diff --git a/src/ontology/reports/doid-subClasses.csv b/src/ontology/reports/doid-subClasses.csv
new file mode 100644
index 0000000..9cc9e46
--- /dev/null
+++ b/src/ontology/reports/doid-subClasses.csv
@@ -0,0 +1,42909 @@
+baseClass,baseLabel,superClass,superLabel
+HP:0003887,Abnormality of the humeral heads,HP:0003063,Abnormality of the humerus
+NCBITaxon:147537,Saccharomycotina,NCBITaxon:716545,saccharomyceta
+DOID:3047,Wissler's syndrome,DOID:225,syndrome
+DOID:11189,pulp degeneration,DOID:5330,dental pulp disease
+UBERON:0001287,proximal convoluted tubule,UBERON:0012275,meso-epithelium
+HP:0010851,EEG with burst suppression,HP:0011198,EEG with generalized epileptiform discharges
+HP:0007545,Congenital palmoplantar keratosis,HP:0000972,Palmoplantar hyperkeratosis
+HP:0005103,Cartilaginous ossification of pinnae,HP:0010766,Ectopic calcification
+UBERON:0016398,lymph node of lower limb,UBERON:0000029,lymph node
+UBERON:2000223,infraorbital 1,UBERON:2000376,infraorbital
+UBERON:0002826,inferior part of vestibular ganglion,UBERON:0000064,organ part
+HP:0002390,Spinal arteriovenous malformation,HP:0002143,Abnormality of the spinal cord
+CL:0000500,follicular epithelial cell,CL:0002371,somatic cell
+HP:0007486,Cavernous hemangioma of the face,HP:0001048,Cavernous hemangioma
+UBERON:0011949,endometrium luminal epithelium,UBERON:0014404,female anatomical structure
+HP:0009230,Osteolytic defects of the proximal phalanx of the 5th finger,HP:0004216,Osteolytic defects of the phalanges of the 5th finger
+CL:0000487,oenocyte,CL:0000151,secretory cell
+UBERON:0014851,chorda tendinea of left ventricle,UBERON:0005994,chordae tendineae
+CL:0002093,secondary polar body,CL:0002090,polar body
+UBERON:0001468,intervertebral joint,UBERON:0004120,mesoderm-derived structure
+HP:0002211,White forelock,HP:0011365,Patchy hypopigmentation of hair
+HP:0004405,Prominent nipples,HP:0004404,Abnormality of the nipple
+HP:0003149,Hyperuricosuria,HP:0003110,Abnormality of urine homeostasis
+HP:0003108,Hyperglycinuria,HP:0010895,Abnormality of glycine metabolism
+UBERON:0003372,pectoral appendage bud ectoderm,UBERON:0010371,ecto-epithelium
+DOID:8354,C3 deficiency,DOID:626,complement deficiency
+UBERON:2001170,vertebral element 4,UBERON:0010913,vertebral element
+HP:0004231,Carpal bone aplasia,HP:0006502,Aplasia/Hypoplasia involving the carpal bones
+HP:0000863,Central diabetes insipidus,HP:0000873,Diabetes insipidus
+DOID:2462,retinal vascular disease,DOID:5679,retinal disease
+UBERON:0004590,sphincter muscle,UBERON:0001630,muscle organ
+UBERON:0015224,interventricular foramen intermedium,UBERON:0004111,anatomical conduit
+HP:0012681,Abnormality of pineal morphology,HP:0012680,Abnormality of the pineal gland
+UBERON:0006305,tunica vasculosa lentis,UBERON:0002050,embryonic structure
+UBERON:0001529,brachiocephalic artery,UBERON:0004573,systemic artery
+HP:0100648,Neoplasm of the tongue,HP:0000157,Abnormality of the tongue
+UBERON:3000451,posterior ramus of pterygoid,UBERON:0010313,neural crest-derived structure
+DOID:0050896,bone squamous cell carcinoma,DOID:2762,bone carcinoma
+DOID:14773,cartilage-hair hypoplasia,DOID:0050737,autosomal recessive disease
+UBERON:0005644,midgut duodenum epithelium,UBERON:0008346,duodenal epithelium
+DOID:11203,Angelucci's syndrome,DOID:11204,allergic conjunctivitis
+HP:0100492,Joint contractures involving the joints of the feet,HP:0100491,Abnormality of the joints of the lower limbs
+UBERON:0010393,T cell domain,UBERON:0010394,lymphocyte domain
+UBERON:0008907,dermal bone,UBERON:0007842,membrane bone
+DOID:6278,ovarian mucinous malignant adenofibroma,DOID:6067,ovarian mucinous neoplasm
+HP:0100630,Neoplasia of the nasopharynx,HP:0100606,Neoplasm of the respiratory system
+HP:0009844,Broad middle phalanx of finger,HP:0009833,Abnormality of the middle phalanges of the hand
+HP:0008598,Mild conductive hearing impairment,HP:0012712,Mild hearing impairment
+UBERON:0013605,layer of lateral geniculate body,UBERON:0000064,organ part
+HP:0006607,Precocious costochondral ossification,HP:0000919,Abnormality of the costochondral junction
+UBERON:0013423,jugal point,UBERON:0006983,anatomical point
+UBERON:2002267,epineural 5,UBERON:2000507,epineural
+HP:0011673,Cardiac hemangioma,HP:0100544,Neoplasm of the heart
+HP:0001377,Limited elbow extension,HP:0001376,Limitation of joint mobility
+HP:0002624,Venous abnormality,HP:0002597,Abnormality of the vasculature
+HP:0009948,Duplication of the distal phalanx of the 2nd finger,HP:0009542,Abnormality of the distal phalanx of the 2nd finger
+UBERON:3010830,spicule,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004534,right testis,UBERON:0015212,lateral structure
+HP:0003860,Diaphyseal sclerosis of the upper limbs,HP:0009808,Anomaly of the upper limb diaphyses
+HP:0009547,Broad phalanges of the 2nd finger,HP:0009541,Abnormality of the phalanges of the 2nd finger
+DOID:625,transient hypogammaglobulinemia,DOID:2583,agammaglobulinemia
+HP:0006921,Axial muscle stiffness,HP:0003552,Muscle stiffness
+DOID:4717,extragonadal germ cell cancer,DOID:2994,germ cell cancer
+UBERON:0004849,respiratory system venous endothelium,UBERON:0001919,endothelium of vein
+HP:0011751,Abnormality of the posterior pituitary,HP:0012503,Abnormality of the pituitary gland
+HP:0100182,Cone-shaped epiphysis of the middle phalanx of the 4th toe,HP:0100068,Cone-shaped epiphyses of the 4th toe
+UBERON:0004915,sphincter of hepatopancreatic ampulla,UBERON:0011185,gastrointestinal sphincter
+HP:0012632,Abnormal intraocular pressure,HP:0012373,Abnormal eye physiology
+HP:0011909,Flattened metacarpal heads,HP:0005916,Abnormal metacarpal morphology
+HP:0001371,Flexion contracture,HP:0011729,Abnormality of joint mobility
+HP:0100746,Macrodactyly of finger,HP:0004099,Macrodactyly
+HP:0010210,Triangular shaped proximal phalanges of the toes,HP:0010184,Abnormality of the proximal phalanges of the toes
+HP:0000762,Decreased nerve conduction velocity,HP:0001311,Abnormal nervous system electrophysiology
+HP:0100165,Small epiphysis of the proximal phalanx of the 3rd toe,HP:0100063,Small epiphyses of the 3rd toe
+UBERON:0001538,posterior tibial artery,UBERON:0007610,tibial artery
+HP:0100073,Pseudoepiphyses of the 4th toe,HP:0010335,Abnormality of the epiphyses of the 4th toe
+HP:0100457,Osteolytic defects of the proximal phalanx of the 5th toe,HP:0010387,Osteolytic defects of the phalanges of the 5th toe
+UBERON:0001224,renal pelvis,UBERON:0004120,mesoderm-derived structure
+HP:0100934,Sclerosis of the proximal phalanx of the 5th toe,HP:0100929,Sclerosis of the phalanges of the 5th toe
+HP:0005274,Prominent nasal tip,HP:0000436,Abnormality of the nasal tip
+UBERON:4200019,preacetabular process,UBERON:0004530,bony projection
+UBERON:2001364,hemal spine,UBERON:0004120,mesoderm-derived structure
+CL:0000986,IgM plasma cell,CL:0000974,long lived plasma cell
+DOID:270,liver sarcoma,DOID:3571,liver cancer
+HP:0011318,Bicoronal synostosis,HP:0004440,Coronal craniosynostosis
+UBERON:0001616,maxillary artery,UBERON:0001637,artery
+UBERON:0005602,dorsal mesogastrium,UBERON:0002050,embryonic structure
+HP:0010679,Elevated tissue non-specific alkaline phosphatase,HP:0003155,Elevated alkaline phosphatase
+UBERON:0013707,iliac spine,UBERON:0013706,bone spine
+HP:0009286,Curved distal phalanx of the 4th finger,HP:0009285,Curved phalanges of the 4th finger
+UBERON:0004268,lower arm connective tissue,UBERON:0003573,arm connective tissue
+HP:0007319,Morphological abnormality of the central nervous system,HP:0002011,Abnormality of the central nervous system
+UBERON:2001193,supraneural 8 bone,UBERON:2000442,supraneural bone
+UBERON:3000941,arciferal girdle,UBERON:0007831,pectoral girdle skeleton
+UBERON:0002290,choroid plexus of fourth ventricle,UBERON:0001886,choroid plexus
+HP:0009062,Infantile axial hypotonia,HP:0008936,Muscular hypotonia of the trunk
+UBERON:3000581,sulcus dentalis of maxilla,UBERON:0000464,anatomical space
+DOID:6201,pericardial mesothelioma,DOID:116,pericardium cancer
+HP:0002088,Abnormality of the lung,HP:0012252,Abnormal respiratory system morphology
+UBERON:0014481,sex skin,UBERON:0000014,zone of skin
+HP:0002862,Bladder carcinoma,HP:0009725,Bladder neoplasm
+UBERON:0014670,distal interphalangeal joint of manual digit 4,UBERON:0014679,distal interphalangeal joint of digit 4
+UBERON:0004265,outflow tract myocardium,UBERON:0002349,myocardium
+DOID:6970,acute inflammation of lacrimal passage,DOID:1400,lacrimal apparatus disease
+UBERON:0002937,parvicellular part of ventral anterior nucleus,UBERON:0003528,brain grey matter
+CL:0000148,melanocyte,CL:0000710,neurecto-epithelial cell
+NCBITaxon:43787,Psychodomorpha,NCBITaxon:7148,Nematocera
+HP:0012553,Hypoplastic thumbnail,HP:0001804,Hypoplastic fingernail
+UBERON:0007687,kidney field,UBERON:0005423,developing anatomical structure
+HP:0007924,Slow decrease in visual acuity,HP:0000529,Progressive visual loss
+UBERON:0005426,lens vesicle,UBERON:0004121,ectoderm-derived structure
+HP:0006060,Tombstone-shaped proximal phalanges,HP:0009834,Abnormality of the proximal phalanges of the hand
+HP:0004338,Abnormality of aromatic amino acid family metabolism,HP:0004337,Abnormality of amino acid metabolism
+HP:0010981,Hypolipoproteinemia,HP:0010979,Abnormality of the level of lipoprotein cholesterol
+UBERON:0011377,femorothoracic muscle,UBERON:0008242,lower back muscle
+CL:1000182,malpighian tubule tip cell,CL:0000423,tip cell
+UBERON:0003535,vagus X nerve trunk,UBERON:0002464,nerve trunk
+DOID:205,hyperostosis,DOID:0080005,bone remodeling disease
+HP:0010199,Patchy sclerosis of the middle phalanges of the toes,HP:0100947,Sclerosis of the middle phalanges of the toes
+UBERON:0011095,vertebra pre-cartilage condensation,UBERON:0015005,vertebra endochondral element
+HP:0003400,Basal lamina 'onion bulb' formation,HP:0003383,Onion bulb formation
+HP:0100402,Duplication of the middle phalanx of the 4th toe,HP:0010379,Duplication of phalanx of the 4th toe
+UBERON:2201614,anal fin middle radial cartilage,UBERON:2201671,anal fin radial cartilage
+DOID:13487,childhood disintegrative disease,DOID:0060040,pervasive developmental disorder
+HP:0003138,Increased blood urea nitrogen (BUN),HP:0002157,Azotemia
+UBERON:2000856,somite 28,UBERON:0002329,somite
+UBERON:2001388,epithelial mesenchymal boundary of regenerating fin/limb,UBERON:0012437,epithelial-mesenchymal boundary
+UBERON:0013592,presylvian sulcus,UBERON:0008334,subarachnoid sulcus
+UBERON:0016403,thoracic wall,UBERON:0000060,anatomical wall
+UBERON:0001587,subclavian vein,UBERON:0001638,vein
+HP:0005638,Decreased anterioposterior diameter of lumbar vertebral bodies,HP:0008473,Narrow anterio-posterior vertebral body diameter
+HP:0000559,Corneal scarring,HP:0007957,Corneal opacity
+DOID:14026,folic acid deficiency anemia,DOID:5113,nutritional deficiency disease
+DOID:649,prion disease,DOID:936,brain disease
+DOID:11793,phthisical cornea,DOID:1237,corneal degeneration
+HP:0006772,Renal angiomyolipoma,HP:0008696,Renal hamartoma
+UBERON:2001280,branchiostegal ray 3,UBERON:2000476,branchiostegal ray
+CL:0000498,inhibitory interneuron,CL:0000099,interneuron
+DOID:0050840,cervical dystonia,DOID:0050836,focal dystonia
+UBERON:0002044,ventral nucleus of posterior commissure,UBERON:0007414,nucleus of midbrain tegmentum
+UBERON:0006448,first lumbar spinal cord segment,UBERON:0007716,lumbar subsegment of spinal cord
+NCBITaxon:42862,Rickettsia felis,NCBITaxon:114277,spotted fever group
+UBERON:0004355,podocyte foot process,UBERON:0006554,urinary system structure
+UBERON:0013153,arachnoid villus,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010154,Irregular epiphysis of the 1st metatarsal,HP:0010118,Irregular epiphyses of the hallux
+UBERON:0001338,urethral gland,UBERON:0002365,exocrine gland
+HP:0005466,Frontal bone hypoplasia,HP:0011218,Abnormal shape of the frontal region
+UBERON:0014759,entopallium,UBERON:0002791,regional part of telencephalon
+UBERON:0002622,preoptic periventricular nucleus,UBERON:0007251,preoptic nucleus
+UBERON:0002592,juxtarestiform body,UBERON:0014649,white matter of medulla oblongata
+DOID:4540,dysgraphia,DOID:0060047,writing disorder
+DOID:3925,steroid lipomatosis,DOID:3153,lipomatosis
+HP:0009614,Bifid proximal phalanx of the thumb,HP:0009613,Duplication of the proximal phalanx of the thumb
+HP:0009658,Aplasia/Hypoplasia of the phalanges of the thumb,HP:0009602,Abnormality of the phalanges of the thumb
+HP:0010204,Broad proximal phalanges of the toes,HP:0010174,Broad phalanx of the toes
+UBERON:2001547,abdominal scute,UBERON:2002294,fish scute
+HP:0009393,Absent epiphyses of the 4th finger,HP:0009174,Abnormality of the epiphyses of the 4th finger
+UBERON:0014613,cervical spinal cord gray matter,UBERON:0002315,gray matter of spinal cord
+HP:0009153,Abnormality of the epiphysis of the proximal phalanx of the 5th finger,HP:0009150,Abnormality of the proximal phalanx of the 5th finger
+UBERON:2005226,median fin proximal radial bone,UBERON:2105226,median fin proximal radial element
+HP:0010469,Aplasia of the testes,HP:0010468,Aplasia/Hypoplasia of the testes
+DOID:9406,hypopituitarism,DOID:53,pituitary gland disease
+DOID:7480,large cell carcinoma with rhabdoid phenotype,DOID:4556,lung large cell carcinoma
+UBERON:0011856,acinus of lactiferous gland,UBERON:0011858,acinus of exocrine gland
+UBERON:0007275,crista of ampulla of posterior semicircular duct of membranous laybrinth,UBERON:0006935,crista ampullaris neuroepithelium
+UBERON:4440010,pelvic fin radial skeleton,UBERON:4300013,paired fin radial skeleton
+HP:0012300,Ureteral agenesis,HP:0000069,Abnormality of the ureter
+UBERON:0004724,medial palpebral ligament,UBERON:0003581,eyelid connective tissue
+HP:0100709,Reduction of oligodendroglia,HP:0100706,Abnormality of the oligodendroglia
+DOID:9848,endolymphatic hydrops,DOID:9847,peripheral vertigo
+HP:0009788,Quadriceps aplasia,HP:0100854,Aplasia of the musculature
+UBERON:0014858,post-larval stage,UBERON:0000069,larval stage
+CL:0000985,IgG plasma cell,CL:0000974,long lived plasma cell
+CL:0000710,neurecto-epithelial cell,CL:0000075,columnar/cuboidal epithelial cell
+HP:0005112,Dilatation of the abdominal aorta,HP:0001724,Aortic dilatation
+HP:0009202,Fragmentation of the epiphysis of the proximal phalanx of the 5th finger,HP:0009153,Abnormality of the epiphysis of the proximal phalanx of the 5th finger
+HP:0009348,Cone-shaped epiphysis of the proximal phalanx of the 3rd finger,HP:0009333,Abnormality of the epiphysis of the proximal phalanx of the 3rd finger
+UBERON:0013559,Brodmann (1909) area 28,UBERON:0013529,Brodmann area
+DOID:5172,endometrium carcinoma in situ,DOID:8719,in situ carcinoma
+UBERON:0001195,inferior pancreaticoduodenal artery,UBERON:0004573,systemic artery
+HP:0006234,Osteolysis involving tarsal bones,HP:0009134,Osteolysis involving bones of the feet
+UBERON:0007124,pharyngeal pouch 3,UBERON:0004117,pharyngeal pouch
+CL:1000287,myocyte of anterior internodal tract,CL:0002096,internodal tract myocyte
+HP:0100575,Neoplasm of the gallbladder,HP:0012437,Abnormal gallbladder morphology
+DOID:9905,follicular mucinosis,DOID:9098,sebaceous gland disease
+HP:0002552,Trichodysplasia,HP:0001595,Abnormality of the hair
+HP:0010272,Fragmentation of the epiphyses of the proximal phalanges of the hand,HP:0010245,Abnormality of the epiphyses of the proximal phalanges of the hand
+HP:0008057,Aplasia/Hypoplasia affecting the fundus,HP:0001098,Abnormality of the fundus
+UBERON:0011675,perichordal ring,UBERON:0004121,ectoderm-derived structure
+UBERON:0002071,stratum lucidum of epidermis,UBERON:0004121,ectoderm-derived structure
+CL:0000424,excretory cell,CL:0000151,secretory cell
+UBERON:0003106,urostyle,UBERON:0002513,endochondral bone
+UBERON:0002363,dura mater,UBERON:0004120,mesoderm-derived structure
+HP:0012178,Reduced natural killer cell activity,HP:0012177,Abnormal natural killer cell physiology
+HP:0100488,Symphalangism of the proximal phalanx of the hallux with the 1st metatarsal,HP:0010091,Symphalangism affecting the proximal phalanx of the hallux
+DOID:13676,posterior scleritis,DOID:13452,scleritis
+DOID:11086,chorioretinal scar,DOID:5679,retinal disease
+HP:0100759,Clubbing of fingers,HP:0001217,Clubbing
+HP:0005264,Abnormality of the gallbladder,HP:0004297,Abnormality of the biliary system
+HP:0011690,Permanent junctional reciprocating tachycardia,HP:0011689,Supraventricular tachycardia with a concealed accessory connection
+UBERON:0006206,iridocorneal angle,UBERON:0000015,anatomical boundary
+UBERON:0002920,callosal sulcus,UBERON:0008334,subarachnoid sulcus
+UBERON:0003395,mesentery of rectum,UBERON:0004854,gastrointestinal system mesentery
+HP:0008519,Abnormality of the coccyx,HP:0000925,Abnormality of the vertebral column
+HP:0010989,Abnormality of the intrinsic pathway,HP:0003256,Abnormality of the coagulation cascade
+UBERON:0002111,artery smooth muscle tissue,UBERON:0004237,blood vessel smooth muscle
+DOID:4303,sarcomatoid basal cell carcinoma,DOID:2513,basal cell carcinoma
+UBERON:0012273,periampullary region of duodenum,UBERON:0004921,subdivision of digestive tract
+UBERON:3000292,medial ramus of pterygoid,UBERON:0010313,neural crest-derived structure
+DOID:3618,epidural neoplasm,DOID:5612,spinal cancer
+UBERON:4100008,pedal claws,UBERON:0009564,distal limb integumentary appendage
+HP:0006067,Multiple carpal ossification centers,HP:0006257,Abnormality of carpal bone ossification
+HP:0002244,Abnormality of the small intestine,HP:0002242,Abnormality of the intestine
+UBERON:0002077,cortex of hair,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0004150,Abnormality of the 3rd finger,HP:0001167,Abnormality of finger
+DOID:5344,testicular yolk sac tumor,DOID:5345,testicular non-seminomatous germ cell cancer
+DOID:3246,embryonal rhabdomyosarcoma,DOID:3247,rhabdomyosarcoma
+UBERON:0011810,collection of feathers,UBERON:0000477,anatomical cluster
+UBERON:0011818,superficial fascia,UBERON:0000479,tissue
+UBERON:0001362,perineal vein,UBERON:0001638,vein
+CL:0000043,mature basophil,CL:0000767,basophil
+UBERON:0008586,tensor veli palatini,UBERON:0015212,lateral structure
+NCBITaxon:52769,Actinomyces gerencseriae,NCBITaxon:1654,Actinomyces
+DOID:2634,cystadenoma,DOID:657,adenoma
+HP:0002656,Epiphyseal dysplasia,HP:0002652,Skeletal dysplasia
+DOID:13507,trigonitis,DOID:1679,cystitis
+DOID:8688,tonsillar pillar cancer,DOID:8557,oropharynx cancer
+DOID:5507,clear cell ependymoma,DOID:4844,benign ependymoma
+CL:0000116,pioneer neuron,CL:0000540,neuron
+HP:0009413,Enlarged epiphyses of the 3rd finger,HP:0009320,Abnormality of the epiphyses of the 3rd finger
+NCBITaxon:766,Rickettsiales,NCBITaxon:28211,Alphaproteobacteria
+UBERON:0010337,mandibular process mesenchyme from head mesenchyme,UBERON:0006905,mandibular process mesenchyme
+UBERON:4300023,interolateral plate,UBERON:0008907,dermal bone
+HP:0100116,Irregular epiphysis of the middle phalanx of the 2nd toe,HP:0100089,Abnormality of the epiphysis of the middle phalanx of the 2nd toe
+UBERON:0008573,lateral crico-arytenoid,UBERON:0010932,crico-arytenoid muscle
+HP:0008002,Abnormality of macular pigmentation,HP:0001103,Abnormality of the macula
+UBERON:0015100,distal tarsal cartilage,UBERON:0010885,hindlimb cartilage element
+UBERON:0001528,radio-ulnar joint,UBERON:0003839,forelimb joint
+UBERON:0004355,podocyte foot process,UBERON:0004120,mesoderm-derived structure
+DOID:11934,head and neck cancer,DOID:0050686,organ system cancer
+UBERON:0001883,olfactory tubercle,UBERON:0004732,segmental subdivision of nervous system
+HP:0009990,Duplication of the proximal phalanx of the 5th finger,HP:0009150,Abnormality of the proximal phalanx of the 5th finger
+HP:0100370,Aplasia/Hypoplasia of the distal phalanx of the 4th toe,HP:0010185,Aplasia/Hypoplasia of the distal phalanges of the toes
+HP:0100647,Graves disease,HP:0011784,Thyrotoxicosis with diffuse goiter
+DOID:5307,urethra clear cell adenocarcinoma,DOID:4910,urethra adenocarcinoma
+HP:0004499,Chronic rhinitis due to narrow nasal airway,HP:0002257,Chronic rhinitis
+UBERON:0001726,papilla of tongue,UBERON:0000064,organ part
+UBERON:0003429,abdomen nerve,UBERON:0003825,nerve of abdominal segment
+DOID:3565,meningioma,DOID:3620,central nervous system cancer
+UBERON:0002322,periventricular nucleus,UBERON:0002308,nucleus of brain
+UBERON:2002044,anterior limb of parapophysis 4,UBERON:0004530,bony projection
+HP:0006694,Early progressive calcific cardiac valvular disease,HP:0005146,Cardiac valve calcification
+CL:0000960,T3 B cell,CL:0000818,transitional stage B cell
+UBERON:0010032,anterior part of tongue,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0009984,medial condyle of femur,UBERON:0009980,condyle of femur
+HP:0100363,Aplasia of the phalanges of the 4th toe,HP:0010371,Aplasia/Hypoplasia of the phalanges of the 4th toe
+CL:0000753,type 1 cone bipolar cell (sensu Mus),CL:0000750,OFF-bipolar cell
+UBERON:3000628,ventral ramus of squamosal,UBERON:0004120,mesoderm-derived structure
+DOID:13186,megaesophagus,DOID:6050,esophageal disease
+HP:0003982,Absent ulna,HP:0009822,Aplasia involving forearm bones
+UBERON:3010624,subarticular sesamoid,UBERON:0012357,digitopodium bone
+UBERON:0014634,ventral nerve root of cervical spinal cord,UBERON:0002260,ventral root of spinal cord
+UBERON:0002869,diffuse reticular nucleus,UBERON:0002680,regional part of metencephalon
+DOID:12084,transient arthropathy,DOID:2092,transient arthritis
+UBERON:0011598,coronoid bone,UBERON:0004768,bone of lower jaw
+HP:0008823,Hypoplastic inferior pubic rami,HP:0003173,Hypoplastic pubic bones
+DOID:8541,Sezary's disease,DOID:0060061,cutaneous T cell lymphoma
+HP:0012519,Hypoplastic posterior communicating artery,HP:0012518,Abnormality of circle of Willis
+HP:0000572,Visual loss,HP:0000505,Visual impairment
+DOID:12689,acoustic neuroma,DOID:3192,neurilemmoma
+UBERON:2002050,Schreckstoff,UBERON:0000470,cell part
+HP:0100851,Abnormal emotion/affect behavior,HP:0000708,Behavioural/Psychiatric Abnormality
+UBERON:2002108,buccal papilla,UBERON:0004121,ectoderm-derived structure
+NCBITaxon:169455,Coelopellini,NCBITaxon:169449,Coelopinae
+UBERON:0004368,Reichert's cartilage,UBERON:0005291,embryonic tissue
+HP:0010064,Symphalangism affecting the phalanges of the hallux,HP:0010057,Abnormality of the phalanges of the hallux
+UBERON:0005081,ureter ureteric bud,UBERON:0000084,ureteric bud
+UBERON:0014524,electromotor division of oculomotor nuclear complex,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:3004,breast myoepithelial neoplasm,DOID:1612,breast cancer
+UBERON:0011804,"feather bud, epidermal component",UBERON:0005153,epithelial bud
+UBERON:0001429,pisiform,UBERON:0007997,sesamoid bone of manus
+DOID:10205,axillary lipoma,DOID:0060097,thoracic benign neoplasm
+HP:0012445,Morphological abnormality of the pyramidal tracts,HP:0002062,Abnormality of the pyramidal tracts
+HP:0002265,Large fleshy ears,HP:0000400,Macrotia
+UBERON:4000070,elasmoid scale,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009983,Partial duplication of the proximal phalanx of the 4th finger,HP:0009974,Partial duplication of the phalanges of the 4th finger
+CL:0002638,bronchioalveolar stem cell,CL:1000351,basal cell of epithelium of respiratory bronchiole
+HP:0000567,Chorioretinal coloboma,HP:0000611,Choroid coloboma
+HP:0007670,Abnormal vestibulo-ocular reflex,HP:0001751,Vestibular dysfunction
+UBERON:0003325,mesenchyme of pinna,UBERON:0003104,mesenchyme
+HP:0011465,Duodenal aganglionosis,HP:0011464,Aganglionosis of the small intestine
+DOID:4371,Schnitzler syndrome,DOID:2916,hypersensitivity reaction type IV disease
+DOID:7927,malignant type A thymoma,DOID:3279,spindle cell thymoma
+UBERON:2001349,stratum opticum,UBERON:0004121,ectoderm-derived structure
+DOID:13295,crater-like holes of optic disc,DOID:1393,visual pathway disease
+UBERON:3010815,m. flexor indicis superficialis proprius,UBERON:0001630,muscle organ
+HP:0005639,Hyperextensible hand joints,HP:0001382,Joint hypermobility
+HP:0008438,Vertebral arch anomaly,HP:0003312,Abnormal form of the vertebral bodies
+DOID:5505,papillary ependymoma,DOID:4844,benign ependymoma
+DOID:663,scrotal angioma,DOID:471,skin hemangioma
+HP:0003468,Abnormality of the vertebrae,HP:0000925,Abnormality of the vertebral column
+HP:0000474,Thickened nuchal skin fold,HP:0000464,Abnormality of the neck
+HP:0006710,Aplasia/Hypoplasia of the clavicles,HP:0006711,Aplasia/Hypoplasia involving bones of the thorax
+DOID:8484,maple bark strippers' lung,DOID:2473,opportunistic mycosis
+HP:0003361,Tryptophanuria,HP:0004365,Abnormality of tryptophan metabolism
+HP:0001931,Hypochromic anemia,HP:0010972,Anemia of inadequate production
+UBERON:0004790,skin mucous gland,UBERON:0000414,mucous gland
+CL:1000453,epithelial cell of intermediate tubule,CL:1000909,kidney loop of henle epithelial cell
+DOID:12055,sarcoid meningitis,DOID:9471,meningitis
+UBERON:0013613,tooth cingulum,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:7266,familiar fallopian tube carcinoma,DOID:1963,fallopian tube carcinoma
+UBERON:0009590,mesenchyme of interdigital region between pedal digits 1 and 2,UBERON:0009596,mesenchyme of interdigital region between digits 1 and 2
+UBERON:0004613,mammalian cervical vertebra 4,UBERON:0002413,cervical vertebra
+DOID:0060153,topographical agnosia,DOID:0060155,visual agnosia
+CL:0000675,female gamete,CL:0000300,gamete
+UBERON:0011206,hinge joint,UBERON:0000982,skeletal joint
+UBERON:0006794,visual processing part of nervous system,UBERON:0011216,organ system subdivision
+UBERON:2002161,ural centrum 4,UBERON:2002085,ural centrum
+UBERON:0005841,cervical spinal cord dorsal column,UBERON:0006079,subdivision of spinal cord dorsal column
+HP:0100544,Neoplasm of the heart,HP:0011793,Neoplasm by anatomical site
+HP:0006315,Single median maxillary incisor,HP:0011064,Abnormal number of incisors
+UBERON:0014694,posterior auricular artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+CL:1001005,glomerular capillary endothelial cell,CL:0002188,glomerular endothelial cell
+DOID:12680,pseudobulbar palsy,DOID:936,brain disease
+UBERON:0009675,facial VII nerve chorda tympani branch,UBERON:0001647,facial nerve
+HP:0001722,High-output congestive heart failure,HP:0001635,Congestive heart failure
+UBERON:4200177,supracondyle tubercle,UBERON:4100000,skeletal element projection
+HP:0000732,Inflexible adherence to routines or rituals,HP:0100851,Abnormal emotion/affect behavior
+UBERON:0012246,thyroid follicular lumen,UBERON:0000464,anatomical space
+HP:0002804,Arthrogryposis multiplex congenita,HP:0002803,Congenital contracture
+UBERON:0010264,hepatopancreas,UBERON:0003408,gland of gut
+DOID:3261,Job's syndrome,DOID:2959,hyperimmunoglobulin syndrome
+HP:0007885,Slowed horizontal saccades,HP:0000514,Slow saccadic eye movements
+UBERON:0010750,prefrontal bone,UBERON:0003462,facial bone
+HP:0000480,Retinal coloboma,HP:0000479,Abnormality of the retina
+DOID:2678,adult mesoblastic nephroma,DOID:154,mixed cell type cancer
+UBERON:0001253,lamina propria of ureter,UBERON:0006554,urinary system structure
+UBERON:0007152,inferior sagittal sinus,UBERON:0003499,brain blood vessel
+HP:0009330,Stippling of the epiphysis of the middle phalanx of the 3rd finger,HP:0009334,Abnormality of the epiphysis of the middle phalanx of the 3rd finger
+UBERON:2001805,articular bone,UBERON:0002513,endochondral bone
+HP:0009662,Abnormality of the epiphysis of the distal phalanx of the thumb,HP:0010243,Abnormality of the epiphyses of the distal phalanx of finger
+HP:0100842,Septo-optic dysplasia,HP:0000609,Optic nerve hypoplasia
+HP:0001285,Spastic tetraparesis,HP:0001257,Spasticity
+HP:0012120,Methylmalonic aciduria,HP:0003215,Dicarboxylic aciduria
+CL:0000706,choroid plexus epithelial cell,CL:0000627,transporting cell
+UBERON:0002289,midbrain cerebral aqueduct,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100181,Bracket epiphysis of the middle phalanx of the 4th toe,HP:0100095,Abnormality of the epiphysis of the middle phalanx of the 4th toe
+HP:0009248,Abnormality of the epiphysis of the proximal phalanx of the 4th finger,HP:0009284,Abnormality of the proximal phalanx of the 4th finger
+HP:0009300,Aplasia/Hypoplasia of the proximal phalanx of the 4th finger,HP:0009408,Aplasia/Hypoplasia of the phalanges of the 4th finger
+DOID:2962,Cockayne syndrome,DOID:37,skin disease
+HP:0004324,Increased body weight,HP:0004323,Abnormality of body weight
+UBERON:2001653,pharyngobranchial 3 tooth,UBERON:0001091,calcareous tooth
+DOID:0050678,Blau syndrome,DOID:0050736,autosomal dominant disease
+DOID:13060,traumatic glaucoma,DOID:1686,glaucoma
+CL:0000645,pituicyte,CL:0000127,astrocyte
+UBERON:0013181,blowhole ligament,UBERON:0008845,nonskeletal ligament
+UBERON:2000587,sphenotic,UBERON:0011164,neurocranium bone
+HP:0007827,Nodular corneal dystrophy,HP:0011494,Generalized opacification of the cornea
+UBERON:0004325,middle phalanx of pedal digit 3,UBERON:0003642,pedal digit 3 phalanx
+UBERON:0006645,adventitia of epididymis,UBERON:0014403,male anatomical structure
+HP:0012052,"Low serum calcitriol (1,25-dihydroxycholecalciferol)",HP:0100511,Abnormality of vitamin D metabolism
+UBERON:0005818,cephalic flexure,UBERON:0005817,neuraxis flexure
+HP:0004001,Medially deficient radial epiphyses,HP:0003999,Abnormality of radial epiphyses
+UBERON:0008591,depressor supercilii,UBERON:0001577,facial nerve muscle
+UBERON:0005562,thymus primordium,UBERON:0003351,pharyngeal epithelium
+UBERON:0001946,inferior colliculus,UBERON:0015212,lateral structure
+HP:0009397,Fragmentation of the epiphyses of the 4th finger,HP:0009174,Abnormality of the epiphyses of the 4th finger
+DOID:4829,adenosquamous cell lung carcinoma,DOID:3908,non-small cell lung carcinoma
+UBERON:2000901,hypaxial region somite 7,UBERON:0003895,hypaxial myotome region
+DOID:6494,pediatric myxoid chondrosarcoma,DOID:5861,myxoid chondrosarcoma
+DOID:8221,upper clivus meningioma,DOID:6517,clivus meningioma
+UBERON:2002003,posterior dentation of dorsal fin spine 2,UBERON:4100000,skeletal element projection
+HP:0100931,Sclerosis of the proximal phalanx of the 2nd toe,HP:0100926,Sclerosis of the phalanges of the 2nd toe
+CL:0000723,somatic stem cell,CL:0002371,somatic cell
+HP:0003204,Intracellular accumulation of autofluorescent lipopigment storage material,HP:0011017,Abnormality of cell physiology
+DOID:12568,dyscalculia,DOID:8927,learning disability
+HP:0009573,Patchy sclerosis of the middle phalanx of the 2nd finger,HP:0100904,Sclerosis of the middle phalanx of the 2nd finger
+UBERON:0002215,synchondrosis,UBERON:0002209,fibrous joint
+HP:0003834,Shoulder dislocation,HP:0003043,Abnormality of the shoulder
+HP:0012510,Extra-axial cerebrospinal fluid accumulation,HP:0002921,Abnormality of the cerebrospinal fluid
+HP:0009023,Abdominal wall muscle weakness,HP:0010991,Abnormality of the abdominal musculature
+CL:1000271,lung ciliated cell,CL:0000064,ciliated cell
+UBERON:0006247,iliac pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+CL:0000945,lymphocyte of B lineage,CL:0000542,lymphocyte
+HP:0007349,Distal motor neuropathy,HP:0002450,Abnormality of the motor neurons
+HP:0007945,Choroidal degeneration,HP:0000610,Abnormality of the choroid
+DOID:0050893,gallbladder adenoma,DOID:0050625,biliary tract neoplasm
+HP:0002475,Meningomyelocele,HP:0002435,Meningocele
+DOID:0050884,triosephosphate isomerase deficiency,DOID:4194,glucose metabolism disease
+HP:0007740,Long eyelashes in irregular rows,HP:0000527,Long eyelashes
+HP:0200022,Choroid plexus papilloma,HP:0100835,Benign neoplasm of the central nervous system
+HP:0002637,Cerebral ischemia,HP:0009145,Abnormality of cerebral artery
+NCBITaxon:1656,Actinomyces viscosus,NCBITaxon:1654,Actinomyces
+UBERON:0002223,endolymphatic sac,UBERON:0006937,inner ear epithelium
+UBERON:4200111,prepelvic fin spine,UBERON:0004529,anatomical projection
+DOID:1930,Laurence-Moon syndrome,DOID:0050737,autosomal recessive disease
+UBERON:0008465,abductor pollicis brevis muscle,UBERON:0001500,muscle of manus
+CL:0002343,decidual natural killer cell,CL:0000824,mature natural killer cell
+UBERON:3010786,pars subvertebralis,UBERON:0008777,hypaxial musclulature
+UBERON:0002877,parasolitary nucleus,UBERON:0007635,nucleus of medulla oblongata
+CL:1000708,ureter adventitial cell,CL:1000601,ureteral cell
+DOID:12972,intrapelvic lymph node leukemic reticuloendotheliosis,DOID:10619,lymph node cancer
+HP:0004919,Galactose intolerance,HP:0004915,Impairment of galactose metabolism
+UBERON:0005607,hyaloid vascular plexus,UBERON:0005629,vascular plexus
+DOID:10393,secondary hypertrophic osteoarthropathy,DOID:381,arthropathy
+UBERON:0002964,dorsal oculomotor nucleus,UBERON:0007414,nucleus of midbrain tegmentum
+UBERON:0000415,artery wall,UBERON:0004120,mesoderm-derived structure
+DOID:9296,cleft lip,DOID:0050567,orofacial cleft
+HP:0012380,Reduced carnitine O-palmitoyltransferase activity,HP:0012379,Abnormal enzyme/coenzyme activity
+UBERON:0013777,skin of palm of manus,UBERON:0013776,skin of palmar/plantar part of autopod
+HP:0007311,Short stepped shuffling gait,HP:0002362,Shuffling gait
+HP:0006166,Tubular metacarpal bones,HP:0005916,Abnormal metacarpal morphology
+HP:0004491,Large posterior fontanelle,HP:0000239,Large fontanelles
+UBERON:0000017,exocrine pancreas,UBERON:0004119,endoderm-derived structure
+UBERON:0006877,vasculature of liver,UBERON:0006876,vasculature of organ
+UBERON:0008594,zygomaticus minor muscle,UBERON:0010437,zygomaticus muscle
+UBERON:0004001,olfactory bulb layer,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:0060022,CD40 ligand deficiency,DOID:628,combined T cell and B cell immunodeficiency
+UBERON:4200020,suprascapular fossa,UBERON:0004704,bone fossa
+DOID:5884,benign intermediate mesothelioma,DOID:2645,benign mesothelioma
+DOID:12342,retroperitoneum carcinoma,DOID:5875,retroperitoneal cancer
+UBERON:0014761,spinal trigeminal tract,UBERON:0007702,tract of brain
+DOID:13138,acute proliferative glomerulonephritis,DOID:2921,glomerulonephritis
+UBERON:0007626,subparaventricular zone,UBERON:0003048,regional part of hypothalamus
+UBERON:2000315,asteriscus,UBERON:0002280,otolith
+HP:0003137,Prolinuria,HP:0010907,Abnormality of proline metabolism
+DOID:3908,non-small cell lung carcinoma,DOID:3905,lung carcinoma
+UBERON:0014950,layer of developing cerebral cortex,UBERON:0005423,developing anatomical structure
+UBERON:0002544,digit,UBERON:0005881,limb outgrowth
+UBERON:0008335,ventrolateral sulcus of medulla oblongata,UBERON:0008334,subarachnoid sulcus
+UBERON:0000920,egg chorion,UBERON:0000478,extraembryonic structure
+DOID:997,uterine inversion,DOID:345,uterine disease
+UBERON:0008880,annelid pygidium,UBERON:0000914,organismal segment
+HP:0100180,Absent epiphysis of the middle phalanx of the 4th toe,HP:0100066,Absent epiphyses of the 4th toe
+UBERON:0010192,genital artery,UBERON:0012254,abdominal aorta artery
+DOID:1967,leiomyosarcoma,DOID:4230,smooth muscle cancer
+HP:0010133,Ivory epiphysis of the proximal phalanx of the hallux,HP:0010119,Ivory epiphyses of the hallux
+DOID:5843,posteroinferior myocardial infarction,DOID:5844,myocardial infarction
+UBERON:0001942,medial habenular nucleus,UBERON:0007692,nucleus of thalamus
+UBERON:0004984,mucosa of seminal vesicle,UBERON:0000344,mucosa
+UBERON:0011048,obturator internus,UBERON:0011043,obturator muscle
+UBERON:0003485,vagina sebaceous gland,UBERON:0001821,sebaceous gland
+HP:0009517,Fragmentation of the epiphysis of the middle phalanx of the 2nd finger,HP:0009500,Abnormality of the epiphysis of the middle phalanx of the 2nd finger
+CL:0002326,luminal epithelial cell of mammary gland,CL:0000069,branched duct epithelial cell
+CL:0002113,B220-low CD38-negative unswitched memory B cell,CL:0002112,B220-positive CD38-negative unswitched memory B cell
+HP:0011484,Posterior synechiae of the anterior chamber,HP:0007833,Anterior chamber synechiae
+HP:0009986,Complete duplication of the phalanges of the 5th finger,HP:0009985,Duplication of phalanx of 5th finger
+UBERON:0006957,submandibular gland primordium epithelium,UBERON:0005291,embryonic tissue
+DOID:5153,atypical neurofibroma,DOID:962,neurofibroma
+UBERON:0007263,intervertebral disk of sixth cervical vertebra,UBERON:0007252,intervertebral disk of cervical vertebra
+UBERON:0005816,posterior tubercle of transverse process of cervical vertebra,UBERON:0004120,mesoderm-derived structure
+HP:0002979,Bowing of the legs,HP:0002814,Abnormality of the lower limb
+HP:0009313,Patchy sclerosis of the proximal phalanx of the 4th finger,HP:0100910,Sclerosis of the proximal phalanx of the 4th finger
+CL:0000666,fenestrated cell,CL:0002371,somatic cell
+HP:0002611,Cholestatic liver disease,HP:0001396,Cholestasis
+HP:0200050,Bracket metacarpal epiphyses,HP:0005913,Abnormality of metacarpal epiphyses
+UBERON:0008923,sublaminar layer S2,UBERON:0009733,sublaminar layers S1 or S2 or S3
+UBERON:0002038,substantia nigra,UBERON:0009661,midbrain nucleus
+DOID:10325,silicosis,DOID:10316,pneumoconiosis
+UBERON:0005625,tubotympanic recess lumen,UBERON:0002553,anatomical cavity
+UBERON:0006854,distal straight tubule postmacula segment,UBERON:0006853,renal cortex tubule
+HP:0001960,Hypokalemic metabolic alkalosis,HP:0001949,Hypokalemic alkalosis
+UBERON:0002785,regional part of lateral hypothalamic region,UBERON:0003048,regional part of hypothalamus
+CL:0000651,mucous neck cell,CL:0000319,mucus secreting cell
+HP:0008482,Asymmetry of spinal facet joints,HP:0003312,Abnormal form of the vertebral bodies
+UBERON:0001826,nasal cavity mucosa,UBERON:0004119,endoderm-derived structure
+UBERON:0006525,left lung alveolar system,UBERON:0004119,endoderm-derived structure
+HP:0012743,Abdominal obesity,HP:0001513,Obesity
+CL:0000644,Bergmann glial cell,CL:0000127,astrocyte
+DOID:7531,anal gland adenocarcinoma,DOID:3447,anus adenocarcinoma
+UBERON:2001378,axial hypoblast,UBERON:0005291,embryonic tissue
+UBERON:0001440,forelimb skeleton,UBERON:0007272,pectoral appendage skeleton
+UBERON:0013518,coccygeal vertebra pre-cartilage condensation,UBERON:0013504,caudal vertebra pre-cartilage condensation
+HP:0100523,Liver abscess,HP:0001392,Abnormality of the liver
+HP:0009242,Osteolytic defects of the distal phalanx of the 5th finger,HP:0009839,Osteolytic defects of the distal phalanges of the hand
+UBERON:0014699,extraembryonic venous system,UBERON:0014701,extraembryonic vascular system
+HP:0100509,Abnormality of vitamin C metabolism,HP:0100508,Abnormality of vitamin metabolism
+CL:0000600,heterokaryon,CL:0000228,multinucleate cell
+HP:0002362,Shuffling gait,HP:0001288,Gait disturbance
+UBERON:0003464,hindlimb bone,UBERON:0015022,hindlimb endochondral element
+DOID:12029,sympathetic ophthalmia,DOID:417,hypersensitivity reaction type II disease
+HP:0002659,Increased susceptibility to fractures,HP:0011843,Abnormality of skeletal physiology
+HP:0003041,Humeroradial synostosis,HP:0100744,Abnormality of the humeroradial joint
+CL:0002667,type 5 otic fibrocyte,CL:0002665,otic fibrocyte
+NCBITaxon:5583,Exophiala,NCBITaxon:82104,mitosporic Herpotrichiellaceae
+UBERON:0015453,subcutaneous lymph node,UBERON:0000029,lymph node
+UBERON:2000993,lateral wall neural rod,UBERON:0004121,ectoderm-derived structure
+UBERON:2001364,hemal spine,UBERON:0002513,endochondral bone
+DOID:9074,systemic lupus erythematosus,DOID:8857,lupus erythematosus
+UBERON:0009961,esophagus smooth muscle longitudinal layer,UBERON:0004120,mesoderm-derived structure
+DOID:0060114,vaginal benign neoplasm,DOID:0060086,female reproductive organ benign neoplasm
+UBERON:0003051,ear vesicle,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:13948,bladder neck obstruction,DOID:365,bladder disease
+DOID:0080037,Worth's syndrome,DOID:205,hyperostosis
+UBERON:4200011,pedal centrale,UBERON:0001447,tarsal bone
+HP:0012011,EEG with occipital focal spike waves,HP:0011197,EEG with focal spike waves
+CL:0000608,zygospore,CL:0000596,sexual spore
+UBERON:2001001,epaxial region somite 13,UBERON:0003900,epaxial myotome region
+HP:0009344,Stippling of the epiphysis of the distal phalanx of the 3rd finger,HP:0009419,Stippling of the epiphyses of the 3rd finger
+DOID:0050132,inflammatory diarrhea,DOID:13250,diarrhea
+DOID:2247,spondylosis,DOID:0080010,bone structure disease
+HP:0007369,Atrophy/Degeneration affecting the cerebrum,HP:0002060,Abnormality of the cerebrum
+HP:0100099,Abnormality of the epiphysis of the proximal phalanx of the 5th toe,HP:0010341,Abnormality of the epiphyses of the 5th toe
+DOID:2682,intracystic papillary adenoma,DOID:2615,papilloma
+DOID:1496,echinococcosis,DOID:883,parasitic helminthiasis infectious disease
+UBERON:0005401,cerebral hemisphere grey matter,UBERON:0011300,gray matter of telencephalon
+CL:0000764,erythroid lineage cell,CL:0000763,myeloid cell
+HP:0011618,Pulmonary situs ambiguus with bilateral morphologic right lungs,HP:0011617,Pulmonary situs ambiguus
+UBERON:3000288,maxillopalatine,UBERON:0008907,dermal bone
+DOID:3777,granuloma annulare,DOID:2723,dermatitis
+DOID:9375,Fuchs' heterochromic uveitis,DOID:225,syndrome
+HP:0000554,Uveitis,HP:0000553,Abnormality of the uvea
+CL:1001016,kidney loop of henle ascending limb epithelial cell,CL:0002305,epithelial cell of distal tubule
+UBERON:0009973,ureterovesical junction,UBERON:0006554,urinary system structure
+HP:0012423,Colonic inertia,HP:0012700,Abnormal large intestine physiology
+UBERON:0006472,Brodmann (1909) area 6,UBERON:0013529,Brodmann area
+HP:0004326,Cachexia,HP:0001824,Weight loss
+HP:0007651,Ectropion of lower eyelids,HP:0000656,Ectropion
+DOID:11541,recurrent corneal erosion,DOID:1237,corneal degeneration
+UBERON:0009495,extrahepatic part of biliary bud,UBERON:0005911,endo-epithelium
+UBERON:0002832,ventral nucleus of trapezoid body,UBERON:0003528,brain grey matter
+CL:0002355,primitive red blood cell,CL:0002417,primitive erythroid lineage cell
+UBERON:0002532,epiblast (generic),UBERON:0002050,embryonic structure
+UBERON:0012129,radial head of humerus,UBERON:0005055,zone of long bone
+CL:0000972,class switched memory B cell,CL:0000787,memory B cell
+HP:0009180,Ulnar deviation of the 5th finger,HP:0009179,Deviation of the 5th finger
+HP:0011387,Enlarged vestibular aqueduct,HP:0011376,Morphological abnormality of the vestibule of the inner ear
+DOID:9471,meningitis,DOID:331,central nervous system disease
+UBERON:0002248,transverse pericardial sinus,UBERON:0010279,pericardial sinus
+UBERON:0004256,hindlimb zeugopod muscle,UBERON:0001383,muscle of leg
+UBERON:0006224,elbow joint primordium,UBERON:0001048,primordium
+UBERON:0002662,medial pes lemniscus,UBERON:0014891,brainstem white matter
+UBERON:0007635,nucleus of medulla oblongata,UBERON:0009662,hindbrain nucleus
+UBERON:0016419,bony part of vertebral arch,UBERON:0005913,zone of bone organ
+HP:0007191,Tropical spastic paraparesis,HP:0002313,Spastic paraparesis
+HP:0010894,Abnormality of serine family amino acid metabolism,HP:0004337,Abnormality of amino acid metabolism
+HP:0001677,Coronary artery disease,HP:0002621,Atherosclerosis
+HP:0000738,Hallucinations,HP:0000708,Behavioural/Psychiatric Abnormality
+UBERON:0010305,region of conjunctiva,UBERON:0004121,ectoderm-derived structure
+HP:0003020,Enlargement of the wrists,HP:0003019,Abnormality of the wrist
+HP:0011046,Agenesis of primary maxillary central incisor,HP:0006293,Agenesis of maxillary central incisor
+UBERON:0008611,scalene muscle,UBERON:0002377,muscle of neck
+UBERON:0003635,pedal digit 5,UBERON:0001466,pedal digit
+DOID:0050433,fatal familial insomnia,DOID:649,prion disease
+UBERON:0003099,cranial neural crest,UBERON:0005291,embryonic tissue
+DOID:8635,uvula cancer,DOID:8578,soft palate cancer
+UBERON:0012118,infraspinatus tendon,UBERON:0000043,tendon
+NCBITaxon:117571,Euteleostomi,NCBITaxon:117570,Teleostomi
+NCBITaxon:7197,Psychodidae,NCBITaxon:41831,Psychodoidea
+UBERON:2102027,pectoral fin proximal radial element 2,UBERON:2101587,pectoral fin proximal radial element
+DOID:5032,pineal gland cancer,DOID:170,endocrine gland cancer
+HP:0010850,EEG with spike-wave complexes,HP:0011198,EEG with generalized epileptiform discharges
+UBERON:0016399,lymph node of upper limb,UBERON:0000029,lymph node
+HP:0009435,Symphalangism of middle phalanx of 3rd finger,HP:0004172,Abnormality of the middle phalanx of the 3rd finger
+UBERON:0001103,diaphragm,UBERON:0003831,respiratory system muscle
+HP:0005063,"Fragmented, irregular epiphyses",HP:0100168,Fragmented epiphyses
+UBERON:0004668,fourth ventricle aperture,UBERON:0004121,ectoderm-derived structure
+DOID:1974,adenosarcoma,DOID:4236,carcinosarcoma
+HP:0003165,Elevated circulating parathyroid hormone (PTH) level,HP:0100530,Abnormality of calcium-phosphate metabolism
+UBERON:0006757,lateral lingual swelling,UBERON:0005423,developing anatomical structure
+DOID:12257,medulloadrenal hyperfunction,DOID:9553,adrenal gland disease
+CL:1000718,kidney inner medulla collecting duct principal cell,CL:1001431,kidney collecting duct principal cell
+UBERON:0008188,tendon of biceps brachii,UBERON:0000043,tendon
+HP:0003259,Elevated serum creatinine,HP:0012100,Abnormal circulating creatinine level
+UBERON:0014764,anatomical line along groove,UBERON:0006800,anatomical line
+UBERON:0001720,cochlear nucleus,UBERON:0002621,regional part of cochlear nuclear complex
+UBERON:0006930,glandular cuboidal epithelium,UBERON:0006799,glandular epithelium
+HP:0011672,Cardiac myxoma,HP:0100544,Neoplasm of the heart
+UBERON:0012138,pedal digit 8,UBERON:0001466,pedal digit
+HP:0009338,Enlarged epiphysis of the distal phalanx of the 3rd finger,HP:0009413,Enlarged epiphyses of the 3rd finger
+DOID:10032,hyperlucent lung,DOID:9675,pulmonary emphysema
+HP:0011729,Abnormality of joint mobility,HP:0001367,Abnormal joint morphology
+HP:0009544,Abnormality of the proximal phalanx of the 2nd finger,HP:0009541,Abnormality of the phalanges of the 2nd finger
+UBERON:2000401,octaval nerve sensory nucleus,UBERON:0007635,nucleus of medulla oblongata
+DOID:5200,urinary tract obstruction,DOID:557,kidney disease
+HP:0009441,Bullet-shaped phalanges of the 3rd finger,HP:0009769,Bullet-shaped phalanges of the hand
+DOID:13250,diarrhea,DOID:77,gastrointestinal system disease
+CL:0002084,Boettcher cell,CL:0002315,supporting cell of cochlea
+UBERON:0010081,future common hepatic duct,UBERON:0005911,endo-epithelium
+UBERON:0007709,superior cerebellar peduncle of pons,UBERON:0002680,regional part of metencephalon
+HP:0005446,Obtuse angle of mandible,HP:0000277,Abnormality of the mandible
+DOID:4656,extraocular retinoblastoma,DOID:768,retinoblastoma
+UBERON:0006678,foramen secundum,UBERON:0004111,anatomical conduit
+UBERON:0007228,vestibular nucleus,UBERON:0000126,cranial nerve nucleus
+UBERON:2101672,dorsal fin radial element,UBERON:0005174,dorsal region organ
+HP:0000221,Furrowed tongue,HP:0000157,Abnormality of the tongue
+UBERON:0010392,B cell domain,UBERON:0010394,lymphocyte domain
+UBERON:0004111,anatomical conduit,UBERON:0000477,anatomical cluster
+HP:0000904,Flaring of rib cage,HP:0000772,Abnormality of the ribs
+HP:0012537,Food intolerance,HP:0001939,Abnormality of metabolism/homeostasis
+HP:0001744,Splenomegaly,HP:0001743,Abnormality of the spleen
+UBERON:0002374,metacarpal bone,UBERON:0003821,metapodium bone
+HP:0010365,Symphalangism affecting the phalanges of the 3rd toe,HP:0100235,Synostosis involving bones of the toes
+UBERON:0003624,manual digit 4,UBERON:0006051,digit 4
+UBERON:0000157,theca interna,UBERON:0014404,female anatomical structure
+HP:0012297,Slender proximal phalanx of finger,HP:0009834,Abnormality of the proximal phalanges of the hand
+UBERON:0013424,lambda,UBERON:0006983,anatomical point
+UBERON:3000651,lamina anterior of maxilla,UBERON:0010313,neural crest-derived structure
+UBERON:0004948,submucosa of left main bronchus,UBERON:0004949,submucosa of main bronchus
+HP:0003679,Pace of progression,HP:0000004,Onset and clinical course
+CL:0000655,secondary oocyte,CL:0000023,oocyte
+UBERON:0001613,occipital artery,UBERON:0001637,artery
+UBERON:0004863,thoracic sympathetic nerve trunk,UBERON:0004295,sympathetic nerve trunk
+DOID:9969,carotenemia,DOID:0060158,acquired metabolic disease
+CL:0000507,endorphin secreting cell,CL:0000167,peptide hormone secreting cell
+UBERON:0004533,left testis,UBERON:0015212,lateral structure
+HP:0010219,Structural foot deformity,HP:0001760,Abnormality of the foot
+UBERON:0016464,dorsum of nose,UBERON:0000064,organ part
+HP:0100804,Ungual fibroma,HP:0100826,Neoplasm of the nail
+HP:0100536,Abnormality of the fascia,HP:0003549,Abnormality of connective tissue
+CL:0000583,alveolar macrophage,CL:1001603,lung macrophage
+UBERON:3000113,crista intermedia,UBERON:0004529,anatomical projection
+HP:0011889,Bleeding with minor or no trauma,HP:0001892,Abnormal bleeding
+UBERON:3000454,postnasal wall,UBERON:0010313,neural crest-derived structure
+UBERON:0000060,anatomical wall,UBERON:0000064,organ part
+HP:0004386,Gastrointestinal inflammation,HP:0012719,Functional abnormality of the gastrointestinal tract
+HP:0100747,Macrodactyly of toe,HP:0004099,Macrodactyly
+UBERON:0002164,tectobulbar tract,UBERON:0002678,regional part of medulla oblongata
+HP:0005982,Reduced phenylalanine hydroxylase activity,HP:0010893,Abnormality of phenylalanine metabolism
+HP:0010211,Duplication of proximal phalanx of toe,HP:0010184,Abnormality of the proximal phalanges of the toes
+UBERON:0013262,remnnant of ductus deferens,UBERON:0014404,female anatomical structure
+HP:0100072,Ivory epiphyses of the 4th toe,HP:0010335,Abnormality of the epiphyses of the 4th toe
+UBERON:0003889,fallopian tube,UBERON:0000025,tube
+HP:0009388,Ivory epiphyses of the 5th finger,HP:0100921,Sclerosis of the phalanges of the 5th finger
+HP:0009615,Complete duplication of the first metacarpal,HP:0010000,Complete duplication of the proximal phalanges of the hand
+HP:0000013,Hypoplasia of the uterus,HP:0008684,Aplasia/hypoplasia of the uterus
+HP:0010474,Bladder stones,HP:0000014,Abnormality of the bladder
+DOID:3331,frontal lobe epilepsy,DOID:2234,focal epilepsy
+UBERON:4000123,odontode tissue,UBERON:0010365,odontoid tissue
+CL:0002418,hemangioblast,CL:0000222,mesodermal cell
+HP:0010810,Long uvula,HP:0000172,Abnormality of the uvula
+UBERON:0015717,smooth muscle tissue layer of ejaculatory duct,UBERON:0014403,male anatomical structure
+UBERON:0004813,seminiferous tubule epithelium,UBERON:0001136,mesothelium
+UBERON:0001912,lobule of lactiferous gland,UBERON:0014404,female anatomical structure
+UBERON:0001985,corneal endothelium,UBERON:0001986,endothelium
+HP:0100600,Penoscrotal transposition,HP:0000036,Abnormality of the penis
+HP:0012475,Specific antibody deficiency,HP:0010701,Abnormal immunoglobulin level
+NCBITaxon:34619,Dermacentor,NCBITaxon:426437,Rhipicephalinae
+DOID:7519,endocervical carcinoma,DOID:2893,cervix carcinoma
+HP:0000859,Hyperaldosteronism,HP:0002717,Adrenal overactivity
+HP:0010103,Short distal phalanx of hallux,HP:0010111,Short phalanx of hallux
+UBERON:0006855,ureter muscle layer,UBERON:0004120,mesoderm-derived structure
+UBERON:0001854,saccule of membranous labyrinth,UBERON:0002518,otolith organ
+DOID:264,hemangiopericytoma,DOID:201,connective tissue cancer
+UBERON:0007801,pygostyle,UBERON:0004120,mesoderm-derived structure
+HP:0009659,Partial absence of thumb,HP:0009601,Aplasia/Hypoplasia of the thumb
+UBERON:0010209,plica semilunaris of conjunctiva,UBERON:0005160,vestigial structure
+UBERON:0005350,lobule simplex,UBERON:0004003,cerebellum hemisphere lobule
+HP:0011275,Recurrent mycobacterium avium complex infections,HP:0011274,Recurrent mycobacterial infections
+HP:0001024,Skin dimple over apex of long bone angulation,HP:0010781,Skin dimples
+UBERON:0005415,zone of polarizing activity of pectoral appendage,UBERON:0003413,pectoral appendage bud mesenchyme
+UBERON:2002172,branchial mesenchyme,UBERON:0005253,head mesenchyme
+UBERON:0003071,eye primordium,UBERON:0010371,ecto-epithelium
+HP:0007239,Congenital encephalopathy,HP:0001298,Encephalopathy
+UBERON:0010364,dermal skeleton,UBERON:0010912,subdivision of skeleton
+UBERON:0001617,mental artery,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:6119,renal pelvis urothelial papilloma,DOID:5975,renal pelvis papillary tumor
+HP:0001262,Somnolence,HP:0004372,Reduced consciousness/confusion
+UBERON:0004321,middle phalanx of manual digit 3,UBERON:0014489,middle phalanx of digit 3
+DOID:407,hepatic tuberculosis,DOID:37,skin disease
+DOID:0050904,salivary gland carcinoma,DOID:8850,salivary gland cancer
+NCBITaxon:43786,Culicimorpha,NCBITaxon:7148,Nematocera
+DOID:3332,haemonchiasis,DOID:1255,trichostrongyloidiasis
+UBERON:0002399,lesser omentum,UBERON:0003688,omentum
+DOID:0050554,X-linked sideroblastic anemia with ataxia,DOID:1441,spinocerebellar ataxia
+HP:0002043,Esophageal stricture,HP:0010450,Esophageal stenosis
+HP:0100554,Hemihypertrophy of upper limb,HP:0100560,Upper limb asymmetry
+UBERON:0002316,white matter,UBERON:0011215,cell part cluster of neuraxis
+UBERON:0004833,lip skeletal muscle,UBERON:0004121,ectoderm-derived structure
+UBERON:2002264,epineural 2,UBERON:2000507,epineural
+UBERON:2001620,lagenar capsule,UBERON:0000477,anatomical cluster
+DOID:8677,perinatal necrotizing enterocolitis,DOID:77,gastrointestinal system disease
+UBERON:0005622,right dorsal aorta,UBERON:0003513,trunk blood vessel
+CL:0002029,Fc-epsilon RIalpha-low mast cell progenitor,CL:0000831,mast cell progenitor
+UBERON:0004269,upper arm connective tissue,UBERON:0003573,arm connective tissue
+UBERON:0015042,manual digit metacarpus endochondral element,UBERON:0015021,forelimb endochondral element
+UBERON:0010266,arthropod hepatopancreas,UBERON:0010264,hepatopancreas
+HP:0006645,Thin clavicles,HP:0000889,Abnormality of the clavicles
+UBERON:0014690,left gastric vein,UBERON:0004450,gastric vein
+HP:0010629,Abnormality of the cortex of the humerus,HP:0003063,Abnormality of the humerus
+HP:0007470,Periarticular subcutaneous nodules,HP:0001482,Subcutaneous nodule
+UBERON:0001947,red nucleus,UBERON:0007414,nucleus of midbrain tegmentum
+UBERON:3000944,pseudoarciferal girdle,UBERON:0007831,pectoral girdle skeleton
+UBERON:0016440,glabella,UBERON:0005913,zone of bone organ
+DOID:0060027,B cell linker protein deficiency,DOID:2583,agammaglobulinemia
+UBERON:0005176,tooth enamel organ,UBERON:0004121,ectoderm-derived structure
+UBERON:0006291,scapula pre-cartilage condensation,UBERON:0005291,embryonic tissue
+HP:0005547,Myeloproliferative disorder,HP:0001909,Leukemia
+UBERON:0007274,crista of ampulla of anterior semicircular duct of membranous laybrinth,UBERON:0006935,crista ampullaris neuroepithelium
+UBERON:2000202,efferent branchial artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:12205,dengue disease,DOID:934,viral infectious disease
+UBERON:0001588,vertebral vein,UBERON:0001638,vein
+HP:0012449,Sacroiliac joint synovitis,HP:0100781,Abnormality of the sacroiliac joint
+DOID:0050643,anonychia congenita,DOID:4123,nail disease
+DOID:9043,uterine cervix leukoplakia,DOID:2253,cervix disease
+DOID:6888,ureter transitional cell carcinoma,DOID:4939,ureter carcinoma
+UBERON:0009654,alveolar artery,UBERON:0000078,mixed ectoderm/mesoderm/endoderm-derived structure
+NCBITaxon:12066,Coxsackievirus,NCBITaxon:90010,unclassified Enterovirus
+UBERON:0002570,medial orbital gyrus,UBERON:0007193,orbital gyrus
+UBERON:0002573,pontine reticular formation,UBERON:0002680,regional part of metencephalon
+UBERON:0014411,greater sciatic notch,UBERON:0014430,sciatic notch
+HP:0008656,Incomplete male pseudohermaphroditism,HP:0000037,Male pseudohermaphroditism
+DOID:11433,middle ear cholesteatoma,DOID:10964,cholesteatoma of middle ear
+DOID:5488,mediastinum synovial sarcoma,DOID:5485,synovial sarcoma
+UBERON:0015103,distal tarsal bone 1 cartilage,UBERON:0010885,hindlimb cartilage element
+DOID:5551,choriocarcinoma of the testis,DOID:5345,testicular non-seminomatous germ cell cancer
+HP:0004388,Microcolon,HP:0100811,Aplasia/Hypoplasia of the colon
+DOID:11077,brucellosis,DOID:0050338,primary bacterial infectious disease
+HP:0005653,Moderate generalized osteoporosis,HP:0000939,Osteoporosis
+HP:0100371,Aplasia/Hypoplasia of the distal phalanx of the 5th toe,HP:0010185,Aplasia/Hypoplasia of the distal phalanges of the toes
+UBERON:0011854,acinus of areolar gland,UBERON:0011846,acinus of sebaceous gland
+NCBITaxon:715989,sordariomyceta,NCBITaxon:716546,leotiomyceta
+HP:0011910,Shortening of all phalanges of fingers,HP:0009803,Short phalanx of finger
+HP:0005376,Recurrent Haemophilus influenzae infections,HP:0005420,Recurrent gram-negative bacterial infections
+UBERON:0002799,fronto-orbital sulcus,UBERON:0014639,frontal sulcus
+UBERON:0010412,epididymal fat pad,UBERON:0005156,reproductive structure
+HP:0011681,Subarterial ventricular septal defect,HP:0001629,Ventricular septal defect
+UBERON:2002077,lateropterygium,UBERON:0010742,bone of pelvic complex
+UBERON:0014387,mesenchyme derived from neural crest,UBERON:0003104,mesenchyme
+UBERON:0013239,future glans penis,UBERON:0013238,future glans
+DOID:5363,myxoid liposarcoma,DOID:3382,liposarcoma
+UBERON:0011857,acinus of lacrimal gland,UBERON:0011858,acinus of exocrine gland
+UBERON:0004190,renal glomerulus vasculature,UBERON:0006544,kidney vasculature
+UBERON:2001059,cranial division of the internal carotid artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0013593,suprasylvian sulcus,UBERON:0008334,subarachnoid sulcus
+HP:0100166,Stippling of the epiphysis of the proximal phalanx of the 3rd toe,HP:0100064,Stippling of the epiphyses of the 3rd toe
+CL:0000416,polytene cell,CL:0000412,polyploid cell
+UBERON:4200124,sternal trabecula,UBERON:4100000,skeletal element projection
+CL:0000724,heterocyst,CL:0000725,nitrogen fixing cell
+UBERON:0004717,Brodmann (1909) area 29,UBERON:0013529,Brodmann area
+HP:0012305,Coarctation of the descending aortic arch,HP:0001680,Coarctation of aorta
+HP:0012115,Hepatitis,HP:0001392,Abnormality of the liver
+HP:0009201,Stippling of the epiphysis of the proximal phalanx of the 5th finger,HP:0009153,Abnormality of the epiphysis of the proximal phalanx of the 5th finger
+HP:0100671,Abnormal trabecular bone morphology,HP:0003330,Abnormal bone structure
+HP:0009349,Enlarged epiphysis of the proximal phalanx of the 3rd finger,HP:0009333,Abnormality of the epiphysis of the proximal phalanx of the 3rd finger
+CL:0000429,imaginal disc cell,CL:0000146,simple columnar epithelial cell
+DOID:4302,cystic basal cell carcinoma,DOID:2513,basal cell carcinoma
+HP:0001800,Hypoplastic toenails,HP:0001792,Small nail
+HP:0006106,Absent trapezoid bone,HP:0004256,Abnormality of the trapezoid bone
+HP:0001169,Broad palm,HP:0100871,Abnormality of the palm
+UBERON:0005585,rhombomere 7 floor plate,UBERON:0005500,rhombomere floor plate
+DOID:5093,thoracic cancer,DOID:0050686,organ system cancer
+HP:0010299,Abnormality of dentin,HP:0011061,Abnormality of dental structure
+DOID:3969,papillary thyroid carcinoma,DOID:3963,thyroid carcinoma
+DOID:4914,esophagus adenocarcinoma,DOID:1107,esophageal carcinoma
+UBERON:2005220,larval melanophore stripe,UBERON:2001463,melanophore stripe
+HP:0000719,Inappropriate behavior,HP:0100851,Abnormal emotion/affect behavior
+HP:0000999,Pyoderma,HP:0005406,Recurrent bacterial skin infections
+UBERON:0007123,pharyngeal pouch 2,UBERON:0004117,pharyngeal pouch
+DOID:3926,mediastinal lipomatosis,DOID:3153,lipomatosis
+UBERON:0005841,cervical spinal cord dorsal column,UBERON:0014614,cervical spinal cord white matter
+DOID:1425,pyoureter,DOID:1426,ureteral disease
+HP:0011599,Mesocardia,HP:0004307,Abnormal anatomic location of the heart
+HP:0010187,Bullet-shaped distal phalanges of the toes,HP:0010182,Abnormality of the distal phalanges of the toes
+DOID:4087,testicular pure germ cell tumor,DOID:5557,testicular germ cell cancer
+HP:0100799,Neoplasm of the middle ear,HP:0011793,Neoplasm by anatomical site
+HP:0002270,Abnormality of the autonomic nervous system,HP:0012639,Abnormality of nervous system morphology
+UBERON:0011219,longissimus lumborum muscle,UBERON:0000392,longissimus muscle
+HP:0009396,Enlarged epiphyses of the 4th finger,HP:0009174,Abnormality of the epiphyses of the 4th finger
+HP:0001468,Aplasia/Hypoplasia involving the musculature of the upper arm,HP:0001467,Aplasia/Hypoplasia involving the musculature of the upper limbs
+NCBITaxon:28556,Pleosporaceae,NCBITaxon:715340,Pleosporineae
+UBERON:0000013,sympathetic nervous system,UBERON:0002410,autonomic nervous system
+HP:0002586,Peritonitis,HP:0002585,Abnormality of the peritoneum
+UBERON:0003917,arthropod fat body,UBERON:0000062,organ
+CL:0000735,lymph gland hemocyte,CL:0000387,hemocyte (sensu Nematoda and Protostomia)
+HP:0100797,Toenail dysplasia,HP:0002164,Nail dysplasia
+UBERON:2000474,intercalar,UBERON:0011164,neurocranium bone
+HP:0010276,Small epiphyses of the proximal phalanges of the hand,HP:0010236,Small epiphyses of the phalanges of the hand
+UBERON:0007192,posterior paracentral gyrus,UBERON:0007190,paracentral gyrus
+DOID:14256,adult-onset Still's disease,DOID:848,arthritis
+UBERON:0008585,levator veli palatini,UBERON:0015212,lateral structure
+DOID:14459,hemangioma of orbit,DOID:255,hemangioma
+DOID:7079,adult cystic teratoma,DOID:5565,adult teratoma
+HP:0010545,Downbeat nystagmus,HP:0010544,Vertical nystagmus
+HP:0005113,Dilatation of the aortic arch,HP:0001724,Aortic dilatation
+HP:0100184,Fragmentation of the epiphysis of the middle phalanx of the 4th toe,HP:0100070,Fragmentation of the epiphyses of the 4th toe
+HP:0001336,Myoclonus,HP:0004305,Involuntary movements
+HP:0009349,Enlarged epiphysis of the proximal phalanx of the 3rd finger,HP:0010271,Enlarged epiphyses of the proximal phalanges of the hand
+HP:0010988,Abnormality of the extrinsic pathway,HP:0003256,Abnormality of the coagulation cascade
+NCBITaxon:11646,Lentivirus,NCBITaxon:327045,Orthoretrovirinae
+HP:0008279,Transient hyperlipidemia,HP:0003077,Hyperlipidemia
+UBERON:0008304,inner chondrogenic layer of perichondrium,UBERON:0002384,connective tissue
+HP:0001433,Hepatosplenomegaly,HP:0001392,Abnormality of the liver
+HP:0003927,Cortical irregularity of humeral diaphysis,HP:0003867,Cortical irregularity (humeral)
+UBERON:0001196,middle colic artery,UBERON:0004573,systemic artery
+HP:0001693,Cardiac shunt,HP:0011025,Abnormality of cardiovascular system physiology
+UBERON:0007120,premolar tooth,UBERON:0013164,molariform tooth
+HP:0012682,Pineal gland calcification,HP:0012681,Abnormality of pineal morphology
+DOID:4916,pituitary carcinoma,DOID:1785,pituitary cancer
+CL:0000167,peptide hormone secreting cell,CL:0000163,endocrine cell
+UBERON:3010084,M. tibialis posticus,UBERON:0010890,pelvic complex muscle
+HP:0009374,Broad phalanges of the 5th finger,HP:0009768,Broad phalanges of the hand
+HP:0011719,Supracardiac total anomalous pulmonary venous connection,HP:0005160,Total anomalous pulmonary venous return
+HP:0010537,Wide cranial sutures,HP:0011329,Abnormality of cranial sutures
+CL:0000748,retinal bipolar neuron,CL:0000103,bipolar neuron
+CL:0000666,fenestrated cell,CL:0000066,epithelial cell
+DOID:10087,gastric leiomyoma,DOID:0050624,gastrointestinal system benign neoplasm
+HP:0004762,Hypoplasia of right ventricle,HP:0001707,Abnormality of the right ventricle
+HP:0100339,Abnormality of the os naviculare pedis,HP:0001850,Abnormality of the tarsal bones
+DOID:557,kidney disease,DOID:18,urinary system disease
+UBERON:0002098,apex of heart,UBERON:0006983,anatomical point
+UBERON:0005115,metanephric cortical collecting duct,UBERON:0004120,mesoderm-derived structure
+UBERON:0002702,middle frontal gyrus,UBERON:0015593,frontal gyrus
+HP:0009331,Triangular epiphysis of the middle phalanx of the 3rd finger,HP:0009334,Abnormality of the epiphysis of the middle phalanx of the 3rd finger
+DOID:4265,angiomyoma,DOID:127,leiomyoma
+UBERON:2000271,radial bone,UBERON:0004376,fin bone
+UBERON:0002313,hippocampus pyramidal layer,UBERON:0002305,layer of hippocampus
+UBERON:0012269,equine hindlimb splint bone,UBERON:0012267,equine splint bone
+HP:0002655,Spondyloepiphyseal dysplasia,HP:0002652,Skeletal dysplasia
+UBERON:0003954,squamoparietal suture,UBERON:0003685,cranial suture
+UBERON:0002269,pupillary membrane,UBERON:0004121,ectoderm-derived structure
+UBERON:0002382,rectus abdominis muscle,UBERON:0003897,axial muscle
+UBERON:0001629,carotid body,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0013556,Brodmann (1909) area 25,UBERON:0013529,Brodmann area
+HP:0010129,Cone-shaped epiphysis of the proximal phalanx of the hallux,HP:0010126,Abnormality of the epiphysis of the proximal phalanx of the hallux
+HP:0003427,Thenar muscle weakness,HP:0002460,Distal muscle weakness
+HP:0100115,Fragmentation of the epiphysis of the middle phalanx of the 2nd toe,HP:0100089,Abnormality of the epiphysis of the middle phalanx of the 2nd toe
+UBERON:0001088,urine,UBERON:0000174,excreta
+UBERON:0016405,pulmonary capillary,UBERON:0003512,lung blood vessel
+UBERON:0003851,diencephalon neural crest,UBERON:0002342,neural crest
+DOID:2145,malignant ovarian cyst,DOID:2394,ovarian cancer
+CL:0002378,immature Vgamma2-positive fetal thymocyte,CL:0002404,fetal thymocyte
+HP:0006538,Recurrent bronchopulmonary infections,HP:0002205,Recurrent respiratory infections
+UBERON:0005408,circumventricular organ,UBERON:0002616,regional part of brain
+HP:0011483,Anterior synechiae of the anterior chamber,HP:0007833,Anterior chamber synechiae
+UBERON:0002941,capsule of red nucleus,UBERON:0014891,brainstem white matter
+CL:1001589,duodenum glandular cell,CL:1001598,small intestine glandular cell
+HP:0001487,Hypopigmented fundi,HP:0001098,Abnormality of the fundus
+DOID:2965,bursitis,DOID:381,arthropathy
+HP:0012285,Abnormal hypothalamus physiology,HP:0000864,Abnormality of the hypothalamus-pituitary axis
+UBERON:0011145,adductor muscle,UBERON:0001630,muscle organ
+UBERON:0011828,areolar tubercle,UBERON:0004121,ectoderm-derived structure
+UBERON:0011971,calcaneofibular ligament,UBERON:0003701,calcaneal tendon
+UBERON:0004691,bulbourethral gland secretion,UBERON:0006530,seminal fluid
+DOID:6961,Bartholin's gland squamous cell carcinoma,DOID:3999,Bartholin's gland carcinoma
+UBERON:2002027,pectoral fin proximal radial bone 2,UBERON:2102027,pectoral fin proximal radial element 2
+UBERON:0010567,manual digit 3 metacarpus pre-cartilage condensation,UBERON:0015045,manual digit 3 metacarpus endochondral element
+HP:0009414,Fragmentation of the epiphyses of the 3rd finger,HP:0009320,Abnormality of the epiphyses of the 3rd finger
+HP:0009224,Triangular epiphysis of the middle phalanx of the 4th finger,HP:0010267,Triangular epiphyses of the middle phalanges of the hand
+DOID:13976,peptic esophagitis,DOID:750,peptic ulcer disease
+UBERON:0001530,common carotid artery plus branches,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0008281,tooth bud,UBERON:0005423,developing anatomical structure
+HP:0010063,Patchy sclerosis of the phalanges of the hallux,HP:0010057,Abnormality of the phalanges of the hallux
+HP:0100259,Postaxial polydactyly,HP:0010442,Polydactyly
+DOID:2030,anxiety disorder,DOID:1561,cognitive disorder
+UBERON:0011298,submucosa of uterine tube,UBERON:0005156,reproductive structure
+UBERON:0004689,naso-frontal vein,UBERON:0001638,vein
+HP:0004180,Short distal phalanx of the 3rd finger,HP:0009461,Short 3rd finger
+UBERON:0001335,prostatic urethra,UBERON:0000063,organ segment
+HP:0009182,Triangular shaped middle phalanx of the 5th finger,HP:0009378,Triangular shaped phalanges of the 5th finger
+DOID:8864,acute monocytic leukemia,DOID:8527,monocytic leukemia
+DOID:3153,lipomatosis,DOID:37,skin disease
+DOID:3497,pancreatic signet ring cell adenocarcinoma,DOID:3498,pancreatic ductal adenocarcinoma
+HP:0000308,Microretrognathia,HP:0000278,Retrognathia
+DOID:289,endometriosis,DOID:229,female reproductive system disease
+HP:0006640,Multiple rib fractures,HP:0000772,Abnormality of the ribs
+UBERON:0009985,lateral condyle of femur,UBERON:0009980,condyle of femur
+DOID:906,peroxisomal disease,DOID:655,inherited metabolic disorder
+UBERON:0013755,arterial blood,UBERON:0000178,blood
+UBERON:0002257,ventral horn of spinal cord,UBERON:0015212,lateral structure
+HP:0008437,Bifid thoracic vertebrae,HP:0003312,Abnormal form of the vertebral bodies
+CL:0000223,endodermal cell,CL:0002321,embryonic cell
+DOID:5504,tanycytic ependymoma,DOID:4844,benign ependymoma
+DOID:8105,extrahepatic bile duct cystadenoma,DOID:5384,bile duct cystadenoma
+UBERON:0003126,trachea,UBERON:0000117,respiratory tube
+HP:0005988,Congenital muscular torticollis,HP:0011006,Abnormality of the musculature of the neck
+HP:0009307,Patchy sclerosis of the middle phalanx of the 4th finger,HP:0009406,Patchy sclerosis of the phalanges of the 4th finger
+UBERON:0004612,mammalian cervical vertebra 3,UBERON:0002413,cervical vertebra
+UBERON:0015226,bulbar spiral septum,UBERON:0002099,cardiac septum
+CL:0000047,neuronal stem cell,CL:0002319,neural cell
+UBERON:0014801,nuchal line,UBERON:0006800,anatomical line
+HP:0009880,Broad distal phalanges of all fingers,HP:0009836,Broad distal phalanx of finger
+UBERON:0014886,distal epiphysis of distal phalanx of manual digit,UBERON:0011979,epiphysis of distal phalanx of manus
+DOID:7312,breast adenomyoepithelial adenosis,DOID:5998,microglandular adenosis
+HP:0100394,Short middle phalanx of the 5th toe,HP:0100368,Short phalanx of the 5th toe
+HP:0002641,Peripheral thrombosis,HP:0001977,Abnormal thrombosis
+UBERON:0004439,proximal epiphysis of middle phalanx of manual digit 5,UBERON:0004421,proximal epiphysis of phalanx of manual digit 5
+CL:1000505,kidney pelvis cell,CL:1000497,kidney cell
+HP:0011853,Serous pericardial effusion,HP:0001698,Pericardial effusion
+HP:0008515,Aplasia/Hypoplasia of the vertebrae,HP:0003468,Abnormality of the vertebrae
+UBERON:0011150,pharyngeal arch derived gill,UBERON:0002535,gill
+UBERON:2000183,central pretectum,UBERON:0003047,regional part of pretectal region
+CL:0000265,anterior like cell,CL:0000263,vegetative cell (sensu Mycetozoa)
+UBERON:0001820,sweat gland,UBERON:0007771,epidermis gland
+HP:0006347,Microdontia of primary teeth,HP:0000691,Microdontia
+UBERON:0007723,interphalangeal joint of manual digit 1,UBERON:0007722,interphalangeal joint of manus
+DOID:452,pleomorphic adenoma,DOID:0050624,gastrointestinal system benign neoplasm
+UBERON:0002999,oral pontine reticular nucleus,UBERON:0003528,brain grey matter
+UBERON:0008924,sublaminar layer S3,UBERON:0009733,sublaminar layers S1 or S2 or S3
+DOID:219,colon cancer,DOID:9256,colorectal cancer
+UBERON:2002002,anterior distal serration of pectoral fin spine,UBERON:4100000,skeletal element projection
+UBERON:0015222,ventral nasal meatus,UBERON:0015216,nasal meatus
+UBERON:0010167,beard,UBERON:0010165,collection of hair on face
+UBERON:0008936,gastropod genital pore,UBERON:0005156,reproductive structure
+HP:0001250,Seizures,HP:0012638,Abnormality of nervous system physiology
+UBERON:2000699,entopterygoid vertical strut,UBERON:4100000,skeletal element projection
+HP:0011468,Facial tics,HP:0005324,Disturbance of facial expression
+UBERON:2000820,presumptive neuron neural tube,UBERON:0002050,embryonic structure
+UBERON:0010294,scleral endothelium,UBERON:0015808,eye epithelium
+UBERON:0005327,mesonephric glomerular epithelium,UBERON:0005330,mesonephric nephron epithelium
+UBERON:0005842,lumbar spinal cord dorsal column,UBERON:0006079,subdivision of spinal cord dorsal column
+DOID:10568,early yaws,DOID:10371,yaws
+UBERON:0008964,abdominal ganglion of visceral hump,UBERON:0000045,ganglion
+HP:0004476,Aplasia cutis congenita over parietal area,HP:0007385,Aplasia cutis congenita of scalp
+HP:0005891,Progressive forearm bowing,HP:0006383,Progressive bowing of long bones
+DOID:6367,acral lentiginous melanoma,DOID:8923,skin melanoma
+HP:0004586,Biconcave vertebral bodies,HP:0003312,Abnormal form of the vertebral bodies
+HP:0010106,Aplasia of the proximal phalanx of the hallux,HP:0010110,Aplasia of the phalanges of the hallux
+HP:0004000,Chevron-shaped/cone-shaped radial epiphyses,HP:0003999,Abnormality of radial epiphyses
+HP:0006886,Impaired distal vibration sensation,HP:0002495,Impaired vibratory sensation
+DOID:520,aortic disease,DOID:0050828,artery disease
+HP:0003502,Mild short stature,HP:0003508,Proportionate short stature
+HP:0009514,Bracket epiphysis of the middle phalanx of the 2nd finger,HP:0009500,Abnormality of the epiphysis of the middle phalanx of the 2nd finger
+HP:0009383,Bracket epiphyses of the 5th finger,HP:0010229,Bracket epiphyses of the phalanges of the hand
+HP:0004787,Fulminant hepatitis,HP:0012115,Hepatitis
+HP:0009212,Stippling of the epiphysis of the middle phalanx of the 5th finger,HP:0004224,Abnormality of the epiphysis of the middle phalanx of the 5th finger
+UBERON:0001292,distal convoluted tubule,UBERON:0006853,renal cortex tubule
+HP:0009458,Aplasia of the proximal phalanx of the 3rd finger,HP:0010242,Aplasia of the proximal phalanges of the hand
+UBERON:0004183,labyrinthine layer blood vessel,UBERON:0005156,reproductive structure
+HP:0004442,Sagittal craniosynostosis,HP:0001363,Craniosynostosis
+HP:0002290,Poliosis,HP:0011365,Patchy hypopigmentation of hair
+HP:0000886,Deformed rib cage,HP:0001547,Abnormality of the rib cage
+UBERON:0006653,glans clitoris,UBERON:0008324,erectile tissue
+UBERON:2000900,hypaxial region somite 4,UBERON:0003895,hypaxial myotome region
+DOID:8419,colloid adenoma,DOID:6204,follicular adenoma
+HP:0003249,Genital ulcers,HP:0012243,Abnormal genital system morphology
+UBERON:0002562,superior frontal sulcus,UBERON:0003022,cerebral cortex lobe
+UBERON:0011588,pre-enamel,UBERON:0010365,odontoid tissue
+UBERON:3010764,laryngeus ventralis,UBERON:0001021,nerve
+DOID:12341,retroperitoneal sarcoma,DOID:5875,retroperitoneal cancer
+HP:0012269,Abnormal muscle glycogen content,HP:0004303,Abnormality of muscle fibers
+UBERON:0002342,neural crest,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0006267,notochordal plate,UBERON:0005291,embryonic tissue
+UBERON:4300033,anterior dorsal fin basal cartilage,UBERON:0007844,cartilage element
+HP:0100091,Abnormality of the epiphysis of the distal phalanx of the 3rd toe,HP:0010329,Abnormality of the epiphyses of the 3rd toe
+UBERON:0002923,posterior parolfactory sulcus,UBERON:0008334,subarachnoid sulcus
+UBERON:2001655,upper pharyngeal 4 tooth,UBERON:0001091,calcareous tooth
+UBERON:0010233,stroma of thyroid gland,UBERON:0010313,neural crest-derived structure
+DOID:2076,vulvar glandular tumor,DOID:1245,vulva cancer
+UBERON:2002215,otic vesicle protrusion,UBERON:0004121,ectoderm-derived structure
+HP:0007517,Palmoplantar cutis laxa,HP:0100871,Abnormality of the palm
+UBERON:0005848,sacral spinal cord lateral column,UBERON:0006078,subdivision of spinal cord lateral column
+HP:0000003,Multicystic kidney dysplasia,HP:0000107,Renal cyst
+UBERON:3000989,pectoral fold,UBERON:3000977,body external integument structure
+UBERON:2002244,supraoptic tract,UBERON:0003544,brain white matter
+DOID:1283,enterocele,DOID:1284,prolapse of female genital organ
+NCBITaxon:11072,Japanese encephalitis virus,NCBITaxon:11071,Japanese encephalitis virus group
+UBERON:3010603,body gland,UBERON:3000977,body external integument structure
+HP:0009447,Aplasia/Hypoplasia of the phalanges of the 3rd finger,HP:0009767,Aplasia/Hypoplasia of the phalanges of the hand
+UBERON:0011014,spinalis capitis muscle,UBERON:0011013,spinalis muscle
+UBERON:0005069,neural fold hinge point,UBERON:0004121,ectoderm-derived structure
+UBERON:0002876,nucleus intercalatus,UBERON:0007635,nucleus of medulla oblongata
+HP:0008774,Aplasia/Hypoplasia of the inner ear,HP:0011390,Morphological abnormality of the inner ear
+HP:0007280,Acute infantile spinal muscular atrophy,HP:0007269,Spinal muscular atrophy
+UBERON:2001428,olfactory rosette,UBERON:0010371,ecto-epithelium
+UBERON:0004983,mucosa of vagina,UBERON:0000344,mucosa
+HP:0000932,Abnormality of the posterior cranial fossa,HP:0002693,Abnormality of the skull base
+UBERON:0002897,cistern of lamina terminalis,UBERON:0004050,subarachnoid cistern
+HP:0000823,Delayed puberty,HP:0008373,Puberty and gonadal disorders
+HP:0100643,Abnormality of nail color,HP:0001597,Abnormality of the nail
+DOID:5152,cellular neurofibroma,DOID:962,neurofibroma
+HP:0001215,Camptodactyly (2nd-5th fingers),HP:0100490,Camptodactyly of finger
+UBERON:2001352,stratum periventriculare,UBERON:0000479,tissue
+DOID:13099,Moyamoya disease,DOID:3527,cerebral arterial disease
+HP:0012349,Abnormal sialylation of N-linked protein glycosylation,HP:0012347,Abnormal protein N-linked glycosylation
+HP:0100946,Sclerosis of the proximal phalanges of the toes,HP:0100924,Sclerosis of the phalanges of the toes
+UBERON:0011595,jaw region,UBERON:0004121,ectoderm-derived structure
+DOID:2649,chondroblastoma,DOID:201,connective tissue cancer
+UBERON:0002113,kidney,UBERON:0005172,abdomen organ
+DOID:5725,rete ovarii cystadenoma,DOID:6837,rete ovarii adenoma
+DOID:6495,adult myxoid chondrosarcoma,DOID:5861,myxoid chondrosarcoma
+UBERON:0010185,rete ovarii,UBERON:0004111,anatomical conduit
+HP:0004492,Widely patent fontanelles and sutures,HP:0000239,Large fontanelles
+UBERON:0000016,endocrine pancreas,UBERON:0004119,endoderm-derived structure
+HP:0000111,Renal juxtaglomerular cell hypertrophy/hyperplasia,HP:0000095,Abnormality of the glomerulus
+HP:0005191,Congenital knee dislocation,HP:0004976,Knee dislocation
+CL:0000159,seromucus secreting cell,CL:0000151,secretory cell
+UBERON:0003533,manual digit skin,UBERON:0015249,digit skin
+UBERON:0013126,vein of abdomen,UBERON:0001638,vein
+UBERON:0014780,palatine aponeurosis,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:0060023,CD40 deficiency,DOID:628,combined T cell and B cell immunodeficiency
+UBERON:0009617,head paraxial mesoderm,UBERON:0006904,head mesenchyme from mesoderm
+DOID:9910,central corneal ulcer,DOID:8463,corneal ulcer
+UBERON:0002481,bone tissue,UBERON:0004755,skeletal tissue
+UBERON:0004706,bulbus cordis,UBERON:0004120,mesoderm-derived structure
+UBERON:0013460,suprainiac fossa,UBERON:0004704,bone fossa
+UBERON:2001694,humerovertebral ligament,UBERON:0008846,skeletal ligament
+UBERON:0015099,distal tarsal bone endochondral element,UBERON:0015050,tarsus endochondral element
+DOID:7463,childhood pleomorphic rhabdomyosarcoma,DOID:3250,pleomorphic rhabdomyosarcoma
+HP:0100623,Abnormality of corpus cavernosum,HP:0000036,Abnormality of the penis
+DOID:799,varicose veins,DOID:866,vein disease
+UBERON:0002578,sublentiform nucleus,UBERON:0011214,nucleus of midbrain tectum
+UBERON:0011320,ligament of temporomandibular joint,UBERON:0010313,neural crest-derived structure
+CL:0001050,"effector CD8-positive, alpha-beta T cell",CL:0000625,"CD8-positive, alpha-beta T cell"
+DOID:288,endometriosis of uterus,DOID:345,uterine disease
+HP:0000201,Pierre-Robin sequence,HP:0000153,Abnormality of the mouth
+HP:0005897,Severe osteoporosis,HP:0000939,Osteoporosis
+HP:0200123,Chronic hepatitis,HP:0012115,Hepatitis
+UBERON:0007822,vomeronasal cartilage,UBERON:0001823,nasal cartilage
+DOID:5826,breast lymphoma,DOID:1612,breast cancer
+HP:0008956,Proximal lower limb amyotrophy,HP:0001441,Abnormality of the musculature of the thigh
+UBERON:0009867,Hatschek's diverticulum,UBERON:0001048,primordium
+UBERON:0000162,cloaca,UBERON:0000481,multi-tissue structure
+HP:0009987,Partial duplication of the phalanges of the 5th finger,HP:0009985,Duplication of phalanx of 5th finger
+UBERON:0010198,carotid duct,UBERON:0003513,trunk blood vessel
+HP:0002930,Thyroid hormone receptor defect,HP:0002926,Abnormality of thyroid physiology
+UBERON:0001446,fibula,UBERON:0015013,fibula endochondral element
+DOID:0050194,Argentine hemorrhagic fever,DOID:934,viral infectious disease
+DOID:4768,epithelial predominant pulmonary blastoma,DOID:4765,pulmonary blastoma
+DOID:10324,anthracosilicosis,DOID:10316,pneumoconiosis
+UBERON:0005630,fetal membrane,UBERON:0005631,extraembryonic membrane
+DOID:0080036,SOST-related sclerosing bone dysplasia,DOID:205,hyperostosis
+HP:0009405,Bullet-shaped phalanges of the 4th finger,HP:0009172,Abnormality of the phalanges of the 4th finger
+HP:0100654,Retrobulbar optic neuritis,HP:0100653,Optic neuritis
+UBERON:2002193,dorsolateral septum,UBERON:0000479,tissue
+UBERON:2005056,palatocerebral vein,UBERON:0009141,craniocervical region vein
+DOID:1355,paranasal sinus lymphoma,DOID:0050619,paranasal sinus cancer
+DOID:0050615,respiratory system cancer,DOID:0050686,organ system cancer
+DOID:0050841,focal hand dystonia,DOID:0050836,focal dystonia
+HP:0009233,Triangular shaped proximal phalanx of the 5th finger,HP:0009378,Triangular shaped phalanges of the 5th finger
+HP:0002516,Increased intracranial pressure,HP:0012640,Abnormality of intracranial pressure
+HP:0005241,Total intestinal aganglionosis,HP:0004362,Abnormality of the enteric ganglia
+UBERON:0006497,interosseous muscle of pes,UBERON:0014378,intrinsic muscle of pes
+UBERON:0002446,patella,UBERON:0001479,sesamoid bone
+HP:0000473,Torticollis,HP:0012179,Craniofacial dystonia
+DOID:1921,Klinefelter's syndrome,DOID:0080014,chromosomal disease
+UBERON:0005911,endo-epithelium,UBERON:0004119,endoderm-derived structure
+CL:0005009,renal principal cell,CL:0002518,kidney epithelial cell
+HP:0006931,Lipoma of corpus callosum,HP:0006866,Midline central nervous system lipomas
+UBERON:0007264,intervertebral disk of seventh cervical vertebra,UBERON:0007252,intervertebral disk of cervical vertebra
+UBERON:0010066,tympanic plate,UBERON:0005913,zone of bone organ
+HP:0009502,Absent epiphysis of the distal phalanx of the 2nd finger,HP:0009488,Absent epiphyses of the 2nd finger
+UBERON:3000816,margo fenestralis,UBERON:0000064,organ part
+HP:0004482,Relative macrocephaly,HP:0000256,Macrocephaly
+HP:0012308,Decreased serum complement C9,HP:0004431,Complement deficiency
+DOID:8179,cervical atypical polypoid adenomyoma,DOID:4995,cervical adenomyoma
+UBERON:0006326,base of arytenoid,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004710,pectoral appendage,UBERON:0004708,paired limb/fin
+CL:0000113,mononuclear phagocyte,CL:0000226,single nucleate cell
+CL:0000006,neuronal receptor cell,CL:0000540,neuron
+HP:0007408,Tegumentary leishmaniasis susceptibility,HP:0005386,Recurrent protozoan infections
+CL:0000607,ascospore,CL:0000596,sexual spore
+DOID:6726,fibrillary astrocytoma,DOID:3069,astrocytoma
+UBERON:0003634,pedal digit 4,UBERON:0001466,pedal digit
+HP:0100098,Abnormality of the epiphysis of the middle phalanx of the 5th toe,HP:0010341,Abnormality of the epiphyses of the 5th toe
+DOID:11198,DiGeorge syndrome,DOID:11200,T cell deficiency
+HP:0100787,Prostate neoplasm,HP:0008775,Abnormality of the prostate
+UBERON:0010071,layer of tympanic membrane,UBERON:0000064,organ part
+HP:0008371,Abnormal metatarsal ossification,HP:0001832,Abnormality of the metatarsal bones
+HP:0003885,Undermodeled humerus,HP:0003063,Abnormality of the humerus
+DOID:1242,globe disease,DOID:5614,eye disease
+UBERON:2205382,dorsal fin proximal radial cartilage 5,UBERON:2105382,dorsal fin proximal radial element 5
+DOID:3813,central nervous system chondroma,DOID:502,central nervous system mesenchymal non-meningothelial tumor
+UBERON:0006473,Brodmann (1909) area 18,UBERON:0013529,Brodmann area
+CL:0002541,chorionic membrane mesenchymal stem cell,CL:0000349,extraembryonic cell
+UBERON:0002833,medial nucleus of trapezoid body,UBERON:0003528,brain grey matter
+DOID:14181,calcific tendinitis,DOID:971,tendinitis
+HP:0010020,Irregular epiphysis of the 1st metacarpal,HP:0009691,Irregular epiphyses of the thumb
+HP:0007410,Palmoplantar hyperhidrosis,HP:0100872,Abnormality of the plantar skin of foot
+HP:0001987,Hyperammonemia,HP:0002157,Azotemia
+DOID:5150,neurofibroma of gallbladder,DOID:962,neurofibroma
+UBERON:0004017,periocular mesenchyme,UBERON:0003104,mesenchyme
+HP:0010105,Short first metatarsal,HP:0010067,Aplasia/Hypoplasia of the 1st metatarsal
+UBERON:0003262,amniotic mesoderm,UBERON:0010333,extraembryonic membrane mesenchyme
+HP:0008255,Transient neonatal diabetes mellitus,HP:0000857,Neonatal insulin-dependent diabetes mellitus
+UBERON:2001915,basibranchial 1 element,UBERON:0013746,basibranchial element
+DOID:11581,phlyctenulosis,DOID:9368,keratoconjunctivitis
+HP:0011966,Elevated plasma citrulline,HP:0011965,Abnormality of citrulline metabolism
+UBERON:0006068,bone of tail,UBERON:0001474,bone element
+DOID:3717,gastric adenocarcinoma,DOID:5517,stomach carcinoma
+UBERON:3000655,processus dorsalis of lamella alaris,UBERON:0010313,neural crest-derived structure
+DOID:429,gynatresia,DOID:229,female reproductive system disease
+HP:0010414,Broad distal phalanx of the 2nd toe,HP:0010348,Broad phalanges of the 2nd toe
+UBERON:0005711,foregut duodenum mesentery,UBERON:0004121,ectoderm-derived structure
+UBERON:0014490,middle phalanx of digit 4,UBERON:0004301,middle phalanx
+HP:0005686,Patchy osteosclerosis,HP:0011001,Increased bone mineral density
+CL:1000397,endothelial cell of venous sinus of red pulp of spleen,CL:0002651,endothelial cell of venous sinus of spleen
+HP:0011557,Double inlet to single ventricle of indeterminate morphology,HP:0001750,Single ventricle
+HP:0011619,Pulmonary situs ambiguus with bilateral morphologic left lungs,HP:0011617,Pulmonary situs ambiguus
+DOID:5678,nerve fibre bundle defect,DOID:5679,retinal disease
+HP:0012683,Pineal cyst,HP:0012681,Abnormality of pineal morphology
+UBERON:2102026,pectoral fin proximal radial element 1,UBERON:2101587,pectoral fin proximal radial element
+UBERON:0004246,outflow tract smooth muscle,UBERON:0001135,smooth muscle tissue
+UBERON:0011200,sacrococcygeal symphysis,UBERON:0001468,intervertebral joint
+DOID:10588,adrenoleukodystrophy,DOID:10579,leukodystrophy
+HP:0001644,Dilated cardiomyopathy,HP:0001638,Cardiomyopathy
+CL:0002600,smooth muscle cell of trachea,CL:0000192,smooth muscle cell
+UBERON:3000583,sulcus for Meckels cartilage,UBERON:0000464,anatomical space
+DOID:1395,schistosomiasis,DOID:883,parasitic helminthiasis infectious disease
+DOID:3650,lactic acidosis,DOID:0060158,acquired metabolic disease
+UBERON:2001392,parapophysis 1,UBERON:0011370,transverse process of atlas
+UBERON:0003397,mesentery of duodenum,UBERON:0003336,serosa of duodenum
+HP:0000501,Glaucoma,HP:0012373,Abnormal eye physiology
+UBERON:0002968,central gray substance of pons,UBERON:0007413,nucleus of pontine reticular formation
+CL:1000376,purkinje myocyte of interventricular septum,CL:0002068,Purkinje myocyte
+HP:0011013,Abnormality of carbohydrate metabolism/homeostasis,HP:0001939,Abnormality of metabolism/homeostasis
+UBERON:0000095,cardiac neural crest,UBERON:0005291,embryonic tissue
+UBERON:0006870,endostyle,UBERON:0006846,surface groove
+HP:0001838,Rocker bottom foot,HP:0008365,Abnormality of the talus
+HP:0011872,Impaired thrombin-induced platelet aggregation,HP:0003540,Impaired platelet aggregation
+UBERON:0012499,serosa of uterine tube,UBERON:0000042,serous membrane
+HP:0001421,Abnormality of the musculature of the hand,HP:0001155,Abnormality of the hand
+CL:1001609,muscle fibroblast,CL:0000057,fibroblast
+UBERON:0011112,tibiofibular joint,UBERON:0002210,syndesmosis
+HP:0009545,Symphalangism of the 2nd finger,HP:0009541,Abnormality of the phalanges of the 2nd finger
+HP:0009913,Aplasia/Hypoplasia of the tragus,HP:0009912,Abnormality of the tragus
+HP:0005873,Polysyndactyly of hallux,HP:0001841,Preaxial foot polydactyly
+UBERON:0011599,lenticular process of incus,UBERON:0004530,bony projection
+UBERON:0001472,vaginal venous plexus,UBERON:0006876,vasculature of organ
+UBERON:3000224,hyobranchial muscle,UBERON:0002376,cranial muscle
+HP:0006170,Chess-pawn distal phalanges,HP:0009832,Abnormality of the distal phalanx of finger
+CL:0002281,type S enteroendocrine cell,CL:0000458,serotonin secreting cell
+UBERON:0003918,kidney mesenchyme,UBERON:0003104,mesenchyme
+UBERON:0001276,epithelium of stomach,UBERON:0003350,epithelium of mucosa
+DOID:5221,chronic polyneuropathy,DOID:1389,polyneuropathy
+HP:0007066,Proximal limb muscle stiffness,HP:0003552,Muscle stiffness
+UBERON:2000544,pectoral fin actinotrichium,UBERON:2000089,actinotrichium
+DOID:2885,benign prostate phyllodes tumor,DOID:0060087,male reproductive organ benign neoplasm
+HP:0009436,Triangular shaped middle phalanx of the 3rd finger,HP:0004172,Abnormality of the middle phalanx of the 3rd finger
+UBERON:0001554,skin of hip,UBERON:0000014,zone of skin
+UBERON:2001230,pharyngeal arch 6 skeleton,UBERON:0010912,subdivision of skeleton
+CL:0008013,cranial visceromotor neuron,CL:0015000,cranial motor neuron
+DOID:3185,spinal cord glioma,DOID:5612,spinal cancer
+CL:0000636,Mueller cell,CL:0000127,astrocyte
+HP:0006450,Multicentric ossification of proximal femoral epiphyses,HP:0010574,Abnormality of the epiphysis of the femoral head
+CL:0000028,CNS neuron (sensu Nematoda and Protostomia),CL:0000540,neuron
+DOID:5112,swayback,DOID:5113,nutritional deficiency disease
+CL:0007011,enteric neuron,CL:0000107,autonomic neuron
+HP:0100071,Irregular epiphyses of the 4th toe,HP:0010335,Abnormality of the epiphyses of the 4th toe
+HP:0004934,Vascular calcification,HP:0002597,Abnormality of the vasculature
+CL:0001058,"plasmacytoid dendritic cell, human",CL:0001056,"dendritic cell, human"
+UBERON:3010451,involuting marginal zone,UBERON:0004879,marginal zone of embryo
+HP:0011933,Elongated superior cerebellar peduncle,HP:0011932,Abnormality of the superior cerebellar peduncle
+HP:0005602,Progressive vitiligo,HP:0001045,Vitiligo
+HP:0011395,Aplasia/Hypoplasia of the cochlea,HP:0008774,Aplasia/Hypoplasia of the inner ear
+UBERON:0001935,ventromedial nucleus of hypothalamus,UBERON:0002951,regional part of intermediate hypothalamic region
+UBERON:0005065,right ventricular compact myocardium,UBERON:0004127,compact layer of ventricle
+DOID:3330,partial sensory epilepsy,DOID:2234,focal epilepsy
+HP:0005183,Pericardial lymphangiectasia,HP:0001697,Abnormality of the pericardium
+UBERON:0003407,cartilage of nasal septum,UBERON:0001823,nasal cartilage
+UBERON:0009672,oronasal membrane,UBERON:0004119,endoderm-derived structure
+HP:0011814,Increased urinary hypoxanthine,HP:0004352,Abnormality of purine metabolism
+UBERON:0014453,gustatory epithelium of palate,UBERON:0002926,gustatory epithelium
+HP:0011888,Bleeding requiring red cell transfusion,HP:0001892,Abnormal bleeding
+DOID:0060209,amyotrophic lateral sclerosis type 18,DOID:332,amyotrophic lateral sclerosis
+UBERON:3000453,posterolateral vomerine process,UBERON:0010313,neural crest-derived structure
+HP:0006089,Palmar hyperhidrosis,HP:0000975,Hyperhidrosis
+HP:0000075,Renal duplication,HP:0012210,Abnormal renal morphology
+HP:0004286,Patchy sclerosis of hand bones,HP:0004281,Irregular sclerosis of hand bones
+UBERON:2000127,antorbital,UBERON:0003462,facial bone
+UBERON:0005448,greater omentum,UBERON:0003688,omentum
+HP:0005008,Large joint dislocations,HP:0001373,Joint dislocation
+DOID:14245,cystoid macular retinal degeneration,DOID:2007,degeneration of macula and posterior pole
+HP:0012331,Abnormal autonomic nervous system morphology,HP:0002270,Abnormality of the autonomic nervous system
+HP:0011049,Agenesis of primary maxillary lateral incisor,HP:0000690,Agenesis of maxillary lateral incisor
+UBERON:0002008,cardiac nerve plexus,UBERON:0004120,mesoderm-derived structure
+UBERON:2000564,pelvic abductor profundus,UBERON:0014795,pelvic appendage muscle
+HP:0100769,Synovitis,HP:0005262,Abnormality of the synovia
+UBERON:0011532,female pubococcygeus muscle,UBERON:0011528,pubococcygeus muscle
+HP:0010534,Transient global amnesia,HP:0002354,Memory impairment
+UBERON:2001939,inter-basipterygium joint,UBERON:0000982,skeletal joint
+DOID:4372,intracranial embolism,DOID:6713,cerebrovascular disease
+HP:0010888,Morbus Koehler,HP:0100339,Abnormality of the os naviculare pedis
+HP:0011336,Bitemporal forceps marks,HP:0000606,Abnormality of the periorbital region
+UBERON:2005311,pronephric glomerular capsule epithelium,UBERON:0000487,simple squamous epithelium
+HP:0009707,Synostosis involving the 4th metacarpal,HP:0010012,Abnormality of the 4th metacarpal
+UBERON:0009013,white fibrocartilage,UBERON:0001995,fibrocartilage
+CL:0010002,epithelial cell of umbilical artery,CL:0000066,epithelial cell
+HP:0010811,Narrow uvula,HP:0000172,Abnormality of the uvula
+UBERON:0006025,interdigital region between digits 4 and 5,UBERON:0006012,interdigital region
+HP:0001735,Acute pancreatitis,HP:0001733,Pancreatitis
+UBERON:0010265,mollusc hepatopancreas,UBERON:0010264,hepatopancreas
+HP:0000147,Polycystic ovaries,HP:0000138,Ovarian cysts
+UBERON:0008424,inguinal mammary gland,UBERON:0005173,abdominal segment organ
+UBERON:0002386,forelimb zeugopod,UBERON:0002471,zeugopod
+HP:0100432,Broad distal phalanx of the 4th toe,HP:0010372,Broad phalanges of the 4th toe
+UBERON:2001467,pharyngeal mesoderm,UBERON:0000926,mesoderm
+UBERON:0004721,crista ampullaris,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0006462,Generalized bone demineralization,HP:0004349,Reduced bone mineral density
+UBERON:0006428,basisphenoid bone,UBERON:0002513,endochondral bone
+DOID:3029,colon mucinous adenocarcinoma,DOID:234,colon adenocarcinoma
+HP:0001126,Cryptophthalmos,HP:0100886,Abnormality of globe location
+UBERON:0013697,exocrine pancreas epithelium,UBERON:0005911,endo-epithelium
+HP:0009693,Pseudoepiphyses of the thumb,HP:0010235,Pseudoepiphyses of the phalanges of the hand
+UBERON:0003512,lung blood vessel,UBERON:0003504,respiratory system blood vessel
+HP:0009972,Duplication of phalanx of 4th finger,HP:0009172,Abnormality of the phalanges of the 4th finger
+HP:0008237,Hypothalamic hypothyroidism,HP:0011787,Central hypothyroidism
+UBERON:0005130,metanephric loop of Henle,UBERON:0005146,metanephric nephron tubule
+UBERON:0002630,body of caudate nucleus,UBERON:0011300,gray matter of telencephalon
+HP:0006634,Osteosclerosis of ribs,HP:0012306,Abnormal rib ossification
+UBERON:0003647,metacarpal bone of digit 3,UBERON:0015045,manual digit 3 metacarpus endochondral element
+CL:2000000,epidermal melanocyte,CL:0000362,epidermal cell
+UBERON:0006714,tibiofibula,UBERON:0004251,hindlimb zeugopod bone
+NCBITaxon:1262365,Tabanoidea,NCBITaxon:43735,Tabanomorpha
+UBERON:0002695,parieto-occipital sulcus,UBERON:0008334,subarachnoid sulcus
+HP:0005923,Abnormalities of the metaphyses of the hand,HP:0001155,Abnormality of the hand
+DOID:8920,leukoplakia of vagina,DOID:121,vaginal disease
+HP:0009736,Tibial pseudoarthrosis,HP:0002992,Abnormality of the tibia
+UBERON:0005826,gracile fasciculus of spinal cord,UBERON:0007699,tract of spinal cord
+UBERON:0002304,layer of dentate gyrus,UBERON:0004121,ectoderm-derived structure
+UBERON:0001793,nerve fiber layer of retina,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0002608,Celiac disease,HP:0002244,Abnormality of the small intestine
+UBERON:0010294,scleral endothelium,UBERON:0001986,endothelium
+UBERON:0004013,egg cylinder,UBERON:0000119,cell layer
+UBERON:0002793,dorsal longitudinal fasciculus of pons,UBERON:0003045,dorsal longitudinal fasciculus
+HP:0002012,Abnormality of the abdominal organs,HP:0001438,Abnormality of the abdomen
+UBERON:0001445,skeleton of pes,UBERON:0006717,autopodial skeleton
+UBERON:0000456,bodily secretion,UBERON:0000463,portion of organism substance
+UBERON:0006651,appendix testis,UBERON:0014403,male anatomical structure
+UBERON:0007097,chordo neural hinge,UBERON:0005291,embryonic tissue
+UBERON:3000294,median prenasal process,UBERON:0010313,neural crest-derived structure
+HP:0003843,Round epiphyses of the upper limbs,HP:0003839,Abnormality involving the epiphyses of the upper limbs
+UBERON:0001205,submucosa of small intestine,UBERON:0009566,intestinal submucosa
+UBERON:0002838,first cervical dorsal root ganglion,UBERON:0002834,cervical dorsal root ganglion
+UBERON:0001268,peritoneal fluid,UBERON:0007794,serous fluid
+UBERON:0001692,basioccipital bone,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3000943,pseudofirmisternal girdle,UBERON:0007831,pectoral girdle skeleton
+DOID:3923,diffuse lipomatosis,DOID:3153,lipomatosis
+HP:0100908,Sclerosis of the proximal phalanx of the 2nd finger,HP:0100918,Sclerosis of the phalanges of the 2nd finger
+DOID:9248,Pallister-Hall syndrome,DOID:0080015,physical disorder
+UBERON:0004388,epiphysis of fibula,UBERON:0001437,epiphysis
+UBERON:0002661,superior frontal gyrus,UBERON:0015593,frontal gyrus
+UBERON:0006290,scapula cartilage element,UBERON:0005291,embryonic tissue
+DOID:5574,VIPoma,DOID:169,neuroendocrine tumor
+UBERON:0004338,proximal phalanx of manual digit 1,UBERON:0003620,manual digit 1 phalanx
+HP:0100592,Peritoneal abscess,HP:0002585,Abnormality of the peritoneum
+UBERON:0013499,glossopharyngeal-vagus IX-X preganglion complex,UBERON:0002050,embryonic structure
+HP:0100215,Cone-shaped epiphysis of the middle phalanx of the 5th toe,HP:0100079,Cone-shaped epiphyses of the 5th toe
+HP:0001789,Hydrops fetalis,HP:0000969,Edema
+UBERON:0001228,renal papilla,UBERON:0004120,mesoderm-derived structure
+DOID:2697,renal adenoma,DOID:731,urinary system benign neoplasm
+UBERON:0005653,upper jaw molar epithelium,UBERON:0015839,molar epithelium
+UBERON:4200123,scapular process,UBERON:4100000,skeletal element projection
+UBERON:0008877,epidermal-dermal junction,UBERON:0005769,basement membrane of epithelium
+CL:0002395,Gr1-high classical monocyte,CL:0000860,classical monocyte
+HP:0004220,Short middle phalanx of the 5th finger,HP:0005819,Short middle phalanx of finger
+HP:0100473,Symphalangism affecting the proximal phalanx of the 3rd toe,HP:0010365,Symphalangism affecting the phalanges of the 3rd toe
+DOID:7903,intracranial chondrosarcoma,DOID:4549,extraosseous chondrosarcoma
+HP:0009346,Absent epiphysis of the proximal phalanx of the 3rd finger,HP:0009333,Abnormality of the epiphysis of the proximal phalanx of the 3rd finger
+UBERON:2002265,epineural 3,UBERON:2000507,epineural
+UBERON:0002411,clitoris,UBERON:0005156,reproductive structure
+UBERON:0011614,basihyal element,UBERON:0010522,replacement element
+HP:0100777,Exostoses,HP:0010622,Neoplasm of the skeletal system
+UBERON:0012100,appendicocostalis muscle,UBERON:0003831,respiratory system muscle
+UBERON:0012488,muscle layer of duodenum,UBERON:0011201,muscle layer of small intestine
+DOID:4964,neurotic disorder,DOID:2030,anxiety disorder
+UBERON:0014691,right gastric vein,UBERON:0004450,gastric vein
+UBERON:3010087,M. tibialis anticus longus,UBERON:0010890,pelvic complex muscle
+HP:0009290,Short distal phalanx of the 4th finger,HP:0009289,Aplasia/Hypoplasia of the distal phalanx of the 4th finger
+HP:0006293,Agenesis of maxillary central incisor,HP:0006289,Agenesis of central incisor
+UBERON:0014686,angular vein,UBERON:0009141,craniocervical region vein
+UBERON:0004707,pharyngula stage,UBERON:0000067,embryo stage part
+HP:0006127,Long proximal phalanx of finger,HP:0009834,Abnormality of the proximal phalanges of the hand
+UBERON:2001829,caudal fin dorsal procurrent ray,UBERON:2001584,caudal procurrent ray
+DOID:11664,nephrosclerosis,DOID:1073,renal hypertension
+UBERON:0003937,sex gland,UBERON:0005156,reproductive structure
+UBERON:0009740,border between sublaminar layers,UBERON:0004121,ectoderm-derived structure
+UBERON:0005171,hepatic duct,UBERON:0002394,bile duct
+UBERON:2001341,intervening zone,UBERON:0004121,ectoderm-derived structure
+UBERON:0002199,integument,UBERON:0003102,surface structure
+HP:0008997,Proximal muscle weakness in upper limbs,HP:0003701,Proximal muscle weakness
+UBERON:0007191,anterior paracentral gyrus,UBERON:0007190,paracentral gyrus
+UBERON:0013594,ectosylvian sulcus,UBERON:0008334,subarachnoid sulcus
+UBERON:0004320,middle phalanx of manual digit 2,UBERON:0014488,middle phalanx of digit 2
+DOID:10661,mediastinum ganglioneuroblastoma,DOID:4691,malignant mediastinal neurogenic neoplasm
+UBERON:2005144,ampullary nerve,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:12155,lymphocytic choriomeningitis,DOID:934,viral infectious disease
+HP:0001958,Nonketotic hypoglycemia,HP:0001943,Hypoglycemia
+DOID:11772,leukocoria,DOID:9799,eye degenerative disease
+UBERON:0002139,subcommissural organ,UBERON:0010134,secretory circumventricular organ
+UBERON:0004347,limb bud,UBERON:0004357,paired limb/fin bud
+HP:0009609,Duplication of the 1st metacarpal,HP:0010006,Duplication of the proximal phalanx of hand
+UBERON:0007651,anatomical junction,UBERON:0000061,anatomical structure
+UBERON:0005493,hyoid muscle,UBERON:0004120,mesoderm-derived structure
+DOID:13300,Scheuermann's disease,DOID:8125,osteochondrosis
+DOID:840,cork-handlers' disease,DOID:841,extrinsic allergic alveolitis
+UBERON:3000670,anterior process of hyoid apparatus,UBERON:4100000,skeletal element projection
+DOID:4086,testicular germ cell tumor non-seminomatous,DOID:5557,testicular germ cell cancer
+DOID:3951,acute myocarditis,DOID:820,myocarditis
+UBERON:0001156,ascending colon,UBERON:0000168,segment of colon
+HP:0009395,Cone-shaped epiphyses of the 4th finger,HP:0009174,Abnormality of the epiphyses of the 4th finger
+UBERON:0001244,internal anal sphincter,UBERON:0004916,anal sphincter
+HP:0011682,Perimembranous ventricular septal defect,HP:0001629,Ventricular septal defect
+UBERON:2001476,sublingual ventral ossification,UBERON:2001275,sublingual
+CL:0002215,type IIb muscle cell,CL:0002212,type II muscle cell
+HP:0010417,Osteolytic defects of the distal phalanx of the 2nd toe,HP:0010351,Osteolytic defects of the phalanges of the 2nd toe
+UBERON:0010193,renal portal vein,UBERON:0003513,trunk blood vessel
+HP:0001396,Cholestasis,HP:0004297,Abnormality of the biliary system
+DOID:13825,squamous blepharitis,DOID:9423,blepharitis
+UBERON:0006004,hair follicle matrix region,UBERON:0004121,ectoderm-derived structure
+UBERON:0013191,ovarian cortex,UBERON:0001851,cortex
+CL:0002368,respiratory epithelial cell,CL:0002076,endo-epithelial cell
+UBERON:0001360,deep circumflex iliac vein,UBERON:0001638,vein
+DOID:8187,gestational uterine corpus choriocarcinoma,DOID:8188,uterine corpus choriocarcinoma
+DOID:3049,Churg-Strauss syndrome,DOID:865,vasculitis
+UBERON:2002063,nuchal plate series,UBERON:0000477,anatomical cluster
+DOID:10791,frontal sinusitis,DOID:0050127,sinusitis
+UBERON:2205225,median fin radial cartilage,UBERON:2105225,median fin radial element
+UBERON:0002935,magnocellular part of ventral anterior nucleus,UBERON:0003528,brain grey matter
+UBERON:0003649,metacarpal bone of digit 5,UBERON:0013585,metapodium bone 5
+HP:0000030,Testicular gonadoblastoma,HP:0000150,Gonadoblastoma
+UBERON:0011213,root of vagus nerve,UBERON:0006843,root of cranial nerve
+HP:0012355,Abnormal mannosylation of N-linked protein glycosylation,HP:0012347,Abnormal protein N-linked glycosylation
+HP:0009411,Bracket epiphyses of the 3rd finger,HP:0009320,Abnormality of the epiphyses of the 3rd finger
+HP:0005272,Prominent nasolabial fold,HP:0005289,Abnormality of the nasolabial region
+UBERON:0002381,pectoralis major,UBERON:0003897,axial muscle
+HP:0001805,Thick nail,HP:0008404,Nail dystrophy
+HP:0100811,Aplasia/Hypoplasia of the colon,HP:0005245,Intestinal hypoplasia
+UBERON:0008305,outer fibrous layer of perichondrium,UBERON:0002384,connective tissue
+HP:0100114,Enlarged epiphysis of the middle phalanx of the 2nd toe,HP:0100089,Abnormality of the epiphysis of the middle phalanx of the 2nd toe
+DOID:11671,hypotrichosis of eyelid,DOID:4535,hypotrichosis
+UBERON:0003850,telencephalon neural crest,UBERON:0002342,neural crest
+UBERON:0002625,median preoptic nucleus,UBERON:0007251,preoptic nucleus
+HP:0009332,Abnormality of the epiphysis of the distal phalanx of the 3rd finger,HP:0009320,Abnormality of the epiphyses of the 3rd finger
+UBERON:0016440,glabella,UBERON:0004120,mesoderm-derived structure
+HP:0005733,Spinal stenosis with reduced interpedicular distance,HP:0003416,Spinal canal stenosis
+HP:0010188,Curved distal phalanges of the toes,HP:0010182,Abnormality of the distal phalanges of the toes
+UBERON:0015842,incisor enamel organ,UBERON:0005176,tooth enamel organ
+DOID:5446,eccrine papillary adenoma,DOID:173,eccrine sweat gland neoplasm
+HP:0007460,Autoamputation of digits,HP:0001155,Abnormality of the hand
+HP:0009566,Short distal phalanx of the 2nd finger,HP:0009536,Short 2nd finger
+UBERON:3010131,orbital cartilages,UBERON:0003933,cranial cartilage
+CL:0002576,perineural cell,CL:0002320,connective tissue cell
+DOID:3127,proctitis,DOID:1285,rectal disease
+UBERON:0001111,intercostal muscle,UBERON:0004120,mesoderm-derived structure
+UBERON:0011585,cell condensation,UBERON:0000061,anatomical structure
+UBERON:0002703,precentral gyrus,UBERON:0015593,frontal gyrus
+UBERON:0001585,anterior vena cava,UBERON:0001638,vein
+HP:0005775,Multiple skeletal anomalies,HP:0002652,Skeletal dysplasia
+UBERON:4300003,urodermal bone,UBERON:0008907,dermal bone
+DOID:7642,cholangiolocellular carcinoma,DOID:4928,intrahepatic cholangiocarcinoma
+HP:0006665,Coat hanger sign of ribs,HP:0000772,Abnormality of the ribs
+UBERON:0013758,cervical os,UBERON:0000161,orifice
+HP:0001498,Carpal bone hypoplasia,HP:0006502,Aplasia/Hypoplasia involving the carpal bones
+HP:0003112,Abnormality of serum amino acid levels,HP:0004337,Abnormality of amino acid metabolism
+HP:0002504,Calcification of the small brain vessels,HP:0002514,Cerebral calcification
+UBERON:0001610,lingual artery,UBERON:0001637,artery
+DOID:8106,cellular phase chronic idiopathic myelofibrosis,DOID:4971,myelofibrosis
+HP:0010128,Bracket epiphysis of the proximal phalanx of the hallux,HP:0010126,Abnormality of the epiphysis of the proximal phalanx of the hallux
+HP:0010062,Osteolytic defects of the phalanges of the hallux,HP:0010057,Abnormality of the phalanges of the hallux
+UBERON:3000492,processus infrafenestralis,UBERON:4100000,skeletal element projection
+UBERON:0013159,epithalamus mantle layer,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009733,Glioma,HP:0100836,Malignant neoplasm of the central nervous system
+DOID:4690,childhood mediastinal neurogenic tumor,DOID:4691,malignant mediastinal neurogenic neoplasm
+UBERON:0001441,hindlimb skeleton,UBERON:0007273,pelvic appendage skeleton
+DOID:2146,ovary sarcoma,DOID:2394,ovarian cancer
+UBERON:0012269,equine hindlimb splint bone,UBERON:0012359,pedal digitopodium bone
+HP:0009981,Partial duplication of the distal phalanx of the 4th finger,HP:0009974,Partial duplication of the phalanges of the 4th finger
+HP:0005643,Short 3rd toe,HP:0001831,Short toe
+UBERON:0008297,pennaceous feather,UBERON:0008292,vaned feather
+DOID:12311,stromal corneal pigmentation,DOID:11547,corneal deposit
+UBERON:0005590,rhombomere 8 roof plate,UBERON:0005502,rhombomere roof plate
+DOID:0050727,tyrosinemia type III,DOID:9275,tyrosinemia
+HP:0000995,Melanocytic nevus,HP:0001000,Abnormality of skin pigmentation
+DOID:688,embryonal cancer,DOID:2994,germ cell cancer
+UBERON:0014379,adductor hallucis muscle,UBERON:0014378,intrinsic muscle of pes
+UBERON:0003496,head blood vessel,UBERON:0001981,blood vessel
+UBERON:0006246,humerus pre-cartilage condensation,UBERON:0010884,forelimb bone pre-cartilage condensation
+UBERON:4200166,interepipodial space,UBERON:0004120,mesoderm-derived structure
+HP:0009166,Fragmentation of the epiphysis of the distal phalanx of the 5th finger,HP:0010250,Fragmentation of the epiphyses of the distal phalanges of the hand
+HP:0007902,Vitreous hemorrhage,HP:0011029,Internal hemorrhage
+HP:0100803,Abnormality of the periungual region,HP:0011356,Regional abnormality of skin
+UBERON:0001495,pectoral muscle,UBERON:0008196,muscle of pectoral girdle
+DOID:5310,glycogen-rich clear cell breast carcinoma,DOID:3458,breast adenocarcinoma
+UBERON:0005116,metanephric descending thin limb,UBERON:0004120,mesoderm-derived structure
+HP:0006729,Retroperitoneal chemodectomas,HP:0011793,Neoplasm by anatomical site
+DOID:6857,pineal region mature teratoma,DOID:5566,mature teratoma
+UBERON:2001648,basihyal tooth plate,UBERON:2001647,pharyngeal tooth plate
+DOID:6161,childhood testicular mixed germ cell tumor,DOID:6082,pediatric testicular germ cell tumor
+CL:0000892,smooth muscle cell derived foam cell,CL:0000891,foam cell
+HP:0000799,Renal steatosis,HP:0012210,Abnormal renal morphology
+HP:0100092,Abnormality of the epiphysis of the middle phalanx of the 3rd toe,HP:0010329,Abnormality of the epiphyses of the 3rd toe
+DOID:13730,malignant renovascular hypertension,DOID:13731,malignant secondary hypertension
+DOID:10718,giardiasis,DOID:2789,parasitic protozoa infectious disease
+HP:0009444,Patchy sclerosis of the phalanges of the 3rd finger,HP:0100919,Sclerosis of the phalanges of the 3rd finger
+DOID:950,dacryoadenitis,DOID:1400,lacrimal apparatus disease
+UBERON:0004879,marginal zone of embryo,UBERON:0002050,embryonic structure
+HP:0100842,Septo-optic dysplasia,HP:0001331,Absent septum pellucidum
+HP:0003388,Easy fatigability,HP:0004302,Functional motor problems.
+CL:0002496,intraepithelial lymphocyte,CL:0002419,mature T cell
+HP:0100258,Preaxial polydactyly,HP:0010442,Polydactyly
+DOID:14107,De Quervain disease,DOID:381,arthropathy
+HP:0004252,Abnormality of the trapezium,HP:0001191,Abnormality of the carpal bones
+UBERON:0002437,cerebral hemisphere white matter,UBERON:0011299,white matter of telencephalon
+HP:0001657,Prolonged QT interval,HP:0003115,Abnormal EKG
+HP:0011215,Hemihypsarrhythmia,HP:0011185,EEG with focal epileptiform discharges
+CL:1000504,kidney medulla cell,CL:1000497,kidney cell
+HP:0011852,Chylopericardium,HP:0001698,Pericardial effusion
+HP:0100760,Clubbing of toes,HP:0010161,Abnormality of the phalanges of the toes
+HP:0007406,Hyperpigmentation of eyelids,HP:0007400,Irregular hyperpigmentation
+UBERON:0012177,skin apocrine gland,UBERON:0008974,apocrine gland
+HP:0010368,Abnormality of the distal phalanx of the 3rd toe,HP:0010182,Abnormality of the distal phalanges of the toes
+UBERON:2001844,ceratohyal-ventral hypohyal joint,UBERON:0000982,skeletal joint
+UBERON:0010575,manual digit 1 phalanx pre-cartilage condensation,UBERON:0010564,manual digit 1 mesenchyme
+UBERON:4000177,dorsal fin lepidotrichium,UBERON:4000172,lepidotrichium
+UBERON:0005677,caecum mesentery,UBERON:0003396,mesentery of colon
+DOID:476,breast hemangioma,DOID:255,hemangioma
+UBERON:0002256,dorsal horn of spinal cord,UBERON:0015212,lateral structure
+DOID:3315,lipoma,DOID:0060084,cell type benign neoplasm
+UBERON:0010700,phalanx pre-cartilage condensation,UBERON:0010702,digit mesenchyme
+DOID:14233,orbital cyst,DOID:930,orbital disease
+UBERON:0001199,mucosa of stomach,UBERON:0004786,gastrointestinal system mucosa
+DOID:5142,vulvar leiomyoma,DOID:0060109,vulvar benign neoplasm
+DOID:12450,pancytopenia,DOID:2355,anemia
+HP:0006009,Broad phalanx,HP:0011297,Abnormality of the digits
+UBERON:0013216,udder,UBERON:0014404,female anatomical structure
+HP:0011478,True anophthalmia,HP:0000528,Anophthalmia
+HP:0006514,Intraalveolar nodular calcifications,HP:0010766,Ectopic calcification
+DOID:6257,chromophil adenoma of the kidney,DOID:2697,renal adenoma
+UBERON:0001336,membranous urethra of male or female,UBERON:0000063,organ segment
+UBERON:0006072,cervical region of vertebral column,UBERON:0006077,subdivision of vertebral column
+HP:0000202,Oral cleft,HP:0000153,Abnormality of the mouth
+UBERON:0002424,oral epithelium,UBERON:0010371,ecto-epithelium
+DOID:14796,Dubowitz Syndrome,DOID:225,syndrome
+UBERON:0003487,skin sebaceous gland,UBERON:0001821,sebaceous gland
+UBERON:0001821,sebaceous gland,UBERON:0007771,epidermis gland
+UBERON:4100004,ischial peduncle,UBERON:0004530,bony projection
+DOID:0050914,large intestine adenoma,DOID:4610,intestinal benign neoplasm
+HP:0009211,Small epiphysis of the middle phalanx of the 5th finger,HP:0004224,Abnormality of the epiphysis of the middle phalanx of the 5th finger
+UBERON:0002590,prepyriform area,UBERON:0002619,regional part of cerebral cortex
+UBERON:0002921,longitudinal fissure,UBERON:0014466,subarachnoid fissure
+CL:0000805,immature single positive thymocyte,CL:0000893,thymocyte
+DOID:10041,dysplastic nevus syndrome,DOID:0050736,autosomal dominant disease
+UBERON:0004649,sphenoid bone pterygoid process,UBERON:4100000,skeletal element projection
+UBERON:0015221,common nasal meatus,UBERON:0015216,nasal meatus
+HP:0011769,Ectopic parathyroid,HP:0011768,Parathyroid dysgenesis
+HP:0004554,Generalized hypertrichosis,HP:0000998,Hypertrichosis
+UBERON:0005130,metanephric loop of Henle,UBERON:0001288,loop of Henle
+UBERON:0003264,mesoderm of yolk sac,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0001632,temporal artery,UBERON:0001637,artery
+DOID:3613,Canavan disease,DOID:10579,leukodystrophy
+UBERON:3010720,ramus hyomandibularis,UBERON:0004529,anatomical projection
+HP:0008633,Absent gonadal tissue,HP:0000812,Abnormal internal genitalia
+NCBITaxon:11604,Puumala virus,NCBITaxon:11598,Hantavirus
+HP:0002654,Multiple epiphyseal dysplasia,HP:0002652,Skeletal dysplasia
+UBERON:0007177,lamina propria of mucosa of colon,UBERON:0011189,lamina propria of large intestine
+HP:0000137,Abnormality of the ovary,HP:0000008,Abnormality of female internal genitalia
+HP:0001847,Long hallux,HP:0001844,Abnormality of the hallux
+UBERON:0011152,dorsal hyoid arch skeleton,UBERON:0010912,subdivision of skeleton
+UBERON:0006266,nasolacrimal groove,UBERON:0005291,embryonic tissue
+UBERON:2000623,basipterygium bone,UBERON:2100623,basipterygium element
+UBERON:4300032,posterior dorsal fin basal cartilage,UBERON:0007844,cartilage element
+UBERON:0005192,deferent duct artery,UBERON:0005156,reproductive structure
+UBERON:0005328,mesonephric comma-shaped body,UBERON:0005330,mesonephric nephron epithelium
+UBERON:2005255,frontal-parietal joint,UBERON:0000982,skeletal joint
+UBERON:0005588,rhombomere 8 floor plate,UBERON:0005500,rhombomere floor plate
+UBERON:0005847,thoracic spinal cord lateral column,UBERON:0006078,subdivision of spinal cord lateral column
+HP:0004021,Lytic defects of radial metaphysis,HP:0003851,Lytic defects in metaphyses of the upper limbs
+CL:0000716,lymph gland crystal cell,CL:0000735,lymph gland hemocyte
+HP:0001970,Tubulointerstitial nephritis,HP:0001969,Tubulointerstitial abnormality
+UBERON:0001970,bile,UBERON:0000456,bodily secretion
+HP:0100796,Orchitis,HP:0000035,Abnormality of the testis
+UBERON:2205379,dorsal fin distal radial cartilage 8,UBERON:2200936,dorsal fin distal radial cartilage
+UBERON:2001666,rudimentary neural arch,UBERON:0003861,neural arch
+UBERON:2000311,adductor mandibulae complex,UBERON:0010959,craniocervical muscle
+HP:0010375,Osteolytic defects of the phalanges of the 4th toe,HP:0010177,Osteolytic defects of the phalanges of the toes
+UBERON:2000735,hemal postzygapophysis,UBERON:0004120,mesoderm-derived structure
+UBERON:0004635,thoracic vertebra 11,UBERON:0002347,thoracic vertebra
+NCBITaxon:13373,Burkholderia mallei,NCBITaxon:111527,pseudomallei group
+DOID:7788,adult spinal cord ependymoma,DOID:5503,spinal cord ependymoma
+CL:0000975,short lived plasma cell,CL:0000786,plasma cell
+UBERON:0001769,iris,UBERON:0000481,multi-tissue structure
+HP:0000329,Facial hemangioma,HP:0001028,Hemangioma
+DOID:0050932,lung mucoepidermoid carcinoma,DOID:3905,lung carcinoma
+HP:0003995,Abnormality of the radial head,HP:0002818,Abnormality of the radius
+HP:0006587,Straight clavicles,HP:0000889,Abnormality of the clavicles
+UBERON:0001813,somatic nerve plexus,UBERON:0001810,nerve plexus
+HP:0100768,Choriocarcinoma,HP:0100728,Germ cell neoplasia
+HP:0011109,Chronic sinusitis,HP:0000246,Sinusitis
+HP:0002167,Neurological speech impairment,HP:0011446,Abnormality of higher mental function
+UBERON:0002439,myenteric nerve plexus,UBERON:0000429,enteric plexus
+UBERON:0003396,mesentery of colon,UBERON:0007826,peritoneal mesentery
+HP:0004633,Lower thoracic kyphosis,HP:0002942,Thoracic kyphosis
+UBERON:0010287,motor root of facial nerve,UBERON:0004674,facial nerve root
+HP:0006375,Dumbbell-shaped femur,HP:0000947,Dumbbell-shaped long bone
+DOID:10605,short bowel syndrome,DOID:5295,intestinal disease
+CL:1000274,trophectodermal cell,CL:0000349,extraembryonic cell
+CL:0002679,natural helper lymphocyte,CL:0000542,lymphocyte
+DOID:1520,colon carcinoma,DOID:219,colon cancer
+HP:0200122,Atypical or prolonged hepatitis,HP:0012115,Hepatitis
+HP:0009399,Ivory epiphyses of the 4th finger,HP:0009174,Abnormality of the epiphyses of the 4th finger
+HP:0009515,Cone-shaped epiphysis of the middle phalanx of the 2nd finger,HP:0009500,Abnormality of the epiphysis of the middle phalanx of the 2nd finger
+UBERON:0015855,ventral ectodermal ridge,UBERON:0002050,embryonic structure
+UBERON:0013645,gular gland,UBERON:0002530,gland
+DOID:5151,plexiform neurofibroma,DOID:962,neurofibroma
+HP:0012348,Decreased galactosylation of N-linked protein glycosylation,HP:0012347,Abnormal protein N-linked glycosylation
+HP:0100947,Sclerosis of the middle phalanges of the toes,HP:0100924,Sclerosis of the phalanges of the toes
+UBERON:0004780,gastrointestinal system lamina propria,UBERON:0000030,lamina propria
+HP:0006180,Crowded carpal bones,HP:0001191,Abnormality of the carpal bones
+HP:0001881,Abnormality of leukocytes,HP:0001871,Abnormality of  blood and blood-forming tissues
+UBERON:0000042,serous membrane,UBERON:0004120,mesoderm-derived structure
+HP:0004784,Juvenile gastrointestinal polyposis,HP:0200008,Intestinal polyposis
+HP:0009164,Abnormal calcification of the carpal bones,HP:0010766,Ectopic calcification
+UBERON:0002652,posterior median eminence,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001691,external ear,UBERON:0015212,lateral structure
+UBERON:0012330,nasal-associated lymphoid tissue,UBERON:0004119,endoderm-derived structure
+HP:0001053,Hypopigmented skin patches,HP:0011355,Localized skin lesion
+UBERON:0005712,midgut duodenum mesentery,UBERON:0004121,ectoderm-derived structure
+UBERON:4200152,os sesamoides tarsale,UBERON:0001447,tarsal bone
+UBERON:0002707,pyramidal tract,UBERON:0001018,axon tract
+UBERON:0003217,neural lobe of neurohypophysis,UBERON:0002784,regional part of diencephalon
+UBERON:0002165,endocardium,UBERON:0005983,heart layer
+UBERON:0002577,pericentral nucleus of inferior colliculus,UBERON:0011214,nucleus of midbrain tectum
+UBERON:0010164,collection of hairs,UBERON:0000477,anatomical cluster
+DOID:9837,hypertropia,DOID:540,strabismus
+UBERON:0008987,renal parenchyma,UBERON:0006554,urinary system structure
+HP:0001428,Somatic mutation,HP:0000005,Mode of inheritance
+HP:0010199,Patchy sclerosis of the middle phalanges of the toes,HP:0010178,Patchy sclerosis of the phalanges of the toes
+UBERON:2000983,somite 9,UBERON:0002329,somite
+UBERON:0002012,pulmonary artery,UBERON:0001637,artery
+HP:0003760,Percussion-induced rapid rolling muscle contractions (PIRC),HP:0010548,Percussion myotonia
+HP:0000303,Mandibular prognathia,HP:0000277,Abnormality of the mandible
+DOID:2373,hereditary elliptocytosis,DOID:74,hematopoietic system disease
+HP:0006964,Cerebral cortical neurodegeneration,HP:0007369,Atrophy/Degeneration affecting the cerebrum
+UBERON:0002898,chiasmatic cistern,UBERON:0004050,subarachnoid cistern
+DOID:2438,dermis tumor,DOID:3165,skin benign neoplasm
+UBERON:0012110,frontal process of zygomatic bone,UBERON:0010313,neural crest-derived structure
+HP:0004481,Progressive macrocephaly,HP:0000256,Macrocephaly
+DOID:0050691,branchiooculofacial syndrome,DOID:0050736,autosomal dominant disease
+DOID:1791,peritoneal carcinoma,DOID:3119,gastrointestinal system cancer
+DOID:4767,classic pulmonary blastoma,DOID:4765,pulmonary blastoma
+UBERON:0001677,sphenoid bone,UBERON:0002513,endochondral bone
+HP:0008678,Renal hypoplasia/aplasia,HP:0012210,Abnormal renal morphology
+DOID:643,progressive multifocal leukoencephalopathy,DOID:934,viral infectious disease
+HP:0001065,Striae distensae,HP:0004334,Dermal atrophy
+UBERON:2005055,median palatocerebral vein,UBERON:0009141,craniocervical region vein
+HP:0002225,Sparse pubic hair,HP:0100133,Abnormality of the pubic hair
+HP:0012453,Bilateral wrist flexion contracture,HP:0001239,Wrist flexion contracture
+DOID:5600,precursor lymphoblastic lymphoma/leukemia,DOID:0060058,lymphoma
+HP:0100237,Proximal symphalangism (feet),HP:0100264,Proximal symphalangism
+DOID:0050842,oculogyric crisis,DOID:0050836,focal dystonia
+UBERON:0013138,coronary ligament of liver,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0005443,filum terminale,UBERON:0000479,tissue
+HP:0100097,Abnormality of the epiphysis of the distal phalanx of the 5th toe,HP:0010341,Abnormality of the epiphyses of the 5th toe
+NCBITaxon:91347,Enterobacteriales,NCBITaxon:1236,Gammaproteobacteria
+UBERON:0013068,palatine torus,UBERON:0010313,neural crest-derived structure
+HP:0006349,Agenesis of permanent teeth,HP:0011044,Abnormal number of permanent teeth
+DOID:10378,disuse amblyopia,DOID:10376,amblyopia
+HP:0100832,Mouches volantes,HP:0004327,Abnormality of the vitreous humor
+HP:0001991,Aplasia/Hypoplasia of toe,HP:0001780,Abnormality of toe
+HP:0003034,Diaphyseal sclerosis,HP:0011001,Increased bone mineral density
+HP:0100383,Aplasia of the middle phalanx of the 5th toe,HP:0100374,Aplasia/Hypoplasia of the middle phalanx of the 5th toe
+UBERON:0008618,subcostal muscle,UBERON:0002426,chest muscle
+UBERON:3000068,cartilago ectochoanalis,UBERON:0003406,cartilage of respiratory system
+CL:0002627,mature astrocyte,CL:0000127,astrocyte
+UBERON:0004019,baroreceptor,UBERON:0000477,anatomical cluster
+UBERON:2000406,parvocellular superficial pretectal nucleus,UBERON:0014450,pretectal nucleus
+UBERON:0004986,mucosa of deferent duct,UBERON:0000344,mucosa
+DOID:1563,dermatomycosis,DOID:0050134,cutaneous mycosis
+HP:0000829,Hypoparathyroidism,HP:0011767,Abnormality of the parathyroid physiology
+HP:0003904,Wide epiphyses of the upper limbs,HP:0003839,Abnormality involving the epiphyses of the upper limbs
+HP:0010360,Broad phalanges of the 3rd toe,HP:0010330,Abnormality of the phalanges of the 3rd toe
+UBERON:0007265,intervertebral disk of axis,UBERON:0007252,intervertebral disk of cervical vertebra
+DOID:11213,acute contagious conjunctivitis,DOID:11184,acute conjunctivitis
+UBERON:0009716,cupular organ,UBERON:0000020,sense organ
+CL:0008002,skeletal muscle fiber,CL:0002372,myotube
+UBERON:0010016,spiral valve of intestine,UBERON:0003978,valve
+HP:0000252,Microcephaly,HP:0000240,Abnormality of skull size
+UBERON:0008925,sublaminar layer S4,UBERON:0009731,sublaminar layers S3 or S4
+DOID:8178,endometrial type cervical adenomyoma,DOID:4995,cervical adenomyoma
+DOID:0050195,Bolivian hemorrhagic fever,DOID:934,viral infectious disease
+UBERON:0005030,mucosa of paranasal sinus,UBERON:0000344,mucosa
+HP:0009427,Triangular shaped distal phalanx of the 3rd finger,HP:0009875,Triangular shaped distal phalanges of the hand
+UBERON:0012320,cervical artery,UBERON:0003502,neck blood vessel
+HP:0009408,Aplasia/Hypoplasia of the phalanges of the 4th finger,HP:0009172,Abnormality of the phalanges of the 4th finger
+UBERON:3000654,pars jugalis,UBERON:0010313,neural crest-derived structure
+UBERON:0010687,pedal digit metatarsal pre-cartilage condensation,UBERON:0015036,pedal digit metatarsal endochondral element
+HP:0009162,Absent middle phalanx of 5th finger,HP:0009161,Aplasia/Hypoplasia of the middle phalanx of the 5th finger
+HP:0001252,Muscular hypotonia,HP:0003808,Abnormal muscle tone
+UBERON:0011202,urachus epithelium,UBERON:0005911,endo-epithelium
+HP:0006329,Alveolar process hypoplasia,HP:0006477,Abnormality of the alveolar ridges
+HP:0011453,Abnormality of the incus,HP:0004452,Abnormality of the middle ear ossicles
+NCBITaxon:30005,Anoplura,NCBITaxon:85819,Phthiraptera
+HP:0010127,Absent epiphysis of the proximal phalanx of the hallux,HP:0010126,Abnormality of the epiphysis of the proximal phalanx of the hallux
+HP:0000772,Abnormality of the ribs,HP:0001547,Abnormality of the rib cage
+UBERON:3010752,lobe,UBERON:0004119,endoderm-derived structure
+UBERON:0002395,talus,UBERON:0011679,proximal tarsal bone
+DOID:2935,Chediak-Higashi syndrome,DOID:0050737,autosomal recessive disease
+DOID:9512,simple chronic conjunctivitis,DOID:2475,chronic conjunctivitis
+HP:0010315,Aplasia/Hypoplasia of the diaphragm,HP:0000775,Abnormality of the diaphragm
+UBERON:0002048,lung,UBERON:0015212,lateral structure
+UBERON:0005184,hair medulla,UBERON:0000958,medulla of organ
+CL:1000073,spinal cord radial glial cell,CL:0000681,radial glial cell
+HP:0003886,Wide humerus,HP:0003063,Abnormality of the humerus
+DOID:6613,vaginal villous adenoma,DOID:5402,vaginal adenoma
+UBERON:0014696,anterior choroidal artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0009662,Abnormality of the epiphysis of the distal phalanx of the thumb,HP:0009617,Abnormality of the distal phalanx of the thumb
+UBERON:0001558,lower respiratory tract,UBERON:0000072,segment of respiratory tract
+DOID:10587,Krabbe disease,DOID:10579,leukodystrophy
+CL:0000725,nitrogen fixing cell,CL:0000003,native cell
+HP:0006369,Irregular patellae,HP:0003045,Abnormality of the patella
+DOID:2449,acromegaly,DOID:2444,hyperpituitarism
+UBERON:0004172,pons reticulospinal tract,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009433,Osteolytic defects of the middle phalanx of the 3rd finger,HP:0004172,Abnormality of the middle phalanx of the 3rd finger
+HP:0005920,Abnormality of the epiphyses of the phalanges of the hand,HP:0005924,Abnormality of the epiphyses of the hand
+HP:0010104,Absent first metatarsal,HP:0010067,Aplasia/Hypoplasia of the 1st metatarsal
+HP:0004452,Abnormality of the middle ear ossicles,HP:0008609,Morphological abnormality of the middle ear
+UBERON:3000817,margo posterior,UBERON:0000064,organ part
+HP:0010041,Short 3rd metacarpal,HP:0010039,Aplasia/Hypoplasia of the 3rd metacarpal
+HP:0000600,Abnormality of the pharynx,HP:0000234,Abnormality of the head
+UBERON:0010017,spiral valve of cystic duct,UBERON:0003978,valve
+HP:0100156,Triangular epiphysis of the middle phalanx of the 3rd toe,HP:0100065,Triangular epiphyses of the 3rd toe
+UBERON:0008840,plantar pad,UBERON:0013623,pedal autopod pad
+UBERON:0005746,primary vitreous humour,UBERON:0010314,structure with developmental contribution from neural crest
+CL:1000708,ureter adventitial cell,CL:0000134,mesenchymal cell
+HP:0009919,Retinoblastoma,HP:0002898,Embryonal neoplasm
+DOID:10030,interstitial emphysema,DOID:9675,pulmonary emphysema
+UBERON:0011944,subintestinal vein,UBERON:0001638,vein
+HP:0002366,Abnormality of the lower motor neuron,HP:0002450,Abnormality of the motor neurons
+HP:0002648,Abnormality of calvarial morphology,HP:0002683,Abnormality of the calvaria
+UBERON:0005403,ventral striatum,UBERON:0011300,gray matter of telencephalon
+HP:0010395,Aplasia/Hypoplasia of the proximal phalanx of the 2nd toe,HP:0010203,Aplasia/Hypoplasia of the proximal phalanges of the toes
+DOID:9561,nasopharyngeal disease,DOID:974,upper respiratory tract disease
+HP:0011556,Double inlet right ventricle,HP:0001750,Single ventricle
+UBERON:3000380,palatoquadrate articular process,UBERON:4100000,skeletal element projection
+CL:0002330,undifferentiated cell of bronchus epithelium,CL:0002328,bronchial epithelial cell
+CL:0000169,type B pancreatic cell,CL:0000083,epithelial cell of pancreas
+UBERON:0003876,subdivision of hippocampus,UBERON:0002619,regional part of cerebral cortex
+HP:0000260,Wide anterior fontanel,HP:0000239,Large fontanelles
+HP:0004276,Exostoses of hand bones,HP:0001155,Abnormality of the hand
+UBERON:0002507,abdominal lymph node,UBERON:0000029,lymph node
+HP:0002652,Skeletal dysplasia,HP:0011842,Abnormality of skeletal morphology
+HP:0004279,Short palm,HP:0005927,Aplasia/Hypoplasia involving bones of the hand
+HP:0000437,Depressed nasal tip,HP:0000436,Abnormality of the nasal tip
+HP:0008407,Hyperconvex thumb nails,HP:0001795,Hyperconvex nail
+HP:0000227,Tongue telangiectasia,HP:0000157,Abnormality of the tongue
+HP:0010512,Adrenal calcification,HP:0011732,Abnormality of adrenal morphology
+UBERON:0004553,forelimb digital artery,UBERON:0003522,manual digit blood vessel
+DOID:8013,penis papillary carcinoma,DOID:5518,penis squamous cell carcinoma
+HP:0000902,Rib fusion,HP:0000772,Abnormality of the ribs
+UBERON:0003265,chorionic mesenchyme,UBERON:0010333,extraembryonic membrane mesenchyme
+UBERON:0013493,abdominal fascia,UBERON:0003567,abdomen connective tissue
+UBERON:0011594,dentary tooth,UBERON:0003268,tooth of lower jaw
+DOID:10323,byssinosis,DOID:10316,pneumoconiosis
+HP:0000472,Long neck,HP:0000464,Abnormality of the neck
+UBERON:0009969,stato-acoustic epithelium,UBERON:0006934,sensory epithelium
+HP:0100790,Hernia,HP:0003549,Abnormality of connective tissue
+UBERON:0012317,vagina orifice,UBERON:0005156,reproductive structure
+HP:0008134,Irregular tarsal ossification,HP:0008369,Abnormal tarsal ossification
+UBERON:0015777,transitional epithelium of prostatic urethra,UBERON:0004787,urethra urothelium
+HP:0100833,Neoplasm of the small intestine,HP:0007378,Neoplasm of the gastrointestinal tract
+HP:0002268,Paroxysmal dystonia,HP:0001332,Dystonia
+UBERON:3010529,ovisac,UBERON:0005156,reproductive structure
+UBERON:0005421,pectoral appendage apical ectodermal ridge,UBERON:0004121,ectoderm-derived structure
+UBERON:3010183,femoral glands,UBERON:3010606,limb glands
+HP:0100389,Short distal phalanx of the 3rd toe,HP:0100366,Short phalanx of the 3rd toe
+HP:0011925,Decreased activity of mitochondrial ATP synthase complex,HP:0008972,Decreased activity of mitochondrial respiratory chain
+HP:0009247,Abnormality of the epiphysis of the middle phalanx of the 4th finger,HP:0010244,Abnormality of the epiphyses of the middle phalanges of the hand
+UBERON:0013628,pollical pad,UBERON:0003533,manual digit skin
+HP:0009179,Deviation of the 5th finger,HP:0004207,Abnormality of the 5th finger
+UBERON:0007377,stratum compactum,UBERON:0004120,mesoderm-derived structure
+UBERON:0001173,biliary tree,UBERON:0004119,endoderm-derived structure
+HP:0100848,Neoplasia of the male external genitalia,HP:0000032,Abnormality of male external genitalia
+UBERON:0009911,lobule,UBERON:0000064,organ part
+UBERON:2001878,rib of vertebra 2,UBERON:0002228,rib
+HP:0000700,Periapical radiolucency,HP:0000164,Abnormality of the teeth
+CL:0000036,epithelial fate stem cell,CL:0000035,single fate stem cell
+DOID:4993,atypical polypoid adenomyoma,DOID:2609,adenomyoma
+DOID:4211,posterior cranial fossa meningioma,DOID:3565,meningioma
+HP:0002277,Horner syndrome,HP:0012332,Abnormal autonomic nervous system physiology
+HP:0100070,Fragmentation of the epiphyses of the 4th toe,HP:0010335,Abnormality of the epiphyses of the 4th toe
+HP:0009157,Ivory epiphysis of the proximal phalanx of the 5th finger,HP:0010274,Ivory epiphyses of the proximal phalanges of the hand
+CL:0001057,"myeloid dendritic cell, human",CL:0001056,"dendritic cell, human"
+CL:0000534,primary interneuron,CL:0000099,interneuron
+CL:0000008,migratory cranial neural crest cell,CL:0000333,migratory neural crest cell
+HP:0012401,Abnormal urine alpha-ketoglutarate concentration,HP:0003110,Abnormality of urine homeostasis
+UBERON:0004643,lateral ventricle ependyma,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3010450,dorso-lateral marginal zone,UBERON:0004879,marginal zone of embryo
+HP:0006257,Abnormality of carpal bone ossification,HP:0001191,Abnormality of the carpal bones
+UBERON:0007179,basal cell layer of urothelium,UBERON:0004119,endoderm-derived structure
+HP:0002639,Budd-Chiari syndrome,HP:0002624,Venous abnormality
+DOID:11695,portal vein thrombosis,DOID:866,vein disease
+UBERON:4200076,trunk armor pectoral fenestra,UBERON:3000755,pectoral girdle opening
+UBERON:0002586,calcarine sulcus,UBERON:0013118,sulcus of brain
+UBERON:0001934,dorsomedial nucleus of hypothalamus,UBERON:0002951,regional part of intermediate hypothalamic region
+UBERON:0011188,lesser tubercle of humerus,UBERON:4100000,skeletal element projection
+UBERON:0004416,proximal epiphysis of metacarpal bone,UBERON:0004390,epiphysis of metacarpal bone
+UBERON:0006811,occipital condyle,UBERON:0005913,zone of bone organ
+HP:0002927,Histidinuria,HP:0010905,Abnormality of histidine metabolism
+UBERON:0011185,gastrointestinal sphincter,UBERON:0004590,sphincter muscle
+UBERON:0010905,clavicle bone primordium,UBERON:0001048,primordium
+DOID:10974,oophoritis,DOID:1100,ovarian disease
+HP:0100776,Recurrent pharyngitis,HP:0002788,Recurrent upper respiratory tract infections
+UBERON:0006326,base of arytenoid,UBERON:0005913,zone of bone organ
+UBERON:0006282,primary head vein,UBERON:0002050,embryonic structure
+HP:0005511,Heinz body anemia,HP:0001878,Hemolytic anemia
+UBERON:0004051,lateral cerebellomedullary cistern,UBERON:0004049,cerebellomedullary cistern
+UBERON:0001277,intestinal epithelium,UBERON:0003350,epithelium of mucosa
+HP:0001399,Hepatic failure,HP:0001410,Decreased liver function
+HP:0200109,Absent/shortened outer dynein arms,HP:0012256,Absent outer dynein arms
+DOID:0060208,amyotrophic lateral sclerosis type 17,DOID:332,amyotrophic lateral sclerosis
+HP:0010968,Abnormality of liposaccharide metabolism,HP:0003119,Abnormality of lipid metabolism
+UBERON:0003499,brain blood vessel,UBERON:0001981,blood vessel
+UBERON:0002716,collateral sulcus,UBERON:0008334,subarachnoid sulcus
+UBERON:0004385,epiphysis of radius,UBERON:0001437,epiphysis
+DOID:10266,subendocardial infarction acute myocardial infarction,DOID:9408,acute myocardial infarction
+UBERON:2001231,pharyngeal arch 4 skeleton,UBERON:0010912,subdivision of skeleton
+HP:0012332,Abnormal autonomic nervous system physiology,HP:0002270,Abnormality of the autonomic nervous system
+HP:0009670,Ivory epiphysis of the proximal phalanx of the thumb,HP:0009692,Ivory epiphyses of the thumb
+HP:0006711,Aplasia/Hypoplasia involving bones of the thorax,HP:0000765,Abnormality of the thorax
+CL:0000970,unswitched memory B cell,CL:0000787,memory B cell
+CL:0000974,long lived plasma cell,CL:0000786,plasma cell
+UBERON:0010362,endoskeleton,UBERON:0010912,subdivision of skeleton
+CL:1001603,lung macrophage,CL:0000235,macrophage
+UBERON:0001599,stapedius muscle,UBERON:0001577,facial nerve muscle
+HP:0011781,Thyroid C cell hyperplasia,HP:0008249,Thyroid hyperplasia
+UBERON:0004526,cardiac muscle tissue of trabecula carnea of left ventricle,UBERON:0003382,cardiac muscle of left ventricle
+DOID:13328,diabetic cataract,DOID:83,cataract
+DOID:10971,acute salpingo-oophoritis,DOID:10973,acute salpingitis
+HP:0000068,Urethral atresia,HP:0000795,Abnormality of the urethra
+HP:0006710,Aplasia/Hypoplasia of the clavicles,HP:0000889,Abnormality of the clavicles
+UBERON:0005352,spermatic cord,UBERON:0000477,anatomical cluster
+DOID:7032,bile duct clear cell adenocarcinoma,DOID:4896,bile duct adenocarcinoma
+CL:0000765,erythroblast,CL:0002242,nucleate cell
+UBERON:0013426,obelion,UBERON:0006983,anatomical point
+HP:0002034,Abnormality of the rectum,HP:0002250,Abnormality of the large intestine
+CL:0002623,acinar cell of salivary gland,CL:1001596,salivary gland glandular cell
+CL:0001047,"CD4-positive, CD25-positive, CCR4-positive, alpha-beta regulatory T cell",CL:0000792,"CD4-positive, CD25-positive, alpha-beta regulatory T cell"
+UBERON:0007267,trachea pre-cartilage rings,UBERON:0009505,associated mesenchyme of trachea
+UBERON:0003571,trachea connective tissue,UBERON:0003580,lower respiratory tract connective tissue
+UBERON:2001553,manubrium,UBERON:0002513,endochondral bone
+HP:0008609,Morphological abnormality of the middle ear,HP:0000370,Abnormality of the middle ear
+HP:0011361,Congenital abnormal hair pattern,HP:0010720,Abnormal hair pattern
+UBERON:2000622,barbel,UBERON:0003102,surface structure
+HP:0002733,Abnormality of the lymph nodes,HP:0100763,Abnormality of the lymphatic system
+HP:0011031,Abnormality of iron homeostasis,HP:0011030,Abnormality of transition element cation homeostasis
+UBERON:1000022,Zymbal's gland,UBERON:0015251,modified sebaceous gland
+HP:0009229,Curved proximal phalanx of the 5th finger,HP:0004214,Curved phalanges of the 5th finger
+UBERON:0003957,Bruch's membrane,UBERON:0000119,cell layer
+UBERON:3000408,pars media plectri,UBERON:0000064,organ part
+DOID:13924,necrotizing ulcerative gingivitis,DOID:3087,gingivitis
+UBERON:0006755,inferior parathyroid gland,UBERON:0004119,endoderm-derived structure
+UBERON:3000582,sulcus dentalis of premaxilla,UBERON:0000464,anatomical space
+DOID:11836,clubfoot,DOID:0080006,bone development disease
+HP:0000930,Elevated imprint of the transverse sinuses,HP:0002693,Abnormality of the skull base
+HP:0010859,Frank breech presentation,HP:0001623,Breech presentation
+HP:0007435,Diffuse palmoplantar keratoderma,HP:0000982,Palmoplantar keratoderma
+DOID:13942,acute gonococcal salpingitis,DOID:10973,acute salpingitis
+DOID:11983,Prader-Willi syndrome,DOID:0080014,chromosomal disease
+HP:0004306,Abnormality of the endocardium,HP:0001627,Abnormality of cardiac morphology
+DOID:11088,asphyxia neonatorum,DOID:1579,respiratory system disease
+UBERON:2000654,rostral motor nucleus of abducens,UBERON:0006331,brainstem nucleus
+DOID:1829,urethral stricture,DOID:12577,urethral obstruction
+HP:0003105,Protuberances at ends of long bones,HP:0011314,Abnormality of long bone morphology
+UBERON:0016412,central part of body of vertebra,UBERON:0005913,zone of bone organ
+HP:0005922,Abnormal hand morphology,HP:0001155,Abnormality of the hand
+UBERON:0008195,tarsometatarsus,UBERON:0005899,pes bone
+UBERON:0002305,layer of hippocampus,UBERON:0004121,ectoderm-derived structure
+UBERON:4200069,sternal keel,UBERON:0005913,zone of bone organ
+HP:0007333,Hypoplasia of the frontal lobes,HP:0006872,Cerebral hypoplasia
+HP:0004311,Abnormality of macrophages,HP:0010974,Abnormality of myeloid leukocytes
+UBERON:0007254,intervertebral disk of thoracic vertebra,UBERON:0005181,thoracic segment organ
+UBERON:0011386,facial modiolus,UBERON:0002385,muscle tissue
+HP:0011343,Moderate global developmental delay,HP:0001263,Global developmental delay
+HP:0011312,Fused nails,HP:0002164,Nail dysplasia
+HP:0011276,Vascular skin abnormality,HP:0011354,Generalized abnormality of skin
+DOID:8670,eating disorder,DOID:0060038,specific developmental disorder
+HP:0003416,Spinal canal stenosis,HP:0000925,Abnormality of the vertebral column
+UBERON:0006650,tunica vaginalis testis,UBERON:0014403,male anatomical structure
+UBERON:0005328,mesonephric comma-shaped body,UBERON:0004198,comma-shaped body
+HP:0003844,Small epiphyses of the upper limbs,HP:0003839,Abnormality involving the epiphyses of the upper limbs
+DOID:6522,mixed cell uveal melanoma,DOID:6039,uveal melanoma
+UBERON:0008449,trochlear notch,UBERON:0005055,zone of long bone
+UBERON:0006218,common atrial chamber,UBERON:0002050,embryonic structure
+UBERON:0006857,interrenal primordium,UBERON:0004120,mesoderm-derived structure
+DOID:4926,bronchiolo-alveolar adenocarcinoma,DOID:3910,lung adenocarcinoma
+HP:0009227,Broad proximal phalanx of the 5th finger,HP:0009852,Broad proximal phalanges of the hand
+HP:0000151,Aplasia of the uterus,HP:0008684,Aplasia/hypoplasia of the uterus
+UBERON:0002484,bone marrow cavity,UBERON:0002553,anatomical cavity
+HP:0010172,Triangular epiphyses of the toes,HP:0010587,Triangular epiphyses
+UBERON:0004337,distal phalanx of manual digit 1,UBERON:0003620,manual digit 1 phalanx
+DOID:11719,oculopharyngeal muscular dystrophy,DOID:9884,muscular dystrophy
+HP:0005320,Lack of facial subcutaneous fat,HP:0003717,Minimal subcutaneous fat
+HP:0006248,Limited wrist movement,HP:0001376,Limitation of joint mobility
+HP:0009674,Triangular epiphysis of the proximal phalanx of the thumb,HP:0009696,Triangular epiphyses of the thumb
+HP:0002476,"Primitive reflexes (palmomental, snout, glabellar)",HP:0100022,Abnormality of movement
+UBERON:0010575,manual digit 1 phalanx pre-cartilage condensation,UBERON:0010586,manual digit phalanx pre-cartilage condensation
+UBERON:0004339,vault of skull,UBERON:0010912,subdivision of skeleton
+UBERON:0002996,nucleus of optic tract,UBERON:0003528,brain grey matter
+DOID:374,nutrition disease,DOID:0060158,acquired metabolic disease
+UBERON:0010848,radius-ulna cartilage element,UBERON:0010883,forelimb cartilage element
+UBERON:0013158,foregut-midgut junction gland,UBERON:0003408,gland of gut
+UBERON:0010753,lymph node secondary follicle,UBERON:0001745,secondary nodular lymphoid tissue
+UBERON:0004118,vasculature of iris,UBERON:0002203,vasculature of eye
+UBERON:0003022,cerebral cortex lobe,UBERON:0002619,regional part of cerebral cortex
+UBERON:0003648,metacarpal bone of digit 4,UBERON:0013584,metapodium bone 4
+UBERON:0001794,inner limiting layer of retina,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0008822,Hypoplastic ischiopubic rami,HP:0003175,Hypoplastic ischia
+HP:0011202,EEG with diffuse acceleration,HP:0002353,EEG abnormality
+HP:0009347,Bracket epiphysis of the proximal phalanx of the 3rd finger,HP:0009333,Abnormality of the epiphysis of the proximal phalanx of the 3rd finger
+UBERON:2002012,dentary foramen,UBERON:0005744,bone foramen
+UBERON:2000766,granular layer valvula cerebelli,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000603,dikaryon,CL:0000600,heterokaryon
+DOID:1852,intrahepatic cholestasis,DOID:13580,cholestasis
+HP:0006818,Type I lissencephaly,HP:0001339,Lissencephaly
+DOID:4305,bone giant cell tumor,DOID:200,giant cell tumor
+HP:0010812,Short uvula,HP:0010293,Aplasia/Hypoplasia of the uvula
+DOID:7475,diverticulitis,DOID:5295,intestinal disease
+DOID:3201,sympathetic neurilemmoma,DOID:2621,autonomic nervous system neoplasm
+UBERON:0002769,superior temporal gyrus,UBERON:0000200,gyrus
+HP:0001188,Hand clenching,HP:0005922,Abnormal hand morphology
+DOID:2508,Takayasu's arteritis,DOID:225,syndrome
+HP:0007449,Confetti-like hypopigmented macules,HP:0009719,Hypomelanotic macules
+DOID:4674,androgen insensitivity syndrome,DOID:3763,hermaphroditism
+UBERON:0013128,bulb of penis,UBERON:0005156,reproductive structure
+HP:0002160,Hyperhomocystinemia,HP:0010919,Abnormality of homocysteine metabolism
+UBERON:0005611,inner canthus,UBERON:0006742,canthus
+HP:0009291,Aplasia of the distal phalanx of the 4th finger,HP:0009289,Aplasia/Hypoplasia of the distal phalanx of the 4th finger
+UBERON:0001693,exoccipital bone,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000787,memory B cell,CL:0000785,mature B cell
+HP:0009503,Bracket epiphysis of the distal phalanx of the 2nd finger,HP:0010247,Bracket epiphyses of the distal phalanges of the hand
+HP:0010121,Small epiphyses of the hallux,HP:0010170,Small epiphyses of the toes
+DOID:13580,cholestasis,DOID:4138,bile duct disease
+UBERON:0013726,posterior talofibular ligament,UBERON:0011970,talofibular ligament
+DOID:4153,spinal chordoma,DOID:3302,chordoma
+UBERON:0013138,coronary ligament of liver,UBERON:0007826,peritoneal mesentery
+UBERON:0009201,nephric duct,UBERON:0006553,renal duct
+UBERON:2001342,presumptive intervening zone,UBERON:0004121,ectoderm-derived structure
+UBERON:0011234,fibrous membrane of synovial tendon sheath,UBERON:0004923,organ component layer
+HP:0005820,Superior rib anomalies,HP:0000772,Abnormality of the ribs
+UBERON:0007276,crista of ampulla of lateral semicircular duct of membranous laybrinth,UBERON:0006935,crista ampullaris neuroepithelium
+CL:0002661,luminal cell of lactiferous terminal ductal lobular unit,CL:0002662,luminal cell of lactiferous duct
+UBERON:0013136,vein of lip,UBERON:0003502,neck blood vessel
+HP:0006160,Irregular metacarpals,HP:0005916,Abnormal metacarpal morphology
+DOID:11781,regular astigmatism,DOID:11782,astigmatism
+DOID:1019,osteomyelitis,DOID:3342,bone inflammation disease
+NCBITaxon:12542,Omsk hemorrhagic fever virus,NCBITaxon:29263,tick-borne encephalitis virus group
+HP:0200058,Angiosarcoma,HP:0100242,Sarcoma
+DOID:0060112,ovarian benign neoplasm,DOID:0060086,female reproductive organ benign neoplasm
+UBERON:0008830,cerebellum internal granule cell layer,UBERON:0002956,granular layer of cerebellar cortex
+HP:0009108,Aplasia/Hypoplasia involving the femoral head and neck,HP:0003366,Abnormality of the femoral neck and head region
+UBERON:0005428,vagal neural crest,UBERON:0005291,embryonic tissue
+HP:0012358,Abnormal protein O-linked glycosylation,HP:0012346,Abnormal protein glycosylation
+HP:0100374,Aplasia/Hypoplasia of the middle phalanx of the 5th toe,HP:0010393,Abnormality of the middle phalanx of the 5th toe
+HP:0011992,Abnormality of neutrophil morphology,HP:0001874,Abnormality of neutrophils
+HP:0100771,Hypoperistalsis,HP:0002579,Gastrointestinal dysmotility
+DOID:10966,lipoid nephrosis,DOID:2921,glomerulonephritis
+UBERON:3010071,cranial crest,UBERON:3000972,head external integument structure
+UBERON:0001532,internal carotid artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0005494,intermediate mesenchyme,UBERON:0004120,mesoderm-derived structure
+UBERON:0005567,rhombomere 1 lateral wall,UBERON:0005501,rhombomere lateral wall
+DOID:3868,melanotic medulloblastoma,DOID:0050902,medulloblastoma
+DOID:9937,chronic dacryocystitis,DOID:9938,dacryocystitis
+DOID:310,MERRF syndrome,DOID:890,mitochondrial encephalomyopathy
+HP:0004006,Round radial epiphyses,HP:0003999,Abnormality of radial epiphyses
+UBERON:0003312,mesenchyme of testis,UBERON:0014403,male anatomical structure
+HP:0009376,Aplasia/Hypoplasia of the phalanges of the 5th finger,HP:0009767,Aplasia/Hypoplasia of the phalanges of the hand
+CL:1000448,epithelial cell of sweat gland,CL:0000362,epidermal cell
+CL:0002095,hilus cell of ovary,CL:0002132,stromal cell of ovary
+HP:0003755,Type 1 fibers relatively smaller than type 2 fibers,HP:0012084,Abnormality of skeletal muscle fiber size
+UBERON:0001935,ventromedial nucleus of hypothalamus,UBERON:0006568,hypothalamic nucleus
+UBERON:0002752,olivocerebellar tract,UBERON:0007702,tract of brain
+HP:0009691,Irregular epiphyses of the thumb,HP:0010233,Irregular epiphyses of the phalanges of the hand
+DOID:5052,melioidosis,DOID:0050338,primary bacterial infectious disease
+UBERON:0000975,sternum,UBERON:0010363,endochondral element
+HP:0011683,Restrictive ventricular septal defect,HP:0001629,Ventricular septal defect
+DOID:5627,adenosquamous gallbladder carcinoma,DOID:4948,gallbladder carcinoma
+CL:1000223,lung neuroendocrine cell,CL:0000165,neuroendocrine cell
+HP:0003612,Positive ferric chloride test,HP:0010893,Abnormality of phenylalanine metabolism
+CL:0002235,luminal cell of prostatic acinus,CL:0002233,epithelial cell of prostatic acinus
+HP:0010344,Deviation/Displacement of the 5th toe,HP:0010322,Abnormality of the 5th toe
+UBERON:0011658,epiplastron,UBERON:0015212,lateral structure
+UBERON:0014409,metacromion,UBERON:4100000,skeletal element projection
+HP:0001504,Metacarpal osteolysis,HP:0002797,Osteolysis
+UBERON:0014644,cerebrocerebellum,UBERON:0002749,regional part of cerebellar cortex
+UBERON:0004887,left lung hilus,UBERON:0004886,lung hilus
+UBERON:0010696,skeleton of pedal acropodium,UBERON:0010543,acropodial skeleton
+HP:0000878,11 pairs of ribs,HP:0000921,Missing ribs
+UBERON:0006922,cervix squamous epithelium,UBERON:0010304,non-keratinized stratified squamous epithelium
+UBERON:0013228,sweat gland of eyelid,UBERON:0013229,eyelid gland
+HP:0100113,Cone-shaped epiphysis of the middle phalanx of the 2nd toe,HP:0100089,Abnormality of the epiphysis of the middle phalanx of the 2nd toe
+CL:0000868,lymph node macrophage,CL:0000867,secondary lymphoid organ macrophage
+DOID:2143,ovarian malignant mesothelioma,DOID:2394,ovarian cancer
+UBERON:0004243,prostate gland smooth muscle,UBERON:0008715,muscle tissue of prostate
+DOID:5749,pulmonary valve disease,DOID:4079,heart valve disease
+DOID:53,pituitary gland disease,DOID:28,endocrine system disease
+HP:0011103,Abnormality of the left ventricular outflow tract,HP:0001711,Abnormality of the left ventricle
+HP:0012675,Iron accumulation in brain,HP:0012443,Abnormality of the brain
+UBERON:0010712,limb skeleton subdivision,UBERON:0010912,subdivision of skeleton
+DOID:8924,autoimmune thrombocytopenic purpura,DOID:8925,primary thrombocytopenia
+DOID:12782,cicatricial ectropion,DOID:1570,ectropion
+DOID:10177,malignant hypertensive renal disease,DOID:1073,renal hypertension
+UBERON:0001165,pyloric antrum,UBERON:0009870,zone of stomach
+DOID:3192,neurilemmoma,DOID:2001,neuroma
+UBERON:0001302,right uterine tube,UBERON:0003889,fallopian tube
+UBERON:0008585,levator veli palatini,UBERON:0003682,palatal muscle
+UBERON:0001277,intestinal epithelium,UBERON:0000485,simple columnar epithelium
+DOID:6160,childhood choriocarcinoma of the testis,DOID:6082,pediatric testicular germ cell tumor
+UBERON:0008433,lumbar vertebral arch,UBERON:0003861,neural arch
+DOID:5479,papillary adenofibroma,DOID:2683,adenofibroma
+DOID:11060,placenta praevia,DOID:780,placenta disease
+HP:0011859,Punctate keratitis,HP:0000491,Keratitis
+HP:0009412,Cone-shaped epiphyses of the 3rd finger,HP:0009320,Abnormality of the epiphyses of the 3rd finger
+UBERON:0010336,mandibular process mesenchyme from neural crest,UBERON:0006905,mandibular process mesenchyme
+DOID:350,mastocytosis,DOID:9500,leukocyte disease
+HP:0012620,Cloacal abnormality,HP:0010866,Abdominal wall defect
+HP:0010517,Ectopic thymus tissue,HP:0000777,Abnormality of the thymus
+UBERON:0000056,ureter,UBERON:0005179,pelvic region organ
+CL:1000472,myoepithelial cell of tertiary lactiferous duct,CL:0000185,myoepithelial cell
+NCBITaxon:780,Rickettsia,NCBITaxon:33988,Rickettsieae
+DOID:302,substance abuse,DOID:303,substance-related disorder
+UBERON:0015885,cymba conchae of pinna,UBERON:0000064,organ part
+CL:1001064,kidney artery smooth muscle cell,CL:0000359,vascular associated smooth muscle cell
+HP:0200128,Biventricular hypertrophy,HP:0001712,Left ventricular hypertrophy
+UBERON:0005769,basement membrane of epithelium,UBERON:0005764,acellular membrane
+DOID:0050934,ovarian clear cell carcinoma,DOID:4001,ovarian carcinoma
+HP:0001414,Microvesicular hepatic steatosis,HP:0001397,Hepatic steatosis
+HP:0009333,Abnormality of the epiphysis of the proximal phalanx of the 3rd finger,HP:0009320,Abnormality of the epiphyses of the 3rd finger
+CL:0000052,totipotent stem cell,CL:0000723,somatic stem cell
+DOID:4409,folliculitis,DOID:2723,dermatitis
+DOID:0050726,tyrosinemia type I,DOID:9275,tyrosinemia
+CL:0002303,pigmented ciliary epithelial cell,CL:0000710,neurecto-epithelial cell
+UBERON:0015843,molar enamel organ,UBERON:0005176,tooth enamel organ
+HP:0001571,Multiple impacted teeth,HP:0011079,Impacted tooth
+HP:0000653,Sparse eyelashes,HP:0200102,Sparse/absent eyelashes
+UBERON:2001843,ceratohyal-dorsal hypohyal joint,UBERON:0000982,skeletal joint
+DOID:0050425,restless legs syndrome,DOID:331,central nervous system disease
+UBERON:4200167,mesial pelvic ridge,UBERON:0004120,mesoderm-derived structure
+UBERON:2005011,pseudobranchial artery,UBERON:0001637,artery
+UBERON:0000316,cervical mucus,UBERON:0000912,mucus
+UBERON:0002820,zona arcuata of basilar membrane of cochlea,UBERON:0005764,acellular membrane
+UBERON:0003132,arthropod hypopharynx,UBERON:0000477,anatomical cluster
+DOID:3128,anus disease,DOID:1285,rectal disease
+UBERON:0001112,latissimus dorsi muscle,UBERON:0004120,mesoderm-derived structure
+HP:0010529,Echolalia,HP:0100851,Abnormal emotion/affect behavior
+UBERON:0001816,autonomic nerve plexus,UBERON:0001810,nerve plexus
+DOID:3314,angiomyolipoma,DOID:0060084,cell type benign neoplasm
+UBERON:0004230,urinary bladder neck smooth muscle,UBERON:0004228,urinary bladder smooth muscle
+UBERON:0003356,epithelium of nasal septum,UBERON:0012275,meso-epithelium
+HP:0010339,Flexion contracture of the 4th toe,HP:0001836,Camptodactyly (feet)
+CL:0002167,olfactory epithelial cell,CL:0000710,neurecto-epithelial cell
+DOID:12657,vestibulocochlear nerve disease,DOID:2889,retrocochlear disease
+UBERON:0006086,stria medullaris,UBERON:0003931,diencephalic white matter
+HP:0009962,Duplication of the distal phalanx of the 3rd finger,HP:0009357,Abnormality of the distal phalanx of the 3rd finger
+DOID:3733,theileriasis,DOID:2789,parasitic protozoa infectious disease
+UBERON:0001264,pancreas,UBERON:0002075,viscus
+UBERON:0005010,mucosa of neck of urinary bladder,UBERON:0001259,mucosa of urinary bladder
+UBERON:0001611,sublingual artery,UBERON:0001637,artery
+UBERON:0007688,anlage,UBERON:0005423,developing anatomical structure
+HP:0009811,Abnormality of the elbow,HP:0009810,Abnormality of the joints of the upper limbs
+DOID:0060171,Dravet Syndrome,DOID:0050703,infancy electroclinical syndrome
+HP:0011851,Hemopericardium,HP:0001698,Pericardial effusion
+NCBITaxon:204428,Chlamydiae,NCBITaxon:51290,Chlamydiae/Verrucomicrobia group
+HP:0005089,Abnormal metaphyseal trabeculation,HP:0000944,Abnormality of the metaphyses
+UBERON:2001867,post-ceratobranchial cartilage,UBERON:0011004,pharyngeal arch cartilage
+UBERON:0009555,short pastern bone,UBERON:0014489,middle phalanx of digit 3
+HP:0000929,Abnormality of the skull,HP:0000234,Abnormality of the head
+UBERON:0001430,distal carpal bone 1,UBERON:0001481,distal carpal bone
+UBERON:0006104,Brodmann (1909) area 36,UBERON:0013529,Brodmann area
+UBERON:0004431,proximal epiphysis of fifth metatarsal bone,UBERON:0004415,proximal epiphysis of metatarsal bone
+DOID:6934,urethra inverted papilloma,DOID:2140,urethral urothelial papilloma
+UBERON:0001125,serratus ventralis,UBERON:0001482,muscle of shoulder
+HP:0007830,Adult-onset night blindness,HP:0000662,Night blindness
+UBERON:0005478,sulcus limitans of neural tube,UBERON:0006846,surface groove
+UBERON:2001392,parapophysis 1,UBERON:0003109,parapophysis
+UBERON:3010557,triangular process,UBERON:0004120,mesoderm-derived structure
+HP:0002687,Abnormality of the frontal sinuses,HP:0000245,Abnormality of the sinuses
+UBERON:0002210,syndesmosis,UBERON:0002209,fibrous joint
+HP:0100054,Triangular epiphyses of the 2nd toe,HP:0010323,Abnormality of the epiphyses of the 2nd toe
+HP:0008629,Pulsatile tinnitus,HP:0000360,Tinnitus
+UBERON:0013691,buttock,UBERON:0015212,lateral structure
+UBERON:0002134,tricuspid valve,UBERON:0005208,right atrium valve
+UBERON:0012453,nerve ending,UBERON:0000477,anatomical cluster
+HP:0005084,Anterior radial head dislocation,HP:0003083,Dislocated radial head
+UBERON:4400001,ceratotrichium,UBERON:4400006,elastoidin fin ray
+UBERON:2001226,basibranchial 4 bone,UBERON:0002513,endochondral bone
+UBERON:0009130,dorsal meso-duodenum,UBERON:0004121,ectoderm-derived structure
+DOID:5126,central nervous system leiomyoma,DOID:0060090,central nervous system organ benign neoplasm
+UBERON:0013159,epithalamus mantle layer,UBERON:0002757,regional part of epithalamus
+UBERON:0003473,thoracic cavity artery,UBERON:0003519,thoracic cavity blood vessel
+UBERON:0001337,spongiose part of urethra,UBERON:0000063,organ segment
+DOID:11981,morbid obesity,DOID:9970,obesity
+UBERON:0001208,submucosa of large intestine,UBERON:0009566,intestinal submucosa
+UBERON:0006073,thoracic region of vertebral column,UBERON:0006077,subdivision of vertebral column
+UBERON:0004366,extraembryonic ectoderm,UBERON:0004121,ectoderm-derived structure
+UBERON:0012268,equine forelimb splint bone,UBERON:0012358,manual digitopodium bone
+UBERON:2005174,ventral liver lobe,UBERON:0004119,endoderm-derived structure
+DOID:2364,post-thrombotic syndrome,DOID:10128,venous insufficiency
+DOID:5476,cervical adenofibroma,DOID:0060110,cervical benign neoplasm
+UBERON:0006307,urogenital membrane,UBERON:0006554,urinary system structure
+UBERON:0002500,zygomatic arch,UBERON:0003462,facial bone
+HP:0002980,Femoral bowing,HP:0002823,Abnormality of the femur
+CL:0002077,ecto-epithelial cell,CL:0002371,somatic cell
+HP:0001522,Death in infancy,HP:0011420,Death
+DOID:2132,brain sarcoma,DOID:1319,brain cancer
+HP:0100436,Bullet-shaped middle phalanx of the 5th toe,HP:0010385,Bullet-shaped phalanges of the 5th toe
+HP:0009210,Pseudoepiphysis of the middle phalanx of the 5th finger,HP:0004224,Abnormality of the epiphysis of the middle phalanx of the 5th finger
+NCBITaxon:480118,Eremoneura,NCBITaxon:43733,Muscomorpha
+UBERON:0001953,presubiculum,UBERON:0004121,ectoderm-derived structure
+CL:0002165,phalangeal cell,CL:0002490,organ of Corti supporting cell
+UBERON:0013677,serrated projection of ctenactinium,UBERON:0014403,male anatomical structure
+HP:0004440,Coronal craniosynostosis,HP:0001363,Craniosynostosis
+HP:0010340,Polydactyly affecting the 4th toe,HP:0010321,Abnormality of the 4th toe
+UBERON:0003303,roof plate of medulla oblongata,UBERON:0003298,roof plate of neural tube
+UBERON:0013595,postlateral sulcus,UBERON:0008334,subarachnoid sulcus
+UBERON:4300019,dorsal fin basal cartilage,UBERON:0007844,cartilage element
+HP:0011108,Recurrent sinusitis,HP:0000246,Sinusitis
+UBERON:0009035,renal straight tubule,UBERON:0001231,nephron tubule
+UBERON:3000569,solum nasi,UBERON:0010313,neural crest-derived structure
+DOID:582,hemoglobinuria,DOID:583,hemolytic anemia
+CL:0000878,central nervous system macrophage,CL:0002319,neural cell
+CL:1001145,interlobular vein cell,CL:1001052,kidney cortex vein cell
+HP:0010568,Hamartoma of the eye,HP:0010566,Hamartoma
+UBERON:0006803,obturator foramen,UBERON:0004111,anatomical conduit
+HP:0003710,Exercise-induced muscle cramps,HP:0003394,Muscle cramps
+NCBITaxon:10405,Orthohepadnavirus,NCBITaxon:10404,Hepadnaviridae
+UBERON:0008259,aboral surface,UBERON:0000475,organism subdivision
+DOID:4253,melorheostosis,DOID:4254,osteosclerosis
+UBERON:0007109,meconium,UBERON:0001988,feces
+HP:0005951,Progressive inspiratory stridor,HP:0005348,Inspiratory stridor
+HP:0009630,Broad proximal phalanx of the thumb,HP:0009844,Broad middle phalanx of finger
+CL:1000322,pancreatic goblet cell,CL:0000160,goblet cell
+HP:0009398,Irregular epiphyses of the 4th finger,HP:0009174,Abnormality of the epiphyses of the 4th finger
+CL:0002251,epithelial cell of alimentary canal,CL:0002076,endo-epithelial cell
+HP:0003043,Abnormality of the shoulder,HP:0000765,Abnormality of the thorax
+HP:0010797,Hemangioblastoma,HP:0100835,Benign neoplasm of the central nervous system
+UBERON:0004634,thoracic vertebra 10,UBERON:0002347,thoracic vertebra
+UBERON:0006005,hair follicle isthmus,UBERON:0004121,ectoderm-derived structure
+DOID:0050911,appendix carcinoid tumor,DOID:11239,appendix cancer
+DOID:11476,osteoporosis,DOID:0080011,bone resorption disease
+UBERON:2001767,pectoral fin lepidotrichium 7,UBERON:4000175,pectoral fin lepidotrichium
+CL:1001572,colon endothelial cell,CL:0011108,colon epithelial cell
+UBERON:0009772,right anterior cardinal vein,UBERON:0015212,lateral structure
+CL:0007005,notochordal cell,CL:0000003,native cell
+UBERON:0001578,orbicularis oculi,UBERON:0004277,eye muscle
+DOID:7506,small intestinal L-cell glucagon-like peptide producing tumor,DOID:10154,small intestine cancer
+DOID:9544,refractory plasma cell neoplasm,DOID:9538,multiple myeloma
+HP:0010701,Abnormal immunoglobulin level,HP:0005368,Abnormality of humoral immunity
+HP:0004376,Neuroblastic tumors,HP:0100836,Malignant neoplasm of the central nervous system
+HP:0008463,Central vertebral hypoplasia,HP:0008417,Vertebral hypoplasia
+UBERON:0010363,endochondral element,UBERON:0004765,skeletal element
+UBERON:0015036,pedal digit metatarsal endochondral element,UBERON:0015063,autopod endochondral element
+HP:0005198,Stiff interphalangeal joints,HP:0001387,Joint stiffness
+UBERON:0006248,incus pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+UBERON:2000924,myotome somite 1,UBERON:0003082,myotome
+UBERON:0005616,mesenteric artery,UBERON:0012254,abdominal aorta artery
+UBERON:0005471,right umbilical vein,UBERON:0002066,umbilical vein
+UBERON:0011153,ventral hyoid arch skeleton,UBERON:0010912,subdivision of skeleton
+HP:0001888,Lymphopenia,HP:0012140,Abnormality of cells of the lymphoid lineage
+HP:0003534,Reduced xanthine dehydrogenase activity,HP:0010933,Abnormality of xanthine metabolism
+CL:0000928,"activated CD4-negative, CD8-negative type I NK T cell",CL:0000924,"CD4-negative, CD8-negative type I NK T cell"
+HP:0007078,Decreased amplitude of sensory action potentials,HP:0003134,Abnormality of peripheral nerve conduction
+DOID:10606,blind loop syndrome,DOID:5295,intestinal disease
+DOID:5337,epulis,DOID:3086,gingival overgrowth
+UBERON:0005329,mesonephric nephron tubule,UBERON:0005330,mesonephric nephron epithelium
+DOID:5775,cavernous hemangioma of colon,DOID:483,cavernous hemangioma
+UBERON:4000171,scapular complex,UBERON:0010912,subdivision of skeleton
+HP:0003248,Gonadal tissue inappropriate for external genitalia or chromosomal sex,HP:0000062,Ambiguous genitalia
+UBERON:0010428,flat bone,UBERON:0001474,bone element
+HP:0002427,Motor aphasia,HP:0002381,Aphasia
+UBERON:0001287,proximal convoluted tubule,UBERON:0006534,renal convoluted tubule
+HP:0000197,Abnormality of parotid gland,HP:0010286,Abnormality of the salivary glands
+HP:0005336,Forehead hyperpigmentation,HP:0007400,Irregular hyperpigmentation
+DOID:0050638,transthyretin amyloidosis,DOID:9120,amyloidosis
+UBERON:3010740,ramus auricularis of the vagus nerve,UBERON:0001759,vagus nerve
+CL:0002081,type II cell of carotid body,CL:0000703,sustentacular cell
+UBERON:0007820,accessory nasal cartilage,UBERON:0001823,nasal cartilage
+UBERON:0004414,proximal epiphysis of phalanx of manus,UBERON:0004447,proximal epiphysis of phalanx
+UBERON:0009871,nephrogenic zone,UBERON:0005423,developing anatomical structure
+HP:0012641,Decreased intracranial pressure,HP:0012640,Abnormality of intracranial pressure
+UBERON:0002754,predorsal bundle,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0006346,Screwdriver-shaped incisors,HP:0011063,Abnormality of incisor morphology
+UBERON:2202028,pectoral fin proximal radial cartilage 3,UBERON:2102028,pectoral fin proximal radial element 3
+UBERON:0004781,gall bladder lamina propria,UBERON:0000030,lamina propria
+HP:0007903,Pigmented paravenous chorioretinal atrophy,HP:0000533,Chorioretinal atrophy
+HP:0100075,Stippling of the epiphyses of the 4th toe,HP:0010171,Epiphyseal stippling of toe phalanges
+UBERON:0001639,hepatic portal vein,UBERON:0002017,portal vein
+HP:0002608,Celiac disease,HP:0100326,Immunologic hypersensitivity
+HP:0009809,Abnormality of upper limb metaphysis,HP:0000944,Abnormality of the metaphyses
+UBERON:2200947,dorsal fin proximal radial cartilage,UBERON:2100947,dorsal fin proximal radial element
+UBERON:0013527,pectoral flipper tubercle,UBERON:0005813,tubercle
+HP:0009059,Congenital generalized lipodystrophy,HP:0009125,Lipodystrophy
+UBERON:0009479,ectoderm of buccopharyngeal membrane,UBERON:0000924,ectoderm
+HP:0004783,Duodenal polyposis,HP:0200008,Intestinal polyposis
+UBERON:2201586,pectoral fin radial cartilage,UBERON:1700006,paired fin radial cartilage
+CL:1001611,cerebellar neuron,CL:0000540,neuron
+UBERON:3000657,dentigerous process,UBERON:0010313,neural crest-derived structure
+HP:0001433,Hepatosplenomegaly,HP:0003271,Visceromegaly
+HP:0009775,Amniotic constriction ring,HP:0011409,Abnormality of placental membranes
+DOID:2917,cryoglobulinemia,DOID:2916,hypersensitivity reaction type IV disease
+HP:0011927,Short digit,HP:0011297,Abnormality of the digits
+UBERON:0002653,gracile fasciculus of medulla,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2001657,upper pharyngeal 5 tooth,UBERON:0001091,calcareous tooth
+UBERON:0002130,cerebellar nuclear complex,UBERON:0000064,organ part
+UBERON:0013706,bone spine,UBERON:0004530,bony projection
+DOID:13709,premature ejaculation,DOID:10132,psychosexual disorder
+HP:0011739,Dexamethasone-suppresible primary hyperaldosteronism,HP:0011736,Primary hyperaldosteronism
+CL:0000637,chromophil cell of anterior pituitary gland,CL:0000167,peptide hormone secreting cell
+NCBITaxon:1659,Actinomyces israelii,NCBITaxon:1654,Actinomyces
+HP:0000108,Renal corticomedullary cysts,HP:0000107,Renal cyst
+UBERON:0005407,sublingual ganglion,UBERON:0001808,parasympathetic ganglion
+DOID:7013,ovarian mucinous cystadenofibroma,DOID:6469,ovarian mucinous adenofibroma
+UBERON:0004787,urethra urothelium,UBERON:0000365,urothelium
+HP:0100818,Long thorax,HP:0100625,Enlarged thorax
+UBERON:0013170,cricoarytenoid ligament,UBERON:0001730,extrinsic ligament of larynx
+HP:0001427,Mitochondrial inheritance,HP:0000005,Mode of inheritance
+DOID:2123,tularemia,DOID:0050338,primary bacterial infectious disease
+UBERON:0013459,stephanion,UBERON:0006983,anatomical point
+UBERON:0006716,mesopodium region,UBERON:0002529,limb segment
+UBERON:0004985,mucosa of ejaculatory duct,UBERON:0000344,mucosa
+HP:0000963,Thin skin,HP:0008065,Aplasia/Hypoplasia of the skin
+HP:0008470,Lower thoracic interpediculate narrowness,HP:0008450,Narrow vertebral interpedicular distance
+UBERON:0014895,somatic muscle,UBERON:0005090,muscle structure
+UBERON:0000053,macula lutea,UBERON:0004121,ectoderm-derived structure
+CL:0002206,brush cell of terminal bronchiole,CL:0002205,brush cell of lobular bronchiole
+DOID:5287,kidney leiomyosarcoma,DOID:4242,kidney sarcoma
+DOID:11269,chronic apical periodontitis,DOID:823,periapical periodontitis
+HP:0100948,Sclerosis of the distal phalanges of the toes,HP:0100924,Sclerosis of the phalanges of the toes
+DOID:8437,intestinal obstruction,DOID:5295,intestinal disease
+UBERON:0002106,spleen,UBERON:0005057,immune organ
+HP:0100859,Superior mesenteric artery aneurysm,HP:0011934,Mesenteric artery aneurysm
+HP:0006548,Pulmonary arteriovenous malformation,HP:0100026,Arteriovenous malformation
+DOID:8177,endocervical type cervical adenomyoma,DOID:4995,cervical adenomyoma
+HP:0006595,Scapulohumeral synostosis,HP:0003063,Abnormality of the humerus
+HP:0010899,Abnormality of aspartate family amino acid metabolism,HP:0004337,Abnormality of amino acid metabolism
+UBERON:0001065,parotid duct,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0011319,disk of temporomandibular joint,UBERON:0007844,cartilage element
+UBERON:0005301,male preputial gland,UBERON:0000359,preputial gland
+UBERON:0011172,retrorubral area,UBERON:0002635,regional part of midbrain tegmentum
+UBERON:0001064,ventral pancreatic duct,UBERON:0002394,bile duct
+NCBITaxon:11308,Orthomyxoviridae,NCBITaxon:35301,ssRNA negative-strand viruses
+NCBITaxon:120793,Mycobacterium avium complex (MAC),NCBITaxon:1763,Mycobacterium
+DOID:4011,prostate transitional cell carcinoma,DOID:10286,prostate carcinoma
+HP:0200026,Ocular pain,HP:0000284,Abnormality of the ocular region
+HP:0002667,Nephroblastoma (Wilms tumor),HP:0011794,Embryonal renal neoplasm
+HP:0001862,Acral ulceration and osteomyelitis leading to autoamputation of the digits (feet),HP:0200042,Skin ulcer
+HP:0011999,Paranoia,HP:0000746,Delusions
+CL:0000133,neurectodermal cell,CL:0000221,ectodermal cell
+HP:0011273,Anisocytosis,HP:0001877,Abnormality of erythrocytes
+UBERON:0009576,medulla oblongata sulcus limitans,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:10377,ametropic amblyopia,DOID:10376,amblyopia
+UBERON:0004140,primary heart field,UBERON:0005291,embryonic tissue
+HP:0003883,Tapered humerus,HP:0003063,Abnormality of the humerus
+UBERON:0001557,upper respiratory tract,UBERON:0000072,segment of respiratory tract
+UBERON:0006471,Brodmann (1909) area 5,UBERON:0013529,Brodmann area
+HP:0011247,Prominent superior crus of antihelix,HP:0011245,Abnormality of superior crus of antihelix
+CL:0001052,"CD8-positive, CXCR3-negative, CCR6-negative, alpha-beta T cell",CL:0000625,"CD8-positive, alpha-beta T cell"
+UBERON:0000935,anterior commissure,UBERON:0005341,ventral commissure
+UBERON:0002896,telodiencephalic fissure,UBERON:0014466,subarachnoid fissure
+DOID:4869,laryngeal adenoid cystic carcinoma,DOID:2600,laryngeal carcinoma
+HP:0004944,Cerebral aneurysm,HP:0009145,Abnormality of cerebral artery
+UBERON:2001665,basibranchial 2 tooth,UBERON:0001091,calcareous tooth
+UBERON:0001883,olfactory tubercle,UBERON:0005813,tubercle
+DOID:11161,neonatal respiratory failure,DOID:11162,respiratory failure
+UBERON:2000479,caudal mesencephalo-cerebellar tract,UBERON:0004121,ectoderm-derived structure
+HP:0100483,Symphalangism of the proximal phalanx of the 2nd toe with the 2nd metatarsal,HP:0010378,Triangular shaped phalanges of the 4th toe
+HP:0002912,Methylmalonic acidemia,HP:0010995,Abnormality of dicarboxylic acid metabolism
+HP:0004875,Neonatal inspiratory stridor,HP:0002643,Neonatal respiratory distress
+UBERON:2205225,median fin radial cartilage,UBERON:2200271,radial cartilage
+DOID:2562,suppurative periapical periodontitis,DOID:823,periapical periodontitis
+HP:0010040,Aplasia of the 3rd metacarpal,HP:0010039,Aplasia/Hypoplasia of the 3rd metacarpal
+UBERON:0009717,coronal organ,UBERON:0000020,sense organ
+DOID:4031,eosinophilic gastroenteritis,DOID:2326,gastroenteritis
+HP:0012706,Elevated brain choline level by MRS,HP:0012705,Abnormal metabolic brain imaging by MRS
+DOID:0050196,Venezuelan hemorrhagic fever,DOID:934,viral infectious disease
+UBERON:0001963,bronchial-associated lymphoid tissue,UBERON:0004119,endoderm-derived structure
+HP:0009407,Triangular shaped phalanges of the 4th finger,HP:0009172,Abnormality of the phalanges of the 4th finger
+UBERON:2002195,epidermal placode,UBERON:0000479,tissue
+HP:0009637,Absent proximal phalanx of thumb,HP:0010239,Aplasia of the middle phalanx of the hand
+DOID:6331,immature teratoma of ovary,DOID:5563,malignant teratoma
+HP:0012313,Heberden's node,HP:0006247,Enlarged interphalangeal joints
+HP:0008559,Hypoplastic superior helix,HP:0008589,Hypoplastic helices
+CL:0000853,olfactory epithelial support cell,CL:0002167,olfactory epithelial cell
+UBERON:3010813,vent glands,UBERON:3010603,body gland
+CL:0000186,myofibroblast cell,CL:0000183,contractile cell
+HP:0011555,Double inlet left ventricle,HP:0001750,Single ventricle
+HP:0009719,Hypomelanotic macules,HP:0001010,Hypopigmentation of the skin
+CL:0000016,male germ line stem cell,CL:0000015,male germ cell
+UBERON:4200110,prepectoral spine,UBERON:0004529,anatomical projection
+UBERON:0002680,regional part of metencephalon,UBERON:0002616,regional part of brain
+DOID:5716,hormone producing pituitary cancer,DOID:1785,pituitary cancer
+HP:0003950,Flared metaphyses (elbow),HP:0003949,Abnormality of the elbow metaphyses
+DOID:2034,encephalomalacia,DOID:936,brain disease
+UBERON:0014695,deep auricular artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0100234,Triangular epiphysis of the proximal phalanx of the 5th toe,HP:0100087,Triangular epiphyses of the 5th toe
+UBERON:0007623,comb and wattle,UBERON:0000021,cutaneous appendage
+UBERON:0011345,pharyngeal raphe,UBERON:0004119,endoderm-derived structure
+UBERON:0010862,dactylopatagium,UBERON:0006012,interdigital region
+UBERON:0009990,medial condyle of tibia,UBERON:0009989,condyle of tibia
+UBERON:0005020,mucosa of tongue,UBERON:0003729,mouth mucosa
+UBERON:0003515,forelimb blood vessel,UBERON:0007300,pectoral appendage blood vessel
+DOID:4394,reticulohistiocytic granuloma,DOID:3405,histiocytosis
+HP:0007944,Intermittent microsaccadic pursuits,HP:0001152,Saccadic smooth pursuit
+HP:0010704,1-2 finger syndactyly,HP:0006101,Finger syndactyly
+UBERON:0011310,masseteric fossa,UBERON:0004120,mesoderm-derived structure
+HP:0004038,Bony spikule of ulnar epiphyseal plate,HP:0004037,Abnormality of the ulnar epiphyses
+UBERON:0002010,celiac nerve plexus,UBERON:0001816,autonomic nerve plexus
+UBERON:0004746,prootic bone,UBERON:0011164,neurocranium bone
+UBERON:3000735,mid-dorsal keel,UBERON:0004120,mesoderm-derived structure
+CL:0000136,fat cell,CL:0000325,stuff accumulating cell
+UBERON:3000818,margo anterior of scapula,UBERON:0000064,organ part
+DOID:13891,bird fancier's lung,DOID:841,extrinsic allergic alveolitis
+UBERON:2002195,epidermal placode,UBERON:0004121,ectoderm-derived structure
+HP:0011870,Impaired arachidonic acid-induced platelet aggregation,HP:0003540,Impaired platelet aggregation
+UBERON:3010454,ventro-lateral marginal zone,UBERON:0004879,marginal zone of embryo
+HP:0000910,Wide-cupped costochondral junctions,HP:0000919,Abnormality of the costochondral junction
+HP:0002540,Inability to walk,HP:0001288,Gait disturbance
+HP:0100728,Germ cell neoplasia,HP:0010785,Gonadal neoplasm
+UBERON:0006588,round ligament of liver,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0009149,Triangular epiphysis of the distal phalanx of the 5th finger,HP:0009392,Triangular epiphyses of the 5th finger
+UBERON:0012119,vinculum tendon of wing,UBERON:0000043,tendon
+CL:0002639,amniotic stem cell,CL:0002323,amniocyte
+HP:0011680,Single ventricle of indeterminate morphology,HP:0001750,Single ventricle
+UBERON:2001252,pharyngobranchial 3 bone,UBERON:2000527,pharyngobranchial bone
+HP:0008777,Abnormality of the vocal cords,HP:0001600,Abnormality of the larynx
+NCBITaxon:119088,Enoplea,NCBITaxon:6231,Nematoda
+CL:0000468,neuroglioblast,CL:0000055,non-terminally differentiated cell
+DOID:2883,prostatic adenoma,DOID:0060087,male reproductive organ benign neoplasm
+HP:0004275,Duplication of hand bones,HP:0001155,Abnormality of the hand
+HP:0200110,Absent paranasal sinuses and mastoids,HP:0000265,Mastoiditis
+HP:0001067,Neurofibromas,HP:0100007,Neoplasm of the peripheral nervous system
+UBERON:0010134,secretory circumventricular organ,UBERON:0005408,circumventricular organ
+UBERON:0000063,organ segment,UBERON:0000064,organ part
+HP:0009434,Patchy sclerosis of the middle phalanx of the 3rd finger,HP:0004172,Abnormality of the middle phalanx of the 3rd finger
+DOID:3254,bile duct rhabdomyosarcoma,DOID:4064,bile duct sarcoma
+UBERON:0007178,muscularis mucosae of colon,UBERON:0001239,muscularis mucosae of large intestine
+HP:0004042,Irregular ulnar metaphysis,HP:0004039,Abnormality of ulnar metaphysis
+DOID:4210,clear cell meningioma,DOID:3565,meningioma
+DOID:10322,berylliosis,DOID:10316,pneumoconiosis
+CL:0010020,cardiac glial cell,CL:0000125,glial cell
+HP:0100938,Sclerosis of the middle phalanx of the 5th toe,HP:0100929,Sclerosis of the phalanges of the 5th toe
+UBERON:0004947,submucosa of right main bronchus,UBERON:0004949,submucosa of main bronchus
+HP:0100770,Hyperperistalsis,HP:0002579,Gastrointestinal dysmotility
+UBERON:3010701,m. latissimus dorsi,UBERON:0010891,pectoral complex muscle
+DOID:5074,malignant ependymoma,DOID:3070,malignant glioma
+UBERON:2001225,basibranchial 3 bone,UBERON:0002513,endochondral bone
+HP:0100467,Patchy sclerosis of the distal phalanx of the 3rd toe,HP:0100940,Sclerosis of the distal phalanx of the 3rd toe
+HP:0009731,Cerebral hamartomata,HP:0100835,Benign neoplasm of the central nervous system
+DOID:11599,Frey Syndrome,DOID:11465,autonomic nervous system disease
+UBERON:0004452,carpal region,UBERON:0006716,mesopodium region
+UBERON:0003315,mesenchyme of ovary,UBERON:0014404,female anatomical structure
+HP:0010042,Aplasia/Hypoplasia of the 4th metacarpal,HP:0010012,Abnormality of the 4th metacarpal
+DOID:1580,diffuse scleroderma,DOID:418,systemic scleroderma
+DOID:6376,hypersplenism,DOID:2529,splenic disease
+UBERON:0002492,sagittal suture,UBERON:0004120,mesoderm-derived structure
+UBERON:0016466,antihelix,UBERON:0000481,multi-tissue structure
+HP:0010341,Abnormality of the epiphyses of the 5th toe,HP:0010160,Abnormality of the epiphyses of the toes
+UBERON:0004666,interventricular septum membranous part,UBERON:0005983,heart layer
+UBERON:2000815,nucleus of medial longitudinal fasciculus of medulla,UBERON:0007635,nucleus of medulla oblongata
+DOID:419,scleroderma,DOID:1575,rheumatic disease
+UBERON:0001490,elbow joint,UBERON:0011139,synovial limb joint
+CL:0000039,germ line cell,CL:0000548,animal cell
+UBERON:0000040,Leydig's organ,UBERON:0004177,hemopoietic organ
+HP:0001465,Amyotrophy involving the shoulder musculature,HP:0001435,Abnormality of the shoulder girdle musculature
+DOID:4013,urethra transitional cell carcinoma,DOID:734,urethra cancer
+HP:0001030,Fragile skin,HP:0011354,Generalized abnormality of skin
+UBERON:0001917,endothelium of artery,UBERON:0004638,blood vessel endothelium
+HP:0007835,S-shaped palpebral fissures,HP:0200005,Abnormal shape of the palpebral fissure
+HP:0002583,Colitis,HP:0002037,Inflammation of the large intestine
+UBERON:3010586,vasa efferentia,UBERON:0006946,efferent duct
+DOID:10908,hydrocephalus,DOID:1443,cerebral degeneration
+HP:0009354,Small epiphysis of the proximal phalanx of the 3rd finger,HP:0010276,Small epiphyses of the proximal phalanges of the hand
+UBERON:0010244,choroid tapetum lucidum,UBERON:0004868,tapetum lucidum of camera-type eye
+UBERON:2001274,coronomeckelian,UBERON:0008907,dermal bone
+CL:0000587,cold sensing thermoreceptor cell,CL:0000205,thermoreceptor cell
+UBERON:0007378,egg yolk,UBERON:0004120,mesoderm-derived structure
+UBERON:3000413,pars palatina of maxilla,UBERON:0004120,mesoderm-derived structure
+UBERON:0009912,anatomical lobe,UBERON:0000064,organ part
+DOID:0050288,penicilliosis,DOID:2473,opportunistic mycosis
+HP:0000322,Short philtrum,HP:0000288,Abnormality of the philtrum
+HP:0005261,Joint hemorrhage,HP:0011029,Internal hemorrhage
+HP:0011802,Hamartoma of tongue,HP:0100648,Neoplasm of the tongue
+UBERON:0012177,skin apocrine gland,UBERON:0002419,skin gland
+UBERON:0001616,maxillary artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0006356,epigastric vein,UBERON:0001638,vein
+HP:0008517,Aplasia/Hypoplasia of the sacrum,HP:0005107,Abnormality of the sacrum
+HP:0005921,Abnormal ossification of hand bones,HP:0001155,Abnormality of the hand
+UBERON:0003291,meninx of hindbrain,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001992,papillary layer of dermis,UBERON:0004121,ectoderm-derived structure
+UBERON:2001519,ceratobranchial 4 cartilage,UBERON:2001902,ceratobranchial 4 element
+UBERON:3010453,ventral marginal zone,UBERON:0004879,marginal zone of embryo
+HP:0011579,Unbalanced atrioventricular canal defect,HP:0006695,Atrioventricular canal defect
+UBERON:0004922,postnatal subventricular zone,UBERON:0004121,ectoderm-derived structure
+DOID:7996,familial glomangioma,DOID:2436,glomangioma
+HP:0006332,Supernumerary maxillary incisor,HP:0011064,Abnormal number of incisors
+UBERON:0015031,pedal digit 1 phalanx endochondral element,UBERON:0015030,pedal digit phalanx endochondral element
+HP:0000815,Hypergonadotropic hypogonadism,HP:0000135,Hypogonadism
+UBERON:0011002,articular cartilage element,UBERON:0011004,pharyngeal arch cartilage
+UBERON:0001436,phalanx of manus,UBERON:0015024,manual digit phalanx endochondral element
+DOID:0050877,pancreatic agenesis,DOID:26,pancreas disease
+UBERON:0010748,lymph node follicle,UBERON:0000444,lymphoid follicle
+UBERON:0001690,ear,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2002122,pouch scale,UBERON:0007380,dermal scale
+UBERON:0001853,utricle of membranous labyrinth,UBERON:0002518,otolith organ
+DOID:11623,dental pulp necrosis,DOID:5330,dental pulp disease
+UBERON:0001269,acetabular part of hip bone,UBERON:0005913,zone of bone organ
+UBERON:0005351,paraflocculus,UBERON:0004003,cerebellum hemisphere lobule
+UBERON:0004386,epiphysis of ulna,UBERON:0001437,epiphysis
+NCBITaxon:34613,Ixodes ricinus,NCBITaxon:6944,Ixodes
+HP:0012579,Minimal change glomerulonephritis,HP:0000099,Glomerulonephritis
+UBERON:0002152,middle cerebellar peduncle,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001741,corniculate cartilage,UBERON:0003583,larynx connective tissue
+UBERON:0002281,vestibular membrane of cochlear duct,UBERON:0000094,membrane organ
+UBERON:0010754,germinal center,UBERON:0001744,lymphoid tissue
+HP:0002170,Intracranial hemorrhage,HP:0100659,Abnormality of the cerebral vasculature
+HP:0001818,Paronychia,HP:0100803,Abnormality of the periungual region
+UBERON:2000089,actinotrichium,UBERON:4400006,elastoidin fin ray
+HP:0011344,Severe global developmental delay,HP:0001263,Global developmental delay
+HP:0003513,Reduced ratio of renal calcium clearance to creatinine clearance,HP:0011280,Abnormality of urine calcium concentration
+UBERON:0010937,salpingopharyngeus muscle,UBERON:0015212,lateral structure
+HP:0005550,Chronic lymphatic leukemia,HP:0005558,Chronic leukemia
+UBERON:0015488,sural nerve,UBERON:0003431,leg nerve
+HP:0010882,Pulmonary valve atresia,HP:0001641,Abnormality of the pulmonary valve
+UBERON:2000707,ventral zone,UBERON:0003048,regional part of hypothalamus
+DOID:8431,physiological polycythemia,DOID:8432,polycythemia
+HP:0011057,Agenesis of second permanent molar,HP:0011055,Agenesis of permanent molar
+UBERON:0012083,lumen of primary bronchus,UBERON:0012082,bronchial lumen
+NCBITaxon:644710,Anisakis simplex complex,NCBITaxon:6268,Anisakis
+DOID:8158,complement component 5 deficiency,DOID:626,complement deficiency
+HP:0005676,Rudimentary postaxial polydactyly of hands,HP:0001162,Postaxial hand polydactyly
+HP:0003279,Coxa magna,HP:0003272,Abnormality of the hip bone
+UBERON:0014521,anterodorsal nucleus of medial geniculate body,UBERON:0015233,nucleus of dorsal thalamus
+DOID:7826,adult papillary meningioma,DOID:5058,rhabdoid meningioma
+HP:0005526,Lymphoid leukemia,HP:0001909,Leukemia
+UBERON:3000386,cultriform process,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003368,epithelium of hard palate,UBERON:0003235,epithelium of upper jaw
+HP:0002355,Difficulty walking,HP:0001288,Gait disturbance
+UBERON:0013725,anterior talofibular ligament,UBERON:0011970,talofibular ligament
+UBERON:0014455,subcutaneous abdominal adipose tissue,UBERON:0002190,subcutaneous adipose tissue
+UBERON:4200098,ischial foot,UBERON:0005913,zone of bone organ
+HP:0003899,Round humeral epiphyses,HP:0003891,Abnormality of the humeral epiphysis
+CL:0000536,secondary motor neuron,CL:0000100,motor neuron
+HP:0000935,Thickened cortex of long bones,HP:0011314,Abnormality of long bone morphology
+DOID:0050453,lissencephaly,DOID:2490,congenital nervous system abnormality
+CL:0002291,X chromosome-bearing sperm cell,CL:0000019,sperm
+CL:0000722,cystoblast,CL:0000586,germ cell
+HP:0010311,Aplasia/Hypoplasia of the breasts,HP:0000769,Abnormality of the breast
+UBERON:2001537,mesocoracoid cartilage,UBERON:0007844,cartilage element
+HP:0009550,Osteolytic defects of the phalanges of the 2nd finger,HP:0009699,Osteolytic defects of the hand bones
+DOID:0060111,fallopian tube benign neoplasm,DOID:0060086,female reproductive organ benign neoplasm
+HP:0002828,Multiple joint contractures,HP:0001371,Flexion contracture
+HP:0001555,Asymmetry of the thorax,HP:0001547,Abnormality of the rib cage
+HP:0009107,Abnormal ossification involving the femoral head and neck,HP:0003366,Abnormality of the femoral neck and head region
+UBERON:0000928,embryonic segment,UBERON:0002050,embryonic structure
+HP:0001508,Failure to thrive,HP:0004325,Decreased body weight
+HP:0011203,EEG with abnormally slow frequencies,HP:0002353,EEG abnormality
+HP:0009744,Abnormality of the spinal dura mater,HP:0010652,Abnormality of the dura mater
+DOID:10646,schizotypal personality disorder,DOID:1510,personality disorder
+HP:0011991,Abnormal neutrophil cell number,HP:0001874,Abnormality of neutrophils
+CL:0000470,digestive enzyme secreting cell,CL:0000154,protein secreting cell
+HP:0000539,Abnormality of refraction,HP:0012373,Abnormal eye physiology
+CL:0002193,myelocyte,CL:0000763,myeloid cell
+UBERON:0014488,middle phalanx of digit 2,UBERON:0004301,middle phalanx
+HP:0012621,Persistent cloaca,HP:0010866,Abdominal wall defect
+DOID:5487,spindle cell synovial sarcoma,DOID:5485,synovial sarcoma
+UBERON:3000367,otic ramus of squamosal,UBERON:4100000,skeletal element projection
+UBERON:0013129,bulb of vestibule,UBERON:0005156,reproductive structure
+HP:0002514,Cerebral calcification,HP:0010766,Ectopic calcification
+CL:0000162,parietal cell,CL:0000161,acid secreting cell
+HP:0004005,Large radial epiphyses,HP:0003999,Abnormality of radial epiphyses
+UBERON:0006858,adrenal/interrenal gland,UBERON:0004120,mesoderm-derived structure
+HP:0012442,Gallbladder dyskinesia,HP:0012396,Biliary dyskinesia
+UBERON:0002879,peritrigeminal nucleus,UBERON:0007635,nucleus of medulla oblongata
+DOID:13357,chondromalacia patellae,DOID:2557,chondromalacia
+UBERON:0001870,frontal cortex,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100610,Maternal hyperphenylalaninemia,HP:0002686,Prenatal maternal abnormality
+UBERON:0011894,lumen of vagina,UBERON:0002558,organ cavity
+DOID:4152,chondroid chordoma,DOID:3302,chordoma
+HP:0009044,Hypoplasia of deltoid muscle,HP:0001464,Aplasia/Hypoplasia involving the shoulder musculature
+UBERON:0008840,plantar pad,UBERON:0013778,skin of sole of pes
+HP:0010343,Aplasia/Hypoplasia of the 5th toe,HP:0010322,Abnormality of the 5th toe
+UBERON:2000564,pelvic abductor profundus,UBERON:0006845,abductor muscle
+UBERON:0001673,central retinal vein,UBERON:0003499,brain blood vessel
+UBERON:0010702,digit mesenchyme,UBERON:0009749,limb mesenchyme
+HP:0010300,Abnormally low-pitched voice,HP:0001608,Abnormality of the voice
+UBERON:0007603,stratified cuboidal epithelium,UBERON:0000486,multilaminar epithelium
+CL:0000828,thromboblast,CL:0000763,myeloid cell
+DOID:3320,Tay-Sachs disease,DOID:3321,gangliosidosis GM2
+NCBITaxon:34384,Arthrodermataceae,NCBITaxon:33183,Onygenales
+UBERON:0010561,pedal digit 5 metatarsal cartilage element,UBERON:0015041,pedal digit 5 metatarsal endochondral element
+UBERON:0001863,scala vestibuli,UBERON:0004120,mesoderm-derived structure
+UBERON:0012270,forestomach-glandular stomach junction,UBERON:0007651,anatomical junction
+UBERON:0008340,nasal bridge,UBERON:0004121,ectoderm-derived structure
+UBERON:0010337,mandibular process mesenchyme from head mesenchyme,UBERON:0006904,head mesenchyme from mesoderm
+HP:0100834,Neoplasm of the large intestine,HP:0007378,Neoplasm of the gastrointestinal tract
+HP:0010622,Neoplasm of the skeletal system,HP:0011793,Neoplasm by anatomical site
+DOID:13481,thanatophoric dysplasia,DOID:2256,osteochondrodysplasia
+HP:0100112,Bracket epiphysis of the middle phalanx of the 2nd toe,HP:0100089,Abnormality of the epiphysis of the middle phalanx of the 2nd toe
+UBERON:0003572,chest connective tissue,UBERON:0003837,thoracic segment connective tissue
+DOID:12197,punctate epithelial keratoconjunctivitis,DOID:9368,keratoconjunctivitis
+DOID:2345,plasma protein metabolism disease,DOID:655,inherited metabolic disorder
+UBERON:0005422,pelvic appendage apical ectodermal ridge,UBERON:0004121,ectoderm-derived structure
+DOID:11870,Pick's disease,DOID:1289,neurodegenerative disease
+UBERON:0010269,filum terminale internum,UBERON:0000479,tissue
+UBERON:0002497,acromion,UBERON:4100000,skeletal element projection
+UBERON:0004546,cribriform plate,UBERON:0010313,neural crest-derived structure
+UBERON:3010089,M. extensor cruris brevis,UBERON:0010890,pelvic complex muscle
+DOID:3587,pancreatic ductal carcinoma,DOID:4905,pancreatic carcinoma
+UBERON:0007806,connecting stalk,UBERON:0004120,mesoderm-derived structure
+UBERON:2205377,dorsal fin distal radial cartilage 6,UBERON:2200936,dorsal fin distal radial cartilage
+UBERON:0001934,dorsomedial nucleus of hypothalamus,UBERON:0006568,hypothalamic nucleus
+UBERON:0005856,developing mesenchymal condensation,UBERON:0011585,cell condensation
+DOID:1787,pericarditis,DOID:0050829,pericardium disease
+HP:0012384,Rhinitis,HP:0000366,Abnormality of the nose
+UBERON:0010688,skeleton of manual acropodium,UBERON:0010543,acropodial skeleton
+CL:1000320,axial mesoderm cell,CL:0002658,glandular cell of the large intestine
+UBERON:0002684,nucleus raphe obscurus,UBERON:0002677,regional part of medullary raphe nuclear complex
+CL:0000961,Bm1 B cell,CL:0002056,Fraction F mature B cell
+UBERON:0009538,mesenchyme of sublingual gland primordium,UBERON:0005253,head mesenchyme
+UBERON:2001701,basibranchial 5 bone,UBERON:0004740,basibranchial bone
+DOID:4994,adenomyoma of uterine corpus,DOID:2609,adenomyoma
+CL:0002305,epithelial cell of distal tubule,CL:1000615,kidney cortex tubule cell
+CL:1000222,stomach neuroendocrine cell,CL:0000165,neuroendocrine cell
+DOID:5635,gastric adenosquamous carcinoma,DOID:5517,stomach carcinoma
+HP:0000987,Atypical scarring of skin,HP:0011354,Generalized abnormality of skin
+UBERON:0001276,epithelium of stomach,UBERON:0000485,simple columnar epithelium
+HP:0005583,Tubular basement membrane disintegration,HP:0000091,Abnormality of the renal tubule
+UBERON:0001956,cartilage of bronchus,UBERON:0001994,hyaline cartilage tissue
+UBERON:3000505,processus pterygoideus of maxilla,UBERON:0010313,neural crest-derived structure
+DOID:11816,vitreous syneresis,DOID:9799,eye degenerative disease
+HP:0005130,Restrictive heart failure,HP:0001635,Congestive heart failure
+DOID:4209,brainstem intraparenchymal clear cell meningioma,DOID:4210,clear cell meningioma
+HP:0010932,Abnormality of nucleobase metabolism,HP:0001939,Abnormality of metabolism/homeostasis
+HP:0010380,Abnormality of the distal phalanx of the 4th toe,HP:0010182,Abnormality of the distal phalanges of the toes
+UBERON:4200048,bicipital crest,UBERON:4100000,skeletal element projection
+UBERON:0006074,lumbar region of vertebral column,UBERON:0006077,subdivision of vertebral column
+HP:0000365,Hearing impairment,HP:0000364,Hearing abnormality
+HP:0001748,Polysplenia,HP:0009799,Supernumerary spleens
+DOID:8072,sarcomatous intrahepatic cholangiocarcinoma,DOID:4928,intrahepatic cholangiocarcinoma
+UBERON:0004363,aortic arch,UBERON:0003469,respiratory system artery
+UBERON:0001158,descending colon,UBERON:0000168,segment of colon
+UBERON:0010373,uncinate process of pancreas,UBERON:0004529,anatomical projection
+HP:0009830,Peripheral neuropathy,HP:0000759,Abnormality of the peripheral nervous system
+UBERON:0001166,pylorus,UBERON:0009870,zone of stomach
+UBERON:0006872,handplate apical ectodermal ridge,UBERON:0004356,apical ectodermal ridge
+HP:0011926,Proximal placement of hallux,HP:0010051,Deviation/Displacement of the hallux
+UBERON:0011930,preganglionic parasympathetic  fiber,UBERON:0011925,preganglionic autonomic fiber
+HP:0100255,Metaphyseal dysplasia,HP:0000944,Abnormality of the metaphyses
+HP:0004565,Severe platyspondyly,HP:0000926,Platyspondyly
+UBERON:0007862,perichordal tissue,UBERON:0004121,ectoderm-derived structure
+UBERON:0002993,inferior central nucleus,UBERON:0003528,brain grey matter
+HP:0009608,Complete duplication of proximal phalanx of the thumb,HP:0009943,Complete duplication of the phalanges of the thumb
+UBERON:0000459,uterine wall,UBERON:0000060,anatomical wall
+HP:0006714,Aplasia/Hypoplasia of the sternum,HP:0006711,Aplasia/Hypoplasia involving bones of the thorax
+HP:0009759,Neck pterygia,HP:0001059,Pterygium
+UBERON:2000673,hypobranchial artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0010230,eyeball of camera-type eye,UBERON:0004121,ectoderm-derived structure
+DOID:8622,measles,DOID:934,viral infectious disease
+CL:0000457,biogenic amine secreting cell,CL:0000163,endocrine cell
+DOID:9358,fibular collateral ligament bursitis,DOID:204,enthesopathy
+UBERON:0008287,feather vane,UBERON:0000477,anatomical cluster
+HP:0005527,Reduced kininogen activity,HP:0005559,Abnormality of the kinin-kallikrein system
+NCBITaxon:32066,Fusobacteria,NCBITaxon:2,Bacteria
+UBERON:3000117,crista subnasalis,UBERON:0004529,anatomical projection
+UBERON:0002407,pericardium,UBERON:0006914,squamous epithelium
+UBERON:0005527,rhombomere 8,UBERON:0001892,rhombomere
+DOID:7817,mixed astrocytoma-ependymoma-oligodendroglioma,DOID:5076,mixed glioma
+UBERON:0003249,epithelium of otic placode,UBERON:0015807,ear epithelium
+UBERON:0008992,chorion frondosum,UBERON:0000478,extraembryonic structure
+UBERON:0006428,basisphenoid bone,UBERON:0003462,facial bone
+HP:0009944,Partial duplication of the phalanges of the thumb,HP:0009999,Partial duplication of the phalanx of hand
+CL:0005005,cyanoblast,CL:0000055,non-terminally differentiated cell
+UBERON:0002519,otolithic membrane,UBERON:0005764,acellular membrane
+HP:0003066,Limited knee extension,HP:0002815,Abnormality of the knees
+UBERON:2001874,basibranchial 2 cartilage,UBERON:2001916,basibranchial 2 element
+UBERON:0008924,sublaminar layer S3,UBERON:0009734,sublaminar layers S2 or S3 or S4
+UBERON:0008586,tensor veli palatini,UBERON:0003682,palatal muscle
+HP:0200016,Acrokeratosis,HP:0011368,Epidermal thickening
+NCBITaxon:451870,Chaetothyriomycetidae,NCBITaxon:147545,Eurotiomycetes
+HP:0100053,Stippling of the epiphyses of the 2nd toe,HP:0010323,Abnormality of the epiphyses of the 2nd toe
+DOID:5831,fallopian tube endometrioid adenocarcinoma,DOID:3706,fallopian tube adenocarcinoma
+HP:0002668,Paraganglioma,HP:0100634,Neuroendocrine neoplasm
+HP:0100245,Desmoid tumors,HP:0007378,Neoplasm of the gastrointestinal tract
+DOID:7891,testicular spermatocytic seminoma,DOID:5834,spermatocytoma
+CL:0002524,disseminated nephrocyte,CL:0002520,nephrocyte
+HP:0009348,Cone-shaped epiphysis of the proximal phalanx of the 3rd finger,HP:0010270,Cone-shaped epiphyses of the proximal phalanges of the hand
+HP:0001812,Hyperconvex fingernails,HP:0001795,Hyperconvex nail
+HP:0012451,Acute constipation,HP:0002019,Constipation
+UBERON:3000494,processus lingualis of pterygoid,UBERON:4100000,skeletal element projection
+DOID:8394,adult type testicular granulosa cell tumor,DOID:5331,testicular granulosa cell tumor
+DOID:5222,acute necrotizing encephalitis,DOID:9588,encephalitis
+UBERON:0014770,palpebral artery,UBERON:0003496,head blood vessel
+CL:0002483,hair follicle melanocyte,CL:2000000,epidermal melanocyte
+NCBITaxon:2049,Actinomycetaceae,NCBITaxon:85005,Actinomycineae
+CL:1000473,myoepithelial cell of quarternary lactiferous duct,CL:0000185,myoepithelial cell
+HP:0100391,Short distal phalanx of the 5th toe,HP:0100368,Short phalanx of the 5th toe
+DOID:5432,bladder papillary transitional cell neoplasm,DOID:5433,urinary tract papillary transitional cell benign neoplasm
+DOID:6032,juvenile type testicular granulosa cell tumor,DOID:5331,testicular granulosa cell tumor
+HP:0000620,Dacrocystitis,HP:0000614,Abnormality of the nasolacrimal system
+DOID:4558,Ludwig's angina,DOID:3488,cellulitis
+DOID:13941,benign paroxysmal positional nystagmus,DOID:9847,peripheral vertigo
+UBERON:0006091,inferior horn of the lateral ventricle,UBERON:0004121,ectoderm-derived structure
+UBERON:2000187,lateral granular eminence,UBERON:0002946,regional part of cerebellum
+UBERON:0004430,proximal epiphysis of fourth metatarsal bone,UBERON:0004415,proximal epiphysis of metatarsal bone
+UBERON:0012294,navicular fossa of spongiose part of urethra,UBERON:0005156,reproductive structure
+UBERON:0011267,quadratojugal bone,UBERON:0002514,intramembranous bone
+HP:0008153,Periodic hypokalemic paresis,HP:0003768,Periodic paralysis
+CL:1001586,mammary gland glandular cell,CL:0000150,glandular epithelial cell
+HP:0002614,Hepatic periportal necrosis,HP:0002605,Hepatic necrosis
+UBERON:0013756,venous blood,UBERON:0000178,blood
+DOID:3741,bladder verrucous squamous cell carcinoma,DOID:3742,bladder squamous cell carcinoma
+HP:0007381,Congenital exfoliative erythroderma,HP:0001019,Erythroderma
+HP:0100347,Tibial deviation of the 5th toe,HP:0010344,Deviation/Displacement of the 5th toe
+UBERON:0004133,salivatory nucleus,UBERON:0002680,regional part of metencephalon
+HP:0002730,Chronic noninfectious lymphadenopathy,HP:0002716,Lymphadenopathy
+HP:0000230,Gingivitis,HP:0000168,Abnormality of the gingiva
+DOID:5703,mixed liposarcoma,DOID:3382,liposarcoma
+DOID:10567,late yaws,DOID:10371,yaws
+HP:0000491,Keratitis,HP:0000481,Abnormality of the cornea
+DOID:9682,yellow fever,DOID:934,viral infectious disease
+UBERON:0003827,thoracic segment bone,UBERON:0003463,trunk bone
+UBERON:0009722,entire pharyngeal arch endoderm,UBERON:0000477,anatomical cluster
+UBERON:2000573,internal cellular layer,UBERON:0000479,tissue
+UBERON:0001431,distal carpal bone 2,UBERON:0001481,distal carpal bone
+UBERON:2001846,inter-ventral hypohyal joint,UBERON:0000982,skeletal joint
+UBERON:0001450,calcaneus,UBERON:0015014,calcaneum endochondral element
+HP:0002945,Intervertebral space narrowing,HP:0005108,Abnormality of the intervertebral disk
+HP:0012305,Coarctation of the descending aortic arch,HP:0012303,Abnormality of the aortic arch
+HP:0000707,Abnormality of the nervous system,HP:0000118,Phenotypic abnormality
+CL:0000648,kidney granular cell,CL:0000154,protein secreting cell
+UBERON:2005072,endocardial ring,UBERON:0004120,mesoderm-derived structure
+UBERON:2001766,pectoral fin lepidotrichium 6,UBERON:4000175,pectoral fin lepidotrichium
+HP:0003378,Axonal degeneration/regeneration,HP:0000764,Peripheral axonal degeneration
+DOID:13731,malignant secondary hypertension,DOID:10824,malignant hypertension
+UBERON:0009771,left anterior cardinal vein,UBERON:0015212,lateral structure
+UBERON:0002258,dorsal funiculus,UBERON:0015212,lateral structure
+UBERON:0013596,brain coronal sulcus,UBERON:0008334,subarachnoid sulcus
+UBERON:0014782,allantois of embryonic urinary system,UBERON:0000481,multi-tissue structure
+HP:0100103,Enlarged epiphysis of the distal phalanx of the 2nd toe,HP:0100047,Enlarged epiphyses of the 2nd toe
+HP:0100507,Folate deficiency,HP:0012335,Abnormality of folate metabolism
+DOID:14472,hantavirus pulmonary syndrome,DOID:934,viral infectious disease
+UBERON:0010738,distal tarsal bone 5,UBERON:0015114,distal tarsal bone 5 endochondral element
+HP:0003423,Thoracolumbar kyphoscoliosis,HP:0002751,Kyphoscoliosis
+DOID:2058,chronic mucocutaneous candidiasis,DOID:1508,candidiasis
+DOID:9352,type 2 diabetes mellitus,DOID:9351,diabetes mellitus
+UBERON:3000454,postnasal wall,UBERON:0010363,endochondral element
+UBERON:0005905,insect labrum,UBERON:0000064,organ part
+UBERON:0011620,basihyal lingual process,UBERON:0004530,bony projection
+HP:0010516,Thymus hyperplasia,HP:0000777,Abnormality of the thymus
+UBERON:0003688,omentum,UBERON:0004120,mesoderm-derived structure
+UBERON:0008258,oral surface,UBERON:0000475,organism subdivision
+DOID:5908,penis verrucous carcinoma,DOID:5518,penis squamous cell carcinoma
+UBERON:0006670,central tendon of diaphragm,UBERON:0000043,tendon
+DOID:2972,renal artery obstruction,DOID:2388,renal artery disease
+HP:0011210,EEG with occipital slowing,HP:0010843,EEG with focal slow activity
+UBERON:4200016,postbranchial lamina,UBERON:0005913,zone of bone organ
+UBERON:0014754,P4 area of pallium (Myxiniformes),UBERON:0002791,regional part of telencephalon
+HP:0008659,Multiple small medullary renal cysts,HP:0100957,Abnormality of the renal medulla
+DOID:0050637,Finnish type amyloidosis,DOID:9120,amyloidosis
+UBERON:0010185,rete ovarii,UBERON:0014404,female anatomical structure
+UBERON:0010682,pedal digit 3 phalanx cartilage element,UBERON:0010685,pedal digit phalanx cartilage element
+UBERON:0013231,sebaceous gland of eyelid,UBERON:0013229,eyelid gland
+CL:0002078,meso-epithelial cell,CL:0002371,somatic cell
+CL:0000311,keratin accumulating cell,CL:0000325,stuff accumulating cell
+UBERON:0006101,Brodmann (1909) area 24,UBERON:0013529,Brodmann area
+HP:0009513,Absent epiphysis of the middle phalanx of the 2nd finger,HP:0009500,Abnormality of the epiphysis of the middle phalanx of the 2nd finger
+UBERON:0002974,molecular layer of cerebellar cortex,UBERON:0004130,cerebellar layer
+HP:0100062,Pseudoepiphyses of the 3rd toe,HP:0010169,Pseudoepiphyses of the toes
+HP:0012032,Lipoma,HP:0012031,Lipomatous tumor
+UBERON:4000159,ossified ligament,UBERON:0001479,sesamoid bone
+HP:0010158,Stippling of the epiphysis of the 1st metatarsal,HP:0010122,Stippling of the epiphyses of the hallux
+DOID:7632,cowper gland carcinoma,DOID:3856,male reproductive organ cancer
+UBERON:0011050,thoracic vertebra 8,UBERON:0002347,thoracic vertebra
+NCBITaxon:11161,Mumps virus,NCBITaxon:39744,Rubulavirus
+CL:0007004,premigratory neural crest cell,CL:0000003,native cell
+UBERON:0005478,sulcus limitans of neural tube,UBERON:0004121,ectoderm-derived structure
+UBERON:0015223,dorsal nasal meatus,UBERON:0015216,nasal meatus
+HP:0011798,Renal oncocytoma,HP:0009726,Renal neoplasm
+UBERON:0005631,extraembryonic membrane,UBERON:0000158,membranous layer
+UBERON:0003530,pedal digit skin,UBERON:0015249,digit skin
+HP:0005197,Generalized morning stiffness,HP:0001387,Joint stiffness
+CL:0000449,brown fat cell,CL:0000136,fat cell
+UBERON:2000276,rostrolateral thalamic nucleus of Butler & Saidel,UBERON:0015234,nucleus of ventral thalamus
+HP:0009478,Symphalangism of the proximal phalanx of the 4th finger with the 4th metatcarpal,HP:0005880,Metacarpophalangeal synostosis
+HP:0012180,Cystic medial necrosis,HP:0011004,Abnormality of the systemic arterial tree
+DOID:3275,thymoma,DOID:3277,thymus cancer
+UBERON:0000999,ejaculatory duct,UBERON:0005904,duct of male reproductive system
+CL:1000296,epithelial cell of urethra,CL:1001320,urethra cell
+UBERON:0005141,metanephric short descending thin limb,UBERON:0005134,metanephric nephron epithelium
+CL:0000929,"CD4-negative, CD8-negative type I NK T cell secreting interferon-gamma",CL:0000924,"CD4-negative, CD8-negative type I NK T cell"
+HP:0008259,Adrenocorticotropin (ACTH) receptor (ACTHR) defect,HP:0011734,Central adrenal insufficiency
+DOID:5338,gingival hypertrophy,DOID:3086,gingival overgrowth
+DOID:5776,cavernous hemangioma of face,DOID:483,cavernous hemangioma
+UBERON:0005574,rhombomere 3 lateral wall,UBERON:0005501,rhombomere lateral wall
+DOID:4659,extracutaneous mastocytoma,DOID:3664,mast cell neoplasm
+HP:0003992,Slender ulna,HP:0003969,Slender forearm bones
+HP:0007613,Spinous keratoses of palms and soles,HP:0000972,Palmoplantar hyperkeratosis
+HP:0003215,Dicarboxylic aciduria,HP:0010995,Abnormality of dicarboxylic acid metabolism
+HP:0001067,Neurofibromas,HP:0010614,Fibroma
+HP:0012048,Oromandibular dystonia,HP:0012179,Craniofacial dystonia
+UBERON:0006470,eighth cervical spinal cord segment,UBERON:0007714,cervical subsegment of spinal cord
+HP:0009328,Pseudoepiphysis of the middle phalanx of the 3rd finger,HP:0010264,Pseudoepiphyses of the middle phalanges of the hand
+UBERON:0007821,lateral nasal cartilage,UBERON:0001823,nasal cartilage
+UBERON:0014616,dorsal nerve root of thoracic spinal cord,UBERON:0009630,root of thoracic nerve
+HP:0009274,Joint contractures of the 4th finger,HP:0004188,Abnormality of the 4th finger
+HP:0005231,Chronic gastritis,HP:0005263,Gastritis
+HP:0012220,Non-caseating epithelioid cell granulomatosis,HP:0002955,Granulomatosis
+DOID:6676,Froelich's syndrome,DOID:1931,hypothalamic disease
+UBERON:3000819,margo clavicularis,UBERON:0000064,organ part
+HP:0009208,Irregular epiphysis of the middle phalanx of the 5th finger,HP:0010262,Irregular epiphyses of the middle phalanges of the hand
+HP:0000934,Chondrocalcinosis,HP:0100685,Abnormality of Sharpey fibers
+UBERON:0001636,posterior cerebral artery,UBERON:0003496,head blood vessel
+HP:0002239,Gastrointestinal hemorrhage,HP:0011029,Internal hemorrhage
+HP:0010257,Absent epiphyses of the middle phalanges of the hand,HP:0010228,Absent epiphyses of the phalanges of the hand
+UBERON:0009676,early telencephalic vesicle,UBERON:0013150,future brain vesicle
+HP:0000340,Sloping forehead,HP:0000290,Abnormality of the forehead
+UBERON:0000022,feather,UBERON:0004121,ectoderm-derived structure
+UBERON:2001433,posterior sclerotic bone,UBERON:0010297,endochondral scleral ossicle
+HP:0011935,Decreased urinary urate,HP:0004369,Decreased purine levels
+UBERON:0014551,CA2 stratum oriens,UBERON:0014567,layer of hippocampal field
+HP:0012546,Skewed maternal X inactivation,HP:0002686,Prenatal maternal abnormality
+HP:0000431,Wide nasal bridge,HP:0000422,Abnormality of the nasal bridge
+NCBITaxon:50557,Insecta,NCBITaxon:6960,Hexapoda
+CL:0002422,enucleated reticulocyte,CL:0000225,anucleate cell
+HP:0009054,Scapuloperoneal myopathy,HP:0001430,Abnormality of the calf musculature
+UBERON:4000107,elasmodine,UBERON:0003585,dermis connective tissue
+UBERON:2002120,orbitosphenoid septum,UBERON:0004120,mesoderm-derived structure
+HP:0001789,Hydrops fetalis,HP:0001197,Abnormality of prenatal development or birth
+HP:0010045,Aplasia/Hypoplasia of the 5th metacarpal,HP:0010013,Abnormality of the 5th metacarpal
+HP:0007655,Eversion of lateral third of lower eyelids,HP:0000656,Ectropion
+UBERON:0000464,anatomical space,UBERON:0000466,immaterial anatomical entity
+UBERON:2002226,preglomerular nucleus,UBERON:0006569,diencephalic nucleus
+DOID:0050427,xeroderma pigmentosum,DOID:0050737,autosomal recessive disease
+UBERON:0010063,tympanic cavity epithelium,UBERON:0007499,epithelial sac
+UBERON:3000459,prearticular coronoid process,UBERON:0010313,neural crest-derived structure
+HP:0009423,Bullet-shaped distal phalanx of the 3rd finger,HP:0009441,Bullet-shaped phalanges of the 3rd finger
+UBERON:0007729,interphalangeal joint of manual digit 2,UBERON:0007722,interphalangeal joint of manus
+UBERON:0001178,visceral peritoneum,UBERON:0004120,mesoderm-derived structure
+CL:0000844,germinal center B cell,CL:0000785,mature B cell
+UBERON:0005302,female preputial gland,UBERON:0000359,preputial gland
+DOID:13781,hypermobility syndrome,DOID:381,arthropathy
+UBERON:0002798,spinothalamic tract of pons,UBERON:0007702,tract of brain
+HP:0006179,Pseudoepiphyses of second metacarpal,HP:0009193,Pseudoepiphyses of the metacarpals
+UBERON:0001339,ischiocavernosus muscle,UBERON:0002379,perineal muscle
+UBERON:0008873,alveolar pore,UBERON:0004111,anatomical conduit
+UBERON:2001312,dorsal anterior lateral line ganglion,UBERON:0004121,ectoderm-derived structure
+UBERON:0001325,muscle of pelvis,UBERON:0005179,pelvic region organ
+HP:0001618,Dysphonia,HP:0002167,Neurological speech impairment
+HP:0008362,Aplasia/Hypoplasia of the hallux,HP:0010760,Absent toe
+UBERON:2002210,mossy fiber,UBERON:0004121,ectoderm-derived structure
+HP:0000196,Lower lip pit,HP:0000178,Abnormality of lower lip
+DOID:7936,precursor T-lymphoblastic lymphoma/leukemia refractory,DOID:712,refractory hematologic cancer
+UBERON:0006856,interrenal gland,UBERON:0004177,hemopoietic organ
+HP:0002594,Pancreatic hypoplasia,HP:0100800,Aplasia/Hypoplasia of the pancreas
+HP:0003884,Triangular humerus,HP:0003063,Abnormality of the humerus
+DOID:7211,fibrous meningioma,DOID:3565,meningioma
+DOID:0050553,JMP syndrome,DOID:0050737,autosomal recessive disease
+HP:0011246,Underdeveloped superior crus of antihelix,HP:0011245,Abnormality of superior crus of antihelix
+UBERON:2001681,cornu mesial process,UBERON:0004120,mesoderm-derived structure
+DOID:11252,microcytic anemia,DOID:2355,anemia
+HP:0200048,Cyanotic episode,HP:0000961,Cyanosis
+UBERON:2202277,pectoral fin distal radial cartilage 1,UBERON:2102277,pectoral fin distal radial element 1
+NCBITaxon:35278,"ssRNA positive-strand viruses, no DNA stage",NCBITaxon:439488,ssRNA viruses
+HP:0009431,Bullet-shaped middle phalanx of the 3rd finger,HP:0004172,Abnormality of the middle phalanx of the 3rd finger
+HP:0000178,Abnormality of lower lip,HP:0000159,Abnormality of the lip
+CL:0011101,chorionic trophoblast cell,CL:0000351,trophoblast cell
+CL:1000449,epithelial cell of nephron,CL:0002518,kidney epithelial cell
+UBERON:0002960,central oculomotor nucleus,UBERON:0007414,nucleus of midbrain tegmentum
+HP:0002480,Hepatic encephalopathy,HP:0001298,Encephalopathy
+UBERON:0004745,parasphenoid,UBERON:0011164,neurocranium bone
+HP:0002384,Focal seizures with impairment of consciousness or awareness,HP:0011146,Dialeptic seizures
+UBERON:0014932,periventricular white matter,UBERON:0002316,white matter
+HP:0012707,Elevated brain lactate level by MRS,HP:0012705,Abnormal metabolic brain imaging by MRS
+UBERON:0001297,serosa of uterus,UBERON:0000042,serous membrane
+HP:0004724,Calcium nephrolithiasis,HP:0000787,Nephrolithiasis
+HP:0009597,Short proximal phalanx of the 2nd finger,HP:0010241,Short proximal phalanx of finger
+UBERON:0003363,epithelium of ductus reuniens,UBERON:0006932,vestibular epithelium
+CL:0002319,neural cell,CL:0000548,animal cell
+DOID:12527,common peroneal nerve lesion,DOID:9473,mononeuritis of lower limb
+DOID:8545,malignant hyperthermia,DOID:630,genetic disease
+CL:0002508,"langerin-negative, CD103-negative lymph node dendritic cell",CL:0000990,conventional dendritic cell
+UBERON:0010931,intermandibularis,UBERON:0001630,muscle organ
+DOID:3596,placental site trophoblastic tumor,DOID:3594,choriocarcinoma
+HP:0012314,Bouchard's node,HP:0006247,Enlarged interphalangeal joints
+CL:0002299,type-2 epithelial cell of thymus,CL:0002364,cortical thymic epithelial cell
+UBERON:0010323,cranial skeletal system,UBERON:0000075,subdivision of skeletal system
+DOID:0060020,reticular dysgenesis,DOID:627,severe combined immunodeficiency
+UBERON:0000331,ileal mucosa,UBERON:0001204,mucosa of small intestine
+HP:0007970,Congenital ptosis,HP:0000508,Ptosis
+DOID:3869,childhood medulloblastoma,DOID:0050902,medulloblastoma
+CL:0000187,muscle cell,CL:0000183,contractile cell
+DOID:10184,spindle cell lipoma,DOID:3315,lipoma
+UBERON:0011164,neurocranium bone,UBERON:0004766,cranial bone
+HP:0009116,Aplasia/Hypoplasia involving bones of the skull,HP:0009122,Aplasia/Hypoplasia affecting bones of the axial skeleton
+HP:0008001,Foveal hyperpigmentation,HP:0008002,Abnormality of macular pigmentation
+UBERON:0000965,lens of camera-type eye,UBERON:0004121,ectoderm-derived structure
+UBERON:0009745,lymph node medullary cord,UBERON:0000061,anatomical structure
+UBERON:0005158,parenchyma of central nervous system,UBERON:0004121,ectoderm-derived structure
+UBERON:3000590,supraorbital flange,UBERON:0004120,mesoderm-derived structure
+UBERON:0006290,scapula cartilage element,UBERON:0015057,scapula endochondral element
+NCBITaxon:37705,Sin Nombre virus,NCBITaxon:11598,Hantavirus
+HP:0009954,Complete duplication of the proximal phalanx of the 2nd finger,HP:0010000,Complete duplication of the proximal phalanges of the hand
+HP:0000998,Hypertrichosis,HP:0011362,Abnormal hair quantity
+CL:0002240,marrow fibroblast,CL:0002092,bone marrow cell
+HP:0009672,Small epiphysis of the proximal phalanx of the thumb,HP:0009694,Small epiphyses of the thumb
+HP:0004041,Cupped ulnar metaphysis,HP:0004039,Abnormality of ulnar metaphysis
+CL:0002437,mature CD8 single-positive thymocyte,CL:0000625,"CD8-positive, alpha-beta T cell"
+HP:0000900,Thickened ribs,HP:0000772,Abnormality of the ribs
+UBERON:0013500,glossopharyngeal-vagus IX-X ganglion complex,UBERON:0001714,cranial ganglion
+HP:0012244,Abnormal sex determination,HP:0012243,Abnormal genital system morphology
+UBERON:0008538,muscle of posterior compartment of thigh,UBERON:0004252,hindlimb stylopod muscle
+UBERON:0008918,ampulla of Lorenzini,UBERON:0003103,compound organ
+DOID:0050197,Brazilian hemorrhagic fever,DOID:934,viral infectious disease
+UBERON:0001081,endocardium of ventricle,UBERON:0012275,meso-epithelium
+DOID:14502,cholesterol ester storage disease,DOID:9455,lipid storage disease
+DOID:1558,angioedema,DOID:37,skin disease
+DOID:10321,baritosis,DOID:10316,pneumoconiosis
+DOID:11328,schizophreniform disorder,DOID:2468,psychotic disorder
+HP:0007407,Excessive skin wrinkling on dorsum of hands and fingers,HP:0007392,Excessive wrinkled skin
+DOID:6102,herpetic gastritis,DOID:2327,viral gastritis
+DOID:9788,myositis fibrosa,DOID:633,myositis
+HP:0007595,Redundant skin in infancy,HP:0001582,Redundant skin
+UBERON:3000656,processus posterodorsalis of lamella alaris,UBERON:0010313,neural crest-derived structure
+UBERON:0011281,nail of pedal digit 4,UBERON:0009567,nail of pedal digit
+UBERON:0011693,extraembryonic portion of umbilical artery,UBERON:0004573,systemic artery
+UBERON:0011202,urachus epithelium,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0010240,zygomatic gland,UBERON:0012102,buccal salivary gland
+DOID:8628,"Hodgkin's lymphoma, lymphocytic depletion",DOID:8567,Hodgkin's lymphoma
+DOID:13389,labia majora carcinoma,DOID:1294,vulva carcinoma
+HP:0009949,Duplication of the middle phalanx of the 2nd finger,HP:0009543,Abnormality of the middle phalanx of the 2nd finger
+UBERON:2005219,choroid plexus vascular circuit,UBERON:0005284,brain vasculature
+CL:0002170,keratinized cell of the oral mucosa,CL:0002336,buccal mucosa cell
+DOID:4939,ureter carcinoma,DOID:11819,ureter cancer
+DOID:13658,infective urethral stricture,DOID:1829,urethral stricture
+HP:0011923,Decreased activity of mitochondrial complex I,HP:0008972,Decreased activity of mitochondrial respiratory chain
+UBERON:0015245,septal olfactory organ,UBERON:0004121,ectoderm-derived structure
+HP:0003951,Irregular metaphyses (elbow),HP:0003949,Abnormality of the elbow metaphyses
+HP:0002859,Rhabdomyosarcoma,HP:0100242,Sarcoma
+UBERON:0004200,kidney pyramid,UBERON:0000064,organ part
+DOID:3721,plasmacytoma,DOID:6536,plasma cell neoplasm
+UBERON:0001432,distal carpal bone 3,UBERON:0015090,distal carpal bone 3 endochondral element
+UBERON:4200099,lateral extrascapular,UBERON:2000663,extrascapula
+HP:0010197,Curved middle phalanges of the toes,HP:0010176,Curved phalanges of the toes
+DOID:0050683,Bothnia retinal dystrophy,DOID:8501,fundus dystrophy
+UBERON:0008277,cnida,UBERON:0000470,cell part
+UBERON:0003980,cerebellum fissure,UBERON:0014466,subarachnoid fissure
+HP:0100247,Recurrent singultus,HP:0000775,Abnormality of the diaphragm
+UBERON:0010135,sensory circumventricular organ,UBERON:0005408,circumventricular organ
+HP:0006775,Multiple myeloma,HP:0004377,Hematological neoplasm
+DOID:0080019,metaphyseal dysplasia,DOID:2256,osteochondrodysplasia
+HP:0010799,Pinealoma,HP:0100835,Benign neoplasm of the central nervous system
+UBERON:0000981,femur,UBERON:0015052,femur endochondral element
+HP:0007394,Prominent superficial blood vessels,HP:0011276,Vascular skin abnormality
+UBERON:0006660,muscle layer,UBERON:0004923,organ component layer
+UBERON:2001950,inter-premaxillary joint,UBERON:0000982,skeletal joint
+UBERON:0004338,proximal phalanx of manual digit 1,UBERON:0002234,proximal phalanx of manus
+DOID:2174,ocular cancer,DOID:0060116,sensory system cancer
+HP:0001464,Aplasia/Hypoplasia involving the shoulder musculature,HP:0001435,Abnormality of the shoulder girdle musculature
+HP:0005576,Tubulointerstitial fibrosis,HP:0001969,Tubulointerstitial abnormality
+HP:0010051,Deviation/Displacement of the hallux,HP:0001844,Abnormality of the hallux
+DOID:11809,bladder neck cancer,DOID:11054,urinary bladder cancer
+CL:0000540,neuron,CL:0000404,electrically signaling cell
+HP:0011871,Impaired ristocetin-induced platelet aggregation,HP:0003540,Impaired platelet aggregation
+UBERON:0001653,facial vein,UBERON:0003502,neck blood vessel
+UBERON:0009116,thymoid,UBERON:0000078,mixed ectoderm/mesoderm/endoderm-derived structure
+HP:0012352,Abnormal fucosylation of protein N-linked glycosylation,HP:0012347,Abnormal protein N-linked glycosylation
+UBERON:0009834,dorsolateral prefrontal cortex,UBERON:0002619,regional part of cerebral cortex
+DOID:14000,rubeosis iridis,DOID:5679,retinal disease
+UBERON:2002215,otic vesicle protrusion,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009882,Short distal phalanx of finger,HP:0009835,Aplasia/Hypoplasia of the distal phalanges of the hand
+UBERON:2001224,basibranchial 2 bone,UBERON:0002513,endochondral bone
+UBERON:0002823,clivus of fovea centralis,UBERON:0000466,immaterial anatomical entity
+UBERON:0008816,embryonic head,UBERON:0002050,embryonic structure
+HP:0007473,Crusting erythematous dermatitis,HP:0011123,Inflammatory abnormality of the skin
+HP:0006773,Cutaneous angiolipomas,HP:0008069,Neoplasm of the skin
+UBERON:0006713,foramen cecum of frontal bone,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010030,Osteolytic defects of the 1st metacarpal,HP:0010009,Abnormality of the 1st metacarpal
+UBERON:0013177,dorsal bursa,UBERON:0015212,lateral structure
+UBERON:0014452,gustatory epithelium of tongue,UBERON:0002926,gustatory epithelium
+UBERON:2007004,epiphysial cluster,UBERON:0000479,tissue
+HP:0007832,Pigmentation of the sclera,HP:0000591,Abnormality of the sclera
+HP:0004953,Abdominal aortic aneurysm,HP:0005112,Dilatation of the abdominal aorta
+HP:0012242,Superior rectus atrophy,HP:0008049,Abnormality of the extraocular muscles
+UBERON:0007722,interphalangeal joint of manus,UBERON:0006658,interphalangeal joint
+HP:0011447,Hyposegmentation of neutrophil nuclei,HP:0011992,Abnormality of neutrophil morphology
+UBERON:0004383,epiphysis of tibia,UBERON:0001437,epiphysis
+DOID:13523,loiasis,DOID:1080,filariasis
+DOID:13239,internal pathological resorption,DOID:13240,tooth resorption
+DOID:13316,exocrine pancreatic insufficiency,DOID:26,pancreas disease
+HP:0200034,Papule,HP:0011355,Localized skin lesion
+UBERON:0003075,neural plate,UBERON:0010371,ecto-epithelium
+CL:0002562,hair germinal matrix cell,CL:0002559,hair follicle cell
+UBERON:2001918,basibranchial 4 element,UBERON:0013746,basibranchial element
+DOID:6445,ovarian endometrioid malignant adenofibroma,DOID:6170,ovarian carcinosarcoma
+CL:0000811,"CD8-positive, alpha-beta thymocyte",CL:0000790,immature alpha-beta T cell
+CL:0000800,mature gamma-delta T cell,CL:0000798,gamma-delta T cell
+DOID:1156,pseudogout,DOID:1222,cartilage disease
+UBERON:0012353,fin skeleton,UBERON:0010912,subdivision of skeleton
+HP:0100803,Abnormality of the periungual region,HP:0001597,Abnormality of the nail
+HP:0004684,Talipes valgus,HP:0003028,Abnormality of the ankles
+DOID:8691,mycosis fungoides,DOID:0060061,cutaneous T cell lymphoma
+UBERON:0005745,optic canal,UBERON:0010313,neural crest-derived structure
+UBERON:0015227,peristaltic circulatory vessel,UBERON:0000025,tube
+UBERON:2002268,epineural 6,UBERON:2000507,epineural
+HP:0012518,Abnormality of circle of Willis,HP:0009145,Abnormality of cerebral artery
+UBERON:0007691,gustatory pore,UBERON:0000161,orifice
+HP:0009708,Synostosis involving the 5th metacarpal,HP:0010013,Abnormality of the 5th metacarpal
+DOID:7902,adult extraosseous chondrosarcoma,DOID:4549,extraosseous chondrosarcoma
+CL:0002108,CD38-negative IgG memory B cell,CL:0001053,IgD-negative memory B cell
+UBERON:0005507,rhombomere 3,UBERON:0001892,rhombomere
+HP:0010388,Patchy sclerosis of the phalanges of the 5th toe,HP:0010342,Abnormality of the phalanges of the 5th toe
+UBERON:0007379,egg,UBERON:0004120,mesoderm-derived structure
+DOID:4524,prostate angiosarcoma,DOID:4054,prostate sarcoma
+UBERON:0014903,primordial vasculature,UBERON:0001048,primordium
+UBERON:3000414,pars palatina of premaxilla,UBERON:0004120,mesoderm-derived structure
+UBERON:0000054,macula,UBERON:0004121,ectoderm-derived structure
+UBERON:0000914,organismal segment,UBERON:0000475,organism subdivision
+CL:0002289,type I taste bud cell,CL:0000703,sustentacular cell
+HP:0001944,Dehydration,HP:0011032,Abnormality of fluid regulation
+DOID:6569,micropapillomatosis labialis,DOID:2071,vulvar squamous papilloma
+UBERON:0002822,macula lutea proper,UBERON:0000064,organ part
+UBERON:0005746,primary vitreous humour,UBERON:0004121,ectoderm-derived structure
+HP:0003117,Abnormality of circulating hormone level,HP:0000818,Abnormality of the endocrine system
+HP:0012578,Membranous nephropathy,HP:0000099,Glomerulonephritis
+HP:0000336,Prominent supraorbital ridges,HP:0100538,Abnormality of the supraorbital ridges
+UBERON:0003406,cartilage of respiratory system,UBERON:0007844,cartilage element
+UBERON:0007801,pygostyle,UBERON:0001474,bone element
+DOID:5348,adult endodermal sinus tumor,DOID:1911,endodermal sinus tumor
+HP:0001677,Coronary artery disease,HP:0100545,Arterial stenosis
+UBERON:3010452,non-involuting marginal zone,UBERON:0004879,marginal zone of embryo
+HP:0100601,Eclampsia,HP:0100603,Toxemia of pregnancy
+HP:0002866,Hypoplastic iliac wings,HP:0011867,Abnormality of the wing of the ilium
+HP:0100551,Neoplasm of the trachea,HP:0100552,Neoplasm of the tracheobronchial system
+UBERON:0003079,floor plate,UBERON:0004121,ectoderm-derived structure
+HP:0004474,Persistent open anterior fontanelle,HP:0001476,Delayed closure of the anterior fontanelle
+HP:0005009,Dumbbell-shaped humerus,HP:0000947,Dumbbell-shaped long bone
+UBERON:0003690,sacrum,UBERON:0005179,pelvic region organ
+DOID:850,lung disease,DOID:0050161,lower respiratory tract disease
+DOID:0050515,paralytic poliomyelitis,DOID:4953,poliomyelitis
+UBERON:0010409,eye surface,UBERON:0003102,surface structure
+HP:0011056,Agenesis of first permanent molar tooth,HP:0011055,Agenesis of permanent molar
+DOID:0050462,Antley-Bixler syndrome,DOID:0050737,autosomal recessive disease
+UBERON:0005215,kidney interstitium,UBERON:0005169,interstitial tissue
+HP:0004826,Folate-unresponsive megaloblastic anemia,HP:0001889,Megaloblastic anemia
+UBERON:0010375,pancreas dorsal primordium,UBERON:0001048,primordium
+HP:0001114,Xanthelasma,HP:0010604,Cyst of the eyelid
+HP:0009950,Complete duplication of the distal phalanx of the 2nd finger,HP:0010001,Complete duplication of the distal phalanges of the hand
+UBERON:0006878,decidua parietalis,UBERON:0000478,extraembryonic structure
+DOID:10538,gastric fundus cancer,DOID:10534,stomach cancer
+DOID:9123,eczema herpeticum,DOID:8566,herpes simplex
+UBERON:4440008,fin radial skeleton,UBERON:0010912,subdivision of skeleton
+UBERON:2002151,vertebral element 11,UBERON:0010913,vertebral element
+HP:0002293,Alopecia of scalp,HP:0001596,Alopecia
+UBERON:0002414,lumbar vertebra,UBERON:0003828,abdominal segment bone
+HP:0009942,Duplication of phalanx of thumb,HP:0009997,Duplication of phalanx of hand
+UBERON:0003398,mesentery of jejunum,UBERON:0003337,serosa of jejunum
+HP:0009745,Spinalarachnoid cyst,HP:0100702,Arachnoid cyst
+DOID:6786,childhood botryoid rhabdomyosarcoma,DOID:3255,botryoid rhabdomyosarcoma
+HP:0001620,High pitched voice,HP:0001608,Abnormality of the voice
+UBERON:0009882,anal column,UBERON:0000064,organ part
+HP:0012679,Widened interpedicular distance,HP:0008438,Vertebral arch anomaly
+UBERON:0001742,epiglottic cartilage,UBERON:0003583,larynx connective tissue
+HP:0000529,Progressive visual loss,HP:0000572,Visual loss
+UBERON:0002366,bulbo-urethral gland,UBERON:0010147,male accessory sex gland
+DOID:5592,breast papillary carcinoma,DOID:3459,breast carcinoma
+HP:0006252,Interphalangeal joint erosions,HP:0006261,Abnormality of phalangeal joints of the hand
+UBERON:0015032,pedal digit 2 phalanx endochondral element,UBERON:0015030,pedal digit phalanx endochondral element
+HP:0000570,Abnormality of saccadic eye movements,HP:0000496,Abnormality of eye movement
+HP:0008236,Isosexual precocious puberty,HP:0000826,Precocious puberty
+UBERON:0002031,epithelium of bronchus,UBERON:0000485,simple columnar epithelium
+HP:0011451,Congenital microcephaly,HP:0000252,Microcephaly
+CL:0002192,metamyelocyte,CL:0000763,myeloid cell
+UBERON:2007050,constrictor dorsalis,UBERON:0011648,jaw muscle
+UBERON:0001769,iris,UBERON:0004121,ectoderm-derived structure
+HP:0009280,Short 4th finger,HP:0009381,Short finger
+HP:0006753,Neoplasm of the stomach,HP:0007378,Neoplasm of the gastrointestinal tract
+UBERON:0006266,nasolacrimal groove,UBERON:0000490,unilaminar epithelium
+UBERON:0006588,round ligament of liver,UBERON:0013139,ligament of liver
+UBERON:0001111,intercostal muscle,UBERON:0002426,chest muscle
+UBERON:3000389,paries nasi,UBERON:0010313,neural crest-derived structure
+HP:0008073,Low maternal serum estriol,HP:0011436,Abnormal maternal serum screening
+HP:0010543,Opsoclonus,HP:0012547,Abnormal involuntary eye movements
+HP:0003903,Broad humeral epiphyses,HP:0003904,Wide epiphyses of the upper limbs
+UBERON:0013764,common crus of semicircular duct,UBERON:0004121,ectoderm-derived structure
+HP:0009477,Proximal/middle symphalangism of 4th finger,HP:0009308,Symphalangism of middle phalanx of 4th finger
+DOID:4151,skull base chordoma,DOID:3302,chordoma
+HP:0001464,Aplasia/Hypoplasia involving the shoulder musculature,HP:0001467,Aplasia/Hypoplasia involving the musculature of the upper limbs
+UBERON:2001450,apical ectodermal ridge pelvic fin,UBERON:0004356,apical ectodermal ridge
+HP:0004621,Enlarged vertebral pedicles,HP:0008438,Vertebral arch anomaly
+UBERON:2001966,epibranchial 5 element,UBERON:2001904,epibranchial element
+UBERON:0000474,female reproductive system,UBERON:0014404,female anatomical structure
+UBERON:0004802,respiratory tract epithelium,UBERON:0005911,endo-epithelium
+HP:0012081,Enlarged cerebellum,HP:0001317,Abnormality of the cerebellum
+HP:0002974,Radioulnar synostosis,HP:0100238,Synostosis involving bones of the upper limbs
+CL:0000300,gamete,CL:0000413,haploid cell
+HP:0010312,Asymmetry of the breasts,HP:0000769,Abnormality of the breast
+DOID:0060110,cervical benign neoplasm,DOID:0060086,female reproductive organ benign neoplasm
+UBERON:0010707,appendage girdle complex,UBERON:0000475,organism subdivision
+NCBITaxon:34383,mitosporic Onygenales,NCBITaxon:33183,Onygenales
+UBERON:0008930,somatosensory cortex,UBERON:0002619,regional part of cerebral cortex
+NCBITaxon:140693,Pulicomorpha,NCBITaxon:7509,Siphonaptera
+DOID:6128,gliomatosis cerebri,DOID:1319,brain cancer
+HP:0000765,Abnormality of the thorax,HP:0009121,Abnormal axial skeleton morphology
+CL:0000926,CD4-positive type I NK T cell secreting interferon-gamma,CL:0000923,CD4-positive type I NK T cell
+HP:0009482,Proximal/middle symphalangism of 3rd finger,HP:0009435,Symphalangism of middle phalanx of 3rd finger
+HP:0003418,Back pain,HP:0000925,Abnormality of the vertebral column
+UBERON:0001192,left gastric artery,UBERON:0004573,systemic artery
+UBERON:0012084,lumen of secondary bronchus,UBERON:0012082,bronchial lumen
+UBERON:0003479,thoracic cavity vein,UBERON:0003519,thoracic cavity blood vessel
+HP:0100569,Abnormal vertebral ossification,HP:0011849,Abnormal bone ossification
+HP:0003846,Wide epiphyseal plates of the upper limbs,HP:0003839,Abnormality involving the epiphyses of the upper limbs
+UBERON:0005710,lower jaw incisor epithelium,UBERON:0003355,epithelium of incisor
+CL:1000698,kidney resident macrophage,CL:0000864,tissue-resident macrophage
+UBERON:3000118,crista supraorbitalis,UBERON:0004529,anatomical projection
+HP:0004004,Irregular radial epiphyses,HP:0003999,Abnormality of radial epiphyses
+HP:0100404,Duplication of the proximal phalanx of the 3rd toe,HP:0010367,Duplication of phalanx of the 3rd toe
+HP:0100384,Absent proximal phalanx of the 3rd toe,HP:0100375,Aplasia/Hypoplasia of the proximal phalanx of the 3rd toe
+HP:0011638,Anomalous origin of left coronary artery from the pulmonary artery,HP:0011637,Anomalous origin of coronary artery from the pulmonary artery
+DOID:10190,liver lipoma,DOID:916,liver neoplasm
+UBERON:3000387,subotic alae,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0007805,synsacrum,UBERON:0004120,mesoderm-derived structure
+HP:0000052,"Urethral atresia, male",HP:0000068,Urethral atresia
+UBERON:0005808,bone tissue of long bone,UBERON:0002481,bone tissue
+UBERON:0000460,major vestibular gland,UBERON:0015212,lateral structure
+HP:0001272,Cerebellar atrophy,HP:0001317,Abnormality of the cerebellum
+HP:0004360,Abnormality of acid-base homeostasis,HP:0001939,Abnormality of metabolism/homeostasis
+HP:0010418,Patchy sclerosis of the distal phalanx of the 2nd toe,HP:0010352,Patchy sclerosis of the phalanges of the 2nd toe
+HP:0007126,Proximal amyotrophy,HP:0003202,Amyotrophy
+DOID:0050454,periventricular nodular heterotopia,DOID:2490,congenital nervous system abnormality
+HP:0009806,Nephrogenic diabetes insipidus,HP:0000873,Diabetes insipidus
+HP:0200141,"Small, conical teeth",HP:0000698,Conical tooth
+UBERON:0003646,metacarpal bone of digit 2,UBERON:0015044,manual digit 2 metacarpus endochondral element
+UBERON:0004252,hindlimb stylopod muscle,UBERON:0001383,muscle of leg
+HP:0010342,Abnormality of the phalanges of the 5th toe,HP:0010322,Abnormality of the 5th toe
+UBERON:0000038,follicular fluid,UBERON:0000463,portion of organism substance
+HP:0012157,Subcortical cerebral atrophy,HP:0007369,Atrophy/Degeneration affecting the cerebrum
+HP:0005927,Aplasia/Hypoplasia involving bones of the hand,HP:0001155,Abnormality of the hand
+UBERON:0007602,stratified columnar epithelium,UBERON:0000486,multilaminar epithelium
+HP:0004785,Malrotation of colon,HP:0002566,Intestinal malrotation
+UBERON:0004108,clivus of occipital bone,UBERON:0004120,mesoderm-derived structure
+UBERON:0001215,inferior mesenteric vein,UBERON:0005617,mesenteric vein
+UBERON:0005792,nephric ridge,UBERON:0005423,developing anatomical structure
+CL:0000113,mononuclear phagocyte,CL:0000518,phagocyte (sensu Vertebrata)
+UBERON:0000976,humerus,UBERON:0004250,upper arm bone
+HP:0005972,Respiratory acidosis,HP:0001941,Acidosis
+UBERON:0008341,columella nasi,UBERON:0004121,ectoderm-derived structure
+UBERON:2002070,internal anterior process of basipterygium,UBERON:0004120,mesoderm-derived structure
+HP:0012060,Acral lentiginous melanoma,HP:0012056,Cutaneous melanoma
+UBERON:0004477,tongue musculature,UBERON:0004121,ectoderm-derived structure
+HP:0100111,Absent epiphysis of the middle phalanx of the 2nd toe,HP:0100089,Abnormality of the epiphysis of the middle phalanx of the 2nd toe
+HP:0005997,Restricted neck movement due to contractures,HP:0001371,Flexion contracture
+CL:0002326,luminal epithelial cell of mammary gland,CL:0002327,mammary gland epithelial cell
+UBERON:3010175,circumferential groove,UBERON:3000981,limb external integument structure
+DOID:7747,pediatric extraocular retinoblastoma,DOID:4656,extraocular retinoblastoma
+UBERON:0001677,sphenoid bone,UBERON:0004120,mesoderm-derived structure
+UBERON:0007807,connecting stalk blood vessel,UBERON:0004120,mesoderm-derived structure
+UBERON:0011627,orbital part of frontal bone,UBERON:0004120,mesoderm-derived structure
+HP:0002582,Chronic atrophic gastritis,HP:0005231,Chronic gastritis
+UBERON:0001157,transverse colon,UBERON:0000168,segment of colon
+CL:0002323,amniocyte,CL:0000349,extraembryonic cell
+HP:0001545,Anteriorly placed anus,HP:0004397,Ectopic anus
+DOID:6652,diffuse idiopathic skeletal hyperostosis,DOID:182,calcinosis
+CL:0002257,epithelial cell of thyroid gland,CL:0002076,endo-epithelial cell
+HP:0006713,Aplasia/Hypoplasia of the scapulae,HP:0000782,Abnormality of the scapula
+CL:0011005,GABAergic interneuron,CL:0000099,interneuron
+UBERON:0009539,mesenchyme of submandibular gland primordium,UBERON:0005253,head mesenchyme
+UBERON:2000390,medial preglomerular nucleus,UBERON:2002226,preglomerular nucleus
+DOID:4995,cervical adenomyoma,DOID:2609,adenomyoma
+UBERON:4200186,distal keel of metacarpal III,UBERON:4100000,skeletal element projection
+UBERON:0013757,capillary blood,UBERON:0000178,blood
+UBERON:0005816,posterior tubercle of transverse process of cervical vertebra,UBERON:4100000,skeletal element projection
+HP:0012140,Abnormality of cells of the lymphoid lineage,HP:0005561,Abnormality of bone marrow cell morphology
+DOID:14448,46 XY gonadal dysgenesis,DOID:14447,gonadal dysgenesis
+UBERON:0003836,abdominal segment skin,UBERON:0001085,skin of trunk
+UBERON:0013694,brain endothelium,UBERON:0001986,endothelium
+UBERON:0002706,posterior nucleus of hypothalamus,UBERON:0006568,hypothalamic nucleus
+HP:0004099,Macrodactyly,HP:0011297,Abnormality of the digits
+UBERON:0005440,ductus arteriosus,UBERON:0003498,heart blood vessel
+UBERON:0001864,scala tympani,UBERON:0004120,mesoderm-derived structure
+HP:0009856,Patchy sclerosis of the proximal phalanges of the hand,HP:0100917,Sclerosis of the proximal phalanges of the hand
+HP:0009410,Absent epiphyses of the 3rd finger,HP:0009320,Abnormality of the epiphyses of the 3rd finger
+UBERON:0002357,serous pericardium,UBERON:0000042,serous membrane
+UBERON:2007061,epibranchial field,UBERON:2007059,neurogenic field
+HP:0008131,Tarsal stippling,HP:0008369,Abnormal tarsal ossification
+UBERON:2001250,pharyngobranchial 2 bone,UBERON:2001911,pharyngobranchial 2 element
+DOID:11693,acute apical periodontitis,DOID:823,periapical periodontitis
+UBERON:0012291,lateral malleolus of fibula,UBERON:0005055,zone of long bone
+UBERON:0006075,sacral region of vertebral column,UBERON:0006077,subdivision of vertebral column
+HP:0100561,Spinal cord lesions,HP:0002143,Abnormality of the spinal cord
+UBERON:3000671,anterolateral process of hyoid plate,UBERON:4100000,skeletal element projection
+UBERON:0003828,abdominal segment bone,UBERON:0003463,trunk bone
+HP:0009248,Abnormality of the epiphysis of the proximal phalanx of the 4th finger,HP:0010245,Abnormality of the epiphyses of the proximal phalanges of the hand
+HP:0100063,Small epiphyses of the 3rd toe,HP:0010170,Small epiphyses of the toes
+CL:1000288,myocyte of atrial branch of anterior internodal tract,CL:0002096,internodal tract myocyte
+CL:0000880,choroid-plexus macrophage,CL:0000878,central nervous system macrophage
+UBERON:0008876,hypodermis skeletal muscle layer,UBERON:0001134,skeletal muscle tissue
+DOID:3490,Noonan syndrome,DOID:0050736,autosomal dominant disease
+UBERON:0001937,lateral hypothalamic nucleus,UBERON:0006568,hypothalamic nucleus
+UBERON:2005097,caudal fin vasculature,UBERON:0007304,appendage vasculature
+UBERON:0009739,border of sublaminar layers S3 and S4,UBERON:0009740,border between sublaminar layers
+UBERON:0008854,root of molar tooth,UBERON:0003677,tooth root
+NCBITaxon:118655,Oropouche virus,NCBITaxon:11572,Orthobunyavirus
+UBERON:0011357,Reissner's fiber,UBERON:0000476,acellular anatomical structure
+UBERON:0013146,venous system of brain,UBERON:0004121,ectoderm-derived structure
+CL:0002306,epithelial cell of proximal tubule,CL:1000615,kidney cortex tubule cell
+DOID:7676,testicular thecoma,DOID:4757,sex cord-stromal neoplasm
+UBERON:0008783,dorsal venous arch,UBERON:0001638,vein
+DOID:3003,nipple neoplasm,DOID:0060082,breast benign neoplasm
+HP:0100684,Salivary gland neoplasm,HP:0100649,Neoplasm of the oral cavity
+HP:0007104,Prolonged somatosensory evoked potentials,HP:0007377,Abnormality of somatosensory evoked potentials
+DOID:5500,cellular ependymoma,DOID:4844,benign ependymoma
+UBERON:0002994,nucleus of pretectal area,UBERON:0003528,brain grey matter
+UBERON:0008923,sublaminar layer S2,UBERON:0009734,sublaminar layers S2 or S3 or S4
+HP:0009154,Triangular epiphysis of the proximal phalanx of the 5th finger,HP:0010278,Triangular epiphyses of the proximal phalanges of the hand
+UBERON:3000886,ypsiloid cartilage,UBERON:0007844,cartilage element
+UBERON:0009950,olfactory bulb plexiform layer,UBERON:0004001,olfactory bulb layer
+HP:0000819,Diabetes mellitus,HP:0000818,Abnormality of the endocrine system
+UBERON:0014859,megalopa stage,UBERON:0014858,post-larval stage
+CL:0002091,primary polar body,CL:0002090,polar body
+UBERON:0002535,gill,UBERON:0000062,organ
+HP:0003559,Muscle hyperirritability,HP:0011804,Abnormality of muscle physiology
+DOID:12905,sialolithiasis,DOID:10854,salivary gland disease
+DOID:420,hypertrichosis,DOID:421,hair disease
+DOID:13655,acquired tear duct stenosis,DOID:1400,lacrimal apparatus disease
+UBERON:0001716,secondary palate,UBERON:0007375,roof of mouth
+CL:0000577,type EC enteroendocrine cell,CL:0002251,epithelial cell of alimentary canal
+DOID:7808,necrotic uveal melanoma,DOID:6039,uveal melanoma
+UBERON:0014698,lacrimal caruncle,UBERON:0010305,region of conjunctiva
+UBERON:0009921,hypophyseal tube,UBERON:0000025,tube
+HP:0100018,Nuclear cataract,HP:0010920,Zonular cataract
+UBERON:0003004,median raphe nucleus,UBERON:0007415,nucleus of midbrain reticular formation
+CL:0000894,DN1 thymic pro-T cell,CL:0000827,pro-T cell
+NCBITaxon:68525,delta/epsilon subdivisions,NCBITaxon:1224,Proteobacteria
+UBERON:0005155,open tracheal system,UBERON:0001004,respiratory system
+CL:0005004,pigment erythroblast,CL:0000055,non-terminally differentiated cell
+HP:0007361,Abnormality of the pons,HP:0011283,Abnormality of the metencephalon
+HP:0001678,Atrioventricular block,HP:0012722,Heart block
+DOID:7962,tamoxifen-Related endometrial Lesion,DOID:1005,endometrial disease
+HP:0003725,Firm muscles,HP:0011805,Abnormality of muscle morphology
+HP:0001217,Clubbing,HP:0011297,Abnormality of the digits
+HP:0003998,Constricted radial neck,HP:0002818,Abnormality of the radius
+HP:0010082,Symphalangism affecting the distal phalanx of the hallux,HP:0010064,Symphalangism affecting the phalanges of the hallux
+HP:0000244,Brachyturricephaly,HP:0000248,Brachycephaly
+HP:0008291,Pituitary corticotropic cell adenoma,HP:0002893,Pituitary adenoma
+UBERON:0008435,vertebral arch of sacral segment,UBERON:0003861,neural arch
+UBERON:0006049,digit 2,UBERON:0002544,digit
+DOID:0080007,bone deterioration disease,DOID:0080010,bone structure disease
+NCBITaxon:213849,Campylobacterales,NCBITaxon:29547,Epsilonproteobacteria
+UBERON:0011922,cochlear basement membrane,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001561,subcostal artery,UBERON:0004573,systemic artery
+DOID:7328,iris spindle cell melanoma,DOID:6037,spindle cell intraocular melanoma
+HP:0010285,Oral synechia,HP:0011830,Abnormality of oral mucosa
+UBERON:0007347,hyperpallium,UBERON:0002791,regional part of telencephalon
+HP:0012450,Chronic constipation,HP:0002019,Constipation
+HP:0007880,Marginal corneal dystrophy,HP:0001131,Corneal dystrophy
+UBERON:3000493,processus internus of pseudoangular,UBERON:4100000,skeletal element projection
+HP:0010834,Trophic changes related to pain,HP:0010832,Abnormality of pain sensation
+UBERON:0007440,stratum intermedium of tooth,UBERON:0004121,ectoderm-derived structure
+CL:1001066,kidney arteriole smooth muscle cell,CL:0000359,vascular associated smooth muscle cell
+HP:0004214,Curved phalanges of the 5th finger,HP:0009770,Curved phalanges of the hand
+CL:0002135,nonkeratinized cell of epidermis,CL:0000362,epidermal cell
+HP:0009611,Bifid distal phalanx of the thumb,HP:0009612,Duplication of the distal phalanx of the thumb
+UBERON:2001012,epaxial region somite 16,UBERON:0003900,epaxial myotome region
+DOID:0050424,familial adenomatous polyposis,DOID:0050736,autosomal dominant disease
+UBERON:2001845,dorsal hypohyal-ventral hypohyal joint,UBERON:0000982,skeletal joint
+HP:0010828,Hemifacial spasm,HP:0003739,Myoclonic spasms
+UBERON:4200169,process 2,UBERON:0004120,mesoderm-derived structure
+UBERON:3000591,suprasphenoid,UBERON:0002513,endochondral bone
+UBERON:3000862,pubo-ischium,UBERON:0004120,mesoderm-derived structure
+HP:0010729,Cherry red spot of the macula,HP:0001103,Abnormality of the macula
+UBERON:0001386,extensor digitorum longus,UBERON:0001383,muscle of leg
+UBERON:0003531,forelimb skin,UBERON:0001419,skin of limb
+UBERON:0006272,oronasal cavity,UBERON:0002553,anatomical cavity
+DOID:5190,cervical Wilms' tumor,DOID:2154,nephroblastoma
+UBERON:2001739,anterior cranial fontanel,UBERON:0002221,fontanelle
+UBERON:0015178,somite border,UBERON:0004120,mesoderm-derived structure
+UBERON:0010842,calcaneum cartilage element,UBERON:0010885,hindlimb cartilage element
+HP:0100346,Fibular deviation of the 5th toe,HP:0010344,Deviation/Displacement of the 5th toe
+DOID:0050695,malignant pleural solitary fibrous tumor,DOID:5158,pleural cancer
+NCBITaxon:451871,Eurotiomycetidae,NCBITaxon:147545,Eurotiomycetes
+HP:0100932,Sclerosis of the proximal phalanx of the 3rd toe,HP:0100927,Sclerosis of the phalanges of the 3rd toe
+UBERON:0010849,tibia cartilage element,UBERON:0015004,tibia endochondral element
+CL:0002090,polar body,CL:0000021,female germ cell
+HP:0008786,Iliac crest serration,HP:0003796,Irregular iliac crest
+DOID:12570,phacolytic glaucoma,DOID:12571,phacogenic glaucoma
+HP:0006929,Hypoglycemic encephalopathy,HP:0001298,Encephalopathy
+UBERON:0009117,indifferent gonad,UBERON:0000991,gonad
+CL:0000846,vestibular dark cell,CL:0000066,epithelial cell
+UBERON:0001228,renal papilla,UBERON:0000064,organ part
+HP:0001222,Spatulate thumbs,HP:0011304,Broad thumb
+UBERON:0006219,deltoid pre-muscle mass,UBERON:0005865,pre-muscle condensation
+UBERON:2002022,dermethmoid,UBERON:0008907,dermal bone
+HP:0007517,Palmoplantar cutis laxa,HP:0100872,Abnormality of the plantar skin of foot
+HP:0200120,Chronic active hepatitis,HP:0200123,Chronic hepatitis
+HP:0012198,Juvenile colonic polyposis,HP:0200008,Intestinal polyposis
+UBERON:0001868,skin of chest,UBERON:0001418,skin of thorax
+HP:0005791,Cortical thickening of long bone diaphyses,HP:0000940,Abnormal diaphysis morphology
+HP:0008755,Laryngotracheomalacia,HP:0002779,Tracheomalacia
+UBERON:0013648,masseteric artery,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009398,Irregular epiphyses of the 4th finger,HP:0010233,Irregular epiphyses of the phalanges of the hand
+UBERON:0002819,apex of cochlea,UBERON:0010313,neural crest-derived structure
+CL:0000309,copper accumulating cell,CL:0000308,metal ion accumulating cell
+DOID:7986,cerebral falx meningioma,DOID:4436,anterior cranial fossa meningioma
+UBERON:0014703,anal membrane ectodermal component,UBERON:0000490,unilaminar epithelium
+UBERON:0010681,pedal digit 2 phalanx cartilage element,UBERON:0010685,pedal digit phalanx cartilage element
+DOID:6812,childhood pilocytic astrocytoma,DOID:4851,pilocytic astrocytoma
+HP:0000300,Oval face,HP:0001999,Abnormal facial shape
+UBERON:2000188,corpus cerebelli,UBERON:0002946,regional part of cerebellum
+UBERON:0004016,dermatome,UBERON:0000490,unilaminar epithelium
+NCBITaxon:1491,Clostridium botulinum,NCBITaxon:1485,Clostridium
+HP:0003868,Cortical thickening (humeral),HP:0000935,Thickened cortex of long bones
+UBERON:0012295,Guérin's valve,UBERON:0005156,reproductive structure
+UBERON:0005564,gonad primordium,UBERON:0000479,tissue
+UBERON:0004810,nephron tubule epithelium,UBERON:0004211,nephron epithelium
+UBERON:0003522,manual digit blood vessel,UBERON:0003523,manus blood vessel
+HP:0002791,Hypoventilation,HP:0002793,Abnormal pattern of respiration
+CL:0002011,Kit-positive macrophage dendritic cell progenitor,CL:0002009,macrophage dendritic cell progenitor
+UBERON:0010747,body of ilium,UBERON:0005913,zone of bone organ
+UBERON:0006290,scapula cartilage element,UBERON:0007844,cartilage element
+UBERON:0008835,hepatic diverticulum,UBERON:0005291,embryonic tissue
+HP:0002883,Hyperventilation,HP:0002793,Abnormal pattern of respiration
+CL:0002402,Peyer's patch B cell,CL:0000822,B-2 B cell
+UBERON:0008833,great auricular nerve,UBERON:0002003,peripheral nerve
+HP:0008434,Hypoplastic cervical vertebrae,HP:0011041,Aplasia/Hypoplasia of the cervical spine
+HP:0100517,Neoplasm of the urethra,HP:0000795,Abnormality of the urethra
+UBERON:0005687,orbitosphenoid cartilage element,UBERON:0003932,cartilage element of chondrocranium
+UBERON:0006691,tentorium cerebelli,UBERON:0004120,mesoderm-derived structure
+UBERON:2000593,superior reticular formation medial column,UBERON:0002579,regional part of medullary reticular formation
+UBERON:0011388,male bulbospongiosus muscle,UBERON:0014403,male anatomical structure
+DOID:6041,choroid spindle cell melanoma,DOID:6438,malignant choroid melanoma
+DOID:8929,atrophic gastritis,DOID:4029,gastritis
+NCBITaxon:266068,Rickettsia sibirica subgroup,NCBITaxon:114277,spotted fever group
+HP:0006817,Aplasia/Hypoplasia of the  cerebellar vermis,HP:0002334,Abnormality of the cerebellar vermis
+DOID:2451,protein S deficiency,DOID:620,blood protein disease
+DOID:5705,spindle cell Liposarcoma,DOID:5690,atypical lipomatous tumor
+HP:0010515,Aplasia/Hypoplasia of the thymus,HP:0000777,Abnormality of the thymus
+UBERON:0003689,sella turcica,UBERON:0004120,mesoderm-derived structure
+HP:0000775,Abnormality of the diaphragm,HP:0012252,Abnormal respiratory system morphology
+CL:1000470,myoepithelial cell of primary lactiferous duct,CL:0000185,myoepithelial cell
+HP:0100627,Displacement of the external urethral meatus,HP:0000036,Abnormality of the penis
+UBERON:0004467,musculature of pharynx,UBERON:0001015,musculature
+DOID:7061,precursor B lymphoblastic lymphoma/leukemia,DOID:707,B-cell lymphoma
+UBERON:0014755,P5 area of pallium (Myxiniformes),UBERON:0002791,regional part of telencephalon
+DOID:0080010,bone structure disease,DOID:0080001,bone disease
+HP:0009204,Bracket epiphysis of the middle phalanx of the 5th finger,HP:0010258,Bracket epiphyses of the middle phalanges of the hand
+CL:0002344,"CD56-negative, CD161-positive immature natural killer cell",CL:0000823,immature natural killer cell
+UBERON:0001971,gastric juice,UBERON:0000456,bodily secretion
+HP:0011722,Mixed total anomalous pulmonary venous connection,HP:0005160,Total anomalous pulmonary venous return
+UBERON:2205378,dorsal fin distal radial cartilage 7,UBERON:2200936,dorsal fin distal radial cartilage
+HP:0001004,Lymphedema,HP:0000969,Edema
+UBERON:2001824,lateral line scale,UBERON:0000073,regional part of nervous system
+HP:0010009,Abnormality of the 1st metacarpal,HP:0009602,Abnormality of the phalanges of the thumb
+HP:0003198,Myopathy,HP:0011805,Abnormality of muscle morphology
+DOID:9822,partial central choroid dystrophy,DOID:9794,hereditary choroidal atrophy
+UBERON:0002752,olivocerebellar tract,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:13081,hemangioma of subcutaneous tissue,DOID:255,hemangioma
+CL:0002442,"CD94-negative, Ly49CI-negative natural killer cell",CL:0002447,CD94-negative natural killer cell
+HP:0002102,Pleuritis,HP:0002103,Abnormality of the pleura
+UBERON:0005904,duct of male reproductive system,UBERON:0005156,reproductive structure
+UBERON:0012364,colloid of thyroid follicle,UBERON:0000463,portion of organism substance
+CL:1000279,smooth muscle cell of large intestine,CL:0002504,enteric smooth muscle cell
+DOID:10794,sphenoid sinusitis,DOID:0050127,sinusitis
+HP:0003784,Type 1 collagen overmodification,HP:0011862,Abnormal bone collagen fibril morphology
+UBERON:0005922,inferior nasal concha,UBERON:0008001,irregular bone
+UBERON:2001974,subtemporal fossa,UBERON:0004704,bone fossa
+UBERON:0009951,main olfactory bulb,UBERON:0002791,regional part of telencephalon
+HP:0011371,Recurrent viral skin infections,HP:0001581,Recurrent skin infections
+HP:0004359,Abnormality of fatty-acid metabolism,HP:0003119,Abnormality of lipid metabolism
+DOID:7839,infiltrating nipple syringomatous adenoma,DOID:3003,nipple neoplasm
+HP:0012398,Peripheral edema,HP:0000969,Edema
+UBERON:2001432,anterior sclerotic bone,UBERON:0010297,endochondral scleral ossicle
+HP:0012507,Weakness of orbicularis oculi muscle,HP:0000301,Abnormality of facial musculature
+NCBITaxon:263,Francisella tularensis,NCBITaxon:262,Francisella
+UBERON:0004013,egg cylinder,UBERON:0005291,embryonic tissue
+CL:0000789,alpha-beta T cell,CL:0000084,T cell
+UBERON:3000759,omosternum,UBERON:0010363,endochondral element
+HP:0005750,Contractures of the joints of the lower limbs,HP:0003121,Limb joint contracture
+DOID:10075,diphyllobothriasis,DOID:883,parasitic helminthiasis infectious disease
+HP:0011757,Posterior pituitary hypoplasia,HP:0011753,Posterior pituitary dysgenesis
+DOID:12711,black piedra,DOID:0050133,superficial mycosis
+UBERON:0004438,proximal epiphysis of middle phalanx of manual digit 4,UBERON:0004420,proximal epiphysis of phalanx of manual digit 4
+HP:0010603,Keratocystic odontogenic tumor,HP:0100612,Odontogenic neoplasm
+UBERON:0002053,zona glomerulosa of adrenal gland,UBERON:0009753,adrenal gland cortex zone
+UBERON:0006102,Brodmann (1909) area 35,UBERON:0013529,Brodmann area
+HP:0011776,Thyroid microfollicular adenoma,HP:0011774,Thyroid follicular adenoma
+UBERON:0004636,thoracic vertebra 12,UBERON:0002347,thoracic vertebra
+HP:0008984,Neck muscle hypoplasia,HP:0009004,Hypoplasia of the musculature
+UBERON:0006007,pre-Botzinger complex,UBERON:0004121,ectoderm-derived structure
+UBERON:0006843,root of cranial nerve,UBERON:0002211,nerve root
+UBERON:0009139,right posterior cardinal vein,UBERON:0015212,lateral structure
+UBERON:0014701,extraembryonic vascular system,UBERON:0004120,mesoderm-derived structure
+DOID:10660,mediastinum neuroblastoma,DOID:4691,malignant mediastinal neurogenic neoplasm
+HP:0012427,Excessive femoral anteversion,HP:0002823,Abnormality of the femur
+UBERON:0000961,thoracic ganglion,UBERON:0001807,paravertebral ganglion
+UBERON:2000926,myotome somite 12,UBERON:0003082,myotome
+UBERON:0002903,lunate sulcus,UBERON:0008334,subarachnoid sulcus
+UBERON:0010728,sphenoid lesser wing pre-cartilage condensation,UBERON:0014387,mesenchyme derived from neural crest
+UBERON:0014550,pyramidal layer of CA3,UBERON:0014567,layer of hippocampal field
+CL:0002354,yolk sac hematopoietic stem cell,CL:0000349,extraembryonic cell
+UBERON:4200033,cleithrum head,UBERON:0004121,ectoderm-derived structure
+DOID:10375,suppression amblyopia,DOID:10376,amblyopia
+DOID:9939,dacryocystocele,DOID:9935,chronic inflammation of lacrimal passage
+DOID:639,acute disseminated encephalomyelitis,DOID:640,encephalomyelitis
+HP:0001377,Limited elbow extension,HP:0002996,Limited elbow movement
+HP:0012134,Dysplastic erythropoesis,HP:0012130,Abnormality of cells of the erythroid lineage
+UBERON:2000120,lateral line ganglion,UBERON:0001714,cranial ganglion
+HP:0100056,Bracket epiphyses of the 3rd toe,HP:0010163,Bracket epiphyses of the toes
+DOID:5478,fallopian tube adenofibroma,DOID:0060111,fallopian tube benign neoplasm
+HP:0002346,Head tremor,HP:0001337,Tremor
+UBERON:0015129,epicardial fat,UBERON:0001013,adipose tissue
+HP:0008352,Impaired platelet adhesion,HP:0011869,Abnormal platelet function
+HP:0009631,Bullet-shaped proximal phalanx of the thumb,HP:0009845,Bullet-shaped middle phalanges of the hand
+UBERON:0014617,ventral nerve root of thoracic spinal cord,UBERON:0009630,root of thoracic nerve
+CL:0002488,trophoblast giant cell,CL:0000351,trophoblast cell
+HP:0000177,Abnormality of upper lip,HP:0000159,Abnormality of the lip
+UBERON:0013713,posterior iliac spine,UBERON:0013707,iliac spine
+HP:0009683,Small epiphysis of the distal phalanx of the thumb,HP:0010254,Small epiphyses of the distal phalanges of the hand
+UBERON:0013693,cerebral cortex neuropil,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005050,liver papillary process,UBERON:0000063,organ segment
+HP:0003974,Absent radius,HP:0003953,Absent ossification/absent forearm bones
+CL:0000665,permanently open valve cell,CL:0000663,valve cell
+HP:0100854,Aplasia of the musculature,HP:0001460,Aplasia/Hypoplasia involving the musculature
+UBERON:0002797,dorsal trigeminal tract,UBERON:0007702,tract of brain
+UBERON:3000659,postchoanal process,UBERON:0010313,neural crest-derived structure
+UBERON:0006524,alveolar system,UBERON:0004119,endoderm-derived structure
+HP:0100870,Plantar telangiectasia,HP:0100585,Teleangiectasia of the skin
+UBERON:0001822,orbital septum,UBERON:0003037,septum
+UBERON:2001659,upper pharyngeal tooth,UBERON:0001091,calcareous tooth
+UBERON:0003279,endothelium of trachea,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0011448,Ankle clonus,HP:0002815,Abnormality of the knees
+UBERON:0010901,tarsometatarsus pre-cartilage condensation,UBERON:0010882,limb bone pre-cartilage condensation
+NCBITaxon:35793,Rickettsia sibirica,NCBITaxon:266068,Rickettsia sibirica subgroup
+CL:1001100,kidney efferent arteriole smooth muscle cell,CL:1001009,kidney efferent arteriole cell
+HP:0002144,Tethered cord,HP:0002143,Abnormality of the spinal cord
+UBERON:0014394,uterine fat pad,UBERON:0005156,reproductive structure
+DOID:628,combined T cell and B cell immunodeficiency,DOID:612,primary immunodeficiency disease
+DOID:648,kuru,DOID:649,prion disease
+HP:0010350,Curved phalanges of the 2nd toe,HP:0010176,Curved phalanges of the toes
+HP:0008142,Delayed calcaneal ossification,HP:0008364,Abnormality of the calcaneus
+DOID:7210,psammomatous meningioma,DOID:3565,meningioma
+HP:0000190,Abnormality of oral frenula,HP:0000163,Abnormality of the oral cavity
+UBERON:0013172,cricotracheal ligament,UBERON:0001730,extrinsic ligament of larynx
+HP:0004688,Irregular tarsal bones,HP:0001850,Abnormality of the tarsal bones
+UBERON:0004454,tarsal region,UBERON:0006716,mesopodium region
+UBERON:0006524,alveolar system,UBERON:0000467,anatomical system
+UBERON:0009075,membrana tympaniformis,UBERON:0004119,endoderm-derived structure
+UBERON:0002746,intermediate periventricular nucleus,UBERON:0002951,regional part of intermediate hypothalamic region
+HP:0006865,Sensorimotor polyneuropathy affecting arms more than legs,HP:0009830,Peripheral neuropathy
+UBERON:0002030,nipple,UBERON:0004121,ectoderm-derived structure
+UBERON:0011245,infra-orbital canal of maxilla,UBERON:0005744,bone foramen
+UBERON:0000489,cavitated compound organ,UBERON:0003103,compound organ
+UBERON:0004943,submucosa of urinary bladder,UBERON:0000009,submucosa
+DOID:0050177,monogenic disease,DOID:630,genetic disease
+HP:0000164,Abnormality of the teeth,HP:0000163,Abnormality of the oral cavity
+DOID:7603,fibrosarcomatous osteosarcoma,DOID:3378,conventional central osteosarcoma
+DOID:10033,cycloplegia,DOID:10034,eye accommodation disease
+UBERON:0002441,cervicothoracic ganglion,UBERON:0001991,cervical ganglion
+CL:0000940,mucosal invariant T cell,CL:0000791,mature alpha-beta T cell
+UBERON:2000083,ventral mesoderm,UBERON:0000926,mesoderm
+HP:0007366,Atrophy/Degeneration affecting the brainstem,HP:0007367,Atrophy/Degeneration affecting the central nervous system
+UBERON:0008809,foramina of scarpa,UBERON:0000464,anatomical space
+UBERON:0007592,ciliated columnar epithelium,UBERON:0007601,ciliated epithelium
+UBERON:0005385,nasal cavity respiratory epithelium,UBERON:0010499,pseudostratified ciliated columnar epithelium
+HP:0100896,Rectal polyposis,HP:0200008,Intestinal polyposis
+UBERON:0008324,erectile tissue,UBERON:0000479,tissue
+UBERON:0003072,optic cup,UBERON:0004121,ectoderm-derived structure
+UBERON:0011167,septomaxilla bone,UBERON:0002514,intramembranous bone
+DOID:8672,viral exanthem,DOID:0050486,exanthem
+DOID:12304,conjunctival pigmentation,DOID:11653,conjunctival deposit
+UBERON:0008959,auditory bulla,UBERON:0004530,bony projection
+UBERON:0006291,scapula pre-cartilage condensation,UBERON:0015057,scapula endochondral element
+DOID:4406,spongiotic dermatitis,DOID:2723,dermatitis
+CL:0000877,splenic tingible body macrophage,CL:0000876,splenic white pulp macrophage
+CL:0000181,metabolising cell,CL:0000003,native cell
+UBERON:0004827,thyroid gland medulla,UBERON:0000958,medulla of organ
+UBERON:0002445,ulnare,UBERON:0001480,proximal carpal bone
+HP:0008396,Chronic monilial nail infection,HP:0001597,Abnormality of the nail
+HP:0009432,Curved middle phalanx of the 3rd finger,HP:0004172,Abnormality of the middle phalanx of the 3rd finger
+UBERON:0006127,funiculus of spinal cord,UBERON:0006133,funiculus of neuraxis
+UBERON:0010690,manual digit 1 epithelium,UBERON:0005227,manual digit epithelium
+HP:0004040,Corner fragments of ulnar metaphysis,HP:0004039,Abnormality of ulnar metaphysis
+UBERON:2000363,hypobranchial bone,UBERON:0002513,endochondral bone
+HP:0004207,Abnormality of the 5th finger,HP:0001167,Abnormality of finger
+DOID:4176,blood group incompatibility,DOID:74,hematopoietic system disease
+UBERON:0004324,middle phalanx of pedal digit 2,UBERON:0014488,middle phalanx of digit 2
+HP:0004752,Congenital atrioventricular dissociation,HP:0011709,Atrioventricular dissociation
+HP:0012708,Reduced brain N-acetyl aspartate level by MRS,HP:0012705,Abnormal metabolic brain imaging by MRS
+DOID:0050198,Chapare hemorrhagic fever,DOID:934,viral infectious disease
+HP:0010045,Aplasia/Hypoplasia of the 5th metacarpal,HP:0005914,Aplasia/Hypoplasia involving the metacarpal bones
+UBERON:0001255,urinary bladder,UBERON:0000489,cavitated compound organ
+DOID:14503,neuronal ceroid lipofuscinosis,DOID:9455,lipid storage disease
+UBERON:0001444,subdivision of head,UBERON:0000475,organism subdivision
+DOID:10320,asbestosis,DOID:10316,pneumoconiosis
+HP:0010221,Pseudoepiphysis of the 2nd metacarpal,HP:0010220,Abnormality of the epiphysis of the 2nd metacarpal
+HP:0007475,Congenital bullous ichthyosiform erythroderma,HP:0007431,Congenital ichthyosiform erythroderma
+DOID:8186,fallopian tube gestational choriocarcinoma,DOID:1963,fallopian tube carcinoma
+UBERON:0011282,nail of pedal digit 5,UBERON:0009567,nail of pedal digit
+UBERON:0005925,ethmoidal process of inferior nasal concha,UBERON:0010313,neural crest-derived structure
+HP:0009339,Fragmentation of the epiphysis of the distal phalanx of the 3rd finger,HP:0009414,Fragmentation of the epiphyses of the 3rd finger
+CL:0002068,Purkinje myocyte,CL:0002086,specialized cardiac myocyte
+UBERON:0008913,perichondral bone,UBERON:0002513,endochondral bone
+HP:0011924,Decreased activity of mitochondrial complex III,HP:0008972,Decreased activity of mitochondrial respiratory chain
+UBERON:0001951,epithelium of nasopharynx,UBERON:0003351,pharyngeal epithelium
+HP:0003952,Sclerotic foci of metaphyses of the elbow,HP:0003949,Abnormality of the elbow metaphyses
+UBERON:0002547,tadpole,UBERON:0002548,larva
+HP:0010333,Flexion contracture of 3rd toe,HP:0005830,Flexion contracture of toe
+HP:0000206,Glossitis,HP:0000157,Abnormality of the tongue
+HP:0005245,Intestinal hypoplasia,HP:0002242,Abnormality of the intestine
+UBERON:0014760,gustatory nucleus,UBERON:0009050,nucleus of solitary tract
+UBERON:0007152,inferior sagittal sinus,UBERON:0006615,venous sinus
+HP:0004813,Post-transfusion thrombocytopenia,HP:0001873,Thrombocytopenia
+UBERON:2001394,neural arch 3,UBERON:0003861,neural arch
+HP:0009671,Pseudoepiphysis of the proximal phalanx of the thumb,HP:0009693,Pseudoepiphyses of the thumb
+HP:0000455,Broad nasal tip,HP:0000463,Anteverted nares
+HP:0001621,Weak voice,HP:0001608,Abnormality of the voice
+UBERON:0006721,alisphenoid bone,UBERON:0015058,alisphenoid endochondral element
+HP:0002450,Abnormality of the motor neurons,HP:0002011,Abnormality of the central nervous system
+HP:0012438,Abnormal gallbladder physiology,HP:0005264,Abnormality of the gallbladder
+UBERON:0000088,trophoblast,UBERON:0002050,embryonic structure
+UBERON:0001288,loop of Henle,UBERON:0007685,region of nephron tubule
+HP:0000561,Absent eyelashes,HP:0200102,Sparse/absent eyelashes
+UBERON:0013110,hydrophid venom,UBERON:0013076,snake venom
+DOID:13031,balanoposthitis,DOID:1529,penile disease
+UBERON:0001915,endothelium of capillary,UBERON:0004638,blood vessel endothelium
+DOID:12369,prolapse of urethra,DOID:1284,prolapse of female genital organ
+HP:0000243,Trigonocephaly,HP:0002648,Abnormality of calvarial morphology
+HP:0100177,Small epiphysis of the distal phalanx of the 4th toe,HP:0100074,Small epiphyses of the 4th toe
+UBERON:4200151,toe disc,UBERON:3000981,limb external integument structure
+HP:0011051,Agenesis of premolar,HP:0001592,Selective tooth agenesis
+HP:0004026,Broad radial metaphysis,HP:0004015,Abnormality of radial metaphyses
+UBERON:0015085,distal carpal bone 1 cartilage,UBERON:0010883,forelimb cartilage element
+UBERON:0012497,muscularis mucosae of rectum,UBERON:0004231,anal region smooth muscle
+UBERON:0013742,wall of crypt of lieberkuhn of large intestine,UBERON:0013740,wall of crypt of lieberkuhn
+HP:0009881,Aplasia of the distal phalanges of the hand,HP:0009835,Aplasia/Hypoplasia of the distal phalanges of the hand
+UBERON:0006260,lingual swellings,UBERON:0010188,protuberance
+UBERON:0003373,ectoderm of footplate,UBERON:0000924,ectoderm
+HP:0010387,Osteolytic defects of the phalanges of the 5th toe,HP:0010342,Abnormality of the phalanges of the 5th toe
+HP:0010031,Patchy sclerosis of the 1st metacarpal,HP:0010009,Abnormality of the 1st metacarpal
+UBERON:0009779,cardiac muscle tissue of right auricle,UBERON:0003379,cardiac muscle of right atrium
+HP:0001973,Autoimmune thrombocytopenia,HP:0002960,Autoimmunity
+HP:0007799,Conjunctival whitish salt-like deposits,HP:0000502,Abnormality of the conjunctiva
+UBERON:0007721,interphalangeal joint of pes,UBERON:0006658,interphalangeal joint
+DOID:4384,orbit alveolar rhabdomyosarcoma,DOID:3259,orbit rhabdomyosarcoma
+HP:0009673,Stippling of the epiphysis of the proximal phalanx of the thumb,HP:0009695,Stippling of the epiphyses of the thumb
+DOID:12239,anal margin squamous cell carcinoma,DOID:4284,anal margin carcinoma
+HP:0002438,Cerebellar malformation,HP:0001317,Abnormality of the cerebellum
+UBERON:0002035,medial preoptic nucleus,UBERON:0006568,hypothalamic nucleus
+UBERON:2001919,basibranchial 5 element,UBERON:0013746,basibranchial element
+DOID:13356,senile ectropion,DOID:1570,ectropion
+DOID:1882,atrial heart septal defect,DOID:1681,heart septal defect
+UBERON:0010234,palatopharyngeus muscle,UBERON:0003682,palatal muscle
+DOID:1070,primary open angle glaucoma,DOID:1067,open-angle glaucoma
+HP:0001232,Nail bed telangiectasia,HP:0001597,Abnormality of the nail
+UBERON:0014860,copepodite stage,UBERON:0000069,larval stage
+UBERON:2002175,rostral octaval nerve motor nucleus,UBERON:2002174,octaval nerve motor nucleus
+DOID:11123,Henoch-Schoenlein purpura,DOID:9809,hypersensitivity vasculitis
+UBERON:0015867,cystic lymph node,UBERON:0015860,visceral abdominal lymph node
+HP:0006695,Atrioventricular canal defect,HP:0001671,Abnormality of the cardiac septa
+UBERON:3000050,braincase and auditory apparatus,UBERON:0000477,anatomical cluster
+HP:0100638,Neoplasia of the pharynx,HP:0100630,Neoplasia of the nasopharynx
+HP:0000341,Narrow forehead,HP:0000290,Abnormality of the forehead
+UBERON:0007215,trabecula cranii,UBERON:0004120,mesoderm-derived structure
+CL:0002507,langerin-positive lymph node dendritic cell,CL:0000990,conventional dendritic cell
+UBERON:0009835,anterior cingulate cortex,UBERON:0002619,regional part of cerebral cortex
+DOID:0060040,pervasive developmental disorder,DOID:0060037,developmental disorder of mental health
+DOID:5076,mixed glioma,DOID:3070,malignant glioma
+HP:0001839,Split foot,HP:0001760,Abnormality of the foot
+UBERON:2001535,median fin cartilage,UBERON:2001457,postcranial axial cartilage
+DOID:981,diffuse secondary choroid atrophy,DOID:980,choroidal sclerosis
+DOID:7585,subglottis squamous cell carcinoma,DOID:7764,subglottis carcinoma
+HP:0006802,Abnormality of the anterior horn cell,HP:0000759,Abnormality of the peripheral nervous system
+UBERON:0009854,digestive tract diverticulum,UBERON:0004921,subdivision of digestive tract
+DOID:1201,trigeminal nerve neoplasm,DOID:338,cranial nerve neoplasm
+DOID:6811,juvenile pilocytic astrocytoma,DOID:6812,childhood pilocytic astrocytoma
+CL:0000570,parafollicular cell,CL:0000710,neurecto-epithelial cell
+UBERON:0007315,internal pudendal artery,UBERON:0007312,pudendal artery
+CL:0000214,synovial cell,CL:0000213,lining cell
+UBERON:0006271,orbital fissure,UBERON:0010313,neural crest-derived structure
+HP:0005608,Bilobate gallbladder,HP:0012437,Abnormal gallbladder morphology
+UBERON:0010676,manual digit 2 phalanx cartilage element,UBERON:0015026,manual digit 2 phalanx endochondral element
+UBERON:0004384,epiphysis of femur,UBERON:0001437,epiphysis
+UBERON:0002494,papillary muscle of heart,UBERON:0004120,mesoderm-derived structure
+UBERON:0012173,middle suprarenal artery,UBERON:0005624,suprarenal artery
+DOID:5628,ampulla of Vater adenosquamous carcinoma,DOID:4932,ampulla of Vater carcinoma
+DOID:3606,ovarian mucinous adenocarcinoma,DOID:3713,ovary adenocarcinoma
+HP:0009758,Pyramidal skinfold extending from the base to the top of the nails,HP:0001597,Abnormality of the nail
+DOID:2877,larynx sarcoma,DOID:2596,larynx cancer
+HP:0003528,Elevated calcitonin,HP:0100530,Abnormality of calcium-phosphate metabolism
+HP:0000647,Sclerocornea,HP:0007957,Corneal opacity
+HP:0011017,Abnormality of cell physiology,HP:0001939,Abnormality of metabolism/homeostasis
+HP:0002495,Impaired vibratory sensation,HP:0003474,Sensory impairment
+UBERON:0002482,lamellar bone,UBERON:0002481,bone tissue
+UBERON:0014378,intrinsic muscle of pes,UBERON:0001498,muscle of pes
+UBERON:0004646,infraorbital artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003623,manual digit 3,UBERON:0006050,digit 3
+HP:0011149,Absence seizures with eyelid myoclonia,HP:0011148,Absence seizures with special features
+HP:0100602,Preeclampsia,HP:0100603,Toxemia of pregnancy
+HP:0011342,Mild global developmental delay,HP:0001263,Global developmental delay
+HP:0002220,Melanin pigment aggregation in hair shafts,HP:0009887,Abnormality of hair pigmentation
+UBERON:0013671,nerve ending of of corpus cavernosum maxillaris,UBERON:0012453,nerve ending
+DOID:13333,hypertrophy of tongue papillae,DOID:10944,tongue disease
+DOID:10610,pancreatic steatorrhea,DOID:26,pancreas disease
+HP:0011882,Decreased platelet P2Y12 receptor,HP:0011878,Abnormal platelet membrane protein expression
+UBERON:0001247,falciform ligament,UBERON:0003281,mesentery of stomach
+HP:0100640,Laryngeal cyst,HP:0001600,Abnormality of the larynx
+HP:0000445,Wide nose,HP:0005105,Abnormal nasal morphology
+DOID:13534,purulent labyrinthitis,DOID:1468,labyrinthitis
+UBERON:0001662,anterior auricular vein,UBERON:0006197,auricular vein
+UBERON:0004412,proximal epiphysis of femur,UBERON:0004384,epiphysis of femur
+UBERON:3010780,pars recta,UBERON:0005156,reproductive structure
+DOID:4651,unilateral retinoblastoma,DOID:768,retinoblastoma
+UBERON:0005458,left umbilical artery,UBERON:0001310,umbilical artery
+UBERON:2002152,vertebral element 12,UBERON:0010913,vertebral element
+UBERON:0001129,subscapularis muscle,UBERON:0001482,muscle of shoulder
+HP:0012019,Lens luxation,HP:0001083,Ectopia lentis
+CL:0005003,leucoblast,CL:0000055,non-terminally differentiated cell
+HP:0000010,Recurrent urinary tract infections,HP:0100577,Urinary bladder inflammation
+HP:0002297,Red hair,HP:0009887,Abnormality of hair pigmentation
+UBERON:0009883,medullary ray,UBERON:0000064,organ part
+UBERON:2001379,pharyngeal ectoderm,UBERON:0004119,endoderm-derived structure
+UBERON:3000580,stylus of pars media plectri,UBERON:0010313,neural crest-derived structure
+HP:0008341,Distal renal tubular acidosis,HP:0001947,Renal tubular acidosis
+HP:0001128,Trichiasis,HP:0000499,Abnormality of the eyelashes
+HP:0010879,Postnatal cystic hygroma,HP:0000476,Cystic hygroma
+UBERON:0003925,photoreceptor inner segment layer,UBERON:0004121,ectoderm-derived structure
+HP:0003552,Muscle stiffness,HP:0011804,Abnormality of muscle physiology
+HP:0004952,Pulmonary arteriovenous fistulas,HP:0004947,Arteriovenous fistula
+HP:0007469,Palmoplantar cutis gyrata,HP:0100872,Abnormality of the plantar skin of foot
+UBERON:0015033,pedal digit 3 phalanx endochondral element,UBERON:0015030,pedal digit phalanx endochondral element
+UBERON:0005195,deferent duct vein,UBERON:0005156,reproductive structure
+UBERON:2000394,molecular layer corpus cerebelli,UBERON:0004121,ectoderm-derived structure
+UBERON:0001569,constrictor muscle of pharynx,UBERON:0000933,pharyngeal muscle
+HP:0200129,Calcific mitral stenosis,HP:0004382,Mitral valve calcification
+HP:0004342,Abnormality of galactoside metabolism,HP:0003649,Abnormality of glycoside metabolism
+UBERON:0013771,intermammary line,UBERON:0006800,anatomical line
+UBERON:0003960,styloid process of temporal bone,UBERON:0010313,neural crest-derived structure
+UBERON:0011831,duct of vestibular gland,UBERON:0000058,duct
+CL:0000015,male germ cell,CL:0000586,germ cell
+HP:0009084,Midline notch of upper alveolar ridge,HP:0006477,Abnormality of the alveolar ridges
+UBERON:0002011,thoracodorsal artery,UBERON:0001637,artery
+UBERON:0009141,craniocervical region vein,UBERON:0013140,systemic vein
+UBERON:2002270,pelvic fin spine,UBERON:4000173,pelvic fin lepidotrichium
+UBERON:2000630,caudal parvocellular preoptic nucleus,UBERON:2002219,parvocellular preoptic nucleus
+UBERON:0004493,cardiac muscle tissue of myocardium,UBERON:0001133,cardiac muscle tissue
+UBERON:0005212,Leydig cell region of testis,UBERON:0014403,male anatomical structure
+HP:0010341,Abnormality of the epiphyses of the 5th toe,HP:0010322,Abnormality of the 5th toe
+UBERON:0013678,anatomical line between inner canthi,UBERON:0006800,anatomical line
+HP:0005010,osteomyelitis leading to amputation due to slow healing fractures,HP:0002754,Osteomyelitis
+UBERON:0011094,vertebra cartilage element,UBERON:0005863,cartilaginous condensation
+HP:0100679,Lack of skin elasticity,HP:0010647,Abnormal elasticity of skin
+HP:0000684,Delayed eruption of teeth,HP:0006292,Abnormality of dental eruption
+UBERON:0001271,pelvic girdle region,UBERON:0015212,lateral structure
+UBERON:1000000,chin ventral margin,UBERON:0004121,ectoderm-derived structure
+DOID:0050556,infantile onset spinocerebellar ataxia,DOID:1441,spinocerebellar ataxia
+HP:0006808,Cerebral hypomyelination,HP:0003429,CNS hypomyelination
+CL:1000488,cholangiocyte,CL:0000069,branched duct epithelial cell
+HP:0003091,Trophic limb changes,HP:0010834,Trophic changes related to pain
+CL:0001027,CD7-negative lymphoid progenitor cell,CL:0001012,CD7-negative lymphoid progenitor OR granulocyte monocyte progenitor
+CL:0000927,CD4-positive type I NK T cell secreting interleukin-4,CL:0000923,CD4-positive type I NK T cell
+UBERON:0010021,dorsal part of pharyngeal pouch 1,UBERON:0000490,unilaminar epithelium
+DOID:5102,inner ear cancer,DOID:833,auditory system cancer
+NCBITaxon:33256,Ascaridoidea,NCBITaxon:6249,Ascaridida
+NCBITaxon:519,Bordetella parapertussis,NCBITaxon:517,Bordetella
+UBERON:0012085,lumen of tertiary bronchus,UBERON:0012082,bronchial lumen
+UBERON:0014385,aryepiglottic fold,UBERON:0015212,lateral structure
+HP:0003881,Humeral sclerosis,HP:0003063,Abnormality of the humerus
+UBERON:0008322,deep artery of clitoris,UBERON:0003520,pelvis blood vessel
+CL:1000697,kidney interstitial suppressor macrophage,CL:0000864,tissue-resident macrophage
+UBERON:0006267,notochordal plate,UBERON:0000490,unilaminar epithelium
+UBERON:3010719,dilated medial process of metacarpal IV,UBERON:4100000,skeletal element projection
+UBERON:2205375,dorsal fin distal radial cartilage 4,UBERON:2200936,dorsal fin distal radial cartilage
+DOID:50,thyroid gland disease,DOID:28,endocrine system disease
+DOID:6331,immature teratoma of ovary,DOID:2155,malignant ovarian germ cell neoplasm
+UBERON:2000337,basioccipital posterodorsal region,UBERON:0011164,neurocranium bone
+UBERON:0013124,left posterior cardinal vein,UBERON:0002065,posterior cardinal vein
+UBERON:0011996,pharyngeal adductor,UBERON:0000933,pharyngeal muscle
+HP:0009250,Absent epiphysis of the distal phalanx of the 4th finger,HP:0009249,Abnormality of the epiphysis of the distal phalanx of the 4th finger
+HP:0010313,Breast hypertrophy,HP:0000769,Abnormality of the breast
+UBERON:2001539,basipterygium cartilage,UBERON:0007844,cartilage element
+HP:0003170,Abnormality of the acetabulum,HP:0001384,Abnormality of the hip joint
+CL:0000814,mature NK T cell,CL:0000791,mature alpha-beta T cell
+HP:0005926,Abnormalities of the cortex of hand bones,HP:0001155,Abnormality of the hand
+UBERON:0001589,internal thoracic vein,UBERON:0001638,vein
+HP:0005802,Coalescence of tarsal bones,HP:0008368,Tarsal synostosis
+UBERON:0004109,cortex of humerus,UBERON:0004120,mesoderm-derived structure
+UBERON:0013489,superficial cervical fascia,UBERON:0004120,mesoderm-derived structure
+UBERON:0004277,eye muscle,UBERON:0010959,craniocervical muscle
+HP:0008527,Congenital sensorineural hearing impairment,HP:0000407,Sensorineural hearing impairment
+UBERON:0013442,postorbital process,UBERON:0004120,mesoderm-derived structure
+UBERON:0013692,inframammary fold,UBERON:0006800,anatomical line
+UBERON:0015161,inferior branch of oculomotor nerve,UBERON:0004121,ectoderm-derived structure
+UBERON:2002071,distal cartilage of internal anterior process of basipterygium,UBERON:0004120,mesoderm-derived structure
+UBERON:0003498,heart blood vessel,UBERON:0005985,coronary vessel
+UBERON:0013143,gastrocnemius vein,UBERON:0001551,vein of hindlimb zeugopod
+UBERON:2000224,quadrate ventral process,UBERON:0010313,neural crest-derived structure
+HP:0005696,Postaxial polydactyly type A,HP:0001162,Postaxial hand polydactyly
+UBERON:0002614,medial part of ventral lateral nucleus,UBERON:0003528,brain grey matter
+DOID:14743,trichorhinophalangeal syndrome type I,DOID:0050736,autosomal dominant disease
+HP:0010066,Duplication of phalanx of hallux,HP:0010057,Abnormality of the phalanges of the hallux
+DOID:2717,bloom syndrome,DOID:0050737,autosomal recessive disease
+HP:0002669,Osteosarcoma,HP:0100242,Sarcoma
+DOID:12361,Graves' disease,DOID:7998,hyperthyroidism
+HP:0011639,Anomalous origin of right coronary artery from the pulmonary artery,HP:0011637,Anomalous origin of coronary artery from the pulmonary artery
+UBERON:0003681,masticatory muscle,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0002094,interstitial cell of ovary,CL:0002132,stromal cell of ovary
+HP:0004729,Acute tubulointerstitial nephritis,HP:0001970,Tubulointerstitial nephritis
+HP:0011467,Absent gallbladder,HP:0011466,Aplasia/Hypoplasia of the gallbladder
+UBERON:2002105,electrosensory lateral line lobe,UBERON:0009662,hindbrain nucleus
+UBERON:3010007,pit organ,UBERON:0004121,ectoderm-derived structure
+DOID:8102,fetal adenoma,DOID:6204,follicular adenoma
+DOID:7675,testicular fibroma,DOID:4757,sex cord-stromal neoplasm
+HP:0008788,Delayed pubic bone ossification,HP:0009105,Abnormal ossification of the pubic bone
+UBERON:4200107,obturator process of ischium,UBERON:0004120,mesoderm-derived structure
+UBERON:0010544,metacarpus skeleton,UBERON:0010546,metapodial skeleton
+DOID:234,colon adenocarcinoma,DOID:1520,colon carcinoma
+UBERON:0005815,anterior tubercle of transverse process of cervical vertebra,UBERON:4100000,skeletal element projection
+UBERON:0004000,tarsal gland acinus,UBERON:0011846,acinus of sebaceous gland
+DOID:0050143,asymptomatic dengue,DOID:12205,dengue disease
+UBERON:0005922,inferior nasal concha,UBERON:0003462,facial bone
+HP:0009676,Bracket epiphysis of the distal phalanx of the thumb,HP:0009687,Bracket epiphyses of the thumb
+DOID:10132,psychosexual disorder,DOID:0060043,sexual disorder
+HP:0009757,Intercrural pterygium,HP:0001059,Pterygium
+CL:1000549,kidney cortex collecting duct epithelial cell,CL:0002681,kidney cortical cell
+UBERON:2005080,anterior mesenteric artery,UBERON:0005616,mesenteric artery
+DOID:11406,choroiditis,DOID:1417,choroid disease
+UBERON:2001971,parapophysis 4,UBERON:0003109,parapophysis
+HP:0000568,Microphthalmos,HP:0100887,Abnormality of globe size
+UBERON:0002226,basilar membrane of cochlea,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002358,peritoneum,UBERON:0000042,serous membrane
+UBERON:2007060,dorsolateral field,UBERON:2007059,neurogenic field
+NCBITaxon:35788,Rickettsia africae,NCBITaxon:114277,spotted fever group
+UBERON:0002421,hippocampal formation,UBERON:0002791,regional part of telencephalon
+DOID:13654,stenosis of lacrimal passage,DOID:1400,lacrimal apparatus disease
+UBERON:0014705,median lingual swelling epithelium,UBERON:0005911,endo-epithelium
+DOID:5774,giant hemangioma,DOID:483,cavernous hemangioma
+UBERON:2001247,epibranchial 3 bone,UBERON:2001907,epibranchial 3 element
+DOID:4527,ovarian angiosarcoma,DOID:2146,ovary sarcoma
+UBERON:0004819,kidney epithelium,UBERON:0006554,urinary system structure
+DOID:1935,Bardet-Biedl syndrome,DOID:0050737,autosomal recessive disease
+UBERON:2002116,epibranchial organ,UBERON:0003103,compound organ
+DOID:6469,ovarian mucinous adenofibroma,DOID:0060112,ovarian benign neoplasm
+CL:1000289,myocyte of atrial septal branch of anterior internodal tract,CL:0002096,internodal tract myocyte
+HP:0003267,Reduced orotidine 5-prime phosphate decarboxylase activity,HP:0004353,Abnormality of pyrimidine metabolism
+HP:0004612,cervical spine segmentation defects,HP:0003422,Vertebral segmentation defect
+UBERON:0009522,lateral lingual swelling epithelium,UBERON:0003929,gut epithelium
+UBERON:0001936,tuberomammillary nucleus,UBERON:0006568,hypothalamic nucleus
+HP:0003897,Irregular ossification of the humeral epiphyses,HP:0003891,Abnormality of the humeral epiphysis
+UBERON:0007354,cartilage of pharyngotympanic tube,UBERON:0003566,head connective tissue
+HP:0009508,Ivory epiphysis of the distal phalanx of the 2nd finger,HP:0009499,Abnormality of the epiphysis of the distal phalanx of the 2nd finger
+HP:0011629,Total absence of the pericardium,HP:0011628,Congenital defect of the pericardium
+HP:0005923,Abnormalities of the metaphyses of the hand,HP:0009809,Abnormality of upper limb metaphysis
+UBERON:0011693,extraembryonic portion of umbilical artery,UBERON:0003520,pelvis blood vessel
+UBERON:0010743,meningeal cluster,UBERON:0004121,ectoderm-derived structure
+UBERON:0005001,mucosa of common hepatic duct,UBERON:0004999,mucosa of biliary tree
+UBERON:0006048,digit 1,UBERON:0002544,digit
+UBERON:0012268,equine forelimb splint bone,UBERON:0012267,equine splint bone
+HP:0002189,Excessive daytime sleepiness,HP:0002360,Sleep disturbance
+HP:0011201,EEG with changes in voltage,HP:0002353,EEG abnormality
+HP:0002666,Pheochromocytoma,HP:0100634,Neuroendocrine neoplasm
+HP:0009593,Peripheral Schwannoma,HP:0100008,Schwannoma
+DOID:13148,acute cystitis,DOID:1679,cystitis
+DOID:12904,mucocele of salivary gland,DOID:10854,salivary gland disease
+CL:0002199,oxyphil cell of parathyroid gland,CL:0002260,epithelial cell of parathyroid gland
+UBERON:0011162,supraoccipital cartilage element,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:2475,chronic conjunctivitis,DOID:6195,conjunctivitis
+HP:0012571,Ureter fissus,HP:0000081,Duplicated collecting system
+HP:0010865,Oppositional defiant disorder,HP:0100851,Abnormal emotion/affect behavior
+CL:1000471,myoepithelial cell of secondary lactiferous duct,CL:0000185,myoepithelial cell
+UBERON:0006076,caudal region of vertebral column,UBERON:0006077,subdivision of vertebral column
+UBERON:0006283,primitive ventricle of heart,UBERON:0005423,developing anatomical structure
+HP:0012131,Abnormal number of erythroid precursors,HP:0012130,Abnormality of cells of the erythroid lineage
+UBERON:0008333,hilum of inferior olivary complex,UBERON:0008332,hilum of neuraxis
+CL:0000762,nucleated thrombocyte,CL:0000226,single nucleate cell
+DOID:0050933,ovarian serous carcinoma,DOID:4001,ovarian carcinoma
+DOID:3702,cervical adenocarcinoma,DOID:2893,cervix carcinoma
+HP:0100019,Cortical cataract,HP:0010920,Zonular cataract
+UBERON:0010684,pedal digit 5 phalanx cartilage element,UBERON:0010685,pedal digit phalanx cartilage element
+UBERON:0002223,endolymphatic sac,UBERON:0007499,epithelial sac
+CL:0000881,perivascular macrophage,CL:0000878,central nervous system macrophage
+UBERON:0010699,manual digit metacarpus cartilage element,UBERON:0010883,forelimb cartilage element
+HP:0002251,Aganglionic megacolon,HP:0004362,Abnormality of the enteric ganglia
+UBERON:2001539,basipterygium cartilage,UBERON:2100623,basipterygium element
+HP:0005715,Flattened knee epiphyses,HP:0003071,Flattened epiphyses
+HP:0002359,Frequent falls,HP:0004302,Functional motor problems.
+UBERON:0013712,anterior iliac spine,UBERON:0013707,iliac spine
+UBERON:0004497,skeletal muscle tissue of gluteus maximus,UBERON:0001134,skeletal muscle tissue
+DOID:13327,anatomical narrow angle borderline glaucoma,DOID:9283,borderline glaucoma
+UBERON:0007260,intervertebral disk of third cervical vertebra,UBERON:0007252,intervertebral disk of cervical vertebra
+UBERON:0001303,left uterine tube,UBERON:0003889,fallopian tube
+HP:0008835,Multicentric femoral head ossification,HP:0009107,Abnormal ossification involving the femoral head and neck
+HP:0000256,Macrocephaly,HP:0000240,Abnormality of skull size
+HP:0008651,Uric acid urolithiasis independent of gout,HP:0000791,Uric acid nephrolithiasis
+DOID:1114,esophagus sarcoma,DOID:5041,esophageal cancer
+DOID:9063,Ritter's disease,DOID:0050339,commensal bacterial infectious disease
+HP:0005338,Sparse lateral eyebrow,HP:0000535,Sparse eyebrow
+HP:0011716,Junctional ectopic tachycardia,HP:0011687,AV nodal tachycardia
+UBERON:0008434,cervical vertebral arch,UBERON:0003861,neural arch
+UBERON:0011756,male genital swelling,UBERON:0014403,male anatomical structure
+CL:0000693,neuroglioform cell,CL:0000691,stellate interneuron
+UBERON:2000663,extrascapula,UBERON:0008907,dermal bone
+UBERON:0014540,lamina of cerebellum,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0001034,Hypermelanotic macule,HP:0007400,Irregular hyperpigmentation
+UBERON:0008283,columnella,UBERON:0000475,organism subdivision
+UBERON:0011577,flexural organ,UBERON:0000481,multi-tissue structure
+UBERON:0010232,placodal ectoderm,UBERON:0004121,ectoderm-derived structure
+DOID:5519,colon squamous cell carcinoma,DOID:1520,colon carcinoma
+HP:0003730,EMG: myotonic runs,HP:0002486,Myotonia
+DOID:10787,premature menopause,DOID:1414,ovarian dysfunction
+UBERON:0005572,rhombomere 2 roof plate,UBERON:0005502,rhombomere roof plate
+UBERON:3010242,nasolabial groove,UBERON:3000972,head external integument structure
+DOID:5701,breast liposarcoma,DOID:3382,liposarcoma
+HP:0007489,Diffuse telangiectasia,HP:0001009,Telangiectasia
+DOID:6899,malignant ovarian mixed epithelial neoplasm,DOID:6211,mixed epithelial tumor of ovary
+NCBITaxon:810,Chlamydia,NCBITaxon:1113537,Chlamydia/Chlamydophila group
+UBERON:0005330,mesonephric nephron epithelium,UBERON:0005103,mesonephric epithelium
+NCBITaxon:119089,Chromadorea,NCBITaxon:6231,Nematoda
+UBERON:0014702,frontonasal process epithelium,UBERON:0000490,unilaminar epithelium
+HP:0007648,Punctate cataract,HP:0010920,Zonular cataract
+DOID:5442,eccrine acrospiroma,DOID:173,eccrine sweat gland neoplasm
+DOID:6571,non-invasive bladder urothelial carcinoma,DOID:4006,bladder transitional cell carcinoma
+DOID:0050759,myotonic dystrophy type 2,DOID:450,myotonic disease
+NCBITaxon:56426,Bartonella clarridgeiae,NCBITaxon:773,Bartonella
+HP:0010421,Duplication of the distal phalanx of the 2nd toe,HP:0010356,Abnormality of the distal phalanx of the 2nd toe
+DOID:5280,gastric leiomyosarcoma,DOID:10534,stomach cancer
+UBERON:0002440,inferior cervical ganglion,UBERON:0001991,cervical ganglion
+UBERON:2002028,pectoral fin proximal radial bone 3,UBERON:2102028,pectoral fin proximal radial element 3
+HP:0003999,Abnormality of radial epiphyses,HP:0002818,Abnormality of the radius
+UBERON:0004724,medial palpebral ligament,UBERON:0000211,ligament
+UBERON:0001673,central retinal vein,UBERON:0001638,vein
+DOID:3644,hypothalamic neoplasm,DOID:3843,diencephalic neoplasm
+UBERON:0014780,palatine aponeurosis,UBERON:0004121,ectoderm-derived structure
+HP:0009506,Fragmentation of the epiphysis of the distal phalanx of the 2nd finger,HP:0010250,Fragmentation of the epiphyses of the distal phalanges of the hand
+DOID:12070,Dieulafoy lesion,DOID:76,stomach disease
+UBERON:0011941,lateral angle of scapula,UBERON:0007172,angle of scapula
+HP:0004234,Bone-in-a-bone appearance of carpal bones,HP:0011001,Increased bone mineral density
+UBERON:0011628,early premaxilla,UBERON:0002050,embryonic structure
+NCBITaxon:36086,Trichuris,NCBITaxon:119093,Trichuridae
+HP:0100482,Proximal/middle symphalangism of 5th toe,HP:0100237,Proximal symphalangism (feet)
+HP:0003296,Hyperthreoninuria,HP:0010900,Abnormality of threonine metabolism
+HP:0001839,Split foot,HP:0100257,Ectrodactyly
+HP:0006989,Dysplastic corpus callosum,HP:0001273,Abnormality of the corpus callosum
+HP:0000126,Hydronephrosis,HP:0010946,Dilatation of the renal pelvis
+UBERON:0001121,longus colli muscle,UBERON:0005178,thoracic cavity organ
+HP:0009155,Cone-shaped epiphysis of the proximal phalanx of the 5th finger,HP:0009384,Cone-shaped epiphyses of the 5th finger
+UBERON:0006916,non-keratinized epithelium of tongue,UBERON:0010304,non-keratinized stratified squamous epithelium
+DOID:4231,histiocytoma,DOID:201,connective tissue cancer
+HP:0009981,Partial duplication of the distal phalanx of the 4th finger,HP:0009975,Duplication of the distal phalanx of the 4th finger
+HP:0008062,Aplasia/Hypoplasia affecting the anterior segment of the eye,HP:0004328,Abnormality of the anterior segment of the eye
+UBERON:0000118,lung bud,UBERON:0005153,epithelial bud
+UBERON:0008858,pyloric canal,UBERON:0009870,zone of stomach
+HP:0009652,Bullet-shaped phalanges of the thumb,HP:0009602,Abnormality of the phalanges of the thumb
+UBERON:0014465,antorbital fenestra,UBERON:0004705,fenestra
+UBERON:0004901,right lung lobar bronchus mesenchyme,UBERON:0004884,lobar bronchus mesenchyme
+DOID:2769,tic disorder,DOID:0060038,specific developmental disorder
+UBERON:0002538,hatching gland,UBERON:0002050,embryonic structure
+UBERON:0000074,renal glomerulus,UBERON:0006554,urinary system structure
+UBERON:0003532,hindlimb skin,UBERON:0001419,skin of limb
+HP:0005217,Duplication of internal organs,HP:0002012,Abnormality of the abdominal organs
+HP:0006986,Upper limb spasticity,HP:0001257,Spasticity
+DOID:5191,stromal predominant kidney Wilms' tumor,DOID:2154,nephroblastoma
+DOID:1943,telogen effluvium,DOID:987,alopecia
+DOID:1397,chronic orbital inflammation,DOID:930,orbital disease
+DOID:4756,testicular Leydig cell tumor,DOID:2696,Leydig cell tumor
+HP:0000232,Everted lower lip vermilion,HP:0000178,Abnormality of lower lip
+UBERON:0010801,calcaneum pre-cartilage condensation,UBERON:0015014,calcaneum endochondral element
+HP:0000238,Hydrocephalus,HP:0002118,Abnormality of the cerebral ventricles
+HP:0010194,Aplasia/Hypoplasia of the middle phalanges of the toes,HP:0010183,Abnormality of the middle phalanges of the toes
+HP:0009606,Complete duplication of distal phalanx of the thumb,HP:0009943,Complete duplication of the phalanges of the thumb
+CL:0015000,cranial motor neuron,CL:0000100,motor neuron
+UBERON:2002001,anterior dentation of pectoral fin spine,UBERON:4100000,skeletal element projection
+UBERON:4300029,dermal neck joint,UBERON:0000982,skeletal joint
+HP:0002099,Asthma,HP:0100326,Immunologic hypersensitivity
+UBERON:2005010,mid cerebral vein,UBERON:0009141,craniocervical region vein
+HP:0009515,Cone-shaped epiphysis of the middle phalanx of the 2nd finger,HP:0010259,Cone-shaped epiphyses of the middle phalanges of the hand
+HP:0005765,Sacral meningocele,HP:0005107,Abnormality of the sacrum
+HP:0001258,Spastic paraplegia,HP:0010550,Paraplegia
+UBERON:0010251,anterior meningeal artery,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010009,Abnormality of the 1st metacarpal,HP:0001163,Abnormality of the metacarpal bones
+DOID:3109,idiopathic CD4-positive T-lymphocytopenia,DOID:614,lymphopenia
+UBERON:0004915,sphincter of hepatopancreatic ampulla,UBERON:0004119,endoderm-derived structure
+UBERON:0014440,ischiopubic ramus,UBERON:0004120,mesoderm-derived structure
+UBERON:0008995,nucleus of cerebellar nuclear complex,UBERON:0002946,regional part of cerebellum
+UBERON:0000966,retina,UBERON:0005388,photoreceptor array
+HP:0001050,Plethora,HP:0001005,Dermatological manifestations of systemic disorders
+HP:0000776,Congenital diaphragmatic hernia,HP:0100790,Hernia
+CL:0000677,gut absorptive cell,CL:0000212,absorptive cell
+UBERON:4000170,median fin skeleton,UBERON:0010912,subdivision of skeleton
+HP:0004256,Abnormality of the trapezoid bone,HP:0001191,Abnormality of the carpal bones
+UBERON:3000059,capsular process,UBERON:0010313,neural crest-derived structure
+UBERON:2001417,pelvic fin distal radial bone 1,UBERON:2101417,pelvic fin distal radial element 1
+HP:0007018,Attention deficit hyperactivity disorder,HP:0000752,Hyperactivity
+NCBITaxon:69826,Ornithodoros savignyi,NCBITaxon:6937,Ornithodoros
+CL:0002345,"CD27-low, CD11b-low immature natural killer cell",CL:0000823,immature natural killer cell
+HP:0011721,Infracardiac total anomalous pulmonary venous connection,HP:0005160,Total anomalous pulmonary venous return
+DOID:1738,small intestine leiomyoma,DOID:7505,small intestine neoplasm
+CL:1000306,fibroblast of tunica adventitia of artery,CL:0002503,adventitial cell
+HP:0009272,Aplasia/Hypoplasia of the 4th finger,HP:0004188,Abnormality of the 4th finger
+UBERON:2001848,ventral hypohyal-urohyal joint,UBERON:0000982,skeletal joint
+UBERON:0002615,ventral tegmental decussation,UBERON:0007418,decussation of neuraxis
+DOID:11031,bullous keratopathy,DOID:2283,keratopathy
+UBERON:0010693,pedal digit 1 epithelium,UBERON:0005226,pedal digit epithelium
+HP:0011775,Thyroid macrofollicular adenoma,HP:0011774,Thyroid follicular adenoma
+HP:0010944,Abnormality of the renal pelvis,HP:0012210,Abnormal renal morphology
+DOID:0050827,rheumatic heart disease,DOID:4079,heart valve disease
+UBERON:0005456,jugular foramen,UBERON:0013685,foramen of skull
+HP:0004443,Lambdoidal craniosynostosis,HP:0001363,Craniosynostosis
+UBERON:0010842,calcaneum cartilage element,UBERON:0015014,calcaneum endochondral element
+UBERON:0010545,metatarsus skeleton,UBERON:0010546,metapodial skeleton
+HP:0003862,Absent humerus,HP:0011849,Abnormal bone ossification
+HP:0000553,Abnormality of the uvea,HP:0012374,Abnormality of the globe
+CL:0000653,glomerular visceral epithelial cell,CL:1000451,epithelial cell of visceral layer of glomerular capsule
+UBERON:0009919,ureter smooth muscle,UBERON:0001135,smooth muscle tissue
+CL:0000445,apoptosis fated cell,CL:0000003,native cell
+UBERON:3010377,unicellular gland,UBERON:0003102,surface structure
+UBERON:0009603,right lung associated mesenchyme,UBERON:0004883,lung mesenchyme
+CL:0000605,fungal asexual spore,CL:0002369,fungal spore
+UBERON:0003457,head bone,UBERON:0007914,head or neck bone
+UBERON:0006692,vertebral canal,UBERON:0004120,mesoderm-derived structure
+HP:0011603,Congenital malformation of the great arteries,HP:0002564,Malformation of the heart and great vessels
+HP:0002533,Abnormal posturing,HP:0100022,Abnormality of movement
+UBERON:0001631,thoracic duct,UBERON:0001473,lymphatic vessel
+CL:1000849,kidney distal convoluted tubule epithelial cell,CL:0002305,epithelial cell of distal tubule
+UBERON:4440011,paired fin lepidotrichium,UBERON:0004375,bone of free limb or fin
+UBERON:0002365,exocrine gland,UBERON:0002530,gland
+HP:0001627,Abnormality of cardiac morphology,HP:0001626,Abnormality of the cardiovascular system
+HP:0100100,Absent epiphysis of the distal phalanx of the 2nd toe,HP:0100088,Abnormality of the epiphysis of the distal phalanx of the 2nd toe
+DOID:10074,hymenolepiasis,DOID:883,parasitic helminthiasis infectious disease
+HP:0010152,Enlarged epiphysis of the 1st metatarsal,HP:0010116,Enlarged epiphyses of the hallux
+UBERON:0015151,Harderian gland duct,UBERON:0010313,neural crest-derived structure
+HP:0011756,Posterior pituitary agenesis,HP:0011753,Posterior pituitary dysgenesis
+HP:0002162,Low posterior hairline,HP:0000464,Abnormality of the neck
+HP:0004039,Abnormality of ulnar metaphysis,HP:0002997,Abnormality of the ulna
+UBERON:0009640,hypophyseal cartilage,UBERON:0003932,cartilage element of chondrocranium
+UBERON:0014756,Wulst,UBERON:0002791,regional part of telencephalon
+DOID:0050485,sennetsu fever,DOID:0050338,primary bacterial infectious disease
+HP:0008444,Posterior wedging of vertebral bodies,HP:0008422,Vertebral wedging
+HP:0001787,Abnormal delivery,HP:0001197,Abnormality of prenatal development or birth
+DOID:0050639,primary cutaneous amyloidosis,DOID:9120,amyloidosis
+UBERON:0010187,female urethral gland,UBERON:0014404,female anatomical structure
+UBERON:0006643,tunica albuginea of testis,UBERON:0006610,tunica albuginea
+HP:0004268,Osteoarthritis of the small joints of the hand,HP:0002758,Osteoarthritis
+UBERON:0003584,mammary gland connective tissue,UBERON:0002384,connective tissue
+HP:0100823,Genital hernia,HP:0100790,Hernia
+CL:1001573,nasopharyngeal epithelial cell,CL:0002631,epithelial cell of upper respiratory tract
+HP:0003396,Syringomyelia,HP:0100561,Spinal cord lesions
+HP:0003199,Decreased muscle mass,HP:0011805,Abnormality of muscle morphology
+HP:0002755,Osteomyelitis due to immunodeficiency,HP:0002721,Immunodeficiency
+UBERON:0001951,epithelium of nasopharynx,UBERON:0004814,upper respiratory tract epithelium
+DOID:14453,farmer's lung,DOID:841,extrinsic allergic alveolitis
+UBERON:2005369,dorsal fin pterygiophore 6,UBERON:2001419,dorsal fin pterygiophore
+UBERON:0004224,vas deferens smooth muscle,UBERON:0006660,muscle layer
+CL:0000664,closable valve cell,CL:0000663,valve cell
+UBERON:2002067,upper hypural set,UBERON:0000477,anatomical cluster
+UBERON:0005253,head mesenchyme,UBERON:0005291,embryonic tissue
+UBERON:0012186,ovary growing follicle,UBERON:0001305,ovarian follicle
+NCBITaxon:11608,Seoul virus,NCBITaxon:11598,Hantavirus
+UBERON:2000927,myotome somite 16,UBERON:0003082,myotome
+UBERON:3000658,prechoanal process,UBERON:0010313,neural crest-derived structure
+HP:0012444,Brain atrophy,HP:0012443,Abnormality of the brain
+CL:1000549,kidney cortex collecting duct epithelial cell,CL:1001225,kidney collecting duct cell
+HP:0012584,Bilateral renal hypoplasia,HP:0000089,Renal hypoplasia
+HP:0005233,Hypoplasia of the gallbladder,HP:0011466,Aplasia/Hypoplasia of the gallbladder
+UBERON:0003026,limitans nucleus,UBERON:0002308,nucleus of brain
+UBERON:0001069,head of pancreas,UBERON:0004119,endoderm-derived structure
+HP:0002226,White eyebrow,HP:0000534,Abnormality of the eyebrow
+HP:0009768,Broad phalanges of the hand,HP:0006009,Broad phalanx
+DOID:12735,hernia of ovary and fallopian tube,DOID:229,female reproductive system disease
+HP:0012211,Abnormal renal physiology,HP:0011277,Abnormality of the urinary system physiology
+UBERON:0009074,syrinx organ,UBERON:0004119,endoderm-derived structure
+UBERON:0003508,pedal digit blood vessel,UBERON:0003521,pes blood vessel
+UBERON:0002054,zona fasciculata of adrenal gland,UBERON:0009753,adrenal gland cortex zone
+UBERON:0005700,upper jaw molar odontogenic papilla,UBERON:0010258,mesenchyme from rhombencephalic neural crest
+DOID:7602,intracortical osteogenic sarcoma,DOID:3378,conventional central osteosarcoma
+HP:0011582,Abdominal ectopia cordis,HP:0001683,Ectopia cordis
+UBERON:0004631,thoracic vertebra 6,UBERON:0002347,thoracic vertebra
+CL:0000935,"CD4-negative, CD8-negative, alpha-beta intraepithelial T cell",CL:0000797,alpha-beta intraepithelial T cell
+HP:0000573,Retinal hemorrhage,HP:0011029,Internal hemorrhage
+CL:0002680,PP cell of intestine,CL:1001516,intestinal enteroendocrine cell
+DOID:13538,cornea squamous cell carcinoma,DOID:6199,cornea cancer
+HP:0010598,Abnormality of the proximal humeral epiphysis,HP:0003891,Abnormality of the humeral epiphysis
+UBERON:0007416,cerebellar peduncle,UBERON:0007417,peduncle of neuraxis
+UBERON:0001243,serosa of intestine,UBERON:0004782,gastrointestinal system serosa
+DOID:3303,notochordal cancer,DOID:184,bone cancer
+UBERON:0006783,layer of superior colliculus,UBERON:0004923,organ component layer
+HP:0003459,Polyclonal elevation of IgM,HP:0003496,Increased IgM level
+DOID:5268,myxoid leiomyosarcoma,DOID:1967,leiomyosarcoma
+HP:0001836,Camptodactyly (feet),HP:0012385,Camptodactyly
+UBERON:0014553,CA3 stratum oriens,UBERON:0014567,layer of hippocampal field
+CL:0002297,type-3 epithelial cell of thymus,CL:0002364,cortical thymic epithelial cell
+HP:0100141,Ivory epiphysis of the distal phalanx of the 3rd toe,HP:0100091,Abnormality of the epiphysis of the distal phalanx of the 3rd toe
+UBERON:0001224,renal pelvis,UBERON:0000063,organ segment
+DOID:4794,ependymoblastoma,DOID:0060103,central nervous system primitive neuroectodermal neoplasm
+DOID:7437,uterus perivascular epithelioid cell tumor,DOID:9460,uterine corpus cancer
+DOID:10536,malignant gastric granular cell tumor,DOID:10534,stomach cancer
+DOID:0050920,tonsil squamous cell carcinoma,DOID:8858,tonsil cancer
+CL:0002005,"CD34-positive, CD38-positive megakaryocyte erythroid progenitor cell",CL:0000050,megakaryocyte-erythroid progenitor cell
+UBERON:2000245,nucleus of the descending root,UBERON:0004132,trigeminal sensory nucleus
+DOID:6641,breast juvenile papillomatosis,DOID:1634,breast papillomatosis
+UBERON:2001614,anal fin middle radial bone,UBERON:2001671,anal fin radial bone
+UBERON:0009149,foramen primum,UBERON:0004111,anatomical conduit
+UBERON:2000714,accessory pretectal nucleus,UBERON:0014450,pretectal nucleus
+UBERON:0002682,abducens nucleus,UBERON:0009662,hindbrain nucleus
+HP:0010947,Abnormality of ductus venosus blood flow,HP:0010948,Abnormality of the fetal cardiovascular system
+DOID:8025,gastric signet ring cell adenocarcinoma,DOID:6217,gastric diffuse adenocarcinoma
+DOID:7491,vulvar proximal-type epithelioid sarcoma,DOID:2096,vulvar sarcoma
+HP:0004590,Hypoplastic sacrum,HP:0008517,Aplasia/Hypoplasia of the sacrum
+HP:0000803,Renal cortical cysts,HP:0011035,Abnormality of the renal cortex
+UBERON:0006641,appendix epididymis,UBERON:0005160,vestigial structure
+UBERON:0013427,occipital bun,UBERON:0005913,zone of bone organ
+HP:0006895,Lower limb hypertonia,HP:0002509,Limb hypertonia
+UBERON:0004858,cellular cartilage,UBERON:0002418,cartilage tissue
+CL:0000999,CD4-positive CD11b-positive dendritic cell,CL:0002465,CD11b-positive dendritic cell
+HP:0011974,Myelofibrosis,HP:0012145,Abnormality of multiple cell lineages in the bone marrow
+UBERON:0008828,presphenoid bone,UBERON:0002513,endochondral bone
+UBERON:0006915,stratified squamous epithelium,UBERON:0006914,squamous epithelium
+HP:0100468,Patchy sclerosis of the distal phalanx of the 4th toe,HP:0100941,Sclerosis of the distal phalanx of the 4th toe
+HP:0009570,Bullet-shaped middle phalanx of the 2nd finger,HP:0009548,Bullet-shaped phalanges of the 2nd finger
+CL:0000785,mature B cell,CL:0000236,B cell
+NCBITaxon:1113537,Chlamydia/Chlamydophila group,NCBITaxon:809,Chlamydiaceae
+DOID:1862,jaw cancer,DOID:184,bone cancer
+HP:0005232,Pancreatic dysplasia,HP:0012090,Abnormality of pancreas morphology
+HP:0000692,Misalignment of teeth,HP:0000164,Abnormality of the teeth
+HP:0011081,Incisor macrodontia,HP:0001572,Macrodontia
+HP:0012749,Focal T2 hypointense brainstem lesion,HP:0012747,Abnormal brainstem MRI signal intensity
+HP:0010034,Short 1st metacarpal,HP:0009660,Short phalanx of the thumb
+UBERON:0004943,submucosa of urinary bladder,UBERON:0006554,urinary system structure
+UBERON:0009991,lateral condyle of tibia,UBERON:0009989,condyle of tibia
+UBERON:0005705,primary palate mesenchyme,UBERON:0006904,head mesenchyme from mesoderm
+UBERON:0015152,gland of orbital region,UBERON:0002530,gland
+UBERON:0004032,podocyte slit diaphragm,UBERON:0006554,urinary system structure
+HP:0200063,Colorectal polyps,HP:0100743,Neoplasm of the rectum
+UBERON:0012360,bone of jaw,UBERON:0003462,facial bone
+UBERON:0004751,hypohyal bone,UBERON:0011613,hypohyal element
+DOID:676,juvenile rheumatoid arthritis,DOID:7148,rheumatoid arthritis
+DOID:5342,childhood endodermal sinus tumor,DOID:1911,endodermal sinus tumor
+UBERON:0013078,venom-injecting tooth,UBERON:0001091,calcareous tooth
+DOID:9123,eczema herpeticum,DOID:37,skin disease
+UBERON:0005655,right lung accessory lobe epithelium,UBERON:0003364,epithelium of right lung
+DOID:11889,female breast nipple and areola cancer,DOID:0050671,female breast cancer
+HP:0010057,Abnormality of the phalanges of the hallux,HP:0001844,Abnormality of the hallux
+UBERON:0004784,heart ventricle wall,UBERON:0004120,mesoderm-derived structure
+DOID:10331,kaolin pneumoconiosis,DOID:10316,pneumoconiosis
+UBERON:3010457,upper blastopore lip,UBERON:3010455,blastopore lip
+HP:0005479,IgE deficiency,HP:0004313,Hypogammaglobulinemia
+DOID:11561,hypertensive retinopathy,DOID:5679,retinal disease
+HP:0009716,Subependymal nodules,HP:0009731,Cerebral hamartomata
+UBERON:0013228,sweat gland of eyelid,UBERON:0003605,eye skin gland
+HP:0007627,Mandibular condyle aplasia,HP:0005790,Short mandibular condyles
+HP:0004025,Spurred radial metaphysis,HP:0004015,Abnormality of radial metaphyses
+UBERON:0004162,pulmonary myocardium,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0000278,Retrognathia,HP:0000277,Abnormality of the mandible
+UBERON:0009476,madreporite,UBERON:0003978,valve
+DOID:7402,L-cell glucagon-like peptide producing tumor,DOID:4148,gastrointestinal neuroendocrine benign tumor
+HP:0008763,No social interaction,HP:0000735,Impaired social interactions
+UBERON:0012459,antler pedicle,UBERON:0005913,zone of bone organ
+UBERON:0002610,cochlear nuclear complex,UBERON:0003528,brain grey matter
+UBERON:0005064,left ventricular trabecular myocardium,UBERON:0004126,trabecular layer of ventricle
+UBERON:0010535,primitive metanephric nephron,UBERON:0005106,metanephric tubule
+HP:0009225,Aplasia of the proximal phalanx of the 5th finger,HP:0010242,Aplasia of the proximal phalanges of the hand
+HP:0007363,Aplasia/Hypoplasia of the pyramidal tract,HP:0002062,Abnormality of the pyramidal tracts
+UBERON:0005073,preganglionic parasympathetic nervous system,UBERON:0000011,parasympathetic nervous system
+HP:0009049,Peroneal muscle atrophy,HP:0001430,Abnormality of the calf musculature
+UBERON:2002117,ovipositor,UBERON:0003103,compound organ
+DOID:10485,esophageal atresia,DOID:6050,esophageal disease
+DOID:8399,trombiculiasis,DOID:7894,mite infestation
+HP:0010707,1-4 finger syndactyly,HP:0006101,Finger syndactyly
+CL:0008010,cranial somatomotor neuron,CL:0015000,cranial motor neuron
+UBERON:3000771,acetabular depression,UBERON:3000767,pelvic girdle opening
+UBERON:0002084,heart left ventricle,UBERON:0002082,cardiac ventricle
+UBERON:2001916,basibranchial 2 element,UBERON:0013746,basibranchial element
+HP:0010247,Bracket epiphyses of the distal phalanges of the hand,HP:0010243,Abnormality of the epiphyses of the distal phalanx of finger
+DOID:0050905,inflammatory myofibroblastic tumor,DOID:3350,mesenchymal cell neoplasm
+UBERON:0001289,descending limb of loop of Henle,UBERON:0007685,region of nephron tubule
+DOID:0050199,Whitewater Arroyo hemorrhagic fever,DOID:934,viral infectious disease
+UBERON:0014695,deep auricular artery,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000152,exocrine cell,CL:0000151,secretory cell
+UBERON:0008331,clitoral smooth muscle,UBERON:0005156,reproductive structure
+UBERON:0012129,radial head of humerus,UBERON:0004120,mesoderm-derived structure
+HP:0100717,Abnormality of the cementum,HP:0011061,Abnormality of dental structure
+HP:0100778,Cryoglobulinemia,HP:0005368,Abnormality of humoral immunity
+HP:0001263,Global developmental delay,HP:0100543,Cognitive impairment
+HP:0100637,Neoplasia of the nose,HP:0100630,Neoplasia of the nasopharynx
+CL:0000768,immature basophil,CL:0002242,nucleate cell
+UBERON:0002749,regional part of cerebellar cortex,UBERON:0002946,regional part of cerebellum
+DOID:5129,simple partial epilepsy,DOID:2234,focal epilepsy
+UBERON:2002075,distal cartilage of external anterior process of basipterygium,UBERON:4100000,skeletal element projection
+DOID:10604,lactose intolerance,DOID:2978,carbohydrate metabolic disorder
+DOID:7134,esophagus small cell carcinoma,DOID:1107,esophageal carcinoma
+UBERON:2000609,ventrolateral nucleus,UBERON:0011214,nucleus of midbrain tectum
+UBERON:0006022,interdigital region between digits 3 and 4,UBERON:0006012,interdigital region
+HP:0008897,Postnatal growth retardation,HP:0001510,Growth delay
+UBERON:0006026,interdigital region between manual digits 1 and 2,UBERON:0006013,interdigital region between manual digits
+DOID:9965,toxoplasmosis,DOID:2113,coccidiosis
+UBERON:0001952,epithelium of oropharynx,UBERON:0003351,pharyngeal epithelium
+HP:0008652,Autonomic erectile dysfunction,HP:0002459,Dysautonomia
+DOID:1099,alpha thalassemia,DOID:10241,thalassemia
+HP:0010386,Curved phalanges of the 5th toe,HP:0010342,Abnormality of the phalanges of the 5th toe
+DOID:14032,malignant parietal pleura tumor,DOID:5158,pleural cancer
+HP:0002718,Recurrent bacterial infections,HP:0002719,Recurrent infections
+DOID:14022,algoneurodystrophy,DOID:1289,neurodegenerative disease
+DOID:7198,maxillary sinus adenoid cystic carcinoma,DOID:1357,maxillary sinus cancer
+UBERON:0000911,chyle,UBERON:0000463,portion of organism substance
+UBERON:0014735,paleocortex,UBERON:0014734,allocortex
+UBERON:0015418,urethra mesenchymal layer,UBERON:0004120,mesoderm-derived structure
+HP:0011335,Frontal hirsutism,HP:0009937,Facial hirsutism
+HP:0008261,Pancreatic islet cell adenoma,HP:0006476,Abnormality of the pancreatic islet cells
+UBERON:0001548,lateral marginal vein,UBERON:0004261,lower leg blood vessel
+HP:0005268,Spontaneous abortion,HP:0001787,Abnormal delivery
+HP:0011093,Molarization of premolar,HP:0011080,Abnormality of premolar morphology
+HP:0011098,Speech apraxia,HP:0002186,Apraxia
+UBERON:0011313,posterior subdivision of masseter,UBERON:0004120,mesoderm-derived structure
+HP:0009347,Bracket epiphysis of the proximal phalanx of the 3rd finger,HP:0010269,Bracket epiphyses of the proximal phalanges of the hand
+UBERON:2000646,anal fin distal radial bone,UBERON:2001671,anal fin radial bone
+UBERON:0001161,body of stomach,UBERON:0009870,zone of stomach
+UBERON:2005012,afferent filamental artery,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0001146,Pigmentary retinal degeneration,HP:0008051,Abnormality of the retinal pigment epithelium
+UBERON:0002034,suprachiasmatic nucleus,UBERON:0006568,hypothalamic nucleus
+UBERON:0001537,anterior tibial artery,UBERON:0007610,tibial artery
+UBERON:0000089,hypoblast (generic),UBERON:0002050,embryonic structure
+UBERON:2000196,dorsal hypohyal bone,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2000425,anterior lateral line nerve,UBERON:0008906,lateral line nerve
+HP:0100327,Cow milk allergy,HP:0012393,Allergy
+UBERON:0001655,submental vein,UBERON:0003502,neck blood vessel
+UBERON:2002176,caudal octaval nerve motor nucleus,UBERON:2002174,octaval nerve motor nucleus
+UBERON:0015868,lymph node of epiploic foramen,UBERON:0015860,visceral abdominal lymph node
+HP:0010400,Patchy sclerosis of the proximal phalanx of the 2nd toe,HP:0010208,Patchy sclerosis of the proximal phalanges of the toes
+NCBITaxon:11286,Lyssavirus,NCBITaxon:11270,Rhabdoviridae
+HP:0009275,Contracture of the distal interphalangeal joint of the 4th finger,HP:0009697,Contractures of the distal interphalangeal joints of the fingers
+HP:0004261,Wide hamate bone,HP:0004242,Broad carpal bones
+UBERON:4200131,trochanteric shelf,UBERON:0004120,mesoderm-derived structure
+UBERON:0008836,liver bud,UBERON:0005423,developing anatomical structure
+HP:0010596,Abnormality of the proximal radial epiphysis,HP:0003946,Abnormality of the epiphyses of the elbow
+DOID:5155,multiple mucosal neuroma,DOID:2001,neuroma
+UBERON:0001733,soft palate,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0001325,Hypoglycemic coma,HP:0001259,Coma
+DOID:5398,lipoadenoma,DOID:657,adenoma
+HP:0000889,Abnormality of the clavicles,HP:0000765,Abnormality of the thorax
+UBERON:0012489,muscle layer of colon,UBERON:0011198,muscle layer of large intestine
+DOID:3103,thoracic outlet syndrome,DOID:178,vascular disease
+UBERON:3010058,annuli,UBERON:3000977,body external integument structure
+DOID:4650,bilateral retinoblastoma,DOID:768,retinoblastoma
+HP:0010891,Morbus Scheuermann,HP:0100323,Juvenile aseptic necrosis
+HP:0008855,Moderate postnatal growth retardation,HP:0008897,Postnatal growth retardation
+HP:0009988,Duplication of the distal phalanx of the 5th finger,HP:0009985,Duplication of phalanx of 5th finger
+HP:0000793,Membranoproliferative glomerulonephritis,HP:0000099,Glomerulonephritis
+HP:0001107,Ocular albinism,HP:0007730,Iris hypopigmentation
+HP:0010633,Partial anosmia,HP:0000458,Anosmia
+DOID:3605,ovarian cystadenocarcinoma,DOID:3713,ovary adenocarcinoma
+DOID:4617,periapical granuloma,DOID:823,periapical periodontitis
+DOID:12297,Vogt-Koyanagi-Harada disease,DOID:417,hypersensitivity reaction type II disease
+UBERON:0010235,uvular muscle,UBERON:0003682,palatal muscle
+UBERON:0013241,embryonic urethral groove,UBERON:0002050,embryonic structure
+HP:0000736,Short attention span,HP:0000708,Behavioural/Psychiatric Abnormality
+HP:0100937,Sclerosis of the middle phalanx of the 4th toe,HP:0100928,Sclerosis of the phalanges of the 4th toe
+UBERON:0004649,sphenoid bone pterygoid process,UBERON:0010313,neural crest-derived structure
+UBERON:0002588,decussation of superior cerebellar peduncle,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0000015,Bladder diverticulum,HP:0000014,Abnormality of the bladder
+UBERON:0001300,scrotum,UBERON:0005156,reproductive structure
+HP:0011189,Bilateral multifocal epileptiform discharges,HP:0010841,Multifocal epileptiform discharges
+UBERON:0001734,palatine uvula,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:14748,Sotos syndrome,DOID:0050737,autosomal recessive disease
+CL:1000082,stretch receptor cell,CL:0000006,neuronal receptor cell
+UBERON:0003642,pedal digit 3 phalanx,UBERON:0001449,phalanx of pes
+UBERON:0010678,manual digit 4 phalanx cartilage element,UBERON:0015028,manual digit 4 phalanx endochondral element
+DOID:0060108,brain glioma,DOID:1319,brain cancer
+UBERON:0006798,efferent nerve,UBERON:0001021,nerve
+HP:0000444,Convex nasal ridge,HP:0005105,Abnormal nasal morphology
+UBERON:0000994,spermathecum,UBERON:0000062,organ
+UBERON:0004455,neurula embryo,UBERON:0000922,embryo
+HP:0010339,Flexion contracture of the 4th toe,HP:0005830,Flexion contracture of toe
+DOID:4877,breast adenoid cystic carcinoma,DOID:3459,breast carcinoma
+UBERON:0010759,equine distal sesamoid,UBERON:0001479,sesamoid bone
+UBERON:3010781,pars convoluta,UBERON:0005156,reproductive structure
+NCBITaxon:42407,Neotoma,NCBITaxon:337963,Neotominae
+UBERON:4300034,antorbital cartilage,UBERON:0004120,mesoderm-derived structure
+UBERON:3000031,ascending process of palatoquadrate,UBERON:0004530,bony projection
+DOID:13778,chancroid,DOID:0050338,primary bacterial infectious disease
+HP:0009296,Bullet-shaped middle phalanx of the 4th finger,HP:0009845,Bullet-shaped middle phalanges of the hand
+HP:0010238,Triangular epiphyses of the phalanges of the hand,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+HP:0011652,Double outlet right ventricle with doubly committed ventricular septal defect without pulmonary stenosis,HP:0001719,Double outlet right ventricle
+HP:0004289,Sclerotic foci in hand bones,HP:0004281,Irregular sclerosis of hand bones
+DOID:5303,cervical clear cell adenocarcinoma,DOID:3702,cervical adenocarcinoma
+UBERON:2000835,sclerotome somite 28,UBERON:0003089,sclerotome
+UBERON:0012297,male urethral crest,UBERON:0005156,reproductive structure
+CL:0005002,xanthoblast,CL:0000055,non-terminally differentiated cell
+UBERON:0006536,male reproductive system fluid/secretion,UBERON:0000463,portion of organism substance
+UBERON:0004754,foramen ovale of heart,UBERON:0000464,anatomical space
+UBERON:0008945,extraembryonic endoderm,UBERON:0005292,extraembryonic tissue
+UBERON:0008777,hypaxial musclulature,UBERON:0004120,mesoderm-derived structure
+HP:0008726,Hypoplasia of the vagina,HP:0011026,Aplasia/Hypoplasia of the vagina
+UBERON:0009719,tunicate siphon,UBERON:0000026,appendage
+UBERON:2007005,hemal prezygapophysis,UBERON:0002513,endochondral bone
+UBERON:0003093,occipital lateral line,UBERON:0010202,lateral line
+UBERON:0001771,pupil,UBERON:0000464,anatomical space
+UBERON:0009977,natal tooth,UBERON:0007115,deciduous tooth
+HP:0010878,Fetal cystic hygroma,HP:0000476,Cystic hygroma
+HP:0010628,Facial palsy,HP:0000301,Abnormality of facial musculature
+UBERON:2001734,posterior process of basipterygium,UBERON:4100000,skeletal element projection
+UBERON:0002483,trabecular bone tissue,UBERON:0002481,bone tissue
+DOID:1148,polydactyly,DOID:0080015,physical disorder
+DOID:0050762,adenylosuccinase lyase deficiency,DOID:9252,amino acid metabolic disorder
+HP:0200143,Megaloblastic erythroid hyperplasia,HP:0012132,Erythroid hyperplasia
+DOID:5101,auricular cancer,DOID:833,auditory system cancer
+HP:0007744,Iridoretinal coloboma,HP:0000612,Iris coloboma
+DOID:3864,adult medulloblastoma,DOID:0050902,medulloblastoma
+DOID:4977,lymphedema,DOID:75,lymphatic system disease
+UBERON:0015109,distal tarsal bone 3 cartilage,UBERON:0010885,hindlimb cartilage element
+UBERON:0006767,head of femur,UBERON:0005055,zone of long bone
+DOID:507,adjustment disorder,DOID:150,disease of mental health
+UBERON:0004114,tympanic cavity,UBERON:0002553,anatomical cavity
+DOID:5748,rheumatic pulmonary valve disease,DOID:5749,pulmonary valve disease
+HP:0004216,Osteolytic defects of the phalanges of the 5th finger,HP:0009771,Osteolytic defects of the phalanges of the hand
+HP:0100233,Stippling of the epiphysis of the proximal phalanx of the 5th toe,HP:0100086,Stippling of the epiphyses of the 5th toe
+CL:1000696,kidney interstitial inflammatory macrophage,CL:0000864,tissue-resident macrophage
+HP:0008046,Abnormality of the retinal vasculature,HP:0008047,Abnormality of the vasculature of the eye
+UBERON:2000410,postcleithrum,UBERON:0007829,pectoral girdle bone
+DOID:0050601,ADULT syndrome,DOID:37,skin disease
+HP:0009104,Aplasia/Hypoplasia of the pubic bone,HP:0003172,Abnormality of the pubic bones
+NCBITaxon:186826,Lactobacillales,NCBITaxon:91061,Bacilli
+UBERON:0003481,tail vein,UBERON:0003524,tail blood vessel
+DOID:4893,middle ear carcinoma,DOID:5099,middle ear cancer
+HP:0003898,Large humeral epiphyses,HP:0003891,Abnormality of the humeral epiphysis
+UBERON:0004492,cardiac muscle tissue of cardiac septum,UBERON:0001133,cardiac muscle tissue
+UBERON:0002181,substantia gelatinosa,UBERON:0000064,organ part
+HP:0008272,Renal tubular lysine transport defect,HP:0000124,Renal tubular dysfunction
+UBERON:0001271,pelvic girdle region,UBERON:0007823,appendage girdle region
+UBERON:0009775,lateral medullary reticular complex,UBERON:0003528,brain grey matter
+UBERON:0001619,ophthalmic artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3010720,ramus hyomandibularis,UBERON:0004732,segmental subdivision of nervous system
+DOID:9977,hallucinogen dependence,DOID:9974,drug dependence
+CL:0002031,hematopoietic lineage restricted progenitor cell,CL:0008001,hematopoietic precursor cell
+UBERON:0005654,lower jaw molar epithelium,UBERON:0015839,molar epithelium
+HP:0009677,Cone-shaped epiphysis of the distal phalanx of the thumb,HP:0009688,Cone-shaped epiphyses of the thumb
+CL:0002265,type D cell of colon,CL:1001516,intestinal enteroendocrine cell
+UBERON:0015034,pedal digit 4 phalanx endochondral element,UBERON:0015030,pedal digit phalanx endochondral element
+HP:0009355,Stippling of the epiphysis of the proximal phalanx of the 3rd finger,HP:0010277,Stippling of the epiphyses of the proximal phalanges of the hand
+HP:0011841,Ventricular flutter,HP:0004756,Ventricular tachycardia
+HP:0000293,Full cheeks,HP:0004426,Abnormality of the cheeks
+HP:0011493,Central opacification of the cornea,HP:0007759,Opacification of the corneal stroma
+UBERON:0014489,middle phalanx of digit 3,UBERON:0004301,middle phalanx
+CL:1000702,kidney pelvis smooth muscle cell,CL:1000505,kidney pelvis cell
+DOID:3436,viral laryngitis,DOID:9396,acute laryngitis
+HP:0100121,Triangular epiphysis of the middle phalanx of the 2nd toe,HP:0100089,Abnormality of the epiphysis of the middle phalanx of the 2nd toe
+DOID:3700,uterine ligament adenocarcinoma,DOID:5727,uterine ligament cancer
+HP:0003882,Slender humerus,HP:0003063,Abnormality of the humerus
+UBERON:2000224,quadrate ventral process,UBERON:4100000,skeletal element projection
+UBERON:0014758,interstitial part of hyperpallium apicale,UBERON:0002791,regional part of telencephalon
+UBERON:0002498,deltopectoral crest,UBERON:0005813,tubercle
+CL:0002064,pancreatic acinar cell,CL:1001599,pancreas exocrine glandular cell
+DOID:2557,chondromalacia,DOID:6227,articular cartilage disease
+DOID:10547,pyloric antrum cancer,DOID:10544,pylorus cancer
+DOID:5408,Paget's disease of bone,DOID:205,hyperostosis
+DOID:1947,trichomoniasis,DOID:2789,parasitic protozoa infectious disease
+UBERON:2000464,otic lateral line,UBERON:2001470,anterior lateral line
+DOID:3522,lateral medullary syndrome,DOID:3523,brain stem infarction
+UBERON:0000428,prostate epithelium,UBERON:0005156,reproductive structure
+UBERON:0003055,periderm,UBERON:0010371,ecto-epithelium
+UBERON:0003585,dermis connective tissue,UBERON:0002384,connective tissue
+HP:0009085,Alveolar ridge overgrowth,HP:0006477,Abnormality of the alveolar ridges
+UBERON:0008835,hepatic diverticulum,UBERON:0009497,epithelium of foregut-midgut junction
+UBERON:3000597,symphysis maxillaris,UBERON:0000064,organ part
+NCBITaxon:426442,Ixodinae,NCBITaxon:6939,Ixodidae
+UBERON:0000011,parasympathetic nervous system,UBERON:0002410,autonomic nervous system
+DOID:538,internuclear ophthalmoplegia,DOID:539,ophthalmoplegia
+HP:0007692,Nonnuclear polymorphic congenital cataract,HP:0000519,Congenital cataract
+HP:0009251,Bracket epiphysis of the distal phalanx of the 4th finger,HP:0009249,Abnormality of the epiphysis of the distal phalanx of the 4th finger
+DOID:12559,idiopathic juvenile osteoporosis,DOID:11476,osteoporosis
+HP:0011089,Double tooth,HP:0006482,Abnormality of dental morphology
+UBERON:2001538,pelvic radial cartilage,UBERON:0007844,cartilage element
+UBERON:0000415,artery wall,UBERON:0000060,anatomical wall
+DOID:12140,Chagas disease,DOID:10113,trypanosomiasis
+HP:0011768,Parathyroid dysgenesis,HP:0011766,Abnormality of the parathyroid morphology
+UBERON:0002301,layer of neocortex,UBERON:0004121,ectoderm-derived structure
+HP:0002032,Esophageal atresia,HP:0002589,Gastrointestinal atresia
+HP:0006438,Enlargement of the distal femoral epiphysis,HP:0010590,Abnormality of the distal femoral epiphysis
+UBERON:0003671,anterior cruciate ligament of knee joint,UBERON:0006659,cruciate ligament of knee
+NCBITaxon:39107,Murinae,NCBITaxon:10066,Muridae
+UBERON:0016412,central part of body of vertebra,UBERON:0004120,mesoderm-derived structure
+HP:0004810,Congenital hypoplastic anemia,HP:0001908,Hypoplastic anemia
+HP:0005111,Dilatation of the ascending aorta,HP:0001724,Aortic dilatation
+UBERON:0011906,muscle head,UBERON:0000064,organ part
+DOID:4065,mixed type rhabdomyosarcoma,DOID:3247,rhabdomyosarcoma
+UBERON:0002667,lateral septal nucleus,UBERON:0009663,telencephalic nucleus
+UBERON:4000074,palaeoniscoid scale,UBERON:4000052,ganoid scale
+UBERON:0013142,soleal vein,UBERON:0001551,vein of hindlimb zeugopod
+UBERON:0010022,ventral part of pharyngeal pouch 1,UBERON:0000490,unilaminar epithelium
+HP:0005780,Absent fourth finger distal interphalangeal crease,HP:0001032,Absent distal interphalangeal creases
+UBERON:0003317,odontogenic papilla of incisor,UBERON:0001763,odontogenic papilla
+HP:0003840,Delayed upper limb epiphyseal ossification,HP:0003839,Abnormality involving the epiphyses of the upper limbs
+DOID:2516,intracranial cavernous angioma,DOID:2517,intracranial structure hemangioma
+UBERON:3010078,M. iliacus externus,UBERON:0010890,pelvic complex muscle
+HP:0003443,Decreased size of nerve terminals,HP:0000759,Abnormality of the peripheral nervous system
+DOID:5691,visual cortex disease,DOID:1393,visual pathway disease
+HP:0000162,Glossoptosis,HP:0000157,Abnormality of the tongue
+HP:0001747,Accessory spleen,HP:0009799,Supernumerary spleens
+UBERON:2205376,dorsal fin distal radial cartilage 5,UBERON:2200936,dorsal fin distal radial cartilage
+HP:0009329,Small epiphysis of the middle phalanx of the 3rd finger,HP:0010265,Small epiphyses of the middle phalanges of the hand
+CL:0000055,non-terminally differentiated cell,CL:0000003,native cell
+HP:0003044,Shoulder flexion contracture,HP:0003043,Abnormality of the shoulder
+UBERON:0004757,rectal gland,UBERON:0003408,gland of gut
+HP:0006392,Increased density of long bones,HP:0011314,Abnormality of long bone morphology
+HP:0100188,Small epiphysis of the middle phalanx of the 4th toe,HP:0100095,Abnormality of the epiphysis of the middle phalanx of the 4th toe
+DOID:12072,pylorospasm,DOID:76,stomach disease
+UBERON:0005902,occipital region,UBERON:0000477,anatomical cluster
+UBERON:0006743,paleodentate of dentate nucleus,UBERON:0003528,brain grey matter
+UBERON:0015162,superior branch of oculomotor nerve,UBERON:0004121,ectoderm-derived structure
+CL:1001517,stomach enteroendocrine cell,CL:0000164,enteroendocrine cell
+CL:0002213,white muscle cell,CL:0000190,fast muscle cell
+CL:0005024,somatomotor neuron,CL:0008014,excitatory motor neuron
+UBERON:0008944,albumen,UBERON:0000463,portion of organism substance
+UBERON:2002072,middle anterior process of basipterygium,UBERON:0004120,mesoderm-derived structure
+HP:0000414,Bulbous nose,HP:0005105,Abnormal nasal morphology
+DOID:13653,stenosis of lacrimal punctum,DOID:1400,lacrimal apparatus disease
+UBERON:3010138,trabecular horn,UBERON:0000064,organ part
+HP:0008944,Distal lower limb amyotrophy,HP:0007210,Lower limb amyotrophy
+UBERON:0004296,respiratory system lymphatic vessel smooth muscle,UBERON:0004232,lymphatic vessel smooth muscle
+DOID:1793,pancreatic cancer,DOID:170,endocrine gland cancer
+UBERON:0012320,cervical artery,UBERON:0001637,artery
+HP:0002672,Gastrointestinal carcinoma,HP:0006749,Malignant gastrointestinal tract tumors
+UBERON:3010177,nuptial pads,UBERON:3000981,limb external integument structure
+HP:0011755,Ectopic posterior pituitary,HP:0011753,Posterior pituitary dysgenesis
+UBERON:0002727,medial medullary lamina of globus pallidus,UBERON:0014532,lamina of cerebral hemisphere
+UBERON:0002498,deltopectoral crest,UBERON:4100000,skeletal element projection
+UBERON:0013770,intermammary cleft,UBERON:0006800,anatomical line
+UBERON:4200181,astragalus head,UBERON:0004120,mesoderm-derived structure
+UBERON:0008879,ligament of pinna,UBERON:0003566,head connective tissue
+UBERON:2005116,secondary posterior lateral line primordium,UBERON:2001157,posterior lateral line primordium
+UBERON:0001159,sigmoid colon,UBERON:0000168,segment of colon
+HP:0012717,Severe conductive hearing impairment,HP:0012714,Severe hearing impairment
+HP:0010234,Ivory epiphyses of the phalanges of the hand,HP:0010583,Ivory epiphyses
+HP:0001847,Long hallux,HP:0010511,Long toe
+UBERON:2001608,autopalatine-lateral ethmoid joint,UBERON:0000982,skeletal joint
+HP:0008587,Mild neurosensory hearing impairment,HP:0000407,Sensorineural hearing impairment
+HP:0003724,Shoulder girdle muscle atrophy,HP:0003797,Limb-girdle muscle atrophy
+UBERON:0010133,neuroendocrine gland,UBERON:0002368,endocrine gland
+HP:0009509,Pseudoepiphysis of the distal phalanx of the 2nd finger,HP:0009499,Abnormality of the epiphysis of the distal phalanx of the 2nd finger
+UBERON:0004751,hypohyal bone,UBERON:0002513,endochondral bone
+UBERON:0004088,ocular region,UBERON:0000477,anatomical cluster
+HP:0006332,Supernumerary maxillary incisor,HP:0011069,Increased number of teeth
+UBERON:0000120,blood brain barrier,UBERON:0000119,cell layer
+UBERON:0010005,placental labyrinth villous,UBERON:0005156,reproductive structure
+HP:0000705,Amelogenesis imperfecta,HP:0000682,Abnormality of dental enamel
+UBERON:2000233,lower oral valve,UBERON:0000479,tissue
+UBERON:0005000,mucosa of common bile duct,UBERON:0004999,mucosa of biliary tree
+CL:1000191,pillar cell,CL:0002490,organ of Corti supporting cell
+HP:0005781,Contractures of the large joints,HP:0001371,Flexion contracture
+DOID:2452,thrombophilia,DOID:1247,blood coagulation disease
+UBERON:0003595,pes connective tissue,UBERON:0003589,hindlimb connective tissue
+UBERON:0002227,spiral organ of cochlea,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0005747,Easily subluxated first metacarpophalangeal joints,HP:0004294,Subluxation of metacarpal phalangeal joints
+UBERON:2007062,olfactory field,UBERON:2007059,neurogenic field
+UBERON:3010075,tympanic fold,UBERON:3000972,head external integument structure
+UBERON:0005498,primitive heart tube,UBERON:0004120,mesoderm-derived structure
+HP:0012572,Ureter duplex,HP:0000081,Duplicated collecting system
+HP:0012583,Unilateral renal hypoplasia,HP:0000089,Renal hypoplasia
+UBERON:0010733,alisphenoid cartilage element,UBERON:0005863,cartilaginous condensation
+HP:0004496,Posterior choanal atresia,HP:0000453,Choanal atresia
+UBERON:0008321,deep artery of penis,UBERON:0003520,pelvis blood vessel
+NCBITaxon:314146,Euarchontoglires,NCBITaxon:9347,Eutheria
+HP:0011695,Cerebellar hemorrhage,HP:0002170,Intracranial hemorrhage
+HP:0001371,Flexion contracture,HP:0003549,Abnormality of connective tissue
+NCBITaxon:1224,Proteobacteria,NCBITaxon:2,Bacteria
+UBERON:2005170,extrahepatic duct,UBERON:0004119,endoderm-derived structure
+HP:0010756,Aplasia/Hypoplasia of the premaxilla,HP:0009117,Aplasia/Hypoplasia of the maxilla
+UBERON:0001939,medial mammillary nucleus,UBERON:0006568,hypothalamic nucleus
+UBERON:2005099,ray vein,UBERON:0007304,appendage vasculature
+HP:0003185,Small sacroiliac notches,HP:0005107,Abnormality of the sacrum
+UBERON:0004496,skeletal muscle tissue of iliacus,UBERON:0001134,skeletal muscle tissue
+UBERON:0005602,dorsal mesogastrium,UBERON:0003281,mesentery of stomach
+HP:0001742,Nasal obstruction,HP:0000366,Abnormality of the nose
+UBERON:0007261,intervertebral disk of fourth cervical vertebra,UBERON:0007252,intervertebral disk of cervical vertebra
+HP:0010781,Skin dimples,HP:0011355,Localized skin lesion
+UBERON:0013703,integumentary projection,UBERON:0004529,anatomical projection
+HP:0010413,Aplasia/Hypoplasia of the distal phalanx of the 2nd toe,HP:0010325,Aplasia/Hypoplasia of the 2nd toe
+UBERON:4300002,palatine prong,UBERON:0010313,neural crest-derived structure
+UBERON:0008925,sublaminar layer S4,UBERON:0009734,sublaminar layers S2 or S3 or S4
+DOID:10971,acute salpingo-oophoritis,DOID:10972,salpingo-oophoritis
+UBERON:0001579,olfactory nerve,UBERON:0001785,cranial nerve
+HP:0001231,Abnormality of the fingernails,HP:0001597,Abnormality of the nail
+UBERON:0005115,metanephric cortical collecting duct,UBERON:0004203,cortical collecting duct
+UBERON:0004902,urogenital sinus epithelium,UBERON:0009846,embryonic cloacal epithelium
+HP:0002657,Spondylometaphyseal dysplasia,HP:0002652,Skeletal dysplasia
+UBERON:2000164,ventral mesenchyme,UBERON:0003104,mesenchyme
+HP:0011404,Lethal short-trunk short stature,HP:0003521,Disproportionate short-trunk short stature
+CL:0000003,native cell,CL:0000000,cell
+UBERON:0008801,parotid gland primordium,UBERON:0001048,primordium
+UBERON:0001040,yolk sac,UBERON:0005631,extraembryonic membrane
+CL:0000263,vegetative cell (sensu Mycetozoa),CL:0000257,Mycetozoan cell
+HP:0007587,Numerous pigmented freckles,HP:0001000,Abnormality of skin pigmentation
+DOID:10201,gallbladder lipoma,DOID:0050625,biliary tract neoplasm
+HP:0008360,Neonatal hypoproteinemia,HP:0003075,Hypoproteinemia
+HP:0003016,Metaphyseal widening,HP:0000944,Abnormality of the metaphyses
+UBERON:0009552,distal segment of manual digit,UBERON:0009551,distal segment of digit
+CL:0002107,IgD-negative CD38-positive IgG memory B cell,CL:0001053,IgD-negative memory B cell
+UBERON:0004354,male inguinal canal,UBERON:0003702,inguinal canal
+DOID:13206,nodular prostate,DOID:11132,prostatic hypertrophy
+HP:0003909,Cortical subperiosteal resorption (humeral metaphyses),HP:0003907,Abnormality of the humeral metaphyses
+CL:0002228,primary lens fiber,CL:0011004,lens fiber cell
+DOID:0050669,spastic cerebral palsy,DOID:1969,cerebral palsy
+HP:0006844,Absent patellar reflexes,HP:0002522,Areflexia of lower limbs
+UBERON:0013398,choroidal gland,UBERON:0004859,eye gland
+UBERON:0000102,lung vasculature,UBERON:0004119,endoderm-derived structure
+UBERON:0010240,zygomatic gland,UBERON:0010241,molar gland
+CL:0007001,skeletogenic cell,CL:0000003,native cell
+HP:0100104,Fragmentation of the epiphysis of the distal phalanx of the 2nd toe,HP:0100048,Fragmentation of the epiphyses of the 2nd toe
+HP:0010659,Patchy variation in bone mineral density,HP:0004349,Reduced bone mineral density
+UBERON:3010778,jugal ramule,UBERON:3010765,ramus mandibularis externus
+UBERON:2002000,posterior dentation of pectoral fin spine,UBERON:4100000,skeletal element projection
+HP:0000636,Upper eyelid coloboma,HP:0000625,Cleft eyelid
+HP:0009756,Popliteal pterygium,HP:0001059,Pterygium
+DOID:5699,kidney liposarcoma,DOID:4242,kidney sarcoma
+UBERON:0000045,ganglion,UBERON:0003714,neural tissue
+UBERON:0004014,labium minora,UBERON:0004084,genital labium
+UBERON:0014401,renal venous blood vessel,UBERON:0003920,venous blood vessel
+UBERON:0002905,intralingual sulcus,UBERON:0008334,subarachnoid sulcus
+UBERON:0006457,first thoracic spinal cord segment,UBERON:0007715,thoracic subsegment of spinal cord
+UBERON:0007349,mesopallium,UBERON:0002791,regional part of telencephalon
+HP:0100481,Proximal/middle symphalangism of 4th toe,HP:0100237,Proximal symphalangism (feet)
+HP:0010069,Bullet-shaped 1st metatarsal,HP:0010054,Abnormality of the first metatarsal
+UBERON:0000113,post-juvenile adult stage,UBERON:0000105,life cycle stage
+DOID:5702,pleomorphic liposarcoma,DOID:3382,liposarcoma
+HP:0002773,Small vertebral bodies,HP:0008479,Hypoplastic vertebral bodies
+UBERON:0002373,palatine tonsil,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0013731,basilar papilla,UBERON:0010314,structure with developmental contribution from neural crest
+CL:1001068,kidney venous system smooth muscle cell,CL:0000359,vascular associated smooth muscle cell
+UBERON:0002669,anterior horizontal limb of lateral sulcus,UBERON:0014639,frontal sulcus
+CL:0002254,epithelial cell of small intestine,CL:0002563,intestinal epithelial cell
+DOID:4644,epidermolysis bullosa simplex,DOID:2730,epidermolysis bullosa
+DOID:9838,cyclotropia,DOID:540,strabismus
+CL:1000703,kidney pelvis urothelial cell,CL:0002518,kidney epithelial cell
+HP:0006466,Ankle contracture,HP:0003028,Abnormality of the ankles
+HP:0010033,Triangular shaped 1st metacarpal,HP:0010009,Abnormality of the 1st metacarpal
+HP:0004341,Abnormality of the vitamin B12 metabolism,HP:0004340,Abnormality of vitamin B metabolism
+UBERON:0001729,oropharynx,UBERON:0000477,anatomical cluster
+HP:0003124,Hypercholesterolemia,HP:0003107,Abnormality of cholesterol metabolism
+HP:0100621,Dysgerminoma,HP:0100620,Germinoma
+UBERON:2001847,dorsal hypohyal-urohyal joint,UBERON:0000982,skeletal joint
+NCBITaxon:204429,Chlamydiia,NCBITaxon:204428,Chlamydiae
+HP:0009167,Irregular epiphysis of the distal phalanx of the 5th finger,HP:0010251,Irregular epiphyses of the distal phalanges of the hand
+UBERON:0006645,adventitia of epididymis,UBERON:0005742,adventitia
+UBERON:0003493,trachea reticular lamina,UBERON:0004119,endoderm-derived structure
+UBERON:0004070,cerebellum vermis lobule,UBERON:0004004,cerebellum lobule
+DOID:5138,leiomyomatosis,DOID:127,leiomyoma
+HP:0006380,Knee flexion contracture,HP:0002815,Abnormality of the knees
+UBERON:0003713,splenic vein,UBERON:0001638,vein
+DOID:9953,B- and T-cell mixed leukemia,DOID:9952,acute lymphocytic leukemia
+UBERON:0014441,ischial ramus,UBERON:0004120,mesoderm-derived structure
+HP:0011760,Pituitary growth hormone cell adenoma,HP:0002893,Pituitary adenoma
+HP:0008410,Subungual hyperkeratotic fragments,HP:0009723,Abnormality of the subungual region
+UBERON:0002120,pronephros,UBERON:0005423,developing anatomical structure
+HP:0011280,Abnormality of urine calcium concentration,HP:0012591,Abnormal urinary electrolyte concentration
+DOID:5232,aortic valve prolapse,DOID:62,aortic valve disease
+UBERON:2001733,mesethmoid ventral diverging lamella,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:4200104,metacarpal extensor pit,UBERON:0004704,bone fossa
+HP:0012363,Decreased sialylation of O-linked protein glycosylation,HP:0012362,Abnormal sialylation of O-linked protein glycosylation
+HP:0005687,Deformed humeral heads,HP:0003871,Deformed humerus
+HP:0000420,Short nasal septum,HP:0000419,Abnormality of the nasal septum
+DOID:355,mast-cell sarcoma,DOID:1115,sarcoma
+HP:0011765,Ectopic anterior pituitary,HP:0010625,Anterior pituitary dysgenesis
+UBERON:3000364,otic plate of pterygoid,UBERON:0004120,mesoderm-derived structure
+HP:0000549,Abnormal conjugate eye movement,HP:0000496,Abnormality of eye movement
+HP:0010601,Abnormality of the proximal ulnar epiphysis,HP:0003946,Abnormality of the epiphyses of the elbow
+HP:0003302,Spondylolisthesis,HP:0000925,Abnormality of the vertebral column
+HP:0100532,Scleritis,HP:0000591,Abnormality of the sclera
+CL:1000507,kidney tubule cell,CL:1000497,kidney cell
+UBERON:0006373,perihilar interstitium,UBERON:0004120,mesoderm-derived structure
+UBERON:0001694,petrous part of temporal bone,UBERON:0010313,neural crest-derived structure
+DOID:11725,Cornelia de Lange syndrome,DOID:630,genetic disease
+UBERON:0005742,adventitia,UBERON:0004923,organ component layer
+UBERON:0014705,median lingual swelling epithelium,UBERON:0000490,unilaminar epithelium
+UBERON:0010683,pedal digit 4 phalanx cartilage element,UBERON:0010685,pedal digit phalanx cartilage element
+DOID:1737,duodenal benign neoplasm,DOID:7505,small intestine neoplasm
+HP:0009273,Deviation of the 4th finger,HP:0004188,Abnormality of the 4th finger
+HP:0012128,Basal ganglia necrosis,HP:0002134,Abnormality of the basal ganglia
+UBERON:0013230,gland of nictitating membrane,UBERON:0013229,eyelid gland
+UBERON:0004698,vena cava endothelium,UBERON:0001919,endothelium of vein
+UBERON:0006100,Brodmann (1909) area 3,UBERON:0013529,Brodmann area
+UBERON:2001804,olfactory nerve foramen,UBERON:0005744,bone foramen
+NCBITaxon:787,Rickettsia australis,NCBITaxon:114277,spotted fever group
+UBERON:0012641,body of tubeworm,UBERON:0000468,multi-cellular organism
+UBERON:0002539,pharyngeal arch,UBERON:0002050,embryonic structure
+CL:1000414,endothelial cell of venule,CL:0002139,endothelial cell of vascular tree
+UBERON:2001876,basibranchial 3 cartilage,UBERON:2001917,basibranchial 3 element
+HP:0007316,Involuntary writhing movements,HP:0004305,Involuntary movements
+UBERON:0014451,tongue taste bud,UBERON:0004121,ectoderm-derived structure
+CL:1000420,myoepithelial cell of terminal lactiferous duct,CL:0000185,myoepithelial cell
+CL:0000930,"CD4-negative, CD8-negative type I NK T cell secreting interleukin-4",CL:0000912,helper T cell
+UBERON:0003007,lateral parabrachial nucleus,UBERON:0007634,parabrachial nucleus
+UBERON:2001571,postovulatory follicle,UBERON:0001305,ovarian follicle
+UBERON:3010039,protandrous hermaphroditic organism,UBERON:0010895,sequential hermaphroditic organism
+UBERON:0001199,mucosa of stomach,UBERON:0009034,stomach region
+DOID:12529,tibial nerve palsy,DOID:9473,mononeuritis of lower limb
+UBERON:0006865,metaphysis of femur,UBERON:0001438,metaphysis
+UBERON:0009602,left lung associated mesenchyme,UBERON:0004883,lung mesenchyme
+DOID:2921,glomerulonephritis,DOID:10952,nephritis
+HP:0001841,Preaxial foot polydactyly,HP:0001844,Abnormality of the hallux
+UBERON:0000473,testis,UBERON:0003135,male reproductive organ
+CL:0000141,cementocyte,CL:0000137,osteocyte
+UBERON:0013642,ring of oral cilia,UBERON:0000062,organ
+HP:0011829,Narrow philtrum,HP:0000288,Abnormality of the philtrum
+UBERON:0007960,scapholunate,UBERON:0001480,proximal carpal bone
+UBERON:0001676,occipital bone,UBERON:0010428,flat bone
+DOID:9667,placental abruption,DOID:780,placenta disease
+UBERON:0005579,rhombomere 5 floor plate,UBERON:0005500,rhombomere floor plate
+HP:0100101,Bracket epiphysis of the distal phalanx of the 2nd toe,HP:0100088,Abnormality of the epiphysis of the distal phalanx of the 2nd toe
+DOID:9937,chronic dacryocystitis,DOID:9935,chronic inflammation of lacrimal passage
+DOID:1863,skull cancer,DOID:184,bone cancer
+HP:0002943,Thoracic scoliosis,HP:0100711,Abnormality of the thoracic spine
+HP:0003839,Abnormality involving the epiphyses of the upper limbs,HP:0002817,Abnormality of the upper limb
+UBERON:0004469,musculature of back,UBERON:0001015,musculature
+UBERON:0003497,abdomen blood vessel,UBERON:0003835,abdominal segment blood vessel
+UBERON:0014757,hyperpallium apicale,UBERON:0002791,regional part of telencephalon
+UBERON:0006214,carpus pre-cartilage condensation,UBERON:0010884,forelimb bone pre-cartilage condensation
+CL:0002346,"Dx5-negative, NK1.1-positive immature natural killer cell",CL:0000823,immature natural killer cell
+UBERON:2001830,caudal fin ventral procurrent ray,UBERON:2001584,caudal procurrent ray
+HP:0007111,Chronic hepatic encephalopathy,HP:0002480,Hepatic encephalopathy
+CL:0007023,flask cell,CL:0000003,native cell
+UBERON:0006169,hindlimb proper dorsal digital arteries,UBERON:0006145,dorsal digital artery of pes
+UBERON:0005608,hyoid artery,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010420,Triangular shaped distal phalanx of the 2nd toe,HP:0010356,Abnormality of the distal phalanx of the 2nd toe
+UBERON:0012444,gastropege,UBERON:0012443,row of scales
+UBERON:0002930,tectopontine tract,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0002519,Hypnagogic hallucinations,HP:0000738,Hallucinations
+UBERON:0010725,accessory navicular bone,UBERON:0005899,pes bone
+UBERON:0006531,oculomotor muscle,UBERON:0001601,extra-ocular muscle
+DOID:371,extracranial neuroblastoma,DOID:769,neuroblastoma
+UBERON:0003489,respiratory system capillary endothelium,UBERON:0004702,respiratory system blood vessel endothelium
+HP:0008756,Bowing of the vocal cords,HP:0008777,Abnormality of the vocal cords
+NCBITaxon:10357,Betaherpesvirinae,NCBITaxon:10292,Herpesviridae
+NCBITaxon:948,Anaplasma phagocytophilum,NCBITaxon:106179,phagocytophilum group
+UBERON:3000830,margo vertebralis,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0011567,Sinus venosus atrial septal defect,HP:0001631,Defect in the atrial septum
+DOID:5171,vaginal endometrial stromal tumor,DOID:119,vaginal cancer
+UBERON:0003507,arm blood vessel,UBERON:0003515,forelimb blood vessel
+UBERON:0002911,parietal operculum,UBERON:0000477,anatomical cluster
+DOID:626,complement deficiency,DOID:612,primary immunodeficiency disease
+HP:0002039,Anorexia,HP:0011458,Abdominal symptom
+HP:0007810,Progressive bifocal chorioretinal atrophy,HP:0000533,Chorioretinal atrophy
+DOID:4662,thalamic disease,DOID:936,brain disease
+HP:0012569,Delayed menarche,HP:0000140,Abnormality of the menstrual cycle
+UBERON:0002597,principal sensory nucleus of trigeminal nerve,UBERON:0006331,brainstem nucleus
+UBERON:0011621,thyrohyoid cartilage,UBERON:0011004,pharyngeal arch cartilage
+HP:0009982,Partial duplication of the middle phalanx of the 4th finger,HP:0009976,Duplication of the middle phalanx of the 4th finger
+DOID:7521,breast myoepitheliosis,DOID:3004,breast myoepithelial neoplasm
+CL:0002016,"CD71-low, GlyA-positive polychromatic erythroblast",CL:0000550,polychromatophilic erythroblast
+DOID:4943,adenocarcinoma in situ,DOID:8719,in situ carcinoma
+UBERON:0002055,zona reticularis of adrenal gland,UBERON:0009753,adrenal gland cortex zone
+UBERON:0010055,stapes cartilage element,UBERON:0011607,hyomandibular cartilage
+UBERON:0004630,thoracic vertebra 5,UBERON:0002347,thoracic vertebra
+UBERON:0002047,pontine raphe nucleus,UBERON:0009662,hindbrain nucleus
+HP:0008158,Hyperapobetalipoproteinemia,HP:0003119,Abnormality of lipid metabolism
+HP:0002298,Absent hair,HP:0011362,Abnormal hair quantity
+NCBITaxon:64899,Dothioraceae,NCBITaxon:5014,Dothideales
+UBERON:0004776,inner renal medulla vasa recta,UBERON:0014401,renal venous blood vessel
+UBERON:0001272,innominate bone,UBERON:0010428,flat bone
+UBERON:2001671,anal fin radial bone,UBERON:2101671,anal fin radial element
+UBERON:0003080,anterior neural tube,UBERON:0005423,developing anatomical structure
+CL:1000307,fibroblast of dense regular elastic tissue,CL:0000057,fibroblast
+HP:0005416,Decreased serum complement factor B,HP:0004431,Complement deficiency
+HP:0004450,Preauricular skin furrow,HP:0000383,Abnormality of periauricular region
+DOID:1856,cherubism,DOID:0050736,autosomal dominant disease
+HP:0001063,Acrocyanosis,HP:0000961,Cyanosis
+UBERON:0014552,CA1 stratum oriens,UBERON:0014567,layer of hippocampal field
+DOID:5516,gastric squamous cell carcinoma,DOID:5517,stomach carcinoma
+CL:0002296,type-4 epithelial cell of thymus,CL:0002364,cortical thymic epithelial cell
+HP:0100140,Irregular epiphysis of the distal phalanx of the 3rd toe,HP:0100091,Abnormality of the epiphysis of the distal phalanx of the 3rd toe
+HP:0009255,Irregular epiphysis of the distal phalanx of the 4th finger,HP:0010251,Irregular epiphyses of the distal phalanges of the hand
+UBERON:0006010,hyaloid canal,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0014768,superior palpebral vein,UBERON:0014769,palpebral vein
+CL:0000439,prolactin secreting cell,CL:0000167,peptide hormone secreting cell
+UBERON:0009679,set of lower jaw teeth,UBERON:0009678,tooth row
+CL:1001568,pulmonary artery endothelial cell,CL:1000413,endothelial cell of artery
+UBERON:2007026,forebrain neural keel,UBERON:0004121,ectoderm-derived structure
+UBERON:0004811,endometrium epithelium,UBERON:0006955,uterine epithelium
+UBERON:0001267,femoral nerve,UBERON:0003431,leg nerve
+UBERON:2000939,middle lateral line neuromast,UBERON:0008904,neuromast
+DOID:2887,prostate leiomyoma,DOID:0060087,male reproductive organ benign neoplasm
+UBERON:0002267,laterodorsal tegmental nucleus,UBERON:0002680,regional part of metencephalon
+HP:0200046,Cat cry,HP:0001608,Abnormality of the voice
+CL:0002006,"Kit-positive, CD34-negative megakaryocyte erythroid progenitor cell",CL:0000050,megakaryocyte-erythroid progenitor cell
+CL:1001607,articular chondrocyte,CL:0000138,chondrocyte
+HP:0009430,Broad middle phalanx of the 3rd finger,HP:0004172,Abnormality of the middle phalanx of the 3rd finger
+UBERON:0001510,skin of knee,UBERON:0001511,skin of leg
+HP:0006535,Recurrent intrapulmonary hemorrhage,HP:0002088,Abnormality of the lung
+UBERON:0000370,adductor magnus,UBERON:0004252,hindlimb stylopod muscle
+HP:0005989,Redundant neck skin,HP:0001582,Redundant skin
+UBERON:2002102,epibranchial series,UBERON:0000477,anatomical cluster
+HP:0004281,Irregular sclerosis of hand bones,HP:0004054,Sclerosis of hand bones
+HP:0011288,EEG with parietal sharp slow waves,HP:0011195,EEG with focal sharp slow waves
+HP:0005527,Reduced kininogen activity,HP:0010989,Abnormality of the intrinsic pathway
+DOID:13822,tetanic cataract,DOID:83,cataract
+DOID:1555,urticaria,DOID:37,skin disease
+UBERON:0002166,endocardium of atrium,UBERON:0002165,endocardium
+HP:0100930,Sclerosis of the phalanges of the hallux,HP:0100924,Sclerosis of the phalanges of the toes
+UBERON:2001941,orbitosphenoid-lateral ethmoid joint,UBERON:0000982,skeletal joint
+UBERON:0009963,antennal gland,UBERON:0009962,excretory gland
+HP:0011454,Abnormality of the malleus,HP:0004452,Abnormality of the middle ear ossicles
+UBERON:2001750,rib of vertebra 6,UBERON:0002228,rib
+UBERON:0010903,tibiotarsus pre-cartilage condensation,UBERON:0010882,limb bone pre-cartilage condensation
+DOID:10020,ampulla of Vater cancer,DOID:10021,duodenum cancer
+HP:0003216,Generalized amyloid deposition,HP:0011034,Amyloidosis
+DOID:4367,apparent mineralocorticoid excess syndrome,DOID:1701,steroid inherited metabolic disorder
+DOID:292,lacrimal system cancer,DOID:2174,ocular cancer
+UBERON:0002758,dorsal nucleus of medial geniculate body,UBERON:0015233,nucleus of dorsal thalamus
+DOID:1526,panniculitis,DOID:631,fibromyalgia
+UBERON:0006171,renal sinus,UBERON:0002558,organ cavity
+HP:0005508,Waldenstrom macroglobulinemia,HP:0005523,Lymphoproliferative disorder
+DOID:5514,breast squamous cell carcinoma,DOID:4680,breast metaplastic carcinoma
+UBERON:0006526,right lung alveolar system,UBERON:0000467,anatomical system
+UBERON:0005710,lower jaw incisor epithelium,UBERON:0010313,neural crest-derived structure
+UBERON:2001675,mesethmoid cornu,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009502,Absent epiphysis of the distal phalanx of the 2nd finger,HP:0010246,Absent epiphyses of the distal phalanges of the hand
+UBERON:0013528,Brodmann (1909) area 11,UBERON:0013529,Brodmann area
+DOID:9317,lymphangitis,DOID:75,lymphatic system disease
+HP:0009754,Fibrous syngnathia,HP:0006477,Abnormality of the alveolar ridges
+DOID:0060203,amyotrophic lateral sclerosis type 12,DOID:332,amyotrophic lateral sclerosis
+UBERON:0004271,outflow tract pericardium,UBERON:0002407,pericardium
+HP:0002183,Phonophobia,HP:0000708,Behavioural/Psychiatric Abnormality
+UBERON:0003330,submucosa of rectum,UBERON:0001208,submucosa of large intestine
+HP:0010560,Undulate clavicles,HP:0000889,Abnormality of the clavicles
+DOID:13664,post-vaccinal encephalitis,DOID:9588,encephalitis
+DOID:13313,pancreatic mucinous ductal ectasia,DOID:26,pancreas disease
+UBERON:2200947,dorsal fin proximal radial cartilage,UBERON:2201672,dorsal fin radial cartilage
+HP:0009570,Bullet-shaped middle phalanx of the 2nd finger,HP:0009845,Bullet-shaped middle phalanges of the hand
+UBERON:0004033,podocyte slit junction,UBERON:0006554,urinary system structure
+DOID:3145,hyperlipoproteinemia type III,DOID:1168,familial hyperlipidemia
+UBERON:0004743,coracoid bone,UBERON:0007829,pectoral girdle bone
+HP:0010246,Absent epiphyses of the distal phalanges of the hand,HP:0010243,Abnormality of the epiphyses of the distal phalanx of finger
+HP:0000246,Sinusitis,HP:0000245,Abnormality of the sinuses
+UBERON:0000004,olfactory apparatus,UBERON:0004121,ectoderm-derived structure
+DOID:8081,myxomatous pattern testicular yolk sac tumor,DOID:5344,testicular yolk sac tumor
+UBERON:0004008,cerebellar plate,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010056,Abnormality of the epiphyses of the hallux,HP:0001844,Abnormality of the hallux
+UBERON:0015420,ureteral valve,UBERON:0003978,valve
+HP:0007628,Mandibular condyle hypoplasia,HP:0005790,Short mandibular condyles
+UBERON:0015792,prostate gland dorsal lobe,UBERON:0001328,lobe of prostate
+CL:0000441,follicle stem cell,CL:0000036,epithelial fate stem cell
+HP:0010857,EEG with periodic abnormalities,HP:0011200,EEG with generalized polymorphic epileptiform discharges
+UBERON:0003251,temporal part of head,UBERON:0001444,subdivision of head
+UBERON:0006209,basioccipital cartilage element,UBERON:0003932,cartilage element of chondrocranium
+HP:0010926,Aculeiform cataract,HP:0100018,Nuclear cataract
+UBERON:0002270,hyaloid artery,UBERON:0001637,artery
+DOID:5677,extragonadal nonseminomatous germ cell tumor,DOID:4717,extragonadal germ cell cancer
+HP:0010385,Bullet-shaped phalanges of the 5th toe,HP:0010342,Abnormality of the phalanges of the 5th toe
+DOID:12171,radial neuropathy,DOID:1188,mononeuropathy
+HP:0002015,Dysphagia,HP:0002031,Abnormality of the esophagus
+HP:0009164,Abnormal calcification of the carpal bones,HP:0010660,Abnormal hand bone ossification
+DOID:0050633,ocular albinism,DOID:5614,eye disease
+HP:0011135,Aplasia/Hypoplasia of the sweat glands,HP:0000971,Abnormality of the sweat gland
+UBERON:0004173,medulla reticulospinal tract,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0006165,median dorsal digital artery for digit 1,UBERON:0006146,dorsal digital artery of manus
+HP:0010024,Epiphyseal stippling of the first metacarpal,HP:0010277,Stippling of the epiphyses of the proximal phalanges of the hand
+UBERON:0002559,medullary reticular formation,UBERON:0015827,brainstem reticular formation
+DOID:6950,combat disorder,DOID:6088,acute stress disorder
+UBERON:0003946,placenta labyrinth,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:2066,vulvar angiokeratoma,DOID:0060109,vulvar benign neoplasm
+UBERON:0010900,tarsometatarsus cartilage element,UBERON:0015064,autopod cartilage
+UBERON:2000068,proneural cluster,UBERON:0002050,embryonic structure
+UBERON:2001917,basibranchial 3 element,UBERON:0013746,basibranchial element
+DOID:8255,vulva fibroepithelial polyp,DOID:6873,skin tag
+DOID:9974,drug dependence,DOID:9973,substance dependence
+CL:0002227,nucleated secondary lens fiber,CL:0002225,secondary lens fiber
+HP:0000625,Cleft eyelid,HP:0000492,Abnormality of the eyelid
+UBERON:0014696,anterior choroidal artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001992,papillary layer of dermis,UBERON:0004120,mesoderm-derived structure
+UBERON:3010047,M. quadratus femoris,UBERON:0010890,pelvic complex muscle
+UBERON:0001654,supra-orbital vein,UBERON:0003502,neck blood vessel
+HP:0012660,Thalamic hypometabolism in FDG PET,HP:0012658,Abnormal brain FDG positron emission tomography
+HP:0001474,Sclerotic scapulae,HP:0000782,Abnormality of the scapula
+UBERON:0002585,central tegmental tract of midbrain,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009717,Cortical tubers,HP:0009731,Cerebral hamartomata
+UBERON:0013173,anterior part of tympanic bone,UBERON:0010313,neural crest-derived structure
+UBERON:2001468,anterior lateral line system,UBERON:0002540,lateral line system
+UBERON:0011203,urachus mesenchyme,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0001788,Premature rupture of membranes,HP:0001787,Abnormal delivery
+UBERON:2002074,external anterior process of basipterygium,UBERON:4100000,skeletal element projection
+UBERON:2105381,dorsal fin proximal radial element 4,UBERON:2100947,dorsal fin proximal radial element
+UBERON:0010677,manual digit 3 phalanx cartilage element,UBERON:0015027,manual digit 3 phalanx endochondral element
+UBERON:4300007,medial pelvic process,UBERON:4100000,skeletal element projection
+UBERON:0009648,eyelid subcutaneous connective tissue,UBERON:0004120,mesoderm-derived structure
+UBERON:2001054,lateral dorsal aorta,UBERON:0001637,artery
+HP:0010359,Aplasia/Hypoplasia of the phalanges of the 3rd toe,HP:0010173,Aplasia/Hypoplasia of the phalanges of the toes
+DOID:13628,favism,DOID:2862,glucosephosphate dehydrogenase deficiency
+UBERON:0005124,metanephric proximal convoluted tubule,UBERON:0001287,proximal convoluted tubule
+HP:0010568,Hamartoma of the eye,HP:0012372,Abnormal eye morphology
+UBERON:0013510,lumbar vertebra pre-cartilage condensation,UBERON:0011095,vertebra pre-cartilage condensation
+HP:0100455,Osteolytic defects of the proximal phalanx of the 3rd toe,HP:0010363,Osteolytic defects of the phalanges of the 3rd toe
+HP:0200128,Biventricular hypertrophy,HP:0001667,Right ventricular hypertrophy
+HP:0012241,Levator palpebrae superioris atrophy,HP:0008049,Abnormality of the extraocular muscles
+HP:0012474,Carotid artery occlusion,HP:0005344,Abnormality of the carotid arteries
+UBERON:0004382,epiphysis of humerus,UBERON:0001437,epiphysis
+HP:0100922,Sclerosis of the phalanges of the thumb,HP:0100899,Sclerosis of the phalanges of the hand
+UBERON:0004499,skeletal muscle tissue of tibialis anterior,UBERON:0001134,skeletal muscle tissue
+UBERON:0003109,parapophysis,UBERON:0001077,transverse process of vertebra
+HP:0012385,Camptodactyly,HP:0001371,Flexion contracture
+HP:0010708,1-5 finger syndactyly,HP:0006101,Finger syndactyly
+UBERON:0011314,anterior subdivision of masseter,UBERON:0004120,mesoderm-derived structure
+UBERON:0011798,tertial remex feather,UBERON:0011795,remex feather
+UBERON:0012520,forelimb epitrochlearis muscle,UBERON:0003662,forelimb muscle
+CL:0002436,mature CD4 single-positive thymocyte,CL:0000624,"CD4-positive, alpha-beta T cell"
+UBERON:0001162,cardia of stomach,UBERON:0009870,zone of stomach
+UBERON:0003843,dental epithelium,UBERON:0010371,ecto-epithelium
+HP:0010392,Abnormality of the distal phalanx of the 5th toe,HP:0010182,Abnormality of the distal phalanges of the toes
+UBERON:0004752,palatoquadrate cartilage,UBERON:0013765,digestive system organ
+CL:0002654,epithelial cell of stratum corneum of esophageal epithelium,CL:0002252,epithelial cell of esophagus
+UBERON:3000671,anterolateral process of hyoid plate,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0000453,decidua basalis,UBERON:0014404,female anatomical structure
+NCBITaxon:37020,Oryzomys palustris,NCBITaxon:29122,Oryzomys
+CL:0000810,"CD4-positive, alpha-beta thymocyte",CL:0000790,immature alpha-beta T cell
+UBERON:0008424,inguinal mammary gland,UBERON:0001911,mammary gland
+HP:0009192,Aplasia/Hypoplasia of the proximal phalanx of the 5th finger,HP:0009376,Aplasia/Hypoplasia of the phalanges of the 5th finger
+UBERON:2001269,regenerating fin/limb,UBERON:0004708,paired limb/fin
+UBERON:0014772,lateral palpebral artery,UBERON:0014770,palpebral artery
+UBERON:0005091,left horn of sinus venosus,UBERON:0002050,embryonic structure
+UBERON:4000173,pelvic fin lepidotrichium,UBERON:4440011,paired fin lepidotrichium
+HP:0008202,Prolactin deficiency,HP:0000830,Anterior hypopituitarism
+UBERON:0013744,wall of crypt of lieberkuhn of small intestine,UBERON:0013740,wall of crypt of lieberkuhn
+HP:0200138,Bilateral choanal atresia/stenosis,HP:0004502,Bilateral choanal atresia
+DOID:2698,nephrogenic adenofibroma,DOID:3116,kidney benign neoplasm
+DOID:10047,nodular malignant melanoma,DOID:8923,skin melanoma
+DOID:7696,lung hilum cancer,DOID:1324,lung cancer
+HP:0008283,Fasting hyperinsulinemia,HP:0000842,Hyperinsulinemia
+UBERON:0003498,heart blood vessel,UBERON:0003834,thoracic segment blood vessel
+DOID:1587,thrombocytopenia due to platelet alloimmunization,DOID:1588,thrombocytopenia
+UBERON:0006123,horizontal limb of the diagonal band,UBERON:0006125,subdivision of diagonal band
+HP:0003682,Variable progression rate,HP:0003679,Pace of progression
+UBERON:0003643,respiratory system arterial blood vessel,UBERON:0003504,respiratory system blood vessel
+UBERON:3010824,processus triangularis of palatoquadrate cartilage,UBERON:0004121,ectoderm-derived structure
+DOID:1928,Williams-Beuren syndrome,DOID:0080014,chromosomal disease
+UBERON:0006749,superior parathyroid gland,UBERON:0001132,parathyroid gland
+UBERON:0006935,crista ampullaris neuroepithelium,UBERON:0006932,vestibular epithelium
+UBERON:0007271,appendage musculature,UBERON:0001015,musculature
+DOID:6595,gastric tubular adenocarcinoma,DOID:3717,gastric adenocarcinoma
+UBERON:4200050,cotyla,UBERON:4100003,articular surface
+UBERON:2002150,vertebral element 10,UBERON:0010913,vertebral element
+UBERON:0007805,synsacrum,UBERON:0003828,abdominal segment bone
+HP:0010890,Morbus Osgood-Schlatter,HP:0100323,Juvenile aseptic necrosis
+UBERON:0001549,dorsal metatarsal vein,UBERON:0004261,lower leg blood vessel
+HP:0009989,Duplication of the middle phalanx of the 5th finger,HP:0009985,Duplication of phalanx of 5th finger
+CL:0005001,iridoblast,CL:0000055,non-terminally differentiated cell
+UBERON:2001232,pharyngeal arch 5 skeleton,UBERON:0010912,subdivision of skeleton
+HP:0010632,Total anosmia,HP:0000458,Anosmia
+UBERON:2005013,concurrent branch afferent branchial artery,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0001575,Mood changes,HP:0100852,Abnormal fear/anxiety-related behavior
+DOID:4297,scimitar syndrome,DOID:1682,congenital heart disease
+UBERON:4200060,ectepicondylar foramen,UBERON:0005744,bone foramen
+UBERON:0011968,radio-carpal joint,UBERON:0001491,wrist joint
+HP:0005019,Diaphyseal thickening,HP:0000940,Abnormal diaphysis morphology
+DOID:7482,petrous apex meningioma,DOID:3565,meningioma
+UBERON:0011238,mesethmoid bone,UBERON:0002513,endochondral bone
+DOID:1293,labia minora carcinoma,DOID:1294,vulva carcinoma
+DOID:10330,slate pneumoconiosis,DOID:10316,pneumoconiosis
+UBERON:0014862,trochophore stage,UBERON:0000069,larval stage
+UBERON:0000126,cranial nerve nucleus,UBERON:0002308,nucleus of brain
+UBERON:0010367,conjunctival vein,UBERON:0004121,ectoderm-derived structure
+HP:0007757,Hypoplasia of choroid,HP:0001122,Aplasia/Hypoplasia of the choroid
+HP:0004414,Abnormality of the pulmonary artery,HP:0004930,Abnormality of the pulmonary vasculature
+UBERON:0003606,limb long bone,UBERON:0002428,limb bone
+DOID:10793,chronic sphenoidal sinusitis,DOID:10794,sphenoid sinusitis
+UBERON:0006876,vasculature of organ,UBERON:0002049,vasculature
+UBERON:0009974,lumen of Rathke's pouch,UBERON:0007473,lumen of epithelial sac
+DOID:4660,indolent systemic mastocytosis,DOID:349,systemic mastocytosis
+HP:0004227,Short distal phalanx of the 5th finger,HP:0009237,Short 5th finger
+DOID:14350,suppurative thyroiditis,DOID:7166,thyroiditis
+HP:0011272,Underdeveloped tragus,HP:0009913,Aplasia/Hypoplasia of the tragus
+DOID:12997,Phlegmonous dacryocystitis,DOID:9938,dacryocystitis
+HP:0004263,Large capitate bone,HP:0004262,Abnormality of the capitate bone
+UBERON:0010309,palpebral bone,UBERON:0003462,facial bone
+DOID:3304,germinoma,DOID:2994,germ cell cancer
+HP:0011637,Anomalous origin of coronary artery from the pulmonary artery,HP:0011636,Abnormal origin of the coronary arteries
+CL:0000954,small pre-B-II cell,CL:0000955,pre-B-II cell
+DOID:14275,atrophic vulva,DOID:2059,vulvar disease
+UBERON:0010586,manual digit phalanx pre-cartilage condensation,UBERON:0010884,forelimb bone pre-cartilage condensation
+UBERON:0006535,skin fluid/secretion,UBERON:0000463,portion of organism substance
+HP:0003329,Hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes,HP:0003328,Abnormal hair laboratory examination
+UBERON:3010599,stratum spongiosum,UBERON:0002067,dermis
+UBERON:0008778,epaxial musclulature,UBERON:0004120,mesoderm-derived structure
+UBERON:0002367,prostate gland,UBERON:0010147,male accessory sex gland
+DOID:5230,hepatoerythropoietic porphyria,DOID:3133,acute porphyria
+UBERON:0005746,primary vitreous humour,UBERON:0010312,immature eye
+HP:0100203,Bracket epiphysis of the distal phalanx of the 5th toe,HP:0100078,Bracket epiphyses of the 5th toe
+HP:0003254,Abnormality of DNA repair,HP:0011017,Abnormality of cell physiology
+UBERON:0010939,zygomaticomandibularis muscle,UBERON:0004120,mesoderm-derived structure
+NCBITaxon:194440,Primate T-lymphotropic virus 1,NCBITaxon:153136,Deltaretrovirus
+UBERON:0011183,corpus spongiosum of penis,UBERON:0014403,male anatomical structure
+HP:0100499,Tibial deviation of toes,HP:0100498,Deviation of toes
+UBERON:2000891,hypaxial region somite 1,UBERON:0003895,hypaxial myotome region
+HP:0002376,Developmental regression,HP:0100543,Cognitive impairment
+UBERON:0010376,pancreas ventral primordium,UBERON:0001048,primordium
+DOID:1933,Rubinstein-Taybi syndrome,DOID:0050736,autosomal dominant disease
+DOID:11752,acute endophthalmitis,DOID:9724,purulent endophthalmitis
+UBERON:0002016,pulmonary vein,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0003490,Defective dehydrogenation of isovaleryl CoA and butyryl CoA,HP:0004359,Abnormality of fatty-acid metabolism
+HP:0100401,Duplication of the middle phalanx of the 3rd toe,HP:0010367,Duplication of phalanx of the 3rd toe
+HP:0009105,Abnormal ossification of the pubic bone,HP:0003172,Abnormality of the pubic bones
+UBERON:0000035,primary ovarian follicle,UBERON:0001305,ovarian follicle
+UBERON:0005687,orbitosphenoid cartilage element,UBERON:0014387,mesenchyme derived from neural crest
+DOID:0050917,lung combined type small cell adenocarcinoma,DOID:5421,lung combined type small cell carcinoma
+UBERON:4300035,supraneural element,UBERON:0004120,mesoderm-derived structure
+CL:0000142,hyalocyte,CL:0000499,stromal cell
+HP:0011653,Double outlet right ventricle with non-committed ventricular septal defect and pulmonary stenosis,HP:0001719,Double outlet right ventricle
+UBERON:2000836,sclerotome somite 30,UBERON:0003089,sclerotome
+UBERON:0002256,dorsal horn of spinal cord,UBERON:0001948,regional part of spinal cord
+HP:0001233,2-3 finger syndactyly,HP:0006101,Finger syndactyly
+NCBITaxon:426441,Amblyomminae,NCBITaxon:6939,Ixodidae
+DOID:11354,stone in bladder diverticulum,DOID:11353,bladder diverticulum
+DOID:3225,tracheal disease,DOID:974,upper respiratory tract disease
+DOID:2780,rectosigmoid junction neoplasm,DOID:1896,sigmoid neoplasm
+UBERON:0001774,muscle of trunk,UBERON:0001630,muscle organ
+HP:0100734,Abnormality of the vertebral epiphyses,HP:0003468,Abnormality of the vertebrae
+HP:0002688,Absent frontal sinuses,HP:0009119,Aplasia/Hypoplasia of the frontal sinuses
+HP:0006335,Persistence of primary teeth,HP:0006481,Abnormality of primary teeth
+HP:0005925,Abnormalities of the diaphyses of the hand,HP:0001155,Abnormality of the hand
+DOID:1634,breast papillomatosis,DOID:0060082,breast benign neoplasm
+HP:0011004,Abnormality of the systemic arterial tree,HP:0002597,Abnormality of the vasculature
+DOID:10600,chronic tic disorder,DOID:2769,tic disorder
+UBERON:0003433,arm nerve,UBERON:0003441,forelimb nerve
+UBERON:0013648,masseteric artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0003564,Folate-dependent fragile site at Xq28,HP:0003220,Abnormality of chromosome stability
+UBERON:0004825,dental lamina,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0006253,Swelling of proximal interphalangeal joints,HP:0006261,Abnormality of phalangeal joints of the hand
+UBERON:0005205,vagina stroma,UBERON:0003891,stroma
+CL:0002266,type D cell of small intestine,CL:1001516,intestinal enteroendocrine cell
+UBERON:0015068,distal carpal endochondral element,UBERON:0015049,carpus endochondral element
+UBERON:0015035,pedal digit 5 phalanx endochondral element,UBERON:0015030,pedal digit phalanx endochondral element
+HP:0005344,Abnormality of the carotid arteries,HP:0011004,Abnormality of the systemic arterial tree
+UBERON:3000509,processus suprafenestralis,UBERON:0010313,neural crest-derived structure
+UBERON:2000226,lateral ethmoid bone,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100120,Stippling of the epiphysis of the middle phalanx of the 2nd toe,HP:0100089,Abnormality of the epiphysis of the middle phalanx of the 2nd toe
+DOID:4209,brainstem intraparenchymal clear cell meningioma,DOID:4211,posterior cranial fossa meningioma
+CL:0002649,epithelial cell of gingival part of viscerocranial mucosa,CL:0002283,ecto-epithelial cell of viscerocranial mucosa
+HP:0006870,Lobar holoprosencephaly,HP:0001360,Holoprosencephaly
+CL:0002253,epithelial cell of large intestine,CL:0002563,intestinal epithelial cell
+DOID:0050331,LADD syndrome,DOID:0050736,autosomal dominant disease
+UBERON:3000405,pars inferior of labyrinth,UBERON:0000064,organ part
+UBERON:0003586,trunk connective tissue,UBERON:0002384,connective tissue
+UBERON:0004340,allantois,UBERON:0005631,extraembryonic membrane
+UBERON:2000269,inferior ventral flexor,UBERON:0000366,flexor muscle
+DOID:12927,screw worm infectious disease,DOID:11080,myiasis
+HP:0005579,Impaired reabsorption of chloride,HP:0011038,Abnormality of renal resorption
+DOID:6858,pineal region immature teratoma,DOID:6856,pineal region teratoma
+UBERON:0002014,inferior hypogastric nerve plexus,UBERON:0001816,autonomic nerve plexus
+UBERON:0009776,intermediate reticular formation,UBERON:0003528,brain grey matter
+UBERON:0004331,proximal phalanx of manual digit 5,UBERON:0002234,proximal phalanx of manus
+HP:0006391,Overtubulated long bones,HP:0011314,Abnormality of long bone morphology
+DOID:6278,ovarian mucinous malignant adenofibroma,DOID:4422,malignant adenofibroma
+CL:0002032,hematopoietic oligopotent progenitor cell,CL:0008001,hematopoietic precursor cell
+CL:0000417,endopolyploid cell,CL:0000412,polyploid cell
+UBERON:0001883,olfactory tubercle,UBERON:0005401,cerebral hemisphere grey matter
+UBERON:0003224,chorion syncytiotrophoblast,UBERON:0000478,extraembryonic structure
+HP:0001460,Aplasia/Hypoplasia involving the musculature,HP:0011805,Abnormality of muscle morphology
+UBERON:0001273,ilium,UBERON:0015212,lateral structure
+CL:1001516,intestinal enteroendocrine cell,CL:0000164,enteroendocrine cell
+UBERON:0000154,posterior region of body,UBERON:0000475,organism subdivision
+CL:0000703,sustentacular cell,CL:0000630,supportive cell
+HP:0002180,Neurodegeneration,HP:0007367,Atrophy/Degeneration affecting the central nervous system
+HP:0001059,Pterygium,HP:0011356,Regional abnormality of skin
+CL:1000703,kidney pelvis urothelial cell,CL:1000505,kidney pelvis cell
+HP:0009071,Inflammatory myopathy,HP:0003198,Myopathy
+NCBITaxon:10407,Hepatitis B virus,NCBITaxon:10405,Orthohepadnavirus
+HP:0010963,Absence of stomach bubble on fetal sonography,HP:0011425,Fetal ultrasound soft marker
+HP:0003155,Elevated alkaline phosphatase,HP:0004379,Abnormality of alkaline phosphatase activity
+HP:0011956,Intestinal lymphoid nodular  hyperplasia,HP:0002242,Abnormality of the intestine
+HP:0001436,Abnormality of the foot musculature,HP:0001437,Abnormality of the musculature of the lower limbs
+DOID:13717,mature cataract,DOID:9669,senile cataract
+UBERON:0011272,embryonic skin basal layer,UBERON:0010371,ecto-epithelium
+HP:0003107,Abnormality of cholesterol metabolism,HP:0003119,Abnormality of lipid metabolism
+UBERON:0006725,spiral ligament,UBERON:0004121,ectoderm-derived structure
+HP:0003895,Flattened humeral epiphyses,HP:0003891,Abnormality of the humeral epiphysis
+UBERON:0003716,recurrent laryngeal nerve,UBERON:0002003,peripheral nerve
+HP:0009294,Absent middle phalanx of 4th finger,HP:0009299,Aplasia/Hypoplasia of the middle phalanx of the 4th finger
+DOID:2155,malignant ovarian germ cell neoplasm,DOID:2156,ovarian germ cell cancer
+CL:0000736,embryonic gland hemocyte,CL:0000387,hemocyte (sensu Nematoda and Protostomia)
+HP:0008045,Enlarged flash visual evoked potentials,HP:0007928,Abnormal flash visual evoked potentials
+HP:0011227,Elevated C-reactive protein level,HP:0010876,Abnormality of circulating protein level
+UBERON:0006259,lens pit,UBERON:0010312,immature eye
+UBERON:0002299,alveolus of lung,UBERON:0004119,endoderm-derived structure
+HP:0010296,Ankyloglossia,HP:0000190,Abnormality of oral frenula
+UBERON:0000982,skeletal joint,UBERON:0004905,articulation
+UBERON:0001658,middle temporal vein,UBERON:0003502,neck blood vessel
+HP:0100189,Stippling of the epiphysis of the middle phalanx of the 4th toe,HP:0100095,Abnormality of the epiphysis of the middle phalanx of the 4th toe
+UBERON:0013695,colon endothelium,UBERON:0001986,endothelium
+HP:0002575,Tracheoesophageal fistula,HP:0002031,Abnormality of the esophagus
+UBERON:4200010,ventral humeral ridge,UBERON:0004530,bony projection
+UBERON:0003342,mucosa of anal canal,UBERON:0004121,ectoderm-derived structure
+UBERON:0006065,hemal arch,UBERON:0004247,bone of dorsum
+UBERON:0014849,hemotrichorial placental membrane,UBERON:0009002,placental membrane
+UBERON:2002073,distal cartilage of middle anterior process of basipterygium,UBERON:0004120,mesoderm-derived structure
+DOID:13209,right bundle branch block,DOID:10273,heart conduction disease
+UBERON:0004940,submucosa of common hepatic duct,UBERON:0004938,submucosa of biliary tree
+HP:0003920,Sloping humeral metaphysis,HP:0003907,Abnormality of the humeral metaphyses
+HP:0011858,Reduced factor IX activity,HP:0010989,Abnormality of the intrinsic pathway
+HP:0000066,Labial hypoplasia,HP:0003241,Genital hypoplasia
+HP:0003841,Fragmented epiphyses of the upper limbs,HP:0003839,Abnormality involving the epiphyses of the upper limbs
+HP:0006413,Broad tibial metaphyses,HP:0006491,Abnormality of the tibial metaphysis
+HP:0100057,Cone-shaped epiphyses of the 3rd toe,HP:0010164,Cone-shaped epiphyses of the toes
+HP:0001440,Synostosis involving metatarsal bones,HP:0001832,Abnormality of the metatarsal bones
+DOID:0050725,tyrosinemia type II,DOID:9275,tyrosinemia
+UBERON:3010560,anterior process of the palatoquadrate,UBERON:0004530,bony projection
+CL:0000900,"naive thymus-derived CD8-positive, alpha-beta T cell",CL:0000898,naive T cell
+HP:0011535,Abnormal atrial arrangement,HP:0011534,Abnormal spatial orientation of the cardiac segments
+CL:1001434,olfactory bulb interneuron,CL:0000101,sensory neuron
+UBERON:0002097,skin of body,UBERON:0004121,ectoderm-derived structure
+HP:0007129,Cerebellar medulloblastoma,HP:0002885,Medulloblastoma
+UBERON:3000909,sulcus proximalis ossis cruris,UBERON:0000064,organ part
+UBERON:2005098,central ray artery,UBERON:0007304,appendage vasculature
+HP:0002530,Axial dystonia,HP:0001332,Dystonia
+UBERON:0014510,omasal lamina,UBERON:0004923,organ component layer
+UBERON:0006755,inferior parathyroid gland,UBERON:0015212,lateral structure
+DOID:3144,cutis laxa,DOID:37,skin disease
+UBERON:0004182,mammary gland cord,UBERON:0005154,epithelial cord
+HP:0006527,Lymphoid interstitial pneumonia,HP:0006530,Interstitial pulmonary disease
+DOID:11266,hemorrhagic fever with renal syndrome,DOID:37,skin disease
+HP:0100356,Contractures of the metatarsophalangeal joint of the 2nd toe,HP:0010327,Flexion contracture of the 2nd toe
+HP:0003121,Limb joint contracture,HP:0001371,Flexion contracture
+UBERON:0005989,atrioventricular septum,UBERON:0010313,neural crest-derived structure
+HP:0000282,Facial edema,HP:0000969,Edema
+DOID:162,cancer,DOID:14566,disease of cellular proliferation
+DOID:11312,Mobitz type II atrioventricular block,DOID:0050822,second-degree atrioventricular block
+CL:0002161,superficial external epithelial cell of tympanic membrane,CL:0002158,external epithelial cell of tympanic membrane
+UBERON:0003698,subtalar joint,UBERON:0008447,intertarsal joint
+UBERON:2002248,supratemporal commissure,UBERON:1500003,lateral line canal lumen
+UBERON:0010347,6th arch mesenchyme from head mesenchyme,UBERON:0010031,6th arch mesenchyme
+UBERON:0002766,fusiform gyrus,UBERON:0000200,gyrus
+UBERON:0011342,surface of mandible,UBERON:0006984,anatomical surface
+UBERON:0014916,velar vocal fold,UBERON:0015212,lateral structure
+UBERON:0015049,carpus endochondral element,UBERON:0015021,forelimb endochondral element
+CL:1001036,vasa recta cell,CL:0002543,vein endothelial cell
+UBERON:2000397,nucleus subglomerulosis,UBERON:0006569,diencephalic nucleus
+UBERON:4200182,lateral tubercle of astragalus,UBERON:0004120,mesoderm-derived structure
+UBERON:0015069,distal carpal cartilage,UBERON:0015064,autopod cartilage
+CL:0000678,commissural neuron,CL:0000540,neuron
+UBERON:2205373,dorsal fin distal radial cartilage 2,UBERON:2200936,dorsal fin distal radial cartilage
+UBERON:0001938,lateral mammillary nucleus,UBERON:0006568,hypothalamic nucleus
+HP:0008094,Widely spaced toes,HP:0001780,Abnormality of toe
+HP:0009690,Fragmentation of the epiphyses of the thumb,HP:0010232,Fragmentation of the epiphyses of the phalanges of the hand
+UBERON:2001762,pectoral fin lepidotrichium 2,UBERON:4000175,pectoral fin lepidotrichium
+DOID:11372,megacolon,DOID:5353,colonic disease
+CL:0000193,cardiac muscle cell (sensu Arthopoda),CL:0000746,cardiac muscle cell
+UBERON:0000101,lobe of lung,UBERON:0004119,endoderm-derived structure
+HP:0100065,Triangular epiphyses of the 3rd toe,HP:0010329,Abnormality of the epiphyses of the 3rd toe
+HP:0007958,Optic atrophy from cranial nerve compression,HP:0001293,Cranial nerve compression
+UBERON:0005003,mucosa of left hepatic duct,UBERON:0004999,mucosa of biliary tree
+UBERON:0003636,manual digit 2 phalanx,UBERON:0015026,manual digit 2 phalanx endochondral element
+CL:0000931,activated type II NK T cell,CL:0000912,helper T cell
+DOID:6364,migraine,DOID:936,brain disease
+CL:0000914,immature NK T cell,CL:0000790,immature alpha-beta T cell
+UBERON:0003383,cardiac muscle of interventricular septum,UBERON:0004667,interventricular septum muscular part
+DOID:3083,chronic obstructive pulmonary disease,DOID:2320,obstructive lung disease
+HP:0003231,Hypertyrosinemia,HP:0010917,Abnormality of tyrosine metabolism
+UBERON:0005922,inferior nasal concha,UBERON:0001762,nasal concha
+HP:0007456,Progressive reticulate hyperpigmentation,HP:0007400,Irregular hyperpigmentation
+UBERON:0004561,proper palmar digital vein,UBERON:0004563,forelimb digital vein
+HP:0006903,Congenital peripheral neuropathy,HP:0009830,Peripheral neuropathy
+DOID:10607,tropical sprue,DOID:5295,intestinal disease
+HP:0010068,Broad first metatarsal,HP:0010054,Abnormality of the first metatarsal
+DOID:436,posterior mediastinum cancer,DOID:5559,mediastinal cancer
+DOID:3021,acute kidney failure,DOID:1074,kidney failure
+HP:0008963,Tibialis muscle weakness,HP:0009053,Distal lower limb muscle weakness
+UBERON:0006761,corneo-scleral junction,UBERON:0007651,anatomical junction
+HP:0008078,Thin metatarsal cortices,HP:0001832,Abnormality of the metatarsal bones
+UBERON:0004295,sympathetic nerve trunk,UBERON:0002464,nerve trunk
+UBERON:0007105,vitelline duct,UBERON:0000025,tube
+HP:0010498,Bipartite patella,HP:0003045,Abnormality of the patella
+UBERON:0009773,renal tubule,UBERON:0006555,excretory tube
+UBERON:0000997,mammalian vulva,UBERON:0000062,organ
+HP:0100918,Sclerosis of the phalanges of the 2nd finger,HP:0009541,Abnormality of the phalanges of the 2nd finger
+UBERON:0000920,egg chorion,UBERON:0000476,acellular anatomical structure
+UBERON:0001697,orbital region,UBERON:0010313,neural crest-derived structure
+UBERON:2000528,interradialis,UBERON:0001630,muscle organ
+UBERON:0004353,female inguinal canal,UBERON:0003702,inguinal canal
+NCBITaxon:639021,Magnaporthales,NCBITaxon:222544,Sordariomycetidae
+HP:0009629,Aplasia/Hypoplasia of the proximal phalanx of the thumb,HP:0009618,Abnormality of the proximal phalanx of the thumb
+UBERON:0001728,nasopharynx,UBERON:0000477,anatomical cluster
+UBERON:2002020,hypomaxilla,UBERON:0011597,bone of upper jaw
+CL:0000801,gamma-delta intraepithelial T cell,CL:0000800,mature gamma-delta T cell
+UBERON:0004742,dentary,UBERON:0004768,bone of lower jaw
+UBERON:3000646,margo libera,UBERON:0004120,mesoderm-derived structure
+UBERON:0003492,bronchus reticular lamina,UBERON:0004119,endoderm-derived structure
+UBERON:2001393,parapophysis 2,UBERON:0003109,parapophysis
+UBERON:0005904,duct of male reproductive system,UBERON:0000058,duct
+UBERON:0004803,penis epithelium,UBERON:0005156,reproductive structure
+HP:0004247,Small scaphoid,HP:0001498,Carpal bone hypoplasia
+UBERON:0004911,epithelium of female gonad,UBERON:0004909,epithelium of gonad
+UBERON:0007497,developing epithelial placode,UBERON:0001048,primordium
+CL:1000454,kidney collecting duct epithelial cell,CL:1000449,epithelial cell of nephron
+UBERON:4300018,ventral marginal cartilage,UBERON:0007844,cartilage element
+UBERON:0005329,mesonephric nephron tubule,UBERON:0000083,mesonephric tubule
+UBERON:0015005,vertebra endochondral element,UBERON:0004120,mesoderm-derived structure
+HP:0000463,Anteverted nares,HP:0005288,Abnormality of the nares
+CL:0000973,IgA memory B cell,CL:0000972,class switched memory B cell
+UBERON:0007826,peritoneal mesentery,UBERON:0002095,mesentery
+UBERON:0002605,precentral operculum,UBERON:0000477,anatomical cluster
+NCBITaxon:716546,leotiomyceta,NCBITaxon:147538,Pezizomycotina
+UBERON:0008203,pelvic cavity,UBERON:0002553,anatomical cavity
+CL:1001142,arcuate vein cell,CL:1001052,kidney cortex vein cell
+UBERON:0013155,1st arch mandibular ectoderm,UBERON:0005291,embryonic tissue
+UBERON:0006456,eighth thoracic spinal cord segment,UBERON:0007715,thoracic subsegment of spinal cord
+CL:0002539,aortic smooth muscle cell,CL:0000359,vascular associated smooth muscle cell
+NCBITaxon:489714,Microsporum gypseum,NCBITaxon:63402,Arthroderma gypseum
+UBERON:0013613,tooth cingulum,UBERON:0004121,ectoderm-derived structure
+HP:0004375,Neoplasm of the nervous system,HP:0000707,Abnormality of the nervous system
+DOID:3710,bladder colloid adenocarcinoma,DOID:3711,bladder adenocarcinoma
+HP:0004966,Medial calcification of large arteries,HP:0012456,Medial arterial calcification
+UBERON:2001055,pronephric duct opening,UBERON:0000464,anatomical space
+UBERON:2205380,dorsal fin proximal radial cartilage 3,UBERON:2105380,dorsal fin proximal radial element 3
+DOID:3616,angiolipoma,DOID:3315,lipoma
+HP:0009205,Cone-shaped epiphysis of the middle phalanx of the 5th finger,HP:0010259,Cone-shaped epiphyses of the middle phalanges of the hand
+UBERON:0011139,synovial limb joint,UBERON:0003657,limb joint
+HP:0003355,Aminoaciduria,HP:0012072,Aciduria
+UBERON:2005115,primary posterior lateral line primordium,UBERON:2001157,posterior lateral line primordium
+UBERON:0010194,hepatic portal system,UBERON:0005806,portal system
+UBERON:0005523,rhombomere 7,UBERON:0001892,rhombomere
+UBERON:0008891,external gill,UBERON:0003102,surface structure
+HP:0010237,Epiphyseal stippling of finger phalanges,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+HP:0009422,Broad distal phalanx of the 3rd finger,HP:0009440,Broad phalanges of the 3rd finger
+NCBITaxon:786,Rickettsia akari,NCBITaxon:114277,spotted fever group
+UBERON:3000865,epileon,UBERON:0004120,mesoderm-derived structure
+DOID:4270,encephalitozoonosis,DOID:4271,microsporidiosis
+HP:0009506,Fragmentation of the epiphysis of the distal phalanx of the 2nd finger,HP:0009499,Abnormality of the epiphysis of the distal phalanx of the 2nd finger
+UBERON:0007728,interphalangeal joint of pedal digit 5,UBERON:0007721,interphalangeal joint of pes
+UBERON:2001357,alar plate midbrain,UBERON:0000479,tissue
+DOID:1756,facial nerve disease,DOID:5656,cranial nerve disease
+UBERON:0001534,right subclavian artery,UBERON:0001533,subclavian artery
+CL:1000419,myoepithelial cell of lactiferous duct,CL:0000068,duct epithelial cell
+UBERON:0002609,spinothalamic tract of midbrain,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0012284,Small proximal tibial epiphyses,HP:0010591,Abnormality of the proximal tibial epiphysis
+DOID:3381,liposarcoma of bone,DOID:3382,liposarcoma
+DOID:5137,pericardium leiomyoma,DOID:127,leiomyoma
+UBERON:0015224,interventricular foramen intermedium,UBERON:0004120,mesoderm-derived structure
+DOID:9799,eye degenerative disease,DOID:5614,eye disease
+HP:0002617,Aneurysm,HP:0002597,Abnormality of the vasculature
+DOID:9954,null-cell leukemia,DOID:9952,acute lymphocytic leukemia
+UBERON:0002906,anterior occipital sulcus,UBERON:0008334,subarachnoid sulcus
+UBERON:3000380,palatoquadrate articular process,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:5704,Sclerosing liposarcoma,DOID:5690,atypical lipomatous tumor
+HP:0007029,Cerebral berry aneurysm,HP:0004944,Cerebral aneurysm
+UBERON:0006653,glans clitoris,UBERON:0014404,female anatomical structure
+DOID:9936,chronic canaliculitis,DOID:9935,chronic inflammation of lacrimal passage
+HP:0100650,Vaginal neoplasm,HP:0010787,Genital neoplasm
+DOID:3962,follicular thyroid carcinoma,DOID:3963,thyroid carcinoma
+UBERON:2001051,caudal division of the internal carotid artery,UBERON:0004573,systemic artery
+HP:0002942,Thoracic kyphosis,HP:0100711,Abnormality of the thoracic spine
+UBERON:0004468,set of muscles of vertebral column,UBERON:0001015,musculature
+UBERON:0011203,urachus mesenchyme,UBERON:0007524,dense mesenchyme tissue
+UBERON:0007715,thoracic subsegment of spinal cord,UBERON:0003038,thoracic spinal cord
+UBERON:0000054,macula,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0014525,subdivision of internal capsule,UBERON:0002437,cerebral hemisphere white matter
+UBERON:0015472,tracheobronchial lymph node,UBERON:0007644,thoracic lymph node
+UBERON:0006374,part of afferent arteriole forming the juxtaglomerular complex,UBERON:0004120,mesoderm-derived structure
+HP:0011009,Acute,HP:0011008,Speed of onset
+UBERON:0015088,distal carpal bone 2 cartilage,UBERON:0015087,distal carpal bone 2 endochondral element
+UBERON:0003959,rete testis,UBERON:0004111,anatomical conduit
+DOID:4889,lymph node tuberculosis,DOID:0050598,extrapulmonary tuberculosis
+HP:0009213,Triangular epiphysis of the middle phalanx of the 5th finger,HP:0004224,Abnormality of the epiphysis of the middle phalanx of the 5th finger
+DOID:13282,intestinal tuberculosis,DOID:404,gastrointestinal tuberculosis
+DOID:2312,nocardiosis,DOID:0050340,opportunistic bacterial infectious disease
+UBERON:2005367,dorsal fin pterygiophore 4,UBERON:2001419,dorsal fin pterygiophore
+NCBITaxon:138948,Human enterovirus A,NCBITaxon:12059,Enterovirus
+HP:0011678,Tetralogy of Fallot with pulmonary atresia and major aortopulmonary collateral arteries,HP:0012516,Tetralogy of Fallot with pulmonary atresia
+HP:0100076,Triangular epiphyses of the 4th toe,HP:0010172,Triangular epiphyses of the toes
+UBERON:0006294,stapes pre-cartilage condensation,UBERON:0015016,stapes endochondral element
+HP:0010978,Abnormality of immune system physiology,HP:0002715,Abnormality of the immune system
+UBERON:0000486,multilaminar epithelium,UBERON:0000483,epithelium
+UBERON:0008896,post-hyoid pharyngeal arch,UBERON:0002539,pharyngeal arch
+NCBITaxon:2759,Eukaryota,NCBITaxon:131567,cellular organisms
+HP:0010056,Abnormality of the epiphyses of the hallux,HP:0010160,Abnormality of the epiphyses of the toes
+CL:0002575,central nervous system pericyte,CL:0000669,pericyte cell
+HP:0100678,Premature skin wrinkling,HP:0011121,Abnormality of skin morphology
+DOID:12528,lesion of sciatic nerve,DOID:9473,mononeuritis of lower limb
+HP:0011370,Recurrent cutaneous fungal infections,HP:0001581,Recurrent skin infections
+HP:0100333,Unilateral cleft lip,HP:0100335,Non-midline cleft lip
+UBERON:0010367,conjunctival vein,UBERON:0009141,craniocervical region vein
+UBERON:0005620,primary palate,UBERON:0007375,roof of mouth
+UBERON:0005327,mesonephric glomerular epithelium,UBERON:0004188,glomerular epithelium
+HP:0011828,Midline sinus of philtrum,HP:0000288,Abnormality of the philtrum
+UBERON:0010499,pseudostratified ciliated columnar epithelium,UBERON:0007592,ciliated columnar epithelium
+HP:0003850,Irregular metaphyses of the upper limbs,HP:0003025,Metaphyseal irregularity
+DOID:2113,coccidiosis,DOID:2789,parasitic protozoa infectious disease
+DOID:11486,Horner's syndrome,DOID:11504,autonomic neuropathy
+UBERON:0002347,thoracic vertebra,UBERON:0004247,bone of dorsum
+UBERON:0010162,post-anal tail tip,UBERON:0000479,tissue
+HP:0009632,Curved proximal phalanx of the thumb,HP:0009846,Curved middle phalanges of the hand
+UBERON:0002276,lamina of spiral limbus,UBERON:0000064,organ part
+UBERON:0016390,auricular lymph node,UBERON:0000029,lymph node
+UBERON:0004661,mandible temporal crest,UBERON:0010313,neural crest-derived structure
+CL:0002609,neuron of cerebral cortex,CL:0010012,cerebral cortex neuron
+UBERON:0003300,roof plate of telencephalon,UBERON:0003298,roof plate of neural tube
+HP:0009849,Symphalangism of middle phalanx of finger,HP:0009833,Abnormality of the middle phalanges of the hand
+DOID:9547,non-secretory myeloma,DOID:9538,multiple myeloma
+UBERON:0005604,hepatic duct extrahepatic part,UBERON:0004822,extrahepatic bile duct epithelium
+UBERON:0014904,intersegmental pulmonary vein,UBERON:0002016,pulmonary vein
+UBERON:0013737,paranigral nucleus,UBERON:0002438,ventral tegmental nucleus
+HP:0100480,Proximal/middle symphalangism of 3rd toe,HP:0100237,Proximal symphalangism (feet)
+DOID:5030,pineal parenchymal tumor of intermediate differentiation,DOID:1664,pineoblastoma
+UBERON:3000367,otic ramus of squamosal,UBERON:0004120,mesoderm-derived structure
+CL:0001018,immature CD8_alpha-low Langerhans cell,CL:0001015,CD8_alpha-low Langerhans cell
+DOID:3827,congenital diaphragmatic hernia,DOID:10481,diaphragm disease
+HP:0100268,Upper lip pit,HP:0000177,Abnormality of upper lip
+UBERON:3000012,angulosplenial coronoid process,UBERON:0010313,neural crest-derived structure
+DOID:1891,optic nerve disease,DOID:5656,cranial nerve disease
+HP:0000490,Deeply set eye,HP:0100886,Abnormality of globe location
+UBERON:2001672,dorsal fin radial bone,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0005987,Multinodular goiter,HP:0005994,Nodular goiter
+HP:0001025,Urticaria,HP:0011276,Vascular skin abnormality
+HP:0001604,Vocal cord paresis,HP:0001609,Hoarse voice
+UBERON:0010582,pedal digit 3 phalanx pre-cartilage condensation,UBERON:0005697,pedal digit 3 mesenchyme
+HP:0009478,Symphalangism of the proximal phalanx of the 4th finger with the 4th metatcarpal,HP:0009707,Synostosis involving the 4th metacarpal
+HP:0007015,Poor gross motor coordination,HP:0002275,Poor motor coordination
+UBERON:0003904,bursal plica,UBERON:0000064,organ part
+HP:0009183,Joint contractures of the 5th finger,HP:0100490,Camptodactyly of finger
+UBERON:0010933,orbicularis oris muscle,UBERON:0001577,facial nerve muscle
+DOID:5524,adenoid squamous cell carcinoma,DOID:37,skin disease
+CL:0002658,glandular cell of the large intestine,CL:0002253,epithelial cell of large intestine
+UBERON:0004775,outer renal medulla vasa recta,UBERON:0014401,renal venous blood vessel
+UBERON:2000592,superficial pelvic adductor,UBERON:0011145,adductor muscle
+DOID:9246,cerebral amyloid angiopathy,DOID:9120,amyloidosis
+HP:0010423,Partial duplication of the proximal phalanx of the 2nd toe,HP:0010428,Partial duplication of phalanx of the 2nd toe
+UBERON:0003431,leg nerve,UBERON:0003442,hindlimb nerve
+UBERON:2001940,vertebra 4-vertebra 5 joint,UBERON:0000982,skeletal joint
+UBERON:3000831,spina acromioidea,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001707,nasal cavity,UBERON:0002553,anatomical cavity
+DOID:2942,bronchiolitis,DOID:850,lung disease
+NCBITaxon:11652,Primate lentivirus group,NCBITaxon:11646,Lentivirus
+UBERON:4300087,mesopterygium bone,UBERON:2001587,pectoral fin proximal radial bone
+UBERON:0005931,primary choana,UBERON:0005423,developing anatomical structure
+HP:0005957,Breathing dysregulation,HP:0002795,Functional respiratory abnormality
+HP:0000022,Abnormality of male internal genitalia,HP:0010461,Abnormality of the male genitalia
+UBERON:0006525,left lung alveolar system,UBERON:0000467,anatomical system
+UBERON:0009709,ventral pancreas,UBERON:0004119,endoderm-derived structure
+UBERON:0013154,1st arch maxillary endoderm,UBERON:0003929,gut epithelium
+UBERON:2002069,distal cartilage of posterior process of basipterygium,UBERON:4100000,skeletal element projection
+UBERON:3010832,occipital segment,UBERON:0005913,zone of bone organ
+UBERON:0004633,thoracic vertebra 9,UBERON:0002347,thoracic vertebra
+NCBITaxon:33154,Opisthokonta,NCBITaxon:2759,Eukaryota
+DOID:4921,eccrine sweat gland cancer,DOID:2095,sweat gland cancer
+UBERON:0010329,paired limb/fin bud mesenchyme,UBERON:0010377,mesenchyme from somatopleure
+UBERON:0002036,striated muscle tissue,UBERON:0002385,muscle tissue
+HP:0011289,EEG with temporal sharp slow waves,HP:0011195,EEG with focal sharp slow waves
+HP:0006121,Acral ulceration leading to autoamputation of digits,HP:0200042,Skin ulcer
+DOID:10813,nasal cavity lymphoma,DOID:10811,nasal cavity cancer
+HP:0000905,Progressive clavicular acroosteolysis,HP:0002797,Osteolysis
+HP:0010055,Broad hallux,HP:0001844,Abnormality of the hallux
+HP:0001045,Vitiligo,HP:0001000,Abnormality of skin pigmentation
+UBERON:0009909,rostral root of abducens nerve,UBERON:0002786,abducens nerve fibers
+UBERON:0009964,crustacean maxillary gland,UBERON:0009962,excretory gland
+UBERON:0002626,head of caudate nucleus,UBERON:0011300,gray matter of telencephalon
+HP:0001074,Atypical nevi in non-sun exposed areas,HP:0003764,Nevus
+DOID:898,polycystic kidney disease,DOID:0050736,autosomal dominant disease
+HP:0004023,Sloping radial metaphysis,HP:0004015,Abnormality of radial metaphyses
+UBERON:2000602,uroneural,UBERON:0004376,fin bone
+UBERON:0001351,lacrimal sac,UBERON:0000063,organ segment
+UBERON:0014555,CA2 stratum radiatum,UBERON:0014567,layer of hippocampal field
+HP:0003450,Axonal regeneration,HP:0000764,Peripheral axonal degeneration
+HP:0100143,Small epiphysis of the distal phalanx of the 3rd toe,HP:0100091,Abnormality of the epiphysis of the distal phalanx of the 3rd toe
+DOID:11424,fallopian tube endometriosis,DOID:1962,fallopian tube disease
+UBERON:0002384,connective tissue,UBERON:0000479,tissue
+UBERON:0012239,urinary bladder vasculature,UBERON:0002201,vasculature of trunk
+HP:0011226,Aplasia/Hypoplasia affecting the eyelid,HP:0000492,Abnormality of the eyelid
+HP:0010925,Nuclear punctate cataract,HP:0100018,Nuclear cataract
+UBERON:0000065,respiratory tract,UBERON:0004119,endoderm-derived structure
+DOID:0050832,pyrimidine metabolic disorder,DOID:655,inherited metabolic disorder
+UBERON:0014787,left extraembryonic umbilical vein,UBERON:0015212,lateral structure
+HP:0000846,Adrenal insufficiency,HP:0011733,Abnormality of adrenal physiology
+CL:0002588,smooth muscle cell of the umbilical vein,CL:0000359,vascular associated smooth muscle cell
+DOID:0060202,amyotrophic lateral sclerosis type 11,DOID:332,amyotrophic lateral sclerosis
+UBERON:0014725,intercalated duct,UBERON:0000058,duct
+UBERON:0000221,supraauricular point,UBERON:0006983,anatomical point
+UBERON:3000259,lamina inferior,UBERON:0004121,ectoderm-derived structure
+HP:0010705,4-5 finger syndactyly,HP:0006101,Finger syndactyly
+HP:0009684,Stippling of the epiphysis of the distal phalanx of the thumb,HP:0010255,Stippling of the epiphyses of the distal phalanges of the hand
+HP:0009403,Triangular epiphyses of the 4th finger,HP:0010238,Triangular epiphyses of the phalanges of the hand
+UBERON:0003383,cardiac muscle of interventricular septum,UBERON:0004492,cardiac muscle tissue of cardiac septum
+UBERON:0002936,magnocellular part of red nucleus,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010949,Abnormality of umbilical vein blood flow,HP:0010948,Abnormality of the fetal cardiovascular system
+DOID:9975,cocaine dependence,DOID:9974,drug dependence
+CL:0002226,non-nucleated secondary lens fiber,CL:0002225,secondary lens fiber
+UBERON:0011194,ophthalmic plexus,UBERON:0001810,nerve plexus
+CL:0000150,glandular epithelial cell,CL:0000151,secretory cell
+DOID:9336,bestiality,DOID:0060044,paraphilia disorder
+CL:1000437,epithelial cell of nasolacrimal duct,CL:1000435,epithelial cell of lacrimal duct
+HP:0001831,Short toe,HP:0001991,Aplasia/Hypoplasia of toe
+UBERON:0004647,liver lobule,UBERON:0000064,organ part
+UBERON:3010496,mandibular artery,UBERON:0001637,artery
+UBERON:0001697,orbital region,UBERON:0015212,lateral structure
+DOID:12273,anisometropia,DOID:9835,refractive error
+UBERON:0014447,feathered facial disc,UBERON:0011810,collection of feathers
+UBERON:0011144,adductor muscle of hip,UBERON:0010890,pelvic complex muscle
+UBERON:0004333,proximal phalanx of pedal digit 2,UBERON:0003641,pedal digit 2 phalanx
+UBERON:2001537,mesocoracoid cartilage,UBERON:4300092,mesocoracoid element
+UBERON:0002759,magnocellular nucleus of medial geniculate body,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0006937,inner ear epithelium,UBERON:0015807,ear epithelium
+HP:0002350,Cerebellar cyst,HP:0002438,Cerebellar malformation
+UBERON:0009010,periurethral tissue,UBERON:0004120,mesoderm-derived structure
+HP:0000360,Tinnitus,HP:0000364,Hearing abnormality
+UBERON:0010310,nictitating membrane lamina,UBERON:0003581,eyelid connective tissue
+UBERON:0000168,segment of colon,UBERON:0004921,subdivision of digestive tract
+CL:0002015,"Kit-negative, Ly-76 high polychromatophilic erythroblast",CL:0000550,polychromatophilic erythroblast
+HP:0007620,Cutaneous leiomyoma,HP:0008069,Neoplasm of the skin
+HP:0008507,Static ophthalmoparesis,HP:0000597,Ophthalmoparesis
+UBERON:0005091,left horn of sinus venosus,UBERON:0015212,lateral structure
+NCBITaxon:781,Rickettsia conorii,NCBITaxon:114277,spotted fever group
+UBERON:2001395,neural arch 4,UBERON:0003861,neural arch
+UBERON:0008611,scalene muscle,UBERON:0003897,axial muscle
+HP:0000097,Focal segmental glomerulosclerosis,HP:0000096,Glomerulosclerosis
+UBERON:4300016,pelvic cartilage,UBERON:0007844,cartilage element
+UBERON:0002023,claustrum of brain,UBERON:0005401,cerebral hemisphere grey matter
+DOID:7551,gonorrhea,DOID:0050338,primary bacterial infectious disease
+UBERON:0008847,ovarian ligament,UBERON:0004120,mesoderm-derived structure
+UBERON:2001997,parietal-supraoccipital,UBERON:0002513,endochondral bone
+CL:1000306,fibroblast of tunica adventitia of artery,CL:0000057,fibroblast
+UBERON:0002069,stratum granulosum of epidermis,UBERON:0013754,integumentary system layer
+HP:0006580,Portal fibrosis,HP:0004297,Abnormality of the biliary system
+UBERON:0001993,reticular layer of dermis,UBERON:0004120,mesoderm-derived structure
+UBERON:0010959,craniocervical muscle,UBERON:0001630,muscle organ
+HP:0009469,Contracture of the distal interphalangeal joint of the 3rd finger,HP:0009319,Joint contractures of the 3rd finger
+UBERON:2001553,manubrium,UBERON:2000461,Weberian ossicle
+UBERON:0004628,thoracic vertebra 3,UBERON:0002347,thoracic vertebra
+DOID:3983,oesophagostomiasis,DOID:883,parasitic helminthiasis infectious disease
+UBERON:0004727,cochlear nerve,UBERON:0004121,ectoderm-derived structure
+HP:0012711,Delayed ossification of vertebral epiphysis,HP:0100569,Abnormal vertebral ossification
+HP:0003880,Sclerotic foci of the humerus,HP:0003881,Humeral sclerosis
+HP:0100593,Calcification of cartilage,HP:0002763,Abnormal cartilage morphology
+CL:1001320,urethra cell,CL:1000600,lower urinary tract cell
+CL:0000434,eccrine cell,CL:0000150,glandular epithelial cell
+UBERON:0005066,right ventricular trabecular myocardium,UBERON:0004126,trabecular layer of ventricle
+UBERON:0002414,lumbar vertebra,UBERON:0015009,lumbar vertebra endochondral element
+UBERON:0015091,distal carpal bone 3 cartilage,UBERON:0015064,autopod cartilage
+HP:0010836,Abnormality of copper homeostasis,HP:0011030,Abnormality of transition element cation homeostasis
+UBERON:0014882,distal epiphysis of distal phalanx of manual digit 2,UBERON:0014886,distal epiphysis of distal phalanx of manual digit
+HP:0001836,Camptodactyly (feet),HP:0001760,Abnormality of the foot
+UBERON:0004661,mandible temporal crest,UBERON:0000064,organ part
+UBERON:0005799,simplex uterus,UBERON:0000995,uterus
+UBERON:0010234,palatopharyngeus muscle,UBERON:0004119,endoderm-derived structure
+HP:0002247,Duodenal atresia,HP:0011100,Intestinal atresia
+HP:0000219,Thin upper lip vermilion,HP:0011339,Abnormality of upper lip vermillion
+UBERON:0008114,joint of girdle,UBERON:0000982,skeletal joint
+UBERON:0015877,parietal pelvic lymph node,UBERON:0015876,pelvic lymph node
+HP:0002343,Normal pressure hydrocephalus,HP:0000238,Hydrocephalus
+HP:0004278,Synostosis involving bones of the hand,HP:0001155,Abnormality of the hand
+HP:0100429,Broad proximal phalanx of the 4th toe,HP:0010372,Broad phalanges of the 4th toe
+UBERON:0006166,lateral dorsal digital artery for digit 5,UBERON:0006146,dorsal digital artery of manus
+DOID:14778,"blepharophimosis, ptosis, and epicanthus inversus syndrome",DOID:0050736,autosomal dominant disease
+UBERON:0002247,uterine horn,UBERON:0014404,female anatomical structure
+DOID:0050850,diabetic encephalopathy,DOID:936,brain disease
+UBERON:0004494,cardiac muscle tissue of papillary muscle,UBERON:0001133,cardiac muscle tissue
+UBERON:0004498,skeletal muscle tissue of quadriceps femoris,UBERON:0001134,skeletal muscle tissue
+HP:0002332,Lack of peer relationships,HP:0000735,Impaired social interactions
+UBERON:2002101,branchiostegal ray series,UBERON:0000477,anatomical cluster
+UBERON:2001051,caudal division of the internal carotid artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0010008,mammalian cotyledon,UBERON:0005156,reproductive structure
+UBERON:3000672,posterolateral process,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005159,pyramid of medulla oblongata,UBERON:0002678,regional part of medulla oblongata
+HP:0010042,Aplasia/Hypoplasia of the 4th metacarpal,HP:0005914,Aplasia/Hypoplasia involving the metacarpal bones
+CL:0002132,stromal cell of ovary,CL:0000499,stromal cell
+UBERON:2000716,afferent branchial artery,UBERON:0003469,respiratory system artery
+UBERON:0015156,terminal branch of ophthalmic artery,UBERON:0004573,systemic artery
+HP:0004788,Intestinal lymphedema,HP:0001004,Lymphedema
+UBERON:0014861,glaucothoe stage,UBERON:0000069,larval stage
+DOID:2080,vulvar trichoepithelioma,DOID:0060109,vulvar benign neoplasm
+HP:0012661,Hypothalamic hypometabolism in FDG PET,HP:0012658,Abnormal brain FDG positron emission tomography
+UBERON:0004297,respiratory system blood vessel smooth muscle,UBERON:0004225,respiratory system smooth muscle
+UBERON:0014773,medial palpebral artery,UBERON:0014770,palpebral artery
+HP:0005180,Tricuspid regurgitation,HP:0001702,Abnormality of the tricuspid valve
+HP:0006735,Renal cortical adenoma,HP:0009726,Renal neoplasm
+HP:0002717,Adrenal overactivity,HP:0011733,Abnormality of adrenal physiology
+HP:0010697,Anterior pyramidal cataract,HP:0001134,Anterior polar cataract
+HP:0009486,Radial deviation of the hand,HP:0009485,Radial deviation of the hand or of fingers of the hand
+HP:0009221,Pseudoepiphysis of the middle phalanx of the 4th finger,HP:0010264,Pseudoepiphyses of the middle phalanges of the hand
+UBERON:0001773,sclera,UBERON:0000064,organ part
+UBERON:0005049,mucosa of infundibulum of uterine tube,UBERON:0000344,mucosa
+UBERON:2105382,dorsal fin proximal radial element 5,UBERON:2100947,dorsal fin proximal radial element
+CL:0000165,neuroendocrine cell,CL:0000710,neurecto-epithelial cell
+UBERON:0003640,pedal digit 1 phalanx,UBERON:0001449,phalanx of pes
+HP:0012166,Skin-picking,HP:0100716,Self-injurious behavior
+HP:0002243,Protein-losing enteropathy,HP:0002244,Abnormality of the small intestine
+UBERON:0004021,spongiotrophoblast layer,UBERON:0000119,cell layer
+DOID:3382,liposarcoma,DOID:3939,lipomatous cancer
+UBERON:4200079,dorsal iliac process,UBERON:0004120,mesoderm-derived structure
+DOID:10587,Krabbe disease,DOID:1927,sphingolipidosis
+UBERON:0000913,interstitial fluid,UBERON:0000463,portion of organism substance
+HP:0006904,Late-onset spinocerebellar degeneration,HP:0002503,Spinocerebellar tract degeneration
+UBERON:0009121,vomeronasal nerve,UBERON:0001785,cranial nerve
+HP:0010630,Abnormality of metatarsal epiphysis,HP:0001832,Abnormality of the metatarsal bones
+UBERON:0007833,osseus semicircular canal,UBERON:0005913,zone of bone organ
+UBERON:2000859,specialized hemal arch and spine,UBERON:0004376,fin bone
+HP:0010122,Stippling of the epiphyses of the hallux,HP:0010171,Epiphyseal stippling of toe phalanges
+DOID:8577,ulcerative colitis,DOID:0060180,colitis
+UBERON:0003518,main bronchus blood vessel,UBERON:0003504,respiratory system blood vessel
+UBERON:0008947,respiratory primordium,UBERON:0001048,primordium
+HP:0010799,Pinealoma,HP:0100836,Malignant neoplasm of the central nervous system
+UBERON:4200129,synarcual region,UBERON:0011676,subdivision of organism along main body axis
+DOID:10880,iliac vein thrombophlebitis,DOID:3875,thrombophlebitis
+UBERON:0001163,lesser curvature of stomach,UBERON:0009870,zone of stomach
+UBERON:0005058,hemolymphoid system gland,UBERON:0002530,gland
+HP:0001694,Right-to-left shunt,HP:0001693,Cardiac shunt
+UBERON:0008311,penile bulb artery,UBERON:0014403,male anatomical structure
+UBERON:0002581,postcentral gyrus,UBERON:0000200,gyrus
+HP:0001038,Warfarin-induced skin necrosis,HP:0001005,Dermatological manifestations of systemic disorders
+UBERON:0001918,endothelium of venule,UBERON:0004638,blood vessel endothelium
+HP:0010956,Fetal megacystis,HP:0010955,Dilatation of the bladder
+UBERON:0006608,corpus cavernosum clitoridis,UBERON:0005156,reproductive structure
+UBERON:0001200,submucosa of stomach,UBERON:0000009,submucosa
+UBERON:0005432,aortic sac,UBERON:0001637,artery
+UBERON:0010348,hyoid pre-muscle mass,UBERON:0004120,mesoderm-derived structure
+UBERON:2001805,articular bone,UBERON:0004768,bone of lower jaw
+UBERON:2000267,primary olfactory fiber layer,UBERON:0000479,tissue
+UBERON:2005150,basal regeneration epithelium of regenerating fin/limb,UBERON:0007567,regenerating anatomical structure
+HP:0100564,Triplomyelia,HP:0100561,Spinal cord lesions
+CL:0002533,immature CD16-positive myeloid dendritic cell,CL:0002532,CD16-positive myeloid dendritic cell
+UBERON:0008307,heart endothelium,UBERON:0004852,cardiovascular system endothelium
+HP:0006560,Biliary hyperplasia,HP:0012440,Abnormal biliary tract morphology
+DOID:13691,dermoid cyst of skin,DOID:2658,dermoid cyst
+UBERON:3000309,narial muscles,UBERON:0002376,cranial muscle
+UBERON:0006124,vertical limb of the diagonal band,UBERON:0006125,subdivision of diagonal band
+HP:0001733,Pancreatitis,HP:0012091,Abnormality of pancreas physiology
+HP:0200151,Cutaneous mastocytosis,HP:0000951,Abnormality of the skin
+DOID:0050929,mucosal melanoma,DOID:1909,melanoma
+HP:0007087,Involuntary jerking movements,HP:0004305,Involuntary movements
+UBERON:0006597,quadrate bone,UBERON:0015212,lateral structure
+DOID:0050289,fusariosis,DOID:2473,opportunistic mycosis
+UBERON:0004676,spinal cord lateral horn,UBERON:0015212,lateral structure
+HP:0003700,Generalized amyotrophy,HP:0003202,Amyotrophy
+HP:0100486,Symphalangism of the proximal phalanx of the 5th toe with the 5th metatarsal,HP:0100475,Symphalangism affecting the proximal phalanx of the 5th toe
+DOID:4843,subependymal glioma,DOID:4844,benign ependymoma
+DOID:13565,neuroaspergillosis,DOID:13564,aspergillosis
+UBERON:0013137,external pudendal artery,UBERON:0007312,pudendal artery
+UBERON:0011613,hypohyal element,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005057,immune organ,UBERON:0000062,organ
+UBERON:0000402,nasal vestibule,UBERON:0002553,anatomical cavity
+HP:0010278,Triangular epiphyses of the proximal phalanges of the hand,HP:0010238,Triangular epiphyses of the phalanges of the hand
+UBERON:0006592,transformed vein,UBERON:0006590,vestigial embryonic structure
+DOID:8556,vallecula cancer,DOID:8557,oropharynx cancer
+HP:0009451,Bullet-shaped proximal phalanx of the 3rd finger,HP:0009853,Bullet-shaped proximal phalanges of the hand
+UBERON:0015807,ear epithelium,UBERON:0000483,epithelium
+HP:0010643,Midnasal atresia,HP:0010644,Midnasal stenosis
+DOID:12986,leukostasis,DOID:9500,leukocyte disease
+UBERON:2001857,hyoidean artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:14351,Riedel's fibrosing thyroiditis,DOID:7166,thyroiditis
+UBERON:4000108,non-mineralized hyaline cartilage tissue,UBERON:0011589,non-mineralized cartilage tissue
+DOID:4551,anus neoplasm,DOID:4610,intestinal benign neoplasm
+UBERON:0001437,epiphysis,UBERON:0005055,zone of long bone
+HP:0100582,Nasal polyposis,HP:0000433,Abnormality of the nasal mucosa
+HP:0004495,Thin anteverted nares,HP:0000463,Anteverted nares
+DOID:10581,metachromatic leukodystrophy,DOID:10579,leukodystrophy
+UBERON:2000767,hypaxial region somite 11,UBERON:0003895,hypaxial myotome region
+HP:0012100,Abnormal circulating creatinine level,HP:0004364,Abnormality of nitrogen compound homeostasis
+UBERON:2001420,anal fin pterygiophore,UBERON:0000477,anatomical cluster
+CL:0002137,type III cell of adrenal cortex,CL:0000593,androgen secreting cell
+UBERON:0006494,apex of arytenoid,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2000837,sclerotome somite 6,UBERON:0003089,sclerotome
+HP:0011654,Double outlet right ventricle with non-committed ventricular septal defect without pulmonary stenosis,HP:0001719,Double outlet right ventricle
+UBERON:0006639,crus penis,UBERON:0005156,reproductive structure
+HP:0002190,Choroid plexus cyst,HP:0007376,Abnormality of the choroid plexus
+UBERON:0002257,ventral horn of spinal cord,UBERON:0001948,regional part of spinal cord
+DOID:0050179,Powassan encephalitis,DOID:934,viral infectious disease
+UBERON:0013450,simian shelf,UBERON:0005913,zone of bone organ
+DOID:4630,inverted transitional papilloma,DOID:2670,transitional papilloma
+UBERON:0006538,respiratory system fluid/secretion,UBERON:0000463,portion of organism substance
+HP:0010342,Abnormality of the phalanges of the 5th toe,HP:0010161,Abnormality of the phalanges of the toes
+UBERON:0008839,palmar pad,UBERON:0013777,skin of palm of manus
+UBERON:4200182,lateral tubercle of astragalus,UBERON:4100000,skeletal element projection
+UBERON:0008866,enamel knot,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010629,Abnormality of the cortex of the humerus,HP:0003103,Abnormal cortical bone morphology
+DOID:10140,dry eye syndrome,DOID:1400,lacrimal apparatus disease
+UBERON:0003095,dorsal lateral line,UBERON:0010202,lateral line
+HP:0006334,Hypoplasia of the primary teeth,HP:0006481,Abnormality of primary teeth
+HP:0007385,Aplasia cutis congenita of scalp,HP:0001057,Aplasia cutis congenita
+HP:0005924,Abnormality of the epiphyses of the hand,HP:0001155,Abnormality of the hand
+HP:0008721,Hypoplastic male genitalia,HP:0000050,Hypoplastic genitalia
+DOID:12642,hiatus hernia,DOID:76,stomach disease
+DOID:1134,gingival recession,DOID:1483,gingival disease
+CL:0000800,mature gamma-delta T cell,CL:0002419,mature T cell
+UBERON:0001272,innominate bone,UBERON:0015212,lateral structure
+HP:0008450,Narrow vertebral interpedicular distance,HP:0008438,Vertebral arch anomaly
+UBERON:0004112,muscle of middle ear,UBERON:0002376,cranial muscle
+UBERON:0005464,median sacral artery,UBERON:0012254,abdominal aorta artery
+UBERON:0014907,intersomitic vessel,UBERON:0001981,blood vessel
+HP:0012372,Abnormal eye morphology,HP:0000478,Abnormality of the eye
+UBERON:0015171,uterine spiral artery,UBERON:0015172,endometrial blood vessel
+HP:0009800,Maternal diabetes,HP:0000819,Diabetes mellitus
+UBERON:0012317,vagina orifice,UBERON:0000161,orifice
+UBERON:0008323,dorsal artery of clitoris,UBERON:0003520,pelvis blood vessel
+HP:0008404,Nail dystrophy,HP:0001597,Abnormality of the nail
+UBERON:0007374,incus cartilage element,UBERON:0011004,pharyngeal arch cartilage
+UBERON:0007642,ligamentum arteriosum,UBERON:0006591,transformed artery
+UBERON:0009778,pleural sac,UBERON:0004119,endoderm-derived structure
+HP:0003392,First dorsal interossei muscle weakness,HP:0002460,Distal muscle weakness
+CL:0000512,paracrine cell,CL:0000151,secretory cell
+HP:0008490,Sacral segmentation defects,HP:0003422,Vertebral segmentation defect
+UBERON:2205374,dorsal fin distal radial cartilage 3,UBERON:2200936,dorsal fin distal radial cartilage
+DOID:0050582,distal hereditary motor neuropathy,DOID:683,motor neuritis
+DOID:12926,hypodermyiasis,DOID:11080,myiasis
+UBERON:0005100,long descending thin limb,UBERON:0004211,nephron epithelium
+UBERON:0009708,dorsal pancreas,UBERON:0004119,endoderm-derived structure
+UBERON:0001967,reticular lamina of epithelium,UBERON:0005764,acellular membrane
+DOID:6857,pineal region mature teratoma,DOID:6856,pineal region teratoma
+CL:0000061,cementoblast,CL:0000151,secretory cell
+UBERON:0002962,adductor pollicis muscle,UBERON:0011145,adductor muscle
+DOID:1562,chromoblastomycosis,DOID:0050135,subcutaneous mycosis
+HP:0006000,Ureteral obstruction,HP:0000069,Abnormality of the ureter
+HP:0010239,Aplasia of the middle phalanx of the hand,HP:0009843,Aplasia/Hypoplasia of the middle phalanges of the hand
+UBERON:0005601,dorsal mesocardium,UBERON:0010277,mesocardium
+UBERON:0011013,spinalis muscle,UBERON:0004120,mesoderm-derived structure
+NCBITaxon:53550,Culicini,NCBITaxon:43817,Culicinae
+UBERON:0011670,pygal plate of carapace,UBERON:0011665,carapace bone
+UBERON:0005206,choroid plexus stroma,UBERON:0003891,stroma
+DOID:11722,myotonic dystrophy type 1,DOID:450,myotonic disease
+HP:0009269,Small epiphysis of the proximal phalanx of the 4th finger,HP:0010276,Small epiphyses of the proximal phalanges of the hand
+UBERON:0005233,medial-nasal process ectoderm,UBERON:0014702,frontonasal process epithelium
+DOID:9206,Barrett's esophagus,DOID:6050,esophageal disease
+UBERON:0000153,anterior region of body,UBERON:0000475,organism subdivision
+DOID:13166,allergic bronchopulmonary aspergillosis,DOID:13564,aspergillosis
+DOID:2476,hereditary spastic paraplegia,DOID:607,paraplegia
+HP:0005265,Abnormality of the jejunum,HP:0002244,Abnormality of the small intestine
+CL:0000098,sensory epithelial cell,CL:0002371,somatic cell
+DOID:12996,acute dacryocystitis,DOID:9938,dacryocystitis
+UBERON:0010679,manual digit 5 phalanx cartilage element,UBERON:0015029,manual digit 5 phalanx endochondral element
+HP:0008223,Compensated hypothyroidism,HP:0000821,Hypothyroidism
+DOID:2280,hidradenitis suppurativa,DOID:2282,hidradenitis
+HP:0003080,Hydroxyprolinuria,HP:0010907,Abnormality of proline metabolism
+HP:0004719,Hyperechogenic kidneys,HP:0012210,Abnormal renal morphology
+HP:0002755,Osteomyelitis due to immunodeficiency,HP:0002754,Osteomyelitis
+UBERON:3000406,pars interna plectri,UBERON:0000064,organ part
+UBERON:0002310,hippocampus fimbria,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003587,limb connective tissue,UBERON:0002384,connective tissue
+CL:0000289,chemotactic amoeboid cell (sensu Mycetozoa),CL:0000732,amoeboid cell
+DOID:13520,neonatal infective mastitis,DOID:10690,mastitis
+HP:0010183,Abnormality of the middle phalanges of the toes,HP:0010161,Abnormality of the phalanges of the toes
+HP:0009295,Short middle phalanx of the 4th finger,HP:0009299,Aplasia/Hypoplasia of the middle phalanx of the 4th finger
+UBERON:0014687,temporal sulcus,UBERON:0013118,sulcus of brain
+UBERON:0012238,ureteric bud trunk,UBERON:0005103,mesonephric epithelium
+HP:0100460,Osteolytic defects of the distal phalanx of the 5th toe,HP:0010387,Osteolytic defects of the phalanges of the 5th toe
+UBERON:0001657,superficial temporal vein,UBERON:0003502,neck blood vessel
+HP:0001829,Foot polydactyly,HP:0001780,Abnormality of toe
+HP:0012204,Recurrent vulvovaginal candidiasis,HP:0002728,Chronic mucocutaneous candidiasis
+HP:0004630,Anterior beaking of thoracic vertebrae,HP:0004568,Beaking of vertebral bodies
+HP:0100855,Triceps hypoplasia,HP:0009784,Aplasia/Hypoplasia of the triceps
+DOID:3644,hypothalamic neoplasm,DOID:368,cerebrum cancer
+HP:0003330,Abnormal bone structure,HP:0011842,Abnormality of skeletal morphology
+UBERON:0004184,prostate gland stroma,UBERON:0003891,stroma
+HP:0009223,Stippling of the epiphysis of the middle phalanx of the 4th finger,HP:0009247,Abnormality of the epiphysis of the middle phalanx of the 4th finger
+UBERON:0004573,systemic artery,UBERON:0001637,artery
+HP:0006397,Lateral displacement of patellae,HP:0003045,Abnormality of the patella
+UBERON:0005478,sulcus limitans of neural tube,UBERON:0002050,embryonic structure
+DOID:10151,malignant neoplasm of short bones of lower limb,DOID:10149,long bones of lower limb cancer
+HP:0003842,Irregular epiphyses of the upper limbs,HP:0003839,Abnormality involving the epiphyses of the upper limbs
+HP:0004008,Sloping radial epiphyses,HP:0003999,Abnormality of radial epiphyses
+HP:0002239,Gastrointestinal hemorrhage,HP:0012719,Functional abnormality of the gastrointestinal tract
+CL:0002168,border cell of cochlea,CL:0002315,supporting cell of cochlea
+HP:0003896,Irregular humeral epiphyses,HP:0003891,Abnormality of the humeral epiphysis
+UBERON:0007355,bony part of pharyngotympanic tube,UBERON:0003566,head connective tissue
+HP:0004364,Abnormality of nitrogen compound homeostasis,HP:0001939,Abnormality of metabolism/homeostasis
+HP:0002563,Constrictive pericarditis,HP:0001701,Pericarditis
+HP:0007024,Pseudobulbar paralysis,HP:0002200,Pseudobulbar signs
+UBERON:0006647,adventitia of ductus deferens,UBERON:0005742,adventitia
+HP:0008393,Congenital curved nail of fourth toe,HP:0008388,Abnormality of the toenail
+HP:0001842,Acroosteolysis (feet),HP:0010177,Osteolytic defects of the phalanges of the toes
+HP:0002918,Hypermagnesemia,HP:0004921,Abnormality of magnesium homeostasis
+UBERON:0016426,proximal interphalangeal joint of little finger,UBERON:0009767,proximal interphalangeal joint
+HP:0100746,Macrodactyly of finger,HP:0001167,Abnormality of finger
+CL:0002160,basal external epithelial cell of tympanic membrane,CL:0002158,external epithelial cell of tympanic membrane
+DOID:5480,ovarian endometrioid adenofibroma,DOID:0060112,ovarian benign neoplasm
+DOID:7961,cervical non-keratinizing squamous cell carcinoma,DOID:3744,cervical squamous cell carcinoma
+UBERON:2002074,external anterior process of basipterygium,UBERON:0004120,mesoderm-derived structure
+UBERON:0011255,Eimer's organ,UBERON:0010314,structure with developmental contribution from neural crest
+NCBITaxon:35789,Rickettsia helvetica,NCBITaxon:114277,spotted fever group
+DOID:1387,hypolipoproteinemia,DOID:3146,lipid metabolism disorder
+DOID:5914,nonencapsulated sclerosing carcinoma,DOID:3969,papillary thyroid carcinoma
+HP:0007291,Posterior fossa cyst,HP:0000932,Abnormality of the posterior cranial fossa
+HP:0006097,3-4 finger syndactyly,HP:0006101,Finger syndactyly
+UBERON:0002555,intermediate hypothalamic region,UBERON:0004121,ectoderm-derived structure
+UBERON:0001049,neural tube,UBERON:0007497,developing epithelial placode
+UBERON:4200183,bicipital tuberosity,UBERON:0004120,mesoderm-derived structure
+UBERON:0011207,iliocostalis lumborum,UBERON:0002251,iliocostalis muscle
+HP:0009961,Partial duplication of the phalanges of the 3rd finger,HP:0009999,Partial duplication of the phalanx of hand
+CL:0001025,"Kit-positive, Sca1-positive common lymphoid progenitor",CL:0001030,CD117-positive common myeloid progenitor OR CD217-positive common lymphoid progenitor
+UBERON:0003356,epithelium of nasal septum,UBERON:0010313,neural crest-derived structure
+UBERON:2001533,pharyngobranchial cartilage,UBERON:0011004,pharyngeal arch cartilage
+HP:0009563,Distal/middle symphalangism of 2nd finger,HP:0009545,Symphalangism of the 2nd finger
+HP:0011359,Dry hair,HP:0010719,Abnormality of hair texture
+UBERON:0007316,deep external pudendal artery,UBERON:0003520,pelvis blood vessel
+HP:0000168,Abnormality of the gingiva,HP:0000163,Abnormality of the oral cavity
+UBERON:0010153,rumen papilla,UBERON:0009034,stomach region
+UBERON:2001733,mesethmoid ventral diverging lamella,UBERON:0004120,mesoderm-derived structure
+HP:0009439,Short middle phalanx of the 3rd finger,HP:0005819,Short middle phalanx of finger
+UBERON:2000438,parhypural,UBERON:0004376,fin bone
+CL:1000223,lung neuroendocrine cell,CL:0000082,epithelial cell of lung
+UBERON:2001761,pectoral fin lepidotrichium 1,UBERON:4000175,pectoral fin lepidotrichium
+HP:0200039,Pustule,HP:0011123,Inflammatory abnormality of the skin
+UBERON:0011201,muscle layer of small intestine,UBERON:0012367,muscle layer of intestine
+UBERON:2001653,pharyngobranchial 3 tooth,UBERON:0004756,dermal skeletal element
+HP:0010657,Patchy reduction of bone mineral density,HP:0004349,Reduced bone mineral density
+HP:0100841,Microgastria,HP:0002577,Abnormality of the stomach
+UBERON:0005002,mucosa of right hepatic duct,UBERON:0004999,mucosa of biliary tree
+NCBITaxon:53527,Culex <subgenus>,NCBITaxon:7174,Culex <genus>
+CL:0000932,type II NK T cell secreting interferon-gamma,CL:0000912,helper T cell
+UBERON:0001450,calcaneus,UBERON:0011679,proximal tarsal bone
+UBERON:0006329,superior pharyngeal constrictor,UBERON:0001569,constrictor muscle of pharynx
+UBERON:2005226,median fin proximal radial bone,UBERON:2005225,median fin radial bone
+UBERON:0008200,forehead,UBERON:0003102,surface structure
+UBERON:0002097,skin of body,UBERON:0000062,organ
+DOID:0060139,color agnosia,DOID:4090,agnosia
+DOID:0060021,DNA ligase IV deficiency,DOID:628,combined T cell and B cell immunodeficiency
+HP:0010067,Aplasia/Hypoplasia of the 1st metatarsal,HP:0010054,Abnormality of the first metatarsal
+UBERON:0005320,mesonephric juxtaglomerular apparatus,UBERON:0004120,mesoderm-derived structure
+UBERON:0007812,post-anal tail,UBERON:0002415,tail
+UBERON:3010241,labial fold,UBERON:3000972,head external integument structure
+HP:0100798,Fingernail dysplasia,HP:0001231,Abnormality of the fingernails
+DOID:11949,Creutzfeldt-Jakob disease,DOID:649,prion disease
+HP:0010499,Patellar subluxation,HP:0003045,Abnormality of the patella
+UBERON:0006351,principal vein of forelimb,UBERON:0006443,prinicipal vein of limb
+DOID:11830,myopia,DOID:9835,refractive error
+DOID:1456,glossitis,DOID:10944,tongue disease
+UBERON:0009743,visceral yolk sac cavity,UBERON:0002050,embryonic structure
+HP:0001920,Renal artery stenosis,HP:0100545,Arterial stenosis
+DOID:11783,necrosis of ear ossicle,DOID:2742,auditory system disease
+UBERON:0012112,ingested food,UBERON:0000463,portion of organism substance
+UBERON:3000647,crista interna,UBERON:0004120,mesoderm-derived structure
+DOID:7757,childhood leukemia,DOID:1240,leukemia
+HP:0011912,Abnormality of the glenoid fossa,HP:0003043,Abnormality of the shoulder
+HP:0007314,White matter neuronal heterotopia,HP:0002282,Heterotopia
+CL:0000784,plasmacytoid dendritic cell,CL:0000451,dendritic cell
+DOID:3525,middle cerebral artery infarction,DOID:3526,cerebral infarction
+UBERON:0006364,ureteric bud tip,UBERON:0000083,mesonephric tubule
+HP:0001015,Prominent superficial veins,HP:0007394,Prominent superficial blood vessels
+UBERON:0004804,oviduct epithelium,UBERON:0005156,reproductive structure
+UBERON:0009129,right atrium endocardium,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:8704,genital herpes,DOID:8566,herpes simplex
+UBERON:0015006,coccygeal vertebra endochondral element,UBERON:0004120,mesoderm-derived structure
+CL:1000313,gastric goblet cell,CL:0002180,mucous cell of stomach
+UBERON:0003711,brachiocephalic vein,UBERON:0001638,vein
+HP:0009188,Pseudoepiphysis of the distal phalanx of the 5th finger,HP:0009198,Abnormality of the epiphysis of the distal phalanx of the 5th finger
+UBERON:0013590,cruciate sulcus,UBERON:0013118,sulcus of brain
+HP:0003643,Sulfite oxidase deficiency,HP:0004339,Abnormality of sulfur amino acid metabolism
+HP:0100186,Ivory epiphysis of the middle phalanx of the 4th toe,HP:0100095,Abnormality of the epiphysis of the middle phalanx of the 4th toe
+UBERON:0010250,middle meningeal artery,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:14320,generalized anxiety disorder,DOID:2030,anxiety disorder
+HP:0100176,Pseudoepiphysis of the distal phalanx of the 4th toe,HP:0100073,Pseudoepiphyses of the 4th toe
+UBERON:0002959,subfascicular nucleus,UBERON:0015233,nucleus of dorsal thalamus
+HP:0100665,Angioedema,HP:0000969,Edema
+UBERON:0010321,skeletal element of eye region,UBERON:0010313,neural crest-derived structure
+DOID:13651,eversion of lacrimal punctum,DOID:1400,lacrimal apparatus disease
+HP:0009391,Stippling of the epiphyses of the 5th finger,HP:0010237,Epiphyseal stippling of finger phalanges
+HP:0005772,Aplasia/Hypoplasia of the tibia,HP:0002992,Abnormality of the tibia
+HP:0011060,Dentinogenesis imperfecta limited to primary teeth,HP:0000703,Dentinogenesis imperfecta
+UBERON:4200118,pubic peduncle,UBERON:0004530,bony projection
+UBERON:0007374,incus cartilage element,UBERON:0005863,cartilaginous condensation
+UBERON:0010195,renal portal system,UBERON:0005806,portal system
+HP:0010236,Small epiphyses of the phalanges of the hand,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+UBERON:0005701,lower jaw molar odontogenic papilla,UBERON:0010258,mesenchyme from rhombencephalic neural crest
+UBERON:2000127,antorbital,UBERON:0008907,dermal bone
+HP:0012252,Abnormal respiratory system morphology,HP:0002086,Abnormality of the respiratory system
+HP:0000543,Optic disc pallor,HP:0000587,Abnormality of the optic nerve
+HP:0100116,Irregular epiphysis of the middle phalanx of the 2nd toe,HP:0100049,Irregular epiphyses of the 2nd toe
+HP:0009507,Irregular epiphysis of the distal phalanx of the 2nd finger,HP:0009499,Abnormality of the epiphysis of the distal phalanx of the 2nd finger
+UBERON:2001769,anal fin lepidotrichium 1,UBERON:4000176,anal fin lepidotrichium
+UBERON:0007727,interphalangeal joint of pedal digit 4,UBERON:0007721,interphalangeal joint of pes
+DOID:9269,maple syrup urine disease,DOID:0060159,organic acidemia
+UBERON:0015795,right lung lobar bronchus epitheium,UBERON:0003364,epithelium of right lung
+UBERON:0003905,bursal follicle,UBERON:0000064,organ part
+HP:0000559,Corneal scarring,HP:0100699,Scarring
+CL:1000891,kidney arterial blood vessel cell,CL:1000854,kidney blood vessel cell
+UBERON:2001765,pectoral fin lepidotrichium 5,UBERON:4000175,pectoral fin lepidotrichium
+HP:0010075,Duplication of the 1st metatarsal,HP:0010066,Duplication of phalanx of hallux
+DOID:9138,stomach carcinoma in situ,DOID:8719,in situ carcinoma
+UBERON:2001792,pharyngobranchial 3 bone uncinate process,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010126,Abnormality of the epiphysis of the proximal phalanx of the hallux,HP:0010056,Abnormality of the epiphyses of the hallux
+HP:0004925,Chronic lactic acidosis,HP:0003128,Lactic acidosis
+UBERON:2000735,hemal postzygapophysis,UBERON:0004247,bone of dorsum
+UBERON:0008933,primary somatosensory cortex,UBERON:0008930,somatosensory cortex
+UBERON:0006328,laryngeal intrinsic muscle,UBERON:0001568,muscle of larynx
+UBERON:0002093,spinal dura mater,UBERON:0003292,meninx of spinal cord
+DOID:7037,childhood immature teratoma of ovary,DOID:6331,immature teratoma of ovary
+HP:0011827,Malaligned philtral ridges,HP:0000288,Abnormality of the philtrum
+UBERON:0006459,third thoracic spinal cord segment,UBERON:0007715,thoracic subsegment of spinal cord
+CL:0007003,preodontoblast,CL:0000055,non-terminally differentiated cell
+HP:0001739,Abnormality of the nasopharynx,HP:0000600,Abnormality of the pharynx
+UBERON:0016410,male breast,UBERON:0000310,breast
+UBERON:0006652,muscular layer of vagina,UBERON:0014404,female anatomical structure
+UBERON:0002456,internal thoracic artery,UBERON:0004573,systemic artery
+UBERON:0008804,stylopharyngeus muscle,UBERON:0003831,respiratory system muscle
+HP:0008922,Childhood-onset short-trunk short stature,HP:0003521,Disproportionate short-trunk short stature
+HP:0010015,Absent epiphysis of the 1st metacarpal,HP:0009686,Absent epiphyses of the thumb
+HP:0012737,Small intestinal polyp,HP:0100833,Neoplasm of the small intestine
+UBERON:2001849,epihyal-branchiostegal ray joint,UBERON:0000982,skeletal joint
+HP:0001257,Spasticity,HP:0001276,Hypertonia
+UBERON:3000866,agger limitans anterior of ilium,UBERON:0004120,mesoderm-derived structure
+UBERON:3000949,posterior ramus of cleithrum,UBERON:0000064,organ part
+DOID:4608,common bile duct neoplasm,DOID:0050625,biliary tract neoplasm
+UBERON:0004660,mandible coronoid process,UBERON:0010313,neural crest-derived structure
+UBERON:2005368,dorsal fin pterygiophore 5,UBERON:2001419,dorsal fin pterygiophore
+HP:0010083,Triangular shaped distal phalanx of the hallux,HP:0010065,Triangular shaped phalanges of the hallux
+UBERON:0004236,arteriole smooth muscle,UBERON:0002111,artery smooth muscle tissue
+CL:0002561,outer root sheath cell,CL:0000362,epidermal cell
+HP:0011079,Impacted tooth,HP:0000706,Unerupted tooth
+DOID:4749,middle cranial fossa meningioma,DOID:3565,meningioma
+UBERON:0015225,atrial foramen intermedium,UBERON:0004120,mesoderm-derived structure
+UBERON:0002501,oval window,UBERON:0004120,mesoderm-derived structure
+UBERON:0013244,vaginal plate,UBERON:0002050,embryonic structure
+HP:0010258,Bracket epiphyses of the middle phalanges of the hand,HP:0010229,Bracket epiphyses of the phalanges of the hand
+HP:0008391,Dystrophic fingernails,HP:0008404,Nail dystrophy
+DOID:4028,angioma serpiginosum,DOID:471,skin hemangioma
+UBERON:0003458,neck bone,UBERON:0007914,head or neck bone
+UBERON:0013732,vestibule of nasal cavity,UBERON:0001349,vestibule
+UBERON:0004119,endoderm-derived structure,UBERON:0000061,anatomical structure
+DOID:13109,bladder leiomyoma,DOID:0050623,bladder benign neoplasm
+CL:0002622,prostate stromal cell,CL:0000499,stromal cell
+HP:0200124,Chronic hepatitis due to cryptospridium infection,HP:0200123,Chronic hepatitis
+UBERON:0016479,fibrous capsule of liver,UBERON:0003893,capsule
+UBERON:0015152,gland of orbital region,UBERON:0010313,neural crest-derived structure
+DOID:3443,mammary Paget's disease,DOID:3458,breast adenocarcinoma
+DOID:2632,papillary serous adenocarcinoma,DOID:3112,papillary adenocarcinoma
+UBERON:0005004,mucosa of right ureter,UBERON:0004980,mucosa of ureter
+HP:0003304,Spondylolysis,HP:0000925,Abnormality of the vertebral column
+HP:0010427,Partial duplication of the middle phalanx of the 2nd toe,HP:0010412,Duplication of the middle phalanx of the 2nd toe
+UBERON:0001069,head of pancreas,UBERON:0000064,organ part
+UBERON:2001470,anterior lateral line,UBERON:0010202,lateral line
+UBERON:0001093,vertebral bone 2,UBERON:0002412,vertebra
+UBERON:0006644,tunica albuginea of ovary,UBERON:0006610,tunica albuginea
+DOID:8303,congenital granular cell tumor,DOID:3350,mesenchymal cell neoplasm
+DOID:0050913,large intestine adenocarcinoma,DOID:5672,large intestine cancer
+HP:0006812,White mater abnormalities in the posterior periventricular region,HP:0002500,Abnormality of the cerebral white matter
+DOID:6612,leukocyte adhesion deficiency,DOID:0050737,autosomal recessive disease
+UBERON:0015089,distal carpal bone 2 pre-cartilage condensation,UBERON:0015087,distal carpal bone 2 endochondral element
+HP:0001351,Jerk-locked premyoclonus spikes,HP:0001311,Abnormal nervous system electrophysiology
+HP:0006689,Bacterial endocarditis,HP:0100584,Endocarditis
+UBERON:0016391,thymic lymph node,UBERON:0000029,lymph node
+UBERON:0002056,inferior suprarenal artery,UBERON:0005624,suprarenal artery
+UBERON:2001709,infraorbital series,UBERON:0000477,anatomical cluster
+UBERON:0004481,musculature of upper limb,UBERON:0004480,musculature of limb
+DOID:0050865,tongue squamous cell carcinoma,DOID:8649,tongue cancer
+UBERON:0012305,marginal cutaneous pouch of ear,UBERON:0001459,skin of external ear
+HP:0001469,Abnormality of the musculature of the pelvis,HP:0003011,Abnormality of the musculature
+UBERON:3000808,parasagittal processes,UBERON:0004120,mesoderm-derived structure
+UBERON:0002799,fronto-orbital sulcus,UBERON:0003022,cerebral cortex lobe
+UBERON:2002068,lower hypural set,UBERON:0000477,anatomical cluster
+HP:0009187,Bracket epiphysis of the distal phalanx of the 5th finger,HP:0009198,Abnormality of the epiphysis of the distal phalanx of the 5th finger
+UBERON:0011950,mammary gland luminal epithelium,UBERON:0004121,ectoderm-derived structure
+HP:0008069,Neoplasm of the skin,HP:0000951,Abnormality of the skin
+HP:0000629,Periorbital fullness,HP:0000606,Abnormality of the periorbital region
+UBERON:0013738,parabrachial pigmental nucleus,UBERON:0002438,ventral tegmental nucleus
+UBERON:4000081,cosmoid scale,UBERON:0007380,dermal scale
+CL:0002294,type-1 epithelial cell of thymus,CL:0002364,cortical thymic epithelial cell
+DOID:5805,subvalvular aortic stenosis,DOID:1712,aortic valve stenosis
+UBERON:0004332,proximal phalanx of pedal digit 1,UBERON:0003640,pedal digit 1 phalanx
+HP:0004259,Abnormality of the hamate bone,HP:0001191,Abnormality of the carpal bones
+UBERON:0005460,left vitelline vein,UBERON:0015212,lateral structure
+UBERON:0012082,bronchial lumen,UBERON:0000464,anatomical space
+UBERON:0001849,membranous labyrinth,UBERON:0000062,organ
+DOID:12785,diabetic polyneuropathy,DOID:9743,diabetic neuropathy
+CL:0002410,pancreatic stellate cell,CL:0000057,fibroblast
+HP:0010196,Bullet-shaped middle phalanges of the toes,HP:0010175,Bullet-shaped phalanges of the toes
+UBERON:2000305,ventral sulcus,UBERON:0004121,ectoderm-derived structure
+NCBITaxon:11234,Measles virus,NCBITaxon:11229,Morbillivirus
+HP:0007204,Diffuse white matter abnormalities,HP:0002500,Abnormality of the cerebral white matter
+HP:0100944,Sclerosis of the distal phalanx of the hallux,HP:0010053,Abnormality of the distal phalanx of the hallux
+UBERON:0009671,nasal fin,UBERON:0004121,ectoderm-derived structure
+UBERON:0001734,palatine uvula,UBERON:0004121,ectoderm-derived structure
+UBERON:0006340,fourth ventricle choroid plexus stroma,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010157,Small epiphysis of the 1st metatarsal,HP:0010121,Small epiphyses of the hallux
+CL:0000402,CNS interneuron,CL:0000099,interneuron
+UBERON:0003301,roof plate of diencephalon,UBERON:0003298,roof plate of neural tube
+HP:0009175,Patchy sclerosis of the middle phalanx of the 5th finger,HP:0100907,Sclerosis of the middle phalanx of the 5th finger
+UBERON:3000523,pterygoid process of palatoquadrate,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0005830,Flexion contracture of toe,HP:0001836,Camptodactyly (feet)
+UBERON:0009908,caudal root of abducens nerve,UBERON:0002786,abducens nerve fibers
+UBERON:0003588,forelimb connective tissue,UBERON:0003587,limb connective tissue
+DOID:0050592,asphyxiating thoracic dystrophy,DOID:0050737,autosomal recessive disease
+UBERON:0009062,posterior air sac,UBERON:0009060,air sac
+UBERON:2005102,presumptive median fin fold,UBERON:0006598,presumptive structure
+DOID:12339,retroperitoneal lymphoma,DOID:5875,retroperitoneal cancer
+DOID:13757,excessive tearing,DOID:1400,lacrimal apparatus disease
+HP:0007378,Neoplasm of the gastrointestinal tract,HP:0011024,Abnormality of the gastrointestinal tract
+HP:0009571,Curved middle phalanx of the 2nd finger,HP:0009549,Curved phalanges of the 2nd finger
+UBERON:0002972,centromedian nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0004434,proximal epiphysis of distal phalanx of manual digit 4,UBERON:0004420,proximal epiphysis of phalanx of manual digit 4
+UBERON:0002760,ventral corticospinal tract,UBERON:0001018,axon tract
+HP:0005364,Severe viral infections,HP:0004429,Recurrent viral infections
+UBERON:0002491,lambdoid suture,UBERON:0004120,mesoderm-derived structure
+HP:0008037,Absent anterior eye chamber,HP:0000593,Abnormality of the anterior chamber
+NCBITaxon:30639,Mastomys,NCBITaxon:39107,Murinae
+UBERON:0004632,thoracic vertebra 7,UBERON:0002347,thoracic vertebra
+CL:0002044,"Kit-positive, integrin beta7-high basophil mast progenitor cell",CL:0002028,basophil mast progenitor cell
+HP:0001328,Specific learning disability,HP:0100543,Cognitive impairment
+DOID:8439,postgastrectomy syndrome,DOID:5295,intestinal disease
+UBERON:0004741,cleithrum,UBERON:0007829,pectoral girdle bone
+HP:0000483,Astigmatism,HP:0000539,Abnormality of refraction
+CL:1000979,ureter smooth muscle cell,CL:1000601,ureteral cell
+UBERON:2000728,somite 2,UBERON:0002329,somite
+UBERON:0009778,pleural sac,UBERON:0015212,lateral structure
+HP:0001780,Abnormality of toe,HP:0001760,Abnormality of the foot
+UBERON:0008924,sublaminar layer S3,UBERON:0009731,sublaminar layers S3 or S4
+UBERON:0014781,stomodeal ectoderm,UBERON:0000483,epithelium
+DOID:10812,nasal cavity olfactory neuroblastoma,DOID:10811,nasal cavity cancer
+UBERON:0005236,osseus labyrinth vestibule,UBERON:0010313,neural crest-derived structure
+UBERON:2002193,dorsolateral septum,UBERON:0004121,ectoderm-derived structure
+UBERON:2001243,epibranchial 1 bone,UBERON:2000658,epibranchial bone
+HP:0010698,Nuclear pulverulent cataract,HP:0010925,Nuclear punctate cataract
+UBERON:0001632,temporal artery,UBERON:0003496,head blood vessel
+HP:0009937,Facial hirsutism,HP:0009889,Localized hirsutism
+UBERON:4000175,pectoral fin lepidotrichium,UBERON:4440011,paired fin lepidotrichium
+DOID:2645,benign mesothelioma,DOID:0060084,cell type benign neoplasm
+HP:0004765,Episodic supraventricular tachycardia,HP:0004755,Supraventricular tachycardia
+CL:0000794,"CD8-positive, alpha-beta cytotoxic T cell",CL:0000910,cytotoxic T cell
+DOID:4166,syphilis,DOID:0050338,primary bacterial infectious disease
+HP:0004022,Sclerotic radial metaphysis with longitudinal striations,HP:0004015,Abnormality of radial metaphyses
+UBERON:2005382,dorsal fin proximal radial bone 5,UBERON:2105382,dorsal fin proximal radial element 5
+DOID:5900,meningeal melanocytoma,DOID:4955,central nervous system melanocytic neoplasm
+CL:0000435,alkali secreting cell,CL:0000151,secretory cell
+UBERON:0003248,epithelium of footplate,UBERON:0000490,unilaminar epithelium
+UBERON:0014554,CA1 stratum radiatum,UBERON:0014567,layer of hippocampal field
+UBERON:0001770,lacrimal canaliculus,UBERON:0000063,organ segment
+HP:0003001,Glomus jugular tumor,HP:0002864,Paraganglioma of head and neck
+HP:0011503,Aplasia of the fovea,HP:0008060,Aplasia/Hypoplasia of the fovea
+UBERON:0004687,lieno-renal ligament,UBERON:0003567,abdomen connective tissue
+HP:0100142,Pseudoepiphysis of the distal phalanx of the 3rd toe,HP:0100091,Abnormality of the epiphysis of the distal phalanx of the 3rd toe
+UBERON:0012337,cauda equina,UBERON:0005162,multi cell component structure
+DOID:10881,"hand, foot and mouth disease",DOID:934,viral infectious disease
+HP:0005682,Talocalcaneal synostosis,HP:0008368,Tarsal synostosis
+CL:1001435,periglomerular cell,CL:1001434,olfactory bulb interneuron
+DOID:0050795,cone dystrophy,DOID:5679,retinal disease
+UBERON:2007028,spinal cord neural keel,UBERON:0004121,ectoderm-derived structure
+HP:0012237,Urocanic aciduria,HP:0010996,Abnormality of monocarboxylic acid metabolism
+HP:0005611,Craniodiaphyseal osteosclerosis,HP:0003034,Diaphyseal sclerosis
+CL:0002589,smooth muscle cell of the brachiocephalic vasculature,CL:0000359,vascular associated smooth muscle cell
+UBERON:0002288,choroid plexus of third ventricle,UBERON:0001886,choroid plexus
+HP:0012501,Abnormality of the brainstem white matter,HP:0002363,Abnormality of the brainstem
+UBERON:2000347,dorsal zone of median tuberal portion of hypothalamus,UBERON:0003048,regional part of hypothalamus
+UBERON:0002127,inferior olivary complex,UBERON:0003528,brain grey matter
+UBERON:0005304,submucous nerve plexus,UBERON:0000429,enteric plexus
+HP:0008288,Nonketotic hyperglycinemia,HP:0002154,Hyperglycinemia
+UBERON:0001742,epiglottic cartilage,UBERON:0001739,laryngeal cartilage
+UBERON:0014611,apex of thoracic spinal cord dorsal horn,UBERON:0006983,anatomical point
+HP:0001441,Abnormality of the musculature of the thigh,HP:0001437,Abnormality of the musculature of the lower limbs
+UBERON:0013617,upper primary molar tooth,UBERON:0013616,primary molar tooth
+UBERON:0001335,prostatic urethra,UBERON:0006554,urinary system structure
+DOID:4196,femoral neuropathy,DOID:1188,mononeuropathy
+UBERON:0008917,ampullary organ,UBERON:0003103,compound organ
+HP:0001288,Gait disturbance,HP:0100022,Abnormality of movement
+DOID:3199,C-P angle neurinoma,DOID:3200,cerebellopontine angle tumor
+UBERON:0014694,posterior auricular artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3010456,lower blastopore lip,UBERON:3010455,blastopore lip
+UBERON:0000479,tissue,UBERON:0010000,multicellular anatomical structure
+HP:0011666,Absent right superior vena cava,HP:0005301,Persistent left superior vena cava
+UBERON:0001623,dorsal nasal artery,UBERON:0015156,terminal branch of ophthalmic artery
+DOID:2348,arteriosclerotic cardiovascular disease,DOID:2349,arteriosclerosis
+UBERON:0006966,heart capillary,UBERON:0003498,heart blood vessel
+DOID:6776,breast myoepithelial carcinoma,DOID:3459,breast carcinoma
+UBERON:0005289,tela choroidea of telencephalic ventricle,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005074,postganglionic parasympathetic nervous system,UBERON:0000011,parasympathetic nervous system
+UBERON:2001223,basibranchial 1 bone,UBERON:0002513,endochondral bone
+DOID:8361,glassy cell variant cervical adenosquamous carcinoma,DOID:5636,cervical adenosquamous carcinoma
+UBERON:0014881,distal epiphysis of distal phalanx of manual digit 1,UBERON:0014886,distal epiphysis of distal phalanx of manual digit
+UBERON:3010528,articular process of palatoquadrate,UBERON:0000064,organ part
+UBERON:0008904,neuromast,UBERON:0000477,anatomical cluster
+UBERON:0005409,gastrointestinal system,UBERON:0000467,anatomical system
+HP:0100253,Abnormality of the medullary cavity of the long bones,HP:0011314,Abnormality of long bone morphology
+UBERON:0005620,primary palate,UBERON:0010313,neural crest-derived structure
+HP:0011171,Simple febrile seizures,HP:0002373,Febrile seizures
+UBERON:2002232,presumptive cardiac ventricle primitive heart tube,UBERON:0002050,embryonic structure
+HP:0010418,Patchy sclerosis of the distal phalanx of the 2nd toe,HP:0010190,Patchy sclerosis of the distal phalanges of the toes
+HP:0011969,Elevated luteinizing hormone,HP:0000837,Gonadotropin excess
+DOID:13756,epiphora due to insufficient drainage,DOID:13757,excessive tearing
+DOID:12190,descending colon cancer,DOID:219,colon cancer
+UBERON:0009673,accessory XI nerve cranial component,UBERON:0001785,cranial nerve
+UBERON:0004380,proximal epiphysis,UBERON:0001437,epiphysis
+DOID:5485,synovial sarcoma,DOID:2706,synovium cancer
+HP:0006751,Paraspinal neurofibromas,HP:0001067,Neurofibromas
+UBERON:0005262,ventricle cardiac jelly,UBERON:0003906,cardiac jelly
+HP:0010706,1-3 finger syndactyly,HP:0006101,Finger syndactyly
+UBERON:0002403,internal intercostal muscle,UBERON:0001111,intercostal muscle
+NCBITaxon:138949,Human enterovirus B,NCBITaxon:12059,Enterovirus
+UBERON:0014672,distal interphalangeal joint of pedal digit 2,UBERON:0014677,distal interphalangeal joint of digit 2
+UBERON:2005410,pars inferior ear,UBERON:0010314,structure with developmental contribution from neural crest
+CL:1000305,fibroblast of connective tissue of glandular part of prostate,CL:0000057,fibroblast
+CL:0002170,keratinized cell of the oral mucosa,CL:0000237,keratinizing barrier epithelial cell
+UBERON:0004627,thoracic vertebra 2,UBERON:0002347,thoracic vertebra
+UBERON:0005325,mesonephric glomerulus,UBERON:0000074,renal glomerulus
+HP:0011314,Abnormality of long bone morphology,HP:0011842,Abnormality of skeletal morphology
+UBERON:0011624,superior horn of thyroid cartilage,UBERON:0011623,horn of thyroid cartilage
+CL:0002298,type-5 epithelial cell of thymus,CL:0002365,medullary thymic epithelial cell
+UBERON:0013154,1st arch maxillary endoderm,UBERON:0005291,embryonic tissue
+DOID:9776,Senile atrophy of choroid,DOID:980,choroidal sclerosis
+UBERON:0014448,feathered ear tuft,UBERON:0011810,collection of feathers
+DOID:4472,mucinous tubular and spindle renal cell carcinoma,DOID:4450,renal cell carcinoma
+UBERON:0006822,proximal epiphysis of ulna,UBERON:0004380,proximal epiphysis
+UBERON:0010233,stroma of thyroid gland,UBERON:0004119,endoderm-derived structure
+DOID:2766,ethmoid sinus adenocarcinoma,DOID:1363,ethmoid sinus cancer
+DOID:5443,clear cell hidradenoma,DOID:3896,hidradenoma
+UBERON:3000446,posterior condyle,UBERON:0005913,zone of bone organ
+HP:0004277,Fractured hand bones,HP:0001155,Abnormality of the hand
+HP:0007935,Juvenile posterior subcapsular lenticular opacities,HP:0007787,Posterior subcapsular cataract
+HP:0006408,Distal tapering femur,HP:0002823,Abnormality of the femur
+UBERON:0006167,forelimb proper dorsal digital arteries,UBERON:0006146,dorsal digital artery of manus
+HP:0003893,Advanced ossification of the humeral epiphysis,HP:0003891,Abnormality of the humeral epiphysis
+HP:0012033,Sacral lipoma,HP:0012032,Lipoma
+HP:0004411,Deviated nasal septum,HP:0000419,Abnormality of the nasal septum
+UBERON:0007744,metacarpophalangeal joint of manual digit 4,UBERON:0003695,metacarpophalangeal joint
+HP:0009274,Joint contractures of the 4th finger,HP:0100490,Camptodactyly of finger
+UBERON:2005011,pseudobranchial artery,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0002442,"CD94-negative, Ly49CI-negative natural killer cell",CL:0002446,Ly49CI-negative natural killer cell
+HP:0009962,Duplication of the distal phalanx of the 3rd finger,HP:0009883,Duplication of the distal phalanx of hand
+UBERON:0006002,vitelline artery,UBERON:0001637,artery
+UBERON:3010049,M. gemellus,UBERON:0010890,pelvic complex muscle
+HP:0012662,Parietal hypometabolism in FDG PET,HP:0012658,Abnormal brain FDG positron emission tomography
+UBERON:0004296,respiratory system lymphatic vessel smooth muscle,UBERON:0004225,respiratory system smooth muscle
+UBERON:0001805,autonomic ganglion,UBERON:0003338,ganglion of peripheral nervous system
+HP:0000062,Ambiguous genitalia,HP:0000811,Abnormal external genitalia
+UBERON:2000139,immature otolith,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004693,Peyer's patch epithelium,UBERON:0001277,intestinal epithelium
+UBERON:0001675,trigeminal ganglion,UBERON:0001800,sensory ganglion
+NCBITaxon:52773,Actinomyces meyeri,NCBITaxon:1654,Actinomyces
+DOID:5467,conjunctival cancer,DOID:2174,ocular cancer
+UBERON:0005048,mucosa of uterine tube,UBERON:0000344,mucosa
+DOID:11750,Bordetella parapertussis whooping cough,DOID:1116,pertussis
+UBERON:2002076,lateral process of basipterygium,UBERON:4100000,skeletal element projection
+UBERON:0002247,uterine horn,UBERON:0005156,reproductive structure
+DOID:0050084,rhinotracheitis,DOID:974,upper respiratory tract disease
+UBERON:0003641,pedal digit 2 phalanx,UBERON:0001449,phalanx of pes
+HP:0011044,Abnormal number of permanent teeth,HP:0006483,Abnormal number of teeth
+UBERON:3000254,lamella alaris,UBERON:0010313,neural crest-derived structure
+DOID:4140,biliary dyskinesia,DOID:4137,common bile duct disease
+HP:0008425,Cuboid-shaped thoracolumbar vertebral bodies,HP:0004634,Cuboid-shaped vertebral bodies
+UBERON:0002074,hair shaft,UBERON:0000021,cutaneous appendage
+UBERON:0009896,oral siphon primordia,UBERON:0009894,siphon primordium
+UBERON:0006770,apophysis,UBERON:0004530,bony projection
+HP:0010475,Cloacal exstrophy,HP:0010866,Abdominal wall defect
+DOID:3205,melanotic neurilemmoma,DOID:3192,neurilemmoma
+UBERON:0001164,greater curvature of stomach,UBERON:0009870,zone of stomach
+HP:0002589,Gastrointestinal atresia,HP:0012718,Morphological abnormality of the gastrointestinal tract
+UBERON:3000792,anterior ramus of cleithrum,UBERON:0004121,ectoderm-derived structure
+UBERON:0015853,dental pulp of median incisor tusk,UBERON:0015837,incisor dental pulp
+UBERON:0005372,hippocampus stratum radiatum,UBERON:0002305,layer of hippocampus
+UBERON:0002225,costal arch,UBERON:0006800,anatomical line
+UBERON:0002434,pituitary stalk,UBERON:0002784,regional part of diencephalon
+HP:0006824,Cranial nerve paralysis,HP:0001291,Abnormality of the cranial nerves
+UBERON:0001919,endothelium of vein,UBERON:0004638,blood vessel endothelium
+UBERON:3010764,laryngeus ventralis,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001293,outer medulla of kidney,UBERON:0000064,organ part
+UBERON:0003480,vein of clitoris,UBERON:0014404,female anatomical structure
+UBERON:0006674,inguinal ring,UBERON:0000064,organ part
+HP:0010406,Bullet-shaped middle phalanx of the 2nd toe,HP:0010349,Bullet-shaped phalanges of the 2nd toe
+CL:0000923,CD4-positive type I NK T cell,CL:0000921,type I NK T cell
+UBERON:2000658,epibranchial bone,UBERON:2001904,epibranchial element
+HP:0001027,"Soft, doughy skin",HP:0000977,Soft skin
+UBERON:0006204,inguinal ligament,UBERON:0000211,ligament
+UBERON:0004892,lobar bronchus alveolar system,UBERON:0000467,anatomical system
+UBERON:0004022,embryonic neuroepithelium,UBERON:0010371,ecto-epithelium
+UBERON:0015143,mesenteric fat pad,UBERON:0004120,mesoderm-derived structure
+HP:0004024,Medially sloping radial metaphysis,HP:0004023,Sloping radial metaphysis
+DOID:4511,breast angiosarcoma,DOID:3017,breast sarcoma
+HP:0100565,Hydromyelia,HP:0100561,Spinal cord lesions
+DOID:9884,muscular dystrophy,DOID:423,myopathy
+UBERON:0001596,intrinsic auricular muscle,UBERON:0001595,auricular muscle
+UBERON:0015482,right hepatic artery,UBERON:0015796,liver blood vessel
+UBERON:0003358,epithelium of soft palate,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0002631,Ascending aortic aneurysm,HP:0012727,Thoracic aortic aneurysm
+CL:0000948,IgE memory B cell,CL:0000972,class switched memory B cell
+CL:1000427,adrenal cortex chromaffin cell,CL:1001601,adrenal gland glandular cell
+HP:0006232,Expanded metacarpals with widened medullary cavities,HP:0005916,Abnormal metacarpal morphology
+UBERON:0011318,capsule of temporomandibular joint,UBERON:0004120,mesoderm-derived structure
+NCBITaxon:241806,Moniliformopses,NCBITaxon:78536,Euphyllophyta
+HP:0010101,Partial duplication of the phalanges of the hallux,HP:0010066,Duplication of phalanx of hallux
+UBERON:0003483,thymus lymphoid tissue,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0003094,infraorbital lateral line,UBERON:0010202,lateral line
+UBERON:0006591,transformed artery,UBERON:0006590,vestigial embryonic structure
+HP:0012485,Abnormal surface-connected open canalicular system,HP:0011875,Abnormal platelet morphology
+UBERON:0000480,anatomical group,UBERON:0000061,anatomical structure
+HP:0009443,Osteolytic defects of the phalanges of the 3rd finger,HP:0009699,Osteolytic defects of the hand bones
+DOID:10458,legionellosis,DOID:0050338,primary bacterial infectious disease
+UBERON:4200012,ectepicondylar flange,UBERON:0004530,bony projection
+UBERON:0014370,extrastriate cortex,UBERON:0010009,aggregate regional part of brain
+UBERON:0009965,coxal gland,UBERON:0009962,excretory gland
+DOID:14018,alcoholic liver cirrhosis,DOID:5082,liver cirrhosis
+DOID:8553,pyoderma gangrenosum,DOID:4223,pyoderma
+HP:0006915,Inability to walk by childhood/adolescence,HP:0002505,Progressive inability to walk
+DOID:10423,acute pericementitis,DOID:824,periodontitis
+DOID:0050516,O'nyong'nyong fever,DOID:934,viral infectious disease
+HP:0000776,Congenital diaphragmatic hernia,HP:0000775,Abnormality of the diaphragm
+UBERON:0010130,autopod plate,UBERON:0002050,embryonic structure
+UBERON:0005178,thoracic cavity organ,UBERON:0005181,thoracic segment organ
+UBERON:3000365,otic process,UBERON:4100000,skeletal element projection
+UBERON:0001438,metaphysis,UBERON:0005055,zone of long bone
+CL:0002647,epithelial cell of anterior palatal part of viscerocranial mucosa,CL:0002283,ecto-epithelial cell of viscerocranial mucosa
+UBERON:2001711,frontal-pterotic joint,UBERON:0000982,skeletal joint
+UBERON:0004808,gastrointestinal system epithelium,UBERON:0000483,epithelium
+HP:0010171,Epiphyseal stippling of toe phalanges,HP:0010655,Epiphyseal stippling
+HP:0100609,Hypermenorrhea,HP:0000140,Abnormality of the menstrual cycle
+UBERON:0013479,lung endothelium,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0009473,Joint contracture of the hand,HP:0001155,Abnormality of the hand
+UBERON:0012373,sympathetic nerve plexus,UBERON:0001816,autonomic nerve plexus
+UBERON:2000657,entopterygoid,UBERON:0011597,bone of upper jaw
+HP:0100838,Recurrent cutaneous abscess formation,HP:0005406,Recurrent bacterial skin infections
+HP:0010123,Triangular epiphyses of the hallux,HP:0010172,Triangular epiphyses of the toes
+HP:0009927,Aplasia of the nose,HP:0009924,Aplasia/Hypoplasia involving the nose
+UBERON:0002498,deltopectoral crest,UBERON:0004120,mesoderm-derived structure
+UBERON:0006537,female reproductive system fluid/secretion,UBERON:0000463,portion of organism substance
+UBERON:3000509,processus suprafenestralis,UBERON:4100000,skeletal element projection
+DOID:6945,inverted follicular keratosis,DOID:6498,seborrheic keratosis
+UBERON:3010306,mitochondrial aggregate,UBERON:0000470,cell part
+HP:0000076,Vesicoureteral reflux,HP:0000009,Functional abnormality of the bladder
+UBERON:2002029,pectoral fin proximal radial bone 4,UBERON:2102029,pectoral fin proximal radial element 4
+HP:0002818,Abnormality of the radius,HP:0002973,Abnormality of the forearm
+DOID:4645,retinal cancer,DOID:2174,ocular cancer
+UBERON:0001686,auditory ossicle,UBERON:0008001,irregular bone
+HP:0012087,Abnormal mitochondrial shape,HP:0008322,Abnormal mitochondrial morphology
+DOID:6286,childhood cerebellar astrocytic neoplasm,DOID:4848,cerebellar astrocytoma
+HP:0005406,Recurrent bacterial skin infections,HP:0002718,Recurrent bacterial infections
+UBERON:0011965,saddle joint,UBERON:0000982,skeletal joint
+DOID:13500,hairy tongue,DOID:10944,tongue disease
+HP:0006805,Large corpus callosum,HP:0200009,Abnormal size of corpus callosum
+UBERON:0011802,feather bud,UBERON:0005423,developing anatomical structure
+HP:0000667,Phthisis bulbi,HP:0012374,Abnormality of the globe
+UBERON:0011630,intertemporal bone,UBERON:0002514,intramembranous bone
+CL:0002140,acinar cell of sebaceous gland,CL:1000448,epithelial cell of sweat gland
+CL:0000701,paraganglia type 2 cell,CL:0000630,supportive cell
+UBERON:0003432,chest nerve,UBERON:0003824,nerve of thoracic segment
+UBERON:0011631,tabular bone,UBERON:0008907,dermal bone
+HP:0100659,Abnormality of the cerebral vasculature,HP:0007319,Morphological abnormality of the central nervous system
+UBERON:0010207,nictitating membrane,UBERON:0010305,region of conjunctiva
+UBERON:0013746,basibranchial element,UBERON:0010363,endochondral element
+DOID:12337,varicocele,DOID:9742,pelvic varices
+HP:0003680,Nonprogressive disorder,HP:0003679,Pace of progression
+UBERON:0010005,placental labyrinth villous,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0010809,Broad uvula,HP:0000172,Abnormality of the uvula
+HP:0005680,Tongue-like lumbar vertebral deformities,HP:0003312,Abnormal form of the vertebral bodies
+UBERON:0010884,forelimb bone pre-cartilage condensation,UBERON:0003859,forelimb mesenchyme
+HP:0011655,Double outlet right ventricle with subaortic ventricular septal defect and pulmonary stenosis,HP:0001719,Double outlet right ventricle
+UBERON:0006856,interrenal gland,UBERON:0005058,hemolymphoid system gland
+HP:0010292,Absent uvula,HP:0010293,Aplasia/Hypoplasia of the uvula
+HP:0006446,Dysplastic patella,HP:0003045,Abnormality of the patella
+HP:0004224,Abnormality of the epiphysis of the middle phalanx of the 5th finger,HP:0010244,Abnormality of the epiphyses of the middle phalanges of the hand
+UBERON:0013403,asterion of skull,UBERON:0006983,anatomical point
+UBERON:0004170,spinal cord ventral commissure,UBERON:0007838,spinal cord white commissure
+DOID:5149,epithelioid neurofibroma,DOID:962,neurofibroma
+UBERON:0003460,arm bone,UBERON:0008962,forelimb bone
+HP:0009576,Absent middle phalanx of 2nd finger,HP:0009535,Aplasia of the 2nd finger
+UBERON:2002258,trituration tooth,UBERON:0001091,calcareous tooth
+CL:0000835,myeloblast,CL:0002242,nucleate cell
+CL:0002037,"CD2-positive, CD5-positive, CD44-positive alpha-beta intraepithelial T cell",CL:0000793,"CD4-positive, alpha-beta intraepithelial T cell"
+UBERON:0003699,pubic symphysis,UBERON:0008114,joint of girdle
+UBERON:0003979,utricle valve,UBERON:0003978,valve
+CL:0000682,M cell of gut,CL:0000473,defensive cell
+HP:0010280,Stomatitis,HP:0011830,Abnormality of oral mucosa
+UBERON:0013221,caudofemoralis,UBERON:0003665,tail muscle
+UBERON:0005671,greater sac mesothelium,UBERON:0001136,mesothelium
+UBERON:0011124,xiphisternal joint,UBERON:0002216,symphysis
+HP:0009977,Duplication of the proximal phalanx of the 4th finger,HP:0009284,Abnormality of the proximal phalanx of the 4th finger
+UBERON:4300018,ventral marginal cartilage,UBERON:0005156,reproductive structure
+HP:0100545,Arterial stenosis,HP:0005114,Abnormalities of the peripheral arteries
+HP:0100288,EMG: myokymic discharges,HP:0003457,EMG abnormality
+HP:0006508,Abnormality of tibial epiphyses,HP:0002992,Abnormality of the tibia
+HP:0004544,Pointed frontal hairline,HP:0000599,Abnormality of the frontal hairline
+CL:0000164,enteroendocrine cell,CL:0000163,endocrine cell
+UBERON:0004611,rib 12,UBERON:0002228,rib
+UBERON:0003003,microfilament,UBERON:0000470,cell part
+UBERON:0006959,mandible angular process,UBERON:0010313,neural crest-derived structure
+HP:0004007,Sclerotic radial epiphyses,HP:0003999,Abnormality of radial epiphyses
+DOID:0050662,bestrophinopathy,DOID:4448,macular degeneration
+UBERON:0013522,subdivision of tube,UBERON:0000064,organ part
+DOID:4708,foramen magnum meningioma,DOID:4437,skull base meningioma
+HP:0008064,Ichthyosis,HP:0011368,Epidermal thickening
+UBERON:1500006,paired fin radial bone,UBERON:1600006,paired fin radial element
+HP:0010650,Premaxillary underdevelopment,HP:0010756,Aplasia/Hypoplasia of the premaxilla
+NCBITaxon:11588,Rift Valley fever virus,NCBITaxon:11584,Phlebovirus
+DOID:10368,epididymis adenocarcinoma,DOID:10366,epididymis cancer
+UBERON:0010584,pedal digit 5 phalanx pre-cartilage condensation,UBERON:0005699,pedal digit 5 mesenchyme
+HP:0001211,Abnormality of the fingertips,HP:0001167,Abnormality of finger
+NCBITaxon:129726,Pseudocowpox virus,NCBITaxon:10257,Parapoxvirus
+DOID:3640,central nervous system teratoma,DOID:4439,central nervous system germ cell tumor
+NCBITaxon:106178,canis group,NCBITaxon:943,Ehrlichia
+CL:0002097,cortical cell of adrenal gland,CL:0000174,steroid hormone secreting cell
+HP:0007933,Broad lateral eyebrow,HP:0011229,Broad eyebrow
+HP:0008653,Crescentic glomerulonephritis,HP:0000099,Glomerulonephritis
+DOID:0060125,heavy chain disease,DOID:2916,hypersensitivity reaction type IV disease
+DOID:10303,sialadenitis,DOID:10854,salivary gland disease
+DOID:5306,bladder clear cell adenocarcinoma,DOID:3711,bladder adenocarcinoma
+CL:0002102,CD38-negative naive B cell,CL:0000788,naive B cell
+UBERON:0013705,fascia of Scarpa,UBERON:0003427,abdominal fat pad
+UBERON:0002189,outer cortex of kidney,UBERON:0001225,cortex of kidney
+HP:0002592,Gastric ulcer,HP:0004398,Peptic ulcer
+HP:0008419,Intervertebral disc degeneration,HP:0005108,Abnormality of the intervertebral disk
+DOID:3671,pericoronitis,DOID:1483,gingival disease
+HP:0002917,Hypomagnesemia,HP:0004921,Abnormality of magnesium homeostasis
+DOID:0060121,integumentary system benign neoplasm,DOID:0060085,organ system benign neoplasm
+UBERON:0001275,pubis,UBERON:0015212,lateral structure
+UBERON:0002230,head of rib,UBERON:0004120,mesoderm-derived structure
+UBERON:0002122,capsule of thymus,UBERON:0003893,capsule
+DOID:589,congenital hemolytic anemia,DOID:583,hemolytic anemia
+HP:0005561,Abnormality of bone marrow cell morphology,HP:0001871,Abnormality of  blood and blood-forming tissues
+CL:0000143,guidepost cell,CL:0000130,neuron associated cell (sensu Nematoda and Protostomia)
+CL:0002212,type II muscle cell,CL:0000190,fast muscle cell
+DOID:5261,heart leiomyosarcoma,DOID:5262,heart sarcoma
+DOID:6203,thyroid hyalinizing trabecular adenoma,DOID:6204,follicular adenoma
+HP:0009224,Triangular epiphysis of the middle phalanx of the 4th finger,HP:0009247,Abnormality of the epiphysis of the middle phalanx of the 4th finger
+UBERON:0002158,principal inferior olivary nucleus,UBERON:0007244,inferior olivary nucleus
+DOID:3852,Peutz-Jeghers syndrome,DOID:5295,intestinal disease
+UBERON:0000319,cytotrophoblast,UBERON:0002050,embryonic structure
+CL:1000349,basal cell of epithelium of bronchus,CL:0002328,bronchial epithelial cell
+CL:0002187,basal cell of epidermis,CL:1000428,stem cell of epidermis
+HP:0000945,Flared irregular metaphyses,HP:0003015,Flared metaphyses
+HP:0006502,Aplasia/Hypoplasia involving the carpal bones,HP:0005927,Aplasia/Hypoplasia involving bones of the hand
+UBERON:0014637,thoracic spinal cord white matter,UBERON:0002318,white matter of spinal cord
+UBERON:0000976,humerus,UBERON:0003607,forelimb long bone
+HP:0002049,Proximal renal tubular acidosis,HP:0001947,Renal tubular acidosis
+CL:0000528,nitrergic neuron,CL:0000540,neuron
+DOID:1682,congenital heart disease,DOID:114,heart disease
+DOID:6231,mature teratoma of the ovary,DOID:5566,mature teratoma
+UBERON:2000589,sulcus ypsiloniformis,UBERON:0004121,ectoderm-derived structure
+UBERON:0007315,internal pudendal artery,UBERON:0003520,pelvis blood vessel
+HP:0010184,Abnormality of the proximal phalanges of the toes,HP:0010161,Abnormality of the phalanges of the toes
+UBERON:0013689,appendix lymphoid tissue,UBERON:0001744,lymphoid tissue
+UBERON:0001376,tensor fasciae latae muscle,UBERON:0002000,gluteal muscle
+UBERON:3010393,mesonephric late distal segment,UBERON:0006554,urinary system structure
+HP:0007448,Hyperkeratosis over edematous areas,HP:0000962,Hyperkeratosis
+UBERON:0013619,upper secondary molar tooth,UBERON:0003666,upper jaw molar
+NCBITaxon:11292,Rabies virus,NCBITaxon:11286,Lyssavirus
+CL:1001021,kidney loop of henle descending limb epithelial cell,CL:1000909,kidney loop of henle epithelial cell
+HP:0000563,Keratoconus,HP:0100689,Decreased corneal thickness
+UBERON:0011170,quadrate-articular joint,UBERON:0011171,jaw joint
+UBERON:0006763,epithelium of conjunctiva,UBERON:0015808,eye epithelium
+UBERON:0005563,trigeminal neural crest,UBERON:0007213,mesenchyme derived from head neural crest
+UBERON:2002075,distal cartilage of external anterior process of basipterygium,UBERON:0004120,mesoderm-derived structure
+HP:0003922,Spurred humeral metaphysis,HP:0003907,Abnormality of the humeral metaphyses
+HP:0008968,Muscle hypertrophy of the lower extremities,HP:0003712,Muscle hypertrophy
+DOID:13352,ego-dystonic sexual orientation,DOID:1234,gender identity disorder
+HP:0005257,Thoracic hypoplasia,HP:0000765,Abnormality of the thorax
+UBERON:0014528,extreme capsule,UBERON:0002437,cerebral hemisphere white matter
+HP:0005216,Chewing difficulties,HP:0002015,Dysphagia
+UBERON:0004448,distal epiphysis of phalanx,UBERON:0004379,distal epiphysis
+HP:0007178,Motor polyneuropathy,HP:0009830,Peripheral neuropathy
+HP:0009656,Symphalangism of the thumb,HP:0009602,Abnormality of the phalanges of the thumb
+CL:0002225,secondary lens fiber,CL:0011004,lens fiber cell
+DOID:9310,nasal cavity neoplasm,DOID:0050621,respiratory system benign neoplasm
+HP:0012716,Moderate conductive hearing impairment,HP:0012713,Moderate hearing impairment
+HP:0012676,Copper accumulation in brain,HP:0012443,Abnormality of the brain
+UBERON:1000021,skin of face,UBERON:0001084,skin of head
+DOID:4073,pancreatic cystadenocarcinoma,DOID:4074,pancreas adenocarcinoma
+NCBITaxon:65647,Ixodes holocyclus,NCBITaxon:6944,Ixodes
+HP:0009648,Triangular shaped distal phalanx of the thumb,HP:0009617,Abnormality of the distal phalanx of the thumb
+HP:0002293,Alopecia of scalp,HP:0100037,Abnormality of the scalp hair
+UBERON:0001733,soft palate,UBERON:0004121,ectoderm-derived structure
+HP:0003530,Glutaric acidemia,HP:0010995,Abnormality of dicarboxylic acid metabolism
+UBERON:0004335,proximal phalanx of pedal digit 4,UBERON:0003862,pedal digit 4 phalanx
+UBERON:2000454,ventral accessory optic nucleus,UBERON:0014450,pretectal nucleus
+HP:0008062,Aplasia/Hypoplasia affecting the anterior segment of the eye,HP:0008056,Aplasia/Hypoplasia affecting the eye
+UBERON:0003955,molar crown,UBERON:0003675,tooth crown
+HP:0012469,Infantile spasms,HP:0011097,Epileptic spasms
+HP:0100837,Atrophodermia vermiculata,HP:0000987,Atypical scarring of skin
+UBERON:0010849,tibia cartilage element,UBERON:0010885,hindlimb cartilage element
+UBERON:0007808,adipose tissue of abdominal region,UBERON:0001013,adipose tissue
+CL:0002069,type II vestibular sensory cell,CL:0000609,vestibular hair cell
+CL:0002568,mesenchymal stem cell of Wharton's jelly,CL:0002569,mesenchymal stem cell of umbilical cord
+HP:0011847,Giant cell tumor of bone,HP:0010622,Neoplasm of the skeletal system
+UBERON:0011642,oral epithelium from ectoderm,UBERON:0002424,oral epithelium
+HP:0001975,Decreased platelet glycoprotein IIb-IIIa,HP:0011878,Abnormal platelet membrane protein expression
+UBERON:2000654,rostral motor nucleus of abducens,UBERON:0009662,hindbrain nucleus
+HP:0100657,Celosomia,HP:0100656,Thoracoabdominal wall defects
+UBERON:3010498,cutaneus artery,UBERON:0001637,artery
+DOID:8411,kidney angiomyolipoma,DOID:3116,kidney benign neoplasm
+UBERON:0011256,rhinarium,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003509,arterial blood vessel,UBERON:0001981,blood vessel
+HP:0100404,Duplication of the proximal phalanx of the 3rd toe,HP:0010211,Duplication of proximal phalanx of toe
+UBERON:2001243,epibranchial 1 bone,UBERON:2001905,epibranchial 1 element
+UBERON:2000734,preural vertebra,UBERON:0001095,caudal vertebra
+HP:0011055,Agenesis of permanent molar,HP:0011054,Agenesis of molar
+UBERON:0003566,head connective tissue,UBERON:0002384,connective tissue
+HP:0002837,Recurrent bronchitis,HP:0012387,Bronchitis
+HP:0004802,Episodic hemolytic anemia,HP:0001878,Hemolytic anemia
+DOID:0050484,aneruptive fever,DOID:11104,spotted fever
+UBERON:4200184,ulnar tuberosity,UBERON:0004120,mesoderm-derived structure
+UBERON:3000288,maxillopalatine,UBERON:0008193,pneumatized bone
+DOID:1156,pseudogout,DOID:848,arthritis
+UBERON:0003440,limb nerve,UBERON:0001021,nerve
+UBERON:2001734,posterior process of basipterygium,UBERON:0004120,mesoderm-derived structure
+HP:0002080,Intention tremor,HP:0001337,Tremor
+HP:0009504,Cone-shaped epiphysis of the distal phalanx of the 2nd finger,HP:0009499,Abnormality of the epiphysis of the distal phalanx of the 2nd finger
+CL:0000769,basophilic metamyelocyte,CL:0000768,immature basophil
+UBERON:0014793,musculature of pectoral complex,UBERON:0001015,musculature
+UBERON:2001764,pectoral fin lepidotrichium 4,UBERON:4000175,pectoral fin lepidotrichium
+UBERON:0004665,seminal vesicle muscle layer,UBERON:0006660,muscle layer
+HP:0005866,Opposable triphalangeal thumb,HP:0001199,Triphalangeal thumb
+HP:0010976,B lymphocytopenia,HP:0010975,Abnormality of B cell number
+HP:0010125,Abnormality of the epiphysis of the 1st metatarsal,HP:0010056,Abnormality of the epiphyses of the hallux
+HP:0006368,Forearm reduction defects,HP:0002973,Abnormality of the forearm
+UBERON:0013206,nasal tentacle,UBERON:0004121,ectoderm-derived structure
+UBERON:0013204,epipubic bone,UBERON:0007830,pelvic girdle bone/zone
+CL:0000933,type II NK T cell secreting interleukin-4,CL:0000912,helper T cell
+UBERON:2001382,epibranchial bone uncinate process,UBERON:4100000,skeletal element projection
+HP:0100187,Pseudoepiphysis of the middle phalanx of the 4th toe,HP:0100095,Abnormality of the epiphysis of the middle phalanx of the 4th toe
+UBERON:0010543,acropodial skeleton,UBERON:0010712,limb skeleton subdivision
+HP:0009638,Short proximal phalanx of thumb,HP:0009660,Short phalanx of the thumb
+HP:0007469,Palmoplantar cutis gyrata,HP:0100871,Abnormality of the palm
+DOID:112,esophageal varix,DOID:866,vein disease
+HP:0009037,Segmental spinal muscular atrophy,HP:0007269,Spinal muscular atrophy
+DOID:8472,localized scleroderma,DOID:419,scleroderma
+HP:0011745,Non-secretory adrenocortical adenoma,HP:0008256,Adrenocortical adenoma
+UBERON:0002595,orbital sulcus,UBERON:0008334,subarachnoid sulcus
+UBERON:0004375,bone of free limb or fin,UBERON:0004120,mesoderm-derived structure
+UBERON:0015160,supraorbital artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0010092,Triangular shaped proximal phalanx of the hallux,HP:0010052,Abnormality of the proximal phalanx of the hallux
+UBERON:0005104,anterior mesonephric tubule,UBERON:0000083,mesonephric tubule
+DOID:9868,intestinal disaccharidase deficiency,DOID:5295,intestinal disease
+DOID:0050614,bronchus carcinoma in situ,DOID:8719,in situ carcinoma
+HP:0100104,Fragmentation of the epiphysis of the distal phalanx of the 2nd toe,HP:0100088,Abnormality of the epiphysis of the distal phalanx of the 2nd toe
+UBERON:3000678,esophageal process,UBERON:4100000,skeletal element projection
+UBERON:0005688,lens vesicle cavity,UBERON:0000464,anatomical space
+DOID:7147,ankylosing spondylitis,DOID:3342,bone inflammation disease
+UBERON:0000052,fornix of brain,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001699,sensory root of facial nerve,UBERON:0010313,neural crest-derived structure
+HP:0100605,Neoplasm of the larynx,HP:0001600,Abnormality of the larynx
+HP:0010016,Bracket epiphysis of the 1st metacarpal,HP:0009687,Bracket epiphyses of the thumb
+UBERON:0006855,ureter muscle layer,UBERON:0006554,urinary system structure
+UBERON:0010680,pedal digit 1 phalanx cartilage element,UBERON:0010685,pedal digit phalanx cartilage element
+CL:0000837,hematopoietic multipotent progenitor cell,CL:0008001,hematopoietic precursor cell
+HP:0005114,Abnormalities of the peripheral arteries,HP:0011004,Abnormality of the systemic arterial tree
+UBERON:0010719,girdle skeleton,UBERON:0010912,subdivision of skeleton
+HP:0002355,Difficulty walking,HP:0004302,Functional motor problems.
+UBERON:0002246,dorsal thoracic nucleus,UBERON:0011777,nucleus of spinal cord
+CL:1000892,kidney capillary endothelial cell,CL:1000854,kidney blood vessel cell
+DOID:11754,siderosis of eye,DOID:9799,eye degenerative disease
+UBERON:2005365,dorsal fin pterygiophore 2,UBERON:2001419,dorsal fin pterygiophore
+UBERON:0004722,deep cervical lymph node,UBERON:0015918,deep lymph node
+CL:0002145,ciliated columnar cell of tracheobronchial tree,CL:0005012,multi-ciliated epithelial cell
+UBERON:0015007,cervical vertebra endochondral element,UBERON:0004120,mesoderm-derived structure
+HP:0010425,Partial duplication of the distal phalanx of the 2nd toe,HP:0010428,Partial duplication of phalanx of the 2nd toe
+UBERON:0008934,secondary somatosensory cortex,UBERON:0008930,somatosensory cortex
+UBERON:0000209,tetrapod frontal bone,UBERON:0011164,neurocranium bone
+HP:0005694,Partial fusion of proximal row of carpal bones,HP:0009702,Carpal synostosis
+UBERON:0006828,trabecula carnea of atrium,UBERON:0002511,trabecula carnea
+HP:0011826,Philtrum with midline raphe,HP:0000288,Abnormality of the philtrum
+UBERON:0013734,rostral linear nucleus,UBERON:0002438,ventral tegmental nucleus
+UBERON:0006458,second thoracic spinal cord segment,UBERON:0007715,thoracic subsegment of spinal cord
+CL:0000175,luteal cell,CL:0000179,progesterone secreting cell
+DOID:10113,trypanosomiasis,DOID:2789,parasitic protozoa infectious disease
+HP:0007858,Chorioretinal lacunae,HP:0000532,Chorioretinal abnormality
+UBERON:0005719,footplate apical ectodermal ridge,UBERON:0004356,apical ectodermal ridge
+UBERON:0010373,uncinate process of pancreas,UBERON:0004119,endoderm-derived structure
+CL:0007002,precementoblast,CL:0000055,non-terminally differentiated cell
+DOID:4033,bacterial gastritis,DOID:4029,gastritis
+UBERON:0005193,ethmoidal artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:10176,neuroretinitis,DOID:1979,focal chorioretinitis
+HP:0010426,Complete duplication of the middle phalanx of the 2nd toe,HP:0010412,Duplication of the middle phalanx of the 2nd toe
+HP:0009305,Distal/middle symphalangism of 4th finger,HP:0001204,Distal symphalangism (hands)
+UBERON:3000015,anterior maxillary process,UBERON:0010313,neural crest-derived structure
+UBERON:0012464,cloacal vent,UBERON:0000161,orifice
+HP:0011345,Moderate expressive language delay,HP:0002474,Expressive language delay
+CL:1001585,appendix glandular cell,CL:1000405,epithelial cell of appendix
+HP:0100662,Chondritis,HP:0002763,Abnormal cartilage morphology
+UBERON:0001092,vertebral bone 1,UBERON:0002412,vertebra
+UBERON:0002552,vestibulocerebellar tract,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009564,Triangular shaped distal phalanx of the 2nd finger,HP:0009546,Triangular shaped phalanges of the 2nd finger
+UBERON:0008446,flexor pollicis longus muscle,UBERON:0004254,forelimb zeugopod muscle
+UBERON:0011737,caudate lobe hepatic sinusoids,UBERON:0009548,hepatic sinusoid of left of lobe of liver
+DOID:11133,prostatic cyst,DOID:11132,prostatic hypertrophy
+DOID:6331,immature teratoma of ovary,DOID:6232,ovarian biphasic or triphasic teratoma
+DOID:5769,verruciform xanthoma of skin,DOID:3345,xanthomatosis
+NCBITaxon:29189,Ammonia,NCBITaxon:69034,Rotaliidae
+UBERON:3000867,agger limitans anterior of ischium,UBERON:0004120,mesoderm-derived structure
+HP:0010421,Duplication of the distal phalanx of the 2nd toe,HP:0010355,Duplication of the phalanges of the 2nd toe
+UBERON:0001964,least splanchnic nerve,UBERON:0003715,splanchnic nerve
+DOID:8009,penis mixed squamous cell carcinoma,DOID:5518,penis squamous cell carcinoma
+CL:0002536,amniotic epithelial cell,CL:0000349,extraembryonic cell
+UBERON:0013136,vein of lip,UBERON:0009141,craniocervical region vein
+CL:0002136,type II cell of adrenal cortex,CL:0002097,cortical cell of adrenal gland
+UBERON:0007324,pancreatic lobe,UBERON:0000064,organ part
+CL:0002560,inner root sheath cell,CL:0000362,epidermal cell
+UBERON:0005125,metanephric proximal straight tubule,UBERON:0005146,metanephric nephron tubule
+UBERON:3010380,outer fin tissue,UBERON:0000479,tissue
+HP:0002121,Absence seizures,HP:0011146,Dialeptic seizures
+HP:0012429,Aplasia/Hypoplasia of the cerebral white matter,HP:0002500,Abnormality of the cerebral white matter
+HP:0000863,Central diabetes insipidus,HP:0011751,Abnormality of the posterior pituitary
+UBERON:0004626,thoracic vertebra 1,UBERON:0002347,thoracic vertebra
+HP:0010690,Mirror image hand polydactyly,HP:0010689,Mirror image polydactyly
+UBERON:1500010,pelvic fin middle radial bone,UBERON:2000508,pelvic fin radial bone
+HP:0001476,Delayed closure of the anterior fontanelle,HP:0000270,Delayed cranial suture closure
+HP:0012680,Abnormality of the pineal gland,HP:0000818,Abnormality of the endocrine system
+UBERON:2001715,caudal principal ray 3,UBERON:2001585,caudal principal ray
+UBERON:4000080,keratin-based scale,UBERON:0007380,dermal scale
+DOID:10591,pre-eclampsia,DOID:10763,hypertension
+HP:0100145,Triangular epiphysis of the distal phalanx of the 3rd toe,HP:0100091,Abnormality of the epiphysis of the distal phalanx of the 3rd toe
+HP:0000918,Scapular exostoses,HP:0000782,Abnormality of the scapula
+DOID:0050712,AGAT deficiency,DOID:0050798,cerebral creatine deficiency syndrome
+UBERON:0011814,non-neurogenic ectodermal placode,UBERON:0005085,ectodermal placode
+CL:0000339,glioblast (sensu Vertebrata),CL:0000030,glioblast
+CL:0002476,bone marrow macrophage,CL:1001610,bone marrow hematopoietic cell
+UBERON:2001887,neural spine 3,UBERON:0001076,neural spine
+UBERON:0005005,mucosa of left ureter,UBERON:0004980,mucosa of ureter
+DOID:4790,medulloepithelioma,DOID:0060103,central nervous system primitive neuroectodermal neoplasm
+HP:0004764,Myxomatous mitral valve degeneration,HP:0001633,Abnormality of the mitral valve
+UBERON:0008194,tibiotarsus,UBERON:0003464,hindlimb bone
+UBERON:2002006,axillary pore,UBERON:0008915,pore
+DOID:12987,agranulocytosis,DOID:615,leukopenia
+UBERON:0011677,trunk vertebra,UBERON:0003463,trunk bone
+UBERON:0004389,epiphysis of metatarsal bone,UBERON:0011973,epiphysis of phalanx of pes
+HP:0007500,Decreased number of sweat glands,HP:0000971,Abnormality of the sweat gland
+DOID:3950,adrenal carcinoma,DOID:3953,adrenal gland cancer
+HP:0004390,Hamartomatous polyps,HP:0005266,Intestinal polyp
+HP:0000605,Supranuclear gaze palsy,HP:0000496,Abnormality of eye movement
+HP:0001092,Absent lacrimal puncta,HP:0011479,Abnormality of the lacrimal punctum
+UBERON:0004482,musculature of lower limb,UBERON:0004480,musculature of limb
+CL:0000222,mesodermal cell,CL:0002321,embryonic cell
+UBERON:0000488,atypical epithelium,UBERON:0000483,epithelium
+UBERON:3000809,accessory articulation,UBERON:0004120,mesoderm-derived structure
+UBERON:0002502,round window of inner ear,UBERON:0004120,mesoderm-derived structure
+UBERON:0005088,sebaceous gland placode,UBERON:0011814,non-neurogenic ectodermal placode
+UBERON:0004458,body cavity or lining,UBERON:0001062,anatomical entity
+UBERON:2002010,hyoideomandibular nerve,UBERON:0001021,nerve
+UBERON:0014444,pubic ramus,UBERON:0004120,mesoderm-derived structure
+HP:0010028,Bullet-shaped 1st metacarpal,HP:0009652,Bullet-shaped phalanges of the thumb
+HP:0003311,Hypoplasia of the odontoid process,HP:0003310,Abnormality of the odontoid process
+HP:0002814,Abnormality of the lower limb,HP:0002813,Abnormality of limb bone morphology
+CL:1000143,lung goblet cell,CL:0000082,epithelial cell of lung
+HP:0001678,Atrioventricular block,HP:0005150,Abnormal atrioventricular conduction
+UBERON:0006919,tongue squamous epithelium,UBERON:0006914,squamous epithelium
+UBERON:0009061,anterior air sac,UBERON:0009060,air sac
+NCBITaxon:203397,Rotaliacea,NCBITaxon:29185,Rotaliida
+UBERON:0005313,mammary duct terminal end bud,UBERON:0004121,ectoderm-derived structure
+DOID:13310,diphtheritic peritonitis,DOID:8283,peritonitis
+HP:0009875,Triangular shaped distal phalanges of the hand,HP:0009832,Abnormality of the distal phalanx of finger
+DOID:0080001,bone disease,DOID:65,connective tissue disease
+HP:0009298,Aplasia of the proximal phalanx of the 4th finger,HP:0010242,Aplasia of the proximal phalanges of the hand
+DOID:5362,focal epithelial hyperplasia,DOID:934,viral infectious disease
+UBERON:0015067,centrale endochondral element,UBERON:0015063,autopod endochondral element
+HP:0011172,Complex febrile seizures,HP:0002373,Febrile seizures
+UBERON:0002359,fibrous pericardium,UBERON:0000094,membrane organ
+UBERON:0005249,metanephric renal pelvis,UBERON:0001224,renal pelvis
+UBERON:0003409,gland of tongue,UBERON:0010047,oral gland
+UBERON:0002016,pulmonary vein,UBERON:0001638,vein
+HP:0010893,Abnormality of phenylalanine metabolism,HP:0004338,Abnormality of aromatic amino acid family metabolism
+UBERON:2002272,ventral caudal procurrent ray 1,UBERON:2001830,caudal fin ventral procurrent ray
+UBERON:0014892,skeletal muscle organ,UBERON:0004120,mesoderm-derived structure
+UBERON:0009672,oronasal membrane,UBERON:0004121,ectoderm-derived structure
+HP:0007016,Corticospinal tract hypoplasia,HP:0007365,Aplasia/Hypoplasia involving the corticospinal tracts
+UBERON:0003073,lens placode,UBERON:0010312,immature eye
+DOID:0060179,Renpenning syndrome,DOID:0050888,syndromic intellectual disability
+UBERON:0006139,plantar digital vein,UBERON:0004564,hindlimb digital vein
+UBERON:0002594,dentatothalamic tract,UBERON:0014891,brainstem white matter
+UBERON:0003302,roof plate of metencephalon,UBERON:0003298,roof plate of neural tube
+HP:0011287,EEG with occipital sharp slow waves,HP:0011195,EEG with focal sharp slow waves
+HP:0200017,White matter agenesis,HP:0012429,Aplasia/Hypoplasia of the cerebral white matter
+UBERON:0010746,iliac blade,UBERON:0005913,zone of bone organ
+HP:0003891,Abnormality of the humeral epiphysis,HP:0003839,Abnormality involving the epiphyses of the upper limbs
+UBERON:3000524,pterygoquadrate,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004998,mucosa of pylorus,UBERON:0001199,mucosa of stomach
+UBERON:0008879,ligament of pinna,UBERON:0008846,skeletal ligament
+UBERON:0006327,laryngeal extrinsic muscle,UBERON:0001568,muscle of larynx
+UBERON:0012127,feather barbicel,UBERON:0004121,ectoderm-derived structure
+HP:0005959,Impaired gluconeogenesis,HP:0011014,Abnormal glucose homeostasis
+UBERON:0010892,mesethmoid element,UBERON:0004765,skeletal element
+UBERON:0001305,ovarian follicle,UBERON:0005156,reproductive structure
+HP:0004021,Lytic defects of radial metaphysis,HP:0004015,Abnormality of radial metaphyses
+UBERON:0013245,sinovaginal bulb,UBERON:0006554,urinary system structure
+UBERON:0008907,dermal bone,UBERON:0004756,dermal skeletal element
+UBERON:0009769,left common cardinal vein,UBERON:0002064,common cardinal vein
+UBERON:2000298,vent,UBERON:0003102,surface structure
+UBERON:0011312,hyoepiglottic muscle,UBERON:0001568,muscle of larynx
+UBERON:0004686,gastro-splenic ligament,UBERON:0003567,abdomen connective tissue
+DOID:2696,Leydig cell tumor,DOID:4757,sex cord-stromal neoplasm
+UBERON:0008000,sesamoid bone of pes,UBERON:0001479,sesamoid bone
+HP:0007560,Unusual dermatoglyphics,HP:0005882,Dermatoglyphic variants
+DOID:1470,major depressive disorder,DOID:1595,endogenous depression
+HP:0011903,Hemoglobin H,HP:0011902,Abnormal hemoglobin
+DOID:4473,sarcomatoid renal cell carcinoma,DOID:4450,renal cell carcinoma
+DOID:9011,larynx carcinoma in situ,DOID:8719,in situ carcinoma
+HP:0000552,Tritanomaly,HP:0011519,Anomalous trichromacy
+UBERON:0011161,spheno-occipital synchondrosis,UBERON:0001725,cranial synchondrosis
+HP:0009963,Duplication of the middle phalanx of the 3rd finger,HP:0010008,Duplication of the middle phalanx of hand
+DOID:8568,infectious mononucleosis,DOID:934,viral infectious disease
+DOID:0060201,amyotrophic lateral sclerosis type 10,DOID:332,amyotrophic lateral sclerosis
+UBERON:0006285,pubic pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+NCBITaxon:11584,Phlebovirus,NCBITaxon:11571,Bunyaviridae
+UBERON:0002634,anterior nucleus of hypothalamus,UBERON:0007251,preoptic nucleus
+UBERON:0005970,brain commissure,UBERON:0001020,nervous system commissure
+DOID:6758,chest wall lymphoma,DOID:5093,thoracic cancer
+HP:0009571,Curved middle phalanx of the 2nd finger,HP:0009846,Curved middle phalanges of the hand
+HP:0001001,Abnormality of subcutaneous fat tissue,HP:0011354,Generalized abnormality of skin
+DOID:1762,cheilitis,DOID:9297,lip disease
+HP:0004798,Recurrent infection of the gastrointestinal tract,HP:0012719,Functional abnormality of the gastrointestinal tract
+CL:0000809,"double-positive, alpha-beta thymocyte",CL:0000790,immature alpha-beta T cell
+UBERON:2001942,autopalatine-maxillary joint,UBERON:0000982,skeletal joint
+UBERON:0009067,abdominal air sac,UBERON:0009062,posterior air sac
+UBERON:3000038,basimandibulare,UBERON:0000479,tissue
+UBERON:3010494,lateral pretrosal artery,UBERON:0001637,artery
+UBERON:0002500,zygomatic arch,UBERON:0011164,neurocranium bone
+UBERON:2001751,rib of vertebra 5,UBERON:0002228,rib
+UBERON:4300089,propterygium bone,UBERON:2001587,pectoral fin proximal radial bone
+DOID:4279,infundibulocystic basal cell carcinoma,DOID:2513,basal cell carcinoma
+HP:0007132,Pallidal degeneration,HP:0002453,Abnormality of the globus pallidus
+UBERON:0005286,tela choroidea of midbrain cerebral aqueduct,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:10882,epidemic pleurodynia,DOID:934,viral infectious disease
+HP:0004679,Large tarsal bones,HP:0001850,Abnormality of the tarsal bones
+UBERON:2007029,hindbrain neural keel,UBERON:0004121,ectoderm-derived structure
+UBERON:0000971,ommatidium,UBERON:0002536,arthropod sensillum
+UBERON:0001374,biceps femoris,UBERON:0004252,hindlimb stylopod muscle
+DOID:0050630,Aland Island eye disease,DOID:5614,eye disease
+CL:0000657,secondary spermatocyte,CL:0000017,spermatocyte
+UBERON:0006345,stapedial artery,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:0060119,pharynx cancer,DOID:3119,gastrointestinal system cancer
+DOID:96,staphyloenterotoxemia,DOID:0050338,primary bacterial infectious disease
+UBERON:0003721,lingual nerve,UBERON:0001021,nerve
+HP:0005096,Distal femoral bowing,HP:0002980,Femoral bowing
+HP:0009847,Osteolytic defects of the middle phalanges of the hand,HP:0009833,Abnormality of the middle phalanges of the hand
+HP:0009704,Chronic CSF lymphocytosis,HP:0200149,CSF lymphocytosis
+UBERON:0003470,artery of upper lip,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000542,lymphocyte,CL:0002242,nucleate cell
+UBERON:0001522,flexor carpi ulnaris muscle,UBERON:0000366,flexor muscle
+UBERON:0011140,superficial part of masseter muscle,UBERON:0004120,mesoderm-derived structure
+CL:1000304,fibroblast of connective tissue of nonglandular part of prostate,CL:0000057,fibroblast
+UBERON:0001633,basilar artery,UBERON:0003496,head blood vessel
+HP:0012163,Carotid artery aneurysm,HP:0005344,Abnormality of the carotid arteries
+HP:0003152,"Increased serum 1,25-dihydroxyvitamin D3",HP:0003117,Abnormality of circulating hormone level
+HP:0011667,Bilateral superior vena cava with bridging vein,HP:0005301,Persistent left superior vena cava
+DOID:4061,testis rhabdomyosarcoma,DOID:4062,testis sarcoma
+UBERON:0010684,pedal digit 5 phalanx cartilage element,UBERON:0015035,pedal digit 5 phalanx endochondral element
+HP:0006339,Conical mandibular incisor,HP:0011065,Conical incisor
+DOID:5588,lung papillary adenocarcinoma,DOID:3910,lung adenocarcinoma
+HP:0009485,Radial deviation of the hand or of fingers of the hand,HP:0009484,Deviation of the hand or of fingers of the hand
+DOID:5264,epithelioid leiomyosarcoma,DOID:1967,leiomyosarcoma
+CL:0000924,"CD4-negative, CD8-negative type I NK T cell",CL:0000921,type I NK T cell
+UBERON:0014557,CA1 stratum lacunosum moleculare,UBERON:0014567,layer of hippocampal field
+UBERON:0002270,hyaloid artery,UBERON:0010312,immature eye
+HP:0008716,Urethrovaginal fistula,HP:0004320,Vaginal fistula
+HP:0010782,Shoulder dimples,HP:0010781,Skin dimples
+UBERON:0005760,urorectal septum,UBERON:0006554,urinary system structure
+DOID:0050768,"mitochondrial complex V (ATP synthase) deficiency, nuclear type 1",DOID:700,mitochondrial metabolism disease
+DOID:0060026,immunoglobulin beta deficiency,DOID:2115,B cell deficiency
+DOID:11991,osteopoikilosis,DOID:4254,osteosclerosis
+HP:0012111,Abnormality of circulating glucocorticoid level,HP:0003117,Abnormality of circulating hormone level
+UBERON:0002536,arthropod sensillum,UBERON:0000020,sense organ
+DOID:13620,patent foramen ovale,DOID:1882,atrial heart septal defect
+UBERON:0009497,epithelium of foregut-midgut junction,UBERON:0005911,endo-epithelium
+HP:0100452,Osteolytic defects of the middle phalanx of the 3rd toe,HP:0010363,Osteolytic defects of the phalanges of the 3rd toe
+UBERON:0005324,mesonephric macula densa,UBERON:0002335,macula densa
+UBERON:0002128,superior olivary complex,UBERON:0003528,brain grey matter
+HP:0012490,Panniculitis,HP:0009124,Abnormality of adipose tissue
+CL:0000494,UV sensitive photoreceptor cell,CL:0000210,photoreceptor cell
+UBERON:0002647,magnocellular part of medial dorsal nucleus,UBERON:0003528,brain grey matter
+UBERON:0005263,outflow tract cardiac jelly,UBERON:0003906,cardiac jelly
+UBERON:0001336,membranous urethra of male or female,UBERON:0006554,urinary system structure
+CL:0002537,amnion mesenchymal stem cell,CL:0000349,extraembryonic cell
+HP:0012152,Foveoschisis,HP:0000493,Abnormality of the fovea
+UBERON:0002434,pituitary stalk,UBERON:0004120,mesoderm-derived structure
+UBERON:3000670,anterior process of hyoid apparatus,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2002016,pharyngobranchial 4 tooth plate,UBERON:2002015,pharyngobranchial tooth plate
+UBERON:0002541,germ ring,UBERON:0002050,embryonic structure
+UBERON:3010515,lateral vein,UBERON:0001638,vein
+UBERON:0002397,maxilla,UBERON:0011597,bone of upper jaw
+HP:0012414,Duodenal atrophy,HP:0002246,Abnormality of the duodenum
+UBERON:0005134,metanephric nephron epithelium,UBERON:0004211,nephron epithelium
+HP:0009276,Contracture of the proximal interphalangeal joint of the 4th finger,HP:0009698,Contractures of the proximal interphalangeal joints of the fingers
+CL:0000495,blue sensitive photoreceptor cell,CL:0000490,photopic photoreceptor cell
+DOID:519,aortitis,DOID:520,aortic disease
+UBERON:0000490,unilaminar epithelium,UBERON:0000483,epithelium
+CL:0002440,Ly49D-positive natural killer cell,CL:0002438,NK1.1-positive natural killer cell
+UBERON:2105380,dorsal fin proximal radial element 3,UBERON:2100947,dorsal fin proximal radial element
+DOID:5289,uterus leiomyosarcoma,DOID:5165,uterine corpus sarcoma
+HP:0012038,Corneal guttata,HP:0011490,Abnormality of Descemet's membrane
+UBERON:4200116,pteroid,UBERON:0008962,forelimb bone
+UBERON:0003483,thymus lymphoid tissue,UBERON:0001744,lymphoid tissue
+HP:0011433,High maternal serum chorionic gonadotropin,HP:0011436,Abnormal maternal serum screening
+UBERON:0013167,cricopharyngeal ligament,UBERON:0001730,extrinsic ligament of larynx
+NCBITaxon:1056966,Aedini,NCBITaxon:43817,Culicinae
+UBERON:0003355,epithelium of incisor,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0007561,Telangiectases in sun-exposed and nonexposed skin,HP:0100585,Teleangiectasia of the skin
+UBERON:2002109,uroneural 2,UBERON:2000602,uroneural
+HP:0010134,Pseudoepiphysis of the proximal phalanx of the hallux,HP:0010120,Pseudoepiphyses of the hallux
+UBERON:2000319,branchiostegal membrane,UBERON:0004119,endoderm-derived structure
+UBERON:0002021,occipital lobe,UBERON:0000477,anatomical cluster
+UBERON:0001301,epididymis,UBERON:0005904,duct of male reproductive system
+UBERON:2000839,sclerotome somite 9,UBERON:0003089,sclerotome
+HP:0004980,Metaphyseal rarefaction,HP:0000944,Abnormality of the metaphyses
+UBERON:0003039,anterior commissure anterior part,UBERON:0005970,brain commissure
+HP:0100672,Vaginal hernia,HP:0000142,Abnormality of the vagina
+UBERON:2002091,median caudal cartilage,UBERON:2001457,postcranial axial cartilage
+DOID:12531,von Willebrand's disease,DOID:2214,inherited blood coagulation disease
+UBERON:0010939,zygomaticomandibularis muscle,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005371,hippocampus stratum oriens,UBERON:0002305,layer of hippocampus
+UBERON:2005411,common crus,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:5213,chronic inflammatory demyelinating polyradiculoneuropathy,DOID:4308,polyradiculoneuropathy
+HP:0000625,Cleft eyelid,HP:0000589,Coloboma
+DOID:870,neuropathy,DOID:863,nervous system disease
+UBERON:0001435,carpal bone,UBERON:0003656,mesopodium bone
+DOID:3762,cytochrome-c oxidase deficiency disease,DOID:700,mitochondrial metabolism disease
+UBERON:0004084,genital labium,UBERON:0005156,reproductive structure
+DOID:3264,subacute leukemia,DOID:1240,leukemia
+HP:0000993,Molluscoid pseudotumors,HP:0011355,Localized skin lesion
+HP:0001941,Acidosis,HP:0004360,Abnormality of acid-base homeostasis
+HP:0012540,Axillary epidermoid cyst,HP:0200040,Epidermoid cyst
+UBERON:0009853,body of uterus,UBERON:0005156,reproductive structure
+UBERON:2005260,fenestrated capillary,UBERON:0004638,blood vessel endothelium
+UBERON:0011625,inferior horn of thyroid cartilage,UBERON:0011623,horn of thyroid cartilage
+UBERON:0003098,optic stalk,UBERON:0004022,embryonic neuroepithelium
+HP:0006193,Thimble-shaped middle phalanges of hand,HP:0009833,Abnormality of the middle phalanges of the hand
+UBERON:0004668,fourth ventricle aperture,UBERON:0000161,orifice
+HP:0006918,Diffuse cerebral sclerosis,HP:0002060,Abnormality of the cerebrum
+UBERON:3000381,paranasal commissure,UBERON:0010313,neural crest-derived structure
+HP:0007748,Irido-fundal coloboma,HP:0000612,Iris coloboma
+UBERON:0014884,distal epiphysis of distal phalanx of manual digit 4,UBERON:0014886,distal epiphysis of distal phalanx of manual digit
+HP:0100562,Diplomyelia,HP:0100561,Spinal cord lesions
+CL:0002571,hepatic mesenchymal stem cell,CL:0002195,hepatic stem cell
+DOID:4798,aggressive systemic mastocytosis,DOID:349,systemic mastocytosis
+HP:0012020,Right aortic arch,HP:0011587,Abnormal branching pattern of the aortic arch
+HP:0001647,Bicuspid aortic valve,HP:0001646,Abnormality of the aortic valve
+UBERON:0000061,anatomical structure,UBERON:0000465,material anatomical entity
+UBERON:0015224,interventricular foramen intermedium,UBERON:0010313,neural crest-derived structure
+CL:0002275,pancreatic PP cell,CL:0000083,epithelial cell of pancreas
+UBERON:0003078,epibranchial placode,UBERON:0009955,neurogenic placode
+UBERON:0006245,humerus cartilage element,UBERON:0010883,forelimb cartilage element
+UBERON:0002958,medial lemniscus of pons,UBERON:0002680,regional part of metencephalon
+UBERON:0007116,primary dentition,UBERON:0003672,dentition
+UBERON:0013152,interventricular foramen of heart,UBERON:0004120,mesoderm-derived structure
+DOID:171,neuroectodermal tumor,DOID:3093,nervous system cancer
+HP:0005415,Decreased number of CD8+ T cells,HP:0005403,T lymphocytopenia
+UBERON:0006762,suspensory ligament of lens,UBERON:0008841,suspensory ligament
+HP:0011139,Gastric duplication,HP:0011140,Gastrointestinal duplication
+HP:0009733,Glioma,HP:0100705,Abnormality of the glial cells
+CL:0000836,promyelocyte,CL:0002242,nucleate cell
+HP:0009500,Abnormality of the epiphysis of the middle phalanx of the 2nd finger,HP:0006263,Abnormality of the epiphyses of the 2nd finger
+UBERON:0006837,tegmen tympani,UBERON:0005913,zone of bone organ
+UBERON:0004619,lumbar vertebra 3,UBERON:0002414,lumbar vertebra
+UBERON:2002218,parallel fiber,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100900,Sclerosis of the distal phalanx of the 2nd finger,HP:0100915,Sclerosis of the distal phalanges of the hand
+UBERON:0001442,skeleton of manus,UBERON:0006717,autopodial skeleton
+HP:0012105,Occipital cortical atrophy,HP:0002120,Cerebral cortical atrophy
+HP:0009771,Osteolytic defects of the phalanges of the hand,HP:0009699,Osteolytic defects of the hand bones
+UBERON:2001622,odontode,UBERON:0000481,multi-tissue structure
+UBERON:0015481,left hepatic artery,UBERON:0015796,liver blood vessel
+HP:0010604,Cyst of the eyelid,HP:0200040,Epidermoid cyst
+DOID:9955,hypoplastic left heart syndrome,DOID:1682,congenital heart disease
+DOID:5212,congenital disorder of glycosylation,DOID:2978,carbohydrate metabolic disorder
+UBERON:0004775,outer renal medulla vasa recta,UBERON:0004726,vasa recta
+UBERON:0004022,embryonic neuroepithelium,UBERON:0005291,embryonic tissue
+UBERON:0007530,migrating mesenchyme population,UBERON:0003104,mesenchyme
+UBERON:0003535,vagus X nerve trunk,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2000596,pelvic fin actinotrichium,UBERON:0004120,mesoderm-derived structure
+NCBITaxon:7158,Aedes <genus>,NCBITaxon:1056966,Aedini
+UBERON:0011366,cleidobrachialis muscle,UBERON:0001630,muscle organ
+UBERON:0010581,pedal digit 2 phalanx pre-cartilage condensation,UBERON:0005696,pedal digit 2 mesenchyme
+HP:0010100,Complete duplication of the phalanges of the hallux,HP:0010066,Duplication of phalanx of hallux
+DOID:1325,bronchus cancer,DOID:0050615,respiratory system cancer
+NCBITaxon:29263,tick-borne encephalitis virus group,NCBITaxon:11051,Flavivirus
+HP:0000099,Glomerulonephritis,HP:0000095,Abnormality of the glomerulus
+UBERON:0012478,cloacal gland,UBERON:0003408,gland of gut
+DOID:3696,acute sanguinous otitis media,DOID:3697,acute transudative otitis media
+CL:0011005,GABAergic interneuron,CL:0000617,GABAergic neuron
+HP:0006449,Distal radial epiphyseal osteolysis,HP:0010597,Abnormality of the distal radial epiphysis
+HP:0000248,Brachycephaly,HP:0002648,Abnormality of calvarial morphology
+HP:0010666,Hypoplasia of the anterior nasal spine,HP:0000327,Hypoplasia of the maxilla
+UBERON:4200135,puboischiadic bar,UBERON:0004120,mesoderm-derived structure
+UBERON:0009878,mesopodial skeleton,UBERON:0010712,limb skeleton subdivision
+HP:0100322,Aplasia of the pyramidal tract,HP:0007363,Aplasia/Hypoplasia of the pyramidal tract
+UBERON:0006453,fifth thoracic spinal cord segment,UBERON:0007715,thoracic subsegment of spinal cord
+HP:0010945,Fetal pyelectasis,HP:0011425,Fetal ultrasound soft marker
+NCBITaxon:163159,Xenopsylla cheopis,NCBITaxon:163158,Xenopsylla
+CL:0002648,epithelial cell of nasal part of viscerocranial mucosa,CL:0002283,ecto-epithelial cell of viscerocranial mucosa
+DOID:2763,ethmoid sinus squamous cell carcinoma,DOID:1363,ethmoid sinus cancer
+UBERON:0011695,embryonic cardiovascular system,UBERON:0004535,cardiovascular system
+DOID:178,vascular disease,DOID:1287,cardiovascular system disease
+UBERON:2001710,opercle-interopercle joint,UBERON:0000982,skeletal joint
+UBERON:0004185,endodermal part of digestive tract,UBERON:0004921,subdivision of digestive tract
+UBERON:0004807,respiratory system epithelium,UBERON:0000483,epithelium
+UBERON:0003996,cervical vertebra 1 arcus anterior,UBERON:0004120,mesoderm-derived structure
+UBERON:0010675,manual digit 1 phalanx cartilage element,UBERON:0015025,manual digit 1 phalanx endochondral element
+HP:0100320,Rosenthal fibres,HP:0100314,Cerebral inclusion bodies
+UBERON:0006762,suspensory ligament of lens,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0011319,disk of temporomandibular joint,UBERON:0004120,mesoderm-derived structure
+UBERON:0006533,rectus extraocular muscle,UBERON:0006531,oculomotor muscle
+UBERON:0002013,superior hypogastric nerve plexus,UBERON:0001816,autonomic nerve plexus
+HP:0002014,Diarrhea,HP:0011458,Abdominal symptom
+UBERON:0004679,dentate gyrus molecular layer,UBERON:0002304,layer of dentate gyrus
+CL:0000604,retinal rod cell,CL:0010009,camera-type eye photoreceptor cell
+CL:0000920,"CD8-positive, CD28-negative, alpha-beta regulatory T cell",CL:0000795,"CD8-positive, alpha-beta regulatory T cell"
+HP:0009053,Distal lower limb muscle weakness,HP:0002460,Distal muscle weakness
+HP:0009568,Aplasia/Hypoplasia of the middle phalanx of the 2nd finger,HP:0009552,Aplasia/Hypoplasia of the phalanges of the 2nd finger
+UBERON:2000636,cerebellar crest,UBERON:0000479,tissue
+UBERON:0010534,primitive mesonephric nephron,UBERON:0010532,primitive nephron
+DOID:13996,small intestine lymphoma,DOID:10154,small intestine cancer
+HP:0012047,Hemeralopia,HP:0000504,Abnormality of vision
+DOID:0050517,Barmah Forest virus disease,DOID:934,viral infectious disease
+CL:0000505,substance P secreting cell,CL:0000167,peptide hormone secreting cell
+UBERON:0005670,greater omentum mesothelium,UBERON:0001136,mesothelium
+UBERON:2000527,pharyngobranchial bone,UBERON:2001909,pharyngobranchial element
+NCBITaxon:11229,Morbillivirus,NCBITaxon:11159,Paramyxovirinae
+UBERON:2000892,hypaxial region somite 12,UBERON:0003895,hypaxial myotome region
+CL:0000646,basal cell,CL:0000036,epithelial fate stem cell
+UBERON:2000769,hypaxial region somite 17,UBERON:0003895,hypaxial myotome region
+CL:0000957,large pre-B-II cell,CL:0000955,pre-B-II cell
+HP:0001421,Abnormality of the musculature of the hand,HP:0001446,Abnormality of the musculature of the upper limbs
+HP:0009141,Depletion of mitochondrial DNA in muscle tissue,HP:0003800,Muscle abnormality related to mitochondrial dysfunction
+UBERON:0004859,eye gland,UBERON:0002530,gland
+UBERON:0015030,pedal digit phalanx endochondral element,UBERON:0015023,phalanx endochondral element
+DOID:9784,trichinosis,DOID:883,parasitic helminthiasis infectious disease
+HP:0100168,Fragmented epiphyses,HP:0005930,Abnormality of the epiphyses
+HP:0011656,Double outlet right ventricle with subaortic ventricular septal defect without pulmonary stenosis,HP:0001719,Double outlet right ventricle
+HP:0007778,Neovascularization of peripheral and posterior retina,HP:0008046,Abnormality of the retinal vasculature
+HP:0007730,Iris hypopigmentation,HP:0008034,Abnormal iris pigmentation
+UBERON:0002226,basilar membrane of cochlea,UBERON:0005764,acellular membrane
+UBERON:0006672,incisive canal,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:3204,neurilemmomatosis,DOID:3192,neurilemmoma
+UBERON:3010772,M. dorsalis trunci,UBERON:0008778,epaxial musclulature
+UBERON:4200184,ulnar tuberosity,UBERON:4100000,skeletal element projection
+HP:0003656,Decreased beta-glucocerebrosidase protein and activity,HP:0004344,Abnormality of cerebrosidase metabolism
+HP:0006897,Cranial nerve VI palsy,HP:0006824,Cranial nerve paralysis
+DOID:4202,brain stem glioma,DOID:4203,brain stem cancer
+UBERON:2001314,posterior lateral line ganglion,UBERON:0004121,ectoderm-derived structure
+UBERON:0007841,furcula,UBERON:0007829,pectoral girdle bone
+UBERON:0011167,septomaxilla bone,UBERON:0008907,dermal bone
+UBERON:0001274,ischium,UBERON:0015212,lateral structure
+HP:0008873,Disproportionate short-limb short stature,HP:0003498,Disproportionate short stature
+HP:0001107,Ocular albinism,HP:0001098,Abnormality of the fundus
+UBERON:2002129,caudal rod,UBERON:0000481,multi-tissue structure
+UBERON:0000349,limbic system,UBERON:0000467,anatomical system
+UBERON:0012350,carpal pad,UBERON:0013622,manual autopod pad
+DOID:8802,trachea carcinoma in situ,DOID:8719,in situ carcinoma
+UBERON:0011687,levator hyomandibulae muscle,UBERON:0001577,facial nerve muscle
+UBERON:2000241,midline column,UBERON:0004121,ectoderm-derived structure
+HP:0009221,Pseudoepiphysis of the middle phalanx of the 4th finger,HP:0009247,Abnormality of the epiphysis of the middle phalanx of the 4th finger
+HP:0009895,Abnormality of the crus of the helix,HP:0011039,Abnormality of the helix
+HP:0003498,Disproportionate short stature,HP:0004322,Short stature
+UBERON:0015788,olfactory apparatus chamber,UBERON:0004121,ectoderm-derived structure
+UBERON:0010842,calcaneum cartilage element,UBERON:0010695,mesenchyme of tarsal region
+HP:0100287,EMG: slow motor conduction,HP:0003457,EMG abnormality
+UBERON:0011952,non-glandular epithelium,UBERON:0000483,epithelium
+CL:0000165,neuroendocrine cell,CL:0000163,endocrine cell
+UBERON:0004610,rib 11,UBERON:0002228,rib
+CL:1000696,kidney interstitial inflammatory macrophage,CL:0000863,inflammatory macrophage
+DOID:0050661,vitelliform macular dystrophy,DOID:4448,macular degeneration
+CL:0000527,efferent neuron,CL:0000540,neuron
+DOID:0050910,cecum adenoma,DOID:1517,cecal benign neoplasm
+HP:0009814,Upper limb peromelia,HP:0009828,Peromelia
+HP:0009818,Amelia involving the lower limbs,HP:0009827,Amelia
+HP:0003894,Delayed humeral epiphyseal ossification,HP:0003891,Abnormality of the humeral epiphysis
+UBERON:0001702,eyelash,UBERON:0001037,strand of hair
+UBERON:0005629,vascular plexus,UBERON:0002049,vasculature
+HP:0002315,Headache,HP:0012638,Abnormality of nervous system physiology
+HP:0200118,Malabsorption of Vitamin B12,HP:0004341,Abnormality of the vitamin B12 metabolism
+DOID:10302,parotid disease,DOID:10854,salivary gland disease
+UBERON:0015087,distal carpal bone 2 endochondral element,UBERON:0015049,carpus endochondral element
+HP:0010695,Sutural cataract,HP:0010920,Zonular cataract
+HP:0009307,Patchy sclerosis of the middle phalanx of the 4th finger,HP:0100906,Sclerosis of the middle phalanx of the 4th finger
+UBERON:0011015,iliac fossa,UBERON:0004120,mesoderm-derived structure
+UBERON:0002231,body of rib,UBERON:0004120,mesoderm-derived structure
+HP:0012106,Rhizomelic leg shortening,HP:0008905,Rhizomelia
+UBERON:0011672,suprapygal plate of carapace,UBERON:0011665,carapace bone
+HP:0002282,Heterotopia,HP:0002269,Abnormality of neuronal migration
+CL:0000411,flatworm hypodermal cell,CL:0000076,squamous epithelial cell
+UBERON:0003615,lung elastic tissue,UBERON:0000114,lung connective tissue
+UBERON:2000342,dorsal inclinator,UBERON:2005276,inclinator muscle
+HP:0005473,Fusion of middle ear ossicles,HP:0004452,Abnormality of the middle ear ossicles
+DOID:0050647,Arts syndrome,DOID:0050735,X-linked disease
+DOID:6524,malignant ciliary body melanoma,DOID:4352,ciliary body cancer
+HP:0003930,Lytic defects of humeral diaphysis,HP:0003926,Abnormality of the humeral diaphysis
+DOID:1800,neuroendocrine carcinoma,DOID:305,carcinoma
+HP:0000029,Testicular atrophy,HP:0000035,Abnormality of the testis
+DOID:10992,acute hemorrhagic leukoencephalitis,DOID:639,acute disseminated encephalomyelitis
+NCBITaxon:11577,La Crosse virus,NCBITaxon:35305,California encephalitis virus
+UBERON:0003682,palatal muscle,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3000400,pars facialis of maxilla,UBERON:0000064,organ part
+UBERON:0003913,tooth-like structure,UBERON:0004765,skeletal element
+HP:0003981,Broad radius,HP:0003971,Broad forearm bones
+NCBITaxon:262,Francisella,NCBITaxon:34064,Francisellaceae
+UBERON:0005348,ansiform lobule,UBERON:0004003,cerebellum hemisphere lobule
+UBERON:2002144,anterior catecholaminergic tract,UBERON:0002316,white matter
+UBERON:0010410,inguinal fat pad,UBERON:0003838,abdominal segment connective tissue
+HP:0002457,Abnormal head movements,HP:0100022,Abnormality of movement
+UBERON:0002722,trochlear nucleus,UBERON:0007414,nucleus of midbrain tegmentum
+DOID:11371,functional diarrhea,DOID:5353,colonic disease
+CL:1000893,kidney venous blood vessel cell,CL:1000854,kidney blood vessel cell
+HP:0012119,Methemoglobinemia,HP:0011902,Abnormal hemoglobin
+NCBITaxon:119093,Trichuridae,NCBITaxon:6329,Trichocephalida
+UBERON:0013213,ossicone,UBERON:0006969,cranial appendage
+CL:0000540,neuron,CL:0000393,electrically responsive cell
+HP:0002138,Subarachnoid hemorrhage,HP:0012703,Abnormality of the subarachnoid space
+NCBITaxon:299467,Leptotrombidium deliense,NCBITaxon:279271,Leptotrombidium
+HP:0002827,Hip dislocation,HP:0001373,Joint dislocation
+DOID:6958,aleukemic monocytic leukemia cutis,DOID:6003,aleukemic leukemia cutis
+HP:0000130,Abnormality of the uterus,HP:0000008,Abnormality of female internal genitalia
+HP:0012388,Acute bronchitis,HP:0012387,Bronchitis
+CL:0000437,gonadtroph,CL:0000438,luteinizing hormone secreting cell
+UBERON:0006044,interdigital region between pedal digits 3 and 4,UBERON:0006014,interdigital region between pedal digits
+DOID:0050663,Bethlem myopathy,DOID:0050557,congenital muscular dystrophy
+UBERON:0002337,endometrial stroma,UBERON:0014404,female anatomical structure
+CL:0000436,vaginal lubricant secreting cell,CL:0000151,secretory cell
+UBERON:2000735,hemal postzygapophysis,UBERON:0002513,endochondral bone
+HP:0010675,Abnormal foot bone ossification,HP:0001760,Abnormality of the foot
+UBERON:0002159,medial accessory inferior olivary nucleus,UBERON:0007244,inferior olivary nucleus
+CL:0000232,erythrocyte,CL:0000764,erythroid lineage cell
+DOID:10044,balloon cell malignant melanoma,DOID:8923,skin melanoma
+UBERON:0003339,ganglion of central nervous system,UBERON:0004121,ectoderm-derived structure
+HP:0003923,Square humeral metaphysis,HP:0003907,Abnormality of the humeral metaphyses
+UBERON:0015849,canine tusk,UBERON:0003674,cuspid
+DOID:11121,pulpitis,DOID:5330,dental pulp disease
+CL:0000778,mononuclear osteoclast,CL:0000092,osteoclast
+HP:0005477,Progressive sclerosis of skull base,HP:0002694,Sclerosis of skull base
+UBERON:0011168,postfrontal bone,UBERON:0003462,facial bone
+UBERON:0008813,helicotrema,UBERON:0000161,orifice
+UBERON:3010217,carotid,UBERON:0001637,artery
+DOID:9723,vitreous abscess,DOID:9720,vitreous disease
+CL:1000444,mesothelial cell of anterior chamber of eye,CL:0002371,somatic cell
+HP:0006064,Limited interphalangeal movement,HP:0001376,Limitation of joint mobility
+UBERON:0008807,coagulating gland,UBERON:0010147,male accessory sex gland
+UBERON:2205372,dorsal fin distal radial cartilage 1,UBERON:2200936,dorsal fin distal radial cartilage
+UBERON:0002914,inferior postcentral sulcus,UBERON:0003022,cerebral cortex lobe
+DOID:0050938,breast lobular carcinoma,DOID:3459,breast carcinoma
+HP:0000737,Irritability,HP:0100851,Abnormal emotion/affect behavior
+HP:0001667,Right ventricular hypertrophy,HP:0001714,Ventricular hypertrophy
+UBERON:0002947,frontal operculum,UBERON:0000477,anatomical cluster
+HP:0007989,Intraretinal exudate,HP:0001147,Retinal exudate
+HP:0003417,Coronal cleft vertebrae,HP:0008428,Vertebral clefting
+UBERON:0005492,hyaloid vessel,UBERON:0010312,immature eye
+HP:0009647,Proximal/distal symphalangism of thumb,HP:0009617,Abnormality of the distal phalanx of the thumb
+UBERON:0001139,common iliac vein,UBERON:0015212,lateral structure
+HP:0001881,Abnormality of leukocytes,HP:0010987,Abnormality of cellular immune system
+DOID:2799,bronchiolitis obliterans,DOID:3082,interstitial lung disease
+HP:0001604,Vocal cord paresis,HP:0008777,Abnormality of the vocal cords
+HP:0000661,Palpebral fissure narrowing on adduction,HP:0000581,Blepharophimosis
+UBERON:0004910,epithelium of male gonad,UBERON:0004909,epithelium of gonad
+CL:0002137,type III cell of adrenal cortex,CL:0002097,cortical cell of adrenal gland
+DOID:7105,epiglottis neoplasm,DOID:8002,supraglottis neoplasm
+HP:0011846,Osteoblastoma,HP:0010622,Neoplasm of the skeletal system
+DOID:1405,primary angle-closure glaucoma,DOID:13550,angle-closure glaucoma
+UBERON:0004006,cerebellum intermediate zone,UBERON:0002749,regional part of cerebellar cortex
+HP:0010223,Pseudoepiphysis of the 3rd metacarpal,HP:0010222,Abnormality of the epiphysis of the 3rd metacarpal
+UBERON:0003903,bursa of Fabricius,UBERON:0011510,cloacal bursa
+DOID:7191,ovarian endometrioid cystadenoma,DOID:3269,ovarian cystadenoma
+UBERON:3000294,median prenasal process,UBERON:0004529,anatomical projection
+UBERON:2002076,lateral process of basipterygium,UBERON:0004120,mesoderm-derived structure
+HP:0000602,Ophthalmoplegia,HP:0000597,Ophthalmoparesis
+DOID:4430,somatostatinoma,DOID:169,neuroendocrine tumor
+UBERON:2001246,epibranchial 2 bone,UBERON:2001906,epibranchial 2 element
+DOID:9820,central gyrate choroidal dystrophy,DOID:9822,partial central choroid dystrophy
+HP:0012657,Abnormal brain positron emission tomography,HP:0012638,Abnormality of nervous system physiology
+UBERON:3000865,epileon,UBERON:0000064,organ part
+HP:0010941,Aplasia of the nasal bone,HP:0010940,Aplasia/Hypoplasia of the nasal bone
+UBERON:2001640,notochordal ossification,UBERON:0008909,perichordal bone
+HP:0001048,Cavernous hemangioma,HP:0001028,Hemangioma
+DOID:2743,pyeloureteritis cystica,DOID:2744,pyelitis
+UBERON:0001508,arch of aorta,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0002630,Fat malabsorption,HP:0002024,Malabsorption
+UBERON:0002392,nasolacrimal duct,UBERON:0004121,ectoderm-derived structure
+UBERON:0001130,vertebral column,UBERON:0004120,mesoderm-derived structure
+UBERON:2001808,facial foramen,UBERON:0005744,bone foramen
+NCBITaxon:783,Rickettsia rickettsii,NCBITaxon:114277,spotted fever group
+HP:0001966,Mesangial abnormality,HP:0000095,Abnormality of the glomerulus
+HP:0009505,Enlarged epiphysis of the distal phalanx of the 2nd finger,HP:0009499,Abnormality of the epiphysis of the distal phalanx of the 2nd finger
+CL:0001060,"hematopoietic oligopotent progenitor cell, lineage-negative",CL:0002032,hematopoietic oligopotent progenitor cell
+DOID:0050753,cerebellar ataxia,DOID:2786,cerebellar disease
+UBERON:0014792,musculature of pelvic complex,UBERON:0001015,musculature
+UBERON:2001763,pectoral fin lepidotrichium 3,UBERON:4000175,pectoral fin lepidotrichium
+UBERON:2000726,somite 14,UBERON:0002329,somite
+CL:0002233,epithelial cell of prostatic acinus,CL:0002231,epithelial cell of prostate
+HP:0001281,Tetany,HP:0011804,Abnormality of muscle physiology
+HP:0004488,Macrocephaly at birth,HP:0000256,Macrocephaly
+HP:0000854,Thyroid adenoma,HP:0100031,Neoplasm of the thyroid gland
+UBERON:0001674,masseteric vein,UBERON:0001638,vein
+HP:0010124,Abnormality of the epiphysis of the distal phalanx of the hallux,HP:0010056,Abnormality of the epiphyses of the hallux
+UBERON:0011576,supra-orbital ridge,UBERON:0003462,facial bone
+UBERON:0010030,ventral part of pharyngeal pouch 5,UBERON:0005911,endo-epithelium
+DOID:8358,pseudoglandular variant testicular seminoma,DOID:5842,testis seminoma
+DOID:4962,pericardial tuberculosis,DOID:0050598,extrapulmonary tuberculosis
+DOID:8826,colon carcinoma in situ,DOID:8719,in situ carcinoma
+HP:0011746,Secretory adrenocortical adenoma,HP:0008256,Adrenocortical adenoma
+DOID:0050839,anismus,DOID:0050836,focal dystonia
+CL:0000452,thyroid hormone secreting cell,CL:0000163,endocrine cell
+UBERON:0005322,mesonephric nephron,UBERON:0004120,mesoderm-derived structure
+HP:0010093,Duplication of the proximal phalanx of the hallux,HP:0010052,Abnormality of the proximal phalanx of the hallux
+UBERON:0005571,rhombomere 2 lateral wall,UBERON:0005501,rhombomere lateral wall
+UBERON:0005575,rhombomere 3 roof plate,UBERON:0005502,rhombomere roof plate
+CL:0001055,"CD14-positive, CD16-low monocyte",CL:0002397,"CD14-positive, CD16-positive monocyte"
+HP:0100105,Irregular epiphysis of the distal phalanx of the 2nd toe,HP:0100088,Abnormality of the epiphysis of the distal phalanx of the 2nd toe
+DOID:5580,pancreatic gastrinoma,DOID:1799,islet cell tumor
+CL:0002665,otic fibrocyte,CL:0000135,fibrocyte
+HP:0004804,Congenital hemolytic anemia,HP:0001878,Hemolytic anemia
+UBERON:0006353,principal vein of hindlimb,UBERON:0006443,prinicipal vein of limb
+UBERON:0006209,basioccipital cartilage element,UBERON:0015048,basioccipital endochondral element
+HP:0100058,Enlarged epiphyses of the 3rd toe,HP:0010165,Enlarged epiphyses of the toes
+CL:0000317,sebum secreting cell,CL:0000151,secretory cell
+DOID:2115,B cell deficiency,DOID:612,primary immunodeficiency disease
+HP:0009653,Curved phalanges of the thumb,HP:0009602,Abnormality of the phalanges of the thumb
+UBERON:0003663,hindlimb muscle,UBERON:0014795,pelvic appendage muscle
+UBERON:0002343,abdomen musculature,UBERON:0004479,musculature of trunk
+UBERON:3000649,anterior process of vomer,UBERON:0004120,mesoderm-derived structure
+HP:0002266,Focal clonic seizures,HP:0011153,Focal motor seizures
+UBERON:0012451,sensory receptor,UBERON:0012453,nerve ending
+UBERON:0013136,vein of lip,UBERON:0003496,head blood vessel
+UBERON:2005366,dorsal fin pterygiophore 3,UBERON:2001419,dorsal fin pterygiophore
+UBERON:0002518,otolith organ,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004806,vas deferens epithelium,UBERON:0005156,reproductive structure
+CL:0002527,immature CD14-positive dermal dendritic cell,CL:0001009,immature dermal dendritic cell
+DOID:14022,algoneurodystrophy,DOID:3223,complex regional pain syndrome
+UBERON:0015008,thoracic vertebra endochondral element,UBERON:0004120,mesoderm-derived structure
+DOID:0050545,visceral heterotaxy,DOID:0080015,physical disorder
+DOID:4990,essential tremor,DOID:480,movement disease
+HP:0007716,Intraocular melanoma,HP:0100012,Neoplasm of the eye
+UBERON:0005605,hepatic duct intrahepatic part,UBERON:0004823,intrahepatic bile duct epithelium
+HP:0010422,Complete duplication of the proximal phalanx of the 2nd toe,HP:0010429,Complete duplication of the phalanges of the 2nd toe
+UBERON:0011755,female labial swelling,UBERON:0014404,female anatomical structure
+NCBITaxon:12059,Enterovirus,NCBITaxon:12058,Picornaviridae
+HP:0000971,Abnormality of the sweat gland,HP:0011138,Abnormality of skin adnexa
+HP:0001449,Duplication of metatarsal bones,HP:0009136,Duplication involving bones of the feet
+HP:0100883,Chorangioma,HP:0100767,Abnormality of the placenta
+UBERON:0005077,neuropore,UBERON:0002050,embryonic structure
+CL:0002620,skin fibroblast,CL:0000057,fibroblast
+HP:0011094,Overbite,HP:0000692,Misalignment of teeth
+HP:0004914,Recurrent infantile hypoglycemia,HP:0001988,Recurrent hypoglycemia
+UBERON:0013628,pollical pad,UBERON:0013622,manual autopod pad
+UBERON:0015708,splenium of the corpus callosum,UBERON:0002791,regional part of telencephalon
+UBERON:2000331,commissure infima of Haller,UBERON:2000318,brainstem and spinal white matter
+DOID:1468,labyrinthitis,DOID:3930,otitis interna
+HP:0007256,Abnormality of pyramidal motor function,HP:0011442,Abnormality of central motor function
+HP:0011346,Mild expressive language delay,HP:0002474,Expressive language delay
+UBERON:0009526,maxillary process mesenchyme,UBERON:0005291,embryonic tissue
+UBERON:0013655,elastica externa of notochord,UBERON:0004121,ectoderm-derived structure
+HP:0009850,Triangular shaped middle phalanges of the hand,HP:0009833,Abnormality of the middle phalanges of the hand
+CL:0000432,reticular cell,CL:0000057,fibroblast
+HP:0009569,Broad middle phalanx of the 2nd finger,HP:0009547,Broad phalanges of the 2nd finger
+HP:0010925,Nuclear punctate cataract,HP:0007648,Punctate cataract
+UBERON:2002168,preural centrum 1 + ural centrum 1 + ural centrum 2,UBERON:0003106,urostyle
+UBERON:2002285,cycloid scale,UBERON:0007380,dermal scale
+CL:0002267,type D cell of stomach,CL:0002659,glandular cell of stomach
+HP:0000632,Lacrimation abnormality,HP:0012373,Abnormal eye physiology
+UBERON:0015783,muscle layer in fatty layer of subcutaneous tissue,UBERON:0001135,smooth muscle tissue
+HP:0002153,Hyperkalemia,HP:0011042,Abnormality of potassium homeostasis
+UBERON:0006672,incisive canal,UBERON:0004121,ectoderm-derived structure
+HP:0009346,Absent epiphysis of the proximal phalanx of the 3rd finger,HP:0010268,Absent epiphyses of the proximal phalanges of the hand
+HP:0010391,Duplication of the phalanges of the 5th toe,HP:0010181,Duplication of phalanx of toe
+UBERON:0008922,sublaminar layer S1,UBERON:0009732,sublaminar layers S1 or S2 or S5
+DOID:12237,bile reflux,DOID:9741,biliary tract disease
+UBERON:0013529,Brodmann area,UBERON:0002619,regional part of cerebral cortex
+HP:0009507,Irregular epiphysis of the distal phalanx of the 2nd finger,HP:0010251,Irregular epiphyses of the distal phalanges of the hand
+UBERON:0004708,paired limb/fin,UBERON:0000026,appendage
+HP:0007715,Weak extraocular muscles,HP:0008049,Abnormality of the extraocular muscles
+HP:0010691,Mirror image foot polydactyly,HP:0010689,Mirror image polydactyly
+UBERON:0011574,mesonephric duct lumen,UBERON:0005082,tube lumen
+HP:0011799,Abnormality of facial soft tissue,HP:0000271,Abnormality of the face
+UBERON:2001714,caudal principal ray 2,UBERON:2001585,caudal principal ray
+CL:0002296,type-4 epithelial cell of thymus,CL:0002365,medullary thymic epithelial cell
+UBERON:0006047,interdigital region between pedal digits 4 and 5,UBERON:0006025,interdigital region between digits 4 and 5
+UBERON:0002934,ventral oculomotor nucleus,UBERON:0007414,nucleus of midbrain tegmentum
+HP:0100144,Stippling of the epiphysis of the distal phalanx of the 3rd toe,HP:0100091,Abnormality of the epiphysis of the distal phalanx of the 3rd toe
+UBERON:0016459,posterior pole of lens,UBERON:0004121,ectoderm-derived structure
+HP:0100314,Cerebral inclusion bodies,HP:0002060,Abnormality of the cerebrum
+CL:0002190,squamous cell of epidermis,CL:0000312,keratinocyte
+UBERON:4000104,ganoine,UBERON:0003585,dermis connective tissue
+UBERON:0002458,spinal artery,UBERON:0004573,systemic artery
+UBERON:0001035,dento-alveolar joint,UBERON:0002213,cartilaginous joint
+HP:0003690,Limb muscle weakness,HP:0001324,Muscle weakness
+UBERON:3000288,maxillopalatine,UBERON:0011597,bone of upper jaw
+DOID:11240,appendiceal neoplasm,DOID:4610,intestinal benign neoplasm
+UBERON:0001604,levator palpebrae superioris,UBERON:0001601,extra-ocular muscle
+UBERON:0010583,pedal digit 4 phalanx pre-cartilage condensation,UBERON:0005698,pedal digit 4 mesenchyme
+CL:0000592,large luteal cell,CL:0000177,testosterone secreting cell
+UBERON:0003639,manual digit 5 phalanx,UBERON:0015029,manual digit 5 phalanx endochondral element
+CL:0002493,strial basal cell,CL:0002491,auditory epithelial cell
+DOID:7819,sphenoorbital meningioma,DOID:4437,skull base meningioma
+NCBITaxon:5809,Sarcocystidae,NCBITaxon:423054,Eimeriorina
+HP:0100957,Abnormality of the renal medulla,HP:0012210,Abnormal renal morphology
+CL:0002533,immature CD16-positive myeloid dendritic cell,CL:0000840,immature conventional dendritic cell
+DOID:3998,Bartholin's gland transitional cell carcinoma,DOID:3999,Bartholin's gland carcinoma
+UBERON:4200139,palatoquadrate element,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0000212,toilet claw,UBERON:0001705,nail
+DOID:10241,thalassemia,DOID:0050737,autosomal recessive disease
+HP:0001633,Abnormality of the mitral valve,HP:0006705,Abnormality of the atrioventricular valves
+CL:0000221,ectodermal cell,CL:0002321,embryonic cell
+UBERON:0000458,endocervix,UBERON:0014404,female anatomical structure
+UBERON:0015827,brainstem reticular formation,UBERON:0002616,regional part of brain
+UBERON:0001448,metatarsal bone,UBERON:0003821,metapodium bone
+HP:0006504,Anomaly of the limb diaphyses,HP:0002813,Abnormality of limb bone morphology
+UBERON:0005089,sweat gland placode,UBERON:0011814,non-neurogenic ectodermal placode
+UBERON:0001130,vertebral column,UBERON:0000075,subdivision of skeletal system
+HP:0010816,Epidermal nevus,HP:0003764,Nevus
+UBERON:0003503,leg blood vessel,UBERON:0003516,hindlimb blood vessel
+HP:0000967,Petechiae,HP:0001933,Subcutaneous hemorrhage
+CL:0000031,neuroblast,CL:0000055,non-terminally differentiated cell
+HP:0000417,Slender nose,HP:0005105,Abnormal nasal morphology
+DOID:0050456,Buruli ulcer disease,DOID:0050338,primary bacterial infectious disease
+UBERON:0003502,neck blood vessel,UBERON:0001981,blood vessel
+DOID:7077,malignant melanocytic peripheral nerve sheath tumor of mediastinum,DOID:5559,mediastinal cancer
+DOID:0050613,bile duct carcinoma in situ,DOID:8719,in situ carcinoma
+CL:0002598,bronchial smooth muscle cell,CL:0000192,smooth muscle cell
+UBERON:0005006,mucosa of renal pelvis,UBERON:0004980,mucosa of ureter
+UBERON:0010052,mucosa of dorsum of tongue,UBERON:0005020,mucosa of tongue
+HP:0008014,Central fundal arteriolar microaneurysms,HP:0000630,Abnormality of retinal arteries
+HP:0008457,Caudal interpedicular narrowing,HP:0008450,Narrow vertebral interpedicular distance
+HP:0009878,Cerebellar ataxia associated with quadrupedal gait,HP:0001288,Gait disturbance
+NCBITaxon:11620,Lassa virus,NCBITaxon:208896,Old world arenaviruses
+UBERON:0010197,trunk of common carotid artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0001095,caudal vertebra,UBERON:0002412,vertebra
+HP:0100644,Melanonychia,HP:0100643,Abnormality of nail color
+UBERON:2000615,adductor arcus palatini,UBERON:0005493,hyoid muscle
+HP:0100555,Asymmetric growth,HP:0001507,Growth abnormality
+DOID:2670,transitional papilloma,DOID:2615,papilloma
+UBERON:3000645,corpus,UBERON:0008907,dermal bone
+UBERON:0002017,portal vein,UBERON:0001638,vein
+NCBITaxon:32524,Amniota,NCBITaxon:32523,Tetrapoda
+HP:0003246,Prominent scrotal raphe,HP:0000045,Abnormality of the scrotum
+UBERON:0010343,2nd arch mesenchyme from head mesenchyme,UBERON:0010360,pharyngeal arch mesenchyme from head mesenchyme
+UBERON:0005561,telencephalon lateral wall,UBERON:0005496,neural tube lateral wall
+UBERON:0005925,ethmoidal process of inferior nasal concha,UBERON:4100000,skeletal element projection
+UBERON:0004346,gubernaculum,UBERON:0003567,abdomen connective tissue
+UBERON:0001338,urethral gland,UBERON:0006554,urinary system structure
+UBERON:0014674,distal interphalangeal joint of pedal digit 4,UBERON:0014679,distal interphalangeal joint of digit 4
+HP:0100828,Increase in T cell number,HP:0011839,Abnormality of T cell number
+UBERON:0005839,thoracic spinal cord dorsal column,UBERON:0014637,thoracic spinal cord white matter
+UBERON:2001655,upper pharyngeal 4 tooth,UBERON:0004756,dermal skeletal element
+UBERON:2002008,neural lamina,UBERON:4100000,skeletal element projection
+DOID:1766,factitious disorder,DOID:150,disease of mental health
+UBERON:0010532,primitive nephron,UBERON:0003914,epithelial tube
+HP:0003308,Cervical subluxation,HP:0003319,Abnormality of the cervical spine
+UBERON:0002190,subcutaneous adipose tissue,UBERON:0001013,adipose tissue
+HP:0006508,Abnormality of tibial epiphyses,HP:0006500,Abnormality involving the epiphyses of the lower limbs
+HP:0009663,Abnormality of the epiphysis of the proximal phalanx of the thumb,HP:0010244,Abnormality of the epiphyses of the middle phalanges of the hand
+DOID:12524,plantar nerve lesion,DOID:9473,mononeuritis of lower limb
+UBERON:0004869,parietal organ,UBERON:0003103,compound organ
+DOID:2096,vulvar sarcoma,DOID:1245,vulva cancer
+DOID:14165,bilateral hyperactive labyrinth,DOID:566,labyrinthine dysfunction
+HP:0001057,Aplasia cutis congenita,HP:0008065,Aplasia/Hypoplasia of the skin
+DOID:7246,lymphoepithelioma-like acinar prostate adenocarcinoma,DOID:2526,prostate adenocarcinoma
+UBERON:0001306,cumulus oophorus,UBERON:0005156,reproductive structure
+HP:0004763,Paroxysmal supraventricular tachycardia,HP:0004755,Supraventricular tachycardia
+UBERON:0013151,choroidal artery,UBERON:0001637,artery
+HP:0004020,Irregular ossification of the radial metaphysis,HP:0004015,Abnormality of radial metaphyses
+UBERON:0001987,placenta,UBERON:0000478,extraembryonic structure
+UBERON:2002279,pectoral fin distal radial bone 2,UBERON:2102279,pectoral fin distal radial element 2
+CL:0000544,slowly adapting mechanoreceptor cell,CL:0000199,mechanoreceptor cell
+DOID:2616,Wolffian duct adenoma,DOID:0050622,reproductive organ benign neoplasm
+HP:0010690,Mirror image hand polydactyly,HP:0001161,Hand polydactyly
+CL:1001571,hippocampal pyramidal neuron,CL:0000598,pyramidal cell
+UBERON:0008978,anal sac,UBERON:0004121,ectoderm-derived structure
+HP:0011225,Epiblepharon,HP:0000492,Abnormality of the eyelid
+CL:0000557,granulocyte monocyte progenitor cell,CL:0001012,CD7-negative lymphoid progenitor OR granulocyte monocyte progenitor
+HP:0011904,Persistence of hemoglobin F,HP:0011902,Abnormal hemoglobin
+UBERON:1600006,paired fin radial element,UBERON:2100271,radial element
+DOID:13958,uterine corpus bizarre leiomyoma,DOID:0060095,uterine benign neoplasm
+CL:0000738,leukocyte,CL:0000988,hematopoietic cell
+HP:0008418,Squared-off platyspondyly,HP:0000926,Platyspondyly
+HP:0008476,Irregular sclerotic endplates,HP:0003301,Irregular vertebral endplates
+UBERON:2001824,lateral line scale,UBERON:0007380,dermal scale
+HP:0010310,Chylothorax,HP:0002202,Pleural effusion
+DOID:7267,lung clear cell carcinoma,DOID:3910,lung adenocarcinoma
+DOID:0060200,amyotrophic lateral sclerosis type 9,DOID:332,amyotrophic lateral sclerosis
+HP:0003357,Thymic hormone decreased,HP:0000777,Abnormality of the thymus
+DOID:6208,mediastinal osteogenic sarcoma,DOID:3357,extraosseous osteosarcoma
+UBERON:2001998,posttemporal-supracleithrum,UBERON:0008907,dermal bone
+UBERON:0000400,jejunal epithelium,UBERON:0013636,epithelium of intestinal villus
+DOID:12387,nephrogenic diabetes insipidus,DOID:11705,impaired renal function disease
+HP:0005025,Hypoplastic distal humeri,HP:0006507,Aplasia/Hypoplasia of the humerus
+UBERON:0001273,ilium,UBERON:0015054,iliac endochondral element
+UBERON:0009066,posterior thoracic air sac,UBERON:0009062,posterior air sac
+UBERON:3000834,posterior lamina recurvata,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0011280,nail of pedal digit 3,UBERON:0009567,nail of pedal digit
+HP:0008031,Posterior Y-sutural cataract,HP:0010695,Sutural cataract
+HP:0002564,Malformation of the heart and great vessels,HP:0001627,Abnormality of cardiac morphology
+DOID:0060109,vulvar benign neoplasm,DOID:0060086,female reproductive organ benign neoplasm
+UBERON:0005298,skin of clitoris,UBERON:0005156,reproductive structure
+UBERON:0005826,gracile fasciculus of spinal cord,UBERON:0005821,gracile fasciculus
+HP:0010875,Chaddock reflex,HP:0007256,Abnormality of pyramidal motor function
+HP:0012535,Abnormal synaptic transmission,HP:0001311,Abnormal nervous system electrophysiology
+CL:0002320,connective tissue cell,CL:0000548,animal cell
+UBERON:4300088,metapterygium bone,UBERON:2001587,pectoral fin proximal radial bone
+UBERON:0015094,distal carpal bone 4 cartilage,UBERON:0015064,autopod cartilage
+UBERON:0002385,muscle tissue,UBERON:0000479,tissue
+DOID:13689,prostate calculus,DOID:47,prostate disease
+HP:0008776,Abnormality of the renal artery,HP:0012210,Abnormal renal morphology
+UBERON:0003466,forelimb zeugopod bone,UBERON:0003460,arm bone
+HP:0008074,Metatarsal periosteal thickening,HP:0001832,Abnormality of the metatarsal bones
+HP:0010352,Patchy sclerosis of the phalanges of the 2nd toe,HP:0010178,Patchy sclerosis of the phalanges of the toes
+HP:0001808,Fragile nails,HP:0001597,Abnormality of the nail
+UBERON:2001254,abdominal scute series,UBERON:0000477,anatomical cluster
+UBERON:3000079,cartilago retronarina,UBERON:0003933,cranial cartilage
+HP:0009983,Partial duplication of the proximal phalanx of the 4th finger,HP:0009977,Duplication of the proximal phalanx of the 4th finger
+HP:0007367,Atrophy/Degeneration affecting the central nervous system,HP:0007319,Morphological abnormality of the central nervous system
+UBERON:0007644,thoracic lymph node,UBERON:0000029,lymph node
+DOID:5957,bladder urachal squamous cell carcinoma,DOID:3742,bladder squamous cell carcinoma
+HP:0005667,Os odontoideum,HP:0003467,Atlantoaxial instability
+HP:0005595,Generalized hyperkeratosis,HP:0000962,Hyperkeratosis
+UBERON:0014788,right extraembryonic umbilical vein,UBERON:0015212,lateral structure
+UBERON:0003861,neural arch,UBERON:0002513,endochondral bone
+UBERON:0009496,intrahepatic part of biliary bud,UBERON:0005911,endo-epithelium
+UBERON:3000538,recessus fenestrae ovalis,UBERON:0004121,ectoderm-derived structure
+UBERON:4300005,aphakic space,UBERON:0000464,anatomical space
+CL:0000656,primary spermatocyte,CL:0000017,spermatocyte
+UBERON:0010894,keratinous tooth,UBERON:0003913,tooth-like structure
+UBERON:0005061,neural groove,UBERON:0005423,developing anatomical structure
+HP:0002986,Radial bowing,HP:0002818,Abnormality of the radius
+HP:0011458,Abdominal symptom,HP:0001438,Abnormality of the abdomen
+UBERON:0001521,flexor carpi radialis muscle,UBERON:0000366,flexor muscle
+UBERON:2002013,ascending limb of ceratobranchial 5 bone,UBERON:0010314,structure with developmental contribution from neural crest
+CL:1000303,fibroblast of areolar connective tissue,CL:0000057,fibroblast
+DOID:3643,sella turcica neoplasm,DOID:3842,skull base neoplasm
+HP:0009514,Bracket epiphysis of the middle phalanx of the 2nd finger,HP:0010258,Bracket epiphyses of the middle phalanges of the hand
+HP:0100917,Sclerosis of the proximal phalanges of the hand,HP:0100899,Sclerosis of the phalanges of the hand
+CL:0000459,norepinephrin secreting cell,CL:0000457,biogenic amine secreting cell
+HP:0000225,Gingival bleeding,HP:0001892,Abnormal bleeding
+HP:0009609,Duplication of the 1st metacarpal,HP:0010009,Abnormality of the 1st metacarpal
+UBERON:0014556,CA3 stratum radiatum,UBERON:0014567,layer of hippocampal field
+DOID:3821,posterior cerebral artery infarction,DOID:3526,cerebral infarction
+HP:0001140,Epibulbar dermoid,HP:0000591,Abnormality of the sclera
+UBERON:0011945,luminal layer of epithelium,UBERON:0000119,cell layer
+DOID:10883,herpangina,DOID:934,viral infectious disease
+UBERON:0001037,strand of hair,UBERON:0004121,ectoderm-derived structure
+UBERON:4200115,presupracleithrum,UBERON:0008907,dermal bone
+UBERON:0016382,prescapular lymph node,UBERON:0002429,cervical lymph node
+NCBITaxon:10088,"Mus <mouse, genus>",NCBITaxon:39107,Murinae
+DOID:1035,natural killer cell leukemia,DOID:1037,lymphoblastic leukemia
+UBERON:0012462,proctodeum portion of cloaca,UBERON:0004120,mesoderm-derived structure
+UBERON:0005796,duplex uterus,UBERON:0000995,uterus
+HP:0006070,Metacarpophalangeal joint contractures,HP:0011911,Abnormality of metacarpophalangeal joint
+UBERON:3000234,inferior prenasal cartilage,UBERON:0010313,neural crest-derived structure
+UBERON:0015878,common iliac lymph node,UBERON:0015877,parietal pelvic lymph node
+HP:0006009,Broad phalanx,HP:0009803,Short phalanx of finger
+UBERON:0004356,apical ectodermal ridge,UBERON:0002050,embryonic structure
+DOID:13147,fungal esophagitis,DOID:11963,esophagitis
+DOID:4428,dyslexia,DOID:13365,reading disorder
+HP:0000429,Abnormality of the nasal alae,HP:0010938,Abnormality of the external nose
+UBERON:0006932,vestibular epithelium,UBERON:0006934,sensory epithelium
+HP:0010022,Pseudoepiphysis of the 1st metacarpal,HP:0009693,Pseudoepiphyses of the thumb
+DOID:6740,cervix small cell carcinoma,DOID:2893,cervix carcinoma
+UBERON:0005092,right horn of sinus venosus,UBERON:0015212,lateral structure
+HP:0006406,Club-shaped proximal femur,HP:0002823,Abnormality of the femur
+DOID:6404,metanephric adenoma,DOID:2697,renal adenoma
+UBERON:0003217,neural lobe of neurohypophysis,UBERON:0004120,mesoderm-derived structure
+UBERON:0001337,spongiose part of urethra,UBERON:0006554,urinary system structure
+UBERON:0003471,artery of lower lip,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0010537,mesonephric nephron progenitor,UBERON:0010536,nephron progenitor
+HP:0012194,Episodic hemiplegia,HP:0002301,Hemiplegia
+UBERON:2001313,ventral anterior lateral line ganglion,UBERON:0004121,ectoderm-derived structure
+UBERON:0013161,left lateral ventricle,UBERON:0002285,telencephalic ventricle
+UBERON:0006789,deep gray layer of superior colliculus,UBERON:0006793,deep layer of superior colliculus
+DOID:0060215,Balo concentric sclerosis,DOID:3213,demyelinating disease
+DOID:2272,vulvovaginal candidiasis,DOID:37,skin disease
+DOID:6525,choroid mixed cell melanoma,DOID:6438,malignant choroid melanoma
+HP:0008625,Severe sensorineural hearing impairment,HP:0012714,Severe hearing impairment
+CL:0000233,platelet,CL:0000458,serotonin secreting cell
+HP:0000517,Abnormality of the lens,HP:0004328,Abnormality of the anterior segment of the eye
+DOID:715,T-cell leukemia,DOID:10747,lymphoid leukemia
+UBERON:0014484,distal phalanx of digit 2,UBERON:0004300,distal phalanx
+HP:0012039,Descemet Membrane Folds,HP:0011490,Abnormality of Descemet's membrane
+UBERON:0014883,distal epiphysis of distal phalanx of manual digit 3,UBERON:0014886,distal epiphysis of distal phalanx of manual digit
+DOID:10526,conjunctival pterygium,DOID:10139,conjunctival degeneration
+DOID:4797,SM-AHNMD,DOID:349,systemic mastocytosis
+UBERON:2002129,caudal rod,UBERON:0004120,mesoderm-derived structure
+UBERON:3010771,ventral sympathetic chain,UBERON:0000407,sympathetic trunk
+UBERON:0005837,fasciculus of spinal cord,UBERON:0001019,nerve fasciculus
+UBERON:0010186,male urethral gland,UBERON:0014403,male anatomical structure
+DOID:14033,malignant visceral pleura tumor,DOID:5158,pleural cancer
+DOID:12192,sigmoid colon cancer,DOID:219,colon cancer
+DOID:0060207,amyotrophic lateral sclerosis type 16,DOID:332,amyotrophic lateral sclerosis
+UBERON:0006311,chamber of eyeball,UBERON:0000064,organ part
+HP:0004367,Abnormality of glycoprotein metabolism,HP:0001939,Abnormality of metabolism/homeostasis
+HP:0006722,Small intestine carcinoid,HP:0100833,Neoplasm of the small intestine
+UBERON:0006948,efferent duct epithelium,UBERON:0005156,reproductive structure
+HP:0004042,Irregular ulnar metaphysis,HP:0003850,Irregular metaphyses of the upper limbs
+HP:0100352,Contractures of the distal interphalangeal joint of the 2nd toe,HP:0010327,Flexion contracture of the 2nd toe
+DOID:893,Wilson disease,DOID:409,liver disease
+UBERON:0012104,sesamoid bone of the peroneus longus muscle,UBERON:0004251,hindlimb zeugopod bone
+HP:0005424,Absent specific antibody response,HP:0005372,Abnormality of B cell physiology
+UBERON:0010227,future cardiac atrium,UBERON:0005423,developing anatomical structure
+UBERON:0004629,thoracic vertebra 4,UBERON:0002347,thoracic vertebra
+CL:0002515,interrenal norepinephrine type cell,CL:0000459,norepinephrin secreting cell
+CL:0000496,green sensitive photoreceptor cell,CL:0000490,photopic photoreceptor cell
+CL:1000415,epithelial cell of gall bladder,CL:0002371,somatic cell
+DOID:1284,prolapse of female genital organ,DOID:229,female reproductive system disease
+HP:0011020,Abnormality of mucopolysaccharide metabolism,HP:0004371,Abnormality of glycosaminoglycan metabolism
+DOID:6025,selective immunoglobulin deficiency disease,DOID:2115,B cell deficiency
+DOID:7,disease of anatomical entity,DOID:4,disease
+CL:1000296,epithelial cell of urethra,CL:0002371,somatic cell
+DOID:0060105,brain medulloblastoma,DOID:1319,brain cancer
+UBERON:0005609,iliac artery,UBERON:0004573,systemic artery
+HP:0002673,Coxa valga,HP:0003367,Abnormality of the femoral neck
+HP:0100563,Diastomatomyelia,HP:0100561,Spinal cord lesions
+UBERON:0002572,principal pretectal nucleus,UBERON:0011214,nucleus of midbrain tectum
+HP:0003005,Ganglioneuroma,HP:0004376,Neuroblastic tumors
+HP:0010352,Patchy sclerosis of the phalanges of the 2nd toe,HP:0100926,Sclerosis of the phalanges of the 2nd toe
+HP:0010389,Symphalangism affecting the phalanges of the 5th toe,HP:0010342,Abnormality of the phalanges of the 5th toe
+HP:0005671,Bilateral intracranial calcifications,HP:0002514,Cerebral calcification
+UBERON:0005148,metanephric S-shaped body,UBERON:0005332,mesonephric S-shaped body
+UBERON:0001740,arytenoid cartilage,UBERON:0001739,laryngeal cartilage
+UBERON:0006671,orbital fat pad,UBERON:0010313,neural crest-derived structure
+UBERON:0000210,tetrapod parietal bone,UBERON:0002514,intramembranous bone
+UBERON:3000586,superior prenasal cartilage,UBERON:0010313,neural crest-derived structure
+UBERON:0006273,otic pit,UBERON:0005423,developing anatomical structure
+UBERON:0013406,bregma,UBERON:0006983,anatomical point
+HP:0005478,Prominent frontal sinuses,HP:0002687,Abnormality of the frontal sinuses
+CL:0000901,Tr1 cell,CL:0000492,CD4-positive helper T cell
+UBERON:0002589,lateral corticospinal tract,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009501,Abnormality of the epiphysis of the proximal phalanx of the 2nd finger,HP:0006263,Abnormality of the epiphyses of the 2nd finger
+CL:1001599,pancreas exocrine glandular cell,CL:0000150,glandular epithelial cell
+DOID:5041,esophageal cancer,DOID:3119,gastrointestinal system cancer
+DOID:9401,epididymo-orchitis,DOID:9402,epididymitis
+UBERON:0001139,common iliac vein,UBERON:0001638,vein
+HP:0004566,Pear-shaped vertebrae,HP:0003312,Abnormal form of the vertebral bodies
+HP:0100901,Sclerosis of the distal phalanx of the 3rd finger,HP:0100915,Sclerosis of the distal phalanges of the hand
+UBERON:0009468,basiotic bone,UBERON:0011164,neurocranium bone
+UBERON:2105385,dorsal fin proximal radial element 8,UBERON:2100947,dorsal fin proximal radial element
+HP:0003073,Hypoalbuminemia,HP:0012116,Abnormal albumin level
+HP:0008857,Neonatal short-trunk short stature,HP:0003521,Disproportionate short-trunk short stature
+UBERON:0006676,muscularis mucosa,UBERON:0001135,smooth muscle tissue
+DOID:0060025,immunoglobulin alpha deficiency,DOID:2115,B cell deficiency
+UBERON:0013514,space surrounding organism,UBERON:0000464,anatomical space
+UBERON:0003966,gonial bone,UBERON:0010313,neural crest-derived structure
+UBERON:0002076,cuticle of hair,UBERON:0000021,cutaneous appendage
+UBERON:0001127,serratus dorsalis inferior muscle,UBERON:0011217,serratus dorsalis muscle
+HP:0000523,Subcapsular cataract,HP:0010696,Polar cataract
+CL:0000641,chromophobe cell,CL:0000163,endocrine cell
+DOID:7233,adult central nervous system embryonal carcinoma,DOID:5349,central nervous system adult germ cell tumor
+UBERON:0006812,mental foramen,UBERON:0005744,bone foramen
+UBERON:0004776,inner renal medulla vasa recta,UBERON:0004726,vasa recta
+UBERON:2001335,supradorsal,UBERON:2001457,postcranial axial cartilage
+HP:0100607,Dysmenorrhea,HP:0000140,Abnormality of the menstrual cycle
+HP:0011026,Aplasia/Hypoplasia of the vagina,HP:0000142,Abnormality of the vagina
+CL:0002232,epithelial cell of prostatic duct,CL:0000072,non-branched duct epithelial cell
+UBERON:0014707,hyoplastron,UBERON:0011657,dermal element of plastron
+UBERON:0004505,skeletal muscle tissue of orbicularis oculi,UBERON:0003269,skeletal muscle tissue of eye
+UBERON:0015777,transitional epithelium of prostatic urethra,UBERON:0000428,prostate epithelium
+DOID:3999,Bartholin's gland carcinoma,DOID:1294,vulva carcinoma
+UBERON:0014703,anal membrane ectodermal component,UBERON:0010371,ecto-epithelium
+DOID:14289,Ebstein anomaly,DOID:0050826,tricuspid valve disease
+UBERON:0007197,hermaphroditic organism,UBERON:0000468,multi-cellular organism
+HP:0001641,Abnormality of the pulmonary valve,HP:0001654,Abnormality of the heart valves
+UBERON:3000810,fissura sagittalis,UBERON:0000064,organ part
+UBERON:3000676,bronchial process,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:8307,early invasive cervical adenocarcinoma,DOID:3702,cervical adenocarcinoma
+UBERON:0005729,pectoral appendage field,UBERON:0005732,paired limb/fin field
+DOID:10989,conjunctival vascular disease,DOID:4251,conjunctival disease
+DOID:0050829,pericardium disease,DOID:1287,cardiovascular system disease
+UBERON:0005350,lobule simplex,UBERON:0014648,hemisphere part of cerebellar posterior lobe
+UBERON:0003654,metatarsal bone of digit 5,UBERON:0013585,metapodium bone 5
+HP:0007862,Retinal calcification,HP:0010766,Ectopic calcification
+HP:0011397,Abnormality of the dorsal column of the spinal cord,HP:0002143,Abnormality of the spinal cord
+UBERON:0002824,vestibular ganglion,UBERON:0001800,sensory ganglion
+DOID:0050782,Zollinger-Ellison Syndrome,DOID:225,syndrome
+HP:0009222,Small epiphysis of the middle phalanx of the 4th finger,HP:0010265,Small epiphyses of the middle phalanges of the hand
+DOID:319,spinal cord disease,DOID:331,central nervous system disease
+UBERON:0006452,fourth thoracic spinal cord segment,UBERON:0007715,thoracic subsegment of spinal cord
+CL:0000373,histoblast,CL:0000146,simple columnar epithelial cell
+UBERON:0006138,plantar digital artery,UBERON:0004554,hindlimb digital artery
+UBERON:0012359,pedal digitopodium bone,UBERON:0005899,pes bone
+HP:0011432,High maternal serum alpha-fetoprotein,HP:0011436,Abnormal maternal serum screening
+UBERON:0005377,olfactory bulb glomerular layer,UBERON:0004001,olfactory bulb layer
+UBERON:0004530,bony projection,UBERON:0004529,anatomical projection
+HP:0005892,Proximal tibial and fibular fusion,HP:0005929,Synostosis involving the tibia
+DOID:2764,ethmoid sinus adenoid cystic carcinoma,DOID:1363,ethmoid sinus cancer
+HP:0010438,Abnormality of the ventricular septum,HP:0001713,Abnormality of cardiac ventricle
+HP:0007455,Adermatoglyphia,HP:0007477,Abnormal dermatoglyphics
+UBERON:0002316,white matter,UBERON:0003714,neural tissue
+HP:0003902,Epiphyseal stippling of the humerus,HP:0003897,Irregular ossification of the humeral epiphyses
+UBERON:3010820,suboccular arch,UBERON:0004121,ectoderm-derived structure
+UBERON:0002355,pelvis,UBERON:0000475,organism subdivision
+UBERON:0003993,interventricular foramen of CNS,UBERON:0004121,ectoderm-derived structure
+CL:0000171,pancreatic A cell,CL:0002067,type A enterocrine cell
+HP:0100684,Salivary gland neoplasm,HP:0010286,Abnormality of the salivary glands
+UBERON:0014389,gustatory papilla of tongue,UBERON:0001726,papilla of tongue
+UBERON:0011369,omotransversarius muscle,UBERON:0001630,muscle organ
+UBERON:0001943,midbrain tegmentum,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0003125,Reduced factor VIII activity,HP:0010989,Abnormality of the intrinsic pathway
+HP:0006263,Abnormality of the epiphyses of the 2nd finger,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+DOID:9870,galactosemia,DOID:2978,carbohydrate metabolic disorder
+UBERON:4200183,bicipital tuberosity,UBERON:4100000,skeletal element projection
+HP:0006852,Episodic generalized hypotonia,HP:0001290,Generalized hypotonia
+HP:0004906,hypernatremic dehydration,HP:0001986,Hypertonic dehydration
+UBERON:0003096,middle lateral line,UBERON:0010202,lateral line
+HP:0000368,"Low-set, posteriorly rotated ears",HP:0000358,Posteriorly rotated ears
+UBERON:0011779,nerve of head region,UBERON:0001021,nerve
+HP:0009772,Patchy sclerosis of the phalanges of the hand,HP:0100899,Sclerosis of the phalanges of the hand
+UBERON:4200014,lateral tuber of ulna,UBERON:0004530,bony projection
+UBERON:0005033,mucosa of gallbladder,UBERON:0004999,mucosa of biliary tree
+CL:0000301,pole cell,CL:0000670,primordial germ cell
+HP:0012095,Multiple joint dislocation,HP:0001373,Joint dislocation
+DOID:2569,retinal drusen,DOID:2007,degeneration of macula and posterior pole
+HP:0009220,Ivory epiphysis of the middle phalanx of the 4th finger,HP:0009247,Abnormality of the epiphysis of the middle phalanx of the 4th finger
+DOID:0050518,Ross River fever,DOID:934,viral infectious disease
+CL:0002540,mesenchymal stem cell of the bone marrow,CL:0002092,bone marrow cell
+CL:0001017,mature CD1a-positive Langerhans cell,CL:0000841,mature conventional dendritic cell
+UBERON:0002399,lesser omentum,UBERON:0002050,embryonic structure
+HP:0008271,Abnormal cartilage collagen on EM,HP:0002763,Abnormal cartilage morphology
+UBERON:0005502,rhombomere roof plate,UBERON:0005291,embryonic tissue
+UBERON:0002550,anterior hypothalamic region,UBERON:0004121,ectoderm-derived structure
+UBERON:2000768,hypaxial region somite 14,UBERON:0003895,hypaxial myotome region
+NCBITaxon:155616,Tremellomycetes,NCBITaxon:5302,Agaricomycotina
+DOID:13677,SAPHO syndrome,DOID:225,syndrome
+UBERON:2002128,cavum sinus imparis,UBERON:0000464,anatomical space
+DOID:8003,alveoli adenoma,DOID:5386,lung adenoma
+DOID:13823,parasitic eyelid infestation,DOID:9423,blepharitis
+UBERON:0002320,glomerular mesangium,UBERON:0004120,mesoderm-derived structure
+DOID:11400,pyelonephritis,DOID:2744,pyelitis
+CL:0000388,tendon cell,CL:0000386,attachment cell
+UBERON:2001874,basibranchial 2 cartilage,UBERON:0013747,basibranchial cartilage
+CL:0000686,cerebrospinal fluid secreting cell,CL:0000075,columnar/cuboidal epithelial cell
+UBERON:0012308,superficial lateral cervical lymph node,UBERON:0012306,lateral cervical lymph node
+HP:0008915,Childhood-onset truncal obesity,HP:0001956,Truncal obesity
+HP:0003010,Prolonged bleeding time,HP:0001872,Abnormality of thrombocytes
+HP:0000412,Prominent ears,HP:0000377,Abnormality of the pinna
+UBERON:0011671,nuchal plate of carapace,UBERON:0011665,carapace bone
+UBERON:0009536,vascular element of left lung,UBERON:0005629,vascular plexus
+UBERON:2000718,epaxial region somite 27,UBERON:0003900,epaxial myotome region
+HP:0002281,Gray matter heterotopias,HP:0002269,Abnormality of neuronal migration
+CL:0001041,"CD8-positive, CXCR3-positive, alpha-beta regulatory T cell",CL:0000795,"CD8-positive, alpha-beta regulatory T cell"
+DOID:5809,childhood parosteal osteogenic sarcoma,DOID:3373,juxtacortical osteosarcoma
+UBERON:0008840,plantar pad,UBERON:0008838,metapodial pad
+UBERON:0005009,mucosa of trigone of urinary bladder,UBERON:0001259,mucosa of urinary bladder
+HP:0009222,Small epiphysis of the middle phalanx of the 4th finger,HP:0009247,Abnormality of the epiphysis of the middle phalanx of the 4th finger
+HP:0010778,Tracheomegaly,HP:0002778,Abnormality of the trachea
+UBERON:0001694,petrous part of temporal bone,UBERON:0004120,mesoderm-derived structure
+HP:0010191,Symphalangism affecting the distal phalanges of the toes,HP:0010179,Symphalangism affecting the phalanges of the toes
+CL:0000492,CD4-positive helper T cell,CL:0000624,"CD4-positive, alpha-beta T cell"
+UBERON:2000895,hypaxial region somite 18,UBERON:0003895,hypaxial myotome region
+HP:0100570,Carcinoid,HP:0100568,Neoplasm of the endocrine system
+HP:0009258,Small epiphysis of the distal phalanx of the 4th finger,HP:0009401,Small epiphyses of the 4th finger
+DOID:10792,chronic maxillary sinusitis,DOID:2051,maxillary sinusitis
+CL:0000526,afferent neuron,CL:0000540,neuron
+UBERON:0007251,preoptic nucleus,UBERON:0006569,diencephalic nucleus
+HP:0009800,Maternal diabetes,HP:0002686,Prenatal maternal abnormality
+UBERON:0014702,frontonasal process epithelium,UBERON:0010371,ecto-epithelium
+DOID:5178,metachronous kidney Wilms' tumor,DOID:2154,nephroblastoma
+DOID:10965,spastic diplegia,DOID:0050669,spastic cerebral palsy
+CL:1000714,kidney cortex collecting duct principal cell,CL:1000549,kidney cortex collecting duct epithelial cell
+UBERON:0009756,spermaceti organ,UBERON:0000062,organ
+UBERON:0002640,cuneocerebellar tract,UBERON:0007702,tract of brain
+UBERON:0011016,pyramidalis,UBERON:0002461,anterior abdominal wall muscle
+HP:0012236,Elevated sweat chloride,HP:0011422,Abnormality of chloride homeostasis
+UBERON:0007242,tunica intima of vein,UBERON:0002523,tunica intima
+UBERON:0006242,gall bladder primordium,UBERON:0001048,primordium
+UBERON:0004314,distal phalanx of manual digit 5,UBERON:0003639,manual digit 5 phalanx
+UBERON:0010389,pterygoid bone,UBERON:0011164,neurocranium bone
+UBERON:0012374,subserosal plexus,UBERON:0000429,enteric plexus
+DOID:11151,cholecystolithiasis,DOID:0000000,gallbladder disease
+CL:0000782,myeloid dendritic cell,CL:0000766,myeloid leukocyte
+CL:0002396,"CD14-low, CD16-positive monocyte",CL:0000875,non-classical monocyte
+UBERON:0002406,pericardial sac,UBERON:0005906,serous sac
+DOID:4731,atrophic rhinitis,DOID:4483,rhinitis
+UBERON:0002811,left frontal lobe,UBERON:0001870,frontal cortex
+HP:0000028,Cryptorchidism,HP:0000035,Abnormality of the testis
+HP:0000099,Glomerulonephritis,HP:0000123,Nephritis
+UBERON:3000401,pars facialis of maxillopalatine,UBERON:0000064,organ part
+UBERON:0010545,metatarsus skeleton,UBERON:0015036,pedal digit metatarsal endochondral element
+HP:0009654,Osteolytic defects of the phalanges of the thumb,HP:0009602,Abnormality of the phalanges of the thumb
+HP:0009997,Duplication of phalanx of hand,HP:0004275,Duplication of hand bones
+UBERON:0005347,copula pyramidis,UBERON:0004003,cerebellum hemisphere lobule
+UBERON:0002244,premaxilla,UBERON:0008907,dermal bone
+HP:0010861,Incomplete breech presentation,HP:0001623,Breech presentation
+UBERON:0008617,innermost intercostal muscle,UBERON:0001111,intercostal muscle
+DOID:3114,serous cystadenocarcinoma,DOID:3111,cystadenocarcinoma
+UBERON:0006648,adventitia of seminal vesicle,UBERON:0005742,adventitia
+NCBITaxon:6942,Amblyomma,NCBITaxon:426441,Amblyomminae
+HP:0010154,Irregular epiphysis of the 1st metatarsal,HP:0010125,Abnormality of the epiphysis of the 1st metatarsal
+HP:0007095,Frontoparietal polymicrogyria,HP:0002126,Polymicrogyria
+UBERON:0016408,corona of glans penis,UBERON:0000064,organ part
+UBERON:3000634,vomerine canal,UBERON:0000064,organ part
+HP:0010658,Patchy changes of bone mineral density,HP:0004348,Abnormality of bone mineral density
+UBERON:2005416,sacculoagenar foramen,UBERON:2005415,inner ear foramen
+HP:0011662,Tricuspid atresia,HP:0001702,Abnormality of the tricuspid valve
+DOID:10400,gonococcal seminal vesiculitis,DOID:9365,vesiculitis
+DOID:8747,subacute myeloid leukemia,DOID:8692,myeloid leukemia
+UBERON:0005395,cortical layer VI,UBERON:0002301,layer of neocortex
+HP:0003832,Abnormality of the tibial plateaux,HP:0002992,Abnormality of the tibia
+UBERON:0006494,apex of arytenoid,UBERON:0001996,elastic cartilage tissue
+HP:0011095,Overjet,HP:0000692,Misalignment of teeth
+UBERON:0003688,omentum,UBERON:0000063,organ segment
+UBERON:2101613,dorsal fin middle radial element,UBERON:2101672,dorsal fin radial element
+UBERON:0011169,postorbital bone,UBERON:0003462,facial bone
+HP:0003931,Periosteal new bone (humeral diaphysis),HP:0003926,Abnormality of the humeral diaphysis
+UBERON:4200010,ventral humeral ridge,UBERON:0004120,mesoderm-derived structure
+CL:0000318,sweat secreting cell,CL:0000150,glandular epithelial cell
+UBERON:0001100,pectoralis minor,UBERON:0001495,pectoral muscle
+UBERON:0013122,distal epiphysis of phalanx of pes,UBERON:0004448,distal epiphysis of phalanx
+UBERON:0007317,superficial external pudendal artery,UBERON:0003520,pelvis blood vessel
+UBERON:3001002,basale commune (tarsal),UBERON:0010721,distal tarsal bone
+UBERON:0011675,perichordal ring,UBERON:0004120,mesoderm-derived structure
+HP:0003462,Elevated 8-dehydrocholesterol,HP:0003107,Abnormality of cholesterol metabolism
+HP:0010123,Triangular epiphyses of the hallux,HP:0010056,Abnormality of the epiphyses of the hallux
+HP:0005432,Transient hypogammaglobulinemia of infancy,HP:0004313,Hypogammaglobulinemia
+UBERON:0010256,4th arch mesenchyme from neural crest,UBERON:0005691,4th arch mesenchyme
+HP:0001073,Cigarette-paper scars,HP:0001075,Atrophic scars
+UBERON:0004466,musculature of leg,UBERON:0004482,musculature of lower limb
+HP:0004580,Anterior scalloping of vertebral bodies,HP:0004586,Biconcave vertebral bodies
+UBERON:0005664,2nd arch endoderm,UBERON:0000925,endoderm
+DOID:10337,glaucomatous atrophy of optic disc,DOID:1686,glaucoma
+UBERON:0005250,stomatodeum gland,UBERON:0002050,embryonic structure
+HP:0010090,Patchy sclerosis of the proximal phalanx of the hallux,HP:0010052,Abnormality of the proximal phalanx of the hallux
+CL:0000474,pericardial nephrocyte,CL:0000519,phagocyte (sensu Nematoda and Protostomia)
+UBERON:0002208,sternebra,UBERON:0002513,endochondral bone
+CL:0000779,multinuclear osteoclast,CL:0000092,osteoclast
+UBERON:0001730,extrinsic ligament of larynx,UBERON:0001743,ligament of larynx
+UBERON:0001058,mushroom body,UBERON:0003339,ganglion of central nervous system
+UBERON:0002915,postcentral sulcus,UBERON:0003022,cerebral cortex lobe
+UBERON:0005077,neuropore,UBERON:0000161,orifice
+UBERON:0005746,primary vitreous humour,UBERON:0002050,embryonic structure
+UBERON:3000905,caput ossis cruris,UBERON:0000064,organ part
+UBERON:0002385,muscle tissue,UBERON:0004120,mesoderm-derived structure
+HP:0010245,Abnormality of the epiphyses of the proximal phalanges of the hand,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+CL:0000293,structural cell,CL:0000003,native cell
+CL:0010007,His-Purkinje system cell,CL:0000003,native cell
+UBERON:0003269,skeletal muscle tissue of eye,UBERON:0001134,skeletal muscle tissue
+UBERON:2000727,somite 17,UBERON:0002329,somite
+HP:0010249,Enlarged epiphyses of the distal phalanges of the hand,HP:0010243,Abnormality of the epiphyses of the distal phalanx of finger
+UBERON:0010847,ulna pre-cartilage condensation,UBERON:0010884,forelimb bone pre-cartilage condensation
+UBERON:0004219,urethra smooth muscle,UBERON:0001135,smooth muscle tissue
+HP:0002580,Volvulus,HP:0002242,Abnormality of the intestine
+HP:0007063,Aplasia of the inferior half of the cerebellar vermis,HP:0006817,Aplasia/Hypoplasia of the  cerebellar vermis
+UBERON:0016419,bony part of vertebral arch,UBERON:0004120,mesoderm-derived structure
+UBERON:0008294,feather barb,UBERON:0013703,integumentary projection
+HP:0008321,Reduced factor X activity,HP:0010990,Abnormality of the common coagulation pathway
+UBERON:0001833,lip,UBERON:0004121,ectoderm-derived structure
+UBERON:0007170,squamous part of occipital bone,UBERON:0004120,mesoderm-derived structure
+UBERON:0004760,gland of anal canal,UBERON:0004121,ectoderm-derived structure
+DOID:3445,scrotal carcinoma,DOID:518,scrotum neoplasm
+CL:0002391,multinucleate blastoconidium,CL:0002386,multinucleate macroconidium
+CL:0002599,smooth muscle cell of the esophagus,CL:0000192,smooth muscle cell
+UBERON:0003568,neck connective tissue,UBERON:0002384,connective tissue
+HP:0000947,Dumbbell-shaped long bone,HP:0003016,Metaphyseal widening
+UBERON:0003641,pedal digit 2 phalanx,UBERON:0015032,pedal digit 2 phalanx endochondral element
+UBERON:0004029,canal of Schlemm,UBERON:0009141,craniocervical region vein
+UBERON:4200186,distal keel of metacarpal III,UBERON:0004120,mesoderm-derived structure
+NCBITaxon:11623,Lymphocytic choriomeningitis virus,NCBITaxon:208896,Old world arenaviruses
+DOID:0060172,juvenile absence epilepsy,DOID:0050705,adolescence-adult electroclinical syndrome
+HP:0011151,Obtundation status,HP:0007270,Atypical absence seizures
+UBERON:0002409,pericardial fluid,UBERON:0007794,serous fluid
+DOID:3752,larynx verrucous carcinoma,DOID:2876,laryngeal squamous cell carcinoma
+HP:0008706,Distal urethral duplication,HP:0000795,Abnormality of the urethra
+HP:0011958,Retinal perforation,HP:0000479,Abnormality of the retina
+HP:0008905,Rhizomelia,HP:0009826,Limb undergrowth
+UBERON:0005800,segment of aorta,UBERON:0000063,organ segment
+UBERON:0010578,manual digit 4 phalanx pre-cartilage condensation,UBERON:0010586,manual digit phalanx pre-cartilage condensation
+HP:0100061,Ivory epiphyses of the 3rd toe,HP:0010329,Abnormality of the epiphyses of the 3rd toe
+UBERON:0001490,elbow joint,UBERON:0003839,forelimb joint
+UBERON:2001965,epibranchial 4 bone uncinate process cartilage,UBERON:0011004,pharyngeal arch cartilage
+CL:0002130,regular interatrial cardiac myocyte,CL:0002098,regular cardiac myocyte
+HP:0011102,Ileal atresia,HP:0011100,Intestinal atresia
+UBERON:0009846,embryonic cloacal epithelium,UBERON:0012481,cloacal epithelium
+HP:0009452,Curved proximal phalanx of the 3rd finger,HP:0009854,Curved proximal phalanges of the hand
+CL:0002619,adult endothelial progenitor cell,CL:0000566,angioblastic mesenchymal cell
+DOID:3478,iris cancer,DOID:3479,uveal cancer
+UBERON:2001952,dentary tooth row,UBERON:0009678,tooth row
+HP:0000212,Gingival overgrowth,HP:0000168,Abnormality of the gingiva
+DOID:349,systemic mastocytosis,DOID:350,mastocytosis
+UBERON:0006960,ovary stroma,UBERON:0003891,stroma
+UBERON:2005093,nasal vein,UBERON:0009141,craniocervical region vein
+HP:0001147,Retinal exudate,HP:0000479,Abnormality of the retina
+CL:0002295,type-6 epithelial cell of thymus,CL:0002365,medullary thymic epithelial cell
+HP:0100864,Short femoral neck,HP:0003367,Abnormality of the femoral neck
+HP:0100911,Sclerosis of the proximal phalanx of the 5th finger,HP:0100921,Sclerosis of the phalanges of the 5th finger
+UBERON:0014501,proximal phalanx of digit 1,UBERON:0004302,proximal phalanx
+CL:1000361,transitional myocyte of interatrial septum,CL:0002073,transitional myocyte
+UBERON:3010192,calcar posterior,UBERON:3000981,limb external integument structure
+CL:0000776,immature neutrophil,CL:0002242,nucleate cell
+UBERON:2000174,caudal cerebellar tract,UBERON:0002317,white matter of cerebellum
+HP:0012281,Chylous ascites,HP:0001541,Ascites
+UBERON:0013249,paroophoron,UBERON:0006590,vestigial embryonic structure
+DOID:1759,American histoplasmosis,DOID:1731,histoplasmosis
+UBERON:1000018,cluster of hairs,UBERON:0010164,collection of hairs
+HP:0001829,Foot polydactyly,HP:0009136,Duplication involving bones of the feet
+UBERON:0003895,hypaxial myotome region,UBERON:0005291,embryonic tissue
+UBERON:0004980,mucosa of ureter,UBERON:0000344,mucosa
+CL:0000529,pigmented epithelial cell,CL:0000710,neurecto-epithelial cell
+HP:0009646,Patchy sclerosis of the distal phalanx of the thumb,HP:0009617,Abnormality of the distal phalanx of the thumb
+UBERON:0003335,serosa of colon,UBERON:0001209,serosa of large intestine
+CL:0000138,chondrocyte,CL:0000153,GAG secreting cell
+UBERON:0002406,pericardial sac,UBERON:0005181,thoracic segment organ
+DOID:5331,testicular granulosa cell tumor,DOID:2999,granulosa cell tumor
+UBERON:0015111,distal tarsal bone 4 endochondral element,UBERON:0015050,tarsus endochondral element
+DOID:0050776,non-specific X-linked mental retardation,DOID:0050889,non-syndromic intellectual disability
+UBERON:0002519,otolithic membrane,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0002246,peripheral blood stem cell,CL:0000080,circulating cell
+UBERON:0001628,posterior communicating artery,UBERON:0015212,lateral structure
+HP:0001369,Arthritis,HP:0001367,Abnormal joint morphology
+UBERON:0008923,sublaminar layer S2,UBERON:0009732,sublaminar layers S1 or S2 or S5
+UBERON:0015009,lumbar vertebra endochondral element,UBERON:0004120,mesoderm-derived structure
+CL:1000491,mesothelial cell of pleura,CL:0000077,mesothelial cell
+HP:0009678,Enlarged epiphysis of the distal phalanx of the thumb,HP:0009689,Enlarged epiphyses of the thumb
+DOID:12465,secondary hyperparathyroidism of renal origin,DOID:12466,secondary hyperparathyroidism
+UBERON:0007029,external covering of organism,UBERON:0000475,organism subdivision
+DOID:2068,Bartholin's gland neoplasm,DOID:2076,vulvar glandular tumor
+UBERON:0001045,midgut,UBERON:0004921,subdivision of digestive tract
+UBERON:2000205,external ventral flexor,UBERON:0000366,flexor muscle
+UBERON:0012503,serosa of fundus of stomach,UBERON:0001201,serosa of stomach
+DOID:12179,tinea corporis,DOID:8913,dermatophytosis
+HP:0005067,Proximal fibular overgrowth,HP:0003099,Fibular overgrowth
+CL:0002662,luminal cell of lactiferous duct,CL:0002326,luminal epithelial cell of mammary gland
+DOID:4903,granular cell carcinoma,DOID:305,carcinoma
+UBERON:0009063,interclavicular air sac,UBERON:0009061,anterior air sac
+UBERON:0001263,pancreatic acinus,UBERON:0004119,endoderm-derived structure
+HP:0009148,Small epiphysis of the distal phalanx of the 5th finger,HP:0009390,Small epiphyses of the 5th finger
+UBERON:0001958,epithelium of terminal bronchiole,UBERON:0002051,epithelium of bronchiole
+UBERON:3000017,anterior process of pars palatina of maxilla,UBERON:0010313,neural crest-derived structure
+HP:0007065,Disorganization of the anterior cerebellar vermis,HP:0002334,Abnormality of the cerebellar vermis
+CL:0002624,paneth cell of the appendix,CL:0000510,paneth cell
+UBERON:0002092,brain dura mater,UBERON:0003547,brain meninx
+UBERON:0005317,pulmonary artery endothelium,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:9256,colorectal cancer,DOID:5672,large intestine cancer
+HP:0005523,Lymphoproliferative disorder,HP:0004377,Hematological neoplasm
+UBERON:0001094,sacral vertebra,UBERON:0002412,vertebra
+UBERON:0013656,dulla,UBERON:0004121,ectoderm-derived structure
+HP:0002683,Abnormality of the calvaria,HP:0000929,Abnormality of the skull
+UBERON:0004667,interventricular septum muscular part,UBERON:0002385,muscle tissue
+UBERON:0007993,ulnar sesamoid bone,UBERON:0003466,forelimb zeugopod bone
+UBERON:0005184,hair medulla,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2000981,somite 29,UBERON:0002329,somite
+DOID:7818,petroclival meningioma,DOID:4437,skull base meningioma
+UBERON:0001263,pancreatic acinus,UBERON:0009842,acinus
+UBERON:3000869,ilial protuberance,UBERON:0004120,mesoderm-derived structure
+HP:0009502,Absent epiphysis of the distal phalanx of the 2nd finger,HP:0009499,Abnormality of the epiphysis of the distal phalanx of the 2nd finger
+HP:0005723,Shoe-shaped sella turcica,HP:0002681,Deformed sella turcica
+DOID:10426,Klippel-Feil syndrome,DOID:0080015,physical disorder
+UBERON:0007371,superior surface of tongue,UBERON:0007367,surface of tongue
+UBERON:3011048,genital system,UBERON:0004120,mesoderm-derived structure
+HP:0011661,Anomalous origin of left pulmonary artery from ascending aorta,HP:0011660,Anomalous origin of one pulmonary artery from ascending aorta
+UBERON:0001460,arm,UBERON:0006058,multi-limb segment region
+UBERON:0015128,subepicardial layer of epicardium,UBERON:0007188,mesothelium of serous pericardium
+DOID:1319,brain cancer,DOID:3620,central nervous system cancer
+DOID:3953,adrenal gland cancer,DOID:170,endocrine gland cancer
+UBERON:0010181,straight venules of kidney,UBERON:0005629,vascular plexus
+UBERON:2005381,dorsal fin proximal radial bone 4,UBERON:2105381,dorsal fin proximal radial element 4
+CL:0000030,glioblast,CL:0000055,non-terminally differentiated cell
+UBERON:2001717,caudal principal ray 5,UBERON:2001585,caudal principal ray
+HP:0008829,Delayed femoral head ossification,HP:0003368,Abnormality of the femoral head
+HP:0009813,Upper limb phocomelia,HP:0006496,Aplasia/Hypoplasia involving bones of the upper limbs
+HP:0000630,Abnormality of retinal arteries,HP:0008046,Abnormality of the retinal vasculature
+UBERON:0002179,lateral funiculus,UBERON:0006127,funiculus of spinal cord
+HP:0100135,Absent epiphysis of the distal phalanx of the 3rd toe,HP:0100091,Abnormality of the epiphysis of the distal phalanx of the 3rd toe
+UBERON:3000384,parasagittal crest,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0000112,juvenile stage,UBERON:0000105,life cycle stage
+NCBITaxon:784,Orientia tsutsugamushi,NCBITaxon:69474,Orientia
+HP:0007566,Index finger dermatoglyphic radial loop,HP:0005882,Dermatoglyphic variants
+HP:0003924,Stippled calcification of humeral metaphysis,HP:0003907,Abnormality of the humeral metaphyses
+HP:0100102,Cone-shaped epiphysis of the distal phalanx of the 2nd toe,HP:0100088,Abnormality of the epiphysis of the distal phalanx of the 2nd toe
+HP:0002126,Polymicrogyria,HP:0002536,Abnormal cortical gyration
+UBERON:0007681,facial neural crest,UBERON:0003099,cranial neural crest
+UBERON:0005378,olfactory bulb granule cell layer,UBERON:0004001,olfactory bulb layer
+NCBITaxon:119225,Protomacleaya,NCBITaxon:190765,Ochlerotatus <genus>
+HP:0012109,Primary angle closure glaucoma,HP:0000501,Glaucoma
+CL:0000019,sperm,CL:0000408,male gamete
+HP:0011890,Prolonged bleeding following procedure,HP:0001892,Abnormal bleeding
+HP:0000493,Abnormality of the fovea,HP:0001103,Abnormality of the macula
+UBERON:0006257,laryngotracheal groove,UBERON:0006846,surface groove
+UBERON:0010344,3rd arch mesenchyme from head mesenchyme,UBERON:0010360,pharyngeal arch mesenchyme from head mesenchyme
+CL:1000708,ureter adventitial cell,CL:0000115,endothelial cell
+UBERON:0004229,urinary bladder trigone smooth muscle,UBERON:0004228,urinary bladder smooth muscle
+DOID:0050035,African tick-bite fever,DOID:11104,spotted fever
+UBERON:0010231,anatomical line between outer ears,UBERON:0006800,anatomical line
+HP:0006505,Abnormality involving the epiphyses of the limbs,HP:0002813,Abnormality of limb bone morphology
+HP:0010868,Ocular dyssynergia,HP:0010867,Dyssynergia
+HP:0007542,Absent pigmentation of the ventral chest,HP:0200098,Absent skin pigmentation
+UBERON:0004721,crista ampullaris,UBERON:0004121,ectoderm-derived structure
+UBERON:0014446,acetabular notch,UBERON:0004120,mesoderm-derived structure
+DOID:1273,respiratory syncytial virus infectious disease,DOID:934,viral infectious disease
+DOID:0050138,podoconiosis,DOID:4976,elephantiasis
+HP:0002914,Hyperchloridura,HP:0012600,Abnormal urine chloride concentration
+HP:0011231,Prominent eyelashes,HP:0000499,Abnormality of the eyelashes
+HP:0200009,Abnormal size of corpus callosum,HP:0001273,Abnormality of the corpus callosum
+HP:0012732,Anorectal anomaly,HP:0012718,Morphological abnormality of the gastrointestinal tract
+HP:0012085,Pyuria,HP:0012614,Abnormal urine cytology
+HP:0011242,Underdeveloped stem of antihelix,HP:0011244,Abnormality of stem of antihelix
+HP:0100054,Triangular epiphyses of the 2nd toe,HP:0010172,Triangular epiphyses of the toes
+HP:0011657,Double outlet right ventricle with subpulmonary ventricular septal defect and pulmonary stenosis,HP:0001719,Double outlet right ventricle
+CL:0002603,astrocyte of the cerebellum,CL:2000005,brain macroglial cell
+HP:0010023,Small epiphysis of the 1st metacarpal,HP:0010276,Small epiphyses of the proximal phalanges of the hand
+HP:0004303,Abnormality of muscle fibers,HP:0011805,Abnormality of muscle morphology
+HP:0007763,Retinal telangiectasia,HP:0001009,Telangiectasia
+DOID:8117,neuronitis,DOID:331,central nervous system disease
+UBERON:0010548,pedal digit 2 metatarsal pre-cartilage condensation,UBERON:0010687,pedal digit metatarsal pre-cartilage condensation
+UBERON:0004042,spleen secondary B follicle,UBERON:0001745,secondary nodular lymphoid tissue
+HP:0011220,Prominent forehead,HP:0000290,Abnormality of the forehead
+HP:0002240,Hepatomegaly,HP:0001392,Abnormality of the liver
+UBERON:0010801,calcaneum pre-cartilage condensation,UBERON:0010886,hindlimb bone pre-cartilage condensation
+UBERON:3010136,M. cruralis,UBERON:0010890,pelvic complex muscle
+HP:0007658,Large hyperpigmented retinal spots,HP:0011512,Hyperpigmentation of the fundus
+HP:0100916,Sclerosis of the middle phalanges of the hand,HP:0100899,Sclerosis of the phalanges of the hand
+UBERON:0007383,enveloping layer of ectoderm,UBERON:0005291,embryonic tissue
+UBERON:0001651,right pulmonary artery,UBERON:0002012,pulmonary artery
+UBERON:2000429,scaphium,UBERON:0005814,arch of atlas
+UBERON:0001307,capsule of ovary,UBERON:0005156,reproductive structure
+HP:0006333,Crowded maxillary incisors,HP:0011062,Misalignment of incisors
+HP:0007695,Abnormal pupillary light reflex,HP:0007686,Abnormal pupillary function
+CL:0002321,embryonic cell,CL:0000548,animal cell
+DOID:3660,wheat allergic reaction,DOID:3044,food allergy
+HP:0005465,Facial hyperostosis,HP:0011821,Abnormality of facial skeleton
+UBERON:4300002,palatine prong,UBERON:4100000,skeletal element projection
+UBERON:3000762,epicoracoid,UBERON:0007844,cartilage element
+UBERON:0001372,psoas minor muscle,UBERON:0008450,psoas muscle
+HP:0004611,Anterior concavity of thoracic vertebrae,HP:0003312,Abnormal form of the vertebral bodies
+HP:0011905,Reduced hemoglobin A,HP:0011902,Abnormal hemoglobin
+UBERON:2000896,hypaxial region somite 20,UBERON:0003895,hypaxial myotome region
+UBERON:0003134,female reproductive organ,UBERON:0014404,female anatomical structure
+HP:0009971,Polydactyly affecting the 4th finger,HP:0004188,Abnormality of the 4th finger
+HP:0008346,Increased red cell sickling tendency,HP:0011895,Anemia due to reduced life span of red cells
+CL:1000546,kidney medulla collecting duct epithelial cell,CL:1000504,kidney medulla cell
+UBERON:0002126,solitary tract nuclear complex,UBERON:0003528,brain grey matter
+DOID:8211,fallopian tube cystadenofibroma,DOID:5478,fallopian tube adenofibroma
+UBERON:0010516,clasper,UBERON:0008811,intromittent organ
+UBERON:0003331,submucosa of colon,UBERON:0001208,submucosa of large intestine
+UBERON:0008332,hilum of neuraxis,UBERON:0002316,white matter
+HP:0006536,Obstructive lung disease,HP:0002088,Abnormality of the lung
+HP:0100077,Absent epiphyses of the 5th toe,HP:0010162,Absent epiphyses of the toes
+UBERON:0005261,atrium cardiac jelly,UBERON:0003906,cardiac jelly
+UBERON:0003069,otic placode,UBERON:0003067,dorsolateral placode
+HP:0009145,Abnormality of cerebral artery,HP:0011004,Abnormality of the systemic arterial tree
+HP:0012717,Severe conductive hearing impairment,HP:0000405,Conductive hearing impairment
+DOID:2999,granulosa cell tumor,DOID:2394,ovarian cancer
+DOID:0050387,nonpapillary renal cell carcinoma,DOID:4455,hereditary renal cell carcinoma
+CL:0000458,serotonin secreting cell,CL:0000457,biogenic amine secreting cell
+DOID:0050528,nonphotosensitive trichothiodystrophy,DOID:0050737,autosomal recessive disease
+HP:0012626,Stage 4 chronic kidney disease,HP:0012622,Chronic kidney disease
+HP:0000274,Small face,HP:0001999,Abnormal facial shape
+UBERON:0003494,respiratory system venule,UBERON:0001979,venule
+HP:0011330,Metopic synostosis,HP:0005556,Abnormality of the metopic suture
+UBERON:0009197,basioccipital pre-cartilage condensation,UBERON:0015048,basioccipital endochondral element
+UBERON:0004951,submucosa of segmental bronchus,UBERON:0001957,submucosa of bronchus
+HP:0000748,Inappropriate laughter,HP:0000719,Inappropriate behavior
+UBERON:3000755,pectoral girdle opening,UBERON:0000464,anatomical space
+UBERON:0010565,manual digit 1 metacarpus pre-cartilage condensation,UBERON:0010575,manual digit 1 phalanx pre-cartilage condensation
+UBERON:0014483,distal phalanx of digit 1,UBERON:0004300,distal phalanx
+UBERON:0011110,humeroulnar joint,UBERON:0003839,forelimb joint
+DOID:0050770,polycystic liver disease,DOID:0050736,autosomal dominant disease
+HP:0008133,Distal tapering of metatarsals,HP:0001832,Abnormality of the metatarsal bones
+HP:0100260,Mesoaxial polydactyly,HP:0010442,Polydactyly
+HP:0001225,Wrist swelling,HP:0003019,Abnormality of the wrist
+UBERON:0004916,anal sphincter,UBERON:0004590,sphincter muscle
+HP:0010155,Ivory epiphysis of the 1st metatarsal,HP:0010119,Ivory epiphyses of the hallux
+HP:0010210,Triangular shaped proximal phalanges of the toes,HP:0010180,Triangular shaped phalanges of the toes
+HP:0008036,Retinal pigmentary dystrophy,HP:0000556,Retinal dystrophy
+DOID:11997,spermatocele,DOID:48,male reproductive system disease
+HP:0008453,Congenital kyphoscoliosis,HP:0002751,Kyphoscoliosis
+HP:0009501,Abnormality of the epiphysis of the proximal phalanx of the 2nd finger,HP:0010245,Abnormality of the epiphyses of the proximal phalanges of the hand
+HP:0000664,Synophrys,HP:0002219,Facial hypertrichosis
+HP:0005321,Mandibulofacial dysostosis,HP:0004439,Craniofacial dysostosis
+HP:0006487,Bowing of the long bones,HP:0006504,Anomaly of the limb diaphyses
+DOID:13548,secondary Parkinson disease,DOID:1289,neurodegenerative disease
+HP:0009821,Forearm undergrowth,HP:0003026,Short long bones
+DOID:0050153,pulmonary aspergilloma,DOID:13564,aspergillosis
+HP:0009591,Abnormality of the vestibulocochlear nerve,HP:0001291,Abnormality of the cranial nerves
+HP:0012608,Hypermagnesiuria,HP:0012607,Abnormal urine magnesium concentration
+DOID:4184,pseudohypoparathyroidism,DOID:896,metal metabolism disorder
+DOID:4123,nail disease,DOID:16,integumentary system disease
+UBERON:3000811,glenoid end of clavicle,UBERON:0000064,organ part
+HP:0005880,Metacarpophalangeal synostosis,HP:0011911,Abnormality of metacarpophalangeal joint
+UBERON:0001977,serum,UBERON:0000179,haemolymphatic fluid
+UBERON:4000146,transient cartilaginous element,UBERON:0007844,cartilage element
+UBERON:0000087,inner cell mass,UBERON:0002050,embryonic structure
+UBERON:0011142,axial ossicle,UBERON:0004120,mesoderm-derived structure
+CL:0000918,Tc2 cell,CL:0000908,"CD8-positive, alpha-beta cytokine secreting effector T cell"
+NCBITaxon:1824,Nocardia asteroides,NCBITaxon:1817,Nocardia
+HP:0012357,Increased mannosylation of N-linked protein glycosylation,HP:0012355,Abnormal mannosylation of N-linked protein glycosylation
+UBERON:0010360,pharyngeal arch mesenchyme from head mesenchyme,UBERON:0004120,mesoderm-derived structure
+HP:0008344,Elevated plasma branched chain amino acids,HP:0010892,Abnormality of branched chain family amino acid metabolism
+DOID:0050332,enlarged vestibular aqueduct,DOID:2742,auditory system disease
+DOID:6293,central nervous system lipoma,DOID:502,central nervous system mesenchymal non-meningothelial tumor
+UBERON:0014559,CA3 stratum lacunosum moleculare,UBERON:0014567,layer of hippocampal field
+DOID:4779,focal embolic glomerulonephritis,DOID:2921,glomerulonephritis
+HP:0002486,Myotonia,HP:0011804,Abnormality of muscle physiology
+UBERON:2000525,intercalarium,UBERON:0000218,vertebral arch of axis
+UBERON:0000004,olfactory apparatus,UBERON:0002268,main olfactory organ
+UBERON:0011946,subluminal layer of epithelium,UBERON:0000119,cell layer
+DOID:0050513,spinal polio,DOID:0050515,paralytic poliomyelitis
+NCBITaxon:426455,Rhipicephalus <subgenus>,NCBITaxon:34630,Rhipicephalus <genus>
+DOID:4471,chromophobe adenocarcinoma,DOID:4450,renal cell carcinoma
+UBERON:0005838,fasciculus of brain,UBERON:0001019,nerve fasciculus
+HP:0004894,Laryngotracheal stenosis,HP:0002777,Tracheal stenosis
+UBERON:0001960,periarterial lymphatic sheath,UBERON:0010393,T cell domain
+UBERON:0004357,paired limb/fin bud,UBERON:0002050,embryonic structure
+DOID:0060206,amyotrophic lateral sclerosis type 15,DOID:332,amyotrophic lateral sclerosis
+HP:0012754,CNS hypermyelination,HP:0011400,Abnormal CNS myelination
+HP:0003892,Absent ossification/Absence of the humeral epiphyses,HP:0003891,Abnormality of the humeral epiphysis
+UBERON:0011921,connecting stalk blood islands,UBERON:0012275,meso-epithelium
+UBERON:0009497,epithelium of foregut-midgut junction,UBERON:0003929,gut epithelium
+DOID:9254,mast-cell leukemia,DOID:1240,leukemia
+UBERON:0009051,gelatinous nucleus of solitary tract,UBERON:0009050,nucleus of solitary tract
+UBERON:0002432,pars intermedia of adenohypophysis,UBERON:0004121,ectoderm-derived structure
+UBERON:2001607,basipterygoid process of parasphenoid,UBERON:4100000,skeletal element projection
+UBERON:0005019,mucosa of palate,UBERON:0003729,mouth mucosa
+DOID:9452,fatty liver disease,DOID:9455,lipid storage disease
+UBERON:0010850,tibia pre-cartilage condensation,UBERON:0010882,limb bone pre-cartilage condensation
+DOID:4858,pineal gland astrocytoma,DOID:5032,pineal gland cancer
+UBERON:0013162,right lateral ventricle,UBERON:0002285,telencephalic ventricle
+HP:0200096,Triangular-shaped open mouth,HP:0000207,Triangular mouth
+UBERON:4200108,outer digit of hand,UBERON:0005451,segment of manus
+UBERON:0003653,metatarsal bone of digit 4,UBERON:0013584,metapodium bone 4
+UBERON:0000908,hippocampal commissure,UBERON:0005340,dorsal telencephalic commissure
+UBERON:0004151,cardiac chamber,UBERON:0004120,mesoderm-derived structure
+UBERON:0010226,future cardiac ventricle,UBERON:0005423,developing anatomical structure
+UBERON:4200016,postbranchial lamina,UBERON:0004530,bony projection
+DOID:3166,leukemoid reaction,DOID:0070004,myeloma
+UBERON:0002572,principal pretectal nucleus,UBERON:0014450,pretectal nucleus
+DOID:4514,thyroid angiosarcoma,DOID:4515,thyroid sarcoma
+UBERON:0013277,remnant of processus vaginalis,UBERON:0014403,male anatomical structure
+UBERON:3010671,ramule palatonasalis,UBERON:0000479,tissue
+UBERON:0015143,mesenteric fat pad,UBERON:0003916,fat pad
+UBERON:0003407,cartilage of nasal septum,UBERON:0004120,mesoderm-derived structure
+HP:0002637,Cerebral ischemia,HP:0100545,Arterial stenosis
+DOID:0060106,brain meningioma,DOID:1319,brain cancer
+UBERON:0005175,chest organ,UBERON:0005181,thoracic segment organ
+UBERON:0002571,external nucleus of inferior colliculus,UBERON:0011214,nucleus of midbrain tectum
+HP:0003006,Neuroblastoma,HP:0004376,Neuroblastic tumors
+UBERON:0010532,primitive nephron,UBERON:0004819,kidney epithelium
+UBERON:0011950,mammary gland luminal epithelium,UBERON:0011945,luminal layer of epithelium
+DOID:9192,dyskinesia of esophagus,DOID:6050,esophageal disease
+UBERON:0003316,mesenchyme of yolk sac,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:5545,anal neuroendocrine tumor,DOID:4551,anus neoplasm
+UBERON:0010055,stapes cartilage element,UBERON:0010313,neural crest-derived structure
+UBERON:0001106,cephalic vein,UBERON:0003507,arm blood vessel
+UBERON:0011024,extrinsic extensor muscle of manus,UBERON:0004254,forelimb zeugopod muscle
+HP:0006980,Progressive leukoencephalopathy,HP:0002352,Leukoencephalopathy
+HP:0012709,Abnormal brain choline/creatine ratio by MRS,HP:0012705,Abnormal metabolic brain imaging by MRS
+HP:0012277,Hypoglycinemia,HP:0003112,Abnormality of serum amino acid levels
+DOID:3206,plexiform schwannoma,DOID:3192,neurilemmoma
+NCBITaxon:34610,Amblyomma variegatum,NCBITaxon:6942,Amblyomma
+HP:0011549,Univentricular heart with absent left sided atrioventricular connection,HP:0011547,Absent left sided atrioventricular connection
+UBERON:0014677,distal interphalangeal joint of digit 2,UBERON:0009768,distal interphalangeal joint
+UBERON:2005014,recurrent branch afferent branchial artery,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:1631,benign breast phyllodes tumor,DOID:0060082,breast benign neoplasm
+HP:0010862,Delayed fine motor development,HP:0001270,Motor delay
+HP:0007750,Hypoplasia of the fovea,HP:0008060,Aplasia/Hypoplasia of the fovea
+DOID:3418,glossopharyngeal nerve disease,DOID:5656,cranial nerve disease
+DOID:1993,rectum cancer,DOID:9256,colorectal cancer
+HP:0009232,Symphalangism affecting the proximal phalanx of the 5th finger,HP:0009857,Symphalangism affecting the proximal phalanges of the hand
+CL:2000001,peripheral blood mononuclear cell,CL:0000080,circulating cell
+DOID:12275,cutaneous diphtheria,DOID:4223,pyoderma
+DOID:14384,parietal lobe neoplasm,DOID:368,cerebrum cancer
+HP:0010943,Echogenic fetal bowel,HP:0011425,Fetal ultrasound soft marker
+HP:0009667,Enlarged epiphysis of the proximal phalanx of the thumb,HP:0009663,Abnormality of the epiphysis of the proximal phalanx of the thumb
+HP:0006858,Impaired distal proprioception,HP:0010831,Impaired proprioception
+UBERON:3000255,lamina anterior of pars facialis,UBERON:0010313,neural crest-derived structure
+CL:0002646,epithelial cell of buccal part of viscerocranial mucosa,CL:0002283,ecto-epithelial cell of viscerocranial mucosa
+DOID:0060024,lambda 5 deficiency,DOID:2115,B cell deficiency
+UBERON:0007274,crista of ampulla of anterior semicircular duct of membranous laybrinth,UBERON:0003238,epithelium of superior semicircular canal
+UBERON:0011768,pineal gland stalk,UBERON:0004121,ectoderm-derived structure
+UBERON:0003470,artery of upper lip,UBERON:0003496,head blood vessel
+HP:0004015,Abnormality of radial metaphyses,HP:0002818,Abnormality of the radius
+UBERON:0008874,pulmonary acinus,UBERON:0010368,pulmonary lobule
+CL:0000642,folliculostellate cell,CL:0000163,endocrine cell
+HP:0012302,Herpes simplex encephalitis,HP:0005353,Susceptibility to herpesvirus
+DOID:12859,choreatic disease,DOID:480,movement disease
+HP:0100608,Metrorrhagia,HP:0000140,Abnormality of the menstrual cycle
+UBERON:0004772,eyelid tarsus,UBERON:0000094,membrane organ
+UBERON:0010401,spleen central arteriole,UBERON:0003497,abdomen blood vessel
+UBERON:2005122,dorsal axial hypoblast,UBERON:0005291,embryonic tissue
+UBERON:0002988,first dorsal interosseous of manus,UBERON:0001503,dorsal interosseous of manus
+UBERON:0004490,cardiac muscle tissue of atrium,UBERON:0001133,cardiac muscle tissue
+HP:0000491,Keratitis,HP:0100533,Inflammatory abnormality of the eye
+DOID:5083,iodine hypothyroidism,DOID:1459,hypothyroidism
+UBERON:0007247,superior olivary nucleus,UBERON:0002680,regional part of metencephalon
+CL:0002236,basal epithelial cell of prostatic duct,CL:0002341,basal cell of prostate epithelium
+UBERON:0002050,embryonic structure,UBERON:0000061,anatomical structure
+HP:0009576,Absent middle phalanx of 2nd finger,HP:0009568,Aplasia/Hypoplasia of the middle phalanx of the 2nd finger
+DOID:890,mitochondrial encephalomyopathy,DOID:699,mitochondrial myopathy
+UBERON:0011590,commissure of diencephalon,UBERON:0005970,brain commissure
+HP:0002135,Basal ganglia calcification,HP:0002514,Cerebral calcification
+UBERON:0003447,digit nerve of manus,UBERON:0003448,manus nerve
+DOID:11233,orbital tenonitis,DOID:11230,acute orbital inflammation
+HP:0011498,Partial aniridia,HP:0000526,Aniridia
+UBERON:0001820,sweat gland,UBERON:0002365,exocrine gland
+NCBITaxon:29908,Sporothrix schenckii,NCBITaxon:29907,Sporothrix
+UBERON:0001736,submandibular gland,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100217,Fragmentation of the epiphysis of the middle phalanx of the 5th toe,HP:0100098,Abnormality of the epiphysis of the middle phalanx of the 5th toe
+UBERON:0009897,right auditory cortex,UBERON:0015212,lateral structure
+UBERON:0007689,thyroid diverticulum,UBERON:0001048,primordium
+UBERON:0006863,proximal metaphysis of femur,UBERON:0006865,metaphysis of femur
+UBERON:0002418,cartilage tissue,UBERON:0004755,skeletal tissue
+HP:0100902,Sclerosis of the distal phalanx of the 4th finger,HP:0100915,Sclerosis of the distal phalanges of the hand
+HP:0003027,Mesomelia,HP:0009826,Limb undergrowth
+UBERON:0002799,fronto-orbital sulcus,UBERON:0008334,subarachnoid sulcus
+HP:0012741,Unilateral cryptorchidism,HP:0000028,Cryptorchidism
+UBERON:0002319,mesangium,UBERON:0006554,urinary system structure
+UBERON:0001311,inferior vesical artery,UBERON:0009027,vesical artery
+HP:0009259,Stippling of the epiphysis of the distal phalanx of the 4th finger,HP:0009402,Stippling of the epiphyses of the 4th finger
+UBERON:0001670,inferior cerebellar vein,UBERON:0001668,cerebellar vein
+HP:0002951,Partial absence of cerebellar vermis,HP:0006817,Aplasia/Hypoplasia of the  cerebellar vermis
+UBERON:2001689,pterygoquadrate cartilage,UBERON:0011004,pharyngeal arch cartilage
+DOID:7806,adult spinal cord glioblastoma multiforme,DOID:3185,spinal cord glioma
+UBERON:0015484,skin of metapodial pad,UBERON:0015790,autopod skin
+HP:0009305,Distal/middle symphalangism of 4th finger,HP:0009308,Symphalangism of middle phalanx of 4th finger
+DOID:11702,dysgammaglobulinemia,DOID:6025,selective immunoglobulin deficiency disease
+UBERON:0001949,gingival epithelium,UBERON:0006915,stratified squamous epithelium
+HP:0006443,Patellar aplasia,HP:0006498,Aplasia/Hypoplasia of the patella
+UBERON:2000614,abductor profundus,UBERON:0006845,abductor muscle
+UBERON:0011368,brachiocephalic muscle,UBERON:0001630,muscle organ
+DOID:6167,prostatic urethral cancer,DOID:736,male urethral cancer
+UBERON:0005485,valve of inferior vena cava,UBERON:0006675,venous valve
+HP:0009182,Triangular shaped middle phalanx of the 5th finger,HP:0004219,Abnormality of the middle phalanx of the 5th finger
+UBERON:0008848,cranial suspensory ligament,UBERON:0005156,reproductive structure
+UBERON:0006909,lumen of digestive tract,UBERON:0000464,anatomical space
+UBERON:0006948,efferent duct epithelium,UBERON:0012275,meso-epithelium
+UBERON:0015458,mediastinal fat pad,UBERON:0003916,fat pad
+UBERON:0006685,pharyngeal tubercle,UBERON:0004119,endoderm-derived structure
+HP:0012627,Pseudoexfoliation,HP:0004328,Abnormality of the anterior segment of the eye
+UBERON:3000677,lateral process of cricoid cartilage,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0008338,Partial functional complement factor D deficiency,HP:0004431,Complement deficiency
+UBERON:0004322,middle phalanx of manual digit 4,UBERON:0014490,middle phalanx of digit 4
+DOID:13566,tibial collateral ligament bursitis,DOID:204,enthesopathy
+CL:0000519,phagocyte (sensu Nematoda and Protostomia),CL:0000234,phagocyte
+UBERON:0001451,navicular bone of pes,UBERON:0012131,centrale
+UBERON:2001160,dorsal scute,UBERON:2002294,fish scute
+UBERON:0011631,tabular bone,UBERON:0002514,intramembranous bone
+UBERON:0004375,bone of free limb or fin,UBERON:0010740,bone of appendage girdle complex
+UBERON:0003988,thymus corticomedullary boundary,UBERON:0000015,anatomical boundary
+UBERON:0006455,seventh thoracic spinal cord segment,UBERON:0007715,thoracic subsegment of spinal cord
+DOID:13912,acquired color blindness,DOID:13399,color blindness
+HP:0011403,Abnormal umbilical cord blood vessels,HP:0010881,Abnormality of the umbilical cord
+UBERON:0011630,intertemporal bone,UBERON:0008907,dermal bone
+UBERON:0005151,metanephric proximal tubule,UBERON:0005146,metanephric nephron tubule
+HP:0100611,Multiple glomerular cysts,HP:0000095,Abnormality of the glomerulus
+UBERON:0006218,common atrial chamber,UBERON:0004120,mesoderm-derived structure
+HP:0005250,High intestinal obstruction,HP:0005214,Intestinal obstruction
+UBERON:0000036,secondary ovarian follicle,UBERON:0001305,ovarian follicle
+HP:0012586,Bilateral renal atrophy,HP:0012585,Renal atrophy
+NCBITaxon:480117,Cyclorrhapha,NCBITaxon:480118,Eremoneura
+UBERON:0010336,mandibular process mesenchyme from neural crest,UBERON:0010258,mesenchyme from rhombencephalic neural crest
+HP:0000250,Dense calvaria,HP:0004330,Increased skull ossification
+UBERON:0002321,extraglomerular mesangium,UBERON:0004120,mesoderm-derived structure
+UBERON:2001483,middle lateral line ganglion,UBERON:2000120,lateral line ganglion
+NCBITaxon:29258,ssDNA viruses,NCBITaxon:10239,Viruses
+DOID:10927,gastrojejunal ulcer,DOID:750,peptic ulcer disease
+UBERON:0010577,manual digit 3 phalanx pre-cartilage condensation,UBERON:0010586,manual digit phalanx pre-cartilage condensation
+UBERON:0002072,hypodermis,UBERON:0004120,mesoderm-derived structure
+HP:0010282,Thin lower lip vermilion,HP:0000233,Thin vermilion border
+UBERON:2001815,nuchal plate,UBERON:0008907,dermal bone
+UBERON:0001905,pineal body,UBERON:0010134,secretory circumventricular organ
+HP:0001297,Stroke,HP:0100659,Abnormality of the cerebral vasculature
+HP:0001771,Achilles tendon contracture,HP:0005109,Abnormality of the Achilles tendon
+HP:0012645,Enlarged peripheral nerve,HP:0000759,Abnormality of the peripheral nervous system
+DOID:2272,vulvovaginal candidiasis,DOID:1508,candidiasis
+HP:0010638,Elevated alkaline phosphatase of hepatic origin,HP:0010679,Elevated tissue non-specific alkaline phosphatase
+UBERON:0006787,middle white layer of superior colliculus,UBERON:0006792,intermediate layer of superior colliculus
+NCBITaxon:6656,Arthropoda,NCBITaxon:88770,Panarthropoda
+HP:0012084,Abnormality of skeletal muscle fiber size,HP:0004303,Abnormality of muscle fibers
+HP:0000703,Dentinogenesis imperfecta,HP:0010299,Abnormality of dentin
+HP:0000411,Protruding ear,HP:0000377,Abnormality of the pinna
+DOID:3095,germ cell and embryonal cancer,DOID:2994,germ cell cancer
+UBERON:0010419,vibrissa follicle,UBERON:0002073,hair follicle
+DOID:1596,mental depression,DOID:3324,mood disorder
+DOID:14400,capillary leak syndrome,DOID:1271,capillary disease
+HP:0010701,Abnormal immunoglobulin level,HP:0005372,Abnormality of B cell physiology
+DOID:4957,meninges hemangiopericytoma,DOID:3565,meningioma
+DOID:4520,cervical endometrial stromal sarcoma,DOID:4521,cervix endometrial stromal tumor
+DOID:9220,central sleep apnea,DOID:0050847,sleep apnea
+UBERON:0001672,anterior cerebral vein,UBERON:0009141,craniocervical region vein
+UBERON:2000894,hypaxial region somite 15,UBERON:0003895,hypaxial myotome region
+UBERON:3000867,agger limitans anterior of ischium,UBERON:0000064,organ part
+DOID:6132,bronchitis,DOID:1176,bronchial disease
+HP:0009960,Complete duplication of the phalanges of the 3rd finger,HP:0009998,Complete duplication of phalanx of hand
+HP:0009570,Bullet-shaped middle phalanx of the 2nd finger,HP:0009543,Abnormality of the middle phalanx of the 2nd finger
+UBERON:0008432,thoracic vertebral foramen,UBERON:0001131,vertebral foramen
+UBERON:3000051,braincase and otic capsule opening,UBERON:0004705,fenestra
+UBERON:0003443,thoracic cavity nerve,UBERON:0001021,nerve
+DOID:0050654,Baller-Gerold syndrome,DOID:11971,synostosis
+HP:0004576,Sclerotic vertebral endplates,HP:0005106,Abnormality of the vertebral endplates
+HP:0004355,Abnormality of proteoglycan metabolism,HP:0011012,Abnormality of polysaccharide metabolism
+DOID:10525,double pterygium,DOID:0002116,pterygium
+HP:0010860,Complete breech presentation,HP:0001623,Breech presentation
+UBERON:0010549,pedal digit 3 metatarsal pre-cartilage condensation,UBERON:0015039,pedal digit 3 metatarsal endochondral element
+DOID:0050626,gastrointestinal neuroendocrine tumor,DOID:3119,gastrointestinal system cancer
+DOID:5223,infertility,DOID:15,reproductive system disease
+DOID:13824,Infective dermatitis of eyelid of types resulting in deformity,DOID:9423,blepharitis
+HP:0002491,Spasticity of facial muscles,HP:0000301,Abnormality of facial musculature
+UBERON:0011251,levator claviculae muscle,UBERON:0003897,axial muscle
+CL:1000715,kidney cortex collecting duct intercalated cell,CL:1000549,kidney cortex collecting duct epithelial cell
+UBERON:0014409,metacromion,UBERON:0004530,bony projection
+DOID:6620,X-linked hyper IgM syndrome,DOID:2959,hyperimmunoglobulin syndrome
+HP:0010332,Deviation/Displacement of the 3rd toe,HP:0010320,Abnormality of the 3rd toe
+DOID:8466,retinal degeneration,DOID:5679,retinal disease
+HP:0005487,Prominent metopic ridge,HP:0005556,Abnormality of the metopic suture
+HP:0003764,Nevus,HP:0011355,Localized skin lesion
+UBERON:0003006,dorsal nucleus of lateral lemniscus,UBERON:0006840,nucleus of lateral lemniscus
+CL:0000691,stellate interneuron,CL:0000099,interneuron
+HP:0011506,Choroidal neovascularization of the macula,HP:0001103,Abnormality of the macula
+HP:0007929,Peripheral retinal detachment,HP:0000541,Retinal detachment
+UBERON:0001987,placenta,UBERON:0014404,female anatomical structure
+UBERON:2001051,caudal division of the internal carotid artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004711,jugular vein,UBERON:0009141,craniocervical region vein
+DOID:4852,pleomorphic xanthoastrocytoma,DOID:3069,astrocytoma
+HP:0005486,Small fontanelles,HP:0011328,Abnormality of fontanelles
+UBERON:0002810,right frontal lobe,UBERON:0001870,frontal cortex
+HP:0011421,Death in adolescence,HP:0011420,Death
+UBERON:0004547,decidua capsularis,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0002755,pyramidal decussation,UBERON:0014649,white matter of medulla oblongata
+CL:0001045,naive CCR4-positive regulatory T cell,CL:0002677,naive regulatory T cell
+DOID:6944,vulvar seborrheic keratosis,DOID:6498,seborrheic keratosis
+NCBITaxon:39824,Klebsiella granulomatis,NCBITaxon:570,Klebsiella
+UBERON:0010047,oral gland,UBERON:0002365,exocrine gland
+UBERON:0011857,acinus of lacrimal gland,UBERON:0010313,neural crest-derived structure
+HP:0010153,Fragmentation of the epiphysis of the 1st metatarsal,HP:0010125,Abnormality of the epiphysis of the 1st metatarsal
+CL:0000697,R4 photoreceptor cell,CL:0000287,eye photoreceptor cell
+DOID:6332,adult malignant hemangiopericytoma,DOID:264,hemangiopericytoma
+UBERON:0011623,horn of thyroid cartilage,UBERON:0004765,skeletal element
+HP:0100162,Irregular epiphysis of the proximal phalanx of the 3rd toe,HP:0100060,Irregular epiphyses of the 3rd toe
+UBERON:0016409,base of glans penis,UBERON:0000064,organ part
+UBERON:0009563,pastern region of limb,UBERON:0002529,limb segment
+UBERON:0004004,cerebellum lobule,UBERON:0002749,regional part of cerebellar cortex
+HP:0100313,Cerebral granulomatosis,HP:0002955,Granulomatosis
+CL:0000051,common lymphoid progenitor,CL:0002032,hematopoietic oligopotent progenitor cell
+UBERON:0001710,lower jaw region,UBERON:0011595,jaw region
+UBERON:0013687,pericranium,UBERON:0002515,periosteum
+DOID:6725,spinal stenosis,DOID:0080007,bone deterioration disease
+CL:1000341,enterocyte of epithelium proper of jejunum,CL:1000339,enterocyte of epithelium proper of small intestine
+HP:0002583,Colitis,HP:0002250,Abnormality of the large intestine
+DOID:3356,localized osteosarcoma,DOID:3347,osteosarcoma
+UBERON:0002108,small intestine,UBERON:0004921,subdivision of digestive tract
+HP:0100879,Enlarged ovaries,HP:0000137,Abnormality of the ovary
+DOID:4235,spindle cell sarcoma,DOID:1115,sarcoma
+HP:0000317,Facial myokymia,HP:0002411,Myokymia
+CL:0002265,type D cell of colon,CL:1001588,colon glandular cell
+UBERON:0002320,glomerular mesangium,UBERON:0003891,stroma
+CL:0000164,enteroendocrine cell,CL:0000150,glandular epithelial cell
+NCBITaxon:129369,Pulicoidea,NCBITaxon:140693,Pulicomorpha
+HP:0000179,Thick lower lip vermilion,HP:0000178,Abnormality of lower lip
+HP:0011508,Macular hole,HP:0011958,Retinal perforation
+HP:0012548,Skeletal muscle fatty infiltration,HP:0011805,Abnormality of muscle morphology
+HP:0004032,Abnormality of the olecranon,HP:0002997,Abnormality of the ulna
+HP:0200055,Small hand,HP:0005927,Aplasia/Hypoplasia involving bones of the hand
+HP:0100534,Episcleritis,HP:0000591,Abnormality of the sclera
+UBERON:0004435,proximal epiphysis of distal phalanx of manual digit 5,UBERON:0004421,proximal epiphysis of phalanx of manual digit 5
+DOID:2061,nodular hidradenoma,DOID:3896,hidradenoma
+HP:0004933,Ascending aortic dissection,HP:0002647,Aortic dissection
+HP:0012730,Aglossia,HP:0010295,Aplasia/Hypoplasia of the tongue
+HP:0002003,Large forehead,HP:0000290,Abnormality of the forehead
+HP:0008441,Herniation of intervertebral nuclei,HP:0005108,Abnormality of the intervertebral disk
+UBERON:0006060,conotruncus,UBERON:0004120,mesoderm-derived structure
+HP:0010244,Abnormality of the epiphyses of the middle phalanges of the hand,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+UBERON:0015020,otic capsule endochondral element,UBERON:0004120,mesoderm-derived structure
+DOID:6381,anterior foramen magnum meningioma,DOID:4708,foramen magnum meningioma
+HP:0004954,Descending aortic aneurysm,HP:0012727,Thoracic aortic aneurysm
+DOID:0080039,axial osteomalacia,DOID:4254,osteosclerosis
+UBERON:0001371,gluteus medius,UBERON:0002000,gluteal muscle
+CL:1001213,arcuate artery endothelial cell,CL:1000413,endothelial cell of artery
+HP:0001971,Hypersplenism,HP:0001743,Abnormality of the spleen
+DOID:13185,esophageal diverticulosis,DOID:6050,esophageal disease
+HP:0010122,Stippling of the epiphyses of the hallux,HP:0010056,Abnormality of the epiphyses of the hallux
+UBERON:0008488,cremaster muscle,UBERON:0005156,reproductive structure
+UBERON:0011157,cuneiform cartilage,UBERON:0003583,larynx connective tissue
+HP:0000485,Megalocornea,HP:0001120,Abnormality of corneal size
+HP:0012727,Thoracic aortic aneurysm,HP:0005112,Dilatation of the abdominal aorta
+HP:0012636,Retinal vein occlusion,HP:0008046,Abnormality of the retinal vasculature
+HP:0008303,Olivary degeneration,HP:0011441,Abnormality of the medulla oblongata
+UBERON:0001385,tibialis anterior,UBERON:0008230,tibialis
+HP:0100202,Absent epiphysis of the distal phalanx of the 5th toe,HP:0100077,Absent epiphyses of the 5th toe
+UBERON:0005665,3rd arch endoderm,UBERON:0000925,endoderm
+DOID:5409,lung small cell carcinoma,DOID:3905,lung carcinoma
+UBERON:0003079,floor plate,UBERON:0000119,cell layer
+DOID:4969,Gerstmann syndrome,DOID:863,nervous system disease
+HP:0010091,Symphalangism affecting the proximal phalanx of the hallux,HP:0010052,Abnormality of the proximal phalanx of the hallux
+UBERON:0003966,gonial bone,UBERON:0003457,head bone
+HP:0100285,EMG: impaired neuromuscular transmission,HP:0003457,EMG abnormality
+UBERON:0003055,periderm,UBERON:0000487,simple squamous epithelium
+CL:0002208,brush cell of bronchus,CL:0002328,bronchial epithelial cell
+UBERON:0013773,right nipple,UBERON:0015212,lateral structure
+UBERON:3000906,sulcus pro musculo extensori cruris brevis,UBERON:0000064,organ part
+HP:0012027,Laryngeal edema,HP:0001600,Abnormality of the larynx
+HP:0001251,Ataxia,HP:0011443,Abnormality of coordination
+DOID:5271,small intestine leiomyosarcoma,DOID:5272,small intestinal sarcoma
+HP:0011352,Severe receptive language delay,HP:0010863,Receptive language delay
+CL:0000910,cytotoxic T cell,CL:0000911,effector T cell
+UBERON:0006686,spinal vein,UBERON:0001638,vein
+HP:0009482,Proximal/middle symphalangism of 3rd finger,HP:0006152,Proximal symphalangism (hands)
+UBERON:2001964,epibranchial 3 bone uncinate process cartilage,UBERON:0011004,pharyngeal arch cartilage
+UBERON:0010846,radius pre-cartilage condensation,UBERON:0010884,forelimb bone pre-cartilage condensation
+DOID:2512,nevoid basal cell carcinoma syndrome,DOID:0050736,autosomal dominant disease
+UBERON:0001708,jaw skeleton,UBERON:0004121,ectoderm-derived structure
+UBERON:0000047,simple eye,UBERON:0000970,eye
+CL:0000340,glioblast (sensu Nematoda and Protostomia),CL:0000130,neuron associated cell (sensu Nematoda and Protostomia)
+DOID:0050901,corpus callosum oligodendroglioma,DOID:3187,brain oligodendroglioma
+HP:0100273,Neoplasm of the colon,HP:0100834,Neoplasm of the large intestine
+HP:0001105,Retinal atrophy,HP:0000479,Abnormality of the retina
+UBERON:0008295,feather barbule,UBERON:0013703,integumentary projection
+DOID:11244,neonatal anemia,DOID:2355,anemia
+DOID:10488,imperforate anus,DOID:0080015,physical disorder
+UBERON:0010295,substantia propria of sclera,UBERON:0003566,head connective tissue
+UBERON:0004760,gland of anal canal,UBERON:0003408,gland of gut
+CL:0000420,syncytial epithelial cell,CL:0000066,epithelial cell
+DOID:10319,mixed mineral dust pneumoconiosis,DOID:10316,pneumoconiosis
+UBERON:0006719,lateral pterygoid muscle,UBERON:0006720,pterygoid muscle
+UBERON:0001744,lymphoid tissue,UBERON:0000479,tissue
+UBERON:0003468,ureteric segment of renal artery,UBERON:0004573,systemic artery
+UBERON:0002304,layer of dentate gyrus,UBERON:0000064,organ part
+UBERON:2000555,opercular flap,UBERON:0003102,surface structure
+HP:0100456,Osteolytic defects of the proximal phalanx of the 4th toe,HP:0010375,Osteolytic defects of the phalanges of the 4th toe
+UBERON:2001152,tooth 3MD,UBERON:2000694,ceratobranchial 5 tooth
+UBERON:0004348,optic eminence,UBERON:0000061,anatomical structure
+UBERON:0000128,olivary body,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3000998,suprarostral cartilage,UBERON:0013765,digestive system organ
+UBERON:0003894,liver primordium,UBERON:0005291,embryonic tissue
+HP:0000968,Ectodermal dysplasia,HP:0011354,Generalized abnormality of skin
+UBERON:0005137,metanephric capsule,UBERON:0004120,mesoderm-derived structure
+HP:0007811,Horizontal pendular nystagmus,HP:0000666,Horizontal nystagmus
+UBERON:0014780,palatine aponeurosis,UBERON:0006614,aponeurosis
+UBERON:2001876,basibranchial 3 cartilage,UBERON:0013747,basibranchial cartilage
+UBERON:0005496,neural tube lateral wall,UBERON:0000060,anatomical wall
+DOID:11201,parathyroid gland disease,DOID:28,endocrine system disease
+UBERON:0004336,proximal phalanx of pedal digit 5,UBERON:0003863,pedal digit 5 phalanx
+HP:0100850,Neoplasia of the penis,HP:0000036,Abnormality of the penis
+DOID:3343,mucolipidosis,DOID:2978,carbohydrate metabolic disorder
+HP:0100062,Pseudoepiphyses of the 3rd toe,HP:0010329,Abnormality of the epiphyses of the 3rd toe
+UBERON:0011895,endomysium,UBERON:0004120,mesoderm-derived structure
+HP:0000585,Band keratopathy,HP:0011493,Central opacification of the cornea
+CL:1000490,mesothelial cell of peritoneum,CL:0000077,mesothelial cell
+UBERON:0006271,orbital fissure,UBERON:0013685,foramen of skull
+UBERON:0007634,parabrachial nucleus,UBERON:0002680,regional part of metencephalon
+DOID:0050419,complement factor I deficiency,DOID:626,complement deficiency
+UBERON:0001367,external anal sphincter,UBERON:0003898,skeletal muscle tissue of trunk
+UBERON:0002222,perichondrium,UBERON:0002384,connective tissue
+HP:0009226,Short proximal phalanx of the 5th finger,HP:0009192,Aplasia/Hypoplasia of the proximal phalanx of the 5th finger
+CL:1000362,transitional myocyte of interventricular septum,CL:0002073,transitional myocyte
+CL:0001010,mature dermal dendritic cell,CL:0001006,dermal dendritic cell
+HP:0006638,Midclavicular aplasia,HP:0006710,Aplasia/Hypoplasia of the clavicles
+UBERON:3010191,calcar anterior,UBERON:3000981,limb external integument structure
+UBERON:0000079,male reproductive system,UBERON:0000990,reproductive system
+UBERON:3000016,anterior nasal wall,UBERON:0010313,neural crest-derived structure
+DOID:3847,papillary craniopharyngioma,DOID:3840,craniopharyngioma
+DOID:3401,inappropriate ADH syndrome,DOID:53,pituitary gland disease
+HP:0000739,Anxiety,HP:0100852,Abnormal fear/anxiety-related behavior
+UBERON:3000440,planum terminale,UBERON:0000064,organ part
+UBERON:4200063,ectocondylar tubercle,UBERON:0004530,bony projection
+CL:0000802,"CD8-alpha alpha positive, gamma-delta intraepithelial T cell",CL:0000801,gamma-delta intraepithelial T cell
+UBERON:0002645,densocellular part of medial dorsal nucleus,UBERON:0003528,brain grey matter
+HP:0009645,Osteolytic defects of the distal phalanx of the thumb,HP:0009617,Abnormality of the distal phalanx of the thumb
+HP:0010588,Premature epimetaphyseal fusion,HP:0005930,Abnormality of the epiphyses
+DOID:12349,primary eye hypotony,DOID:790,ocular hypotension
+DOID:8137,thymus clear cell carcinoma,DOID:3284,thymic carcinoma
+HP:0003831,Age-dependent penetrance,HP:0003829,Incomplete penetrance
+UBERON:3010235,nuchal groove,UBERON:0006846,surface groove
+CL:0002131,regular ventricular cardiac myocyte,CL:0002098,regular cardiac myocyte
+UBERON:0001933,retrochiasmatic area,UBERON:0000064,organ part
+UBERON:0012239,urinary bladder vasculature,UBERON:0006554,urinary system structure
+HP:0005791,Cortical thickening of long bone diaphyses,HP:0000935,Thickened cortex of long bones
+HP:0010424,Complete duplication of the distal phalanx of the 2nd toe,HP:0010429,Complete duplication of the phalanges of the 2nd toe
+HP:0100568,Neoplasm of the endocrine system,HP:0000818,Abnormality of the endocrine system
+UBERON:0005269,renal cortex vein,UBERON:0013126,vein of abdomen
+UBERON:3000348,os basale,UBERON:0000477,anatomical cluster
+UBERON:0005305,thyroid follicle,UBERON:0004119,endoderm-derived structure
+UBERON:0000159,anal canal,UBERON:0004111,anatomical conduit
+HP:0100789,Torus palatinus,HP:0100737,Abnormality of the hard palate
+UBERON:0002955,rhomboidal nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0006670,central tendon of diaphragm,UBERON:0003837,thoracic segment connective tissue
+CL:0000137,osteocyte,CL:0001035,bone cell
+UBERON:0004649,sphenoid bone pterygoid process,UBERON:0015212,lateral structure
+UBERON:0009620,tail bud paraxial mesoderm,UBERON:0005291,embryonic tissue
+UBERON:2002261,dorsal fin spine,UBERON:4200070,median fin spine
+UBERON:0001755,distal part of styloid process of temporal bone,UBERON:0004119,endoderm-derived structure
+DOID:5376,skin pilomatrix carcinoma,DOID:3451,skin carcinoma
+UBERON:0005079,eggshell,UBERON:0002050,embryonic structure
+UBERON:0001312,superior vesical artery,UBERON:0003513,trunk blood vessel
+UBERON:0015079,proximal carpal cartilage,UBERON:0010883,forelimb cartilage element
+DOID:8787,disseminated chorioretinitis,DOID:8886,chorioretinitis
+UBERON:0009142,entire embryonic mesenchyme,UBERON:0000477,anatomical cluster
+HP:0010574,Abnormality of the epiphysis of the femoral head,HP:0003368,Abnormality of the femoral head
+UBERON:0013629,hallical pad,UBERON:0003530,pedal digit skin
+DOID:7827,adult extraosseous osteosarcoma,DOID:184,bone cancer
+UBERON:0013280,diaphysis of tibia,UBERON:0004120,mesoderm-derived structure
+HP:0003376,Steppage gait,HP:0001288,Gait disturbance
+UBERON:0014720,interlobar duct,UBERON:0000058,duct
+HP:0009503,Bracket epiphysis of the distal phalanx of the 2nd finger,HP:0009499,Abnormality of the epiphysis of the distal phalanx of the 2nd finger
+UBERON:0009962,excretory gland,UBERON:0006554,urinary system structure
+CL:0002058,Gr1-low non-classical monocyte,CL:0002398,"Gr1-positive, CD43-positive monocyte"
+HP:0007466,Midfrontal capillary hemangioma,HP:0000996,Facial capillary hemangioma
+HP:0000706,Unerupted tooth,HP:0006292,Abnormality of dental eruption
+UBERON:0001201,serosa of stomach,UBERON:0004782,gastrointestinal system serosa
+UBERON:0013207,entepicondylar foramen,UBERON:0004120,mesoderm-derived structure
+NCBITaxon:11041,Rubella virus,NCBITaxon:11040,Rubivirus
+UBERON:0003311,floor plate of medulla oblongata,UBERON:0002678,regional part of medulla oblongata
+HP:0009802,Aplasia of the phalanges of the hand,HP:0009767,Aplasia/Hypoplasia of the phalanges of the hand
+DOID:0050202,lujo hemorrhagic fever,DOID:934,viral infectious disease
+DOID:423,myopathy,DOID:66,muscle tissue disease
+HP:0100336,Bilateral cleft lip,HP:0100335,Non-midline cleft lip
+HP:0001904,Autoimmune neutropenia,HP:0001875,Neutropenia
+DOID:13368,tinea profunda,DOID:12179,tinea corporis
+DOID:1393,visual pathway disease,DOID:5614,eye disease
+UBERON:2005015,afferent lamellar arteriole,UBERON:0003469,respiratory system artery
+UBERON:2001716,caudal principal ray 4,UBERON:2001585,caudal principal ray
+HP:0009737,Lisch nodules,HP:0000525,Abnormality of the iris
+CL:0002072,nodal myocyte,CL:0002086,specialized cardiac myocyte
+DOID:4030,eosinophilic gastritis,DOID:4029,gastritis
+HP:0100103,Enlarged epiphysis of the distal phalanx of the 2nd toe,HP:0100088,Abnormality of the epiphysis of the distal phalanx of the 2nd toe
+CL:0000338,neuroblast (sensu Nematoda and Protostomia),CL:0000031,neuroblast
+HP:0011064,Abnormal number of incisors,HP:0006483,Abnormal number of teeth
+UBERON:0004917,urethral sphincter,UBERON:0004590,sphincter muscle
+UBERON:0014634,ventral nerve root of cervical spinal cord,UBERON:0009632,root of cervical nerve
+HP:0008473,Narrow anterio-posterior vertebral body diameter,HP:0002773,Small vertebral bodies
+UBERON:0000152,pelvic fin,UBERON:0002534,paired fin
+UBERON:0002004,trunk of sciatic nerve,UBERON:0001147,trunk of peripheral nerve
+UBERON:0006067,musculature of hindlimb zeugopod,UBERON:0004466,musculature of leg
+UBERON:0000030,lamina propria,UBERON:0004923,organ component layer
+UBERON:2000658,epibranchial bone,UBERON:0002513,endochondral bone
+UBERON:0003530,pedal digit skin,UBERON:0001513,skin of pes
+DOID:5474,ovarian serous adenofibroma,DOID:0060112,ovarian benign neoplasm
+UBERON:0014464,renal fat pad,UBERON:0006554,urinary system structure
+UBERON:0000070,pupal stage,UBERON:0000092,post-embryonic stage
+HP:0012108,Primary open angle glaucoma,HP:0000501,Glaucoma
+DOID:0050919,trachea mucoepidermoid carcinoma,DOID:4876,trachea carcinoma
+UBERON:2000982,somite 6,UBERON:0002329,somite
+UBERON:0013495,barbed keratin-coated spine,UBERON:0013494,keratin-coated spine
+UBERON:2001467,pharyngeal mesoderm,UBERON:0004119,endoderm-derived structure
+HP:0009160,Absent epiphysis of the proximal phalanx of the 5th finger,HP:0009153,Abnormality of the epiphysis of the proximal phalanx of the 5th finger
+HP:0003002,Breast carcinoma,HP:0100013,Neoplasm of the breast
+DOID:6944,vulvar seborrheic keratosis,DOID:2072,vulvar squamous tumor
+HP:0008800,Limited hip movement,HP:0001376,Limitation of joint mobility
+UBERON:3000945,inscriptional rib,UBERON:0000064,organ part
+HP:0200000,Dysharmonic bone age,HP:0000927,Abnormality of skeletal maturation
+DOID:988,mitral valve prolapse,DOID:61,mitral valve disease
+UBERON:0002963,caudal pontine reticular nucleus,UBERON:0007413,nucleus of pontine reticular formation
+CL:0005020,lymphangioblast,CL:0000048,multi fate stem cell
+UBERON:0010134,secretory circumventricular organ,UBERON:0010133,neuroendocrine gland
+DOID:6552,gastric small cell carcinoma,DOID:5517,stomach carcinoma
+DOID:2456,blepharoconjunctivitis,DOID:9423,blepharitis
+HP:0001308,Tongue fasciculations,HP:0002380,Fasciculations
+UBERON:3000832,anterior lamina recurvata,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0008647,Pubertal developmental failure in females,HP:0008197,Absence of pubertal development
+NCBITaxon:169440,Coelopidae,NCBITaxon:43750,Sciomyzoidea
+UBERON:0005492,hyaloid vessel,UBERON:0002050,embryonic structure
+HP:0009814,Upper limb peromelia,HP:0006496,Aplasia/Hypoplasia involving bones of the upper limbs
+UBERON:0003504,respiratory system blood vessel,UBERON:0001981,blood vessel
+CL:0010022,cardiac neuron,CL:0002494,cardiocyte
+DOID:7571,malignant cystic nephroma,DOID:263,kidney cancer
+DOID:3024,prostatic acinar adenocarcinoma,DOID:2526,prostate adenocarcinoma
+CL:0000857,slow muscle myoblast,CL:0000515,skeletal muscle myoblast
+HP:0011385,Absent internal auditory canal,HP:0011384,Abnormality of the internal auditory canal
+UBERON:2001030,epaxial region somite 21,UBERON:0003900,epaxial myotome region
+UBERON:0003287,midgut region of duodenum,UBERON:0004921,subdivision of digestive tract
+HP:0008542,Low-frequency hearing loss,HP:0000365,Hearing impairment
+UBERON:0006260,lingual swellings,UBERON:0004121,ectoderm-derived structure
+HP:0002996,Limited elbow movement,HP:0001376,Limitation of joint mobility
+UBERON:3000413,pars palatina of maxilla,UBERON:0010313,neural crest-derived structure
+HP:0011658,Double outlet right ventricle with subpulmonary ventricular septal defect without pulmonary stenosis,HP:0001719,Double outlet right ventricle
+UBERON:2001879,rib of vertebra 1,UBERON:0002228,rib
+CL:0000235,macrophage,CL:0000234,phagocyte
+UBERON:0010345,4th arch mesenchyme from head mesenchyme,UBERON:0010360,pharyngeal arch mesenchyme from head mesenchyme
+CL:0000196,flight muscle cell,CL:0008003,somatic muscle myotube
+DOID:4418,cutaneous fibrous histiocytoma,DOID:2438,dermis tumor
+HP:0011337,Abnormality of mouth size,HP:0000153,Abnormality of the mouth
+UBERON:0007703,spinothalamic tract,UBERON:0007702,tract of brain
+UBERON:0010547,pedal digit 1 metatarsal pre-cartilage condensation,UBERON:0010687,pedal digit metatarsal pre-cartilage condensation
+UBERON:2001657,upper pharyngeal 5 tooth,UBERON:0004756,dermal skeletal element
+HP:0011221,Vertical forehead creases,HP:0000290,Abnormality of the forehead
+HP:0200030,Punctate vasculitis skin lesions,HP:0200029,Vasculitis in the skin
+HP:0010869,Asynergia,HP:0010867,Dyssynergia
+HP:0100915,Sclerosis of the distal phalanges of the hand,HP:0100899,Sclerosis of the phalanges of the hand
+UBERON:0009853,body of uterus,UBERON:0000064,organ part
+UBERON:0002743,basal forebrain,UBERON:0002780,regional part of forebrain
+CL:0002429,CD69-positive double-positive thymocyte,CL:0000809,"double-positive, alpha-beta thymocyte"
+HP:0004030,Patchy sclerosis of radial diaphysis,HP:0004027,Abnormality of radial diaphysis
+UBERON:2001825,urohyal lateral process,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004228,urinary bladder smooth muscle,UBERON:0006554,urinary system structure
+UBERON:0011263,femoral gland,UBERON:0003297,gland of integumental system
+HP:0012130,Abnormality of cells of the erythroid lineage,HP:0005561,Abnormality of bone marrow cell morphology
+DOID:4512,conventional angiosarcoma,DOID:0001816,angiosarcoma
+UBERON:3000443,plectral apparatus,UBERON:0001686,auditory ossicle
+UBERON:2001581,ural centrum 2,UBERON:0004247,bone of dorsum
+UBERON:3000189,foramen orbitonasale laterale,UBERON:3000316,nasal opening
+DOID:10208,chondroid lipoma,DOID:3315,lipoma
+HP:0011565,Common atrium,HP:0005120,Abnormality of cardiac atrium
+HP:0001873,Thrombocytopenia,HP:0011873,Abnormal platelet count
+DOID:11797,chronic laryngitis,DOID:3437,laryngitis
+UBERON:0000084,ureteric bud,UBERON:0000083,mesonephric tubule
+UBERON:0015841,molar dental lamina,UBERON:0004825,dental lamina
+HP:0004915,Impairment of galactose metabolism,HP:0011013,Abnormality of carbohydrate metabolism/homeostasis
+DOID:0060118,thoracic disease,DOID:7,disease of anatomical entity
+HP:0010802,Perioral hyperpigmentation,HP:0000153,Abnormality of the mouth
+HP:0004378,Abnormality of the anus,HP:0012732,Anorectal anomaly
+UBERON:2005259,continuous capillary,UBERON:0001982,capillary
+DOID:1650,female breast axillary tail cancer,DOID:0050671,female breast cancer
+UBERON:0005998,tricuspid valve cusp,UBERON:0006009,cusp of cardiac valve
+HP:0011947,Respiratory tract infection,HP:0002088,Abnormality of the lung
+HP:0010369,Abnormality of the middle phalanx of the 3rd toe,HP:0010183,Abnormality of the middle phalanges of the toes
+UBERON:3000527,quadrate process of palatoquadrate,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002436,primary visual cortex,UBERON:0013529,Brodmann area
+HP:0012625,Stage 3 chronic kidney disease,HP:0012622,Chronic kidney disease
+HP:0004927,Pulmonary artery dilatation,HP:0004414,Abnormality of the pulmonary artery
+UBERON:0006846,surface groove,UBERON:0000061,anatomical structure
+HP:0005549,Congenital neutropenia,HP:0001875,Neutropenia
+UBERON:2005411,common crus,UBERON:0000058,duct
+HP:0100521,Neoplasm of the thymus,HP:0011793,Neoplasm by anatomical site
+UBERON:0004945,submucosa of neck of urinary bladder,UBERON:0004943,submucosa of urinary bladder
+HP:0008107,Plantar crease between first and second toes,HP:0001869,Deep plantar creases
+CL:1000335,enterocyte of epithelium of intestinal villus,CL:1000334,enterocyte of epithelium of small intestine
+UBERON:0004952,submucosa of bronchiole,UBERON:0001957,submucosa of bronchus
+DOID:10852,middle ear cholesterol granuloma,DOID:10754,otitis media
+UBERON:0003310,floor plate of metencephalon,UBERON:0002680,regional part of metencephalon
+HP:0200044,Porokeratosis,HP:0011368,Epidermal thickening
+HP:0100731,Transverse facial cleft,HP:0002006,Facial cleft
+UBERON:0011870,pisotriquetral joint,UBERON:0011132,intercarpal joint
+HP:0100372,Aplasia/Hypoplasia of the middle phalanx of the 3rd toe,HP:0010369,Abnormality of the middle phalanx of the 3rd toe
+DOID:7787,breast osteosarcoma,DOID:3017,breast sarcoma
+HP:0001099,Fundus atrophy,HP:0001098,Abnormality of the fundus
+HP:0011363,Abnormality of hair growth rate,HP:0001595,Abnormality of the hair
+UBERON:0015156,terminal branch of ophthalmic artery,UBERON:0010314,structure with developmental contribution from neural crest
+CL:1000324,duodenal goblet cell,CL:1001589,duodenum glandular cell
+UBERON:0002426,chest muscle,UBERON:0005175,chest organ
+UBERON:0003471,artery of lower lip,UBERON:0003496,head blood vessel
+DOID:10290,prostate lymphoma,DOID:10283,prostate cancer
+UBERON:0015800,taenia tectum of brain,UBERON:0002437,cerebral hemisphere white matter
+HP:0200116,Distal ileal atresia,HP:0011102,Ileal atresia
+DOID:0060205,amyotrophic lateral sclerosis type 14,DOID:332,amyotrophic lateral sclerosis
+UBERON:0007222,late adult stage,UBERON:0000113,post-juvenile adult stage
+HP:0009948,Duplication of the distal phalanx of the 2nd finger,HP:0009883,Duplication of the distal phalanx of hand
+HP:0009701,Metacarpal synostosis,HP:0001163,Abnormality of the metacarpal bones
+DOID:9544,refractory plasma cell neoplasm,DOID:712,refractory hematologic cancer
+DOID:9384,gonococcal iridocyclitis,DOID:9383,iridocyclitis
+DOID:2691,myoma,DOID:461,muscle benign neoplasm
+UBERON:0005687,orbitosphenoid cartilage element,UBERON:0005863,cartilaginous condensation
+CL:0000153,GAG secreting cell,CL:0000447,carbohydrate secreting cell
+HP:0010248,Cone-shaped epiphyses of the distal phalanges of the hand,HP:0010243,Abnormality of the epiphyses of the distal phalanx of finger
+UBERON:0001523,flexor digitorum profundus,UBERON:0000366,flexor muscle
+UBERON:0008488,cremaster muscle,UBERON:0014403,male anatomical structure
+UBERON:0009505,associated mesenchyme of trachea,UBERON:0004119,endoderm-derived structure
+HP:0011383,Enlarged semicircular canal,HP:0011380,Morphological abnormality of the semicircular canal
+UBERON:0004819,kidney epithelium,UBERON:0000483,epithelium
+UBERON:0001578,orbicularis oculi,UBERON:0001577,facial nerve muscle
+HP:0000275,Narrow face,HP:0001999,Abnormal facial shape
+HP:0006574,Hepatic arteriovenous malformation,HP:0006707,Abnormality of the hepatic vasculature
+HP:0001674,Complete atrioventricular canal defect,HP:0006695,Atrioventricular canal defect
+HP:0008676,Congenital megaureter,HP:0000069,Abnormality of the ureter
+UBERON:0014558,CA2 stratum lacunosum moleculare,UBERON:0014567,layer of hippocampal field
+UBERON:0007993,ulnar sesamoid bone,UBERON:0011141,appendicular ossicle
+DOID:4778,proliferative glomerulonephritis,DOID:2921,glomerulonephritis
+HP:0010855,EEG with localized low amplitude activity,HP:0011201,EEG with changes in voltage
+UBERON:2000102,dorsal fin fold,UBERON:0000481,multi-tissue structure
+UBERON:0004883,lung mesenchyme,UBERON:0003104,mesenchyme
+UBERON:0011111,humeroradial joint,UBERON:0003839,forelimb joint
+UBERON:4300037,bony fin ray,UBERON:0004376,fin bone
+DOID:8936,plantar fascial fibromatosis,DOID:65,connective tissue disease
+DOID:0050514,bulbospinal polio,DOID:0050515,paralytic poliomyelitis
+UBERON:0001312,superior vesical artery,UBERON:0009027,vesical artery
+HP:0100312,Cerebral germinoma,HP:0100836,Malignant neoplasm of the central nervous system
+UBERON:0012464,cloacal vent,UBERON:0004120,mesoderm-derived structure
+UBERON:3000884,epipubis,UBERON:0000064,organ part
+UBERON:0005798,bicornuate uterus,UBERON:0000995,uterus
+CL:0000580,neutrophilic myelocyte,CL:0002193,myelocyte
+UBERON:0001752,enamel,UBERON:0010365,odontoid tissue
+UBERON:2000226,lateral ethmoid bone,UBERON:0011164,neurocranium bone
+HP:0009424,Osteolytic defects of the distal phalanx of the 3rd finger,HP:0009443,Osteolytic defects of the phalanges of the 3rd finger
+UBERON:4200052,crista tibiofibularis,UBERON:4100000,skeletal element projection
+DOID:9091,REM sleep behavior disorder,DOID:535,sleep disorder
+DOID:9584,Venezuelan equine encephalitis,DOID:934,viral infectious disease
+HP:0001963,Abnormal speech discrimination,HP:0000364,Hearing abnormality
+HP:0009117,Aplasia/Hypoplasia of the maxilla,HP:0000326,Abnormality of the maxilla
+UBERON:3010794,oral ramule,UBERON:3010765,ramus mandibularis externus
+HP:0012609,Hypomagnesiuria,HP:0012607,Abnormal urine magnesium concentration
+HP:0100485,Symphalangism of the proximal phalanx of the 4th toe with the 4th metatarsal,HP:0100474,Symphalangism affecting the proximal phalanx of the 4th toe
+HP:0100719,Lens coloboma,HP:0000589,Coloboma
+UBERON:0004825,dental lamina,UBERON:0010371,ecto-epithelium
+UBERON:0002433,pars tuberalis of adenohypophysis,UBERON:0004121,ectoderm-derived structure
+UBERON:0001694,petrous part of temporal bone,UBERON:0005913,zone of bone organ
+HP:0008665,Clitoral hypertrophy,HP:0000056,Abnormality of the clitoris
+UBERON:2001947,hyomandibular-otic region joint,UBERON:0000982,skeletal joint
+CL:0002461,CD103-positive dendritic cell,CL:0000766,myeloid leukocyte
+UBERON:0002747,neodentate part of dentate nucleus,UBERON:0003528,brain grey matter
+CL:1001597,seminal vesicle glandular cell,CL:0000150,glandular epithelial cell
+UBERON:0012074,bony part of hard palate,UBERON:0004121,ectoderm-derived structure
+DOID:3614,Kallmann syndrome,DOID:1924,hypogonadism
+DOID:6451,central nervous system fibrosarcoma,DOID:2133,central nervous system sarcoma
+UBERON:0012332,broad ligament of uterus,UBERON:0000211,ligament
+NCBITaxon:776,Coxiella <Bacteria>,NCBITaxon:118968,Coxiellaceae
+UBERON:0014486,distal phalanx of digit 4,UBERON:0004300,distal phalanx
+UBERON:2105383,dorsal fin proximal radial element 6,UBERON:2100947,dorsal fin proximal radial element
+NCBITaxon:12091,Hepatovirus,NCBITaxon:12058,Picornaviridae
+UBERON:0014885,distal epiphysis of distal phalanx of manual digit 5,UBERON:0014886,distal epiphysis of distal phalanx of manual digit
+HP:0008964,Nonprogressive muscular atrophy,HP:0003202,Amyotrophy
+UBERON:0002032,areola,UBERON:0004121,ectoderm-derived structure
+UBERON:0000407,sympathetic trunk,UBERON:0000062,organ
+HP:0100232,Small epiphysis of the proximal phalanx of the 5th toe,HP:0100085,Small epiphyses of the 5th toe
+CL:0002089,nuocyte,CL:0000738,leukocyte
+UBERON:0005099,short descending thin limb,UBERON:0006914,squamous epithelium
+UBERON:0010386,peyer's patch follicle,UBERON:0000444,lymphoid follicle
+HP:0011968,Feeding difficulties,HP:0011458,Abdominal symptom
+DOID:3426,vestibular disease,DOID:4539,labyrinthine disease
+HP:0200032,Kayser-Fleischer ring,HP:0007957,Corneal opacity
+HP:0008071,Maternal hypertension,HP:0100603,Toxemia of pregnancy
+UBERON:2001671,anal fin radial bone,UBERON:2005225,median fin radial bone
+UBERON:0008832,outer spiral sulcus,UBERON:0002277,spiral sulcus
+UBERON:2002004,anterior dentation of dorsal fin spine 2,UBERON:0004529,anatomical projection
+HP:0200131,Ostium secundum atrial septal defect,HP:0001684,Secundum atrial septal defect
+HP:0100920,Sclerosis of the phalanges of the 4th finger,HP:0009172,Abnormality of the phalanges of the 4th finger
+HP:0010152,Enlarged epiphysis of the 1st metatarsal,HP:0010125,Abnormality of the epiphysis of the 1st metatarsal
+UBERON:0002600,limbic lobe,UBERON:0003022,cerebral cortex lobe
+UBERON:3000673,posteromedial process,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0010205,mesencephalic vein,UBERON:0001638,vein
+UBERON:2001578,anterior dorsomedial process of autopalatine,UBERON:0004530,bony projection
+UBERON:0005943,hair root sheath matrix,UBERON:0010314,structure with developmental contribution from neural crest
+CL:1000301,fibroblast of subepithelial connective tissue of prostatic gland,CL:0000057,fibroblast
+UBERON:0002995,substantia nigra pars lateralis,UBERON:0002950,regional part of midbrain
+HP:0012404,Abnormal urine citrate concentration,HP:0003110,Abnormality of urine homeostasis
+UBERON:3010804,ramus ventral,UBERON:3010115,posterior lateral line nerve (PLLN)
+UBERON:0001112,latissimus dorsi muscle,UBERON:0001482,muscle of shoulder
+DOID:2843,long QT syndrome,DOID:0050739,autosomal genetic disease
+HP:0003282,Low alkaline phosphatase,HP:0004379,Abnormality of alkaline phosphatase activity
+DOID:12307,anterior corneal pigmentation,DOID:10123,pigmentation disease
+UBERON:0008444,webbed manual digit,UBERON:0008443,webbed digit
+DOID:0060018,CD3gamma deficiency,DOID:627,severe combined immunodeficiency
+UBERON:0005321,mesonephric smooth muscle tissue,UBERON:0001135,smooth muscle tissue
+DOID:10272,left bundle branch hemiblock,DOID:10273,heart conduction disease
+DOID:7031,glottis squamous cell carcinoma,DOID:2599,glottis carcinoma
+HP:0009668,Fragmentation of the epiphysis of the proximal phalanx of the thumb,HP:0009663,Abnormality of the epiphysis of the proximal phalanx of the thumb
+DOID:11342,arcus senilis,DOID:11343,scleral disease
+UBERON:2001745,premaxilla replacement tooth trench,UBERON:2001744,replacement tooth trench
+HP:0001009,Telangiectasia,HP:0011276,Vascular skin abnormality
+HP:0010024,Epiphyseal stippling of the first metacarpal,HP:0009195,Epiphyseal stippling of the metacarpals
+HP:0012104,Parietal cortical atrophy,HP:0002120,Cerebral cortical atrophy
+UBERON:0001631,thoracic duct,UBERON:0004120,mesoderm-derived structure
+HP:0100816,Lip hyperpigmentation,HP:0000159,Abnormality of the lip
+UBERON:0010507,layer of dura mater,UBERON:0004120,mesoderm-derived structure
+UBERON:0011951,prostate luminal epithelium,UBERON:0011945,luminal layer of epithelium
+DOID:1388,Tangier disease,DOID:1387,hypolipoproteinemia
+UBERON:0012487,vaginal sphincter,UBERON:0004590,sphincter muscle
+DOID:13406,pulmonary sarcoidosis,DOID:3082,interstitial lung disease
+DOID:14452,hypokalemic periodic paralysis,DOID:1029,familial periodic paralysis
+HP:0001386,Joint swelling,HP:0000969,Edema
+UBERON:2005015,afferent lamellar arteriole,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009547,Broad phalanges of the 2nd finger,HP:0009768,Broad phalanges of the hand
+UBERON:0003244,epithelium of mammary gland,UBERON:0010371,ecto-epithelium
+DOID:4207,childhood infratentorial neoplasm,DOID:4203,brain stem cancer
+UBERON:0003966,gonial bone,UBERON:0002513,endochondral bone
+UBERON:2001999,posterior cleithral process,UBERON:0004121,ectoderm-derived structure
+CL:1000329,tracheal goblet cell,CL:0000307,tracheal epithelial cell
+CL:0000518,phagocyte (sensu Vertebrata),CL:0000234,phagocyte
+UBERON:0003489,respiratory system capillary endothelium,UBERON:0001915,endothelium of capillary
+UBERON:0001641,transverse sinus,UBERON:0006615,venous sinus
+DOID:11234,orbital cellulitis,DOID:11230,acute orbital inflammation
+UBERON:0009090,outer medulla vasa recta descending limb,UBERON:0004120,mesoderm-derived structure
+DOID:3197,schwannoma of twelfth cranial nerve,DOID:3198,hypoglossal nerve neoplasm
+UBERON:0003038,thoracic spinal cord,UBERON:0005844,spinal cord segment
+UBERON:0002413,cervical vertebra,UBERON:0015007,cervical vertebra endochondral element
+HP:0100903,Sclerosis of the distal phalanx of the 5th finger,HP:0100915,Sclerosis of the distal phalanges of the hand
+HP:0003077,Hyperlipidemia,HP:0003119,Abnormality of lipid metabolism
+DOID:1380,endometrial cancer,DOID:363,uterine cancer
+HP:0000060,Clitoral hypoplasia,HP:0003241,Genital hypoplasia
+UBERON:3000883,recessus coccygealis,UBERON:0000064,organ part
+UBERON:0015172,endometrial blood vessel,UBERON:0001981,blood vessel
+HP:0100059,Fragmentation of the epiphyses of the 3rd toe,HP:0010166,Fragmentation of the epiphyses of the toes
+UBERON:2005036,supraintestinal artery,UBERON:0001637,artery
+HP:0002959,Impaired Ig class switch recombination,HP:0005372,Abnormality of B cell physiology
+DOID:3201,sympathetic neurilemmoma,DOID:3192,neurilemmoma
+UBERON:0011022,flexor hallucis brevis muscle,UBERON:0014378,intrinsic muscle of pes
+UBERON:0001473,lymphatic vessel,UBERON:0000055,vessel
+UBERON:0003610,heart elastic tissue,UBERON:0004120,mesoderm-derived structure
+UBERON:0011640,palatoglossal arch,UBERON:0000477,anatomical cluster
+UBERON:0014705,median lingual swelling epithelium,UBERON:0010371,ecto-epithelium
+DOID:4557,oral leukoedema,DOID:403,mouth disease
+UBERON:0010338,1st arch maxillary mesenchyme from head mesenchyme,UBERON:0010045,1st arch maxillary mesenchyme
+HP:0005090,Lateral femoral bowing,HP:0002980,Femoral bowing
+UBERON:0011614,basihyal element,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001743,ligament of larynx,UBERON:0003583,larynx connective tissue
+HP:0009577,Short middle phalanx of the 2nd finger,HP:0009568,Aplasia/Hypoplasia of the middle phalanx of the 2nd finger
+UBERON:0010219,thyroid pre-cartilage condensation,UBERON:0010213,laryngeal pre-cartilage condensation
+UBERON:0015084,distal carpal bone 1 endochondral element,UBERON:0015049,carpus endochondral element
+HP:0100681,Esophageal duplication,HP:0002031,Abnormality of the esophagus
+HP:0002786,Tracheobronchomalacia,HP:0002779,Tracheomalacia
+HP:0003126,Low-molecular-weight proteinuria,HP:0000093,Proteinuria
+UBERON:3010369,branchial arch skeleton,UBERON:0000477,anatomical cluster
+HP:0000803,Renal cortical cysts,HP:0000107,Renal cyst
+HP:0100375,Aplasia/Hypoplasia of the proximal phalanx of the 3rd toe,HP:0010370,Abnormality of the proximal phalanx of the 3rd toe
+DOID:612,primary immunodeficiency disease,DOID:2914,immune system disease
+UBERON:0010535,primitive metanephric nephron,UBERON:0010532,primitive nephron
+UBERON:0010234,palatopharyngeus muscle,UBERON:0015212,lateral structure
+UBERON:0006454,sixth thoracic spinal cord segment,UBERON:0007715,thoracic subsegment of spinal cord
+HP:0011494,Generalized opacification of the cornea,HP:0007759,Opacification of the corneal stroma
+HP:0009220,Ivory epiphysis of the middle phalanx of the 4th finger,HP:0009399,Ivory epiphyses of the 4th finger
+CL:0000235,macrophage,CL:0000766,myeloid leukocyte
+HP:0011241,Serpiginous stem of antihelix,HP:0011244,Abnormality of stem of antihelix
+UBERON:0006219,deltoid pre-muscle mass,UBERON:0004120,mesoderm-derived structure
+UBERON:0000022,feather,UBERON:0000021,cutaneous appendage
+DOID:7086,multicentric papillary thyroid carcinoma,DOID:3969,papillary thyroid carcinoma
+HP:0010833,Spontaneous pain sensation,HP:0010832,Abnormality of pain sensation
+UBERON:0000037,tertiary ovarian follicle,UBERON:0001305,ovarian follicle
+NCBITaxon:43920,Chrysopsinae,NCBITaxon:7205,Tabanidae
+DOID:9603,intravascular fasciitis,DOID:7327,pseudosarcomatous fibromatosis
+CL:1000343,paneth cell of epithelium of small intestine,CL:0000510,paneth cell
+DOID:0050467,erythrokeratodermia variabilis,DOID:37,skin disease
+DOID:10499,orbital granuloma,DOID:1397,chronic orbital inflammation
+HP:0004717,Axial malrotation of the kidney,HP:0004712,Renal malrotation
+DOID:5176,renal Wilms' tumor,DOID:2154,nephroblastoma
+UBERON:0010576,manual digit 2 phalanx pre-cartilage condensation,UBERON:0010586,manual digit phalanx pre-cartilage condensation
+NCBITaxon:297308,Ixodoidea,NCBITaxon:6935,Ixodida
+UBERON:0003887,intraembryonic coelom,UBERON:0003886,body cavity precursor
+CL:0002237,luminal epithelial cell of prostatic duct,CL:0002340,luminal cell of prostate epithelium
+UBERON:0008922,sublaminar layer S1,UBERON:0009737,sublaminar layers S1 or S2 or S3 or S4
+UBERON:0008926,sublaminar layer S5,UBERON:0009736,sublaminar layers S3 or S4 or S5
+UBERON:0009972,ureteropelvic junction,UBERON:0007651,anatomical junction
+HP:0010431,Short phalanx of the 2nd toe,HP:0010347,Aplasia/Hypoplasia of the phalanges of the 2nd toe
+UBERON:0011647,depressor mandibulae muscle,UBERON:0001577,facial nerve muscle
+DOID:3607,appendix mucinous cystadenocarcinoma,DOID:3608,appendix adenocarcinoma
+DOID:6823,pancreatoblastoma,DOID:4905,pancreatic carcinoma
+HP:0010639,Elevated alkaline phosphatase of bone origin,HP:0010679,Elevated tissue non-specific alkaline phosphatase
+UBERON:0003438,iris nerve,UBERON:0001647,facial nerve
+DOID:10125,acute hydrops keratoconus,DOID:10126,keratoconus
+NCBITaxon:5810,Toxoplasma,NCBITaxon:5809,Sarcocystidae
+UBERON:0010054,malleus cartilage element,UBERON:0011004,pharyngeal arch cartilage
+HP:0010954,Hypoplastic right heart,HP:0001961,Hypoplastic heart
+DOID:2565,macular corneal dystrophy,DOID:2566,corneal dystrophy
+DOID:4025,steatitis,DOID:5113,nutritional deficiency disease
+UBERON:3010832,occipital segment,UBERON:0004120,mesoderm-derived structure
+UBERON:0001671,temporal vein,UBERON:0009141,craniocervical region vein
+UBERON:0013182,core of melon organ,UBERON:0000479,tissue
+UBERON:0008873,alveolar pore,UBERON:0004119,endoderm-derived structure
+CL:0000952,preBCR-positive large pre-B-II cell,CL:0000957,large pre-B-II cell
+UBERON:0006725,spiral ligament,UBERON:0000211,ligament
+UBERON:2000587,sphenotic,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0006213,Thin proximal phalanges with broad epiphyses,HP:0009834,Abnormality of the proximal phalanges of the hand
+DOID:4113,uterine corpus adenosarcoma,DOID:1974,adenosarcoma
+UBERON:0013496,unbarbed keratin-coated spine,UBERON:0013494,keratin-coated spine
+UBERON:3000907,eminentia arcuata,UBERON:0000064,organ part
+DOID:7514,Wolffian adnexal neoplasm,DOID:5727,uterine ligament cancer
+UBERON:0007132,head kidney,UBERON:0005172,abdomen organ
+UBERON:0003549,brain pia mater,UBERON:0003547,brain meninx
+HP:0000498,Blepharitis,HP:0100533,Inflammatory abnormality of the eye
+UBERON:0005710,lower jaw incisor epithelium,UBERON:0003843,dental epithelium
+DOID:9388,lens-induced iridocyclitis,DOID:9383,iridocyclitis
+UBERON:0001248,hilum of spleen,UBERON:0004120,mesoderm-derived structure
+HP:0002878,Early respiratory failure,HP:0002093,Respiratory insufficiency
+UBERON:0006687,median sacral vein,UBERON:0001638,vein
+UBERON:0014887,distal epiphysis of distal phalanx of digit,UBERON:0004448,distal epiphysis of phalanx
+HP:0003640,Foam cells in visceral organs and CNS,HP:0003651,Foam cells
+HP:0009430,Broad middle phalanx of the 3rd finger,HP:0009440,Broad phalanges of the 3rd finger
+UBERON:3010584,mandibular arch neural crest,UBERON:0002050,embryonic structure
+UBERON:0005626,ventral mesogastrium,UBERON:0002050,embryonic structure
+UBERON:0006788,middle gray layer of superior colliculus,UBERON:0006792,intermediate layer of superior colliculus
+HP:0010331,Aplasia/Hypoplasia of the 3rd toe,HP:0010320,Abnormality of the 3rd toe
+CL:0000239,brush border epithelial cell,CL:0000075,columnar/cuboidal epithelial cell
+HP:0009582,Bullet-shaped proximal phalanx of the 2nd finger,HP:0009853,Bullet-shaped proximal phalanges of the hand
+DOID:2583,agammaglobulinemia,DOID:620,blood protein disease
+UBERON:0004120,mesoderm-derived structure,UBERON:0000061,anatomical structure
+DOID:2320,obstructive lung disease,DOID:850,lung disease
+HP:0003950,Flared metaphyses (elbow),HP:0003849,Flared metaphyses of the upper limbs
+HP:0011505,Cystoid macular edema,HP:0001103,Abnormality of the macula
+HP:0009390,Small epiphyses of the 5th finger,HP:0010236,Small epiphyses of the phalanges of the hand
+CL:1000695,kidney interstitial alternatively activated macrophage,CL:0000864,tissue-resident macrophage
+UBERON:0000349,limbic system,UBERON:0004121,ectoderm-derived structure
+UBERON:0008976,snake venom gland,UBERON:0011579,venom gland
+UBERON:0004696,venous system smooth muscle,UBERON:0004237,blood vessel smooth muscle
+DOID:4851,pilocytic astrocytoma,DOID:3069,astrocytoma
+HP:0008516,Abnormality of the vertebral spinous processes,HP:0003312,Abnormal form of the vertebral bodies
+HP:0012078,Motor conduction block,HP:0000762,Decreased nerve conduction velocity
+UBERON:0005908,conjunctival sac,UBERON:0004121,ectoderm-derived structure
+CL:1000411,endothelial cell of peyer's patch,CL:0000115,endothelial cell
+UBERON:0015247,bifurcation of trachea,UBERON:0000064,organ part
+UBERON:0002683,rhinal sulcus,UBERON:0013118,sulcus of brain
+UBERON:0005186,outer renal medulla collecting duct,UBERON:0005185,renal medulla collecting duct
+HP:0010288,Abnormality of the sublingual glands,HP:0010286,Abnormality of the salivary glands
+UBERON:0002869,diffuse reticular nucleus,UBERON:0006331,brainstem nucleus
+HP:0012234,Agranulocytosis,HP:0001913,Granulocytopenia
+HP:0002384,Focal seizures with impairment of consciousness or awareness,HP:0007359,Focal seizures
+UBERON:0013156,1st arch mandibular endoderm,UBERON:0003929,gut epithelium
+HP:0006337,Premature eruption of permanent teeth,HP:0006288,Advanced eruption of teeth
+UBERON:2000593,superior reticular formation medial column,UBERON:0007635,nucleus of medulla oblongata
+HP:0002419,Molar tooth sign on MRI,HP:0002418,Abnormality of the midbrain
+HP:0100063,Small epiphyses of the 3rd toe,HP:0010329,Abnormality of the epiphyses of the 3rd toe
+UBERON:2001672,dorsal fin radial bone,UBERON:2101672,dorsal fin radial element
+HP:0010121,Small epiphyses of the hallux,HP:0010056,Abnormality of the epiphyses of the hallux
+HP:0008456,C2-C3 subluxation,HP:0003308,Cervical subluxation
+UBERON:0006244,hip joint primordium,UBERON:0001048,primordium
+CL:0000988,hematopoietic cell,CL:0000548,animal cell
+HP:0000831,Insulin-resistant diabetes mellitus,HP:0000855,Insulin resistance
+DOID:12661,tooth ankylosis,DOID:214,teeth hard tissue disease
+HP:0001889,Megaloblastic anemia,HP:0001972,Macrocytic anemia
+HP:0006059,Cone-shaped metacarpal epiphyses,HP:0010579,Cone-shaped epiphysis
+CL:1000342,enterocyte of epithelium proper of ileum,CL:1000339,enterocyte of epithelium proper of small intestine
+DOID:13258,typhoid fever,DOID:0050338,primary bacterial infectious disease
+UBERON:4200016,postbranchial lamina,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002321,extraglomerular mesangium,UBERON:0003891,stroma
+UBERON:3000949,posterior ramus of cleithrum,UBERON:0004120,mesoderm-derived structure
+CL:0001011,immature interstitial dendritic cell,CL:0000840,immature conventional dendritic cell
+CL:0000161,acid secreting cell,CL:0000151,secretory cell
+HP:0100284,EMG: myotonic discharges,HP:0003457,EMG abnormality
+UBERON:0003959,rete testis,UBERON:0005156,reproductive structure
+UBERON:3000660,margo choanalis,UBERON:0004120,mesoderm-derived structure
+CL:0001051,"CD4-positive, CXCR3-negative, CCR6-negative, alpha-beta T cell",CL:0000624,"CD4-positive, alpha-beta T cell"
+HP:0010675,Abnormal foot bone ossification,HP:0011849,Abnormal bone ossification
+UBERON:0013772,left nipple,UBERON:0015212,lateral structure
+UBERON:2000084,yolk,UBERON:0002050,embryonic structure
+HP:0010243,Abnormality of the epiphyses of the distal phalanx of finger,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+UBERON:0010334,maxillary process mesenchyme from neural crest,UBERON:0010258,mesenchyme from rhombencephalic neural crest
+HP:0001101,Iritis,HP:0000525,Abnormality of the iris
+UBERON:0011612,hypohyal cartilage,UBERON:0011613,hypohyal element
+HP:0009681,Ivory epiphysis of the distal phalanx of the thumb,HP:0010252,Ivory epiphyses of the distal phalanges of the hand
+NCBITaxon:90964,Staphylococcaceae,NCBITaxon:1385,Bacillales
+UBERON:0013670,midline of corpus cavernosum maxillaris,UBERON:0006800,anatomical line
+HP:0100962,Shyness,HP:0012433,Abnormal social behavior
+UBERON:0009888,Koller's sickle,UBERON:0002050,embryonic structure
+DOID:602,cancerophobia,DOID:0060048,nosophobia
+NCBITaxon:147550,Sordariomycetes,NCBITaxon:715989,sordariomyceta
+UBERON:0000378,tongue muscle,UBERON:0010959,craniocervical muscle
+UBERON:0001706,nasal septum,UBERON:0003037,septum
+UBERON:2000337,basioccipital posterodorsal region,UBERON:0002513,endochondral bone
+DOID:10602,steatorrhea,DOID:5295,intestinal disease
+UBERON:0004818,terminal bronchus epithelium,UBERON:0002031,epithelium of bronchus
+UBERON:0007377,stratum compactum,UBERON:0013754,integumentary system layer
+NCBITaxon:118969,Legionellales,NCBITaxon:1236,Gammaproteobacteria
+DOID:403,mouth disease,DOID:77,gastrointestinal system disease
+HP:0007362,Aplasia/Hypoplasia of the brainstem,HP:0002363,Abnormality of the brainstem
+UBERON:0006718,medial pterygoid muscle,UBERON:0006720,pterygoid muscle
+DOID:9245,Alagille syndrome,DOID:409,liver disease
+HP:0010064,Symphalangism affecting the phalanges of the hallux,HP:0100235,Synostosis involving bones of the toes
+HP:0100157,Absent epiphysis of the proximal phalanx of the 3rd toe,HP:0100093,Abnormality of the epiphysis of the proximal phalanx of the 3rd toe
+HP:0009967,Complete duplication of the proximal phalanx of the 3rd finger,HP:0009964,Duplication of the proximal phalanx of the 3rd finger
+UBERON:0001763,odontogenic papilla,UBERON:0005856,developing mesenchymal condensation
+DOID:4037,necrotizing gastritis,DOID:4029,gastritis
+CL:1000349,basal cell of epithelium of bronchus,CL:0002329,basal epithelial cell of tracheobronchial tree
+UBERON:0014848,tendon of quadriceps femoris,UBERON:0000043,tendon
+UBERON:0001292,distal convoluted tubule,UBERON:0006534,renal convoluted tubule
+CL:0000589,cochlear inner hair cell,CL:0000202,auditory hair cell
+CL:1000697,kidney interstitial suppressor macrophage,CL:0000862,suppressor macrophage
+HP:0001841,Preaxial foot polydactyly,HP:0100258,Preaxial polydactyly
+UBERON:4200012,ectepicondylar flange,UBERON:0004120,mesoderm-derived structure
+UBERON:2001151,tooth 4MD,UBERON:2000694,ceratobranchial 5 tooth
+UBERON:0006061,process of vertebra,UBERON:0004120,mesoderm-derived structure
+DOID:4892,middle ear adenocarcinoma,DOID:4893,middle ear carcinoma
+UBERON:2001809,trigeminal foramen,UBERON:0005744,bone foramen
+UBERON:0008799,transverse palatine fold,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0002430,"CD4-intermediate, CD8-positive double-positive thymocyte",CL:0000809,"double-positive, alpha-beta thymocyte"
+UBERON:0011940,arrector pili muscle of vibrissa,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0002232,epithelial cell of prostatic duct,CL:0002231,epithelial cell of prostate
+UBERON:2100623,basipterygium element,UBERON:0010363,endochondral element
+CL:0000185,myoepithelial cell,CL:0000075,columnar/cuboidal epithelial cell
+HP:0001376,Limitation of joint mobility,HP:0011729,Abnormality of joint mobility
+UBERON:0000078,mixed ectoderm/mesoderm/endoderm-derived structure,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0007876,Juvenile cortical cataract,HP:0001118,Juvenile cataract
+HP:0007450,Increased groin pigmentation with raindrop depigmentation,HP:0007400,Irregular hyperpigmentation
+DOID:899,choledochal cyst,DOID:4138,bile duct disease
+UBERON:0006047,interdigital region between pedal digits 4 and 5,UBERON:0006014,interdigital region between pedal digits
+DOID:12382,complex partial epilepsy,DOID:2234,focal epilepsy
+UBERON:0006011,hyaloid vein,UBERON:0009141,craniocervical region vein
+HP:0009277,Contracture of the metacarpophalangeal joint of the 4th finger,HP:0009274,Joint contractures of the 4th finger
+HP:0100137,Cone-shaped epiphysis of the distal phalanx of the 3rd toe,HP:0100091,Abnormality of the epiphysis of the distal phalanx of the 3rd toe
+HP:0003862,Absent humerus,HP:0006507,Aplasia/Hypoplasia of the humerus
+UBERON:4400006,elastoidin fin ray,UBERON:4400005,fin ray
+UBERON:0002077,cortex of hair,UBERON:0001851,cortex
+HP:0100768,Choriocarcinoma,HP:0100767,Abnormality of the placenta
+NCBITaxon:7742,Vertebrata <Metazoa>,NCBITaxon:89593,Craniata <chordata>
+UBERON:0009846,embryonic cloacal epithelium,UBERON:0006554,urinary system structure
+HP:0003460,Total immunoglobulin A deficiency,HP:0002720,IgA deficiency
+UBERON:0010961,erector spinae pre-muscle mass,UBERON:0004120,mesoderm-derived structure
+HP:0006226,Osteoarthritis of the first carpometacarpal joint,HP:0004268,Osteoarthritis of the small joints of the hand
+HP:0000159,Abnormality of the lip,HP:0000153,Abnormality of the mouth
+DOID:12223,specific bursitis often of occupational origin,DOID:2965,bursitis
+DOID:5468,biliary papillomatosis,DOID:0050625,biliary tract neoplasm
+HP:0009761,Anterior clefting of vertebral bodies,HP:0008428,Vertebral clefting
+HP:0010587,Triangular epiphyses,HP:0005930,Abnormality of the epiphyses
+HP:0004036,Long styloid process,HP:0004035,Abnormality of the styloid process
+DOID:7177,anal canal squamous cell carcinoma,DOID:0050688,anal canal cancer
+UBERON:0011859,internal acoustic meatus,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100539,Periorbital edema,HP:0000606,Abnormality of the periorbital region
+DOID:0050903,parietal lobe ependymoma,DOID:14384,parietal lobe neoplasm
+UBERON:2001793,pharyngobranchial 4 bone uncinate process,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009147,Enlarged epiphysis of the distal phalanx of the 5th finger,HP:0009198,Abnormality of the epiphysis of the distal phalanx of the 5th finger
+HP:0005301,Persistent left superior vena cava,HP:0005345,Abnormality of the vena cava
+HP:0012624,Stage 2 chronic kidney disease,HP:0012622,Chronic kidney disease
+UBERON:0015142,falciform fat,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0002194,capsule of lymph node,UBERON:0003893,capsule
+UBERON:0010574,manual digit 5 metacarpus cartilage element,UBERON:0015047,manual digit 5 metacarpus endochondral element
+HP:0003865,Bowed humerus,HP:0006488,Bowing of the arm
+HP:0009270,Stippling of the epiphysis of the proximal phalanx of the 4th finger,HP:0010277,Stippling of the epiphyses of the proximal phalanges of the hand
+HP:0008434,Hypoplastic cervical vertebrae,HP:0008417,Vertebral hypoplasia
+DOID:13574,cortical senile cataract,DOID:9669,senile cataract
+DOID:3253,embryonal extrahepatic bile duct rhabdomyosarcoma,DOID:3254,bile duct rhabdomyosarcoma
+HP:0009225,Aplasia of the proximal phalanx of the 5th finger,HP:0009192,Aplasia/Hypoplasia of the proximal phalanx of the 5th finger
+UBERON:0015169,tapetum,UBERON:0000479,tissue
+UBERON:0006232,facio-acoustic VII-VIII preganglion complex,UBERON:0010313,neural crest-derived structure
+HP:0007165,Periventricular gray matter heterotopia,HP:0002281,Gray matter heterotopias
+DOID:819,mediastinitis,DOID:65,connective tissue disease
+DOID:4064,bile duct sarcoma,DOID:4606,bile duct cancer
+HP:0009964,Duplication of the proximal phalanx of the 3rd finger,HP:0010006,Duplication of the proximal phalanx of hand
+UBERON:0010249,posterior meningeal artery,UBERON:0003474,meningeal artery
+UBERON:0009127,epibranchial ganglion,UBERON:0004121,ectoderm-derived structure
+UBERON:3000441,planum triangulare,UBERON:0000064,organ part
+HP:0010023,Small epiphysis of the 1st metacarpal,HP:0009694,Small epiphyses of the thumb
+DOID:3499,gallbladder signet ring cell adenocarcinoma,DOID:3500,gallbladder adenocarcinoma
+HP:0003319,Abnormality of the cervical spine,HP:0000925,Abnormality of the vertebral column
+UBERON:0000484,simple cuboidal epithelium,UBERON:0010077,cuboidal epithelium
+UBERON:0011827,areolar gland,UBERON:0001821,sebaceous gland
+UBERON:0011831,duct of vestibular gland,UBERON:0014404,female anatomical structure
+UBERON:0002328,notochord,UBERON:0004121,ectoderm-derived structure
+DOID:4853,pilocytic astrocytoma of cerebellum,DOID:4848,cerebellar astrocytoma
+UBERON:0015923,superficial parotid lymph node,UBERON:0015857,parotid lymph node
+HP:0005104,Hypoplastic nasal septum,HP:0009935,Aplasia/Hypoplasia of the nasal septum
+CL:0002263,transitional cell of parathyroid gland,CL:0002260,epithelial cell of parathyroid gland
+UBERON:0002126,solitary tract nuclear complex,UBERON:0007245,nuclear complex of neuraxis
+DOID:5389,oxyphilic adenoma,DOID:0060089,endocrine organ benign neoplasm
+UBERON:0010951,interscutular muscle,UBERON:0002376,cranial muscle
+UBERON:0005486,venous dural sinus,UBERON:0003499,brain blood vessel
+DOID:1925,Coffin-Siris syndrome,DOID:630,genetic disease
+NCBITaxon:32525,Theria <Mammalia>,NCBITaxon:40674,Mammalia
+UBERON:2005014,recurrent branch afferent branchial artery,UBERON:0003469,respiratory system artery
+DOID:13742,neurofibroma of spinal cord,DOID:962,neurofibroma
+UBERON:0000945,stomach,UBERON:0010039,food storage organ
+HP:0100088,Abnormality of the epiphysis of the distal phalanx of the 2nd toe,HP:0010323,Abnormality of the epiphyses of the 2nd toe
+DOID:5324,fallopian tube germ cell cancer,DOID:1964,fallopian tube cancer
+UBERON:0004563,forelimb digital vein,UBERON:0004562,digital vein
+HP:0004822,Atypical elliptocytosis,HP:0004445,Elliptocytosis
+UBERON:2002262,anal fin spine,UBERON:4200070,median fin spine
+HP:0009254,Fragmentation of the epiphysis of the distal phalanx of the 4th finger,HP:0010250,Fragmentation of the epiphyses of the distal phalanges of the hand
+DOID:2149,urogenital tuberculosis,DOID:0050598,extrapulmonary tuberculosis
+UBERON:0011160,nasal suture,UBERON:0009199,facial suture
+HP:0100313,Cerebral granulomatosis,HP:0002060,Abnormality of the cerebrum
+DOID:10779,septic myocarditis,DOID:3951,acute myocarditis
+UBERON:0014503,proximal phalanx of digit 3,UBERON:0004302,proximal phalanx
+DOID:0050623,bladder benign neoplasm,DOID:731,urinary system benign neoplasm
+HP:0007769,Peripheral retinal degeneration,HP:0000546,Retinal degeneration
+UBERON:0010292,episcleral layer of eyeball,UBERON:0010291,layer of sclera
+UBERON:0011636,surangular bone,UBERON:0008907,dermal bone
+HP:0011443,Abnormality of coordination,HP:0011442,Abnormality of central motor function
+DOID:125,vagina leiomyoma,DOID:0060114,vaginal benign neoplasm
+DOID:551,toxic pneumonitis,DOID:552,pneumonia
+CL:0000803,CD4-negative CD8-negative gamma-delta intraepithelial T cell,CL:0000801,gamma-delta intraepithelial T cell
+UBERON:0006168,hindlimb common dorsal digital arteries,UBERON:0006145,dorsal digital artery of pes
+UBERON:0013615,koniocellular layer of dorsal nucleus of lateral geniculate body,UBERON:0013605,layer of lateral geniculate body
+UBERON:0004360,cauda epididymis,UBERON:0005156,reproductive structure
+DOID:1056,oculocerebrorenal syndrome,DOID:0050735,X-linked disease
+UBERON:0002788,anterior nuclear group,UBERON:0015233,nucleus of dorsal thalamus
+DOID:8138,thymus sarcomatoid carcinoma,DOID:3284,thymic carcinoma
+UBERON:0000975,sternum,UBERON:0005181,thoracic segment organ
+UBERON:0006858,adrenal/interrenal gland,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0000459,uterine wall,UBERON:0014404,female anatomical structure
+CL:0000090,female germ line stem cell (sensu Vertebrata),CL:0000085,germ line stem cell (sensu Vertebrata)
+HP:0012175,Resistance to activated protein C,HP:0003256,Abnormality of the coagulation cascade
+HP:0003312,Abnormal form of the vertebral bodies,HP:0003468,Abnormality of the vertebrae
+UBERON:0007230,lateral vestibular nucleus,UBERON:0007228,vestibular nucleus
+HP:0002048,Renal cortical atrophy,HP:0012585,Renal atrophy
+UBERON:3010060,centrale (fore),UBERON:0015049,carpus endochondral element
+UBERON:0014731,haversian canal,UBERON:0005744,bone foramen
+UBERON:0004904,nerve connecting eye with brain,UBERON:0001021,nerve
+CL:0002134,stromal cell of ovarian medulla,CL:0002132,stromal cell of ovary
+HP:0100218,Irregular epiphysis of the middle phalanx of the 5th toe,HP:0100098,Abnormality of the epiphysis of the middle phalanx of the 5th toe
+DOID:5569,malignant syringoma,DOID:4921,eccrine sweat gland cancer
+HP:0010397,Bullet-shaped proximal phalanx of the 2nd toe,HP:0010205,Bullet-shaped proximal phalanges of the toes
+UBERON:0010570,manual digit 1 metacarpus cartilage element,UBERON:0010699,manual digit metacarpus cartilage element
+HP:0010648,Dermal translucency,HP:0011121,Abnormality of skin morphology
+UBERON:0000151,pectoral fin,UBERON:0002534,paired fin
+UBERON:3010587,hyoid arch neural crest,UBERON:0002342,neural crest
+CL:0000246,Mauthner neuron,CL:0000099,interneuron
+DOID:0050354,infant botulism,DOID:11976,botulism
+UBERON:0004788,kidney pelvis urothelium,UBERON:0004819,kidney epithelium
+UBERON:0003548,forebrain meninges,UBERON:0003547,brain meninx
+HP:0100919,Sclerosis of the phalanges of the 3rd finger,HP:0100899,Sclerosis of the phalanges of the hand
+HP:0008111,Broad distal hallux,HP:0010055,Broad hallux
+UBERON:2001997,parietal-supraoccipital,UBERON:0008907,dermal bone
+UBERON:0006012,interdigital region,UBERON:0010858,inter limb-segment region
+DOID:13098,central retinal artery occlusion,DOID:8483,retinal artery occlusion
+UBERON:0006121,hemispheric lobule VIII,UBERON:0004003,cerebellum hemisphere lobule
+HP:0100101,Bracket epiphysis of the distal phalanx of the 2nd toe,HP:0100045,Bracket epiphyses of the 2nd toe
+DOID:7284,skene gland carcinoma,DOID:14059,paraurethral gland cancer
+HP:0006187,Fusion of midphalangeal joints,HP:0009773,Symphalangism affecting the phalanges of the hand
+HP:0003043,Abnormality of the shoulder,HP:0011844,Abnormal appendicular skeleton morphology
+UBERON:0001600,tensor tympani,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0004214,Curved phalanges of the 5th finger,HP:0004095,Curved fingers
+HP:0002209,Sparse scalp hair,HP:0008070,Sparse hair
+UBERON:0002113,kidney,UBERON:0006554,urinary system structure
+UBERON:0005335,chorioallantoic membrane,UBERON:0005631,extraembryonic membrane
+DOID:9893,periodontosis,DOID:1091,tooth disease
+CL:0000897,"CD4-positive, alpha-beta memory T cell",CL:0000813,memory T cell
+HP:0010472,Abnormality of the heme biosynthetic pathway,HP:0001939,Abnormality of metabolism/homeostasis
+HP:0100736,Abnormality of the soft palate,HP:0000174,Abnormality of the palate
+HP:0011386,Narrow internal auditory canal,HP:0011384,Abnormality of the internal auditory canal
+UBERON:0003286,foregut region of duodenum,UBERON:0004921,subdivision of digestive tract
+UBERON:0014635,dorsal nerve root of cervical spinal cord,UBERON:0009632,root of cervical nerve
+CL:0001016,immature CD1a-positive Langerhans cell,CL:0001014,CD1a-positive Langerhans cell
+DOID:0050465,Muir-Torre syndrome,DOID:3883,Lynch syndrome
+UBERON:4300006,scale row,UBERON:0000477,anatomical cluster
+UBERON:0014779,liver reticuloendothelial system,UBERON:0004119,endoderm-derived structure
+HP:0008442,Vertebral hyperostosis,HP:0100774,Hyperostosis
+HP:0009980,Complete duplication of the proximal phalanx of the 4th finger,HP:0009977,Duplication of the proximal phalanx of the 4th finger
+UBERON:0006984,anatomical surface,UBERON:0000466,immaterial anatomical entity
+DOID:7520,periductal breast myoepitheliosis,DOID:7521,breast myoepitheliosis
+HP:0006690,Myocardial calcification,HP:0011915,Cardiovascular calcification
+DOID:1115,sarcoma,DOID:0050687,cell type cancer
+DOID:13999,contact blepharoconjunctivitis,DOID:2456,blepharoconjunctivitis
+UBERON:0009861,ascidian neural complex,UBERON:0002530,gland
+UBERON:0016458,esophageal hiatus,UBERON:0000161,orifice
+UBERON:2000534,lateral longitudinal fasciculus,UBERON:2000318,brainstem and spinal white matter
+UBERON:0010243,merocrine gland,UBERON:0002530,gland
+UBERON:3010795,preopercular ramule,UBERON:3010765,ramus mandibularis externus
+DOID:1116,pertussis,DOID:0050339,commensal bacterial infectious disease
+UBERON:3010751,ramus muscularis of vagus nerve,UBERON:0000479,tissue
+HP:0010470,Supernumerary testes,HP:0000035,Abnormality of the testis
+UBERON:0002660,medial longitudinal fasciculus of midbrain,UBERON:0002309,medial longitudinal fasciculus
+UBERON:0002902,occipital pole,UBERON:0009899,pole of cerebral hemisphere
+HP:0011316,Left unicoronal synostosis,HP:0011318,Bicoronal synostosis
+UBERON:2001629,otic sensory canal,UBERON:2001612,sensory canal
+UBERON:3010519,Jacobson's vein,UBERON:0001638,vein
+DOID:2256,osteochondrodysplasia,DOID:0080006,bone development disease
+DOID:11231,orbital periostitis,DOID:11230,acute orbital inflammation
+UBERON:0009089,inner medulla vasa recta descending limb,UBERON:0000064,organ part
+NCBITaxon:6329,Trichocephalida,NCBITaxon:33218,Enoplia
+UBERON:0003546,distal convoluted tubule macula densa,UBERON:0002335,macula densa
+HP:0001795,Hyperconvex nail,HP:0002164,Nail dysplasia
+HP:0004251,Lunate-triquetral fusion,HP:0004248,Abnormality of the lunate bone
+UBERON:4200128,synarcual region of vertebral column,UBERON:0006077,subdivision of vertebral column
+DOID:845,cyclothymic disorder,DOID:3312,bipolar disorder
+UBERON:0002584,regional part of vestibular nuclear complex,UBERON:0002678,regional part of medulla oblongata
+HP:0200018,Protanomaly,HP:0000642,Red-green dyschromatopsia
+DOID:12799,mucopolysaccharidosis II,DOID:12798,mucopolysaccharidosis
+HP:0002958,Immune dysregulation,HP:0010978,Abnormality of immune system physiology
+CL:0000858,fast muscle myoblast,CL:0000515,skeletal muscle myoblast
+UBERON:0001715,oculomotor nuclear complex,UBERON:0003528,brain grey matter
+UBERON:2001810,supraorbital sensory canal,UBERON:2001612,sensory canal
+HP:0000540,Hypermetropia,HP:0000539,Abnormality of refraction
+HP:0011362,Abnormal hair quantity,HP:0001595,Abnormality of the hair
+DOID:8274,synovial angioma,DOID:469,deep angioma
+HP:0006799,Basal ganglia cysts,HP:0002134,Abnormality of the basal ganglia
+DOID:4513,gallbladder angiosarcoma,DOID:0001816,angiosarcoma
+DOID:0060037,developmental disorder of mental health,DOID:150,disease of mental health
+UBERON:0014704,pleuroperitoneal canal lumen,UBERON:0000464,anatomical space
+HP:0002149,Hyperuricemia,HP:0004368,Increased purine levels
+NCBITaxon:171,Leptospira,NCBITaxon:170,Leptospiraceae
+HP:0009670,Ivory epiphysis of the proximal phalanx of the thumb,HP:0009663,Abnormality of the epiphysis of the proximal phalanx of the thumb
+UBERON:0014791,musculature of forelimb stylopod,UBERON:0004474,musculature of arm
+HP:0011566,Cor triatriatum dexter,HP:0005120,Abnormality of cardiac atrium
+DOID:9821,choroideremia,DOID:1417,choroid disease
+UBERON:0001996,elastic cartilage tissue,UBERON:0011589,non-mineralized cartilage tissue
+NCBITaxon:772,Bartonellaceae,NCBITaxon:356,Rhizobiales
+UBERON:0014692,superficial epigastric vein,UBERON:0006356,epigastric vein
+DOID:9132,liver carcinoma in situ,DOID:8719,in situ carcinoma
+DOID:4955,central nervous system melanocytic neoplasm,DOID:3620,central nervous system cancer
+HP:0002267,Exaggerated startle response,HP:0002071,Abnormality of extrapyramidal motor function
+UBERON:0004994,mucosa of fundus of stomach,UBERON:0001199,mucosa of stomach
+HP:0003841,Fragmented epiphyses of the upper limbs,HP:0100168,Fragmented epiphyses
+CL:0002110,B220-low CD38-positive naive B cell,CL:0002109,B220-positive CD38-positive naive B cell
+DOID:14064,acute poststreptococcal glomerulonephritis,DOID:2921,glomerulonephritis
+UBERON:2002147,arrector muscle,UBERON:0001630,muscle organ
+UBERON:2001826,urohyal median process,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0001626,Abnormality of the cardiovascular system,HP:0000118,Phenotypic abnormality
+DOID:4777,exudative glomerulonephritis,DOID:2921,glomerulonephritis
+UBERON:0011309,body of mandible,UBERON:0005913,zone of bone organ
+HP:0007361,Abnormality of the pons,HP:0002363,Abnormality of the brainstem
+DOID:0060019,coronin-1A deficiency,DOID:627,severe combined immunodeficiency
+UBERON:0001018,axon tract,UBERON:0000122,neuron projection bundle
+HP:0001654,Abnormality of the heart valves,HP:0002564,Malformation of the heart and great vessels
+HP:0005267,Premature delivery because of cervical insufficiency or membrane fragility,HP:0001622,Premature birth
+UBERON:0006970,bony core of horn,UBERON:0004530,bony projection
+DOID:1542,head and neck carcinoma,DOID:11934,head and neck cancer
+UBERON:2000898,hypaxial region somite 26,UBERON:0003895,hypaxial myotome region
+HP:0100566,Amyelia,HP:0100561,Spinal cord lesions
+UBERON:0003640,pedal digit 1 phalanx,UBERON:0015031,pedal digit 1 phalanx endochondral element
+UBERON:3010770,dorsal sympathetic chain,UBERON:0000407,sympathetic trunk
+UBERON:0005797,bipartite uterus,UBERON:0000995,uterus
+UBERON:0002587,nucleus subceruleus,UBERON:0002308,nucleus of brain
+UBERON:0002664,lateral part of medial mammillary nucleus,UBERON:0003528,brain grey matter
+HP:0100229,Irregular epiphysis of the proximal phalanx of the 5th toe,HP:0100082,Irregular epiphyses of the 5th toe
+DOID:4685,lacrimal gland mucoepidermoid carcinoma,DOID:293,lacrimal gland carcinoma
+UBERON:2000286,superficial lateralis,UBERON:0001774,muscle of trunk
+UBERON:0001751,dentine,UBERON:0010365,odontoid tissue
+CL:0002004,"CD34-negative, GlyA-negative proerythroblast",CL:0000547,proerythroblast
+UBERON:0008342,intestinal villus of duodenum,UBERON:0001213,intestinal villus
+DOID:0060204,amyotrophic lateral sclerosis type 13,DOID:332,amyotrophic lateral sclerosis
+UBERON:0009869,Hatschek's right diverticulum,UBERON:0009867,Hatschek's diverticulum
+HP:0009425,Patchy sclerosis of the distal phalanx of the 3rd finger,HP:0009444,Patchy sclerosis of the phalanges of the 3rd finger
+UBERON:0004799,trachea basal lamina,UBERON:0004798,respiratory system basal lamina
+UBERON:0006664,greater palatine artery,UBERON:0001637,artery
+UBERON:0006654,perineal body,UBERON:0007651,anatomical junction
+UBERON:0008863,stomach smooth muscle outer longitudinal layer,UBERON:0004120,mesoderm-derived structure
+UBERON:0003604,trachea cartilage,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0011351,Moderate receptive language delay,HP:0010863,Receptive language delay
+HP:0001005,Dermatological manifestations of systemic disorders,HP:0011354,Generalized abnormality of skin
+UBERON:0011777,nucleus of spinal cord,UBERON:0001948,regional part of spinal cord
+HP:0007603,Freckles in sun-exposed areas,HP:0005586,Hyperpigmentation in sun-exposed areas
+UBERON:0009009,carotid sinus nerve,UBERON:0001021,nerve
+UBERON:2005067,bulbus arteriosus middle layer,UBERON:0000481,multi-tissue structure
+DOID:3247,rhabdomyosarcoma,DOID:4043,skeletal muscle cancer
+UBERON:2001274,coronomeckelian,UBERON:4000134,ossified tendon
+DOID:14248,chronic atticoantral disease,DOID:14247,chronic purulent otitis media
+NCBITaxon:6271,Pseudoterranova decipiens,NCBITaxon:6270,Pseudoterranova
+HP:0000276,Long face,HP:0001999,Abnormal facial shape
+UBERON:0009140,right subcardinal vein,UBERON:0006296,subcardinal vein
+UBERON:2000139,immature otolith,UBERON:0004121,ectoderm-derived structure
+CL:0002145,ciliated columnar cell of tracheobronchial tree,CL:0002202,epithelial cell of tracheobronchial tree
+UBERON:0002029,epithelium of gall bladder,UBERON:0000485,simple columnar epithelium
+UBERON:0003651,metatarsal bone of digit 2,UBERON:0015038,pedal digit 2 metatarsal endochondral element
+HP:0010854,EEG with generalized low amplitude activity,HP:0011201,EEG with changes in voltage
+HP:0006650,Thickening of the lateral border of the scapula,HP:0000782,Abnormality of the scapula
+UBERON:3000543,retroarticular process,UBERON:0004530,bony projection
+UBERON:0014485,distal phalanx of digit 3,UBERON:0004300,distal phalanx
+HP:0009463,Ulnar deviation of the 3rd finger,HP:0009465,Ulnar deviation of finger
+UBERON:2002249,ctenius,UBERON:0013703,integumentary projection
+HP:0000657,Oculomotor apraxia,HP:0000496,Abnormality of eye movement
+HP:0011500,Polycoria,HP:0000615,Abnormality of the pupil
+HP:0010521,Gait apraxia,HP:0001288,Gait disturbance
+UBERON:4300110,lateral ethmoid cartilage,UBERON:4300111,lateral ethmoid element
+UBERON:4300115,sucking disc,UBERON:0003097,dorsal fin
+DOID:7960,malignant spiradenoma,DOID:4921,eccrine sweat gland cancer
+DOID:6406,double outlet right ventricle,DOID:1657,ventricular septal defect
+UBERON:0010264,hepatopancreas,UBERON:0006925,digestive gland
+DOID:6423,childhood central nervous system mature teratoma,DOID:6017,central nervous system mature teratoma
+CL:0000376,humidity receptor cell,CL:0000006,neuronal receptor cell
+UBERON:0004508,skeletal muscle tissue of levator palpebrae superioris,UBERON:0003269,skeletal muscle tissue of eye
+UBERON:3010750,descending branch of the vagus nerve,UBERON:0000479,tissue
+DOID:4769,pleuropulmonary blastoma,DOID:4765,pulmonary blastoma
+HP:0100877,Renal diverticulum,HP:0004742,Abnormality of the renal collecting system
+DOID:12732,intermediate uveitis,DOID:13141,uveitis
+DOID:5621,histiocytic and dendritic cell cancer,DOID:2531,hematologic cancer
+UBERON:0007589,ciliated columnar oviduct epithelium,UBERON:0007592,ciliated columnar epithelium
+CL:0002285,type III taste bud cell,CL:1000428,stem cell of epidermis
+HP:0000836,Hyperthyroidism,HP:0002926,Abnormality of thyroid physiology
+UBERON:0006091,inferior horn of the lateral ventricle,UBERON:0010314,structure with developmental contribution from neural crest
+CL:1000300,fibroblast of outer membrane of prostatic capsule,CL:0000057,fibroblast
+HP:0003354,Hyperthreoninemia,HP:0003112,Abnormality of serum amino acid levels
+UBERON:0004053,external male genitalia,UBERON:0003135,male reproductive organ
+UBERON:0006860,swim bladder,UBERON:0000489,cavitated compound organ
+CL:0002462,adipose dendritic cell,CL:0000766,myeloid leukocyte
+HP:0000951,Abnormality of the skin,HP:0001574,Abnormality of the integument
+UBERON:0001956,cartilage of bronchus,UBERON:0003603,lower respiratory tract cartilage
+CL:1001598,small intestine glandular cell,CL:0000150,glandular epithelial cell
+UBERON:0014638,lumbar spinal cord dorsal horn,UBERON:0002256,dorsal horn of spinal cord
+UBERON:0001412,common palmar digital vein,UBERON:0004563,forelimb digital vein
+UBERON:0011358,infundibular organ,UBERON:0000073,regional part of nervous system
+HP:0009665,Bracket epiphysis of the proximal phalanx of the thumb,HP:0009663,Abnormality of the epiphysis of the proximal phalanx of the thumb
+UBERON:3000809,accessory articulation,UBERON:0000477,anatomical cluster
+UBERON:0005816,posterior tubercle of transverse process of cervical vertebra,UBERON:0005813,tubercle
+UBERON:0001126,serratus dorsalis superior muscle,UBERON:0011217,serratus dorsalis muscle
+HP:0100612,Odontogenic neoplasm,HP:0100649,Neoplasm of the oral cavity
+HP:0100518,Dysuria,HP:0000009,Functional abnormality of the bladder
+HP:0003142,Excessive purine production,HP:0004368,Increased purine levels
+UBERON:0005746,primary vitreous humour,UBERON:0000476,acellular anatomical structure
+UBERON:2005072,endocardial ring,UBERON:0000479,tissue
+HP:0008518,Aplasia/Hypoplasia involving the vertebral column,HP:0009122,Aplasia/Hypoplasia affecting bones of the axial skeleton
+HP:0007302,Bipolar affective disorder,HP:0000716,Depression
+HP:0100513,Vitamin E deficiency,HP:0100514,Abnormality of vitamin E metabolism
+HP:0008702,Absent internal genitalia,HP:0000812,Abnormal internal genitalia
+HP:0011147,Typical absence seizures,HP:0002121,Absence seizures
+DOID:2784,lung sarcoma,DOID:1324,lung cancer
+DOID:14451,hyperkalemic periodic paralysis,DOID:1029,familial periodic paralysis
+HP:0010151,Cone-shaped epiphysis of the 1st metatarsal,HP:0010125,Abnormality of the epiphysis of the 1st metatarsal
+CL:0000382,scolopidium,CL:0000378,support cell (sensu Nematoda and Protostomia)
+UBERON:0001575,extrinsic muscle of tongue,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0010852,fibula pre-cartilage condensation,UBERON:0010882,limb bone pre-cartilage condensation
+DOID:6477,invasive bladder transitional cell carcinoma,DOID:4006,bladder transitional cell carcinoma
+DOID:12804,mucopolysaccharidosis IV,DOID:12798,mucopolysaccharidosis
+HP:0010832,Abnormality of pain sensation,HP:0003474,Sensory impairment
+UBERON:0003475,ureteric vein,UBERON:0001638,vein
+UBERON:0014876,distal epiphysis of distal phalanx of pedal digit,UBERON:0011976,epiphysis of distal phalanx of pes
+HP:0009261,Absent epiphysis of the proximal phalanx of the 4th finger,HP:0009393,Absent epiphyses of the 4th finger
+UBERON:2005088,posterior mesenteric artery,UBERON:0005616,mesenteric artery
+HP:0100178,Stippling of the epiphysis of the distal phalanx of the 4th toe,HP:0100075,Stippling of the epiphyses of the 4th toe
+CL:0002660,luminal cell of acinus of lactiferous gland,CL:0002326,luminal epithelial cell of mammary gland
+HP:0100215,Cone-shaped epiphysis of the middle phalanx of the 5th toe,HP:0100098,Abnormality of the epiphysis of the middle phalanx of the 5th toe
+UBERON:4300117,pelvic fin soft ray,UBERON:2005228,segmented lepidotrichium
+UBERON:2105384,dorsal fin proximal radial element 7,UBERON:2100947,dorsal fin proximal radial element
+HP:0010041,Short 3rd metacarpal,HP:0010049,Short metacarpal
+UBERON:0001332,prepuce of penis,UBERON:0014403,male anatomical structure
+UBERON:0000946,cardial valve,UBERON:0003978,valve
+DOID:10112,sleeping sickness,DOID:10113,trypanosomiasis
+NCBITaxon:10335,Human herpesvirus 3,NCBITaxon:10319,Varicellovirus
+DOID:0000000,gallbladder disease,DOID:77,gastrointestinal system disease
+HP:0000727,Frontal lobe dementia,HP:0000726,Dementia
+UBERON:0008995,nucleus of cerebellar nuclear complex,UBERON:0009662,hindbrain nucleus
+UBERON:0011679,proximal tarsal bone,UBERON:0014395,proximal mesopodial bone
+CL:0000389,socket cell (sensu Nematoda),CL:0000619,support cell (sensu Nematoda)
+HP:0009635,Symphalangism of proximal phalanx of  thumb,HP:0009656,Symphalangism of the thumb
+UBERON:0002052,capsule of adrenal gland,UBERON:0003893,capsule
+DOID:7574,pancreatic intraductal papillary-colloid carcinoma,DOID:7575,pancreatic intraductal papillary-mucinous neoplasm
+DOID:3528,anterior cerebral artery infarction,DOID:3526,cerebral infarction
+UBERON:0007747,metacarpophalangeal joint of manual digit 5,UBERON:0003695,metacarpophalangeal joint
+UBERON:0008251,water vascular system,UBERON:0000467,anatomical system
+UBERON:0014679,distal interphalangeal joint of digit 4,UBERON:0009768,distal interphalangeal joint
+DOID:4206,childhood brain stem neoplasm,DOID:4203,brain stem cancer
+UBERON:2005415,inner ear foramen,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:705,leber hereditary optic neuropathy,DOID:1891,optic nerve disease
+DOID:5386,lung adenoma,DOID:3683,lung benign neoplasm
+UBERON:0001917,endothelium of artery,UBERON:0003915,endothelial tube
+HP:0003550,Predominantly lower limb lymphedema,HP:0001004,Lymphedema
+UBERON:0007764,paramedian reticular nucleus,UBERON:0007635,nucleus of medulla oblongata
+DOID:6872,spinal cord primitive neuroectodermal neoplasm,DOID:5612,spinal cancer
+HP:0011134,Low-grade fever,HP:0001945,Fever
+UBERON:0002270,hyaloid artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0008445,webbed pedal digit,UBERON:0008443,webbed digit
+HP:0100844,Pancreatic fistula,HP:0012090,Abnormality of pancreas morphology
+HP:0004097,Deviation of finger,HP:0009484,Deviation of the hand or of fingers of the hand
+DOID:7444,diffuse intraductal papillomatosis,DOID:2615,papilloma
+DOID:13910,red color blindness,DOID:13399,color blindness
+DOID:4915,basophilic carcinoma,DOID:4916,pituitary carcinoma
+CL:0011109,hypocretin-secreting neuron,CL:0000540,neuron
+UBERON:3010193,prepollical protuberances,UBERON:3000981,limb external integument structure
+UBERON:2001089,myoseptum,UBERON:0000476,acellular anatomical structure
+HP:0000139,Uterine prolapse,HP:0000130,Abnormality of the uterus
+UBERON:0006655,septum of scrotum,UBERON:0005156,reproductive structure
+HP:0002350,Cerebellar cyst,HP:0010576,Intracranial cystic lesion
+HP:0010645,Aplasia of the distal phalanges of the toes,HP:0010185,Aplasia/Hypoplasia of the distal phalanges of the toes
+DOID:12369,prolapse of urethra,DOID:732,urethral disease
+DOID:9478,postpartum depression,DOID:1595,endogenous depression
+UBERON:0007719,bone of reproductive structure,UBERON:0005156,reproductive structure
+DOID:8663,aryepiglottic fold cancer,DOID:8533,hypopharynx cancer
+CL:0000988,hematopoietic cell,CL:0002371,somatic cell
+UBERON:0004241,main bronchus smooth muscle,UBERON:0004242,bronchus smooth muscle
+UBERON:0011535,chondroglossus muscle,UBERON:0002385,muscle tissue
+CL:0000869,tonsillar macrophage,CL:0000884,mucosa-associated lymphoid tissue macrophage
+DOID:3260,spindle cell rhabdomyosarcoma,DOID:3246,embryonal rhabdomyosarcoma
+DOID:6706,tubular variant testicular seminoma,DOID:5842,testis seminoma
+NCBITaxon:3290,Polypodiopsida,NCBITaxon:241806,Moniliformopses
+HP:0007867,Restrictive partial external ophthalmoplegia,HP:0007936,Restrictive external ophthalmoplegia
+NCBITaxon:5811,Toxoplasma gondii,NCBITaxon:5810,Toxoplasma
+UBERON:0005721,pronephric mesoderm,UBERON:0000926,mesoderm
+UBERON:0008925,sublaminar layer S4,UBERON:0009736,sublaminar layers S3 or S4 or S5
+UBERON:0006594,chorda gubernaculum,UBERON:0006590,vestigial embryonic structure
+CL:1001580,hippocampus glial cell,CL:1001579,cerebral cortex glial cell
+HP:0002254,Intermittent diarrhea,HP:0002014,Diarrhea
+HP:0010483,Amniotic constriction rings of arms,HP:0009775,Amniotic constriction ring
+UBERON:0007243,tunica media of vein,UBERON:0002522,tunica media
+DOID:7578,breast scirrhous carcinoma,DOID:3459,breast carcinoma
+HP:0001260,Dysarthria,HP:0002167,Neurological speech impairment
+UBERON:0009091,vasa recta ascending limb,UBERON:0004120,mesoderm-derived structure
+UBERON:0001051,hypopharynx,UBERON:0004119,endoderm-derived structure
+UBERON:0004369,Reichert's membrane,UBERON:0000478,extraembryonic structure
+UBERON:0001155,colon,UBERON:0004921,subdivision of digestive tract
+UBERON:0004564,hindlimb digital vein,UBERON:0004562,digital vein
+HP:0009583,Curved proximal phalanx of the 2nd finger,HP:0009854,Curved proximal phalanges of the hand
+HP:0009453,Osteolytic defects of the proximal phalanx of the 3rd finger,HP:0009443,Osteolytic defects of the phalanges of the 3rd finger
+UBERON:3000012,angulosplenial coronoid process,UBERON:0004120,mesoderm-derived structure
+UBERON:0003665,tail muscle,UBERON:0004518,muscle of vertebral column
+DOID:14353,acute thyroiditis,DOID:7166,thyroiditis
+HP:0011808,Decreased patellar reflex,HP:0002600,Hyporeflexia of lower limbs
+UBERON:2002020,hypomaxilla,UBERON:0008907,dermal bone
+UBERON:0005286,tela choroidea of midbrain cerebral aqueduct,UBERON:0004121,ectoderm-derived structure
+UBERON:0001436,phalanx of manus,UBERON:0003607,forelimb long bone
+UBERON:0010547,pedal digit 1 metatarsal pre-cartilage condensation,UBERON:0010580,pedal digit 1 phalanx pre-cartilage condensation
+HP:0000833,Glucose intolerance,HP:0001952,Abnormal glucose tolerance
+DOID:3840,craniopharyngioma,DOID:0060090,central nervous system organ benign neoplasm
+DOID:0060156,visual verbal agnosia,DOID:0060155,visual agnosia
+UBERON:0010297,endochondral scleral ossicle,UBERON:0010290,scleral ossicle
+UBERON:2000261,pharyngohyoid,UBERON:0000933,pharyngeal muscle
+HP:0004502,Bilateral choanal atresia,HP:0000453,Choanal atresia
+HP:0011240,Prominent stem of antihelix,HP:0011244,Abnormality of stem of antihelix
+UBERON:0003243,epithelium of cochlear duct,UBERON:0006937,inner ear epithelium
+UBERON:2201613,dorsal fin middle radial cartilage,UBERON:2101613,dorsal fin middle radial element
+UBERON:0002870,dorsal motor nucleus of vagus nerve,UBERON:0011778,motor nucleus of vagal nerve
+CL:0000992,immature CD11c-low plasmacytoid dendritic cell,CL:0000989,CD11c-low plasmacytoid dendritic cell
+CL:0005010,renal intercalated cell,CL:0002518,kidney epithelial cell
+HP:0004273,Cupped metaphyses of hand bones,HP:0005923,Abnormalities of the metaphyses of the hand
+UBERON:0006692,vertebral canal,UBERON:0004111,anatomical conduit
+DOID:3071,gliosarcoma,DOID:3068,glioblastoma multiforme
+UBERON:0013707,iliac spine,UBERON:0004120,mesoderm-derived structure
+HP:0010680,Elevated alkaline phosphatase of renal origin,HP:0012211,Abnormal renal physiology
+HP:0009592,Astrocytoma,HP:0009733,Glioma
+UBERON:3010394,mesonephric late proximal tubule,UBERON:0006553,renal duct
+DOID:0050141,intestinal botulism,DOID:11976,botulism
+HP:0005215,Frequent Giardia lamblia infestation,HP:0004798,Recurrent infection of the gastrointestinal tract
+UBERON:0007373,inferior surface of tongue,UBERON:0007367,surface of tongue
+HP:0010430,Aplasia of the phalanges of the 2nd toe,HP:0010347,Aplasia/Hypoplasia of the phalanges of the 2nd toe
+CL:1001428,bladder urothelial cell,CL:1001319,bladder cell
+HP:0010506,Abnormal plantar dermatoglyphics,HP:0100872,Abnormality of the plantar skin of foot
+HP:0005302,Carotid artery tortuosity,HP:0005344,Abnormality of the carotid arteries
+UBERON:0008943,headfoot,UBERON:0000475,organism subdivision
+HP:0010330,Abnormality of the phalanges of the 3rd toe,HP:0010320,Abnormality of the 3rd toe
+HP:0002344,Progressive neurologic deterioration,HP:0001268,Mental deterioration
+UBERON:3000020,anterolateral process of frontoparietal,UBERON:0004121,ectoderm-derived structure
+UBERON:0009133,pleuroperitoneal membrane,UBERON:0005291,embryonic tissue
+HP:0009726,Renal neoplasm,HP:0000077,Abnormality of the kidney
+UBERON:0005881,limb outgrowth,UBERON:0002529,limb segment
+CL:0000202,auditory hair cell,CL:0002374,ear hair cell
+DOID:10040,malignant eyelid melanoma,DOID:8923,skin melanoma
+DOID:8428,breast apocrine carcinoma in situ,DOID:8791,breast carcinoma in situ
+HP:0003492,High urinary gonadotropins (primary hypogonadism),HP:0003117,Abnormality of circulating hormone level
+DOID:5379,hemoglobin E disease,DOID:2860,hemoglobinopathy
+HP:0005557,Abnormality of the zygomatic arch,HP:0000309,Abnormality of the midface
+CL:0000132,corneal endothelial cell,CL:0000076,squamous epithelial cell
+CL:0000510,paneth cell,CL:0000150,glandular epithelial cell
+UBERON:0007574,apical epidermal cap,UBERON:0007567,regenerating anatomical structure
+HP:0002928,Decreased activity of the pyruvate dehydrogenase (PDH) complex,HP:0003287,Abnormality of mitochondrial metabolism
+DOID:0050150,Pontiac fever,DOID:10458,legionellosis
+DOID:3846,adamantinous craniopharyngioma,DOID:3840,craniopharyngioma
+HP:0007201,Cerebral artery atherosclerosis,HP:0002621,Atherosclerosis
+DOID:7875,adult xanthogranuloma,DOID:4330,non-langerhans-cell histiocytosis
+HP:0005521,Disseminated intravascular coagulation,HP:0001977,Abnormal thrombosis
+UBERON:0003105,dorsal lateral plate region,UBERON:0004120,mesoderm-derived structure
+UBERON:3000908,sulcus distalis ossis cruris,UBERON:0000064,organ part
+DOID:3875,thrombophlebitis,DOID:864,phlebitis
+HP:0000035,Abnormality of the testis,HP:0000022,Abnormality of male internal genitalia
+UBERON:0005119,metanephric glomerular mesangium,UBERON:0002320,glomerular mesangium
+UBERON:0002191,subiculum,UBERON:0002791,regional part of telencephalon
+UBERON:3000467,preorbital process of the pars facialis of the maxilla,UBERON:4100000,skeletal element projection
+HP:0100060,Irregular epiphyses of the 3rd toe,HP:0010167,Irregular epiphyses of the toes
+UBERON:0001249,spleen lymphoid follicle,UBERON:0004120,mesoderm-derived structure
+CL:0000460,glucocorticoid secreting cell,CL:0000174,steroid hormone secreting cell
+UBERON:0002206,mammillary body,UBERON:0000064,organ part
+HP:0100960,Asymmetric ventricles,HP:0002118,Abnormality of the cerebral ventricles
+CL:0000842,mononuclear cell,CL:0002087,nongranular leukocyte
+HP:0000020,Urinary incontinence,HP:0000009,Functional abnormality of the bladder
+UBERON:2000337,basioccipital posterodorsal region,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001452,distal tarsal bone 1,UBERON:0015102,distal tarsal bone 1 endochondral element
+UBERON:0005392,cortical layer III,UBERON:0002301,layer of neocortex
+HP:0009642,Broad distal phalanx of the thumb,HP:0009836,Broad distal phalanx of finger
+UBERON:0012336,perianal skin,UBERON:0003836,abdominal segment skin
+UBERON:0004121,ectoderm-derived structure,UBERON:0000061,anatomical structure
+DOID:9053,bladder carcinoma in situ,DOID:8719,in situ carcinoma
+DOID:4233,clear cell sarcoma,DOID:1115,sarcoma
+HP:0001089,Iris atrophy,HP:0000525,Abnormality of the iris
+UBERON:0004924,submucosa of pharynx,UBERON:0004119,endoderm-derived structure
+HP:0100653,Optic neuritis,HP:0000587,Abnormality of the optic nerve
+DOID:8336,childhood choriocarcinoma of the ovary,DOID:6084,pediatric ovarian germ cell tumor
+UBERON:2101614,anal fin middle radial element,UBERON:2101671,anal fin radial element
+HP:0000542,Impaired ocular adduction,HP:0000496,Abnormality of eye movement
+DOID:4730,vasomotor rhinitis,DOID:4483,rhinitis
+UBERON:0003002,medial lemniscus,UBERON:0003001,lemniscus
+CL:0000953,preBCR-negative large pre-B-II cell,CL:0000957,large pre-B-II cell
+UBERON:2000589,sulcus ypsiloniformis,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0005531,Biphenotypic acute leukaemia,HP:0002488,Acute leukemia
+UBERON:0004776,inner renal medulla vasa recta,UBERON:0013126,vein of abdomen
+HP:0009675,Absent epiphysis of the distal phalanx of the thumb,HP:0009662,Abnormality of the epiphysis of the distal phalanx of the thumb
+UBERON:0005979,crista terminalis,UBERON:0000064,organ part
+UBERON:0001386,extensor digitorum longus,UBERON:0000311,extensor muscle
+UBERON:0003517,kidney blood vessel,UBERON:0006554,urinary system structure
+UBERON:4300026,anterior ventrolateral plate,UBERON:0007829,pectoral girdle bone
+HP:0100064,Stippling of the epiphyses of the 3rd toe,HP:0010329,Abnormality of the epiphyses of the 3rd toe
+HP:0001587,Primary ovarian failure,HP:0000137,Abnormality of the ovary
+NCBITaxon:10279,Molluscum contagiosum virus,NCBITaxon:10278,Molluscipoxvirus
+UBERON:0001193,hepatic artery,UBERON:0001637,artery
+HP:0010120,Pseudoepiphyses of the hallux,HP:0010056,Abnormality of the epiphyses of the hallux
+HP:0007654,Retinal striation,HP:0000479,Abnormality of the retina
+UBERON:0001757,pinna,UBERON:0001444,subdivision of head
+HP:0001308,Tongue fasciculations,HP:0010546,Muscle fibrillation
+DOID:10071,larynx squamous papilloma,DOID:2598,laryngeal benign neoplasm
+UBERON:0008834,prostomium,UBERON:0000914,organismal segment
+HP:0010029,Curved 1st metacarpal,HP:0009653,Curved phalanges of the thumb
+UBERON:2205380,dorsal fin proximal radial cartilage 3,UBERON:2200947,dorsal fin proximal radial cartilage
+HP:0008519,Abnormality of the coccyx,HP:0002644,Abnormality of pelvic girdle bone morphology
+UBERON:0003537,left lung alveolar duct,UBERON:0002173,pulmonary alveolar duct
+UBERON:0011774,utriculosaccular duct,UBERON:0000025,tube
+HP:0100108,Small epiphysis of the distal phalanx of the 2nd toe,HP:0100088,Abnormality of the epiphysis of the distal phalanx of the 2nd toe
+DOID:11164,band keratopathy,DOID:1237,corneal degeneration
+UBERON:0001891,midbrain,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0004172,Abnormality of the middle phalanx of the 3rd finger,HP:0009316,Abnormality of the phalanges of the 3rd finger
+NCBITaxon:83138,Anystina,NCBITaxon:6947,Prostigmata
+UBERON:0015784,duct of olfactory gland,UBERON:0004121,ectoderm-derived structure
+HP:0100283,EMG: continuous motor unit activity at rest,HP:0003457,EMG abnormality
+UBERON:0005196,spleen germinal center,UBERON:0004120,mesoderm-derived structure
+UBERON:3000661,crista vomeri,UBERON:0004120,mesoderm-derived structure
+HP:0010017,Cone-shaped epiphysis of the 1st metacarpal,HP:0009688,Cone-shaped epiphyses of the thumb
+CL:0000327,extracellular matrix secreting cell,CL:0000499,stromal cell
+UBERON:0002862,third sacral dorsal root ganglion,UBERON:0002837,sacral dorsal root ganglion
+UBERON:0005187,inner renal medulla collecting duct,UBERON:0005185,renal medulla collecting duct
+HP:0009122,Aplasia/Hypoplasia affecting bones of the axial skeleton,HP:0009121,Abnormal axial skeleton morphology
+UBERON:0003970,placental labyrinth vasculature,UBERON:0014404,female anatomical structure
+NCBITaxon:92251,Trombiculidae,NCBITaxon:92088,Trombiculoidea
+HP:0011911,Abnormality of metacarpophalangeal joint,HP:0001163,Abnormality of the metacarpal bones
+DOID:5726,uterine ligament papillary cystadenoma,DOID:5727,uterine ligament cancer
+UBERON:0003074,mesonephric duct,UBERON:0009201,nephric duct
+UBERON:3000155,extremitas anterior,UBERON:0000064,organ part
+DOID:2214,inherited blood coagulation disease,DOID:1247,blood coagulation disease
+DOID:603,AIDS phobia,DOID:0060048,nosophobia
+DOID:2494,angiodysplasia,DOID:178,vascular disease
+UBERON:0004390,epiphysis of metacarpal bone,UBERON:0004120,mesoderm-derived structure
+HP:0001103,Abnormality of the macula,HP:0000479,Abnormality of the retina
+HP:0002304,Akinesia,HP:0002374,Diminished movement
+DOID:5016,hepatocellular clear cell carcinoma,DOID:684,hepatocellular carcinoma
+DOID:841,extrinsic allergic alveolitis,DOID:3082,interstitial lung disease
+UBERON:0010937,salpingopharyngeus muscle,UBERON:0003831,respiratory system muscle
+UBERON:0002235,tubercle of rib,UBERON:0004120,mesoderm-derived structure
+CL:0002586,retinal pigment epithelial cell,CL:0000066,epithelial cell
+DOID:5861,myxoid chondrosarcoma,DOID:3371,chondrosarcoma
+HP:0002584,Intestinal bleeding,HP:0002239,Gastrointestinal hemorrhage
+HP:0009217,Enlarged epiphysis of the middle phalanx of the 4th finger,HP:0010260,Enlarged epiphyses of the middle phalanges of the hand
+HP:0001924,Sideroblastic anemia,HP:0010972,Anemia of inadequate production
+DOID:11695,portal vein thrombosis,DOID:272,hepatic vascular disease
+UBERON:0001019,nerve fasciculus,UBERON:0000122,neuron projection bundle
+HP:0002172,Postural instability,HP:0100022,Abnormality of movement
+UBERON:0013445,pterygomaxillary fissure,UBERON:0006800,anatomical line
+UBERON:4200029,adductor crest,UBERON:4100000,skeletal element projection
+UBERON:0000983,metatarsus region,UBERON:0008784,lower limb segment
+HP:0000044,Hypogonadotrophic hypogonadism,HP:0000135,Hypogonadism
+UBERON:0006983,anatomical point,UBERON:0000466,immaterial anatomical entity
+HP:0005017,polyarticular chondrocalcinosis,HP:0000934,Chondrocalcinosis
+HP:0010255,Stippling of the epiphyses of the distal phalanges of the hand,HP:0010237,Epiphyseal stippling of finger phalanges
+DOID:11671,hypotrichosis of eyelid,DOID:10120,eyelid degenerative disease
+DOID:8305,nonossifying fibromyxoid tumor,DOID:3350,mesenchymal cell neoplasm
+HP:0003213,Deficient excision of UV-induced pyrimidine dimers in DNA,HP:0004353,Abnormality of pyrimidine metabolism
+DOID:14683,Binder syndrome,DOID:2163,nasal cavity disease
+HP:0001116,Macular coloboma,HP:0001103,Abnormality of the macula
+DOID:8702,cheek mucosa cancer,DOID:8618,oral cavity cancer
+UBERON:0004639,afferent arteriole,UBERON:0003644,kidney arterial blood vessel
+DOID:4878,esophageal adenoid cystic carcinoma,DOID:1107,esophageal carcinoma
+UBERON:2005068,bulbus arteriosus inner layer,UBERON:0000481,multi-tissue structure
+CL:0000749,ON-bipolar cell,CL:0000748,retinal bipolar neuron
+UBERON:0011510,cloacal bursa,UBERON:0000064,organ part
+DOID:9169,Wiskott-Aldrich syndrome,DOID:0050735,X-linked disease
+UBERON:0005170,ovary stratum granulosum,UBERON:0014404,female anatomical structure
+DOID:4433,pancreatic delta cell neoplasm,DOID:1799,islet cell tumor
+HP:0100307,Cerebellar hemisphere hypoplasia,HP:0001321,Cerebellar hypoplasia
+HP:0010078,Bullet-shaped distal phalanx of the hallux,HP:0010060,Bullet-shaped phalanges of the hallux
+HP:0007517,Palmoplantar cutis laxa,HP:0007605,Excessive wrinkling of palmar skin
+HP:0006409,Progressive leg bowing,HP:0006383,Progressive bowing of long bones
+HP:0001191,Abnormality of the carpal bones,HP:0003019,Abnormality of the wrist
+CL:0000437,gonadtroph,CL:0000639,basophil cell of pars distalis of adenohypophysis
+UBERON:0009050,nucleus of solitary tract,UBERON:0007635,nucleus of medulla oblongata
+UBERON:0015252,coat hair follicle,UBERON:0002073,hair follicle
+HP:0000847,Abnormality of renin-angiotensin system,HP:0000818,Abnormality of the endocrine system
+UBERON:0013156,1st arch mandibular endoderm,UBERON:0005291,embryonic tissue
+DOID:8122,pseudovascular skin squamous cell carcinoma,DOID:3151,skin squamous cell carcinoma
+UBERON:4300017,rostrodermethmoid,UBERON:0011164,neurocranium bone
+DOID:14230,scleromalacia perforans,DOID:11343,scleral disease
+HP:0100031,Neoplasm of the thyroid gland,HP:0011772,Abnormality of thyroid morphology
+UBERON:0010962,extensor pre-muscle mass,UBERON:0004120,mesoderm-derived structure
+UBERON:3000677,lateral process of cricoid cartilage,UBERON:4100000,skeletal element projection
+UBERON:0004913,hepatopancreatic ampulla,UBERON:0003928,digestive system duct
+DOID:9988,tertiary neurosyphilis,DOID:8200,tertiary syphilis
+HP:0002974,Radioulnar synostosis,HP:0002997,Abnormality of the ulna
+CL:0011102,parasympathetic neuron,CL:0000107,autonomic neuron
+DOID:7088,columnar cell variant papillary carcinoma,DOID:3969,papillary thyroid carcinoma
+HP:0002133,Status epilepticus,HP:0001250,Seizures
+DOID:6997,intermediate cell type ciliary body melanoma,DOID:6524,malignant ciliary body melanoma
+UBERON:0002569,transverse temporal sulcus,UBERON:0013118,sulcus of brain
+HP:0001870,Acroosteolysis of distal phalanges (feet),HP:0010189,Osteolytic defects of the distal phalanges of the toes
+CL:0000912,helper T cell,CL:0000911,effector T cell
+UBERON:0004666,interventricular septum membranous part,UBERON:0010313,neural crest-derived structure
+HP:0010159,Triangular epiphysis of the 1st metatarsal,HP:0010123,Triangular epiphyses of the hallux
+UBERON:0010579,manual digit 5 phalanx pre-cartilage condensation,UBERON:0010586,manual digit phalanx pre-cartilage condensation
+HP:0008843,Hip osteoarthritis,HP:0002758,Osteoarthritis
+UBERON:0001149,bare area of liver,UBERON:0000466,immaterial anatomical entity
+UBERON:0004239,small intestine smooth muscle,UBERON:0004221,intestine smooth muscle
+HP:0001840,Metatarsus adductus,HP:0001832,Abnormality of the metatarsal bones
+HP:0100950,Long chain 3 hydroxyacyl coA dehydrogenase deficiency,HP:0010964,Abnormality of long-chain fatty-acid metabolism
+UBERON:0010255,3rd arch mesenchyme from neural crest,UBERON:0005690,3rd arch mesenchyme
+UBERON:0010330,eyelid mesenchyme,UBERON:0003314,eye mesenchyme
+HP:0012623,Stage 1 chronic kidney disease,HP:0012622,Chronic kidney disease
+UBERON:0010847,ulna pre-cartilage condensation,UBERON:0015003,ulna endochondral element
+UBERON:0010560,pedal digit 4 metatarsal cartilage element,UBERON:0015040,pedal digit 4 metatarsal endochondral element
+DOID:3354,fibrosarcoma of bone,DOID:3347,osteosarcoma
+DOID:6867,mediastinal gray zone lymphoma,DOID:6868,mediastinal malignant lymphoma
+UBERON:0002457,intersomitic artery,UBERON:0001637,artery
+HP:0000277,Abnormality of the mandible,HP:0011821,Abnormality of facial skeleton
+DOID:9261,nasopharynx carcinoma,DOID:0060119,pharynx cancer
+HP:0007308,Extrapyramidal dyskinesia,HP:0002071,Abnormality of extrapyramidal motor function
+HP:0001097,Keratoconjunctivitis sicca,HP:0001096,Keratoconjunctivitis
+UBERON:0014502,proximal phalanx of digit 2,UBERON:0004302,proximal phalanx
+HP:0003160,Abnormal isoelectric focusing of serum transferrin,HP:0012347,Abnormal protein N-linked glycosylation
+UBERON:0015064,autopod cartilage,UBERON:0015063,autopod endochondral element
+HP:0100380,Aplasia of the distal phalanx of the 5th toe,HP:0100371,Aplasia/Hypoplasia of the distal phalanx of the 5th toe
+DOID:5469,biliary tract intraductal papillary mucinous neoplasm,DOID:0050625,biliary tract neoplasm
+HP:0001433,Hepatosplenomegaly,HP:0001743,Abnormality of the spleen
+HP:0012556,Hyperbetaalaninemia,HP:0004337,Abnormality of amino acid metabolism
+UBERON:0010680,pedal digit 1 phalanx cartilage element,UBERON:0010562,pedal digit 1 mesenchyme
+UBERON:0014708,costal plate of carapace,UBERON:0015212,lateral structure
+HP:0004302,Functional motor problems.,HP:0011804,Abnormality of muscle physiology
+DOID:13641,exfoliation syndrome,DOID:12571,phacogenic glaucoma
+HP:0011338,Abnormality of mouth shape,HP:0000153,Abnormality of the mouth
+UBERON:0002127,inferior olivary complex,UBERON:0007245,nuclear complex of neuraxis
+NCBITaxon:7178,Culex tritaeniorhynchus,NCBITaxon:53527,Culex <subgenus>
+UBERON:2001659,upper pharyngeal tooth,UBERON:0004756,dermal skeletal element
+UBERON:0010950,styloauricular muscle,UBERON:0002376,cranial muscle
+UBERON:0005102,late distal convoluted tubule,UBERON:0012275,meso-epithelium
+UBERON:0013237,genital papilla of vulva,UBERON:0014404,female anatomical structure
+UBERON:0010573,manual digit 4 metacarpus cartilage element,UBERON:0010678,manual digit 4 phalanx cartilage element
+UBERON:0003028,commissure of inferior colliculus,UBERON:0005970,brain commissure
+UBERON:0005977,ansiform lobule crus II,UBERON:0014648,hemisphere part of cerebellar posterior lobe
+HP:0007893,Progressive retinal degeneration,HP:0000546,Retinal degeneration
+HP:0007801,Fishnet retinal pigmentation,HP:0011512,Hyperpigmentation of the fundus
+HP:0012046,Areflexia of upper limbs,HP:0001284,Areflexia
+UBERON:0005890,gonad germinal epithelium,UBERON:0004909,epithelium of gonad
+HP:0002100,Recurrent aspiration pneumonia,HP:0011951,Aspiration pneumonia
+UBERON:3000018,anterior ramus of pterygoid,UBERON:0010313,neural crest-derived structure
+HP:0000320,Bird-like facies,HP:0001999,Abnormal facial shape
+HP:0008577,Underfolded helix,HP:0008544,Abnormally folded helix
+DOID:6845,infiltrating ureter transitional cell carcinoma,DOID:6888,ureter transitional cell carcinoma
+UBERON:0011637,prearticular bone,UBERON:0008907,dermal bone
+DOID:0050818,transcobalamin II deficiency,DOID:0050731,vitamin B12 deficiency
+UBERON:0004086,brain ventricle,UBERON:0003947,brain ventricle/choroid plexus
+HP:0100003,Peritoneal mesothelioma,HP:0100016,Abnormality of the mesentery
+CL:0000738,leukocyte,CL:0000219,motile cell
+HP:0005063,"Fragmented, irregular epiphyses",HP:0010582,Irregular epiphyses
+UBERON:0003689,sella turcica,UBERON:0010313,neural crest-derived structure
+UBERON:2000980,somite 25,UBERON:0002329,somite
+HP:0001891,Iron deficiency anemia,HP:0001931,Hypochromic anemia
+UBERON:2002271,ventral caudal procurrent ray 2,UBERON:2001830,caudal fin ventral procurrent ray
+DOID:8567,Hodgkin's lymphoma,DOID:0060058,lymphoma
+NCBITaxon:10319,Varicellovirus,NCBITaxon:10293,Alphaherpesvirinae
+DOID:6579,chest wall bone cancer,DOID:184,bone cancer
+UBERON:0011899,epimysium,UBERON:0004120,mesoderm-derived structure
+HP:0010348,Broad phalanges of the 2nd toe,HP:0010324,Abnormality of phalanx of the 2nd toe
+CL:1000718,kidney inner medulla collecting duct principal cell,CL:1000547,kidney inner medulla collecting duct epithelial cell
+NCBITaxon:78536,Euphyllophyta,NCBITaxon:58023,Tracheophyta
+UBERON:0002277,spiral sulcus,UBERON:0000093,sulcus
+HP:0010426,Complete duplication of the middle phalanx of the 2nd toe,HP:0010429,Complete duplication of the phalanges of the 2nd toe
+HP:0003038,Fibular hypoplasia,HP:0006492,Aplasia/Hypoplasia of the fibula
+UBERON:2002280,pectoral fin distal radial bone 3,UBERON:2001588,pectoral fin distal radial bone
+UBERON:0010039,food storage organ,UBERON:0013765,digestive system organ
+NCBITaxon:121221,Pediculidae,NCBITaxon:30005,Anoplura
+UBERON:0001046,hindgut,UBERON:0004921,subdivision of digestive tract
+UBERON:0013278,canal of Nuck,UBERON:0014404,female anatomical structure
+HP:0009812,Amelia involving the upper limbs,HP:0006496,Aplasia/Hypoplasia involving bones of the upper limbs
+NCBITaxon:481,Neisseriaceae,NCBITaxon:206351,Neisseriales
+HP:0100136,Bracket epiphysis of the distal phalanx of the 3rd toe,HP:0100091,Abnormality of the epiphysis of the distal phalanx of the 3rd toe
+CL:0010020,cardiac glial cell,CL:0002494,cardiocyte
+UBERON:2100508,pelvic fin radial element,UBERON:1600006,paired fin radial element
+UBERON:0010571,manual digit 2 metacarpus cartilage element,UBERON:0010699,manual digit metacarpus cartilage element
+CL:0008001,hematopoietic precursor cell,CL:0000988,hematopoietic cell
+UBERON:1000010,mole,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010647,Abnormal elasticity of skin,HP:0011121,Abnormality of skin morphology
+UBERON:0010844,clavicle pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+DOID:7587,supraglottis squamous cell carcinoma,DOID:7763,carcinoma of supraglottis
+UBERON:2102277,pectoral fin distal radial element 1,UBERON:2101588,pectoral fin distal radial element
+DOID:6536,plasma cell neoplasm,DOID:706,mature B-cell neoplasm
+UBERON:0013655,elastica externa of notochord,UBERON:0004120,mesoderm-derived structure
+UBERON:0012401,small intestine smooth muscle circular layer,UBERON:0004120,mesoderm-derived structure
+DOID:2468,psychotic disorder,DOID:1561,cognitive disorder
+HP:0002161,Hyperlysinemia,HP:0003112,Abnormality of serum amino acid levels
+DOID:3417,glossopharyngeal nerve neoplasm,DOID:338,cranial nerve neoplasm
+HP:0100540,Palpebral edema,HP:0000492,Abnormality of the eyelid
+HP:0000185,Cleft soft palate,HP:0000202,Oral cleft
+HP:0002120,Cerebral cortical atrophy,HP:0002059,Cerebral atrophy
+UBERON:0001617,mental artery,UBERON:0003496,head blood vessel
+HP:0012041,Decreased fertility in males,HP:0000144,Decreased fertility
+UBERON:0003521,pes blood vessel,UBERON:0003516,hindlimb blood vessel
+UBERON:0004297,respiratory system blood vessel smooth muscle,UBERON:0004237,blood vessel smooth muscle
+UBERON:0013742,wall of crypt of lieberkuhn of large intestine,UBERON:0001278,epithelium of large intestine
+UBERON:0002120,pronephros,UBERON:0004120,mesoderm-derived structure
+CL:0000937,pre-natural killer cell,CL:0000623,natural killer cell
+UBERON:2001224,basibranchial 2 bone,UBERON:2001916,basibranchial 2 element
+UBERON:2000928,myotome somite 19,UBERON:0003082,myotome
+HP:0004250,Proximally placed lunate,HP:0004248,Abnormality of the lunate bone
+HP:0003429,CNS hypomyelination,HP:0011400,Abnormal CNS myelination
+HP:0004430,Severe combined immunodeficiency,HP:0005387,Combined immunodeficiency
+UBERON:0001480,proximal carpal bone,UBERON:0014395,proximal mesopodial bone
+HP:0004818,Paroxysmal nocturnal hemoglobinuria,HP:0003641,Hemoglobinuria
+HP:0000610,Abnormality of the choroid,HP:0001098,Abnormality of the fundus
+CL:0000289,chemotactic amoeboid cell (sensu Mycetozoa),CL:0000263,vegetative cell (sensu Mycetozoa)
+HP:0002444,Hypothalamic hamartoma,HP:0009731,Cerebral hamartomata
+DOID:11457,brain compression,DOID:936,brain disease
+HP:0001548,Overgrowth,HP:0001507,Growth abnormality
+CL:0002317,external limiting cell of vestibular epithelium,CL:0002316,supporting cell of vestibular epithelium
+HP:0007053,Pontocerebellar hypoplasia,HP:0001321,Cerebellar hypoplasia
+UBERON:0004924,submucosa of pharynx,UBERON:0004777,respiratory system submucosa
+HP:0002902,Hyponatremia,HP:0010931,Abnormality of sodium homeostasis
+UBERON:0002866,caudal part of spinal trigeminal nucleus,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:6977,pancreatic cholera,DOID:1428,endocrine pancreas disease
+UBERON:0010408,ocular angle artery,UBERON:0003496,head blood vessel
+HP:0009222,Small epiphysis of the middle phalanx of the 4th finger,HP:0009401,Small epiphyses of the 4th finger
+DOID:7050,thymus basaloid carcinoma,DOID:5530,thymus squamous cell carcinoma
+UBERON:0004233,lower respiratory tract smooth muscle,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0011317,Right unicoronal synostosis,HP:0011318,Bicoronal synostosis
+DOID:11232,orbital osteomyelitis,DOID:11230,acute orbital inflammation
+HP:0000609,Optic nerve hypoplasia,HP:0002977,Aplasia/Hypoplasia involving the central nervous system
+UBERON:0001652,left pulmonary artery,UBERON:0002012,pulmonary artery
+HP:0003938,Synostosis involving the elbow,HP:0100238,Synostosis involving bones of the upper limbs
+UBERON:0010253,1st arch maxillary mesenchyme from neural crest,UBERON:0010045,1st arch maxillary mesenchyme
+UBERON:0004950,submucosa of lobar bronchus,UBERON:0001957,submucosa of bronchus
+UBERON:0004457,cavity lining,UBERON:0004458,body cavity or lining
+HP:0009238,Aplasia of the 5th finger,HP:0009380,Aplasia of the fingers
+HP:0004227,Short distal phalanx of the 5th finger,HP:0009239,Aplasia/Hypoplasia of the distal phalanx of the 5th finger
+UBERON:3010614,cartilago lateralis of aryngo-tracheal chamber,UBERON:0001739,laryngeal cartilage
+CL:0000443,calcitonin secreting cell,CL:0000167,peptide hormone secreting cell
+HP:0100737,Abnormality of the hard palate,HP:0000174,Abnormality of the palate
+NCBITaxon:5152,Ophiostomataceae,NCBITaxon:5151,Ophiostomatales
+CL:0001044,"effector CD4-positive, alpha-beta T cell",CL:0000911,effector T cell
+UBERON:2000897,hypaxial region somite 23,UBERON:0003895,hypaxial myotome region
+HP:0100464,Patchy sclerosis of the proximal phalanx of the 3rd toe,HP:0100932,Sclerosis of the proximal phalanx of the 3rd toe
+DOID:2776,adamantinoma,DOID:184,bone cancer
+UBERON:0009972,ureteropelvic junction,UBERON:0006554,urinary system structure
+UBERON:0006960,ovary stroma,UBERON:0005156,reproductive structure
+HP:0009420,Triangular epiphyses of the 3rd finger,HP:0010238,Triangular epiphyses of the phalanges of the hand
+UBERON:0010204,tail vasculature,UBERON:0002049,vasculature
+HP:0100053,Stippling of the epiphyses of the 2nd toe,HP:0010171,Epiphyseal stippling of toe phalanges
+UBERON:0010697,pedal digit metatarsal cartilage element,UBERON:0010885,hindlimb cartilage element
+UBERON:0002952,intermediate acoustic stria,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0012287,Hypothalamic luteinizing hormone-releasing hormone deficiency,HP:0012285,Abnormal hypothalamus physiology
+HP:0009671,Pseudoepiphysis of the proximal phalanx of the thumb,HP:0009663,Abnormality of the epiphysis of the proximal phalanx of the thumb
+UBERON:0001321,obturator vein,UBERON:0001638,vein
+HP:0008591,Congenital conductive hearing impairment,HP:0000405,Conductive hearing impairment
+HP:0008204,Precocious puberty with Sertoli cell tumor,HP:0100619,Sertoli cell neoplasm
+HP:0005041,Irregular capital femoral epiphysis,HP:0010574,Abnormality of the epiphysis of the femoral head
+UBERON:0010212,laryngeal apparatus,UBERON:0000467,anatomical system
+HP:0009509,Pseudoepiphysis of the distal phalanx of the 2nd finger,HP:0009495,Pseudoepiphyses of the 2nd finger
+HP:0011043,Abnormality of circulating adrenocorticotropin level,HP:0003117,Abnormality of circulating hormone level
+DOID:1352,paranasal sinus disease,DOID:2825,nose disease
+CL:0000998,CD8_alpha-negative CD11b-negative dendritic cell,CL:0000766,myeloid leukocyte
+HP:0100634,Neuroendocrine neoplasm,HP:0100568,Neoplasm of the endocrine system
+UBERON:0010557,pedal digit 1 metatarsal cartilage element,UBERON:0010680,pedal digit 1 phalanx cartilage element
+UBERON:0002509,mesenteric lymph node,UBERON:0004120,mesoderm-derived structure
+HP:0011381,Aplasia of the semicircular canal,HP:0011380,Morphological abnormality of the semicircular canal
+UBERON:2002106,eminentia granularis,UBERON:0002946,regional part of cerebellum
+UBERON:0008861,pyloric gastric gland,UBERON:0000325,gastric gland
+HP:0000992,Cutaneous photosensitivity,HP:0011354,Generalized abnormality of skin
+HP:0100017,Capsular cataract,HP:0000518,Cataract
+DOID:2401,clitoris cancer,DOID:1245,vulva cancer
+DOID:12932,endomyocardial fibrosis,DOID:397,restrictive cardiomyopathy
+UBERON:0005698,pedal digit 4 mesenchyme,UBERON:0005255,pedal digit mesenchyme
+DOID:4776,rapidly progressive glomerulonephritis,DOID:2921,glomerulonephritis
+UBERON:0004848,respiratory system arterial endothelium,UBERON:0001917,endothelium of artery
+DOID:13025,retinopathy of prematurity,DOID:5679,retinal disease
+UBERON:0008803,skin of cheek,UBERON:1000021,skin of face
+DOID:3608,appendix adenocarcinoma,DOID:4902,appendix carcinoma
+UBERON:0015703,rostrum of corpus callosum,UBERON:0002791,regional part of telencephalon
+UBERON:0004179,prostate glandular acinus,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0001384,primary motor cortex,UBERON:0002619,regional part of cerebral cortex
+DOID:446,hyperaldosteronism,DOID:3947,adrenal gland hyperfunction
+DOID:12098,trigeminal neuralgia,DOID:561,trigeminal nerve disease
+CL:1001016,kidney loop of henle ascending limb epithelial cell,CL:1000909,kidney loop of henle epithelial cell
+HP:0001974,Leukocytosis,HP:0011893,Abnormal leukocyte count
+HP:0003490,Defective dehydrogenation of isovaleryl CoA and butyryl CoA,HP:0004357,Abnormality of leucine metabolism
+CL:0000582,neutrophilic metamyelocyte,CL:0002192,metamyelocyte
+HP:0100401,Duplication of the middle phalanx of the 3rd toe,HP:0010369,Abnormality of the middle phalanx of the 3rd toe
+UBERON:0004926,submucosa of cystic duct,UBERON:0004938,submucosa of biliary tree
+UBERON:0009709,ventral pancreas,UBERON:0002368,endocrine gland
+HP:0009139,Osteolysis involving bones of the lower limbs,HP:0002797,Osteolysis
+UBERON:0009868,Hatschek's left diverticulum,UBERON:0009867,Hatschek's diverticulum
+UBERON:0009971,principal gastric gland,UBERON:0000325,gastric gland
+HP:0010260,Enlarged epiphyses of the middle phalanges of the hand,HP:0010231,Enlarged epiphyses of the phalanges of the hand
+HP:0008499,High-grade hypermetropia,HP:0000540,Hypermetropia
+HP:0100918,Sclerosis of the phalanges of the 2nd finger,HP:0100899,Sclerosis of the phalanges of the hand
+UBERON:0007991,proximal sesamoid bone of manus,UBERON:0007997,sesamoid bone of manus
+HP:0011350,Mild receptive language delay,HP:0010863,Receptive language delay
+HP:0010420,Triangular shaped distal phalanx of the 2nd toe,HP:0010354,Triangular shaped phalanges of the 2nd toe
+HP:0002277,Horner syndrome,HP:0000508,Ptosis
+UBERON:0004446,epiphysis of phalanx,UBERON:0001437,epiphysis
+UBERON:0007794,serous fluid,UBERON:0007779,transduate
+HP:0008439,Lumbar hemivertebrae,HP:0002937,Hemivertebrae
+UBERON:2001604,lateral ethmoid palatine process,UBERON:4100000,skeletal element projection
+UBERON:0006277,pleuropericardial canals,UBERON:0005423,developing anatomical structure
+HP:0004233,Advanced ossification of carpal bones,HP:0006257,Abnormality of carpal bone ossification
+HP:0006880,Cerebellar hemangioblastoma,HP:0001317,Abnormality of the cerebellum
+DOID:3747,esophagus verrucous carcinoma,DOID:3748,esophagus squamous cell carcinoma
+UBERON:3010516,cutaneus magnus,UBERON:0001638,vein
+UBERON:0003605,eye skin gland,UBERON:0004859,eye gland
+DOID:2095,sweat gland cancer,DOID:4159,skin cancer
+UBERON:2005295,axial blood vessel,UBERON:2001073,axial vasculature
+UBERON:0013696,tonsil epithelium,UBERON:0003351,pharyngeal epithelium
+DOID:11355,bladder calculus,DOID:365,bladder disease
+UBERON:0002275,reticular formation,UBERON:0000073,regional part of nervous system
+UBERON:2000211,gill lamella,UBERON:0004119,endoderm-derived structure
+UBERON:0011830,duct of lesser vestibular gland,UBERON:0011831,duct of vestibular gland
+HP:0009194,Small epiphyses of the metacarpals,HP:0010585,Small epiphyses
+HP:0007302,Bipolar affective disorder,HP:0100754,Mania
+HP:0009464,Ulnar deviation of the 2nd finger,HP:0009465,Ulnar deviation of finger
+DOID:10250,louping ill,DOID:934,viral infectious disease
+DOID:5373,retroperitoneal hemangiopericytoma,DOID:264,hemangiopericytoma
+CL:0000016,male germ line stem cell,CL:0000014,germ line stem cell
+HP:0001031,Subcutaneous lipoma,HP:0001012,Multiple lipomas
+UBERON:0011576,supra-orbital ridge,UBERON:0008907,dermal bone
+UBERON:0010678,manual digit 4 phalanx cartilage element,UBERON:0005694,manual digit 4 mesenchyme
+UBERON:2000116,macula lagena,UBERON:0000054,macula
+HP:0008357,Reduced factor XIII activity,HP:0010990,Abnormality of the common coagulation pathway
+HP:0004387,Enterocolitis,HP:0004386,Gastrointestinal inflammation
+HP:0008541,Superiorly displaced ears,HP:0000357,Abnormal location of ears
+UBERON:0013139,ligament of liver,UBERON:0004119,endoderm-derived structure
+DOID:4671,freemartinism,DOID:1923,sex differentiation disease
+DOID:4251,conjunctival disease,DOID:5614,eye disease
+DOID:12002,trachea sarcoma,DOID:11920,tracheal cancer
+HP:0005571,Increased renal tubular phosphate reabsorption,HP:0011038,Abnormality of renal resorption
+UBERON:0003694,atlanto-axial joint,UBERON:0000982,skeletal joint
+UBERON:0008939,pedal ganglion,UBERON:0000045,ganglion
+HP:0010150,Bracket epiphysis of the 1st metatarsal,HP:0010125,Abnormality of the epiphysis of the 1st metatarsal
+HP:0006121,Acral ulceration leading to autoamputation of digits,HP:0007460,Autoamputation of digits
+HP:0000096,Glomerulosclerosis,HP:0000095,Abnormality of the glomerulus
+UBERON:0005370,hippocampus stratum lacunosum,UBERON:0002305,layer of hippocampus
+HP:0100335,Non-midline cleft lip,HP:0000204,Cleft upper lip
+UBERON:0008804,stylopharyngeus muscle,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0012071,palate bone,UBERON:0008907,dermal bone
+DOID:5782,tympanic membrane disease,DOID:5100,middle ear disease
+UBERON:2002017,anterior limb of ceratobranchial 5 bone,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0001136,Retinal arteriolar tortuosity,HP:0000630,Abnormality of retinal arteries
+CL:0000454,epinephrine secreting cell,CL:0000457,biogenic amine secreting cell
+HP:0000176,Submucous cleft hard palate,HP:0000175,Cleft palate
+HP:0002275,Poor motor coordination,HP:0011443,Abnormality of coordination
+HP:0010230,Cone-shaped epiphyses of the phalanges of the hand,HP:0010579,Cone-shaped epiphysis
+HP:0006576,Hepatic vascular malformations,HP:0006707,Abnormality of the hepatic vasculature
+UBERON:0002736,lateral nuclear group of thalamus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0002048,lung,UBERON:0005178,thoracic cavity organ
+DOID:12305,Bloch-Sulzberger syndrome,DOID:10123,pigmentation disease
+HP:0009666,Cone-shaped epiphysis of the proximal phalanx of the thumb,HP:0009663,Abnormality of the epiphysis of the proximal phalanx of the thumb
+CL:0002035,Slamf1-negative multipotent progenitor cell,CL:0000837,hematopoietic multipotent progenitor cell
+HP:0003413,Atlantoaxial abnormality,HP:0000925,Abnormality of the vertebral column
+UBERON:0001331,skin of penis,UBERON:0014403,male anatomical structure
+UBERON:3000538,recessus fenestrae ovalis,UBERON:0000064,organ part
+DOID:14270,ascending cholangitis,DOID:9446,cholangitis
+UBERON:0011904,gastrolith,UBERON:0000476,acellular anatomical structure
+DOID:2133,central nervous system sarcoma,DOID:3620,central nervous system cancer
+UBERON:0005815,anterior tubercle of transverse process of cervical vertebra,UBERON:0005813,tubercle
+HP:0009228,Bullet-shaped proximal phalanx of the 5th finger,HP:0009853,Bullet-shaped proximal phalanges of the hand
+UBERON:0002722,trochlear nucleus,UBERON:0000126,cranial nerve nucleus
+HP:0006492,Aplasia/Hypoplasia of the fibula,HP:0002991,Abnormality of the fibula
+UBERON:0011332,extrinsic tongue pre-muscle mass,UBERON:0004120,mesoderm-derived structure
+DOID:1386,abetalipoproteinemia,DOID:1387,hypolipoproteinemia
+CL:0000993,mature CD11c-low plasmacytoid dendritic cell,CL:0000989,CD11c-low plasmacytoid dendritic cell
+CL:0001046,memory CCR4-positive regulatory T cell,CL:0002678,memory regulatory T cell
+CL:1000699,kidney resident dendritic cell,CL:0001007,interstitial dendritic cell
+UBERON:0012485,cloacal villus,UBERON:0004923,organ component layer
+HP:0007906,Increased intraocular pressure,HP:0000501,Glaucoma
+HP:0011148,Absence seizures with special features,HP:0002121,Absence seizures
+UBERON:0006364,ureteric bud tip,UBERON:0007499,epithelial sac
+HP:0010808,Protruding tongue,HP:0000157,Abnormality of the tongue
+UBERON:0008924,sublaminar layer S3,UBERON:0009737,sublaminar layers S1 or S2 or S3 or S4
+UBERON:4200150,accessory foramina,UBERON:0004120,mesoderm-derived structure
+UBERON:2002018,anterior limb of ceratobranchial 5 cartilage,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0011649,levator operculi,UBERON:0001577,facial nerve muscle
+CL:1001036,vasa recta cell,CL:1000892,kidney capillary endothelial cell
+DOID:12803,Sly syndrome,DOID:12798,mucopolysaccharidosis
+UBERON:0011879,mesorchium,UBERON:0005156,reproductive structure
+UBERON:0011168,postfrontal bone,UBERON:0008907,dermal bone
+DOID:1468,labyrinthitis,DOID:3426,vestibular disease
+HP:0002707,Palate telangiectasia,HP:0000228,Oral cavity teleangiectasia
+UBERON:3000475,presumptive integument,UBERON:0006598,presumptive structure
+UBERON:2000693,tangential nucleus,UBERON:2000401,octaval nerve sensory nucleus
+UBERON:0004618,lumbar vertebra 2,UBERON:0002414,lumbar vertebra
+DOID:2538,Landau-Kleffner syndrome,DOID:0050704,childhood electroclinical syndrome
+UBERON:4300116,dorsal fin soft ray,UBERON:2005228,segmented lepidotrichium
+CL:0001013,mature interstitial dendritic cell,CL:0000841,mature conventional dendritic cell
+DOID:5567,ovarian germ cell teratoma,DOID:2156,ovarian germ cell cancer
+HP:0011175,Versive seizures,HP:0011167,Focal tonic seizures
+UBERON:3011120,early proximal tubule,UBERON:0002050,embryonic structure
+HP:0005093,Absent proximal radial epiphyses,HP:0010577,Absent epiphyses
+DOID:10778,fiedler's myocarditis,DOID:3951,acute myocarditis
+HP:0002557,Hypoplastic nipples,HP:0006709,Aplasia/Hypoplasia of the nipples
+DOID:3234,central nervous system lymphoma,DOID:3620,central nervous system cancer
+UBERON:0002377,muscle of neck,UBERON:0010959,craniocervical muscle
+HP:0000136,Bifid uterus,HP:0000130,Abnormality of the uterus
+CL:1000022,mesonephric nephron tubule epithelial cell,CL:1000494,epithelial cell of renal tubule
+HP:0004320,Vaginal fistula,HP:0000142,Abnormality of the vagina
+NCBITaxon:11628,Machupo virus,NCBITaxon:208897,New world arenaviruses
+DOID:0050600,ABCD syndrome,DOID:37,skin disease
+UBERON:0013754,integumentary system layer,UBERON:0004923,organ component layer
+DOID:8660,postcricoid region cancer,DOID:8533,hypopharynx cancer
+UBERON:0003562,midbrain dura mater,UBERON:0003288,meninx of midbrain
+HP:0008703,Gonadal calcification,HP:0000812,Abnormal internal genitalia
+DOID:4715,gastric neuroendocrine neoplasm,DOID:4148,gastrointestinal neuroendocrine benign tumor
+DOID:13374,fibrodysplasia ossificans progressiva,DOID:65,connective tissue disease
+DOID:13317,hyperinsulinemic hypoglycemia,DOID:2978,carbohydrate metabolic disorder
+HP:0010347,Aplasia/Hypoplasia of the phalanges of the 2nd toe,HP:0010324,Abnormality of phalanx of the 2nd toe
+UBERON:0001179,peritoneal cavity,UBERON:0002323,coelemic cavity lumen
+DOID:5583,lung giant cell carcinoma,DOID:4556,lung large cell carcinoma
+UBERON:0002728,entorhinal area,UBERON:0000064,organ part
+UBERON:0009585,interdigital region mesenchyme,UBERON:0009749,limb mesenchyme
+DOID:210,heel spur,DOID:203,exostosis
+UBERON:0006849,scapula,UBERON:0007829,pectoral girdle bone
+HP:0012734,Ketotic hypoglycemia,HP:0001943,Hypoglycemia
+UBERON:0007691,gustatory pore,UBERON:0004119,endoderm-derived structure
+HP:0009140,Synostosis involving bones of the feet,HP:0009138,Synostosis involving bones of the lower limbs
+UBERON:0009908,caudal root of abducens nerve,UBERON:0004121,ectoderm-derived structure
+UBERON:0011363,cranial lymph vasculature,UBERON:0004536,lymph vasculature
+DOID:1088,meningocele,DOID:0080016,spina bifida
+HP:0100216,Enlarged epiphysis of the middle phalanx of the 5th toe,HP:0100098,Abnormality of the epiphysis of the middle phalanx of the 5th toe
+UBERON:0009578,myelencephalon sulcus limitans,UBERON:0005478,sulcus limitans of neural tube
+UBERON:0006864,distal metaphysis of femur,UBERON:0006865,metaphysis of femur
+UBERON:0009898,left auditory cortex,UBERON:0015212,lateral structure
+UBERON:0009010,periurethral tissue,UBERON:0000479,tissue
+DOID:5003,eunuchism,DOID:1924,hypogonadism
+DOID:13911,achromatopsia,DOID:13399,color blindness
+UBERON:2000910,medial forebrain bundle telencephalon,UBERON:0003931,diencephalic white matter
+UBERON:0015142,falciform fat,UBERON:0003427,abdominal fat pad
+DOID:11343,scleral disease,DOID:5614,eye disease
+UBERON:0005869,maxillary process of inferior nasal concha,UBERON:0010313,neural crest-derived structure
+UBERON:0001262,wall of intestine,UBERON:0000328,gut wall
+HP:0011879,Decreased platelet glycoprotein Ib-IX-V,HP:0011878,Abnormal platelet membrane protein expression
+UBERON:0010020,tubotympanic recess epithelium,UBERON:0007499,epithelial sac
+NCBITaxon:46839,Colorado tick fever virus,NCBITaxon:10911,Coltivirus
+UBERON:0007830,pelvic girdle bone/zone,UBERON:0005913,zone of bone organ
+HP:0009676,Bracket epiphysis of the distal phalanx of the thumb,HP:0009662,Abnormality of the epiphysis of the distal phalanx of the thumb
+UBERON:3000859,foramen perforans carpi,UBERON:0005744,bone foramen
+UBERON:4300108,lepidotrichial segment,UBERON:0004120,mesoderm-derived structure
+UBERON:0005651,pedal digit 4 epithelium,UBERON:0005226,pedal digit epithelium
+DOID:12395,spastic entropion,DOID:12397,entropion
+HP:0008660,Renotubular dysgenesis,HP:0000091,Abnormality of the renal tubule
+CL:0002235,luminal cell of prostatic acinus,CL:0002340,luminal cell of prostate epithelium
+UBERON:0001331,skin of penis,UBERON:0005156,reproductive structure
+UBERON:0002150,superior cerebellar peduncle,UBERON:0007416,cerebellar peduncle
+UBERON:0010925,median thyrohyoid ligament,UBERON:0010921,thyrohyoid ligament
+CL:0002223,anterior lens cell,CL:0002224,lens epithelial cell
+HP:0010595,Abnormality of the distal fibular epiphysis,HP:0010593,Abnormality of fibular epiphyses
+UBERON:0007037,mechanosensory system,UBERON:0001032,sensory system
+UBERON:0009092,inner medulla vasa recta ascending limb,UBERON:0004120,mesoderm-derived structure
+HP:0009233,Triangular shaped proximal phalanx of the 5th finger,HP:0009858,Triangular shaped proximal phalanges of the hand
+HP:0009729,Cardiac rhabdomyoma,HP:0100544,Neoplasm of the heart
+UBERON:0005287,tela choroidea of fourth ventricle,UBERON:0004121,ectoderm-derived structure
+CL:0001032,cortical granule cell,CL:0000120,granule cell
+UBERON:0008882,spinal cord commissure,UBERON:0007699,tract of spinal cord
+DOID:5378,hemoglobin D disease,DOID:2860,hemoglobinopathy
+UBERON:2005338,posterior recess,UBERON:0000464,anatomical space
+UBERON:0010298,intramembranous scleral ossicle,UBERON:0010290,scleral ossicle
+UBERON:0006656,deep dorsal vein of penis,UBERON:0005156,reproductive structure
+HP:0001734,Annular pancreas,HP:0012090,Abnormality of pancreas morphology
+UBERON:0011060,perilymphatic channel,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2000399,secondary gustatory nucleus trigeminal nuclei,UBERON:0004132,trigeminal sensory nucleus
+UBERON:0005642,ultimobranchial body epithelium,UBERON:0005911,endo-epithelium
+UBERON:2001793,pharyngobranchial 4 bone uncinate process,UBERON:4100000,skeletal element projection
+UBERON:3000628,ventral ramus of squamosal,UBERON:0010313,neural crest-derived structure
+UBERON:0002863,fifth sacral dorsal root ganglion,UBERON:0002837,sacral dorsal root ganglion
+HP:0006470,Thin long bone diaphyses,HP:0006504,Anomaly of the limb diaphyses
+HP:0100887,Abnormality of globe size,HP:0012374,Abnormality of the globe
+CL:0002264,type A cell of stomach,CL:0002659,glandular cell of stomach
+DOID:11573,listeriosis,DOID:0050338,primary bacterial infectious disease
+HP:0003237,Increased IgG level,HP:0010702,Hypergammaglobulinemia
+DOID:3203,macrocystic neurilemmoma,DOID:3192,neurilemmoma
+HP:0006145,Central Y-shaped metacarpal,HP:0006042,Y-shaped metacarpals
+HP:0100419,Partial duplication of the middle phalanx of the 3rd toe,HP:0100401,Duplication of the middle phalanx of the 3rd toe
+DOID:790,ocular hypotension,DOID:5614,eye disease
+HP:0012534,Dysesthesia,HP:0003401,Paresthesia
+HP:0002773,Small vertebral bodies,HP:0003312,Abnormal form of the vertebral bodies
+UBERON:0000002,uterine cervix,UBERON:0014404,female anatomical structure
+UBERON:0003108,suspensorium,UBERON:0010912,subdivision of skeleton
+UBERON:0008291,down feather,UBERON:0000022,feather
+HP:0009510,Small epiphysis of the distal phalanx of the 2nd finger,HP:0010254,Small epiphyses of the distal phalanges of the hand
+HP:0000317,Facial myokymia,HP:0000301,Abnormality of facial musculature
+UBERON:0010403,cortical marginal zone,UBERON:0005423,developing anatomical structure
+UBERON:0001041,foregut,UBERON:0004921,subdivision of digestive tract
+DOID:11984,hypertrophic cardiomyopathy,DOID:0050736,autosomal dominant disease
+DOID:2673,cystic nephroma,DOID:3116,kidney benign neoplasm
+UBERON:3000469,presumptive central nervous system,UBERON:3000477,presumptive nervous system
+HP:0009384,Cone-shaped epiphyses of the 5th finger,HP:0010230,Cone-shaped epiphyses of the phalanges of the hand
+DOID:9253,gastrointestinal stromal tumor,DOID:3119,gastrointestinal system cancer
+HP:0100845,Anaphylactic shock,HP:0100326,Immunologic hypersensitivity
+DOID:8725,vascular dementia,DOID:1307,dementia
+UBERON:0012398,large intestine smooth muscle circular layer,UBERON:0004120,mesoderm-derived structure
+UBERON:0006649,suspensory ligament of ovary,UBERON:0008841,suspensory ligament
+HP:0012373,Abnormal eye physiology,HP:0000478,Abnormality of the eye
+HP:0002607,Bowel incontinence,HP:0012700,Abnormal large intestine physiology
+CL:0001011,immature interstitial dendritic cell,CL:0001007,interstitial dendritic cell
+UBERON:0007275,crista of ampulla of posterior semicircular duct of membranous laybrinth,UBERON:0003239,epithelium of posterior semicircular canal
+NCBITaxon:5593,Microascaceae,NCBITaxon:5592,Microascales
+HP:0005892,Proximal tibial and fibular fusion,HP:0005928,Synostosis involving the fibula
+HP:0010565,Aplasia/Hypoplasia of the Epiglottis,HP:0005483,Abnormality of the epiglottis
+HP:0000924,Abnormality of the skeletal system,HP:0000118,Phenotypic abnormality
+NCBITaxon:125204,mitosporic Dothioraceae,NCBITaxon:64899,Dothioraceae
+HP:0003678,Rapidly progressive,HP:0003679,Pace of progression
+HP:0011642,Abnormality of the coronary sinus,HP:0005120,Abnormality of cardiac atrium
+CL:0010006,cardiac blood vessel endothelial cell,CL:0010008,cardiac endothelial cell
+UBERON:0003106,urostyle,UBERON:0004120,mesoderm-derived structure
+UBERON:0012283,femoral fat pad,UBERON:0004266,upper leg connective tissue
+UBERON:2101588,pectoral fin distal radial element,UBERON:2101586,pectoral fin radial element
+UBERON:3010188,outer metacarpal tubercle,UBERON:0005813,tubercle
+HP:0011165,Visual auras,HP:0011157,Auras
+HP:0007481,Hyperpigmented nevi,HP:0000995,Melanocytic nevus
+UBERON:0004814,upper respiratory tract epithelium,UBERON:0004802,respiratory tract epithelium
+DOID:11315,African histoplasmosis,DOID:1731,histoplasmosis
+HP:0002665,Lymphoma,HP:0004377,Hematological neoplasm
+UBERON:0013617,upper primary molar tooth,UBERON:0003666,upper jaw molar
+CL:0000694,R3 photoreceptor cell,CL:0000287,eye photoreceptor cell
+HP:0002642,Arteriovenous fistulas of celiac and mesenteric vessels,HP:0002624,Venous abnormality
+HP:0005990,Thyroid hypoplasia,HP:0008188,Thyroid dysgenesis
+DOID:7319,axonal neuropathy,DOID:870,neuropathy
+HP:0100702,Arachnoid cyst,HP:0100700,Abnormality of the arachnoid mater
+HP:0011341,Long upper lip,HP:0000177,Abnormality of upper lip
+UBERON:0009641,ansa lenticularis,UBERON:0002791,regional part of telencephalon
+UBERON:3010525,frontoparietal fenestra,UBERON:3000051,braincase and otic capsule opening
+UBERON:0013487,epidermal ridge of digit,UBERON:0004121,ectoderm-derived structure
+UBERON:0001227,minor calyx,UBERON:0006517,kidney calyx
+UBERON:0012080,patella cartilage element,UBERON:0015022,hindlimb endochondral element
+UBERON:0003594,pelvis connective tissue,UBERON:0003838,abdominal segment connective tissue
+UBERON:0010574,manual digit 5 metacarpus cartilage element,UBERON:0010679,manual digit 5 phalanx cartilage element
+UBERON:0015082,proximal tarsal cartilage,UBERON:0010885,hindlimb cartilage element
+UBERON:0002772,olfactory sulcus,UBERON:0003022,cerebral cortex lobe
+HP:0009013,Congenital absence of gluteal muscles,HP:0001443,Abnormality of the gluteal musculature
+UBERON:0004381,skeleton of limb,UBERON:0010712,limb skeleton subdivision
+HP:0007024,Pseudobulbar paralysis,HP:0001260,Dysarthria
+HP:0006574,Hepatic arteriovenous malformation,HP:0100026,Arteriovenous malformation
+UBERON:3000036,basal process of palatoquadrate,UBERON:4100000,skeletal element projection
+CL:0002390,uninucleate blastconidium,CL:0002385,blastoconidium
+UBERON:0005271,juxtamedullary cortex,UBERON:0006554,urinary system structure
+HP:0003311,Hypoplasia of the odontoid process,HP:0008518,Aplasia/Hypoplasia involving the vertebral column
+DOID:14272,pericholangitis,DOID:9446,cholangitis
+UBERON:0016481,bronchial lymph node,UBERON:0000029,lymph node
+DOID:1907,malignant fibroxanthoma,DOID:4231,histiocytoma
+UBERON:0009692,lumen of pharyngotympanic tube,UBERON:0002558,organ cavity
+HP:0006251,Limited wrist extension,HP:0006248,Limited wrist movement
+HP:0002997,Abnormality of the ulna,HP:0002973,Abnormality of the forearm
+UBERON:0004775,outer renal medulla vasa recta,UBERON:0013126,vein of abdomen
+UBERON:0006632,musculo-phrenic artery,UBERON:0004573,systemic artery
+HP:0012150,Single lineage myelodysplasia,HP:0002863,Myelodysplasia
+HP:0007529,Hidrotic ectodermal dysplasia,HP:0000968,Ectodermal dysplasia
+HP:0001305,Dandy-Walker malformation,HP:0001320,Cerebellar vermis hypoplasia
+UBERON:2001864,basibranchial 1 cartilage,UBERON:2001915,basibranchial 1 element
+CL:1001100,kidney efferent arteriole smooth muscle cell,CL:1001066,kidney arteriole smooth muscle cell
+HP:0009007,Hypoplastic biceps,HP:0009782,Aplasia/Hypoplasia of the biceps
+UBERON:0013526,otocyst lumen,UBERON:0002553,anatomical cavity
+UBERON:2002257,premaxilla dentigerous process,UBERON:0010313,neural crest-derived structure
+HP:0011574,Imperforate atrioventricular valve,HP:0006705,Abnormality of the atrioventricular valves
+HP:0002788,Recurrent upper respiratory tract infections,HP:0001739,Abnormality of the nasopharynx
+HP:0009149,Triangular epiphysis of the distal phalanx of the 5th finger,HP:0009198,Abnormality of the epiphysis of the distal phalanx of the 5th finger
+DOID:10070,larynx leiomyoma,DOID:2598,laryngeal benign neoplasm
+HP:0012335,Abnormality of folate metabolism,HP:0004340,Abnormality of vitamin B metabolism
+UBERON:0012125,dermatological-muscosal system,UBERON:0000467,anatomical system
+CL:0000050,megakaryocyte-erythroid progenitor cell,CL:0002032,hematopoietic oligopotent progenitor cell
+UBERON:0009502,ventral mesentery of mesentery of foregut-midgut junction,UBERON:0009483,mesentery of foregut-midgut junction
+DOID:5015,hepatocellular fibrolamellar carcinoma,DOID:684,hepatocellular carcinoma
+DOID:9699,ophthalmia neonatorum,DOID:9700,bacterial conjunctivitis
+DOID:9700,bacterial conjunctivitis,DOID:6195,conjunctivitis
+UBERON:2000616,adductor profundus,UBERON:0011145,adductor muscle
+UBERON:0012087,air capillary of parabronchus,UBERON:0000061,anatomical structure
+DOID:12641,displacement of cardia through esophageal hiatus,DOID:12642,hiatus hernia
+UBERON:0014522,dorsolateral oculomotor nucleus,UBERON:0007414,nucleus of midbrain tegmentum
+HP:0100109,Stippling of the epiphysis of the distal phalanx of the 2nd toe,HP:0100088,Abnormality of the epiphysis of the distal phalanx of the 2nd toe
+UBERON:0003250,rectus capitis lateralis,UBERON:0004518,muscle of vertebral column
+UBERON:0012480,cloacal mucosa,UBERON:0000344,mucosa
+CL:0000533,primary motor neuron,CL:0000530,primary neuron
+UBERON:0015785,acinus of olfactory gland,UBERON:0004121,ectoderm-derived structure
+HP:0012364,Decreased urinary potassium,HP:0012598,Abnormal urine potassium concentration
+UBERON:2001577,premaxilla ascending process,UBERON:0004120,mesoderm-derived structure
+HP:0100453,Osteolytic defects of the middle phalanx of the 4th toe,HP:0010375,Osteolytic defects of the phalanges of the 4th toe
+UBERON:0013201,olfactory pathway,UBERON:0000122,neuron projection bundle
+HP:0009334,Abnormality of the epiphysis of the middle phalanx of the 3rd finger,HP:0009320,Abnormality of the epiphyses of the 3rd finger
+UBERON:2000704,ventral pelvic arrector,UBERON:0014795,pelvic appendage muscle
+CL:0000234,phagocyte,CL:0000473,defensive cell
+HP:0100329,Tarsometatarsal synostosis,HP:0008368,Tarsal synostosis
+UBERON:0003418,mesenchyme of submandibular gland,UBERON:0003324,mesenchyme of lower jaw
+DOID:13819,lymphogranuloma venereum,DOID:0050339,commensal bacterial infectious disease
+UBERON:0003662,forelimb muscle,UBERON:0014794,pectoral appendage muscle
+HP:0008242,Pseudohypoaldosteronism,HP:0011733,Abnormality of adrenal physiology
+UBERON:2001842,epihyal-ceratohyal joint,UBERON:0000982,skeletal joint
+HP:0009672,Small epiphysis of the proximal phalanx of the thumb,HP:0009663,Abnormality of the epiphysis of the proximal phalanx of the thumb
+DOID:3108,ascaridiasis,DOID:883,parasitic helminthiasis infectious disease
+DOID:9997,peripartum cardiomyopathy,DOID:12930,dilated cardiomyopathy
+UBERON:0013455,spheno-petrosal fissure,UBERON:0006800,anatomical line
+HP:0007200,Episodic hypersomnia,HP:0100786,Hypersomnia
+UBERON:0010889,ectethmoid,UBERON:0004120,mesoderm-derived structure
+UBERON:0000326,pancreatic juice,UBERON:0000456,bodily secretion
+DOID:2213,hemorrhagic disease,DOID:1247,blood coagulation disease
+DOID:4752,multiple system atrophy,DOID:0050890,synucleinopathy
+UBERON:0006256,knee joint primordium,UBERON:0002050,embryonic structure
+UBERON:0006590,vestigial embryonic structure,UBERON:0000061,anatomical structure
+UBERON:0012141,manual digitopodium region,UBERON:0005451,segment of manus
+DOID:3492,mixed connective tissue disease,DOID:854,collagen disease
+UBERON:0005800,segment of aorta,UBERON:0004120,mesoderm-derived structure
+UBERON:0016401,pancreaticoduodenal lymph node,UBERON:0015860,visceral abdominal lymph node
+HP:0001102,Angioid streaks of the retina,HP:0000479,Abnormality of the retina
+UBERON:0004645,urinary bladder urothelium,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0004914,duodenal papilla,UBERON:0000063,organ segment
+HP:0004661,Frontalis muscle weakness,HP:0010628,Facial palsy
+DOID:3919,pancreatic serous cystic neoplasm,DOID:1795,tumor of exocrine pancreas
+HP:0012387,Bronchitis,HP:0011947,Respiratory tract infection
+HP:0000912,Sprengel anomaly,HP:0000782,Abnormality of the scapula
+UBERON:0003326,mesenchyme of mammary gland,UBERON:0005156,reproductive structure
+DOID:0080053,Albright's hereditary osteodystrophy,DOID:4184,pseudohypoparathyroidism
+DOID:4845,pilomyxoid astrocytoma,DOID:3069,astrocytoma
+UBERON:3000676,bronchial process,UBERON:4100000,skeletal element projection
+DOID:0050292,primary systemic mycosis,DOID:0050136,systemic mycosis
+UBERON:3000662,processus posterior of parasphenoid,UBERON:0004120,mesoderm-derived structure
+HP:0006931,Lipoma of corpus callosum,HP:0001273,Abnormality of the corpus callosum
+HP:0006383,Progressive bowing of long bones,HP:0006487,Bowing of the long bones
+UBERON:0006845,abductor muscle,UBERON:0001630,muscle organ
+CL:0002167,olfactory epithelial cell,CL:0000098,sensory epithelial cell
+UBERON:2005256,intervillus pockets,UBERON:0000479,tissue
+HP:0011934,Mesenteric artery aneurysm,HP:0002636,Aneurysm of an abdominal artery
+DOID:9395,croup,DOID:1579,respiratory system disease
+DOID:2669,Pacinian tumor,DOID:962,neurofibroma
+DOID:2223,platelet storage pool deficiency,DOID:2218,blood platelet disease
+HP:0006641,Prominent floating ribs,HP:0000772,Abnormality of the ribs
+HP:0000479,Abnormality of the retina,HP:0001098,Abnormality of the fundus
+CL:0000190,fast muscle cell,CL:0008002,skeletal muscle fiber
+UBERON:0002374,metacarpal bone,UBERON:0015042,manual digit metacarpus endochondral element
+UBERON:0001930,paraventricular nucleus of hypothalamus,UBERON:0006568,hypothalamic nucleus
+UBERON:0005928,external naris,UBERON:0003102,surface structure
+UBERON:2000074,somite 26,UBERON:0002329,somite
+HP:0010830,Impaired tactile sensation,HP:0003474,Sensory impairment
+HP:0005466,Frontal bone hypoplasia,HP:0002692,Hypoplastic facial bones
+UBERON:0001504,lumbrical muscle of pes,UBERON:0014378,intrinsic muscle of pes
+HP:0007020,Progressive spastic paraplegia,HP:0001258,Spastic paraplegia
+HP:0009513,Absent epiphysis of the middle phalanx of the 2nd finger,HP:0010257,Absent epiphyses of the middle phalanges of the hand
+HP:0009195,Epiphyseal stippling of the metacarpals,HP:0010660,Abnormal hand bone ossification
+DOID:10247,pleurisy,DOID:1532,pleural disease
+UBERON:0002236,costal cartilage,UBERON:0004120,mesoderm-derived structure
+HP:0003265,Neonatal hyperbilirubinemia,HP:0002904,Hyperbilirubinemia
+UBERON:0005391,cortical layer II,UBERON:0002301,layer of neocortex
+DOID:0060132,amusia,DOID:4090,agnosia
+UBERON:0002454,dorsal metacarpal artery,UBERON:0001637,artery
+UBERON:0005295,sex cord,UBERON:0005154,epithelial cord
+UBERON:0015244,accessory olfactory bulb granule cell layer,UBERON:0004001,olfactory bulb layer
+UBERON:0004982,mucosa of epiglottis,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0006571,Reduced number of intrahepatic bile ducts,HP:0011040,Abnormality of the intrahepatic bile duct
+CL:0002518,kidney epithelial cell,CL:0000066,epithelial cell
+DOID:817,interstitial myocarditis,DOID:820,myocarditis
+DOID:2785,Dandy-Walker syndrome,DOID:2786,cerebellar disease
+HP:0100465,Patchy sclerosis of the proximal phalanx of the 4th toe,HP:0100933,Sclerosis of the proximal phalanx of the 4th toe
+UBERON:0013587,fused metacarpal bones 3 and 4,UBERON:0002374,metacarpal bone
+UBERON:0002298,brainstem,UBERON:0002616,regional part of brain
+UBERON:4200014,lateral tuber of ulna,UBERON:0004120,mesoderm-derived structure
+HP:0006781,Hurthle cell thyroid adenoma,HP:0000854,Thyroid adenoma
+UBERON:2201586,pectoral fin radial cartilage,UBERON:2101586,pectoral fin radial element
+CL:0011103,sympathetic neuron,CL:0000107,autonomic neuron
+UBERON:0011268,sublingua,UBERON:0004121,ectoderm-derived structure
+HP:0006129,Drumstick terminal phalanges,HP:0009832,Abnormality of the distal phalanx of finger
+HP:0008659,Multiple small medullary renal cysts,HP:0000107,Renal cyst
+UBERON:2001406,kinethmoid bone,UBERON:0008907,dermal bone
+UBERON:0003153,head capsule,UBERON:0000477,anatomical cluster
+UBERON:0003501,retina blood vessel,UBERON:0004121,ectoderm-derived structure
+DOID:882,heterophyiasis,DOID:883,parasitic helminthiasis infectious disease
+DOID:3491,Turner syndrome,DOID:14447,gonadal dysgenesis
+CL:0002278,GIP cell,CL:0000167,peptide hormone secreting cell
+HP:0007461,Hemangiomatosis,HP:0001028,Hemangioma
+HP:0004681,Deep longitudinal plantar crease,HP:0001869,Deep plantar creases
+CL:1000348,basal cell of epithelium of trachea,CL:0000307,tracheal epithelial cell
+HP:0002629,Gastrointestinal arteriovenous malformation,HP:0004296,Abnormality of gastrointestinal vasculature
+DOID:13382,megaloblastic anemia,DOID:2361,macrocytic anemia
+HP:0004962,Thoracic aorta calcification,HP:0004963,Calcification of the aorta
+CL:0000029,neuron neural crest derived,CL:0000540,neuron
+UBERON:0002350,conducting system of heart,UBERON:0010131,conducting tissue of heart
+UBERON:0014931,periungual skin,UBERON:0015249,digit skin
+UBERON:0001722,medial vestibular nucleus,UBERON:0007228,vestibular nucleus
+UBERON:0007690,early pharyngeal endoderm,UBERON:0004119,endoderm-derived structure
+UBERON:2001713,caudal principal ray 1,UBERON:2001585,caudal principal ray
+UBERON:0004536,lymph vasculature,UBERON:0002049,vasculature
+UBERON:0002977,triangular septal nucleus,UBERON:0009663,telencephalic nucleus
+UBERON:0001295,endometrium,UBERON:0005156,reproductive structure
+HP:0100139,Fragmentation of the epiphysis of the distal phalanx of the 3rd toe,HP:0100091,Abnormality of the epiphysis of the distal phalanx of the 3rd toe
+UBERON:0000144,trochlea of humerus,UBERON:0004120,mesoderm-derived structure
+HP:0002097,Emphysema,HP:0002088,Abnormality of the lung
+HP:0100106,Ivory epiphysis of the distal phalanx of the 2nd toe,HP:0100088,Abnormality of the epiphysis of the distal phalanx of the 2nd toe
+DOID:4112,cervical carcinosarcoma,DOID:4362,cervical cancer
+HP:0004037,Abnormality of the ulnar epiphyses,HP:0002997,Abnormality of the ulna
+CL:0000734,embryonic gland plasmatocyte,CL:0000736,embryonic gland hemocyte
+HP:0006450,Multicentric ossification of proximal femoral epiphyses,HP:0009107,Abnormal ossification involving the femoral head and neck
+UBERON:0011221,ora serrata of retina,UBERON:0004121,ectoderm-derived structure
+DOID:3502,ampulla of Vater adenocarcinoma,DOID:4932,ampulla of Vater carcinoma
+UBERON:4200016,postbranchial lamina,UBERON:0004120,mesoderm-derived structure
+UBERON:0014705,median lingual swelling epithelium,UBERON:0003929,gut epithelium
+DOID:7089,tall cell variant papillary carcinoma,DOID:3969,papillary thyroid carcinoma
+UBERON:0015109,distal tarsal bone 3 cartilage,UBERON:0015108,distal tarsal bone 3 endochondral element
+UBERON:0005691,4th arch mesenchyme,UBERON:0009494,pharyngeal arch mesenchymal region
+UBERON:0014707,hyoplastron,UBERON:0015212,lateral structure
+DOID:461,muscle benign neoplasm,DOID:423,myopathy
+CL:0002489,double negative thymocyte,CL:0000893,thymocyte
+UBERON:2001223,basibranchial 1 bone,UBERON:0004740,basibranchial bone
+HP:0100472,Symphalangism affecting the middle phalanx of the 5th toe,HP:0010389,Symphalangism affecting the phalanges of the 5th toe
+DOID:4084,testicular trophoblastic tumor,DOID:4087,testicular pure germ cell tumor
+UBERON:0005101,early distal convoluted tubule,UBERON:0012275,meso-epithelium
+HP:0007096,Hypoplasia of the optic tract,HP:0011000,Aplasia/Hypoplasia of the optic tract
+UBERON:0001634,mesencephalic artery,UBERON:0001637,artery
+UBERON:0005034,mucosa of right main bronchus,UBERON:0005036,mucosa of main bronchus
+UBERON:0011218,spinalis cervicis muscle,UBERON:0011013,spinalis muscle
+UBERON:0002448,fungiform papilla,UBERON:0014389,gustatory papilla of tongue
+HP:0003086,Acromesomelia,HP:0003027,Mesomelia
+DOID:2516,intracranial cavernous angioma,DOID:483,cavernous hemangioma
+NCBITaxon:41831,Psychodoidea,NCBITaxon:43787,Psychodomorpha
+DOID:14464,neuroleptic malignant syndrome,DOID:481,central nervous system hereditary degenerative disease
+HP:0000832,Primary hypothyroidism,HP:0000821,Hypothyroidism
+HP:0004220,Short middle phalanx of the 5th finger,HP:0009237,Short 5th finger
+UBERON:0011677,trunk vertebra,UBERON:0004451,trunk or cervical vertebra
+DOID:4035,lymphocytic gastritis,DOID:4029,gastritis
+HP:0005237,Degenerative liver disease,HP:0001392,Abnormality of the liver
+UBERON:2007008,ventral intermandibularis anterior,UBERON:0001630,muscle organ
+HP:0004278,Synostosis involving bones of the hand,HP:0100238,Synostosis involving bones of the upper limbs
+UBERON:3010094,quadratoethmoid process,UBERON:0004121,ectoderm-derived structure
+UBERON:0004529,anatomical projection,UBERON:0000063,organ segment
+DOID:0050268,ophthalmomyiasis,DOID:11080,myiasis
+UBERON:0005455,interventricular groove,UBERON:0006846,surface groove
+HP:0002395,Lower limb hyperreflexia,HP:0001347,Hyperreflexia
+HP:0100792,Acantholysis,HP:0011124,Abnormality of epidermal morphology
+UBERON:0000160,intestine,UBERON:0004921,subdivision of digestive tract
+UBERON:0009121,vomeronasal nerve,UBERON:0004121,ectoderm-derived structure
+DOID:1909,melanoma,DOID:0050687,cell type cancer
+UBERON:0008436,thoracic vertebral arch,UBERON:0004247,bone of dorsum
+DOID:6517,clivus meningioma,DOID:4211,posterior cranial fossa meningioma
+DOID:10699,paragonimiasis,DOID:883,parasitic helminthiasis infectious disease
+UBERON:0000931,proctodeum,UBERON:0004121,ectoderm-derived structure
+UBERON:0006248,incus pre-cartilage condensation,UBERON:0015017,incus endochondral element
+HP:0010655,Epiphyseal stippling,HP:0010656,Abnormal epiphyseal ossification
+UBERON:0013169,vestibular ligament,UBERON:0006325,laryngeal intrinsic ligament
+HP:0001712,Left ventricular hypertrophy,HP:0001714,Ventricular hypertrophy
+CL:1000337,enterocyte of epithelium of duodenal gland,CL:0000584,enterocyte
+DOID:2457,giant papillary conjunctivitis,DOID:2458,papillary conjunctivitis
+HP:0000217,Xerostomia,HP:0100755,Abnormality of salivation
+UBERON:4300028,posterior ventrolateral plate,UBERON:0007829,pectoral girdle bone
+DOID:5394,prolactinoma,DOID:5395,functioning pituitary adenoma
+UBERON:0002128,superior olivary complex,UBERON:0007245,nuclear complex of neuraxis
+UBERON:0006608,corpus cavernosum clitoridis,UBERON:0006609,corpus cavernosum
+UBERON:0006791,superficial layer of superior colliculus,UBERON:0006783,layer of superior colliculus
+UBERON:2000422,retroarticular,UBERON:0002513,endochondral bone
+CL:1000719,kidney inner medulla collecting duct intercalated cell,CL:1000547,kidney inner medulla collecting duct epithelial cell
+UBERON:0005015,mucosa of prostatic urethra,UBERON:0005013,mucosa of male urethra
+UBERON:0004741,cleithrum,UBERON:0008907,dermal bone
+UBERON:0000172,vomit,UBERON:0000463,portion of organism substance
+DOID:5815,cerebral lymphoma,DOID:368,cerebrum cancer
+HP:0011668,Bilateral superior vena cava with no bridging vein,HP:0005301,Persistent left superior vena cava
+HP:0008468,Abnormal sacral segmentation,HP:0003422,Vertebral segmentation defect
+HP:0007707,Congenital primary aphakia,HP:0008063,Aplasia/Hypoplasia of the lens
+UBERON:3010704,levator mandibulae longus,UBERON:0011648,jaw muscle
+CL:0000405,neuroepidermoblast,CL:0000338,neuroblast (sensu Nematoda and Protostomia)
+DOID:13249,pneumatosis cystoides intestinalis,DOID:5295,intestinal disease
+UBERON:2002164,caudal principal ray set,UBERON:0000477,anatomical cluster
+HP:0006499,Abnormality of femoral epiphyses,HP:0002823,Abnormality of the femur
+CL:0000337,neuroblast (sensu Vertebrata),CL:0000031,neuroblast
+UBERON:0005619,secondary palatal shelf,UBERON:0004121,ectoderm-derived structure
+HP:0010351,Osteolytic defects of the phalanges of the 2nd toe,HP:0010177,Osteolytic defects of the phalanges of the toes
+DOID:4880,kidney clear cell sarcoma,DOID:4242,kidney sarcoma
+HP:0000321,Square face,HP:0001999,Abnormal facial shape
+CL:0002397,"CD14-positive, CD16-positive monocyte",CL:0001054,CD14-positive monocyte
+UBERON:0004021,spongiotrophoblast layer,UBERON:0014404,female anatomical structure
+UBERON:0002219,subfornical organ,UBERON:0002663,septal nuclear complex
+HP:0001093,Optic nerve dysplasia,HP:0000587,Abnormality of the optic nerve
+HP:0009579,Proximal/middle symphalangism of the 2nd finger,HP:0009574,Symphalangism of middle phalanx of 2nd finger
+UBERON:2005126,intestinal bulb epithelium,UBERON:0001277,intestinal epithelium
+CL:0002457,epidermal Langerhans cell,CL:0002465,CD11b-positive dendritic cell
+HP:0000565,Esotropia,HP:0000486,Strabismus
+HP:0002020,Gastroesophageal reflux,HP:0002031,Abnormality of the esophagus
+UBERON:0010726,os vesalianum manus,UBERON:0001481,distal carpal bone
+HP:0010818,Generalized tonic seizures,HP:0002197,Generalized seizures
+UBERON:0010750,prefrontal bone,UBERON:0008907,dermal bone
+UBERON:0004096,odontoid process of cervical vertebra 2,UBERON:0004530,bony projection
+HP:0010398,Curved proximal phalanx of the 2nd toe,HP:0010350,Curved phalanges of the 2nd toe
+HP:0011496,Corneal neovascularization,HP:0000481,Abnormality of the cornea
+UBERON:0006183,mesonephric glomerular capillary,UBERON:0004212,glomerular capillary
+UBERON:0003611,respiratory system elastic tissue,UBERON:0002521,elastic tissue
+UBERON:0005493,hyoid muscle,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:3110,papillary cystadenocarcinoma,DOID:3111,cystadenocarcinoma
+CL:0002398,"Gr1-positive, CD43-positive monocyte",CL:0001022,CD115-positive monocyte
+DOID:10772,thrombotic thrombocytopenic purpura,DOID:2452,thrombophilia
+DOID:6103,thoracic spinal canal and spinal cord meningioma,DOID:1140,spinal canal and spinal cord meningioma
+HP:0009980,Complete duplication of the proximal phalanx of the 4th finger,HP:0010000,Complete duplication of the proximal phalanges of the hand
+HP:0007691,Short curly eyelashes,HP:0000499,Abnormality of the eyelashes
+CL:1000385,type 2 vestibular sensory cell of epithelium of crista of ampulla of semicircular duct of membranous labyrinth,CL:0002069,type II vestibular sensory cell
+HP:0008297,Transient hyperphenylalaninemia,HP:0010893,Abnormality of phenylalanine metabolism
+CL:0000547,proerythroblast,CL:0002242,nucleate cell
+HP:0100508,Abnormality of vitamin metabolism,HP:0001939,Abnormality of metabolism/homeostasis
+HP:0100779,Urogenital sinus anomaly,HP:0000795,Abnormality of the urethra
+UBERON:3010517,ventral abdominal vein,UBERON:0001638,vein
+UBERON:0002124,medulla of thymus,UBERON:0000958,medulla of organ
+HP:0004293,Synostosis of second metacarpal-trapezoid,HP:0009702,Carpal synostosis
+HP:0100963,Hyperesthesia,HP:0000763,Sensory neuropathy
+CL:0000934,"CD4-positive, alpha-beta cytotoxic T cell",CL:0000624,"CD4-positive, alpha-beta T cell"
+HP:0007554,Confetti hypopigmentation pattern of lower leg skin,HP:0001010,Hypopigmentation of the skin
+UBERON:2000929,myotome somite 21,UBERON:0003082,myotome
+DOID:10399,seminal vesicle chronic gonorrhea,DOID:10400,gonococcal seminal vesiculitis
+DOID:4415,fibrous histiocytoma,DOID:4231,histiocytoma
+UBERON:0004114,tympanic cavity,UBERON:0005082,tube lumen
+UBERON:0004791,thymus trabecula,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+CL:0001030,CD117-positive common myeloid progenitor OR CD217-positive common lymphoid progenitor,CL:0001060,"hematopoietic oligopotent progenitor cell, lineage-negative"
+HP:0010370,Abnormality of the proximal phalanx of the 3rd toe,HP:0010184,Abnormality of the proximal phalanges of the toes
+UBERON:0001742,epiglottic cartilage,UBERON:0013765,digestive system organ
+HP:0004003,Medially flattened radial epiphyses,HP:0004002,Flattened radial epiphyses
+UBERON:0001897,dorsal plus ventral thalamus,UBERON:0002784,regional part of diencephalon
+UBERON:0008838,metapodial pad,UBERON:0012348,autopod pad
+DOID:9273,citrullinemia,DOID:9267,urea cycle disorder
+DOID:11717,neonatal diabetes mellitus,DOID:9351,diabetes mellitus
+CL:0002222,vertebrate lens cell,CL:0000066,epithelial cell
+UBERON:0000102,lung vasculature,UBERON:0002201,vasculature of trunk
+UBERON:2001619,post-otic sensory canal,UBERON:2001612,sensory canal
+HP:0009720,Adenoma sebaceum,HP:0011799,Abnormality of facial soft tissue
+UBERON:0009580,diencephalon mantle layer,UBERON:0005883,neural tube lateral wall mantle layer
+UBERON:0010551,pedal digit 5 metatarsal pre-cartilage condensation,UBERON:0015041,pedal digit 5 metatarsal endochondral element
+UBERON:3000078,cartilago prootico-occipitalis,UBERON:0003933,cranial cartilage
+HP:0005607,Abnormality of the tracheobronchial system,HP:0002087,Abnormality of the upper respiratory tract
+UBERON:0012402,small intestine smooth muscle longitudinal layer,UBERON:0004120,mesoderm-derived structure
+UBERON:0004478,musculature of larynx,UBERON:0004119,endoderm-derived structure
+UBERON:3000414,pars palatina of premaxilla,UBERON:0010313,neural crest-derived structure
+UBERON:0000972,antenna,UBERON:0000026,appendage
+HP:0003758,Reduced subcutaneous adipose tissue,HP:0009124,Abnormality of adipose tissue
+DOID:8369,adult malignant schwannoma,DOID:5940,malignant peripheral nerve sheath tumor
+UBERON:0007241,tunica adventitia of vein,UBERON:0005734,tunica adventitia of blood vessel
+UBERON:2001586,pectoral fin radial bone,UBERON:2101586,pectoral fin radial element
+UBERON:0010533,metanephros cortex,UBERON:0004120,mesoderm-derived structure
+UBERON:2002255,ocular side,UBERON:0000475,organism subdivision
+DOID:6337,cerebellopontine angle meningioma,DOID:3200,cerebellopontine angle tumor
+UBERON:0015840,incisor dental lamina,UBERON:0004825,dental lamina
+UBERON:2000991,epaxial region somite 10,UBERON:0003900,epaxial myotome region
+UBERON:3000440,planum terminale,UBERON:0010313,neural crest-derived structure
+DOID:3651,pyruvate carboxylase deficiency disease,DOID:2978,carbohydrate metabolic disorder
+UBERON:0000015,anatomical boundary,UBERON:0000466,immaterial anatomical entity
+UBERON:0005986,left branch of atrioventricular bundle,UBERON:0004493,cardiac muscle tissue of myocardium
+HP:0001682,Subaortic stenosis,HP:0011103,Abnormality of the left ventricular outflow tract
+UBERON:2005410,pars inferior ear,UBERON:0000477,anatomical cluster
+UBERON:0005317,pulmonary artery endothelium,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0006564,Fluctuating hepatomegaly,HP:0002240,Hepatomegaly
+DOID:14731,Weaver syndrome,DOID:0080015,physical disorder
+UBERON:0001940,supramammillary nucleus,UBERON:0002789,regional part of posterior hypothalamic region
+UBERON:0013068,palatine torus,UBERON:0005913,zone of bone organ
+UBERON:0006353,principal vein of hindlimb,UBERON:0003516,hindlimb blood vessel
+HP:0008762,Repetitive compulsive behavior,HP:0000733,Stereotypic behavior
+UBERON:0002369,adrenal gland,UBERON:0006858,adrenal/interrenal gland
+DOID:5813,purine nucleoside phosphorylase deficiency,DOID:628,combined T cell and B cell immunodeficiency
+DOID:13026,lobomycosis,DOID:1563,dermatomycosis
+DOID:0050785,progressive relapsing multiple sclerosis,DOID:2377,multiple sclerosis
+DOID:9972,hypervitaminosis A,DOID:654,overnutrition
+UBERON:4300008,epipleural series,UBERON:0000477,anatomical cluster
+UBERON:0006222,future diencephalon,UBERON:0004121,ectoderm-derived structure
+HP:0010018,Enlarged epiphysis of the 1st metacarpal,HP:0009689,Enlarged epiphyses of the thumb
+UBERON:0009708,dorsal pancreas,UBERON:0002368,endocrine gland
+UBERON:0003990,spinal cord motor column,UBERON:0004121,ectoderm-derived structure
+CL:0000829,basophilic myeloblast,CL:0000835,myeloblast
+DOID:10234,histoplasmosis pericarditis,DOID:1787,pericarditis
+UBERON:0007805,synsacrum,UBERON:0005179,pelvic region organ
+UBERON:0001203,muscularis mucosae of stomach,UBERON:0006676,muscularis mucosa
+DOID:0050567,orofacial cleft,DOID:0080015,physical disorder
+DOID:1039,prolymphocytic leukemia,DOID:1040,chronic lymphocytic leukemia
+UBERON:2005225,median fin radial bone,UBERON:2000271,radial bone
+UBERON:2001603,maxilla ascending process,UBERON:4100000,skeletal element projection
+HP:0005559,Abnormality of the kinin-kallikrein system,HP:0010876,Abnormality of circulating protein level
+UBERON:0005397,brain arachnoid mater,UBERON:0002362,arachnoid mater
+UBERON:3010045,centrale 1,UBERON:0015050,tarsus endochondral element
+CL:1001572,colon endothelial cell,CL:0000115,endothelial cell
+HP:0001382,Joint hypermobility,HP:0011729,Abnormality of joint mobility
+DOID:0050522,Balkan hemorrhagic fever,DOID:11266,hemorrhagic fever with renal syndrome
+HP:0011382,Hypoplasia of the semicircular canal,HP:0011380,Morphological abnormality of the semicircular canal
+UBERON:0009065,anterior thoracic air sac,UBERON:0009061,anterior air sac
+NCBITaxon:33317,Protostomia,NCBITaxon:33213,Bilateria
+UBERON:0001601,extra-ocular muscle,UBERON:0010313,neural crest-derived structure
+UBERON:2005412,transverse canal,UBERON:0000058,duct
+UBERON:0009689,anterior inferior cerebellar artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3000477,presumptive nervous system,UBERON:0006598,presumptive structure
+UBERON:0001101,external jugular vein,UBERON:0004711,jugular vein
+DOID:0060116,sensory system cancer,DOID:3093,nervous system cancer
+HP:0009231,Patchy sclerosis of the proximal phalanx of the 5th finger,HP:0009856,Patchy sclerosis of the proximal phalanges of the hand
+HP:0002591,Polyphagia,HP:0100738,Abnormal eating behavior
+UBERON:0010902,tibiotarsus cartilage element,UBERON:0010885,hindlimb cartilage element
+UBERON:0010260,umbilical blood vessel,UBERON:0001981,blood vessel
+UBERON:0002241,chondrocranium,UBERON:0011159,primary subdivision of cranial skeletal system
+DOID:2007,degeneration of macula and posterior pole,DOID:4448,macular degeneration
+UBERON:0002671,pallidotegmental fasciculus,UBERON:0007702,tract of brain
+CL:1000321,large intestine crypt goblet cell,CL:1000320,axial mesoderm cell
+HP:0100910,Sclerosis of the proximal phalanx of the 4th finger,HP:0100920,Sclerosis of the phalanges of the 4th finger
+DOID:11988,conjunctival concretion,DOID:11653,conjunctival deposit
+HP:0007164,Slowed slurred speech,HP:0001350,Slurred speech
+UBERON:0004370,anterior limiting lamina of cornea,UBERON:0010313,neural crest-derived structure
+HP:0010384,Broad phalanges of the 5th toe,HP:0010342,Abnormality of the phalanges of the 5th toe
+UBERON:0003390,mesothelium of pleural cavity,UBERON:0001136,mesothelium
+HP:0006532,Recurrent pneumonia,HP:0002783,Recurrent lower respiratory tract infections
+CL:1000596,inner renal cortex cell,CL:0002681,kidney cortical cell
+UBERON:0011860,collagen fibril,UBERON:0000476,acellular anatomical structure
+UBERON:0014898,lamina terminalis of ischium,UBERON:0004120,mesoderm-derived structure
+CL:0002592,smooth muscle cell of the coronary artery,CL:0002494,cardiocyte
+HP:0007602,Complex palmar dermatoglyphic pattern,HP:0001018,Abnormal palmar dermatoglyphics
+HP:0003826,Stillbirth,HP:0011420,Death
+HP:0010316,Ebstein's anomaly of the tricuspid valve,HP:0001702,Abnormality of the tricuspid valve
+UBERON:0009115,thoracic thymus,UBERON:0005178,thoracic cavity organ
+UBERON:0002636,lateral pulvinar nucleus,UBERON:0015233,nucleus of dorsal thalamus
+NCBITaxon:6269,Anisakis simplex,NCBITaxon:644710,Anisakis simplex complex
+HP:0005266,Intestinal polyp,HP:0007378,Neoplasm of the gastrointestinal tract
+CL:0000999,CD4-positive CD11b-positive dendritic cell,CL:0000766,myeloid leukocyte
+UBERON:0003959,rete testis,UBERON:0014403,male anatomical structure
+HP:0007397,Axillary apocrine gland hypoplasia,HP:0011135,Aplasia/Hypoplasia of the sweat glands
+UBERON:0003523,manus blood vessel,UBERON:0003515,forelimb blood vessel
+UBERON:0001991,cervical ganglion,UBERON:0001807,paravertebral ganglion
+UBERON:2002014,ascending limb of ceratobranchial 5 cartilage,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0007301,Oromotor apraxia,HP:0002186,Apraxia
+UBERON:0006669,alveolar canal,UBERON:0005744,bone foramen
+DOID:2964,periarthritis,DOID:2965,bursitis
+DOID:4432,pancreatic somatostatinoma,DOID:1799,islet cell tumor
+UBERON:0004996,mucosa of cardia of stomach,UBERON:0001199,mucosa of stomach
+UBERON:0001642,superior sagittal sinus,UBERON:0006615,venous sinus
+UBERON:0007132,head kidney,UBERON:0004177,hemopoietic organ
+UBERON:0008294,feather barb,UBERON:0004121,ectoderm-derived structure
+UBERON:2005378,dorsal fin distal radial bone 7,UBERON:2105378,dorsal fin distal radial element 7
+UBERON:2002277,pectoral fin distal radial bone 1,UBERON:2102277,pectoral fin distal radial element 1
+HP:0000643,Blepharospasm,HP:0012179,Craniofacial dystonia
+UBERON:0005699,pedal digit 5 mesenchyme,UBERON:0005255,pedal digit mesenchyme
+HP:0010939,Abnormality of the nasal bone,HP:0010937,Abnormality of the nasal skeleton
+UBERON:0004227,kidney pelvis smooth muscle,UBERON:0009919,ureter smooth muscle
+UBERON:0014785,levator cloacae,UBERON:0014783,cloacal muscle
+HP:0008399,Circumungual hyperkeratosis,HP:0100803,Abnormality of the periungual region
+UBERON:0003925,photoreceptor inner segment layer,UBERON:0000479,tissue
+DOID:7511,breast intraductal papillomatosis,DOID:1634,breast papillomatosis
+UBERON:0014886,distal epiphysis of distal phalanx of manual digit,UBERON:0014887,distal epiphysis of distal phalanx of digit
+UBERON:0002615,ventral tegmental decussation,UBERON:0014891,brainstem white matter
+UBERON:0010384,lumen of laryngopharynx,UBERON:0000464,anatomical space
+UBERON:0002394,bile duct,UBERON:0003928,digestive system duct
+HP:0002317,Unsteady gait,HP:0001288,Gait disturbance
+HP:0001738,Exocrine pancreatic insufficiency,HP:0012091,Abnormality of pancreas physiology
+UBERON:3010437,post-anal gut,UBERON:0004119,endoderm-derived structure
+UBERON:2000288,supracarinalis,UBERON:0001774,muscle of trunk
+HP:0003646,Bicarbonaturia,HP:0011279,Abnormality of urine bicarbonate concentration
+HP:0009229,Curved proximal phalanx of the 5th finger,HP:0009854,Curved proximal phalanges of the hand
+HP:0003452,Increased serum iron,HP:0011031,Abnormality of iron homeostasis
+UBERON:0001753,cementum,UBERON:0010365,odontoid tissue
+UBERON:2001768,retractor tentaculi,UBERON:0002376,cranial muscle
+UBERON:0003484,eye sebaceous gland,UBERON:0003605,eye skin gland
+NCBITaxon:29547,Epsilonproteobacteria,NCBITaxon:68525,delta/epsilon subdivisions
+CL:1000380,type 1 vestibular sensory cell of epithelium of macula of saccule of membranous labyrinth,CL:0002070,type I vestibular sensory cell
+UBERON:0013233,supraorbital gland,UBERON:0012278,gland of nasal mucosa
+UBERON:0001423,radius bone,UBERON:0015001,radius endochondral element
+HP:0006466,Ankle contracture,HP:0005750,Contractures of the joints of the lower limbs
+DOID:12001,tracheal lymphoma,DOID:11920,tracheal cancer
+UBERON:3000131,dilatatio alaris,UBERON:0010313,neural crest-derived structure
+UBERON:0010953,nasalis muscle,UBERON:0015212,lateral structure
+HP:0009223,Stippling of the epiphysis of the middle phalanx of the 4th finger,HP:0009402,Stippling of the epiphyses of the 4th finger
+CL:0000380,thecogen cell,CL:0000378,support cell (sensu Nematoda and Protostomia)
+DOID:9948,residual stage corticosteroid-induced glaucoma,DOID:9946,steroid-induced glaucoma
+UBERON:0005092,right horn of sinus venosus,UBERON:0002050,embryonic structure
+CL:0002127,innate effector T cell,CL:0000911,effector T cell
+CL:0000497,red sensitive photoreceptor cell,CL:0000490,photopic photoreceptor cell
+UBERON:0004617,lumbar vertebra 1,UBERON:0002414,lumbar vertebra
+UBERON:0001526,extensor carpi ulnaris muscle,UBERON:0011024,extrinsic extensor muscle of manus
+UBERON:0002109,pair of nares,UBERON:0004121,ectoderm-derived structure
+DOID:12304,conjunctival pigmentation,DOID:10123,pigmentation disease
+UBERON:0014487,distal phalanx of digit 5,UBERON:0004300,distal phalanx
+UBERON:0006231,facial bone primordium,UBERON:0007842,membrane bone
+HP:0010043,Aplasia of the 4th metacarpal,HP:0010048,Aplasia of metacarpal bones
+UBERON:2001240,ceratobranchial 4 bone,UBERON:2001902,ceratobranchial 4 element
+HP:0005266,Intestinal polyp,HP:0002242,Abnormality of the intestine
+CL:1001610,bone marrow hematopoietic cell,CL:0002092,bone marrow cell
+CL:0000160,goblet cell,CL:0000150,glandular epithelial cell
+UBERON:0016378,ileocecocolic lymph node,UBERON:0000029,lymph node
+HP:0010111,Short phalanx of hallux,HP:0010109,Short hallux
+DOID:14271,acute cholangitis,DOID:9446,cholangitis
+HP:0009566,Short distal phalanx of the 2nd finger,HP:0009882,Short distal phalanx of finger
+UBERON:0000086,zona pellucida,UBERON:0005156,reproductive structure
+UBERON:0009895,atrial siphon primordia,UBERON:0009894,siphon primordium
+UBERON:0012477,dorsal part of neck,UBERON:0005434,cervical region
+HP:0100852,Abnormal fear/anxiety-related behavior,HP:0100851,Abnormal emotion/affect behavior
+UBERON:2001672,dorsal fin radial bone,UBERON:2005225,median fin radial bone
+UBERON:0014387,mesenchyme derived from neural crest,UBERON:0010313,neural crest-derived structure
+UBERON:0003221,phalanx,UBERON:0015023,phalanx endochondral element
+UBERON:0003264,mesoderm of yolk sac,UBERON:0000926,mesoderm
+UBERON:0015454,pancreatic fat pad,UBERON:0003916,fat pad
+UBERON:0004326,middle phalanx of pedal digit 4,UBERON:0014490,middle phalanx of digit 4
+CL:0002335,brown preadipocyte,CL:0002334,preadipocyte
+UBERON:0002685,anteroventral nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0003968,peripheral lymph node,UBERON:0000029,lymph node
+DOID:4483,rhinitis,DOID:2163,nasal cavity disease
+DOID:1508,candidiasis,DOID:2473,opportunistic mycosis
+UBERON:0011169,postorbital bone,UBERON:0008907,dermal bone
+HP:0003980,Pseudarthrosis of the radius,HP:0002818,Abnormality of the radius
+UBERON:0004150,coronary sinus valve,UBERON:0000946,cardial valve
+UBERON:0010546,metapodial skeleton,UBERON:0010712,limb skeleton subdivision
+UBERON:0002112,smooth muscle of esophagus,UBERON:0001135,smooth muscle tissue
+UBERON:0009577,metencephalon sulcus limitans,UBERON:0005478,sulcus limitans of neural tube
+HP:0001770,Toe syndactyly,HP:0001780,Abnormality of toe
+UBERON:0003942,somatic sensory system,UBERON:0001032,sensory system
+UBERON:2000734,preural vertebra,UBERON:0004376,fin bone
+HP:0010314,Premature thelarche,HP:0000826,Precocious puberty
+CL:0002036,Slamf1-positive multipotent progenitor cell,CL:0000837,hematopoietic multipotent progenitor cell
+DOID:668,myositis ossificans,DOID:633,myositis
+CL:1000322,pancreatic goblet cell,CL:1001599,pancreas exocrine glandular cell
+HP:0002857,Genu valgum,HP:0002979,Bowing of the legs
+HP:0005045,diaphyseal cortical sclerosis,HP:0003034,Diaphyseal sclerosis
+HP:0009812,Amelia involving the upper limbs,HP:0009827,Amelia
+UBERON:0010370,tibial vein,UBERON:0001638,vein
+UBERON:0005307,chorion-containing eggshell,UBERON:0005079,eggshell
+HP:0000546,Retinal degeneration,HP:0000479,Abnormality of the retina
+UBERON:0005650,pedal digit 3 epithelium,UBERON:0005226,pedal digit epithelium
+DOID:13145,benign renovascular hypertension,DOID:13143,benign secondary hypertension
+HP:0003926,Abnormality of the humeral diaphysis,HP:0009808,Anomaly of the upper limb diaphyses
+DOID:5209,benign struma ovarii,DOID:2640,struma ovarii
+UBERON:0008798,rugal fold of vagina,UBERON:0014404,female anatomical structure
+CL:0000642,folliculostellate cell,CL:0000630,supportive cell
+HP:0002787,Tracheal calcification,HP:0002778,Abnormality of the trachea
+HP:0010594,Abnormality of the proximal fibular epiphysis,HP:0010593,Abnormality of fibular epiphyses
+DOID:13143,benign secondary hypertension,DOID:11130,secondary hypertension
+HP:0008784,Wide capital femoral epiphyses,HP:0010574,Abnormality of the epiphysis of the femoral head
+HP:0005701,Multiple enchondromatosis,HP:0002763,Abnormal cartilage morphology
+HP:0002068,Neuromuscular dysphagia,HP:0002015,Dysphagia
+UBERON:2001796,epibranchial 2 bone uncinate process,UBERON:2001382,epibranchial bone uncinate process
+UBERON:2002257,premaxilla dentigerous process,UBERON:4100000,skeletal element projection
+HP:0008449,Progressive cervical vertebral spine fusion,HP:0002949,Fused cervical vertebrae
+UBERON:0003596,ankle connective tissue,UBERON:0003595,pes connective tissue
+UBERON:0014444,pubic ramus,UBERON:0005913,zone of bone organ
+HP:0003860,Diaphyseal sclerosis of the upper limbs,HP:0003034,Diaphyseal sclerosis
+HP:0001226,Acral ulceration and osteomyelitis leading to autoamputation of digits,HP:0007460,Autoamputation of digits
+UBERON:0001261,lamina propria of urinary bladder,UBERON:0004120,mesoderm-derived structure
+DOID:2701,nodular tenosynovitis,DOID:0060123,connective tissue benign neoplasm
+HP:0009574,Symphalangism of middle phalanx of 2nd finger,HP:0009543,Abnormality of the middle phalanx of the 2nd finger
+UBERON:0015232,nematode pharynx,UBERON:0001041,foregut
+UBERON:0011088,ligament of knee joint,UBERON:0008846,skeletal ligament
+HP:0011901,Dysfibrinogenemia,HP:0011898,Abnormality of circulating fibrinogen
+DOID:655,inherited metabolic disorder,DOID:0014667,disease of metabolism
+UBERON:0010389,pterygoid bone,UBERON:0002513,endochondral bone
+DOID:3202,neurilemmoma of the fifth cranial nerve,DOID:3192,neurilemmoma
+HP:0006414,Distal tibial bowing,HP:0003028,Abnormality of the ankles
+UBERON:0003933,cranial cartilage,UBERON:0007844,cartilage element
+NCBITaxon:42068,Pneumocystis jirovecii,NCBITaxon:4753,Pneumocystis
+DOID:6590,spondylitis,DOID:1123,spondyloarthropathy
+HP:0200135,Macrocephaly due to hydrocephalus,HP:0000238,Hydrocephalus
+DOID:13814,hypoglossal nerve disease,DOID:3418,glossopharyngeal nerve disease
+UBERON:2005018,efferent filamental artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003247,epithelium of forearm,UBERON:0010371,ecto-epithelium
+UBERON:0010926,lateral thyrohyoid ligament,UBERON:0010921,thyrohyoid ligament
+UBERON:0013653,velar skeleton,UBERON:0010912,subdivision of skeleton
+DOID:0050450,Gitelman syndrome,DOID:447,renal tubular transport disease
+UBERON:3000743,sacral condyle,UBERON:0004120,mesoderm-derived structure
+UBERON:0003304,mesoderm blood island,UBERON:0003061,blood island
+HP:0007574,Generalized bronze hyperpigmentation,HP:0007440,Generalized hyperpigmentation
+UBERON:2000090,apical ectodermal ridge dorsal fin,UBERON:0004356,apical ectodermal ridge
+CL:1001596,salivary gland glandular cell,CL:0000150,glandular epithelial cell
+UBERON:0001695,squamous part of temporal bone,UBERON:0011164,neurocranium bone
+DOID:5099,middle ear cancer,DOID:833,auditory system cancer
+UBERON:0009909,rostral root of abducens nerve,UBERON:0004121,ectoderm-derived structure
+DOID:0050760,X-linked myopathy with excessive autophagy,DOID:423,myopathy
+UBERON:0013685,foramen of skull,UBERON:0005744,bone foramen
+HP:0010488,Aplasia/Hypoplasia of the palmar creases,HP:0010490,Abnormality of the palmar creases
+UBERON:0002772,olfactory sulcus,UBERON:0013118,sulcus of brain
+CL:0001031,cerebellar granule cell,CL:0000120,granule cell
+DOID:5313,vulvar alveolar soft part sarcoma,DOID:2096,vulvar sarcoma
+HP:0001400,Hepatic abscesses due to immunodeficiency,HP:0100523,Liver abscess
+DOID:2583,agammaglobulinemia,DOID:2115,B cell deficiency
+CL:0000446,chief cell of parathyroid gland,CL:0002260,epithelial cell of parathyroid gland
+UBERON:0003690,sacrum,UBERON:0003828,abdominal segment bone
+UBERON:0001851,cortex,UBERON:0000064,organ part
+UBERON:0003861,neural arch,UBERON:0010358,arch of centrum of vertebra
+UBERON:0004266,upper leg connective tissue,UBERON:0003569,leg connective tissue
+UBERON:0008866,enamel knot,UBERON:0000477,anatomical cluster
+HP:0001965,Abnormality of the scalp,HP:0000234,Abnormality of the head
+DOID:4961,bone marrow disease,DOID:74,hematopoietic system disease
+HP:0008000,Decreased corneal reflex,HP:0000481,Abnormality of the cornea
+UBERON:2201672,dorsal fin radial cartilage,UBERON:2205225,median fin radial cartilage
+UBERON:2101587,pectoral fin proximal radial element,UBERON:2101586,pectoral fin radial element
+UBERON:3010187,inner metacarpal tubercle,UBERON:0005813,tubercle
+CL:0000579,border follicle cell,CL:0000477,follicle cell
+UBERON:0015789,cranial or facial muscle,UBERON:0002376,cranial muscle
+DOID:14146,ureterolithiasis,DOID:1426,ureteral disease
+HP:0008061,Aplasia/Hypoplasia affecting the retina,HP:0008057,Aplasia/Hypoplasia affecting the fundus
+DOID:13386,gastrointestinal anthrax,DOID:7427,anthrax disease
+UBERON:3000434,planum antorbitale,UBERON:0003406,cartilage of respiratory system
+UBERON:0013730,mycetome,UBERON:0000062,organ
+UBERON:0008923,sublaminar layer S2,UBERON:0009737,sublaminar layers S1 or S2 or S3 or S4
+UBERON:4000052,ganoid scale,UBERON:0007380,dermal scale
+CL:0002650,epithelial cell of paranasal sinus part of viscerocranial mucosa,CL:0002283,ecto-epithelial cell of viscerocranial mucosa
+DOID:12802,mucopolysaccharidosis I,DOID:12798,mucopolysaccharidosis
+DOID:6481,bladder signet ring cell adenocarcinoma,DOID:3711,bladder adenocarcinoma
+DOID:0080016,spina bifida,DOID:0080015,physical disorder
+UBERON:0003437,eyelid nerve,UBERON:0001647,facial nerve
+UBERON:0001439,compact bone tissue,UBERON:0002481,bone tissue
+DOID:9650,pathologic nystagmus,DOID:1279,ocular motility disease
+HP:0008848,Moderately short stature,HP:0003508,Proportionate short stature
+CL:0000865,gastrointestinal tract (lamina propria) macrophage,CL:0000885,gut-associated lymphoid tissue macrophage
+NCBITaxon:5302,Agaricomycotina,NCBITaxon:5204,Basidiomycota
+DOID:2856,euthyroid sick syndrome,DOID:50,thyroid gland disease
+UBERON:0009093,outer medulla vasa recta ascending limb,UBERON:0004120,mesoderm-derived structure
+HP:0001948,Alkalosis,HP:0004360,Abnormality of acid-base homeostasis
+UBERON:0000426,extravillous trophoblast,UBERON:0002050,embryonic structure
+UBERON:0001659,transverse facial vein,UBERON:0009141,craniocervical region vein
+HP:0006114,Multiple palmar creases,HP:0010490,Abnormality of the palmar creases
+HP:0007915,Polymorphous posterior corneal dystrophy,HP:0011489,Abnormal migration of corneal endothelium
+UBERON:2005409,pars superior ear,UBERON:0004121,ectoderm-derived structure
+UBERON:0012399,large intestine smooth muscle longitudinal layer,UBERON:0004120,mesoderm-derived structure
+UBERON:0002193,hemolymphoid system,UBERON:0000467,anatomical system
+HP:0008306,Abnormal iron deposition in mitochondria,HP:0003287,Abnormality of mitochondrial metabolism
+HP:0005535,Exercise-induced hemolysis,HP:0001878,Hemolytic anemia
+UBERON:0005288,tela choroidea of third ventricle,UBERON:0004121,ectoderm-derived structure
+CL:0001016,immature CD1a-positive Langerhans cell,CL:0000840,immature conventional dendritic cell
+UBERON:0001304,germinal epithelium of ovary,UBERON:0000484,simple cuboidal epithelium
+UBERON:0012150,skeleton of digitopodium,UBERON:0010712,limb skeleton subdivision
+UBERON:0001072,inferior vena cava,UBERON:0004087,vena cava
+HP:0002007,Frontal bossing,HP:0000290,Abnormality of the forehead
+DOID:6947,sphenoidal sinus neoplasm,DOID:1350,paranasal sinus neoplasm
+UBERON:0011364,cleidocephalicus muscle,UBERON:0001630,muscle organ
+DOID:12638,hypertrophic pyloric stenosis,DOID:12639,pyloric stenosis
+DOID:9389,infectious anterior uveitis,DOID:9383,iridocyclitis
+UBERON:0015410,heart plus pericardium,UBERON:0005178,thoracic cavity organ
+DOID:0050848,obstructive sleep apnea,DOID:0050847,sleep apnea
+HP:0008394,Congenital onychodystrophy,HP:0002164,Nail dysplasia
+UBERON:0009668,ventral mesentery,UBERON:0002050,embryonic structure
+HP:0009682,Pseudoepiphysis of the distal phalanx of the thumb,HP:0010253,Pseudoepiphyses of the distal phalanges of the hand
+UBERON:4300024,spinal plate,UBERON:0007829,pectoral girdle bone
+HP:0001946,Ketosis,HP:0001939,Abnormality of metabolism/homeostasis
+UBERON:0011951,prostate luminal epithelium,UBERON:0014403,male anatomical structure
+DOID:5057,papillary meningioma of the cerebellum,DOID:5058,rhabdoid meningioma
+CL:0000501,granulosa cell,CL:0000174,steroid hormone secreting cell
+UBERON:0001226,major calyx,UBERON:0006517,kidney calyx
+HP:0002812,Coxa vara,HP:0003367,Abnormality of the femoral neck
+HP:0001166,Arachnodactyly,HP:0001238,Slender finger
+UBERON:3010118,quadrato-orbital commissure,UBERON:0000064,organ part
+HP:0003882,Slender humerus,HP:0003100,Slender long bone
+UBERON:0010682,pedal digit 3 phalanx cartilage element,UBERON:0015033,pedal digit 3 phalanx endochondral element
+DOID:809,cocaine abuse,DOID:302,substance abuse
+UBERON:0002617,pars postrema of ventral lateral nucleus,UBERON:0003528,brain grey matter
+UBERON:0010903,tibiotarsus pre-cartilage condensation,UBERON:0010886,hindlimb bone pre-cartilage condensation
+DOID:1975,thymus lipoma,DOID:0060092,immune system organ benign neoplasm
+HP:0000895,Hooked clavicles,HP:0000889,Abnormality of the clavicles
+DOID:3183,childhood oligodendroglioma,DOID:3181,oligodendroglioma
+UBERON:0001325,muscle of pelvis,UBERON:0003833,abdominal segment muscle
+UBERON:0004983,mucosa of vagina,UBERON:0005156,reproductive structure
+UBERON:0010752,exoccipital cartilage element,UBERON:0003932,cartilage element of chondrocranium
+UBERON:0013655,elastica externa of notochord,UBERON:0000479,tissue
+UBERON:0002860,first sacral dorsal root ganglion,UBERON:0002837,sacral dorsal root ganglion
+UBERON:2001841,interhyal-epihyal joint,UBERON:0000982,skeletal joint
+UBERON:0010366,conjunctival vasculature,UBERON:0002203,vasculature of eye
+HP:0007097,Cranial nerve motor loss,HP:0001291,Abnormality of the cranial nerves
+UBERON:2000532,lateral division,UBERON:0002946,regional part of cerebellum
+HP:0005612,Arthrogryposis-like hand anomaly,HP:0005684,Distal arthrogryposis
+UBERON:0003072,optic cup,UBERON:0000481,multi-tissue structure
+DOID:3107,toxascariasis,DOID:883,parasitic helminthiasis infectious disease
+DOID:5179,mixed cell type kidney Wilms' tumor,DOID:2154,nephroblastoma
+HP:0001900,Increased hemoglobin,HP:0001901,Polycythemia
+UBERON:0002247,uterine horn,UBERON:0000064,organ part
+CL:0000626,olfactory granule cell,CL:0012001,neuron of the forebrain
+DOID:2212,coagulation protein disease,DOID:1247,blood coagulation disease
+UBERON:0010078,optic choroid vascular plexus,UBERON:0002203,vasculature of eye
+DOID:13089,intracranial arterial disease,DOID:6713,cerebrovascular disease
+HP:0009650,Short distal phalanx of the thumb,HP:0009641,Aplasia/Hypoplasia of the distal phalanx of the thumb
+HP:0011223,Metopic depression,HP:0005556,Abnormality of the metopic suture
+HP:0007074,Thick corpus callosum,HP:0001273,Abnormality of the corpus callosum
+HP:0009148,Small epiphysis of the distal phalanx of the 5th finger,HP:0009198,Abnormality of the epiphysis of the distal phalanx of the 5th finger
+HP:0001140,Epibulbar dermoid,HP:0000481,Abnormality of the cornea
+UBERON:0005394,cortical layer V,UBERON:0002301,layer of neocortex
+HP:0010082,Symphalangism affecting the distal phalanx of the hallux,HP:0010191,Symphalangism affecting the distal phalanges of the toes
+HP:0009581,Broad proximal phalanx of the 2nd finger,HP:0009852,Broad proximal phalanges of the hand
+UBERON:0001229,renal corpuscle,UBERON:0000481,multi-tissue structure
+HP:0005776,Carpal bone malsegmentation,HP:0001191,Abnormality of the carpal bones
+CL:0002391,multinucleate blastoconidium,CL:0002385,blastoconidium
+UBERON:0008428,ceratoglossus,UBERON:0004121,ectoderm-derived structure
+DOID:11055,pasteurellosis,DOID:0050338,primary bacterial infectious disease
+HP:0011390,Morphological abnormality of the inner ear,HP:0000359,Abnormality of the inner ear
+CL:0005012,multi-ciliated epithelial cell,CL:0000066,epithelial cell
+DOID:3450,cutaneous Paget's disease,DOID:3451,skin carcinoma
+HP:0004322,Short stature,HP:0000002,Abnormality of body height
+UBERON:0009072,ventrobronchus,UBERON:0002185,bronchus
+HP:0010151,Cone-shaped epiphysis of the 1st metatarsal,HP:0010630,Abnormality of metatarsal epiphysis
+HP:0006367,Crumpled long bones,HP:0011314,Abnormality of long bone morphology
+UBERON:0012317,vagina orifice,UBERON:0014404,female anatomical structure
+UBERON:0002631,cerebral crus,UBERON:0002950,regional part of midbrain
+UBERON:0006649,suspensory ligament of ovary,UBERON:0002095,mesentery
+UBERON:2005031,dorsal longitudinal vein,UBERON:0001638,vein
+UBERON:2002009,medial cartilage of palatine,UBERON:0004121,ectoderm-derived structure
+HP:0003019,Abnormality of the wrist,HP:0009810,Abnormality of the joints of the upper limbs
+UBERON:2005015,afferent lamellar arteriole,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0004396,Poor appetite,HP:0011458,Abdominal symptom
+HP:0008368,Tarsal synostosis,HP:0100266,Synostosis of carpals/tarsals
+UBERON:0008888,vesical venous plexus,UBERON:0002201,vasculature of trunk
+UBERON:2100623,basipterygium element,UBERON:0004120,mesoderm-derived structure
+HP:0008833,Irregular acetabular roof,HP:0003170,Abnormality of the acetabulum
+HP:0100560,Upper limb asymmetry,HP:0002817,Abnormality of the upper limb
+HP:0003849,Flared metaphyses of the upper limbs,HP:0003015,Flared metaphyses
+UBERON:0006491,fifth cervical spinal cord segment,UBERON:0007714,cervical subsegment of spinal cord
+HP:0007446,Palmoplantar blistering,HP:0011356,Regional abnormality of skin
+HP:0007616,Nevus flammeus nuchae,HP:0001052,Nevus flammeus
+UBERON:0002720,mammillary peduncle,UBERON:0003931,diencephalic white matter
+UBERON:0002295,scala media,UBERON:0004120,mesoderm-derived structure
+DOID:7188,autoimmune thyroiditis,DOID:0060005,autoimmune disease of endocrine system
+UBERON:2001994,gill raker row,UBERON:0000477,anatomical cluster
+UBERON:0006257,laryngotracheal groove,UBERON:0002050,embryonic structure
+DOID:539,ophthalmoplegia,DOID:1279,ocular motility disease
+DOID:1251,tuberculous epididymitis,DOID:2149,urogenital tuberculosis
+HP:0000520,Proptosis,HP:0100886,Abnormality of globe location
+DOID:4434,small intestine neuroendocrine neoplasm,DOID:7505,small intestine neoplasm
+DOID:3639,spinal cord intramedullary teratoma,DOID:5612,spinal cancer
+DOID:8536,herpes zoster,DOID:37,skin disease
+HP:0009456,Triangular shaped proximal phalanx of the 3rd finger,HP:0009446,Triangular shaped phalanges of the 3rd finger
+CL:0000898,naive T cell,CL:0002419,mature T cell
+HP:0009278,Ulnar deviation of the 4th finger,HP:0009273,Deviation of the 4th finger
+HP:0004361,Abnormality of circulating leptin level,HP:0003117,Abnormality of circulating hormone level
+DOID:14365,systemic primary carnitine deficiency disease,DOID:9252,amino acid metabolic disorder
+HP:0010637,Conjunctival amyloidosis,HP:0000502,Abnormality of the conjunctiva
+HP:0000218,High palate,HP:0000174,Abnormality of the palate
+UBERON:0015149,ventral hair,UBERON:0001037,strand of hair
+HP:0008363,Aplasia/Hypoplasia of the tarsal bones,HP:0006494,Aplasia/Hypoplasia involving bones of the feet
+HP:0003677,Slow progression,HP:0003679,Pace of progression
+UBERON:0010501,pseudostratified smooth columnar epithelium,UBERON:0010498,pseudostratified columnar epithelium
+HP:0011955,Hepatic granulomatosis,HP:0002955,Granulomatosis
+HP:0004026,Broad radial metaphysis,HP:0003981,Broad radius
+UBERON:0003972,placenta junctional zone,UBERON:0014404,female anatomical structure
+HP:0010711,1-2 toe syndactyly,HP:0001770,Toe syndactyly
+UBERON:0002623,cerebral peduncle,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0011164,Vegetative auras,HP:0011157,Auras
+HP:0011834,Moyamoya phenomenon,HP:0012518,Abnormality of circle of Willis
+HP:0100061,Ivory epiphyses of the 3rd toe,HP:0010168,Ivory epiphyses of the toes
+CL:0002431,"CD4-positive, CD8-intermediate double-positive thymocyte",CL:0000809,"double-positive, alpha-beta thymocyte"
+UBERON:0001035,dento-alveolar joint,UBERON:0002209,fibrous joint
+UBERON:0009976,hypothalamo-hypophyseal system,UBERON:0005806,portal system
+CL:0002277,type I enteroendocrine cell,CL:0000167,peptide hormone secreting cell
+HP:0012647,Abnormal inflammatory response,HP:0010978,Abnormality of immune system physiology
+HP:0010831,Impaired proprioception,HP:0003474,Sensory impairment
+UBERON:4200140,prepollical element,UBERON:0015049,carpus endochondral element
+UBERON:0016402,colic lymph node,UBERON:0015860,visceral abdominal lymph node
+UBERON:0001244,internal anal sphincter,UBERON:0012368,circular muscle layer
+UBERON:0004183,labyrinthine layer blood vessel,UBERON:0014404,female anatomical structure
+HP:0002834,Flared femoral metaphysis,HP:0003063,Abnormality of the humerus
+HP:0005155,Ventricular escape rhythms,HP:0004308,Ventricular arrhythmia
+HP:0100733,Neoplasm of the parathyroid gland,HP:0100568,Neoplasm of the endocrine system
+DOID:3352,malignant fibrous histiocytoma of bone,DOID:3347,osteosarcoma
+HP:0003184,Decreased hip abduction,HP:0008800,Limited hip movement
+HP:0100138,Enlarged epiphysis of the distal phalanx of the 3rd toe,HP:0100091,Abnormality of the epiphysis of the distal phalanx of the 3rd toe
+UBERON:4000138,ligamentous replacement element,UBERON:0010522,replacement element
+UBERON:3000644,processus lingularis of nasal skeleton,UBERON:0004529,anatomical projection
+HP:0011753,Posterior pituitary dysgenesis,HP:0011751,Abnormality of the posterior pituitary
+UBERON:0006217,cloacal membrane,UBERON:0000481,multi-tissue structure
+UBERON:0005879,pharyngeal cleft,UBERON:0005291,embryonic tissue
+UBERON:0005044,mucosa of pharyngotympanic tube,UBERON:0005026,mucosa of middle ear
+DOID:5820,composite lymphoma,DOID:707,B-cell lymphoma
+UBERON:0002369,adrenal gland,UBERON:0015212,lateral structure
+UBERON:3000329,oblique cartilage,UBERON:0010313,neural crest-derived structure
+UBERON:0005690,3rd arch mesenchyme,UBERON:0009494,pharyngeal arch mesenchymal region
+UBERON:0004387,epiphysis of phalanx of manus,UBERON:0004446,epiphysis of phalanx
+UBERON:0010437,zygomaticus muscle,UBERON:0001577,facial nerve muscle
+UBERON:0001721,inferior vestibular nucleus,UBERON:0007228,vestibular nucleus
+UBERON:0013638,horny papilla of tongue,UBERON:0001726,papilla of tongue
+UBERON:0005336,capillary layer of choroid,UBERON:0004923,organ component layer
+HP:0007721,Saccular conjunctival aneurysms,HP:0008054,Abnormality of the vasculature of the conjunctiva
+UBERON:0014675,distal interphalangeal joint of pedal digit 5,UBERON:0007728,interphalangeal joint of pedal digit 5
+UBERON:0009000,ischial spine,UBERON:0013706,bone spine
+UBERON:0001597,masseter muscle,UBERON:0003681,masticatory muscle
+HP:0005401,Recurrent candida infections,HP:0002841,Recurrent fungal infections
+DOID:11831,cortical blindness,DOID:5691,visual cortex disease
+UBERON:2005019,efferent lamellar arteriole,UBERON:0003469,respiratory system artery
+UBERON:0003449,tail intervertebral disc,UBERON:0001066,intervertebral disk
+HP:0007232,Spinocerebellar tract disease in lower limbs,HP:0002503,Spinocerebellar tract degeneration
+UBERON:0001296,myometrium,UBERON:0005156,reproductive structure
+UBERON:0004245,oviduct smooth muscle,UBERON:0005156,reproductive structure
+DOID:14080,glucocorticoid-remediable aldosteronism,DOID:446,hyperaldosteronism
+CL:1000546,kidney medulla collecting duct epithelial cell,CL:1001225,kidney collecting duct cell
+HP:0003269,Sudanophilic leukodystrophy,HP:0002415,Leukodystrophy
+UBERON:0015130,connective tissue of prostate,UBERON:0011822,dense irregular connective tissue
+DOID:4034,fungal gastritis,DOID:4029,gastritis
+HP:0100107,Pseudoepiphysis of the distal phalanx of the 2nd toe,HP:0100088,Abnormality of the epiphysis of the distal phalanx of the 2nd toe
+UBERON:0001282,intralobular bile duct,UBERON:0014716,interlobular duct
+UBERON:3010583,basibranchial I,UBERON:0004740,basibranchial bone
+UBERON:0001388,gastrocnemius,UBERON:0004256,hindlimb zeugopod muscle
+UBERON:0002214,macula of utricle of membranous labyrinth,UBERON:0000054,macula
+DOID:2518,orchitis,DOID:2519,testicular disease
+UBERON:0011635,splenial bone,UBERON:0008907,dermal bone
+UBERON:0010124,future inferior salivatory nucleus,UBERON:0002020,gray matter of neuraxis
+UBERON:4100011,postacetabular buttress,UBERON:0004120,mesoderm-derived structure
+UBERON:2000379,lateral forebrain bundle diencephalon,UBERON:0003931,diencephalic white matter
+DOID:7007,childhood cerebral astrocytoma,DOID:368,cerebrum cancer
+HP:0006092,Malaligned carpal bone,HP:0001191,Abnormality of the carpal bones
+HP:0004614,spina bifida occulta at S1,HP:0003298,Spina bifida occulta
+DOID:3748,esophagus squamous cell carcinoma,DOID:1107,esophageal carcinoma
+HP:0006607,Precocious costochondral ossification,HP:0004348,Abnormality of bone mineral density
+CL:0000825,pro-NK cell,CL:0000838,lymphoid lineage restricted progenitor cell
+DOID:11685,inflamed seborrheic keratosis,DOID:6498,seborrheic keratosis
+UBERON:0012401,small intestine smooth muscle circular layer,UBERON:0012368,circular muscle layer
+CL:0000855,sensory hair cell,CL:0000199,mechanoreceptor cell
+CL:1000467,chromaffin cell of left ovary,CL:1000465,chromaffin cell of ovary
+HP:0100009,Intracranial meningioma,HP:0002858,Meningioma
+HP:0006357,Premature loss of permanent teeth,HP:0006480,Premature loss of teeth
+HP:0007436,Hair-nail ectodermal dysplasia,HP:0000968,Ectodermal dysplasia
+HP:0100872,Abnormality of the plantar skin of foot,HP:0011356,Regional abnormality of skin
+UBERON:0005987,right branch of atrioventricular bundle,UBERON:0004493,cardiac muscle tissue of myocardium
+UBERON:0003865,distal phalanx of manus,UBERON:0001436,phalanx of manus
+DOID:0050105,endothrix infectious disease,DOID:4337,tinea capitis
+UBERON:0003973,nasal concha of ethmoid bone,UBERON:0001762,nasal concha
+UBERON:2001730,caudal principal ray 18,UBERON:2001585,caudal principal ray
+HP:0004458,Dilatated internal auditory canal,HP:0011384,Abnormality of the internal auditory canal
+CL:0000864,tissue-resident macrophage,CL:0000235,macrophage
+HP:0000388,Otitis media,HP:0000370,Abnormality of the middle ear
+UBERON:0002393,pharyngotympanic tube,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005641,otocyst epithelium,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0000981,femur,UBERON:0003826,upper leg bone
+HP:0010838,High nonceruloplasmin-bound serum copper,HP:0010836,Abnormality of copper homeostasis
+HP:0012436,Nonocclusive coronary artery disease,HP:0001677,Coronary artery disease
+UBERON:2001886,neural spine 2,UBERON:0001076,neural spine
+UBERON:0014504,proximal phalanx of digit 4,UBERON:0004302,proximal phalanx
+DOID:6530,cortical thymoma,DOID:3282,dendritic cell thymoma
+DOID:5525,anal squamous cell carcinoma,DOID:4908,anal carcinoma
+UBERON:3000687,processus confluens,UBERON:0000064,organ part
+UBERON:3000432,pila metoptica,UBERON:0003932,cartilage element of chondrocranium
+DOID:268,liver angiosarcoma,DOID:0001816,angiosarcoma
+UBERON:2001403,supraethmoid,UBERON:0008907,dermal bone
+UBERON:0013168,thyroepiglottic ligament,UBERON:0006325,laryngeal intrinsic ligament
+UBERON:0002714,rubrospinal tract,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0002037,Inflammation of the large intestine,HP:0002242,Abnormality of the intestine
+CL:0000511,androgen binding protein secreting cell,CL:0000154,protein secreting cell
+UBERON:0007499,epithelial sac,UBERON:0009856,sac
+UBERON:0003976,saccule duct,UBERON:0000025,tube
+HP:0011298,Prominent digit pad,HP:0011356,Regional abnormality of skin
+HP:0010710,3-5 finger syndactyly,HP:0006101,Finger syndactyly
+DOID:0050631,Allan-Herndon-Dudley syndrome,DOID:0050735,X-linked disease
+UBERON:0010272,hyoid apparatus,UBERON:0010314,structure with developmental contribution from neural crest
+CL:1000384,type 2 vestibular sensory cell of epithelium of macula of saccule of membranous labyrinth,CL:0002069,type II vestibular sensory cell
+DOID:8590,acute vascular insufficiency of intestine,DOID:5295,intestinal disease
+UBERON:0006792,intermediate layer of superior colliculus,UBERON:0006783,layer of superior colliculus
+NCBITaxon:7205,Tabanidae,NCBITaxon:1262365,Tabanoidea
+DOID:4295,follicular basal cell carcinoma,DOID:2513,basal cell carcinoma
+HP:0011669,Left superior vena cava draining directly to the left atrium,HP:0005301,Persistent left superior vena cava
+UBERON:0005035,mucosa of left main bronchus,UBERON:0005036,mucosa of main bronchus
+HP:0001890,Autoimmune hemolytic anemia,HP:0002960,Autoimmunity
+UBERON:0008521,gluteus minimus,UBERON:0002000,gluteal muscle
+UBERON:0011380,female external urethral sphincter,UBERON:0014404,female anatomical structure
+UBERON:0004208,nephrogenic mesenchyme,UBERON:0003104,mesenchyme
+UBERON:0006189,mesonephric connecting tubule,UBERON:0005097,renal connecting tubule
+DOID:0060131,alexithymia,DOID:4090,agnosia
+CL:0002133,stromal cell of ovarian cortex,CL:0002132,stromal cell of ovary
+UBERON:0010507,layer of dura mater,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004857,skeletal muscle connective tissue,UBERON:0002384,connective tissue
+HP:0008955,Progressive distal muscular atrophy,HP:0003693,Distal amyotrophy
+UBERON:0001064,ventral pancreatic duct,UBERON:0007329,pancreatic duct
+UBERON:0010157,sphenoparietal suture,UBERON:0003685,cranial suture
+DOID:851,Bartholin's duct cyst,DOID:229,female reproductive system disease
+UBERON:2001813,preopercular sensory canal,UBERON:2001612,sensory canal
+DOID:8969,tonsillar fossa cancer,DOID:8557,oropharynx cancer
+UBERON:0003642,pedal digit 3 phalanx,UBERON:0015033,pedal digit 3 phalanx endochondral element
+HP:0001070,Mottled pigmentation,HP:0001000,Abnormality of skin pigmentation
+DOID:1727,retinal vein occlusion,DOID:1729,retinal vascular occlusion
+UBERON:0002563,central nucleus of inferior colliculus,UBERON:0002917,regional part of inferior colliculus
+DOID:5285,breast leiomyosarcoma,DOID:3017,breast sarcoma
+HP:0010819,Atonic seizures,HP:0002197,Generalized seizures
+NCBITaxon:6854,Arachnida,NCBITaxon:6843,Chelicerata
+UBERON:4300032,posterior dorsal fin basal cartilage,UBERON:0005174,dorsal region organ
+UBERON:0003619,aorta tunica intima,UBERON:0002523,tunica intima
+UBERON:4300081,mesopterygium element,UBERON:2101587,pectoral fin proximal radial element
+UBERON:0012307,anterior cervical lymph node,UBERON:0002429,cervical lymph node
+UBERON:3010765,ramus mandibularis externus,UBERON:3010109,anteroventral lateral line nerve (AVLLN)
+HP:0005918,Abnormality of phalanx of finger,HP:0001167,Abnormality of finger
+HP:0008097,Partial fusion of tarsals,HP:0008368,Tarsal synostosis
+HP:0010049,Short metacarpal,HP:0005914,Aplasia/Hypoplasia involving the metacarpal bones
+UBERON:2005269,hypophyseal fenestra,UBERON:0005744,bone foramen
+UBERON:0004742,dentary,UBERON:0008907,dermal bone
+HP:0000522,Alacrima,HP:0000633,Decreased lacrimation
+HP:0009346,Absent epiphysis of the proximal phalanx of the 3rd finger,HP:0009410,Absent epiphyses of the 3rd finger
+HP:0004825,Increased hemoglobin oxygen affinity,HP:0001877,Abnormality of erythrocytes
+HP:0003411,Irregular proximal femoral metaphyses,HP:0003366,Abnormality of the femoral neck and head region
+HP:0009541,Abnormality of the phalanges of the 2nd finger,HP:0004100,Abnormality of the 2nd finger
+HP:0004571,Widening of cervical spinal canal,HP:0003319,Abnormality of the cervical spine
+UBERON:0002591,oral part of spinal trigeminal nucleus,UBERON:0003528,brain grey matter
+DOID:11716,prediabetes syndrome,DOID:9351,diabetes mellitus
+HP:0010149,Absent epiphysis of the 1st metatarsal,HP:0010113,Absent epiphyses of the hallux
+CL:1000085,stratified non keratinized epithelial stem cell,CL:0000357,stratified epithelial stem cell
+UBERON:0010083,future dermis,UBERON:0003104,mesenchyme
+UBERON:2102279,pectoral fin distal radial element 2,UBERON:2101588,pectoral fin distal radial element
+CL:0000500,follicular epithelial cell,CL:0000066,epithelial cell
+UBERON:0007240,tunica adventitia of artery,UBERON:0005734,tunica adventitia of blood vessel
+HP:0003465,Elevated 8(9)-cholestenol,HP:0003107,Abnormality of cholesterol metabolism
+UBERON:0004658,mandible head,UBERON:0005913,zone of bone organ
+HP:0100463,Patchy sclerosis of the middle phalanx of the 5th toe,HP:0010388,Patchy sclerosis of the phalanges of the 5th toe
+UBERON:0004054,internal male genitalia,UBERON:0003135,male reproductive organ
+DOID:1858,McCune Albright syndrome,DOID:0050736,autosomal dominant disease
+HP:0003352,Endopolyploidy on chromosome studies of bone marrow,HP:0002916,Abnormality of chromosome segregation
+UBERON:0010271,musculus retractor bulbi,UBERON:0001601,extra-ocular muscle
+HP:0012454,Unilateral wrist flexion contracture,HP:0001239,Wrist flexion contracture
+DOID:6228,peritoneal serous papillary adenocarcinoma,DOID:4901,peritoneal serous adenocarcinoma
+UBERON:0011647,depressor mandibulae muscle,UBERON:0011648,jaw muscle
+HP:0011499,Mydriasis,HP:0000615,Abnormality of the pupil
+UBERON:0001976,epithelium of esophagus,UBERON:0003929,gut epithelium
+DOID:4948,gallbladder carcinoma,DOID:3121,gallbladder cancer
+UBERON:2002217,parasphenoid-pterosphenoid joint,UBERON:0000982,skeletal joint
+UBERON:0002192,ventricular system choroidal fissure,UBERON:0000464,anatomical space
+UBERON:0013479,lung endothelium,UBERON:0000115,lung epithelium
+UBERON:0001447,tarsal bone,UBERON:0015050,tarsus endochondral element
+DOID:14749,methylmalonic acidemia,DOID:0060159,organic acidemia
+DOID:0060036,intrinsic cardiomyopathy,DOID:0050700,cardiomyopathy
+DOID:2025,gestational choriocarcinoma,DOID:3594,choriocarcinoma
+UBERON:2001885,neural spine 1,UBERON:0001076,neural spine
+DOID:0050784,primary progressive multiple sclerosis,DOID:2377,multiple sclerosis
+UBERON:0009581,midbrain mantle layer,UBERON:0005883,neural tube lateral wall mantle layer
+HP:0001737,Pancreatic cysts,HP:0012090,Abnormality of pancreas morphology
+DOID:9971,hypervitaminosis D,DOID:654,overnutrition
+UBERON:0013472,upper esophagus,UBERON:0004921,subdivision of digestive tract
+UBERON:0001761,future foramen cecum,UBERON:0005423,developing anatomical structure
+HP:0003015,Flared metaphyses,HP:0003016,Metaphyseal widening
+UBERON:0006276,perioptic mesenchyme,UBERON:0010312,immature eye
+NCBITaxon:7164,Anopheles <genus>,NCBITaxon:43816,Anophelinae
+UBERON:3010489,muscular artery,UBERON:0001637,artery
+DOID:8051,bladder papillary clear cell adenocarcinoma,DOID:5306,bladder clear cell adenocarcinoma
+HP:0007690,Map-dot-fingerprint corneal dystrophy,HP:0200020,Corneal erosions
+HP:0200037,skin vesicle,HP:0011355,Localized skin lesion
+UBERON:0001989,superior cervical ganglion,UBERON:0001991,cervical ganglion
+UBERON:0005908,conjunctival sac,UBERON:0005906,serous sac
+UBERON:0003827,thoracic segment bone,UBERON:0005181,thoracic segment organ
+DOID:3343,mucolipidosis,DOID:3211,lysosomal storage disease
+HP:0011449,Knee clonus,HP:0002169,Clonus
+UBERON:0001010,diaphysis of ulna,UBERON:0004120,mesoderm-derived structure
+CL:0000792,"CD4-positive, CD25-positive, alpha-beta regulatory T cell",CL:0000815,regulatory T cell
+UBERON:0009064,cervical air sac,UBERON:0009061,anterior air sac
+HP:0010395,Aplasia/Hypoplasia of the proximal phalanx of the 2nd toe,HP:0010347,Aplasia/Hypoplasia of the phalanges of the 2nd toe
+UBERON:2000175,posterior lateral line nerve,UBERON:0008906,lateral line nerve
+HP:0006698,Ventricular aneurysm,HP:0002617,Aneurysm
+UBERON:0007993,ulnar sesamoid bone,UBERON:0001479,sesamoid bone
+DOID:11353,bladder diverticulum,DOID:365,bladder disease
+UBERON:0004616,mammalian cervical vertebra 7,UBERON:0002413,cervical vertebra
+HP:0100250,Meningeal calcification,HP:0002514,Cerebral calcification
+HP:0000032,Abnormality of male external genitalia,HP:0000811,Abnormal external genitalia
+HP:0009191,Ivory epiphyses of the metacarpals,HP:0011001,Increased bone mineral density
+DOID:5511,dysgerminoma of ovary,DOID:4441,dysgerminoma
+UBERON:0014784,transverse cloacal muscle,UBERON:0014783,cloacal muscle
+HP:0009417,Pseudoepiphyses of the 3rd finger,HP:0010235,Pseudoepiphyses of the phalanges of the hand
+HP:0010321,Abnormality of the 4th toe,HP:0001780,Abnormality of toe
+DOID:13549,interval angle-closure glaucoma,DOID:1405,primary angle-closure glaucoma
+UBERON:2000899,hypaxial region somite 29,UBERON:0003895,hypaxial myotome region
+DOID:2799,bronchiolitis obliterans,DOID:2320,obstructive lung disease
+CL:0002314,external supporting cell of vestibular epithelium,CL:0002316,supporting cell of vestibular epithelium
+HP:0006709,Aplasia/Hypoplasia of the nipples,HP:0004404,Abnormality of the nipple
+HP:0003482,EMG: axonal abnormality,HP:0003457,EMG abnormality
+CL:0000101,sensory neuron,CL:0000526,afferent neuron
+UBERON:0000948,heart,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002637,ventral anterior nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0002692,medullary raphe nuclear complex,UBERON:0003528,brain grey matter
+UBERON:0010341,1st arch mesenchyme from head mesenchyme,UBERON:0010360,pharyngeal arch mesenchyme from head mesenchyme
+DOID:11354,stone in bladder diverticulum,DOID:11355,bladder calculus
+UBERON:0011951,prostate luminal epithelium,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0001765,mammary duct,UBERON:0003914,epithelial tube
+HP:0009963,Duplication of the middle phalanx of the 3rd finger,HP:0009959,Duplication of phalanx of 3rd finger
+DOID:713,HCL-V,DOID:285,hairy cell leukemia
+HP:0100102,Cone-shaped epiphysis of the distal phalanx of the 2nd toe,HP:0100046,Cone-shaped epiphyses of the 2nd toe
+UBERON:1000019,top of head,UBERON:0001444,subdivision of head
+CL:0000917,Tc1 cell,CL:0000908,"CD8-positive, alpha-beta cytokine secreting effector T cell"
+DOID:6405,ovarian papillary cystadenoma,DOID:3269,ovarian cystadenoma
+UBERON:0004995,mucosa of body of stomach,UBERON:0001199,mucosa of stomach
+HP:0010668,Abnormality of the zygomatic bone,HP:0005557,Abnormality of the zygomatic arch
+UBERON:0008295,feather barbule,UBERON:0004121,ectoderm-derived structure
+UBERON:3000428,perilymphatic system,UBERON:0001032,sensory system
+UBERON:0001104,anterior jugular vein,UBERON:0004711,jugular vein
+UBERON:0001307,capsule of ovary,UBERON:0003893,capsule
+UBERON:0012925,bronchial bud,UBERON:0005153,epithelial bud
+DOID:0050576,Senior-Loken syndrome,DOID:0050737,autosomal recessive disease
+UBERON:0008902,lateral recess of third vetricle,UBERON:0000464,anatomical space
+UBERON:0011922,cochlear basement membrane,UBERON:0004121,ectoderm-derived structure
+HP:0009664,Absent epiphysis of the proximal phalanx of the thumb,HP:0009663,Abnormality of the epiphysis of the proximal phalanx of the thumb
+DOID:10603,glucose intolerance,DOID:4195,hyperglycemia
+HP:0009261,Absent epiphysis of the proximal phalanx of the 4th finger,HP:0010268,Absent epiphyses of the proximal phalanges of the hand
+UBERON:0010351,otic capsule cartilage element,UBERON:0005863,cartilaginous condensation
+HP:0001857,Short distal phalanx of toe,HP:0010185,Aplasia/Hypoplasia of the distal phalanges of the toes
+UBERON:0010032,anterior part of tongue,UBERON:0004121,ectoderm-derived structure
+CL:0000732,amoeboid cell,CL:0000219,motile cell
+DOID:3773,third ventricle chordoid glioma,DOID:3541,cerebral ventricle cancer
+UBERON:3010229,costal grooves,UBERON:3000977,body external integument structure
+UBERON:2002229,presumptive atrium primitive heart tube,UBERON:0000481,multi-tissue structure
+UBERON:3000649,anterior process of vomer,UBERON:0004530,bony projection
+HP:0007344,Atrophy/Degeneration involving the spinal cord,HP:0007367,Atrophy/Degeneration affecting the central nervous system
+HP:0010657,Patchy reduction of bone mineral density,HP:0010658,Patchy changes of bone mineral density
+UBERON:3010259,phallodeum,UBERON:0008811,intromittent organ
+DOID:1927,sphingolipidosis,DOID:9455,lipid storage disease
+UBERON:0001610,lingual artery,UBERON:0003496,head blood vessel
+UBERON:0005625,tubotympanic recess lumen,UBERON:0007473,lumen of epithelial sac
+DOID:5240,retinal hemangioblastoma,DOID:4645,retinal cancer
+HP:0002054,Heavy supraorbital ridges,HP:0000336,Prominent supraorbital ridges
+UBERON:0003248,epithelium of footplate,UBERON:0010371,ecto-epithelium
+HP:0006230,Unilateral oligodactyly,HP:0001180,Oligodactyly (hands)
+UBERON:0002152,middle cerebellar peduncle,UBERON:0007416,cerebellar peduncle
+UBERON:0006282,primary head vein,UBERON:0009141,craniocervical region vein
+UBERON:0006790,deep white layer of superior colliculus,UBERON:0006786,white matter of superior colliculus
+CL:1000716,kidney outer medulla collecting duct principal cell,CL:1000548,kidney outer medulla collecting duct epithelial cell
+UBERON:0004457,cavity lining,UBERON:0004923,organ component layer
+HP:0007850,Retinal vascular proliferation,HP:0008046,Abnormality of the retinal vasculature
+UBERON:0001840,semicircular canal,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001844,cochlea,UBERON:0010313,neural crest-derived structure
+HP:0100775,Dural ectasia,HP:0010303,Abnormality of the spinal meninges
+NCBITaxon:712,Pasteurellaceae,NCBITaxon:135625,Pasteurellales
+UBERON:0001562,digastric muscle,UBERON:0001577,facial nerve muscle
+NCBITaxon:51291,Chlamydiales,NCBITaxon:204429,Chlamydiia
+DOID:4079,heart valve disease,DOID:114,heart disease
+HP:0100351,Contractures of the proximal interphalangeal joint of the 5th toe,HP:0010345,Flexion contracture of the 5th toe
+DOID:8543,"Hodgkin's lymphoma, lymphocytic-histiocytic predominance",DOID:8567,Hodgkin's lymphoma
+DOID:2781,rectosigmoid cancer,DOID:2782,rectosigmoid junction cancer
+UBERON:3010144,odontoids,UBERON:0004121,ectoderm-derived structure
+UBERON:0002616,regional part of brain,UBERON:0000073,regional part of nervous system
+HP:0001852,Sandal gap,HP:0001780,Abnormality of toe
+HP:0012670,Orthostatic syncope,HP:0001279,Syncope
+UBERON:0012262,manual minor digit (Aves),UBERON:0002389,manual digit
+UBERON:2001095,immature macula,UBERON:0005423,developing anatomical structure
+HP:0100147,Bracket epiphysis of the middle phalanx of the 3rd toe,HP:0100056,Bracket epiphyses of the 3rd toe
+CL:0011002,lateral motor column neuron,CL:0011001,spinal cord motor neuron
+DOID:5236,subungual glomus tumor,DOID:2431,glomus tumor
+UBERON:0004792,secretion of endocrine pancreas,UBERON:0004795,pancreas secretion
+HP:0000200,Short lingual frenulum,HP:0000190,Abnormality of oral frenula
+UBERON:0000057,urethra,UBERON:0000062,organ
+DOID:0050826,tricuspid valve disease,DOID:4079,heart valve disease
+DOID:12698,gynecomastia,DOID:10688,hypertrophy of breast
+UBERON:2000540,magnocellular octaval nucleus,UBERON:2000401,octaval nerve sensory nucleus
+CL:1001474,medium spiny neuron,CL:0000540,neuron
+DOID:5208,malignant struma ovarii,DOID:2640,struma ovarii
+DOID:1556,arthus reaction,DOID:1557,hypersensitivity reaction type III disease
+DOID:13777,epidermodysplasia verruciformis,DOID:0050737,autosomal recessive disease
+UBERON:0008293,filoplume feather,UBERON:0000022,feather
+UBERON:2001786,unbranched dorsal fin ray,UBERON:4000177,dorsal fin lepidotrichium
+UBERON:2000937,hypaxial region somite 13,UBERON:0003895,hypaxial myotome region
+HP:0008497,Congenital craniofacial dysostosis,HP:0004439,Craniofacial dysostosis
+DOID:7910,maxillary sinus squamous cell carcinoma,DOID:1357,maxillary sinus cancer
+HP:0011965,Abnormality of citrulline metabolism,HP:0004337,Abnormality of amino acid metabolism
+DOID:7497,brain ependymoma,DOID:0060108,brain glioma
+HP:0001996,Chronic metabolic acidosis,HP:0012468,Chronic acidosis
+HP:0003981,Broad radius,HP:0002818,Abnormality of the radius
+DOID:1342,congenital hypoplastic anemia,DOID:12449,aplastic anemia
+UBERON:0005093,cement gland,UBERON:0002050,embryonic structure
+DOID:2977,primary hyperoxaluria,DOID:557,kidney disease
+UBERON:3000192,foramen perilymphaticum,UBERON:3000051,braincase and otic capsule opening
+HP:0005768,2-4 toe cutaneous syndactyly,HP:0010621,Cutaneous syndactyly of toes
+UBERON:0011676,subdivision of organism along main body axis,UBERON:0000475,organism subdivision
+UBERON:0001035,dento-alveolar joint,UBERON:0004121,ectoderm-derived structure
+UBERON:0001333,male urethra,UBERON:0014403,male anatomical structure
+UBERON:0002528,sacral lymph node,UBERON:0000029,lymph node
+DOID:10175,optic papillitis,DOID:1210,optic neuritis
+HP:0007227,Macrogyria,HP:0002536,Abnormal cortical gyration
+CL:0000423,tip cell,CL:0000422,mitogenic signaling cell
+DOID:2460,anterior dislocation of lens,DOID:1242,globe disease
+UBERON:0006461,second sacral spinal cord segment,UBERON:0007717,sacral subsegment of spinal cord
+DOID:12753,corneal staphyloma,DOID:10124,corneal disease
+UBERON:0001567,cheek,UBERON:0001444,subdivision of head
+HP:0011900,Hypofibrinogenemia,HP:0011898,Abnormality of circulating fibrinogen
+HP:0009660,Short phalanx of the thumb,HP:0009658,Aplasia/Hypoplasia of the phalanges of the thumb
+CL:0002205,brush cell of lobular bronchiole,CL:0000082,epithelial cell of lung
+DOID:4323,epidermolytic acanthoma,DOID:174,acanthoma
+DOID:4719,bone giant cell sarcoma,DOID:2705,malignant giant cell tumor
+DOID:1324,lung cancer,DOID:0050615,respiratory system cancer
+UBERON:0013138,coronary ligament of liver,UBERON:0013139,ligament of liver
+UBERON:0000351,nuchal ligament,UBERON:0004267,back connective tissue
+UBERON:4200018,calcaneal tuber,UBERON:4100000,skeletal element projection
+UBERON:2101416,pelvic fin distal radial element 3,UBERON:1600008,pelvic fin distal radial element
+HP:0100035,Phonic tics,HP:0100033,Tics
+UBERON:0002604,ventral nucleus of lateral lemniscus,UBERON:0009662,hindbrain nucleus
+UBERON:0006668,carotid canal,UBERON:0005744,bone foramen
+DOID:5551,choriocarcinoma of the testis,DOID:4084,testicular trophoblastic tumor
+HP:0006959,Proximal spinal muscular atrophy,HP:0007269,Spinal muscular atrophy
+UBERON:0004331,proximal phalanx of manual digit 5,UBERON:0003639,manual digit 5 phalanx
+CL:1001593,parathyroid glandular cell,CL:0000150,glandular epithelial cell
+DOID:5631,endometrial adenosquamous carcinoma,DOID:2871,endometrial carcinoma
+HP:0010599,Abnormality of the distal humeral epiphysis,HP:0003946,Abnormality of the epiphyses of the elbow
+UBERON:0001297,serosa of uterus,UBERON:0005156,reproductive structure
+DOID:5810,adenosine deaminase deficiency,DOID:627,severe combined immunodeficiency
+UBERON:0011185,gastrointestinal sphincter,UBERON:0013765,digestive system organ
+UBERON:4200098,ischial foot,UBERON:0004120,mesoderm-derived structure
+HP:0005688,Dysplastic distal thumb phalanges with a central hole,HP:0009617,Abnormality of the distal phalanx of the thumb
+CL:0000067,ciliated epithelial cell,CL:0000075,columnar/cuboidal epithelial cell
+HP:0009902,Cleft helix,HP:0011039,Abnormality of the helix
+CL:0000018,spermatid,CL:0000015,male germ cell
+UBERON:0003450,upper jaw incisor,UBERON:0001098,incisor tooth
+UBERON:0011830,duct of lesser vestibular gland,UBERON:0006555,excretory tube
+UBERON:0005910,transitional epithelium,UBERON:0000486,multilaminar epithelium
+DOID:2450,central retinal vein occlusion,DOID:1729,retinal vascular occlusion
+UBERON:0001904,habenula,UBERON:0002757,regional part of epithalamus
+UBERON:0010009,aggregate regional part of brain,UBERON:0002616,regional part of brain
+DOID:7281,uterine corpus adenocarcinofibroma,DOID:4114,uterine body mixed cancer
+UBERON:0002170,upper lobe of right lung,UBERON:0006518,right lung lobe
+HP:0008390,Recurrent loss of toenails and fingernails,HP:0001597,Abnormality of the nail
+DOID:0080032,craniodiaphyseal dysplasia,DOID:4254,osteosclerosis
+UBERON:0003421,mesenchyme of vomeronasal organ,UBERON:0009891,facial mesenchyme
+CL:0000510,paneth cell,CL:0002563,intestinal epithelial cell
+HP:0004245,Comma-shaped scaphoid,HP:0004235,Comma-shaped carpal bones
+UBERON:0002911,parietal operculum,UBERON:0003022,cerebral cortex lobe
+CL:0000991,CD11c-negative plasmacytoid dendritic cell,CL:0000784,plasmacytoid dendritic cell
+HP:0002893,Pituitary adenoma,HP:0011750,Neoplasm of the anterior pituitary
+UBERON:3000678,esophageal process,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0002519,interrenal epithelial cell,CL:0002518,kidney epithelial cell
+UBERON:0005997,tricuspid valve anulus,UBERON:0006008,fibrous ring of heart
+HP:0010019,Fragmentation of the epiphysis of the 1st metacarpal,HP:0010014,Abnormality of the epiphysis of the 1st metacarpal
+CL:0000969,regulatory B cell,CL:0000785,mature B cell
+HP:0009378,Triangular shaped phalanges of the 5th finger,HP:0009774,Triangular shaped phalanges of the hand
+UBERON:3000744,urostyle cotyle,UBERON:0004120,mesoderm-derived structure
+DOID:334,histrionic personality disorder,DOID:1510,personality disorder
+HP:0012374,Abnormality of the globe,HP:0012372,Abnormal eye morphology
+HP:0010620,Malar prominence,HP:0012369,Malar anomaly
+HP:0011749,Adrenocorticotropic hormone excess,HP:0010514,Hyperpituitarism
+UBERON:2001253,neural arch 2,UBERON:0003861,neural arch
+UBERON:0005591,diencephalon lateral wall,UBERON:0005496,neural tube lateral wall
+DOID:1417,choroid disease,DOID:3480,uveal disease
+DOID:3186,adult oligodendroglioma,DOID:3181,oligodendroglioma
+UBERON:0014505,proximal phalanx of digit 5,UBERON:0004302,proximal phalanx
+CL:0002224,lens epithelial cell,CL:0000075,columnar/cuboidal epithelial cell
+HP:0007838,Progressive ptosis,HP:0000508,Ptosis
+UBERON:2001611,quadrate posterodorsal process,UBERON:0010313,neural crest-derived structure
+UBERON:0016416,anterior chest,UBERON:0000475,organism subdivision
+HP:0009575,Triangular shaped middle phalanx of the 2nd finger,HP:0009543,Abnormality of the middle phalanx of the 2nd finger
+UBERON:0010741,bone of pectoral complex,UBERON:0010740,bone of appendage girdle complex
+DOID:827,ureter tuberculosis,DOID:2149,urogenital tuberculosis
+DOID:8544,chronic fatigue syndrome,DOID:225,syndrome
+DOID:11204,allergic conjunctivitis,DOID:2475,chronic conjunctivitis
+DOID:12139,dysthymic disorder,DOID:3324,mood disorder
+UBERON:0007267,trachea pre-cartilage rings,UBERON:0005866,pre-cartilage condensation
+UBERON:0005760,urorectal septum,UBERON:0003037,septum
+HP:0001705,Right ventricular outlet obstruction,HP:0001707,Abnormality of the right ventricle
+UBERON:2005019,efferent lamellar arteriole,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0002405,gamma-delta thymocyte,CL:0002489,double negative thymocyte
+DOID:0050916,bronchus mucoepidermoid carcinoma,DOID:1325,bronchus cancer
+HP:0003390,Sensory axonal neuropathy,HP:0003477,Peripheral axonal neuropathy
+UBERON:3000292,medial ramus of pterygoid,UBERON:4100000,skeletal element projection
+UBERON:0013128,bulb of penis,UBERON:0014403,male anatomical structure
+UBERON:0003310,floor plate of metencephalon,UBERON:0003306,floor plate of neural tube
+DOID:12801,mucopolysaccharidosis III,DOID:12798,mucopolysaccharidosis
+UBERON:0001928,preoptic area,UBERON:0002784,regional part of diencephalon
+UBERON:0005662,4th arch ectoderm,UBERON:0000924,ectoderm
+HP:0009643,Bullet-shaped distal phalanx of the thumb,HP:0009837,Bullet-shaped distal phalanges of the hand
+CL:0001024,"CD34-positive, CD38-negative hematopoietic stem cell",CL:0000037,hematopoietic stem cell
+HP:0000956,Acanthosis nigricans,HP:0011368,Epidermal thickening
+HP:0005248,Intrahepatic biliary atresia,HP:0011040,Abnormality of the intrahepatic bile duct
+HP:0003276,Pelvic exostoses,HP:0100777,Exostoses
+DOID:6901,familiar ovarian carcinoma,DOID:2152,ovary epithelial cancer
+HP:0000679,Taurodontia,HP:0006486,Abnormality of the dental root
+HP:0009462,Radial deviation of the 3rd finger,HP:0009466,Radial deviation of finger
+UBERON:0005289,tela choroidea of telencephalic ventricle,UBERON:0004121,ectoderm-derived structure
+DOID:0050072,adiaspiromycosis,DOID:0050292,primary systemic mycosis
+UBERON:0003682,palatal muscle,UBERON:0004121,ectoderm-derived structure
+DOID:0050886,Troyer syndrome,DOID:2476,hereditary spastic paraplegia
+HP:0100390,Short distal phalanx of the 4th toe,HP:0100367,Short phalanx of the 4th toe
+DOID:14319,pleuropneumonia,DOID:552,pneumonia
+HP:0004035,Abnormality of the styloid process,HP:0002997,Abnormality of the ulna
+CL:0008013,cranial visceromotor neuron,CL:0005025,visceromotor neuron
+UBERON:0011673,plastron scute,UBERON:0008201,scute
+UBERON:4200031,caudalipuboischiotibialis,UBERON:0001630,muscle organ
+HP:0006829,Severe muscular hypotonia,HP:0001252,Muscular hypotonia
+HP:0003390,Sensory axonal neuropathy,HP:0000763,Sensory neuropathy
+HP:0006280,Chronic pancreatitis,HP:0001733,Pancreatitis
+HP:0100747,Macrodactyly of toe,HP:0001780,Abnormality of toe
+UBERON:0003050,olfactory placode,UBERON:0010371,ecto-epithelium
+HP:0000383,Abnormality of periauricular region,HP:0000356,Abnormality of the outer ear
+DOID:1076,chronic pyelonephritis,DOID:11400,pyelonephritis
+UBERON:0006932,vestibular epithelium,UBERON:0006937,inner ear epithelium
+UBERON:0007302,pectoral appendage vasculature,UBERON:0007304,appendage vasculature
+DOID:3142,leg dermatosis,DOID:37,skin disease
+NCBITaxon:34390,Epidermophyton,NCBITaxon:34385,mitosporic Arthrodermataceae
+UBERON:0003614,blood vessel elastic tissue,UBERON:0004120,mesoderm-derived structure
+UBERON:4300025,posterior dorsolateral plate,UBERON:0007829,pectoral girdle bone
+UBERON:0016392,mastoid lymph node,UBERON:0015870,lymph node of head
+UBERON:0003947,brain ventricle/choroid plexus,UBERON:0004121,ectoderm-derived structure
+UBERON:0004312,distal phalanx of manual digit 3,UBERON:0014485,distal phalanx of digit 3
+UBERON:0004316,distal phalanx of pedal digit 2,UBERON:0014484,distal phalanx of digit 2
+DOID:778,delusional disorder,DOID:2468,psychotic disorder
+UBERON:0008311,penile bulb artery,UBERON:0005156,reproductive structure
+DOID:11594,ring staphyloma,DOID:11595,scleral staphyloma
+HP:0000896,Rib exostoses,HP:0100777,Exostoses
+HP:0007441,Hyperpigmented/hypopigmented macules,HP:0012733,Macule
+DOID:3666,cutaneous solitary mastocytoma,DOID:3664,mast cell neoplasm
+HP:0003529,Parathormone-independent increased renal tubular calcium reabsorption,HP:0003110,Abnormality of urine homeostasis
+UBERON:0005393,cortical layer IV,UBERON:0002301,layer of neocortex
+UBERON:0001043,esophagus,UBERON:0004921,subdivision of digestive tract
+UBERON:0008199,chin,UBERON:0003102,surface structure
+DOID:8203,sacral spinal canal and spinal cord meningioma,DOID:1140,spinal canal and spinal cord meningioma
+UBERON:0003978,valve,UBERON:0000064,organ part
+HP:0007634,Nonarteritic anterior ischemic optic neuropathy,HP:0001138,Optic neuropathy
+HP:0001849,Oligodactyly (feet),HP:0010760,Absent toe
+HP:0100312,Cerebral germinoma,HP:0100835,Benign neoplasm of the central nervous system
+NCBITaxon:28450,Burkholderia pseudomallei,NCBITaxon:111527,pseudomallei group
+CL:0000531,primary sensory neuron,CL:0000530,primary neuron
+UBERON:0011167,septomaxilla bone,UBERON:0003462,facial bone
+DOID:3274,proliferative type fibrocystic change of breast,DOID:10354,breast fibrocystic disease
+CL:0000186,myofibroblast cell,CL:0000548,animal cell
+HP:0011154,Focal autonomic seizures,HP:0007359,Focal seizures
+UBERON:0005251,yolk sac cavity,UBERON:0002553,anatomical cavity
+HP:0009835,Aplasia/Hypoplasia of the distal phalanges of the hand,HP:0009767,Aplasia/Hypoplasia of the phalanges of the hand
+HP:0000166,Severe periodontitis,HP:0000704,Periodontitis
+UBERON:0002139,subcommissural organ,UBERON:0002966,regional part of midbrain tectum
+HP:0010383,Aplasia/Hypoplasia of the phalanges of the 5th toe,HP:0010342,Abnormality of the phalanges of the 5th toe
+HP:0010109,Short hallux,HP:0008362,Aplasia/Hypoplasia of the hallux
+UBERON:0003246,epithelium of endolymphatic sac,UBERON:0006937,inner ear epithelium
+UBERON:2005014,recurrent branch afferent branchial artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0009571,Curved middle phalanx of the 2nd finger,HP:0009543,Abnormality of the middle phalanx of the 2nd finger
+NCBITaxon:92088,Trombiculoidea,NCBITaxon:83141,Parasitengona
+DOID:0080049,acromesomelic dysplasia,DOID:2256,osteochondrodysplasia
+HP:0002460,Distal muscle weakness,HP:0001324,Muscle weakness
+HP:0008569,"Microtia, second degree",HP:0008551,Microtia
+UBERON:0001312,superior vesical artery,UBERON:0015212,lateral structure
+UBERON:0007501,arborizing epithelial duct system,UBERON:0007499,epithelial sac
+HP:0010660,Abnormal hand bone ossification,HP:0001155,Abnormality of the hand
+UBERON:0004812,male prepuce epithelium,UBERON:0004803,penis epithelium
+UBERON:0004816,larynx epithelium,UBERON:0004802,respiratory tract epithelium
+UBERON:0010853,capitulum of humerus,UBERON:0005055,zone of long bone
+HP:0009198,Abnormality of the epiphysis of the distal phalanx of the 5th finger,HP:0010243,Abnormality of the epiphyses of the distal phalanx of finger
+HP:0001822,Hallux valgus,HP:0010051,Deviation/Displacement of the hallux
+UBERON:0000945,stomach,UBERON:0004921,subdivision of digestive tract
+HP:0003252,Anteriorly displaced genitalia,HP:0012243,Abnormal genital system morphology
+UBERON:0006583,statocyst,UBERON:0000020,sense organ
+NCBITaxon:499556,Chapare virus,NCBITaxon:208897,New world arenaviruses
+UBERON:0014674,distal interphalangeal joint of pedal digit 4,UBERON:0007727,interphalangeal joint of pedal digit 4
+UBERON:0003474,meningeal artery,UBERON:0001637,artery
+HP:0012233,Intramuscular hematoma,HP:0011805,Abnormality of muscle morphology
+UBERON:0013442,postorbital process,UBERON:0004121,ectoderm-derived structure
+DOID:0050463,campomelic dysplasia,DOID:2256,osteochondrodysplasia
+UBERON:0001598,temporalis muscle,UBERON:0003681,masticatory muscle
+HP:0002059,Cerebral atrophy,HP:0007369,Atrophy/Degeneration affecting the cerebrum
+HP:0004761,Post-angioplasty coronary artery restenosis,HP:0001677,Coronary artery disease
+CL:1000450,epithelial cell of glomerular capsule,CL:1000510,kidney glomerular epithelial cell
+UBERON:3000017,anterior process of pars palatina of maxilla,UBERON:0004120,mesoderm-derived structure
+UBERON:0001614,superficial temporal artery,UBERON:0001632,temporal artery
+DOID:4175,Rh isoimmunization,DOID:4176,blood group incompatibility
+UBERON:0007111,Douglas' pouch,UBERON:0004120,mesoderm-derived structure
+UBERON:0003276,skeleton of embryo,UBERON:0001434,skeletal system
+UBERON:0004700,arterial system endothelium,UBERON:0004852,cardiovascular system endothelium
+UBERON:0011581,platypus calcaneus spur,UBERON:0008784,lower limb segment
+UBERON:0001984,crypt of lieberkuhn of large intestine,UBERON:0001983,crypt of Lieberkuhn
+DOID:14095,boutonneuse fever,DOID:11104,spotted fever
+UBERON:2001256,lateral floor plate,UBERON:0004121,ectoderm-derived structure
+CL:0000891,foam cell,CL:0000003,native cell
+UBERON:0004984,mucosa of seminal vesicle,UBERON:0005156,reproductive structure
+UBERON:2001610,quadrate dorsal process,UBERON:0010313,neural crest-derived structure
+CL:0000575,corneal epithelial cell,CL:0000076,squamous epithelial cell
+HP:0009106,Abnormal pelvis bone ossification,HP:0011849,Abnormal bone ossification
+UBERON:0002861,second sacral dorsal root ganglion,UBERON:0002837,sacral dorsal root ganglion
+UBERON:0010014,epigonal organ,UBERON:0004177,hemopoietic organ
+UBERON:0002326,lamina propria of urethra,UBERON:0004120,mesoderm-derived structure
+UBERON:0005711,foregut duodenum mesentery,UBERON:0003397,mesentery of duodenum
+HP:0100463,Patchy sclerosis of the middle phalanx of the 5th toe,HP:0010199,Patchy sclerosis of the middle phalanges of the toes
+UBERON:0006490,fourth cervical spinal cord segment,UBERON:0007714,cervical subsegment of spinal cord
+HP:0001511,Intrauterine growth retardation,HP:0001510,Growth delay
+UBERON:0005356,Rathke's pouch,UBERON:0010371,ecto-epithelium
+UBERON:0000071,death stage,UBERON:0000105,life cycle stage
+UBERON:0000401,mandibular ramus,UBERON:0004120,mesoderm-derived structure
+UBERON:2001022,myotome somite 9,UBERON:0003082,myotome
+UBERON:0001350,coccyx,UBERON:0008001,irregular bone
+HP:0002277,Horner syndrome,HP:0000616,Miosis
+UBERON:0004747,supraoccipital bone,UBERON:0015015,supraoccipital endochondral element
+DOID:0050814,temtamy preaxial brachydactyly syndrome,DOID:0050737,autosomal recessive disease
+DOID:0060010,Omenn syndrome,DOID:628,combined T cell and B cell immunodeficiency
+UBERON:0015148,tail hair,UBERON:0001037,strand of hair
+HP:0000288,Abnormality of the philtrum,HP:0000153,Abnormality of the mouth
+UBERON:0001894,diencephalon,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0008264,echinopluteus larval stage,UBERON:0000069,larval stage
+UBERON:2001617,trunk sensory canal,UBERON:2001612,sensory canal
+DOID:1289,neurodegenerative disease,DOID:331,central nervous system disease
+HP:0003676,Progressive disorder,HP:0003679,Pace of progression
+UBERON:0002269,pupillary membrane,UBERON:0002050,embryonic structure
+CL:0002304,non-pigmented ciliary epithelial cell,CL:0000710,neurecto-epithelial cell
+HP:0008669,Abnormal spermatogenesis,HP:0000025,Functional abnormality of male internal genitalia
+HP:0002813,Abnormality of limb bone morphology,HP:0011844,Abnormal appendicular skeleton morphology
+DOID:2326,gastroenteritis,DOID:77,gastrointestinal system disease
+DOID:5385,mixed cell adenoma,DOID:657,adenoma
+HP:0010712,1-4 toe syndactyly,HP:0001770,Toe syndactyly
+HP:0011163,Somatosensory auras,HP:0011157,Auras
+NCBITaxon:5234,Tremellales,NCBITaxon:155616,Tremellomycetes
+UBERON:0002800,spinal trigeminal tract of pons,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0000946,cardial valve,UBERON:0010313,neural crest-derived structure
+UBERON:0001348,brown adipose tissue,UBERON:0001013,adipose tissue
+UBERON:0007383,enveloping layer of ectoderm,UBERON:0010371,ecto-epithelium
+HP:0008819,Narrow femoral neck,HP:0003367,Abnormality of the femoral neck
+UBERON:0002328,notochord,UBERON:0004120,mesoderm-derived structure
+HP:0003464,Abnormal cholesterol homeostasis,HP:0003107,Abnormality of cholesterol metabolism
+CL:0002502,type M enteroendocrine cell,CL:1001598,small intestine glandular cell
+HP:0001040,Multiple pterygia,HP:0001059,Pterygium
+UBERON:0010214,cricoid pre-cartilage condensation,UBERON:0010213,laryngeal pre-cartilage condensation
+UBERON:0006793,deep layer of superior colliculus,UBERON:0006783,layer of superior colliculus
+DOID:9597,Krukenberg carcinoma,DOID:2152,ovary epithelial cancer
+HP:0000728,Impaired ability to form peer relationships,HP:0000735,Impaired social interactions
+UBERON:2005018,efferent filamental artery,UBERON:0003469,respiratory system artery
+UBERON:0005666,4th arch endoderm,UBERON:0000925,endoderm
+CL:1000339,enterocyte of epithelium proper of small intestine,CL:1000334,enterocyte of epithelium of small intestine
+HP:0010513,Pituitary calcification,HP:0002514,Cerebral calcification
+DOID:3351,bone angioendothelial sarcoma,DOID:3347,osteosarcoma
+HP:0100816,Lip hyperpigmentation,HP:0007400,Irregular hyperpigmentation
+UBERON:0001170,mesentery of small intestine,UBERON:0007826,peritoneal mesentery
+UBERON:0004746,prootic bone,UBERON:0010313,neural crest-derived structure
+HP:0005518,Erythrocyte macrocytosis,HP:0001877,Abnormality of erythrocytes
+UBERON:0013632,sesamoid cartilage,UBERON:0007844,cartilage element
+HP:0000699,Diastema,HP:0000692,Misalignment of teeth
+UBERON:0002648,anterior median eminence,UBERON:0004120,mesoderm-derived structure
+DOID:1195,ischemic neuropathy,DOID:870,neuropathy
+UBERON:0005439,definitive endoderm,UBERON:0002050,embryonic structure
+HP:0011752,Neoplasm of the posterior pituitary,HP:0011751,Abnormality of the posterior pituitary
+DOID:585,nephrolithiasis,DOID:557,kidney disease
+DOID:9726,vitreous detachment,DOID:9720,vitreous disease
+CL:0002509,"CD103-positive, langerin-positive lymph node dendritic cell",CL:0002461,CD103-positive dendritic cell
+UBERON:0010547,pedal digit 1 metatarsal pre-cartilage condensation,UBERON:0015037,pedal digit 1 metatarsal endochondral element
+HP:0009500,Abnormality of the epiphysis of the middle phalanx of the 2nd finger,HP:0010244,Abnormality of the epiphyses of the middle phalanges of the hand
+UBERON:0002579,regional part of medullary reticular formation,UBERON:0002678,regional part of medulla oblongata
+UBERON:0011305,superficial part of temporalis,UBERON:0003681,masticatory muscle
+UBERON:0004495,skeletal muscle tissue of diaphragm,UBERON:0003898,skeletal muscle tissue of trunk
+DOID:4230,smooth muscle cancer,DOID:4045,muscle cancer
+HP:0001557,Prenatal movement abnormality,HP:0001197,Abnormality of prenatal development or birth
+HP:0006555,Diffuse hepatic steatosis,HP:0001397,Hepatic steatosis
+DOID:3674,kidney rhabdoid cancer,DOID:3672,rhabdoid cancer
+HP:0008544,Abnormally folded helix,HP:0011039,Abnormality of the helix
+UBERON:0002423,hepatobiliary system,UBERON:0000467,anatomical system
+DOID:7347,ovarian stromal hyperthecosis,DOID:1100,ovarian disease
+UBERON:0013639,mechanical papilla of tongue,UBERON:0001726,papilla of tongue
+HP:0005310,Large vessel vasculitis,HP:0002633,Vasculitis
+HP:0004796,Gastrointestinal obstruction,HP:0012719,Functional abnormality of the gastrointestinal tract
+UBERON:0006207,aortico-pulmonary spiral septum,UBERON:0004142,outflow tract septum
+UBERON:0007169,short head of biceps brachii,UBERON:0011906,muscle head
+DOID:11832,visual epilepsy,DOID:5691,visual cortex disease
+HP:0002209,Sparse scalp hair,HP:0100037,Abnormality of the scalp hair
+HP:0009881,Aplasia of the distal phalanges of the hand,HP:0009802,Aplasia of the phalanges of the hand
+UBERON:0004615,mammalian cervical vertebra 6,UBERON:0002413,cervical vertebra
+DOID:0060134,apperceptive agnosia,DOID:4090,agnosia
+HP:0007366,Atrophy/Degeneration affecting the brainstem,HP:0002363,Abnormality of the brainstem
+CL:1000478,transitional myocyte of sinoatrial node,CL:1000409,myocyte of sinoatrial node
+UBERON:0000012,somatic nervous system,UBERON:0011216,organ system subdivision
+UBERON:0006659,cruciate ligament of knee,UBERON:0011088,ligament of knee joint
+HP:0100610,Maternal hyperphenylalaninemia,HP:0010893,Abnormality of phenylalanine metabolism
+HP:0009553,Abnormality of the hairline,HP:0100037,Abnormality of the scalp hair
+DOID:0080030,"spondyloepimetaphyseal dysplasia, Missouri type",DOID:0080027,spondyloepimetaphyseal dysplasia
+HP:0011470,Nasogastric tube feeding in infancy,HP:0008872,Feeding difficulties in infancy
+HP:0006702,Spontaneous coronary artery dissection,HP:0006704,Abnormality of the coronary arteries
+UBERON:0003076,posterior neural tube,UBERON:0005423,developing anatomical structure
+DOID:12978,Plasmodium vivax malaria,DOID:12365,malaria
+DOID:7213,transitional meningioma,DOID:3565,meningioma
+UBERON:0003023,pontine tegmentum,UBERON:0004121,ectoderm-derived structure
+HP:0100220,Pseudoepiphysis of the middle phalanx of the 5th toe,HP:0100084,Pseudoepiphyses of the 5th toe
+UBERON:0006261,male genital tubercle,UBERON:0011757,differentiated genital tubercle
+UBERON:4100012,postacetabular zone,UBERON:0004120,mesoderm-derived structure
+HP:0000135,Hypogonadism,HP:0000080,Abnormality of genital physiology
+NCBITaxon:447135,Myodes glareolus,NCBITaxon:447134,Myodes
+HP:0004395,Malnutrition,HP:0011458,Abdominal symptom
+UBERON:0002474,cerebellar peduncular complex,UBERON:0003035,regional part of cerebellar white matter
+UBERON:0003453,large intestine Peyer's patch,UBERON:0001211,Peyer's patch
+UBERON:0001734,palatine uvula,UBERON:0000477,anatomical cluster
+CL:0000826,pro-B cell,CL:0000838,lymphoid lineage restricted progenitor cell
+CL:0000632,hepatic stellate cell,CL:0000327,extracellular matrix secreting cell
+DOID:4183,pseudopseudohypoparathyroidism,DOID:4184,pseudohypoparathyroidism
+HP:0010025,Triangular epiphysis of the 1st metacarpal,HP:0010278,Triangular epiphyses of the proximal phalanges of the hand
+CL:1000466,chromaffin cell of right ovary,CL:1000465,chromaffin cell of ovary
+UBERON:0002910,posterior ascending limb of lateral sulcus,UBERON:0003022,cerebral cortex lobe
+UBERON:0002069,stratum granulosum of epidermis,UBERON:0004121,ectoderm-derived structure
+UBERON:0001210,muscularis mucosae of small intestine,UBERON:0004239,small intestine smooth muscle
+DOID:10127,cerebral artery occlusion,DOID:6713,cerebrovascular disease
+HP:0008348,Immunoglobulin IgG2 deficiency,HP:0004315,IgG deficiency
+DOID:11557,acute serous otitis media,DOID:3697,acute transudative otitis media
+UBERON:0003864,middle phalanx of manus,UBERON:0001436,phalanx of manus
+HP:0005949,Apneic episodes in infancy,HP:0002104,Apnea
+DOID:4294,adenoid basal cell carcinoma,DOID:2513,basal cell carcinoma
+UBERON:2001225,basibranchial 3 bone,UBERON:2001917,basibranchial 3 element
+UBERON:0006349,epigastric artery,UBERON:0001637,artery
+HP:0010082,Symphalangism affecting the distal phalanx of the hallux,HP:0010091,Symphalangism affecting the proximal phalanx of the hallux
+UBERON:0006351,principal vein of forelimb,UBERON:0003515,forelimb blood vessel
+UBERON:0002993,inferior central nucleus,UBERON:0007413,nucleus of pontine reticular formation
+HP:0010377,Symphalangism affecting the phalanges of the 4th toe,HP:0100235,Synostosis involving bones of the toes
+DOID:7567,vulvar clear cell hidradenocarcinoma,DOID:1294,vulva carcinoma
+UBERON:0005976,ansiform lobule crus I,UBERON:0014648,hemisphere part of cerebellar posterior lobe
+UBERON:0011346,palatine raphe,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0001598,Concave nail,HP:0002164,Nail dysplasia
+HP:0010448,Colonic atresia,HP:0002250,Abnormality of the large intestine
+UBERON:0002301,layer of neocortex,UBERON:0000064,organ part
+HP:0008011,Peripheral opacification of the cornea,HP:0007759,Opacification of the corneal stroma
+HP:0010839,Increased urinary copper concentration,HP:0010836,Abnormality of copper homeostasis
+DOID:5625,esophageal adenosquamous carcinoma,DOID:1107,esophageal carcinoma
+DOID:0050668,alcohol-related birth defect,DOID:0050696,fetal alcohol spectrum disorder
+UBERON:0014789,embryo portion of umbilical vein,UBERON:0001638,vein
+DOID:6090,adult leptomeningeal melanoma,DOID:6085,meningeal melanoma
+UBERON:0010125,future superior salivatory nucleus,UBERON:0002020,gray matter of neuraxis
+NCBITaxon:34476,mitosporic Tremellales,NCBITaxon:5234,Tremellales
+UBERON:4200018,calcaneal tuber,UBERON:0004120,mesoderm-derived structure
+UBERON:3000431,pila antoptica,UBERON:0003932,cartilage element of chondrocranium
+DOID:180,ossifying fibroma,DOID:0060094,bone benign neoplasm
+UBERON:0006009,cusp of cardiac valve,UBERON:0000064,organ part
+HP:0003584,Late onset,HP:0003581,Adult onset
+UBERON:0002629,triangular part of inferior frontal gyrus,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3010621,constrictor laryngis anterior,UBERON:3000224,hyobranchial muscle
+UBERON:2000710,viscerosensory commissural nucleus of Cajal,UBERON:0007635,nucleus of medulla oblongata
+UBERON:2000429,scaphium,UBERON:0003861,neural arch
+DOID:2151,malignant ovarian surface epithelial-stromal neoplasm,DOID:2152,ovary epithelial cancer
+HP:0006028,Metaphyseal cupping of metacarpals,HP:0003021,Metaphyseal cupping
+UBERON:0001856,semicircular duct,UBERON:0000025,tube
+CL:1000383,type 2 vestibular sensory cell of epithelium of macula of utricle of membranous labyrinth,CL:0002069,type II vestibular sensory cell
+HP:0010390,Triangular shaped phalanges of the 5th toe,HP:0010180,Triangular shaped phalanges of the toes
+UBERON:2001225,basibranchial 3 bone,UBERON:0004740,basibranchial bone
+UBERON:0001090,synovial fluid,UBERON:0007794,serous fluid
+UBERON:0010522,replacement element,UBERON:0004765,skeletal element
+DOID:13419,neurogenic bowel,DOID:5295,intestinal disease
+UBERON:0000363,reticuloendothelial system,UBERON:0000467,anatomical system
+HP:0010048,Aplasia of metacarpal bones,HP:0005914,Aplasia/Hypoplasia involving the metacarpal bones
+UBERON:0002245,cerebellar hemisphere,UBERON:0002749,regional part of cerebellar cortex
+UBERON:0004802,respiratory tract epithelium,UBERON:0004807,respiratory system epithelium
+UBERON:0013245,sinovaginal bulb,UBERON:0002050,embryonic structure
+UBERON:0005103,mesonephric epithelium,UBERON:0012275,meso-epithelium
+DOID:1754,mitral valve stenosis,DOID:61,mitral valve disease
+CL:0000979,IgG memory B cell,CL:0000972,class switched memory B cell
+UBERON:0002493,uterine artery,UBERON:0001637,artery
+DOID:7586,supraglottis verrucous carcinoma,DOID:7587,supraglottis squamous cell carcinoma
+DOID:3165,skin benign neoplasm,DOID:0060121,integumentary system benign neoplasm
+UBERON:0006767,head of femur,UBERON:0004120,mesoderm-derived structure
+UBERON:0001451,navicular bone of pes,UBERON:0001447,tarsal bone
+UBERON:0006810,olecranon,UBERON:0004120,mesoderm-derived structure
+DOID:9271,ornithine carbamoyltransferase deficiency,DOID:9267,urea cycle disorder
+UBERON:0013720,dartos muscle of labia majora,UBERON:0013718,dartos muscle
+HP:0009309,Triangular shaped middle phalanx of the 4th finger,HP:0009850,Triangular shaped middle phalanges of the hand
+UBERON:2007055,pillar of the lateral semicircular canal,UBERON:0004120,mesoderm-derived structure
+UBERON:0010156,sphenofrontal suture,UBERON:0003685,cranial suture
+UBERON:2001814,mandibular sensory canal,UBERON:2001612,sensory canal
+HP:0005011,Mesomelic arm shortening,HP:0003027,Mesomelia
+UBERON:4200120,puboischiadic plate,UBERON:0005913,zone of bone organ
+HP:0100289,Abnormality of pattern reversal visual evoked potentials,HP:0000649,Abnormality of vision evoked potentials
+DOID:1222,cartilage disease,DOID:6227,articular cartilage disease
+UBERON:0001472,vaginal venous plexus,UBERON:0001593,venous plexus
+UBERON:0002715,spinal trigeminal tract of medulla,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0008420,buccal epithelium,UBERON:0002424,oral epithelium
+HP:0100288,EMG: myokymic discharges,HP:0002411,Myokymia
+HP:0004305,Involuntary movements,HP:0011804,Abnormality of muscle physiology
+DOID:337,spinal accessory nerve neoplasm,DOID:338,cranial nerve neoplasm
+UBERON:0006197,auricular vein,UBERON:0009141,craniocervical region vein
+DOID:4189,mutism,DOID:92,speech disorder
+CL:0000595,enucleate erythrocyte,CL:0000225,anucleate cell
+HP:0004409,Hyposmia,HP:0004408,Abnormality of the sense of smell
+UBERON:2001226,basibranchial 4 bone,UBERON:0004740,basibranchial bone
+HP:0000090,Nephronophthisis,HP:0100957,Abnormality of the renal medulla
+HP:0100631,Neoplasm of the adrenal gland,HP:0100568,Neoplasm of the endocrine system
+HP:0000405,Conductive hearing impairment,HP:0011452,Functional abnormality of the middle ear
+UBERON:0000174,excreta,UBERON:0000463,portion of organism substance
+UBERON:0008798,rugal fold of vagina,UBERON:0005156,reproductive structure
+HP:0009499,Abnormality of the epiphysis of the distal phalanx of the 2nd finger,HP:0009542,Abnormality of the distal phalanx of the 2nd finger
+HP:0001106,Periorbital hyperpigmentation,HP:0000606,Abnormality of the periorbital region
+UBERON:0013543,Brodmann (1909) area 12,UBERON:0013529,Brodmann area
+HP:0009803,Short phalanx of finger,HP:0009767,Aplasia/Hypoplasia of the phalanges of the hand
+UBERON:2002118,scale radius,UBERON:0000464,anatomical space
+HP:0005146,Cardiac valve calcification,HP:0001654,Abnormality of the heart valves
+HP:0010393,Abnormality of the middle phalanx of the 5th toe,HP:0010183,Abnormality of the middle phalanges of the toes
+CL:0002428,double-positive blast,CL:0000809,"double-positive, alpha-beta thymocyte"
+HP:0005254,Unilateral chest hypoplasia,HP:0005257,Thoracic hypoplasia
+UBERON:3000748,suprascapula,UBERON:0007844,cartilage element
+UBERON:0011289,pharyngobasilar fascia,UBERON:0004119,endoderm-derived structure
+UBERON:2205383,dorsal fin proximal radial cartilage 6,UBERON:2200947,dorsal fin proximal radial cartilage
+HP:0002635,Atheromatosis,HP:0002621,Atherosclerosis
+UBERON:0005610,iliac vein,UBERON:0001638,vein
+CL:0000779,multinuclear osteoclast,CL:0000228,multinucleate cell
+DOID:10808,gastric ulcer,DOID:750,peptic ulcer disease
+HP:0003949,Abnormality of the elbow metaphyses,HP:0009811,Abnormality of the elbow
+HP:0100133,Abnormality of the pubic hair,HP:0009888,Abnormality of secondary sexual hair
+HP:0010483,Amniotic constriction rings of arms,HP:0002817,Abnormality of the upper limb
+HP:0009928,Thick nasal alae,HP:0000429,Abnormality of the nasal alae
+UBERON:2001929,epioccipital posterior process,UBERON:0004120,mesoderm-derived structure
+UBERON:0002229,interparietal bone,UBERON:0008907,dermal bone
+DOID:0050783,secondary progressive multiple sclerosis,DOID:2377,multiple sclerosis
+UBERON:2001437,ductus communicans,UBERON:0000058,duct
+DOID:9970,obesity,DOID:654,overnutrition
+CL:0000096,mature neutrophil,CL:0002242,nucleate cell
+UBERON:0010975,external oblique pre-muscle mass,UBERON:0005865,pre-muscle condensation
+UBERON:0010724,lateral tubercle of talus,UBERON:0005813,tubercle
+DOID:12705,Friedreich ataxia,DOID:1441,spinocerebellar ataxia
+UBERON:4300033,anterior dorsal fin basal cartilage,UBERON:0005174,dorsal region organ
+CL:0002285,type III taste bud cell,CL:0000048,multi fate stem cell
+UBERON:0003613,cardiovascular system elastic tissue,UBERON:0002521,elastic tissue
+UBERON:0003618,aorta tunica media,UBERON:0002522,tunica media
+UBERON:0006245,humerus cartilage element,UBERON:0010881,limb cartilage element
+UBERON:0001320,iliolumbar vein,UBERON:0001638,vein
+HP:0100268,Upper lip pit,HP:0100269,Paramedian lip pit
+CL:0002203,Brush cell of epithelium proper of large intestine,CL:0002204,brush cell
+DOID:8050,bladder tubulo-cystic clear cell adenocarcinoma,DOID:5306,bladder clear cell adenocarcinoma
+UBERON:0008252,tube foot ampulla,UBERON:0003913,tooth-like structure
+DOID:9182,pemphigus,DOID:8502,bullous skin disease
+HP:0200036,Skin nodule,HP:0011355,Localized skin lesion
+UBERON:0011217,serratus dorsalis muscle,UBERON:0004518,muscle of vertebral column
+HP:0010434,Aplasia of the middle phalanx of the 2nd toe,HP:0100388,Aplasia of the proximal phalanges of the toes
+UBERON:0005986,left branch of atrioventricular bundle,UBERON:0015212,lateral structure
+DOID:2929,Newcastle disease,DOID:934,viral infectious disease
+HP:0000668,Hypodontia,HP:0009804,Reduced number of teeth
+HP:0006913,Frontal cortical atrophy,HP:0002120,Cerebral cortical atrophy
+HP:0010035,Aplasia of the 1st metacarpal,HP:0010026,Aplasia/Hypoplasia of the 1st metacarpal
+UBERON:0002546,cranial placode,UBERON:0005085,ectodermal placode
+DOID:11801,protein-energy malnutrition,DOID:5113,nutritional deficiency disease
+CL:0000767,basophil,CL:0000094,granulocyte
+UBERON:0005043,mucosa of nasolacrimal duct,UBERON:0000344,mucosa
+CL:1000327,appendix goblet cell,CL:1000320,axial mesoderm cell
+UBERON:0010574,manual digit 5 metacarpus cartilage element,UBERON:0010699,manual digit metacarpus cartilage element
+UBERON:0011667,pleural plate of carapace,UBERON:0011665,carapace bone
+HP:0007709,Band-shaped corneal dystrophy,HP:0001131,Corneal dystrophy
+UBERON:2002202,intermediate nucleus,UBERON:0006569,diencephalic nucleus
+UBERON:0001993,reticular layer of dermis,UBERON:0013754,integumentary system layer
+CL:0000017,spermatocyte,CL:0000015,male germ cell
+UBERON:0008522,nasal muscle,UBERON:0003831,respiratory system muscle
+HP:0012694,Enlarged thalamic volume,HP:0012693,Abnormal thalamic size
+UBERON:0006497,interosseous muscle of pes,UBERON:0006508,interosseous muscle
+UBERON:2001784,autopalatine-vomer joint,UBERON:0000982,skeletal joint
+HP:0010429,Complete duplication of the phalanges of the 2nd toe,HP:0010355,Duplication of the phalanges of the 2nd toe
+HP:0011586,Thoracoabdominal ectopia cordis,HP:0001683,Ectopia cordis
+DOID:9617,orthostatic proteinuria,DOID:557,kidney disease
+UBERON:2001821,notochord posterior region,UBERON:0000479,tissue
+HP:0001355,Megalencephaly,HP:0002060,Abnormality of the cerebrum
+DOID:3689,brachial plexus neuritis,DOID:3690,brachial plexus neuropathy
+UBERON:0009504,associated mesenchyme of main bronchus,UBERON:0004119,endoderm-derived structure
+HP:0000482,Microcornea,HP:0001120,Abnormality of corneal size
+HP:0011448,Ankle clonus,HP:0002169,Clonus
+DOID:4562,subacute bacterial endocarditis,DOID:0060000,infective endocarditis
+UBERON:0001605,ciliary muscle,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:4200132,tuber,UBERON:0004529,anatomical projection
+UBERON:0011249,appendicular skeletal system,UBERON:0000075,subdivision of skeletal system
+NCBITaxon:73229,Emmonsia,NCBITaxon:34383,mitosporic Onygenales
+UBERON:0002628,tail of caudate nucleus,UBERON:0011300,gray matter of telencephalon
+UBERON:0004944,submucosa of trigone of urinary bladder,UBERON:0004943,submucosa of urinary bladder
+UBERON:0002739,medial dorsal nucleus of thalamus,UBERON:0015233,nucleus of dorsal thalamus
+HP:0005787,Lumbar platyspondyly,HP:0000926,Platyspondyly
+DOID:8464,flat retinoschisis,DOID:8465,retinoschisis
+HP:0001156,Brachydactyly syndrome,HP:0011927,Short digit
+UBERON:0013436,porion,UBERON:0006983,anatomical point
+HP:0000403,Recurrent otitis media,HP:0002719,Recurrent infections
+DOID:7141,prostate small cell carcinoma,DOID:10286,prostate carcinoma
+UBERON:0010308,os opticus,UBERON:0010298,intramembranous scleral ossicle
+DOID:7042,ciliary body epithelioid cell melanoma,DOID:6524,malignant ciliary body melanoma
+CL:0000614,basophilic myelocyte,CL:0000768,immature basophil
+HP:0011173,Hypokinetic seizures,HP:0011153,Focal motor seizures
+HP:0012289,Facial neoplasm,HP:0012288,Neoplasm of head and neck
+HP:0005291,Inflammatory arteriopathy,HP:0002633,Vasculitis
+UBERON:2000363,hypobranchial bone,UBERON:2001893,hypobranchial element
+HP:0009962,Duplication of the distal phalanx of the 3rd finger,HP:0009959,Duplication of phalanx of 3rd finger
+UBERON:0002430,lateral hypothalamic area,UBERON:0004121,ectoderm-derived structure
+UBERON:0001405,spinalis thoracis muscle,UBERON:0011013,spinalis muscle
+HP:0006610,Wide intermamillary distance,HP:0004404,Abnormality of the nipple
+HP:0007370,Aplasia/Hypoplasia of the corpus callosum,HP:0007364,Aplasia/Hypoplasia of the cerebrum
+UBERON:4000172,lepidotrichium,UBERON:4300037,bony fin ray
+UBERON:0003479,thoracic cavity vein,UBERON:0001638,vein
+UBERON:0001890,forebrain,UBERON:0002616,regional part of brain
+HP:0001444,Autosomal dominant somatic cell mutation,HP:0000006,Autosomal dominant inheritance
+UBERON:0004671,gyrus rectus,UBERON:0003022,cerebral cortex lobe
+UBERON:3010528,articular process of palatoquadrate,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3010830,spicule,UBERON:0000064,organ part
+UBERON:0004021,spongiotrophoblast layer,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0010322,Abnormality of the 5th toe,HP:0001780,Abnormality of toe
+UBERON:0001584,left subclavian artery,UBERON:0001533,subclavian artery
+UBERON:0012261,manual major digit (Aves),UBERON:0002389,manual digit
+UBERON:0010127,future dorsal motor nucleus of vagus,UBERON:0002020,gray matter of neuraxis
+UBERON:0009016,ciliary stroma,UBERON:0004121,ectoderm-derived structure
+CL:0000536,secondary motor neuron,CL:0000535,secondary neuron
+HP:0010756,Aplasia/Hypoplasia of the premaxilla,HP:0010758,Abnormality of the premaxilla
+DOID:3876,colonic pseudo-obstruction,DOID:3877,functional colonic disease
+UBERON:0002638,medial pulvinar nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0003994,pelvic ligament,UBERON:0003594,pelvis connective tissue
+UBERON:0010732,alisphenoid pre-cartilage condensation,UBERON:0007213,mesenchyme derived from head neural crest
+UBERON:2001994,gill raker row,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0006278,pleuropericardial folds,UBERON:0005423,developing anatomical structure
+UBERON:2001546,neural spine 4,UBERON:0001076,neural spine
+DOID:4680,breast metaplastic carcinoma,DOID:3459,breast carcinoma
+CL:1000717,kidney outer medulla collecting duct intercalated cell,CL:1000548,kidney outer medulla collecting duct epithelial cell
+NCBITaxon:10278,Molluscipoxvirus,NCBITaxon:10241,Chordopoxvirinae
+HP:0007158,Progressive extrapyramidal muscular rigidity,HP:0007076,Extrapyramidal muscular rigidity
+UBERON:2000307,vestibulolateralis lobe,UBERON:0002946,regional part of cerebellum
+HP:0100204,Cone-shaped epiphysis of the distal phalanx of the 5th toe,HP:0100079,Cone-shaped epiphyses of the 5th toe
+UBERON:0004016,dermatome,UBERON:0012275,meso-epithelium
+UBERON:0013659,spongiose tissue of corpus cavernosum maxillaris,UBERON:0008324,erectile tissue
+DOID:10579,leukodystrophy,DOID:1443,cerebral degeneration
+UBERON:0010031,6th arch mesenchyme,UBERON:0009494,pharyngeal arch mesenchymal region
+HP:0005767,1-2 toe complete cutaneous syndactyly,HP:0010621,Cutaneous syndactyly of toes
+UBERON:0009661,midbrain nucleus,UBERON:0002950,regional part of midbrain
+HP:0011723,Congenital malformation of the right heart,HP:0002564,Malformation of the heart and great vessels
+UBERON:0002376,cranial muscle,UBERON:0010959,craniocervical muscle
+UBERON:0010033,posterior part of tongue,UBERON:0004121,ectoderm-derived structure
+UBERON:0006460,first sacral spinal cord segment,UBERON:0007717,sacral subsegment of spinal cord
+UBERON:0006468,twelfth thoracic spinal cord segment,UBERON:0007715,thoracic subsegment of spinal cord
+HP:0100498,Deviation of toes,HP:0001780,Abnormality of toe
+HP:0005292,Intimal thickening in the coronary arteries,HP:0006704,Abnormality of the coronary arteries
+HP:0003189,Long nose,HP:0005105,Abnormal nasal morphology
+CL:0002260,epithelial cell of parathyroid gland,CL:1001593,parathyroid glandular cell
+UBERON:2101415,pelvic fin distal radial element 2,UBERON:1600008,pelvic fin distal radial element
+HP:0009332,Abnormality of the epiphysis of the distal phalanx of the 3rd finger,HP:0010243,Abnormality of the epiphyses of the distal phalanx of finger
+UBERON:0008292,vaned feather,UBERON:0000022,feather
+HP:0003737,Mitochondrial myopathy,HP:0003800,Muscle abnormality related to mitochondrial dysfunction
+UBERON:2001785,branched dorsal fin ray,UBERON:4000177,dorsal fin lepidotrichium
+HP:0000845,Growth hormone excess,HP:0010514,Hyperpituitarism
+HP:0009545,Symphalangism of the 2nd finger,HP:0009700,Synostosis involving bones of the fingers
+UBERON:0000390,lens nucleus,UBERON:0004121,ectoderm-derived structure
+HP:0010438,Abnormality of the ventricular septum,HP:0001671,Abnormality of the cardiac septa
+HP:0001915,Aplastic anemia,HP:0001876,Pancytopenia
+CL:0000243,glial cell (sensu Vertebrata),CL:0000125,glial cell
+UBERON:0014450,pretectal nucleus,UBERON:0003047,regional part of pretectal region
+HP:0000961,Cyanosis,HP:0002795,Functional respiratory abnormality
+HP:0100904,Sclerosis of the middle phalanx of the 2nd finger,HP:0100916,Sclerosis of the middle phalanges of the hand
+DOID:14043,neonatal myasthenia gravis,DOID:437,myasthenia gravis
+HP:0006582,Reye syndrome-like episodes,HP:0001392,Abnormality of the liver
+UBERON:2001137,ventral tooth row,UBERON:0009678,tooth row
+HP:0002245,Meckel diverticulum,HP:0001549,Abnormality of the ileum
+HP:0008315,Decreased plasma free carnitine,HP:0003234,Decreased plasma carnitine
+DOID:9599,proliferative fasciitis,DOID:9598,fasciitis
+DOID:10657,colonic lymphangioma,DOID:235,colonic benign neoplasm
+HP:0002822,Hyperplasia of the femoral trochanters,HP:0003366,Abnormality of the femoral neck and head region
+UBERON:0002475,saphenous nerve,UBERON:0002003,peripheral nerve
+NCBITaxon:10880,Reoviridae,NCBITaxon:35325,dsRNA viruses
+HP:0011659,Tetralogy of Fallot with absent pulmonary valve,HP:0001636,Tetralogy of Fallot
+UBERON:2000913,molecular layer valvula cerebelli,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0002875,Exertional dyspnea,HP:0002094,Dyspnea
+DOID:0050486,exanthem,DOID:37,skin disease
+UBERON:0009571,ventral midline,UBERON:0002050,embryonic structure
+DOID:4324,acantholytic acanthoma,DOID:174,acanthoma
+DOID:2526,prostate adenocarcinoma,DOID:10286,prostate carcinoma
+UBERON:0014607,thoracic spinal cord lateral horn,UBERON:0004676,spinal cord lateral horn
+UBERON:0003984,uterine tube infundibulum,UBERON:0013515,subdivision of uterine tube
+HP:0003777,Pili torti,HP:0003328,Abnormal hair laboratory examination
+UBERON:0002196,adenohypophysis,UBERON:0004121,ectoderm-derived structure
+DOID:10236,exhibitionism,DOID:0060044,paraphilia disorder
+UBERON:0000179,haemolymphatic fluid,UBERON:0006314,bodily fluid
+HP:0011508,Macular hole,HP:0001103,Abnormality of the macula
+HP:0002435,Meningocele,HP:0010651,Abnormality of the meninges
+UBERON:0011922,cochlear basement membrane,UBERON:0005769,basement membrane of epithelium
+DOID:6988,peripheral epithelioid sarcoma,DOID:6193,epithelioid sarcoma
+CL:1000708,ureter adventitial cell,CL:0002503,adventitial cell
+CL:0002250,intestinal crypt stem cell,CL:0002563,intestinal epithelial cell
+UBERON:0010371,ecto-epithelium,UBERON:0000483,epithelium
+UBERON:4000134,ossified tendon,UBERON:0001479,sesamoid bone
+UBERON:0010399,spleen trabecular artery,UBERON:0003497,abdomen blood vessel
+HP:0100631,Neoplasm of the adrenal gland,HP:0011732,Abnormality of adrenal morphology
+HP:0100886,Abnormality of globe location,HP:0012374,Abnormality of the globe
+NCBITaxon:157540,Zygodontomys,NCBITaxon:40141,Sigmodontinae
+UBERON:2000311,adductor mandibulae complex,UBERON:0011145,adductor muscle
+DOID:0060173,Timothy syndrome,DOID:0050736,autosomal dominant disease
+HP:0006530,Interstitial pulmonary disease,HP:0002088,Abnormality of the lung
+HP:0100068,Cone-shaped epiphyses of the 4th toe,HP:0010164,Cone-shaped epiphyses of the toes
+UBERON:0013199,stria of neuraxis,UBERON:0002316,white matter
+DOID:12995,conduct disorder,DOID:0060038,specific developmental disorder
+UBERON:0005652,pedal digit 5 epithelium,UBERON:0005226,pedal digit epithelium
+DOID:1984,rectal neoplasm,DOID:4610,intestinal benign neoplasm
+UBERON:0002912,marginal sulcus,UBERON:0003022,cerebral cortex lobe
+UBERON:0006445,caudal middle frontal gyrus,UBERON:0003022,cerebral cortex lobe
+CL:0000192,smooth muscle cell,CL:0008007,visceral muscle cell
+UBERON:2000394,molecular layer corpus cerebelli,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0013448,sagittal keel,UBERON:0005913,zone of bone organ
+HP:0010506,Abnormal plantar dermatoglyphics,HP:0007477,Abnormal dermatoglyphics
+HP:0100226,Cone-shaped epiphysis of the proximal phalanx of the 5th toe,HP:0100079,Cone-shaped epiphyses of the 5th toe
+CL:1001033,peritubular capillary endothelial cell,CL:1000892,kidney capillary endothelial cell
+UBERON:0003280,endothelium of main bronchus,UBERON:0001986,endothelium
+HP:0010018,Enlarged epiphysis of the 1st metacarpal,HP:0010014,Abnormality of the epiphysis of the 1st metacarpal
+HP:0010929,Abnormality of cation homeostasis,HP:0003111,Abnormality of ion homeostasis
+DOID:6230,childhood teratoma of the ovary,DOID:6084,pediatric ovarian germ cell tumor
+DOID:12800,mucopolysaccharidosis VI,DOID:12798,mucopolysaccharidosis
+UBERON:0003393,mesentery of urinary system,UBERON:0006554,urinary system structure
+NCBITaxon:59140,Myzomyia,NCBITaxon:44534,Cellia <subgenus>
+HP:0009511,Stippling of the epiphysis of the distal phalanx of the 2nd finger,HP:0010255,Stippling of the epiphyses of the distal phalanges of the hand
+CL:0000968,Be cell,CL:0000785,mature B cell
+UBERON:0004821,pulmonary alveolus epithelium,UBERON:0000487,simple squamous epithelium
+HP:0002236,Frontal upsweep of hair,HP:0010721,Abnormal hair whorl
+UBERON:0002578,sublentiform nucleus,UBERON:0014450,pretectal nucleus
+DOID:10456,tonsillitis,DOID:974,upper respiratory tract disease
+HP:0008769,Dull facial expression,HP:0004673,Decreased facial expression
+UBERON:0004453,metacarpus region,UBERON:0005451,segment of manus
+UBERON:0011861,aorta collagen fibril,UBERON:0004120,mesoderm-derived structure
+HP:0011883,Abnormal platelet granules,HP:0011875,Abnormal platelet morphology
+UBERON:0003282,mesentery of heart,UBERON:0005983,heart layer
+UBERON:0003451,lower jaw incisor,UBERON:0001098,incisor tooth
+NCBITaxon:46607,Andes virus,NCBITaxon:11598,Hantavirus
+DOID:2641,ovarian germ cell monodermal and highly specialized teratoma,DOID:5207,monodermal teratoma
+UBERON:0001905,pineal body,UBERON:0002757,regional part of epithalamus
+UBERON:0010228,ruminal fluid,UBERON:0000463,portion of organism substance
+UBERON:2002077,lateropterygium,UBERON:0004376,fin bone
+UBERON:0004413,proximal epiphysis of radius,UBERON:0004385,epiphysis of radius
+CL:0000420,syncytial epithelial cell,CL:0000228,multinucleate cell
+HP:0100417,Partial duplication of the distal phalanx of the 4th toe,HP:0100399,Duplication of the distal phalanx of the 4th toe
+HP:0100625,Enlarged thorax,HP:0001547,Abnormality of the rib cage
+HP:0004347,Weakness of muscles of respiration,HP:0001324,Muscle weakness
+HP:0009679,Fragmentation of the epiphysis of the distal phalanx of the thumb,HP:0009662,Abnormality of the epiphysis of the distal phalanx of the thumb
+HP:0000007,Autosomal recessive inheritance,HP:0000005,Mode of inheritance
+HP:0000149,Ovarian gonadoblastoma,HP:0000150,Gonadoblastoma
+UBERON:0003849,mesencephalic neural crest,UBERON:0003099,cranial neural crest
+HP:0009899,Prominent crus of helix,HP:0009895,Abnormality of the crus of the helix
+HP:0001197,Abnormality of prenatal development or birth,HP:0000118,Phenotypic abnormality
+UBERON:0004404,distal epiphysis of humerus,UBERON:0004382,epiphysis of humerus
+DOID:0080033,craniometaphyseal dysplasia,DOID:4254,osteosclerosis
+UBERON:0005712,midgut duodenum mesentery,UBERON:0003397,mesentery of duodenum
+HP:0010249,Enlarged epiphyses of the distal phalanges of the hand,HP:0010231,Enlarged epiphyses of the phalanges of the hand
+UBERON:0009586,mesenchyme of interdigital region between manual digits 1 and 2,UBERON:0009600,mesenchyme of interdigital region of manus
+HP:0003145,Decreased adenosylcobalamin,HP:0004341,Abnormality of the vitamin B12 metabolism
+UBERON:2001314,posterior lateral line ganglion,UBERON:2000120,lateral line ganglion
+CL:0002360,AGM hematopoietic stem cell,CL:0002352,gestational hematopoietic stem cell
+HP:0009466,Radial deviation of finger,HP:0009485,Radial deviation of the hand or of fingers of the hand
+UBERON:0008851,ectoplacental cavity,UBERON:0000464,anatomical space
+UBERON:0006589,round ligament of uterus,UBERON:0004120,mesoderm-derived structure
+UBERON:3000745,webbing of bone,UBERON:0004120,mesoderm-derived structure
+CL:0000041,mature eosinophil,CL:0000771,eosinophil
+CL:0000182,hepatocyte,CL:0002371,somatic cell
+UBERON:0010901,tarsometatarsus pre-cartilage condensation,UBERON:0010886,hindlimb bone pre-cartilage condensation
+UBERON:2000171,interhyal bone,UBERON:0002513,endochondral bone
+UBERON:0006950,stellate reticulum,UBERON:0003843,dental epithelium
+HP:0100488,Symphalangism of the proximal phalanx of the hallux with the 1st metatarsal,HP:0001440,Synostosis involving metatarsal bones
+UBERON:0011666,peripheral plate of carapace,UBERON:0011665,carapace bone
+UBERON:2001052,primordial hindbrain channel,UBERON:0009141,craniocervical region vein
+DOID:1901,vagina sarcoma,DOID:119,vaginal cancer
+DOID:6271,gastric cardia adenocarcinoma,DOID:6270,gastric cardia carcinoma
+UBERON:0007282,presumptive segmental plate,UBERON:0006598,presumptive structure
+HP:0005756,Neonatal epiphyseal stippling,HP:0010655,Epiphyseal stippling
+CL:0001022,CD115-positive monocyte,CL:0000839,myeloid lineage restricted progenitor cell
+UBERON:0000078,mixed ectoderm/mesoderm/endoderm-derived structure,UBERON:0004121,ectoderm-derived structure
+HP:0011153,Focal motor seizures,HP:0007359,Focal seizures
+HP:0010564,Bifid epiglottis,HP:0005483,Abnormality of the epiglottis
+HP:0000260,Wide anterior fontanel,HP:0000236,Abnormality of the anterior fontanelle
+UBERON:0005050,liver papillary process,UBERON:0004119,endoderm-derived structure
+UBERON:0001733,soft palate,UBERON:0000477,anatomical cluster
+CL:0002143,dark chief cell of parathyroid cell,CL:0000446,chief cell of parathyroid gland
+CL:0000947,IgE plasma cell,CL:0000974,long lived plasma cell
+UBERON:0001311,inferior vesical artery,UBERON:0015212,lateral structure
+HP:0009426,Distal/middle symphalangism of 3rd finger,HP:0009445,Symphalangism of the 3rd finger
+UBERON:0004436,proximal epiphysis of middle phalanx of manual digit 2,UBERON:0004418,proximal epiphysis of phalanx of manual digit 2
+UBERON:3000619,tympanosquamosal,UBERON:0000064,organ part
+UBERON:0004815,lower respiratory tract epithelium,UBERON:0004802,respiratory tract epithelium
+HP:0009318,Aplasia/Hypoplasia of the 3rd finger,HP:0004150,Abnormality of the 3rd finger
+DOID:13120,protein-deficiency anemia,DOID:13121,deficiency anemia
+UBERON:0011619,stylohyoid bone,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0014542,cervical spinal cord central canal,UBERON:0014538,subdivision of spinal cord central canal
+DOID:13133,HELLP syndrome,DOID:1588,thrombocytopenia
+UBERON:0008925,sublaminar layer S4,UBERON:0009735,sublaminar layers S1 or S3 or S4
+UBERON:0001754,dental pulp,UBERON:0010313,neural crest-derived structure
+UBERON:0009751,cardiac mesenchyme,UBERON:0000477,anatomical cluster
+HP:0009461,Short 3rd finger,HP:0009318,Aplasia/Hypoplasia of the 3rd finger
+DOID:4860,brain stem astrocytic neoplasm,DOID:4202,brain stem glioma
+UBERON:0009095,tip of renal papilla,UBERON:0004120,mesoderm-derived structure
+UBERON:0005455,interventricular groove,UBERON:0004120,mesoderm-derived structure
+UBERON:0005023,mucosa of oropharynx,UBERON:0004786,gastrointestinal system mucosa
+UBERON:0001703,neurocranium,UBERON:0011158,primary subdivision of skull
+DOID:14319,pleuropneumonia,DOID:10247,pleurisy
+UBERON:0005282,ventricular system of brain,UBERON:0004121,ectoderm-derived structure
+UBERON:0010548,pedal digit 2 metatarsal pre-cartilage condensation,UBERON:0010581,pedal digit 2 phalanx pre-cartilage condensation
+UBERON:0012103,suspensory ligament of breast,UBERON:0014404,female anatomical structure
+UBERON:0014705,median lingual swelling epithelium,UBERON:0005291,embryonic tissue
+CL:0000187,muscle cell,CL:0000548,animal cell
+UBERON:0011674,carapace scute,UBERON:0008201,scute
+HP:0008414,Lumbar kyphosis in infancy,HP:0008454,Lumbar kyphosis
+NCBITaxon:28211,Alphaproteobacteria,NCBITaxon:1224,Proteobacteria
+HP:0009572,Osteolytic defects of the middle phalanx of the 2nd finger,HP:0009543,Abnormality of the middle phalanx of the 2nd finger
+UBERON:0002574,regional part of inferior olivary complex,UBERON:0002678,regional part of medulla oblongata
+UBERON:0003051,ear vesicle,UBERON:0010371,ecto-epithelium
+HP:0007720,Flat cornea,HP:0100691,Abnormality of the curvature of the cornea
+HP:0004384,Type I truncus arteriosus,HP:0001660,Truncus arteriosus
+UBERON:0004854,gastrointestinal system mesentery,UBERON:0002095,mesentery
+DOID:12466,secondary hyperparathyroidism,DOID:13543,hyperparathyroidism
+UBERON:0008331,clitoral smooth muscle,UBERON:0001135,smooth muscle tissue
+DOID:833,auditory system cancer,DOID:0060116,sensory system cancer
+HP:0002076,Migraine,HP:0002315,Headache
+HP:0010111,Short phalanx of hallux,HP:0010746,Hypoplasia of the phalanges of the toes
+UBERON:0011380,female external urethral sphincter,UBERON:0005156,reproductive structure
+HP:0100036,Pseudo-fractures,HP:0003103,Abnormal cortical bone morphology
+UBERON:0004896,right lung accessory lobe lobar bronchus,UBERON:0003404,lobar bronchus of right lung
+DOID:11920,tracheal cancer,DOID:0050615,respiratory system cancer
+NCBITaxon:80840,Burkholderiales,NCBITaxon:28216,Betaproteobacteria
+HP:0003028,Abnormality of the ankles,HP:0100491,Abnormality of the joints of the lower limbs
+UBERON:3000018,anterior ramus of pterygoid,UBERON:0004120,mesoderm-derived structure
+UBERON:0011007,endocardium of right auricle,UBERON:0011005,endocardium of auricle
+UBERON:0004491,cardiac muscle tissue of interatrial septum,UBERON:0004492,cardiac muscle tissue of cardiac septum
+UBERON:0005642,ultimobranchial body epithelium,UBERON:0000490,unilaminar epithelium
+DOID:9993,hypoglycemia,DOID:4194,glucose metabolism disease
+UBERON:0014636,thoracic spinal cord gray matter,UBERON:0002315,gray matter of spinal cord
+UBERON:0003690,sacrum,UBERON:0004120,mesoderm-derived structure
+DOID:1999,chronic eustachian salpingitis,DOID:2000,otosalpingitis
+HP:0005227,Adenomatous colonic polyposis,HP:0100273,Neoplasm of the colon
+UBERON:0000041,odontode scale,UBERON:0004756,dermal skeletal element
+UBERON:0004985,mucosa of ejaculatory duct,UBERON:0005156,reproductive structure
+HP:0009107,Abnormal ossification involving the femoral head and neck,HP:0011849,Abnormal bone ossification
+CL:0002597,smooth muscle cell of bladder,CL:1001319,bladder cell
+CL:0000592,large luteal cell,CL:0000175,luteal cell
+UBERON:3000904,apophysis distalis of tibiofibula,UBERON:0000064,organ part
+HP:0003301,Irregular vertebral endplates,HP:0005106,Abnormality of the vertebral endplates
+CL:0000091,Kupffer cell,CL:0000864,tissue-resident macrophage
+DOID:0001816,angiosarcoma,DOID:1115,sarcoma
+UBERON:0002422,fourth ventricle,UBERON:0004086,brain ventricle
+UBERON:0005357,brain ependyma,UBERON:0010371,ecto-epithelium
+UBERON:0002404,transversus thoracis,UBERON:0002426,chest muscle
+UBERON:0005708,lower jaw incisor odontogenic papilla,UBERON:0003317,odontogenic papilla of incisor
+DOID:2730,epidermolysis bullosa,DOID:2731,vesiculobullous skin disease
+UBERON:0012648,ampulla of uterine tube,UBERON:0005156,reproductive structure
+HP:0012435,Ventral shortening of foreskin,HP:0100587,Abnormality of the preputium
+DOID:9808,Goodpasture syndrome,DOID:417,hypersensitivity reaction type II disease
+UBERON:0008804,stylopharyngeus muscle,UBERON:0000933,pharyngeal muscle
+UBERON:0004646,infraorbital artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+NCBITaxon:29178,Foraminifera,NCBITaxon:543769,Rhizaria
+HP:0007335,Recurrent encephalopathy,HP:0001298,Encephalopathy
+HP:0007340,Lower limb muscle weakness,HP:0003690,Limb muscle weakness
+UBERON:0015056,ischial endochondral element,UBERON:0010363,endochondral element
+UBERON:2005375,dorsal fin distal radial bone 4,UBERON:2105375,dorsal fin distal radial element 4
+UBERON:2002014,ascending limb of ceratobranchial 5 cartilage,UBERON:4100000,skeletal element projection
+HP:0003469,Peripheral dysmyelination,HP:0003130,Abnormal peripheral myelination
+UBERON:0000019,camera-type eye,UBERON:0000047,simple eye
+UBERON:0001619,ophthalmic artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0009286,Curved distal phalanx of the 4th finger,HP:0009282,Abnormality of the distal phalanx of the 4th finger
+UBERON:0005984,subendocardium layer,UBERON:0005983,heart layer
+HP:0007686,Abnormal pupillary function,HP:0000615,Abnormality of the pupil
+CL:0001010,mature dermal dendritic cell,CL:0000841,mature conventional dendritic cell
+DOID:0050279,conidiobolomycosis,DOID:37,skin disease
+DOID:5526,middle ear squamous cell carcinoma,DOID:4893,middle ear carcinoma
+CL:0002579,omentum preadipocyte,CL:0002334,preadipocyte
+HP:0012547,Abnormal involuntary eye movements,HP:0000496,Abnormality of eye movement
+NCBITaxon:694009,Severe acute respiratory syndrome-related coronavirus,NCBITaxon:694002,Betacoronavirus
+UBERON:2001257,medial floor plate,UBERON:0004121,ectoderm-derived structure
+DOID:0050152,aspiration pneumonia,DOID:874,bacterial pneumonia
+CL:0002506,liver CD103-positive dendritic cell,CL:0002461,CD103-positive dendritic cell
+HP:0011959,Unilateral hypoplasia of pectoralis major muscle,HP:0011957,Abnormality of the  pectoral muscle
+HP:0001638,Cardiomyopathy,HP:0001637,Abnormality of the myocardium
+HP:0011675,Arrhythmia,HP:0011025,Abnormality of cardiovascular system physiology
+UBERON:2001615,sphenotic spine,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003419,mesenchyme of parotid,UBERON:0003324,mesenchyme of lower jaw
+UBERON:0008430,lumbar vertebral foramen,UBERON:0001131,vertebral foramen
+DOID:1270,hereditary hemorrhagic telangiectasia,DOID:0050736,autosomal dominant disease
+UBERON:0010727,sutural bone,UBERON:0010428,flat bone
+CL:1000447,epithelial cell of stratum germinativum of esophagus,CL:0000646,basal cell
+UBERON:0010559,pedal digit 3 metatarsal cartilage element,UBERON:0015039,pedal digit 3 metatarsal endochondral element
+UBERON:0003103,compound organ,UBERON:0000062,organ
+HP:0001997,Gout,HP:0002149,Hyperuricemia
+HP:0011930,Hyperextensible skin of chest,HP:0007458,Focal hyperextensible skin
+UBERON:0001347,white adipose tissue,UBERON:0001013,adipose tissue
+UBERON:0004346,gubernaculum,UBERON:0006590,vestigial embryonic structure
+HP:0003535,3-Methylglutaconic aciduria,HP:0003355,Aminoaciduria
+UBERON:4300022,anteroventral plate,UBERON:0007829,pectoral girdle bone
+HP:0100060,Irregular epiphyses of the 3rd toe,HP:0010329,Abnormality of the epiphyses of the 3rd toe
+UBERON:0001931,lateral preoptic nucleus,UBERON:0006568,hypothalamic nucleus
+HP:0100720,Hypoplasia of the ear cartilage,HP:0000377,Abnormality of the pinna
+DOID:9912,hydrocele,DOID:48,male reproductive system disease
+HP:0004122,Midline defect of the nose,HP:0005105,Abnormal nasal morphology
+UBERON:0004732,segmental subdivision of nervous system,UBERON:0000063,organ segment
+DOID:9888,alternating esotropia,DOID:9840,esotropia
+HP:0200110,Absent paranasal sinuses and mastoids,HP:0002689,Absent paranasal sinuses
+DOID:0060095,uterine benign neoplasm,DOID:0060086,female reproductive organ benign neoplasm
+UBERON:0001891,midbrain,UBERON:0002616,regional part of brain
+HP:0100334,Unilateral cleft palate,HP:0100338,Non-midline cleft palate
+DOID:749,active peptic ulcer disease,DOID:750,peptic ulcer disease
+HP:0002692,Hypoplastic facial bones,HP:0011821,Abnormality of facial skeleton
+CL:1000338,enterocyte of epithelium of crypt of lieberkuhn of small intestine,CL:1000334,enterocyte of epithelium of small intestine
+DOID:0060133,anosognosia,DOID:4090,agnosia
+HP:0008433,Reversed usual vertebral column curves,HP:0000925,Abnormality of the vertebral column
+DOID:0050577,Sensenbrenner syndrome,DOID:0050737,autosomal recessive disease
+UBERON:0011359,urophysis,UBERON:0004121,ectoderm-derived structure
+UBERON:0001895,metencephalon,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005905,insect labrum,UBERON:0004121,ectoderm-derived structure
+HP:0011720,Cardiac total anomalous pulmonary venous connection,HP:0005160,Total anomalous pulmonary venous return
+DOID:565,bilateral hypoactive labyrinth,DOID:566,labyrinthine dysfunction
+DOID:5190,cervical Wilms' tumor,DOID:4112,cervical carcinosarcoma
+UBERON:0002317,white matter of cerebellum,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004713,corpus cavernosum penis,UBERON:0005156,reproductive structure
+HP:0012570,Synovial sarcoma,HP:0100242,Sarcoma
+HP:0100690,Mosaic central corneal dystrophy,HP:0007836,Mosaic corneal dystrophy
+HP:0002378,Hand tremor,HP:0001337,Tremor
+CL:0000479,vasopressin stimulating hormone secreting cell,CL:0000167,peptide hormone secreting cell
+UBERON:2001820,posterior nuchal plate,UBERON:0002513,endochondral bone
+HP:0006247,Enlarged interphalangeal joints,HP:0006261,Abnormality of phalangeal joints of the hand
+UBERON:0003975,internal female genitalia,UBERON:0004175,internal genitalia
+UBERON:0013740,wall of crypt of lieberkuhn,UBERON:0011184,epithelium of crypt of lieberkuhn
+HP:0011281,Abnormality of urine catecholamine concentration,HP:0003110,Abnormality of urine homeostasis
+HP:0000621,Entropion,HP:0000492,Abnormality of the eyelid
+UBERON:0004135,distal tubule,UBERON:0007685,region of nephron tubule
+HP:0007703,Abnormal retinal pigmentation,HP:0008051,Abnormality of the retinal pigment epithelium
+CL:0000706,choroid plexus epithelial cell,CL:0002319,neural cell
+UBERON:2002018,anterior limb of ceratobranchial 5 cartilage,UBERON:4100000,skeletal element projection
+UBERON:0004614,mammalian cervical vertebra 5,UBERON:0002413,cervical vertebra
+HP:0100556,Hemiatrophy,HP:0100555,Asymmetric growth
+UBERON:0004235,mammary gland smooth muscle,UBERON:0005156,reproductive structure
+UBERON:0011976,epiphysis of distal phalanx of pes,UBERON:0004446,epiphysis of phalanx
+HP:0004527,large clumps of pigment irregularly distributed along hair shaft,HP:0002220,Melanin pigment aggregation in hair shafts
+HP:0002165,Pterygium formation (nails),HP:0001597,Abnormality of the nail
+HP:0011401,Delayed peripheral myelination,HP:0012448,Delayed myelination
+DOID:2074,intestinal perforation,DOID:5295,intestinal disease
+HP:0100367,Short phalanx of the 4th toe,HP:0010337,Aplasia/Hypoplasia of the 4th toe
+HP:0010621,Cutaneous syndactyly of toes,HP:0012725,Cutaneous syndactyly
+DOID:5047,neurohypophysis granular cell tumor,DOID:5048,posterior pituitary gland neoplasm
+DOID:7212,meningothelial meningioma,DOID:3565,meningioma
+HP:0200020,Corneal erosions,HP:0011495,Abnormality of corneal epithelium
+DOID:5258,granular cell leiomyosarcoma,DOID:1967,leiomyosarcoma
+DOID:12657,vestibulocochlear nerve disease,DOID:5656,cranial nerve disease
+HP:0002640,Hypertension associated with pheochromocytoma,HP:0000822,Hypertension
+UBERON:0005852,thoracic spinal cord ventral column,UBERON:0014637,thoracic spinal cord white matter
+UBERON:0003338,ganglion of peripheral nervous system,UBERON:0000045,ganglion
+UBERON:0011306,deep part of temporalis,UBERON:0003681,masticatory muscle
+UBERON:0012275,meso-epithelium,UBERON:0004120,mesoderm-derived structure
+UBERON:0006665,accessory hemiazygos vein,UBERON:0001638,vein
+UBERON:0002378,muscle of abdomen,UBERON:0003833,abdominal segment muscle
+HP:0000169,Gingival fibromatosis,HP:0010614,Fibroma
+HP:0005463,Elongated sella turcica,HP:0002681,Deformed sella turcica
+NCBITaxon:40272,Roseolovirus,NCBITaxon:10357,Betaherpesvirinae
+HP:0100584,Endocarditis,HP:0004306,Abnormality of the endocardium
+UBERON:2002256,blind side,UBERON:0000475,organism subdivision
+NCBITaxon:85819,Phthiraptera,NCBITaxon:33342,Paraneoptera
+UBERON:0010172,bulb of aorta,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0005258,Pectoral muscle hypoplasia/aplasia,HP:0001435,Abnormality of the shoulder girdle musculature
+UBERON:0011092,right pelvic girdle region,UBERON:0001271,pelvic girdle region
+UBERON:0008454,rectus capitis posterior major,UBERON:0004518,muscle of vertebral column
+UBERON:0010531,metanephros induced blastemal cells,UBERON:0005423,developing anatomical structure
+DOID:4293,clear cell basal cell carcinoma,DOID:2513,basal cell carcinoma
+CL:0000563,endospore,CL:0000520,prokaryotic cell
+UBERON:0008274,mollusc venom,UBERON:0007113,venom
+UBERON:0010424,distal segment of rib,UBERON:0005055,zone of long bone
+UBERON:0001152,cystic duct,UBERON:0003703,extrahepatic bile duct
+UBERON:0004537,blood vasculature,UBERON:0002049,vasculature
+HP:0008233,Decreased serum progesterone,HP:0008373,Puberty and gonadal disorders
+HP:0010748,Ectopic lacrimal punctum,HP:0011479,Abnormality of the lacrimal punctum
+HP:0010040,Aplasia of the 3rd metacarpal,HP:0010048,Aplasia of metacarpal bones
+HP:0010044,Short 4th metacarpal,HP:0010049,Short metacarpal
+UBERON:0006038,interdigital region between pedal digits 1 and 2,UBERON:0006016,interdigital region between digits 1 and 2
+UBERON:0010071,layer of tympanic membrane,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0003458,EMG: myopathic abnormalities,HP:0003457,EMG abnormality
+HP:0011471,Gastrostomy tube feeding in infancy,HP:0008872,Feeding difficulties in infancy
+DOID:338,cranial nerve neoplasm,DOID:3620,central nervous system cancer
+UBERON:3010585,basibranchial II,UBERON:0004740,basibranchial bone
+HP:0009722,Dental enamel pits,HP:0000682,Abnormality of dental enamel
+DOID:0050667,alcohol-related neurodevelopmental disorder,DOID:0050696,fetal alcohol spectrum disorder
+HP:0010383,Aplasia/Hypoplasia of the phalanges of the 5th toe,HP:0010173,Aplasia/Hypoplasia of the phalanges of the toes
+UBERON:0010126,future nucleus ambiguus,UBERON:0002020,gray matter of neuraxis
+CL:0002454,"Cd4-negative, CD8_alpha-negative, CD11b-positive dendritic cell",CL:0002465,CD11b-positive dendritic cell
+UBERON:4200019,preacetabular process,UBERON:0004120,mesoderm-derived structure
+UBERON:0001737,larynx,UBERON:0000477,anatomical cluster
+CL:0000827,pro-T cell,CL:0000838,lymphoid lineage restricted progenitor cell
+UBERON:0004825,dental lamina,UBERON:0000957,lamina
+DOID:2983,anuria,DOID:557,kidney disease
+HP:0200136,Oral-pharyngeal dysphagia,HP:0002015,Dysphagia
+UBERON:0001855,cochlear duct of membranous labyrinth,UBERON:0000025,tube
+HP:0011989,Ectopic ossification in ligament tissue,HP:0011986,Ectopic ossification
+UBERON:2001224,basibranchial 2 bone,UBERON:0004740,basibranchial bone
+HP:0003115,Abnormal EKG,HP:0011025,Abnormality of cardiovascular system physiology
+UBERON:0013540,Brodmann (1909) area 9,UBERON:0013529,Brodmann area
+UBERON:0004316,distal phalanx of pedal digit 2,UBERON:0003867,distal phalanx of pes
+DOID:368,cerebrum cancer,DOID:1659,supratentorial cancer
+UBERON:0004465,musculature of neck,UBERON:0008229,craniocervical region musculature
+UBERON:2002039,dilatator fossa,UBERON:0004704,bone fossa
+UBERON:0005095,kidney rudiment,UBERON:0005423,developing anatomical structure
+HP:0009551,Patchy sclerosis of the phalanges of the 2nd finger,HP:0100918,Sclerosis of the phalanges of the 2nd finger
+HP:0006086,Thin metacarpal cortices,HP:0005916,Abnormal metacarpal morphology
+HP:0100219,Ivory epiphysis of the middle phalanx of the 5th toe,HP:0100098,Abnormality of the epiphysis of the middle phalanx of the 5th toe
+UBERON:0006811,occipital condyle,UBERON:0004120,mesoderm-derived structure
+HP:0003946,Abnormality of the epiphyses of the elbow,HP:0009811,Abnormality of the elbow
+DOID:13248,mucocele of appendix,DOID:5295,intestinal disease
+HP:0009152,Abnormality of the epiphyses of the 5th finger,HP:0004207,Abnormality of the 5th finger
+DOID:12574,posterior uveitis,DOID:12030,panuveitis
+HP:0012066,Increased urinary disaccharide excretion,HP:0010471,Oligosacchariduria
+UBERON:2002165,caudal procurrent ray set,UBERON:0000477,anatomical cluster
+HP:0009343,Small epiphysis of the distal phalanx of the 3rd finger,HP:0010254,Small epiphyses of the distal phalanges of the hand
+UBERON:0010908,paraglossale,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000426,scaffold cell,CL:0000445,apoptosis fated cell
+DOID:3692,anal canal adenocarcinoma,DOID:0050688,anal canal cancer
+DOID:0050752,amyotrophic lateral sclerosis type 8,DOID:332,amyotrophic lateral sclerosis
+UBERON:4200187,hyperphalangy of manus,UBERON:0002389,manual digit
+CL:1000083,stratified keratinized epithelial stem cell,CL:0000357,stratified epithelial stem cell
+HP:0009522,Stippling of the epiphysis of the middle phalanx of the 2nd finger,HP:0009500,Abnormality of the epiphysis of the middle phalanx of the 2nd finger
+HP:0100837,Atrophodermia vermiculata,HP:0011799,Abnormality of facial soft tissue
+CL:0002087,nongranular leukocyte,CL:0000738,leukocyte
+DOID:4051,alveolar rhabdomyosarcoma,DOID:3247,rhabdomyosarcoma
+UBERON:0002682,abducens nucleus,UBERON:0000126,cranial nerve nucleus
+HP:0008054,Abnormality of the vasculature of the conjunctiva,HP:0000502,Abnormality of the conjunctiva
+UBERON:0013241,embryonic urethral groove,UBERON:0005156,reproductive structure
+UBERON:3000730,foramen nutritium,UBERON:0010276,vertebral column opening
+UBERON:0002032,areola,UBERON:0000475,organism subdivision
+DOID:13521,tetanus neonatorum,DOID:11338,tetanus
+HP:0011495,Abnormality of corneal epithelium,HP:0000481,Abnormality of the cornea
+DOID:4003,Schneiderian carcinoma,DOID:1357,maxillary sinus cancer
+HP:0007446,Palmoplantar blistering,HP:0100872,Abnormality of the plantar skin of foot
+HP:0000851,Congenital hypothyroidism,HP:0000821,Hypothyroidism
+UBERON:0000173,amniotic fluid,UBERON:0000463,portion of organism substance
+DOID:4744,placenta accreta,DOID:780,placenta disease
+CL:0002427,resting double-positive thymocyte,CL:0000809,"double-positive, alpha-beta thymocyte"
+UBERON:0012179,bone of pelvis,UBERON:0005179,pelvic region organ
+HP:0100179,Triangular epiphysis of the distal phalanx of the 4th toe,HP:0100076,Triangular epiphyses of the 4th toe
+UBERON:0010572,manual digit 3 metacarpus cartilage element,UBERON:0015045,manual digit 3 metacarpus endochondral element
+HP:0010197,Curved middle phalanges of the toes,HP:0010183,Abnormality of the middle phalanges of the toes
+UBERON:2205384,dorsal fin proximal radial cartilage 7,UBERON:2200947,dorsal fin proximal radial cartilage
+UBERON:0005015,mucosa of prostatic urethra,UBERON:0005156,reproductive structure
+HP:0007872,Choroidal hemangiomata,HP:0000610,Abnormality of the choroid
+UBERON:0001898,hypothalamus,UBERON:0002784,regional part of diencephalon
+UBERON:0011391,perineal nerve,UBERON:0003444,pelvis nerve
+DOID:12797,hallucinogen abuse,DOID:302,substance abuse
+UBERON:0001762,nasal concha,UBERON:0004120,mesoderm-derived structure
+UBERON:0011974,epiphysis of proximal phalanx of pes,UBERON:0004446,epiphysis of phalanx
+HP:0010484,Hypertrophy of the upper limb,HP:0002817,Abnormality of the upper limb
+UBERON:0010368,pulmonary lobule,UBERON:0004119,endoderm-derived structure
+CL:0000702,R5 photoreceptor cell,CL:0000488,visible light photoreceptor cell
+UBERON:0010159,occipitomastoid suture,UBERON:0003685,cranial suture
+UBERON:0005432,aortic sac,UBERON:0002050,embryonic structure
+UBERON:0014786,extraembryonic umbilical vein,UBERON:0001638,vein
+HP:0000324,Facial asymmetry,HP:0001999,Abnormal facial shape
+UBERON:0004677,spinal cord gray commissure,UBERON:0008882,spinal cord commissure
+DOID:5238,benign perivascular tumor,DOID:0060091,cardiovascular organ benign neoplasm
+UBERON:0002627,capsule of medial geniculate body,UBERON:0003931,diencephalic white matter
+UBERON:0004130,cerebellar layer,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0012490,muscle layer of anal canal,UBERON:0011198,muscle layer of large intestine
+UBERON:2002111,prootic bulla,UBERON:0000481,multi-tissue structure
+UBERON:0008978,anal sac,UBERON:0000064,organ part
+HP:0010428,Partial duplication of phalanx of the 2nd toe,HP:0010355,Duplication of the phalanges of the 2nd toe
+DOID:12028,Conn's syndrome,DOID:656,adrenal adenoma
+HP:0200035,Skin plaque,HP:0011355,Localized skin lesion
+HP:0000331,Small chin,HP:0000306,Abnormality of the chin
+HP:0011748,Adrenocorticotropic hormone deficiency,HP:0000830,Anterior hypopituitarism
+UBERON:0002607,superior rostral sulcus,UBERON:0003022,cerebral cortex lobe
+UBERON:0014567,layer of hippocampal field,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3000441,planum triangulare,UBERON:0010313,neural crest-derived structure
+DOID:10435,purulent acute otitis media,DOID:11506,suppurative otitis media
+CL:0000726,chlamydospore,CL:0000605,fungal asexual spore
+UBERON:0001352,external acoustic meatus,UBERON:0004111,anatomical conduit
+HP:0010034,Short 1st metacarpal,HP:0010026,Aplasia/Hypoplasia of the 1st metacarpal
+DOID:6648,adult pineoblastoma,DOID:5031,adult pineal parenchymal tumor
+UBERON:0001478,teres major muscle,UBERON:0010467,teres muscle
+CL:1001591,oviduct glandular cell,CL:0000150,glandular epithelial cell
+UBERON:0011006,endocardium of left auricle,UBERON:0011005,endocardium of auricle
+UBERON:0001832,sublingual gland,UBERON:0001829,major salivary gland
+UBERON:0006060,conotruncus,UBERON:0002050,embryonic structure
+UBERON:0002142,pedunculopontine tegmental nucleus,UBERON:0007415,nucleus of midbrain reticular formation
+HP:0011885,Hemorrhage of the eye,HP:0011029,Internal hemorrhage
+HP:0004235,Comma-shaped carpal bones,HP:0006014,Abnormally shaped carpal bones
+HP:0001595,Abnormality of the hair,HP:0011138,Abnormality of skin adnexa
+HP:0100227,Enlarged epiphysis of the proximal phalanx of the 5th toe,HP:0100080,Enlarged epiphyses of the 5th toe
+CL:0002083,type I cell of adrenal medulla,CL:0000459,norepinephrin secreting cell
+DOID:0050746,mantle cell lymphoma,DOID:707,B-cell lymphoma
+DOID:11383,cryptorchidism,DOID:0080015,physical disorder
+HP:0012695,Decreased thalamic volume,HP:0012693,Abnormal thalamic size
+DOID:10526,conjunctival pterygium,DOID:0002116,pterygium
+UBERON:0013141,capillary bed,UBERON:0007502,epithelial plexus
+UBERON:0012133,lateral-intermediate intercuneiform joint,UBERON:0012132,intercuneiform joint
+UBERON:0008969,dental follicle,UBERON:0005087,tooth placode
+UBERON:0001910,medial forebrain bundle,UBERON:0005838,fasciculus of brain
+HP:0008179,Decreased electrooculogram (EOG),HP:0000512,Abnormal electroretinogram
+HP:0011585,Thoracic ectopia cordis,HP:0001683,Ectopia cordis
+HP:0010003,Partial duplication of the proximal phalanges of the hand,HP:0010006,Duplication of the proximal phalanx of hand
+UBERON:0003314,eye mesenchyme,UBERON:0009891,facial mesenchyme
+HP:0100462,Patchy sclerosis of the middle phalanx of the 4th toe,HP:0010199,Patchy sclerosis of the middle phalanges of the toes
+DOID:5568,mediastinum teratoma,DOID:5559,mediastinal cancer
+DOID:4006,bladder transitional cell carcinoma,DOID:4007,bladder carcinoma
+UBERON:0001363,great saphenous vein,UBERON:0007318,saphenous vein
+HP:0009961,Partial duplication of the phalanges of the 3rd finger,HP:0009959,Duplication of phalanx of 3rd finger
+UBERON:0011287,rostral organ,UBERON:0010520,head electric organ
+DOID:711,refractory hairy cell leukemia,DOID:285,hairy cell leukemia
+DOID:3372,chondroblastic osteosarcoma,DOID:3347,osteosarcoma
+UBERON:0006428,basisphenoid bone,UBERON:0011164,neurocranium bone
+UBERON:0003393,mesentery of urinary system,UBERON:0002095,mesentery
+CL:0000612,eosinophilic myelocyte,CL:0002193,myelocyte
+HP:0200071,Peripheral vitreoretinal degeneration,HP:0000655,Vitreoretinal degeneration
+UBERON:0013523,lateral vaginal canal,UBERON:0015212,lateral structure
+HP:0008760,Violent behavior,HP:0006919,"Abnormal aggressive, impulsive or violent behavior"
+UBERON:0002653,gracile fasciculus of medulla,UBERON:0005838,fasciculus of brain
+HP:0009439,Short middle phalanx of the 3rd finger,HP:0009437,Aplasia/Hypoplasia of the middle phalanx of the 3rd finger
+HP:0011710,Bundle branch block,HP:0012722,Heart block
+HP:0011921,Exudative pleural effusion,HP:0002202,Pleural effusion
+UBERON:0003565,hindbrain dura mater,UBERON:0003291,meninx of hindbrain
+HP:0100280,Crohn's disease,HP:0100281,Chronic colitis
+UBERON:0001464,hip,UBERON:0000475,organism subdivision
+DOID:3637,childhood spinal cord tumor,DOID:5612,spinal cancer
+HP:0006524,Tracheobronchial leiomyomatosis,HP:0005607,Abnormality of the tracheobronchial system
+UBERON:2001811,infraorbital sensory canal,UBERON:2001612,sensory canal
+UBERON:2001139,mediodorsal tooth row,UBERON:0009678,tooth row
+UBERON:3010178,finger glands,UBERON:3010606,limb glands
+DOID:0050488,early congenital syphilis,DOID:9856,congenital syphilis
+UBERON:0004652,humerus diaphysis,UBERON:0004769,diaphysis
+UBERON:2000211,gill lamella,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0010405,spinal cord lateral motor column,UBERON:0001948,regional part of spinal cord
+DOID:8584,Burkitt lymphoma,DOID:706,mature B-cell neoplasm
+UBERON:3010227,costal protuberances,UBERON:3000977,body external integument structure
+CL:0000343,visual pigment cell (sensu Vertebrata),CL:0000149,visual pigment cell
+UBERON:0009194,basisphenoid cartilage condenstion,UBERON:0005863,cartilaginous condensation
+UBERON:0001781,layer of retina,UBERON:0004923,organ component layer
+UBERON:0006463,fourth sacral spinal cord segment,UBERON:0007717,sacral subsegment of spinal cord
+UBERON:0000332,yellow bone marrow,UBERON:0002371,bone marrow
+UBERON:0009499,parietal of mesothelium of pericardio-peritoneal canal,UBERON:0007185,pericardio-peritoneal canal mesothelium
+CL:0000183,contractile cell,CL:0000003,native cell
+UBERON:0001291,thick ascending limb of loop of Henle,UBERON:0008408,distal tubular epithelium
+UBERON:3010240,Nobelian rod,UBERON:0005156,reproductive structure
+HP:0000933,Posterior fossa cyst at the fourth ventricle,HP:0007291,Posterior fossa cyst
+UBERON:2001613,dorsal fin middle radial bone,UBERON:2001672,dorsal fin radial bone
+UBERON:0004870,superficial cervical lymph node,UBERON:0015917,superficial lymph node
+UBERON:2000033,intermediate cell mass of mesoderm,UBERON:0004120,mesoderm-derived structure
+UBERON:0005202,distal straight tubule macula densa,UBERON:0002335,macula densa
+CL:1001036,vasa recta cell,CL:1000893,kidney venous blood vessel cell
+UBERON:0001012,head of radius,UBERON:0004120,mesoderm-derived structure
+HP:0005003,Aplasia/Hypoplasia of the capital femoral epiphysis,HP:0010577,Absent epiphyses
+HP:0005278,Hypoplastic nasal tip,HP:0000436,Abnormality of the nasal tip
+UBERON:4200084,preaxial centrale,UBERON:0012131,centrale
+UBERON:0014686,angular vein,UBERON:0003496,head blood vessel
+UBERON:0002829,dorsal cochlear nucleus,UBERON:0001720,cochlear nucleus
+UBERON:0012480,cloacal mucosa,UBERON:0004120,mesoderm-derived structure
+HP:0006563,Malformation of the hepatic ductal plate,HP:0004297,Abnormality of the biliary system
+UBERON:2007001,dorso-rostral cluster,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3000079,cartilago retronarina,UBERON:0010313,neural crest-derived structure
+UBERON:2001665,basibranchial 2 tooth,UBERON:0004756,dermal skeletal element
+DOID:5812,MHC class II deficiency,DOID:627,severe combined immunodeficiency
+DOID:0050068,pestis minor,DOID:10773,bubonic plague
+UBERON:0003926,photoreceptor outer segment layer,UBERON:0000479,tissue
+UBERON:0002525,brachial lymph node,UBERON:0000029,lymph node
+HP:0012700,Abnormal large intestine physiology,HP:0002250,Abnormality of the large intestine
+HP:0000652,Lower eyelid coloboma,HP:0000625,Cleft eyelid
+UBERON:0015329,respiratory system basement membrane,UBERON:0005769,basement membrane of epithelium
+HP:0100109,Stippling of the epiphysis of the distal phalanx of the 2nd toe,HP:0100053,Stippling of the epiphyses of the 2nd toe
+HP:0100515,Pollakisuria,HP:0000009,Functional abnormality of the bladder
+UBERON:0004548,left eye,UBERON:0015212,lateral structure
+HP:0006561,Lipid accumulation in hepatocytes,HP:0001392,Abnormality of the liver
+UBERON:0011060,perilymphatic channel,UBERON:0000025,tube
+HP:0011174,Hyperkinetic seizures,HP:0011153,Focal motor seizures
+HP:0002834,Flared femoral metaphysis,HP:0006489,Abnormality of the femoral metaphysis
+UBERON:0010733,alisphenoid cartilage element,UBERON:0007213,mesenchyme derived from head neural crest
+HP:0001786,Narrow foot,HP:0001760,Abnormality of the foot
+UBERON:0003682,palatal muscle,UBERON:0013765,digestive system organ
+UBERON:0002417,abdominal segment of trunk,UBERON:0009569,subdivision of trunk
+UBERON:0007721,interphalangeal joint of pes,UBERON:0001487,pes joint
+DOID:12123,postinflammatory pulmonary fibrosis,DOID:3770,pulmonary fibrosis
+DOID:2975,cystic kidney,DOID:557,kidney disease
+UBERON:0003422,mesenchyme of umbilical cord,UBERON:0004120,mesoderm-derived structure
+DOID:1129,pituitary apoplexy,DOID:1130,pituitary infarct
+UBERON:0003650,metatarsal bone of digit 1,UBERON:0015037,pedal digit 1 metatarsal endochondral element
+DOID:0050816,urofacial syndrome,DOID:0050737,autosomal recessive disease
+DOID:13088,periventricular leukomalacia,DOID:2034,encephalomalacia
+CL:0000031,neuroblast,CL:0000047,neuronal stem cell
+HP:0000657,Oculomotor apraxia,HP:0002186,Apraxia
+UBERON:0014396,interscapular fat pad,UBERON:0003579,shoulder connective tissue
+HP:0010242,Aplasia of the proximal phalanges of the hand,HP:0009380,Aplasia of the fingers
+UBERON:0010853,capitulum of humerus,UBERON:0004120,mesoderm-derived structure
+UBERON:0003343,mucosa of oral region,UBERON:0003729,mouth mucosa
+UBERON:0010372,uncinate process of ethmoid,UBERON:0010313,neural crest-derived structure
+HP:0007768,Central retinal vessel vascular tortuosity,HP:0000631,Retinal arterial tortuosity
+UBERON:0010034,copula linguae,UBERON:0004121,ectoderm-derived structure
+CL:1000681,kidney cortex interstitial cell,CL:0002584,renal cortical epithelial cell
+UBERON:4000177,dorsal fin lepidotrichium,UBERON:0004247,bone of dorsum
+HP:0001997,Gout,HP:0001369,Arthritis
+HP:0003435,Cold-induced hand cramps,HP:0003449,Cold-induced muscle cramps
+UBERON:0005271,juxtamedullary cortex,UBERON:0000064,organ part
+HP:0010659,Patchy variation in bone mineral density,HP:0010658,Patchy changes of bone mineral density
+HP:0007230,Decreased distal sensory nerve action potential,HP:0007078,Decreased amplitude of sensory action potentials
+UBERON:0001612,facial artery,UBERON:0003496,head blood vessel
+DOID:4321,large cell acanthoma,DOID:174,acanthoma
+UBERON:0002929,dentate gyrus pyramidal layer,UBERON:0002304,layer of dentate gyrus
+UBERON:0013132,penicillar arteriole,UBERON:0003497,abdomen blood vessel
+UBERON:2001172,roofing cartilage,UBERON:2001457,postcranial axial cartilage
+HP:0010841,Multifocal epileptiform discharges,HP:0011185,EEG with focal epileptiform discharges
+UBERON:0001932,arcuate nucleus of hypothalamus,UBERON:0006568,hypothalamic nucleus
+UBERON:3010127,fringe on postaxial edge of Finger IV,UBERON:3010123,finger fringes
+HP:0012716,Moderate conductive hearing impairment,HP:0000405,Conductive hearing impairment
+DOID:8557,oropharynx cancer,DOID:0060119,pharynx cancer
+UBERON:0008897,fin,UBERON:0000026,appendage
+UBERON:0001144,testicular vein,UBERON:0015212,lateral structure
+HP:0000297,Facial hypotonia,HP:0001252,Muscular hypotonia
+UBERON:4200175,supraglenoid region,UBERON:0005913,zone of bone organ
+DOID:0060219,lymph node adenoid cystic carcinoma,DOID:10619,lymph node cancer
+UBERON:0015895,proximal deep inguinal lymph node,UBERON:0009006,deep inguinal lymph node
+UBERON:0005049,mucosa of infundibulum of uterine tube,UBERON:0014404,female anatomical structure
+UBERON:0003476,respiratory system venous blood vessel,UBERON:0001638,vein
+HP:0000426,Prominent nasal bridge,HP:0000422,Abnormality of the nasal bridge
+UBERON:2001961,ceratobranchial 5 bone distal cartilage,UBERON:4000003,permanent cartilage
+UBERON:0001095,caudal vertebra,UBERON:0004247,bone of dorsum
+HP:0100905,Sclerosis of the middle phalanx of the 3rd finger,HP:0100916,Sclerosis of the middle phalanges of the hand
+UBERON:2002141,annular ligament,UBERON:0008846,skeletal ligament
+UBERON:0001661,deep temporal vein,UBERON:0001671,temporal vein
+HP:0010885,Aseptic necrosis,HP:0011843,Abnormality of skeletal physiology
+HP:0003927,Cortical irregularity of humeral diaphysis,HP:0003926,Abnormality of the humeral diaphysis
+UBERON:0006054,surface of occiput,UBERON:0006056,posterior surface of head
+CL:0000594,skeletal muscle satellite cell,CL:0000188,skeletal muscle cell
+UBERON:0005636,caecum epithelium,UBERON:0000397,colonic epithelium
+UBERON:0003046,ventral acoustic stria,UBERON:0002316,white matter
+UBERON:0001535,vertebral artery,UBERON:0002458,spinal artery
+HP:0009062,Infantile axial hypotonia,HP:0008947,Infantile muscular hypotonia
+HP:0007618,Subcutaneous calcification,HP:0010766,Ectopic calcification
+UBERON:0006265,mural trophectoderm,UBERON:0000478,extraembryonic structure
+UBERON:0004550,gastroesophageal sphincter,UBERON:0011185,gastrointestinal sphincter
+HP:0100131,Stippling of the epiphysis of the proximal phalanx of the 2nd toe,HP:0100053,Stippling of the epiphyses of the 2nd toe
+CL:0002327,mammary gland epithelial cell,CL:0000066,epithelial cell
+UBERON:0001964,least splanchnic nerve,UBERON:0003429,abdomen nerve
+CL:1000334,enterocyte of epithelium of small intestine,CL:0000584,enterocyte
+HP:0100411,Complete duplication of the middle phalanx of the 4th toe,HP:0100402,Duplication of the middle phalanx of the 4th toe
+UBERON:0005068,neural rod,UBERON:0005423,developing anatomical structure
+UBERON:0008596,mentalis,UBERON:0013765,digestive system organ
+UBERON:0005314,alveolar primary septum,UBERON:0004821,pulmonary alveolus epithelium
+CL:1000382,type 2 vestibular sensory cell of stato-acoustic epithelium,CL:0002069,type II vestibular sensory cell
+UBERON:2000549,posttemporal,UBERON:0011164,neurocranium bone
+UBERON:0005400,telencephalon arachnoid mater,UBERON:0003289,meninx of telencephalon
+DOID:0050644,arterial calcification of infancy,DOID:178,vascular disease
+HP:0003422,Vertebral segmentation defect,HP:0003468,Abnormality of the vertebrae
+HP:0010874,Tendon xanthomatosis,HP:0000991,Xanthomatosis
+HP:0007526,Hypopigmented skin patches on arms,HP:0001053,Hypopigmented skin patches
+HP:0010017,Cone-shaped epiphysis of the 1st metacarpal,HP:0010014,Abnormality of the epiphysis of the 1st metacarpal
+HP:0002857,Genu valgum,HP:0002815,Abnormality of the knees
+HP:0010079,Curved distal phalanx of the hallux,HP:0010061,Curved phalanges of the hallux
+DOID:4531,mucoepidermoid carcinoma,DOID:0050904,salivary gland carcinoma
+CL:0000925,activated CD4-positive type I NK T cell,CL:0000923,CD4-positive type I NK T cell
+HP:0011507,Macular flecks,HP:0001103,Abnormality of the macula
+UBERON:0006044,interdigital region between pedal digits 3 and 4,UBERON:0006022,interdigital region between digits 3 and 4
+NCBITaxon:6029,Microsporidia,NCBITaxon:4751,Fungi
+HP:0000790,Hematuria,HP:0012614,Abnormal urine cytology
+UBERON:0002002,interchondral joint,UBERON:0002001,joint of rib
+HP:0010533,Spasmus nutans,HP:0012043,Pendular nystagmus
+UBERON:0013474,middle part of esophagus,UBERON:0004921,subdivision of digestive tract
+UBERON:2002002,anterior distal serration of pectoral fin spine,UBERON:0004121,ectoderm-derived structure
+UBERON:0010889,ectethmoid,UBERON:0010313,neural crest-derived structure
+HP:0009573,Patchy sclerosis of the middle phalanx of the 2nd finger,HP:0009543,Abnormality of the middle phalanx of the 2nd finger
+UBERON:3000386,cultriform process,UBERON:0004121,ectoderm-derived structure
+CL:0000886,nasal and broncial associated lymphoid tissue macrophage,CL:0000884,mucosa-associated lymphoid tissue macrophage
+UBERON:2000448,tertiary gustatory nucleus,UBERON:0006569,diencephalic nucleus
+HP:0009333,Abnormality of the epiphysis of the proximal phalanx of the 3rd finger,HP:0009358,Abnormality of the proximal phalanx of the 3rd finger
+UBERON:0005457,left thymus lobe,UBERON:0005483,thymus lobe
+HP:0005230,Biliary tract obstruction,HP:0012440,Abnormal biliary tract morphology
+UBERON:0010421,spleen B cell corona,UBERON:0004120,mesoderm-derived structure
+UBERON:0009582,spinal cord lateral wall,UBERON:0005496,neural tube lateral wall
+UBERON:0005676,right lung accessory lobe endothelium,UBERON:0005655,right lung accessory lobe epithelium
+UBERON:0003855,gonad mesenchyme,UBERON:0005156,reproductive structure
+DOID:12449,aplastic anemia,DOID:2355,anemia
+UBERON:0006446,rostral middle frontal gyrus,UBERON:0003022,cerebral cortex lobe
+DOID:1279,ocular motility disease,DOID:5656,cranial nerve disease
+UBERON:0013447,sagittal crest,UBERON:0005913,zone of bone organ
+DOID:4209,brainstem intraparenchymal clear cell meningioma,DOID:4203,brain stem cancer
+UBERON:0002370,thymus,UBERON:0002368,endocrine gland
+HP:0010119,Ivory epiphyses of the hallux,HP:0010056,Abnormality of the epiphyses of the hallux
+HP:0000970,Anhidrosis,HP:0000971,Abnormality of the sweat gland
+HP:0005348,Inspiratory stridor,HP:0010307,Stridor
+HP:0001880,Eosinophilia,HP:0001879,Abnormality of eosinophils
+DOID:0050549,Saldino-Noonan syndrome,DOID:225,syndrome
+UBERON:0001866,sebum,UBERON:0000456,bodily secretion
+UBERON:0004999,mucosa of biliary tree,UBERON:0004119,endoderm-derived structure
+UBERON:0007359,ruminant forestomach,UBERON:0011954,stomach non-glandular region
+UBERON:0009654,alveolar artery,UBERON:0003496,head blood vessel
+UBERON:0011769,cartilaginous projection,UBERON:0004529,anatomical projection
+UBERON:0001299,glans penis,UBERON:0005156,reproductive structure
+UBERON:2000232,lateral semicircular canal primordium,UBERON:2002215,otic vesicle protrusion
+HP:0007925,Lacrimal duct aplasia,HP:0011481,Abnormality of the lacrimal duct
+CL:0002390,uninucleate blastconidium,CL:0002384,uninucleate macroconidium
+HP:0100532,Scleritis,HP:0100533,Inflammatory abnormality of the eye
+HP:0009121,Abnormal axial skeleton morphology,HP:0011842,Abnormality of skeletal morphology
+HP:0100485,Symphalangism of the proximal phalanx of the 4th toe with the 4th metatarsal,HP:0001440,Synostosis involving metatarsal bones
+UBERON:0011358,infundibular organ,UBERON:0004121,ectoderm-derived structure
+DOID:12858,Huntington's disease,DOID:1289,neurodegenerative disease
+UBERON:3010179,web glands,UBERON:3010606,limb glands
+HP:0100599,Diphallia,HP:0000036,Abnormality of the penis
+UBERON:0003135,male reproductive organ,UBERON:0014403,male anatomical structure
+HP:0008663,Renal sarcoma,HP:0009726,Renal neoplasm
+UBERON:0001181,inferior recess of lesser sac,UBERON:0004458,body cavity or lining
+UBERON:0000414,mucous gland,UBERON:0002365,exocrine gland
+HP:0003153,Cystathioninuria,HP:0004339,Abnormality of sulfur amino acid metabolism
+HP:0000006,Autosomal dominant inheritance,HP:0000005,Mode of inheritance
+DOID:6741,bilateral breast cancer,DOID:3459,breast carcinoma
+DOID:3140,scleredema adultorum,DOID:37,skin disease
+UBERON:0002913,intraparietal sulcus,UBERON:0003022,cerebral cortex lobe
+DOID:7428,pineal region germinoma,DOID:1660,malignant pineal area germ cell neoplasm
+HP:0001195,Single umbilical artery,HP:0011425,Fetal ultrasound soft marker
+UBERON:3000237,infrarostral cartilage,UBERON:0013765,digestive system organ
+CL:0002313,endocrine-paracrine cell of prostate gland,CL:0000150,glandular epithelial cell
+HP:0006706,Cystic liver disease,HP:0001392,Abnormality of the liver
+CL:0000724,heterocyst,CL:0000520,prokaryotic cell
+UBERON:0006925,digestive gland,UBERON:0013765,digestive system organ
+DOID:5530,thymus squamous cell carcinoma,DOID:3284,thymic carcinoma
+UBERON:0001966,substantia nigra pars reticulata,UBERON:0004121,ectoderm-derived structure
+HP:0006501,Aplasia/Hypoplasia of the radius,HP:0002818,Abnormality of the radius
+HP:0009450,Broad proximal phalanx of the 3rd finger,HP:0009852,Broad proximal phalanges of the hand
+HP:0009460,Aplasia of the 3rd finger,HP:0009318,Aplasia/Hypoplasia of the 3rd finger
+UBERON:3000746,urostyle ridge,UBERON:0004120,mesoderm-derived structure
+HP:0100373,Aplasia/Hypoplasia of the middle phalanx of the 4th toe,HP:0010371,Aplasia/Hypoplasia of the phalanges of the 4th toe
+CL:0000978,IgM short lived plasma cell,CL:0000975,short lived plasma cell
+CL:0000242,Merkel cell,CL:0000123,neuron associated cell (sensu Vertebrata)
+DOID:2855,hyperthyroxinemia,DOID:50,thyroid gland disease
+CL:0000125,glial cell,CL:0000095,neuron associated cell
+DOID:1003,pelvic inflammatory disease,DOID:229,female reproductive system disease
+UBERON:2005044,optic artery,UBERON:0003496,head blood vessel
+DOID:5599,precursor T-lymphoblastic lymphoma/leukemia,DOID:5600,precursor lymphoblastic lymphoma/leukemia
+HP:0001204,Distal symphalangism (hands),HP:0009773,Symphalangism affecting the phalanges of the hand
+HP:0001117,Sudden central visual loss,HP:0001123,Visual field defect
+CL:0002475,lymphoid MHC-II-negative non-classical monocyte,CL:0002469,MHC-II-negative classical monocyte
+UBERON:0014767,left crus of diaphragm,UBERON:0014765,crus of diaphragm
+UBERON:0007283,presumptive shield,UBERON:0006598,presumptive structure
+UBERON:0002012,pulmonary artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0010221,laryngeal associated mesenchyme,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2002078,hypural plate,UBERON:0004376,fin bone
+UBERON:0001281,hepatic sinusoid,UBERON:0015796,liver blood vessel
+DOID:0080047,pseudoachondroplasia,DOID:2256,osteochondrodysplasia
+UBERON:0014286,dorsal cap of Kooy,UBERON:0002574,regional part of inferior olivary complex
+HP:0007412,Macular hyperpigmented dermopathy,HP:0001034,Hypermelanotic macule
+UBERON:0001556,lower urinary tract,UBERON:0000477,anatomical cluster
+DOID:11329,ainhum,DOID:65,connective tissue disease
+UBERON:0004433,proximal epiphysis of distal phalanx of manual digit 3,UBERON:0004419,proximal epiphysis of phalanx of manual digit 3
+HP:0010645,Aplasia of the distal phalanges of the toes,HP:0010745,Aplasia of the phalanges of the toes
+UBERON:0005302,female preputial gland,UBERON:0005398,female reproductive gland
+HP:0009149,Triangular epiphysis of the distal phalanx of the 5th finger,HP:0010256,Triangular epiphyses of the distal phalanges of the hand
+CL:0000628,photosynthetic cell,CL:0000003,native cell
+UBERON:0006231,facial bone primordium,UBERON:0003462,facial bone
+UBERON:0009587,mesenchyme of interdigital region between manual digits 2 and 3,UBERON:0009600,mesenchyme of interdigital region of manus
+CL:0002234,basal cell of prostatic acinus,CL:0002233,epithelial cell of prostatic acinus
+HP:0008216,Adrenal gland dysgenesis,HP:0011732,Abnormality of adrenal morphology
+HP:0007537,Severe photosensitivity,HP:0000992,Cutaneous photosensitivity
+UBERON:0001190,ovarian artery,UBERON:0001637,artery
+UBERON:0006721,alisphenoid bone,UBERON:0003462,facial bone
+UBERON:0005731,fin field,UBERON:0005732,paired limb/fin field
+HP:0011286,Total colonic aganglionosis,HP:0002251,Aganglionic megacolon
+UBERON:0003645,metacarpal bone of digit 1,UBERON:0002374,metacarpal bone
+UBERON:0006252,intersubcardinal venous anastomosis,UBERON:0002050,embryonic structure
+UBERON:0000176,oronasal secretion,UBERON:0000463,portion of organism substance
+DOID:4292,morpheaform basal cell carcinoma,DOID:2513,basal cell carcinoma
+UBERON:0003472,cerebellar artery,UBERON:0001637,artery
+CL:0002284,type X enteroendocrine cell,CL:0000164,enteroendocrine cell
+DOID:8501,fundus dystrophy,DOID:5614,eye disease
+HP:0004220,Short middle phalanx of the 5th finger,HP:0009161,Aplasia/Hypoplasia of the middle phalanx of the 5th finger
+UBERON:2000211,gill lamella,UBERON:0000481,multi-tissue structure
+UBERON:0010370,tibial vein,UBERON:0003503,leg blood vessel
+CL:1000340,enterocyte of epithelium proper of duodenum,CL:1000339,enterocyte of epithelium proper of small intestine
+UBERON:0009207,geschmacksstreifen,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001912,lobule of lactiferous gland,UBERON:0005156,reproductive structure
+UBERON:0001899,epithalamus,UBERON:0002784,regional part of diencephalon
+UBERON:0013139,ligament of liver,UBERON:0003567,abdomen connective tissue
+UBERON:3000547,rostral process,UBERON:4100000,skeletal element projection
+DOID:8060,frontal sinus inverted papilloma,DOID:1361,frontal sinus neoplasm
+HP:0009535,Aplasia of the 2nd finger,HP:0006264,Aplasia/Hypoplasia of the 2nd finger
+DOID:13589,female infertility of uterine origin,DOID:345,uterine disease
+HP:0009714,Abnormality of the epididymis,HP:0000022,Abnormality of male internal genitalia
+UBERON:0010074,chromaffin system,UBERON:0010313,neural crest-derived structure
+UBERON:0012282,mammary fat pad,UBERON:0004180,mammary gland fat
+HP:0001331,Absent septum pellucidum,HP:0007375,Abnormality of the septum pellucidum
+HP:0009929,Abnormality of the columella,HP:0010938,Abnormality of the external nose
+UBERON:0002326,lamina propria of urethra,UBERON:0000030,lamina propria
+UBERON:0011246,procoracoid bone,UBERON:0007829,pectoral girdle bone
+DOID:0050588,muscular dystrophy-dystroglycanopathy,DOID:0050557,congenital muscular dystrophy
+DOID:5772,central nervous system hematologic cancer,DOID:3620,central nervous system cancer
+UBERON:2105225,median fin radial element,UBERON:2100271,radial element
+HP:0010254,Small epiphyses of the distal phalanges of the hand,HP:0010236,Small epiphyses of the phalanges of the hand
+UBERON:0013223,alveolar gland,UBERON:0002530,gland
+HP:0010291,Prominent palatine ridges,HP:0000174,Abnormality of the palate
+UBERON:2201614,anal fin middle radial cartilage,UBERON:2101614,anal fin middle radial element
+HP:0100245,Desmoid tumors,HP:0100244,Fibrosarcoma
+HP:0011492,Abnormality of corneal stroma,HP:0000481,Abnormality of the cornea
+DOID:823,periapical periodontitis,DOID:824,periodontitis
+UBERON:0009738,border of sublaminar layers S1 and S2,UBERON:0009740,border between sublaminar layers
+HP:0002324,Hydranencephaly,HP:0002323,Anencephaly
+DOID:9125,lower gum cancer,DOID:8602,gum cancer
+HP:0009319,Joint contractures of the 3rd finger,HP:0004150,Abnormality of the 3rd finger
+UBERON:2001343,telencephalon diencephalon boundary,UBERON:0006800,anatomical line
+UBERON:0008856,stomach muscularis externa,UBERON:0004222,stomach smooth muscle
+UBERON:0006847,cerebellar commissure,UBERON:0001020,nervous system commissure
+UBERON:0014543,lumbar spinal cord central canal,UBERON:0014538,subdivision of spinal cord central canal
+DOID:7542,osteosarcoma arising in bone Paget's disease,DOID:3376,bone osteosarcoma
+HP:0002219,Facial hypertrichosis,HP:0000998,Hypertrichosis
+UBERON:0010309,palpebral bone,UBERON:0010321,skeletal element of eye region
+HP:0011844,Abnormal appendicular skeleton morphology,HP:0011842,Abnormality of skeletal morphology
+UBERON:4000051,lepidosteoid scale,UBERON:4000052,ganoid scale
+UBERON:0002515,periosteum,UBERON:0000158,membranous layer
+UBERON:0005123,metanephric prebend segment,UBERON:0004207,prebend segment
+HP:0002032,Esophageal atresia,HP:0002031,Abnormality of the esophagus
+HP:0003477,Peripheral axonal neuropathy,HP:0000764,Peripheral axonal degeneration
+HP:0005937,Respiratory function loss,HP:0002093,Respiratory insufficiency
+CL:0000075,columnar/cuboidal epithelial cell,CL:0002371,somatic cell
+HP:0004798,Recurrent infection of the gastrointestinal tract,HP:0002719,Recurrent infections
+UBERON:0015055,pubic endochondral element,UBERON:0010363,endochondral element
+HP:0009218,Fragmentation of the epiphysis of the middle phalanx of the 4th finger,HP:0010261,Fragmentation of the epiphyses of the middle phalanges of the hand
+DOID:0060136,associative agnosia,DOID:4090,agnosia
+HP:0009454,Patchy sclerosis of the proximal phalanx of the 3rd finger,HP:0009444,Patchy sclerosis of the phalanges of the 3rd finger
+UBERON:0001620,central retinal artery,UBERON:0001637,artery
+DOID:9065,leishmaniasis,DOID:2789,parasitic protozoa infectious disease
+UBERON:2000474,intercalar,UBERON:0007842,membrane bone
+CL:0002578,mesenteric preadipocyte,CL:0002334,preadipocyte
+DOID:12253,testicular lymphoma,DOID:2998,testicular cancer
+UBERON:0012358,manual digitopodium bone,UBERON:0005897,manus bone
+DOID:318,progressive muscular atrophy,DOID:231,motor neuron disease
+HP:0012125,Prostate cancer,HP:0100787,Prostate neoplasm
+HP:0100579,Mucosal telangiectasiae,HP:0001009,Telangiectasia
+CL:1001587,uterine cervix glandular cell,CL:1001591,oviduct glandular cell
+DOID:4588,secretory meningioma,DOID:3565,meningioma
+HP:0001790,Nonimmune hydrops fetalis,HP:0001789,Hydrops fetalis
+UBERON:0002985,ventral nucleus of medial geniculate body,UBERON:0015233,nucleus of dorsal thalamus
+HP:0010025,Triangular epiphysis of the 1st metacarpal,HP:0009696,Triangular epiphyses of the thumb
+HP:0010608,Hordeolum internum,HP:0010606,Hordeolum
+HP:0003960,Exostoses of the forearm bones,HP:0100777,Exostoses
+UBERON:2000810,myotome somite 7,UBERON:0003082,myotome
+UBERON:0005019,mucosa of palate,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001370,gluteus maximus,UBERON:0002000,gluteal muscle
+UBERON:0010880,gular fold,UBERON:0010854,skin of front of neck
+DOID:3198,hypoglossal nerve neoplasm,DOID:338,cranial nerve neoplasm
+UBERON:0006544,kidney vasculature,UBERON:0006876,vasculature of organ
+UBERON:2002023,second preethmoid,UBERON:0002513,endochondral bone
+HP:0009649,Aplasia of the distal phalanx of the thumb,HP:0009659,Partial absence of thumb
+HP:0001698,Pericardial effusion,HP:0001697,Abnormality of the pericardium
+UBERON:0011198,muscle layer of large intestine,UBERON:0012367,muscle layer of intestine
+HP:0010669,Cheekbone underdevelopment,HP:0010668,Abnormality of the zygomatic bone
+DOID:1143,exotropia,DOID:540,strabismus
+HP:0009735,Spinal neurofibromas,HP:0001067,Neurofibromas
+UBERON:0000353,parenchyma,UBERON:0000064,organ part
+UBERON:3000844,sulcus longitudinalis,UBERON:0000064,organ part
+NCBITaxon:452563,Davidiellaceae,NCBITaxon:134362,Capnodiales
+UBERON:0001725,cranial synchondrosis,UBERON:0002215,synchondrosis
+HP:0009279,Radial deviation of the 4th finger,HP:0009273,Deviation of the 4th finger
+UBERON:0006230,extrinsic ocular pre-muscle mass,UBERON:0006904,head mesenchyme from mesoderm
+DOID:0050278,basidiobolomycosis,DOID:37,skin disease
+CL:0000163,endocrine cell,CL:0000151,secretory cell
+UBERON:0001358,perineal artery,UBERON:0004573,systemic artery
+HP:0003749,Pelvic girdle muscle weakness,HP:0001445,Abnormality of the hip-girdle musculature
+HP:0011754,Pituicytoma,HP:0011752,Neoplasm of the posterior pituitary
+UBERON:0002640,cuneocerebellar tract,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001136,mesothelium,UBERON:0012275,meso-epithelium
+UBERON:0004986,mucosa of deferent duct,UBERON:0005156,reproductive structure
+UBERON:2000522,inferior hyohyoid,UBERON:0005493,hyoid muscle
+UBERON:2001616,lateral ethmoid wing,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0004840,Hypochromic microcytic anemia,HP:0001935,Microcytic anemia
+UBERON:0008431,sacral foramen,UBERON:0001131,vertebral foramen
+DOID:0050608,Askin's tumor,DOID:3369,peripheral primitive neuroectodermal tumor
+HP:0009164,Abnormal calcification of the carpal bones,HP:0001191,Abnormality of the carpal bones
+HP:0008058,Aplasia/Hypoplasia of the optic nerve,HP:0000587,Abnormality of the optic nerve
+HP:0007736,Pericentral retinal dystrophy,HP:0000556,Retinal dystrophy
+DOID:12241,beta thalassemia,DOID:10241,thalassemia
+DOID:421,hair disease,DOID:16,integumentary system disease
+HP:0009574,Symphalangism of middle phalanx of 2nd finger,HP:0009849,Symphalangism of middle phalanx of finger
+UBERON:4300023,interolateral plate,UBERON:0007829,pectoral girdle bone
+UBERON:0008863,stomach smooth muscle outer longitudinal layer,UBERON:0012369,longitudinal muscle layer
+UBERON:0001680,lacrimal bone,UBERON:0008001,irregular bone
+NCBITaxon:35305,California encephalitis virus,NCBITaxon:11572,Orthobunyavirus
+CL:0000525,syncytiotrophoblast cell,CL:0000228,multinucleate cell
+HP:0010486,Abnormality of the hypothenar eminence,HP:0001421,Abnormality of the musculature of the hand
+UBERON:0003724,musculocutaneous nerve,UBERON:0002003,peripheral nerve
+DOID:4084,testicular trophoblastic tumor,DOID:4086,testicular germ cell tumor non-seminomatous
+HP:0006562,Viral hepatitis,HP:0012115,Hepatitis
+HP:0002572,Episodic vomiting,HP:0002013,Vomiting
+DOID:1340,pure red-cell aplasia,DOID:12449,aplastic anemia
+DOID:0050692,Brody myopathy,DOID:440,neuromuscular disease
+UBERON:0006255,ischial pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+DOID:2556,relapsing polychondritis,DOID:1222,cartilage disease
+DOID:7378,pituitary hypoplasia,DOID:53,pituitary gland disease
+UBERON:2002017,anterior limb of ceratobranchial 5 bone,UBERON:4100000,skeletal element projection
+HP:0009455,Symphalangism affecting the proximal phalanx of the 3rd finger,HP:0009445,Symphalangism of the 3rd finger
+HP:0010644,Midnasal stenosis,HP:0010641,Abnormality of the midnasal cavity
+DOID:2237,hepatitis,DOID:409,liver disease
+UBERON:0000010,peripheral nervous system,UBERON:0011216,organ system subdivision
+UBERON:0011856,acinus of lactiferous gland,UBERON:0004121,ectoderm-derived structure
+HP:0002164,Nail dysplasia,HP:0001597,Abnormality of the nail
+DOID:4500,hypokalemia,DOID:0050032,mineral metabolism disease
+HP:0009724,Subungual fibromas,HP:0009723,Abnormality of the subungual region
+HP:0100907,Sclerosis of the middle phalanx of the 5th finger,HP:0100921,Sclerosis of the phalanges of the 5th finger
+UBERON:0001795,inner plexiform layer of retina,UBERON:0003902,retinal neural layer
+DOID:0050449,pachyonychia congenita,DOID:0050736,autosomal dominant disease
+UBERON:0010081,future common hepatic duct,UBERON:0007497,developing epithelial placode
+HP:0001417,X-linked inheritance,HP:0010985,Gonosomal inheritance
+UBERON:3010793,m. ypsiloideus anterior,UBERON:0008777,hypaxial musclulature
+HP:0007859,Congenital horizontal nystagmus,HP:0000666,Horizontal nystagmus
+UBERON:0012402,small intestine smooth muscle longitudinal layer,UBERON:0012369,longitudinal muscle layer
+CL:0000478,oxytocin stimulating hormone secreting cell,CL:0000167,peptide hormone secreting cell
+DOID:1123,spondyloarthropathy,DOID:381,arthropathy
+HP:0004422,Biparietal narrowing,HP:0002648,Abnormality of calvarial morphology
+CL:0002398,"Gr1-positive, CD43-positive monocyte",CL:0002393,intermediate monocyte
+DOID:8488,polyhydramnios,DOID:780,placenta disease
+UBERON:0002565,olivary pretectal nucleus,UBERON:0003528,brain grey matter
+HP:0000683,Grayish enamel,HP:0000682,Abnormality of dental enamel
+UBERON:3010209,keratinous claw,UBERON:3000981,limb external integument structure
+DOID:3209,junctional epidermolysis bullosa,DOID:2730,epidermolysis bullosa
+UBERON:0004136,intermediate tubule,UBERON:0007685,region of nephron tubule
+HP:0012336,Reduced cerebrospinal fluid 5-methyltetrahydrofolate concentration,HP:0012335,Abnormality of folate metabolism
+CL:0000861,elicited macrophage,CL:0000235,macrophage
+UBERON:0009879,tarsal skeleton,UBERON:0009878,mesopodial skeleton
+UBERON:0006347,communicating artery,UBERON:0001637,artery
+HP:0011070,Abnormality of molar morphology,HP:0011077,Abnormality of molar
+HP:0002256,Small bowel diverticula,HP:0005222,Bowel diverticulosis
+DOID:7565,vulvar eccrine porocarcinoma,DOID:1294,vulva carcinoma
+UBERON:0002392,nasolacrimal duct,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010002,Complete duplication of the middle phalanges of the hand,HP:0009998,Complete duplication of phalanx of hand
+UBERON:0007610,tibial artery,UBERON:0001637,artery
+UBERON:0001801,anterior segment of eyeball,UBERON:0000063,organ segment
+UBERON:0011975,epiphysis of middle phalanx of pes,UBERON:0004446,epiphysis of phalanx
+UBERON:4200139,palatoquadrate element,UBERON:0010363,endochondral element
+UBERON:0004923,organ component layer,UBERON:0000064,organ part
+DOID:0050666,partial fetal alcohol syndrome,DOID:0050696,fetal alcohol spectrum disorder
+CL:1000050,lateral line nerve glial cell,CL:0000125,glial cell
+HP:0100424,Partial duplication of the proximal phalanx of the 5th toe,HP:0100406,Duplication of the proximal phalanx of the 5th toe
+HP:0006387,Wide distal femoral metaphysis,HP:0006489,Abnormality of the femoral metaphysis
+HP:0007425,Hyperextensible skin of face,HP:0007458,Focal hyperextensible skin
+UBERON:0009116,thymoid,UBERON:0005057,immune organ
+HP:0011615,Abnormality of pulmonary situs,HP:0012252,Abnormal respiratory system morphology
+UBERON:0011307,suprazygomatic part of temporalis,UBERON:0003681,masticatory muscle
+DOID:14066,acute diffuse nephritis,DOID:4781,diffuse glomerulonephritis
+DOID:2982,perinephritis,DOID:557,kidney disease
+HP:0001265,Hyporeflexia,HP:0001315,Reduced tendon reflexes
+DOID:11684,melanoacanthoma,DOID:6498,seborrheic keratosis
+HP:0007965,Absence of visual evoked potentials,HP:0000649,Abnormality of vision evoked potentials
+UBERON:4200103,median extrascapular,UBERON:2000663,extrascapula
+DOID:4060,breast rhabdomyosarcoma,DOID:3017,breast sarcoma
+HP:0010740,Osteopathia striata,HP:0000944,Abnormality of the metaphyses
+HP:0100636,Pulmonary paraglioma,HP:0002668,Paraganglioma
+CL:0002339,prostate stem cell,CL:0000048,multi fate stem cell
+HP:0002996,Limited elbow movement,HP:0009811,Abnormality of the elbow
+HP:0011988,Ectopic ossification in tendon tissue,HP:0011986,Ectopic ossification
+UBERON:0010173,sinotubular junction,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2001731,caudal principal ray 19,UBERON:2001585,caudal principal ray
+UBERON:0011093,left pelvic girdle region,UBERON:0001271,pelvic girdle region
+UBERON:0008455,rectus capitis posterior minor,UBERON:0004518,muscle of vertebral column
+HP:0010427,Partial duplication of the middle phalanx of the 2nd toe,HP:0010428,Partial duplication of phalanx of the 2nd toe
+UBERON:0004148,cardiac vein,UBERON:0005194,thoracic vein
+HP:0000132,Menorrhagia,HP:0001892,Abnormal bleeding
+UBERON:0008715,muscle tissue of prostate,UBERON:0014403,male anatomical structure
+HP:0010031,Patchy sclerosis of the 1st metacarpal,HP:0009856,Patchy sclerosis of the proximal phalanges of the hand
+HP:0010920,Zonular cataract,HP:0000518,Cataract
+HP:0009134,Osteolysis involving bones of the feet,HP:0009139,Osteolysis involving bones of the lower limbs
+UBERON:0001655,submental vein,UBERON:0009141,craniocervical region vein
+HP:0009644,Curved distal phalanx of the thumb,HP:0009838,Curved distal phalanges of the hand
+UBERON:0009639,body of sphenoid,UBERON:0003462,facial bone
+DOID:3558,duodenal obstruction,DOID:4072,duodenal disease
+DOID:0050774,rapadilino syndrome,DOID:0050737,autosomal recessive disease
+CL:0000060,odontoblast,CL:0000055,non-terminally differentiated cell
+UBERON:0001389,soleus muscle,UBERON:0004256,hindlimb zeugopod muscle
+DOID:11257,social phobia,DOID:591,phobic disorder
+UBERON:0009583,spinal cord mantle layer,UBERON:0005883,neural tube lateral wall mantle layer
+HP:0006637,Sternal punctate calcifications,HP:0000766,Abnormality of the sternum
+HP:0100021,Cerebral palsy,HP:0100022,Abnormality of movement
+HP:0010380,Abnormality of the distal phalanx of the 4th toe,HP:0010336,Abnormality of the phalanges of the 4th toe
+DOID:5309,epithelial-myoepithelial carcinoma,DOID:8850,salivary gland cancer
+DOID:13139,crescentic glomerulonephritis,DOID:13138,acute proliferative glomerulonephritis
+UBERON:0005267,renal cortex collecting duct,UBERON:0001232,collecting duct of renal tubule
+NCBITaxon:31704,Human coxsackievirus A16,NCBITaxon:138948,Human enterovirus A
+UBERON:0006923,vagina squamous epithelium,UBERON:0001344,epithelium of vagina
+HP:0100959,Dense metaphyseal bands,HP:0000944,Abnormality of the metaphyses
+UBERON:0003977,utricle duct,UBERON:0000025,tube
+UBERON:0006722,manubrium of malleus,UBERON:0010313,neural crest-derived structure
+DOID:3691,anal colloid adenocarcinoma,DOID:3447,anus adenocarcinoma
+DOID:331,central nervous system disease,DOID:863,nervous system disease
+UBERON:0012306,lateral cervical lymph node,UBERON:0002429,cervical lymph node
+CL:0000690,R2 photoreceptor cell,CL:0000287,eye photoreceptor cell
+HP:0009177,Proximal/middle symphalangism of 5th finger,HP:0009232,Symphalangism affecting the proximal phalanx of the 5th finger
+UBERON:0010048,Duvernoy's gland,UBERON:0010047,oral gland
+DOID:1761,Melkersson-Rosenthal syndrome,DOID:1756,facial nerve disease
+HP:0100153,Pseudoepiphysis of the middle phalanx of the 3rd toe,HP:0100062,Pseudoepiphyses of the 3rd toe
+UBERON:0000987,haltere,UBERON:0000026,appendage
+DOID:2251,hypertrophic elongation of cervix,DOID:2253,cervix disease
+UBERON:0007228,vestibular nucleus,UBERON:0002584,regional part of vestibular nuclear complex
+UBERON:0013541,Brodmann (1909) area 10,UBERON:0013529,Brodmann area
+UBERON:0003394,mesentery of hindgut,UBERON:0002095,mesentery
+UBERON:0004315,distal phalanx of pedal digit 1,UBERON:0003867,distal phalanx of pes
+UBERON:0011165,crico-esophageal tendon,UBERON:0008845,nonskeletal ligament
+UBERON:2205381,dorsal fin proximal radial cartilage 4,UBERON:2200947,dorsal fin proximal radial cartilage
+HP:0009786,Aplasia/Hypoplasia of the musculature of the thigh,HP:0001460,Aplasia/Hypoplasia involving the musculature
+NCBITaxon:1513,Clostridium tetani,NCBITaxon:1485,Clostridium
+DOID:4510,aorta angiosarcoma,DOID:175,vascular cancer
+UBERON:0001467,shoulder,UBERON:0000475,organism subdivision
+UBERON:0010069,outer epithelial layer of tympanic membrane,UBERON:0009647,tympanic membrane epithelium
+UBERON:0006679,carina of trachea,UBERON:0003604,trachea cartilage
+HP:0001345,Psychotic mentation,HP:0000709,Psychosis
+UBERON:0011390,pudendal nerve,UBERON:0003444,pelvis nerve
+UBERON:0012243,nuptial pad,UBERON:0003102,surface structure
+UBERON:0012068,right lung middle lobe bronchiole,UBERON:0003538,right lung bronchiole
+HP:0007262,Symmetric peripheral demyelination,HP:0011096,Peripheral demyelination
+HP:0004352,Abnormality of purine metabolism,HP:0010932,Abnormality of nucleobase metabolism
+DOID:8042,testis polyembryoma,DOID:5556,testicular malignant germ cell cancer
+UBERON:0009494,pharyngeal arch mesenchymal region,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:4200048,bicipital crest,UBERON:0004530,bony projection
+DOID:1243,labia minora cancer,DOID:1245,vulva cancer
+HP:0009523,Triangular epiphysis of the middle phalanx of the 2nd finger,HP:0009500,Abnormality of the epiphysis of the middle phalanx of the 2nd finger
+UBERON:4100016,posterior process of ilium,UBERON:0004120,mesoderm-derived structure
+DOID:767,muscular atrophy,DOID:423,myopathy
+UBERON:3000813,sulcus pro cartilagine praecoracoidealis,UBERON:0000464,anatomical space
+HP:0005223,Duplicated colon,HP:0002250,Abnormality of the large intestine
+NCBITaxon:337687,Muroidea,NCBITaxon:33553,Sciurognathi
+UBERON:0008438,webbed interdigital region between manual digits,UBERON:0006013,interdigital region between manual digits
+CL:0000658,cuticle secreting cell,CL:0000066,epithelial cell
+UBERON:0006662,musculo-phrenic vein,UBERON:0001638,vein
+UBERON:0000074,renal glomerulus,UBERON:0000064,organ part
+HP:0003183,Wide pubic symphysis,HP:0003172,Abnormality of the pubic bones
+UBERON:0014371,future telencephalon,UBERON:0000481,multi-tissue structure
+UBERON:3000870,preacetabular expansion,UBERON:0004120,mesoderm-derived structure
+UBERON:0013632,sesamoid cartilage,UBERON:0013631,sesamoid element
+UBERON:0004736,metanephric glomerulus,UBERON:0000074,renal glomerulus
+CL:0000795,"CD8-positive, alpha-beta regulatory T cell",CL:0000815,regulatory T cell
+UBERON:0004749,blastodisc,UBERON:0002050,embryonic structure
+HP:0006437,Disproportionate prominence of the femoral medial condyle,HP:0002823,Abnormality of the femur
+HP:0010198,Osteolytic defects of the middle phalanges of the toes,HP:0010183,Abnormality of the middle phalanges of the toes
+HP:0000183,Difficulty in tongue movements,HP:0000182,Movement abnormality of the tongue
+UBERON:0008979,carcass,UBERON:0000468,multi-cellular organism
+UBERON:0011362,cranial blood vasculature,UBERON:0004537,blood vasculature
+HP:0008789,Cone-shaped capital femoral epiphysis,HP:0010579,Cone-shaped epiphysis
+UBERON:0003631,pedal digit 1,UBERON:0001466,pedal digit
+UBERON:0009005,femorotibial joint,UBERON:0003840,hindlimb joint
+HP:0011620,Abnormality of abdominal situs,HP:0001438,Abnormality of the abdomen
+CL:0005013,single ciliated epithelial cell,CL:0000066,epithelial cell
+UBERON:0013704,notochordal canal,UBERON:0004111,anatomical conduit
+UBERON:0002045,cuneate nucleus,UBERON:0007635,nucleus of medulla oblongata
+HP:0004749,Atrial flutter,HP:0001692,Primary atrial arrhythmia
+UBERON:0010158,sphenozygomatic suture,UBERON:0003685,cranial suture
+UBERON:0010572,manual digit 3 metacarpus cartilage element,UBERON:0010699,manual digit metacarpus cartilage element
+UBERON:0003681,masticatory muscle,UBERON:0011648,jaw muscle
+UBERON:0002145,interpeduncular nucleus,UBERON:0007414,nucleus of midbrain tegmentum
+UBERON:0002325,epithelium of urethra,UBERON:0012275,meso-epithelium
+UBERON:0001334,female urethra,UBERON:0014404,female anatomical structure
+UBERON:0000081,metanephros,UBERON:0002113,kidney
+UBERON:2001857,hyoidean artery,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:4278,scrotum basal cell carcinoma,DOID:3445,scrotal carcinoma
+CL:0000916,dendritic epidermal T cell,CL:0000800,mature gamma-delta T cell
+DOID:0050830,peripheral artery disease,DOID:0050828,artery disease
+HP:0010021,Ivory epiphysis of the 1st metacarpal,HP:0009692,Ivory epiphyses of the thumb
+UBERON:0004791,thymus trabecula,UBERON:0000440,trabecula
+CL:0000065,ependymal cell,CL:0000710,neurecto-epithelial cell
+HP:0011584,Thoracocervical ectopia cordis,HP:0001683,Ectopia cordis
+HP:0007299,Dysfunction of lateral corticospinal tracts,HP:0002493,Corticospinal tract dysfunction
+UBERON:3000400,pars facialis of maxilla,UBERON:0004120,mesoderm-derived structure
+UBERON:0003273,skeletal muscle tissue of tongue,UBERON:0001134,skeletal muscle tissue
+CL:1000612,kidney corpuscule cell,CL:1000449,epithelial cell of nephron
+UBERON:0005869,maxillary process of inferior nasal concha,UBERON:0004120,mesoderm-derived structure
+UBERON:0014410,fibularis quartus,UBERON:0009132,peroneus
+HP:0011744,Secondary hypercorticolism,HP:0001578,Hypercortisolism
+UBERON:3010529,ovisac,UBERON:0014404,female anatomical structure
+UBERON:0015917,superficial lymph node,UBERON:0000029,lymph node
+UBERON:0003589,hindlimb connective tissue,UBERON:0003587,limb connective tissue
+CL:1001592,gall bladder glandular cell,CL:0000150,glandular epithelial cell
+HP:0007002,Motor axonal neuropathy,HP:0003477,Peripheral axonal neuropathy
+HP:0009193,Pseudoepiphyses of the metacarpals,HP:0004288,Pseudoepiphyses of hand bones
+HP:0000954,Single transverse palmar crease,HP:0010490,Abnormality of the palmar creases
+UBERON:3010700,levator mandibulae externus,UBERON:0011648,jaw muscle
+HP:0010646,Cervical spine instability,HP:0003319,Abnormality of the cervical spine
+UBERON:0006587,ligamentum venosum,UBERON:0006592,transformed vein
+HP:0010015,Absent epiphysis of the 1st metacarpal,HP:0010268,Absent epiphyses of the proximal phalanges of the hand
+UBERON:0003820,prostate bud,UBERON:0005153,epithelial bud
+UBERON:0009780,cardiac muscle tissue of left auricle,UBERON:0003380,cardiac muscle of left atrium
+HP:0004236,Irregular carpal bones,HP:0006014,Abnormally shaped carpal bones
+NCBITaxon:6939,Ixodidae,NCBITaxon:297308,Ixodoidea
+HP:0009262,Bracket epiphysis of the proximal phalanx of the 4th finger,HP:0010269,Bracket epiphyses of the proximal phalanges of the hand
+HP:0000325,Triangular face,HP:0001999,Abnormal facial shape
+UBERON:0000080,mesonephros,UBERON:0004120,mesoderm-derived structure
+UBERON:2002043,posterior limb of parapophysis 4,UBERON:4100000,skeletal element projection
+UBERON:0006566,left ventricle myocardium,UBERON:0001083,myocardium of ventricle
+UBERON:0013473,lower esophagus,UBERON:0004921,subdivision of digestive tract
+DOID:0050747,lymphoplasmacytic lymphoma,DOID:707,B-cell lymphoma
+HP:0006737,Extraadrenal pheochromocytoma,HP:0002666,Pheochromocytoma
+UBERON:0010977,flexor pre-muscle mass,UBERON:0005865,pre-muscle condensation
+DOID:11818,ureteric orifice cancer,DOID:11819,ureter cancer
+HP:0100458,Osteolytic defects of the distal phalanx of the 3rd toe,HP:0010363,Osteolytic defects of the phalanges of the 3rd toe
+HP:0008722,Urethral diverticulum,HP:0000795,Abnormality of the urethra
+HP:0012628,Abnormality of the suspensory ligament of lens,HP:0012374,Abnormality of the globe
+UBERON:0006813,nasal skeleton,UBERON:0000075,subdivision of skeletal system
+HP:0005303,Aortic arch calcification,HP:0004962,Thoracic aorta calcification
+HP:0000191,Accessory oral frenulum,HP:0000190,Abnormality of oral frenula
+UBERON:0006270,optic pit,UBERON:0002050,embryonic structure
+UBERON:0015214,arcuate ligament,UBERON:0000211,ligament
+HP:0100461,Patchy sclerosis of the middle phalanx of the 3rd toe,HP:0010199,Patchy sclerosis of the middle phalanges of the toes
+HP:0009960,Complete duplication of the phalanges of the 3rd finger,HP:0009959,Duplication of phalanx of 3rd finger
+UBERON:2001457,postcranial axial cartilage,UBERON:0004120,mesoderm-derived structure
+DOID:13938,amenorrhea,DOID:229,female reproductive system disease
+UBERON:0009002,placental membrane,UBERON:0014404,female anatomical structure
+HP:0004417,Intermittent claudication,HP:0002621,Atherosclerosis
+HP:0003848,Cupped metaphyses of the upper limbs,HP:0009809,Abnormality of upper limb metaphysis
+DOID:8233,inflammatory liposarcoma,DOID:5690,atypical lipomatous tumor
+UBERON:0005045,mucosa of ethmoidal sinus,UBERON:0000344,mucosa
+CL:0000446,chief cell of parathyroid gland,CL:0000167,peptide hormone secreting cell
+UBERON:0011669,neural plate of carapace,UBERON:0011665,carapace bone
+UBERON:2001812,preoperculo-mandibular sensory canal,UBERON:2001612,sensory canal
+UBERON:0011606,hyomandibular bone,UBERON:0002513,endochondral bone
+DOID:2575,barbiturate dependence,DOID:9974,drug dependence
+HP:0007291,Posterior fossa cyst,HP:0010576,Intracranial cystic lesion
+HP:0011524,Iris melanoma,HP:0007716,Intraocular melanoma
+DOID:2798,bronchiolitis obliterans organizing pneumonia,DOID:2320,obstructive lung disease
+UBERON:3000074,cartilago orbitalis,UBERON:0003933,cranial cartilage
+DOID:1373,endometrial stromal nodule,DOID:0060095,uterine benign neoplasm
+HP:0009056,Loss of subcutaneous adipose tissue from upper limbs,HP:0003635,Loss of subcutaneous adipose tissue in limbs
+DOID:12308,Dubin-Johnson syndrome,DOID:2741,bilirubin metabolic disorder
+DOID:4450,renal cell carcinoma,DOID:4451,renal carcinoma
+UBERON:0008715,muscle tissue of prostate,UBERON:0005156,reproductive structure
+UBERON:0010297,endochondral scleral ossicle,UBERON:0002513,endochondral bone
+UBERON:0003214,mammary gland alveolus,UBERON:0004121,ectoderm-derived structure
+UBERON:0002323,coelemic cavity lumen,UBERON:0004458,body cavity or lining
+UBERON:0006857,interrenal primordium,UBERON:0000481,multi-tissue structure
+DOID:8283,peritonitis,DOID:77,gastrointestinal system disease
+CL:1000369,transitional myocyte of septal division of left branch of atrioventricular bundle,CL:1000370,transitional myocyte of left branch of atrioventricular bundle
+UBERON:0010038,fundic gastric gland,UBERON:0000325,gastric gland
+UBERON:0002354,purkinje fiber,UBERON:0010131,conducting tissue of heart
+UBERON:3010720,ramus hyomandibularis,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0013741,base of crypt of lieberkuhn of large intestine,UBERON:0001278,epithelium of large intestine
+CL:0002502,type M enteroendocrine cell,CL:0002272,motilin secreting cell
+UBERON:0001277,intestinal epithelium,UBERON:0003929,gut epithelium
+UBERON:2002040,inter-coracoid joint,UBERON:0008114,joint of girdle
+DOID:3617,epidural spinal canal angiolipoma,DOID:3616,angiolipoma
+UBERON:0000435,lateral tuberal nucleus,UBERON:0002785,regional part of lateral hypothalamic region
+UBERON:0009775,lateral medullary reticular complex,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:0050851,glomerulosclerosis,DOID:2921,glomerulonephritis
+DOID:0050548,hereditary sensory neuropathy,DOID:0060053,peripheral neuropathy
+UBERON:0005975,hair follicle bulge,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:8230,intrahepatic biliary papillomatosis,DOID:5468,biliary papillomatosis
+UBERON:0002244,premaxilla,UBERON:0011597,bone of upper jaw
+HP:0004218,Symphalangism of the 5th finger,HP:0009773,Symphalangism affecting the phalanges of the hand
+UBERON:0002396,vomer,UBERON:0008001,irregular bone
+UBERON:2002003,posterior dentation of dorsal fin spine 2,UBERON:0004121,ectoderm-derived structure
+DOID:2410,skin granular cell tumor,DOID:3165,skin benign neoplasm
+HP:0009162,Absent middle phalanx of 5th finger,HP:0009238,Aplasia of the 5th finger
+UBERON:3000363,otic ligament,UBERON:0003566,head connective tissue
+UBERON:0001973,substance of tooth,UBERON:0000463,portion of organism substance
+HP:0002621,Atherosclerosis,HP:0002634,Arteriosclerosis
+HP:0009508,Ivory epiphysis of the distal phalanx of the 2nd finger,HP:0009494,Ivory epiphyses of the 2nd finger
+UBERON:0005145,metanephric comma-shaped body,UBERON:0005146,metanephric nephron tubule
+UBERON:0016467,antitragus,UBERON:0000481,multi-tissue structure
+UBERON:0011797,secondary remex feather,UBERON:0011795,remex feather
+UBERON:0003889,fallopian tube,UBERON:0014404,female anatomical structure
+HP:0003616,Premature separation of centromeric heterochromatin,HP:0200024,Premature chromatid separation
+HP:0100553,Hemihypertrophy of lower limb,HP:0002814,Abnormality of the lower limb
+UBERON:0005414,zone of polarizing activity,UBERON:0010329,paired limb/fin bud mesenchyme
+UBERON:0001357,inferior rectal artery,UBERON:0001637,artery
+HP:0002208,Coarse hair,HP:0010719,Abnormality of hair texture
+UBERON:0015058,alisphenoid endochondral element,UBERON:0010363,endochondral element
+HP:0009230,Osteolytic defects of the proximal phalanx of the 5th finger,HP:0009855,Osteolytic defects of the proximal phalanges of the hand
+UBERON:0001094,sacral vertebra,UBERON:0004247,bone of dorsum
+DOID:5842,testis seminoma,DOID:5556,testicular malignant germ cell cancer
+UBERON:0007162,lateral arcuate ligament,UBERON:0015214,arcuate ligament
+HP:0000658,Eyelid apraxia,HP:0002186,Apraxia
+UBERON:0009550,endoderm of foregut-midgut junction,UBERON:0000925,endoderm
+HP:0004618,Sandwich appearance of vertebral bodies,HP:0003312,Abnormal form of the vertebral bodies
+CL:0000279,prestalk 0 cell,CL:0000269,prestalk cell
+CL:0000875,non-classical monocyte,CL:0000576,monocyte
+UBERON:0004209,renal vesicle,UBERON:0007503,epithelial vesicle
+CL:0000100,motor neuron,CL:0000527,efferent neuron
+DOID:4160,differentiating neuroblastoma,DOID:769,neuroblastoma
+HP:0006879,Pontocerebellar atrophy,HP:0001272,Cerebellar atrophy
+UBERON:0004141,heart tube,UBERON:0003914,epithelial tube
+HP:0004426,Abnormality of the cheeks,HP:0000309,Abnormality of the midface
+UBERON:0001679,ethmoid bone,UBERON:0003462,facial bone
+DOID:13576,twin-to-twin transfusion syndrome,DOID:11244,neonatal anemia
+HP:0010440,Ectopic accesory toe-like appendage,HP:0001829,Foot polydactyly
+DOID:0050696,fetal alcohol spectrum disorder,DOID:0080015,physical disorder
+HP:0000481,Abnormality of the cornea,HP:0004328,Abnormality of the anterior segment of the eye
+HP:0011325,Pansynostosis,HP:0011324,Multiple suture craniosynostosis
+DOID:0050175,tick-borne encephalitis,DOID:934,viral infectious disease
+DOID:4322,pilar sheath acanthoma,DOID:174,acanthoma
+UBERON:0002928,dentate gyrus polymorphic layer,UBERON:0002304,layer of dentate gyrus
+DOID:9339,urethral false passage,DOID:732,urethral disease
+CL:0002337,keratinocyte stem cell,CL:0000312,keratinocyte
+CL:0002150,epithelioid macrophage,CL:0000235,macrophage
+HP:0006440,Increased density of long bone diaphyses,HP:0006392,Increased density of long bones
+DOID:12362,thyrotoxic exophthalmos,DOID:12359,endocrine exophthalmos
+HP:0006707,Abnormality of the hepatic vasculature,HP:0001392,Abnormality of the liver
+CL:0000092,osteoclast,CL:0001035,bone cell
+HP:0100783,Breast aplasia,HP:0010311,Aplasia/Hypoplasia of the breasts
+UBERON:0001506,brachialis muscle,UBERON:0001499,muscle of arm
+UBERON:0002712,premammillary nucleus,UBERON:0002789,regional part of posterior hypothalamic region
+UBERON:0005048,mucosa of uterine tube,UBERON:0014404,female anatomical structure
+UBERON:2007033,forebrain midbrain boundary neural rod,UBERON:0006800,anatomical line
+UBERON:0008290,afterfeather,UBERON:0004121,ectoderm-derived structure
+UBERON:0004322,middle phalanx of manual digit 4,UBERON:0003638,manual digit 4 phalanx
+UBERON:0002597,principal sensory nucleus of trigeminal nerve,UBERON:0004132,trigeminal sensory nucleus
+DOID:7234,pancreatic colloid cystadenocarcinoma,DOID:4073,pancreatic cystadenocarcinoma
+CL:0000058,chondroblast,CL:0002320,connective tissue cell
+HP:0012088,Abnormal urinary odor,HP:0003110,Abnormality of urine homeostasis
+UBERON:0008839,palmar pad,UBERON:0008838,metapodial pad
+UBERON:4200033,cleithrum head,UBERON:0005913,zone of bone organ
+HP:0002835,Aspiration,HP:0002795,Functional respiratory abnormality
+UBERON:0002009,pulmonary nerve plexus,UBERON:0001816,autonomic nerve plexus
+DOID:1811,reflex sympathetic dystrophy,DOID:3223,complex regional pain syndrome
+UBERON:0002040,bronchial artery,UBERON:0004573,systemic artery
+DOID:3981,pantothenate kinase-associated neurodegeneration,DOID:1289,neurodegenerative disease
+UBERON:3010014,inguinal glands,UBERON:3010603,body gland
+UBERON:0009774,embryonic midbrain hindbrain boundary,UBERON:0006800,anatomical line
+HP:0000381,Stapes ankylosis,HP:0008628,Abnormality of the stapes
+UBERON:0009193,sphenoid cartilage element,UBERON:0005863,cartilaginous condensation
+UBERON:0006462,third sacral spinal cord segment,UBERON:0007717,sacral subsegment of spinal cord
+UBERON:1500008,pelvic fin distal radial bone,UBERON:1600008,pelvic fin distal radial element
+UBERON:0011914,pubioischiotibialis muscle,UBERON:0004252,hindlimb stylopod muscle
+UBERON:0004793,secretion of exocrine pancreas,UBERON:0004795,pancreas secretion
+UBERON:0007693,caroticotympanic artery,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000679,glutamatergic neuron,CL:0000151,secretory cell
+UBERON:0008877,epidermal-dermal junction,UBERON:0004121,ectoderm-derived structure
+UBERON:0012652,colorectum,UBERON:0004921,subdivision of digestive tract
+HP:0100418,Partial duplication of the distal phalanx of the 5th toe,HP:0100400,Duplication of the distal phalanx of the 5th toe
+HP:0003193,Allergic rhinitis,HP:0012393,Allergy
+UBERON:4200130,tibial facet of astragalus,UBERON:4100003,articular surface
+UBERON:0016423,compact bone of diaphysis,UBERON:0001439,compact bone tissue
+HP:0001708,Right ventricular failure,HP:0001707,Abnormality of the right ventricle
+HP:0005692,Joint hyperflexibility,HP:0001382,Joint hypermobility
+HP:0010019,Fragmentation of the epiphysis of the 1st metacarpal,HP:0009189,Fragmentation of the metacarpal epiphyses
+UBERON:4200019,preacetabular process,UBERON:4100000,skeletal element projection
+DOID:3508,stricture or kinking of ureter,DOID:557,kidney disease
+UBERON:0001577,facial nerve muscle,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010118,Irregular epiphyses of the hallux,HP:0010056,Abnormality of the epiphyses of the hallux
+HP:0100034,Motor tics,HP:0100033,Tics
+HP:0100111,Absent epiphysis of the middle phalanx of the 2nd toe,HP:0100044,Absent epiphyses of the 2nd toe
+HP:0010016,Bracket epiphysis of the 1st metacarpal,HP:0010014,Abnormality of the epiphysis of the 1st metacarpal
+HP:0005259,Abnormal facility in opposing the shoulders,HP:0001547,Abnormality of the rib cage
+UBERON:0013129,bulb of vestibule,UBERON:0014404,female anatomical structure
+HP:0100370,Aplasia/Hypoplasia of the distal phalanx of the 4th toe,HP:0010371,Aplasia/Hypoplasia of the phalanges of the 4th toe
+NCBITaxon:7509,Siphonaptera,NCBITaxon:33392,Endopterygota
+HP:0009157,Ivory epiphysis of the proximal phalanx of the 5th finger,HP:0009388,Ivory epiphyses of the 5th finger
+UBERON:0002347,thoracic vertebra,UBERON:0002412,vertebra
+UBERON:0005279,nail bed of toe,UBERON:0005277,dorsal skin of toe
+UBERON:2000507,epineural,UBERON:2000526,intermuscular bone
+HP:0003434,Sensory ataxic neuropathy,HP:0000763,Sensory neuropathy
+UBERON:2000654,rostral motor nucleus of abducens,UBERON:0002680,regional part of metencephalon
+UBERON:0013614,fasciculus aberans,UBERON:0005838,fasciculus of brain
+HP:0011939,3-4 finger cutaneous syndactyly,HP:0010554,Cutaneous finger syndactyly
+HP:0008083,2nd-5th toe middle phalangeal hypoplasia,HP:0003795,Short middle phalanx of toe
+HP:0001141,Severe visual impairment,HP:0000505,Visual impairment
+UBERON:0010679,manual digit 5 phalanx cartilage element,UBERON:0005695,manual digit 5 mesenchyme
+UBERON:0012076,tibiotalar joint,UBERON:0001488,ankle joint
+DOID:3772,intraventricular meningioma,DOID:3541,cerebral ventricle cancer
+UBERON:0006211,buccopharyngeal membrane,UBERON:0003037,septum
+HP:0100896,Rectal polyposis,HP:0100743,Neoplasm of the rectum
+CL:0000885,gut-associated lymphoid tissue macrophage,CL:0000884,mucosa-associated lymphoid tissue macrophage
+UBERON:0004535,cardiovascular system,UBERON:0000467,anatomical system
+HP:0009677,Cone-shaped epiphysis of the distal phalanx of the thumb,HP:0009662,Abnormality of the epiphysis of the distal phalanx of the thumb
+HP:0005343,Hypoplasia of the bladder,HP:0010476,Aplasia/Hypoplasia of the bladder
+UBERON:0000401,mandibular ramus,UBERON:0005913,zone of bone organ
+HP:0009897,Horizontal crus of helix,HP:0009895,Abnormality of the crus of the helix
+DOID:0050700,cardiomyopathy,DOID:114,heart disease
+HP:0000939,Osteoporosis,HP:0004349,Reduced bone mineral density
+UBERON:2001474,sublingual dorsal and ventral separate,UBERON:0000477,anatomical cluster
+UBERON:0003501,retina blood vessel,UBERON:0003496,head blood vessel
+HP:0006733,Acute megakaryocytic leukemia,HP:0002488,Acute leukemia
+UBERON:0002681,anteromedial nucleus of thalamus,UBERON:0015233,nucleus of dorsal thalamus
+HP:0008327,Microscopic nephrocalcinosis,HP:0000121,Nephrocalcinosis
+UBERON:0011025,aryepiglotticus muscle,UBERON:0001568,muscle of larynx
+HP:0000771,Gynecomastia,HP:0000769,Abnormality of the breast
+UBERON:1000023,spleen pulp,UBERON:0000064,organ part
+UBERON:0002650,paralaminar part of medial dorsal nucleus,UBERON:0002020,gray matter of neuraxis
+HP:0010327,Flexion contracture of the 2nd toe,HP:0001836,Camptodactyly (feet)
+DOID:680,tauopathy,DOID:1289,neurodegenerative disease
+UBERON:0014766,right crus of diaphragm,UBERON:0014765,crus of diaphragm
+HP:0100486,Symphalangism of the proximal phalanx of the 5th toe with the 5th metatarsal,HP:0001440,Synostosis involving metatarsal bones
+UBERON:0001341,lesser sac,UBERON:0004458,body cavity or lining
+UBERON:0002413,cervical vertebra,UBERON:0004247,bone of dorsum
+UBERON:0004702,respiratory system blood vessel endothelium,UBERON:0004638,blood vessel endothelium
+UBERON:2001792,pharyngobranchial 3 bone uncinate process,UBERON:4100000,skeletal element projection
+UBERON:3000387,subotic alae,UBERON:0004121,ectoderm-derived structure
+CL:0000462,adepithelial cell,CL:0000680,muscle precursor cell
+UBERON:0008281,tooth bud,UBERON:0010371,ecto-epithelium
+UBERON:0003229,epithelium of elbow,UBERON:0010371,ecto-epithelium
+UBERON:0002171,lower lobe of right lung,UBERON:0006518,right lung lobe
+UBERON:0015080,proximal carpal bone pre-cartilage condensation,UBERON:0015078,proximal carpal endochondral element
+HP:0004673,Decreased facial expression,HP:0005346,Abnormal facial expression
+HP:0007376,Abnormality of the choroid plexus,HP:0002118,Abnormality of the cerebral ventricles
+UBERON:0012287,Rathkes pouch epithelium,UBERON:0011642,oral epithelium from ectoderm
+UBERON:0005358,ventricle of nervous system,UBERON:0000064,organ part
+UBERON:0003277,skeleton of upper jaw,UBERON:0004121,ectoderm-derived structure
+UBERON:0003311,floor plate of medulla oblongata,UBERON:0003306,floor plate of neural tube
+UBERON:0007500,epithelial tube open at both ends,UBERON:0003914,epithelial tube
+DOID:6939,childhood brain meningioma,DOID:0060106,brain meningioma
+DOID:2338,mandibular cancer,DOID:1862,jaw cancer
+DOID:8771,contagious pustular dermatitis,DOID:934,viral infectious disease
+HP:0010505,Limitation of movement at ankles,HP:0001376,Limitation of joint mobility
+UBERON:2000610,vertical myoseptum,UBERON:2001089,myoseptum
+UBERON:0001198,superior suprarenal artery,UBERON:0005624,suprarenal artery
+DOID:12712,nephronophthisis,DOID:0050737,autosomal recessive disease
+HP:0007083,Hyperactive patellar reflex,HP:0002395,Lower limb hyperreflexia
+DOID:5936,ovarian mixed germ cell neoplasm,DOID:3306,mixed germ cell cancer
+HP:0002253,Colonic diverticulosis,HP:0005222,Bowel diverticulosis
+HP:0012190,T-cell lymphoma,HP:0012539,Non-Hodgkin lymphoma
+CL:0002474,lymphoid MHC-II-negative classical monocyte,CL:0002469,MHC-II-negative classical monocyte
+UBERON:0014440,ischiopubic ramus,UBERON:0005913,zone of bone organ
+UBERON:0002732,longitudinal pontine fibers,UBERON:0007702,tract of brain
+DOID:3693,ampulla of Vater mucinous adenocarcinoma,DOID:3502,ampulla of Vater adenocarcinoma
+NCBITaxon:694002,Betacoronavirus,NCBITaxon:693995,Coronavirinae
+DOID:4336,tinea favosa,DOID:4337,tinea capitis
+UBERON:0002635,regional part of midbrain tegmentum,UBERON:0002950,regional part of midbrain
+UBERON:0001265,trabecula of spleen,UBERON:0004120,mesoderm-derived structure
+UBERON:0003417,mesenchyme of soft palate,UBERON:0003323,mesenchyme of upper jaw
+UBERON:2005019,efferent lamellar arteriole,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0002090,postcranial axial skeleton,UBERON:0004120,mesoderm-derived structure
+CL:1001431,kidney collecting duct principal cell,CL:0005009,renal principal cell
+HP:0003310,Abnormality of the odontoid process,HP:0000925,Abnormality of the vertebral column
+UBERON:0010424,distal segment of rib,UBERON:0004120,mesoderm-derived structure
+UBERON:0011313,posterior subdivision of masseter,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000818,transitional stage B cell,CL:0000236,B cell
+HP:0000933,Posterior fossa cyst at the fourth ventricle,HP:0007109,Periventricular cysts
+CL:0000627,transporting cell,CL:0000003,native cell
+HP:0200073,Respiratory insufficiency due to defective ciliary clearance,HP:0002093,Respiratory insufficiency
+UBERON:0009588,mesenchyme of interdigital region between manual digits 3 and 4,UBERON:0009600,mesenchyme of interdigital region of manus
+HP:0010033,Triangular shaped 1st metacarpal,HP:0009657,Triangular shaped phalanges of the thumb
+UBERON:0002389,manual digit,UBERON:0008785,upper limb segment
+DOID:4291,fibroepithelial basal cell carcinoma,DOID:2513,basal cell carcinoma
+UBERON:0013442,postorbital process,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0008200,Primary hyperparathyroidism,HP:0000843,Hyperparathyroidism
+UBERON:0016478,liver stroma,UBERON:0003567,abdomen connective tissue
+UBERON:0009740,border between sublaminar layers,UBERON:0004923,organ component layer
+HP:0011920,Transudative pleural effusion,HP:0002202,Pleural effusion
+HP:0002752,Sparse bone trabeculae,HP:0100671,Abnormal trabecular bone morphology
+UBERON:0005906,serous sac,UBERON:0000062,organ
+UBERON:0002198,neurohypophysis,UBERON:0002784,regional part of diencephalon
+UBERON:0003221,phalanx,UBERON:0012357,digitopodium bone
+UBERON:0007170,squamous part of occipital bone,UBERON:0005913,zone of bone organ
+DOID:4696,intraneural perineurioma,DOID:4697,perineurioma
+UBERON:0005252,omental bursa cavity,UBERON:0002553,anatomical cavity
+HP:0009276,Contracture of the proximal interphalangeal joint of the 4th finger,HP:0009274,Joint contractures of the 4th finger
+UBERON:0010586,manual digit phalanx pre-cartilage condensation,UBERON:0015024,manual digit phalanx endochondral element
+HP:0002131,Episodic ataxia,HP:0001251,Ataxia
+CL:0000590,small luteal cell,CL:0000175,luteal cell
+HP:0001495,Carpal osteolysis,HP:0001191,Abnormality of the carpal bones
+UBERON:0003456,respiratory system lymphatic vessel,UBERON:0001473,lymphatic vessel
+DOID:7549,ceruminoma,DOID:5876,apocrine sweat gland neoplasm
+UBERON:0008857,stomach smooth muscle circular layer,UBERON:0004222,stomach smooth muscle
+HP:0004466,Prolonged brainstem auditory evoked potentials,HP:0006958,Abnormal auditory evoked potentials
+HP:0003344,3-Methylglutaric aciduria,HP:0003535,3-Methylglutaconic aciduria
+UBERON:0001819,palpebral fissure,UBERON:0004121,ectoderm-derived structure
+UBERON:3000438,planum internasale,UBERON:0003406,cartilage of respiratory system
+UBERON:0003646,metacarpal bone of digit 2,UBERON:0002374,metacarpal bone
+UBERON:0005726,chemosensory system,UBERON:0001032,sensory system
+UBERON:0003473,thoracic cavity artery,UBERON:0001637,artery
+UBERON:3000085,cavum inferius,UBERON:0001707,nasal cavity
+UBERON:0001817,lacrimal gland,UBERON:0002365,exocrine gland
+NCBITaxon:6201,Cyclophyllidea,NCBITaxon:6200,Eucestoda
+UBERON:0009591,mesenchyme of interdigital region between pedal digits 2 and 3,UBERON:0009597,mesenchyme of interdigital region between digits 2 and 3
+DOID:620,blood protein disease,DOID:74,hematopoietic system disease
+UBERON:0012648,ampulla of uterine tube,UBERON:0014404,female anatomical structure
+CL:0002339,prostate stem cell,CL:0002341,basal cell of prostate epithelium
+HP:0001061,Acne,HP:0011123,Inflammatory abnormality of the skin
+UBERON:0005284,brain vasculature,UBERON:0004121,ectoderm-derived structure
+UBERON:0004701,venous system endothelium,UBERON:0004852,cardiovascular system endothelium
+DOID:633,myositis,DOID:423,myopathy
+NCBITaxon:426439,Haemaphysalinae,NCBITaxon:6939,Ixodidae
+UBERON:3000605,tentacular foramen,UBERON:0011773,upper jaw opening
+DOID:0050671,female breast cancer,DOID:1612,breast cancer
+HP:0100146,Absent epiphysis of the middle phalanx of the 3rd toe,HP:0100055,Absent epiphyses of the 3rd toe
+HP:0000272,Malar flattening,HP:0005557,Abnormality of the zygomatic arch
+HP:0100399,Duplication of the distal phalanx of the 4th toe,HP:0010379,Duplication of phalanx of the 4th toe
+CL:1001437,hair-down neuron,CL:0002487,cutaneous/subcutaneous mechanoreceptor cell
+UBERON:0010266,arthropod hepatopancreas,UBERON:0005057,immune organ
+UBERON:0004315,distal phalanx of pedal digit 1,UBERON:0014483,distal phalanx of digit 1
+UBERON:0002251,iliocostalis muscle,UBERON:0004120,mesoderm-derived structure
+UBERON:0007647,ectomeninx,UBERON:0007645,future meninx
+HP:0009185,Contracture of the proximal interphalangeal joint of the 5th finger,HP:0009698,Contractures of the proximal interphalangeal joints of the fingers
+HP:0006644,Thoracic dysplasia,HP:0001547,Abnormality of the rib cage
+HP:0002836,Bladder exstrophy,HP:0100548,Exstrophy
+DOID:6162,childhood embryonal testis carcinoma,DOID:6082,pediatric testicular germ cell tumor
+HP:0007076,Extrapyramidal muscular rigidity,HP:0002071,Abnormality of extrapyramidal motor function
+DOID:750,peptic ulcer disease,DOID:77,gastrointestinal system disease
+HP:0001637,Abnormality of the myocardium,HP:0002564,Malformation of the heart and great vessels
+HP:0003467,Atlantoaxial instability,HP:0003413,Atlantoaxial abnormality
+HP:0010195,Broad middle phalanges of the toes,HP:0010183,Abnormality of the middle phalanges of the toes
+UBERON:0000006,islet of Langerhans,UBERON:0000064,organ part
+UBERON:0009980,condyle of femur,UBERON:0005055,zone of long bone
+HP:0004447,Poikilocytosis,HP:0001877,Abnormality of erythrocytes
+CL:0000188,skeletal muscle cell,CL:0002371,somatic cell
+DOID:13168,prepuce cancer,DOID:4159,skin cancer
+UBERON:0006451,fourth lumbar spinal cord segment,UBERON:0007716,lumbar subsegment of spinal cord
+UBERON:0011741,cardiac valve leaflet,UBERON:0000064,organ part
+DOID:9278,hyperargininemia,DOID:9267,urea cycle disorder
+DOID:4038,granulomatous gastritis,DOID:4029,gastritis
+UBERON:0001893,telencephalon,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0010801,calcaneum pre-cartilage condensation,UBERON:0010695,mesenchyme of tarsal region
+UBERON:2001236,hypobranchial 2 bone,UBERON:2000363,hypobranchial bone
+NCBITaxon:83136,Trombidiformes,NCBITaxon:6946,Acariformes
+DOID:3306,mixed germ cell cancer,DOID:2994,germ cell cancer
+HP:0000339,Pugilistic facies,HP:0000280,Coarse facial features
+UBERON:0011222,intra-ocular muscle,UBERON:0004120,mesoderm-derived structure
+UBERON:0011533,"abductor pollicis, radioulna-prepollox",UBERON:0003662,forelimb muscle
+HP:0011510,Drusen,HP:0001103,Abnormality of the macula
+UBERON:3010563,craniopalatine foramina,UBERON:3000051,braincase and otic capsule opening
+UBERON:3000678,esophageal process,UBERON:0000072,segment of respiratory tract
+UBERON:0003638,manual digit 4 phalanx,UBERON:0015028,manual digit 4 phalanx endochondral element
+UBERON:0001678,temporal bone,UBERON:0003462,facial bone
+HP:0100132,Triangular epiphysis of the proximal phalanx of the 2nd toe,HP:0100054,Triangular epiphyses of the 2nd toe
+HP:0009157,Ivory epiphysis of the proximal phalanx of the 5th finger,HP:0009153,Abnormality of the epiphysis of the proximal phalanx of the 5th finger
+DOID:5750,uterine corpus serous adenocarcinoma,DOID:9460,uterine corpus cancer
+HP:0010802,Perioral hyperpigmentation,HP:0001000,Abnormality of skin pigmentation
+UBERON:3010195,lateral appendix,UBERON:0004121,ectoderm-derived structure
+CL:0000225,anucleate cell,CL:0000003,native cell
+UBERON:0014620,cervical spinal cord dorsal horn,UBERON:0002256,dorsal horn of spinal cord
+UBERON:4200009,hypochordal lepidotrichium,UBERON:4000174,caudal fin lepidotrichium
+UBERON:2000411,posterior crista primordium,UBERON:0003239,epithelium of posterior semicircular canal
+HP:0011730,Abnormality of central sensory function,HP:0012638,Abnormality of nervous system physiology
+UBERON:0014371,future telencephalon,UBERON:0002050,embryonic structure
+UBERON:0014850,hemomonochorial placental membrane,UBERON:0009002,placental membrane
+HP:0012515,Hip flexor weakness,HP:0003749,Pelvic girdle muscle weakness
+UBERON:0005617,mesenteric vein,UBERON:0001638,vein
+HP:0009219,Irregular epiphysis of the middle phalanx of the 4th finger,HP:0010262,Irregular epiphyses of the middle phalanges of the hand
+UBERON:0004547,decidua capsularis,UBERON:0000478,extraembryonic structure
+HP:0000633,Decreased lacrimation,HP:0000632,Lacrimation abnormality
+UBERON:2001586,pectoral fin radial bone,UBERON:0010741,bone of pectoral complex
+CL:0000692,terminal Schwann cell,CL:0000630,supportive cell
+HP:0100085,Small epiphyses of the 5th toe,HP:0010170,Small epiphyses of the toes
+HP:0001334,Communicating hydrocephalus,HP:0000238,Hydrocephalus
+CL:1001006,kidney afferent arteriole cell,CL:1000612,kidney corpuscule cell
+HP:0003761,Calcinosis,HP:0011805,Abnormality of muscle morphology
+HP:0004789,Lactose intolerance,HP:0002024,Malabsorption
+UBERON:0007833,osseus semicircular canal,UBERON:0010313,neural crest-derived structure
+UBERON:4200161,mesomere 5,UBERON:4200160,mesomere (fin)
+UBERON:2001364,hemal spine,UBERON:0004247,bone of dorsum
+UBERON:2000268,anal fin proximal radial bone,UBERON:2001671,anal fin radial bone
+UBERON:0001053,neurohemal organ,UBERON:0000062,organ
+DOID:0050530,intermediate spinal muscular atrophy,DOID:12377,spinal muscular atrophy
+HP:0004100,Abnormality of the 2nd finger,HP:0001167,Abnormality of finger
+UBERON:3000280,margo mandibularis of pterygoid,UBERON:0004120,mesoderm-derived structure
+UBERON:3010564,carotid foramina,UBERON:3000051,braincase and otic capsule opening
+DOID:10349,solitary cyst of breast,DOID:10350,breast cyst
+HP:0012304,Hypoplastic aortic arch,HP:0012303,Abnormality of the aortic arch
+HP:0005674,Metacarpophalangeal camptodactyly,HP:0100490,Camptodactyly of finger
+UBERON:0011310,masseteric fossa,UBERON:0010313,neural crest-derived structure
+UBERON:0000125,neural nucleus,UBERON:0000073,regional part of nervous system
+HP:0001015,Prominent superficial veins,HP:0002624,Venous abnormality
+HP:0002292,Frontal balding,HP:0011360,Acquired abnormal hair pattern
+UBERON:3000181,foramen acusticum maius,UBERON:0005744,bone foramen
+DOID:11851,indeterminate leprosy,DOID:1024,leprosy
+HP:0011860,Metaphyseal dappling,HP:0004979,Metaphyseal sclerosis
+CL:0000606,macroconidium,CL:0000599,conidium
+UBERON:0001630,muscle organ,UBERON:0005090,muscle structure
+UBERON:0004426,proximal epiphysis of fifth metacarpal bone,UBERON:0011104,epiphysis of fifth metacarpal bone
+HP:0012158,Carotid artery dissection,HP:0005344,Abnormality of the carotid arteries
+HP:0009512,Triangular epiphysis of the distal phalanx of the 2nd finger,HP:0010256,Triangular epiphyses of the distal phalanges of the hand
+UBERON:0004319,distal phalanx of pedal digit 5,UBERON:0003867,distal phalanx of pes
+UBERON:4200079,dorsal iliac process,UBERON:0004530,bony projection
+CL:0000448,white fat cell,CL:0000136,fat cell
+DOID:0050487,bacterial exanthem,DOID:0050486,exanthem
+UBERON:0016435,chest wall,UBERON:0000060,anatomical wall
+HP:0002740,Recurrent E. coli infections,HP:0005420,Recurrent gram-negative bacterial infections
+UBERON:0001654,supra-orbital vein,UBERON:0009141,craniocervical region vein
+HP:0007187,Focal lissencephaly,HP:0001339,Lissencephaly
+UBERON:0005423,developing anatomical structure,UBERON:0000465,material anatomical entity
+HP:0002446,Astrocytosis,HP:0100705,Abnormality of the glial cells
+DOID:0060135,apraxia,DOID:4090,agnosia
+HP:0002921,Abnormality of the cerebrospinal fluid,HP:0002011,Abnormality of the central nervous system
+UBERON:2001059,cranial division of the internal carotid artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0006952,outer dental epithelium,UBERON:0003843,dental epithelium
+HP:0100848,Neoplasia of the male external genitalia,HP:0010787,Genital neoplasm
+DOID:0050665,fetal alcohol syndrome,DOID:0050696,fetal alcohol spectrum disorder
+HP:0006460,Increased laxity of ankles,HP:0003028,Abnormality of the ankles
+UBERON:2000239,mesocoracoid bone,UBERON:0002513,endochondral bone
+UBERON:0003454,small intestine Peyer's patch,UBERON:0001211,Peyer's patch
+UBERON:0014915,genu of facial nerve,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003018,parvicellular part of ventral posteromedial nucleus,UBERON:0003528,brain grey matter
+DOID:2981,kidney papillary necrosis,DOID:557,kidney disease
+UBERON:3010620,dilatator laryngis,UBERON:3000224,hyobranchial muscle
+DOID:1965,fallopian tube leiomyosarcoma,DOID:1964,fallopian tube cancer
+HP:0001635,Congestive heart failure,HP:0011025,Abnormality of cardiovascular system physiology
+DOID:885,fascioliasis,DOID:883,parasitic helminthiasis infectious disease
+DOID:11563,retinal vasculitis,DOID:865,vasculitis
+HP:0010743,Short metatarsal,HP:0003026,Short long bones
+HP:0001480,Freckling,HP:0001000,Abnormality of skin pigmentation
+HP:0007238,Nonarteriosclerotic cerebral calcification,HP:0002514,Cerebral calcification
+DOID:853,polymyalgia rheumatica,DOID:854,collagen disease
+HP:0011987,Ectopic ossification in muscle tissue,HP:0011986,Ectopic ossification
+UBERON:0005990,aortic valve cusp,UBERON:0006009,cusp of cardiac valve
+HP:0004797,Multiple small bowel atresias,HP:0011100,Intestinal atresia
+HP:0100568,Neoplasm of the endocrine system,HP:0011793,Neoplasm by anatomical site
+DOID:13369,tinea manuum,DOID:8913,dermatophytosis
+HP:0012045,Retinal flecks,HP:0000479,Abnormality of the retina
+HP:0011320,Unilambdoid synostosis,HP:0004443,Lambdoidal craniosynostosis
+DOID:0050641,Rh deficiency syndrome,DOID:583,hemolytic anemia
+UBERON:0010398,spleen marginal sinus,UBERON:0001959,white pulp of spleen
+UBERON:0001802,posterior segment of eyeball,UBERON:0000063,organ segment
+UBERON:2005268,preopercle horizontal limb-symplectic joint,UBERON:0000982,skeletal joint
+UBERON:0010169,moustache,UBERON:0004121,ectoderm-derived structure
+UBERON:0015161,inferior branch of oculomotor nerve,UBERON:0001021,nerve
+NCBITaxon:352061,Ornithodorinae,NCBITaxon:6936,Argasidae
+UBERON:0013512,row of feathers,UBERON:0000477,anatomical cluster
+UBERON:0002134,tricuspid valve,UBERON:0002133,atrioventricular valve
+UBERON:0002950,regional part of midbrain,UBERON:0002616,regional part of brain
+HP:0009520,Pseudoepiphysis of the middle phalanx of the 2nd finger,HP:0009500,Abnormality of the epiphysis of the middle phalanx of the 2nd finger
+UBERON:4200007,transverse pelvic ridge,UBERON:0000064,organ part
+UBERON:0002411,clitoris,UBERON:0014404,female anatomical structure
+NCBITaxon:9347,Eutheria,NCBITaxon:32525,Theria <Mammalia>
+UBERON:4200061,epicercal tail,UBERON:4000164,caudal fin
+UBERON:3010797,m. ypsiloideus posterior,UBERON:0008777,hypaxial musclulature
+HP:0100615,Ovarian neoplasm,HP:0000137,Abnormality of the ovary
+UBERON:0010548,pedal digit 2 metatarsal pre-cartilage condensation,UBERON:0015038,pedal digit 2 metatarsal endochondral element
+HP:0010139,Bracket epiphysis of the distal phalanx of the hallux,HP:0010124,Abnormality of the epiphysis of the distal phalanx of the hallux
+DOID:4454,childhood kidney cell carcinoma,DOID:4450,renal cell carcinoma
+DOID:5643,urethral villous adenoma,DOID:730,urethral benign neoplasm
+HP:0100899,Sclerosis of the phalanges of the hand,HP:0004054,Sclerosis of hand bones
+UBERON:0001886,choroid plexus,UBERON:0005284,brain vasculature
+CL:0011110,histaminergic neuron,CL:0002274,histamine secreting cell
+DOID:4188,echolalia,DOID:92,speech disorder
+UBERON:4200047,attachment site,UBERON:0000061,anatomical structure
+DOID:13774,Addison's disease,DOID:10493,adrenal cortical hypofunction
+CL:0000120,granule cell,CL:0000117,CNS neuron (sensu Vertebrata)
+HP:0001658,Myocardial infarction,HP:0001677,Coronary artery disease
+UBERON:0000210,tetrapod parietal bone,UBERON:0010428,flat bone
+HP:0100145,Triangular epiphysis of the distal phalanx of the 3rd toe,HP:0100065,Triangular epiphyses of the 3rd toe
+UBERON:0013502,5th arch mesenchyme,UBERON:0009494,pharyngeal arch mesenchymal region
+UBERON:2205382,dorsal fin proximal radial cartilage 5,UBERON:2200947,dorsal fin proximal radial cartilage
+UBERON:0011246,procoracoid bone,UBERON:0011248,procoracoid element
+HP:0009987,Partial duplication of the phalanges of the 5th finger,HP:0009999,Partial duplication of the phalanx of hand
+HP:0004353,Abnormality of pyrimidine metabolism,HP:0010932,Abnormality of nucleobase metabolism
+UBERON:0002072,hypodermis,UBERON:0002384,connective tissue
+UBERON:0000080,mesonephros,UBERON:0002113,kidney
+UBERON:0014702,frontonasal process epithelium,UBERON:0005291,embryonic tissue
+HP:0007698,Retinal pigment epithelial atrophy,HP:0007894,Hypopigmentation of the fundus
+UBERON:0003254,amniotic ectoderm,UBERON:0000490,unilaminar epithelium
+HP:0011199,EEG with generalized sharp slow waves,HP:0011198,EEG with generalized epileptiform discharges
+UBERON:0006465,ninth thoracic spinal cord segment,UBERON:0007715,thoracic subsegment of spinal cord
+HP:0001998,Neonatal hypoglycemia,HP:0001943,Hypoglycemia
+DOID:1770,toxic megacolon,DOID:11372,megacolon
+HP:0009634,Patchy sclerosis of the proximal phalanx of the thumb,HP:0009655,Patchy sclerosis of the phalanges of the thumb
+CL:1000442,urothelial cell of trigone of urinary bladder,CL:0000731,urothelial cell
+UBERON:0001143,hepatic vein,UBERON:0015796,liver blood vessel
+UBERON:0004982,mucosa of epiglottis,UBERON:0004987,mucosa of laryngopharynx
+NCBITaxon:11040,Rubivirus,NCBITaxon:11018,Togaviridae
+UBERON:0002328,notochord,UBERON:0000481,multi-tissue structure
+UBERON:0005167,papillary duct,UBERON:0001232,collecting duct of renal tubule
+UBERON:0004318,distal phalanx of pedal digit 4,UBERON:0003867,distal phalanx of pes
+HP:0007162,Diffuse demyelination of the cerebral white matter,HP:0007305,CNS demyelination
+DOID:4050,mediastinum sarcoma,DOID:5559,mediastinal cancer
+UBERON:2005377,dorsal fin distal radial bone 6,UBERON:2105377,dorsal fin distal radial element 6
+HP:0000922,Posterior rib cupping,HP:0000887,Cupped ribs
+UBERON:0001260,serosa of urinary bladder,UBERON:0000042,serous membrane
+UBERON:0002567,basal part of pons,UBERON:0000477,anatomical cluster
+UBERON:0002008,cardiac nerve plexus,UBERON:0001816,autonomic nerve plexus
+UBERON:0009054,open circulatory system,UBERON:0001009,circulatory system
+DOID:2078,chondroid syringoma of the vulva,DOID:2079,eccrine mixed tumor of skin
+UBERON:0010573,manual digit 4 metacarpus cartilage element,UBERON:0010699,manual digit metacarpus cartilage element
+UBERON:0011287,rostral organ,UBERON:0004120,mesoderm-derived structure
+HP:0001806,Onycholysis,HP:0001597,Abnormality of the nail
+HP:0009275,Contracture of the distal interphalangeal joint of the 4th finger,HP:0009274,Joint contractures of the 4th finger
+HP:0012310,Abnormal monocyte count,HP:0012144,Abnormality of cells of the monocyte/macrophage lineage
+UBERON:0001237,paraaortic body,UBERON:0000062,organ
+DOID:7609,parathyroid transitional clear cell adenoma,DOID:7608,parathyroid adenoma
+UBERON:0008598,risorius muscle,UBERON:0001577,facial nerve muscle
+UBERON:2001873,head sensory canal system,UBERON:0002540,lateral line system
+UBERON:0003960,styloid process of temporal bone,UBERON:0004119,endoderm-derived structure
+UBERON:0002718,solitary tract,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0006663,hemiazygos vein,UBERON:0001638,vein
+HP:0011583,Cervical ectopia cordis,HP:0001683,Ectopia cordis
+HP:0009469,Contracture of the distal interphalangeal joint of the 3rd finger,HP:0009697,Contractures of the distal interphalangeal joints of the fingers
+HP:0007941,Limited extraocular movements,HP:0008049,Abnormality of the extraocular muscles
+UBERON:0006444,annulus fibrosus,UBERON:0001995,fibrocartilage
+UBERON:3000405,pars inferior of labyrinth,UBERON:0004121,ectoderm-derived structure
+UBERON:3000401,pars facialis of maxillopalatine,UBERON:0004120,mesoderm-derived structure
+UBERON:0007425,decussation of diencephalon,UBERON:0007418,decussation of neuraxis
+HP:0009198,Abnormality of the epiphysis of the distal phalanx of the 5th finger,HP:0009152,Abnormality of the epiphyses of the 5th finger
+HP:0000121,Nephrocalcinosis,HP:0012210,Abnormal renal morphology
+UBERON:3000871,fossula tuberis superioris,UBERON:0004120,mesoderm-derived structure
+HP:0009243,Patchy sclerosis of the distal phalanx of the 5th finger,HP:0009377,Patchy sclerosis of the phalanges of the 5th finger
+HP:0004416,Precocious atherosclerosis,HP:0002621,Atherosclerosis
+HP:0002234,Early balding,HP:0011360,Acquired abnormal hair pattern
+HP:0000528,Anophthalmia,HP:0100887,Abnormality of globe size
+UBERON:0001469,sternoclavicular joint,UBERON:0011108,synovial joint of pectoral girdle
+UBERON:0012294,navicular fossa of spongiose part of urethra,UBERON:0006554,urinary system structure
+UBERON:0015918,deep lymph node,UBERON:0000029,lymph node
+UBERON:0002999,oral pontine reticular nucleus,UBERON:0007413,nucleus of pontine reticular formation
+DOID:11044,gastroschisis,DOID:0080015,physical disorder
+HP:0002817,Abnormality of the upper limb,HP:0002813,Abnormality of limb bone morphology
+DOID:5334,paraphimosis,DOID:2712,phimosis
+HP:0012191,B-cell lymphoma,HP:0012539,Non-Hodgkin lymphoma
+DOID:0050700,cardiomyopathy,DOID:423,myopathy
+HP:0005952,Decreased pulmonary function,HP:0002795,Functional respiratory abnormality
+UBERON:0002479,dorsal lateral geniculate nucleus,UBERON:0015233,nucleus of dorsal thalamus
+NCBITaxon:226665,Rickettsia heilongjiangensis,NCBITaxon:114277,spotted fever group
+CL:0002231,epithelial cell of prostate,CL:0002076,endo-epithelial cell
+CL:0001017,mature CD1a-positive Langerhans cell,CL:0001014,CD1a-positive Langerhans cell
+UBERON:0006567,right ventricle myocardium,UBERON:0001083,myocardium of ventricle
+HP:0011750,Neoplasm of the anterior pituitary,HP:0100568,Neoplasm of the endocrine system
+HP:0010759,Premaxillary Prominence,HP:0010758,Abnormality of the premaxilla
+CL:1000691,kidney interstitial myofibroblast,CL:1000500,kidney interstitial cell
+UBERON:0005224,pancreas tail parenchyma,UBERON:0004119,endoderm-derived structure
+DOID:630,genetic disease,DOID:4,disease
+UBERON:3000977,body external integument structure,UBERON:3000961,external integument structure
+DOID:9898,villonodular synovitis,DOID:381,arthropathy
+HP:0009838,Curved distal phalanges of the hand,HP:0009770,Curved phalanges of the hand
+DOID:13094,branch retinal artery occlusion,DOID:8483,retinal artery occlusion
+UBERON:0005987,right branch of atrioventricular bundle,UBERON:0015212,lateral structure
+UBERON:3000873,pars cylindriformis ilei,UBERON:0004120,mesoderm-derived structure
+DOID:0050495,exanthema subitum,DOID:934,viral infectious disease
+UBERON:3010205,postminimus,UBERON:0015050,tarsus endochondral element
+UBERON:0001850,lacrimal duct,UBERON:0000058,duct
+HP:0012238,Hyperchylomicronemia,HP:0010980,Hyperlipoproteinemia
+DOID:801,hemarthrosis,DOID:381,arthropathy
+UBERON:0009119,branchial basket,UBERON:0010912,subdivision of skeleton
+DOID:3855,seminal vesicle tumor,DOID:0060087,male reproductive organ benign neoplasm
+HP:0003945,Irregular articular surfaces of the elbow joints,HP:0009811,Abnormality of the elbow
+UBERON:0008953,lower lobe of left lung,UBERON:0008951,left lung lobe
+UBERON:0000081,metanephros,UBERON:0004120,mesoderm-derived structure
+DOID:0050748,marginal zone B-cell lymphoma,DOID:707,B-cell lymphoma
+HP:0011260,Darwin notch of helix,HP:0009902,Cleft helix
+UBERON:2000642,decussation of the medial octavolateralis nucleus,UBERON:2000318,brainstem and spinal white matter
+HP:0010135,Small epiphysis of the proximal phalanx of the hallux,HP:0010121,Small epiphyses of the hallux
+HP:0010058,Aplasia/Hypoplasia of the phalanges of the hallux,HP:0008362,Aplasia/Hypoplasia of the hallux
+DOID:0050328,congenital hypothyroidism,DOID:1459,hypothyroidism
+HP:0001152,Saccadic smooth pursuit,HP:0000617,Abnormality of ocular smooth pursuit
+UBERON:0013677,serrated projection of ctenactinium,UBERON:0005156,reproductive structure
+UBERON:0011796,primary remex feather,UBERON:0011795,remex feather
+UBERON:2002027,pectoral fin proximal radial bone 2,UBERON:2001587,pectoral fin proximal radial bone
+HP:0000923,Beaded ribs,HP:0000772,Abnormality of the ribs
+UBERON:0012081,patella pre-cartilage condensation,UBERON:0003321,mesenchyme of knee
+UBERON:0015040,pedal digit 4 metatarsal endochondral element,UBERON:0015036,pedal digit metatarsal endochondral element
+UBERON:0011147,Verson's gland,UBERON:0004121,ectoderm-derived structure
+UBERON:0003683,rotator cuff,UBERON:0000477,anatomical cluster
+UBERON:0006929,glandular columnar epithelium,UBERON:0000485,simple columnar epithelium
+UBERON:0005121,metanephric long descending thin limb bend,UBERON:0004206,long descending thin limb bend
+CL:1001214,arcuate artery smooth muscle cell,CL:1001135,arcuate artery cell
+UBERON:0003257,yolk sac endoderm,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:5830,cervical endometrioid adenocarcinoma,DOID:3702,cervical adenocarcinoma
+HP:0009262,Bracket epiphysis of the proximal phalanx of the 4th finger,HP:0009394,Bracket epiphyses of the 4th finger
+HP:0003849,Flared metaphyses of the upper limbs,HP:0009809,Abnormality of upper limb metaphysis
+UBERON:0010683,pedal digit 4 phalanx cartilage element,UBERON:0015034,pedal digit 4 phalanx endochondral element
+UBERON:0011677,trunk vertebra,UBERON:0004247,bone of dorsum
+UBERON:0012248,cervical mucosa,UBERON:0005156,reproductive structure
+HP:0005709,2-3 toe cutaneous syndactyly,HP:0010621,Cutaneous syndactyly of toes
+UBERON:0003414,mesenchyme of mandible,UBERON:0006904,head mesenchyme from mesoderm
+DOID:11120,psychologic dyspareunia,DOID:10132,psychosexual disorder
+UBERON:0013476,dermal layer of tongue,UBERON:0004923,organ component layer
+UBERON:0001997,olfactory epithelium,UBERON:0005384,nasal cavity epithelium
+UBERON:0006936,thymus subcapsular epithelium,UBERON:0003846,thymus epithelium
+HP:0012633,Asymmetry of intraocular pressure,HP:0012632,Abnormal intraocular pressure
+HP:0000541,Retinal detachment,HP:0000479,Abnormality of the retina
+HP:0002083,Migraine without aura,HP:0002076,Migraine
+HP:0000726,Dementia,HP:0001268,Mental deterioration
+DOID:12397,entropion,DOID:530,eyelid disease
+UBERON:0001143,hepatic vein,UBERON:0013126,vein of abdomen
+CL:2000005,brain macroglial cell,CL:0000128,oligodendrocyte
+UBERON:0000171,respiration organ,UBERON:0000062,organ
+UBERON:0006743,paleodentate of dentate nucleus,UBERON:0002946,regional part of cerebellum
+UBERON:0010399,spleen trabecular artery,UBERON:0004573,systemic artery
+HP:0100669,Abnormal pigmentation of oral cavity,HP:0000163,Abnormality of the oral cavity
+DOID:3227,tracheal stenosis,DOID:3225,tracheal disease
+UBERON:0003608,hindlimb long bone,UBERON:0003464,hindlimb bone
+HP:0006366,Adductor longus contractures,HP:0005750,Contractures of the joints of the lower limbs
+DOID:2780,rectosigmoid junction neoplasm,DOID:1984,rectal neoplasm
+UBERON:0003856,odontogenic mesenchyme,UBERON:0007213,mesenchyme derived from head neural crest
+UBERON:0002314,midbrain tectum,UBERON:0002950,regional part of midbrain
+HP:0010212,Flexion contracture of the hallux,HP:0001836,Camptodactyly (feet)
+UBERON:0009776,intermediate reticular formation,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000057,fibroblast,CL:0002320,connective tissue cell
+UBERON:0012482,submucosa of cloaca,UBERON:0004120,mesoderm-derived structure
+UBERON:0000465,material anatomical entity,UBERON:0001062,anatomical entity
+UBERON:0007161,medial arcuate ligament,UBERON:0015214,arcuate ligament
+UBERON:0014908,cerebellopontine angle,UBERON:0004121,ectoderm-derived structure
+HP:0010331,Aplasia/Hypoplasia of the 3rd toe,HP:0010760,Absent toe
+UBERON:0001822,orbital septum,UBERON:0000094,membrane organ
+HP:0012164,Asterixis,HP:0100022,Abnormality of movement
+DOID:8661,lip carcinoma in situ,DOID:8719,in situ carcinoma
+UBERON:0005193,ethmoidal artery,UBERON:0003496,head blood vessel
+DOID:2411,granular cell tumor,DOID:3165,skin benign neoplasm
+CL:1000381,type 1 vestibular sensory cell of epithelium of crista of ampulla of semicircular duct of membranous labyrinth,CL:0002070,type I vestibular sensory cell
+UBERON:0002174,middle lobe of right lung,UBERON:0006518,right lung lobe
+DOID:0050625,biliary tract neoplasm,DOID:3117,hepatobiliary benign neoplasm
+DOID:9923,developmental coordination disorder,DOID:0060038,specific developmental disorder
+UBERON:0013175,nasal air sac,UBERON:0002553,anatomical cavity
+HP:0000074,Ureteropelvic junction obstruction,HP:0000071,Ureteral stenosis
+HP:0001746,Asplenia,HP:0010451,Aplasia/Hypoplasia of the spleen
+UBERON:0001682,palatine bone,UBERON:0008001,irregular bone
+HP:0011122,Abnormality of skin physiology,HP:0011354,Generalized abnormality of skin
+DOID:7959,duodenal gastrinoma,DOID:10021,duodenum cancer
+HP:0010015,Absent epiphysis of the 1st metacarpal,HP:0010014,Abnormality of the epiphysis of the 1st metacarpal
+HP:0100057,Cone-shaped epiphyses of the 3rd toe,HP:0010329,Abnormality of the epiphyses of the 3rd toe
+DOID:2920,membranoproliferative glomerulonephritis,DOID:2921,glomerulonephritis
+UBERON:3010424,right channel of ventral aorta,UBERON:0004573,systemic artery
+HP:0005085,limited knee flexion/extension,HP:0003066,Limited knee extension
+UBERON:0011876,body of tongue,UBERON:0000064,organ part
+HP:0007543,Epidermal hyperkeratosis,HP:0000962,Hyperkeratosis
+UBERON:4000059,avascular GAG-rich matrix,UBERON:0000479,tissue
+UBERON:0005886,post-hyoid pharyngeal arch skeleton,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0009055,closed circulatory system,UBERON:0001009,circulatory system
+HP:0009930,Asymmetry of the nares,HP:0005288,Abnormality of the nares
+HP:0006581,Depletion of mitochondrial DNA in liver,HP:0001392,Abnormality of the liver
+DOID:407,hepatic tuberculosis,DOID:404,gastrointestinal tuberculosis
+UBERON:0007284,presumptive neural plate,UBERON:0006598,presumptive structure
+UBERON:4200162,mesomere 4,UBERON:4200160,mesomere (fin)
+CL:0002303,pigmented ciliary epithelial cell,CL:0000067,ciliated epithelial cell
+UBERON:0014916,velar vocal fold,UBERON:0013765,digestive system organ
+DOID:11424,fallopian tube endometriosis,DOID:289,endometriosis
+DOID:4586,familial meningioma,DOID:3565,meningioma
+HP:0011651,Double outlet right ventricle with doubly committed ventricular septal defect and pulmonary stenosis,HP:0001719,Double outlet right ventricle
+HP:0003487,Babinski sign,HP:0007256,Abnormality of pyramidal motor function
+UBERON:0010055,stapes cartilage element,UBERON:0015016,stapes endochondral element
+UBERON:2001523,hypobranchial 4 cartilage,UBERON:2001522,hypobranchial cartilage
+UBERON:0011950,mammary gland luminal epithelium,UBERON:0014404,female anatomical structure
+HP:0007552,Abnormal subcutaneous fat tissue distribution,HP:0001001,Abnormality of subcutaneous fat tissue
+CL:0000594,skeletal muscle satellite cell,CL:0000035,single fate stem cell
+HP:0100199,Small epiphysis of the proximal phalanx of the 4th toe,HP:0100074,Small epiphyses of the 4th toe
+HP:0010117,Fragmentation of the epiphyses of the hallux,HP:0010056,Abnormality of the epiphyses of the hallux
+DOID:0060159,organic acidemia,DOID:9252,amino acid metabolic disorder
+HP:0100847,Palmoplantar pustules,HP:0200039,Pustule
+HP:0002953,Vertebral compression fractures,HP:0003468,Abnormality of the vertebrae
+UBERON:2001028,hypurapophysis,UBERON:0004120,mesoderm-derived structure
+UBERON:0006588,round ligament of liver,UBERON:0006592,transformed vein
+DOID:8000,frontal convexity meningioma,DOID:6114,cerebral convexity meningioma
+HP:0000414,Bulbous nose,HP:0000436,Abnormality of the nasal tip
+DOID:12246,histoplasmosis meningitis,DOID:11608,fungal meningitis
+UBERON:2001647,pharyngeal tooth plate,UBERON:0008907,dermal bone
+UBERON:0003948,blood-air barrier,UBERON:0000119,cell layer
+DOID:8133,epiglottis cancer,DOID:13476,supraglottis cancer
+DOID:12750,cyclosporiasis,DOID:2113,coccidiosis
+UBERON:0010241,molar gland,UBERON:0001830,minor salivary gland
+UBERON:0001253,lamina propria of ureter,UBERON:0000030,lamina propria
+UBERON:2001969,inner mental barbel,UBERON:2002024,mental barbel
+HP:0002186,Apraxia,HP:0011446,Abnormality of higher mental function
+HP:0009601,Aplasia/Hypoplasia of the thumb,HP:0006265,Aplasia/Hypoplasia of fingers
+HP:0000938,Osteopenia,HP:0004349,Reduced bone mineral density
+UBERON:0001290,proximal straight tubule,UBERON:0008404,proximale tubular epithelium
+UBERON:0003992,fourth ventricle lateral aperture,UBERON:0004668,fourth ventricle aperture
+UBERON:0005817,neuraxis flexure,UBERON:0000064,organ part
+UBERON:0003648,metacarpal bone of digit 4,UBERON:0002374,metacarpal bone
+HP:0001052,Nevus flammeus,HP:0100026,Arteriovenous malformation
+UBERON:0009657,labial artery,UBERON:0001637,artery
+CL:0000584,enterocyte,CL:0002563,intestinal epithelial cell
+UBERON:2001774,anal fin lepidotrichium 6,UBERON:4000176,anal fin lepidotrichium
+UBERON:0006836,medial tibial tarsal bone,UBERON:0001447,tarsal bone
+DOID:2478,spinocerebellar degeneration,DOID:1289,neurodegenerative disease
+DOID:2973,kidney cortex necrosis,DOID:557,kidney disease
+UBERON:0004655,zygomatic process of temporal bone,UBERON:4100000,skeletal element projection
+UBERON:0005702,optic eminence mesenchyme,UBERON:0003104,mesenchyme
+UBERON:0013131,lobe of tail,UBERON:0000064,organ part
+UBERON:0002733,intralaminar nuclear group,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0002669,anterior horizontal limb of lateral sulcus,UBERON:0008334,subarachnoid sulcus
+DOID:13603,obstructive jaundice,DOID:13580,cholestasis
+HP:0007485,Absence of subcutaneous fat,HP:0003758,Reduced subcutaneous adipose tissue
+HP:0001445,Abnormality of the hip-girdle musculature,HP:0001469,Abnormality of the musculature of the pelvis
+HP:0003256,Abnormality of the coagulation cascade,HP:0001928,Abnormality of coagulation
+UBERON:0005269,renal cortex vein,UBERON:0014401,renal venous blood vessel
+DOID:5730,salpingitis isthmica nodosa,DOID:5731,chronic salpingitis
+HP:0002831,Long coccyx,HP:0008519,Abnormality of the coccyx
+DOID:0060005,autoimmune disease of endocrine system,DOID:417,hypersensitivity reaction type II disease
+CL:1001107,kidney loop of henle thin ascending limb epithelial cell,CL:1001016,kidney loop of henle ascending limb epithelial cell
+UBERON:0013208,Grueneberg ganglion,UBERON:0000045,ganglion
+UBERON:2005018,efferent filamental artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:10341,chronic meningitis,DOID:9471,meningitis
+UBERON:0001714,cranial ganglion,UBERON:0000045,ganglion
+HP:0004941,Extrahepatic portal hypertension,HP:0001409,Portal hypertension
+HP:0009678,Enlarged epiphysis of the distal phalanx of the thumb,HP:0009662,Abnormality of the epiphysis of the distal phalanx of the thumb
+CL:0000136,fat cell,CL:0002320,connective tissue cell
+UBERON:0006097,ventral external arcuate fiber bundle,UBERON:0002678,regional part of medulla oblongata
+UBERON:0010425,internal naris,UBERON:0000003,naris
+HP:0009898,Underdeveloped crus of the helix,HP:0009895,Abnormality of the crus of the helix
+UBERON:3010128,taeniae tecti marginalis,UBERON:0003932,cartilage element of chondrocranium
+UBERON:0007802,uropygial gland,UBERON:0002365,exocrine gland
+HP:0002827,Hip dislocation,HP:0001384,Abnormality of the hip joint
+HP:0011284,Short-segment aganglionic megacolon,HP:0002251,Aganglionic megacolon
+UBERON:0001242,intestinal mucosa,UBERON:0004786,gastrointestinal system mucosa
+UBERON:0004105,subungual region,UBERON:0004121,ectoderm-derived structure
+HP:0002910,Elevated hepatic transaminases,HP:0001392,Abnormality of the liver
+DOID:4290,adamantinoid basal cell epithelioma,DOID:2513,basal cell carcinoma
+CL:0002282,type TG enteroendocrine cell,CL:0000164,enteroendocrine cell
+HP:0001750,Single ventricle,HP:0001713,Abnormality of cardiac ventricle
+HP:0100437,Bullet-shaped proximal phalanx of the 3rd toe,HP:0010361,Bullet-shaped phalanges of the 3rd toe
+UBERON:0005031,mucosa of upper lip,UBERON:0010314,structure with developmental contribution from neural crest
+CL:1001582,lateral ventricle neuron,CL:0000540,neuron
+UBERON:3000396,pars dentalis of maxilla,UBERON:0004120,mesoderm-derived structure
+UBERON:0006517,kidney calyx,UBERON:0006554,urinary system structure
+UBERON:0000461,minor vestibular gland,UBERON:0010187,female urethral gland
+UBERON:0000039,follicular antrum,UBERON:0000464,anatomical space
+DOID:3419,optic nerve neoplasm,DOID:338,cranial nerve neoplasm
+CL:0002337,keratinocyte stem cell,CL:0000048,multi fate stem cell
+DOID:4119,intestinal neuroendocrine benign tumor,DOID:4610,intestinal benign neoplasm
+HP:0003261,Increased IgA level,HP:0010702,Hypergammaglobulinemia
+HP:0005885,Absent ossification of cervical and thoracic vertebral bodies,HP:0004599,Absent or minimally ossified vertebral bodies
+HP:0008366,Contractures involving the joints of the feet,HP:0001760,Abnormality of the foot
+UBERON:0014541,thoracic spinal cord central canal,UBERON:0014538,subdivision of spinal cord central canal
+UBERON:0005200,thoracic mammary gland,UBERON:0005175,chest organ
+UBERON:0005993,pulmonary valve anulus,UBERON:0006008,fibrous ring of heart
+HP:0011078,Abnormality of canine,HP:0000164,Abnormality of the teeth
+UBERON:0001755,distal part of styloid process of temporal bone,UBERON:0010313,neural crest-derived structure
+HP:0100826,Neoplasm of the nail,HP:0011793,Neoplasm by anatomical site
+CL:0000073,barrier epithelial cell,CL:0002371,somatic cell
+HP:0010083,Triangular shaped distal phalanx of the hallux,HP:0010192,Triangular shaped distal phalanges of the toes
+UBERON:0010927,thyroepiglotticus muscle,UBERON:0001568,muscle of larynx
+UBERON:0002197,median eminence of neurohypophysis,UBERON:0002784,regional part of diencephalon
+UBERON:0002233,tectorial membrane of cochlea,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2001242,ceratobranchial 2 bone,UBERON:2001900,ceratobranchial 2 element
+UBERON:0004045,tailgut,UBERON:0002050,embryonic structure
+HP:0009549,Curved phalanges of the 2nd finger,HP:0009541,Abnormality of the phalanges of the 2nd finger
+DOID:2154,nephroblastoma,DOID:263,kidney cancer
+UBERON:0009034,stomach region,UBERON:0000064,organ part
+NCBITaxon:426438,Hyalomminae,NCBITaxon:6939,Ixodidae
+UBERON:3000368,otoccipital,UBERON:0002513,endochondral bone
+DOID:14336,estrogen excess,DOID:1414,ovarian dysfunction
+UBERON:0013698,strand of pubic hair,UBERON:0001037,strand of hair
+HP:0003849,Flared metaphyses of the upper limbs,HP:0003856,Upper limb metaphyseal widening
+UBERON:0015063,autopod endochondral element,UBERON:0015061,limb endochondral element
+UBERON:0001266,splenic cord,UBERON:0004120,mesoderm-derived structure
+UBERON:0006542,outer medulla outer stripe loop of henle,UBERON:0001288,loop of Henle
+DOID:1074,kidney failure,DOID:557,kidney disease
+UBERON:0005689,2nd arch mesenchyme,UBERON:0009494,pharyngeal arch mesenchymal region
+UBERON:4300109,proximal segment of caudal ray,UBERON:4300108,lepidotrichial segment
+HP:0001274,Agenesis of corpus callosum,HP:0007370,Aplasia/Hypoplasia of the corpus callosum
+UBERON:0006725,spiral ligament,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0006134,nerve fiber,UBERON:0000470,cell part
+HP:0002645,Wormian bones,HP:0011329,Abnormality of cranial sutures
+HP:0003532,Ornithinuria,HP:0003355,Aminoaciduria
+UBERON:0001373,sartorius muscle,UBERON:0001630,muscle organ
+HP:0001204,Distal symphalangism (hands),HP:0009832,Abnormality of the distal phalanx of finger
+UBERON:0005733,limb field,UBERON:0005732,paired limb/fin field
+UBERON:0003647,metacarpal bone of digit 3,UBERON:0002374,metacarpal bone
+CL:0001658,visual pigment cell (sensu Nematoda and Protostomia),CL:0000341,pigment cell (sensu Nematoda and Protostomia)
+UBERON:0004739,pronephric glomerulus,UBERON:0000074,renal glomerulus
+UBERON:0014647,hemisphere part of cerebellar anterior lobe,UBERON:0002749,regional part of cerebellar cortex
+HP:0002868,Narrow iliac wings,HP:0011867,Abnormality of the wing of the ilium
+UBERON:0008330,vestibulum vaginae,UBERON:0001349,vestibule
+UBERON:0002412,vertebra,UBERON:0015005,vertebra endochondral element
+UBERON:3010754,ramus recurrens,UBERON:0004529,anatomical projection
+HP:0100946,Sclerosis of the proximal phalanges of the toes,HP:0010184,Abnormality of the proximal phalanges of the toes
+UBERON:0003536,right lung alveolar duct,UBERON:0002173,pulmonary alveolar duct
+DOID:5630,Bartholin's gland adenosquamous carcinoma,DOID:3999,Bartholin's gland carcinoma
+UBERON:0004747,supraoccipital bone,UBERON:0010314,structure with developmental contribution from neural crest
+NCBITaxon:1660,Actinomyces odontolyticus,NCBITaxon:1654,Actinomyces
+CL:0000026,invertebrate nurse cell,CL:0000412,polyploid cell
+DOID:5090,sternum cancer,DOID:184,bone cancer
+HP:0001251,Ataxia,HP:0001317,Abnormality of the cerebellum
+CL:0002080,pancreatic centro-acinar cell,CL:1001433,epithelial cell of exocrine pancreas
+NCBITaxon:63402,Arthroderma gypseum,NCBITaxon:63399,Arthroderma
+DOID:5253,conventional leiomyosarcoma,DOID:1967,leiomyosarcoma
+DOID:10194,kidney lipoma,DOID:3116,kidney benign neoplasm
+HP:0007573,Late onset atopic dermatitis,HP:0001047,Atopic dermatitis
+UBERON:2002112,preural 3 vertebra,UBERON:2000734,preural vertebra
+DOID:14081,toxic labyrinthitis,DOID:1468,labyrinthitis
+HP:0000988,Skin rash,HP:0011123,Inflammatory abnormality of the skin
+DOID:5214,demyelinating polyneuropathy,DOID:1389,polyneuropathy
+HP:0011232,Infra-orbital fold,HP:0000315,Abnormality of the orbital region
+CL:1001436,hair-tylotrich neuron,CL:0002487,cutaneous/subcutaneous mechanoreceptor cell
+DOID:4370,stomach diverticulosis,DOID:76,stomach disease
+UBERON:0012301,female membranous urethra,UBERON:0001336,membranous urethra of male or female
+UBERON:4300021,anterolateral plate,UBERON:0007829,pectoral girdle bone
+UBERON:0003647,metacarpal bone of digit 3,UBERON:0013583,metapodium bone 3
+DOID:607,paraplegia,DOID:331,central nervous system disease
+UBERON:0007646,endomeninx,UBERON:0007645,future meninx
+DOID:12175,dyshormonogenic goiter,DOID:12176,goiter
+UBERON:0001717,spinal nucleus of trigeminal nerve,UBERON:0004132,trigeminal sensory nucleus
+UBERON:0005708,lower jaw incisor odontogenic papilla,UBERON:0009891,facial mesenchyme
+UBERON:3000086,cavum internasale,UBERON:0001707,nasal cavity
+DOID:9473,mononeuritis of lower limb,DOID:1802,mononeuritis
+DOID:8654,"Hodgkin's lymphoma, mixed cellularity",DOID:8567,Hodgkin's lymphoma
+UBERON:0015057,scapula endochondral element,UBERON:0010363,endochondral element
+HP:0010196,Bullet-shaped middle phalanges of the toes,HP:0010183,Abnormality of the middle phalanges of the toes
+CL:0000123,neuron associated cell (sensu Vertebrata),CL:0000095,neuron associated cell
+DOID:0060138,autotopagnosia,DOID:4090,agnosia
+HP:0008998,Pectoralis hypoplasia,HP:0005258,Pectoral muscle hypoplasia/aplasia
+UBERON:0006450,second lumbar spinal cord segment,UBERON:0007716,lumbar subsegment of spinal cord
+UBERON:0000992,female gonad,UBERON:0000991,gonad
+NCBITaxon:4891,Saccharomycetes,NCBITaxon:147537,Saccharomycotina
+UBERON:0014450,pretectal nucleus,UBERON:0002308,nucleus of brain
+UBERON:0008000,sesamoid bone of pes,UBERON:0011141,appendicular ossicle
+UBERON:0006063,cartilaginous neural arch,UBERON:0002050,embryonic structure
+UBERON:0001793,nerve fiber layer of retina,UBERON:0003902,retinal neural layer
+UBERON:0006639,crus penis,UBERON:0014403,male anatomical structure
+HP:0000958,Dry skin,HP:0011121,Abnormality of skin morphology
+UBERON:0005362,vagus X ganglion,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0004575,fusion of midcervical facet joints,HP:0002949,Fused cervical vertebrae
+DOID:7983,breast malignant eccrine spiradenoma,DOID:1612,breast cancer
+DOID:0050801,androgenic alopecia,DOID:987,alopecia
+DOID:4455,hereditary renal cell carcinoma,DOID:4450,renal cell carcinoma
+DOID:7926,epithelial malignant thymoma,DOID:3282,dendritic cell thymoma
+HP:0000882,Hypoplastic scapulae,HP:0006713,Aplasia/Hypoplasia of the scapulae
+UBERON:0006724,osseus spiral lamina,UBERON:0010313,neural crest-derived structure
+UBERON:0004363,aortic arch,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:3000180,foramen acusticum anterius,UBERON:0005744,bone foramen
+UBERON:0006606,mandibular symphysis,UBERON:0002216,symphysis
+UBERON:0002563,central nucleus of inferior colliculus,UBERON:0003528,brain grey matter
+UBERON:0008922,sublaminar layer S1,UBERON:0009735,sublaminar layers S1 or S3 or S4
+UBERON:0003117,pharyngeal arch 6,UBERON:0002539,pharyngeal arch
+DOID:8643,duodenitis,DOID:5295,intestinal disease
+DOID:14500,fucosidosis,DOID:3211,lysosomal storage disease
+HP:0100613,Death in early adulthood,HP:0011420,Death
+UBERON:0003620,manual digit 1 phalanx,UBERON:0001436,phalanx of manus
+DOID:7997,thyrotoxicosis,DOID:50,thyroid gland disease
+UBERON:0010026,ventral part of pharyngeal pouch 3,UBERON:0005291,embryonic tissue
+HP:0010008,Duplication of the middle phalanx of hand,HP:0009834,Abnormality of the proximal phalanges of the hand
+UBERON:2200936,dorsal fin distal radial cartilage,UBERON:2100936,dorsal fin distal radial element
+NCBITaxon:6208,Taeniidae,NCBITaxon:6201,Cyclophyllidea
+UBERON:3000846,element Y of fore mesopodium,UBERON:0000064,organ part
+UBERON:0002129,cerebellar cortex,UBERON:0000064,organ part
+UBERON:0006806,entepicondyle of humerus,UBERON:0009978,epicondyle
+HP:0010000,Complete duplication of the proximal phalanges of the hand,HP:0009998,Complete duplication of phalanx of hand
+DOID:8339,intestinal variant cervical mucinous adenocarcinoma,DOID:3701,cervical mucinous adenocarcinoma
+UBERON:4200030,antitrochanter,UBERON:0004120,mesoderm-derived structure
+UBERON:0010375,pancreas dorsal primordium,UBERON:0002050,embryonic structure
+UBERON:0006948,efferent duct epithelium,UBERON:0014403,male anatomical structure
+UBERON:3000101,hyale,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0005626,Posterior fusion of lumbosacral vertebrae,HP:0002948,Vertebral fusion
+UBERON:2001996,maxillary canal,UBERON:0000481,multi-tissue structure
+UBERON:2005341,medial longitudinal catecholaminergic tract,UBERON:0002316,white matter
+HP:0011616,Pulmonary situs inversus,HP:0011615,Abnormality of pulmonary situs
+UBERON:0007707,superior cerebellar peduncle of midbrain,UBERON:0003035,regional part of cerebellar white matter
+UBERON:0010930,interhyoideus,UBERON:0005493,hyoid muscle
+DOID:9839,accommodative esotropia,DOID:9840,esotropia
+UBERON:3000281,margo orbitalis of maxilla,UBERON:0004120,mesoderm-derived structure
+HP:0012264,Absent central microtubular pair morphology of motile cilia,HP:0005938,Abnormal respiratory motile cilium morphology
+UBERON:0011782,feather follicle,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0010955,trapezius pre-muscle mass,UBERON:0010258,mesenchyme from rhombencephalic neural crest
+HP:0004271,Cortical thickening of hand bones,HP:0005926,Abnormalities of the cortex of hand bones
+HP:0100067,Bracket epiphyses of the 4th toe,HP:0010163,Bracket epiphyses of the toes
+DOID:10003,sensorineural hearing loss,DOID:2952,inner ear disease
+DOID:700,mitochondrial metabolism disease,DOID:655,inherited metabolic disorder
+HP:0200113,Aphalangy of hands and feet,HP:0009776,Adactyly
+HP:0011305,Partial absence of toe,HP:0010760,Absent toe
+UBERON:0001830,minor salivary gland,UBERON:0001044,salivary gland
+HP:0007818,Central heterochromia,HP:0001100,Heterochromia iridis
+UBERON:0012196,right superior intercostal vein,UBERON:0012194,superior intercostal vein
+HP:0100190,Triangular epiphysis of the middle phalanx of the 4th toe,HP:0100076,Triangular epiphyses of the 4th toe
+HP:0003040,Arthropathy,HP:0001367,Abnormal joint morphology
+DOID:4242,kidney sarcoma,DOID:263,kidney cancer
+HP:0001120,Abnormality of corneal size,HP:0000481,Abnormality of the cornea
+UBERON:0001653,facial vein,UBERON:0009141,craniocervical region vein
+HP:0000534,Abnormality of the eyebrow,HP:0000284,Abnormality of the ocular region
+HP:0005229,Jejunoileal ulceration,HP:0001549,Abnormality of the ileum
+UBERON:0007250,lingual tonsil,UBERON:0002372,tonsil
+DOID:0050117,disease by infectious agent,DOID:4,disease
+UBERON:0006951,inner dental epithelium,UBERON:0003843,dental epithelium
+HP:0009189,Fragmentation of the metacarpal epiphyses,HP:0005913,Abnormality of metacarpal epiphyses
+HP:0010377,Symphalangism affecting the phalanges of the 4th toe,HP:0010179,Symphalangism affecting the phalanges of the toes
+UBERON:0010883,forelimb cartilage element,UBERON:0007844,cartilage element
+UBERON:0013731,basilar papilla,UBERON:0000020,sense organ
+CL:0000465,cardioblast (sensu Arthropoda),CL:0010021,cardiac myoblast
+UBERON:0010013,lower beak,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004703,dorsal thalamus,UBERON:0002784,regional part of diencephalon
+HP:0004963,Calcification of the aorta,HP:0003207,Arterial calcification
+HP:0010446,Tricuspid stenosis,HP:0001702,Abnormality of the tricuspid valve
+UBERON:0014288,dorsal accessory olive,UBERON:0002574,regional part of inferior olivary complex
+UBERON:0003339,ganglion of central nervous system,UBERON:0000045,ganglion
+HP:0001163,Abnormality of the metacarpal bones,HP:0001155,Abnormality of the hand
+HP:0006402,Distal shortening of limbs,HP:0009826,Limb undergrowth
+DOID:884,metagonimiasis,DOID:883,parasitic helminthiasis infectious disease
+UBERON:0010347,6th arch mesenchyme from head mesenchyme,UBERON:0010360,pharyngeal arch mesenchyme from head mesenchyme
+CL:0002449,CD94-positive Ly49CI-positive natural killer cell,CL:0002441,CD94-positive natural killer cell
+UBERON:0003374,chorionic ectoderm,UBERON:0004120,mesoderm-derived structure
+UBERON:2002116,epibranchial organ,UBERON:0013765,digestive system organ
+HP:0100043,Broad 5th toe,HP:0010322,Abnormality of the 5th toe
+UBERON:3000570,spatium sacculare,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:11054,urinary bladder cancer,DOID:3996,urinary system cancer
+UBERON:2002005,canal plate,UBERON:0008907,dermal bone
+UBERON:0002016,pulmonary vein,UBERON:0013768,great vessel of heart
+HP:0002741,Recurrent Serratia marcescens infections,HP:0005420,Recurrent gram-negative bacterial infections
+HP:0002071,Abnormality of extrapyramidal motor function,HP:0011442,Abnormality of central motor function
+UBERON:0008441,webbed manus,UBERON:0008440,webbed autopod
+UBERON:0004517,smooth muscle tissue of respiratory bronchiole,UBERON:0004515,smooth muscle tissue of bronchiole
+HP:0002323,Anencephaly,HP:0007364,Aplasia/Hypoplasia of the cerebrum
+HP:0002099,Asthma,HP:0002088,Abnormality of the lung
+HP:0012516,Tetralogy of Fallot with pulmonary atresia,HP:0001636,Tetralogy of Fallot
+HP:0008513,Bilateral conductive hearing impairment,HP:0000405,Conductive hearing impairment
+UBERON:0002881,sublingual nucleus,UBERON:0007635,nucleus of medulla oblongata
+DOID:12265,chronic salpingo-oophoritis,DOID:5731,chronic salpingitis
+HP:0009521,Small epiphysis of the middle phalanx of the 2nd finger,HP:0009500,Abnormality of the epiphysis of the middle phalanx of the 2nd finger
+UBERON:0005156,reproductive structure,UBERON:0004120,mesoderm-derived structure
+DOID:8036,childhood ovarian embryonal carcinoma,DOID:5681,ovarian embryonal carcinoma
+DOID:12581,olecranon bursitis,DOID:12223,specific bursitis often of occupational origin
+UBERON:0014916,velar vocal fold,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003019,oral part of ventral posterolateral nucleus,UBERON:0003528,brain grey matter
+DOID:8893,psoriasis,DOID:37,skin disease
+UBERON:0003712,cavernous sinus,UBERON:0005486,venous dural sinus
+HP:0007123,Subcortical dementia,HP:0000726,Dementia
+CL:1001561,vomeronasal sensory neuron,CL:0000101,sensory neuron
+HP:0006134,Enlarged metacarpal epiphyses,HP:0005913,Abnormality of metacarpal epiphyses
+UBERON:0001498,muscle of pes,UBERON:0003663,hindlimb muscle
+CL:0000121,Purkinje cell,CL:0000117,CNS neuron (sensu Vertebrata)
+HP:0010349,Bullet-shaped phalanges of the 2nd toe,HP:0010324,Abnormality of phalanx of the 2nd toe
+HP:0000204,Cleft upper lip,HP:0000202,Oral cleft
+HP:0009916,Anisocoria,HP:0000615,Abnormality of the pupil
+UBERON:4300116,dorsal fin soft ray,UBERON:4000177,dorsal fin lepidotrichium
+DOID:11811,urinary bladder posterior wall cancer,DOID:11054,urinary bladder cancer
+HP:0005845,4th finger camptodactyly,HP:0009274,Joint contractures of the 4th finger
+HP:0010110,Aplasia of the phalanges of the hallux,HP:0010745,Aplasia of the phalanges of the toes
+DOID:2093,vulvar melanoma,DOID:1245,vulva cancer
+HP:0011074,Localized hypoplasia of dental enamel,HP:0006297,Hypoplasia of dental enamel
+HP:0010922,Membranous cataract,HP:0000518,Cataract
+HP:0010084,Duplication of the distal phalanx of the hallux,HP:0010193,Duplication of distal phalanx of toe
+HP:0006485,Agenesis of incisor,HP:0011064,Abnormal number of incisors
+HP:0002745,Oral leukoplakia,HP:0011830,Abnormality of oral mucosa
+UBERON:0015241,parapineal organ,UBERON:0004121,ectoderm-derived structure
+HP:0003162,Fasting hypoglycemia,HP:0003117,Abnormality of circulating hormone level
+UBERON:0005642,ultimobranchial body epithelium,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3000644,processus lingularis of nasal skeleton,UBERON:0010313,neural crest-derived structure
+UBERON:0015162,superior branch of oculomotor nerve,UBERON:0001021,nerve
+HP:0005995,Decreased adipose tissue around neck,HP:0003758,Reduced subcutaneous adipose tissue
+UBERON:0005750,glomerular parietal epithelium,UBERON:0004188,glomerular epithelium
+HP:0100228,Fragmentation of the epiphysis of the proximal phalanx of the 5th toe,HP:0100081,Fragmentation of the epiphyses of the 5th toe
+HP:0001531,Failure to thrive in infancy,HP:0001508,Failure to thrive
+UBERON:2001855,hyomandibular condyle for the opercle,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004027,chorionic plate,UBERON:0000479,tissue
+UBERON:0011809,inner epidermal layer of feather follicle,UBERON:0011807,epidermis of feather follicle
+UBERON:0002539,pharyngeal arch,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100948,Sclerosis of the distal phalanges of the toes,HP:0010182,Abnormality of the distal phalanges of the toes
+UBERON:2001872,trunk sensory canal system,UBERON:0002540,lateral line system
+HP:0002865,Medullary thyroid carcinoma,HP:0002890,Thyroid carcinoma
+UBERON:0003216,hard palate,UBERON:0004121,ectoderm-derived structure
+CL:0000817,precursor B cell,CL:0000236,B cell
+UBERON:0005018,mucosa of nasal septum,UBERON:0010313,neural crest-derived structure
+UBERON:3000543,retroarticular process,UBERON:0010313,neural crest-derived structure
+UBERON:0014872,distal epiphysis of distal phalanx of pedal digit 2,UBERON:0014876,distal epiphysis of distal phalanx of pedal digit
+HP:0008169,Reduced factor VII activity,HP:0010988,Abnormality of the extrinsic pathway
+UBERON:0010273,zone of hyoid bone,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0011896,Subconjunctival hemorrhage,HP:0011885,Hemorrhage of the eye
+HP:0004279,Short palm,HP:0100871,Abnormality of the palm
+CL:0002347,"CD27-high, CD11b-high natural killer cell",CL:0002426,"CD11b-positive, CD27-positive natural killer cell"
+UBERON:3010528,articular process of palatoquadrate,UBERON:0004121,ectoderm-derived structure
+DOID:5603,acute T cell leukemia,DOID:715,T-cell leukemia
+UBERON:1000014,right part of face,UBERON:0001444,subdivision of head
+HP:0005290,Internal carotid artery hypoplasia,HP:0005344,Abnormality of the carotid arteries
+UBERON:0004317,distal phalanx of pedal digit 3,UBERON:0003867,distal phalanx of pes
+UBERON:0004768,bone of lower jaw,UBERON:0012360,bone of jaw
+CL:1001590,epididymis glandular cell,CL:0000150,glandular epithelial cell
+UBERON:2000623,basipterygium bone,UBERON:0007830,pelvic girdle bone/zone
+NCBITaxon:6204,Taenia solium,NCBITaxon:6202,Taenia
+UBERON:2001719,caudal principal ray 7,UBERON:2001585,caudal principal ray
+CL:0002373,growth hormone releasing hormone secreting cell,CL:0000167,peptide hormone secreting cell
+UBERON:0009857,cavum septum pellucidum,UBERON:0000464,anatomical space
+DOID:2300,spondylolysis,DOID:0080010,bone structure disease
+CL:0000233,platelet,CL:0000763,myeloid cell
+UBERON:0014890,right hemisphere of cerebellum,UBERON:0002245,cerebellar hemisphere
+UBERON:0013629,hallical pad,UBERON:0013623,pedal autopod pad
+HP:0009416,Ivory epiphyses of the 3rd finger,HP:0010234,Ivory epiphyses of the phalanges of the hand
+HP:0001805,Thick nail,HP:0001597,Abnormality of the nail
+UBERON:0006320,inferior oblique extraocular muscle,UBERON:0006532,oblique extraocular muscle
+UBERON:2001695,mediopharyngobranchial,UBERON:0011004,pharyngeal arch cartilage
+DOID:7612,childhood intracortical osteosarcoma,DOID:7602,intracortical osteogenic sarcoma
+UBERON:0008597,depressor anguli oris muscle,UBERON:0001577,facial nerve muscle
+CL:0002558,fibroblast of villous mesenchyme,CL:0000349,extraembryonic cell
+DOID:9743,diabetic neuropathy,DOID:870,neuropathy
+UBERON:0001628,posterior communicating artery,UBERON:0006347,communicating artery
+HP:0005984,Elevated maternal serum alpha-fetoprotein,HP:0006254,Elevated alpha-fetoprotein
+DOID:14092,renal artery atheroma,DOID:2388,renal artery disease
+UBERON:3000668,hyoglossal sinus,UBERON:0000464,anatomical space
+HP:0006454,Severely delayed patellae ossification,HP:0011849,Abnormal bone ossification
+UBERON:0009000,ischial spine,UBERON:4100000,skeletal element projection
+DOID:13934,facial paralysis,DOID:1756,facial nerve disease
+UBERON:2002102,epibranchial series,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0011495,rectus thoracis muscle,UBERON:0014398,respiratory muscle
+DOID:1564,fungal infectious disease,DOID:0050117,disease by infectious agent
+UBERON:0002682,abducens nucleus,UBERON:0002680,regional part of metencephalon
+CL:0002334,preadipocyte,CL:0000057,fibroblast
+UBERON:3000872,collum ilei,UBERON:0004120,mesoderm-derived structure
+HP:0008988,Pelvic girdle muscle atrophy,HP:0001471,Aplasia/Hypoplasia of the musculature of the pelvis
+DOID:0050719,cerebral folate receptor alpha deficiency,DOID:0050718,vitamin metabolic disorder
+UBERON:0009291,cartilaginous vertebral centrum,UBERON:0007844,cartilage element
+UBERON:0008453,rectus capitis anterior,UBERON:0004518,muscle of vertebral column
+UBERON:0003689,sella turcica,UBERON:0005913,zone of bone organ
+UBERON:0006204,inguinal ligament,UBERON:0003567,abdomen connective tissue
+DOID:6001,breast fibrosarcoma,DOID:3017,breast sarcoma
+UBERON:0010571,manual digit 2 metacarpus cartilage element,UBERON:0010676,manual digit 2 phalanx cartilage element
+HP:0008024,Congenital nuclear cataract,HP:0000519,Congenital cataract
+HP:0012103,Abnormality of the mitochondrion,HP:0011017,Abnormality of cell physiology
+DOID:5957,bladder urachal squamous cell carcinoma,DOID:5958,bladder urachal carcinoma
+HP:0003514,Deficiency or absence of cytochrome b(-245),HP:0003287,Abnormality of mitochondrial metabolism
+UBERON:0003633,pedal digit 3,UBERON:0001466,pedal digit
+HP:0003829,Incomplete penetrance,HP:0003812,Phenotypic variability
+UBERON:0001831,parotid gland,UBERON:0001829,major salivary gland
+UBERON:0008246,pyloric stomach,UBERON:0004921,subdivision of digestive tract
+DOID:2043,hepatitis B,DOID:37,skin disease
+HP:0100389,Short distal phalanx of the 3rd toe,HP:0100369,Aplasia/Hypoplasia of the distal phalanx of the 3rd toe
+HP:0006891,Thick cerebral cortex,HP:0002538,Abnormality of the cerebral cortex
+UBERON:0010535,primitive metanephric nephron,UBERON:0005110,metanephric nephron
+HP:0000163,Abnormality of the oral cavity,HP:0000153,Abnormality of the mouth
+UBERON:0007914,head or neck bone,UBERON:0001474,bone element
+CL:0002521,subcutaneous fat cell,CL:0000136,fat cell
+HP:0005743,Avascular necrosis of the capital femoral epiphysis,HP:0100323,Juvenile aseptic necrosis
+UBERON:0001293,outer medulla of kidney,UBERON:0006554,urinary system structure
+CL:0000593,androgen secreting cell,CL:0000174,steroid hormone secreting cell
+UBERON:2002114,cotylephore,UBERON:0000481,multi-tissue structure
+DOID:0050925,small intestine carcinoid neuroendocrine tumor,DOID:10154,small intestine cancer
+HP:0007348,Hypoplasia of the pyramidal tract,HP:0007363,Aplasia/Hypoplasia of the pyramidal tract
+UBERON:0002719,spino-olivary tract,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3000570,spatium sacculare,UBERON:0004121,ectoderm-derived structure
+CL:0002509,"CD103-positive, langerin-positive lymph node dendritic cell",CL:0002507,langerin-positive lymph node dendritic cell
+UBERON:0002734,superior temporal sulcus,UBERON:0003022,cerebral cortex lobe
+UBERON:0010250,middle meningeal artery,UBERON:0003474,meningeal artery
+HP:0007146,Bilateral basal ganglia lesions,HP:0002134,Abnormality of the basal ganglia
+UBERON:2002026,pectoral fin proximal radial bone 1,UBERON:2001587,pectoral fin proximal radial bone
+HP:0010409,Patchy sclerosis of the middle phalanx of the 2nd toe,HP:0010199,Patchy sclerosis of the middle phalanges of the toes
+UBERON:0003991,fourth ventricle median aperture,UBERON:0004668,fourth ventricle aperture
+HP:0009760,Antecubital pterygium,HP:0001059,Pterygium
+HP:0011420,Death,HP:0000004,Onset and clinical course
+HP:0100466,Patchy sclerosis of the proximal phalanx of the 5th toe,HP:0010388,Patchy sclerosis of the phalanges of the 5th toe
+UBERON:3000874,crista ischii,UBERON:0004120,mesoderm-derived structure
+NCBITaxon:85009,Propionibacterineae,NCBITaxon:2037,Actinomycetales
+DOID:6082,pediatric testicular germ cell tumor,DOID:6053,pediatric germ cell cancer
+CL:1001213,arcuate artery endothelial cell,CL:1001135,arcuate artery cell
+UBERON:0012104,sesamoid bone of the peroneus longus muscle,UBERON:0001479,sesamoid bone
+UBERON:0000200,gyrus,UBERON:0000064,organ part
+UBERON:0012295,Guérin's valve,UBERON:0006554,urinary system structure
+UBERON:0000026,appendage,UBERON:0000475,organism subdivision
+UBERON:0007257,intervertebral disk of sacral vertebra,UBERON:2001457,postcranial axial cartilage
+UBERON:2001190,Weberian vertebra,UBERON:0002412,vertebra
+HP:0002335,Agenesis of cerebellar vermis,HP:0006817,Aplasia/Hypoplasia of the  cerebellar vermis
+CL:0000226,single nucleate cell,CL:0002242,nucleate cell
+HP:0000561,Absent eyelashes,HP:0002298,Absent hair
+UBERON:0003367,epithelium of vomeronasal organ,UBERON:0010371,ecto-epithelium
+UBERON:0001063,flocculus,UBERON:0002749,regional part of cerebellar cortex
+DOID:14463,cavernous hemangioma of orbit,DOID:483,cavernous hemangioma
+UBERON:0014453,gustatory epithelium of palate,UBERON:0011642,oral epithelium from ectoderm
+UBERON:0005973,blood-inner ear barrier,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0001301,Chronic sensorineural polyneuropathy,HP:0009830,Peripheral neuropathy
+UBERON:0009149,foramen primum,UBERON:0004120,mesoderm-derived structure
+UBERON:0012442,epiploic foramen,UBERON:0000464,anatomical space
+UBERON:0002793,dorsal longitudinal fasciculus of pons,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009113,Diaphragmatic weakness,HP:0001324,Muscle weakness
+HP:0009344,Stippling of the epiphysis of the distal phalanx of the 3rd finger,HP:0010255,Stippling of the epiphyses of the distal phalanges of the hand
+DOID:8476,Whipple disease,DOID:5295,intestinal disease
+CL:0007019,epidermal mucus secreting cell,CL:0000319,mucus secreting cell
+UBERON:2001532,sublingual dorsal cartilage,UBERON:2001544,sublingual cartilage
+UBERON:0000082,adult mammalian kidney,UBERON:0004120,mesoderm-derived structure
+UBERON:0005925,ethmoidal process of inferior nasal concha,UBERON:0004530,bony projection
+UBERON:0001459,skin of external ear,UBERON:0001084,skin of head
+DOID:3939,lipomatous cancer,DOID:201,connective tissue cancer
+HP:0003959,Deformed forearm bones,HP:0002973,Abnormality of the forearm
+UBERON:0006289,rib pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+DOID:14705,Pfeiffer syndrome,DOID:12960,acrocephalosyndactylia
+HP:0005868,Metaphyseal enchondromatosis,HP:0000944,Abnormality of the metaphyses
+UBERON:0012134,medial-intermediate intercuneiform joint,UBERON:0012132,intercuneiform joint
+UBERON:3010780,pars recta,UBERON:0014404,female anatomical structure
+UBERON:0006164,forelimb common dorsal digital arteries,UBERON:0006146,dorsal digital artery of manus
+HP:0007802,Granular corneal dystrophy,HP:0001131,Corneal dystrophy
+DOID:10944,tongue disease,DOID:403,mouth disease
+UBERON:0001695,squamous part of temporal bone,UBERON:0002514,intramembranous bone
+UBERON:0013621,lower secondary molar tooth,UBERON:0013618,secondary molar tooth
+DOID:8869,neuromyelitis optica,DOID:331,central nervous system disease
+HP:0100292,Amyloidosis of peripheral nerves,HP:0011034,Amyloidosis
+UBERON:0003053,ventricular zone,UBERON:0000477,anatomical cluster
+HP:0004059,Radial club hand,HP:0006501,Aplasia/Hypoplasia of the radius
+UBERON:0001355,deep femoral artery,UBERON:0001637,artery
+HP:0006257,Abnormality of carpal bone ossification,HP:0010660,Abnormal hand bone ossification
+UBERON:0010051,dorsal patch of Leydig's organ,UBERON:0004120,mesoderm-derived structure
+HP:0009467,Radial deviation of the 2nd finger,HP:0009466,Radial deviation of finger
+DOID:13909,red-green color blindness,DOID:13399,color blindness
+HP:0007663,Decreased central vision,HP:0000572,Visual loss
+HP:0011140,Gastrointestinal duplication,HP:0012718,Morphological abnormality of the gastrointestinal tract
+UBERON:0002118,right ovary,UBERON:0000992,female gonad
+UBERON:0004549,right eye,UBERON:0015212,lateral structure
+DOID:7607,chief cell adenoma,DOID:7608,parathyroid adenoma
+HP:0010741,Edema of the lower limbs,HP:0000969,Edema
+DOID:0080045,Kniest dysplasia,DOID:2256,osteochondrodysplasia
+HP:0004274,Deficient ossification of hand bones,HP:0005921,Abnormal ossification of hand bones
+UBERON:0006208,auditory hillocks,UBERON:0002050,embryonic structure
+HP:0010000,Complete duplication of the proximal phalanges of the hand,HP:0010006,Duplication of the proximal phalanx of hand
+UBERON:2001828,primordial ligament,UBERON:0008846,skeletal ligament
+UBERON:0002320,glomerular mesangium,UBERON:0006554,urinary system structure
+UBERON:0011298,submucosa of uterine tube,UBERON:0014404,female anatomical structure
+HP:0010551,Paraplegia/paraparesis,HP:0010549,Paralysis due to lesions of the principle motor tracts
+HP:0004469,Chronic bronchitis,HP:0012387,Bronchitis
+HP:0012646,Retractile testis,HP:0000035,Abnormality of the testis
+DOID:11853,monocular exotropia,DOID:1143,exotropia
+HP:0008265,Mitochondrial lysine transport defect,HP:0003287,Abnormality of mitochondrial metabolism
+DOID:0050585,congenital generalized lipodystrophy,DOID:811,lipodystrophy
+UBERON:2005020,central artery,UBERON:0003499,brain blood vessel
+UBERON:3010754,ramus recurrens,UBERON:0004732,segmental subdivision of nervous system
+UBERON:0010721,distal tarsal bone,UBERON:0001447,tarsal bone
+UBERON:2001960,ceratobranchial 4 bone distal cartilage,UBERON:4000003,permanent cartilage
+UBERON:0006345,stapedial artery,UBERON:0001637,artery
+UBERON:0005839,thoracic spinal cord dorsal column,UBERON:0006079,subdivision of spinal cord dorsal column
+UBERON:0004883,lung mesenchyme,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0003846,thymus epithelium,UBERON:0012275,meso-epithelium
+HP:0010873,Cervical spinal cord atrophy,HP:0006827,Atrophy of the spinal cord
+HP:0012086,Abnormal urinary color,HP:0003110,Abnormality of urine homeostasis
+UBERON:0000466,immaterial anatomical entity,UBERON:0001062,anatomical entity
+HP:0001007,Hirsutism,HP:0011362,Abnormal hair quantity
+DOID:10460,nasopharyngitis,DOID:9561,nasopharyngeal disease
+DOID:5535,gallbladder squamous cell carcinoma,DOID:4948,gallbladder carcinoma
+HP:0009743,Distichiasis,HP:0008496,Multiple rows of eyelashes
+UBERON:0009521,anal membrane endodermal component,UBERON:0005911,endo-epithelium
+UBERON:0006226,endolymphatic appendage,UBERON:0002050,embryonic structure
+HP:0005587,Profuse pigmented skin lesions,HP:0001000,Abnormality of skin pigmentation
+HP:0011179,Beta-EEG,HP:0011202,EEG with diffuse acceleration
+UBERON:0006220,diencephalic part of interventricular foramen,UBERON:0004121,ectoderm-derived structure
+HP:0011376,Morphological abnormality of the vestibule of the inner ear,HP:0011390,Morphological abnormality of the inner ear
+DOID:265,spleen angiosarcoma,DOID:0001816,angiosarcoma
+HP:0004910,Bicarbonate-wasting renal tubular acidosis,HP:0001947,Renal tubular acidosis
+UBERON:0011263,femoral gland,UBERON:0002365,exocrine gland
+HP:0000467,Neck muscle weakness,HP:0011006,Abnormality of the musculature of the neck
+HP:0004380,Aortic valve calcification,HP:0001646,Abnormality of the aortic valve
+HP:0006500,Abnormality involving the epiphyses of the lower limbs,HP:0006505,Abnormality involving the epiphyses of the limbs
+UBERON:0001683,jugal bone,UBERON:0008001,irregular bone
+UBERON:2001609,pharyngobranchial 2 bone uncinate process,UBERON:4100000,skeletal element projection
+HP:0011121,Abnormality of skin morphology,HP:0011354,Generalized abnormality of skin
+HP:0000975,Hyperhidrosis,HP:0000971,Abnormality of the sweat gland
+HP:0000790,Hematuria,HP:0012211,Abnormal renal physiology
+HP:0003333,Increased serum beta-hexosaminidase,HP:0004345,Abnormality of ganglioside metabolism
+UBERON:2001226,basibranchial 4 bone,UBERON:2001918,basibranchial 4 element
+UBERON:0003066,pharyngeal arch 2,UBERON:0002539,pharyngeal arch
+HP:0009348,Cone-shaped epiphysis of the proximal phalanx of the 3rd finger,HP:0009412,Cone-shaped epiphyses of the 3rd finger
+UBERON:0009060,air sac,UBERON:0000061,anatomical structure
+UBERON:0010900,tarsometatarsus cartilage element,UBERON:0010885,hindlimb cartilage element
+HP:0008435,Absent in utero ossification of vertebral bodies,HP:0004606,Unossified vertebral bodies
+UBERON:0004516,smooth muscle tissue of terminal bronchiole,UBERON:0004515,smooth muscle tissue of bronchiole
+HP:0001470,Sex-limited autosomal dominant,HP:0000006,Autosomal dominant inheritance
+UBERON:2007004,epiphysial cluster,UBERON:0004121,ectoderm-derived structure
+HP:0012371,Midface prominence,HP:0000309,Abnormality of the midface
+HP:0002795,Functional respiratory abnormality,HP:0002086,Abnormality of the respiratory system
+UBERON:3010463,animal cap,UBERON:0002050,embryonic structure
+UBERON:0005329,mesonephric nephron tubule,UBERON:0001231,nephron tubule
+UBERON:0007285,presumptive paraxial mesoderm,UBERON:0006598,presumptive structure
+HP:0009976,Duplication of the middle phalanx of the 4th finger,HP:0009283,Abnormality of the middle phalanx of the 4th finger
+HP:0010789,Abnormality of the Leydig cells,HP:0000035,Abnormality of the testis
+NCBITaxon:81093,Magnaporthaceae,NCBITaxon:639021,Magnaporthales
+UBERON:0004520,striated muscle tissue of prostate,UBERON:0008715,muscle tissue of prostate
+UBERON:0002728,entorhinal area,UBERON:0004121,ectoderm-derived structure
+UBERON:0004418,proximal epiphysis of phalanx of manual digit 2,UBERON:0004414,proximal epiphysis of phalanx of manus
+UBERON:2002077,lateropterygium,UBERON:0004375,bone of free limb or fin
+HP:0007920,Congenital chorioretinal dystrophy,HP:0001135,Chorioretinal dystrophy
+HP:0004968,Recurrent cerebral hemorrhage,HP:0001342,Cerebral hemorrhage
+UBERON:0015030,pedal digit phalanx endochondral element,UBERON:0015022,hindlimb endochondral element
+HP:0003688,Decreased activity of cytochrome C oxidase in muscle tissue,HP:0003800,Muscle abnormality related to mitochondrial dysfunction
+HP:0003351,Decreased circulating renin level,HP:0000847,Abnormality of renin-angiotensin system
+UBERON:0000423,eccrine sweat gland,UBERON:0001820,sweat gland
+UBERON:3000467,preorbital process of the pars facialis of the maxilla,UBERON:0004120,mesoderm-derived structure
+HP:0005472,Orbital craniosynostosis,HP:0001363,Craniosynostosis
+HP:0004912,Hypophosphatemic rickets,HP:0002748,Rickets
+UBERON:2001968,outer mental barbel,UBERON:2002024,mental barbel
+DOID:0050581,brachydactyly,DOID:1934,dysostosis
+UBERON:0004851,aorta endothelium,UBERON:0004638,blood vessel endothelium
+UBERON:0005315,alveolar secondary septum,UBERON:0004821,pulmonary alveolus epithelium
+UBERON:2001999,posterior cleithral process,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2201613,dorsal fin middle radial cartilage,UBERON:2201672,dorsal fin radial cartilage
+DOID:11976,botulism,DOID:0050338,primary bacterial infectious disease
+UBERON:0001145,ovarian vein,UBERON:0015212,lateral structure
+UBERON:0002709,posterior nuclear complex of thalamus,UBERON:0015233,nucleus of dorsal thalamus
+DOID:7492,central epithelioid sarcoma,DOID:6193,epithelioid sarcoma
+UBERON:2001773,anal fin lepidotrichium 5,UBERON:4000176,anal fin lepidotrichium
+UBERON:2000203,rhinosphenoid,UBERON:0003462,facial bone
+HP:0100058,Enlarged epiphyses of the 3rd toe,HP:0010329,Abnormality of the epiphyses of the 3rd toe
+DOID:2378,relapsing-remitting multiple sclerosis,DOID:2377,multiple sclerosis
+HP:0012729,Saccular descending thoracic aortic aneurysm,HP:0004954,Descending aortic aneurysm
+UBERON:0001693,exoccipital bone,UBERON:0011164,neurocranium bone
+HP:0006261,Abnormality of phalangeal joints of the hand,HP:0005918,Abnormality of phalanx of finger
+UBERON:0014690,left gastric vein,UBERON:0015212,lateral structure
+HP:0002187,"Intellectual disability, profound",HP:0001249,Intellectual disability
+HP:0009392,Triangular epiphyses of the 5th finger,HP:0010238,Triangular epiphyses of the phalanges of the hand
+UBERON:0002239,floating rib,UBERON:0002238,false rib
+HP:0009931,Enlarged naris,HP:0005288,Abnormality of the nares
+HP:0010601,Abnormality of the proximal ulnar epiphysis,HP:0004037,Abnormality of the ulnar epiphyses
+CL:0002536,amniotic epithelial cell,CL:0000066,epithelial cell
+HP:0003980,Pseudarthrosis of the radius,HP:0003965,Pseudarthrosis of the forearm bones
+CL:0000786,plasma cell,CL:0000946,antibody secreting cell
+UBERON:0006585,vestibular organ,UBERON:0000062,organ
+HP:0100393,Short middle phalanx of the 4th toe,HP:0100367,Short phalanx of the 4th toe
+UBERON:0008929,sublaminar layers S4 or S5,UBERON:0008921,substratum of layer of retina
+HP:0100650,Vaginal neoplasm,HP:0000142,Abnormality of the vagina
+UBERON:0004870,superficial cervical lymph node,UBERON:0003968,peripheral lymph node
+CL:0002147,clear chief cell of parathyroid cell,CL:0000446,chief cell of parathyroid gland
+DOID:5976,occlusion precerebral artery,DOID:6713,cerebrovascular disease
+HP:0011546,Abnormal atrioventricular connection,HP:0011545,Abnormal connection of the cardiac segments
+HP:0011659,Tetralogy of Fallot with absent pulmonary valve,HP:0005134,Absence of the pulmonary valve
+HP:0005100,premature birth following premature rupture of fetal membranes,HP:0001788,Premature rupture of membranes
+UBERON:0011967,costotransverse joint,UBERON:0004120,mesoderm-derived structure
+HP:0009946,Polydactyly affecting the 2nd finger,HP:0006159,Mesoaxial hand polydactyly
+UBERON:0003649,metacarpal bone of digit 5,UBERON:0002374,metacarpal bone
+UBERON:2001279,branchiostegal ray 1,UBERON:2000476,branchiostegal ray
+NCBITaxon:33511,Deuterostomia,NCBITaxon:33213,Bilateria
+UBERON:0001846,internal ear,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:2059,vulvar disease,DOID:229,female reproductive system disease
+UBERON:0014648,hemisphere part of cerebellar posterior lobe,UBERON:0002749,regional part of cerebellar cortex
+UBERON:0004654,temporal process of zygomatic bone,UBERON:4100000,skeletal element projection
+NCBITaxon:38946,Paracoccidioides,NCBITaxon:34383,mitosporic Onygenales
+UBERON:0003669,fascia lata,UBERON:0004266,upper leg connective tissue
+UBERON:0009593,mesenchyme of interdigital region between pedal digits 4 and 5,UBERON:0009599,mesenchyme of interdigital region between digits 4 and 5
+UBERON:0008187,hypertrophic cartilage zone,UBERON:0002418,cartilage tissue
+UBERON:0005273,nail bed,UBERON:0005275,dorsal skin of digit
+HP:0008181,Abetalipoproteinemia,HP:0003563,Hypobetalipoproteinemia
+UBERON:3000903,tibial crest,UBERON:0004120,mesoderm-derived structure
+UBERON:0001926,lateral geniculate body,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0005989,atrioventricular septum,UBERON:0002099,cardiac septum
+UBERON:0008791,rugal fold of stomach,UBERON:0008790,rugal fold
+CL:1000352,basal cell of epithelium of lobular bronchiole,CL:1000349,basal cell of epithelium of bronchus
+DOID:7327,pseudosarcomatous fibromatosis,DOID:9598,fasciitis
+DOID:312,tenosynovitis of foot and ankle,DOID:970,tenosynovitis
+HP:0004737,Global glomerulosclerosis,HP:0000096,Glomerulosclerosis
+UBERON:0003862,pedal digit 4 phalanx,UBERON:0015034,pedal digit 4 phalanx endochondral element
+UBERON:2000309,E-YSL,UBERON:0005291,embryonic tissue
+HP:0009356,Triangular epiphysis of the proximal phalanx of the 3rd finger,HP:0009420,Triangular epiphyses of the 3rd finger
+HP:0004736,Crossed fused renal ectopia,HP:0000086,Ectopic kidney
+HP:0005513,Increased megakaryocyte count,HP:0012143,Abnormality of cells of the megakaryocyte lineage
+UBERON:0010129,femur cartilage element,UBERON:0010885,hindlimb cartilage element
+HP:0003083,Dislocated radial head,HP:0003995,Abnormality of the radial head
+UBERON:2001415,pelvic fin distal radial bone 2,UBERON:2101415,pelvic fin distal radial element 2
+UBERON:0011156,facial skeleton,UBERON:0011158,primary subdivision of skull
+HP:0006615,Absent in utero rib ossification,HP:0012306,Abnormal rib ossification
+HP:0000078,Abnormality of the genital system,HP:0000119,Abnormality of the genitourinary system
+UBERON:1000023,spleen pulp,UBERON:0004120,mesoderm-derived structure
+CL:0000374,trichogen cell,CL:0000463,epidermal cell (sensu arthropoda)
+HP:0011285,Long-segment aganglionic megacolon,HP:0002251,Aganglionic megacolon
+HP:0007268,Aprosencephaly,HP:0007364,Aplasia/Hypoplasia of the cerebrum
+UBERON:0004222,stomach smooth muscle,UBERON:0004226,gastrointestinal system smooth muscle
+UBERON:0011940,arrector pili muscle of vibrissa,UBERON:0002033,arrector muscle of hair
+CL:0002281,type S enteroendocrine cell,CL:0000164,enteroendocrine cell
+HP:0003986,Exostoses of the radius,HP:0002818,Abnormality of the radius
+CL:0000010,cultured cell,CL:0000578,experimentally modified cell in vitro
+UBERON:0013198,cocoon,UBERON:0000463,portion of organism substance
+UBERON:2001430,pneumatic duct,UBERON:0003928,digestive system duct
+DOID:6345,malignant melanocytic neoplasm of the peripheral nerve sheath,DOID:5940,malignant peripheral nerve sheath tumor
+UBERON:3010837,Apical Supplementary Element,UBERON:0010931,intermandibularis
+UBERON:2005170,extrahepatic duct,UBERON:0003928,digestive system duct
+HP:0003948,Irregular epiphyses of the elbow,HP:0003842,Irregular epiphyses of the upper limbs
+DOID:10595,Charcot-Marie-Tooth disease,DOID:440,neuromuscular disease
+CL:1000315,endocardial cushion cell,CL:1000313,gastric goblet cell
+DOID:5897,ovarian clear cell adenofibroma,DOID:0060112,ovarian benign neoplasm
+DOID:5125,extrahepatic bile duct leiomyoma,DOID:0050624,gastrointestinal system benign neoplasm
+HP:0004307,Abnormal anatomic location of the heart,HP:0002564,Malformation of the heart and great vessels
+DOID:4404,occupational dermatitis,DOID:2773,contact dermatitis
+UBERON:0005709,upper jaw incisor epithelium,UBERON:0003355,epithelium of incisor
+UBERON:0006541,outer medulla inner stripe loop of henle,UBERON:0001288,loop of Henle
+UBERON:3000397,pars dentalis of premaxilla,UBERON:0004120,mesoderm-derived structure
+UBERON:0014287,medial accessory olive,UBERON:0002574,regional part of inferior olivary complex
+HP:0010858,EEG with hyperventilation-induced epileptiform discharges,HP:0011182,Epileptiform EEG discharges
+UBERON:0003563,telencephalon dura mater,UBERON:0003289,meninx of telencephalon
+UBERON:0009917,kidney corticomedullary boundary,UBERON:0000015,anatomical boundary
+DOID:979,angioid streaks of choroid,DOID:980,choroidal sclerosis
+UBERON:0001245,anus,UBERON:0004121,ectoderm-derived structure
+HP:0007132,Pallidal degeneration,HP:0012157,Subcortical cerebral atrophy
+DOID:4867,cervical adenoid cystic carcinoma,DOID:2893,cervix carcinoma
+HP:0003939,Humeroulnar synostosis,HP:0100745,Abnormality of the humeroulnar joint
+HP:0010159,Triangular epiphysis of the 1st metatarsal,HP:0010125,Abnormality of the epiphysis of the 1st metatarsal
+HP:0008151,Prolonged prothrombin time,HP:0012200,Abnormality of prothrombin
+CL:0002234,basal cell of prostatic acinus,CL:0002341,basal cell of prostate epithelium
+HP:0010770,Pilonidal fistula,HP:0010767,Sacrococcygeal pilonidal abnormality
+HP:0008573,Low-frequency sensorineural hearing impairment,HP:0000407,Sensorineural hearing impairment
+HP:0001310,Dysmetria,HP:0001251,Ataxia
+HP:0009732,Plexiform neurofibroma,HP:0001067,Neurofibromas
+UBERON:0008713,pectoral girdle and thoracic body wall skeletal muscle,UBERON:0001134,skeletal muscle tissue
+DOID:12714,Ellis-Van Creveld syndrome,DOID:0050737,autosomal recessive disease
+HP:0009263,Cone-shaped epiphysis of the proximal phalanx of the 4th finger,HP:0010270,Cone-shaped epiphyses of the proximal phalanges of the hand
+HP:0010005,Partial duplication of the middle phalanges of the hand,HP:0009999,Partial duplication of the phalanx of hand
+HP:0100211,Stippling of the epiphysis of the distal phalanx of the 5th toe,HP:0100097,Abnormality of the epiphysis of the distal phalanx of the 5th toe
+UBERON:0001689,malleus bone,UBERON:0015018,malleus endochondral element
+UBERON:3000993,otic and occipital,UBERON:0000064,organ part
+UBERON:0011859,internal acoustic meatus,UBERON:0004121,ectoderm-derived structure
+CL:0001018,immature CD8_alpha-low Langerhans cell,CL:0000840,immature conventional dendritic cell
+NCBITaxon:426437,Rhipicephalinae,NCBITaxon:6939,Ixodidae
+UBERON:3010802,courtship gland,UBERON:0004121,ectoderm-derived structure
+UBERON:2005344,preopticohypothalamic tract,UBERON:0002316,white matter
+DOID:580,acute urate nephropathy,DOID:557,kidney disease
+DOID:4917,villous adenocarcinoma,DOID:299,adenocarcinoma
+HP:0009244,Distal/middle symphalangism of 5th finger,HP:0001204,Distal symphalangism (hands)
+DOID:2891,thyroid adenoma,DOID:0060089,endocrine organ benign neoplasm
+HP:0100530,Abnormality of calcium-phosphate metabolism,HP:0001939,Abnormality of metabolism/homeostasis
+UBERON:2002185,climbing fiber,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0014639,frontal sulcus,UBERON:0013118,sulcus of brain
+NCBITaxon:186540,Sudan ebolavirus,NCBITaxon:186536,Ebolavirus
+DOID:2148,tuberculous oophoritis,DOID:2149,urogenital tuberculosis
+UBERON:0002794,medial longitudinal fasciculus of pons,UBERON:0002309,medial longitudinal fasciculus
+UBERON:0014837,pectoantebrachialis,UBERON:0001495,pectoral muscle
+UBERON:3000183,foramen acusticum posterius,UBERON:0005744,bone foramen
+DOID:12294,atypical depressive disorder,DOID:3324,mood disorder
+HP:0007446,Palmoplantar blistering,HP:0100871,Abnormality of the palm
+UBERON:4200159,ventral ridge system,UBERON:0004120,mesoderm-derived structure
+UBERON:0000323,late embryo,UBERON:0000922,embryo
+UBERON:0013278,canal of Nuck,UBERON:0006590,vestigial embryonic structure
+DOID:0050923,spindle epithelial tumor with thymus-like differentiation tumor,DOID:3963,thyroid carcinoma
+UBERON:0003971,interfrontal bone,UBERON:0003462,facial bone
+HP:0005947,Decreased sensitivity to hypoxemia,HP:0005957,Breathing dysregulation
+UBERON:0006958,great vein of heart,UBERON:0004148,cardiac vein
+HP:0002141,Gait imbalance,HP:0001288,Gait disturbance
+UBERON:0000177,pus,UBERON:0000463,portion of organism substance
+DOID:7598,cervical lymphoepithelioma-like carcinoma,DOID:3744,cervical squamous cell carcinoma
+UBERON:0004805,seminal vesicle epithelium,UBERON:0004910,epithelium of male gonad
+HP:0002721,Immunodeficiency,HP:0010978,Abnormality of immune system physiology
+HP:0002869,Flared iliac wings,HP:0011867,Abnormality of the wing of the ilium
+UBERON:0007843,uncinate process of ribs,UBERON:0004120,mesoderm-derived structure
+HP:0100251,Lipomas of the central neryous system,HP:0001012,Multiple lipomas
+HP:0002033,Poor suck,HP:0008872,Feeding difficulties in infancy
+UBERON:0003700,temporomandibular joint,UBERON:0015212,lateral structure
+DOID:0060137,auditory agnosia,DOID:4090,agnosia
+CL:0000186,myofibroblast cell,CL:0002371,somatic cell
+HP:0011647,Postductal coarctation of the aorta,HP:0012305,Coarctation of the descending aortic arch
+DOID:1240,leukemia,DOID:2531,hematologic cancer
+UBERON:0002180,ventral funiculus,UBERON:0006127,funiculus of spinal cord
+UBERON:0001191,common iliac artery,UBERON:0012254,abdominal aorta artery
+HP:0011058,Generalized periodontitis,HP:0000704,Periodontitis
+HP:0009287,Curved middle phalanx of the 4th finger,HP:0009283,Abnormality of the middle phalanx of the 4th finger
+DOID:8534,gastroesophageal reflux disease,DOID:77,gastrointestinal system disease
+DOID:9883,Becker muscular dystrophy,DOID:9884,muscular dystrophy
+HP:0011157,Auras,HP:0007359,Focal seizures
+UBERON:0003729,mouth mucosa,UBERON:0004121,ectoderm-derived structure
+UBERON:0005673,left lung endothelium,UBERON:0001986,endothelium
+CL:0000679,glutamatergic neuron,CL:0000540,neuron
+HP:0100639,Erectile abnormalities,HP:0000036,Abnormality of the penis
+HP:0005429,Recurrent systemic pyogenic infections,HP:0002718,Recurrent bacterial infections
+DOID:7922,benign mediastinal neurilemmoma,DOID:955,benign neurilemmoma
+DOID:8432,polycythemia,DOID:4961,bone marrow disease
+UBERON:0016397,submental lymph node,UBERON:0015870,lymph node of head
+HP:0011317,Right unicoronal synostosis,HP:0011315,Unicoronal synostosis
+DOID:9370,exophthalmos,DOID:5614,eye disease
+DOID:10207,paratesticular lipoma,DOID:0050622,reproductive organ benign neoplasm
+UBERON:0010025,dorsal part of pharyngeal pouch 3,UBERON:0005291,embryonic tissue
+CL:0002517,interrenal epinephrin secreting cell,CL:0000454,epinephrine secreting cell
+UBERON:3010499,coeliaco-mesenteric artery,UBERON:0001637,artery
+DOID:2626,choroid plexus papilloma,DOID:2615,papilloma
+UBERON:0002689,supraoptic crest,UBERON:0010135,sensory circumventricular organ
+UBERON:2000527,pharyngobranchial bone,UBERON:0002513,endochondral bone
+NCBITaxon:41819,Ceratopogonidae,NCBITaxon:41828,Chironomoidea
+UBERON:2000642,decussation of the medial octavolateralis nucleus,UBERON:0014649,white matter of medulla oblongata
+UBERON:0008945,extraembryonic endoderm,UBERON:0000490,unilaminar epithelium
+UBERON:0004720,cerebellar vermis,UBERON:0002749,regional part of cerebellar cortex
+HP:0100363,Aplasia of the phalanges of the 4th toe,HP:0010337,Aplasia/Hypoplasia of the 4th toe
+UBERON:0012072,palatal part of dermatocranium,UBERON:0000075,subdivision of skeletal system
+UBERON:0002551,interstitial nucleus of Cajal,UBERON:0007414,nucleus of midbrain tegmentum
+HP:0000473,Torticollis,HP:0011442,Abnormality of central motor function
+HP:0100450,Curved distal phalanx of the 4th toe,HP:0010374,Curved phalanges of the 4th toe
+UBERON:0013166,vallecula of cerebellum,UBERON:0004121,ectoderm-derived structure
+UBERON:0004166,superior reticular formation,UBERON:0002559,medullary reticular formation
+UBERON:3010011,axillary glands,UBERON:3010603,body gland
+DOID:7600,infiltrating bladder lymphoepithelioma-like carcinoma,DOID:6477,invasive bladder transitional cell carcinoma
+CL:0000096,mature neutrophil,CL:0000234,phagocyte
+HP:0009204,Bracket epiphysis of the middle phalanx of the 5th finger,HP:0004224,Abnormality of the epiphysis of the middle phalanx of the 5th finger
+UBERON:0001718,mesencephalic nucleus of trigeminal nerve,UBERON:0004132,trigeminal sensory nucleus
+HP:0002418,Abnormality of the midbrain,HP:0002363,Abnormality of the brainstem
+UBERON:0001245,anus,UBERON:0000161,orifice
+CL:0000099,interneuron,CL:0000540,neuron
+UBERON:0000044,dorsal root ganglion,UBERON:0001800,sensory ganglion
+HP:0002162,Low posterior hairline,HP:0009553,Abnormality of the hairline
+DOID:7998,hyperthyroidism,DOID:50,thyroid gland disease
+DOID:3282,dendritic cell thymoma,DOID:3275,thymoma
+UBERON:0002648,anterior median eminence,UBERON:0002784,regional part of diencephalon
+UBERON:0011238,mesethmoid bone,UBERON:0011164,neurocranium bone
+DOID:8338,villoglandular variant cervical mucinous adenocarcinoma,DOID:3701,cervical mucinous adenocarcinoma
+HP:0009301,Short proximal phalanx of the 4th finger,HP:0010241,Short proximal phalanx of finger
+UBERON:3000647,crista interna,UBERON:0010313,neural crest-derived structure
+UBERON:0002334,submandibular duct,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002212,macula of saccule of membranous labyrinth,UBERON:0000054,macula
+UBERON:0003694,atlanto-axial joint,UBERON:0004120,mesoderm-derived structure
+HP:0001106,Periorbital hyperpigmentation,HP:0001000,Abnormality of skin pigmentation
+UBERON:0005275,dorsal skin of digit,UBERON:0015249,digit skin
+HP:0002013,Vomiting,HP:0002017,Nausea and vomiting
+CL:0000295,somatotropin secreting cell,CL:0000167,peptide hormone secreting cell
+HP:0004272,Cortical thinning of hand bones,HP:0005926,Abnormalities of the cortex of hand bones
+HP:0002778,Abnormality of the trachea,HP:0005607,Abnormality of the tracheobronchial system
+HP:0009159,Small epiphysis of the proximal phalanx of the 5th finger,HP:0009153,Abnormality of the epiphysis of the proximal phalanx of the 5th finger
+DOID:3829,pituitary adenoma,DOID:0060089,endocrine organ benign neoplasm
+DOID:1963,fallopian tube carcinoma,DOID:1964,fallopian tube cancer
+CL:0002279,type L enteroendocrine cell,CL:0000167,peptide hormone secreting cell
+UBERON:0007145,dome of diaphragm,UBERON:0000064,organ part
+UBERON:2000711,DEL,UBERON:0002050,embryonic structure
+UBERON:0003985,major sublingual duct,UBERON:0001838,sublingual duct
+HP:0010116,Enlarged epiphyses of the hallux,HP:0010056,Abnormality of the epiphyses of the hallux
+HP:0006189,Prominent interdigital folds,HP:0001018,Abnormal palmar dermatoglyphics
+UBERON:0009654,alveolar artery,UBERON:0001637,artery
+DOID:3805,porokeratosis,DOID:161,keratosis
+UBERON:0004744,articular/anguloarticular,UBERON:0008907,dermal bone
+HP:0006789,Mitochondrial encephalopathy,HP:0001298,Encephalopathy
+CL:0000870,Peyer's patch macrophage,CL:0000885,gut-associated lymphoid tissue macrophage
+UBERON:0004023,ganglionic eminence,UBERON:0005423,developing anatomical structure
+HP:0009645,Osteolytic defects of the distal phalanx of the thumb,HP:0009839,Osteolytic defects of the distal phalanges of the hand
+DOID:9537,Lassa fever,DOID:934,viral infectious disease
+HP:0007957,Corneal opacity,HP:0000481,Abnormality of the cornea
+HP:0010001,Complete duplication of the distal phalanges of the hand,HP:0009998,Complete duplication of phalanx of hand
+UBERON:0015172,endometrial blood vessel,UBERON:0005156,reproductive structure
+UBERON:0010376,pancreas ventral primordium,UBERON:0002050,embryonic structure
+HP:0008666,Impaired histidine renal tubular absorption,HP:0000124,Renal tubular dysfunction
+UBERON:0011646,patagialis muscle,UBERON:0008196,muscle of pectoral girdle
+UBERON:0001957,submucosa of bronchus,UBERON:0004777,respiratory system submucosa
+UBERON:0001982,capillary,UBERON:0001981,blood vessel
+HP:0011617,Pulmonary situs ambiguus,HP:0011615,Abnormality of pulmonary situs
+DOID:12581,olecranon bursitis,DOID:204,enthesopathy
+UBERON:3000282,margo orbitalis of pterygoid,UBERON:0004120,mesoderm-derived structure
+UBERON:3010566,prootic foramen,UBERON:3000051,braincase and otic capsule opening
+CL:0000533,primary motor neuron,CL:0000100,motor neuron
+UBERON:0007712,fourth thoracic spinal ganglion,UBERON:0002835,thoracic dorsal root ganglion
+UBERON:0003395,mesentery of rectum,UBERON:0003334,serosa of rectum
+DOID:201,connective tissue cancer,DOID:0060100,musculoskeletal system cancer
+UBERON:0009697,epithelium of appendix,UBERON:0005636,caecum epithelium
+DOID:12357,viral labyrinthitis,DOID:1468,labyrinthitis
+DOID:0050922,gastrointestinal carcinoma,DOID:3119,gastrointestinal system cancer
+UBERON:0011932,pilosebaceous unit,UBERON:0000477,anatomical cluster
+HP:0009432,Curved middle phalanx of the 3rd finger,HP:0009442,Curved phalanges of the 3rd finger
+UBERON:0010549,pedal digit 3 metatarsal pre-cartilage condensation,UBERON:0010687,pedal digit metatarsal pre-cartilage condensation
+DOID:5520,head and neck squamous cell carcinoma,DOID:1542,head and neck carcinoma
+HP:0004646,Hypoplasia of the nasal bone,HP:0009924,Aplasia/Hypoplasia involving the nose
+UBERON:0003288,meninx of midbrain,UBERON:0003547,brain meninx
+UBERON:0008442,webbed pes,UBERON:0008440,webbed autopod
+UBERON:0005745,optic canal,UBERON:0013685,foramen of skull
+DOID:0060011,recombinase activating gene 1 deficiency,DOID:627,severe combined immunodeficiency
+HP:0006330,Rotated maxillary central incisors,HP:0000676,Abnormality of the incisor
+HP:0000134,Female hypogonadism,HP:0000135,Hypogonadism
+CL:0002166,epithelial cell of Malassez,CL:0002251,epithelial cell of alimentary canal
+UBERON:0002500,zygomatic arch,UBERON:0015212,lateral structure
+UBERON:0011808,outer epidermal layer of feather follicle,UBERON:0011807,epidermis of feather follicle
+UBERON:0007187,pericardial parietal mesothelium,UBERON:0007140,parietal mesothelium
+HP:0001680,Coarctation of aorta,HP:0001679,Abnormality of the aorta
+UBERON:0000946,cardial valve,UBERON:0004120,mesoderm-derived structure
+CL:1001599,pancreas exocrine glandular cell,CL:1001433,epithelial cell of exocrine pancreas
+UBERON:0006723,cochlear modiolus,UBERON:0010313,neural crest-derived structure
+UBERON:0010251,anterior meningeal artery,UBERON:0003474,meningeal artery
+HP:0009600,Flexion contracture of thumb,HP:0100490,Camptodactyly of finger
+DOID:3750,urethra squamous cell carcinoma,DOID:734,urethra cancer
+UBERON:0010049,supralabial gland,UBERON:0010047,oral gland
+UBERON:0001275,pubis,UBERON:0002513,endochondral bone
+UBERON:0005215,kidney interstitium,UBERON:0003567,abdomen connective tissue
+DOID:2580,rhizomelic chondrodysplasia punctata,DOID:630,genetic disease
+HP:0001360,Holoprosencephaly,HP:0002060,Abnormality of the cerebrum
+UBERON:0005992,pulmonary valve cusp,UBERON:0006009,cusp of cardiac valve
+UBERON:0010751,squamous part of temporal bone primordium,UBERON:0001048,primordium
+DOID:11812,bladder sarcoma,DOID:11054,urinary bladder cancer
+HP:0000640,Gaze-evoked nystagmus,HP:0000639,Nystagmus
+UBERON:0005809,cortex of manus bone,UBERON:0004120,mesoderm-derived structure
+UBERON:0006804,reticular tissue,UBERON:0011825,loose connective tissue
+UBERON:0001709,upper jaw region,UBERON:0011595,jaw region
+UBERON:0012328,penile spine,UBERON:0000479,tissue
+UBERON:4200133,crest,UBERON:0004529,anatomical projection
+UBERON:2001948,anal-fin hook,UBERON:0004121,ectoderm-derived structure
+CL:0002056,Fraction F mature B cell,CL:0000822,B-2 B cell
+DOID:4504,central nervous system angiosarcoma,DOID:2133,central nervous system sarcoma
+HP:0000631,Retinal arterial tortuosity,HP:0000630,Abnormality of retinal arteries
+UBERON:3000655,processus dorsalis of lamella alaris,UBERON:4100000,skeletal element projection
+UBERON:0003228,supinator muscle,UBERON:0004254,forelimb zeugopod muscle
+DOID:3620,central nervous system cancer,DOID:3093,nervous system cancer
+HP:0010318,Aplasia/Hypoplasia of the abdominal wall musculature,HP:0010991,Abnormality of the abdominal musculature
+UBERON:0016459,posterior pole of lens,UBERON:0000064,organ part
+HP:0009767,Aplasia/Hypoplasia of the phalanges of the hand,HP:0005918,Abnormality of phalanx of finger
+UBERON:0010293,suprachoroid lamina,UBERON:0010291,layer of sclera
+HP:0008717,Unilateral renal atrophy,HP:0012585,Renal atrophy
+HP:0100423,Partial duplication of the proximal phalanx of the 4th toe,HP:0100405,Duplication of the proximal phalanx of the 4th toe
+HP:0003206,Decreased activity of NADPH oxidase,HP:0004358,Abnormality of superoxide metabolism
+UBERON:0000970,eye,UBERON:0000020,sense organ
+HP:0010896,Hypersarcosinemia,HP:0010898,Abnormality of sarcosine metabolism
+HP:0010024,Epiphyseal stippling of the first metacarpal,HP:0009695,Stippling of the epiphyses of the thumb
+UBERON:0003034,central dorsal nucleus,UBERON:0015233,nucleus of dorsal thalamus
+DOID:566,labyrinthine dysfunction,DOID:3426,vestibular disease
+UBERON:2001587,pectoral fin proximal radial bone,UBERON:2101587,pectoral fin proximal radial element
+UBERON:2001361,basiventral,UBERON:2001457,postcranial axial cartilage
+UBERON:0014871,distal epiphysis of distal phalanx of pedal digit 1,UBERON:0014876,distal epiphysis of distal phalanx of pedal digit
+UBERON:1700006,paired fin radial cartilage,UBERON:2200271,radial cartilage
+CL:0000122,stellate cell,CL:0000117,CNS neuron (sensu Vertebrata)
+UBERON:3000446,posterior condyle,UBERON:0010313,neural crest-derived structure
+UBERON:0004444,proximal epiphysis of distal phalanx of manual digit 1,UBERON:0011979,epiphysis of distal phalanx of manus
+HP:0009917,Persistent pupillary membrane,HP:0000615,Abnormality of the pupil
+HP:0100152,Ivory epiphysis of the middle phalanx of the 3rd toe,HP:0100061,Ivory epiphyses of the 3rd toe
+HP:0000680,Delayed eruption of primary teeth,HP:0000684,Delayed eruption of teeth
+UBERON:1000013,nose vertex,UBERON:0001444,subdivision of head
+DOID:47,prostate disease,DOID:48,male reproductive system disease
+UBERON:0002210,syndesmosis,UBERON:0002213,cartilaginous joint
+UBERON:0007254,intervertebral disk of thoracic vertebra,UBERON:2001457,postcranial axial cartilage
+UBERON:0011267,quadratojugal bone,UBERON:0011597,bone of upper jaw
+UBERON:2005135,primary dental epithelium,UBERON:0003843,dental epithelium
+HP:0012753,T2 hypointense basal ganglia,HP:0012751,Abnormal basal ganglia MRI signal intensity
+UBERON:2001718,caudal principal ray 6,UBERON:2001585,caudal principal ray
+UBERON:0003632,pedal digit 2,UBERON:0001466,pedal digit
+HP:0010016,Bracket epiphysis of the 1st metacarpal,HP:0010269,Bracket epiphyses of the proximal phalanges of the hand
+HP:0003828,Variable expressivity,HP:0003812,Phenotypic variability
+UBERON:0003371,pelvic appendage bud ectoderm,UBERON:0000490,unilaminar epithelium
+HP:0005652,Cortical sclerosis,HP:0003103,Abnormal cortical bone morphology
+UBERON:0000082,adult mammalian kidney,UBERON:0002113,kidney
+UBERON:0005107,metanephric cap,UBERON:0005423,developing anatomical structure
+UBERON:0006321,superior oblique extraocular muscle,UBERON:0006532,oblique extraocular muscle
+UBERON:0002119,left ovary,UBERON:0000992,female gonad
+DOID:0050563,nonsyndromic deafness,DOID:2742,auditory system disease
+HP:0007352,Cerebellar calcifications,HP:0010766,Ectopic calcification
+UBERON:0005473,sacral region,UBERON:0011676,subdivision of organism along main body axis
+DOID:3764,Denys-Drash syndrome,DOID:0050736,autosomal dominant disease
+UBERON:0005148,metanephric S-shaped body,UBERON:0005146,metanephric nephron tubule
+HP:0003048,Radial head subluxation,HP:0003042,Elbow dislocation
+UBERON:0013188,monkey lips dorsal bursa complex,UBERON:0015212,lateral structure
+UBERON:2000240,metapterygoid,UBERON:0011597,bone of upper jaw
+UBERON:2001129,pharyngeal pouches 2-6,UBERON:0004117,pharyngeal pouch
+DOID:7165,subacute thyroiditis,DOID:7166,thyroiditis
+UBERON:0001601,extra-ocular muscle,UBERON:0004120,mesoderm-derived structure
+UBERON:2002223,pillar of the semicircular canal,UBERON:0000479,tissue
+UBERON:0008839,palmar pad,UBERON:0013622,manual autopod pad
+UBERON:0014797,hypobranchial group muscle,UBERON:0004120,mesoderm-derived structure
+DOID:10123,pigmentation disease,DOID:37,skin disease
+UBERON:0013501,cloacal sphincter,UBERON:0014783,cloacal muscle
+HP:0012147,Reduced quantity of Von Willebrand factor,HP:0012146,Abnormality of  von Willebrand factor
+HP:0004290,Sclerosis of hand bones with transverse striations,HP:0004281,Irregular sclerosis of hand bones
+NCBITaxon:693762,Schizaeales,NCBITaxon:3290,Polypodiopsida
+UBERON:0010380,enteric nerve,UBERON:0001021,nerve
+UBERON:0010733,alisphenoid cartilage element,UBERON:0006904,head mesenchyme from mesoderm
+UBERON:0008266,periodontal ligament,UBERON:0008846,skeletal ligament
+NCBITaxon:147541,Dothideomycetes,NCBITaxon:715962,dothideomyceta
+UBERON:0001543,popliteal lymph node,UBERON:0016398,lymph node of lower limb
+HP:0006499,Abnormality of femoral epiphyses,HP:0006500,Abnormality involving the epiphyses of the lower limbs
+DOID:0060072,benign neoplasm,DOID:14566,disease of cellular proliferation
+HP:0000315,Abnormality of the orbital region,HP:0000271,Abnormality of the face
+UBERON:0006871,footplate,UBERON:0010130,autopod plate
+HP:0001830,Postaxial foot polydactyly,HP:0010322,Abnormality of the 5th toe
+NCBITaxon:137,Spirochaetaceae,NCBITaxon:136,Spirochaetales
+DOID:1067,open-angle glaucoma,DOID:1686,glaucoma
+DOID:3146,lipid metabolism disorder,DOID:655,inherited metabolic disorder
+UBERON:0008927,sublaminar layers S1 or S2,UBERON:0008921,substratum of layer of retina
+UBERON:0001458,skin of lip,UBERON:0001084,skin of head
+UBERON:2002044,anterior limb of parapophysis 4,UBERON:4100000,skeletal element projection
+UBERON:3010820,suboccular arch,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0003958,Cross-fusion of the forearm bones,HP:0002973,Abnormality of the forearm
+HP:0009813,Upper limb phocomelia,HP:0009829,Phocomelia
+UBERON:0007276,crista of ampulla of lateral semicircular duct of membranous laybrinth,UBERON:0003240,epithelium of lateral semicircular canal
+UBERON:0015886,root of nail,UBERON:0004121,ectoderm-derived structure
+HP:0009407,Triangular shaped phalanges of the 4th finger,HP:0009774,Triangular shaped phalanges of the hand
+UBERON:0006618,atrium auricular region,UBERON:0000481,multi-tissue structure
+DOID:4186,articulation disorder,DOID:92,speech disorder
+UBERON:1000017,tip of external ear,UBERON:0001444,subdivision of head
+DOID:1875,impotence,DOID:1529,penile disease
+DOID:4045,muscle cancer,DOID:0060100,musculoskeletal system cancer
+CL:0000005,fibroblast neural crest derived,CL:0000057,fibroblast
+HP:0009291,Aplasia of the distal phalanx of the 4th finger,HP:0009881,Aplasia of the distal phalanges of the hand
+HP:0002156,Homocystinuria,HP:0003355,Aminoaciduria
+UBERON:0010898,gastralium,UBERON:0008907,dermal bone
+HP:0000589,Coloboma,HP:0012372,Abnormal eye morphology
+DOID:0050557,congenital muscular dystrophy,DOID:9884,muscular dystrophy
+HP:0000292,Loss of facial adipose tissue,HP:0000291,Abnormality of facial adipose tissue
+NCBITaxon:186801,Clostridia,NCBITaxon:1239,Firmicutes
+UBERON:0012296,urethral crest,UBERON:0006554,urinary system structure
+DOID:1742,drug psychosis,DOID:1203,drug-induced mental disorder
+UBERON:0004321,middle phalanx of manual digit 3,UBERON:0003637,manual digit 3 phalanx
+NCBITaxon:10243,Cowpox virus,NCBITaxon:10242,Orthopoxvirus
+DOID:4702,mongolian spot,DOID:37,skin disease
+HP:0011644,Coronary sinus diverticulum,HP:0011642,Abnormality of the coronary sinus
+UBERON:0004544,epididymis epithelium,UBERON:0005156,reproductive structure
+CL:1001009,kidney efferent arteriole cell,CL:1000612,kidney corpuscule cell
+UBERON:0002794,medial longitudinal fasciculus of pons,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0005439,Maxillozygomatic hypoplasia,HP:0010669,Cheekbone underdevelopment
+HP:0002089,Pulmonary hypoplasia,HP:0006703,Aplasia/Hypoplasia of the lungs
+DOID:6643,Baastrup's syndrome,DOID:1123,spondyloarthropathy
+HP:0006256,Abnormality of hand joint mobility,HP:0001155,Abnormality of the hand
+NCBITaxon:5501,Coccidioides immitis,NCBITaxon:5500,Coccidioides
+HP:0000590,Progressive external ophthalmoplegia,HP:0000544,External ophthalmoplegia
+HP:0007922,Hypermyelinated retinal fibers,HP:0000479,Abnormality of the retina
+UBERON:0006199,posterior auricular vein,UBERON:0006197,auricular vein
+UBERON:0007529,loose mesenchyme tissue,UBERON:0003104,mesenchyme
+HP:0012307,Spatulate ribs,HP:0000885,Broad ribs
+NCBITaxon:11103,Hepatitis C virus,NCBITaxon:11102,Hepacivirus
+UBERON:0006306,ulna cartilage element,UBERON:0010883,forelimb cartilage element
+HP:0009316,Abnormality of the phalanges of the 3rd finger,HP:0005918,Abnormality of phalanx of finger
+UBERON:0001328,lobe of prostate,UBERON:0005156,reproductive structure
+UBERON:0001974,lamina propria of esophagus,UBERON:0000030,lamina propria
+UBERON:3000875,spina pelvis posterior,UBERON:0004120,mesoderm-derived structure
+CL:0000335,mesenchyme condensation cell,CL:0000134,mesenchymal cell
+HP:0004020,Irregular ossification of the radial metaphysis,HP:0011849,Abnormal bone ossification
+UBERON:0005336,capillary layer of choroid,UBERON:0004121,ectoderm-derived structure
+UBERON:0006651,appendix testis,UBERON:0006590,vestigial embryonic structure
+DOID:2951,motion sickness,DOID:2952,inner ear disease
+HP:0003947,Delayed elbow epiphyseal ossification,HP:0003840,Delayed upper limb epiphyseal ossification
+DOID:0060073,lymphatic system cancer,DOID:0060083,immune system cancer
+HP:0008030,Retinal arteritis,HP:0000630,Abnormality of retinal arteries
+HP:0011949,Acute infectious pneumonia,HP:0011948,Acute respiratory tract infection
+DOID:9462,cholesteatoma of external ear,DOID:869,cholesteatoma
+UBERON:2000297,vagal lobe,UBERON:0007635,nucleus of medulla oblongata
+HP:0009755,Ankyloblepharon,HP:0000492,Abnormality of the eyelid
+UBERON:0012260,alular digit,UBERON:0002389,manual digit
+UBERON:4200134,antimere,UBERON:0000475,organism subdivision
+DOID:8644,gastroduodenitis,DOID:77,gastrointestinal system disease
+DOID:0060168,histidinemia,DOID:9265,histidine metabolism disease
+UBERON:0009522,lateral lingual swelling epithelium,UBERON:0005291,embryonic tissue
+HP:0010402,Triangular shaped proximal phalanx of the 2nd toe,HP:0010354,Triangular shaped phalanges of the 2nd toe
+UBERON:0001172,hepatic acinus,UBERON:0004119,endoderm-derived structure
+CL:0005014,auditory epithelial support cell,CL:0002491,auditory epithelial cell
+DOID:0080044,hypochondrogenesis,DOID:2256,osteochondrodysplasia
+UBERON:0002497,acromion,UBERON:0004530,bony projection
+UBERON:0005494,intermediate mesenchyme,UBERON:0005256,trunk mesenchyme
+UBERON:0002321,extraglomerular mesangium,UBERON:0006554,urinary system structure
+UBERON:0004313,distal phalanx of manual digit 4,UBERON:0014486,distal phalanx of digit 4
+UBERON:0007567,regenerating anatomical structure,UBERON:0000061,anatomical structure
+UBERON:0008892,internal gill,UBERON:0002535,gill
+HP:0000123,Nephritis,HP:0012211,Abnormal renal physiology
+CL:0010001,stromal cell of bone marrow,CL:0002092,bone marrow cell
+HP:0007508,Punctate palmar and solar hyperkeratosis,HP:0000962,Hyperkeratosis
+DOID:6262,follicular dendritic cell sarcoma,DOID:7849,dendritic cell sarcoma
+UBERON:0008345,ileal epithelium,UBERON:0013636,epithelium of intestinal villus
+HP:0001591,Bell-shaped thorax,HP:0001547,Abnormality of the rib cage
+UBERON:0001356,medial circumflex femoral artery,UBERON:0001637,artery
+UBERON:0015059,orbitosphenoid endochondral element,UBERON:0010363,endochondral element
+UBERON:4000162,median fin,UBERON:0008897,fin
+UBERON:0015453,subcutaneous lymph node,UBERON:0004120,mesoderm-derived structure
+NCBITaxon:6947,Prostigmata,NCBITaxon:83136,Trombidiformes
+UBERON:0005884,hyoid arch skeleton,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0010009,camera-type eye photoreceptor cell,CL:0000287,eye photoreceptor cell
+UBERON:0002583,commissure of superior colliculus,UBERON:0005970,brain commissure
+CL:0000577,type EC enteroendocrine cell,CL:0000458,serotonin secreting cell
+HP:0008454,Lumbar kyphosis,HP:0100712,Abnormality of the lumbar spine
+UBERON:0001496,ascending aorta,UBERON:0001515,thoracic aorta
+UBERON:0004417,proximal epiphysis of phalanx of manual digit 1,UBERON:0004414,proximal epiphysis of phalanx of manus
+UBERON:2000250,opercle,UBERON:0008907,dermal bone
+DOID:9765,emphysematous cholecystitis,DOID:1949,cholecystitis
+HP:0005449,Bridged sella turcica,HP:0002681,Deformed sella turcica
+UBERON:0008867,trabecular network of bone,UBERON:0000479,tissue
+DOID:4584,choroid plexus meningioma,DOID:3565,meningioma
+UBERON:0000024,forelimb wing,UBERON:0000023,wing
+UBERON:0006467,eleventh thoracic spinal cord segment,UBERON:0007715,thoracic subsegment of spinal cord
+HP:0010742,Edema of the upper limbs,HP:0000969,Edema
+UBERON:0001847,lobule of pinna,UBERON:0001444,subdivision of head
+UBERON:0010298,intramembranous scleral ossicle,UBERON:0002514,intramembranous bone
+HP:0100004,Pericardial mesothelioma,HP:0001697,Abnormality of the pericardium
+UBERON:3000763,epicoracoid bridge,UBERON:0000064,organ part
+UBERON:3010735,ramus anterior of CN VIII,UBERON:0004732,segmental subdivision of nervous system
+HP:0012245,Sex reversal,HP:0012244,Abnormal sex determination
+UBERON:4200080,fibular crest,UBERON:4100000,skeletal element projection
+UBERON:0004312,distal phalanx of manual digit 3,UBERON:0003865,distal phalanx of manus
+UBERON:0003633,pedal digit 3,UBERON:0006050,digit 3
+DOID:5866,juxtacortical chondrosarcoma,DOID:3371,chondrosarcoma
+UBERON:0001692,basioccipital bone,UBERON:0011164,neurocranium bone
+UBERON:0004145,outflow tract,UBERON:0004111,anatomical conduit
+HP:0000809,Urinary tract atresia,HP:0000079,Abnormality of the urinary system
+HP:0009281,Aplasia of the 4th finger,HP:0009380,Aplasia of the fingers
+UBERON:0006087,internal arcuate fiber bundle,UBERON:0000122,neuron projection bundle
+UBERON:0016425,epiphyseal plate of radius,UBERON:0002516,epiphyseal plate
+UBERON:0002880,pontobulbar nucleus,UBERON:0007635,nucleus of medulla oblongata
+DOID:7136,ampulla of Vater small cell carcinoma,DOID:4932,ampulla of Vater carcinoma
+UBERON:3010464,animal cap inner layer,UBERON:0002050,embryonic structure
+HP:0009257,Pseudoepiphysis of the distal phalanx of the 4th finger,HP:0009400,Pseudoepiphyses of the 4th finger
+CL:0002534,mature CD16-positive myeloid dendritic cell,CL:0002532,CD16-positive myeloid dendritic cell
+HP:0010788,Testicular neoplasm,HP:0000035,Abnormality of the testis
+HP:0009565,Aplasia of the distal phalanx of the 2nd finger,HP:0009881,Aplasia of the distal phalanges of the hand
+DOID:11235,chronic adhesive otitis media,DOID:2742,auditory system disease
+DOID:559,acute pyelonephritis,DOID:11400,pyelonephritis
+HP:0000642,Red-green dyschromatopsia,HP:0007641,Dyschromatopsia
+CL:0002196,hepatic oval stem cell,CL:0002195,hepatic stem cell
+UBERON:0015027,manual digit 3 phalanx endochondral element,UBERON:0015024,manual digit phalanx endochondral element
+UBERON:0004364,ectoplacental cone,UBERON:0005423,developing anatomical structure
+HP:0004891,Recurrent infections due to aspiration,HP:0002205,Recurrent respiratory infections
+CL:1000375,myocardial endocrine cell of septal division of left branch of atrioventricular bundle,CL:0002074,myocardial endocrine cell
+HP:0002803,Congenital contracture,HP:0001371,Flexion contracture
+HP:0003079,Defective DNA repair after ultraviolet radiation damage,HP:0003254,Abnormality of DNA repair
+UBERON:0011255,Eimer's organ,UBERON:0000020,sense organ
+HP:0004603,Hyperconvex vertebral body endplates,HP:0005106,Abnormality of the vertebral endplates
+DOID:11512,hepatic vein thrombosis,DOID:272,hepatic vascular disease
+UBERON:0003079,floor plate,UBERON:0005291,embryonic tissue
+UBERON:0016422,compact bone of long bone,UBERON:0001439,compact bone tissue
+HP:0004552,Scarring alopecia of scalp,HP:0000987,Atypical scarring of skin
+HP:0003939,Humeroulnar synostosis,HP:0003938,Synostosis involving the elbow
+UBERON:0015181,neck of tooth,UBERON:0004121,ectoderm-derived structure
+CL:0000631,labyrinth supporting cell,CL:0000630,supportive cell
+UBERON:0005995,mitral valve anulus,UBERON:0006008,fibrous ring of heart
+HP:0100059,Fragmentation of the epiphyses of the 3rd toe,HP:0010329,Abnormality of the epiphyses of the 3rd toe
+UBERON:0005029,mucosa of lacrimal canaliculus,UBERON:0004121,ectoderm-derived structure
+HP:0012728,Fusiform descending thoracic aortic aneurysm,HP:0004954,Descending aortic aneurysm
+HP:0010394,Abnormality of the proximal phalanx of the 5th toe,HP:0010184,Abnormality of the proximal phalanges of the toes
+HP:0009671,Pseudoepiphysis of the proximal phalanx of the thumb,HP:0010264,Pseudoepiphyses of the middle phalanges of the hand
+UBERON:2005376,dorsal fin distal radial bone 5,UBERON:2105376,dorsal fin distal radial element 5
+HP:0200018,Protanomaly,HP:0011519,Anomalous trichromacy
+UBERON:0009566,intestinal submucosa,UBERON:0000009,submucosa
+UBERON:0003658,hip muscle,UBERON:0010890,pelvic complex muscle
+DOID:13196,lingual goiter,DOID:12176,goiter
+UBERON:2002163,ural vertebra 1,UBERON:2002162,ural vertebra
+UBERON:0012135,prepollex skeleton,UBERON:0010712,limb skeleton subdivision
+HP:0009968,Partial duplication of the distal phalanx of the 3rd finger,HP:0009961,Partial duplication of the phalanges of the 3rd finger
+CL:0002535,epithelial cell of cervix,CL:0000066,epithelial cell
+UBERON:0007763,cerebellum culmen,UBERON:0004070,cerebellum vermis lobule
+UBERON:0001791,inner nuclear layer of retina,UBERON:0003902,retinal neural layer
+UBERON:0007286,presumptive floor plate,UBERON:0006598,presumptive structure
+UBERON:0002735,transverse pontine fibers,UBERON:0007702,tract of brain
+HP:0007947,Pericentral retinitis pigmentosa,HP:0000510,Retinitis pigmentosa
+UBERON:0011150,pharyngeal arch derived gill,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0001443,Abnormality of the gluteal musculature,HP:0001469,Abnormality of the musculature of the pelvis
+UBERON:0008928,sublaminar layers S2 or S3,UBERON:0008921,substratum of layer of retina
+UBERON:0008798,rugal fold of vagina,UBERON:0008790,rugal fold
+DOID:0080011,bone resorption disease,DOID:0080005,bone remodeling disease
+DOID:11367,congenital aphakia,DOID:110,lens disease
+HP:0010442,Polydactyly,HP:0011297,Abnormality of the digits
+HP:0010680,Elevated alkaline phosphatase of renal origin,HP:0010679,Elevated tissue non-specific alkaline phosphatase
+HP:0010256,Triangular epiphyses of the distal phalanges of the hand,HP:0010238,Triangular epiphyses of the phalanges of the hand
+DOID:5727,uterine ligament cancer,DOID:363,uterine cancer
+UBERON:0001336,membranous urethra of male or female,UBERON:0004120,mesoderm-derived structure
+CL:0000134,mesenchymal cell,CL:0002320,connective tissue cell
+UBERON:0005208,right atrium valve,UBERON:0004120,mesoderm-derived structure
+HP:0006026,Rounded epiphyses,HP:0005924,Abnormality of the epiphyses of the hand
+HP:0100052,Small epiphyses of the 2nd toe,HP:0010170,Small epiphyses of the toes
+UBERON:0004405,distal epiphysis of tibia,UBERON:0004383,epiphysis of tibia
+DOID:4795,Tay-Sachs disease AB variant,DOID:3321,gangliosidosis GM2
+UBERON:2001827,premaxillary-maxillary ligament,UBERON:0008846,skeletal ligament
+DOID:10487,Hirschsprung's disease,DOID:11372,megacolon
+HP:0005613,Aplasia/hypoplasia of the femur,HP:0002823,Abnormality of the femur
+UBERON:0009470,postsphenoidal bone,UBERON:0003462,facial bone
+HP:0002198,Dilated fourth ventricle,HP:0010950,Abnormality of the fourth ventricle
+UBERON:0003556,forebrain arachnoid mater,UBERON:0002362,arachnoid mater
+DOID:4267,akinetic mutism,DOID:936,brain disease
+UBERON:2001525,hypobranchial 2 cartilage,UBERON:2001522,hypobranchial cartilage
+CL:0000329,oxygen accumulating cell,CL:0000003,native cell
+DOID:14039,POEMS syndrome,DOID:2916,hypersensitivity reaction type IV disease
+HP:0010444,Pulmonary insufficiency,HP:0001641,Abnormality of the pulmonary valve
+CL:0002280,type N enteroendocrine cell,CL:0000164,enteroendocrine cell
+HP:0001492,Axenfeld anomaly,HP:0007700,Anterior segment dysgenesis
+UBERON:0002106,spleen,UBERON:0002075,viscus
+DOID:13743,spinal cord lipoma,DOID:5612,spinal cancer
+HP:0012235,Drug-induced agranulocytosis,HP:0012234,Agranulocytosis
+UBERON:0005274,proximal nail bed,UBERON:0005275,dorsal skin of digit
+UBERON:0005278,nail bed of finger,UBERON:0005276,dorsal skin of finger
+UBERON:3000904,apophysis distalis of tibiofibula,UBERON:0004120,mesoderm-derived structure
+DOID:3213,demyelinating disease,DOID:1289,neurodegenerative disease
+HP:0002415,Leukodystrophy,HP:0011400,Abnormal CNS myelination
+HP:0011059,Localized periodontitis,HP:0000704,Periodontitis
+UBERON:0007148,lumen of hindgut,UBERON:0000464,anatomical space
+UBERON:3000543,retroarticular process,UBERON:4100000,skeletal element projection
+HP:0100766,Abnormality of the lymphatic vessels,HP:0100763,Abnormality of the lymphatic system
+HP:0002526,Deficit in nonword repetition,HP:0002167,Neurological speech impairment
+DOID:5728,diffuse peritoneal leiomyomatosis,DOID:5138,leiomyomatosis
+HP:0003779,Antegonial notching of mandible,HP:0010753,Midline defect of mandible
+UBERON:0008775,proximal epiphysis of fibula,UBERON:0004388,epiphysis of fibula
+DOID:10742,cerebral lipidosis,DOID:1443,cerebral degeneration
+UBERON:0003644,kidney arterial blood vessel,UBERON:0003509,arterial blood vessel
+NCBITaxon:28216,Betaproteobacteria,NCBITaxon:1224,Proteobacteria
+DOID:7214,noninvasive malignant thymoma,DOID:3275,thymoma
+UBERON:0007351,nucleus isthmo-opticus,UBERON:0002791,regional part of telencephalon
+UBERON:0001338,urethral gland,UBERON:0004120,mesoderm-derived structure
+CL:0002200,oxyphil cell of thyroid,CL:0002198,oncocyte
+DOID:0050635,alternating hemiplegia of childhood,DOID:10969,hemiplegia
+UBERON:0015454,pancreatic fat pad,UBERON:0003586,trunk connective tissue
+UBERON:0006145,dorsal digital artery of pes,UBERON:0006163,dorsal digital artery
+DOID:10986,discitis,DOID:1222,cartilage disease
+HP:0010158,Stippling of the epiphysis of the 1st metatarsal,HP:0010125,Abnormality of the epiphysis of the 1st metatarsal
+HP:0000557,Buphthalmos,HP:0001087,Congenital glaucoma
+HP:0100362,Aplasia of the phalanges of the 3rd toe,HP:0010745,Aplasia of the phalanges of the toes
+UBERON:0011597,bone of upper jaw,UBERON:0012360,bone of jaw
+DOID:7825,chronic toxic polyneuropathy,DOID:5221,chronic polyneuropathy
+UBERON:0004657,mandible condylar process,UBERON:4100000,skeletal element projection
+UBERON:0015479,scrotum skin,UBERON:0000014,zone of skin
+DOID:10459,common cold,DOID:974,upper respiratory tract disease
+HP:0100867,Duodenal stenosis,HP:0002246,Abnormality of the duodenum
+DOID:0014667,disease of metabolism,DOID:4,disease
+DOID:7807,choroid necrotic melanoma,DOID:7808,necrotic uveal melanoma
+UBERON:0006729,liver perisinusoidal space,UBERON:0000464,anatomical space
+HP:0010004,Partial duplication of the distal phalanges of the hand,HP:0009999,Partial duplication of the phalanx of hand
+DOID:5576,inhibited male orgasm,DOID:48,male reproductive system disease
+UBERON:0001068,skin of back,UBERON:0001085,skin of trunk
+HP:0002356,Writer's cramp,HP:0004373,Focal dystonia
+CL:1000314,gastric cardiac gland goblet cell,CL:1000313,gastric goblet cell
+DOID:0050777,Joubert syndrome,DOID:0050737,autosomal recessive disease
+NCBITaxon:543,Enterobacteriaceae,NCBITaxon:91347,Enterobacteriales
+UBERON:0001927,medial geniculate body,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:3010759,ramus buccal,UBERON:3010105,anterodorsal lateral line nerve (ADLLN)
+UBERON:0014441,ischial ramus,UBERON:0005913,zone of bone organ
+DOID:2234,focal epilepsy,DOID:1826,epilepsy syndrome
+CL:1000312,bronchial goblet cell,CL:0002370,respiratory goblet cell
+UBERON:0002414,lumbar vertebra,UBERON:0004247,bone of dorsum
+HP:0010699,Triangular nuclear cataract,HP:0100018,Nuclear cataract
+UBERON:2001257,medial floor plate,UBERON:0005291,embryonic tissue
+HP:0003956,Bowed forearm bones,HP:0006488,Bowing of the arm
+HP:0009308,Symphalangism of middle phalanx of 4th finger,HP:0009849,Symphalangism of middle phalanx of finger
+DOID:11037,dissociative amnesia,DOID:10935,dissociative disorder
+HP:0012379,Abnormal enzyme/coenzyme activity,HP:0001939,Abnormality of metabolism/homeostasis
+DOID:3076,adult astrocytic tumour,DOID:3069,astrocytoma
+HP:0012604,Hyponatriuria,HP:0012603,Abnormal urine sodium concentration
+UBERON:0006852,glomerular visceral epithelium,UBERON:0004188,glomerular epithelium
+UBERON:1000024,parenchyma of spleen,UBERON:0004120,mesoderm-derived structure
+UBERON:0008924,sublaminar layer S3,UBERON:0009735,sublaminar layers S1 or S3 or S4
+UBERON:0005805,dorsal aorta,UBERON:0000947,aorta
+UBERON:0013277,remnant of processus vaginalis,UBERON:0006590,vestigial embryonic structure
+DOID:0050572,cone-rod dystrophy,DOID:8466,retinal degeneration
+UBERON:2005026,primary head sinus,UBERON:0003496,head blood vessel
+DOID:4633,nasal cavity inverting papilloma,DOID:9310,nasal cavity neoplasm
+HP:0006441,Lateral humeral condyle aplasia,HP:0003063,Abnormality of the humerus
+UBERON:0010291,layer of sclera,UBERON:0004121,ectoderm-derived structure
+UBERON:3010838,Anterolateral Supplementary Element,UBERON:0010931,intermandibularis
+UBERON:3000036,basal process of palatoquadrate,UBERON:0004530,bony projection
+DOID:5113,nutritional deficiency disease,DOID:374,nutrition disease
+UBERON:0006598,presumptive structure,UBERON:0005423,developing anatomical structure
+HP:0010807,Open bite,HP:0000692,Misalignment of teeth
+HP:0000421,Epistaxis,HP:0001892,Abnormal bleeding
+UBERON:0001354,inferior epigastric artery,UBERON:0004573,systemic artery
+UBERON:2005343,endohypothalamic tract,UBERON:0002316,white matter
+HP:0010384,Broad phalanges of the 5th toe,HP:0010174,Broad phalanx of the toes
+CL:0000209,taste receptor cell,CL:0000362,epidermal cell
+UBERON:0005672,right lung endothelium,UBERON:0001986,endothelium
+UBERON:2005038,supraintestinal vein,UBERON:0001638,vein
+UBERON:0005332,mesonephric S-shaped body,UBERON:0010534,primitive mesonephric nephron
+HP:0006313,Widely spaced primary teeth,HP:0006481,Abnormality of primary teeth
+UBERON:0006912,urinary bladder muscularis mucosa,UBERON:0006676,muscularis mucosa
+UBERON:2001063,posterior caudal vein,UBERON:0003481,tail vein
+UBERON:0002336,corpus callosum,UBERON:0005340,dorsal telencephalic commissure
+UBERON:3010092,basitrabecular process,UBERON:0004530,bony projection
+UBERON:0007311,sputum,UBERON:0006538,respiratory system fluid/secretion
+UBERON:3000437,planum conchale,UBERON:0003406,cartilage of respiratory system
+HP:0010771,Pilonidal abscess,HP:0010767,Sacrococcygeal pilonidal abnormality
+UBERON:2000274,rostral octaval nerve sensory nucleus,UBERON:2000401,octaval nerve sensory nucleus
+UBERON:0002397,maxilla,UBERON:0002514,intramembranous bone
+UBERON:0004233,lower respiratory tract smooth muscle,UBERON:0004225,respiratory system smooth muscle
+CL:1001285,vasa recta descending limb cell,CL:1001036,vasa recta cell
+UBERON:0010127,future dorsal motor nucleus of vagus,UBERON:0000125,neural nucleus
+HP:0000169,Gingival fibromatosis,HP:0000168,Abnormality of the gingiva
+UBERON:2001020,myotome somite 30,UBERON:0003082,myotome
+DOID:9682,yellow fever,DOID:37,skin disease
+UBERON:0006517,kidney calyx,UBERON:0000063,organ segment
+UBERON:0005106,metanephric tubule,UBERON:0003914,epithelial tube
+HP:0002312,Clumsiness,HP:0002311,Incoordination
+UBERON:0000411,visual cortex,UBERON:0002619,regional part of cerebral cortex
+UBERON:0006869,electric organ,UBERON:0000062,organ
+UBERON:0002432,pars intermedia of adenohypophysis,UBERON:0000064,organ part
+UBERON:2002013,ascending limb of ceratobranchial 5 bone,UBERON:4100000,skeletal element projection
+HP:0002845,Increased number of peripheral CD3+ T cells,HP:0100828,Increase in T cell number
+UBERON:3010116,lower eyelid texture,UBERON:3000972,head external integument structure
+CL:0000187,muscle cell,CL:0002371,somatic cell
+UBERON:0007383,enveloping layer of ectoderm,UBERON:0000490,unilaminar epithelium
+HP:0011646,Juxtaductal coarctation of the aorta,HP:0012305,Coarctation of the descending aortic arch
+HP:0100212,Triangular epiphysis of the distal phalanx of the 5th toe,HP:0100097,Abnormality of the epiphysis of the distal phalanx of the 5th toe
+HP:0100856,Poorly ossified vertebrae,HP:0004599,Absent or minimally ossified vertebral bodies
+HP:0005253,Increased anterioposterior diameter of thorax,HP:0100625,Enlarged thorax
+UBERON:0002141,parvocellular oculomotor nucleus,UBERON:0007414,nucleus of midbrain tegmentum
+CL:0011112,magnocellular neurosecretory cell,CL:0000540,neuron
+UBERON:2001233,hypobranchial 1 bone,UBERON:2000363,hypobranchial bone
+UBERON:0007308,pronephric distal early tubule,UBERON:0005310,pronephric nephron tubule
+UBERON:0010418,urethral opening,UBERON:0006554,urinary system structure
+DOID:7516,childhood central nervous system mixed germ cell tumor,DOID:6052,central nervous system childhood germ cell tumor
+HP:0008528,Long hairs growing from helix of pinna,HP:0011039,Abnormality of the helix
+DOID:13027,transient global amnesia,DOID:10914,amnestic disorder
+HP:0001719,Double outlet right ventricle,HP:0001710,Conotruncal defect
+UBERON:0004358,caput epididymis,UBERON:0005156,reproductive structure
+DOID:2907,Goldenhar syndrome,DOID:225,syndrome
+UBERON:2201588,pectoral fin distal radial cartilage,UBERON:2201586,pectoral fin radial cartilage
+HP:0000580,Pigmentary retinopathy,HP:0000479,Abnormality of the retina
+HP:0009130,Hand muscle atrophy,HP:0007149,Distal upper limb amyotrophy
+UBERON:0005707,upper jaw incisor odontogenic papilla,UBERON:0003317,odontogenic papilla of incisor
+DOID:133,vaginal mullerian papilloma,DOID:134,vaginal glandular tumor
+HP:0011316,Left unicoronal synostosis,HP:0011315,Unicoronal synostosis
+UBERON:0001591,thymic vein,UBERON:0001638,vein
+HP:0012079,Abnormality of central motor conduction,HP:0011442,Abnormality of central motor function
+UBERON:0010024,ventral part of pharyngeal pouch 2,UBERON:0005291,embryonic tissue
+HP:0005830,Flexion contracture of toe,HP:0008366,Contractures involving the joints of the feet
+HP:0009308,Symphalangism of middle phalanx of 4th finger,HP:0004197,Symphalangism of the 4th finger
+CL:0002121,CD24-negative CD38-negative IgG-negative class switched memory B cell,CL:0002118,CD38-negative IgG-negative class switched memory B cell
+HP:0012366,Basilar invagination,HP:0000932,Abnormality of the posterior cranial fossa
+CL:0002676,neural crest derived neuroblast,CL:0000337,neuroblast (sensu Vertebrata)
+UBERON:2000526,intermuscular bone,UBERON:0002513,endochondral bone
+UBERON:2000910,medial forebrain bundle telencephalon,UBERON:2000597,telencephalic tracts
+UBERON:0012175,acoustico-facial VII-VIII ganglion complex,UBERON:0010313,neural crest-derived structure
+NCBITaxon:1773,Mycobacterium tuberculosis,NCBITaxon:77643,Mycobacterium tuberculosis complex
+UBERON:0013758,cervical os,UBERON:0005156,reproductive structure
+UBERON:0006174,pronephric sinus,UBERON:0006171,renal sinus
+DOID:1726,partial of retinal vein occlusion,DOID:1727,retinal vein occlusion
+UBERON:0011688,pre-enameloid,UBERON:0010365,odontoid tissue
+UBERON:0011534,abductor pollicis muscle,UBERON:0003662,forelimb muscle
+HP:0003149,Hyperuricosuria,HP:0004368,Increased purine levels
+UBERON:0015599,genu of corpus callosum,UBERON:0002791,regional part of telencephalon
+DOID:11629,pelvic muscle wasting,DOID:1284,prolapse of female genital organ
+UBERON:0000410,bronchial mucosa,UBERON:0004119,endoderm-derived structure
+UBERON:0011910,gastrocnemius externus,UBERON:0004256,hindlimb zeugopod muscle
+DOID:12287,Crimean-Congo hemorrhagic fever,DOID:934,viral infectious disease
+UBERON:0009116,thymoid,UBERON:0005058,hemolymphoid system gland
+UBERON:3000281,margo orbitalis of maxilla,UBERON:0000064,organ part
+DOID:13964,Morgagni cataract,DOID:9669,senile cataract
+HP:0005920,Abnormality of the epiphyses of the phalanges of the hand,HP:0005918,Abnormality of phalanx of finger
+HP:0007427,Reticulated skin pigmentation,HP:0001000,Abnormality of skin pigmentation
+UBERON:0014609,thoracic spinal cord dorsal horn,UBERON:0002256,dorsal horn of spinal cord
+UBERON:0006006,metoptic pilar,UBERON:0004120,mesoderm-derived structure
+UBERON:2002029,pectoral fin proximal radial bone 4,UBERON:2001587,pectoral fin proximal radial bone
+UBERON:0014547,sacral spinal cord central canal,UBERON:0014538,subdivision of spinal cord central canal
+CL:0000025,egg cell,CL:0000675,female gamete
+HP:0009203,Absent epiphysis of the middle phalanx of the 5th finger,HP:0004224,Abnormality of the epiphysis of the middle phalanx of the 5th finger
+UBERON:0003008,dorsal longitudinal fasciculus of hypothalamus,UBERON:0003045,dorsal longitudinal fasciculus
+HP:0010619,Fibroma of the breast,HP:0100013,Neoplasm of the breast
+HP:0100086,Stippling of the epiphyses of the 5th toe,HP:0010171,Epiphyseal stippling of toe phalanges
+HP:0010396,Broad proximal phalanx of the 2nd toe,HP:0010348,Broad phalanges of the 2nd toe
+CL:0000079,stratified epithelial cell,CL:0002371,somatic cell
+UBERON:0004320,middle phalanx of manual digit 2,UBERON:0003636,manual digit 2 phalanx
+CL:0000389,socket cell (sensu Nematoda),CL:0000658,cuticle secreting cell
+HP:0002232,Patchy alopecia,HP:0001596,Alopecia
+CL:0002270,type EC2 enteroendocrine cell,CL:0000577,type EC enteroendocrine cell
+UBERON:0004106,crus of ear,UBERON:0001867,cartilage of external ear
+HP:0012021,Persistent patent ductus venosus,HP:0010948,Abnormality of the fetal cardiovascular system
+NCBITaxon:119060,Burkholderiaceae,NCBITaxon:80840,Burkholderiales
+UBERON:3000646,margo libera,UBERON:0010313,neural crest-derived structure
+UBERON:0001896,medulla oblongata,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0000689,Dental malocclusion,HP:0000692,Misalignment of teeth
+CL:0000872,splenic marginal zone macrophage,CL:0000871,splenic macrophage
+HP:0009768,Broad phalanges of the hand,HP:0005918,Abnormality of phalanx of finger
+CL:0000718,cone cell (sensu Endopterygota),CL:0000306,crystallin accumulating cell
+UBERON:0010011,collection of basal ganglia,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0014458,female bulbospongiosus muscle,UBERON:0014404,female anatomical structure
+UBERON:0012073,tooth of palatine bone,UBERON:0012070,palatal tooth
+UBERON:0002981,pulvinar nucleus,UBERON:0015233,nucleus of dorsal thalamus
+CL:0000684,littoral cell of liver,CL:0000182,hepatocyte
+CL:0000828,thromboblast,CL:0000839,myeloid lineage restricted progenitor cell
+UBERON:2000324,caudal periventricular hypothalamus,UBERON:0006568,hypothalamic nucleus
+UBERON:0013769,uterine lumen,UBERON:0002558,organ cavity
+UBERON:3000182,foramen acusticum minus,UBERON:0005744,bone foramen
+UBERON:3000449,posterior maxillary process dorsal process,UBERON:0010313,neural crest-derived structure
+UBERON:0003986,minor sublingual duct,UBERON:0001838,sublingual duct
+HP:0010115,Cone-shaped epiphyses of the hallux,HP:0010056,Abnormality of the epiphyses of the hallux
+DOID:0050664,Bietti crystalline corneoretinal dystrophy,DOID:8466,retinal degeneration
+DOID:8179,cervical atypical polypoid adenomyoma,DOID:4993,atypical polypoid adenomyoma
+CL:0002255,stromal cell of endometrium,CL:0002149,epithelial cell of uterus
+HP:0008635,Hypertrophy of the urinary bladder,HP:0000014,Abnormality of the bladder
+UBERON:0001070,external carotid artery,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0003083,Dislocated radial head,HP:0100744,Abnormality of the humeroradial joint
+DOID:1509,avoidant personality disorder,DOID:1510,personality disorder
+UBERON:0002153,fastigial nucleus,UBERON:0008995,nucleus of cerebellar nuclear complex
+UBERON:0015793,induseum griseum,UBERON:0002437,cerebral hemisphere white matter
+HP:0002444,Hypothalamic hamartoma,HP:0012286,Abnormal hypothalamus morphology
+DOID:3283,invasive malignant thymoma,DOID:3275,thymoma
+UBERON:2205385,dorsal fin proximal radial cartilage 8,UBERON:2200947,dorsal fin proximal radial cartilage
+HP:0000599,Abnormality of the frontal hairline,HP:0000290,Abnormality of the forehead
+DOID:12125,neurotrophic keratoconjunctivitis,DOID:9368,keratoconjunctivitis
+HP:0009397,Fragmentation of the epiphyses of the 4th finger,HP:0010232,Fragmentation of the epiphyses of the phalanges of the hand
+HP:0001403,Macrovesicular hepatic steatosis,HP:0001397,Hepatic steatosis
+UBERON:0013468,zygomatic fossa,UBERON:0008789,cranial fossa
+CL:0000705,R6 photoreceptor cell,CL:0000488,visible light photoreceptor cell
+HP:0010837,Decreased serum ceruloplasmin,HP:0010836,Abnormality of copper homeostasis
+UBERON:0007709,superior cerebellar peduncle of pons,UBERON:0003035,regional part of cerebellar white matter
+CL:0002184,basal proper cell of olfactory epithelium,CL:0002169,basal cell of olfactory epithelium
+UBERON:0000429,enteric plexus,UBERON:0001816,autonomic nerve plexus
+UBERON:0011288,stomochord,UBERON:0000481,multi-tissue structure
+UBERON:0010123,future facial nucleus,UBERON:0002020,gray matter of neuraxis
+UBERON:3000283,margo orbitalis of squamosal,UBERON:0004120,mesoderm-derived structure
+HP:0001639,Hypertrophic cardiomyopathy,HP:0001638,Cardiomyopathy
+UBERON:2001703,infraorbital 8,UBERON:2000376,infraorbital
+HP:0005880,Metacarpophalangeal synostosis,HP:0009701,Metacarpal synostosis
+HP:0012462,Chin myoclonus,HP:0001336,Myoclonus
+HP:0002273,Tetraparesis,HP:0010549,Paralysis due to lesions of the principle motor tracts
+HP:0005116,Arterial tortuosity,HP:0011004,Abnormality of the systemic arterial tree
+UBERON:0012176,comb,UBERON:0000021,cutaneous appendage
+UBERON:2000498,dilator operculi,UBERON:0011648,jaw muscle
+UBERON:0005054,dorsal nerve cord,UBERON:0004121,ectoderm-derived structure
+UBERON:0004488,musculature of pes,UBERON:0004482,musculature of lower limb
+DOID:6199,cornea cancer,DOID:2174,ocular cancer
+UBERON:0009655,auricular artery,UBERON:0001637,artery
+HP:0008072,Maternal virilization in pregnancy,HP:0002686,Prenatal maternal abnormality
+UBERON:0001449,phalanx of pes,UBERON:0015030,pedal digit phalanx endochondral element
+UBERON:0006790,deep white layer of superior colliculus,UBERON:0006793,deep layer of superior colliculus
+UBERON:0000162,cloaca,UBERON:0004120,mesoderm-derived structure
+CL:0000613,basophil progenitor cell,CL:0002191,granulocytopoietic cell
+UBERON:0006955,uterine epithelium,UBERON:0004804,oviduct epithelium
+HP:0004839,Pyropoikilocytosis,HP:0004447,Poikilocytosis
+UBERON:0009866,Hatschek's nephridium,UBERON:0006554,urinary system structure
+HP:0100377,Aplasia/Hypoplasia of the proximal phalanx of the 5th toe,HP:0010343,Aplasia/Hypoplasia of the 5th toe
+UBERON:0010389,pterygoid bone,UBERON:0012071,palate bone
+UBERON:0014740,dorsal pallium,UBERON:0002791,regional part of telencephalon
+DOID:0060012,recombinase activating gene 2 deficiency,DOID:627,severe combined immunodeficiency
+HP:0009965,Complete duplication of the distal phalanx of the 3rd finger,HP:0009962,Duplication of the distal phalanx of the 3rd finger
+HP:0010731,Extension of eyebrows towards upper eyelid,HP:0011229,Broad eyebrow
+NCBITaxon:86056,Rhinocladiella mackenziei,NCBITaxon:5587,Rhinocladiella
+HP:0012129,Abnormality of bone marrow stromal cells,HP:0005561,Abnormality of bone marrow cell morphology
+UBERON:0005268,renal cortex artery,UBERON:0001637,artery
+UBERON:3010465,animal cap outer layer,UBERON:0002050,embryonic structure
+DOID:320,vascular myelopathy,DOID:319,spinal cord disease
+UBERON:0010885,hindlimb cartilage element,UBERON:0007844,cartilage element
+UBERON:0014509,distal sesamoid impar ligament,UBERON:0008846,skeletal ligament
+HP:0009990,Duplication of the proximal phalanx of the 5th finger,HP:0009985,Duplication of phalanx of 5th finger
+CL:1001571,hippocampal pyramidal neuron,CL:0002608,hippocampal neuron
+UBERON:0003424,mesenchyme of hard palate,UBERON:0003323,mesenchyme of upper jaw
+HP:0000499,Abnormality of the eyelashes,HP:0001595,Abnormality of the hair
+HP:0010263,Ivory epiphyses of the middle phalanges of the hand,HP:0010234,Ivory epiphyses of the phalanges of the hand
+HP:0004993,Slender long bones with narrow diaphyses,HP:0003100,Slender long bone
+DOID:4944,gastroesophageal junction adenocarcinoma,DOID:3119,gastrointestinal system cancer
+DOID:883,parasitic helminthiasis infectious disease,DOID:1398,parasitic infectious disease
+DOID:14679,VACTERL association,DOID:225,syndrome
+UBERON:0010056,future tongue,UBERON:0013765,digestive system organ
+CL:0002562,hair germinal matrix cell,CL:0000362,epidermal cell
+HP:0100242,Sarcoma,HP:0011792,Neoplasm by histology
+HP:0010027,Broad 1st metacarpal,HP:0001230,Broad metacarpals
+DOID:3744,cervical squamous cell carcinoma,DOID:2893,cervix carcinoma
+UBERON:0012327,pearly penile papule,UBERON:0000479,tissue
+UBERON:0010359,pharyngeal arch mesenchyme from neural crest,UBERON:0014387,mesenchyme derived from neural crest
+UBERON:0006959,mandible angular process,UBERON:0004530,bony projection
+DOID:8941,seborrheic infantile dermatitis,DOID:8741,seborrheic dermatitis
+HP:0001115,Posterior polar cataract,HP:0010696,Polar cataract
+HP:0100559,Lower limb asymmetry,HP:0100555,Asymmetric growth
+HP:0002578,Gastroparesis,HP:0002577,Abnormality of the stomach
+NCBITaxon:1239,Firmicutes,NCBITaxon:2,Bacteria
+HP:0009642,Broad distal phalanx of the thumb,HP:0011304,Broad thumb
+HP:0011400,Abnormal CNS myelination,HP:0012447,Abnormal myelination
+DOID:9146,visceral leishmaniasis,DOID:9065,leishmaniasis
+UBERON:0001185,right renal artery,UBERON:0001184,renal artery
+HP:0009975,Duplication of the distal phalanx of the 4th finger,HP:0009282,Abnormality of the distal phalanx of the 4th finger
+UBERON:0005418,hindlimb bud,UBERON:0005420,pelvic appendage bud
+HP:0008736,Hypoplasia of penis,HP:0000036,Abnormality of the penis
+UBERON:0010001,cell cluster organ,UBERON:0000062,organ
+UBERON:0010294,scleral endothelium,UBERON:0010291,layer of sclera
+UBERON:0002135,mitral valve,UBERON:0002133,atrioventricular valve
+DOID:8566,herpes simplex,DOID:934,viral infectious disease
+UBERON:0006466,tenth thoracic spinal cord segment,UBERON:0007715,thoracic subsegment of spinal cord
+UBERON:2005279,enteric circular muscle,UBERON:0001135,smooth muscle tissue
+HP:0010897,Hypersarcosinuria,HP:0010898,Abnormality of sarcosine metabolism
+UBERON:0003472,cerebellar artery,UBERON:0003496,head blood vessel
+HP:0011803,Bifid nose,HP:0004122,Midline defect of the nose
+UBERON:0001693,exoccipital bone,UBERON:0002513,endochondral bone
+UBERON:0003008,dorsal longitudinal fasciculus of hypothalamus,UBERON:0003931,diencephalic white matter
+UBERON:3000792,anterior ramus of cleithrum,UBERON:0004530,bony projection
+CL:0000959,T2 B cell,CL:0000818,transitional stage B cell
+UBERON:0013217,zygomatic plate,UBERON:4100000,skeletal element projection
+DOID:4247,coronary restenosis,DOID:4248,coronary stenosis
+UBERON:0011635,splenial bone,UBERON:0004768,bone of lower jaw
+HP:0009918,Ectopia pupillae,HP:0000615,Abnormality of the pupil
+HP:0004463,Absent brainstem auditory responses,HP:0006958,Abnormal auditory evoked potentials
+DOID:6865,oxyphilic endometrial endometrioid adenocarcinoma,DOID:2870,endometrial adenocarcinoma
+HP:0008772,Aplasia/Hypoplasia of the external ear,HP:0000356,Abnormality of the outer ear
+UBERON:0013691,buttock,UBERON:0000475,organism subdivision
+HP:0011150,Myoclonic absences,HP:0011148,Absence seizures with special features
+UBERON:4100013,postcoracoid,UBERON:0010363,endochondral element
+DOID:14546,sphenoidal sinus cancer,DOID:0050619,paranasal sinus cancer
+UBERON:0004260,upper arm blood vessel,UBERON:0003507,arm blood vessel
+HP:0003665,Amyotrophy of the musculature of the pelvis,HP:0008988,Pelvic girdle muscle atrophy
+UBERON:0014798,clavotrapezius muscle,UBERON:0002380,trapezius muscle
+CL:0000671,centripetally migrating follicle cell,CL:0000477,follicle cell
+UBERON:0011247,procoracoid cartilage,UBERON:0011248,procoracoid element
+CL:0002099,type I cell of adrenal cortex,CL:0000456,mineralocorticoid secreting cell
+UBERON:0010054,malleus cartilage element,UBERON:0014387,mesenchyme derived from neural crest
+DOID:8731,carotid body cancer,DOID:175,vascular cancer
+HP:0010047,Short 5th metacarpal,HP:0010049,Short metacarpal
+CL:0001035,bone cell,CL:0000548,animal cell
+UBERON:2005174,ventral liver lobe,UBERON:0000481,multi-tissue structure
+UBERON:0005921,middle nasal concha,UBERON:0003973,nasal concha of ethmoid bone
+UBERON:0005400,telencephalon arachnoid mater,UBERON:0003556,forebrain arachnoid mater
+DOID:14133,Masters-Allen syndrome,DOID:229,female reproductive system disease
+HP:0011747,Abnormality of the anterior pituitary,HP:0012503,Abnormality of the pituitary gland
+HP:0004223,Ivory epiphysis of the distal phalanx of the 5th finger,HP:0009388,Ivory epiphyses of the 5th finger
+DOID:3495,extrahepatic bile duct adenocarcinoma,DOID:4682,extrahepatic bile duct carcinoma
+HP:0002491,Spasticity of facial muscles,HP:0001257,Spasticity
+HP:0010136,Stippling of the epiphysis of the proximal phalanx of the hallux,HP:0010122,Stippling of the epiphyses of the hallux
+HP:0009633,Osteolytic defects of the proximal phalanx of the thumb,HP:0009654,Osteolytic defects of the phalanges of the thumb
+UBERON:0001659,transverse facial vein,UBERON:0003496,head blood vessel
+HP:0005227,Adenomatous colonic polyposis,HP:0200008,Intestinal polyposis
+DOID:9280,carbamoyl phosphate synthetase I deficiency disease,DOID:9252,amino acid metabolic disorder
+UBERON:0013191,ovarian cortex,UBERON:0005156,reproductive structure
+UBERON:0014874,distal epiphysis of distal phalanx of pedal digit 4,UBERON:0014876,distal epiphysis of distal phalanx of pedal digit
+UBERON:0002653,gracile fasciculus of medulla,UBERON:0005821,gracile fasciculus
+UBERON:0005140,metanephric short nephron,UBERON:0005110,metanephric nephron
+HP:0010391,Duplication of the phalanges of the 5th toe,HP:0010342,Abnormality of the phalanges of the 5th toe
+DOID:13864,trochlear nerve disease,DOID:5656,cranial nerve disease
+UBERON:0004164,branchiomeric muscle,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:5546,femoral cancer,DOID:184,bone cancer
+UBERON:4400000,metapterygium cartilage,UBERON:2201587,pectoral fin proximal radial cartilage
+UBERON:1000016,tip of snout,UBERON:0001444,subdivision of head
+NCBITaxon:85007,Corynebacterineae,NCBITaxon:2037,Actinomycetales
+UBERON:0011094,vertebra cartilage element,UBERON:0015005,vertebra endochondral element
+DOID:8761,megakaryocytic leukemia,DOID:1240,leukemia
+HP:0004808,Acute myeloid leukemia,HP:0002488,Acute leukemia
+HP:0011897,Neutrophillia,HP:0011991,Abnormal neutrophil cell number
+UBERON:0002953,lateral lemniscus,UBERON:0003544,brain white matter
+UBERON:0004562,digital vein,UBERON:0003514,limb blood vessel
+UBERON:0007255,intervertebral disk of lumbar vertebra,UBERON:2001457,postcranial axial cartilage
+HP:0005177,Premature arteriosclerosis,HP:0002634,Arteriosclerosis
+DOID:0060071,pre-malignant neoplasm,DOID:14566,disease of cellular proliferation
+NCBITaxon:6206,Taenia saginata,NCBITaxon:6202,Taenia
+UBERON:0004719,kidney arcuate vein,UBERON:0014401,renal venous blood vessel
+UBERON:0012420,coprodeum,UBERON:0004120,mesoderm-derived structure
+HP:0011643,Coronary sinus atrial septal defect,HP:0011642,Abnormality of the coronary sinus
+UBERON:0003372,pectoral appendage bud ectoderm,UBERON:0000490,unilaminar epithelium
+UBERON:0002791,regional part of telencephalon,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003328,mesenchyme of footplate,UBERON:0010377,mesenchyme from somatopleure
+DOID:240,iris disease,DOID:3480,uveal disease
+UBERON:0005657,crus commune epithelium,UBERON:0006932,vestibular epithelium
+UBERON:2005054,inner optic circle,UBERON:0004120,mesoderm-derived structure
+HP:0011048,Agenesis of permanent mandibular central incisor,HP:0006355,Agenesis of mandibular central incisor
+DOID:13949,interstitial cystitis,DOID:1679,cystitis
+HP:0003957,Cortical thickening of the forearm bones,HP:0002973,Abnormality of the forearm
+UBERON:0015785,acinus of olfactory gland,UBERON:0004119,endoderm-derived structure
+UBERON:0013193,parakeratinized epithelium,UBERON:0000488,atypical epithelium
+HP:0002597,Abnormality of the vasculature,HP:0001626,Abnormality of the cardiovascular system
+UBERON:0007805,synsacrum,UBERON:0004247,bone of dorsum
+UBERON:0005149,metanephric connecting tubule,UBERON:0005146,metanephric nephron tubule
+HP:0008239,Adrenal medullary hypoplasia,HP:0000835,Adrenal hypoplasia
+HP:0006593,Anomalous rib insertion to vertebrae,HP:0000772,Abnormality of the ribs
+UBERON:0001946,inferior colliculus,UBERON:0002966,regional part of midbrain tectum
+HP:0004963,Calcification of the aorta,HP:0001679,Abnormality of the aorta
+UBERON:0001715,oculomotor nuclear complex,UBERON:0007245,nuclear complex of neuraxis
+DOID:5262,heart sarcoma,DOID:117,heart cancer
+UBERON:0009643,central tegmental tract,UBERON:0007702,tract of brain
+UBERON:0003273,skeletal muscle tissue of tongue,UBERON:0004121,ectoderm-derived structure
+HP:0006790,Cerebral cortex with spongiform changes,HP:0002538,Abnormality of the cerebral cortex
+HP:0010549,Paralysis due to lesions of the principle motor tracts,HP:0007256,Abnormality of pyramidal motor function
+UBERON:0004188,glomerular epithelium,UBERON:0004211,nephron epithelium
+CL:1000367,transitional myocyte of posterior internodal tract,CL:1000480,transitional myocyte of internodal tract
+CL:0000444,obliquely striated muscle cell,CL:0000737,striated muscle cell
+UBERON:0002665,supracallosal gyrus,UBERON:0003022,cerebral cortex lobe
+HP:0009263,Cone-shaped epiphysis of the proximal phalanx of the 4th finger,HP:0009395,Cone-shaped epiphyses of the 4th finger
+HP:0008275,Abnormal cone-mediated electroretinogram,HP:0000512,Abnormal electroretinogram
+UBERON:0010573,manual digit 4 metacarpus cartilage element,UBERON:0015046,manual digit 4 metacarpus endochondral element
+DOID:12265,chronic salpingo-oophoritis,DOID:10972,salpingo-oophoritis
+UBERON:2000549,posttemporal,UBERON:0008907,dermal bone
+HP:0007258,Severe demyelination of the white matter,HP:0007305,CNS demyelination
+UBERON:0007862,perichordal tissue,UBERON:0002384,connective tissue
+CL:0002122,B220-positive CD38-positive IgG-negative class switched memory B cell,CL:0002119,CD38-positive IgG-negative class switched memory B cell
+HP:0011740,Glucocortocoid-insensitive primary hyperaldosteronism,HP:0011736,Primary hyperaldosteronism
+HP:0010933,Abnormality of xanthine metabolism,HP:0004352,Abnormality of purine metabolism
+DOID:5949,angiokeratoma circumscriptum,DOID:3165,skin benign neoplasm
+UBERON:2001536,pharyngobranchial 2 cartilage,UBERON:2001911,pharyngobranchial 2 element
+UBERON:0004731,neuromere,UBERON:0002050,embryonic structure
+DOID:1701,steroid inherited metabolic disorder,DOID:3146,lipid metabolism disorder
+UBERON:0008248,echinoderm pyloric cecum,UBERON:0004921,subdivision of digestive tract
+UBERON:0008954,lingula of left lung,UBERON:0000072,segment of respiratory tract
+CL:0000275,prestalk B cell,CL:0000269,prestalk cell
+UBERON:0008831,inner spiral sulcus,UBERON:0002277,spiral sulcus
+UBERON:0001171,portal lobule,UBERON:0004119,endoderm-derived structure
+DOID:13127,gonococcal spondylitis,DOID:6590,spondylitis
+DOID:0080043,achondrogenesis,DOID:2256,osteochondrodysplasia
+UBERON:0011980,intratarsal joint,UBERON:0001488,ankle joint
+UBERON:0007250,lingual tonsil,UBERON:0004121,ectoderm-derived structure
+HP:0012723,Sinoatrial block,HP:0011702,Abnormal electrophysiology of sinoatrial node origin
+UBERON:2000419,pterosphenoid,UBERON:0011164,neurocranium bone
+UBERON:2002251,epural 3,UBERON:2000660,epural
+UBERON:2002028,pectoral fin proximal radial bone 3,UBERON:2001587,pectoral fin proximal radial bone
+UBERON:0005700,upper jaw molar odontogenic papilla,UBERON:0003323,mesenchyme of upper jaw
+UBERON:0002518,otolith organ,UBERON:0000062,organ
+HP:0012386,Absent hallux,HP:0008362,Aplasia/Hypoplasia of the hallux
+HP:0005213,Pancreatic calcification,HP:0010766,Ectopic calcification
+CL:0000860,classical monocyte,CL:0000234,phagocyte
+UBERON:3000876,spina pelvis anterior,UBERON:0004120,mesoderm-derived structure
+UBERON:0002518,otolith organ,UBERON:0004121,ectoderm-derived structure
+DOID:1526,panniculitis,DOID:37,skin disease
+HP:0000307,Pointed chin,HP:0000306,Abnormality of the chin
+CL:1000418,myoepithelial cell of lactiferous alveolus,CL:1000416,myoepithelial cell of lactiferous gland
+HP:0006070,Metacarpophalangeal joint contractures,HP:0100490,Camptodactyly of finger
+HP:0007401,Noninflammatory macular atrophy,HP:0000608,Macular degeneration
+UBERON:0001932,arcuate nucleus of hypothalamus,UBERON:0002951,regional part of intermediate hypothalamic region
+UBERON:0003079,floor plate,UBERON:0004120,mesoderm-derived structure
+UBERON:0009645,ampullary gland,UBERON:0005399,male reproductive gland
+UBERON:0005563,trigeminal neural crest,UBERON:0003099,cranial neural crest
+HP:0006429,Broad femoral neck,HP:0003367,Abnormality of the femoral neck
+DOID:10027,tabes dorsalis,DOID:9988,tertiary neurosyphilis
+UBERON:2002235,presumptive ventral mesoderm,UBERON:0006603,presumptive mesoderm
+DOID:4621,holoprosencephaly,DOID:2490,congenital nervous system abnormality
+CL:1000600,lower urinary tract cell,CL:0000548,animal cell
+UBERON:0002244,premaxilla,UBERON:0002514,intramembranous bone
+UBERON:0003105,dorsal lateral plate region,UBERON:0005291,embryonic tissue
+UBERON:0008428,ceratoglossus,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009577,Short middle phalanx of the 2nd finger,HP:0005819,Short middle phalanx of finger
+HP:0100362,Aplasia of the phalanges of the 3rd toe,HP:0010359,Aplasia/Hypoplasia of the phalanges of the 3rd toe
+HP:0100410,Complete duplication of the middle phalanx of the 3rd toe,HP:0100401,Duplication of the middle phalanx of the 3rd toe
+NCBITaxon:747,Pasteurella multocida,NCBITaxon:745,Pasteurella
+HP:0009989,Duplication of the middle phalanx of the 5th finger,HP:0004219,Abnormality of the middle phalanx of the 5th finger
+UBERON:0006266,nasolacrimal groove,UBERON:0010371,ecto-epithelium
+HP:0009964,Duplication of the proximal phalanx of the 3rd finger,HP:0009959,Duplication of phalanx of 3rd finger
+DOID:4678,thymus mucoepidermoid carcinoma,DOID:3284,thymic carcinoma
+UBERON:0006294,stapes pre-cartilage condensation,UBERON:0007213,mesenchyme derived from head neural crest
+HP:0011029,Internal hemorrhage,HP:0001892,Abnormal bleeding
+UBERON:0015041,pedal digit 5 metatarsal endochondral element,UBERON:0015036,pedal digit metatarsal endochondral element
+DOID:6170,ovarian carcinosarcoma,DOID:2151,malignant ovarian surface epithelial-stromal neoplasm
+DOID:3488,cellulitis,DOID:37,skin disease
+HP:0100843,Glioblastoma,HP:0009592,Astrocytoma
+HP:0001947,Renal tubular acidosis,HP:0001941,Acidosis
+HP:0003994,Dislocated wrist,HP:0003019,Abnormality of the wrist
+UBERON:2001949,caudal-fin hook,UBERON:0004121,ectoderm-derived structure
+DOID:10854,salivary gland disease,DOID:403,mouth disease
+DOID:5088,mixed epithelial stromal tumour,DOID:154,mixed cell type cancer
+HP:0009566,Short distal phalanx of the 2nd finger,HP:0009557,Aplasia/Hypoplasia of the distal phalanx of the 2nd finger
+HP:0012686,Increased pineal volume,HP:0012684,Abnormal pineal volume
+UBERON:0010467,teres muscle,UBERON:0001482,muscle of shoulder
+HP:0002553,Highly arched eyebrow,HP:0000534,Abnormality of the eyebrow
+HP:0000480,Retinal coloboma,HP:0000589,Coloboma
+CL:0000670,primordial germ cell,CL:0000039,germ line cell
+UBERON:0005313,mammary duct terminal end bud,UBERON:0005156,reproductive structure
+HP:0100213,Absent epiphysis of the middle phalanx of the 5th toe,HP:0100098,Abnormality of the epiphysis of the middle phalanx of the 5th toe
+HP:0008012,Congenital myopia,HP:0000545,Myopia
+HP:0004524,Temporal hypotrichosis,HP:0011361,Congenital abnormal hair pattern
+HP:0011435,Low maternal serum PAPP-A,HP:0011436,Abnormal maternal serum screening
+DOID:5492,biphasic synovial sarcoma,DOID:5485,synovial sarcoma
+HP:0003733,Thigh hypertrophy,HP:0008968,Muscle hypertrophy of the lower extremities
+CL:1000484,purkinje myocyte of atrioventricular bundle,CL:0002068,Purkinje myocyte
+HP:0100055,Absent epiphyses of the 3rd toe,HP:0010162,Absent epiphyses of the toes
+HP:0000639,Nystagmus,HP:0012547,Abnormal involuntary eye movements
+UBERON:0005879,pharyngeal cleft,UBERON:0006846,surface groove
+DOID:4436,anterior cranial fossa meningioma,DOID:3565,meningioma
+UBERON:0004714,septum pellucidum,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010248,Cone-shaped epiphyses of the distal phalanges of the hand,HP:0010230,Cone-shaped epiphyses of the phalanges of the hand
+UBERON:0014650,dorsal hypothalamic nucleus,UBERON:0006568,hypothalamic nucleus
+UBERON:0004651,scapula spine,UBERON:0005913,zone of bone organ
+UBERON:0003527,kidney capillary,UBERON:0003517,kidney blood vessel
+DOID:8719,in situ carcinoma,DOID:0060071,pre-malignant neoplasm
+UBERON:0008346,duodenal epithelium,UBERON:0013636,epithelium of intestinal villus
+UBERON:0005411,bony otic capsule,UBERON:0003566,head connective tissue
+UBERON:0004311,distal phalanx of manual digit 2,UBERON:0003865,distal phalanx of manus
+DOID:0080020,Jansen's metaphyseal chondrodysplasia,DOID:0080019,metaphyseal dysplasia
+NCBITaxon:33743,Kyasanur forest disease virus,NCBITaxon:29263,tick-borne encephalitis virus group
+UBERON:0010700,phalanx pre-cartilage condensation,UBERON:0015023,phalanx endochondral element
+CL:0000241,stratified cuboidal epithelial cell,CL:0000079,stratified epithelial cell
+UBERON:2005385,dorsal fin proximal radial bone 8,UBERON:2105385,dorsal fin proximal radial element 8
+CL:0002247,pleural macrophage,CL:0000864,tissue-resident macrophage
+UBERON:0012485,cloacal villus,UBERON:0004120,mesoderm-derived structure
+UBERON:0005007,mucosa of major calyx,UBERON:0005006,mucosa of renal pelvis
+HP:0100799,Neoplasm of the middle ear,HP:0000370,Abnormality of the middle ear
+HP:0006851,Symmetric spinal nerve root neurofibromas,HP:0009735,Spinal neurofibromas
+HP:0010600,Abnormality of the distal ulnar epiphysis,HP:0004037,Abnormality of the ulnar epiphyses
+UBERON:0000369,corpus striatum,UBERON:0002616,regional part of brain
+HP:0012293,Abnormal genital pigmentation,HP:0000811,Abnormal external genitalia
+HP:0009116,Aplasia/Hypoplasia involving bones of the skull,HP:0000929,Abnormality of the skull
+UBERON:0001295,endometrium,UBERON:0004923,organ component layer
+HP:0009160,Absent epiphysis of the proximal phalanx of the 5th finger,HP:0009382,Absent epiphyses of the 5th finger
+HP:0006234,Osteolysis involving tarsal bones,HP:0001850,Abnormality of the tarsal bones
+UBERON:2001293,posterior kidney,UBERON:0003103,compound organ
+DOID:9766,xanthogranulomatous cholecystitis,DOID:1949,cholecystitis
+UBERON:0015028,manual digit 4 phalanx endochondral element,UBERON:0015024,manual digit phalanx endochondral element
+UBERON:0010302,amnioserosa,UBERON:0010303,extraembryonic epithelium
+HP:0009298,Aplasia of the proximal phalanx of the 4th finger,HP:0009300,Aplasia/Hypoplasia of the proximal phalanx of the 4th finger
+DOID:10300,Raynaud disease,DOID:341,peripheral vascular disease
+UBERON:0009853,body of uterus,UBERON:0014404,female anatomical structure
+UBERON:0014640,occipital gyrus,UBERON:0003022,cerebral cortex lobe
+HP:0008054,Abnormality of the vasculature of the conjunctiva,HP:0008047,Abnormality of the vasculature of the eye
+HP:0011054,Agenesis of molar,HP:0011077,Abnormality of molar
+UBERON:0001685,hyoid bone,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0011164,neurocranium bone,UBERON:0004120,mesoderm-derived structure
+DOID:12030,panuveitis,DOID:13141,uveitis
+UBERON:0003351,pharyngeal epithelium,UBERON:0005911,endo-epithelium
+UBERON:2001524,hypobranchial 1 cartilage,UBERON:2001522,hypobranchial cartilage
+UBERON:0001685,hyoid bone,UBERON:0008001,irregular bone
+UBERON:0002360,meninx,UBERON:0004121,ectoderm-derived structure
+UBERON:0001274,ischium,UBERON:0002513,endochondral bone
+UBERON:2001960,ceratobranchial 4 bone distal cartilage,UBERON:0011004,pharyngeal arch cartilage
+UBERON:0014686,angular vein,UBERON:0003502,neck blood vessel
+DOID:3558,duodenal obstruction,DOID:8437,intestinal obstruction
+DOID:12894,Sjogren's syndrome,DOID:417,hypersensitivity reaction type II disease
+UBERON:2001929,epioccipital posterior process,UBERON:0004530,bony projection
+DOID:7665,non-gestational ovarian choriocarcinoma,DOID:5351,ovarian primitive germ cell tumor
+UBERON:0002154,lateral reticular nucleus,UBERON:0002579,regional part of medullary reticular formation
+UBERON:0000365,urothelium,UBERON:0005910,transitional epithelium
+DOID:5867,clear cell chondrosarcoma,DOID:3371,chondrosarcoma
+UBERON:2007015,posterior presumptive neural plate,UBERON:0005291,embryonic tissue
+UBERON:0004880,chordamesoderm,UBERON:0005423,developing anatomical structure
+DOID:13197,nodular goiter,DOID:12176,goiter
+UBERON:0010212,laryngeal apparatus,UBERON:0004119,endoderm-derived structure
+NCBITaxon:11908,Human T-lymphotropic virus 1,NCBITaxon:194440,Primate T-lymphotropic virus 1
+HP:0009969,Partial duplication of the middle phalanx of the 3rd finger,HP:0009961,Partial duplication of the phalanges of the 3rd finger
+HP:0011892,Vitamin K deficiency,HP:0100831,Abnormality of vitamin K metabolism
+HP:0003423,Thoracolumbar kyphoscoliosis,HP:0002944,Thoracolumbar scoliosis
+HP:0000656,Ectropion,HP:0000492,Abnormality of the eyelid
+HP:0100765,Abnormality of the tonsils,HP:0100763,Abnormality of the lymphatic system
+HP:0007069,Profound static encephalopathy,HP:0007030,Nonprogressive encephalopathy
+UBERON:0007287,presumptive bulbus arteriosus,UBERON:0006598,presumptive structure
+CL:1000804,kidney outer medulla interstitial cell,CL:1000616,kidney outer medulla cell
+DOID:0050570,congenital disorder of glycosylation type I,DOID:5212,congenital disorder of glycosylation
+HP:0009175,Patchy sclerosis of the middle phalanx of the 5th finger,HP:0009848,Patchy sclerosis of the middle phalanges of the hand
+UBERON:0015085,distal carpal bone 1 cartilage,UBERON:0015084,distal carpal bone 1 endochondral element
+UBERON:0001180,superior recess of lesser sac,UBERON:0004458,body cavity or lining
+HP:0005833,Joint swelling onset late infancy,HP:0001386,Joint swelling
+HP:0003639,Elevated urinary epinephrine,HP:0011976,Elevated urinary catecholamines
+HP:0009983,Partial duplication of the proximal phalanx of the 4th finger,HP:0010003,Partial duplication of the proximal phalanges of the hand
+UBERON:2001186,collagenous dermal stroma,UBERON:0000476,acellular anatomical structure
+UBERON:0003557,midbrain arachnoid mater,UBERON:0002362,arachnoid mater
+DOID:8083,classic congenital mesoblastic nephroma,DOID:4773,congenital mesoblastic nephroma
+DOID:6354,CLL/SLL,DOID:1040,chronic lymphocytic leukemia
+UBERON:0006673,mandibular canal,UBERON:0005744,bone foramen
+UBERON:2001775,anal fin lepidotrichium 7,UBERON:4000176,anal fin lepidotrichium
+HP:0012539,Non-Hodgkin lymphoma,HP:0002665,Lymphoma
+DOID:3877,functional colonic disease,DOID:5353,colonic disease
+HP:0002671,Basal cell carcinoma,HP:0008069,Neoplasm of the skin
+DOID:8389,lumbar plexus neoplasm,DOID:4693,nerve plexus neoplasm
+UBERON:0003327,mesenchyme of forearm,UBERON:0003859,forelimb mesenchyme
+UBERON:0007147,lumen of midgut,UBERON:0000464,anatomical space
+UBERON:0005211,renal medulla interstitium,UBERON:0005215,kidney interstitium
+UBERON:0000642,suspensory ligament of duodenum,UBERON:0008841,suspensory ligament
+UBERON:0001328,lobe of prostate,UBERON:0000064,organ part
+UBERON:2001256,lateral floor plate,UBERON:0005291,embryonic tissue
+DOID:13121,deficiency anemia,DOID:2355,anemia
+UBERON:0015766,epithelium of duct of salivary gland,UBERON:0004809,salivary gland epithelium
+CL:1000615,kidney cortex tubule cell,CL:0002584,renal cortical epithelial cell
+NCBITaxon:227859,SARS coronavirus,NCBITaxon:694009,Severe acute respiratory syndrome-related coronavirus
+HP:0009703,Synostosis involving the 1st metacarpal,HP:0009656,Symphalangism of the thumb
+HP:0009002,Loss of truncal subcutaneous adipose tissue,HP:0008887,Adipose tissue loss
+CL:0002060,melanophage,CL:0000864,tissue-resident macrophage
+HP:0010157,Small epiphysis of the 1st metatarsal,HP:0010125,Abnormality of the epiphysis of the 1st metatarsal
+DOID:2297,leptospirosis,DOID:37,skin disease
+CL:0011112,magnocellular neurosecretory cell,CL:0000167,peptide hormone secreting cell
+HP:0100363,Aplasia of the phalanges of the 4th toe,HP:0010745,Aplasia of the phalanges of the toes
+HP:0011945,Bronchiolitis obliterans organizing pneumonia,HP:0006530,Interstitial pulmonary disease
+UBERON:0010141,primitive sex cord of indifferent gonad,UBERON:0005295,sex cord
+DOID:9427,hypertensive encephalopathy,DOID:9428,intracranial hypertension
+UBERON:0011108,synovial joint of pectoral girdle,UBERON:0002217,synovial joint
+HP:0100922,Sclerosis of the phalanges of the thumb,HP:0009602,Abnormality of the phalanges of the thumb
+UBERON:0009537,vascular element of right lung,UBERON:0005629,vascular plexus
+UBERON:3000905,caput ossis cruris,UBERON:0004120,mesoderm-derived structure
+UBERON:0009646,lumbar sympathetic nerve trunk,UBERON:0004295,sympathetic nerve trunk
+HP:0010003,Partial duplication of the proximal phalanges of the hand,HP:0009999,Partial duplication of the phalanx of hand
+HP:0009985,Duplication of phalanx of 5th finger,HP:0004213,Abnormality of the phalanges of the 5th finger
+DOID:0050778,Meckel syndrome,DOID:0050737,autosomal recessive disease
+HP:0006753,Neoplasm of the stomach,HP:0002577,Abnormality of the stomach
+UBERON:0010174,Schweigger-Seidel sheath,UBERON:0000064,organ part
+HP:0000077,Abnormality of the kidney,HP:0010935,Abnormality of the upper urinary tract
+HP:0010698,Nuclear pulverulent cataract,HP:0100018,Nuclear cataract
+UBERON:0012074,bony part of hard palate,UBERON:0000075,subdivision of skeletal system
+HP:0008281,Acute hyperammonemia,HP:0001987,Hyperammonemia
+HP:0010949,Abnormality of umbilical vein blood flow,HP:0011403,Abnormal umbilical cord blood vessels
+UBERON:0006310,vitelline venous plexus,UBERON:0002050,embryonic structure
+UBERON:2001788,pelvic splint,UBERON:0004376,fin bone
+HP:0011562,Straddling atrioventricular valve,HP:0011546,Abnormal atrioventricular connection
+DOID:11038,depersonalization disorder,DOID:10935,dissociative disorder
+UBERON:3000282,margo orbitalis of pterygoid,UBERON:0000064,organ part
+DOID:2051,maxillary sinusitis,DOID:0050127,sinusitis
+UBERON:0006146,dorsal digital artery of manus,UBERON:0006163,dorsal digital artery
+HP:0003444,EMG: chronic denervation signs,HP:0003445,EMG: neuropathic changes
+DOID:0050489,multinodular goiter,DOID:12176,goiter
+HP:0009548,Bullet-shaped phalanges of the 2nd finger,HP:0009769,Bullet-shaped phalanges of the hand
+UBERON:0009618,trunk paraxial mesoderm,UBERON:0005256,trunk mesenchyme
+UBERON:0000942,frontal nerve (branch of ophthalmic),UBERON:0001021,nerve
+UBERON:3000601,tectum nasi,UBERON:0010363,endochondral element
+HP:0009159,Small epiphysis of the proximal phalanx of the 5th finger,HP:0010276,Small epiphyses of the proximal phalanges of the hand
+UBERON:0004008,cerebellar plate,UBERON:0010371,ecto-epithelium
+UBERON:0001501,lumbrical muscle of manus,UBERON:0014375,intrinsic muscle of manus
+UBERON:2005027,posterior cerebral vein,UBERON:0003496,head blood vessel
+HP:0003652,Recurrent myoglobinuria,HP:0002913,Myoglobinuria
+UBERON:0003162,lateral ocellus,UBERON:0003161,dorsal ocellus
+UBERON:0011253,gland of anal sac,UBERON:0011252,scent gland
+UBERON:0003544,brain white matter,UBERON:0002316,white matter
+UBERON:0010704,parenchyma of quadrate lobe of liver,UBERON:0005221,liver right lobe parenchyma
+HP:0009536,Short 2nd finger,HP:0006264,Aplasia/Hypoplasia of the 2nd finger
+HP:0003696,Absent epiphysis of the distal phalanx of the 5th finger,HP:0009198,Abnormality of the epiphysis of the distal phalanx of the 5th finger
+UBERON:0003822,forelimb stylopod,UBERON:0002472,stylopod
+UBERON:0001173,biliary tree,UBERON:0013765,digestive system organ
+HP:0009986,Complete duplication of the phalanges of the 5th finger,HP:0009998,Complete duplication of phalanx of hand
+UBERON:0005331,mesonephric renal vesicle,UBERON:0005330,mesonephric nephron epithelium
+UBERON:0006228,exoccipital pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+DOID:0050805,glioblastoma mesenchymal subtype,DOID:3068,glioblastoma multiforme
+DOID:0050444,infantile refsum disease,DOID:906,peroxisomal disease
+UBERON:0005850,lumbar spinal cord lateral column,UBERON:0006078,subdivision of spinal cord lateral column
+HP:0100395,Short proximal phalanx of the 3rd toe,HP:0100366,Short phalanx of the 3rd toe
+UBERON:0013699,strand of axillary hair,UBERON:0001037,strand of hair
+UBERON:0001280,liver parenchyma,UBERON:0004119,endoderm-derived structure
+UBERON:0002609,spinothalamic tract of midbrain,UBERON:0007702,tract of brain
+CL:0002050,Fraction C' precursor B cell,CL:0000817,precursor B cell
+UBERON:0002413,cervical vertebra,UBERON:0003458,neck bone
+DOID:7030,bronchial mucus gland adenoma,DOID:5391,bronchus adenoma
+DOID:6192,inflammatory MFH,DOID:1907,malignant fibroxanthoma
+HP:0012605,Hypernatriuria,HP:0012603,Abnormal urine sodium concentration
+HP:0008232,Elevated follicle stimulating hormone,HP:0000837,Gonadotropin excess
+HP:0005954,Pulmonary capillary hemangiomatosis,HP:0005306,Capillary hemangiomas
+CL:0000546,T-helper 2 cell,CL:0001051,"CD4-positive, CXCR3-negative, CCR6-negative, alpha-beta T cell"
+DOID:8007,Pancoast tumor,DOID:1324,lung cancer
+HP:0000273,Facial grimacing,HP:0005324,Disturbance of facial expression
+UBERON:4200032,clavicle blade,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2001021,myotome somite 6,UBERON:0003082,myotome
+UBERON:0011166,patellofemoral joint,UBERON:0003840,hindlimb joint
+UBERON:0002342,neural crest,UBERON:0010316,germ layer / neural crest
+UBERON:0010023,dorsal part of pharyngeal pouch 2,UBERON:0005291,embryonic tissue
+UBERON:0002433,pars tuberalis of adenohypophysis,UBERON:0000064,organ part
+DOID:6175,mediastinal neurilemmoma,DOID:4691,malignant mediastinal neurogenic neoplasm
+HP:0004854,Intermittent thrombocytopenia,HP:0001873,Thrombocytopenia
+DOID:0060123,connective tissue benign neoplasm,DOID:0060099,musculoskeletal system benign neoplasm
+DOID:2021,placenta cancer,DOID:120,female reproductive organ cancer
+UBERON:2101819,dorsal fin proximal radial element 2,UBERON:2100947,dorsal fin proximal radial element
+UBERON:0000086,zona pellucida,UBERON:0000476,acellular anatomical structure
+HP:0100540,Palpebral edema,HP:0100539,Periorbital edema
+HP:0006326,Buried teeth encased in mucopolysaccharide,HP:0000164,Abnormality of the teeth
+UBERON:0002521,elastic tissue,UBERON:0002384,connective tissue
+DOID:7915,cervical spinal canal and spinal cord meningioma,DOID:1140,spinal canal and spinal cord meningioma
+UBERON:0003127,open tracheal system trachea,UBERON:0001005,respiratory airway
+UBERON:0007846,dense regular connective tissue,UBERON:0011823,dense connective tissue
+UBERON:0001269,acetabular part of hip bone,UBERON:0004120,mesoderm-derived structure
+HP:0006628,Absent sternal ossification,HP:0011863,Abnormal sternal ossification
+UBERON:0013247,male paramesonephric duct,UBERON:0005156,reproductive structure
+UBERON:0003469,respiratory system artery,UBERON:0001637,artery
+DOID:0050907,mixed extragonadal germ cell cancer,DOID:3306,mixed germ cell cancer
+CL:1001432,kidney collecting duct intercalated cell,CL:1000454,kidney collecting duct epithelial cell
+NCBITaxon:85003,Actinobacteridae,NCBITaxon:1760,Actinobacteria <class>
+HP:0010072,Patchy sclerosis of the 1st metatarsal,HP:0010208,Patchy sclerosis of the proximal phalanges of the toes
+HP:0008211,Parathyroid agenesis,HP:0011768,Parathyroid dysgenesis
+HP:0001100,Heterochromia iridis,HP:0008034,Abnormal iris pigmentation
+UBERON:0002136,hilus of dentate gyrus,UBERON:0005401,cerebral hemisphere grey matter
+UBERON:2201587,pectoral fin proximal radial cartilage,UBERON:2201586,pectoral fin radial cartilage
+CL:0002221,keratinized squamous cell of esophagus,CL:0000237,keratinizing barrier epithelial cell
+UBERON:0012302,male membranous urethra,UBERON:0001336,membranous urethra of male or female
+CL:1000416,myoepithelial cell of lactiferous gland,CL:0002327,mammary gland epithelial cell
+HP:0002524,Cataplexy,HP:0012638,Abnormality of nervous system physiology
+UBERON:0004274,lateral ventricle choroid plexus epithelium,UBERON:0004643,lateral ventricle ependyma
+HP:0100087,Triangular epiphyses of the 5th toe,HP:0010172,Triangular epiphyses of the toes
+HP:0003570,Molybdenum cofactor deficiency,HP:0001939,Abnormality of metabolism/homeostasis
+DOID:1399,primary lacrimal atrophy,DOID:1400,lacrimal apparatus disease
+UBERON:0001852,endolymph,UBERON:0006586,otolymph
+CL:0002120,CD24-positive CD38-negative IgG-negative class switched memory B cell,CL:0002118,CD38-negative IgG-negative class switched memory B cell
+UBERON:0005075,forebrain-midbrain boundary,UBERON:0000015,anatomical boundary
+UBERON:0001792,ganglionic layer of retina,UBERON:0003902,retinal neural layer
+HP:0008421,Tall lumbar vertebral bodies,HP:0004570,Increased vertebral height
+UBERON:3000640,arcus praeoccipitalis,UBERON:0003933,cranial cartilage
+DOID:11428,endometriosis of intestine,DOID:289,endometriosis
+DOID:13963,nuclear senile cataract,DOID:9669,senile cataract
+UBERON:0005628,ileal artery,UBERON:0004573,systemic artery
+UBERON:0004359,corpus epididymis,UBERON:0005156,reproductive structure
+UBERON:4200126,supraacetabular rim,UBERON:4100000,skeletal element projection
+UBERON:0014781,stomodeal ectoderm,UBERON:0005291,embryonic tissue
+HP:0007937,Honeycomb retinal degeneration,HP:0000546,Retinal degeneration
+HP:0012023,Galactosuria,HP:0004915,Impairment of galactose metabolism
+UBERON:0001592,bronchial vein,UBERON:0001638,vein
+HP:0100024,Conspicuously happy disposition,HP:0100851,Abnormal emotion/affect behavior
+DOID:5368,Wolffian duct adenocarcinoma,DOID:3702,cervical adenocarcinoma
+DOID:11428,endometriosis of intestine,DOID:5295,intestinal disease
+HP:0009046,Difficulty running,HP:0004302,Functional motor problems.
+UBERON:3000089,cavum principale,UBERON:0001707,nasal cavity
+DOID:0050204,Epstein-Barr virus hepatitis,DOID:1884,viral hepatitis
+DOID:5058,rhabdoid meningioma,DOID:3565,meningioma
+UBERON:2001382,epibranchial bone uncinate process,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003222,flexor digitorum superficialis,UBERON:0004254,forelimb zeugopod muscle
+DOID:0050798,cerebral creatine deficiency syndrome,DOID:9252,amino acid metabolic disorder
+HP:0003221,Chromosomal breakage induced by crosslinking agents,HP:0003220,Abnormality of chromosome stability
+DOID:14550,root resorption,DOID:13240,tooth resorption
+HP:0009769,Bullet-shaped phalanges of the hand,HP:0005918,Abnormality of phalanx of finger
+DOID:11364,lens subluxation,DOID:110,lens disease
+UBERON:0001540,peroneal artery,UBERON:0001637,artery
+DOID:10152,Meckel's diverticulum cancer,DOID:10153,ileum cancer
+UBERON:2000629,caudal motor nucleus of abducens,UBERON:0009662,hindbrain nucleus
+NCBITaxon:260963,Avulavirus,NCBITaxon:11159,Paramyxovirinae
+HP:0001609,Hoarse voice,HP:0001608,Abnormality of the voice
+HP:0008261,Pancreatic islet cell adenoma,HP:0002894,Neoplasm of the pancreas
+UBERON:0003078,epibranchial placode,UBERON:0005291,embryonic tissue
+HP:0100779,Urogenital sinus anomaly,HP:0000142,Abnormality of the vagina
+UBERON:0003646,metacarpal bone of digit 2,UBERON:0013582,metapodium bone 2
+UBERON:2000376,infraorbital,UBERON:0003462,facial bone
+HP:0100238,Synostosis involving bones of the upper limbs,HP:0100240,Synostosis of joints
+UBERON:0009612,forebrain midbrain boundary neural plate,UBERON:0006800,anatomical line
+UBERON:3000448,posterior maxillary process,UBERON:0010313,neural crest-derived structure
+HP:0005445,Widened posterior fossa,HP:0000932,Abnormality of the posterior cranial fossa
+UBERON:0010579,manual digit 5 phalanx pre-cartilage condensation,UBERON:0005695,manual digit 5 mesenchyme
+UBERON:0001239,muscularis mucosae of large intestine,UBERON:0004220,large intestine smooth muscle
+CL:0002183,stem cell of gastric gland,CL:0000048,multi fate stem cell
+UBERON:0001493,axillary nerve,UBERON:0003433,arm nerve
+UBERON:0001244,internal anal sphincter,UBERON:0007521,smooth muscle sphincter
+UBERON:0007252,intervertebral disk of cervical vertebra,UBERON:0005174,dorsal region organ
+HP:0100784,Peripheral arteriovenous fistula,HP:0004947,Arteriovenous fistula
+HP:0001848,Calcaneovalgus deformity,HP:0008364,Abnormality of the calcaneus
+HP:0002230,Generalized hirsutism,HP:0001007,Hirsutism
+UBERON:0005099,short descending thin limb,UBERON:0004211,nephron epithelium
+UBERON:0006807,ectepicondyle of humerus,UBERON:0009978,epicondyle
+UBERON:0009639,body of sphenoid,UBERON:0002513,endochondral bone
+UBERON:0000170,pair of lungs,UBERON:0004119,endoderm-derived structure
+UBERON:4200033,cleithrum head,UBERON:0004120,mesoderm-derived structure
+UBERON:0001925,ventral lateral nucleus,UBERON:0015234,nucleus of ventral thalamus
+HP:0006119,Proximal tapering of metacarpals,HP:0005916,Abnormal metacarpal morphology
+UBERON:3000649,anterior process of vomer,UBERON:0010313,neural crest-derived structure
+HP:0011186,Focal epileptiform discharges with limited propagation to contralateral hemisphere,HP:0011185,EEG with focal epileptiform discharges
+UBERON:0006082,fundus of urinary bladder,UBERON:0004120,mesoderm-derived structure
+DOID:8659,chickenpox,DOID:37,skin disease
+UBERON:0007773,scrotal sweat gland,UBERON:0001820,sweat gland
+UBERON:0002982,inferior pulvinar nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:2000586,preural 2 vertebra,UBERON:2000734,preural vertebra
+DOID:2097,vulval Paget's disease,DOID:2098,vulva adenocarcinoma
+UBERON:0010129,femur cartilage element,UBERON:0015052,femur endochondral element
+HP:0003783,Externally rotated/abducted legs,HP:0002814,Abnormality of the lower limb
+UBERON:0011741,cardiac valve leaflet,UBERON:0004120,mesoderm-derived structure
+HP:0012602,Renal chloride wasting,HP:0012600,Abnormal urine chloride concentration
+UBERON:0004333,proximal phalanx of pedal digit 2,UBERON:0003868,proximal phalanx of pes
+UBERON:0001499,muscle of arm,UBERON:0003662,forelimb muscle
+UBERON:0006058,multi-limb segment region,UBERON:0000477,anatomical cluster
+DOID:0060060,non-Hodgkin lymphoma,DOID:0060058,lymphoma
+UBERON:0014782,allantois of embryonic urinary system,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0200149,CSF lymphocytosis,HP:0012229,CSF pleocytosis
+UBERON:0013177,dorsal bursa,UBERON:0001013,adipose tissue
+UBERON:1000001,collection of hairs on vertex,UBERON:0014382,collection of hairs on head or neck
+UBERON:0002430,lateral hypothalamic area,UBERON:0000477,anatomical cluster
+UBERON:0008859,cardiac gastric gland,UBERON:0000325,gastric gland
+HP:0007722,Loss of retinal pigment epithelium,HP:0008051,Abnormality of the retinal pigment epithelium
+CL:0000401,macrophage (sensu Diptera),CL:0000394,plasmatocyte
+UBERON:3010707,m. dorsalis scapulae,UBERON:0010891,pectoral complex muscle
+DOID:3463,breast disease,DOID:0060118,thoracic disease
+UBERON:0010982,latissimus dorsi pre-muscle mass,UBERON:0004120,mesoderm-derived structure
+HP:0010227,Pseudoepiphysis of the 5th metacarpal,HP:0010226,Abnormality of the epiphysis of the 5th metacarpal
+DOID:4938,ureter adenocarcinoma,DOID:4939,ureter carcinoma
+UBERON:0000203,pallium,UBERON:0011300,gray matter of telencephalon
+UBERON:0015174,helicine artery of penis,UBERON:0005156,reproductive structure
+CL:1000299,fibroblast of connective tissue of prostate,CL:0000057,fibroblast
+DOID:7501,pediatric infratentorial ependymoma,DOID:4706,infratentorial cancer
+UBERON:0002882,supraspinal nucleus,UBERON:0007635,nucleus of medulla oblongata
+HP:0100906,Sclerosis of the middle phalanx of the 4th finger,HP:0100920,Sclerosis of the phalanges of the 4th finger
+CL:1000427,adrenal cortex chromaffin cell,CL:1000426,chromaffin cell of adrenal gland
+UBERON:3000284,margo tympanicus of pterygoid,UBERON:0004120,mesoderm-derived structure
+DOID:1002,endometritis,DOID:1005,endometrial disease
+HP:0200101,Decreased/absent ankle reflexes,HP:0002522,Areflexia of lower limbs
+HP:0000250,Dense calvaria,HP:0002683,Abnormality of the calvaria
+HP:0009946,Polydactyly affecting the 2nd finger,HP:0004100,Abnormality of the 2nd finger
+UBERON:2000952,sclerotome somite 1,UBERON:0003089,sclerotome
+HP:0002604,Gastrointestinal telangiectasia,HP:0004296,Abnormality of gastrointestinal vasculature
+UBERON:0010277,mesocardium,UBERON:0002050,embryonic structure
+CL:0000958,T1 B cell,CL:0000818,transitional stage B cell
+HP:0100198,Pseudoepiphysis of the proximal phalanx of the 4th toe,HP:0100073,Pseudoepiphyses of the 4th toe
+CL:0000372,tormogen cell,CL:0000463,epidermal cell (sensu arthropoda)
+HP:0009353,Pseudoepiphysis of the proximal phalanx of the 3rd finger,HP:0009417,Pseudoepiphyses of the 3rd finger
+HP:0005212,Anal mucosal leukoplakia,HP:0004378,Abnormality of the anus
+UBERON:2000251,adipose fin,UBERON:4000162,median fin
+DOID:12170,radial nerve lesion,DOID:572,mononeuritis of upper limb and mononeuritis multiplex
+UBERON:0013069,popliteal area,UBERON:0005055,zone of long bone
+UBERON:0013244,vaginal plate,UBERON:0006554,urinary system structure
+CL:1000441,epithelial cell of viscerocranial mucosa,CL:0000066,epithelial cell
+UBERON:0004110,midnasal cavity,UBERON:0002553,anatomical cavity
+UBERON:0014741,lateral pallium,UBERON:0002791,regional part of telencephalon
+HP:0000627,Posterior embryotoxon,HP:0008048,Abnormality of the line of Schwalbe
+UBERON:0002380,trapezius muscle,UBERON:0001482,muscle of shoulder
+NCBITaxon:27973,Encephalitozoon hellem,NCBITaxon:6033,Encephalitozoon
+DOID:0060013,gamma chain deficiency,DOID:627,severe combined immunodeficiency
+DOID:8426,follicular infundibulum tumor,DOID:5375,hair follicle neoplasm
+HP:0008258,Congenital adrenal hyperplasia,HP:0008221,Adrenal hyperplasia
+UBERON:0001186,left renal artery,UBERON:0001184,renal artery
+CL:0000839,myeloid lineage restricted progenitor cell,CL:0002031,hematopoietic lineage restricted progenitor cell
+UBERON:0007380,dermal scale,UBERON:0004120,mesoderm-derived structure
+DOID:1569,mechanical ectropion,DOID:1570,ectropion
+UBERON:0000948,heart,UBERON:0004120,mesoderm-derived structure
+DOID:7144,laryngeal small cell carcinoma,DOID:2600,laryngeal carcinoma
+DOID:8110,periampullary adenocarcinoma,DOID:3502,ampulla of Vater adenocarcinoma
+CL:1000695,kidney interstitial alternatively activated macrophage,CL:1000500,kidney interstitial cell
+DOID:7076,lipid-rich breast carcinoma,DOID:6741,bilateral breast cancer
+HP:0006727,T-cell acute lymphoblastic leukemias,HP:0006721,Acute lymphatic leukemia
+DOID:0050718,vitamin metabolic disorder,DOID:655,inherited metabolic disorder
+UBERON:0002605,precentral operculum,UBERON:0003022,cerebral cortex lobe
+HP:0010390,Triangular shaped phalanges of the 5th toe,HP:0010342,Abnormality of the phalanges of the 5th toe
+UBERON:0002519,otolithic membrane,UBERON:0004121,ectoderm-derived structure
+CL:1001214,arcuate artery smooth muscle cell,CL:1001064,kidney artery smooth muscle cell
+HP:0012621,Persistent cloaca,HP:0012620,Cloacal abnormality
+DOID:7236,pancreatic invasive mucinous cystadenocarcinoma,DOID:7234,pancreatic colloid cystadenocarcinoma
+UBERON:0009952,dentate gyrus subgranular zone,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100292,Amyloidosis of peripheral nerves,HP:0000759,Abnormality of the peripheral nervous system
+UBERON:0014799,acromiotrapezius muscle,UBERON:0002380,trapezius muscle
+HP:0000982,Palmoplantar keratoderma,HP:0000962,Hyperkeratosis
+UBERON:4200022,extracleithrum,UBERON:0008907,dermal bone
+HP:0009907,Attached earlobe,HP:0000363,Abnormality of earlobe
+UBERON:3000038,basimandibulare,UBERON:0010313,neural crest-derived structure
+HP:0008230,Decreased testosterone in males,HP:0008373,Puberty and gonadal disorders
+UBERON:3000657,dentigerous process,UBERON:4100000,skeletal element projection
+HP:0000870,Prolactin excess,HP:0010514,Hyperpituitarism
+HP:0008477,Poorly ossified cervical vertebrae,HP:0100856,Poorly ossified vertebrae
+HP:0100469,Patchy sclerosis of the distal phalanx of the 5th toe,HP:0100942,Sclerosis of the distal phalanx of the 5th toe
+UBERON:0002144,peripeduncular nucleus,UBERON:0007414,nucleus of midbrain tegmentum
+HP:0011393,Aplasia of the vestibular nerve.,HP:0011392,Abnormality of the vestibular nerve
+UBERON:0000922,embryo,UBERON:0000468,multi-cellular organism
+UBERON:0010295,substantia propria of sclera,UBERON:0010291,layer of sclera
+DOID:857,multiple carboxylase deficiency,DOID:2978,carbohydrate metabolic disorder
+UBERON:2001696,gongyloid cartilage,UBERON:0011004,pharyngeal arch cartilage
+UBERON:0016480,interlobular stroma of liver,UBERON:0016478,liver stroma
+UBERON:2001702,infraorbital 7,UBERON:2000376,infraorbital
+DOID:0060079,Her2-receptor positive breast cancer,DOID:1612,breast cancer
+UBERON:0004447,proximal epiphysis of phalanx,UBERON:0004446,epiphysis of phalanx
+HP:0005236,Chronic calcifying pancreatitis,HP:0001733,Pancreatitis
+UBERON:0003494,respiratory system venule,UBERON:0003504,respiratory system blood vessel
+UBERON:0001556,lower urinary tract,UBERON:0006554,urinary system structure
+UBERON:2000602,uroneural,UBERON:0003861,neural arch
+UBERON:0001411,basilic vein,UBERON:0001638,vein
+UBERON:0005113,metanephric cortex mesenchyme,UBERON:0003104,mesenchyme
+DOID:7694,bladder urachal adenocarcinoma,DOID:3711,bladder adenocarcinoma
+UBERON:0013192,ovarian medulla,UBERON:0005156,reproductive structure
+UBERON:0014873,distal epiphysis of distal phalanx of pedal digit 3,UBERON:0014876,distal epiphysis of distal phalanx of pedal digit
+DOID:0050547,familial medullary thyroid carcinoma,DOID:0050736,autosomal dominant disease
+UBERON:0009678,tooth row,UBERON:0003672,dentition
+HP:0010592,Abnormality of the distal tibial epiphysis,HP:0006508,Abnormality of tibial epiphyses
+DOID:5746,ovarian serous cystadenocarcinoma,DOID:5744,ovary serous adenocarcinoma
+UBERON:0003938,sensory dissociation area,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005352,spermatic cord,UBERON:0014403,male anatomical structure
+NCBITaxon:157541,Zygodontomys brevicauda,NCBITaxon:157540,Zygodontomys
+HP:0000820,Abnormality of the thyroid gland,HP:0000818,Abnormality of the endocrine system
+HP:0011086,Dentinogenesis imperfecta of primary and permanent teeth,HP:0000703,Dentinogenesis imperfecta
+HP:0006432,Trapezoidal distal femoral condyles,HP:0002823,Abnormality of the femur
+HP:0005190,Proximal finger joint hyperextensibility,HP:0001187,Hyperextensibility of the finger joints
+HP:0000064,Hypoplastic labia minora,HP:0000066,Labial hypoplasia
+UBERON:3000036,basal process of palatoquadrate,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010308,Asternia,HP:0006714,Aplasia/Hypoplasia of the sternum
+UBERON:0015796,liver blood vessel,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0009966,Complete duplication of the middle phalanx of the 3rd finger,HP:0009963,Duplication of the middle phalanx of the 3rd finger
+UBERON:0012421,urodeum,UBERON:0004120,mesoderm-derived structure
+DOID:6961,Bartholin's gland squamous cell carcinoma,DOID:2101,vulva squamous cell carcinoma
+UBERON:4300036,supraneural cartilage,UBERON:2001457,postcranial axial cartilage
+CL:0002544,aortic endothelial cell,CL:1000413,endothelial cell of artery
+UBERON:0009779,cardiac muscle tissue of right auricle,UBERON:0003378,cardiac muscle of auricular region
+HP:0100672,Vaginal hernia,HP:0100823,Genital hernia
+UBERON:0003844,upper eyelid epithelium,UBERON:0015808,eye epithelium
+UBERON:0015153,medial gland of orbital region,UBERON:0015152,gland of orbital region
+HP:0009436,Triangular shaped middle phalanx of the 3rd finger,HP:0009850,Triangular shaped middle phalanges of the hand
+HP:0000544,External ophthalmoplegia,HP:0000602,Ophthalmoplegia
+UBERON:0001446,fibula,UBERON:0004251,hindlimb zeugopod bone
+HP:0000616,Miosis,HP:0000615,Abnormality of the pupil
+HP:0011548,Absent right sided atrioventricular connection,HP:0011546,Abnormal atrioventricular connection
+CL:0000541,melanoblast,CL:0000710,neurecto-epithelial cell
+UBERON:0004101,nasolabial region,UBERON:0004121,ectoderm-derived structure
+UBERON:0014593,tuberomammillary nucleus dorsal part,UBERON:0002785,regional part of lateral hypothalamic region
+CL:0000921,type I NK T cell,CL:0000814,mature NK T cell
+DOID:2643,perivascular epithelioid cell tumor,DOID:3316,perivascular tumor
+UBERON:0012075,replacement bone,UBERON:0001474,bone element
+HP:0009674,Triangular epiphysis of the proximal phalanx of the thumb,HP:0010267,Triangular epiphyses of the middle phalanges of the hand
+HP:0010501,Limitation of knee mobility,HP:0001376,Limitation of joint mobility
+UBERON:0004025,lateral ganglionic eminence,UBERON:0005423,developing anatomical structure
+UBERON:0005496,neural tube lateral wall,UBERON:0002050,embryonic structure
+HP:0004237,Large carpal bones,HP:0006014,Abnormally shaped carpal bones
+UBERON:0008955,middle lobe of lung,UBERON:0000101,lobe of lung
+UBERON:0006355,superior vesical vein,UBERON:0002460,vesical vein
+NCBITaxon:7157,Culicidae,NCBITaxon:41827,Culicoidea
+HP:0001597,Abnormality of the nail,HP:0011138,Abnormality of skin adnexa
+HP:0011557,Double inlet to single ventricle of indeterminate morphology,HP:0011554,Double inlet atrioventricular connection
+HP:0012267,Absent ciliary axoneme radial spokes,HP:0005938,Abnormal respiratory motile cilium morphology
+HP:0003421,Platyspondyly (childhood),HP:0000926,Platyspondyly
+UBERON:0015029,manual digit 5 phalanx endochondral element,UBERON:0015024,manual digit phalanx endochondral element
+HP:0009936,Narrow nasal septum,HP:0000419,Abnormality of the nasal septum
+HP:0011472,Abnormality of small intestinal villus morphology,HP:0002244,Abnormality of the small intestine
+UBERON:3010781,pars convoluta,UBERON:0014404,female anatomical structure
+UBERON:0011154,gular region,UBERON:0003102,surface structure
+UBERON:0004376,fin bone,UBERON:0001474,bone element
+UBERON:2002250,epural 2,UBERON:2000660,epural
+UBERON:0015788,olfactory apparatus chamber,UBERON:0015787,upper respiratory conduit
+HP:0009638,Short proximal phalanx of thumb,HP:0009629,Aplasia/Hypoplasia of the proximal phalanx of the thumb
+UBERON:0001357,inferior rectal artery,UBERON:0003835,abdominal segment blood vessel
+HP:0002058,Myopathic facies,HP:0010628,Facial palsy
+HP:0012026,Hyperornithinemia,HP:0012025,Abnormality of ornithine metabolism
+UBERON:0004099,joint space of elbow,UBERON:0000464,anatomical space
+UBERON:0002715,spinal trigeminal tract of medulla,UBERON:0014761,spinal trigeminal tract
+HP:0002992,Abnormality of the tibia,HP:0002981,Abnormality of the calf
+UBERON:0013157,1st arch maxillary-mandibular cleft,UBERON:0005879,pharyngeal cleft
+NCBITaxon:34630,Rhipicephalus <genus>,NCBITaxon:426437,Rhipicephalinae
+UBERON:0009145,pharyngeal region,UBERON:0005423,developing anatomical structure
+UBERON:2000437,caudal fin actinotrichium,UBERON:2000089,actinotrichium
+UBERON:0005303,hypogastric nerve,UBERON:0001816,autonomic nerve plexus
+DOID:7202,intermediate malignant teratoma,DOID:5563,malignant teratoma
+UBERON:0007288,presumptive forebrain midbrain boundary,UBERON:0006598,presumptive structure
+HP:0011434,Low maternal serum chorionic gonadotropin,HP:0011436,Abnormal maternal serum screening
+CL:1000601,ureteral cell,CL:0000548,animal cell
+HP:0006510,Chronic obstructive pulmonary disease,HP:0006536,Obstructive lung disease
+CL:1000483,purkinje myocyte of internodal tract,CL:0002068,Purkinje myocyte
+CL:0002672,retinal progenitor cell,CL:0000048,multi fate stem cell
+HP:0007021,Pain insensitivity,HP:0007328,Impaired pain sensation
+UBERON:0010400,spleen trabecular vein,UBERON:0013126,vein of abdomen
+DOID:4974,actinobacillosis,DOID:0050339,commensal bacterial infectious disease
+HP:0005841,Calcific stippling of infantile cartilaginous skeleton,HP:0011849,Abnormal bone ossification
+HP:0009055,Generalized limb muscle atrophy,HP:0003700,Generalized amyotrophy
+CL:0000484,connective tissue type mast cell,CL:0002320,connective tissue cell
+UBERON:0006290,scapula cartilage element,UBERON:0005863,cartilaginous condensation
+HP:0001284,Areflexia,HP:0001315,Reduced tendon reflexes
+NCBITaxon:11050,Flaviviridae,NCBITaxon:35278,"ssRNA positive-strand viruses, no DNA stage"
+UBERON:0006342,left subhepatic recess,UBERON:0006442,subhepatic recess
+DOID:6339,vulvar eccrine adenocarcinoma,DOID:2098,vulva adenocarcinoma
+DOID:0050147,otomycosis,DOID:9463,otitis externa
+UBERON:0007385,pectoral appendage lymph vessel,UBERON:0007384,appendage lymph vessel
+DOID:11719,oculopharyngeal muscular dystrophy,DOID:929,myopathy of extraocular muscle
+DOID:936,brain disease,DOID:331,central nervous system disease
+UBERON:0004359,corpus epididymis,UBERON:0014403,male anatomical structure
+DOID:2473,opportunistic mycosis,DOID:0050136,systemic mycosis
+UBERON:3000948,articular process,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0012363,thyroid follicle epithelium,UBERON:0005911,endo-epithelium
+HP:0002880,Respiratory difficulties,HP:0002795,Functional respiratory abnormality
+DOID:4960,bone marrow cancer,DOID:2531,hematologic cancer
+UBERON:3000877,intumescentia bilateralis inferior,UBERON:0004120,mesoderm-derived structure
+DOID:1272,telangiectasis,DOID:341,peripheral vascular disease
+DOID:12685,mixed receptive-expressive language disorder,DOID:2033,communication disorder
+CL:1000419,myoepithelial cell of lactiferous duct,CL:1000416,myoepithelial cell of lactiferous gland
+UBERON:0007843,uncinate process of ribs,UBERON:0005055,zone of long bone
+UBERON:0007357,proventriculus,UBERON:0011953,stomach glandular region
+HP:0012685,Decreased pineal volume,HP:0012684,Abnormal pineal volume
+UBERON:0004784,heart ventricle wall,UBERON:0000060,anatomical wall
+UBERON:2005267,erector muscle,UBERON:0001134,skeletal muscle tissue
+UBERON:0005281,ventricular system of central nervous system,UBERON:0004121,ectoderm-derived structure
+CL:1000804,kidney outer medulla interstitial cell,CL:1000682,kidney medulla interstitial cell
+UBERON:4000120,mineralized avascular GAG-rich matrix,UBERON:4000020,mineralized extracellular matrix
+UBERON:0000325,gastric gland,UBERON:0003294,gland of foregut
+HP:0007105,Infantile encephalopathy,HP:0001298,Encephalopathy
+UBERON:0007299,choroid plexus of tectal ventricle,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:0050279,conidiobolomycosis,DOID:0050135,subcutaneous mycosis
+HP:0003956,Bowed forearm bones,HP:0002973,Abnormality of the forearm
+DOID:7360,solid pattern testicular yolk sac tumor,DOID:5344,testicular yolk sac tumor
+UBERON:2000088,YSL,UBERON:0002050,embryonic structure
+HP:0100477,Symphalangism affecting the distal phalanx of the 4th toe,HP:0010377,Symphalangism affecting the phalanges of the 4th toe
+UBERON:0006934,sensory epithelium,UBERON:0000488,atypical epithelium
+UBERON:2000573,internal cellular layer,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003212,gustatory organ,UBERON:0000005,chemosensory organ
+HP:0001011,Diaphoresis (with pheochromocytoma),HP:0001005,Dermatological manifestations of systemic disorders
+UBERON:0010246,choroidal guanine tapetum,UBERON:0010244,choroid tapetum lucidum
+UBERON:0006267,notochordal plate,UBERON:0010371,ecto-epithelium
+HP:0003140,T-wave inversion in the right precordial leads,HP:0010872,EKG: T-wave inversion
+UBERON:0000200,gyrus,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0004240,Sclerotic foci within carpal bones,HP:0009164,Abnormal calcification of the carpal bones
+HP:0005950,Partial laryngeal atresia,HP:0008750,Laryngeal atresia
+UBERON:0005027,mucosa of frontal sinus,UBERON:0000344,mucosa
+HP:0000877,Insulin-resistant diabetes mellitus at puberty,HP:0000831,Insulin-resistant diabetes mellitus
+DOID:0080021,Schmid metaphyseal chondrodysplasia,DOID:0080019,metaphyseal dysplasia
+DOID:11481,constrictive pericarditis,DOID:1787,pericarditis
+UBERON:2001533,pharyngobranchial cartilage,UBERON:2001909,pharyngobranchial element
+HP:0011942,Increased urinary sulfite,HP:0004369,Decreased purine levels
+HP:0010502,Fibular bowing,HP:0002991,Abnormality of the fibula
+HP:0100214,Bracket epiphysis of the middle phalanx of the 5th toe,HP:0100098,Abnormality of the epiphysis of the middle phalanx of the 5th toe
+HP:0002401,Stroke-like episodes,HP:0001297,Stroke
+HP:0011437,Maternal autoimmune disease,HP:0002686,Prenatal maternal abnormality
+DOID:4454,childhood kidney cell carcinoma,DOID:3675,childhood kidney neoplasm
+DOID:7430,childhood germ cell brain tumor,DOID:6052,central nervous system childhood germ cell tumor
+DOID:10913,benign essential hypertension,DOID:10825,essential hypertension
+CL:0011006,lugaro cell,CL:1001611,cerebellar neuron
+UBERON:0004419,proximal epiphysis of phalanx of manual digit 3,UBERON:0004414,proximal epiphysis of phalanx of manus
+HP:0009179,Deviation of the 5th finger,HP:0004097,Deviation of finger
+DOID:11832,visual epilepsy,DOID:1826,epilepsy syndrome
+UBERON:2002000,posterior dentation of pectoral fin spine,UBERON:0004121,ectoderm-derived structure
+HP:0009170,Osteolytic defects of the middle phalanx of the 5th finger,HP:0009847,Osteolytic defects of the middle phalanges of the hand
+HP:0009608,Complete duplication of proximal phalanx of the thumb,HP:0009613,Duplication of the proximal phalanx of the thumb
+UBERON:0012181,tonsil crypt,UBERON:0013696,tonsil epithelium
+HP:0006938,Impaired vibration sensation at ankles,HP:0002166,Impaired vibration sensation in the lower limbs
+UBERON:0003700,temporomandibular joint,UBERON:0004120,mesoderm-derived structure
+HP:0100269,Paramedian lip pit,HP:0100267,Lip pit
+UBERON:2000576,pterotic,UBERON:0002513,endochondral bone
+DOID:3672,rhabdoid cancer,DOID:3675,childhood kidney neoplasm
+UBERON:0001599,stapedius muscle,UBERON:0004113,muscle of auditory ossicle
+DOID:5488,mediastinum synovial sarcoma,DOID:4050,mediastinum sarcoma
+HP:0002642,Arteriovenous fistulas of celiac and mesenteric vessels,HP:0004947,Arteriovenous fistula
+UBERON:0014864,caterpillar stage,UBERON:0000069,larval stage
+UBERON:0004314,distal phalanx of manual digit 5,UBERON:0003865,distal phalanx of manus
+UBERON:0002366,bulbo-urethral gland,UBERON:0010186,male urethral gland
+UBERON:0002054,zona fasciculata of adrenal gland,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0007872,Choroidal hemangiomata,HP:0001028,Hemangioma
+UBERON:0010701,phalanx cartilage element,UBERON:0015023,phalanx endochondral element
+UBERON:0008444,webbed manual digit,UBERON:0002389,manual digit
+UBERON:0012486,muscle layer of cloaca,UBERON:0004120,mesoderm-derived structure
+HP:0005003,Aplasia/Hypoplasia of the capital femoral epiphysis,HP:0010574,Abnormality of the epiphysis of the femoral head
+DOID:864,phlebitis,DOID:866,vein disease
+NCBITaxon:121739,Lacazia,NCBITaxon:34383,mitosporic Onygenales
+UBERON:0006089,dorsal external arcuate fiber bundle,UBERON:0000122,neuron projection bundle
+HP:0100764,Lymphangioma,HP:0100763,Abnormality of the lymphatic system
+CL:0002322,embryonic stem cell,CL:0002321,embryonic cell
+HP:0004898,Persistent lactic acidosis,HP:0003128,Lactic acidosis
+DOID:3328,temporal lobe epilepsy,DOID:2234,focal epilepsy
+HP:0009837,Bullet-shaped distal phalanges of the hand,HP:0009769,Bullet-shaped phalanges of the hand
+UBERON:0002522,tunica media,UBERON:0004797,blood vessel layer
+CL:0000083,epithelial cell of pancreas,CL:0000066,epithelial cell
+UBERON:0012136,prehallux,UBERON:0008784,lower limb segment
+UBERON:0015086,distal carpal bone 1 pre-cartilage condensation,UBERON:0015084,distal carpal bone 1 endochondral element
+UBERON:2001592,claustrum bone,UBERON:2000461,Weberian ossicle
+UBERON:0006246,humerus pre-cartilage condensation,UBERON:0010882,limb bone pre-cartilage condensation
+HP:0001266,Choreoathetosis,HP:0002072,Chorea
+UBERON:4200170,process 3,UBERON:0004120,mesoderm-derived structure
+UBERON:0007730,interphalangeal joint of manual digit 3,UBERON:0007722,interphalangeal joint of manus
+UBERON:0001692,basioccipital bone,UBERON:0002513,endochondral bone
+UBERON:0011795,remex feather,UBERON:0011793,flight feather
+UBERON:0001862,vestibular labyrinth,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0003648,Lacticaciduria,HP:0003128,Lactic acidosis
+UBERON:0000007,pituitary gland,UBERON:0003296,gland of diencephalon
+HP:0100559,Lower limb asymmetry,HP:0002814,Abnormality of the lower limb
+UBERON:0006672,incisive canal,UBERON:0005744,bone foramen
+HP:0009231,Patchy sclerosis of the proximal phalanx of the 5th finger,HP:0100911,Sclerosis of the proximal phalanx of the 5th finger
+UBERON:0011107,synovial joint of pelvic girdle,UBERON:0002217,synovial joint
+HP:0009586,Symphalangism affecting the proximal phalanx of the 2nd finger,HP:0009857,Symphalangism affecting the proximal phalanges of the hand
+UBERON:0014691,right gastric vein,UBERON:0015212,lateral structure
+HP:0009271,Triangular epiphysis of the proximal phalanx of the 4th finger,HP:0010278,Triangular epiphyses of the proximal phalanges of the hand
+DOID:0050147,otomycosis,DOID:37,skin disease
+UBERON:0002805,right limbic lobe,UBERON:0002600,limbic lobe
+HP:0008066,Abnormal blistering of the skin,HP:0011121,Abnormality of skin morphology
+HP:0010212,Flexion contracture of the hallux,HP:0001844,Abnormality of the hallux
+DOID:0050571,congenital disorder of glycosylation type II,DOID:5212,congenital disorder of glycosylation
+NCBITaxon:40674,Mammalia,NCBITaxon:32524,Amniota
+HP:0009699,Osteolytic defects of the hand bones,HP:0001155,Abnormality of the hand
+HP:0004394,Multiple gastric polyps,HP:0006753,Neoplasm of the stomach
+HP:0000467,Neck muscle weakness,HP:0001324,Muscle weakness
+NCBITaxon:36827,Clostridium botulinum B,NCBITaxon:1491,Clostridium botulinum
+CL:0002157,endosteal cell,CL:0001035,bone cell
+DOID:1826,epilepsy syndrome,DOID:936,brain disease
+UBERON:0005220,pancreas head parenchyma,UBERON:0004119,endoderm-derived structure
+UBERON:0000947,aorta,UBERON:0003509,arterial blood vessel
+UBERON:2000488,ceratobranchial bone,UBERON:0002513,endochondral bone
+CL:0002642,epithelial cell of esophageal cardiac gland,CL:0002657,glandular cell of esophagus
+HP:0008052,Abnormal retinal folds,HP:0000479,Abnormality of the retina
+HP:0002084,Encephalocele,HP:0011815,Cephalocele
+HP:0011946,Bronchiolitis obliterans,HP:0006530,Interstitial pulmonary disease
+UBERON:0002386,forelimb zeugopod,UBERON:0008785,upper limb segment
+NCBITaxon:730,Haemophilus ducreyi,NCBITaxon:724,Haemophilus
+UBERON:0002291,central canal of spinal cord,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:14784,olivopontocerebellar atrophy,DOID:1441,spinocerebellar ataxia
+HP:0001400,Hepatic abscesses due to immunodeficiency,HP:0002721,Immunodeficiency
+HP:0009016,Upper limb muscle hypoplasia,HP:0009004,Hypoplasia of the musculature
+UBERON:0001453,distal tarsal bone 2,UBERON:0015105,distal tarsal bone 2 endochondral element
+HP:0007772,Impaired smooth pursuit,HP:0000617,Abnormality of ocular smooth pursuit
+NCBITaxon:1392,Bacillus anthracis,NCBITaxon:86661,Bacillus cereus group
+CL:0000240,stratified squamous epithelial cell,CL:0000079,stratified epithelial cell
+CL:0000653,glomerular visceral epithelial cell,CL:0002522,renal filtration cell
+DOID:10398,pneumonic plague,DOID:3482,plague
+HP:0011190,Uni- and bilateral multifocal epileptiform discharges,HP:0010841,Multifocal epileptiform discharges
+UBERON:3010836,Posterolateral Supplementary Element,UBERON:0010931,intermandibularis
+UBERON:0005276,dorsal skin of finger,UBERON:0005275,dorsal skin of digit
+HP:0100634,Neuroendocrine neoplasm,HP:0100007,Neoplasm of the peripheral nervous system
+HP:0006712,Aplasia/Hypoplasia of the ribs,HP:0000772,Abnormality of the ribs
+UBERON:3000906,sulcus pro musculo extensori cruris brevis,UBERON:0004120,mesoderm-derived structure
+UBERON:0015837,incisor dental pulp,UBERON:0001754,dental pulp
+CL:2000002,decidua cell,CL:0000003,native cell
+HP:0100534,Episcleritis,HP:0100533,Inflammatory abnormality of the eye
+UBERON:0002062,endocardial cushion,UBERON:0014387,mesenchyme derived from neural crest
+NCBITaxon:131221,Streptophytina,NCBITaxon:35493,Streptophyta
+DOID:12883,hypochondriasis,DOID:4737,somatoform disorder
+HP:0001783,Broad metatarsal,HP:0001832,Abnormality of the metatarsal bones
+DOID:7928,testis refractory cancer,DOID:5556,testicular malignant germ cell cancer
+HP:0011561,Overriding atrioventricular valve,HP:0011546,Abnormal atrioventricular connection
+UBERON:3000283,margo orbitalis of squamosal,UBERON:0000064,organ part
+UBERON:0011314,anterior subdivision of masseter,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005470,right umbilical artery,UBERON:0001310,umbilical artery
+UBERON:0011318,capsule of temporomandibular joint,UBERON:0010313,neural crest-derived structure
+DOID:2513,basal cell carcinoma,DOID:3451,skin carcinoma
+DOID:3825,Shwartzman phenomenon,DOID:865,vasculitis
+HP:0005661,Salmonella osteomyelitis,HP:0002754,Osteomyelitis
+HP:0010345,Flexion contracture of the 5th toe,HP:0010322,Abnormality of the 5th toe
+UBERON:0009688,posterior inferior cerebellar artery,UBERON:0004573,systemic artery
+DOID:1556,arthus reaction,DOID:1555,urticaria
+UBERON:0002477,medial globus pallidus,UBERON:0005401,cerebral hemisphere grey matter
+UBERON:0001502,interosseous muscle of manus,UBERON:0014375,intrinsic muscle of manus
+NCBITaxon:33183,Onygenales,NCBITaxon:451871,Eurotiomycetidae
+HP:0200054,Monodactyly (feet),HP:0001849,Oligodactyly (feet)
+UBERON:0001636,posterior cerebral artery,UBERON:0015212,lateral structure
+UBERON:0011213,root of vagus nerve,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0012448,Delayed myelination,HP:0012447,Abnormal myelination
+UBERON:0003996,cervical vertebra 1 arcus anterior,UBERON:4100000,skeletal element projection
+HP:0005967,Mixed respiratory and metabolic acidosis,HP:0001942,Metabolic acidosis
+UBERON:0009592,mesenchyme of interdigital region between pedal digits 3 and 4,UBERON:0009598,mesenchyme of interdigital region between digits 3 and 4
+DOID:8188,uterine corpus choriocarcinoma,DOID:3594,choriocarcinoma
+DOID:0050660,Beare-Stevenson cutis gyrata syndrome,DOID:0050736,autosomal dominant disease
+HP:0100210,Small epiphysis of the distal phalanx of the 5th toe,HP:0100097,Abnormality of the epiphysis of the distal phalanx of the 5th toe
+DOID:0050779,hydrolethalus syndrome,DOID:0050737,autosomal recessive disease
+DOID:0050806,glioblastoma neural subtype,DOID:3068,glioblastoma multiforme
+DOID:7763,carcinoma of supraglottis,DOID:13476,supraglottis cancer
+HP:0008687,Hypoplasia of the prostate,HP:0008775,Abnormality of the prostate
+UBERON:0002465,lymphoid system,UBERON:0000477,anatomical cluster
+UBERON:0003637,manual digit 3 phalanx,UBERON:0015027,manual digit 3 phalanx endochondral element
+DOID:2043,hepatitis B,DOID:934,viral infectious disease
+CL:0002352,gestational hematopoietic stem cell,CL:0000037,hematopoietic stem cell
+HP:0012606,Renal sodium wasting,HP:0012603,Abnormal urine sodium concentration
+HP:0005109,Abnormality of the Achilles tendon,HP:0100261,Abnormal tendon morphology
+UBERON:0002907,superior postcentral sulcus,UBERON:0003022,cerebral cortex lobe
+CL:0002633,respiratory basal cell,CL:0002368,respiratory epithelial cell
+HP:0006619,Anterior rib punctate calcifications,HP:0012306,Abnormal rib ossification
+UBERON:0014838,xiphihumeralis,UBERON:0001495,pectoral muscle
+UBERON:0000428,prostate epithelium,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:5741,pancreatic vasoactive intestinal peptide producing tumor,DOID:1799,islet cell tumor
+UBERON:2000542,medial column,UBERON:0000477,anatomical cluster
+DOID:1586,rheumatic fever,DOID:65,connective tissue disease
+HP:0012338,Abnormal energy expenditure,HP:0012337,Abnormal homeostasis
+UBERON:4200033,cleithrum head,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:6428,cervical adenoid basal carcinoma,DOID:2893,cervix carcinoma
+CL:0010012,cerebral cortex neuron,CL:0000540,neuron
+HP:0100383,Aplasia of the middle phalanx of the 5th toe,HP:0100387,Aplasia of the middle phalanges of the toes
+UBERON:0004368,Reichert's cartilage,UBERON:0002418,cartilage tissue
+HP:0001283,Bulbar palsy,HP:0001324,Muscle weakness
+HP:0010008,Duplication of the middle phalanx of hand,HP:0009833,Abnormality of the middle phalanges of the hand
+HP:0002470,Nonprogressive cerebellar ataxia,HP:0001251,Ataxia
+UBERON:0004186,olfactory bulb mitral cell layer,UBERON:0004001,olfactory bulb layer
+DOID:1777,unilateral hyperactive labyrinth,DOID:566,labyrinthine dysfunction
+HP:0012239,Atransferrinemia,HP:0010876,Abnormality of circulating protein level
+UBERON:0013248,paradidymis,UBERON:0005156,reproductive structure
+DOID:14720,type I Ehlers-Danlos syndrome,DOID:13359,Ehlers-Danlos syndrome
+HP:0010051,Deviation/Displacement of the hallux,HP:0100498,Deviation of toes
+UBERON:2000469,anterior semicircular canal primordium,UBERON:2002215,otic vesicle protrusion
+UBERON:0010328,limb bud mesenchyme,UBERON:0010329,paired limb/fin bud mesenchyme
+UBERON:0003894,liver primordium,UBERON:0009497,epithelium of foregut-midgut junction
+UBERON:4200125,supraacetabular crest,UBERON:4100000,skeletal element projection
+HP:0010156,Pseudoepiphysis of the 1st metatarsal,HP:0010125,Abnormality of the epiphysis of the 1st metatarsal
+HP:0010490,Abnormality of the palmar creases,HP:0001018,Abnormal palmar dermatoglyphics
+HP:0009431,Bullet-shaped middle phalanx of the 3rd finger,HP:0009441,Bullet-shaped phalanges of the 3rd finger
+UBERON:0011997,coelom,UBERON:0000481,multi-tissue structure
+UBERON:0006691,tentorium cerebelli,UBERON:0000064,organ part
+DOID:0050879,fragile X-associated tremor/ataxia syndrome,DOID:0050735,X-linked disease
+HP:0003009,Enhanced neurotoxicity of vincristine,HP:0000759,Abnormality of the peripheral nervous system
+UBERON:0010289,scleral cartilage,UBERON:0010296,scleral skeletal element
+HP:0009934,Supernumerary nostrils,HP:0005288,Abnormality of the nares
+UBERON:0001042,chordate pharynx,UBERON:0004185,endodermal part of digestive tract
+DOID:13476,supraglottis cancer,DOID:2596,larynx cancer
+DOID:11202,primary hyperparathyroidism,DOID:13543,hyperparathyroidism
+HP:0008339,Diaminoaciduria,HP:0003355,Aminoaciduria
+DOID:10655,lipoma of colon,DOID:6460,large intestine lipoma
+UBERON:0002143,dorsal tegmental nucleus,UBERON:0007414,nucleus of midbrain tegmentum
+DOID:402,oral tuberculosis,DOID:404,gastrointestinal tuberculosis
+UBERON:2005034,parachordal vessel,UBERON:0003481,tail vein
+UBERON:2001235,hypobranchial 3 bone,UBERON:2000363,hypobranchial bone
+NCBITaxon:337963,Neotominae,NCBITaxon:337677,Cricetidae
+UBERON:0010896,piston cartilage,UBERON:0002418,cartilage tissue
+HP:0000448,Prominent nose,HP:0005105,Abnormal nasal morphology
+HP:0002176,Spinal cord compression,HP:0002143,Abnormality of the spinal cord
+UBERON:0002278,perilymphatic space,UBERON:0002553,anatomical cavity
+HP:0004890,Elevated pulmonary artery pressure,HP:0004414,Abnormality of the pulmonary artery
+UBERON:3010562,suboccular foramen,UBERON:3000051,braincase and otic capsule opening
+UBERON:0011683,adductor mandibulae,UBERON:0011145,adductor muscle
+HP:0009580,Aplasia/Hypoplasia of the proximal phalanx of the 2nd finger,HP:0009552,Aplasia/Hypoplasia of the phalanges of the 2nd finger
+DOID:10550,acute eustachian salpingitis,DOID:2000,otosalpingitis
+DOID:2050,acute maxillary sinusitis,DOID:2051,maxillary sinusitis
+CL:0000476,thyrotroph,CL:0000639,basophil cell of pars distalis of adenohypophysis
+DOID:888,fasciolopsiasis,DOID:883,parasitic helminthiasis infectious disease
+HP:0008326,Vitamin B6 deficiency,HP:0004340,Abnormality of vitamin B metabolism
+CL:0000955,pre-B-II cell,CL:0000817,precursor B cell
+UBERON:3000773,ilial ridge,UBERON:4100000,skeletal element projection
+DOID:12537,hypermobility of coccyx,DOID:1123,spondyloarthropathy
+UBERON:0003386,smooth muscle of eye,UBERON:0004121,ectoderm-derived structure
+UBERON:0009191,sphenoid bone pre-cartilage condensation,UBERON:0014387,mesenchyme derived from neural crest
+UBERON:2001963,hypobranchial 2 bone distal cartilage,UBERON:0011004,pharyngeal arch cartilage
+HP:0012024,Hypergalactosemia,HP:0004915,Impairment of galactose metabolism
+HP:0002404,Thickened superior cerebellar peduncle,HP:0011932,Abnormality of the superior cerebellar peduncle
+UBERON:0012241,male urethral meatus,UBERON:0014403,male anatomical structure
+UBERON:0012278,gland of nasal mucosa,UBERON:0002365,exocrine gland
+DOID:0060092,immune system organ benign neoplasm,DOID:0060085,organ system benign neoplasm
+DOID:12177,common variable immunodeficiency,DOID:2583,agammaglobulinemia
+UBERON:0001492,radial nerve,UBERON:0003433,arm nerve
+DOID:3281,combined thymoma,DOID:3275,thymoma
+UBERON:0010572,manual digit 3 metacarpus cartilage element,UBERON:0010677,manual digit 3 phalanx cartilage element
+HP:0009429,Aplasia of the distal phalanx of the 3rd finger,HP:0009460,Aplasia of the 3rd finger
+UBERON:0010685,pedal digit phalanx cartilage element,UBERON:0005255,pedal digit mesenchyme
+HP:0001406,Intrahepatic cholestasis,HP:0001396,Cholestasis
+HP:0002574,Episodic abdominal pain,HP:0002027,Abdominal pain
+DOID:5224,acute hemorrhagic encephalitis,DOID:9588,encephalitis
+HP:0012212,Abnormal glomerular filtration rate,HP:0012211,Abnormal renal physiology
+UBERON:3010190,tibial protuberances,UBERON:3000981,limb external integument structure
+CL:1001108,kidney loop of henle medullary thick ascending limb epithelial cell,CL:1001106,kidney loop of henle thick ascending limb epithelial cell
+CL:0000692,terminal Schwann cell,CL:0002376,non-myelinating Schwann cell
+UBERON:0002642,cuneate fasciculus of medulla,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3000570,spatium sacculare,UBERON:0000064,organ part
+UBERON:0002255,vomeronasal organ,UBERON:0000020,sense organ
+HP:0100026,Arteriovenous malformation,HP:0002597,Abnormality of the vasculature
+CL:0002604,astrocyte of the hippocampus,CL:0002605,astrocyte of the cerebral cortex
+UBERON:2001989,mandibular-hyoid median cartilage,UBERON:0011004,pharyngeal arch cartilage
+HP:0005645,Intervertebral disk calcification,HP:0010766,Ectopic calcification
+UBERON:4000146,transient cartilaginous element,UBERON:0010363,endochondral element
+UBERON:0003077,paraxial mesoderm,UBERON:0005291,embryonic tissue
+UBERON:0006008,fibrous ring of heart,UBERON:0004120,mesoderm-derived structure
+NCBITaxon:6944,Ixodes,NCBITaxon:426442,Ixodinae
+UBERON:0007830,pelvic girdle bone/zone,UBERON:0007828,girdle bone/zone
+UBERON:0000977,pleura,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0007007,Cavitation of the basal ganglia,HP:0002134,Abnormality of the basal ganglia
+HP:0100744,Abnormality of the humeroradial joint,HP:0009811,Abnormality of the elbow
+DOID:1219,dicrocoeliasis,DOID:883,parasitic helminthiasis infectious disease
+UBERON:2007014,anterior presumptive neural plate,UBERON:0005291,embryonic tissue
+UBERON:0008962,forelimb bone,UBERON:0015021,forelimb endochondral element
+UBERON:2001908,epibranchial 4 element,UBERON:2001904,epibranchial element
+UBERON:0003560,spinal cord arachnoid mater,UBERON:0003292,meninx of spinal cord
+HP:0001138,Optic neuropathy,HP:0000587,Abnormality of the optic nerve
+UBERON:0004024,medial ganglionic eminence,UBERON:0005423,developing anatomical structure
+DOID:2733,skin atrophy,DOID:37,skin disease
+HP:0000535,Sparse eyebrow,HP:0100840,Aplasia/Hypoplasia of the eyebrow
+HP:0012059,Lentigo maligna melanoma,HP:0012056,Cutaneous melanoma
+UBERON:0004096,odontoid process of cervical vertebra 2,UBERON:0004120,mesoderm-derived structure
+UBERON:0014430,sciatic notch,UBERON:0005744,bone foramen
+UBERON:2007023,posterior neural keel,UBERON:0004121,ectoderm-derived structure
+UBERON:3000648,crista praeopercularis,UBERON:0010313,neural crest-derived structure
+UBERON:0009128,lateral line placode,UBERON:0003067,dorsolateral placode
+UBERON:0005106,metanephric tubule,UBERON:0005108,metanephric epithelium
+HP:0100711,Abnormality of the thoracic spine,HP:0000925,Abnormality of the vertebral column
+HP:0011263,Forward facing earlobe,HP:0000363,Abnormality of earlobe
+DOID:2825,nose disease,DOID:974,upper respiratory tract disease
+HP:0100459,Osteolytic defects of the distal phalanx of the 4th toe,HP:0010375,Osteolytic defects of the phalanges of the 4th toe
+DOID:12307,anterior corneal pigmentation,DOID:11547,corneal deposit
+HP:0010923,Anterior subcapsular cataract,HP:0000523,Subcapsular cataract
+UBERON:0002983,lateral posterior nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0001778,ciliary epithelium,UBERON:0000488,atypical epithelium
+DOID:14225,acute frontal sinusitis,DOID:10791,frontal sinusitis
+CL:1001431,kidney collecting duct principal cell,CL:1000454,kidney collecting duct epithelial cell
+UBERON:0010898,gastralium,UBERON:0003828,abdominal segment bone
+CL:0000422,mitogenic signaling cell,CL:0000003,native cell
+DOID:3241,lipid pneumonia,DOID:3240,aspiration pneumonitis
+UBERON:2001588,pectoral fin distal radial bone,UBERON:2101588,pectoral fin distal radial element
+HP:0012601,Hypochloriduria,HP:0012600,Abnormal urine chloride concentration
+UBERON:0011800,dermal pulp of feather shaft,UBERON:0000479,tissue
+UBERON:2001118,urogenital papilla,UBERON:0003102,surface structure
+UBERON:3000547,rostral process,UBERON:0010313,neural crest-derived structure
+DOID:5913,brachial plexus neoplasm,DOID:4693,nerve plexus neoplasm
+UBERON:0004334,proximal phalanx of pedal digit 3,UBERON:0003868,proximal phalanx of pes
+HP:0001423,X-linked dominant inheritance,HP:0001417,X-linked inheritance
+HP:0200141,"Small, conical teeth",HP:0000691,Microdontia
+DOID:10095,intracranial abscess,DOID:331,central nervous system disease
+CL:0002518,kidney epithelial cell,CL:1000497,kidney cell
+CL:0000707,R7 photoreceptor cell,CL:0000494,UV sensitive photoreceptor cell
+CL:0002565,iris pigment epithelial cell,CL:0000066,epithelial cell
+UBERON:0014933,periventricular gray matter,UBERON:0002020,gray matter of neuraxis
+CL:0000696,PP cell,CL:0000164,enteroendocrine cell
+DOID:11199,hypoparathyroidism,DOID:417,hypersensitivity reaction type II disease
+UBERON:0004152,bulbus arteriosus,UBERON:0004151,cardiac chamber
+DOID:7401,colonic L-cell glucagon-like peptide producing tumor,DOID:219,colon cancer
+DOID:0050790,fibular hypoplasia and complex brachydactyly,DOID:0050737,autosomal recessive disease
+HP:0007642,Congenital stationary night blindness,HP:0000662,Night blindness
+UBERON:0002215,synchondrosis,UBERON:0002213,cartilaginous joint
+UBERON:2002133,dorsal organ,UBERON:0003102,surface structure
+UBERON:0016394,anterior auricular lymph node,UBERON:0016393,deep parotid lymph node
+UBERON:0003922,pancreatic bud,UBERON:0005291,embryonic tissue
+DOID:0060150,astereognosia,DOID:4090,agnosia
+UBERON:0002125,lobule of thymus,UBERON:0000064,organ part
+DOID:363,uterine cancer,DOID:120,female reproductive organ cancer
+CL:0007016,adaxial cell,CL:0000680,muscle precursor cell
+UBERON:0007119,neck of femur,UBERON:0004120,mesoderm-derived structure
+UBERON:4200034,cnemial crest,UBERON:0004120,mesoderm-derived structure
+UBERON:0010070,intermediate layer of tympanic membrane,UBERON:0010071,layer of tympanic membrane
+UBERON:0006725,spiral ligament,UBERON:0003566,head connective tissue
+HP:0003774,Stage 5 chronic kidney disease,HP:0012622,Chronic kidney disease
+HP:0010505,Limitation of movement at ankles,HP:0003028,Abnormality of the ankles
+HP:0009669,Irregular epiphysis of the proximal phalanx of the thumb,HP:0009663,Abnormality of the epiphysis of the proximal phalanx of the thumb
+HP:0005346,Abnormal facial expression,HP:0000271,Abnormality of the face
+UBERON:2002225,posterior pronephric duct,UBERON:0006553,renal duct
+UBERON:0002047,pontine raphe nucleus,UBERON:0002680,regional part of metencephalon
+DOID:4830,adenosquamous carcinoma,DOID:1749,squamous cell carcinoma
+DOID:3575,cavernous sinus thrombosis,DOID:3572,intracranial sinus thrombosis
+UBERON:2001705,infraorbital 10,UBERON:2000376,infraorbital
+HP:0006568,Increased hepatic glycogen content,HP:0001392,Abnormality of the liver
+UBERON:2007002,ventro-rostral cluster,UBERON:0006569,diencephalic nucleus
+DOID:8288,clear cell squamous cell skin carcinoma,DOID:3151,skin squamous cell carcinoma
+UBERON:0000077,mixed endoderm/mesoderm-derived structure,UBERON:0004119,endoderm-derived structure
+DOID:13002,subclavian steal syndrome,DOID:225,syndrome
+DOID:3723,solitary plasmacytoma of chest wall,DOID:3721,plasmacytoma
+UBERON:0004052,quadrigeminal cistern,UBERON:0004050,subarachnoid cistern
+NCBITaxon:35237,"dsDNA viruses, no RNA stage",NCBITaxon:10239,Viruses
+UBERON:0004665,seminal vesicle muscle layer,UBERON:0005156,reproductive structure
+UBERON:0005240,basal plate medulla oblongata,UBERON:0004064,neural tube basal plate
+HP:0004885,Episodic respiratory distress,HP:0002098,Respiratory distress
+UBERON:0011933,vibrissa unit,UBERON:0000477,anatomical cluster
+HP:0003805,Rimmed vacuoles,HP:0004303,Abnormality of muscle fibers
+HP:0000848,Increased circulating renin level,HP:0000847,Abnormality of renin-angiotensin system
+DOID:9577,neonatal candidiasis,DOID:1508,candidiasis
+UBERON:3010668,ramules cutaneous,UBERON:0001021,nerve
+UBERON:0010983,levator scapulae pre-muscle mass,UBERON:0004120,mesoderm-derived structure
+UBERON:3000656,processus posterodorsalis of lamella alaris,UBERON:4100000,skeletal element projection
+DOID:699,mitochondrial myopathy,DOID:423,myopathy
+DOID:13227,retinal dystrophies primarily involving Bruch's membrane,DOID:8501,fundus dystrophy
+DOID:0060014,CD45 deficiency,DOID:627,severe combined immunodeficiency
+DOID:10824,malignant hypertension,DOID:10763,hypertension
+DOID:10933,obsessive-compulsive disorder,DOID:2030,anxiety disorder
+CL:0002617,adipocyte of breast,CL:0000136,fat cell
+HP:0005302,Carotid artery tortuosity,HP:0005116,Arterial tortuosity
+HP:0004695,Calcaneal epiphyseal stippling,HP:0010655,Epiphyseal stippling
+CL:1000468,myoepithelial cell of acinus of lactiferous gland,CL:1000416,myoepithelial cell of lactiferous gland
+UBERON:0002973,parahippocampal gyrus,UBERON:0000200,gyrus
+HP:0010382,Abnormality of the proximal phalanx of the 4th toe,HP:0010336,Abnormality of the phalanges of the 4th toe
+DOID:0060078,progesterone-receptor negative breast cancer,DOID:1612,breast cancer
+UBERON:2000953,sclerotome somite 12,UBERON:0003089,sclerotome
+UBERON:0001798,vitreous body,UBERON:0004121,ectoderm-derived structure
+DOID:5401,water-clear cell adenoma,DOID:657,adenoma
+HP:0001167,Abnormality of finger,HP:0001155,Abnormality of the hand
+UBERON:0001133,cardiac muscle tissue,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:5276,esophagus leiomyosarcoma,DOID:1114,esophagus sarcoma
+HP:0008744,Abnormality of the aryepiglottic fold,HP:0001600,Abnormality of the larynx
+UBERON:0002915,postcentral sulcus,UBERON:0013118,sulcus of brain
+UBERON:2001865,basibranchial 4 cartilage,UBERON:2001918,basibranchial 4 element
+DOID:7693,abdominal aortic aneurysm,DOID:3627,aortic aneurysm
+UBERON:0010524,fibularis tertius,UBERON:0009132,peroneus
+UBERON:0004162,pulmonary myocardium,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009839,Osteolytic defects of the distal phalanges of the hand,HP:0009771,Osteolytic defects of the phalanges of the hand
+HP:0008808,High iliac wings,HP:0011867,Abnormality of the wing of the ilium
+HP:0006385,Short lower limbs,HP:0009816,Lower limb undergrowth
+UBERON:2005113,dorsal lateral line neuromast,UBERON:0008904,neuromast
+DOID:1517,cecal benign neoplasm,DOID:4610,intestinal benign neoplasm
+CL:0000695,Cajal-Retzius cell,CL:0000117,CNS neuron (sensu Vertebrata)
+UBERON:0000351,nuchal ligament,UBERON:0003568,neck connective tissue
+DOID:7237,pancreatic non-invasive mucinous cystadenocarcinoma,DOID:7234,pancreatic colloid cystadenocarcinoma
+UBERON:0012299,mucosa of urethra,UBERON:0006554,urinary system structure
+UBERON:0011251,levator claviculae muscle,UBERON:0002377,muscle of neck
+HP:0011464,Aganglionosis of the small intestine,HP:0004362,Abnormality of the enteric ganglia
+UBERON:0001629,carotid body,UBERON:0000062,organ
+UBERON:0003668,synovial bursa,UBERON:0000062,organ
+DOID:10744,broad ligament malignant neoplasm,DOID:11747,uterine adnexa cancer
+CL:0000577,type EC enteroendocrine cell,CL:0000166,chromaffin cell
+UBERON:0010985,rhomboid pre-muscle mass,UBERON:0004120,mesoderm-derived structure
+HP:0009906,Aplasia/Hypoplasia of the earlobes,HP:0000363,Abnormality of earlobe
+HP:0012188,Hyperemesis gravidarum,HP:0002686,Prenatal maternal abnormality
+UBERON:2001584,caudal procurrent ray,UBERON:4000174,caudal fin lepidotrichium
+UBERON:0003289,meninx of telencephalon,UBERON:0003548,forebrain meninges
+CL:0002384,uninucleate macroconidium,CL:0002381,uninucleate conidium
+UBERON:0009470,postsphenoidal bone,UBERON:0011164,neurocranium bone
+HP:0002710,Commissural lip pit,HP:0100267,Lip pit
+UBERON:0000959,optic chiasma,UBERON:0004121,ectoderm-derived structure
+UBERON:0000964,cornea,UBERON:0010313,neural crest-derived structure
+DOID:0050745,diffuse large B-cell lymphoma,DOID:707,B-cell lymphoma
+UBERON:0001298,psoas major muscle,UBERON:0008450,psoas muscle
+UBERON:0007416,cerebellar peduncle,UBERON:0014891,brainstem white matter
+CL:0002545,thoracic aorta endothelial cell,CL:0002544,aortic endothelial cell
+UBERON:0004217,upper arm nerve,UBERON:0003433,arm nerve
+HP:0010002,Complete duplication of the middle phalanges of the hand,HP:0010008,Duplication of the middle phalanx of hand
+HP:0001830,Postaxial foot polydactyly,HP:0001829,Foot polydactyly
+UBERON:0001531,right common carotid artery plus branches,UBERON:0001530,common carotid artery plus branches
+DOID:7639,malignant granular cell skin tumor,DOID:5274,malignant dermis tumor
+UBERON:0001929,supraoptic nucleus,UBERON:0006568,hypothalamic nucleus
+UBERON:0002768,vestibulospinal tract,UBERON:0007702,tract of brain
+UBERON:0011637,prearticular bone,UBERON:0004768,bone of lower jaw
+HP:0010591,Abnormality of the proximal tibial epiphysis,HP:0006508,Abnormality of tibial epiphyses
+CL:0000066,epithelial cell,CL:0000548,animal cell
+HP:0009321,Absent epiphysis of the middle phalanx of the 3rd finger,HP:0009410,Absent epiphyses of the 3rd finger
+HP:0004942,Aortic aneurysm,HP:0001724,Aortic dilatation
+NCBITaxon:5204,Basidiomycota,NCBITaxon:451864,Dikarya
+UBERON:2200646,anal fin distal radial cartilage,UBERON:2201671,anal fin radial cartilage
+UBERON:2000690,supraoptic commissure,UBERON:0003931,diencephalic white matter
+HP:0004631,Decreased cervical spine flexion due to contractures of posterior cervical muscles,HP:0001371,Flexion contracture
+HP:0009411,Bracket epiphyses of the 3rd finger,HP:0010229,Bracket epiphyses of the phalanges of the hand
+CL:1000365,transitional myocyte of atrial septal branch of anterior internodal tract,CL:1000480,transitional myocyte of internodal tract
+UBERON:0010732,alisphenoid pre-cartilage condensation,UBERON:0006904,head mesenchyme from mesoderm
+DOID:1837,diabetic ketoacidosis,DOID:9352,type 2 diabetes mellitus
+HP:0009457,Aplasia/Hypoplasia of the proximal phalanx of the 3rd finger,HP:0009447,Aplasia/Hypoplasia of the phalanges of the 3rd finger
+UBERON:0013622,manual autopod pad,UBERON:0001519,skin of manus
+HP:0010409,Patchy sclerosis of the middle phalanx of the 2nd toe,HP:0100935,Sclerosis of the middle phalanx of the 2nd toe
+HP:0005005,"Femoral bowing present at birth, straightening with time",HP:0002980,Femoral bowing
+HP:0012061,Urinary excretion of sialylated oligosaccharides,HP:0010471,Oligosacchariduria
+HP:0011394,Hypoplasia of the vestibular nerve,HP:0011392,Abnormality of the vestibular nerve
+HP:0003345,Elevated urinary norepinephrine,HP:0011976,Elevated urinary catecholamines
+UBERON:0001568,muscle of larynx,UBERON:0002377,muscle of neck
+DOID:1214,tympanosclerosis,DOID:5782,tympanic membrane disease
+HP:0007791,Patchy atrophy of the retinal pigment epithelium,HP:0007698,Retinal pigment epithelial atrophy
+DOID:9307,rectal prolapse,DOID:1285,rectal disease
+UBERON:0003845,lower eyelid epithelium,UBERON:0015808,eye epithelium
+HP:0011725,Chaotic multifocal atrial tachycardia,HP:0001692,Primary atrial arrhythmia
+UBERON:0015154,lateral gland of orbital region,UBERON:0015152,gland of orbital region
+HP:0011547,Absent left sided atrioventricular connection,HP:0011546,Abnormal atrioventricular connection
+HP:0002793,Abnormal pattern of respiration,HP:0002795,Functional respiratory abnormality
+HP:0012231,Exudative retinal detachment,HP:0000541,Retinal detachment
+DOID:8239,lower clivus meningioma,DOID:6517,clivus meningioma
+HP:0009637,Absent proximal phalanx of thumb,HP:0009629,Aplasia/Hypoplasia of the proximal phalanx of the thumb
+UBERON:2001788,pelvic splint,UBERON:0008907,dermal bone
+CL:0002204,brush cell,CL:0002076,endo-epithelial cell
+HP:0000752,Hyperactivity,HP:0100022,Abnormality of movement
+HP:0011271,Prominent tragus,HP:0009912,Abnormality of the tragus
+UBERON:4300036,supraneural cartilage,UBERON:4300035,supraneural element
+UBERON:0012187,frontal artery,UBERON:0015156,terminal branch of ophthalmic artery
+UBERON:0006655,septum of scrotum,UBERON:0003037,septum
+UBERON:0002337,endometrial stroma,UBERON:0005156,reproductive structure
+CL:0001009,immature dermal dendritic cell,CL:0001006,dermal dendritic cell
+UBERON:0005276,dorsal skin of finger,UBERON:0003533,manual digit skin
+HP:0011556,Double inlet right ventricle,HP:0011554,Double inlet atrioventricular connection
+UBERON:0008404,proximale tubular epithelium,UBERON:0004810,nephron tubule epithelium
+DOID:417,hypersensitivity reaction type II disease,DOID:0060056,hypersensitivity reaction disease
+UBERON:0002926,gustatory epithelium,UBERON:0006934,sensory epithelium
+HP:0011200,EEG with generalized polymorphic epileptiform discharges,HP:0011198,EEG with generalized epileptiform discharges
+HP:0100574,Biliary tract neoplasm,HP:0007378,Neoplasm of the gastrointestinal tract
+UBERON:0013641,external cheek pouch,UBERON:0008802,cheek pouch
+HP:0000911,Flat glenoid fossa,HP:0011912,Abnormality of the glenoid fossa
+DOID:3669,intermittent claudication,DOID:2349,arteriosclerosis
+UBERON:0002908,subparietal sulcus,UBERON:0003022,cerebral cortex lobe
+HP:0000407,Sensorineural hearing impairment,HP:0011389,Functional abnormality of the inner ear
+UBERON:0005236,osseus labyrinth vestibule,UBERON:0004120,mesoderm-derived structure
+HP:0100550,Rupture of tendons,HP:0100261,Abnormal tendon morphology
+NCBITaxon:44534,Cellia <subgenus>,NCBITaxon:7164,Anopheles <genus>
+DOID:0050251,coenurosis,DOID:883,parasitic helminthiasis infectious disease
+DOID:3486,necrobiosis lipoidica,DOID:37,skin disease
+CL:0000922,type II NK T cell,CL:0000814,mature NK T cell
+HP:0007708,Absent inner eyelashes,HP:0000561,Absent eyelashes
+DOID:2842,Jervell-Lange Nielsen syndrome,DOID:2843,long QT syndrome
+UBERON:0004132,trigeminal sensory nucleus,UBERON:0002925,trigeminal nucleus
+HP:0001326,EEG with irregular generalized spike and wave complexes,HP:0010850,EEG with spike-wave complexes
+UBERON:4200096,intercondylar fossa,UBERON:0004704,bone fossa
+CL:0000440,melanocyte stimulating hormone secreting cell,CL:0000167,peptide hormone secreting cell
+UBERON:0004547,decidua capsularis,UBERON:0005156,reproductive structure
+UBERON:4100016,posterior process of ilium,UBERON:4100000,skeletal element projection
+UBERON:4200180,semilunate carpal,UBERON:0001435,carpal bone
+UBERON:0007289,presumptive rhombomere 1,UBERON:0006598,presumptive structure
+DOID:2047,hepatitis D,DOID:37,skin disease
+CL:0002494,cardiocyte,CL:0002371,somatic cell
+UBERON:0002744,hilum of dentate nucleus,UBERON:0003544,brain white matter
+UBERON:0010928,cricopharyngeus muscle,UBERON:0004120,mesoderm-derived structure
+CL:1000803,kidney inner medulla interstitial cell,CL:1000682,kidney medulla interstitial cell
+UBERON:2001179,epidermal superficial stratum,UBERON:0000479,tissue
+HP:0009067,Progressive spinal muscular atrophy,HP:0007269,Spinal muscular atrophy
+HP:0009145,Abnormality of cerebral artery,HP:0100659,Abnormality of the cerebral vasculature
+NCBITaxon:5579,Aureobasidium,NCBITaxon:125204,mitosporic Dothioraceae
+DOID:2700,mucinous adenofibroma,DOID:2683,adenofibroma
+HP:0011929,Hypersegmentation of proximal phalanx of third finger,HP:0009358,Abnormality of the proximal phalanx of the 3rd finger
+UBERON:0006246,humerus pre-cartilage condensation,UBERON:0005258,upper arm mesenchyme
+UBERON:0002335,macula densa,UBERON:0000064,organ part
+HP:0003074,Hyperglycemia,HP:0011015,Abnormality of blood glucose concentration
+HP:0007605,Excessive wrinkling of palmar skin,HP:0007392,Excessive wrinkled skin
+DOID:0050693,Brooke-Spiegler syndrome,DOID:0050736,autosomal dominant disease
+DOID:5777,rectum neuroendocrine neoplasm,DOID:1984,rectal neoplasm
+DOID:0050632,oculocutaneous albinism,DOID:0050737,autosomal recessive disease
+UBERON:0007386,pelvic appendage lymph vessel,UBERON:0007384,appendage lymph vessel
+HP:0010745,Aplasia of the phalanges of the toes,HP:0010173,Aplasia/Hypoplasia of the phalanges of the toes
+HP:0004280,Irregular ossification of hand bones,HP:0010660,Abnormal hand bone ossification
+HP:0100800,Aplasia/Hypoplasia of the pancreas,HP:0012094,Abnormal pancreas size
+UBERON:0013630,short bone,UBERON:0001474,bone element
+UBERON:4200089,fibular facet of the calcaneum,UBERON:4100003,articular surface
+DOID:5330,dental pulp disease,DOID:1091,tooth disease
+UBERON:3000878,intumescentia bilateralis superior,UBERON:0004120,mesoderm-derived structure
+HP:0009290,Short distal phalanx of the 4th finger,HP:0009882,Short distal phalanx of finger
+DOID:1751,malignant conjunctiva melanoma,DOID:5467,conjunctival cancer
+UBERON:0001586,internal jugular vein,UBERON:0004711,jugular vein
+HP:0100013,Neoplasm of the breast,HP:0011793,Neoplasm by anatomical site
+CL:0000014,germ line stem cell,CL:0000039,germ line cell
+UBERON:2000526,intermuscular bone,UBERON:0004120,mesoderm-derived structure
+DOID:0050800,creatine transporter deficiency,DOID:0050798,cerebral creatine deficiency syndrome
+DOID:10366,epididymis cancer,DOID:3856,male reproductive organ cancer
+CL:0002559,hair follicle cell,CL:0002371,somatic cell
+HP:0004795,Hamartomatous stomach polyps,HP:0004390,Hamartomatous polyps
+DOID:9074,systemic lupus erythematosus,DOID:65,connective tissue disease
+DOID:0060015,interleukin-7 receptor alpha deficiency,DOID:627,severe combined immunodeficiency
+UBERON:0012378,muscle layer of urinary bladder,UBERON:0006660,muscle layer
+HP:0011948,Acute respiratory tract infection,HP:0011947,Respiratory tract infection
+UBERON:0002797,dorsal trigeminal tract,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0001854,Gout (feet),HP:0001997,Gout
+CL:0002513,Vgamma5-positive CD8alpha alpha positive gamma-delta intraepithelial T cell,CL:0000802,"CD8-alpha alpha positive, gamma-delta intraepithelial T cell"
+HP:0009131,Abnormality of the musculature of the thorax,HP:0003011,Abnormality of the musculature
+UBERON:2001821,notochord posterior region,UBERON:0004120,mesoderm-derived structure
+HP:0009441,Bullet-shaped phalanges of the 3rd finger,HP:0009316,Abnormality of the phalanges of the 3rd finger
+HP:0010526,Dysgraphia,HP:0002167,Neurological speech impairment
+UBERON:3000393,pars amphibiorum,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:2139,paraurethral gland neoplasm,DOID:730,urethral benign neoplasm
+DOID:0050278,basidiobolomycosis,DOID:0050135,subcutaneous mycosis
+UBERON:0003062,primitive knot,UBERON:0002050,embryonic structure
+NCBITaxon:11617,Arenaviridae,NCBITaxon:35301,ssRNA negative-strand viruses
+DOID:136,vaginal carcinosarcoma,DOID:0050918,vaginal carcinoma
+UBERON:0011171,jaw joint,UBERON:0002217,synovial joint
+UBERON:0010575,manual digit 1 phalanx pre-cartilage condensation,UBERON:0015025,manual digit 1 phalanx endochondral element
+HP:0009685,Triangular epiphysis of the distal phalanx of the thumb,HP:0010256,Triangular epiphyses of the distal phalanges of the hand
+UBERON:3010736,ramus posterior of CN VIII,UBERON:0004732,segmental subdivision of nervous system
+HP:0003063,Abnormality of the humerus,HP:0001454,Abnormality of the upper arm
+DOID:8149,malignant childhood germ cell neoplasm,DOID:6053,pediatric germ cell cancer
+UBERON:0008925,sublaminar layer S4,UBERON:0009737,sublaminar layers S1 or S2 or S3 or S4
+UBERON:0005026,mucosa of middle ear,UBERON:0000344,mucosa
+UBERON:0014863,veliger stage,UBERON:0000069,larval stage
+HP:0003987,Fractured ulna,HP:0002997,Abnormality of the ulna
+UBERON:0007358,abomasum,UBERON:0011953,stomach glandular region
+HP:0100829,Galactorrhea,HP:0000769,Abnormality of the breast
+HP:0006292,Abnormality of dental eruption,HP:0000164,Abnormality of the teeth
+DOID:13195,nontoxic goiter,DOID:12176,goiter
+UBERON:0010059,hypoglossal cord,UBERON:0004121,ectoderm-derived structure
+UBERON:2001269,regenerating fin/limb,UBERON:0007567,regenerating anatomical structure
+UBERON:0000375,mandibular nerve,UBERON:0004732,segmental subdivision of nervous system
+HP:0007854,Glaucomatous visual field defect,HP:0001123,Visual field defect
+UBERON:0003017,substantia innominata,UBERON:0009663,telencephalic nucleus
+CL:0000202,auditory hair cell,CL:0002491,auditory epithelial cell
+DOID:14179,Bruton-type agammaglobulinemia,DOID:2583,agammaglobulinemia
+UBERON:0002686,angular gyrus,UBERON:0000200,gyrus
+DOID:4928,intrahepatic cholangiocarcinoma,DOID:4947,cholangiocarcinoma
+UBERON:2001746,dentary replacement tooth trench,UBERON:2001744,replacement tooth trench
+DOID:0050828,artery disease,DOID:178,vascular disease
+HP:0003456,Low urinary cyclic AMP response to PTH administration,HP:0003117,Abnormality of circulating hormone level
+DOID:3327,partial motor epilepsy,DOID:2234,focal epilepsy
+HP:0011676,Tetralogy of Fallot with absent subarterial conus,HP:0001636,Tetralogy of Fallot
+HP:0007617,"Fine, reticulate skin pigmentation",HP:0001000,Abnormality of skin pigmentation
+HP:0009178,Symphalangism of middle phalanx of 5th finger,HP:0009849,Symphalangism of middle phalanx of finger
+DOID:0080041,hypochondroplasia,DOID:2256,osteochondrodysplasia
+HP:0009726,Renal neoplasm,HP:0010786,Urinary tract neoplasm
+DOID:379,external ear disease,DOID:2742,auditory system disease
+CL:0002300,type-7 epithelial cell of thymus,CL:0002365,medullary thymic epithelial cell
+UBERON:0011794,rectrix feather,UBERON:0011793,flight feather
+HP:0008677,Congenital nephrotic syndrome,HP:0000100,Nephrotic syndrome
+UBERON:0001016,nervous system,UBERON:0000467,anatomical system
+UBERON:2000979,hypaxial region somite 24,UBERON:0003895,hypaxial myotome region
+NCBITaxon:82105,Cladophialophora,NCBITaxon:82104,mitosporic Herpotrichiellaceae
+HP:0008014,Central fundal arteriolar microaneurysms,HP:0002617,Aneurysm
+UBERON:0004318,distal phalanx of pedal digit 4,UBERON:0014486,distal phalanx of digit 4
+HP:0200126,Amyolid cardiomyopathy,HP:0011034,Amyloidosis
+HP:0010035,Aplasia of the 1st metacarpal,HP:0009659,Partial absence of thumb
+DOID:5529,lacrimal gland squamous cell carcinoma,DOID:293,lacrimal gland carcinoma
+UBERON:2001735,scapular foramen,UBERON:0005744,bone foramen
+DOID:2998,testicular cancer,DOID:3856,male reproductive organ cancer
+UBERON:0004313,distal phalanx of manual digit 4,UBERON:0003865,distal phalanx of manus
+UBERON:0011388,male bulbospongiosus muscle,UBERON:0005156,reproductive structure
+DOID:9779,bowel dysfunction,DOID:5295,intestinal disease
+DOID:0080022,McKusick type metaphyseal dysplasia,DOID:0080019,metaphyseal dysplasia
+HP:0000027,Azoospermia,HP:0008669,Abnormal spermatogenesis
+UBERON:2001274,coronomeckelian,UBERON:0004768,bone of lower jaw
+UBERON:0002055,zona reticularis of adrenal gland,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:12169,carpal tunnel syndrome,DOID:573,nerve compression syndrome
+UBERON:0008712,stylohyoid muscle,UBERON:0008571,suprahyoid muscle
+UBERON:0007257,intervertebral disk of sacral vertebra,UBERON:0005179,pelvic region organ
+UBERON:0007301,appendage blood vessel,UBERON:0001981,blood vessel
+HP:0010025,Triangular epiphysis of the 1st metacarpal,HP:0009171,Triangular epiphyses of the metacarpals
+DOID:11335,sarcoidosis,DOID:2916,hypersensitivity reaction type IV disease
+HP:0009191,Ivory epiphyses of the metacarpals,HP:0010583,Ivory epiphyses
+HP:0009385,Enlarged epiphyses of the 5th finger,HP:0010231,Enlarged epiphyses of the phalanges of the hand
+DOID:0050481,endemic typhus,DOID:11256,typhus
+UBERON:0010740,bone of appendage girdle complex,UBERON:0001474,bone element
+UBERON:0001790,outer plexiform layer of retina,UBERON:0003902,retinal neural layer
+HP:0009412,Cone-shaped epiphyses of the 3rd finger,HP:0010230,Cone-shaped epiphyses of the phalanges of the hand
+HP:0004897,Stress/infection-induced lactic acidosis,HP:0003128,Lactic acidosis
+CL:0002404,fetal thymocyte,CL:0000893,thymocyte
+UBERON:2000716,afferent branchial artery,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:4677,keratitis,DOID:10124,corneal disease
+HP:0002728,Chronic mucocutaneous candidiasis,HP:0011370,Recurrent cutaneous fungal infections
+UBERON:2002001,anterior dentation of pectoral fin spine,UBERON:0004121,ectoderm-derived structure
+UBERON:0005363,inferior vagus X ganglion,UBERON:0010313,neural crest-derived structure
+CL:0002052,Fraction D precursor B cell,CL:0000817,precursor B cell
+DOID:11427,endosalpingiosis,DOID:289,endometriosis
+UBERON:0006494,apex of arytenoid,UBERON:0003583,larynx connective tissue
+UBERON:2100936,dorsal fin distal radial element,UBERON:2101672,dorsal fin radial element
+UBERON:0003643,respiratory system arterial blood vessel,UBERON:0003509,arterial blood vessel
+UBERON:4200011,pedal centrale,UBERON:0012131,centrale
+HP:0002920,Decreased circulating ACTH level,HP:0011043,Abnormality of circulating adrenocorticotropin level
+HP:0002861,Melanoma,HP:0011792,Neoplasm by histology
+UBERON:0004546,cribriform plate,UBERON:0005913,zone of bone organ
+UBERON:0012104,sesamoid bone of the peroneus longus muscle,UBERON:0011141,appendicular ossicle
+UBERON:2001526,hypobranchial 3 cartilage,UBERON:2001522,hypobranchial cartilage
+UBERON:0006431,xiphoid process bone,UBERON:0004120,mesoderm-derived structure
+CL:0000080,circulating cell,CL:0000003,native cell
+HP:0009734,Optic glioma,HP:0009733,Glioma
+HP:0004592,Thoracic platyspondyly,HP:0000926,Platyspondyly
+UBERON:2001962,hypobranchial 1 bone distal cartilage,UBERON:0011004,pharyngeal arch cartilage
+DOID:4844,benign ependymoma,DOID:0060101,benign glioma
+UBERON:0001457,skin of eyelid,UBERON:1000021,skin of face
+DOID:7505,small intestine neoplasm,DOID:4610,intestinal benign neoplasm
+UBERON:0005132,metanephric long nephron,UBERON:0004194,long nephron
+UBERON:0010850,tibia pre-cartilage condensation,UBERON:0015004,tibia endochondral element
+UBERON:0006292,shoulder joint primordium,UBERON:0005856,developing mesenchymal condensation
+DOID:3280,mixed type thymoma,DOID:3275,thymoma
+UBERON:0000058,duct,UBERON:0000025,tube
+CL:0002174,follicular cell of ovary,CL:0002078,meso-epithelial cell
+UBERON:0006976,peptonephridium,UBERON:0013765,digestive system organ
+CL:1000410,myocyte of atrioventricular node,CL:0002072,nodal myocyte
+HP:0002749,Osteomalacia,HP:0004349,Reduced bone mineral density
+HP:0011368,Epidermal thickening,HP:0001072,Thickened skin
+UBERON:0012255,inferior phrenic artery,UBERON:0002057,phrenic artery
+DOID:1227,neutropenia,DOID:12987,agranulocytosis
+NCBITaxon:76804,Nidovirales,NCBITaxon:35278,"ssRNA positive-strand viruses, no DNA stage"
+UBERON:0011357,Reissner's fiber,UBERON:0004121,ectoderm-derived structure
+UBERON:0007825,reticular membrane of spiral organ,UBERON:0004121,ectoderm-derived structure
+HP:0009840,Patchy sclerosis of the distal phalanges of the hand,HP:0100915,Sclerosis of the distal phalanges of the hand
+DOID:0050817,Stargardt disease,DOID:10871,age related macular degeneration
+HP:0100434,Bullet-shaped middle phalanx of the 3rd toe,HP:0010361,Bullet-shaped phalanges of the 3rd toe
+DOID:496,spindle cell hemangioma,DOID:255,hemangioma
+UBERON:0003426,dermis adipose tissue,UBERON:0003585,dermis connective tissue
+UBERON:0014396,interscapular fat pad,UBERON:0003916,fat pad
+HP:0009440,Broad phalanges of the 3rd finger,HP:0009316,Abnormality of the phalanges of the 3rd finger
+UBERON:0003723,vestibular nerve,UBERON:0004121,ectoderm-derived structure
+HP:0009214,Absent epiphysis of the middle phalanx of the 4th finger,HP:0010257,Absent epiphyses of the middle phalanges of the hand
+DOID:1761,Melkersson-Rosenthal syndrome,DOID:1762,cheilitis
+HP:0003307,Hyperlordosis,HP:0010674,Abnormality of the curvature of the vertebral column
+UBERON:0011106,cruciate ligament of atlas,UBERON:0000211,ligament
+UBERON:4200171,process 4,UBERON:0004120,mesoderm-derived structure
+UBERON:0001773,sclera,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003559,hindbrain arachnoid mater,UBERON:0002362,arachnoid mater
+UBERON:0015180,neck of talus,UBERON:0004120,mesoderm-derived structure
+UBERON:0007823,appendage girdle region,UBERON:0000475,organism subdivision
+UBERON:0005121,metanephric long descending thin limb bend,UBERON:0004120,mesoderm-derived structure
+CL:0002641,epithelial cell of esophageal gland proper,CL:0002657,glandular cell of esophagus
+HP:0008051,Abnormality of the retinal pigment epithelium,HP:0000479,Abnormality of the retina
+NCBITaxon:85005,Actinomycineae,NCBITaxon:2037,Actinomycetales
+UBERON:0001965,substantia nigra pars compacta,UBERON:0004121,ectoderm-derived structure
+UBERON:2002120,orbitosphenoid septum,UBERON:0003037,septum
+HP:0006767,Pituitary prolactin cell adenoma,HP:0002893,Pituitary adenoma
+HP:0005537,Decreased mean platelet volume,HP:0011876,Abnormal platelet volume
+UBERON:0014917,pouch sphincter,UBERON:0005156,reproductive structure
+UBERON:0006106,cochlear canal,UBERON:0010313,neural crest-derived structure
+HP:0002786,Tracheobronchomalacia,HP:0002780,Bronchomalacia
+CL:1001319,bladder cell,CL:1000600,lower urinary tract cell
+DOID:418,systemic scleroderma,DOID:37,skin disease
+CL:0000218,myelinating Schwann cell,CL:0002573,Schwann cell
+DOID:9496,unilateral hypoactive labyrinth,DOID:566,labyrinthine dysfunction
+UBERON:0002051,epithelium of bronchiole,UBERON:0003350,epithelium of mucosa
+HP:0100947,Sclerosis of the middle phalanges of the toes,HP:0010183,Abnormality of the middle phalanges of the toes
+UBERON:0011820,atrioventricular region,UBERON:0000481,multi-tissue structure
+HP:0006254,Elevated alpha-fetoprotein,HP:0010876,Abnormality of circulating protein level
+NCBITaxon:11053,Dengue virus 1,NCBITaxon:12637,Dengue virus
+HP:0008231,Macronodular adrenal hyperplasia,HP:0008221,Adrenal hyperplasia
+HP:0010540,Advanced pneumatization of cranial sinuses,HP:0000245,Abnormality of the sinuses
+HP:0005720,Shortening of all metacarpals,HP:0010049,Short metacarpal
+CL:0002316,supporting cell of vestibular epithelium,CL:0005014,auditory epithelial support cell
+CL:0002267,type D cell of stomach,CL:0000502,type D enteroendocrine cell
+UBERON:0014670,distal interphalangeal joint of manual digit 4,UBERON:0007731,interphalangeal joint of manual digit 4
+DOID:0050431,arrhythmogenic right ventricular cardiomyopathy,DOID:0060036,intrinsic cardiomyopathy
+UBERON:0006440,os clitoris,UBERON:0014404,female anatomical structure
+UBERON:0005032,mucosa of lower lip,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009680,Irregular epiphysis of the distal phalanx of the thumb,HP:0009691,Irregular epiphyses of the thumb
+UBERON:0004090,periorbital region,UBERON:0000477,anatomical cluster
+UBERON:0003415,mesenchyme of nasal septum,UBERON:0014387,mesenchyme derived from neural crest
+UBERON:0002542,scale,UBERON:0003102,surface structure
+UBERON:0009949,humeral diverticulum of clavicular air sac,UBERON:0004120,mesoderm-derived structure
+UBERON:0003039,anterior commissure anterior part,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0009689,anterior inferior cerebellar artery,UBERON:0004573,systemic artery
+NCBITaxon:43741,Acalyptratae,NCBITaxon:43738,Schizophora
+UBERON:0002476,lateral globus pallidus,UBERON:0005401,cerebral hemisphere grey matter
+UBERON:2000267,primary olfactory fiber layer,UBERON:0004121,ectoderm-derived structure
+HP:0000301,Abnormality of facial musculature,HP:0011799,Abnormality of facial soft tissue
+HP:0012246,Oculomotor nerve palsy,HP:0001291,Abnormality of the cranial nerves
+UBERON:0011007,endocardium of right auricle,UBERON:0009129,right atrium endocardium
+HP:0001312,Giant somatosensory evoked potentials,HP:0007377,Abnormality of somatosensory evoked potentials
+UBERON:0002462,erector spinae muscle group,UBERON:0003897,axial muscle
+HP:0008093,Short 4th toe,HP:0001831,Short toe
+UBERON:0005277,dorsal skin of toe,UBERON:0005275,dorsal skin of digit
+UBERON:3000907,eminentia arcuata,UBERON:0004120,mesoderm-derived structure
+DOID:12549,hepatitis A,DOID:37,skin disease
+UBERON:0001922,parafascicular nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0008572,posterior crico-arytenoid,UBERON:0010932,crico-arytenoid muscle
+DOID:14402,critical illness polyneuropathy,DOID:2537,inflammatory and toxic neuropathy
+UBERON:2000398,nucleus isthmi,UBERON:0007635,nucleus of medulla oblongata
+CL:0000082,epithelial cell of lung,CL:0000066,epithelial cell
+CL:0002350,endocardial cell,CL:0010008,cardiac endothelial cell
+UBERON:3000284,margo tympanicus of pterygoid,UBERON:0000064,organ part
+HP:0200056,Macular scarring,HP:0100699,Scarring
+DOID:2409,rhinosporidiosis,DOID:0050291,parasitic Ichthyosporea infectious disease
+HP:0006585,Congenital pseudarthrosis of the clavicle,HP:0005864,Pseudoarthrosis
+DOID:11242,plethora of newborn,DOID:8432,polycythemia
+CL:0002632,epithelial cell of lower respiratory tract,CL:0002368,respiratory epithelial cell
+UBERON:0003091,thyroid primordium,UBERON:0000479,tissue
+HP:0006719,Benign gastrointestinal tract tumors,HP:0007378,Neoplasm of the gastrointestinal tract
+HP:0012189,Hodgkin lymphoma,HP:0002665,Lymphoma
+HP:0012523,Oral aversion,HP:0100738,Abnormal eating behavior
+DOID:0070004,myeloma,DOID:4960,bone marrow cancer
+HP:0010479,Patent urachus,HP:0010478,Abnormality of the urachus
+DOID:5629,adenosquamous colon carcinoma,DOID:1520,colon carcinoma
+HP:0009299,Aplasia/Hypoplasia of the middle phalanx of the 4th finger,HP:0009408,Aplasia/Hypoplasia of the phalanges of the 4th finger
+HP:0002035,Rectal prolapse,HP:0002034,Abnormality of the rectum
+HP:0000098,Tall stature,HP:0000002,Abnormality of body height
+NCBITaxon:1385,Bacillales,NCBITaxon:91061,Bacilli
+HP:0002696,Abnormality of the parietal bone,HP:0002648,Abnormality of calvarial morphology
+HP:0100382,Aplasia of the middle phalanx of the 4th toe,HP:0100387,Aplasia of the middle phalanges of the toes
+DOID:6686,Achard syndrome,DOID:225,syndrome
+DOID:8651,Hodgkin's granuloma,DOID:8567,Hodgkin's lymphoma
+HP:0100828,Increase in T cell number,HP:0100827,Lymphocytosis
+DOID:0060094,bone benign neoplasm,DOID:0060123,connective tissue benign neoplasm
+UBERON:0010706,parenchyma of caudate lobe of liver,UBERON:0005221,liver right lobe parenchyma
+HP:0010795,Cerebellar glioma,HP:0009733,Glioma
+DOID:3677,pulmonary plasma cell granuloma,DOID:850,lung disease
+DOID:0050809,mucopolysaccharidosis IX,DOID:12798,mucopolysaccharidosis
+UBERON:2001234,hypobranchial 4 bone,UBERON:2000363,hypobranchial bone
+HP:0005609,Gallbladder dysfunction,HP:0012438,Abnormal gallbladder physiology
+UBERON:0006222,future diencephalon,UBERON:0002050,embryonic structure
+DOID:2527,nephrosis,DOID:557,kidney disease
+HP:0000434,Nasal mucosa telangiectasia,HP:0100579,Mucosal telangiectasiae
+UBERON:3000676,bronchial process,UBERON:0000072,segment of respiratory tract
+DOID:5572,Beckwith-Wiedemann syndrome,DOID:0080014,chromosomal disease
+UBERON:0007145,dome of diaphragm,UBERON:0004120,mesoderm-derived structure
+UBERON:0002984,lateral dorsal nucleus,UBERON:0015233,nucleus of dorsal thalamus
+HP:0010399,Osteolytic defects of the proximal phalanx of the 2nd toe,HP:0010351,Osteolytic defects of the phalanges of the 2nd toe
+HP:0010607,Hordeolum externum,HP:0010606,Hordeolum
+NCBITaxon:36826,Clostridium botulinum A,NCBITaxon:1491,Clostridium botulinum
+HP:0010155,Ivory epiphysis of the 1st metatarsal,HP:0010125,Abnormality of the epiphysis of the 1st metatarsal
+UBERON:0001998,sternocostal joint,UBERON:0002217,synovial joint
+HP:0010266,Stippling of the epiphyses of the middle phalanges of the hand,HP:0010237,Epiphyseal stippling of finger phalanges
+NCBITaxon:28568,Trichocomaceae,NCBITaxon:5042,Eurotiales
+UBERON:0006967,horn,UBERON:0006969,cranial appendage
+UBERON:0001590,pericardiacophrenic vein,UBERON:0001638,vein
+DOID:13731,malignant secondary hypertension,DOID:11130,secondary hypertension
+HP:0010814,Abnormal position of hair whorl,HP:0010721,Abnormal hair whorl
+HP:0001791,Fetal ascites,HP:0001541,Ascites
+CL:0000214,synovial cell,CL:0000153,GAG secreting cell
+NCBITaxon:43816,Anophelinae,NCBITaxon:7157,Culicidae
+UBERON:3000087,cavum medius,UBERON:0001707,nasal cavity
+CL:0002531,mature CD1a-positive dermal dendritic cell,CL:0001010,mature dermal dendritic cell
+HP:0100093,Abnormality of the epiphysis of the proximal phalanx of the 3rd toe,HP:0010329,Abnormality of the epiphyses of the 3rd toe
+UBERON:0001368,obturator externus,UBERON:0011144,adductor muscle of hip
+UBERON:0001688,incus bone,UBERON:0015017,incus endochondral element
+UBERON:0011250,autopod bone,UBERON:0015063,autopod endochondral element
+UBERON:0004714,septum pellucidum,UBERON:0004121,ectoderm-derived structure
+UBERON:2001861,epibranchial 3-pharyngobranchial 3 joint,UBERON:0000982,skeletal joint
+CL:0000482,juvenile hormone secreting cell,CL:0000163,endocrine cell
+HP:0003247,Overgrowth of external genitalia,HP:0000811,Abnormal external genitalia
+UBERON:0002345,descending thoracic aorta,UBERON:0004120,mesoderm-derived structure
+UBERON:0013249,paroophoron,UBERON:0005156,reproductive structure
+HP:0011560,Mitral atresia,HP:0011546,Abnormal atrioventricular connection
+HP:0009631,Bullet-shaped proximal phalanx of the thumb,HP:0009652,Bullet-shaped phalanges of the thumb
+HP:0100958,Narrow foramen obturatorium,HP:0003172,Abnormality of the pubic bones
+UBERON:4200102,median dorsal plate,UBERON:0007829,pectoral girdle bone
+HP:0009104,Aplasia/Hypoplasia of the pubic bone,HP:0009103,Aplasia/Hypoplasia involving the pelvis
+UBERON:0012115,dental comb,UBERON:0009678,tooth row
+UBERON:0002240,spinal cord,UBERON:0005174,dorsal region organ
+UBERON:0002980,opercular part of inferior frontal gyrus,UBERON:0004121,ectoderm-derived structure
+NCBITaxon:5550,Trichophyton,NCBITaxon:34385,mitosporic Arthrodermataceae
+HP:0004046,Spurred ulnar metaphysis,HP:0003855,Spurred metaphyses of the upper limbs
+CL:0000956,pre-B-I cell,CL:0000817,precursor B cell
+HP:0008797,Early ossification of capital femoral epiphyses,HP:0009107,Abnormal ossification involving the femoral head and neck
+HP:0010602,Type 2 muscle fiber predominance,HP:0004303,Abnormality of muscle fibers
+UBERON:0003555,spinal cord pia mater,UBERON:0002361,pia mater
+UBERON:0011683,adductor mandibulae,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002466,intestine secretion,UBERON:0000456,bodily secretion
+HP:0002349,Focal seizures without impairment of consciousness or awareness,HP:0007359,Focal seizures
+HP:0200117,Recurrent upper and lower respiratory tract infections,HP:0002783,Recurrent lower respiratory tract infections
+HP:0001539,Omphalocele,HP:0004299,Hernia of the abdominal wall
+UBERON:0013144,vein of genicular venous plexus,UBERON:0003503,leg blood vessel
+DOID:0060091,cardiovascular organ benign neoplasm,DOID:0060085,organ system benign neoplasm
+DOID:7365,Kimura disease,DOID:37,skin disease
+CL:1000377,dense-core granulated cell of epithelium of trachea,CL:0000307,tracheal epithelial cell
+CL:0000078,peridermal cell,CL:0002371,somatic cell
+UBERON:0007168,long head of biceps brachii,UBERON:0011906,muscle head
+UBERON:0009715,stomodeal lumen,UBERON:0000464,anatomical space
+CL:0000647,multinucleated giant cell,CL:0000228,multinucleate cell
+HP:0009602,Abnormality of the phalanges of the thumb,HP:0009774,Triangular shaped phalanges of the hand
+HP:0012217,Increased urinary porphobilinogen,HP:0010472,Abnormality of the heme biosynthetic pathway
+UBERON:0011085,palatoquadrate arch,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0011436,Abnormal maternal serum screening,HP:0002686,Prenatal maternal abnormality
+DOID:0050803,glioblastoma classical subtype,DOID:3068,glioblastoma multiforme
+UBERON:2000239,mesocoracoid bone,UBERON:0007829,pectoral girdle bone
+UBERON:0006544,kidney vasculature,UBERON:0006554,urinary system structure
+CL:1001109,kidney loop of henle cortical thick ascending limb epithelial cell,CL:1001106,kidney loop of henle thick ascending limb epithelial cell
+UBERON:0001382,pectineus muscle,UBERON:0011144,adductor muscle of hip
+DOID:1931,hypothalamic disease,DOID:936,brain disease
+UBERON:0004705,fenestra,UBERON:0002553,anatomical cavity
+HP:0100633,Esophagitis,HP:0004386,Gastrointestinal inflammation
+DOID:5518,penis squamous cell carcinoma,DOID:3449,penis carcinoma
+HP:0004010,Small radial epiphyses,HP:0003999,Abnormality of radial epiphyses
+UBERON:2000666,filamental artery,UBERON:0003469,respiratory system artery
+HP:0003581,Adult onset,HP:0011007,Age of onset
+HP:0005325,Extension of hair growth on temples to lateral eyebrow,HP:0000599,Abnormality of the frontal hairline
+UBERON:3000234,inferior prenasal cartilage,UBERON:0003933,cranial cartilage
+CL:0002481,peritubular myoid cell,CL:0002625,seminiferous tubule epithelial cell
+UBERON:0012124,avian scapholunar bone,UBERON:0001480,proximal carpal bone
+HP:0000896,Rib exostoses,HP:0000772,Abnormality of the ribs
+UBERON:0001508,arch of aorta,UBERON:0001515,thoracic aorta
+UBERON:0013076,snake venom,UBERON:0007113,venom
+UBERON:4300083,propterygium element,UBERON:2101587,pectoral fin proximal radial element
+CL:0000182,hepatocyte,CL:0000066,epithelial cell
+HP:0011429,Short fetal humerus length,HP:0011425,Fetal ultrasound soft marker
+HP:0100874,Thick hair,HP:0011357,Abnormality of hair density
+HP:0009184,Contracture of the distal interphalangeal joint of the 5th finger,HP:0009697,Contractures of the distal interphalangeal joints of the fingers
+HP:0100745,Abnormality of the humeroulnar joint,HP:0009811,Abnormality of the elbow
+HP:0012080,Cerebellar granular layer atrophy,HP:0001272,Cerebellar atrophy
+HP:0009603,Deviation/Displacement of the thumb,HP:0004097,Deviation of finger
+CL:0000699,paraganglial type 1 cell,CL:0000165,neuroendocrine cell
+UBERON:0013510,lumbar vertebra pre-cartilage condensation,UBERON:0015009,lumbar vertebra endochondral element
+DOID:1218,echinostomiasis,DOID:883,parasitic helminthiasis infectious disease
+HP:0004232,Accessory carpal bones,HP:0001191,Abnormality of the carpal bones
+UBERON:2000499,dorsal arrector,UBERON:0014794,pectoral appendage muscle
+HP:0001685,Myocardial fibrosis,HP:0001637,Abnormality of the myocardium
+CL:0000611,eosinophil progenitor cell,CL:0002191,granulocytopoietic cell
+HP:0012005,Deja vu,HP:0012004,Mnemonic auras
+HP:0100881,Congenital mesoblastic nephroma,HP:0002898,Embryonal neoplasm
+DOID:1029,familial periodic paralysis,DOID:423,myopathy
+UBERON:0010928,cricopharyngeus muscle,UBERON:0001630,muscle organ
+HP:0010641,Abnormality of the midnasal cavity,HP:0010640,Abnormality of the nasal cavity
+UBERON:0000123,endoneurium,UBERON:0000470,cell part
+HP:0012058,Nodular melanoma,HP:0012056,Cutaneous melanoma
+UBERON:0015137,tertiary lactiferous duct,UBERON:0001765,mammary duct
+HP:0000606,Abnormality of the periorbital region,HP:0000271,Abnormality of the face
+DOID:6037,spindle cell intraocular melanoma,DOID:1752,ocular melanoma
+DOID:5225,von Economo's disease,DOID:9588,encephalitis
+CL:0002470,MHC-II-positive classical monocyte,CL:0002395,Gr1-high classical monocyte
+UBERON:0004817,lacrimal gland epithelium,UBERON:0015808,eye epithelium
+UBERON:0010000,multicellular anatomical structure,UBERON:0000061,anatomical structure
+HP:0100712,Abnormality of the lumbar spine,HP:0000925,Abnormality of the vertebral column
+DOID:0050539,Charcot-Marie-Tooth disease type 2,DOID:10595,Charcot-Marie-Tooth disease
+HP:0008189,Insulin insensitivity,HP:0011014,Abnormal glucose homeostasis
+UBERON:2001704,infraorbital 9,UBERON:2000376,infraorbital
+HP:0006014,Abnormally shaped carpal bones,HP:0001191,Abnormality of the carpal bones
+UBERON:0001342,mesovarium,UBERON:0014404,female anatomical structure
+UBERON:0001772,corneal epithelium,UBERON:0010313,neural crest-derived structure
+UBERON:0010053,echolocation organ,UBERON:0000062,organ
+UBERON:0006009,cusp of cardiac valve,UBERON:0004120,mesoderm-derived structure
+DOID:6438,malignant choroid melanoma,DOID:12759,choroid cancer
+CL:0000791,mature alpha-beta T cell,CL:0002419,mature T cell
+UBERON:0005410,cartilaginous otic capsule,UBERON:0014387,mesenchyme derived from neural crest
+HP:0000995,Melanocytic nevus,HP:0003764,Nevus
+HP:0009208,Irregular epiphysis of the middle phalanx of the 5th finger,HP:0004224,Abnormality of the epiphysis of the middle phalanx of the 5th finger
+UBERON:0014610,thoracic spinal cord ventral horn,UBERON:0002257,ventral horn of spinal cord
+UBERON:0012248,cervical mucosa,UBERON:0014404,female anatomical structure
+HP:0008509,Aged leonine appearance,HP:0007495,Prematurely aged appearance
+HP:0100176,Pseudoepiphysis of the distal phalanx of the 4th toe,HP:0100094,Abnormality of the epiphysis of the distal phalanx of the 4th toe
+CL:0002366,myometrial cell,CL:0002601,uterine smooth muscle cell
+UBERON:0002642,cuneate fasciculus of medulla,UBERON:0005832,cuneate fasciculus
+UBERON:2005013,concurrent branch afferent branchial artery,UBERON:0003469,respiratory system artery
+HP:0002742,Recurrent Klebsiella infections,HP:0005420,Recurrent gram-negative bacterial infections
+HP:0010085,Aplasia/Hypoplasia of the proximal phalanx of the hallux,HP:0010194,Aplasia/Hypoplasia of the middle phalanges of the toes
+DOID:3973,thyroid medullary carcinoma,DOID:3962,follicular thyroid carcinoma
+UBERON:0009986,lateral epicondyle of femur,UBERON:0005055,zone of long bone
+UBERON:0016395,infra-auricular lymph node,UBERON:0016393,deep parotid lymph node
+UBERON:0002154,lateral reticular nucleus,UBERON:0007635,nucleus of medulla oblongata
+NCBITaxon:58839,Encephalitozoon intestinalis,NCBITaxon:6033,Encephalitozoon
+CL:0000715,embryonic crystal cell,CL:0000736,embryonic gland hemocyte
+UBERON:0002564,lateral orbital gyrus,UBERON:0007193,orbital gyrus
+UBERON:0003404,lobar bronchus of right lung,UBERON:0002183,lobar bronchus
+CL:0008015,inhibitory motor neuron,CL:0000100,motor neuron
+DOID:13948,bladder neck obstruction,DOID:12577,urethral obstruction
+CL:1001451,sensory neuron of dorsal root ganglion,CL:0009000,sensory neuron of spinal nerve
+UBERON:2007024,anterior neural keel,UBERON:0004121,ectoderm-derived structure
+HP:0010677,Enuresis nocturna,HP:0000805,Enuresis
+CL:0000638,acidophil cell of pars distalis of adenohypophysis,CL:0000637,chromophil cell of anterior pituitary gland
+DOID:14292,vulvar dystrophy,DOID:2059,vulvar disease
+CL:0008006,muscle founder cell,CL:0000056,myoblast
+UBERON:0001118,lobe of thyroid gland,UBERON:0015212,lateral structure
+DOID:3576,sagittal sinus thrombosis,DOID:3572,intracranial sinus thrombosis
+DOID:3113,papillary carcinoma,DOID:305,carcinoma
+UBERON:0003495,respiratory system arteriole,UBERON:0003643,respiratory system arterial blood vessel
+UBERON:0010703,forelimb zeugopod skeleton,UBERON:0011584,zeugopodial skeleton
+CL:0000259,aggregate cell,CL:0000263,vegetative cell (sensu Mycetozoa)
+CL:0002395,Gr1-high classical monocyte,CL:0001022,CD115-positive monocyte
+HP:0009629,Aplasia/Hypoplasia of the proximal phalanx of the thumb,HP:0009658,Aplasia/Hypoplasia of the phalanges of the thumb
+DOID:3737,verrucous carcinoma,DOID:1749,squamous cell carcinoma
+DOID:3722,solitary osseous plasmacytoma,DOID:3721,plasmacytoma
+UBERON:0002786,abducens nerve fibers,UBERON:0006843,root of cranial nerve
+UBERON:0002308,nucleus of brain,UBERON:0002616,regional part of brain
+UBERON:0001260,serosa of urinary bladder,UBERON:0006554,urinary system structure
+HP:0006297,Hypoplasia of dental enamel,HP:0000682,Abnormality of dental enamel
+HP:0009221,Pseudoepiphysis of the middle phalanx of the 4th finger,HP:0009400,Pseudoepiphyses of the 4th finger
+UBERON:0007770,osphradium,UBERON:0002268,main olfactory organ
+HP:0000370,Abnormality of the middle ear,HP:0000598,Abnormality of the ear
+HP:0005374,Cellular immunodeficiency,HP:0002721,Immunodeficiency
+UBERON:0010728,sphenoid lesser wing pre-cartilage condensation,UBERON:0015059,orbitosphenoid endochondral element
+UBERON:3000586,superior prenasal cartilage,UBERON:0003933,cranial cartilage
+HP:0003474,Sensory impairment,HP:0009830,Peripheral neuropathy
+NCBITaxon:768,Anaplasma,NCBITaxon:942,Anaplasmataceae
+UBERON:0009521,anal membrane endodermal component,UBERON:0000490,unilaminar epithelium
+UBERON:0010570,manual digit 1 metacarpus cartilage element,UBERON:0010675,manual digit 1 phalanx cartilage element
+UBERON:0015125,anterior internodal tract,UBERON:0009966,internodal tract
+HP:0009747,Lumbosacral hirsutism,HP:0009889,Localized hirsutism
+CL:0002306,epithelial cell of proximal tubule,CL:0002078,meso-epithelial cell
+HP:0007596,Painful subcutaneous lipomas,HP:0001031,Subcutaneous lipoma
+UBERON:0010984,pectoral pre-muscle mass,UBERON:0004120,mesoderm-derived structure
+DOID:7169,lung occult large cell carcinoma,DOID:4556,lung large cell carcinoma
+UBERON:0003470,artery of upper lip,UBERON:0004573,systemic artery
+CL:0002616,perirenal adipocyte cell,CL:0000136,fat cell
+UBERON:0007634,parabrachial nucleus,UBERON:0006331,brainstem nucleus
+DOID:9240,erythromelalgia,DOID:341,peripheral vascular disease
+DOID:7004,ACTH-secreting pituitary adenoma,DOID:5395,functioning pituitary adenoma
+HP:0006503,Aplasia/Hypoplasia involving forearm bones,HP:0002973,Abnormality of the forearm
+DOID:0060077,progesterone-receptor positive breast cancer,DOID:1612,breast cancer
+UBERON:2002294,fish scute,UBERON:0008907,dermal bone
+UBERON:2000954,sclerotome somite 15,UBERON:0003089,sclerotome
+HP:0010137,Triangular epiphysis of the proximal phalanx of the hallux,HP:0010123,Triangular epiphyses of the hallux
+HP:0010431,Short phalanx of the 2nd toe,HP:0010325,Aplasia/Hypoplasia of the 2nd toe
+UBERON:0005667,connecting stalk mesoderm,UBERON:0004120,mesoderm-derived structure
+DOID:4636,submandibular adenitis,DOID:4637,cervical adenitis
+UBERON:0006489,second cervical spinal cord segment,UBERON:0007714,cervical subsegment of spinal cord
+UBERON:0007195,stroma of bone marrow,UBERON:0004120,mesoderm-derived structure
+UBERON:0009742,proamniotic cavity,UBERON:0002553,anatomical cavity
+HP:0000631,Retinal arterial tortuosity,HP:0005116,Arterial tortuosity
+HP:0000139,Uterine prolapse,HP:0100823,Genital hernia
+UBERON:0011236,deep fascia,UBERON:0008982,fascia
+HP:0005924,Abnormality of the epiphyses of the hand,HP:0003839,Abnormality involving the epiphyses of the upper limbs
+HP:0004357,Abnormality of leucine metabolism,HP:0010892,Abnormality of branched chain family amino acid metabolism
+UBERON:0005483,thymus lobe,UBERON:0015212,lateral structure
+UBERON:0010002,pulmonary neuroendocrine body,UBERON:0004119,endoderm-derived structure
+HP:0010473,Porphyrinuria,HP:0010472,Abnormality of the heme biosynthetic pathway
+UBERON:0004909,epithelium of gonad,UBERON:0005156,reproductive structure
+UBERON:0009910,posterior lateral plate mesoderm,UBERON:0004120,mesoderm-derived structure
+HP:0009959,Duplication of phalanx of 3rd finger,HP:0009316,Abnormality of the phalanges of the 3rd finger
+UBERON:0010986,serratus ventralis pre-muscle mass,UBERON:0004120,mesoderm-derived structure
+HP:0012476,Specific pneumococcal antibody deficiency,HP:0012475,Specific antibody deficiency
+UBERON:2001979,hyomandibula-metapterygoid joint,UBERON:0000982,skeletal joint
+HP:0003165,Elevated circulating parathyroid hormone (PTH) level,HP:0003117,Abnormality of circulating hormone level
+DOID:2327,viral gastritis,DOID:4029,gastritis
+UBERON:0004702,respiratory system blood vessel endothelium,UBERON:0004807,respiratory system epithelium
+DOID:4481,allergic rhinitis,DOID:4483,rhinitis
+UBERON:0014797,hypobranchial group muscle,UBERON:0001630,muscle organ
+HP:0004809,Neonatal alloimmune thrombocytopenia,HP:0001873,Thrombocytopenia
+UBERON:0006319,spinal cord reticular nucleus,UBERON:0011777,nucleus of spinal cord
+UBERON:0005312,primary ureteric bud,UBERON:0000084,ureteric bud
+HP:0004421,Elevated systolic blood pressure,HP:0000822,Hypertension
+HP:0007524,Atypical neurofibromatosis,HP:0001067,Neurofibromas
+UBERON:0004414,proximal epiphysis of phalanx of manus,UBERON:0004387,epiphysis of phalanx of manus
+UBERON:0002510,anterior fontanel,UBERON:0002221,fontanelle
+UBERON:0007233,4 cell stage,UBERON:0000067,embryo stage part
+HP:0001996,Chronic metabolic acidosis,HP:0001942,Metabolic acidosis
+UBERON:2001664,basibranchial 2 tooth plate,UBERON:2001647,pharyngeal tooth plate
+HP:0008110,Equinovarus deformity,HP:0001760,Abnormality of the foot
+HP:0002720,IgA deficiency,HP:0004313,Hypogammaglobulinemia
+DOID:0050694,Brown-Vialetto-Van Laere syndrome,DOID:0050736,autosomal dominant disease
+UBERON:0004216,lower arm nerve,UBERON:0003433,arm nerve
+DOID:14444,sclerosing keratitis,DOID:9858,deep keratitis
+HP:0001711,Abnormality of the left ventricle,HP:0001713,Abnormality of cardiac ventricle
+HP:0006705,Abnormality of the atrioventricular valves,HP:0002564,Malformation of the heart and great vessels
+UBERON:2000466,anal depressor,UBERON:2005270,depressor muscle
+UBERON:0004126,trabecular layer of ventricle,UBERON:0004124,myocardium trabecular layer
+HP:0007286,Horizontal jerk nystagmus,HP:0000666,Horizontal nystagmus
+UBERON:0010054,malleus cartilage element,UBERON:0015018,malleus endochondral element
+NCBITaxon:517,Bordetella,NCBITaxon:506,Alcaligenaceae
+DOID:10754,otitis media,DOID:5100,middle ear disease
+UBERON:2001408,infraorbital 3,UBERON:2000376,infraorbital
+UBERON:0011636,surangular bone,UBERON:0004768,bone of lower jaw
+UBERON:0006502,plantar foot interosseous muscle,UBERON:0006497,interosseous muscle of pes
+UBERON:2002103,ceratobranchial series,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0012487,vaginal sphincter,UBERON:0014404,female anatomical structure
+UBERON:0009092,inner medulla vasa recta ascending limb,UBERON:0006554,urinary system structure
+HP:0002858,Meningioma,HP:0100835,Benign neoplasm of the central nervous system
+UBERON:0005996,mitral valve cusp,UBERON:0006009,cusp of cardiac valve
+CL:0002041,immature NK T cell stage III,CL:0000914,immature NK T cell
+HP:0008188,Thyroid dysgenesis,HP:0011772,Abnormality of thyroid morphology
+UBERON:0001447,tarsal bone,UBERON:0005899,pes bone
+UBERON:0014506,distal interphalangeal joint of digit 3,UBERON:0009768,distal interphalangeal joint
+CL:1000366,transitional myocyte of middle internodal tract,CL:1000480,transitional myocyte of internodal tract
+NCBITaxon:11052,Dengue virus group,NCBITaxon:11051,Flavivirus
+UBERON:1500006,paired fin radial bone,UBERON:2000271,radial bone
+UBERON:2001948,anal-fin hook,UBERON:0004120,mesoderm-derived structure
+UBERON:0001248,hilum of spleen,UBERON:0004885,hilum
+HP:0100371,Aplasia/Hypoplasia of the distal phalanx of the 5th toe,HP:0010392,Abnormality of the distal phalanx of the 5th toe
+UBERON:2000234,macula neglecta,UBERON:0000054,macula
+HP:0008672,Calcium oxalate nephrolithiasis,HP:0004724,Calcium nephrolithiasis
+DOID:11289,ventilation pneumonitis,DOID:841,extrinsic allergic alveolitis
+HP:0008675,Enlarged polycystic ovaries,HP:0100879,Enlarged ovaries
+DOID:0050480,epidemic typhus,DOID:11256,typhus
+NCBITaxon:11571,Bunyaviridae,NCBITaxon:35301,ssRNA negative-strand viruses
+UBERON:0003221,phalanx,UBERON:0003606,limb long bone
+UBERON:0005436,common hepatic artery,UBERON:0004573,systemic artery
+HP:0004935,Pulmonary artery atresia,HP:0004414,Abnormality of the pulmonary artery
+HP:0001151,Impaired horizontal smooth pursuit,HP:0007772,Impaired smooth pursuit
+DOID:5419,schizophrenia,DOID:2468,psychotic disorder
+UBERON:0000095,cardiac neural crest,UBERON:0004121,ectoderm-derived structure
+CL:0000591,warmth sensing thermoreceptor cell,CL:0000205,thermoreceptor cell
+HP:0011555,Double inlet left ventricle,HP:0011554,Double inlet atrioventricular connection
+UBERON:0015212,lateral structure,UBERON:0000061,anatomical structure
+HP:0100039,Thickened cortex of bones,HP:0003103,Abnormal cortical bone morphology
+HP:0001008,Accumulation of melanosomes in melanocytes,HP:0011125,Abnormality of dermal melanosomes
+UBERON:0013194,orthokeratinized epithelium,UBERON:0000488,atypical epithelium
+UBERON:0011091,skeleton of left pelvic girdle,UBERON:0007832,pelvic girdle skeleton
+CL:1000691,kidney interstitial myofibroblast,CL:0000186,myofibroblast cell
+UBERON:0003952,anterior stroma of cornea,UBERON:0010313,neural crest-derived structure
+UBERON:0003030,posterior nucleus of thalamus,UBERON:0015233,nucleus of dorsal thalamus
+DOID:9281,phenylketonuria,DOID:9252,amino acid metabolic disorder
+UBERON:2002108,buccal papilla,UBERON:2001995,papilla
+HP:0004033,Curved olecranon,HP:0004032,Abnormality of the olecranon
+UBERON:3000329,oblique cartilage,UBERON:0003406,cartilage of respiratory system
+HP:0009301,Short proximal phalanx of the 4th finger,HP:0009280,Short 4th finger
+HP:0002792,Reduced vital capacity,HP:0002795,Functional respiratory abnormality
+HP:0012230,Rhegmatogenous retinal detachment,HP:0000541,Retinal detachment
+UBERON:2001898,ceratobranchial element,UBERON:0010363,endochondral element
+UBERON:0010279,pericardial sinus,UBERON:0002553,anatomical cavity
+DOID:3571,liver cancer,DOID:3119,gastrointestinal system cancer
+HP:0011837,Partial IgA deficiency,HP:0002720,IgA deficiency
+HP:0009793,Presacral teratoma,HP:0005107,Abnormality of the sacrum
+HP:0006673,Reduced systolic function,HP:0001635,Congestive heart failure
+HP:0008144,Flattening of the talar dome,HP:0001850,Abnormality of the tarsal bones
+UBERON:0001137,dorsum,UBERON:0000475,organism subdivision
+UBERON:0015846,incisor mesenchyme,UBERON:0003856,odontogenic mesenchyme
+DOID:3615,infiltrating angiolipoma,DOID:3616,angiolipoma
+HP:0011759,Pituitary gonadotropic cell adenoma,HP:0002893,Pituitary adenoma
+UBERON:0010056,future tongue,UBERON:0005423,developing anatomical structure
+UBERON:3000667,pars reuniens,UBERON:0000064,organ part
+HP:0001653,Mitral regurgitation,HP:0001633,Abnormality of the mitral valve
+DOID:6405,ovarian papillary cystadenoma,DOID:6214,ovarian papillary neoplasm
+DOID:5143,large bowel leiomyoma,DOID:4610,intestinal benign neoplasm
+UBERON:0000388,epiglottis,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004178,aorta smooth muscle tissue,UBERON:0004237,blood vessel smooth muscle
+UBERON:0013454,spheno-maxillary fossa,UBERON:0004704,bone fossa
+HP:0001917,Renal amyloidosis,HP:0011034,Amyloidosis
+UBERON:0002390,hematopoietic system,UBERON:0000467,anatomical system
+HP:0006302,Dagger-shaped pulp calcifications,HP:0002514,Cerebral calcification
+UBERON:3000672,posterolateral process,UBERON:0004529,anatomical projection
+UBERON:0005472,right vitelline vein,UBERON:0005487,vitelline vein
+HP:0010521,Gait apraxia,HP:0002186,Apraxia
+NCBITaxon:73230,Emmonsia crescens,NCBITaxon:73229,Emmonsia
+NCBITaxon:6072,Eumetazoa,NCBITaxon:33208,Metazoa
+HP:0004523,Long eyebrows,HP:0000534,Abnormality of the eyebrow
+CL:1000693,kidney interstitial fibrocyte,CL:1000500,kidney interstitial cell
+HP:0005409,Markedly reduced T cell function,HP:0005435,Impaired T cell function
+UBERON:0002914,inferior postcentral sulcus,UBERON:0013118,sulcus of brain
+UBERON:0002909,posterior subcentral sulcus,UBERON:0003022,cerebral cortex lobe
+UBERON:0016442,median palatine suture,UBERON:0003685,cranial suture
+DOID:265,spleen angiosarcoma,DOID:672,spleen cancer
+DOID:9976,heroin dependence,DOID:2559,opiate dependence
+DOID:0050250,philophthalmiasis,DOID:883,parasitic helminthiasis infectious disease
+UBERON:2001921,adipose eyelid,UBERON:0003102,surface structure
+DOID:48,male reproductive system disease,DOID:15,reproductive system disease
+UBERON:0007771,epidermis gland,UBERON:0002419,skin gland
+UBERON:3000660,margo choanalis,UBERON:0010313,neural crest-derived structure
+HP:0009565,Aplasia of the distal phalanx of the 2nd finger,HP:0009557,Aplasia/Hypoplasia of the distal phalanx of the 2nd finger
+UBERON:0005498,primitive heart tube,UBERON:0002050,embryonic structure
+HP:0009713,Spinal hemangioblastoma,HP:0010797,Hemangioblastoma
+HP:0007233,Clusters of axonal regeneration,HP:0003450,Axonal regeneration
+UBERON:0012172,stomach primordium,UBERON:0001048,primordium
+HP:0003879,Pseudarthrosis (humeral),HP:0003063,Abnormality of the humerus
+UBERON:3000680,manubrium of hyale,UBERON:0000064,organ part
+CL:0000594,skeletal muscle satellite cell,CL:0000680,muscle precursor cell
+HP:0006717,Peripheral neuroepithelioma,HP:0100007,Neoplasm of the peripheral nervous system
+DOID:12119,hemosiderosis,DOID:2351,iron metabolism disease
+CL:0002079,pancreatic ductal cell,CL:1001433,epithelial cell of exocrine pancreas
+UBERON:0004719,kidney arcuate vein,UBERON:0013126,vein of abdomen
+UBERON:0006862,diaphysis of femur,UBERON:0004120,mesoderm-derived structure
+UBERON:0005118,metanephric early distal convoluted tubule,UBERON:0005134,metanephric nephron epithelium
+HP:0003286,Cystathioninemia,HP:0004339,Abnormality of sulfur amino acid metabolism
+UBERON:3010824,processus triangularis of palatoquadrate cartilage,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005437,conus medullaris,UBERON:0005844,spinal cord segment
+HP:0004002,Flattened radial epiphyses,HP:0003071,Flattened epiphyses
+DOID:2702,pigmented villonodular synovitis,DOID:2703,synovitis
+HP:0010915,Abnormality of pyruvate family amino acid metabolism,HP:0004337,Abnormality of amino acid metabolism
+UBERON:2001652,pharyngobranchial 3 tooth plate,UBERON:2002015,pharyngobranchial tooth plate
+HP:0100469,Patchy sclerosis of the distal phalanx of the 5th toe,HP:0010388,Patchy sclerosis of the phalanges of the 5th toe
+HP:0012607,Abnormal urine magnesium concentration,HP:0012591,Abnormal urinary electrolyte concentration
+UBERON:0002295,scala media,UBERON:0010313,neural crest-derived structure
+UBERON:0004040,cortical intermediate zone,UBERON:0014950,layer of developing cerebral cortex
+UBERON:0003565,hindbrain dura mater,UBERON:0002092,brain dura mater
+HP:0002549,Deficit in phonologic short-term memory,HP:0002354,Memory impairment
+UBERON:0001966,substantia nigra pars reticulata,UBERON:0000064,organ part
+UBERON:4200030,antitrochanter,UBERON:0005913,zone of bone organ
+DOID:0060016,CD3delta deficiency,DOID:627,severe combined immunodeficiency
+CL:0002441,CD94-positive natural killer cell,CL:0002438,NK1.1-positive natural killer cell
+DOID:5672,large intestine cancer,DOID:10155,intestinal cancer
+UBERON:0002798,spinothalamic tract of pons,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002428,limb bone,UBERON:0004375,bone of free limb or fin
+CL:0002514,Vgamma5-negative CD8alpha alpha positive gamma-delta intraepithelial T cell,CL:0000802,"CD8-alpha alpha positive, gamma-delta intraepithelial T cell"
+HP:0011182,Epileptiform EEG discharges,HP:0002353,EEG abnormality
+UBERON:0010737,distal tarsal bone 4,UBERON:0015111,distal tarsal bone 4 endochondral element
+HP:0007369,Atrophy/Degeneration affecting the cerebrum,HP:0012444,Brain atrophy
+HP:0009442,Curved phalanges of the 3rd finger,HP:0009316,Abnormality of the phalanges of the 3rd finger
+DOID:9159,gas gangrene,DOID:0050339,commensal bacterial infectious disease
+HP:0011047,Agenesis of primary mandibular central incisor,HP:0006355,Agenesis of mandibular central incisor
+UBERON:0008433,lumbar vertebral arch,UBERON:0004247,bone of dorsum
+UBERON:0011315,digastric branch of facial nerve,UBERON:0001647,facial nerve
+UBERON:0001043,esophagus,UBERON:0005178,thoracic cavity organ
+HP:0002677,Small foramen magnum,HP:0002699,Abnormality of the foramen magnum
+HP:0009390,Small epiphyses of the 5th finger,HP:0009152,Abnormality of the epiphyses of the 5th finger
+HP:0006765,Chondrosarcoma,HP:0100242,Sarcoma
+HP:0100015,Stahl ear,HP:0011235,Additional crus of antihelix
+HP:0006714,Aplasia/Hypoplasia of the sternum,HP:0000766,Abnormality of the sternum
+HP:0010746,Hypoplasia of the phalanges of the toes,HP:0010173,Aplasia/Hypoplasia of the phalanges of the toes
+HP:0005665,Massively thickened long bone cortices,HP:0000935,Thickened cortex of long bones
+HP:0002808,Kyphosis,HP:0010674,Abnormality of the curvature of the vertebral column
+UBERON:0004083,cerebellum vermis lobule X,UBERON:0004070,cerebellum vermis lobule
+DOID:0050866,oral squamous cell carcinoma,DOID:8618,oral cavity cancer
+UBERON:3000879,incisura terminalis,UBERON:0004120,mesoderm-derived structure
+HP:0009791,Bifid sacrum,HP:0005107,Abnormality of the sacrum
+DOID:3577,Sertoli cell tumor,DOID:4757,sex cord-stromal neoplasm
+UBERON:0004275,third ventricle choroid plexus epithelium,UBERON:0004642,third ventricle ependyma
+HP:0100241,Ectopic respiratory mucosa,HP:0012253,Abnormal respiratory epithelium morphology
+UBERON:0014915,genu of facial nerve,UBERON:0007702,tract of brain
+HP:0011270,Duplicated tragus,HP:0009912,Abnormality of the tragus
+UBERON:0002749,regional part of cerebellar cortex,UBERON:0003528,brain grey matter
+HP:0007758,Congenital visual impairment,HP:0000505,Visual impairment
+UBERON:0010029,dorsal part of pharyngeal pouch 5,UBERON:0005291,embryonic tissue
+HP:0001051,Seborrheic dermatitis,HP:0000964,Eczema
+DOID:3873,nodular medulloblastoma,DOID:0050902,medulloblastoma
+HP:0010689,Mirror image polydactyly,HP:0010442,Polydactyly
+HP:0010142,Fragmentation of the epiphysis of the distal phalanx of the hallux,HP:0010117,Fragmentation of the epiphyses of the hallux
+HP:0003272,Abnormality of the hip bone,HP:0100491,Abnormality of the joints of the lower limbs
+UBERON:0001296,myometrium,UBERON:0004923,organ component layer
+HP:0003651,Foam cells,HP:0002621,Atherosclerosis
+NCBITaxon:88770,Panarthropoda,NCBITaxon:1206794,Ecdysozoa
+UBERON:0005449,greater sac,UBERON:0000481,multi-tissue structure
+UBERON:0009695,epithelium of laryngopharynx,UBERON:0003351,pharyngeal epithelium
+CL:1000612,kidney corpuscule cell,CL:0002584,renal cortical epithelial cell
+UBERON:0001860,endolymphatic duct,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0010248,choroidal tapetum fibrosum,UBERON:0010244,choroid tapetum lucidum
+CL:1000839,kidney proximal straight tubule epithelial cell,CL:1000616,kidney outer medulla cell
+UBERON:0008844,gubernaculum (female),UBERON:0014404,female anatomical structure
+UBERON:0005029,mucosa of lacrimal canaliculus,UBERON:0000344,mucosa
+UBERON:0010681,pedal digit 2 phalanx cartilage element,UBERON:0015032,pedal digit 2 phalanx endochondral element
+UBERON:0004196,proximal convoluted tubule segment 1,UBERON:0006554,urinary system structure
+HP:0002748,Rickets,HP:0004349,Reduced bone mineral density
+UBERON:2002263,epineural 1,UBERON:2000507,epineural
+UBERON:0004129,growth plate cartilage,UBERON:0002418,cartilage tissue
+UBERON:0010239,spiral colon,UBERON:0000168,segment of colon
+UBERON:0000990,reproductive system,UBERON:0000467,anatomical system
+HP:0009932,Single naris,HP:0005288,Abnormality of the nares
+HP:0006958,Abnormal auditory evoked potentials,HP:0001311,Abnormal nervous system electrophysiology
+UBERON:0007699,tract of spinal cord,UBERON:0001018,axon tract
+UBERON:0008911,chondral bone,UBERON:0012075,replacement bone
+DOID:13575,non-renal secondary hyperparathyroidism,DOID:13543,hyperparathyroidism
+HP:0000447,Pear-shaped nose,HP:0005105,Abnormal nasal morphology
+HP:0001155,Abnormality of the hand,HP:0002817,Abnormality of the upper limb
+NCBITaxon:777,Coxiella burnetii,NCBITaxon:776,Coxiella <Bacteria>
+HP:0011677,Tetralogy of Fallot with atrioventricular canal defect,HP:0001636,Tetralogy of Fallot
+UBERON:0010550,pedal digit 4 metatarsal pre-cartilage condensation,UBERON:0015040,pedal digit 4 metatarsal endochondral element
+UBERON:0003426,dermis adipose tissue,UBERON:0001013,adipose tissue
+HP:0006511,Laryngeal stridor,HP:0001600,Abnormality of the larynx
+HP:0006483,Abnormal number of teeth,HP:0000164,Abnormality of the teeth
+UBERON:0010015,ventral patch of Leydig's organ,UBERON:0000064,organ part
+UBERON:0005734,tunica adventitia of blood vessel,UBERON:0005742,adventitia
+UBERON:0001117,caudate lobe of liver,UBERON:0001114,right lobe of liver
+UBERON:0011961,articular capsule of hip joint,UBERON:0001484,articular capsule
+UBERON:0001449,phalanx of pes,UBERON:0003221,phalanx
+DOID:8082,cellular congenital mesoblastic nephroma,DOID:4773,congenital mesoblastic nephroma
+HP:0012176,Abnormality of natural killer cells,HP:0004332,Abnormality of lymphocytes
+CL:0000750,OFF-bipolar cell,CL:0000748,retinal bipolar neuron
+UBERON:2001961,ceratobranchial 5 bone distal cartilage,UBERON:0011004,pharyngeal arch cartilage
+UBERON:0008924,sublaminar layer S3,UBERON:0009736,sublaminar layers S3 or S4 or S5
+UBERON:3010693,ramus posterior profundus of V3,UBERON:0004529,anatomical projection
+UBERON:0011754,genital swelling,UBERON:0000481,multi-tissue structure
+UBERON:0004103,alveolar ridge,UBERON:0004121,ectoderm-derived structure
+UBERON:0012490,muscle layer of anal canal,UBERON:0004121,ectoderm-derived structure
+DOID:3133,acute porphyria,DOID:13268,porphyria
+DOID:4931,nasal cavity carcinoma,DOID:10811,nasal cavity cancer
+HP:0003339,Pyrimidine-responsive megaloblastic anemia,HP:0001889,Megaloblastic anemia
+HP:0008007,Primary congenital glaucoma,HP:0001087,Congenital glaucoma
+HP:0100177,Small epiphysis of the distal phalanx of the 4th toe,HP:0100094,Abnormality of the epiphysis of the distal phalanx of the 4th toe
+HP:0100042,Broad 4th toe,HP:0010321,Abnormality of the 4th toe
+UBERON:0003564,diencephalon dura mater,UBERON:0003290,meninx of diencephalon
+UBERON:0002682,abducens nucleus,UBERON:0006331,brainstem nucleus
+UBERON:0006786,white matter of superior colliculus,UBERON:0003544,brain white matter
+HP:0008127,Bipartite calcaneus,HP:0008364,Abnormality of the calcaneus
+HP:0000977,Soft skin,HP:0010647,Abnormal elasticity of skin
+UBERON:3010080,snout protuberances,UBERON:3000972,head external integument structure
+HP:0100392,Short middle phalanx of the 3rd toe,HP:0100366,Short phalanx of the 3rd toe
+HP:0100396,Short proximal phalanx of the 4th toe,HP:0100367,Short phalanx of the 4th toe
+DOID:3709,rectum mucinous adenocarcinoma,DOID:1996,rectum adenocarcinoma
+UBERON:2001951,skin flap,UBERON:0003102,surface structure
+UBERON:0005889,zygote cortex,UBERON:0000470,cell part
+UBERON:0003983,conus arteriosus,UBERON:0004151,cardiac chamber
+UBERON:0013694,brain endothelium,UBERON:0010371,ecto-epithelium
+UBERON:0011599,lenticular process of incus,UBERON:4100000,skeletal element projection
+UBERON:0000065,respiratory tract,UBERON:0001005,respiratory airway
+UBERON:0011085,palatoquadrate arch,UBERON:0010912,subdivision of skeleton
+HP:0011563,Abnormal ventriculo-arterial connection,HP:0011545,Abnormal connection of the cardiac segments
+HP:0012406,Hypercitraturia,HP:0012404,Abnormal urine citrate concentration
+HP:0007468,Perifollicular hyperkeratosis,HP:0000962,Hyperkeratosis
+UBERON:0010697,pedal digit metatarsal cartilage element,UBERON:0015064,autopod cartilage
+UBERON:0010509,strand of pelage hair,UBERON:0001037,strand of hair
+UBERON:4200172,neck of humerus,UBERON:0004120,mesoderm-derived structure
+UBERON:0008000,sesamoid bone of pes,UBERON:0005899,pes bone
+UBERON:0001900,ventral thalamus,UBERON:0002784,regional part of diencephalon
+DOID:4535,hypotrichosis,DOID:421,hair disease
+DOID:14744,Partington syndrome,DOID:225,syndrome
+HP:0004058,Monodactyly (hands),HP:0001180,Oligodactyly (hands)
+HP:0006379,Proximal tibial hypopolasia,HP:0005736,Short tibia
+UBERON:0005122,metanephric macula densa,UBERON:0004120,mesoderm-derived structure
+HP:0003566,Increased serum prostaglandin E2,HP:0011023,Abnormality of prostaglandin metabolism
+HP:0010754,Abnormality of the temporomandibular joint,HP:0000277,Abnormality of the mandible
+DOID:1068,juvenile glaucoma,DOID:1067,open-angle glaucoma
+UBERON:0004221,intestine smooth muscle,UBERON:0004226,gastrointestinal system smooth muscle
+HP:0012135,Abnormality of cells of the granulocytic lineage,HP:0005561,Abnormality of bone marrow cell morphology
+UBERON:0005991,aortic valve anulus,UBERON:0006008,fibrous ring of heart
+DOID:5773,oral submucous fibrosis,DOID:403,mouth disease
+HP:0100055,Absent epiphyses of the 3rd toe,HP:0010329,Abnormality of the epiphyses of the 3rd toe
+HP:0005926,Abnormalities of the cortex of hand bones,HP:0003103,Abnormal cortical bone morphology
+UBERON:0010511,strand of awl hair,UBERON:0010509,strand of pelage hair
+UBERON:0001230,glomerular capsule,UBERON:0006554,urinary system structure
+UBERON:0006288,rib cartilage element,UBERON:0004120,mesoderm-derived structure
+HP:0003258,Glyoxalase deficiency,HP:0011013,Abnormality of carbohydrate metabolism/homeostasis
+HP:0100554,Hemihypertrophy of upper limb,HP:0001528,Hemihypertrophy
+UBERON:0004010,primary muscle spindle,UBERON:0003718,muscle spindle
+CL:0000040,monoblast,CL:0002194,monopoietic cell
+HP:0011857,Plasmacytoma,HP:0004377,Hematological neoplasm
+HP:0100375,Aplasia/Hypoplasia of the proximal phalanx of the 3rd toe,HP:0010331,Aplasia/Hypoplasia of the 3rd toe
+HP:0006892,Frontotemporal cerebral atrophy,HP:0002059,Cerebral atrophy
+HP:0012716,Moderate conductive hearing impairment,HP:0012712,Mild hearing impairment
+UBERON:0002624,orbital part of inferior frontal gyrus,UBERON:0003022,cerebral cortex lobe
+DOID:12176,goiter,DOID:50,thyroid gland disease
+CL:0002510,"CD103-negative, langerin-positive lymph node dendritic cell",CL:0002507,langerin-positive lymph node dendritic cell
+UBERON:0002754,predorsal bundle,UBERON:0005838,fasciculus of brain
+UBERON:0001863,scala vestibuli,UBERON:0010313,neural crest-derived structure
+CL:0002631,epithelial cell of upper respiratory tract,CL:0002368,respiratory epithelial cell
+HP:0009506,Fragmentation of the epiphysis of the distal phalanx of the 2nd finger,HP:0009492,Fragmentation of the epiphyses of the 2nd finger
+HP:0001859,Distal symphalangism (feet),HP:0010179,Symphalangism affecting the phalanges of the toes
+UBERON:4200114,prepubic process,UBERON:0004120,mesoderm-derived structure
+DOID:184,bone cancer,DOID:201,connective tissue cancer
+CL:0002191,granulocytopoietic cell,CL:0000839,myeloid lineage restricted progenitor cell
+UBERON:0014602,paraventricular nucleus of the hypothalamus descending division,UBERON:0003048,regional part of hypothalamus
+UBERON:2005012,afferent filamental artery,UBERON:0003469,respiratory system artery
+HP:0005659,Thoracic kyphoscoliosis,HP:0002943,Thoracic scoliosis
+UBERON:0010512,strand of guard hair,UBERON:0010509,strand of pelage hair
+HP:0003326,Myalgia,HP:0011804,Abnormality of muscle physiology
+HP:0009594,Retinal hamartoma,HP:0010568,Hamartoma of the eye
+UBERON:0001150,body of pancreas,UBERON:0000064,organ part
+UBERON:3000908,sulcus distalis ossis cruris,UBERON:0004120,mesoderm-derived structure
+HP:0001756,Vestibular hypofunction,HP:0001751,Vestibular dysfunction
+HP:0009415,Irregular epiphyses of the 3rd finger,HP:0010233,Irregular epiphyses of the phalanges of the hand
+UBERON:0001049,neural tube,UBERON:0003914,epithelial tube
+UBERON:0004487,musculature of forelimb zeugopod,UBERON:0004474,musculature of arm
+UBERON:3000662,processus posterior of parasphenoid,UBERON:0004121,ectoderm-derived structure
+HP:0002311,Incoordination,HP:0011443,Abnormality of coordination
+UBERON:0002374,metacarpal bone,UBERON:0012358,manual digitopodium bone
+DOID:5251,inflammatory leiomyosarcoma,DOID:1967,leiomyosarcoma
+UBERON:0007652,esophageal sphincter,UBERON:0003832,esophagus muscle
+UBERON:0003863,pedal digit 5 phalanx,UBERON:0015035,pedal digit 5 phalanx endochondral element
+DOID:11558,acute allergic serous otitis media,DOID:11557,acute serous otitis media
+DOID:9008,psoriatic arthritis,DOID:225,syndrome
+DOID:3093,nervous system cancer,DOID:0050686,organ system cancer
+HP:0100377,Aplasia/Hypoplasia of the proximal phalanx of the 5th toe,HP:0010383,Aplasia/Hypoplasia of the phalanges of the 5th toe
+CL:0002033,short term hematopoietic stem cell,CL:0001008,Kit and Sca1-positive hematopoietic stem cell
+CL:0000169,type B pancreatic cell,CL:0000168,insulin secreting cell
+HP:0012439,Abnormal biliary tract physiology,HP:0001080,Biliary tract abnormality
+UBERON:2001606,caudal scute,UBERON:2002294,fish scute
+HP:0006289,Agenesis of central incisor,HP:0006485,Agenesis of incisor
+HP:0005452,Obliteration of frontal sinuses,HP:0002687,Abnormality of the frontal sinuses
+UBERON:2001416,pelvic fin distal radial bone 3,UBERON:2101416,pelvic fin distal radial element 3
+DOID:4548,extraskeletal mesenchymal chondrosarcoma,DOID:4549,extraosseous chondrosarcoma
+HP:0007986,Increased retinal vascularity,HP:0008046,Abnormality of the retinal vasculature
+UBERON:0014532,lamina of cerebral hemisphere,UBERON:0014530,lamina of neuraxis
+DOID:9631,Pelger-Huet anomaly,DOID:0050736,autosomal dominant disease
+UBERON:0008848,cranial suspensory ligament,UBERON:0014403,male anatomical structure
+HP:0002528,Granulovacuolar degeneration,HP:0002060,Abnormality of the cerebrum
+HP:0009489,Bracket epiphyses of the 2nd finger,HP:0006263,Abnormality of the epiphyses of the 2nd finger
+HP:0003154,Increased circulating ACTH level,HP:0011043,Abnormality of circulating adrenocorticotropin level
+DOID:11766,blind hypotensive eye,DOID:9799,eye degenerative disease
+DOID:0050168,autoimmune polyendocrine syndrome type 2,DOID:14040,autoimmune polyendocrine syndrome
+CL:0000967,Bm5 B cell,CL:0001053,IgD-negative memory B cell
+HP:0010796,Brainstem glioma,HP:0009733,Glioma
+DOID:5838,extragonadal seminoma,DOID:4440,seminoma
+UBERON:2101818,dorsal fin proximal radial element 1,UBERON:2100947,dorsal fin proximal radial element
+UBERON:0005570,rhombomere 2 floor plate,UBERON:0005500,rhombomere floor plate
+UBERON:0005578,rhombomere 4 roof plate,UBERON:0005502,rhombomere roof plate
+UBERON:0001923,central medial nucleus,UBERON:0015233,nucleus of dorsal thalamus
+HP:0009341,Ivory epiphysis of the distal phalanx of the 3rd finger,HP:0010252,Ivory epiphyses of the distal phalanges of the hand
+UBERON:0000995,uterus,UBERON:0013515,subdivision of uterine tube
+UBERON:2001062,primitive mesencephalic artery,UBERON:0001637,artery
+DOID:0050926,jejunal adenocarcinoma,DOID:13499,jejunal cancer
+UBERON:4300030,flexor caudalis muscle,UBERON:0001630,muscle organ
+HP:0005650,Cutaneous syndactyly between fingers 2 and 5,HP:0010554,Cutaneous finger syndactyly
+UBERON:0001563,longus capitis muscle,UBERON:0008549,prevertebral muscle of neck
+UBERON:0001772,corneal epithelium,UBERON:0000488,atypical epithelium
+CL:1000850,macula densa epithelial cell,CL:1000618,juxtaglomerular complex cell
+HP:0007906,Increased intraocular pressure,HP:0012632,Abnormal intraocular pressure
+UBERON:0001107,sternohyoid muscle,UBERON:0008523,infrahyoid muscle
+UBERON:2000814,opercular lateral line neuromast,UBERON:0008904,neuromast
+HP:0006889,"Intellectual disability, borderline",HP:0001249,Intellectual disability
+DOID:7152,prostate stromal sarcoma,DOID:4054,prostate sarcoma
+DOID:9720,vitreous disease,DOID:1492,eye and adnexa disease
+HP:0009679,Fragmentation of the epiphysis of the distal phalanx of the thumb,HP:0010250,Fragmentation of the epiphyses of the distal phalanges of the hand
+HP:0004299,Hernia of the abdominal wall,HP:0010866,Abdominal wall defect
+UBERON:0010578,manual digit 4 phalanx pre-cartilage condensation,UBERON:0005694,manual digit 4 mesenchyme
+UBERON:0010709,pelvic complex,UBERON:0010707,appendage girdle complex
+NCBITaxon:177872,VEEV complex,NCBITaxon:11019,Alphavirus
+DOID:5862,localized chondrosarcoma,DOID:3371,chondrosarcoma
+UBERON:0002203,vasculature of eye,UBERON:0006876,vasculature of organ
+UBERON:0016396,intraglandular lymph node,UBERON:0016393,deep parotid lymph node
+UBERON:2000497,pelvic adductor profundus,UBERON:0011145,adductor muscle
+DOID:3357,extraosseous osteosarcoma,DOID:3347,osteosarcoma
+UBERON:0006835,arthropod oviduct,UBERON:0014404,female anatomical structure
+DOID:11330,erysipelas,DOID:2723,dermatitis
+HP:0012322,Perifolliculitis,HP:0011123,Inflammatory abnormality of the skin
+UBERON:0003895,hypaxial myotome region,UBERON:0001134,skeletal muscle tissue
+HP:0009153,Abnormality of the epiphysis of the proximal phalanx of the 5th finger,HP:0010245,Abnormality of the epiphyses of the proximal phalanges of the hand
+HP:0002093,Respiratory insufficiency,HP:0002088,Abnormality of the lung
+CL:1000803,kidney inner medulla interstitial cell,CL:1000617,kidney inner medulla cell
+UBERON:0007113,venom,UBERON:0000456,bodily secretion
+UBERON:2001860,epibranchial 4-upper pharyngeal toothplate joint,UBERON:0000982,skeletal joint
+UBERON:0006223,dorsal meso-oesophagus,UBERON:0002050,embryonic structure
+HP:0011511,Macular schisis,HP:0001103,Abnormality of the macula
+DOID:13269,hereditary coproporphyria,DOID:3133,acute porphyria
+DOID:8504,impetigo,DOID:4223,pyoderma
+UBERON:0008438,webbed interdigital region between manual digits,UBERON:0006015,webbed interdigital region
+UBERON:3000677,lateral process of cricoid cartilage,UBERON:0000072,segment of respiratory tract
+HP:0005880,Metacarpophalangeal synostosis,HP:0009700,Synostosis involving bones of the fingers
+HP:0009427,Triangular shaped distal phalanx of the 3rd finger,HP:0009446,Triangular shaped phalanges of the 3rd finger
+UBERON:0001677,sphenoid bone,UBERON:0003462,facial bone
+HP:0004374,Hemiplegia/hemiparesis,HP:0010549,Paralysis due to lesions of the principle motor tracts
+UBERON:0003696,metatarsophalangeal joint,UBERON:0001487,pes joint
+HP:0010475,Cloacal exstrophy,HP:0012620,Cloacal abnormality
+HP:0004366,Abnormality of glycolysis,HP:0011013,Abnormality of carbohydrate metabolism/homeostasis
+UBERON:0011684,levator palatoquadrati,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:486,glomeruloid hemangioma,DOID:255,hemangioma
+UBERON:0004082,cerebellum vermis lobule VIII,UBERON:0004070,cerebellum vermis lobule
+UBERON:0005215,kidney interstitium,UBERON:0006554,urinary system structure
+UBERON:3000896,foveal depression,UBERON:0004704,bone fossa
+DOID:949,chronic dacryoadenitis,DOID:950,dacryoadenitis
+UBERON:3000088,cavum praenasale,UBERON:0001707,nasal cavity
+UBERON:1000004,collection of hair on ear,UBERON:0014382,collection of hairs on head or neck
+UBERON:0015280,pancreas left lobe,UBERON:0015212,lateral structure
+UBERON:2001906,epibranchial 2 element,UBERON:2001904,epibranchial element
+CL:1000309,epicardial adipocyte,CL:0002494,cardiocyte
+HP:0011972,Hypoglycorrhachia,HP:0002921,Abnormality of the cerebrospinal fluid
+HP:0012574,Mesangial proliferation,HP:0001966,Mesangial abnormality
+UBERON:3000650,processus frontalis of maxilla,UBERON:4100000,skeletal element projection
+UBERON:0015136,secondary lactiferous duct,UBERON:0001765,mammary duct
+UBERON:0010939,zygomaticomandibularis muscle,UBERON:0010959,craniocervical muscle
+UBERON:0001687,stapes bone,UBERON:0015016,stapes endochondral element
+DOID:0050804,glioblastoma proneural subtype,DOID:3068,glioblastoma multiforme
+UBERON:3000177,flange of quadratojugal,UBERON:4100000,skeletal element projection
+UBERON:0015081,proximal tarsal bone endochondral element,UBERON:0015050,tarsus endochondral element
+UBERON:0011528,pubococcygeus muscle,UBERON:0001325,muscle of pelvis
+HP:0002034,Abnormality of the rectum,HP:0012732,Anorectal anomaly
+HP:0005819,Short middle phalanx of finger,HP:0009843,Aplasia/Hypoplasia of the middle phalanges of the hand
+UBERON:0004704,bone fossa,UBERON:0002553,anatomical cavity
+DOID:0050538,Charcot-Marie-Tooth disease type 1,DOID:10595,Charcot-Marie-Tooth disease
+HP:0000368,"Low-set, posteriorly rotated ears",HP:0000369,Low-set ears
+DOID:9620,vesicoureteral reflux,DOID:1426,ureteral disease
+UBERON:0001079,superior articular process of vertebra,UBERON:0006062,articular process of vertebra
+UBERON:2000955,sclerotome somite 18,UBERON:0003089,sclerotome
+HP:0011042,Abnormality of potassium homeostasis,HP:0010930,Abnormality of monovalent inorganic cation homeostasis
+HP:0007777,Chorioretinal scars,HP:0000532,Chorioretinal abnormality
+UBERON:4300082,metapterygium element,UBERON:2101587,pectoral fin proximal radial element
+DOID:4055,ectomesenchymoma,DOID:502,central nervous system mesenchymal non-meningothelial tumor
+UBERON:0004332,proximal phalanx of pedal digit 1,UBERON:0003868,proximal phalanx of pes
+HP:0011428,Short fetal femur length,HP:0011425,Fetal ultrasound soft marker
+UBERON:0009193,sphenoid cartilage element,UBERON:0014387,mesenchyme derived from neural crest
+NCBITaxon:1648,Erysipelothrix rhusiopathiae,NCBITaxon:1647,Erysipelothrix
+NCBITaxon:10116,Rattus norvegicus,NCBITaxon:10114,Rattus
+UBERON:4000166,anal fin skeleton,UBERON:4000170,median fin skeleton
+DOID:5382,Bartholin's gland adenoma,DOID:2068,Bartholin's gland neoplasm
+UBERON:0001740,arytenoid cartilage,UBERON:0015212,lateral structure
+HP:0011029,Internal hemorrhage,HP:0011028,Abnormality of blood circulation
+UBERON:0007642,ligamentum arteriosum,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0001494,ulnar nerve,UBERON:0003433,arm nerve
+HP:0100381,Absent middle phalanx of the 3rd toe,HP:0100387,Aplasia of the middle phalanges of the toes
+HP:0009672,Small epiphysis of the proximal phalanx of the thumb,HP:0010265,Small epiphyses of the middle phalanges of the hand
+UBERON:0011931,nasal hair,UBERON:0010171,strand of hair of face
+UBERON:0002560,temporal operculum,UBERON:0000477,anatomical cluster
+CL:1000742,glomerular mesangial cell,CL:1000746,glomerular cell
+HP:0009768,Broad phalanges of the hand,HP:0001500,Broad finger
+UBERON:0002724,limen of insula,UBERON:0000464,anatomical space
+DOID:7379,adrenal medulla carcinoma,DOID:5719,adrenal medulla cancer
+DOID:7455,hypogonadotropism,DOID:2277,gonadal disease
+DOID:3906,bronchial neoplasm,DOID:0050621,respiratory system benign neoplasm
+UBERON:0002820,zona arcuata of basilar membrane of cochlea,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002824,vestibular ganglion,UBERON:0010313,neural crest-derived structure
+DOID:4542,basophil adenoma,DOID:3829,pituitary adenoma
+UBERON:4200169,process 2,UBERON:4100000,skeletal element projection
+UBERON:3000002,alary cartilage,UBERON:0010313,neural crest-derived structure
+DOID:11239,appendix cancer,DOID:10155,intestinal cancer
+HP:0012291,Tracheal neoplasm,HP:0012288,Neoplasm of head and neck
+UBERON:0006293,spleen primordium,UBERON:0003104,mesenchyme
+DOID:13074,tinea unguium,DOID:8913,dermatophytosis
+HP:0007271,Occipital myelomeningocele,HP:0002436,Occipital meningocele
+HP:0100491,Abnormality of the joints of the lower limbs,HP:0001367,Abnormal joint morphology
+DOID:4847,cauda equina neoplasm,DOID:5612,spinal cancer
+HP:0009207,Fragmentation of the epiphysis of the middle phalanx of the 5th finger,HP:0004224,Abnormality of the epiphysis of the middle phalanx of the 5th finger
+HP:0010813,Abnormal number of hair whorls,HP:0010721,Abnormal hair whorl
+UBERON:0006795,arthropod optic lobe,UBERON:0004121,ectoderm-derived structure
+HP:0003803,Type 1 muscle fiber predominance,HP:0004303,Abnormality of muscle fibers
+DOID:3379,metachronous osteosarcoma of the bone,DOID:3347,osteosarcoma
+UBERON:0007303,pharyngeal vasculature,UBERON:0004119,endoderm-derived structure
+HP:0008214,Decreased serum estradiol,HP:0008373,Puberty and gonadal disorders
+UBERON:2002000,posterior dentation of pectoral fin spine,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009237,Short 5th finger,HP:0009381,Short finger
+UBERON:0004098,tibial plateaux,UBERON:0004120,mesoderm-derived structure
+HP:0003431,Decreased motor nerve conduction velocity,HP:0000762,Decreased nerve conduction velocity
+UBERON:0003405,lobar bronchus of left lung,UBERON:0002183,lobar bronchus
+CL:0008014,excitatory motor neuron,CL:0000100,motor neuron
+CL:1000979,ureter smooth muscle cell,CL:0000192,smooth muscle cell
+UBERON:2007025,midbrain neural keel,UBERON:0004121,ectoderm-derived structure
+HP:0012040,Corneal stromal edema,HP:0011492,Abnormality of corneal stroma
+HP:0006956,Dilation of lateral ventricles,HP:0002119,Ventriculomegaly
+CL:0002615,adipocyte of omentum tissue,CL:0000136,fat cell
+UBERON:0001249,spleen lymphoid follicle,UBERON:0000444,lymphoid follicle
+HP:0007993,Malformed lacrimal ducts,HP:0011481,Abnormality of the lacrimal duct
+DOID:13068,renal osteodystrophy,DOID:11705,impaired renal function disease
+UBERON:0008582,superior longitudinal muscle of tongue,UBERON:0001576,intrinsic muscle of tongue
+HP:0100802,Malposition of the stomach,HP:0002577,Abnormality of the stomach
+DOID:8398,osteoarthritis,DOID:848,arthritis
+UBERON:0002962,adductor pollicis muscle,UBERON:0001500,muscle of manus
+DOID:0060076,estrogen-receptor negative breast cancer,DOID:1612,breast cancer
+UBERON:0014918,retrosplenial granular cortex,UBERON:0002619,regional part of cerebral cortex
+UBERON:0003031,submedial nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:2001404,preethmoid bone,UBERON:0011164,neurocranium bone
+CL:0002012,Kit-low proerythroblast,CL:0000547,proerythroblast
+UBERON:0006488,third cervical spinal cord segment,UBERON:0007714,cervical subsegment of spinal cord
+UBERON:0001261,lamina propria of urinary bladder,UBERON:0006554,urinary system structure
+HP:0002253,Colonic diverticulosis,HP:0002250,Abnormality of the large intestine
+UBERON:1000012,nose anterior margin,UBERON:0001444,subdivision of head
+UBERON:0012075,replacement bone,UBERON:0010522,replacement element
+UBERON:0001476,deltoid,UBERON:0004120,mesoderm-derived structure
+UBERON:2202280,pectoral fin distal radial cartilage 3,UBERON:2102280,pectoral fin distal radial element 3
+HP:0010622,Neoplasm of the skeletal system,HP:0011842,Abnormality of skeletal morphology
+UBERON:0009522,lateral lingual swelling epithelium,UBERON:0000490,unilaminar epithelium
+HP:0005359,Aplasia of the thymus,HP:0010515,Aplasia/Hypoplasia of the thymus
+UBERON:0004258,back blood vessel,UBERON:0001981,blood vessel
+UBERON:2000212,granular eminence,UBERON:0002946,regional part of cerebellum
+HP:0004823,Anisopoikilocytosis,HP:0004447,Poikilocytosis
+UBERON:0001126,serratus dorsalis superior muscle,UBERON:0003830,thoracic segment muscle
+UBERON:0009987,medial epicondyle of femur,UBERON:0005055,zone of long bone
+HP:0007598,Bilateral single transverse palmar creases,HP:0000954,Single transverse palmar crease
+DOID:0060152,time agnosia,DOID:4090,agnosia
+UBERON:4200036,internal trochanter,UBERON:0004120,mesoderm-derived structure
+HP:0000291,Abnormality of facial adipose tissue,HP:0009124,Abnormality of adipose tissue
+HP:0011874,Heparin-induced thrombocytopenia,HP:0001873,Thrombocytopenia
+DOID:5665,external ear cancer,DOID:833,auditory system cancer
+UBERON:2005228,segmented lepidotrichium,UBERON:4000172,lepidotrichium
+UBERON:0015834,duodenum lamina propria,UBERON:0001238,lamina propria of small intestine
+DOID:3783,Coffin-Lowry syndrome,DOID:0050735,X-linked disease
+UBERON:0003699,pubic symphysis,UBERON:0004120,mesoderm-derived structure
+HP:0003236,Elevated serum creatine phosphokinase,HP:0011021,Abnormality of circulating enzyme level
+DOID:0050680,Boomerang dysplasia,DOID:2256,osteochondrodysplasia
+HP:0011413,Shoulder dystocia,HP:0001787,Abnormal delivery
+CL:0002417,primitive erythroid lineage cell,CL:0000764,erythroid lineage cell
+CL:0000838,lymphoid lineage restricted progenitor cell,CL:0002031,hematopoietic lineage restricted progenitor cell
+CL:0000419,seam cell,CL:0000036,epithelial fate stem cell
+UBERON:0006088,inferior parietal cortex,UBERON:0003022,cerebral cortex lobe
+HP:0100788,Fused lips,HP:0000159,Abnormality of the lip
+NCBITaxon:89940,Cladophialophora bantiana,NCBITaxon:82105,Cladophialophora
+UBERON:0007232,2 cell stage,UBERON:0000067,embryo stage part
+HP:0010430,Aplasia of the phalanges of the 2nd toe,HP:0010325,Aplasia/Hypoplasia of the 2nd toe
+HP:0009162,Absent middle phalanx of 5th finger,HP:0010239,Aplasia of the middle phalanx of the hand
+UBERON:2007013,preplacodal ectoderm,UBERON:0005497,non-neural ectoderm
+UBERON:0013605,layer of lateral geniculate body,UBERON:0004121,ectoderm-derived structure
+UBERON:0003367,epithelium of vomeronasal organ,UBERON:0004807,respiratory system epithelium
+UBERON:0009196,indifferent external genitalia,UBERON:0004176,external genitalia
+UBERON:0003729,mouth mucosa,UBERON:0000344,mucosa
+UBERON:2001407,infraorbital 2,UBERON:2000376,infraorbital
+HP:0009837,Bullet-shaped distal phalanges of the hand,HP:0009832,Abnormality of the distal phalanx of finger
+UBERON:0011237,visceral fascia,UBERON:0008982,fascia
+HP:0005613,Aplasia/hypoplasia of the femur,HP:0006493,Aplasia/Hypoplasia involving bones of the lower limbs
+CL:1000363,transitional myocyte of atrial branch of anterior internodal tract,CL:1000480,transitional myocyte of internodal tract
+HP:0012089,Arteritis,HP:0011004,Abnormality of the systemic arterial tree
+UBERON:0009856,sac,UBERON:0000061,anatomical structure
+UBERON:0004474,musculature of arm,UBERON:0004481,musculature of upper limb
+CL:0007021,alarm substance cell,CL:0000151,secretory cell
+HP:0009158,Enlarged epiphysis of the proximal phalanx of the 5th finger,HP:0009385,Enlarged epiphyses of the 5th finger
+UBERON:0004180,mammary gland fat,UBERON:0001013,adipose tissue
+UBERON:4300108,lepidotrichial segment,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3010170,ungual flap,UBERON:3000981,limb external integument structure
+UBERON:0002549,ventral trigeminal tract,UBERON:0004171,trigeminothalamic tract
+CL:0000180,estradiol secreting cell,CL:0000174,steroid hormone secreting cell
+UBERON:0003471,artery of lower lip,UBERON:0004573,systemic artery
+HP:0003164,Hypothalamic gonadotropin-releasing hormone (GNRH) deficiency,HP:0003117,Abnormality of circulating hormone level
+UBERON:0015171,uterine spiral artery,UBERON:0002493,uterine artery
+UBERON:0008266,periodontal ligament,UBERON:0010313,neural crest-derived structure
+CL:0002455,CD8_alpha-negative plasmactyoid dendritic cell,CL:0000989,CD11c-low plasmacytoid dendritic cell
+UBERON:0000446,septum of telencephalon,UBERON:0000477,anatomical cluster
+UBERON:0007635,nucleus of medulla oblongata,UBERON:0006331,brainstem nucleus
+NCBITaxon:138,Borrelia,NCBITaxon:137,Spirochaetaceae
+DOID:0060084,cell type benign neoplasm,DOID:0060072,benign neoplasm
+CL:0000850,serotonergic neuron,CL:0000540,neuron
+UBERON:0008957,sequestrum,UBERON:0000064,organ part
+HP:0005419,Decreased T cell activation,HP:0011840,Abnormality of T cell physiology
+UBERON:0003025,brachium of inferior colliculus,UBERON:0003544,brain white matter
+CL:0002656,glandular cell of endometrium,CL:1001591,oviduct glandular cell
+DOID:5536,sarcomatoid squamous cell skin carcinoma,DOID:3151,skin squamous cell carcinoma
+UBERON:0001511,skin of leg,UBERON:0003532,hindlimb skin
+HP:0003542,Increased serum pyruvate,HP:0004366,Abnormality of glycolysis
+DOID:10780,primary polycythemia,DOID:8432,polycythemia
+UBERON:0005608,hyoid artery,UBERON:0001637,artery
+HP:0012359,Abnormal fucosylation of O-linked protein glycosylation,HP:0012358,Abnormal protein O-linked glycosylation
+CL:0002349,"CD27-high, CD11b-low natural killer cell",CL:0002426,"CD11b-positive, CD27-positive natural killer cell"
+HP:0007783,Butterfly retinal pigment epithelial dystrophy,HP:0011512,Hyperpigmentation of the fundus
+DOID:13544,low tension glaucoma,DOID:1067,open-angle glaucoma
+UBERON:2000216,infracarinalis,UBERON:0001774,muscle of trunk
+HP:0003898,Large humeral epiphyses,HP:0010580,Enlarged epiphyses
+CL:0002042,immature NK T cell stage IV,CL:0000914,immature NK T cell
+HP:0009354,Small epiphysis of the proximal phalanx of the 3rd finger,HP:0009418,Small epiphyses of the 3rd finger
+UBERON:0002520,submandibular lymph node,UBERON:0003968,peripheral lymph node
+HP:0007676,Hypoplasia of the iris,HP:0008053,Aplasia/Hypoplasia of the iris
+UBERON:2002232,presumptive cardiac ventricle primitive heart tube,UBERON:0004120,mesoderm-derived structure
+UBERON:0004446,epiphysis of phalanx,UBERON:0004120,mesoderm-derived structure
+UBERON:0005491,glossopharyngeal neural crest,UBERON:0003099,cranial neural crest
+DOID:1036,chronic leukemia,DOID:1240,leukemia
+UBERON:0010987,sterno-mastoid pre-muscle mass,UBERON:0004120,mesoderm-derived structure
+UBERON:0002770,posterior hypothalamic region,UBERON:0004121,ectoderm-derived structure
+HP:0001293,Cranial nerve compression,HP:0001291,Abnormality of the cranial nerves
+UBERON:0002469,esophagus mucosa,UBERON:0000344,mucosa
+UBERON:2000476,branchiostegal ray,UBERON:0008907,dermal bone
+HP:0000873,Diabetes insipidus,HP:0000818,Abnormality of the endocrine system
+DOID:5418,schizoaffective disorder,DOID:2468,psychotic disorder
+UBERON:0004085,labium majora,UBERON:0004084,genital labium
+HP:0000030,Testicular gonadoblastoma,HP:0010788,Testicular neoplasm
+UBERON:0008397,tracheobronchial epithelium,UBERON:0004802,respiratory tract epithelium
+DOID:5340,anterograde amnesia,DOID:10914,amnestic disorder
+HP:0010015,Absent epiphysis of the 1st metacarpal,HP:0009196,Absent metacarpal epiphyses
+UBERON:0001414,median cubital vein,UBERON:0001638,vein
+HP:0008305,Exercise-induced myoglobinuria,HP:0002913,Myoglobinuria
+UBERON:0001654,supra-orbital vein,UBERON:0003496,head blood vessel
+UBERON:0008971,left colon,UBERON:0000064,organ part
+CL:1000692,kidney interstitial fibroblast,CL:1000500,kidney interstitial cell
+UBERON:0015480,proper hepatic artery,UBERON:0004573,systemic artery
+UBERON:0003278,skeleton of lower jaw,UBERON:0010313,neural crest-derived structure
+HP:0001457,Abnormality of the musculature of the upper arm,HP:0001446,Abnormality of the musculature of the upper limbs
+NCBITaxon:11270,Rhabdoviridae,NCBITaxon:11157,Mononegavirales
+HP:0004034,Irregular olecranon,HP:0004032,Abnormality of the olecranon
+DOID:0050810,biotin deficiency,DOID:5113,nutritional deficiency disease
+HP:0005831,Type B brachydactyly,HP:0001156,Brachydactyly syndrome
+UBERON:0007252,intervertebral disk of cervical vertebra,UBERON:0001066,intervertebral disk
+UBERON:0001118,lobe of thyroid gland,UBERON:0004119,endoderm-derived structure
+UBERON:0014692,superficial epigastric vein,UBERON:0004261,lower leg blood vessel
+UBERON:0009093,outer medulla vasa recta ascending limb,UBERON:0006554,urinary system structure
+DOID:9877,urethral gland abscess,DOID:732,urethral disease
+UBERON:0002129,cerebellar cortex,UBERON:0004121,ectoderm-derived structure
+UBERON:0010727,sutural bone,UBERON:0004766,cranial bone
+HP:0001196,Short umbilical cord,HP:0010881,Abnormality of the umbilical cord
+UBERON:0003635,pedal digit 5,UBERON:0006052,digit 5
+DOID:0060046,aphasia,DOID:93,language disorder
+UBERON:0002789,regional part of posterior hypothalamic region,UBERON:0003048,regional part of hypothalamus
+UBERON:2001949,caudal-fin hook,UBERON:0004120,mesoderm-derived structure
+HP:0011758,Pituitary acidophilic stem cell adenoma,HP:0002893,Pituitary adenoma
+UBERON:0004026,caudal ganglionic eminence,UBERON:0005423,developing anatomical structure
+HP:0001519,Disproportionate tall stature,HP:0000098,Tall stature
+HP:0009271,Triangular epiphysis of the proximal phalanx of the 4th finger,HP:0009403,Triangular epiphyses of the 4th finger
+CL:0000420,syncytial epithelial cell,CL:0002371,somatic cell
+UBERON:0004452,carpal region,UBERON:0008785,upper limb segment
+HP:0002092,Pulmonary hypertension,HP:0002088,Abnormality of the lung
+UBERON:0015016,stapes endochondral element,UBERON:0010363,endochondral element
+UBERON:0002688,supramarginal gyrus,UBERON:0000200,gyrus
+UBERON:0001291,thick ascending limb of loop of Henle,UBERON:0004135,distal tubule
+DOID:6163,familial renal papillary carcinoma,DOID:4455,hereditary renal cell carcinoma
+HP:0100462,Patchy sclerosis of the middle phalanx of the 4th toe,HP:0100937,Sclerosis of the middle phalanx of the 4th toe
+UBERON:0001565,geniohyoid muscle,UBERON:0011151,jaw depressor muscle
+DOID:9723,vitreous abscess,DOID:9724,purulent endophthalmitis
+HP:0009966,Complete duplication of the middle phalanx of the 3rd finger,HP:0010002,Complete duplication of the middle phalanges of the hand
+DOID:5233,glomangiosarcoma,DOID:2431,glomus tumor
+HP:0005900,Fifth metacarpal with ulnar notch,HP:0010013,Abnormality of the 5th metacarpal
+CL:0002450,tether cell,CL:0002374,ear hair cell
+HP:0011772,Abnormality of thyroid morphology,HP:0000820,Abnormality of the thyroid gland
+NCBITaxon:1236,Gammaproteobacteria,NCBITaxon:1224,Proteobacteria
+UBERON:2001341,intervening zone,UBERON:0000477,anatomical cluster
+UBERON:0002326,lamina propria of urethra,UBERON:0006554,urinary system structure
+UBERON:0004665,seminal vesicle muscle layer,UBERON:0014403,male anatomical structure
+UBERON:0002559,medullary reticular formation,UBERON:0002678,regional part of medulla oblongata
+HP:0000558,Rieger anomaly,HP:0007700,Anterior segment dysgenesis
+UBERON:0006858,adrenal/interrenal gland,UBERON:0002368,endocrine gland
+DOID:14522,partial arterial retinal occlusion,DOID:8483,retinal artery occlusion
+UBERON:0008891,external gill,UBERON:0002535,gill
+NCBITaxon:12080,Human poliovirus 1,NCBITaxon:138950,Human enterovirus C
+DOID:9507,ethmoid sinusitis,DOID:0050127,sinusitis
+DOID:5723,optic atrophy,DOID:1891,optic nerve disease
+UBERON:2001737,coracoid foramen,UBERON:0005744,bone foramen
+UBERON:0014594,tuberomammillary nucleus ventral part,UBERON:0002785,regional part of lateral hypothalamic region
+HP:0000242,Parietal bossing,HP:0002696,Abnormality of the parietal bone
+HP:0010076,Aplasia/Hypoplasia of the distal phalanx of the hallux,HP:0010053,Abnormality of the distal phalanx of the hallux
+UBERON:0000431,ventral medial complex of thalamus,UBERON:0002784,regional part of diencephalon
+UBERON:0004197,proximal convoluted tubule segment 2,UBERON:0006554,urinary system structure
+DOID:3405,histiocytosis,DOID:75,lymphatic system disease
+HP:0100710,Impulsivity,HP:0006919,"Abnormal aggressive, impulsive or violent behavior"
+HP:0010678,Enuresis diurna,HP:0000805,Enuresis
+UBERON:2000603,valvula cerebelli,UBERON:0002946,regional part of cerebellum
+CL:0000532,CAP motoneuron,CL:0000533,primary motor neuron
+CL:0002332,ciliated cell of the bronchus,CL:0002328,bronchial epithelial cell
+UBERON:3000966,angulosplenial,UBERON:0004768,bone of lower jaw
+CL:0002155,echinocyte,CL:0000595,enucleate erythrocyte
+UBERON:0010030,ventral part of pharyngeal pouch 5,UBERON:0000490,unilaminar epithelium
+NCBITaxon:5596,Pseudallescheria,NCBITaxon:5593,Microascaceae
+UBERON:0002844,eighth cervical dorsal root ganglion,UBERON:0002834,cervical dorsal root ganglion
+UBERON:0010983,levator scapulae pre-muscle mass,UBERON:0005865,pre-muscle condensation
+UBERON:2001707,infraorbital 12,UBERON:2000376,infraorbital
+UBERON:0002208,sternebra,UBERON:0003827,thoracic segment bone
+UBERON:0001071,superficial cervical artery,UBERON:0012320,cervical artery
+UBERON:0006003,integumentary adnexa,UBERON:0000064,organ part
+DOID:2640,struma ovarii,DOID:2641,ovarian germ cell monodermal and highly specialized teratoma
+HP:0004222,Cone-shaped epiphysis of the distal phalanx of the 5th finger,HP:0009384,Cone-shaped epiphyses of the 5th finger
+UBERON:0012239,urinary bladder vasculature,UBERON:0004120,mesoderm-derived structure
+CL:0002209,intermediate epitheliocyte,CL:0002202,epithelial cell of tracheobronchial tree
+HP:0001135,Chorioretinal dystrophy,HP:0000532,Chorioretinal abnormality
+CL:0002575,central nervous system pericyte,CL:0002319,neural cell
+HP:0100474,Symphalangism affecting the proximal phalanx of the 4th toe,HP:0010377,Symphalangism affecting the phalanges of the 4th toe
+UBERON:0002162,area postrema,UBERON:0010135,sensory circumventricular organ
+HP:0006743,Embryonal rhabdomyosarcoma,HP:0002898,Embryonal neoplasm
+UBERON:0002666,mesencephalic tract of trigeminal nerve,UBERON:0014891,brainstem white matter
+UBERON:0005978,olfactory bulb outer nerve layer,UBERON:0004001,olfactory bulb layer
+UBERON:0000440,trabecula,UBERON:0000064,organ part
+HP:0009790,Hemisacrum (S2-S5),HP:0005107,Abnormality of the sacrum
+CL:0000831,mast cell progenitor,CL:0000763,myeloid cell
+UBERON:0002110,gallbladder,UBERON:0004119,endoderm-derived structure
+UBERON:0010041,median ovary,UBERON:0000992,female gonad
+HP:0006248,Limited wrist movement,HP:0003019,Abnormality of the wrist
+UBERON:0001017,central nervous system,UBERON:0004121,ectoderm-derived structure
+HP:0003022,Hypoplasia of the ulna,HP:0009821,Forearm undergrowth
+DOID:0050897,bone chondrosarcoma,DOID:3371,chondrosarcoma
+HP:0006488,Bowing of the arm,HP:0002817,Abnormality of the upper limb
+HP:0006755,Cutaneous leiomyosarcoma,HP:0008069,Neoplasm of the skin
+HP:0001810,Dystrophic toenail,HP:0008388,Abnormality of the toenail
+HP:0003219,Ethylmalonic aciduria,HP:0003215,Dicarboxylic aciduria
+HP:0001688,Sinus bradycardia,HP:0011702,Abnormal electrophysiology of sinoatrial node origin
+HP:0005837,Joint dislocations in young adult,HP:0001373,Joint dislocation
+UBERON:0008445,webbed pedal digit,UBERON:0001466,pedal digit
+HP:0009696,Triangular epiphyses of the thumb,HP:0010238,Triangular epiphyses of the phalanges of the hand
+CL:0002509,"CD103-positive, langerin-positive lymph node dendritic cell",CL:0002454,"Cd4-negative, CD8_alpha-negative, CD11b-positive dendritic cell"
+UBERON:0009040,deep circumflex iliac artery,UBERON:0009026,iliac circumflex artery
+UBERON:2005011,pseudobranchial artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0200007,Abnormal size of the palpebral fissures,HP:0008050,Abnormality of the palpebral fissures
+UBERON:0006108,corticomedial nuclear complex,UBERON:0005401,cerebral hemisphere grey matter
+UBERON:0011094,vertebra cartilage element,UBERON:0010913,vertebral element
+UBERON:0011316,nerve to stylohyoid from facial nerve,UBERON:0001647,facial nerve
+HP:0007034,Generalized hyperreflexia,HP:0001347,Hyperreflexia
+UBERON:0010247,choroidal tapetum cellulosum,UBERON:0010244,choroid tapetum lucidum
+UBERON:0014386,vertebral endplate,UBERON:0005913,zone of bone organ
+HP:0004241,Stippled calcification in carpal bones,HP:0009164,Abnormal calcification of the carpal bones
+HP:0100154,Small epiphysis of the middle phalanx of the 3rd toe,HP:0100063,Small epiphyses of the 3rd toe
+HP:0007570,Hyperkeratosis lenticularis perstans,HP:0000962,Hyperkeratosis
+UBERON:0011302,tunicate tunic,UBERON:0003102,surface structure
+UBERON:3010393,mesonephric late distal segment,UBERON:0000064,organ part
+HP:0100056,Bracket epiphyses of the 3rd toe,HP:0010329,Abnormality of the epiphyses of the 3rd toe
+UBERON:0002053,zona glomerulosa of adrenal gland,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0001961,Hypoplastic heart,HP:0002564,Malformation of the heart and great vessels
+UBERON:0010028,ventral part of pharyngeal pouch 4,UBERON:0005291,embryonic tissue
+UBERON:0003408,gland of gut,UBERON:0002530,gland
+UBERON:0001656,retromandibular vein,UBERON:0001653,facial vein
+HP:0011136,Aplasia of the sweat glands,HP:0011135,Aplasia/Hypoplasia of the sweat glands
+HP:0008970,Scapulohumeral muscular dystrophy,HP:0003560,Muscular dystrophy
+DOID:0060017,CD3epsilon deficiency,DOID:627,severe combined immunodeficiency
+HP:0100438,Bullet-shaped proximal phalanx of the 4th toe,HP:0010373,Bullet-shaped phalanges of the 4th toe
+DOID:6193,epithelioid sarcoma,DOID:3350,mesenchymal cell neoplasm
+HP:0002044,Zollinger-Ellison syndrome,HP:0007378,Neoplasm of the gastrointestinal tract
+HP:0009552,Aplasia/Hypoplasia of the phalanges of the 2nd finger,HP:0009541,Abnormality of the phalanges of the 2nd finger
+UBERON:0011627,orbital part of frontal bone,UBERON:0005913,zone of bone organ
+DOID:5996,blunt duct adenosis of breast,DOID:5998,microglandular adenosis
+UBERON:0001895,metencephalon,UBERON:0004733,segmental subdivision of hindbrain
+UBERON:0005612,intercostal artery,UBERON:0003834,thoracic segment blood vessel
+HP:0010401,Symphalangism affecting the proximal phalanx of the 2nd toe,HP:0010353,Symphalangism affecting the phalanges of the 2nd toe
+UBERON:3000934,foramen perforans tarsi,UBERON:0004120,mesoderm-derived structure
+HP:0006937,Impaired distal tactile sensation,HP:0010830,Impaired tactile sensation
+CL:0001033,hippocampal granule cell,CL:0001032,cortical granule cell
+UBERON:0003723,vestibular nerve,UBERON:0001785,cranial nerve
+UBERON:0000166,oral opening,UBERON:0000161,orifice
+UBERON:2007059,neurogenic field,UBERON:0000479,tissue
+DOID:11503,diabetic autonomic neuropathy,DOID:11504,autonomic neuropathy
+UBERON:0005195,deferent duct vein,UBERON:0014403,male anatomical structure
+UBERON:0011319,disk of temporomandibular joint,UBERON:0010313,neural crest-derived structure
+HP:0007365,Aplasia/Hypoplasia involving the corticospinal tracts,HP:0002492,Abnormality of the corticospinal tract
+DOID:3074,giant cell glioblastoma,DOID:3068,glioblastoma multiforme
+UBERON:0002958,medial lemniscus of pons,UBERON:0014891,brainstem white matter
+DOID:0060166,bipolar ll disorder,DOID:3312,bipolar disorder
+HP:0007141,Sensorimotor neuropathy,HP:0009830,Peripheral neuropathy
+UBERON:0001861,ductus reuniens,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0006856,interrenal gland,UBERON:0006858,adrenal/interrenal gland
+HP:0004945,Extracranial internal carotid artery dissection,HP:0012159,Internal carotid artery dissection
+NCBITaxon:11118,Coronaviridae,NCBITaxon:76804,Nidovirales
+HP:0000499,Abnormality of the eyelashes,HP:0000492,Abnormality of the eyelid
+HP:0005986,Limitation of neck motion,HP:0000464,Abnormality of the neck
+UBERON:0005028,mucosa of maxillary sinus,UBERON:0000344,mucosa
+HP:0004293,Synostosis of second metacarpal-trapezoid,HP:0009705,Synostosis involving the 2nd metacarpal
+HP:0012049,Laryngeal dystonia,HP:0001618,Dysphonia
+UBERON:0005640,right lung caudal lobe epithelium,UBERON:0003364,epithelium of right lung
+UBERON:0012116,nutrient foramen conduit,UBERON:0005744,bone foramen
+UBERON:2000482,caudal tuberal nucleus,UBERON:0006569,diencephalic nucleus
+UBERON:3010197,lateral recess,UBERON:0000464,anatomical space
+HP:0010241,Short proximal phalanx of finger,HP:0009381,Short finger
+UBERON:0006016,interdigital region between digits 1 and 2,UBERON:0006012,interdigital region
+HP:0009460,Aplasia of the 3rd finger,HP:0009380,Aplasia of the fingers
+CL:1000359,microfold cell of epithelium proper of appendix,CL:1000405,epithelial cell of appendix
+UBERON:3000778,supracoracoid foramen,UBERON:3000755,pectoral girdle opening
+DOID:0060043,sexual disorder,DOID:150,disease of mental health
+HP:0005347,Cartilaginous trachea,HP:0002778,Abnormality of the trachea
+HP:0003928,Cortical thickening of humeral diaphysis,HP:0003926,Abnormality of the humeral diaphysis
+UBERON:0014394,uterine fat pad,UBERON:0003916,fat pad
+UBERON:0002523,tunica intima,UBERON:0004797,blood vessel layer
+HP:0002031,Abnormality of the esophagus,HP:0012718,Morphological abnormality of the gastrointestinal tract
+CL:0000342,pigment cell (sensu Vertebrata),CL:0000147,pigment cell
+CL:0000068,duct epithelial cell,CL:0002371,somatic cell
+UBERON:2001788,pelvic splint,UBERON:0004375,bone of free limb or fin
+DOID:0050847,sleep apnea,DOID:535,sleep disorder
+UBERON:0008457,superior articular process of sacral vertebra,UBERON:0001079,superior articular process of vertebra
+HP:0001467,Aplasia/Hypoplasia involving the musculature of the upper limbs,HP:0001460,Aplasia/Hypoplasia involving the musculature
+UBERON:0000409,serous gland,UBERON:0002365,exocrine gland
+UBERON:0004058,biliary ductule,UBERON:0004119,endoderm-derived structure
+UBERON:0011960,articular capsule of glenohumeral joint,UBERON:0001484,articular capsule
+UBERON:2001675,mesethmoid cornu,UBERON:4100000,skeletal element projection
+UBERON:0004311,distal phalanx of manual digit 2,UBERON:0014484,distal phalanx of digit 2
+UBERON:0006724,osseus spiral lamina,UBERON:0005913,zone of bone organ
+HP:0006960,Choroid plexus calcification,HP:0007376,Abnormality of the choroid plexus
+DOID:92,speech disorder,DOID:2033,communication disorder
+HP:0007886,Absent extraocular muscles,HP:0008049,Abnormality of the extraocular muscles
+HP:0000655,Vitreoretinal degeneration,HP:0000546,Retinal degeneration
+UBERON:0013656,dulla,UBERON:0000481,multi-tissue structure
+NCBITaxon:11632,Retroviridae,NCBITaxon:35268,Retro-transcribing viruses
+DOID:3617,epidural spinal canal angiolipoma,DOID:3618,epidural neoplasm
+UBERON:0010351,otic capsule cartilage element,UBERON:0015020,otic capsule endochondral element
+HP:0009572,Osteolytic defects of the middle phalanx of the 2nd finger,HP:0009550,Osteolytic defects of the phalanges of the 2nd finger
+UBERON:0003518,main bronchus blood vessel,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0011990,Abnormality of neutrophil physiology,HP:0001874,Abnormality of neutrophils
+UBERON:0008953,lower lobe of left lung,UBERON:0008949,lower lobe of lung
+UBERON:0002653,gracile fasciculus of medulla,UBERON:0007702,tract of brain
+UBERON:0002156,nucleus raphe magnus,UBERON:0007635,nucleus of medulla oblongata
+HP:0008675,Enlarged polycystic ovaries,HP:0000147,Polycystic ovaries
+UBERON:0001612,facial artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+CL:0002322,embryonic stem cell,CL:0000034,stem cell
+HP:0000225,Gingival bleeding,HP:0000168,Abnormality of the gingiva
+HP:0009154,Triangular epiphysis of the proximal phalanx of the 5th finger,HP:0009392,Triangular epiphyses of the 5th finger
+UBERON:0004820,bile duct epithelium,UBERON:0005911,endo-epithelium
+DOID:3559,pseudomyxoma peritonei,DOID:11239,appendix cancer
+HP:0011679,Tetralogy of Fallot with pulmonary stenosis,HP:0001636,Tetralogy of Fallot
+NCBITaxon:75739,Eucoccidiorida,NCBITaxon:5796,Coccidia
+HP:0004305,Involuntary movements,HP:0100022,Abnormality of movement
+HP:0000196,Lower lip pit,HP:0100269,Paramedian lip pit
+HP:0002942,Thoracic kyphosis,HP:0002808,Kyphosis
+HP:0001820,Leukonychia,HP:0100643,Abnormality of nail color
+HP:0012405,Hypocitraturia,HP:0012404,Abnormal urine citrate concentration
+UBERON:0002025,stratum basale of epidermis,UBERON:0004121,ectoderm-derived structure
+CL:0002141,active chief cell of parathyroid gland,CL:0000446,chief cell of parathyroid gland
+UBERON:0004379,distal epiphysis,UBERON:0001437,epiphysis
+DOID:10865,abducens nerve disease,DOID:3817,cranial nerve palsy
+HP:0003993,Broad ulna,HP:0003971,Broad forearm bones
+UBERON:0013442,postorbital process,UBERON:0005913,zone of bone organ
+UBERON:0001736,submandibular gland,UBERON:0001829,major salivary gland
+HP:0004197,Symphalangism of the 4th finger,HP:0009700,Synostosis involving bones of the fingers
+CL:1000155,malpighian tubule stellate cell,CL:0000122,stellate cell
+UBERON:0008982,fascia,UBERON:0007846,dense regular connective tissue
+UBERON:0006787,middle white layer of superior colliculus,UBERON:0006786,white matter of superior colliculus
+HP:0010753,Midline defect of mandible,HP:0000277,Abnormality of the mandible
+HP:0004354,Abnormality of carboxylic acid metabolism,HP:0001939,Abnormality of metabolism/homeostasis
+DOID:1217,fascioloidiasis,DOID:883,parasitic helminthiasis infectious disease
+UBERON:0014601,paraventricular nucleus of the hypothalamus magnocellular division - posterior magnocellular part,UBERON:0003048,regional part of hypothalamus
+DOID:5608,dental pulp calcification,DOID:5330,dental pulp disease
+HP:0004377,Hematological neoplasm,HP:0001871,Abnormality of  blood and blood-forming tissues
+HP:0003985,Exostoses of the ulna,HP:0002997,Abnormality of the ulna
+UBERON:0010510,strand of auchene hair,UBERON:0010509,strand of pelage hair
+DOID:2088,outlet dysfunction constipation,DOID:2089,constipation
+UBERON:3010081,interorbital fold,UBERON:3000972,head external integument structure
+HP:0008794,Dysplastic iliac wings,HP:0011867,Abnormality of the wing of the ilium
+UBERON:0004011,secondary muscle spindle,UBERON:0003718,muscle spindle
+HP:0009198,Abnormality of the epiphysis of the distal phalanx of the 5th finger,HP:0004225,Abnormality of the distal phalanx of the 5th finger
+HP:0009150,Abnormality of the proximal phalanx of the 5th finger,HP:0004213,Abnormality of the phalanges of the 5th finger
+HP:0010727,Spontaneous rupture of the globe,HP:0012374,Abnormality of the globe
+UBERON:0007827,external nose,UBERON:0004121,ectoderm-derived structure
+HP:0011396,Abnormality of the cochlear nerve,HP:0011391,Morphological abnormality of the nerves of the inner ear
+HP:0001132,Lens subluxation,HP:0001083,Ectopia lentis
+DOID:15,reproductive system disease,DOID:7,disease of anatomical entity
+CL:1001127,outer renal medulla vasa recta cell,CL:1000616,kidney outer medulla cell
+HP:0003241,Genital hypoplasia,HP:0000811,Abnormal external genitalia
+UBERON:0010701,phalanx cartilage element,UBERON:0005863,cartilaginous condensation
+UBERON:0015036,pedal digit metatarsal endochondral element,UBERON:0015022,hindlimb endochondral element
+UBERON:0010686,manual digit phalanx cartilage element,UBERON:0015024,manual digit phalanx endochondral element
+UBERON:0000383,musculature of body,UBERON:0000467,anatomical system
+UBERON:4200173,dorsal ridge,UBERON:0004120,mesoderm-derived structure
+UBERON:0001686,auditory ossicle,UBERON:0010313,neural crest-derived structure
+DOID:2790,necatoriasis,DOID:883,parasitic helminthiasis infectious disease
+UBERON:0016400,infrapatellar fat pad,UBERON:0003916,fat pad
+UBERON:0015875,heel,UBERON:0005445,segment of pes
+UBERON:0004177,hemopoietic organ,UBERON:0004120,mesoderm-derived structure
+UBERON:0005123,metanephric prebend segment,UBERON:0004120,mesoderm-derived structure
+UBERON:0002407,pericardium,UBERON:0004457,cavity lining
+UBERON:2000704,ventral pelvic arrector,UBERON:2002147,arrector muscle
+HP:0010012,Abnormality of the 4th metacarpal,HP:0001163,Abnormality of the metacarpal bones
+DOID:7707,rectum signet ring adenocarcinoma,DOID:1996,rectum adenocarcinoma
+HP:0003011,Abnormality of the musculature,HP:0000118,Phenotypic abnormality
+HP:0009587,Triangular shaped proximal phalanx of the 2nd finger,HP:0009858,Triangular shaped proximal phalanges of the hand
+UBERON:0006059,falx cerebri,UBERON:0000064,organ part
+UBERON:0006289,rib pre-cartilage condensation,UBERON:0004120,mesoderm-derived structure
+UBERON:0001151,tail of pancreas,UBERON:0000064,organ part
+UBERON:0012482,submucosa of cloaca,UBERON:0000009,submucosa
+UBERON:0002334,submandibular duct,UBERON:0001837,duct of salivary gland
+UBERON:0015838,molar dental pulp,UBERON:0001754,dental pulp
+NCBITaxon:6249,Ascaridida,NCBITaxon:119089,Chromadorea
+HP:0009541,Abnormality of the phalanges of the 2nd finger,HP:0005918,Abnormality of phalanx of finger
+UBERON:0012254,abdominal aorta artery,UBERON:0004573,systemic artery
+UBERON:0002049,vasculature,UBERON:0000477,anatomical cluster
+HP:0009969,Partial duplication of the middle phalanx of the 3rd finger,HP:0010005,Partial duplication of the middle phalanges of the hand
+DOID:9007,sudden infant death syndrome,DOID:225,syndrome
+HP:0010544,Vertical nystagmus,HP:0000639,Nystagmus
+DOID:3079,juvenile astrocytoma,DOID:3069,astrocytoma
+UBERON:2000813,infraorbital lateral line neuromast,UBERON:0008904,neuromast
+DOID:8108,fibroepithelial polyp of urethra,DOID:6873,skin tag
+UBERON:0003930,atrioventricular canal endocardium,UBERON:0002050,embryonic structure
+HP:0011983,Brown pigment gallstones,HP:0011981,Pigment gallstones
+DOID:12550,hepatic coma,DOID:13413,hepatic encephalopathy
+UBERON:4000168,dorsal fin skeleton,UBERON:4000170,median fin skeleton
+DOID:7518,inhibited female orgasm,DOID:229,female reproductive system disease
+HP:0004552,Scarring alopecia of scalp,HP:0002293,Alopecia of scalp
+UBERON:0015848,incisor tusk,UBERON:0001098,incisor tooth
+UBERON:0010708,pectoral complex,UBERON:0010707,appendage girdle complex
+HP:0011400,Abnormal CNS myelination,HP:0002011,Abnormality of the central nervous system
+UBERON:2000497,pelvic adductor profundus,UBERON:0014795,pelvic appendage muscle
+UBERON:2001511,interhyal cartilage,UBERON:2001892,interhyal element
+UBERON:0002782,medial superior olivary nucleus,UBERON:0007247,superior olivary nucleus
+HP:0010027,Broad 1st metacarpal,HP:0009852,Broad proximal phalanges of the hand
+UBERON:0014640,occipital gyrus,UBERON:0000200,gyrus
+UBERON:3000909,sulcus proximalis ossis cruris,UBERON:0004120,mesoderm-derived structure
+HP:0001405,Periportal fibrosis,HP:0001395,Hepatic fibrosis
+UBERON:0002174,middle lobe of right lung,UBERON:0008955,middle lobe of lung
+UBERON:0001924,paracentral nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:2001888,supraneural 1 bone,UBERON:2000442,supraneural bone
+HP:0007365,Aplasia/Hypoplasia involving the corticospinal tracts,HP:0002977,Aplasia/Hypoplasia involving the central nervous system
+HP:0010102,Aplasia of the distal phalanx of the hallux,HP:0010076,Aplasia/Hypoplasia of the distal phalanx of the hallux
+UBERON:0000996,vagina,UBERON:0013515,subdivision of uterine tube
+CL:0002237,luminal epithelial cell of prostatic duct,CL:0000068,duct epithelial cell
+HP:0005187,Progressive joint destruction,HP:0001367,Abnormal joint morphology
+UBERON:0012198,intercostal space,UBERON:0000464,anatomical space
+UBERON:0001648,vestibulocochlear nerve,UBERON:0004121,ectoderm-derived structure
+HP:0006749,Malignant gastrointestinal tract tumors,HP:0007378,Neoplasm of the gastrointestinal tract
+UBERON:0007844,cartilage element,UBERON:0004765,skeletal element
+UBERON:0005417,forelimb bud,UBERON:0004347,limb bud
+HP:0002599,Head titubation,HP:0001337,Tremor
+DOID:12164,Blessig's cysts,DOID:12161,peripheral retinal degeneration
+HP:0009673,Stippling of the epiphysis of the proximal phalanx of the thumb,HP:0009663,Abnormality of the epiphysis of the proximal phalanx of the thumb
+UBERON:0001108,omohyoid muscle,UBERON:0008523,infrahyoid muscle
+NCBITaxon:186802,Clostridiales,NCBITaxon:186801,Clostridia
+CL:0002034,long term hematopoietic stem cell,CL:0001008,Kit and Sca1-positive hematopoietic stem cell
+HP:0008959,Distal upper limb muscle weakness,HP:0002460,Distal muscle weakness
+CL:0000531,primary sensory neuron,CL:0000101,sensory neuron
+HP:0002636,Aneurysm of an abdominal artery,HP:0011004,Abnormality of the systemic arterial tree
+HP:0007269,Spinal muscular atrophy,HP:0003202,Amyotrophy
+DOID:681,progressive bulbar palsy,DOID:231,motor neuron disease
+UBERON:0014699,extraembryonic venous system,UBERON:0004582,venous system
+UBERON:4200117,pubic boot,UBERON:0004120,mesoderm-derived structure
+HP:0001537,Umbilical hernia,HP:0004299,Hernia of the abdominal wall
+UBERON:0011464,levator nasolabialis muscle,UBERON:0006821,cutaneous muscle
+DOID:12731,pars planitis,DOID:8886,chorioretinitis
+UBERON:0001949,gingival epithelium,UBERON:0002424,oral epithelium
+UBERON:0005430,ansa cervicalis,UBERON:0001147,trunk of peripheral nerve
+DOID:7945,adult central nervous system mixed germ cell tumor,DOID:5349,central nervous system adult germ cell tumor
+HP:0011183,EEG with hyperventilation-induced focal epileptiform discharges,HP:0010858,EEG with hyperventilation-induced epileptiform discharges
+CL:1000490,mesothelial cell of peritoneum,CL:0002371,somatic cell
+NCBITaxon:177873,EEEV complex,NCBITaxon:11019,Alphavirus
+UBERON:0002347,thoracic vertebra,UBERON:0015008,thoracic vertebra endochondral element
+UBERON:3000512,processus zygomatico-maxillaris,UBERON:0010313,neural crest-derived structure
+HP:0001841,Preaxial foot polydactyly,HP:0001829,Foot polydactyly
+UBERON:0006834,uterus or analog,UBERON:0014404,female anatomical structure
+UBERON:0006330,anterior lingual gland,UBERON:0001830,minor salivary gland
+HP:0009933,Narrow naris,HP:0005288,Abnormality of the nares
+HP:0008866,Failure to thrive secondary to recurrent infections,HP:0002719,Recurrent infections
+UBERON:0005340,dorsal telencephalic commissure,UBERON:0005970,brain commissure
+HP:0011152,Early onset absence seizures,HP:0011147,Typical absence seizures
+DOID:11180,non-suppurative otitis media,DOID:10754,otitis media
+HP:0011995,Atrial septal aneurysm,HP:0011994,Abnormality of the atrial septum
+HP:0010419,Symphalangism affecting the distal phalanx of the 2nd toe,HP:0010410,Symphalangism affecting the middle phalanx of the 2nd toe
+HP:0009914,Cyclopia,HP:0100886,Abnormality of globe location
+HP:0003840,Delayed upper limb epiphyseal ossification,HP:0002663,Delayed epiphyseal ossification
+UBERON:0008439,webbed interdigital region between pedal digits,UBERON:0006015,webbed interdigital region
+UBERON:0003631,pedal digit 1,UBERON:0006048,digit 1
+DOID:6232,ovarian biphasic or triphasic teratoma,DOID:5567,ovarian germ cell teratoma
+UBERON:0014482,ischial callosity,UBERON:0001415,skin of pelvis
+UBERON:0004563,forelimb digital vein,UBERON:0003523,manus blood vessel
+UBERON:0013693,cerebral cortex neuropil,UBERON:0002606,neuropil
+DOID:1255,trichostrongyloidiasis,DOID:883,parasitic helminthiasis infectious disease
+HP:0011427,Enlarged fetal cisterna magna,HP:0011425,Fetal ultrasound soft marker
+UBERON:0004081,cerebellum vermis lobule VII,UBERON:0004070,cerebellum vermis lobule
+UBERON:0014509,distal sesamoid impar ligament,UBERON:0015791,digit connective tissue
+UBERON:0001465,knee,UBERON:0008784,lower limb segment
+HP:0009352,Ivory epiphysis of the proximal phalanx of the 3rd finger,HP:0009416,Ivory epiphyses of the 3rd finger
+UBERON:0009032,right pulmonary vein,UBERON:0002016,pulmonary vein
+UBERON:0001379,vastus lateralis,UBERON:0001377,quadriceps femoris
+UBERON:0010027,dorsal part of pharyngeal pouch 4,UBERON:0005291,embryonic tissue
+DOID:11608,fungal meningitis,DOID:9471,meningitis
+UBERON:3010392,mesonephric early proximal tubule,UBERON:0004120,mesoderm-derived structure
+HP:0100558,Hemiatrophy of upper limb,HP:0100556,Hemiatrophy
+UBERON:2001863,inter-hypobranchial 3 joint,UBERON:0000982,skeletal joint
+UBERON:0008195,tarsometatarsus,UBERON:0015012,tarsometatarsus endochondral element
+HP:0010359,Aplasia/Hypoplasia of the phalanges of the 3rd toe,HP:0010330,Abnormality of the phalanges of the 3rd toe
+DOID:11595,scleral staphyloma,DOID:11343,scleral disease
+HP:0010185,Aplasia/Hypoplasia of the distal phalanges of the toes,HP:0010760,Absent toe
+CL:0002018,"CD71-negative, GlyA-positive orthochromatic erythroblast",CL:0000552,orthochromatic erythroblast
+DOID:11450,allergic cutaneous vasculitis,DOID:9809,hypersensitivity vasculitis
+HP:0001161,Hand polydactyly,HP:0010442,Polydactyly
+UBERON:4300103,rudimentary pectoral fin ray,UBERON:4000175,pectoral fin lepidotrichium
+UBERON:2005415,inner ear foramen,UBERON:0005744,bone foramen
+CL:0000926,CD4-positive type I NK T cell secreting interferon-gamma,CL:0000912,helper T cell
+CL:0002626,immature astrocyte,CL:0000127,astrocyte
+UBERON:0004489,musculature of manus,UBERON:0004481,musculature of upper limb
+UBERON:0003480,vein of clitoris,UBERON:0005156,reproductive structure
+UBERON:4000167,caudal fin skeleton,UBERON:4000170,median fin skeleton
+HP:0009206,Enlarged epiphysis of the middle phalanx of the 5th finger,HP:0004224,Abnormality of the epiphysis of the middle phalanx of the 5th finger
+UBERON:0011871,nasomaxillary suture,UBERON:0003685,cranial suture
+DOID:8741,seborrheic dermatitis,DOID:2723,dermatitis
+DOID:172,clear cell acanthoma,DOID:3165,skin benign neoplasm
+DOID:4299,infiltrative basal cell carcinoma,DOID:2513,basal cell carcinoma
+HP:0003405,Diffuse axonal swelling,HP:0000759,Abnormality of the peripheral nervous system
+HP:0000303,Mandibular prognathia,HP:0000306,Abnormality of the chin
+HP:0010309,Bifid sternum,HP:0000766,Abnormality of the sternum
+HP:0100174,Irregular epiphysis of the distal phalanx of the 4th toe,HP:0100094,Abnormality of the epiphysis of the distal phalanx of the 4th toe
+UBERON:2001907,epibranchial 3 element,UBERON:2001904,epibranchial element
+UBERON:0006906,ala of nose,UBERON:0015212,lateral structure
+HP:0005147,Bidirectional ventricular ectopy,HP:0004308,Ventricular arrhythmia
+UBERON:0001472,vaginal venous plexus,UBERON:0005156,reproductive structure
+CL:0000534,primary interneuron,CL:0000530,primary neuron
+HP:0008039,Subepithelial corneal opacities,HP:0007727,Opacification of the corneal epithelium
+HP:0001604,Vocal cord paresis,HP:0000759,Abnormality of the peripheral nervous system
+CL:0002273,type ECL enteroendocrine cell,CL:0000577,type EC enteroendocrine cell
+DOID:11028,pseudopterygium,DOID:10139,conjunctival degeneration
+UBERON:2001585,caudal principal ray,UBERON:4000174,caudal fin lepidotrichium
+UBERON:0001680,lacrimal bone,UBERON:0008907,dermal bone
+CL:0002456,CD8_alpha-positive plasmactyoid dendritic cell,CL:0000989,CD11c-low plasmacytoid dendritic cell
+UBERON:0009191,sphenoid bone pre-cartilage condensation,UBERON:0004120,mesoderm-derived structure
+UBERON:0011244,perpendicular plate of ethmoid,UBERON:0010313,neural crest-derived structure
+UBERON:0001410,common palmar digital artery,UBERON:0006141,palmar digital artery
+HP:0009307,Patchy sclerosis of the middle phalanx of the 4th finger,HP:0009848,Patchy sclerosis of the middle phalanges of the hand
+UBERON:0006861,diaphysis proper,UBERON:0005055,zone of long bone
+HP:0011621,Gerbode ventricular septal defect,HP:0001629,Ventricular septal defect
+UBERON:4300112,distal segment of caudal ray,UBERON:4300108,lepidotrichial segment
+HP:0004889,Intermittent episodes of respiratory insufficiency due to muscle weakness,HP:0002747,Respiratory insufficiency due to muscle weakness
+HP:0009575,Triangular shaped middle phalanx of the 2nd finger,HP:0009546,Triangular shaped phalanges of the 2nd finger
+UBERON:0001106,cephalic vein,UBERON:0001638,vein
+DOID:8135,gallbladder lymphoma,DOID:3121,gallbladder cancer
+DOID:3454,brain infarction,DOID:6713,cerebrovascular disease
+UBERON:0000382,apocrine sweat gland,UBERON:0010243,merocrine gland
+DOID:9574,choanal atresia,DOID:2163,nasal cavity disease
+HP:0012290,Mouth neoplasm,HP:0012288,Neoplasm of head and neck
+UBERON:2001403,supraethmoid,UBERON:0011164,neurocranium bone
+HP:0000824,Growth hormone deficiency,HP:0000830,Anterior hypopituitarism
+UBERON:0012481,cloacal epithelium,UBERON:0003929,gut epithelium
+HP:0000919,Abnormality of the costochondral junction,HP:0000772,Abnormality of the ribs
+HP:0100065,Triangular epiphyses of the 3rd toe,HP:0010172,Triangular epiphyses of the toes
+UBERON:0003855,gonad mesenchyme,UBERON:0003104,mesenchyme
+UBERON:0007685,region of nephron tubule,UBERON:0004810,nephron tubule epithelium
+HP:0009648,Triangular shaped distal phalanx of the thumb,HP:0009657,Triangular shaped phalanges of the thumb
+HP:0002103,Abnormality of the pleura,HP:0002088,Abnormality of the lung
+HP:0100224,Absent epiphysis of the proximal phalanx of the 5th toe,HP:0100077,Absent epiphyses of the 5th toe
+DOID:3933,anterior compartment syndrome,DOID:682,compartment syndrome
+CL:0000545,T-helper 1 cell,CL:0000492,CD4-positive helper T cell
+UBERON:0006796,cephalopod optic lobe,UBERON:0004121,ectoderm-derived structure
+UBERON:0012130,olecranon fossa,UBERON:0004120,mesoderm-derived structure
+UBERON:0005087,tooth placode,UBERON:0011814,non-neurogenic ectodermal placode
+DOID:5272,small intestinal sarcoma,DOID:10154,small intestine cancer
+UBERON:0002712,premammillary nucleus,UBERON:0006568,hypothalamic nucleus
+HP:0000143,Rectovaginal fistula,HP:0100590,Rectal fistula
+HP:0007973,Retinal dysplasia,HP:0000479,Abnormality of the retina
+CL:0002305,epithelial cell of distal tubule,CL:0002078,meso-epithelial cell
+HP:0100485,Symphalangism of the proximal phalanx of the 4th toe with the 4th metatarsal,HP:0010366,Triangular shaped phalanges of the 3rd toe
+HP:0003867,Cortical irregularity (humeral),HP:0005731,Cortical irregularity
+DOID:0060151,tactile agnosia,DOID:4090,agnosia
+CL:0002548,cardiac fibroblast,CL:0002494,cardiocyte
+UBERON:0005025,mucosa of uvula,UBERON:0005024,mucosa of soft palate
+DOID:6693,testicular monophasic choriocarcinoma,DOID:5551,choriocarcinoma of the testis
+HP:0001981,Schistocytosis,HP:0004447,Poikilocytosis
+UBERON:0014778,cell group,UBERON:0000480,anatomical group
+HP:0011412,Ventouse delivery,HP:0001787,Abnormal delivery
+UBERON:2001706,infraorbital 11,UBERON:2000376,infraorbital
+CL:0002502,type M enteroendocrine cell,CL:1001516,intestinal enteroendocrine cell
+UBERON:0011238,mesethmoid bone,UBERON:0010892,mesethmoid element
+DOID:0060075,estrogen-receptor positive breast cancer,DOID:1612,breast cancer
+HP:0004637,Decreased cervical spine mobility,HP:0003319,Abnormality of the cervical spine
+HP:0009203,Absent epiphysis of the middle phalanx of the 5th finger,HP:0009382,Absent epiphyses of the 5th finger
+UBERON:0006959,mandible angular process,UBERON:0004120,mesoderm-derived structure
+UBERON:0009114,cervical thymus,UBERON:0002370,thymus
+UBERON:0001340,dorsal artery of penis,UBERON:0014403,male anatomical structure
+CL:0000851,neuromast mantle cell,CL:0002319,neural cell
+HP:0010005,Partial duplication of the middle phalanges of the hand,HP:0010008,Duplication of the middle phalanx of hand
+UBERON:0012120,vinculum of tendon,UBERON:0000043,tendon
+HP:0009572,Osteolytic defects of the middle phalanx of the 2nd finger,HP:0009847,Osteolytic defects of the middle phalanges of the hand
+UBERON:0006670,central tendon of diaphragm,UBERON:0004120,mesoderm-derived structure
+DOID:14507,peripheral degeneration of cornea,DOID:1237,corneal degeneration
+DOID:83,cataract,DOID:110,lens disease
+DOID:6804,colon Kaposi sarcoma,DOID:5260,colon sarcoma
+UBERON:1000011,labial commissure,UBERON:0001444,subdivision of head
+DOID:0060185,Clostridium difficile colitis,DOID:0060180,colitis
+DOID:0050912,colon adenoma,DOID:235,colonic benign neoplasm
+HP:0009297,Osteolytic defects of the middle phalanx of the 4th finger,HP:0004195,Osteolytic defects of the phalanges of the 4th finger
+UBERON:0010760,supraglenoid tubercle,UBERON:0005813,tubercle
+HP:0009453,Osteolytic defects of the proximal phalanx of the 3rd finger,HP:0009855,Osteolytic defects of the proximal phalanges of the hand
+UBERON:0009643,central tegmental tract,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009410,Absent epiphyses of the 3rd finger,HP:0010228,Absent epiphyses of the phalanges of the hand
+DOID:5761,vulvar sebaceous carcinoma,DOID:1294,vulva carcinoma
+UBERON:0002216,symphysis,UBERON:0002213,cartilaginous joint
+UBERON:0005181,thoracic segment organ,UBERON:0005177,trunk organ
+HP:0009882,Short distal phalanx of finger,HP:0009803,Short phalanx of finger
+HP:0006882,Severe hydrocephalus,HP:0000238,Hydrocephalus
+DOID:11994,atrophy of testis,DOID:2519,testicular disease
+UBERON:0009988,condyle of humerus,UBERON:0005055,zone of long bone
+CL:0002372,myotube,CL:0000737,striated muscle cell
+CL:0000228,multinucleate cell,CL:0002242,nucleate cell
+UBERON:2002001,anterior dentation of pectoral fin spine,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:4200037,supinator process,UBERON:0004120,mesoderm-derived structure
+HP:0003895,Flattened humeral epiphyses,HP:0003071,Flattened epiphyses
+HP:0006209,Partial-complete absence of 5th phalanges,HP:0006262,Aplasia/Hypoplasia of the 5th finger
+UBERON:4200080,fibular crest,UBERON:0004120,mesoderm-derived structure
+HP:0001558,Decreased fetal movement,HP:0001557,Prenatal movement abnormality
+UBERON:2000608,ventral transverse,UBERON:0000933,pharyngeal muscle
+UBERON:0002486,glottis,UBERON:0004119,endoderm-derived structure
+DOID:2599,glottis carcinoma,DOID:2595,glottis cancer
+CL:0005023,branchiomotor neuron,CL:0015000,cranial motor neuron
+HP:0007760,Crystalline corneal dystrophy,HP:0007856,Punctate opacification of the cornea
+HP:0100586,Aseptic leukocyturia,HP:0012085,Pyuria
+UBERON:0002916,central sulcus,UBERON:0013118,sulcus of brain
+UBERON:0003994,pelvic ligament,UBERON:0000211,ligament
+NCBITaxon:34395,Chaetothyriales,NCBITaxon:451870,Chaetothyriomycetidae
+DOID:952,acute dacryoadenitis,DOID:950,dacryoadenitis
+HP:0006147,Progressive fusion 2nd-5th pip joints,HP:0009773,Symphalangism affecting the phalanges of the hand
+DOID:12376,juvenile spinal muscular atrophy,DOID:0060160,survival motor neuron spinal muscular atrophy
+CL:1000364,transitional myocyte of anterior internodal tract,CL:1000480,transitional myocyte of internodal tract
+HP:0010345,Flexion contracture of the 5th toe,HP:0001836,Camptodactyly (feet)
+DOID:1849,cannabis dependence,DOID:9977,hallucinogen dependence
+UBERON:0015127,posterior internodal tract,UBERON:0009966,internodal tract
+HP:0000691,Microdontia,HP:0006482,Abnormality of dental morphology
+DOID:9407,strictly posterior acute myocardial infarction,DOID:9408,acute myocardial infarction
+DOID:12318,corneal granular dystrophy,DOID:2566,corneal dystrophy
+UBERON:0015228,circulatory organ,UBERON:0003103,compound organ
+UBERON:0006201,dorsal cerebral vein,UBERON:0001663,cerebral vein
+UBERON:0004086,brain ventricle,UBERON:0005358,ventricle of nervous system
+CL:0002374,ear hair cell,CL:0000855,sensory hair cell
+HP:0006442,Hypoplasia of proximal fibula,HP:0003038,Fibular hypoplasia
+UBERON:4200039,supraacetabular buttress,UBERON:0004120,mesoderm-derived structure
+UBERON:0003996,cervical vertebra 1 arcus anterior,UBERON:0004530,bony projection
+DOID:0060085,organ system benign neoplasm,DOID:0060072,benign neoplasm
+UBERON:0002339,epithelium of lobar bronchus,UBERON:0000115,lung epithelium
+UBERON:0008958,cetacean involucrum,UBERON:0000064,organ part
+DOID:1924,hypogonadism,DOID:2277,gonadal disease
+UBERON:3000131,dilatatio alaris,UBERON:0000064,organ part
+UBERON:0013644,duodenal ampulla,UBERON:0004921,subdivision of digestive tract
+UBERON:0010321,skeletal element of eye region,UBERON:0004765,skeletal element
+HP:0000791,Uric acid nephrolithiasis,HP:0000787,Nephrolithiasis
+DOID:1400,lacrimal apparatus disease,DOID:5614,eye disease
+HP:0008523,Posterior helix pit,HP:0011039,Abnormality of the helix
+UBERON:0005212,Leydig cell region of testis,UBERON:0005169,interstitial tissue
+UBERON:3001010,body tubercle,UBERON:3000977,body external integument structure
+HP:0002725,Systemic lupus erythematosus,HP:0002960,Autoimmunity
+HP:0010073,Synostosis involving the 1st metatarsal,HP:0010209,Symphalangism affecting the proximal phalanges of the toes
+DOID:13003,vertebrobasilar insufficiency,DOID:224,transient cerebral ischemia
+DOID:13482,Proteus syndrome,DOID:0080015,physical disorder
+CL:0002067,type A enterocrine cell,CL:0000164,enteroendocrine cell
+UBERON:3010369,branchial arch skeleton,UBERON:0002050,embryonic structure
+HP:0009692,Ivory epiphyses of the thumb,HP:0100922,Sclerosis of the phalanges of the thumb
+HP:0009838,Curved distal phalanges of the hand,HP:0009832,Abnormality of the distal phalanx of finger
+CL:0002348,"CD27-low, CD11b-high natural killer cell",CL:0002426,"CD11b-positive, CD27-positive natural killer cell"
+HP:0002714,Downturned corners of mouth,HP:0011338,Abnormality of mouth shape
+DOID:8243,meningeal melanomatosis,DOID:4955,central nervous system melanocytic neoplasm
+UBERON:3000610,trochlear foramen,UBERON:3000051,braincase and otic capsule opening
+UBERON:0005417,forelimb bud,UBERON:0005419,pectoral appendage bud
+UBERON:0001367,external anal sphincter,UBERON:0004832,anal region skeletal muscle
+UBERON:2000352,external cellular layer,UBERON:0000479,tissue
+UBERON:0002591,oral part of spinal trigeminal nucleus,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0006535,Recurrent intrapulmonary hemorrhage,HP:0011029,Internal hemorrhage
+DOID:1677,low implantation of placenta,DOID:11060,placenta praevia
+HP:0009166,Fragmentation of the epiphysis of the distal phalanx of the 5th finger,HP:0009386,Fragmentation of the epiphyses of the 5th finger
+DOID:4143,orbital cancer,DOID:184,bone cancer
+DOID:1037,lymphoblastic leukemia,DOID:1240,leukemia
+UBERON:2001476,sublingual ventral ossification,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0012420,Meconium stained amniotic fluid,HP:0001560,Abnormality of the amniotic fluid
+HP:0003701,Proximal muscle weakness,HP:0001324,Muscle weakness
+NCBITaxon:7147,Diptera,NCBITaxon:33392,Endopterygota
+UBERON:0010988,teres major pre-muscle mass,UBERON:0004120,mesoderm-derived structure
+DOID:8925,primary thrombocytopenia,DOID:0060050,autoimmune disease of blood
+DOID:0080050,"acromesomelic dysplasia, Maroteaux type",DOID:0080049,acromesomelic dysplasia
+UBERON:0006611,exoskeleton,UBERON:0000477,anatomical cluster
+UBERON:0015015,supraoccipital endochondral element,UBERON:0010363,endochondral element
+UBERON:0011528,pubococcygeus muscle,UBERON:0003897,axial muscle
+HP:0010017,Cone-shaped epiphysis of the 1st metacarpal,HP:0010270,Cone-shaped epiphyses of the proximal phalanges of the hand
+CL:0002634,epithelial cell of anal column,CL:0002253,epithelial cell of large intestine
+UBERON:0015114,distal tarsal bone 5 endochondral element,UBERON:0015050,tarsus endochondral element
+HP:0001939,Abnormality of metabolism/homeostasis,HP:0000118,Phenotypic abnormality
+HP:0100751,Esophageal neoplasm,HP:0012288,Neoplasm of head and neck
+HP:0100687,Polyotia,HP:0000356,Abnormality of the outer ear
+DOID:5509,pediatric ependymoma,DOID:5074,malignant ependymoma
+UBERON:0015418,urethra mesenchymal layer,UBERON:0006554,urinary system structure
+HP:0001714,Ventricular hypertrophy,HP:0001713,Abnormality of cardiac ventricle
+UBERON:0008972,right colon,UBERON:0000064,organ part
+HP:0003180,Flat acetabular roof,HP:0003170,Abnormality of the acetabulum
+CL:0007022,micropylar cell,CL:0000548,animal cell
+DOID:2997,Sertoli-Leydig cell tumor,DOID:4757,sex cord-stromal neoplasm
+DOID:3720,extramedullary plasmacytoma,DOID:3721,plasmacytoma
+HP:0010927,Abnormality of divalent inorganic cation homeostasis,HP:0010929,Abnormality of cation homeostasis
+DOID:2064,vulvar syringoma,DOID:0060109,vulvar benign neoplasm
+HP:0010303,Abnormality of the spinal meninges,HP:0010651,Abnormality of the meninges
+HP:0010394,Abnormality of the proximal phalanx of the 5th toe,HP:0010342,Abnormality of the phalanges of the 5th toe
+HP:0003558,Viral infection-induced rhabdomyolysis,HP:0003201,Rhabdomyolysis
+UBERON:0011595,jaw region,UBERON:0000477,anatomical cluster
+HP:0012211,Abnormal renal physiology,HP:0000077,Abnormality of the kidney
+UBERON:2001237,ceratobranchial 1 bone,UBERON:2000488,ceratobranchial bone
+DOID:0050256,angiostrongyliasis,DOID:883,parasitic helminthiasis infectious disease
+HP:0001033,Facial flushing after alcohol intake,HP:0001005,Dermatological manifestations of systemic disorders
+HP:0007668,Impaired pursuit initiation and maintenance,HP:0000617,Abnormality of ocular smooth pursuit
+HP:0100048,Fragmentation of the epiphyses of the 2nd toe,HP:0010323,Abnormality of the epiphyses of the 2nd toe
+DOID:901,liver lymphoma,DOID:3571,liver cancer
+HP:0100367,Short phalanx of the 4th toe,HP:0010371,Aplasia/Hypoplasia of the phalanges of the 4th toe
+UBERON:0003316,mesenchyme of yolk sac,UBERON:0010333,extraembryonic membrane mesenchyme
+UBERON:0001907,zona incerta,UBERON:0015234,nucleus of ventral thalamus
+UBERON:3000663,parahyoid,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005865,pre-muscle condensation,UBERON:0005856,developing mesenchymal condensation
+UBERON:0005614,lens anterior epithelium,UBERON:0001803,epithelium of lens
+UBERON:0008788,posterior cranial fossa,UBERON:0008789,cranial fossa
+HP:0002411,Myokymia,HP:0100022,Abnormality of movement
+HP:0005173,Calcific aortic valve stenosis,HP:0001650,Aortic valve stenosis
+UBERON:2001241,ceratobranchial 3 bone,UBERON:2001901,ceratobranchial 3 element
+NCBITaxon:11157,Mononegavirales,NCBITaxon:35301,ssRNA negative-strand viruses
+HP:0003877,Oval transradiancy (humeral),HP:0003063,Abnormality of the humerus
+UBERON:0010982,latissimus dorsi pre-muscle mass,UBERON:0005865,pre-muscle condensation
+UBERON:0009601,mesenchyme of interdigital region of pes,UBERON:0003860,hindlimb mesenchyme
+UBERON:0012069,epithelium-associated lymphoid tissue,UBERON:0001744,lymphoid tissue
+HP:0005360,Susceptibility to chickenpox,HP:0004429,Recurrent viral infections
+UBERON:0003321,mesenchyme of knee,UBERON:0003860,hindlimb mesenchyme
+UBERON:0004756,dermal skeletal element,UBERON:0004765,skeletal element
+UBERON:0000053,macula lutea,UBERON:0000064,organ part
+UBERON:0001655,submental vein,UBERON:0003496,head blood vessel
+HP:0005565,Reduced renal corticomedullary differentiation,HP:0005932,Abnormal renal corticomedullary differentiation
+HP:0008749,Laryngeal hypoplasia,HP:0001600,Abnormality of the larynx
+DOID:4723,intracranial hypotension,DOID:936,brain disease
+UBERON:0009952,dentate gyrus subgranular zone,UBERON:0004121,ectoderm-derived structure
+UBERON:0001010,diaphysis of ulna,UBERON:0004769,diaphysis
+UBERON:2001866,basibranchial 5 cartilage,UBERON:2001919,basibranchial 5 element
+DOID:5438,extrahepatic bile duct adenoma,DOID:5381,bile duct adenoma
+HP:0009303,Osteolytic defects of the distal phalanx of the 4th finger,HP:0009282,Abnormality of the distal phalanx of the 4th finger
+HP:0010531,Spinal myoclonus,HP:0001336,Myoclonus
+DOID:0050751,T-cell large granular lymphocyte leukemia,DOID:1040,chronic lymphocytic leukemia
+DOID:6088,acute stress disorder,DOID:2030,anxiety disorder
+UBERON:2001526,hypobranchial 3 cartilage,UBERON:2001896,hypobranchial 3 element
+UBERON:0004327,middle phalanx of pedal digit 5,UBERON:0014491,middle phalanx of digit 5
+DOID:0060097,thoracic benign neoplasm,DOID:0060085,organ system benign neoplasm
+HP:0010077,Broad distal phalanx of the hallux,HP:0010053,Abnormality of the distal phalanx of the hallux
+DOID:6474,childhood teratocarcinoma of the testis,DOID:6161,childhood testicular mixed germ cell tumor
+HP:0003560,Muscular dystrophy,HP:0011805,Abnormality of muscle morphology
+UBERON:0002757,regional part of epithalamus,UBERON:0002784,regional part of diencephalon
+CL:1001434,olfactory bulb interneuron,CL:0012001,neuron of the forebrain
+HP:0000413,Atresia of the external auditory canal,HP:0000372,Abnormality of the auditory canal
+UBERON:3000664,hyoid plate,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100089,Abnormality of the epiphysis of the middle phalanx of the 2nd toe,HP:0010323,Abnormality of the epiphyses of the 2nd toe
+HP:0003057,Tetraamelia,HP:0009827,Amelia
+HP:0009966,Complete duplication of the middle phalanx of the 3rd finger,HP:0009960,Complete duplication of the phalanges of the 3rd finger
+UBERON:0013262,remnnant of ductus deferens,UBERON:0006590,vestigial embryonic structure
+HP:0011389,Functional abnormality of the inner ear,HP:0000359,Abnormality of the inner ear
+UBERON:0002601,fasciolar gyrus,UBERON:0000200,gyrus
+UBERON:0011607,hyomandibular cartilage,UBERON:0011004,pharyngeal arch cartilage
+HP:0000185,Cleft soft palate,HP:0100736,Abnormality of the soft palate
+UBERON:0003900,epaxial myotome region,UBERON:0001134,skeletal muscle tissue
+HP:0004365,Abnormality of tryptophan metabolism,HP:0004338,Abnormality of aromatic amino acid family metabolism
+DOID:5757,endocervicitis,DOID:2568,cervicitis
+UBERON:2002000,posterior dentation of pectoral fin spine,UBERON:0004120,mesoderm-derived structure
+DOID:6951,telangiectatic osteogenic sarcoma,DOID:3378,conventional central osteosarcoma
+DOID:4053,rectum rhabdomyosarcoma,DOID:1995,rectum sarcoma
+HP:0003240,Increased phosphoribosylpyrophosphate (PRPP) synthetase,HP:0010932,Abnormality of nucleobase metabolism
+UBERON:0013229,eyelid gland,UBERON:0004121,ectoderm-derived structure
+UBERON:0006800,anatomical line,UBERON:0000015,anatomical boundary
+HP:0009259,Stippling of the epiphysis of the distal phalanx of the 4th finger,HP:0009249,Abnormality of the epiphysis of the distal phalanx of the 4th finger
+HP:0006062,5th finger camptodactyly,HP:0009183,Joint contractures of the 5th finger
+DOID:7140,Bartholin's gland small cell carcinoma,DOID:3999,Bartholin's gland carcinoma
+HP:0010910,Hypervalinemia,HP:0010914,Abnormality of valine metabolism
+HP:0010880,Increased nuchal translucency,HP:0001197,Abnormality of prenatal development or birth
+UBERON:0000358,blastocyst,UBERON:0002050,embryonic structure
+DOID:8680,alcoholic gastritis,DOID:4029,gastritis
+DOID:10039,late congenital syphilis,DOID:9856,congenital syphilis
+HP:0005534,Transient myeloproliferative syndrome,HP:0005547,Myeloproliferative disorder
+UBERON:0011862,pulmonary collagen fibril,UBERON:0011860,collagen fibril
+UBERON:0004878,distal visceral endoderm,UBERON:0000478,extraembryonic structure
+DOID:540,strabismus,DOID:1279,ocular motility disease
+UBERON:0006209,basioccipital cartilage element,UBERON:0005863,cartilaginous condensation
+UBERON:0000044,dorsal root ganglion,UBERON:0003338,ganglion of peripheral nervous system
+UBERON:0001040,yolk sac,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0004331,Decreased skull ossification,HP:0011849,Abnormal bone ossification
+UBERON:0003897,axial muscle,UBERON:0001630,muscle organ
+UBERON:0016478,liver stroma,UBERON:0003891,stroma
+HP:0011741,Secondary hyperaldosteronism,HP:0000859,Hyperaldosteronism
+UBERON:2001126,noninvoluting endocytic marginal cell cluster,UBERON:0005291,embryonic tissue
+HP:0002571,Achalasia,HP:0002031,Abnormality of the esophagus
+HP:0009188,Pseudoepiphysis of the distal phalanx of the 5th finger,HP:0009389,Pseudoepiphyses of the 5th finger
+HP:0011512,Hyperpigmentation of the fundus,HP:0008051,Abnormality of the retinal pigment epithelium
+HP:0003654,Reduced dihydropyrimidine dehydrogenase activity,HP:0004353,Abnormality of pyrimidine metabolism
+HP:0009413,Enlarged epiphyses of the 3rd finger,HP:0010231,Enlarged epiphyses of the phalanges of the hand
+UBERON:0004829,urethra skeletal muscle,UBERON:0001134,skeletal muscle tissue
+UBERON:0003585,dermis connective tissue,UBERON:0004120,mesoderm-derived structure
+UBERON:2001248,dorsal scute series,UBERON:0000477,anatomical cluster
+NCBITaxon:11618,Arenavirus,NCBITaxon:11617,Arenaviridae
+DOID:0060169,benign familial infantile epilepsy,DOID:0050703,infancy electroclinical syndrome
+HP:0009720,Adenoma sebaceum,HP:0008069,Neoplasm of the skin
+UBERON:0009041,superficial circumflex iliac artery,UBERON:0009026,iliac circumflex artery
+UBERON:2002053,bony plate,UBERON:0008907,dermal bone
+HP:0002198,Dilated fourth ventricle,HP:0002119,Ventriculomegaly
+DOID:12698,gynecomastia,DOID:1923,sex differentiation disease
+UBERON:3010115,posterior lateral line nerve (PLLN),UBERON:0008906,lateral line nerve
+UBERON:0010699,manual digit metacarpus cartilage element,UBERON:0015064,autopod cartilage
+UBERON:0004745,parasphenoid,UBERON:0012071,palate bone
+HP:0007915,Polymorphous posterior corneal dystrophy,HP:0011491,Reduced number of corneal endothelial cells
+UBERON:0004072,cerebellum globose nucleus,UBERON:0002946,regional part of cerebellum
+UBERON:0004406,distal epiphysis of femur,UBERON:0004384,epiphysis of femur
+DOID:8955,sideroblastic anemia,DOID:12449,aplastic anemia
+HP:0007852,Pericentral pigmentary retinopathy,HP:0000580,Pigmentary retinopathy
+DOID:0050004,seminal vesicle acute gonorrhea,DOID:10400,gonococcal seminal vesiculitis
+HP:0008354,Factor X activation deficiency,HP:0008321,Reduced factor X activity
+UBERON:0002340,epithelium of main bronchus,UBERON:0002031,epithelium of bronchus
+DOID:0050831,familial encephalopathy with neuroserpin inclusion bodies,DOID:1289,neurodegenerative disease
+HP:0012339,Increased resting energy expenditure,HP:0012338,Abnormal energy expenditure
+DOID:14184,polyneuropathy due to drug,DOID:2537,inflammatory and toxic neuropathy
+HP:0008774,Aplasia/Hypoplasia of the inner ear,HP:0008771,Aplasia/Hypoplasia of the ear
+CL:1001428,bladder urothelial cell,CL:0000731,urothelial cell
+CL:0000467,adrenocorticotropic hormone secreting cell,CL:0000167,peptide hormone secreting cell
+UBERON:0003420,mesenchyme of sublingual gland,UBERON:0004121,ectoderm-derived structure
+HP:0004390,Hamartomatous polyps,HP:0010566,Hamartoma
+DOID:5513,Pediculus humanus corporis infestation,DOID:5502,lice infestation
+DOID:4661,multiple chemical sensitivity,DOID:225,syndrome
+UBERON:0005870,olfactory pit,UBERON:0005423,developing anatomical structure
+CL:0002443,Ly49CI-positive natural killer cell,CL:0002438,NK1.1-positive natural killer cell
+HP:0010046,Aplasia of the 5th metacarpal,HP:0010048,Aplasia of metacarpal bones
+HP:0005927,Aplasia/Hypoplasia involving bones of the hand,HP:0006496,Aplasia/Hypoplasia involving bones of the upper limbs
+UBERON:0006358,vasa hyaloidea propria,UBERON:0004120,mesoderm-derived structure
+DOID:4201,peroneal neuropathy,DOID:1188,mononeuropathy
+UBERON:0001619,ophthalmic artery,UBERON:0004573,systemic artery
+UBERON:0003467,sesamoid bone of gastrocnemius,UBERON:0011141,appendicular ossicle
+UBERON:0000046,stemma,UBERON:0000047,simple eye
+HP:0002195,Dysgenesis of the cerebellar vermis,HP:0002334,Abnormality of the cerebellar vermis
+UBERON:0005018,mucosa of nasal septum,UBERON:0000078,mixed ectoderm/mesoderm/endoderm-derived structure
+DOID:5999,apocrine adenosis of breast,DOID:5997,non-proliferative fibrocystic change of the breast
+CL:0000341,pigment cell (sensu Nematoda and Protostomia),CL:0000147,pigment cell
+UBERON:0008435,vertebral arch of sacral segment,UBERON:0004247,bone of dorsum
+HP:0002961,Dysgammaglobulinemia,HP:0004313,Hypogammaglobulinemia
+UBERON:0004223,vagina smooth muscle,UBERON:0005156,reproductive structure
+HP:0008598,Mild conductive hearing impairment,HP:0000405,Conductive hearing impairment
+HP:0009392,Triangular epiphyses of the 5th finger,HP:0009152,Abnormality of the epiphyses of the 5th finger
+UBERON:2001357,alar plate midbrain,UBERON:0004121,ectoderm-derived structure
+NCBITaxon:33630,Alveolata,NCBITaxon:2759,Eukaryota
+UBERON:0001273,ilium,UBERON:0002513,endochondral bone
+UBERON:0014682,tooth whorl,UBERON:0009678,tooth row
+UBERON:0001678,temporal bone,UBERON:0015212,lateral structure
+HP:0004619,Lumbar kyphoscoliosis,HP:0004626,Lumbar scoliosis
+UBERON:0004987,mucosa of laryngopharynx,UBERON:0000355,pharyngeal mucosa
+UBERON:0001893,telencephalon,UBERON:0002780,regional part of forebrain
+UBERON:0011133,intermetatarsal joint,UBERON:0001487,pes joint
+HP:0004420,Arterial thrombosis,HP:0001977,Abnormal thrombosis
+UBERON:0005149,metanephric connecting tubule,UBERON:0005097,renal connecting tubule
+HP:0100357,Contractures of the metatarsophalangeal joint of the 3rd toe,HP:0010333,Flexion contracture of 3rd toe
+HP:0002600,Hyporeflexia of lower limbs,HP:0001265,Hyporeflexia
+UBERON:0011242,ethmoid cartilage,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0003929,Ground glass opacity of humeral diaphysis,HP:0003926,Abnormality of the humeral diaphysis
+UBERON:0002969,inferior temporal sulcus,UBERON:0014687,temporal sulcus
+UBERON:0008888,vesical venous plexus,UBERON:0004120,mesoderm-derived structure
+UBERON:0015828,cerebellum ventricular layer,UBERON:0004130,cerebellar layer
+UBERON:0008456,superior articular process of lumbar vertebra,UBERON:0001079,superior articular process of vertebra
+NCBITaxon:29122,Oryzomys,NCBITaxon:40141,Sigmodontinae
+HP:0005815,Supernumerary ribs,HP:0009144,Supernumerary bones of the axial skeleton
+CL:0002246,peripheral blood stem cell,CL:0000037,hematopoietic stem cell
+UBERON:0001519,skin of manus,UBERON:0003531,forelimb skin
+HP:0009537,Flexion contracture of the 2nd finger,HP:0100490,Camptodactyly of finger
+UBERON:0003420,mesenchyme of sublingual gland,UBERON:0003104,mesenchyme
+UBERON:0006811,occipital condyle,UBERON:0010314,structure with developmental contribution from neural crest
+CL:1000310,adipocyte of epicardial fat of right ventricle,CL:1000309,epicardial adipocyte
+UBERON:0006555,excretory tube,UBERON:0006554,urinary system structure
+UBERON:0006228,exoccipital pre-cartilage condensation,UBERON:0015051,exoccipital endochondral element
+HP:0010071,Osteolytic defects of the 1st metatarsal,HP:0010062,Osteolytic defects of the phalanges of the hallux
+DOID:1066,residual stage of open angle glaucoma,DOID:1067,open-angle glaucoma
+UBERON:2001779,pelvic fin lepidotrichium 4,UBERON:4000173,pelvic fin lepidotrichium
+UBERON:0010076,network of trabecular spaces in bone tissue,UBERON:0000464,anatomical space
+HP:0010740,Osteopathia striata,HP:0011314,Abnormality of long bone morphology
+UBERON:0011379,male external urethral sphincter,UBERON:0005156,reproductive structure
+DOID:8607,herpetic whitlow,DOID:8566,herpes simplex
+UBERON:0013657,hump,UBERON:0000481,multi-tissue structure
+CL:0002262,endothelial cell of sinusoid,CL:0000115,endothelial cell
+UBERON:0004637,otic capsule,UBERON:0003462,facial bone
+HP:0011986,Ectopic ossification,HP:0011849,Abnormal bone ossification
+CL:0000772,immature eosinophil,CL:0002242,nucleate cell
+HP:0012351,Increased sialylation of N-linked protein glycosylation,HP:0012349,Abnormal sialylation of N-linked protein glycosylation
+UBERON:0015078,proximal carpal endochondral element,UBERON:0015049,carpus endochondral element
+CL:0002625,seminiferous tubule epithelial cell,CL:0000077,mesothelial cell
+UBERON:0002155,gigantocellular nucleus,UBERON:0007635,nucleus of medulla oblongata
+UBERON:0012481,cloacal epithelium,UBERON:0012275,meso-epithelium
+DOID:13622,campylobacteriosis,DOID:0050338,primary bacterial infectious disease
+HP:0009467,Radial deviation of the 2nd finger,HP:0009468,Deviation of the 2nd finger
+UBERON:0001925,ventral lateral nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0011152,dorsal hyoid arch skeleton,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010953,Noncommunicating hydrocephalus,HP:0000238,Hydrocephalus
+DOID:7133,gallbladder small cell carcinoma,DOID:4948,gallbladder carcinoma
+UBERON:0006107,basolateral amygdaloid nuclear complex,UBERON:0005401,cerebral hemisphere grey matter
+UBERON:0002026,stratum spinosum of epidermis,UBERON:0004121,ectoderm-derived structure
+UBERON:0013506,cervical vertebra pre-cartilage condensation,UBERON:0011095,vertebra pre-cartilage condensation
+UBERON:0000974,neck,UBERON:0000475,organism subdivision
+UBERON:0000200,gyrus,UBERON:0004121,ectoderm-derived structure
+UBERON:0015477,axillary fat pad,UBERON:0003916,fat pad
+UBERON:0002643,decussation of medial lemniscus,UBERON:0007418,decussation of neuraxis
+HP:0001850,Abnormality of the tarsal bones,HP:0001760,Abnormality of the foot
+HP:0008593,Prominent antitragus,HP:0009896,Abnormality of the antitragus
+HP:0002425,Anarthria,HP:0002167,Neurological speech impairment
+UBERON:3000413,pars palatina of maxilla,UBERON:0000064,organ part
+UBERON:0011846,acinus of sebaceous gland,UBERON:0011858,acinus of exocrine gland
+HP:0006407,Irregular distal femoral epiphysis,HP:0010590,Abnormality of the distal femoral epiphysis
+UBERON:0014940,cerebral cortex subventricular zone,UBERON:0014950,layer of developing cerebral cortex
+UBERON:0002202,submucosa of trachea,UBERON:0004777,respiratory system submucosa
+CL:1000308,fibrocyte of adventitia of ureter,CL:0000135,fibrocyte
+DOID:0050266,tungiasis,DOID:4110,parasitic ectoparasitic infectious disease
+UBERON:0000211,ligament,UBERON:0007846,dense regular connective tissue
+DOID:93,language disorder,DOID:2033,communication disorder
+UBERON:0010714,iliac cartilage element,UBERON:0015054,iliac endochondral element
+DOID:10863,paralytic squint,DOID:540,strabismus
+DOID:14183,alcoholic neuropathy,DOID:2537,inflammatory and toxic neuropathy
+HP:0001144,Orbital cyst,HP:0000315,Abnormality of the orbital region
+CL:0002434,"CD24-positive, CD8 single-positive thymocyte",CL:0000811,"CD8-positive, alpha-beta thymocyte"
+HP:0012620,Cloacal abnormality,HP:0000119,Abnormality of the genitourinary system
+UBERON:0002125,lobule of thymus,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0003984,Posteriorly dislocated ulna,HP:0002997,Abnormality of the ulna
+UBERON:0010314,structure with developmental contribution from neural crest,UBERON:0000061,anatomical structure
+CL:0002490,organ of Corti supporting cell,CL:0002315,supporting cell of cochlea
+HP:0010220,Abnormality of the epiphysis of the 2nd metacarpal,HP:0010010,Abnormality of the 2nd metacarpal
+UBERON:0010313,neural crest-derived structure,UBERON:0010314,structure with developmental contribution from neural crest
+CL:1000353,microfold cell of epithelium of small intestine,CL:0002254,epithelial cell of small intestine
+UBERON:0006834,uterus or analog,UBERON:0005156,reproductive structure
+HP:0006185,Enlarged proximal interphalangeal joints,HP:0006247,Enlarged interphalangeal joints
+CL:0001000,CD8_alpha-positive CD11b-negative dendritic cell,CL:0000766,myeloid leukocyte
+UBERON:0014390,muscle layer of ileum,UBERON:0011201,muscle layer of small intestine
+UBERON:0007153,superior epigastric artery,UBERON:0004573,systemic artery
+DOID:1100,ovarian disease,DOID:229,female reproductive system disease
+HP:0011010,Chronic,HP:0011008,Speed of onset
+HP:0011391,Morphological abnormality of the nerves of the inner ear,HP:0011390,Morphological abnormality of the inner ear
+UBERON:0001319,vaginal vein,UBERON:0014404,female anatomical structure
+CL:0002051,CD38-high pre-BCR positive cell,CL:0000952,preBCR-positive large pre-B-II cell
+DOID:7263,selective IgD deficiency disease,DOID:6025,selective immunoglobulin deficiency disease
+DOID:6085,meningeal melanoma,DOID:6086,malignant leptomeningeal tumor
+DOID:6089,pediatric leptomeningeal melanoma,DOID:6085,meningeal melanoma
+HP:0010463,Aplasia of the ovary,HP:0010462,Aplasia/Hypoplasia of the ovary
+DOID:12287,Crimean-Congo hemorrhagic fever,DOID:37,skin disease
+UBERON:0000439,arachnoid trabecula,UBERON:0000440,trabecula
+CL:0000773,eosinophilic metamyelocyte,CL:0002192,metamyelocyte
+UBERON:0005440,ductus arteriosus,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+CL:2000000,epidermal melanocyte,CL:0002484,epithelial melanocyte
+UBERON:0000481,multi-tissue structure,UBERON:0010000,multicellular anatomical structure
+HP:0011982,Black pigment gallstones,HP:0011981,Pigment gallstones
+DOID:10841,Eastern equine encephalitis,DOID:934,viral infectious disease
+UBERON:4000182,suprabranchial fin,UBERON:0002534,paired fin
+UBERON:0002657,posterior parahippocampal gyrus,UBERON:0000200,gyrus
+HP:0004782,Hypotrichosis of the scalp,HP:0001006,Hypotrichosis
+HP:0010013,Abnormality of the 5th metacarpal,HP:0001163,Abnormality of the metacarpal bones
+HP:0008942,Acute rhabdomyolysis,HP:0003201,Rhabdomyolysis
+UBERON:0001663,cerebral vein,UBERON:0001638,vein
+HP:0011789,Thyroid-stimulating hormone receptor (TSHR) defect,HP:0002926,Abnormality of thyroid physiology
+DOID:12971,hereditary spherocytosis,DOID:589,congenital hemolytic anemia
+UBERON:0004008,cerebellar plate,UBERON:0005291,embryonic tissue
+HP:0011229,Broad eyebrow,HP:0000534,Abnormality of the eyebrow
+HP:0010099,Partial duplication of the 1st metatarsal,HP:0010101,Partial duplication of the phalanges of the hallux
+UBERON:0001880,bed nucleus of stria terminalis,UBERON:0009663,telencephalic nucleus
+HP:0009289,Aplasia/Hypoplasia of the distal phalanx of the 4th finger,HP:0009282,Abnormality of the distal phalanx of the 4th finger
+DOID:2992,prostate neuroendocrine neoplasm,DOID:10283,prostate cancer
+UBERON:0005326,mesonephric glomerulus vasculature,UBERON:0004190,renal glomerulus vasculature
+DOID:3911,progeria,DOID:0050737,autosomal recessive disease
+UBERON:0008847,ovarian ligament,UBERON:0008845,nonskeletal ligament
+UBERON:0007829,pectoral girdle bone,UBERON:0007828,girdle bone/zone
+UBERON:4200046,astragalo-calcaneal canal,UBERON:0004705,fenestra
+HP:0010094,Complete duplication of the proximal phalanx of the hallux,HP:0010093,Duplication of the proximal phalanx of the hallux
+HP:0006480,Premature loss of teeth,HP:0000164,Abnormality of the teeth
+UBERON:0008257,radial sesamoid,UBERON:0001435,carpal bone
+HP:0001122,Aplasia/Hypoplasia of the choroid,HP:0008057,Aplasia/Hypoplasia affecting the fundus
+UBERON:0006430,xiphoid cartilage,UBERON:0000398,cartilage tissue of sternum
+DOID:7820,sphenocavernous meningioma,DOID:4437,skull base meningioma
+DOID:3138,acanthosis nigricans,DOID:10123,pigmentation disease
+UBERON:0009473,parapodium,UBERON:0000026,appendage
+UBERON:0005899,pes bone,UBERON:0003464,hindlimb bone
+DOID:3078,grade III astrocytoma,DOID:3069,astrocytoma
+HP:0006887,"Intellectual disability, progressive",HP:0001249,Intellectual disability
+HP:0100069,Enlarged epiphyses of the 4th toe,HP:0010165,Enlarged epiphyses of the toes
+UBERON:0007631,accessory olfactory bulb glomerular layer,UBERON:0011215,cell part cluster of neuraxis
+UBERON:0009589,mesenchyme of interdigital region between manual digits 4 and 5,UBERON:0009600,mesenchyme of interdigital region of manus
+HP:0000326,Abnormality of the maxilla,HP:0000309,Abnormality of the midface
+UBERON:0006723,cochlear modiolus,UBERON:0005913,zone of bone organ
+NCBITaxon:11676,Human immunodeficiency virus 1,NCBITaxon:11652,Primate lentivirus group
+HP:0009772,Patchy sclerosis of the phalanges of the hand,HP:0004286,Patchy sclerosis of hand bones
+HP:0005262,Abnormality of the synovia,HP:0001367,Abnormal joint morphology
+HP:0002123,Generalized myoclonic seizures,HP:0002197,Generalized seizures
+HP:0012253,Abnormal respiratory epithelium morphology,HP:0012252,Abnormal respiratory system morphology
+UBERON:0002399,lesser omentum,UBERON:0009034,stomach region
+HP:0100834,Neoplasm of the large intestine,HP:0002250,Abnormality of the large intestine
+DOID:3644,hypothalamic neoplasm,DOID:1931,hypothalamic disease
+UBERON:0007683,lateral mesenchyme derived from mesoderm,UBERON:0005256,trunk mesenchyme
+HP:0009711,Retinal hemangioblastoma,HP:0010797,Hemangioblastoma
+HP:0010243,Abnormality of the epiphyses of the distal phalanx of finger,HP:0009832,Abnormality of the distal phalanx of finger
+HP:0100483,Symphalangism of the proximal phalanx of the 2nd toe with the 2nd metatarsal,HP:0001440,Synostosis involving metatarsal bones
+DOID:4918,renal pelvis adenocarcinoma,DOID:4919,renal pelvis carcinoma
+HP:0007364,Aplasia/Hypoplasia of the cerebrum,HP:0002977,Aplasia/Hypoplasia involving the central nervous system
+DOID:5288,larynx leiomyosarcoma,DOID:2877,larynx sarcoma
+CL:0002236,basal epithelial cell of prostatic duct,CL:0000068,duct epithelial cell
+HP:0011728,Elbow clonus,HP:0002169,Clonus
+DOID:12165,retinal lattice degeneration,DOID:12161,peripheral retinal degeneration
+HP:0009421,Aplasia/Hypoplasia of the distal phalanx of the 3rd finger,HP:0009447,Aplasia/Hypoplasia of the phalanges of the 3rd finger
+HP:0100366,Short phalanx of the 3rd toe,HP:0010746,Hypoplasia of the phalanges of the toes
+HP:0100013,Neoplasm of the breast,HP:0000769,Abnormality of the breast
+DOID:11080,myiasis,DOID:4110,parasitic ectoparasitic infectious disease
+UBERON:2000358,granular layer corpus cerebelli,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003945,somatic motor system,UBERON:0000061,anatomical structure
+UBERON:0004080,cerebellum vermis lobule VI,UBERON:0004070,cerebellum vermis lobule
+HP:0003159,Hyperoxaluria,HP:0001992,Organic aciduria
+UBERON:4200118,pubic peduncle,UBERON:0004120,mesoderm-derived structure
+UBERON:0002251,iliocostalis muscle,UBERON:0003897,axial muscle
+DOID:7457,enterobiasis,DOID:883,parasitic helminthiasis infectious disease
+HP:0005978,Type II diabetes mellitus,HP:0000819,Diabetes mellitus
+NCBITaxon:43817,Culicinae,NCBITaxon:7157,Culicidae
+HP:0011184,EEG with hyperventilation-induced generalized epileptiform discharges,HP:0010858,EEG with hyperventilation-induced epileptiform discharges
+HP:0000264,Abnormality of the mastoid,HP:0000929,Abnormality of the skull
+HP:0003295,Impaired FSH and LH secretion,HP:0003117,Abnormality of circulating hormone level
+HP:0002037,Inflammation of the large intestine,HP:0004386,Gastrointestinal inflammation
+DOID:6098,thalamic neoplasm,DOID:3843,diencephalic neoplasm
+HP:0010088,Curved proximal phalanx of the hallux,HP:0010061,Curved phalanges of the hallux
+CL:0002071,enterocyte of epithelium of large intestine,CL:0000584,enterocyte
+HP:0009792,Teratoma,HP:0002898,Embryonal neoplasm
+DOID:192,sex cord-gonadal stromal tumor,DOID:193,reproductive organ cancer
+NCBITaxon:6033,Encephalitozoon,NCBITaxon:36734,Unikaryonidae
+UBERON:2000004,anterior axial hypoblast,UBERON:0005291,embryonic tissue
+DOID:14777,benign familial neonatal epilepsy,DOID:0050702,neonatal period electroclinical syndrome
+HP:0002850,IgM deficiency,HP:0004313,Hypogammaglobulinemia
+HP:0010329,Abnormality of the epiphyses of the 3rd toe,HP:0010160,Abnormality of the epiphyses of the toes
+CL:0002017,"Kit-negative, Ly-76 high orthochromatophilic erythroblasts",CL:0000552,orthochromatic erythroblast
+HP:0001681,Angina pectoris,HP:0001677,Coronary artery disease
+HP:0009674,Triangular epiphysis of the proximal phalanx of the thumb,HP:0009663,Abnormality of the epiphysis of the proximal phalanx of the thumb
+UBERON:0001109,sternothyroid muscle,UBERON:0008523,infrahyoid muscle
+DOID:2047,hepatitis D,DOID:934,viral infectious disease
+HP:0004293,Synostosis of second metacarpal-trapezoid,HP:0100328,Carpometacarpal synostosis
+HP:0011426,Fetal choroid plexus cysts,HP:0011425,Fetal ultrasound soft marker
+UBERON:0008857,stomach smooth muscle circular layer,UBERON:0012368,circular muscle layer
+DOID:8392,reticular pattern testicular yolk sac tumor,DOID:5344,testicular yolk sac tumor
+HP:0009721,Shagreen patch,HP:0100898,Connective tissue nevi
+DOID:10616,acute cervicitis,DOID:2568,cervicitis
+NCBITaxon:45219,Guanarito virus,NCBITaxon:208897,New world arenaviruses
+HP:0100375,Aplasia/Hypoplasia of the proximal phalanx of the 3rd toe,HP:0010203,Aplasia/Hypoplasia of the proximal phalanges of the toes
+CL:0000038,erythroid progenitor cell,CL:0000839,myeloid lineage restricted progenitor cell
+HP:0007006,Dorsal column degeneration,HP:0011397,Abnormality of the dorsal column of the spinal cord
+CL:1000491,mesothelial cell of pleura,CL:0002371,somatic cell
+NCBITaxon:177874,WEEV complex,NCBITaxon:11019,Alphavirus
+HP:0002937,Hemivertebrae,HP:0003312,Abnormal form of the vertebral bodies
+UBERON:0010680,pedal digit 1 phalanx cartilage element,UBERON:0015031,pedal digit 1 phalanx endochondral element
+UBERON:0008952,upper lobe of left lung,UBERON:0008948,upper lobe of lung
+DOID:0060154,verbal auditory agnosia,DOID:4090,agnosia
+HP:0100557,Hemiatrophy of lower limb,HP:0100556,Hemiatrophy
+UBERON:2001651,pharyngobranchial 2 tooth,UBERON:0001091,calcareous tooth
+DOID:12919,Plasmodium ovale malaria,DOID:12365,malaria
+UBERON:0006234,femur pre-cartilage condensation,UBERON:0010886,hindlimb bone pre-cartilage condensation
+CL:0000407,scolopidial ligament cell,CL:0000384,ligament cell
+UBERON:0005341,ventral commissure,UBERON:0005970,brain commissure
+CL:1000317,intestinal villus goblet cell,CL:1000495,small intestine goblet cell
+DOID:11868,chronic erythremia,DOID:1240,leukemia
+UBERON:2001862,epibranchial 3-pharyngobranchial 4 joint,UBERON:0000982,skeletal joint
+HP:0100699,Scarring,HP:0003549,Abnormality of connective tissue
+DOID:5302,uterine ligament clear cell adenocarcinoma,DOID:3700,uterine ligament adenocarcinoma
+DOID:2347,generalized atherosclerosis,DOID:1936,atherosclerosis
+CL:0002590,smooth muscle cell of the brain vasculature,CL:0000359,vascular associated smooth muscle cell
+UBERON:0002099,cardiac septum,UBERON:0004120,mesoderm-derived structure
+CL:0000306,crystallin accumulating cell,CL:0000325,stuff accumulating cell
+HP:0003908,Corner spurs (humeral metaphyses),HP:0003922,Spurred humeral metaphysis
+HP:0004909,hypokalemic hypochloremic metabolic alkalosis,HP:0001960,Hypokalemic metabolic alkalosis
+HP:0004472,Mandibular hyperostosis,HP:0005465,Facial hyperostosis
+CL:0000927,CD4-positive type I NK T cell secreting interleukin-4,CL:0000912,helper T cell
+UBERON:0010046,entire pharyngeal arch associated mesenchyme,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009270,Stippling of the epiphysis of the proximal phalanx of the 4th finger,HP:0009248,Abnormality of the epiphysis of the proximal phalanx of the 4th finger
+UBERON:0004247,bone of dorsum,UBERON:0001474,bone element
+HP:0011369,Mongolian blue spot,HP:0001034,Hypermelanotic macule
+UBERON:0011765,jugular lymph sac,UBERON:0005423,developing anatomical structure
+DOID:4320,non-gestational choriocarcinoma,DOID:3594,choriocarcinoma
+HP:0007488,Diffuse skin atrophy,HP:0004334,Dermal atrophy
+UBERON:0001310,umbilical artery,UBERON:0001637,artery
+UBERON:0001466,pedal digit,UBERON:0008784,lower limb segment
+HP:0009205,Cone-shaped epiphysis of the middle phalanx of the 5th finger,HP:0004224,Abnormality of the epiphysis of the middle phalanx of the 5th finger
+CL:1001516,intestinal enteroendocrine cell,CL:0002563,intestinal epithelial cell
+HP:0009240,Broad distal phalanx of the 5th finger,HP:0009374,Broad phalanges of the 5th finger
+DOID:3148,dermal unilateral segmental cavernous angioma,DOID:483,cavernous hemangioma
+HP:0003406,Peripheral nerve compression,HP:0000759,Abnormality of the peripheral nervous system
+UBERON:0005991,aortic valve anulus,UBERON:0010313,neural crest-derived structure
+UBERON:0015281,pancreas right lobe,UBERON:0015212,lateral structure
+NCBITaxon:135625,Pasteurellales,NCBITaxon:1236,Gammaproteobacteria
+DOID:8956,cowpox,DOID:934,viral infectious disease
+DOID:13649,polyneuropathy in collagen vascular disease,DOID:2537,inflammatory and toxic neuropathy
+UBERON:3010393,mesonephric late distal segment,UBERON:0004120,mesoderm-derived structure
+UBERON:0002660,medial longitudinal fasciculus of midbrain,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003706,laryngeal vocal fold,UBERON:0015212,lateral structure
+HP:0005562,Multiple renal cysts,HP:0000107,Renal cyst
+UBERON:0002463,hamstring muscle,UBERON:0001630,muscle organ
+UBERON:0001616,maxillary artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:11360,Phlebotomus fever,DOID:934,viral infectious disease
+UBERON:0015138,quarternary lactiferous duct,UBERON:0001765,mammary duct
+UBERON:0001681,nasal bone,UBERON:0008907,dermal bone
+HP:0012542,Onychauxis,HP:0001805,Thick nail
+NCBITaxon:951,Neorickettsia sennetsu,NCBITaxon:33993,Neorickettsia
+DOID:11634,myxedema,DOID:1459,hypothyroidism
+HP:0100808,Gastric diverticulum,HP:0002577,Abnormality of the stomach
+DOID:13146,esophageal candidiasis,DOID:1508,candidiasis
+UBERON:0002348,epicardium,UBERON:0004120,mesoderm-derived structure
+HP:0006573,Acute hepatic steatosis,HP:0001397,Hepatic steatosis
+HP:0010130,Enlarged epiphysis of the proximal phalanx of the hallux,HP:0010126,Abnormality of the epiphysis of the proximal phalanx of the hallux
+HP:0010138,Absent epiphysis of the distal phalanx of the hallux,HP:0010124,Abnormality of the epiphysis of the distal phalanx of the hallux
+UBERON:3010565,pila preoptica,UBERON:0003932,cartilage element of chondrocranium
+UBERON:0002075,viscus,UBERON:0005177,trunk organ
+UBERON:0013610,inferior olive ventral accessory nucleus,UBERON:0007244,inferior olivary nucleus
+UBERON:4100005,second phalanx,UBERON:0003221,phalanx
+HP:0001054,Numerous nevi,HP:0010566,Hamartoma
+UBERON:0004528,alveolar ridge of mandible,UBERON:0004120,mesoderm-derived structure
+UBERON:0003499,brain blood vessel,UBERON:0004121,ectoderm-derived structure
+UBERON:4100004,ischial peduncle,UBERON:4100000,skeletal element projection
+CL:0002272,motilin secreting cell,CL:0000167,peptide hormone secreting cell
+HP:0010610,Palmar pits,HP:0100276,Skin pits
+CL:2000004,pituitary gland cell,CL:0002319,neural cell
+UBERON:0001681,nasal bone,UBERON:0010428,flat bone
+DOID:4360,epithelioid cell melanoma,DOID:1909,melanoma
+HP:0100175,Ivory epiphysis of the distal phalanx of the 4th toe,HP:0100094,Abnormality of the epiphysis of the distal phalanx of the 4th toe
+DOID:4627,ideomotor apraxia,DOID:0060135,apraxia
+HP:0003647,Electron transfer flavoprotein-ubiquinone oxidoreductase defect,HP:0003287,Abnormality of mitochondrial metabolism
+HP:0009347,Bracket epiphysis of the proximal phalanx of the 3rd finger,HP:0009411,Bracket epiphyses of the 3rd finger
+UBERON:3010018,M. glutaeus magnus,UBERON:0010890,pelvic complex muscle
+UBERON:0012167,buccal fat pad,UBERON:0003916,fat pad
+UBERON:0009864,ascidian neural gland,UBERON:0000064,organ part
+UBERON:0004715,annulus fibrosus disci intervertebralis,UBERON:0004120,mesoderm-derived structure
+DOID:2828,acalculous cholecystitis,DOID:1949,cholecystitis
+UBERON:0005296,ovary sex cord,UBERON:0005295,sex cord
+UBERON:0014787,left extraembryonic umbilical vein,UBERON:0014786,extraembryonic umbilical vein
+UBERON:0011321,masseteric nerve,UBERON:0002003,peripheral nerve
+HP:0000046,Scrotal hypoplasia,HP:0000050,Hypoplastic genitalia
+UBERON:2001303,vagal ganglion 2,UBERON:0009127,epibranchial ganglion
+UBERON:0002965,rostral intralaminar nuclear group,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0005141,metanephric short descending thin limb,UBERON:0005099,short descending thin limb
+UBERON:0002646,dorsal longitudinal fasciculus of medulla,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:3030,mucinous adenocarcinoma,DOID:299,adenocarcinoma
+DOID:9931,Waterhouse-Friderichsen syndrome,DOID:9553,adrenal gland disease
+HP:0011411,Forceps delivery,HP:0001787,Abnormal delivery
+UBERON:0002826,inferior part of vestibular ganglion,UBERON:0010313,neural crest-derived structure
+UBERON:0006667,pituitary fossa,UBERON:0002553,anatomical cavity
+HP:0011622,Inlet ventricular septal defect,HP:0001629,Ventricular septal defect
+HP:0008430,Anterior beaking of lumbar vertebrae,HP:0004568,Beaking of vertebral bodies
+DOID:6607,nervous system hibernoma,DOID:3093,nervous system cancer
+DOID:4991,optic nerve astrocytoma,DOID:4992,optic nerve glioma
+HP:0007606,Multiple cutaneous malignancies,HP:0008069,Neoplasm of the skin
+UBERON:0005835,cuneate fasciculus of spinal cord,UBERON:0005832,cuneate fasciculus
+HP:0002967,Cubitus valgus,HP:0009811,Abnormality of the elbow
+UBERON:0002372,tonsil,UBERON:0004119,endoderm-derived structure
+CL:0000766,myeloid leukocyte,CL:0000738,leukocyte
+UBERON:0015420,ureteral valve,UBERON:0004120,mesoderm-derived structure
+UBERON:0009115,thoracic thymus,UBERON:0002370,thymus
+HP:0001125,Hemianopic blurring of vision,HP:0000505,Visual impairment
+CL:0002380,oospore,CL:0000605,fungal asexual spore
+HP:0007809,Punctate corneal dystrophy,HP:0001131,Corneal dystrophy
+DOID:10915,Wernicke-Korsakoff syndrome,DOID:5113,nutritional deficiency disease
+HP:0009835,Aplasia/Hypoplasia of the distal phalanges of the hand,HP:0009832,Abnormality of the distal phalanx of finger
+HP:0012049,Laryngeal dystonia,HP:0004373,Focal dystonia
+UBERON:0011110,humeroulnar joint,UBERON:0011139,synovial limb joint
+UBERON:0009095,tip of renal papilla,UBERON:0006554,urinary system structure
+DOID:0060186,chemical colitis,DOID:0060180,colitis
+DOID:7643,acantholytic squamous cell skin carcinoma,DOID:3151,skin squamous cell carcinoma
+UBERON:0012322,ascending cervical artery,UBERON:0012320,cervical artery
+UBERON:0000368,adductor brevis,UBERON:0011144,adductor muscle of hip
+HP:0008309,Medium chain dicarboxylic aciduria,HP:0003215,Dicarboxylic aciduria
+UBERON:0004235,mammary gland smooth muscle,UBERON:0014404,female anatomical structure
+UBERON:0009669,embryonic cloacal lumen,UBERON:0012463,cloacal lumen
+UBERON:0010057,hypopharyngeal eminence,UBERON:0005423,developing anatomical structure
+UBERON:2000455,ventral flexor,UBERON:0000366,flexor muscle
+CL:0007010,preosteoblast,CL:0000055,non-terminally differentiated cell
+CL:0002597,smooth muscle cell of bladder,CL:0000192,smooth muscle cell
+UBERON:0012296,urethral crest,UBERON:0004120,mesoderm-derived structure
+UBERON:0008584,vertical muscle of tongue,UBERON:0001576,intrinsic muscle of tongue
+DOID:1923,sex differentiation disease,DOID:2277,gonadal disease
+DOID:12148,alveolar echinococcosis,DOID:1496,echinococcosis
+UBERON:0008459,superior articular process of cervical vertebra,UBERON:0001079,superior articular process of vertebra
+HP:0008113,Multiple plantar creases,HP:0100872,Abnormality of the plantar skin of foot
+CL:0000852,neuromast support cell,CL:0002319,neural cell
+UBERON:0000056,ureter,UBERON:0015212,lateral structure
+HP:0005619,Thoracolumbar kyphosis,HP:0100712,Abnormality of the lumbar spine
+HP:0010694,Lamellar pulverulent cataract,HP:0007971,Lamellar cataract
+UBERON:2001406,kinethmoid bone,UBERON:0011164,neurocranium bone
+DOID:9341,urethral diverticulum,DOID:732,urethral disease
+DOID:2582,acatalasia,DOID:906,peroxisomal disease
+UBERON:0004198,comma-shaped body,UBERON:0001231,nephron tubule
+UBERON:2001981,vertebral element 7,UBERON:0010913,vertebral element
+HP:0003477,Peripheral axonal neuropathy,HP:0009830,Peripheral neuropathy
+UBERON:0001478,teres major muscle,UBERON:0004120,mesoderm-derived structure
+UBERON:0011202,urachus epithelium,UBERON:0003914,epithelial tube
+UBERON:0013173,anterior part of tympanic bone,UBERON:0005913,zone of bone organ
+HP:0009253,Enlarged epiphysis of the distal phalanx of the 4th finger,HP:0009396,Enlarged epiphyses of the 4th finger
+HP:0002980,Femoral bowing,HP:0002979,Bowing of the legs
+UBERON:0015126,middle internodal tract,UBERON:0009966,internodal tract
+HP:0011779,Anaplastic thyroid carcinoma,HP:0002890,Thyroid carcinoma
+UBERON:0004240,gall bladder smooth muscle,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0009989,condyle of tibia,UBERON:0005055,zone of long bone
+UBERON:0003829,urethra muscle,UBERON:0006554,urinary system structure
+DOID:10440,mycotic corneal ulcer,DOID:8463,corneal ulcer
+HP:0003547,Shoulder girdle muscle weakness,HP:0003325,Limb-girdle muscle weakness
+UBERON:0004151,cardiac chamber,UBERON:0000064,organ part
+CL:0000617,GABAergic neuron,CL:0000161,acid secreting cell
+UBERON:0002604,ventral nucleus of lateral lemniscus,UBERON:0006331,brainstem nucleus
+HP:0002933,Ventral hernia,HP:0004299,Hernia of the abdominal wall
+UBERON:0005226,pedal digit epithelium,UBERON:0010371,ecto-epithelium
+UBERON:0001230,glomerular capsule,UBERON:0000064,organ part
+UBERON:4200081,hypocleideum,UBERON:0004120,mesoderm-derived structure
+UBERON:0012067,primary bronchiole,UBERON:0002186,bronchiole
+DOID:11030,corneal edema,DOID:10124,corneal disease
+UBERON:0007234,4-8 cell stage,UBERON:0000067,embryo stage part
+HP:0007307,Rapid neurologic deterioration,HP:0002344,Progressive neurologic deterioration
+DOID:5577,gastrinoma,DOID:169,neuroendocrine tumor
+UBERON:0013700,axial musculature,UBERON:0001015,musculature
+UBERON:0014772,lateral palpebral artery,UBERON:0004573,systemic artery
+HP:0100412,Complete duplication of the middle phalanx of the 5th toe,HP:0100403,Duplication of the middle phalanx of the 5th toe
+UBERON:0002000,gluteal muscle,UBERON:0001497,muscle of pelvic girdle
+DOID:4550,anal gland neoplasm,DOID:4551,anus neoplasm
+UBERON:0012349,digital pad,UBERON:0012348,autopod pad
+UBERON:2001409,infraorbital 4,UBERON:2000376,infraorbital
+HP:0010634,Total hyposmia,HP:0004409,Hyposmia
+HP:0008047,Abnormality of the vasculature of the eye,HP:0012374,Abnormality of the globe
+UBERON:4100003,articular surface,UBERON:0006984,anatomical surface
+DOID:11871,macular keratitis,DOID:4677,keratitis
+UBERON:0001906,subthalamic nucleus,UBERON:0015234,nucleus of ventral thalamus
+UBERON:0010225,thalamic complex,UBERON:0002784,regional part of diencephalon
+HP:0009909,Uplifted earlobe,HP:0000363,Abnormality of earlobe
+UBERON:0010940,belly of digastric,UBERON:0004120,mesoderm-derived structure
+DOID:0050560,Walker-Warburg syndrome,DOID:0050557,congenital muscular dystrophy
+UBERON:2001949,caudal-fin hook,UBERON:4100000,skeletal element projection
+DOID:13110,bladder squamous papilloma,DOID:0050623,bladder benign neoplasm
+HP:0004660,Hypoplasia of facial musculature,HP:0000301,Abnormality of facial musculature
+UBERON:0011283,epoophoron,UBERON:0005156,reproductive structure
+UBERON:0013262,remnnant of ductus deferens,UBERON:0005156,reproductive structure
+DOID:3818,photoallergic dermatitis,DOID:3159,photosensitivity disease
+DOID:0050701,electroclinical syndrome,DOID:1826,epilepsy syndrome
+DOID:1371,uterine corpus adenomatoid tumor,DOID:0060095,uterine benign neoplasm
+UBERON:0001513,skin of pes,UBERON:0003532,hindlimb skin
+UBERON:0013736,interfascicular linear nucleus,UBERON:0002308,nucleus of brain
+UBERON:0005031,mucosa of upper lip,UBERON:0003729,mouth mucosa
+UBERON:0003953,posterior stroma of cornea,UBERON:0010313,neural crest-derived structure
+UBERON:3000880,crista hypertrophica ischium,UBERON:4100000,skeletal element projection
+HP:0010026,Aplasia/Hypoplasia of the 1st metacarpal,HP:0005914,Aplasia/Hypoplasia involving the metacarpal bones
+CL:0007018,epidermal ciliary cell,CL:0000064,ciliated cell
+HP:0004047,Wide ulnar metaphysis,HP:0003856,Upper limb metaphyseal widening
+UBERON:0004747,supraoccipital bone,UBERON:0011164,neurocranium bone
+HP:0007984,Reduced amplitude of b-wave (ERG),HP:0000512,Abnormal electroretinogram
+CL:0002449,CD94-positive Ly49CI-positive natural killer cell,CL:0002443,Ly49CI-positive natural killer cell
+HP:0010393,Abnormality of the middle phalanx of the 5th toe,HP:0010342,Abnormality of the phalanges of the 5th toe
+HP:0006584,Small abnormally formed scapulae,HP:0000882,Hypoplastic scapulae
+DOID:0050537,posterior polar cataract,DOID:83,cataract
+UBERON:0008253,Aristotle's lantern,UBERON:0004121,ectoderm-derived structure
+UBERON:0010170,region of neural crest,UBERON:0002050,embryonic structure
+UBERON:0003484,eye sebaceous gland,UBERON:0003487,skin sebaceous gland
+DOID:12170,radial nerve lesion,DOID:12171,radial neuropathy
+HP:0012210,Abnormal renal morphology,HP:0000077,Abnormality of the kidney
+UBERON:0002957,caudal central oculomotor nucleus,UBERON:0007414,nucleus of midbrain tegmentum
+UBERON:0012479,urodeal gland,UBERON:0012478,cloacal gland
+HP:0100047,Enlarged epiphyses of the 2nd toe,HP:0010323,Abnormality of the epiphyses of the 2nd toe
+UBERON:0001415,skin of pelvis,UBERON:0003836,abdominal segment skin
+HP:0012721,Venous malformation,HP:0002624,Venous abnormality
+UBERON:0010343,2nd arch mesenchyme from head mesenchyme,UBERON:0005689,2nd arch mesenchyme
+UBERON:0001099,subcostal vein,UBERON:0001638,vein
+UBERON:0010989,transverospinalis pre-muscle mass,UBERON:0004120,mesoderm-derived structure
+UBERON:0011786,ramus of feather barbule,UBERON:0004121,ectoderm-derived structure
+DOID:0080051,"acromesomelic dysplasia, Hunter-Thompson type",DOID:0080049,acromesomelic dysplasia
+UBERON:0015085,distal carpal bone 1 cartilage,UBERON:0015064,autopod cartilage
+DOID:7553,infiltrating bladder urothelial carcinoma sarcomatoid variant,DOID:6477,invasive bladder transitional cell carcinoma
+UBERON:0004109,cortex of humerus,UBERON:0001439,compact bone tissue
+UBERON:0003561,forebrain dura mater,UBERON:0003548,forebrain meninges
+UBERON:0000955,brain,UBERON:0004121,ectoderm-derived structure
+HP:0011185,EEG with focal epileptiform discharges,HP:0002353,EEG abnormality
+UBERON:0002204,musculoskeletal system,UBERON:0000467,anatomical system
+HP:0009122,Aplasia/Hypoplasia affecting bones of the axial skeleton,HP:0009115,Aplasia/Hypoplasia involving the skeleton
+HP:0011868,Sciatica,HP:0003418,Back pain
+HP:0010523,Alexia,HP:0002167,Neurological speech impairment
+UBERON:0006464,fifth sacral spinal cord segment,UBERON:0007717,sacral subsegment of spinal cord
+UBERON:2001787,pectoral fin spine,UBERON:4200075,fin spine
+HP:0003343,Glutathione synthetase deficiency,HP:0001939,Abnormality of metabolism/homeostasis
+UBERON:0008339,microvascular endothelium,UBERON:0004852,cardiovascular system endothelium
+UBERON:0014618,middle frontal sulcus,UBERON:0014639,frontal sulcus
+HP:0005564,Absence of renal corticomedullary differentiation,HP:0005932,Abnormal renal corticomedullary differentiation
+DOID:4724,brain edema,DOID:936,brain disease
+DOID:14529,external pathological resorption,DOID:13240,tooth resorption
+HP:0009302,Bullet-shaped distal phalanx of the 4th finger,HP:0009282,Abnormality of the distal phalanx of the 4th finger
+UBERON:0001622,lacrimal artery,UBERON:0010314,structure with developmental contribution from neural crest
+NCBITaxon:44556,Phlebotomus <subgenus>,NCBITaxon:13203,Phlebotomus <genus>
+DOID:12901,necrotizing sialometaplasia,DOID:10854,salivary gland disease
+DOID:5554,childhood neoplasm of the testis,DOID:2998,testicular cancer
+UBERON:0007990,proximal sesamoid bone of pes,UBERON:0008000,sesamoid bone of pes
+DOID:0060044,paraphilia disorder,DOID:0060043,sexual disorder
+HP:0005208,Secretory diarrhea,HP:0002014,Diarrhea
+HP:0008290,Partial complement factor H deficiency,HP:0005369,Decreased serum complement factor H
+UBERON:0003938,sensory dissociation area,UBERON:0004121,ectoderm-derived structure
+HP:0001984,Intolerance to protein,HP:0012537,Food intolerance
+UBERON:3000661,crista vomeri,UBERON:0010313,neural crest-derived structure
+HP:0003217,Hyperglutaminemia,HP:0003112,Abnormality of serum amino acid levels
+DOID:3526,cerebral infarction,DOID:3454,brain infarction
+HP:0000497,Globe retraction and deviation on abduction,HP:0011347,Abnormality of ocular abduction
+UBERON:0005615,lens equatorial epithelium,UBERON:0001803,epithelium of lens
+HP:0009967,Complete duplication of the proximal phalanx of the 3rd finger,HP:0009960,Complete duplication of the phalanges of the 3rd finger
+HP:0005389,Depletion of components of the alternative complement pathway,HP:0005482,Abnormality of the alternate complement pathway
+UBERON:0015018,malleus endochondral element,UBERON:0010363,endochondral element
+HP:0008034,Abnormal iris pigmentation,HP:0000525,Abnormality of the iris
+HP:0006498,Aplasia/Hypoplasia of the patella,HP:0003045,Abnormality of the patella
+UBERON:0004132,trigeminal sensory nucleus,UBERON:0000126,cranial nerve nucleus
+HP:0003878,Periosteal new bone (humeral),HP:0003063,Abnormality of the humerus
+UBERON:0010229,ruminant esophageal groove,UBERON:0006846,surface groove
+UBERON:0008799,transverse palatine fold,UBERON:0008790,rugal fold
+UBERON:0003708,carotid sinus,UBERON:0001530,common carotid artery plus branches
+DOID:4448,macular degeneration,DOID:8466,retinal degeneration
+UBERON:0000407,sympathetic trunk,UBERON:0015212,lateral structure
+DOID:11339,pneumocystosis,DOID:2473,opportunistic mycosis
+UBERON:3000155,extremitas anterior,UBERON:0010313,neural crest-derived structure
+UBERON:2000940,posterior lateral line neuromast,UBERON:0008904,neuromast
+DOID:2810,middle lobe syndrome,DOID:850,lung disease
+UBERON:0013649,fused tarsals 1 and 2,UBERON:0010721,distal tarsal bone
+HP:0003521,Disproportionate short-trunk short stature,HP:0009121,Abnormal axial skeleton morphology
+DOID:12514,retinal perforation,DOID:5327,retinal detachment
+CL:0000574,erythrophore,CL:0000147,pigment cell
+UBERON:3010589,cloacal papilla,UBERON:0004120,mesoderm-derived structure
+UBERON:0013133,superior phrenic artery,UBERON:0003834,thoracic segment blood vessel
+HP:0008587,Mild neurosensory hearing impairment,HP:0012712,Mild hearing impairment
+HP:0000124,Renal tubular dysfunction,HP:0012211,Abnormal renal physiology
+UBERON:0006685,pharyngeal tubercle,UBERON:0005813,tubercle
+DOID:7764,subglottis carcinoma,DOID:11472,subglottis cancer
+UBERON:0014592,anterior nucleus of hypothalamus dorsal part,UBERON:0002784,regional part of diencephalon
+UBERON:0011861,aorta collagen fibril,UBERON:0011860,collagen fibril
+HP:0003144,Increased serum serotonin,HP:0003117,Abnormality of circulating hormone level
+DOID:12403,tinea pedis,DOID:8913,dermatophytosis
+UBERON:0001500,muscle of manus,UBERON:0003662,forelimb muscle
+UBERON:1000013,nose vertex,UBERON:0004121,ectoderm-derived structure
+CL:0002438,NK1.1-positive natural killer cell,CL:0000824,mature natural killer cell
+HP:0002334,Abnormality of the cerebellar vermis,HP:0002438,Cerebellar malformation
+UBERON:2001125,organizer inducing center,UBERON:0005291,embryonic tissue
+UBERON:0010154,inner lining mucosa of the abomasum,UBERON:0006931,stomach glandular region mucosa
+UBERON:3000185,foramen endolymphaticum,UBERON:3000051,braincase and otic capsule opening
+UBERON:3010070,M. ileo-fibularis,UBERON:0010890,pelvic complex muscle
+HP:0009836,Broad distal phalanx of finger,HP:0009768,Broad phalanges of the hand
+HP:0000158,Macroglossia,HP:0000157,Abnormality of the tongue
+HP:0005249,Functional intestinal obstruction,HP:0004796,Gastrointestinal obstruction
+UBERON:2002001,anterior dentation of pectoral fin spine,UBERON:0004120,mesoderm-derived structure
+UBERON:0010311,scleral sesamoid bone,UBERON:0001479,sesamoid bone
+HP:0012742,Thin fingernail,HP:0001231,Abnormality of the fingernails
+UBERON:0002901,posterior calcarine sulcus,UBERON:0013118,sulcus of brain
+HP:0200108,Shortened outer dynein arms,HP:0200106,Absent/shortened dynein arms
+HP:0002002,Deep philtrum,HP:0000288,Abnormality of the philtrum
+DOID:0050734,congenital intrinsic factor deficiency,DOID:0050731,vitamin B12 deficiency
+UBERON:0004073,cerebellum interpositus nucleus,UBERON:0002946,regional part of cerebellum
+DOID:11975,coloboma of optic nerve,DOID:1393,visual pathway disease
+UBERON:4300102,postcleithral scale,UBERON:0007380,dermal scale
+HP:0004047,Wide ulnar metaphysis,HP:0004039,Abnormality of ulnar metaphysis
+HP:0007430,Generalized edema,HP:0000969,Edema
+HP:0009427,Triangular shaped distal phalanx of the 3rd finger,HP:0009357,Abnormality of the distal phalanx of the 3rd finger
+CL:0000710,neurecto-epithelial cell,CL:0002077,ecto-epithelial cell
+UBERON:3000949,posterior ramus of cleithrum,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0006678,foramen secundum,UBERON:0004120,mesoderm-derived structure
+UBERON:0002341,epithelium of segmental bronchus,UBERON:0002031,epithelium of bronchus
+UBERON:0007613,extensor digitorum lateralis muscle,UBERON:0011024,extrinsic extensor muscle of manus
+HP:0010693,Pulverulent Cataract,HP:0007648,Punctate cataract
+HP:0001581,Recurrent skin infections,HP:0011123,Inflammatory abnormality of the skin
+DOID:7921,benign mediastinal psammomatous neurilemmoma,DOID:7922,benign mediastinal neurilemmoma
+HP:0100484,Symphalangism of the proximal phalanx of the 3rd toe with the 3rd metatarsal,HP:0010390,Triangular shaped phalanges of the 5th toe
+HP:0009017,Loss of gluteal subcutaneous adipose tissue,HP:0008887,Adipose tissue loss
+CL:0011000,dorsal horn interneuron,CL:0002611,neuron of the dorsal spinal cord
+UBERON:0010571,manual digit 2 metacarpus cartilage element,UBERON:0015044,manual digit 2 metacarpus endochondral element
+DOID:10011,thyroid lymphoma,DOID:1781,thyroid cancer
+DOID:2354,myelophthisic anemia,DOID:12449,aplastic anemia
+HP:0009129,Upper limb amyotrophy,HP:0002817,Abnormality of the upper limb
+HP:0011274,Recurrent mycobacterial infections,HP:0002718,Recurrent bacterial infections
+HP:0010503,Fibular duplication,HP:0002991,Abnormality of the fibula
+UBERON:0006779,superficial white layer of superior colliculus,UBERON:0006791,superficial layer of superior colliculus
+CL:0002444,Ly49H-positive natural killer cell,CL:0002438,NK1.1-positive natural killer cell
+UBERON:0012428,proximal convoluted tubule brush border,UBERON:0004120,mesoderm-derived structure
+HP:0008028,Cystoid macular degeneration,HP:0000608,Macular degeneration
+UBERON:0005764,acellular membrane,UBERON:0000476,acellular anatomical structure
+UBERON:2001302,vagal ganglion 1,UBERON:0009127,epibranchial ganglion
+HP:0010432,Absent distal phalanx of the 2nd toe,HP:0010645,Aplasia of the distal phalanges of the toes
+DOID:5494,epithelioid cell synovial sarcoma,DOID:5485,synovial sarcoma
+UBERON:0011359,urophysis,UBERON:0005174,dorsal region organ
+UBERON:0014375,intrinsic muscle of manus,UBERON:0001500,muscle of manus
+UBERON:0000155,theca cell layer,UBERON:0005156,reproductive structure
+UBERON:0011166,patellofemoral joint,UBERON:0011139,synovial limb joint
+UBERON:0014706,primitive renal collecting duct system,UBERON:0007501,arborizing epithelial duct system
+UBERON:0006865,metaphysis of femur,UBERON:0004120,mesoderm-derived structure
+UBERON:0006301,telencephalic part of interventricular foramen,UBERON:0004111,anatomical conduit
+UBERON:0004652,humerus diaphysis,UBERON:0004120,mesoderm-derived structure
+UBERON:0008434,cervical vertebral arch,UBERON:0004247,bone of dorsum
+CL:0000905,"effector memory CD4-positive, alpha-beta T cell",CL:0000897,"CD4-positive, alpha-beta memory T cell"
+UBERON:0004224,vas deferens smooth muscle,UBERON:0005156,reproductive structure
+DOID:3347,osteosarcoma,DOID:184,bone cancer
+DOID:12895,keratoconjunctivitis sicca,DOID:10140,dry eye syndrome
+DOID:8923,skin melanoma,DOID:4159,skin cancer
+CL:0000820,B-1a B cell,CL:0000819,B-1 B cell
+DOID:780,placenta disease,DOID:345,uterine disease
+DOID:106,pleural tuberculosis,DOID:0050598,extrapulmonary tuberculosis
+HP:0009391,Stippling of the epiphyses of the 5th finger,HP:0009152,Abnormality of the epiphyses of the 5th finger
+UBERON:0002931,dorsal septal nucleus,UBERON:0009663,telencephalic nucleus
+DOID:8208,lung superior sulcus carcinoma,DOID:8007,Pancoast tumor
+HP:0010530,Palatal myoclonus,HP:0001336,Myoclonus
+UBERON:0001340,dorsal artery of penis,UBERON:0003520,pelvis blood vessel
+UBERON:2002166,pseudourostyle,UBERON:0004120,mesoderm-derived structure
+HP:0009634,Patchy sclerosis of the proximal phalanx of the thumb,HP:0100913,Sclerosis of the proximal phalanx of the thumb
+UBERON:0001876,amygdala,UBERON:0005401,cerebral hemisphere grey matter
+UBERON:0002387,pes,UBERON:0008784,lower limb segment
+DOID:5896,ovarian clear cell cystadenofibroma,DOID:5897,ovarian clear cell adenofibroma
+HP:0000055,Abnormality of female external genitalia,HP:0000811,Abnormal external genitalia
+UBERON:2001531,epibranchial 4 cartilage,UBERON:2001908,epibranchial 4 element
+HP:0003808,Abnormal muscle tone,HP:0011804,Abnormality of muscle physiology
+UBERON:0011391,perineal nerve,UBERON:0002003,peripheral nerve
+HP:0012350,Decreased sialylation of N-linked protein glycosylation,HP:0012349,Abnormal sialylation of N-linked protein glycosylation
+UBERON:0010259,1st arch mesenchyme from neural crest,UBERON:0010042,1st arch mesenchyme
+UBERON:0010411,retroperitoneal fat pad,UBERON:0003427,abdominal fat pad
+UBERON:0000206,pharyngeal gill,UBERON:0002535,gill
+HP:0002912,Methylmalonic acidemia,HP:0004341,Abnormality of the vitamin B12 metabolism
+NCBITaxon:162997,Culex annulirostris,NCBITaxon:53527,Culex <subgenus>
+UBERON:0001894,diencephalon,UBERON:0002780,regional part of forebrain
+DOID:7664,endometrial mixed adenocarcinoma,DOID:2870,endometrial adenocarcinoma
+UBERON:0002633,motor nucleus of trigeminal nerve,UBERON:0009662,hindbrain nucleus
+HP:0008227,Pituitary resistance to thyroid hormone,HP:0011747,Abnormality of the anterior pituitary
+UBERON:2000203,rhinosphenoid,UBERON:0011164,neurocranium bone
+UBERON:0000163,embryonic cloaca,UBERON:0006554,urinary system structure
+HP:0100150,Fragmentation of the epiphysis of the middle phalanx of the 3rd toe,HP:0100059,Fragmentation of the epiphyses of the 3rd toe
+UBERON:0005832,cuneate fasciculus,UBERON:0001018,axon tract
+UBERON:3000003,alary process of premaxilla,UBERON:4100000,skeletal element projection
+CL:0002082,type II cell of adrenal medulla,CL:0000454,epinephrine secreting cell
+UBERON:2001825,urohyal lateral process,UBERON:0004120,mesoderm-derived structure
+UBERON:0005682,right lung accessory lobe bronchiole,UBERON:0003538,right lung bronchiole
+HP:0006482,Abnormality of dental morphology,HP:0000164,Abnormality of the teeth
+UBERON:0004363,aortic arch,UBERON:0003496,head blood vessel
+DOID:4163,ganglioneuroblastoma,DOID:769,neuroblastoma
+HP:0011110,Tonsillitis,HP:0100765,Abnormality of the tonsils
+HP:0100572,Fibrous cardiac diverticulum,HP:0100571,Cardiac diverticulum
+HP:0100376,Aplasia/Hypoplasia of the proximal phalanx of the 4th toe,HP:0010382,Abnormality of the proximal phalanx of the 4th toe
+HP:0005645,Intervertebral disk calcification,HP:0005108,Abnormality of the intervertebral disk
+UBERON:0004432,proximal epiphysis of distal phalanx of manual digit 2,UBERON:0004418,proximal epiphysis of phalanx of manual digit 2
+HP:0009555,Hypoplasia of the pharynx,HP:0000600,Abnormality of the pharynx
+CL:1000311,adipocyte of epicardial fat of left ventricle,CL:1000309,epicardial adipocyte
+HP:0009310,Broad proximal phalanx of the 4th finger,HP:0009404,Broad phalanges of the 4th finger
+UBERON:0004358,caput epididymis,UBERON:0014403,male anatomical structure
+HP:0010251,Irregular epiphyses of the distal phalanges of the hand,HP:0010243,Abnormality of the epiphyses of the distal phalanx of finger
+DOID:13832,patent ductus arteriosus,DOID:1682,congenital heart disease
+HP:0012097,Intracranial dermoid cyst,HP:0010576,Intracranial cystic lesion
+UBERON:0005111,metanephric pyramid,UBERON:0004200,kidney pyramid
+CL:0000792,"CD4-positive, CD25-positive, alpha-beta regulatory T cell",CL:0000624,"CD4-positive, alpha-beta T cell"
+UBERON:2001778,pelvic fin lepidotrichium 3,UBERON:4000173,pelvic fin lepidotrichium
+UBERON:0004262,upper leg skin,UBERON:0001511,skin of leg
+HP:0009477,Proximal/middle symphalangism of 4th finger,HP:0009314,Symphalangism affecting the proximal phalanx of the 4th finger
+UBERON:2000165,inferior lobe,UBERON:0003048,regional part of hypothalamus
+HP:0000630,Abnormality of retinal arteries,HP:0011004,Abnormality of the systemic arterial tree
+DOID:614,lymphopenia,DOID:615,leukopenia
+DOID:4334,splenic manifestation of prolymphocytic leukemia,DOID:710,splenic manifestation of leukemia
+DOID:13407,hypercalcemic sarcoidosis,DOID:11335,sarcoidosis
+DOID:2340,craniosynostosis,DOID:11971,synostosis
+DOID:3503,breast signet ring cell adenocarcinoma,DOID:3458,breast adenocarcinoma
+HP:0008551,Microtia,HP:0008772,Aplasia/Hypoplasia of the external ear
+DOID:5729,intravenous leiomyomatosis,DOID:5138,leiomyomatosis
+HP:0008684,Aplasia/hypoplasia of the uterus,HP:0000130,Abnormality of the uterus
+UBERON:0000049,spherical lensed eye,UBERON:0000047,simple eye
+DOID:66,muscle tissue disease,DOID:0080000,muscular disease
+DOID:2595,glottis cancer,DOID:2596,larynx cancer
+CL:0002182,surface mucosal cell of stomach,CL:0002180,mucous cell of stomach
+UBERON:0002593,orbital operculum,UBERON:0000477,anatomical cluster
+HP:0002193,Pseudobulbar behavioral symptoms,HP:0002200,Pseudobulbar signs
+UBERON:3000414,pars palatina of premaxilla,UBERON:0000064,organ part
+HP:0009981,Partial duplication of the distal phalanx of the 4th finger,HP:0010004,Partial duplication of the distal phalanges of the hand
+UBERON:0001066,intervertebral disk,UBERON:0011135,intervertebral cartilage
+HP:0003383,Onion bulb formation,HP:0003130,Abnormal peripheral myelination
+DOID:4080,tricuspid valve insufficiency,DOID:0050826,tricuspid valve disease
+UBERON:0003129,skull,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0015844,molar dental papilla,UBERON:0001763,odontogenic papilla
+UBERON:0004317,distal phalanx of pedal digit 3,UBERON:0014485,distal phalanx of digit 3
+HP:0010877,Unilateral strabismus,HP:0000486,Strabismus
+CL:0002529,CD1a-positive dermal dendritic cell,CL:0001006,dermal dendritic cell
+UBERON:0009771,left anterior cardinal vein,UBERON:0003087,anterior cardinal vein
+DOID:4374,silo filler's disease,DOID:850,lung disease
+HP:0010317,Scapular aplasia,HP:0006713,Aplasia/Hypoplasia of the scapulae
+HP:0100233,Stippling of the epiphysis of the proximal phalanx of the 5th toe,HP:0100099,Abnormality of the epiphysis of the proximal phalanx of the 5th toe
+HP:0001572,Macrodontia,HP:0006482,Abnormality of dental morphology
+HP:0010010,Abnormality of the 2nd metacarpal,HP:0001163,Abnormality of the metacarpal bones
+CL:0002435,"CD69-positive, CD8-positive single-positive thymocyte",CL:0000811,"CD8-positive, alpha-beta thymocyte"
+DOID:11197,serous conjunctivitis except viral,DOID:11184,acute conjunctivitis
+UBERON:2000558,posterior macula,UBERON:0000054,macula
+HP:0009303,Osteolytic defects of the distal phalanx of the 4th finger,HP:0004195,Osteolytic defects of the phalanges of the 4th finger
+DOID:0060057,gluten allergic reaction,DOID:3044,food allergy
+DOID:8259,bulbomembranous urethral cancer,DOID:736,male urethral cancer
+UBERON:0006835,arthropod oviduct,UBERON:0005156,reproductive structure
+UBERON:0011153,ventral hyoid arch skeleton,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009438,Absent middle phalanx of 3rd finger,HP:0009460,Aplasia of the 3rd finger
+UBERON:0000372,extensor digitorum brevis,UBERON:0001498,muscle of pes
+UBERON:0005055,zone of long bone,UBERON:0005913,zone of bone organ
+UBERON:0010311,scleral sesamoid bone,UBERON:0003462,facial bone
+CL:0001042,T-helper 22 cell,CL:0000492,CD4-positive helper T cell
+UBERON:0004363,aortic arch,UBERON:0002050,embryonic structure
+UBERON:2000438,parhypural,UBERON:2001364,hemal spine
+NCBITaxon:11176,Newcastle disease virus,NCBITaxon:260963,Avulavirus
+UBERON:0002499,cochlear labyrinth,UBERON:0004121,ectoderm-derived structure
+UBERON:0011847,acinus of parotid gland,UBERON:0011858,acinus of exocrine gland
+UBERON:0006878,decidua parietalis,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:660,adrenal cortex cancer,DOID:3953,adrenal gland cancer
+UBERON:0000912,mucus,UBERON:0000456,bodily secretion
+HP:0004432,Agammaglobulinemia,HP:0004313,Hypogammaglobulinemia
+UBERON:0010388,proximal segment of rib,UBERON:0004120,mesoderm-derived structure
+DOID:10842,Murray Valley encephalitis,DOID:934,viral infectious disease
+UBERON:0015112,distal tarsal bone 4 cartilage,UBERON:0015064,autopod cartilage
+HP:0002108,Spontaneous pneumothorax,HP:0002107,Pneumothorax
+UBERON:0006288,rib cartilage element,UBERON:0007844,cartilage element
+UBERON:0001594,azygos vein,UBERON:0001638,vein
+UBERON:0014603,paraventricular nucleus of the hypothalamus magnocellular division,UBERON:0003048,regional part of hypothalamus
+UBERON:0006920,esophagus squamous epithelium,UBERON:0006914,squamous epithelium
+UBERON:0004261,lower leg blood vessel,UBERON:0003503,leg blood vessel
+UBERON:3000783,fovea capitis of humerus,UBERON:0005055,zone of long bone
+HP:0002504,Calcification of the small brain vessels,HP:0004934,Vascular calcification
+DOID:14286,neurogenic arthropathy,DOID:381,arthropathy
+CL:0002572,vertebral mesenchymal stem cell,CL:0001035,bone cell
+HP:0011228,Horizontal eyebrow,HP:0000534,Abnormality of the eyebrow
+UBERON:0001881,island of calleja,UBERON:0009663,telencephalic nucleus
+HP:0012205,Globozoospermia,HP:0008669,Abnormal spermatogenesis
+HP:0007363,Aplasia/Hypoplasia of the pyramidal tract,HP:0002977,Aplasia/Hypoplasia involving the central nervous system
+UBERON:0004666,interventricular septum membranous part,UBERON:0000158,membranous layer
+UBERON:3000776,glenoid foramen,UBERON:3000755,pectoral girdle opening
+DOID:7474,malignant pleural mesothelioma,DOID:5158,pleural cancer
+DOID:9173,submandibular gland cancer,DOID:8850,salivary gland cancer
+UBERON:0002165,endocardium,UBERON:0002523,tunica intima
+HP:0010095,Partial duplication of the proximal phalanx of the hallux,HP:0010093,Duplication of the proximal phalanx of the hallux
+UBERON:2005013,concurrent branch afferent branchial artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0006481,Abnormality of primary teeth,HP:0000164,Abnormality of the teeth
+HP:0011011,Subacute,HP:0011008,Speed of onset
+HP:0000745,Diminished motivation,HP:0100851,Abnormal emotion/affect behavior
+UBERON:0009687,middle cardiac vein,UBERON:0004148,cardiac vein
+UBERON:0005356,Rathke's pouch,UBERON:0005423,developing anatomical structure
+HP:0004250,Proximally placed lunate,HP:0004239,Proximally placed carpal bones
+HP:0009108,Aplasia/Hypoplasia involving the femoral head and neck,HP:0009103,Aplasia/Hypoplasia involving the pelvis
+UBERON:0003707,sinus of Valsalva,UBERON:0004120,mesoderm-derived structure
+HP:0000295,Doll-like facies,HP:0001999,Abnormal facial shape
+UBERON:0011807,epidermis of feather follicle,UBERON:0000479,tissue
+CL:0000928,"activated CD4-negative, CD8-negative type I NK T cell",CL:0000912,helper T cell
+UBERON:0001864,scala tympani,UBERON:0010313,neural crest-derived structure
+CL:1000368,transitional myocyte of anterior division of left branch of atrioventricular bundle,CL:1000370,transitional myocyte of left branch of atrioventricular bundle
+HP:0010072,Patchy sclerosis of the 1st metatarsal,HP:0010063,Patchy sclerosis of the phalanges of the hallux
+HP:0008033,Congenital exotropia,HP:0000577,Exotropia
+UBERON:0009127,epibranchial ganglion,UBERON:0001714,cranial ganglion
+HP:0005066,Cone-shaped epiphyses fused within their metaphyses,HP:0010579,Cone-shaped epiphysis
+UBERON:3000810,fissura sagittalis,UBERON:0004120,mesoderm-derived structure
+UBERON:0001716,secondary palate,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:670,amphetamine abuse,DOID:302,substance abuse
+HP:0005261,Joint hemorrhage,HP:0001367,Abnormal joint morphology
+DOID:533,thymus gland disease,DOID:75,lymphatic system disease
+UBERON:0006765,left anterior vena cava,UBERON:0001638,vein
+HP:0011589,Common origin of the right brachiocephalic artery and left common carotid artery,HP:0011587,Abnormal branching pattern of the aortic arch
+HP:0010495,Amniotic constriction rings of legs,HP:0002814,Abnormality of the lower limb
+HP:0100484,Symphalangism of the proximal phalanx of the 3rd toe with the 3rd metatarsal,HP:0001440,Synostosis involving metatarsal bones
+UBERON:0008523,infrahyoid muscle,UBERON:0005493,hyoid muscle
+DOID:10790,chronic frontal sinusitis,DOID:10791,frontal sinusitis
+HP:0006543,Cardiorespiratory arrest,HP:0005943,Respiratory arrest
+UBERON:0006570,trabecula carnea of right ventricle,UBERON:0002511,trabecula carnea
+HP:0100915,Sclerosis of the distal phalanges of the hand,HP:0009832,Abnormality of the distal phalanx of finger
+DOID:6505,vaginal spindle cell epithelioma,DOID:135,benign vaginal carcinosarcoma
+UBERON:0005396,carotid artery segment,UBERON:0004573,systemic artery
+UBERON:0011345,pharyngeal raphe,UBERON:0003570,respiratory system connective tissue
+HP:0010064,Symphalangism affecting the phalanges of the hallux,HP:0010179,Symphalangism affecting the phalanges of the toes
+UBERON:0004715,annulus fibrosus disci intervertebralis,UBERON:0006444,annulus fibrosus
+DOID:1670,Behcet's syndrome arthropathy,DOID:381,arthropathy
+DOID:7713,tuberculum sellae meningioma,DOID:3643,sella turcica neoplasm
+HP:0005437,Recurrent infections in infancy and early childhood,HP:0002719,Recurrent infections
+DOID:6230,childhood teratoma of the ovary,DOID:5567,ovarian germ cell teratoma
+UBERON:0013417,epicranium,UBERON:0000477,anatomical cluster
+HP:0100367,Short phalanx of the 4th toe,HP:0010746,Hypoplasia of the phalanges of the toes
+HP:0100448,Curved proximal phalanx of the 5th toe,HP:0010386,Curved phalanges of the 5th toe
+HP:0010412,Duplication of the middle phalanx of the 2nd toe,HP:0010357,Abnormality of the middle phalanx of the 2nd toe
+HP:0009507,Irregular epiphysis of the distal phalanx of the 2nd finger,HP:0009493,Irregular epiphyses of the 2nd finger
+UBERON:0005686,caecum dorsal mesentery,UBERON:0002296,dorsal mesentery
+DOID:3413,alpha-mannosidosis,DOID:3211,lysosomal storage disease
+CL:0002487,cutaneous/subcutaneous mechanoreceptor cell,CL:0000199,mechanoreceptor cell
+UBERON:0002620,tuber cinereum,UBERON:0000477,anatomical cluster
+DOID:12549,hepatitis A,DOID:934,viral infectious disease
+HP:0002366,Abnormality of the lower motor neuron,HP:0000759,Abnormality of the peripheral nervous system
+DOID:2431,glomus tumor,DOID:3850,hemangiopericytic tumor
+HP:0012558,Abnormal T3/T4 ratio,HP:0002926,Abnormality of thyroid physiology
+HP:0011915,Cardiovascular calcification,HP:0010766,Ectopic calcification
+CL:0002063,type II pneumocyte,CL:0000157,surfactant secreting cell
+UBERON:0006919,tongue squamous epithelium,UBERON:0002424,oral epithelium
+UBERON:0005994,chordae tendineae,UBERON:0010313,neural crest-derived structure
+HP:0011012,Abnormality of polysaccharide metabolism,HP:0011013,Abnormality of carbohydrate metabolism/homeostasis
+DOID:12120,pulmonary alveolar proteinosis,DOID:850,lung disease
+HP:0009730,Rhabdomyoma,HP:0009728,Neoplasm of striated muscle
+HP:0000658,Eyelid apraxia,HP:0000492,Abnormality of the eyelid
+HP:0200001,Dysharmonic accelerated bone age,HP:0200000,Dysharmonic bone age
+UBERON:0008537,quadratus femoris,UBERON:0002000,gluteal muscle
+UBERON:4200159,ventral ridge system,UBERON:0005055,zone of long bone
+CL:0002411,"Vgamma1.1-positive, Vdelta6.3-negative thymocyte",CL:0002405,gamma-delta thymocyte
+UBERON:3000394,pars articularis of mandibular arch,UBERON:0010313,neural crest-derived structure
+DOID:0060066,pyridoxine-responsive sideroblastic anemia,DOID:8955,sideroblastic anemia
+UBERON:3000280,margo mandibularis of pterygoid,UBERON:0000064,organ part
+UBERON:0009505,associated mesenchyme of trachea,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000707,R7 photoreceptor cell,CL:0000287,eye photoreceptor cell
+CL:0000378,support cell (sensu Nematoda and Protostomia),CL:0000630,supportive cell
+UBERON:4200106,muscle scar,UBERON:4200047,attachment site
+UBERON:0001536,left common carotid artery plus branches,UBERON:0001530,common carotid artery plus branches
+CL:0000669,pericyte cell,CL:0002320,connective tissue cell
+UBERON:0014533,medullary lamina of thalamus,UBERON:0014531,lamina of diencephalon
+UBERON:4200119,pubis-ischium contact,UBERON:0004120,mesoderm-derived structure
+DOID:3892,insulinoma,DOID:1799,islet cell tumor
+UBERON:0003210,blood-cerebrospinal fluid barrier,UBERON:0000119,cell layer
+DOID:13564,aspergillosis,DOID:2473,opportunistic mycosis
+UBERON:0015220,inferior nasal meatus,UBERON:0015216,nasal meatus
+UBERON:0002138,habenulo-interpeduncular tract,UBERON:0005838,fasciculus of brain
+UBERON:1000014,right part of face,UBERON:0015212,lateral structure
+HP:0001308,Tongue fasciculations,HP:0000157,Abnormality of the tongue
+NCBITaxon:177875,SFV complex,NCBITaxon:11019,Alphavirus
+UBERON:2001905,epibranchial 1 element,UBERON:2001904,epibranchial element
+DOID:6245,renal oncocytoma,DOID:3116,kidney benign neoplasm
+DOID:11996,spermatic cord torsion,DOID:2519,testicular disease
+HP:0200134,Epileptic encephalopathy,HP:0001298,Encephalopathy
+DOID:0050838,segmental dystonia,DOID:543,dystonia
+DOID:8578,soft palate cancer,DOID:8618,oral cavity cancer
+CL:0002271,type EC1 enteroendocrine cell,CL:0000577,type EC enteroendocrine cell
+HP:0100122,Absent epiphysis of the proximal phalanx of the 2nd toe,HP:0100044,Absent epiphyses of the 2nd toe
+DOID:10952,nephritis,DOID:557,kidney disease
+HP:0000026,Male hypogonadism,HP:0000135,Hypogonadism
+DOID:3017,breast sarcoma,DOID:1612,breast cancer
+DOID:6688,autoimmune lymphoproliferative syndrome,DOID:2916,hypersensitivity reaction type IV disease
+UBERON:3000870,preacetabular expansion,UBERON:0005913,zone of bone organ
+UBERON:0004527,alveolar process of maxilla,UBERON:0004120,mesoderm-derived structure
+DOID:2671,transitional cell carcinoma,DOID:305,carcinoma
+UBERON:0004747,supraoccipital bone,UBERON:0002513,endochondral bone
+UBERON:3000401,pars facialis of maxillopalatine,UBERON:0010313,neural crest-derived structure
+HP:0009271,Triangular epiphysis of the proximal phalanx of the 4th finger,HP:0009248,Abnormality of the epiphysis of the proximal phalanx of the 4th finger
+UBERON:0012399,large intestine smooth muscle longitudinal layer,UBERON:0012369,longitudinal muscle layer
+CL:0002008,"CD34-positive, CD38-positive eosinophil progenitor cell",CL:0000611,eosinophil progenitor cell
+HP:0002093,Respiratory insufficiency,HP:0002795,Functional respiratory abnormality
+HP:0002101,Abnormal lung lobation,HP:0002088,Abnormality of the lung
+UBERON:0005667,connecting stalk mesoderm,UBERON:0000478,extraembryonic structure
+DOID:0050606,acrokeratosis verruciformis,DOID:161,keratosis
+UBERON:0012070,palatal tooth,UBERON:0003267,tooth of upper jaw
+HP:0009488,Absent epiphyses of the 2nd finger,HP:0006263,Abnormality of the epiphyses of the 2nd finger
+HP:0008940,Generalized lymphadenopathy,HP:0002716,Lymphadenopathy
+HP:0011839,Abnormality of T cell number,HP:0002843,Abnormality of T cells
+CL:0002255,stromal cell of endometrium,CL:0000499,stromal cell
+UBERON:0001178,visceral peritoneum,UBERON:0000064,organ part
+UBERON:0007375,roof of mouth,UBERON:0000481,multi-tissue structure
+UBERON:2005379,dorsal fin distal radial bone 8,UBERON:2105379,dorsal fin distal radial element 8
+UBERON:3010394,mesonephric late proximal tubule,UBERON:0004120,mesoderm-derived structure
+DOID:119,vaginal cancer,DOID:120,female reproductive organ cancer
+UBERON:4200081,hypocleideum,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0008081,Valgus foot deformity,HP:0001760,Abnormality of the foot
+UBERON:0005788,lamina rara interna,UBERON:0000476,acellular anatomical structure
+HP:0009848,Patchy sclerosis of the middle phalanges of the hand,HP:0100916,Sclerosis of the middle phalanges of the hand
+UBERON:0006742,canthus,UBERON:0004121,ectoderm-derived structure
+UBERON:0003073,lens placode,UBERON:0011814,non-neurogenic ectodermal placode
+DOID:11633,thyroid hormone resistance syndrome,DOID:1459,hypothyroidism
+DOID:4117,vaginal adenosarcoma,DOID:136,vaginal carcinosarcoma
+CL:0000717,fusimotor neuron,CL:0000100,motor neuron
+DOID:0060189,ileitis,DOID:8778,Crohn's disease
+DOID:12162,pseudoretinitis pigmentosa,DOID:12161,peripheral retinal degeneration
+CL:0002591,smooth muscle cell of the pulmonary artery,CL:0000359,vascular associated smooth muscle cell
+HP:0006521,Pulmonary lymphangiectasia,HP:0006529,Abnormal pulmonary lymphatics
+UBERON:2202279,pectoral fin distal radial cartilage 2,UBERON:2102279,pectoral fin distal radial element 2
+UBERON:3000003,alary process of premaxilla,UBERON:0010313,neural crest-derived structure
+UBERON:4200174,distal condyle of humerus,UBERON:0009988,condyle of humerus
+UBERON:0004581,systemic venous system,UBERON:0002049,vasculature
+UBERON:0000092,post-embryonic stage,UBERON:0000105,life cycle stage
+UBERON:0011909,gastrocnemius internus,UBERON:0004256,hindlimb zeugopod muscle
+HP:0010692,2-5 finger syndactyly,HP:0006101,Finger syndactyly
+CL:0000219,motile cell,CL:0000003,native cell
+DOID:0060067,Pearson syndrome,DOID:700,mitochondrial metabolism disease
+DOID:0050491,meningovascular neurosyphilis,DOID:9988,tertiary neurosyphilis
+HP:0012082,Cerebellar Purkinje layer atrophy,HP:0001272,Cerebellar atrophy
+UBERON:0012311,deep anterior cervical lymph node,UBERON:0012307,anterior cervical lymph node
+UBERON:0010128,future pterygopalatine ganglion,UBERON:0001808,parasympathetic ganglion
+HP:0009993,Complete duplication of the proximal phalanx of the 5th finger,HP:0009990,Duplication of the proximal phalanx of the 5th finger
+DOID:636,central pontine myelinolysis,DOID:936,brain disease
+DOID:10016,Wagenmann-Froboese syndrome,DOID:0050736,autosomal dominant disease
+DOID:7750,adult brain ependymoma,DOID:7497,brain ependymoma
+UBERON:0013515,subdivision of uterine tube,UBERON:0005156,reproductive structure
+HP:0100240,Synostosis of joints,HP:0011729,Abnormality of joint mobility
+UBERON:0006646,muscle layer of epididymis,UBERON:0006660,muscle layer
+HP:0005129,Congenital hypertrophy of left ventricle,HP:0001712,Left ventricular hypertrophy
+UBERON:2001304,vagal ganglion 3,UBERON:0009127,epibranchial ganglion
+HP:0003789,Minicore (multicore) myopathy,HP:0003198,Myopathy
+HP:0100372,Aplasia/Hypoplasia of the middle phalanx of the 3rd toe,HP:0010331,Aplasia/Hypoplasia of the 3rd toe
+UBERON:2005021,cerebellar central artery,UBERON:2005020,central artery
+DOID:1495,cystic echinococcosis,DOID:1496,echinococcosis
+UBERON:0009193,sphenoid cartilage element,UBERON:0004120,mesoderm-derived structure
+UBERON:0008583,transverse muscle of tongue,UBERON:0001576,intrinsic muscle of tongue
+UBERON:0002825,superior part of vestibular ganglion,UBERON:0010313,neural crest-derived structure
+HP:0004014,Broad radial epiphyseal plate,HP:0003999,Abnormality of radial epiphyses
+HP:0011623,Muscular ventricular septal defect,HP:0001629,Ventricular septal defect
+UBERON:0015423,hilar portion of hepatic duct,UBERON:0005171,hepatic duct
+UBERON:0000446,septum of telencephalon,UBERON:0004121,ectoderm-derived structure
+UBERON:3000832,anterior lamina recurvata,UBERON:0004121,ectoderm-derived structure
+CL:0000510,paneth cell,CL:0000323,lysozyme secreting cell
+UBERON:0004335,proximal phalanx of pedal digit 4,UBERON:0003868,proximal phalanx of pes
+DOID:12064,mediastinum neurofibroma,DOID:4691,malignant mediastinal neurogenic neoplasm
+DOID:0060155,visual agnosia,DOID:4090,agnosia
+HP:0009673,Stippling of the epiphysis of the proximal phalanx of the thumb,HP:0010266,Stippling of the epiphyses of the middle phalanges of the hand
+DOID:5453,pulmonary venoocclusive disease,DOID:6432,pulmonary hypertension
+UBERON:2001471,posterior lateral line system,UBERON:0002540,lateral line system
+UBERON:0009992,cranial sensory ganglion,UBERON:0001714,cranial ganglion
+UBERON:0005297,testis sex cord,UBERON:0005295,sex cord
+DOID:3534,Lafora disease,DOID:891,progressive myoclonus epilepsy
+UBERON:0005873,2nd arch pharyngeal cleft,UBERON:0005879,pharyngeal cleft
+HP:0006095,Wide tufts of distal phalanges,HP:0006200,Widened distal phalanges
+UBERON:0005349,paramedian lobule,UBERON:0004070,cerebellum vermis lobule
+HP:0010337,Aplasia/Hypoplasia of the 4th toe,HP:0010760,Absent toe
+DOID:9060,pityriasis versicolor,DOID:0050133,superficial mycosis
+HP:0001452,Autosomal dominant contiguous gene syndrome,HP:0001466,Contiguous gene syndrome
+UBERON:0002648,anterior median eminence,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010683,Low tissue non-specific alkaline phosphatase,HP:0003282,Low alkaline phosphatase
+CL:0010008,cardiac endothelial cell,CL:0000115,endothelial cell
+HP:0012110,Hypoplasia of the pons,HP:0007361,Abnormality of the pons
+UBERON:0006911,digestive system fluid or secretion,UBERON:0000463,portion of organism substance
+HP:0100573,Muscular cardiac diverticulum,HP:0100571,Cardiac diverticulum
+CL:0002282,type TG enteroendocrine cell,CL:0000509,gastrin secreting cell
+DOID:5547,pulmonary artery choriocarcinoma,DOID:175,vascular cancer
+UBERON:0001346,vaginal hymen,UBERON:0014404,female anatomical structure
+HP:0011072,Rootless teeth,HP:0006486,Abnormality of the dental root
+HP:0011347,Abnormality of ocular abduction,HP:0000496,Abnormality of eye movement
+HP:0007829,Diffuse retinal cone degeneration,HP:0000546,Retinal degeneration
+UBERON:0009664,gut mesentery,UBERON:0000477,anatomical cluster
+UBERON:0002621,regional part of cochlear nuclear complex,UBERON:0002678,regional part of medulla oblongata
+HP:0005764,Polyarticular arthritis,HP:0005195,Polyarticular arthropathy
+HP:0009836,Broad distal phalanx of finger,HP:0009832,Abnormality of the distal phalanx of finger
+HP:0007404,Nonepidermolytic palmoplantar keratoderma,HP:0000982,Palmoplantar keratoderma
+UBERON:0005062,neural fold,UBERON:0010371,ecto-epithelium
+UBERON:0004778,larynx submucosa,UBERON:0004119,endoderm-derived structure
+DOID:3376,bone osteosarcoma,DOID:3347,osteosarcoma
+HP:0010340,Polydactyly affecting the 4th toe,HP:0010112,Mesoaxial foot polydactyly
+UBERON:2001982,vertebral element 8,UBERON:0010913,vertebral element
+UBERON:4300017,rostrodermethmoid,UBERON:0008907,dermal bone
+DOID:10823,malignant essential hypertension,DOID:10824,malignant hypertension
+HP:0003809,"Nearly complete absence of metabolically active adipose tissue (subcutaneous, intraabdominal, intrathoracic)",HP:0009124,Abnormality of adipose tissue
+HP:0001473,Metatarsal osteolysis,HP:0009134,Osteolysis involving bones of the feet
+DOID:12639,pyloric stenosis,DOID:3122,gastric outlet obstruction
+UBERON:0003052,midbrain-hindbrain boundary,UBERON:0007651,anatomical junction
+UBERON:4300101,dorsal fin ceratotrichial spine,UBERON:0005174,dorsal region organ
+DOID:3821,posterior cerebral artery infarction,DOID:3527,cerebral arterial disease
+UBERON:2001948,anal-fin hook,UBERON:4100000,skeletal element projection
+HP:0012028,Hepatocellular adenoma,HP:0002896,Neoplasm of the liver
+HP:0009715,Papillary cystadenoma of the epididymis,HP:0009714,Abnormality of the epididymis
+UBERON:2002011,lateral fontanel of frontal,UBERON:0002221,fontanelle
+UBERON:0003133,reproductive organ,UBERON:0005156,reproductive structure
+HP:0010303,Abnormality of the spinal meninges,HP:0002143,Abnormality of the spinal cord
+HP:0100393,Short middle phalanx of the 4th toe,HP:0100373,Aplasia/Hypoplasia of the middle phalanx of the 4th toe
+UBERON:0014769,palpebral vein,UBERON:0009141,craniocervical region vein
+UBERON:0015048,basioccipital endochondral element,UBERON:0004120,mesoderm-derived structure
+UBERON:0005227,manual digit epithelium,UBERON:0010371,ecto-epithelium
+UBERON:2001534,pharyngobranchial 3 cartilage,UBERON:2001912,pharyngobranchial 3 element
+UBERON:0015110,distal tarsal bone 3 pre-cartilage condensation,UBERON:0015108,distal tarsal bone 3 endochondral element
+HP:0100731,Transverse facial cleft,HP:0011338,Abnormality of mouth shape
+HP:0010284,Intra-oral hyperpigmentation,HP:0100669,Abnormal pigmentation of oral cavity
+HP:0011855,Pharyngeal edema,HP:0000600,Abnormality of the pharynx
+UBERON:0005192,deferent duct artery,UBERON:0014403,male anatomical structure
+UBERON:0000044,dorsal root ganglion,UBERON:0010313,neural crest-derived structure
+UBERON:0014773,medial palpebral artery,UBERON:0004573,systemic artery
+UBERON:0013073,rattle,UBERON:0004529,anatomical projection
+HP:0010106,Aplasia of the proximal phalanx of the hallux,HP:0100388,Aplasia of the proximal phalanges of the toes
+NCBITaxon:121224,Pediculus humanus corporis,NCBITaxon:121225,Pediculus humanus
+CL:0002221,keratinized squamous cell of esophagus,CL:0002252,epithelial cell of esophagus
+HP:0010635,Partial hyposmia,HP:0004409,Hyposmia
+UBERON:2001300,vagal placode 4,UBERON:0003078,epibranchial placode
+DOID:0050254,acanthocephaliasis,DOID:883,parasitic helminthiasis infectious disease
+CL:1001567,lung endothelial cell,CL:0002139,endothelial cell of vascular tree
+HP:0100046,Cone-shaped epiphyses of the 2nd toe,HP:0010323,Abnormality of the epiphyses of the 2nd toe
+UBERON:0002235,tubercle of rib,UBERON:4100000,skeletal element projection
+HP:0009545,Symphalangism of the 2nd finger,HP:0009773,Symphalangism affecting the phalanges of the hand
+HP:0009908,Anterior creases of earlobe,HP:0000363,Abnormality of earlobe
+UBERON:0007163,superior nasal meatus,UBERON:0015216,nasal meatus
+DOID:2893,cervix carcinoma,DOID:4362,cervical cancer
+UBERON:3010447,M. extensor digitorum communis longus,UBERON:0010891,pectoral complex muscle
+UBERON:4100011,postacetabular buttress,UBERON:4100000,skeletal element projection
+UBERON:0006802,acetabular rim,UBERON:0005913,zone of bone organ
+UBERON:0015214,arcuate ligament,UBERON:0003570,respiratory system connective tissue
+UBERON:0009130,dorsal meso-duodenum,UBERON:0002050,embryonic structure
+HP:0005910,Rhomboid or triangular shaped 5th finger middle phalanx,HP:0009182,Triangular shaped middle phalanx of the 5th finger
+HP:0003875,Lytic defects (humeral),HP:0003063,Abnormality of the humerus
+UBERON:2005373,dorsal fin distal radial bone 2,UBERON:2105373,dorsal fin distal radial element 2
+HP:0011410,Caesarian section,HP:0001787,Abnormal delivery
+HP:0010993,Abnormality of the cerebral subcortex,HP:0002060,Abnormality of the cerebrum
+UBERON:0011602,gingiva of lower jaw,UBERON:0001828,gingiva
+UBERON:0001413,brachial vein,UBERON:0001638,vein
+UBERON:4300096,anal fin pterygiophore 1,UBERON:2001420,anal fin pterygiophore
+CL:1000358,microfold cell of epithelium proper of ileum,CL:1000353,microfold cell of epithelium of small intestine
+HP:0100819,Intestinal fistula,HP:0002242,Abnormality of the intestine
+DOID:4772,mesoblastic nephroma,DOID:263,kidney cancer
+UBERON:0003302,roof plate of metencephalon,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005835,cuneate fasciculus of spinal cord,UBERON:0005837,fasciculus of spinal cord
+HP:0005648,Bilateral ulnar hypoplasia,HP:0003022,Hypoplasia of the ulna
+UBERON:0005701,lower jaw molar odontogenic papilla,UBERON:0003324,mesenchyme of lower jaw
+HP:0005913,Abnormality of metacarpal epiphyses,HP:0001163,Abnormality of the metacarpal bones
+HP:0004828,Refractory anemia with ringed sideroblasts,HP:0012150,Single lineage myelodysplasia
+HP:0012603,Abnormal urine sodium concentration,HP:0012591,Abnormal urinary electrolyte concentration
+HP:0004000,Chevron-shaped/cone-shaped radial epiphyses,HP:0010579,Cone-shaped epiphysis
+CL:0002086,specialized cardiac myocyte,CL:0000746,cardiac muscle cell
+UBERON:0014604,paraventricular nucleus of the hypothalamus parvicellular division,UBERON:0003048,regional part of hypothalamus
+UBERON:0001416,skin of abdomen,UBERON:0003836,abdominal segment skin
+UBERON:0003561,forebrain dura mater,UBERON:0002092,brain dura mater
+HP:0008347,Decreased activity of mitochondrial complex IV,HP:0008972,Decreased activity of mitochondrial respiratory chain
+DOID:0080052,"acromesomelic dysplasia, Grebe type",DOID:0080049,acromesomelic dysplasia
+HP:0005304,Hypoplastic pulmonary veins,HP:0004930,Abnormality of the pulmonary vasculature
+UBERON:0003001,lemniscus,UBERON:0002616,regional part of brain
+UBERON:0013145,accessory saphenous vein,UBERON:0007318,saphenous vein
+CL:0002214,type IIa muscle cell,CL:0002210,red muscle cell
+CL:0002479,F4/80-positive adipose macrophage,CL:0002477,adipose macrophage
+HP:0002091,Restrictive lung disease,HP:0002088,Abnormality of the lung
+UBERON:4300003,urodermal bone,UBERON:0004376,fin bone
+UBERON:0015017,incus endochondral element,UBERON:0010363,endochondral element
+HP:0006514,Intraalveolar nodular calcifications,HP:0002088,Abnormality of the lung
+HP:0011358,Generalized hypopigmentation of hair,HP:0005599,Hypopigmentation of hair
+UBERON:0001292,distal convoluted tubule,UBERON:0004135,distal tubule
+HP:0006400,Absent knee epiphyses,HP:0010577,Absent epiphyses
+HP:0012133,Erythroid hypoplasia,HP:0012131,Abnormal number of erythroid precursors
+UBERON:0006214,carpus pre-cartilage condensation,UBERON:0010882,limb bone pre-cartilage condensation
+UBERON:3000597,symphysis maxillaris,UBERON:0004121,ectoderm-derived structure
+DOID:12259,hemophilia B,DOID:2214,inherited blood coagulation disease
+UBERON:3010653,ramus nasalis medialis,UBERON:0004529,anatomical projection
+UBERON:0001119,right lobe of thyroid gland,UBERON:0001118,lobe of thyroid gland
+UBERON:3000032,auditory muscles,UBERON:0002376,cranial muscle
+DOID:1525,nodular nonsuppurative panniculitis,DOID:1526,panniculitis
+UBERON:0015058,alisphenoid endochondral element,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3010560,anterior process of the palatoquadrate,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0200065,Choroidoretinal degeneration,HP:0000532,Chorioretinal abnormality
+HP:0009257,Pseudoepiphysis of the distal phalanx of the 4th finger,HP:0009249,Abnormality of the epiphysis of the distal phalanx of the 4th finger
+HP:0003782,Eunuchoid habitus,HP:0004323,Abnormality of body weight
+DOID:7079,adult cystic teratoma,DOID:2660,cystic teratoma
+HP:0011106,Hypovolemia,HP:0011104,Abnormality of blood volume homeostasis
+HP:0009242,Osteolytic defects of the distal phalanx of the 5th finger,HP:0004216,Osteolytic defects of the phalanges of the 5th finger
+UBERON:0003027,cingulate cortex,UBERON:0003022,cerebral cortex lobe
+UBERON:2001239,ceratobranchial 5 bone,UBERON:2000488,ceratobranchial bone
+UBERON:3010202,tail base gland,UBERON:3000982,tail external integument structure
+UBERON:0012621,muscle of Aristotle's lantern,UBERON:0004121,ectoderm-derived structure
+UBERON:0007475,matrix-based tissue,UBERON:0000479,tissue
+UBERON:0012348,autopod pad,UBERON:0015790,autopod skin
+UBERON:3000720,stegochordal,UBERON:0001075,vertebral centrum
+HP:0004261,Wide hamate bone,HP:0004260,Large hamate bone
+UBERON:4100012,postacetabular zone,UBERON:0005913,zone of bone organ
+UBERON:1500009,pelvic fin basipterygial radial,UBERON:2000508,pelvic fin radial bone
+HP:0006863,Severe expressive language delay,HP:0002474,Expressive language delay
+HP:0011743,Adrenal gland agenesis,HP:0008216,Adrenal gland dysgenesis
+UBERON:0011869,pisiform joint,UBERON:0011132,intercarpal joint
+HP:0004487,Acrobrachycephaly,HP:0000248,Brachycephaly
+DOID:10461,dentin caries,DOID:216,dental caries
+UBERON:0002951,regional part of intermediate hypothalamic region,UBERON:0003048,regional part of hypothalamus
+HP:0008733,Dysplastic testes,HP:0000035,Abnormality of the testis
+HP:0005891,Progressive forearm bowing,HP:0003956,Bowed forearm bones
+UBERON:0002260,ventral root of spinal cord,UBERON:0009623,spinal nerve root
+CL:0002506,liver CD103-positive dendritic cell,CL:0002454,"Cd4-negative, CD8_alpha-negative, CD11b-positive dendritic cell"
+UBERON:2001708,dermosphenotic,UBERON:2000376,infraorbital
+DOID:13364,chronobiology disease,DOID:863,nervous system disease
+HP:0000055,Abnormality of female external genitalia,HP:0010460,Abnormality of the female genitalia
+UBERON:0006245,humerus cartilage element,UBERON:0005258,upper arm mesenchyme
+UBERON:0001170,mesentery of small intestine,UBERON:0004854,gastrointestinal system mesentery
+UBERON:0003998,hyoid bone lesser horn,UBERON:0004119,endoderm-derived structure
+HP:0004920,Phenylpyruvic acidemia,HP:0001941,Acidosis
+HP:0012466,Chronic respiratory acidosis,HP:0005972,Respiratory acidosis
+UBERON:0005234,optic eminence ectoderm,UBERON:0000924,ectoderm
+HP:0009305,Distal/middle symphalangism of 4th finger,HP:0009282,Abnormality of the distal phalanx of the 4th finger
+HP:0012500,Verrucous papule,HP:0200034,Papule
+HP:0002946,Supernumerary vertebrae,HP:0009144,Supernumerary bones of the axial skeleton
+UBERON:2001523,hypobranchial 4 cartilage,UBERON:2001897,hypobranchial 4 element
+UBERON:0006849,scapula,UBERON:0002513,endochondral bone
+UBERON:0007612,extensor digitorum communis,UBERON:0011024,extrinsic extensor muscle of manus
+UBERON:0009647,tympanic membrane epithelium,UBERON:0010071,layer of tympanic membrane
+HP:0009478,Symphalangism of the proximal phalanx of the 4th finger with the 4th metatcarpal,HP:0009314,Symphalangism affecting the proximal phalanx of the 4th finger
+UBERON:2000196,dorsal hypohyal bone,UBERON:0002513,endochondral bone
+HP:0100481,Proximal/middle symphalangism of 4th toe,HP:0010390,Triangular shaped phalanges of the 5th toe
+UBERON:3000365,otic process,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:7103,diaphragma sellae meningioma,DOID:4437,skull base meningioma
+UBERON:0010536,nephron progenitor,UBERON:0000479,tissue
+DOID:6337,cerebellopontine angle meningioma,DOID:4211,posterior cranial fossa meningioma
+HP:0000592,Blue sclerae,HP:0000591,Abnormality of the sclera
+UBERON:0008435,vertebral arch of sacral segment,UBERON:0005179,pelvic region organ
+UBERON:0014539,precommissural fornix of forebrain,UBERON:0000052,fornix of brain
+UBERON:0013719,dartos muscle of scrotum,UBERON:0013718,dartos muscle
+UBERON:0003367,epithelium of vomeronasal organ,UBERON:0000490,unilaminar epithelium
+UBERON:0011977,epiphysis of proximal phalanx of manus,UBERON:0004387,epiphysis of phalanx of manus
+UBERON:0003686,tooth socket,UBERON:0002553,anatomical cavity
+UBERON:0003533,manual digit skin,UBERON:0001519,skin of manus
+HP:0005852,Limited elbow extension and supination,HP:0001377,Limited elbow extension
+UBERON:0001267,femoral nerve,UBERON:0002003,peripheral nerve
+UBERON:2002002,anterior distal serration of pectoral fin spine,UBERON:0004120,mesoderm-derived structure
+HP:0002982,Tibial bowing,HP:0002992,Abnormality of the tibia
+UBERON:0002900,transverse occipital sulcus,UBERON:0013118,sulcus of brain
+UBERON:2005012,afferent filamental artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0200107,Shortened inner dynein arms,HP:0200106,Absent/shortened dynein arms
+UBERON:0013508,thoracic vertebra pre-cartilage condensation,UBERON:0011095,vertebra pre-cartilage condensation
+UBERON:0006061,process of vertebra,UBERON:4100000,skeletal element projection
+DOID:1025,tuberculoid leprosy,DOID:1024,leprosy
+UBERON:0000072,segment of respiratory tract,UBERON:0004119,endoderm-derived structure
+DOID:6291,cerebral hemisphere lipoma,DOID:368,cerebrum cancer
+UBERON:0008549,prevertebral muscle of neck,UBERON:0014892,skeletal muscle organ
+HP:0004046,Spurred ulnar metaphysis,HP:0004039,Abnormality of ulnar metaphysis
+HP:0002511,Alzheimer disease,HP:0002011,Abnormality of the central nervous system
+UBERON:0015050,tarsus endochondral element,UBERON:0015063,autopod endochondral element
+HP:0009428,Curved distal phalanx of the 3rd finger,HP:0009357,Abnormality of the distal phalanx of the 3rd finger
+DOID:13790,acute tympanitis,DOID:5782,tympanic membrane disease
+HP:0200113,Aphalangy of hands and feet,HP:0005886,Aphalangy of the hands
+UBERON:0003274,mesothelium of omental bursa,UBERON:0001136,mesothelium
+UBERON:0004445,proximal epiphysis of proximal phalanx of manual digit 1,UBERON:0011977,epiphysis of proximal phalanx of manus
+UBERON:0010395,lymph node primary follicle,UBERON:0010422,primary nodular lymphoid tissue
+HP:0002121,Absence seizures,HP:0002197,Generalized seizures
+UBERON:0011864,tendon collagen fibril,UBERON:0011860,collagen fibril
+DOID:1358,maxillary sinus neoplasm,DOID:1350,paranasal sinus neoplasm
+HP:0002359,Frequent falls,HP:0002311,Incoordination
+HP:0009377,Patchy sclerosis of the phalanges of the 5th finger,HP:0100921,Sclerosis of the phalanges of the 5th finger
+CL:0000463,epidermal cell (sensu arthropoda),CL:0000362,epidermal cell
+UBERON:0011390,pudendal nerve,UBERON:0002003,peripheral nerve
+DOID:6553,posterior foramen magnum meningioma,DOID:4708,foramen magnum meningioma
+UBERON:0001884,phrenic nerve,UBERON:0002003,peripheral nerve
+DOID:7994,central nervous system osteosarcoma,DOID:502,central nervous system mesenchymal non-meningothelial tumor
+UBERON:0005293,cerebellum lobe,UBERON:0002749,regional part of cerebellar cortex
+UBERON:0012429,hemopoietic tissue,UBERON:0004120,mesoderm-derived structure
+DOID:5495,monophasic synovial sarcoma,DOID:5485,synovial sarcoma
+DOID:646,viral encephalitis,DOID:9588,encephalitis
+UBERON:0000156,theca externa,UBERON:0005156,reproductive structure
+HP:0009632,Curved proximal phalanx of the thumb,HP:0009618,Abnormality of the proximal phalanx of the thumb
+HP:0010529,Echolalia,HP:0002167,Neurological speech impairment
+HP:0004269,Subluxation of the small joints of the hand,HP:0006261,Abnormality of phalangeal joints of the hand
+DOID:1572,normal pressure hydrocephalus,DOID:1573,communicating hydrocephalus
+CL:0000904,"central memory CD4-positive, alpha-beta T cell",CL:0000897,"CD4-positive, alpha-beta memory T cell"
+DOID:3816,glossopharyngeal nerve paralysis,DOID:3418,glossopharyngeal nerve disease
+HP:0010846,EEG with persistent abnormal rhythmic activity,HP:0011176,EEG with constitutional variants
+UBERON:0011134,nonsynovial joint,UBERON:0000982,skeletal joint
+CL:0000832,eosinophilic myeloblast,CL:0000835,myeloblast
+UBERON:0003298,roof plate of neural tube,UBERON:0004121,ectoderm-derived structure
+HP:0008747,Cartilaginous ossification of larynx,HP:0001600,Abnormality of the larynx
+UBERON:0004125,myocardial compact layer,UBERON:0004123,myocardial layer
+DOID:418,systemic scleroderma,DOID:419,scleroderma
+UBERON:2002241,Purkinje cell layer valvula cerebelli,UBERON:0000479,tissue
+UBERON:0008269,nacre,UBERON:0004755,skeletal tissue
+UBERON:0010273,zone of hyoid bone,UBERON:0005913,zone of bone organ
+HP:0005882,Dermatoglyphic variants,HP:0001018,Abnormal palmar dermatoglyphics
+HP:0006585,Congenital pseudarthrosis of the clavicle,HP:0006710,Aplasia/Hypoplasia of the clavicles
+UBERON:0007355,bony part of pharyngotympanic tube,UBERON:0002481,bone tissue
+DOID:11766,blind hypotensive eye,DOID:790,ocular hypotension
+UBERON:3010125,musculus levator bulbi,UBERON:0001601,extra-ocular muscle
+CL:0000559,promonocyte,CL:0002194,monopoietic cell
+UBERON:0002886,lateral amygdaloid nucleus,UBERON:0002619,regional part of cerebral cortex
+HP:0001028,Hemangioma,HP:0008069,Neoplasm of the skin
+HP:0003565,Elevated erythrocyte sedimentation rate,HP:0001939,Abnormality of metabolism/homeostasis
+UBERON:0004329,proximal phalanx of manual digit 3,UBERON:0003637,manual digit 3 phalanx
+HP:0009573,Patchy sclerosis of the middle phalanx of the 2nd finger,HP:0009551,Patchy sclerosis of the phalanges of the 2nd finger
+HP:0000554,Uveitis,HP:0100533,Inflammatory abnormality of the eye
+HP:0011313,Narrow nail,HP:0002164,Nail dysplasia
+DOID:3181,oligodendroglioma,DOID:3070,malignant glioma
+UBERON:0001259,mucosa of urinary bladder,UBERON:0000344,mucosa
+UBERON:0000205,papula,UBERON:0002535,gill
+CL:0002445,Ly49D-negative natural killer cell,CL:0002438,NK1.1-positive natural killer cell
+HP:0009832,Abnormality of the distal phalanx of finger,HP:0005918,Abnormality of phalanx of finger
+HP:0002999,Patellar dislocation,HP:0003045,Abnormality of the patella
+UBERON:0008937,visceral hump,UBERON:0000475,organism subdivision
+UBERON:0015053,humerus endochondral element,UBERON:0015021,forelimb endochondral element
+DOID:7824,spinal multifocal clear cell meningioma,DOID:1140,spinal canal and spinal cord meningioma
+UBERON:0013718,dartos muscle,UBERON:0008982,fascia
+UBERON:0000048,pinhole eye,UBERON:0000047,simple eye
+CL:1001126,inner renal medulla vasa recta cell,CL:1000617,kidney inner medulla cell
+UBERON:2000508,pelvic fin radial bone,UBERON:1500006,paired fin radial bone
+CL:0011106,GABAnergic interplexiform cell,CL:0011104,interplexiform cell
+CL:0000879,meningeal macrophage,CL:0000878,central nervous system macrophage
+UBERON:0004190,renal glomerulus vasculature,UBERON:0004120,mesoderm-derived structure
+UBERON:0004437,proximal epiphysis of middle phalanx of manual digit 3,UBERON:0004419,proximal epiphysis of phalanx of manual digit 3
+UBERON:0005893,leg bone,UBERON:0003464,hindlimb bone
+UBERON:0001394,axillary artery,UBERON:0000063,organ segment
+HP:0003380,Decreased number of peripheral myelinated nerve fibers,HP:0003130,Abnormal peripheral myelination
+DOID:1252,trichuriasis,DOID:883,parasitic helminthiasis infectious disease
+UBERON:0005062,neural fold,UBERON:0005157,epithelial fold
+UBERON:0014400,hepatic sinusoidal space,UBERON:0014399,sinusoidal space
+HP:0010250,Fragmentation of the epiphyses of the distal phalanges of the hand,HP:0010243,Abnormality of the epiphyses of the distal phalanx of finger
+HP:0100695,Lipedema,HP:0009126,Increased adipose tissue
+NCBITaxon:423054,Eimeriorina,NCBITaxon:75739,Eucoccidiorida
+CL:1001602,cerebral cortex endothelial cell,CL:0000115,endothelial cell
+CL:0000836,promyelocyte,CL:0000763,myeloid cell
+HP:0012096,Intracranial epidermoid cyst,HP:0010576,Intracranial cystic lesion
+HP:0009456,Triangular shaped proximal phalanx of the 3rd finger,HP:0009858,Triangular shaped proximal phalanges of the hand
+HP:0007477,Abnormal dermatoglyphics,HP:0011356,Regional abnormality of skin
+UBERON:2001588,pectoral fin distal radial bone,UBERON:2001586,pectoral fin radial bone
+HP:0100038,Slow-growing scalp hair,HP:0002217,Slow-growing hair
+UBERON:0010056,future tongue,UBERON:0004121,ectoderm-derived structure
+HP:0003270,Abdominal distention,HP:0011458,Abdominal symptom
+UBERON:0004608,rib 9,UBERON:0002228,rib
+UBERON:0002643,decussation of medial lemniscus,UBERON:0014649,white matter of medulla oblongata
+DOID:13406,pulmonary sarcoidosis,DOID:11335,sarcoidosis
+UBERON:0006019,interdigital region between digits 2 and 3,UBERON:0006012,interdigital region
+UBERON:0007298,pronephric proximal convoluted tubule,UBERON:0006173,pronephric proximal tubule
+DOID:8633,chronic intestinal vascular insufficiency,DOID:5295,intestinal disease
+HP:0003148,Elevated serum acid phosphatase,HP:0004356,Abnormality of lysosomal metabolism
+UBERON:2001826,urohyal median process,UBERON:0004120,mesoderm-derived structure
+DOID:0060157,diffuse alopecia areata,DOID:986,alopecia areata
+CL:1001606,foreskin keratinocyte,CL:0000312,keratinocyte
+DOID:656,adrenal adenoma,DOID:0060089,endocrine organ benign neoplasm
+HP:0001600,Abnormality of the larynx,HP:0002087,Abnormality of the upper respiratory tract
+CL:0002183,stem cell of gastric gland,CL:0002180,mucous cell of stomach
+UBERON:0003422,mesenchyme of umbilical cord,UBERON:0003104,mesenchyme
+DOID:1749,squamous cell carcinoma,DOID:305,carcinoma
+HP:0012409,Cortical nephrocalcinosis,HP:0000121,Nephrocalcinosis
+CL:0000086,germ line stem cell (sensu Nematoda and Protostomia),CL:0000014,germ line stem cell
+UBERON:4200000,medial blade of ilium,UBERON:0004120,mesoderm-derived structure
+UBERON:0001491,wrist joint,UBERON:0001489,manus joint
+UBERON:0002137,aortic valve,UBERON:0005623,semi-lunar valve
+UBERON:0001660,maxillary vein,UBERON:0003502,neck blood vessel
+HP:0000509,Conjunctivitis,HP:0000502,Abnormality of the conjunctiva
+CL:0000793,"CD4-positive, alpha-beta intraepithelial T cell",CL:0000624,"CD4-positive, alpha-beta T cell"
+HP:0008185,Precocious puberty in males,HP:0000826,Precocious puberty
+HP:0010011,Abnormality of the 3rd metacarpal,HP:0001163,Abnormality of the metacarpal bones
+UBERON:0016475,skin of forehead,UBERON:1000021,skin of face
+HP:0006490,Abnormality of lower-limb metaphyses,HP:0000944,Abnormality of the metaphyses
+UBERON:0003860,hindlimb mesenchyme,UBERON:0009749,limb mesenchyme
+UBERON:0015051,exoccipital endochondral element,UBERON:0010363,endochondral element
+UBERON:0004328,proximal phalanx of manual digit 2,UBERON:0003636,manual digit 2 phalanx
+HP:0002548,Parkinsonism with favorable response to dopaminergic medication,HP:0001300,Parkinsonism
+UBERON:0002157,nucleus raphe pallidus,UBERON:0007635,nucleus of medulla oblongata
+DOID:5834,spermatocytoma,DOID:4440,seminoma
+UBERON:2000461,Weberian ossicle,UBERON:0004120,mesoderm-derived structure
+DOID:4976,elephantiasis,DOID:4977,lymphedema
+DOID:1802,mononeuritis,DOID:1188,mononeuropathy
+CL:0002458,langerin-positive dermal dendritic cell,CL:0002461,CD103-positive dendritic cell
+HP:0100916,Sclerosis of the middle phalanges of the hand,HP:0009833,Abnormality of the middle phalanges of the hand
+UBERON:3000397,pars dentalis of premaxilla,UBERON:0010313,neural crest-derived structure
+HP:0006646,Costal cartilage calcification,HP:0100593,Calcification of cartilage
+DOID:14670,"hypertelorism, microtia, facial clefting syndrome",DOID:0050737,autosomal recessive disease
+UBERON:0008815,pharyngeal slit,UBERON:0000062,organ
+UBERON:0014531,lamina of diencephalon,UBERON:0003931,diencephalic white matter
+HP:0003095,Septic arthritis,HP:0001369,Arthritis
+UBERON:0013733,caudal linear nucleus,UBERON:0002308,nucleus of brain
+DOID:4439,central nervous system germ cell tumor,DOID:3620,central nervous system cancer
+UBERON:0013478,cecal tonsil,UBERON:0001962,gut-associated lymphoid tissue
+HP:0009562,Patchy sclerosis of the distal phalanx of the 2nd finger,HP:0100900,Sclerosis of the distal phalanx of the 2nd finger
+UBERON:3000948,articular process,UBERON:0004530,bony projection
+UBERON:4200088,iliac peduncle of the pubis,UBERON:4100000,skeletal element projection
+HP:0100021,Cerebral palsy,HP:0011442,Abnormality of central motor function
+HP:0010265,Small epiphyses of the middle phalanges of the hand,HP:0010236,Small epiphyses of the phalanges of the hand
+UBERON:0001987,placenta,UBERON:0005156,reproductive structure
+HP:0004792,Rectoperineal fistula,HP:0100590,Rectal fistula
+HP:0100225,Bracket epiphysis of the proximal phalanx of the 5th toe,HP:0100078,Bracket epiphyses of the 5th toe
+UBERON:0009772,right anterior cardinal vein,UBERON:0003087,anterior cardinal vein
+UBERON:0013153,arachnoid villus,UBERON:0004529,anatomical projection
+UBERON:0001723,tongue,UBERON:0000020,sense organ
+HP:0100604,Neoplasm of the lip,HP:0000159,Abnormality of the lip
+HP:0100234,Triangular epiphysis of the proximal phalanx of the 5th toe,HP:0100099,Abnormality of the epiphysis of the proximal phalanx of the 5th toe
+HP:0005590,Spotty hypopigmentation,HP:0001053,Hypopigmented skin patches
+DOID:5240,retinal hemangioblastoma,DOID:5241,hemangioblastoma
+HP:0011588,Cervical aortic arch,HP:0011587,Abnormal branching pattern of the aortic arch
+UBERON:0006041,interdigital region between pedal digits 2 and 3,UBERON:0006014,interdigital region between pedal digits
+DOID:9369,orbital plasma cell granuloma,DOID:929,myopathy of extraocular muscle
+HP:0100172,Enlarged epiphysis of the distal phalanx of the 4th toe,HP:0100069,Enlarged epiphyses of the 4th toe
+HP:0007362,Aplasia/Hypoplasia of the brainstem,HP:0002977,Aplasia/Hypoplasia involving the central nervous system
+UBERON:2001059,cranial division of the internal carotid artery,UBERON:0004573,systemic artery
+UBERON:0014523,oculomotor division of oculomotor nuclear complex,UBERON:0007245,nuclear complex of neuraxis
+UBERON:0001777,substantia propria of cornea,UBERON:0003891,stroma
+HP:0001290,Generalized hypotonia,HP:0001252,Muscular hypotonia
+HP:0002947,Cervical kyphosis,HP:0005905,Abnormal cervical curvature
+HP:0008682,Acute tubular necrosis,HP:0000091,Abnormality of the renal tubule
+HP:0009710,Chilblain lesions,HP:0001167,Abnormality of finger
+HP:0006531,Pleural lymphangiectasia,HP:0002103,Abnormality of the pleura
+HP:0009112,Absent left hemidiaphragm,HP:0009109,Denervation of the diaphragm
+CL:0000503,theca cell,CL:0000593,androgen secreting cell
+HP:0010411,Triangular shaped middle phalanx of the 2nd toe,HP:0010357,Abnormality of the middle phalanx of the 2nd toe
+UBERON:2000296,uncrossed tecto-bulbar tract,UBERON:0002164,tectobulbar tract
+UBERON:0003071,eye primordium,UBERON:0005291,embryonic tissue
+CL:0000929,"CD4-negative, CD8-negative type I NK T cell secreting interferon-gamma",CL:0000912,helper T cell
+HP:0009562,Patchy sclerosis of the distal phalanx of the 2nd finger,HP:0009840,Patchy sclerosis of the distal phalanges of the hand
+CL:0002372,myotube,CL:0000228,multinucleate cell
+HP:0010399,Osteolytic defects of the proximal phalanx of the 2nd toe,HP:0010358,Abnormality of the proximal phalanx of the 2nd toe
+DOID:10843,Western equine encephalitis,DOID:934,viral infectious disease
+DOID:13238,Haverhill fever,DOID:0050338,primary bacterial infectious disease
+HP:0011953,Pulmonary lymphoma,HP:0100526,Neoplasm of the lungs
+DOID:5118,ovarian cystic teratoma,DOID:2660,cystic teratoma
+DOID:929,myopathy of extraocular muscle,DOID:930,orbital disease
+DOID:7097,macrocystic pattern testicular yolk sac tumor,DOID:5344,testicular yolk sac tumor
+UBERON:0012498,serosa of appendix,UBERON:0003335,serosa of colon
+HP:0000764,Peripheral axonal degeneration,HP:0000759,Abnormality of the peripheral nervous system
+UBERON:0003384,skeletal muscle tissue of pharynx,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0013226,accessory lacrimal gland,UBERON:0001817,lacrimal gland
+HP:0100337,Bilateral cleft palate,HP:0100338,Non-midline cleft palate
+DOID:0050921,pharynx squamous cell carcinoma,DOID:0060119,pharynx cancer
+HP:0006803,Vivid hallucinations,HP:0000738,Hallucinations
+DOID:2957,pulmonary tuberculosis,DOID:399,tuberculosis
+HP:0100849,Neoplasia of the scrotum,HP:0000045,Abnormality of the scrotum
+UBERON:0001270,bony pelvis,UBERON:0000075,subdivision of skeletal system
+HP:0012642,Cerebellar agenesis,HP:0007360,Aplasia/Hypoplasia of the cerebellum
+UBERON:0007702,tract of brain,UBERON:0001018,axon tract
+UBERON:0001882,nucleus accumbens,UBERON:0009663,telencephalic nucleus
+HP:0009985,Duplication of phalanx of 5th finger,HP:0009997,Duplication of phalanx of hand
+DOID:12841,ancylostomiasis,DOID:883,parasitic helminthiasis infectious disease
+HP:0000222,Gingival hyperkeratosis,HP:0000168,Abnormality of the gingiva
+UBERON:0015112,distal tarsal bone 4 cartilage,UBERON:0010885,hindlimb cartilage element
+CL:0000486,garland cell,CL:0000227,binucleate cell
+CL:0000570,parafollicular cell,CL:0000443,calcitonin secreting cell
+UBERON:0011782,feather follicle,UBERON:0000481,multi-tissue structure
+UBERON:0010759,equine distal sesamoid,UBERON:0011141,appendicular ossicle
+UBERON:0005418,hindlimb bud,UBERON:0004347,limb bud
+UBERON:0005346,cerebellum vermis lobule VIIb,UBERON:0004081,cerebellum vermis lobule VII
+HP:0009632,Curved proximal phalanx of the thumb,HP:0009653,Curved phalanges of the thumb
+HP:0004961,Pulmonary artery sling,HP:0004414,Abnormality of the pulmonary artery
+DOID:0050890,synucleinopathy,DOID:1289,neurodegenerative disease
+UBERON:0012437,epithelial-mesenchymal boundary,UBERON:0006677,surface of epithelium
+HP:0003974,Absent radius,HP:0006501,Aplasia/Hypoplasia of the radius
+UBERON:0009475,ampullar siphon,UBERON:0000026,appendage
+UBERON:2001164,supraneural 6 bone,UBERON:2000442,supraneural bone
+DOID:9742,pelvic varices,DOID:799,varicose veins
+UBERON:0000050,simple eye with multiple lenses,UBERON:0000047,simple eye
+DOID:8505,dermatitis herpetiformis,DOID:8502,bullous skin disease
+UBERON:2000701,ventral arrector,UBERON:2002147,arrector muscle
+UBERON:0003115,pharyngeal arch 4,UBERON:0002539,pharyngeal arch
+HP:0004540,"Congenital, generalized hypertrichosis",HP:0000998,Hypertrichosis
+DOID:9550,indolent myeloma,DOID:9538,multiple myeloma
+DOID:8683,myeloid sarcoma,DOID:2531,hematologic cancer
+UBERON:0006766,right anterior vena cava,UBERON:0001638,vein
+HP:0008568,Vestibular areflexia,HP:0007670,Abnormal vestibulo-ocular reflex
+HP:0001379,Degenerative joint disease,HP:0001367,Abnormal joint morphology
+UBERON:0007779,transduate,UBERON:0006314,bodily fluid
+UBERON:2007032,midbrain neural rod,UBERON:0005291,embryonic tissue
+HP:0200138,Bilateral choanal atresia/stenosis,HP:0000452,Choanal stenosis
+UBERON:0014914,blood-testis barrier,UBERON:0000119,cell layer
+DOID:0060088,vestibular gland benign neoplasm,DOID:0060086,female reproductive organ benign neoplasm
+HP:0003740,Myotonia with warm-up phenomenon,HP:0002486,Myotonia
+HP:0005143,Anomalous origin of right pulmonary artery from ascending aorta,HP:0011660,Anomalous origin of one pulmonary artery from ascending aorta
+HP:0010222,Abnormality of the epiphysis of the 3rd metacarpal,HP:0010011,Abnormality of the 3rd metacarpal
+HP:0010496,Hypertrophy of the lower limb,HP:0002814,Abnormality of the lower limb
+UBERON:0002396,vomer,UBERON:0003462,facial bone
+UBERON:0014277,piriform cortex layer 1,UBERON:0002791,regional part of telencephalon
+HP:0004955,Generalized arterial tortuosity,HP:0005116,Arterial tortuosity
+HP:0002972,Reduced delayed hypersensitivity,HP:0002963,Abnormal delayed hypersensitivity skin test
+UBERON:0006213,carpus cartilage element,UBERON:0010881,limb cartilage element
+HP:0009979,Complete duplication of the middle phalanx of the 4th finger,HP:0009976,Duplication of the middle phalanx of the 4th finger
+UBERON:4300105,caudal vertebra 1,UBERON:0001095,caudal vertebra
+DOID:11429,endometriosis of pelvic peritoneum,DOID:289,endometriosis
+UBERON:0010306,bulbar conjunctiva,UBERON:0010305,region of conjunctiva
+HP:0003907,Abnormality of the humeral metaphyses,HP:0009809,Abnormality of upper limb metaphysis
+UBERON:0014459,temporal fenestra,UBERON:0004705,fenestra
+UBERON:0004938,submucosa of biliary tree,UBERON:0000009,submucosa
+HP:0006834,Developmental stagnation at onset of seizures,HP:0007281,Developmental stagnation
+UBERON:0009506,associated mesenchyme of middle ear,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100368,Short phalanx of the 5th toe,HP:0010746,Hypoplasia of the phalanges of the toes
+UBERON:0002737,lateral inferior limiting sulcus,UBERON:0003022,cerebral cortex lobe
+UBERON:2001770,anal fin lepidotrichium 2,UBERON:4000176,anal fin lepidotrichium
+DOID:2498,tooth erosion,DOID:214,teeth hard tissue disease
+HP:0007033,Cerebellar dysplasia,HP:0001317,Abnormality of the cerebellum
+HP:0006762,Renal pelvic carcinoma,HP:0009726,Renal neoplasm
+UBERON:0007862,perichordal tissue,UBERON:0004120,mesoderm-derived structure
+HP:0009241,Bullet-shaped distal phalanx of the 5th finger,HP:0009375,Bullet-shaped phalanges of the 5th finger
+UBERON:0012324,transverse cervical artery,UBERON:0012320,cervical artery
+DOID:8093,maxillary sinus Schneiderian papilloma,DOID:1358,maxillary sinus neoplasm
+UBERON:0009600,mesenchyme of interdigital region of manus,UBERON:0003859,forelimb mesenchyme
+UBERON:2002214,os suspensorium medial flange,UBERON:0002513,endochondral bone
+HP:0005620,Hypermobility of interphalangeal joints,HP:0001382,Joint hypermobility
+UBERON:0000915,thoracic segment of trunk,UBERON:0011676,subdivision of organism along main body axis
+UBERON:2005265,hyomandibula-opercle joint,UBERON:0000982,skeletal joint
+DOID:3016,breast malignant phyllodes tumor,DOID:1612,breast cancer
+HP:0100461,Patchy sclerosis of the middle phalanx of the 3rd toe,HP:0100936,Sclerosis of the middle phalanx of the 3rd toe
+HP:0009536,Short 2nd finger,HP:0009381,Short finger
+HP:0001344,Absent speech,HP:0002167,Neurological speech impairment
+DOID:0060188,jejunoileitis,DOID:8778,Crohn's disease
+CL:0002412,"Vgamma1.1-positive, Vdelta6.3-positive thymocyte",CL:0002405,gamma-delta thymocyte
+UBERON:0010375,pancreas dorsal primordium,UBERON:0000481,multi-tissue structure
+UBERON:0003306,floor plate of neural tube,UBERON:0000073,regional part of nervous system
+UBERON:0000069,larval stage,UBERON:0000092,post-embryonic stage
+HP:0000744,Low frustration tolerance,HP:0100851,Abnormal emotion/affect behavior
+UBERON:0006090,glossopharyngeal nerve fiber bundle,UBERON:0002678,regional part of medulla oblongata
+HP:0009564,Triangular shaped distal phalanx of the 2nd finger,HP:0009875,Triangular shaped distal phalanges of the hand
+HP:0001018,Abnormal palmar dermatoglyphics,HP:0100871,Abnormality of the palm
+UBERON:0011806,dermis of feather follicle,UBERON:0000479,tissue
+UBERON:3000400,pars facialis of maxilla,UBERON:0010313,neural crest-derived structure
+CL:0002007,"Kit-low, CD34-positive eosinophil progenitor cell",CL:0000611,eosinophil progenitor cell
+CL:0001012,CD7-negative lymphoid progenitor OR granulocyte monocyte progenitor,CL:0001060,"hematopoietic oligopotent progenitor cell, lineage-negative"
+HP:0002810,Dumbbell-shaped metaphyses,HP:0000944,Abnormality of the metaphyses
+HP:0005548,Megakaryocytopenia,HP:0012143,Abnormality of cells of the megakaryocyte lineage
+DOID:678,progressive supranuclear palsy,DOID:480,movement disease
+HP:0010035,Aplasia of the 1st metacarpal,HP:0010242,Aplasia of the proximal phalanges of the hand
+HP:0002907,Microscopic hematuria,HP:0000790,Hematuria
+UBERON:0007606,ciliated stratified columnar epithelium,UBERON:0007601,ciliated epithelium
+HP:0000972,Palmoplantar hyperkeratosis,HP:0010765,Palmar hyperkeratosis
+DOID:3305,teratocarcinoma,DOID:3306,mixed germ cell cancer
+UBERON:0005787,lamina densa of glomerular basement membrane,UBERON:0000476,acellular anatomical structure
+UBERON:0002442,axillary nerve trunk,UBERON:0001147,trunk of peripheral nerve
+HP:0009342,Pseudoepiphysis of the distal phalanx of the 3rd finger,HP:0010253,Pseudoepiphyses of the distal phalanges of the hand
+HP:0100290,Abnormality of peripheral somatosensory evoked potentials,HP:0007377,Abnormality of somatosensory evoked potentials
+UBERON:0005467,platysma,UBERON:0004253,skin muscle
+HP:0011726,Persistent fetal circulation,HP:0010948,Abnormality of the fetal cardiovascular system
+UBERON:0002563,central nucleus of inferior colliculus,UBERON:0011214,nucleus of midbrain tectum
+UBERON:0008194,tibiotarsus,UBERON:0015011,tibiotarsus endochondral element
+UBERON:0011775,vagus nerve nucleus,UBERON:0009662,hindbrain nucleus
+UBERON:0005228,upper arm epithelium,UBERON:0010371,ecto-epithelium
+HP:0011096,Peripheral demyelination,HP:0003130,Abnormal peripheral myelination
+DOID:12163,senile reticular retinal degeneration,DOID:12161,peripheral retinal degeneration
+CL:0011105,dopamanergic interplexiform cell,CL:0011104,interplexiform cell
+CL:0002592,smooth muscle cell of the coronary artery,CL:0000359,vascular associated smooth muscle cell
+HP:0004327,Abnormality of the vitreous humor,HP:0004329,Abnormality of the posterior segment of the eye
+HP:0006711,Aplasia/Hypoplasia involving bones of the thorax,HP:0009122,Aplasia/Hypoplasia affecting bones of the axial skeleton
+HP:0000095,Abnormality of the glomerulus,HP:0012575,Abnormality of the nephron
+UBERON:0012356,pedal acropodium region,UBERON:0005445,segment of pes
+UBERON:0005420,pelvic appendage bud,UBERON:0004357,paired limb/fin bud
+DOID:4066,anus rhabdomyosarcoma,DOID:4067,anus sarcoma
+DOID:437,myasthenia gravis,DOID:438,autoimmune disease of the nervous system
+HP:0000418,Narrow nasal ridge,HP:0011119,Abnormality of the nasal dorsum
+UBERON:0006849,scapula,UBERON:0015057,scapula endochondral element
+UBERON:0009968,primitive superior sagittal sinus,UBERON:0001638,vein
+UBERON:0005993,pulmonary valve anulus,UBERON:0010313,neural crest-derived structure
+UBERON:0014374,embryoid body,UBERON:0002050,embryonic structure
+HP:0100175,Ivory epiphysis of the distal phalanx of the 4th toe,HP:0100072,Ivory epiphyses of the 4th toe
+HP:0000297,Facial hypotonia,HP:0000301,Abnormality of facial musculature
+HP:0011943,Increased urinary thiosulfate,HP:0004369,Decreased purine levels
+DOID:13402,skin sarcoidosis,DOID:37,skin disease
+UBERON:0001274,ischium,UBERON:0008202,bone of hip region
+DOID:0050458,juvenile myelomonocytic leukemia,DOID:4972,myelodysplastic myeloproliferative cancer
+UBERON:4300012,clavus,UBERON:0000026,appendage
+UBERON:3010735,ramus anterior of CN VIII,UBERON:0004121,ectoderm-derived structure
+HP:0009794,Branchial anomaly,HP:0000464,Abnormality of the neck
+HP:0011265,Cleft earlobe,HP:0000363,Abnormality of earlobe
+HP:0001552,Barrel-shaped chest,HP:0100625,Enlarged thorax
+UBERON:0006785,gray matter of superior colliculus,UBERON:0003528,brain grey matter
+UBERON:0003920,venous blood vessel,UBERON:0001981,blood vessel
+DOID:0060065,pyridoxine-refractory autosomal recessive sideroblastic anemia,DOID:8955,sideroblastic anemia
+UBERON:0006289,rib pre-cartilage condensation,UBERON:0005181,thoracic segment organ
+UBERON:2001522,hypobranchial cartilage,UBERON:0011004,pharyngeal arch cartilage
+HP:0003182,Shallow acetabular fossae,HP:0003170,Abnormality of the acetabulum
+UBERON:0006658,interphalangeal joint,UBERON:0003841,autopod joint
+HP:0011322,Right unilambdoid synostosis,HP:0011320,Unilambdoid synostosis
+HP:0007700,Anterior segment dysgenesis,HP:0000593,Abnormality of the anterior chamber
+UBERON:0004336,proximal phalanx of pedal digit 5,UBERON:0003868,proximal phalanx of pes
+UBERON:2001039,sclerotome somite 19,UBERON:0003089,sclerotome
+DOID:2089,constipation,DOID:9779,bowel dysfunction
+UBERON:0001855,cochlear duct of membranous labyrinth,UBERON:0004121,ectoderm-derived structure
+UBERON:2005025,dorsal longitudinal anastomotic vessel,UBERON:0003513,trunk blood vessel
+HP:0005474,Decreased calvarial ossification,HP:0002683,Abnormality of the calvaria
+CL:0012000,astrocyte of the forebrain,CL:0000127,astrocyte
+CL:1000497,kidney cell,CL:0002371,somatic cell
+UBERON:0010084,future diaphragm,UBERON:0000481,multi-tissue structure
+UBERON:3010665,ramule palatinus,UBERON:3010661,ramus nasalis internus
+UBERON:0005866,pre-cartilage condensation,UBERON:0005856,developing mesenchymal condensation
+UBERON:0005928,external naris,UBERON:0004121,ectoderm-derived structure
+UBERON:3000516,pseudobasal process,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0011204,EEG with continuous slow activity,HP:0010845,EEG with generalized slow activity
+UBERON:0005176,tooth enamel organ,UBERON:0000481,multi-tissue structure
+HP:0008607,Progressive conductive hearing impairment,HP:0000405,Conductive hearing impairment
+CL:0000776,immature neutrophil,CL:0000775,neutrophil
+UBERON:2001305,vagal ganglion 4,UBERON:0009127,epibranchial ganglion
+UBERON:2000859,specialized hemal arch and spine,UBERON:0002513,endochondral bone
+HP:0010614,Fibroma,HP:0012316,Fibrous tissue neoplasm
+HP:0009169,Broad middle phalanx of the 5th finger,HP:0009374,Broad phalanges of the 5th finger
+UBERON:0003858,lower eyelid mesenchyme,UBERON:0010330,eyelid mesenchyme
+UBERON:0014671,distal interphalangeal joint of manural digit 5,UBERON:0007732,interphalangeal joint of manual digit 5
+DOID:5157,benign pleural mesothelioma,DOID:2645,benign mesothelioma
+HP:0009115,Aplasia/Hypoplasia involving the skeleton,HP:0011842,Abnormality of skeletal morphology
+CL:1000703,kidney pelvis urothelial cell,CL:1000706,ureter urothelial cell
+UBERON:0010721,distal tarsal bone,UBERON:0015099,distal tarsal bone endochondral element
+DOID:5855,anteroseptal myocardial infarction,DOID:5844,myocardial infarction
+CL:0002176,secondary follicular cell of ovary,CL:0002174,follicular cell of ovary
+HP:0100364,Aplasia of the phalanges of the 5th toe,HP:0010745,Aplasia of the phalanges of the toes
+HP:0010585,Small epiphyses,HP:0005930,Abnormality of the epiphyses
+UBERON:0001948,regional part of spinal cord,UBERON:0004121,ectoderm-derived structure
+UBERON:0013631,sesamoid element,UBERON:0010911,ossicle
+UBERON:0002325,epithelium of urethra,UBERON:0006555,excretory tube
+UBERON:0006553,renal duct,UBERON:0006555,excretory tube
+UBERON:0005493,hyoid muscle,UBERON:0002377,muscle of neck
+UBERON:0010713,paired fin skeleton,UBERON:0012353,fin skeleton
+UBERON:0005903,duct of seminal vesicle,UBERON:0005904,duct of male reproductive system
+UBERON:3000590,supraorbital flange,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0006051,Metacarpal periosteal thickening,HP:0001163,Abnormality of the metacarpal bones
+HP:0012600,Abnormal urine chloride concentration,HP:0012591,Abnormal urinary electrolyte concentration
+HP:0012254,Ewing's sarcoma,HP:0100242,Sarcoma
+HP:0005110,Atrial fibrillation,HP:0001692,Primary atrial arrhythmia
+DOID:9551,smoldering myeloma,DOID:9538,multiple myeloma
+HP:0004844,Coombs-positive hemolytic anemia,HP:0001878,Hemolytic anemia
+HP:0004225,Abnormality of the distal phalanx of the 5th finger,HP:0004213,Abnormality of the phalanges of the 5th finger
+HP:0011071,Abnormality of permanent molar morphology,HP:0011070,Abnormality of molar morphology
+HP:0009546,Triangular shaped phalanges of the 2nd finger,HP:0009774,Triangular shaped phalanges of the hand
+DOID:14669,acrodysostosis,DOID:1934,dysostosis
+UBERON:2000039,median axial vein,UBERON:0001638,vein
+UBERON:0011950,mammary gland luminal epithelium,UBERON:0005156,reproductive structure
+HP:0010747,Medial flaring of the eyebrow,HP:0000534,Abnormality of the eyebrow
+HP:0001472,Familial predisposition,HP:0000005,Mode of inheritance
+UBERON:4100010,post-glenoid process,UBERON:4100000,skeletal element projection
+CL:0002363,keratocyte,CL:0000005,fibroblast neural crest derived
+CL:0000570,parafollicular cell,CL:0000458,serotonin secreting cell
+HP:0012487,Cerebellopontine angle arachnoid cyst,HP:0100702,Arachnoid cyst
+UBERON:0002261,dorsal root of spinal cord,UBERON:0009623,spinal nerve root
+HP:0009239,Aplasia/Hypoplasia of the distal phalanx of the 5th finger,HP:0004225,Abnormality of the distal phalanx of the 5th finger
+UBERON:0013244,vaginal plate,UBERON:0004120,mesoderm-derived structure
+UBERON:0010421,spleen B cell corona,UBERON:0010755,secondary follicle corona
+NCBITaxon:447134,Myodes,NCBITaxon:39087,Arvicolinae
+DOID:1932,Angelman syndrome,DOID:0080014,chromosomal disease
+UBERON:0003540,right lung terminal bronchiole,UBERON:0002187,terminal bronchiole
+DOID:5403,microcystic adenoma,DOID:657,adenoma
+DOID:13240,tooth resorption,DOID:214,teeth hard tissue disease
+HP:0012467,Acute respiratory acidosis,HP:0005972,Respiratory acidosis
+UBERON:0005879,pharyngeal cleft,UBERON:0000490,unilaminar epithelium
+HP:0100079,Cone-shaped epiphyses of the 5th toe,HP:0010341,Abnormality of the epiphyses of the 5th toe
+HP:0009099,Median cleft palate,HP:0000175,Cleft palate
+UBERON:2000289,preopercle horizontal limb,UBERON:0008907,dermal bone
+DOID:399,tuberculosis,DOID:0050338,primary bacterial infectious disease
+UBERON:2002033,prootic-pterosphenoid joint,UBERON:0000982,skeletal joint
+UBERON:0004722,deep cervical lymph node,UBERON:0002429,cervical lymph node
+HP:0012261,Abnormal respiratory motile cilium physiology,HP:0002795,Functional respiratory abnormality
+UBERON:0007627,magnocellular nucleus of stria terminalis,UBERON:0009663,telencephalic nucleus
+DOID:1969,cerebral palsy,DOID:936,brain disease
+DOID:11227,acute hemorrhagic conjunctivitis,DOID:934,viral infectious disease
+DOID:1062,Fanconi syndrome,DOID:447,renal tubular transport disease
+CL:0002416,"mature Vgamma1.1-positive, Vdelta6.3-positive thymocyte",CL:0002412,"Vgamma1.1-positive, Vdelta6.3-positive thymocyte"
+HP:0002136,Broad-based gait,HP:0001288,Gait disturbance
+HP:0005168,Elevated right atrial pressure,HP:0005120,Abnormality of cardiac atrium
+HP:0100045,Bracket epiphyses of the 2nd toe,HP:0010323,Abnormality of the epiphyses of the 2nd toe
+UBERON:0000199,neck of radius,UBERON:0005055,zone of long bone
+DOID:0050796,achalasia microcephaly syndrome,DOID:0050737,autosomal recessive disease
+UBERON:2001475,sublingual dorsal ossification,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:12326,chronic pulmonary heart disease,DOID:8515,Cor pulmonale
+CL:0002501,type D1 enteroendocrine cell,CL:0002268,P/D1 enteroendocrine cell
+UBERON:3000664,hyoid plate,UBERON:0000064,organ part
+HP:0002681,Deformed sella turcica,HP:0002679,Abnormality of the sella turcica
+UBERON:0012376,retromolar triangle,UBERON:0000479,tissue
+HP:0003174,Abnormality of the ischium,HP:0003272,Abnormality of the hip bone
+HP:0003109,Hyperphosphaturia,HP:0012599,Abnormal urine phosphate concentration
+UBERON:0013494,keratin-coated spine,UBERON:0001037,strand of hair
+UBERON:0014689,middle temporal sulcus,UBERON:0003022,cerebral cortex lobe
+HP:0100223,Triangular epiphysis of the middle phalanx of the 5th toe,HP:0100087,Triangular epiphyses of the 5th toe
+UBERON:0004453,metacarpus region,UBERON:0009877,metapodium region
+CL:0000774,band form eosinophil,CL:0000772,immature eosinophil
+UBERON:0007236,8 cell stage,UBERON:0000067,embryo stage part
+UBERON:0002021,occipital lobe,UBERON:0004121,ectoderm-derived structure
+DOID:2718,hemopneumothorax,DOID:1673,pneumothorax
+UBERON:3000467,preorbital process of the pars facialis of the maxilla,UBERON:0010313,neural crest-derived structure
+UBERON:0011090,skeleton of right pelvic girdle,UBERON:0007832,pelvic girdle skeleton
+UBERON:0013695,colon endothelium,UBERON:0000397,colonic epithelium
+UBERON:0006568,hypothalamic nucleus,UBERON:0003048,regional part of hypothalamus
+UBERON:2001038,sclerotome somite 16,UBERON:0003089,sclerotome
+HP:0005465,Facial hyperostosis,HP:0004493,Craniofacial hyperostosis
+HP:0004358,Abnormality of superoxide metabolism,HP:0001939,Abnormality of metabolism/homeostasis
+HP:0001171,Split hand,HP:0100257,Ectrodactyly
+UBERON:0007657,anular ligament of radius,UBERON:0000211,ligament
+UBERON:0011865,corneal stroma collagen fibril,UBERON:0011860,collagen fibril
+CL:1001097,kidney afferent arteriole smooth muscle cell,CL:1001006,kidney afferent arteriole cell
+UBERON:0006133,funiculus of neuraxis,UBERON:0000122,neuron projection bundle
+UBERON:0003562,midbrain dura mater,UBERON:0002092,brain dura mater
+HP:0012008,Illusory auras,HP:0012002,Experiential auras
+UBERON:3000662,processus posterior of parasphenoid,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2000629,caudal motor nucleus of abducens,UBERON:0006331,brainstem nucleus
+HP:0006572,Subacute progressive viral hepatitis,HP:0006562,Viral hepatitis
+HP:0002888,Ependymoma,HP:0009733,Glioma
+UBERON:1500008,pelvic fin distal radial bone,UBERON:2000508,pelvic fin radial bone
+HP:0003158,Hyposthenuria,HP:0003110,Abnormality of urine homeostasis
+UBERON:0005481,tentorial sinus,UBERON:0001638,vein
+UBERON:0005932,bulb of hair follicle,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2002223,pillar of the semicircular canal,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002238,false rib,UBERON:0002228,rib
+UBERON:0003553,diencephalon pia mater,UBERON:0003550,forebrain pia mater
+UBERON:0007625,pigment epithelium of eye,UBERON:0000483,epithelium
+HP:0009969,Partial duplication of the middle phalanx of the 3rd finger,HP:0009963,Duplication of the middle phalanx of the 3rd finger
+HP:0009219,Irregular epiphysis of the middle phalanx of the 4th finger,HP:0009398,Irregular epiphyses of the 4th finger
+CL:0002478,F4/80-negative adipose macrophage,CL:0002477,adipose macrophage
+UBERON:0006114,lateral occipital cortex,UBERON:0003022,cerebral cortex lobe
+UBERON:0006612,shell,UBERON:0000477,anatomical cluster
+UBERON:0005502,rhombomere roof plate,UBERON:0004121,ectoderm-derived structure
+HP:0100857,Flat sella turcica,HP:0002681,Deformed sella turcica
+UBERON:0003244,epithelium of mammary gland,UBERON:0005156,reproductive structure
+CL:0002342,circulating endothelial cell,CL:0000115,endothelial cell
+HP:0003876,Osteoporotic humerus,HP:0003063,Abnormality of the humerus
+UBERON:0001779,iris stroma,UBERON:0003891,stroma
+DOID:322,myelitis,DOID:331,central nervous system disease
+HP:0009126,Increased adipose tissue,HP:0009124,Abnormality of adipose tissue
+HP:0009935,Aplasia/Hypoplasia of the nasal septum,HP:0000419,Abnormality of the nasal septum
+HP:0009947,Duplication of the proximal phalanx of the 2nd finger,HP:0009945,Duplication of phalanx of 2nd finger
+HP:0003099,Fibular overgrowth,HP:0002991,Abnormality of the fibula
+HP:0006528,Chronic lung disease,HP:0002088,Abnormality of the lung
+UBERON:0002933,nucleus of anterior commissure,UBERON:0009663,telencephalic nucleus
+HP:0003298,Spina bifida occulta,HP:0002414,Spina bifida
+UBERON:0006236,tetrapod frontal bone primordium,UBERON:0001048,primordium
+CL:0000688,perijunctional fibroblast,CL:0000057,fibroblast
+HP:0011105,Hypervolemia,HP:0011104,Abnormality of blood volume homeostasis
+HP:0006288,Advanced eruption of teeth,HP:0006292,Abnormality of dental eruption
+UBERON:3010201,dorsal tail tubercle,UBERON:3000982,tail external integument structure
+HP:0002488,Acute leukemia,HP:0001909,Leukemia
+UBERON:0003910,splenic sinusoid,UBERON:0003909,sinusoid
+HP:0010982,Polygenic inheritance,HP:0001426,Multifactorial inheritance
+DOID:0050308,Alkhurma hemorrhagic fever,DOID:11320,Kyasanur forest disease
+HP:0009330,Stippling of the epiphysis of the middle phalanx of the 3rd finger,HP:0009419,Stippling of the epiphyses of the 3rd finger
+DOID:0050837,multifocal dystonia,DOID:543,dystonia
+DOID:3924,main bronchus cancer,DOID:1324,lung cancer
+HP:0009576,Absent middle phalanx of 2nd finger,HP:0010239,Aplasia of the middle phalanx of the hand
+HP:0100435,Bullet-shaped middle phalanx of the 4th toe,HP:0010373,Bullet-shaped phalanges of the 4th toe
+HP:0003571,Propionicacidemia,HP:0001941,Acidosis
+NCBITaxon:206160,Sandfly fever Naples virus,NCBITaxon:11584,Phlebovirus
+HP:0011032,Abnormality of fluid regulation,HP:0001939,Abnormality of metabolism/homeostasis
+UBERON:0001642,superior sagittal sinus,UBERON:0004121,ectoderm-derived structure
+UBERON:0000040,Leydig's organ,UBERON:0005057,immune organ
+DOID:5996,blunt duct adenosis of breast,DOID:5997,non-proliferative fibrocystic change of the breast
+UBERON:0011004,pharyngeal arch cartilage,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005295,sex cord,UBERON:0005291,embryonic tissue
+HP:0001718,Mitral stenosis,HP:0001633,Abnormality of the mitral valve
+HP:0012083,Ubiquitin-positive cerebral inclusion bodies,HP:0100314,Cerebral inclusion bodies
+HP:0002218,Silver-gray hair,HP:0011358,Generalized hypopigmentation of hair
+UBERON:3000673,posteromedial process,UBERON:0004529,anatomical projection
+HP:0100467,Patchy sclerosis of the distal phalanx of the 3rd toe,HP:0010190,Patchy sclerosis of the distal phalanges of the toes
+HP:0001123,Visual field defect,HP:0000504,Abnormality of vision
+UBERON:0007502,epithelial plexus,UBERON:0003914,epithelial tube
+DOID:1245,vulva cancer,DOID:120,female reproductive organ cancer
+HP:0012566,Premature epimetaphyseal fusion in radius,HP:0010588,Premature epimetaphyseal fusion
+HP:0004045,Sloping ulnar metaphysis,HP:0004039,Abnormality of ulnar metaphysis
+HP:0009258,Small epiphysis of the distal phalanx of the 4th finger,HP:0009249,Abnormality of the epiphysis of the distal phalanx of the 4th finger
+HP:0009304,Patchy sclerosis of the distal phalanx of the 4th finger,HP:0009282,Abnormality of the distal phalanx of the 4th finger
+UBERON:0002078,right cardiac atrium,UBERON:0002081,cardiac atrium
+HP:0008515,Aplasia/Hypoplasia of the vertebrae,HP:0008518,Aplasia/Hypoplasia involving the vertebral column
+DOID:6171,uterine carcinosarcoma,DOID:4114,uterine body mixed cancer
+HP:0010353,Symphalangism affecting the phalanges of the 2nd toe,HP:0100235,Synostosis involving bones of the toes
+HP:0007868,Age-related macular degeneration,HP:0000608,Macular degeneration
+HP:0003798,Nemaline bodies,HP:0100303,Muscle fiber cytoplasmatic inclusion bodies
+DOID:0050253,mesocestoidiasis,DOID:883,parasitic helminthiasis infectious disease
+UBERON:0004264,lower leg skin,UBERON:0001511,skin of leg
+UBERON:0006923,vagina squamous epithelium,UBERON:0006915,stratified squamous epithelium
+HP:0007041,Chronic lymphocytic meningitis,HP:0001287,Meningitis
+HP:0100238,Synostosis involving bones of the upper limbs,HP:0009810,Abnormality of the joints of the upper limbs
+UBERON:0013412,crotaphion,UBERON:0006983,anatomical point
+DOID:10969,hemiplegia,DOID:331,central nervous system disease
+UBERON:0005207,tonsil capsule,UBERON:0003893,capsule
+UBERON:0009200,limb epidermis,UBERON:0001003,skin epidermis
+HP:0012093,Abnormality of endocrine pancreas physiology,HP:0012091,Abnormality of pancreas physiology
+DOID:1328,Rift Valley fever,DOID:37,skin disease
+UBERON:0000093,sulcus,UBERON:0000464,anatomical space
+UBERON:0010057,hypopharyngeal eminence,UBERON:0004121,ectoderm-derived structure
+HP:0008125,Second metatarsal posteriorly placed,HP:0001832,Abnormality of the metatarsal bones
+UBERON:0004868,tapetum lucidum of camera-type eye,UBERON:0015169,tapetum
+HP:0001709,Third degree atrioventricular block,HP:0001678,Atrioventricular block
+UBERON:0011978,epiphysis of middle phalanx of manus,UBERON:0004387,epiphysis of phalanx of manus
+HP:0007428,Telangiectasia of the oral mucosa,HP:0000228,Oral cavity teleangiectasia
+HP:0003209,Decreased pyruvate carboxylase activity,HP:0000816,Abnormality of Krebs cycle metabolism
+DOID:490,hemangioma of lung,DOID:255,hemangioma
+HP:0001476,Delayed closure of the anterior fontanelle,HP:0000236,Abnormality of the anterior fontanelle
+UBERON:0005606,hyaloid cavity,UBERON:0002553,anatomical cavity
+HP:0009631,Bullet-shaped proximal phalanx of the thumb,HP:0009618,Abnormality of the proximal phalanx of the thumb
+UBERON:0001424,ulna,UBERON:0003607,forelimb long bone
+HP:0100386,Aplasia of the proximal phalanx of the 5th toe,HP:0100388,Aplasia of the proximal phalanges of the toes
+UBERON:2000974,somite 10,UBERON:0002329,somite
+HP:0011145,Symptomatic seizures,HP:0001250,Seizures
+HP:0008475,Hypoplastic sacral vertebrae,HP:0004590,Hypoplastic sacrum
+UBERON:0015079,proximal carpal cartilage,UBERON:0015078,proximal carpal endochondral element
+UBERON:0009024,adrenal gland X zone,UBERON:0014404,female anatomical structure
+HP:0010471,Oligosacchariduria,HP:0011013,Abnormality of carbohydrate metabolism/homeostasis
+CL:1000357,microfold cell of epithelium proper of jejunum,CL:1000353,microfold cell of epithelium of small intestine
+UBERON:0005146,metanephric nephron tubule,UBERON:0001231,nephron tubule
+HP:0100006,Neoplasm of the central nervous system,HP:0002011,Abnormality of the central nervous system
+HP:0003557,Increased variability in muscle fiber diameter,HP:0012084,Abnormality of skeletal muscle fiber size
+UBERON:0013250,vesicular appendage of epoophoron,UBERON:0014404,female anatomical structure
+DOID:13791,myringitis bullosa hemorrhagica,DOID:5782,tympanic membrane disease
+NCBITaxon:10292,Herpesviridae,NCBITaxon:548681,Herpesvirales
+UBERON:0003062,primitive knot,UBERON:0010188,protuberance
+HP:0000826,Precocious puberty,HP:0100000,Early onset of sexual maturation
+DOID:0050849,periampullary adenoma,DOID:10022,ampulla of vater neoplasm
+UBERON:0011863,bone collagen fibril,UBERON:0011860,collagen fibril
+UBERON:0011359,urophysis,UBERON:0010133,neuroendocrine gland
+UBERON:0011611,ceratohyal bone,UBERON:0011609,ceratohyal element
+UBERON:0002190,subcutaneous adipose tissue,UBERON:0004120,mesoderm-derived structure
+NCBITaxon:37816,Rickettsia honei,NCBITaxon:114277,spotted fever group
+DOID:0050792,multiple cutaneous and mucosal venous malformations,DOID:0050736,autosomal dominant disease
+HP:0002982,Tibial bowing,HP:0002979,Bowing of the legs
+HP:0012303,Abnormality of the aortic arch,HP:0001679,Abnormality of the aorta
+HP:0009019,Progressive loss of facial adipose tissue,HP:0000292,Loss of facial adipose tissue
+HP:0011438,Maternal teratogenic exposure,HP:0002686,Prenatal maternal abnormality
+UBERON:1000024,parenchyma of spleen,UBERON:0000353,parenchyma
+DOID:0050145,adenoiditis,DOID:974,upper respiratory tract disease
+CL:0000236,B cell,CL:0000945,lymphocyte of B lineage
+DOID:9432,renal glycosuria,DOID:447,renal tubular transport disease
+HP:0004712,Renal malrotation,HP:0012210,Abnormal renal morphology
+UBERON:2000629,caudal motor nucleus of abducens,UBERON:0002680,regional part of metencephalon
+DOID:1992,rectum malignant melanoma,DOID:1993,rectum cancer
+HP:0009992,Complete duplication of the middle phalanx of the 5th finger,HP:0009986,Complete duplication of the phalanges of the 5th finger
+UBERON:3000395,pars basilaris,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2002003,posterior dentation of dorsal fin spine 2,UBERON:0004120,mesoderm-derived structure
+UBERON:0009138,right common cardinal vein,UBERON:0002064,common cardinal vein
+HP:0010605,Chalazion,HP:0010604,Cyst of the eyelid
+CL:0000561,amacrine cell,CL:0000099,interneuron
+HP:0004398,Peptic ulcer,HP:0012719,Functional abnormality of the gastrointestinal tract
+HP:0001763,Pes planus,HP:0001760,Abnormality of the foot
+UBERON:0011244,perpendicular plate of ethmoid,UBERON:0005913,zone of bone organ
+DOID:6654,childhood central nervous system immature teratoma,DOID:6019,central nervous system immature teratoma
+UBERON:0000933,pharyngeal muscle,UBERON:0001630,muscle organ
+DOID:7894,mite infestation,DOID:4110,parasitic ectoparasitic infectious disease
+HP:0011822,Broad chin,HP:0000306,Abnormality of the chin
+UBERON:0013620,lower primary molar tooth,UBERON:0013616,primary molar tooth
+UBERON:0007166,left dome of diaphragm,UBERON:0007145,dome of diaphragm
+DOID:6285,heart lipoma,DOID:0060091,cardiovascular organ benign neoplasm
+UBERON:4200112,prepectoral space,UBERON:0004120,mesoderm-derived structure
+UBERON:0001629,carotid body,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000751,rod bipolar cell,CL:0000749,ON-bipolar cell
+UBERON:0006688,sublingual caruncle,UBERON:0004121,ectoderm-derived structure
+HP:0012437,Abnormal gallbladder morphology,HP:0005264,Abnormality of the gallbladder
+UBERON:0004886,lung hilus,UBERON:0004119,endoderm-derived structure
+HP:0004836,Acute promyelocytic leukemia,HP:0002488,Acute leukemia
+HP:0010997,Chromosomal breakage induced by ionizing radiation,HP:0003220,Abnormality of chromosome stability
+HP:0010494,Acromelia of the lower limbs,HP:0010884,Acromelia
+UBERON:0005845,caudal segment of spinal cord,UBERON:0005844,spinal cord segment
+HP:0006378,Osteolysis of patellae,HP:0009139,Osteolysis involving bones of the lower limbs
+UBERON:0004163,anterior ectodermal midgut,UBERON:0004121,ectoderm-derived structure
+UBERON:0014454,visceral abdominal adipose tissue,UBERON:0007808,adipose tissue of abdominal region
+HP:0003989,Notched ulna,HP:0002997,Abnormality of the ulna
+UBERON:0015922,accessory mandibular lymph node,UBERON:0015871,facial lymph node
+CL:0002446,Ly49CI-negative natural killer cell,CL:0002438,NK1.1-positive natural killer cell
+HP:0009118,Aplasia/Hypoplasia of the mandible,HP:0009116,Aplasia/Hypoplasia involving bones of the skull
+HP:0009833,Abnormality of the middle phalanges of the hand,HP:0005918,Abnormality of phalanx of finger
+UBERON:0006878,decidua parietalis,UBERON:0005156,reproductive structure
+DOID:13405,cardiac sarcoidosis,DOID:11335,sarcoidosis
+UBERON:0011868,midcarpal joint,UBERON:0011132,intercarpal joint
+UBERON:0013462,sylvian point,UBERON:0006983,anatomical point
+UBERON:0010932,crico-arytenoid muscle,UBERON:0006328,laryngeal intrinsic muscle
+UBERON:0005872,1st arch pharyngeal cleft,UBERON:0005879,pharyngeal cleft
+UBERON:0000157,theca interna,UBERON:0005156,reproductive structure
+UBERON:2000182,central caudal thalamic nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:2001251,pharyngobranchial 4 cartilage,UBERON:2001533,pharyngobranchial cartilage
+UBERON:0015077,centrale cartilage,UBERON:0015067,centrale endochondral element
+UBERON:0005609,iliac artery,UBERON:0003520,pelvis blood vessel
+UBERON:0011627,orbital part of frontal bone,UBERON:0004121,ectoderm-derived structure
+UBERON:0013212,anal sac gland secretion,UBERON:0000456,bodily secretion
+DOID:6175,mediastinal neurilemmoma,DOID:956,peripheral nerve schwannoma
+HP:0012726,Episodic hypokalemia,HP:0002900,Hypokalemia
+UBERON:0004654,temporal process of zygomatic bone,UBERON:0004120,mesoderm-derived structure
+UBERON:0011214,nucleus of midbrain tectum,UBERON:0002966,regional part of midbrain tectum
+DOID:11502,mitral valve insufficiency,DOID:61,mitral valve disease
+CL:0008008,striated visceral muscle cell,CL:0008007,visceral muscle cell
+UBERON:0001235,adrenal cortex,UBERON:0001851,cortex
+HP:0012408,Medullary nephrocalcinosis,HP:0000121,Nephrocalcinosis
+HP:0008263,Thyroid defect in oxidation and organification of iodide,HP:0002926,Abnormality of thyroid physiology
+DOID:5926,extrahepatic bile duct small cell adenocarcinoma,DOID:3495,extrahepatic bile duct adenocarcinoma
+NCBITaxon:1206794,Ecdysozoa,NCBITaxon:33317,Protostomia
+HP:0000152,Abnormality of head and neck,HP:0000118,Phenotypic abnormality
+UBERON:0005116,metanephric descending thin limb,UBERON:0005096,descending thin limb
+HP:0011973,Paroxysmal lethargy,HP:0001254,Lethargy
+HP:0006110,Shortening of all middle phalanges of the fingers,HP:0005819,Short middle phalanx of finger
+UBERON:0002800,spinal trigeminal tract of pons,UBERON:0014761,spinal trigeminal tract
+UBERON:0003974,upper part of vagina,UBERON:0013515,subdivision of uterine tube
+HP:0005879,Congenital finger flexion contractures,HP:0100490,Camptodactyly of finger
+UBERON:0002887,basal amygdaloid nucleus,UBERON:0002619,regional part of cerebral cortex
+HP:0100178,Stippling of the epiphysis of the distal phalanx of the 4th toe,HP:0100094,Abnormality of the epiphysis of the distal phalanx of the 4th toe
+HP:0012377,Hemianopsia,HP:0000505,Visual impairment
+NCBITaxon:11051,Flavivirus,NCBITaxon:11050,Flaviviridae
+NCBITaxon:7180,Haemagogus <genus>,NCBITaxon:1056966,Aedini
+UBERON:2001587,pectoral fin proximal radial bone,UBERON:2001586,pectoral fin radial bone
+HP:0003749,Pelvic girdle muscle weakness,HP:0003325,Limb-girdle muscle weakness
+DOID:10254,strawberry gallbladder,DOID:0000000,gallbladder disease
+UBERON:0004607,rib 7,UBERON:0002228,rib
+DOID:10611,protein-losing enteropathy,DOID:5295,intestinal disease
+HP:0012697,Small basal ganglia,HP:0002134,Abnormality of the basal ganglia
+UBERON:0005573,rhombomere 3 floor plate,UBERON:0005500,rhombomere floor plate
+UBERON:0005577,rhombomere 4 lateral wall,UBERON:0005501,rhombomere lateral wall
+HP:0200064,Asymmetry of iris pigmentation,HP:0008034,Abnormal iris pigmentation
+CL:0002189,granular cell of epidermis,CL:0000312,keratinocyte
+UBERON:0015050,tarsus endochondral element,UBERON:0015022,hindlimb endochondral element
+HP:0010143,Irregular epiphysis of the distal phalanx of the hallux,HP:0010118,Irregular epiphyses of the hallux
+UBERON:0007280,presumptive endocardium,UBERON:0006598,presumptive structure
+UBERON:0011596,future lower lip,UBERON:0003236,epithelium of lower jaw
+HP:0000872,Hashimoto thyroiditis,HP:0100646,Thyroiditis
+CL:0002265,type D cell of colon,CL:0000502,type D enteroendocrine cell
+HP:0012422,Villous hypertrophy of choroid plexus,HP:0007376,Abnormality of the choroid plexus
+HP:0008619,Bilateral sensorineural hearing impairment,HP:0000407,Sensorineural hearing impairment
+HP:0001264,Spastic diplegia,HP:0001257,Spasticity
+DOID:4411,hepatitis E,DOID:934,viral infectious disease
+HP:0007623,Pigmentation anomalies of sun-exposed skin,HP:0001000,Abnormality of skin pigmentation
+DOID:10289,prostate malignant phyllodes tumor,DOID:10283,prostate cancer
+CL:1000479,purkinje myocyte of atrioventricular node,CL:0002068,Purkinje myocyte
+HP:0010324,Abnormality of phalanx of the 2nd toe,HP:0010161,Abnormality of the phalanges of the toes
+HP:0011062,Misalignment of incisors,HP:0000692,Misalignment of teeth
+UBERON:2000430,secondary gustatory tract,UBERON:0014649,white matter of medulla oblongata
+HP:0012580,Calcium phosphate nephrolithiasis,HP:0004724,Calcium nephrolithiasis
+UBERON:0005737,swim bladder tunica externa,UBERON:0005742,adventitia
+UBERON:0000005,chemosensory organ,UBERON:0000020,sense organ
+HP:0001551,Abnormality of the umbilicus,HP:0004298,Abnormality of the abdominal wall
+UBERON:0006905,mandibular process mesenchyme,UBERON:0010314,structure with developmental contribution from neural crest
+NCBITaxon:10780,Parvoviridae,NCBITaxon:29258,ssDNA viruses
+CL:0000085,germ line stem cell (sensu Vertebrata),CL:0000014,germ line stem cell
+UBERON:0007185,pericardio-peritoneal canal mesothelium,UBERON:0005291,embryonic tissue
+UBERON:0004407,distal epiphysis of radius,UBERON:0004385,epiphysis of radius
+HP:0001907,Thromboembolism,HP:0001977,Abnormal thrombosis
+UBERON:0013127,pulmonary venous system,UBERON:0002049,vasculature
+HP:0009199,Irregular epiphysis of the proximal phalanx of the 5th finger,HP:0009153,Abnormality of the epiphysis of the proximal phalanx of the 5th finger
+UBERON:2000637,claustrum cartilage,UBERON:2000461,Weberian ossicle
+CL:0000216,Sertoli cell,CL:0002625,seminiferous tubule epithelial cell
+HP:0009304,Patchy sclerosis of the distal phalanx of the 4th finger,HP:0100902,Sclerosis of the distal phalanx of the 4th finger
+DOID:934,viral infectious disease,DOID:0050117,disease by infectious agent
+UBERON:0004769,diaphysis,UBERON:0005055,zone of long bone
+DOID:14284,patellofemoral pain syndrome,DOID:381,arthropathy
+HP:0011191,Unilateral multifocal epileptiform discharges,HP:0010841,Multifocal epileptiform discharges
+HP:0100201,Triangular epiphysis of the proximal phalanx of the 4th toe,HP:0100096,Abnormality of the epiphysis of the proximal phalanx of the 4th toe
+HP:0012160,Intracranial internal carotid artery dissection,HP:0012159,Internal carotid artery dissection
+HP:0006268,Fluctuating splenomegaly,HP:0001744,Splenomegaly
+HP:0007369,Atrophy/Degeneration affecting the cerebrum,HP:0002977,Aplasia/Hypoplasia involving the central nervous system
+UBERON:0006683,posterior fontanelle,UBERON:0002221,fontanelle
+UBERON:0015115,distal tarsal bone 5 cartilage,UBERON:0010885,hindlimb cartilage element
+HP:0003948,Irregular epiphyses of the elbow,HP:0003946,Abnormality of the epiphyses of the elbow
+UBERON:0000090,blastocele,UBERON:0002553,anatomical cavity
+UBERON:2002087,pectoral axillary process,UBERON:0010741,bone of pectoral complex
+UBERON:3000396,pars dentalis of maxilla,UBERON:0010313,neural crest-derived structure
+HP:0012622,Chronic kidney disease,HP:0000083,Renal insufficiency
+HP:0001349,Facial diplegia,HP:0010628,Facial palsy
+UBERON:0001607,sphincter pupillae,UBERON:0007521,smooth muscle sphincter
+UBERON:0010675,manual digit 1 phalanx cartilage element,UBERON:0010564,manual digit 1 mesenchyme
+CL:0000094,granulocyte,CL:0000766,myeloid leukocyte
+DOID:7958,sarcomatoid penile squamous cell carcinoma,DOID:5518,penis squamous cell carcinoma
+NCBITaxon:1809,Mycobacterium ulcerans,NCBITaxon:1763,Mycobacterium
+UBERON:4200001,postpubis,UBERON:0004120,mesoderm-derived structure
+UBERON:2002240,Purkinje cell layer corpus cerebelli,UBERON:0000479,tissue
+HP:0004016,Cupped radial metaphyses,HP:0003848,Cupped metaphyses of the upper limbs
+UBERON:0003070,trigeminal placode,UBERON:0003067,dorsolateral placode
+UBERON:0014531,lamina of diencephalon,UBERON:0014530,lamina of neuraxis
+DOID:5140,gallbladder leiomyoma,DOID:127,leiomyoma
+HP:0012187,Increased erythrocyte protoporphyrin concentration,HP:0010472,Abnormality of the heme biosynthetic pathway
+UBERON:0005730,pelvic appendage field,UBERON:0005732,paired limb/fin field
+UBERON:0015010,sacral vertebra endochondral element,UBERON:0004120,mesoderm-derived structure
+HP:0011219,Short face,HP:0001999,Abnormal facial shape
+HP:0011818,Nasofrontal encephalocele,HP:0007330,Frontal encephalocele
+HP:0010954,Hypoplastic right heart,HP:0011723,Congenital malformation of the right heart
+HP:0002474,Expressive language delay,HP:0000750,Delayed speech and language development
+UBERON:0014371,future telencephalon,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009310,Broad proximal phalanx of the 4th finger,HP:0009852,Broad proximal phalanges of the hand
+DOID:0050167,autoimmune polyendocrine syndrome type 1,DOID:14040,autoimmune polyendocrine syndrome
+UBERON:0002120,pronephros,UBERON:0002113,kidney
+HP:0009799,Supernumerary spleens,HP:0001743,Abnormality of the spleen
+HP:0007326,Progressive choreoathetosis,HP:0001266,Choreoathetosis
+UBERON:0014842,pubioischiofemoralis muscle,UBERON:0001630,muscle organ
+NCBITaxon:10241,Chordopoxvirinae,NCBITaxon:10240,Poxviridae
+DOID:0050527,familial hypertriglyceridemia,DOID:3146,lipid metabolism disorder
+UBERON:2000601,pretectal periventricular nucleus,UBERON:0006569,diencephalic nucleus
+HP:0012369,Malar anomaly,HP:0000309,Abnormality of the midface
+HP:0010676,Mechanical ileus,HP:0002595,Ileus
+UBERON:0014606,infundibular stem,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3010072,M. pyriformis,UBERON:0010890,pelvic complex muscle
+UBERON:0014524,electromotor division of oculomotor nuclear complex,UBERON:0007245,nuclear complex of neuraxis
+UBERON:0008439,webbed interdigital region between pedal digits,UBERON:0006014,interdigital region between pedal digits
+UBERON:0001078,pedicle of vertebra,UBERON:0006061,process of vertebra
+UBERON:0010062,pharyngotympanic tube epithelium,UBERON:0015813,middle ear epithelium
+HP:0012725,Cutaneous syndactyly,HP:0001159,Syndactyly
+UBERON:0006813,nasal skeleton,UBERON:0010313,neural crest-derived structure
+CL:0002218,immature dendritic epithelial T cell precursor,CL:0002404,fetal thymocyte
+NCBITaxon:773,Bartonella,NCBITaxon:772,Bartonellaceae
+UBERON:0009474,ascidian ampulla,UBERON:0000026,appendage
+HP:0010410,Symphalangism affecting the middle phalanx of the 2nd toe,HP:0010357,Abnormality of the middle phalanx of the 2nd toe
+UBERON:2002292,epaxial basal fulcrum,UBERON:2002082,basal fulcrum
+UBERON:0010375,pancreas dorsal primordium,UBERON:0002365,exocrine gland
+HP:0004054,Sclerosis of hand bones,HP:0011001,Increased bone mineral density
+HP:0001962,Palpitations,HP:0011675,Arrhythmia
+UBERON:0002376,cranial muscle,UBERON:0004120,mesoderm-derived structure
+DOID:10844,Japanese encephalitis,DOID:934,viral infectious disease
+UBERON:0001493,axillary nerve,UBERON:0002003,peripheral nerve
+UBERON:2000176,lateral entopeduncular nucleus,UBERON:0009663,telencephalic nucleus
+CL:0000568,APUD cell,CL:0000165,neuroendocrine cell
+CL:0000835,myeloblast,CL:0000763,myeloid cell
+HP:0009797,Cholesteatoma,HP:0008609,Morphological abnormality of the middle ear
+CL:1001216,interlobulary artery endothelial cell,CL:1000413,endothelial cell of artery
+UBERON:4300014,dorsal cleithrum,UBERON:0008907,dermal bone
+HP:0008067,Abnormally lax or hyperextensible skin,HP:0010647,Abnormal elasticity of skin
+UBERON:0015054,iliac endochondral element,UBERON:0010363,endochondral element
+UBERON:0000021,cutaneous appendage,UBERON:0013703,integumentary projection
+HP:0010541,Cutis gyrata of scalp,HP:0011356,Regional abnormality of skin
+DOID:255,hemangioma,DOID:0060084,cell type benign neoplasm
+UBERON:0010861,propatagium,UBERON:0010858,inter limb-segment region
+UBERON:3010085,postrictal protuberances,UBERON:3000972,head external integument structure
+HP:0009965,Complete duplication of the distal phalanx of the 3rd finger,HP:0009960,Complete duplication of the phalanges of the 3rd finger
+DOID:114,heart disease,DOID:1287,cardiovascular system disease
+HP:0009656,Symphalangism of the thumb,HP:0009700,Synostosis involving bones of the fingers
+HP:0011170,Myoclonic atonic seizures,HP:0002123,Generalized myoclonic seizures
+CL:1001123,kidney outer medulla peritubular capillary cell,CL:1000616,kidney outer medulla cell
+UBERON:0008522,nasal muscle,UBERON:0004121,ectoderm-derived structure
+UBERON:0005345,cerebellum vermis lobule VIIa,UBERON:0004081,cerebellum vermis lobule VII
+DOID:5199,ureteral obstruction,DOID:1426,ureteral disease
+UBERON:0000371,syncytiotrophoblast,UBERON:0002050,embryonic structure
+UBERON:4200177,supracondyle tubercle,UBERON:0004120,mesoderm-derived structure
+CL:0000705,R6 photoreceptor cell,CL:0000287,eye photoreceptor cell
+UBERON:2001163,supraneural 7 bone,UBERON:2000442,supraneural bone
+DOID:0050568,spondylocostal dysostosis,DOID:1934,dysostosis
+DOID:7532,squamous papillomatosis,DOID:0050624,gastrointestinal system benign neoplasm
+UBERON:0004442,proximal epiphysis of proximal phalanx of manual digit 4,UBERON:0011977,epiphysis of proximal phalanx of manus
+DOID:8506,bullous pemphigoid,DOID:8502,bullous skin disease
+HP:0007979,Gaze-evoked horizontal nystagmus,HP:0000640,Gaze-evoked nystagmus
+UBERON:0010147,male accessory sex gland,UBERON:0005399,male reproductive gland
+HP:0100231,Pseudoepiphysis of the proximal phalanx of the 5th toe,HP:0100099,Abnormality of the epiphysis of the proximal phalanx of the 5th toe
+UBERON:2001169,vertebral element 3,UBERON:0010913,vertebral element
+UBERON:0005980,pectinate muscle,UBERON:0004120,mesoderm-derived structure
+UBERON:2001790,dorsal fin spine 2,UBERON:2002261,dorsal fin spine
+UBERON:0001906,subthalamic nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:2007031,anterior neural rod,UBERON:0005291,embryonic tissue
+UBERON:0004685,middle temporal area,UBERON:0002619,regional part of cerebral cortex
+HP:0001650,Aortic valve stenosis,HP:0001646,Abnormality of the aortic valve
+UBERON:0014471,primary fissure of cerebellum,UBERON:0003980,cerebellum fissure
+HP:0010497,Sirenomelia,HP:0002814,Abnormality of the lower limb
+HP:0007330,Frontal encephalocele,HP:0002084,Encephalocele
+HP:0009414,Fragmentation of the epiphyses of the 3rd finger,HP:0010232,Fragmentation of the epiphyses of the phalanges of the hand
+UBERON:0002827,auditory ganglion,UBERON:0010313,neural crest-derived structure
+DOID:3390,palmoplantar keratosis,DOID:161,keratosis
+DOID:2908,Treacher Collins syndrome,DOID:0050736,autosomal dominant disease
+UBERON:0002872,inferior salivatory nucleus,UBERON:0004133,salivatory nucleus
+DOID:3350,mesenchymal cell neoplasm,DOID:0050687,cell type cancer
+CL:0000168,insulin secreting cell,CL:0000167,peptide hormone secreting cell
+HP:0011156,Focal autonomic seizures without altered responsiveness,HP:0011154,Focal autonomic seizures
+UBERON:0004071,cerebellum emboliform nucleus,UBERON:0002946,regional part of cerebellum
+CL:0000854,interneuromast cell,CL:0000133,neurectodermal cell
+UBERON:3000834,posterior lamina recurvata,UBERON:0004121,ectoderm-derived structure
+UBERON:0006275,pericardio-peritoneal canal,UBERON:0002050,embryonic structure
+UBERON:2001877,neural arch 1,UBERON:0003861,neural arch
+HP:0004742,Abnormality of the renal collecting system,HP:0012210,Abnormal renal morphology
+UBERON:0006671,orbital fat pad,UBERON:0003916,fat pad
+NCBITaxon:11599,Hantaan virus,NCBITaxon:11598,Hantavirus
+HP:0007411,Hypoplastic-absent sebaceous glands,HP:0008065,Aplasia/Hypoplasia of the skin
+UBERON:0005489,anterior interventricular sulcus,UBERON:0005455,interventricular groove
+UBERON:0003116,pharyngeal arch 5,UBERON:0002539,pharyngeal arch
+DOID:5540,fallopian tube squamous cell carcinoma,DOID:1963,fallopian tube carcinoma
+UBERON:2205226,median fin proximal radial cartilage,UBERON:2105226,median fin proximal radial element
+HP:0002159,Heparan sulfate excretion in urine,HP:0008155,Mucopolysacchariduria
+HP:0100044,Absent epiphyses of the 2nd toe,HP:0010323,Abnormality of the epiphyses of the 2nd toe
+UBERON:0002233,tectorial membrane of cochlea,UBERON:0004121,ectoderm-derived structure
+UBERON:0006505,palmar hand interosseous muscle,UBERON:0001502,interosseous muscle of manus
+CL:1000493,mesothelial cell of visceral pleura,CL:0000082,epithelial cell of lung
+CL:0000343,visual pigment cell (sensu Vertebrata),CL:0000342,pigment cell (sensu Vertebrata)
+HP:0008376,"Nasal, dysarthic speech",HP:0001260,Dysarthria
+HP:0009244,Distal/middle symphalangism of 5th finger,HP:0004218,Symphalangism of the 5th finger
+UBERON:0003898,skeletal muscle tissue of trunk,UBERON:0001134,skeletal muscle tissue
+UBERON:2005264,supraoccipital-parietal joint,UBERON:0000982,skeletal joint
+DOID:1381,fox fordyce disease,DOID:1383,sweat gland disease
+CL:1000394,myoepithelial cell of intralobular lactiferous duct,CL:0000185,myoepithelial cell
+DOID:11907,ecthyma,DOID:8504,impetigo
+HP:0002900,Hypokalemia,HP:0011042,Abnormality of potassium homeostasis
+HP:0009216,Cone-shaped epiphysis of the middle phalanx of the 4th finger,HP:0010259,Cone-shaped epiphyses of the middle phalanges of the hand
+UBERON:0011805,cavity of feather follicle,UBERON:0002553,anatomical cavity
+UBERON:0005911,endo-epithelium,UBERON:0000483,epithelium
+UBERON:0001544,popliteal vein,UBERON:0001638,vein
+HP:0004926,Orthostatic hypotension due to autonomic dysfunction,HP:0001278,Orthostatic hypotension
+HP:0009426,Distal/middle symphalangism of 3rd finger,HP:0001204,Distal symphalangism (hands)
+UBERON:0005738,swim bladder tunica interna,UBERON:0005742,adventitia
+HP:0008245,Pituitary hypothyroidism,HP:0000830,Anterior hypopituitarism
+UBERON:0010051,dorsal patch of Leydig's organ,UBERON:0000064,organ part
+UBERON:0010242,anterior buccal gland,UBERON:0010241,molar gland
+HP:0010398,Curved proximal phalanx of the 2nd toe,HP:0010358,Abnormality of the proximal phalanx of the 2nd toe
+HP:0012531,Pain,HP:0012638,Abnormality of nervous system physiology
+UBERON:0011685,preorbitalis muscle,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0006988,Alobar holoprosencephaly,HP:0001360,Holoprosencephaly
+UBERON:0006080,segment of white matter of spinal cord,UBERON:0002318,white matter of spinal cord
+HP:0000346,Whistling appearance,HP:0000205,Pursed lips
+HP:0007900,Hypoplastic lacrimal duct,HP:0011481,Abnormality of the lacrimal duct
+UBERON:0006239,future central tendon,UBERON:0000043,tendon
+HP:0100726,Kaposi's sarcoma,HP:0005353,Susceptibility to herpesvirus
+HP:0008993,Increased intraabdominal fat,HP:0009126,Increased adipose tissue
+UBERON:0004640,efferent arteriole,UBERON:0001980,arteriole
+HP:0000768,Pectus carinatum,HP:0000766,Abnormality of the sternum
+UBERON:0009482,associated mesenchyme of foregut-midgut junction,UBERON:0003104,mesenchyme
+HP:0008643,Nephroblastomatosis,HP:0011794,Embryonal renal neoplasm
+UBERON:0004472,musculature of chest,UBERON:0004464,musculature of thorax
+UBERON:0015880,external iliac lymph node,UBERON:0015877,parietal pelvic lymph node
+HP:0004012,Premature fusion of the radial epiphyseal plates,HP:0003999,Abnormality of radial epiphyses
+UBERON:0005229,lower leg epithelium,UBERON:0010371,ecto-epithelium
+HP:0004226,Curved distal phalanx of the 5th finger,HP:0009838,Curved distal phalanges of the hand
+UBERON:2002219,parvocellular preoptic nucleus,UBERON:0006569,diencephalic nucleus
+HP:0006467,Limited shoulder movement,HP:0003043,Abnormality of the shoulder
+UBERON:0000165,mouth,UBERON:0004906,ectodermal part of digestive tract
+HP:0004960,Absent pulmonary artery,HP:0004414,Abnormality of the pulmonary artery
+UBERON:0006288,rib cartilage element,UBERON:0005181,thoracic segment organ
+CL:0000177,testosterone secreting cell,CL:0000593,androgen secreting cell
+UBERON:0004109,cortex of humerus,UBERON:0005808,bone tissue of long bone
+UBERON:2001530,epibranchial 2 cartilage,UBERON:2001527,epibranchial cartilage
+UBERON:2001342,presumptive intervening zone,UBERON:0002050,embryonic structure
+HP:0001026,Penetrating foot ulcers,HP:0200042,Skin ulcer
+UBERON:0004226,gastrointestinal system smooth muscle,UBERON:0001135,smooth muscle tissue
+UBERON:0000980,trochanter,UBERON:0005055,zone of long bone
+HP:0009351,Irregular epiphysis of the proximal phalanx of the 3rd finger,HP:0009415,Irregular epiphyses of the 3rd finger
+HP:0005829,Maldevelopment of radioulnar joint,HP:0003059,Abnormality of the radioulnar joints
+UBERON:4200051,cotyloid notch,UBERON:0004120,mesoderm-derived structure
+HP:0011919,Pleural empyema,HP:0002202,Pleural effusion
+UBERON:0006279,pleuroperitoneal canal,UBERON:0005291,embryonic tissue
+DOID:11507,rumination disorder,DOID:8670,eating disorder
+UBERON:3010736,ramus posterior of CN VIII,UBERON:0004121,ectoderm-derived structure
+UBERON:0002649,dorsolateral fasciculus of medulla,UBERON:0014649,white matter of medulla oblongata
+UBERON:0003041,trigeminal nerve fibers,UBERON:0006134,nerve fiber
+UBERON:0014788,right extraembryonic umbilical vein,UBERON:0014786,extraembryonic umbilical vein
+HP:0004937,Pulmonary artery aneurysm,HP:0004414,Abnormality of the pulmonary artery
+UBERON:2001183,dermal superficial region,UBERON:0004120,mesoderm-derived structure
+DOID:12558,chronic progressive external ophthalmoplegia,DOID:699,mitochondrial myopathy
+UBERON:0006776,annular epiphysis,UBERON:0005913,zone of bone organ
+UBERON:0010412,epididymal fat pad,UBERON:0014403,male anatomical structure
+HP:0009535,Aplasia of the 2nd finger,HP:0009380,Aplasia of the fingers
+CL:0000504,enterochromaffin-like cell,CL:0000164,enteroendocrine cell
+HP:0008991,Exercise-induced leg cramps,HP:0003710,Exercise-induced muscle cramps
+DOID:0060064,sideroblastic anemia with spinocerebellar ataxia,DOID:8955,sideroblastic anemia
+HP:0004017,Exostoses of the radial metaphysis,HP:0003986,Exostoses of the radius
+UBERON:0014462,ptychocyst,UBERON:0008277,cnida
+HP:0100521,Neoplasm of the thymus,HP:0000777,Abnormality of the thymus
+UBERON:0010560,pedal digit 4 metatarsal cartilage element,UBERON:0010683,pedal digit 4 phalanx cartilage element
+DOID:10481,diaphragm disease,DOID:0080000,muscular disease
+HP:0011321,Left unilambdoid synostosis,HP:0011320,Unilambdoid synostosis
+HP:0100413,Complete duplication of the proximal phalanx of the 3rd toe,HP:0100404,Duplication of the proximal phalanx of the 3rd toe
+NCBITaxon:35493,Streptophyta,NCBITaxon:33090,Viridiplantae
+DOID:7132,urinary bladder small cell neuroendocrine carcinoma,DOID:4007,bladder carcinoma
+UBERON:0002975,medial oculomotor nucleus,UBERON:0007414,nucleus of midbrain tegmentum
+UBERON:0015485,choledocho-duodenal junction,UBERON:0007651,anatomical junction
+NCBITaxon:181088,Haemaphysalis flava,NCBITaxon:34622,Haemaphysalis
+UBERON:0001210,muscularis mucosae of small intestine,UBERON:0001240,muscularis mucosae of intestine
+CL:0000486,garland cell,CL:0002520,nephrocyte
+UBERON:0001856,semicircular duct,UBERON:0004121,ectoderm-derived structure
+UBERON:0006788,middle gray layer of superior colliculus,UBERON:0006785,gray matter of superior colliculus
+DOID:8161,thyroid hurthle cell carcinoma,DOID:3963,thyroid carcinoma
+UBERON:0006795,arthropod optic lobe,UBERON:0006794,visual processing part of nervous system
+HP:0001119,Keratoglobus,HP:0100689,Decreased corneal thickness
+HP:0009254,Fragmentation of the epiphysis of the distal phalanx of the 4th finger,HP:0009397,Fragmentation of the epiphyses of the 4th finger
+UBERON:3010073,centrale 2,UBERON:0012131,centrale
+DOID:12401,intermittent explosive disorder,DOID:10937,impulse control disorder
+DOID:11638,presbyopia,DOID:9835,refractive error
+HP:0005507,Hemoglobin Barts,HP:0011902,Abnormal hemoglobin
+HP:0011205,EEG with intermittent slow activity,HP:0010845,EEG with generalized slow activity
+UBERON:0015088,distal carpal bone 2 cartilage,UBERON:0015064,autopod cartilage
+DOID:7426,cutaneous anthrax,DOID:7427,anthrax disease
+UBERON:0007800,proatlas,UBERON:0002413,cervical vertebra
+UBERON:0005413,spinocerebellar tract,UBERON:0001018,axon tract
+UBERON:0011322,mylohyoid nerve,UBERON:0002003,peripheral nerve
+HP:0010301,Spinal dysraphism,HP:0002143,Abnormality of the spinal cord
+UBERON:0007215,trabecula cranii,UBERON:0003932,cartilage element of chondrocranium
+HP:0000228,Oral cavity teleangiectasia,HP:0011830,Abnormality of oral mucosa
+UBERON:0011156,facial skeleton,UBERON:0010313,neural crest-derived structure
+UBERON:0009195,anal membrane,UBERON:0004120,mesoderm-derived structure
+UBERON:0003857,upper eyelid mesenchyme,UBERON:0010330,eyelid mesenchyme
+UBERON:0003707,sinus of Valsalva,UBERON:0000064,organ part
+HP:0012392,Jaw hyporeflexia,HP:0001265,Hyporeflexia
+UBERON:0001750,lacrimal apparatus,UBERON:0004121,ectoderm-derived structure
+HP:0001195,Single umbilical artery,HP:0011403,Abnormal umbilical cord blood vessels
+UBERON:0002755,pyramidal decussation,UBERON:0007418,decussation of neuraxis
+DOID:5854,silent myocardial infarction,DOID:5844,myocardial infarction
+DOID:1172,hyperlipoproteinemia type IV,DOID:1168,familial hyperlipidemia
+HP:0006619,Anterior rib punctate calcifications,HP:0010766,Ectopic calcification
+UBERON:0001037,strand of hair,UBERON:0000021,cutaneous appendage
+UBERON:0001094,sacral vertebra,UBERON:0015010,sacral vertebra endochondral element
+HP:0010584,Pseudoepiphyses,HP:0005930,Abnormality of the epiphyses
+UBERON:0011299,white matter of telencephalon,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0013677,serrated projection of ctenactinium,UBERON:0004530,bony projection
+DOID:2060,vulvar nodular hidradenoma,DOID:0060109,vulvar benign neoplasm
+DOID:999,eosinophilia,DOID:9500,leukocyte disease
+HP:0002107,Pneumothorax,HP:0002088,Abnormality of the lung
+DOID:1294,vulva carcinoma,DOID:1245,vulva cancer
+HP:0012704,Widened subarachnoid space,HP:0012703,Abnormality of the subarachnoid space
+UBERON:0008817,thymus primordium endoderm,UBERON:0004119,endoderm-derived structure
+CL:0002415,"immature Vgamma1.1-positive, Vdelta6.3-positive thymocyte",CL:0002412,"Vgamma1.1-positive, Vdelta6.3-positive thymocyte"
+HP:0012030,Increased urinary cortisol level,HP:0012029,Abnormality of urine hormone level
+HP:0007479,Congenital nonbullous ichthyosiform erythroderma,HP:0007431,Congenital ichthyosiform erythroderma
+HP:0005182,Bicuspid pulmonary valve,HP:0001641,Abnormality of the pulmonary valve
+UBERON:0000073,regional part of nervous system,UBERON:0000481,multi-tissue structure
+HP:0100007,Neoplasm of the peripheral nervous system,HP:0004375,Neoplasm of the nervous system
+UBERON:0008942,gastropod cerebral ganglion,UBERON:0000045,ganglion
+HP:0100489,Proximal/middle symphalangism of 2nd toe,HP:0010366,Triangular shaped phalanges of the 3rd toe
+UBERON:3010118,quadrato-orbital commissure,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:3860,cerebellar vermis medulloblastoma,DOID:0060104,cerebellar medulloblastoma
+UBERON:0003294,gland of foregut,UBERON:0003408,gland of gut
+DOID:8153,fibroosseous pseudotumor of digits,DOID:0060094,bone benign neoplasm
+DOID:10825,essential hypertension,DOID:10763,hypertension
+HP:0005186,Synovial hypertrophy,HP:0005262,Abnormality of the synovia
+UBERON:0005875,4th arch pharyngeal cleft,UBERON:0005879,pharyngeal cleft
+CL:1000398,endothelial cell of hepatic sinusoid,CL:0000182,hepatocyte
+HP:0012488,Intraventricular arachnoid cyst,HP:0100702,Arachnoid cyst
+HP:0009589,Bilateral vestibular Schwannoma,HP:0009588,Vestibular Schwannoma
+HP:0000849,Adrenocortical abnormality,HP:0011732,Abnormality of adrenal morphology
+HP:0011602,Midline direction of ventricular apex,HP:0011600,Abnormal direction of ventricular apex
+UBERON:0006442,subhepatic recess,UBERON:0002553,anatomical cavity
+HP:0000148,Vaginal atresia,HP:0000142,Abnormality of the vagina
+UBERON:0003455,inner renal medulla loop of henle,UBERON:0001288,loop of Henle
+HP:0100078,Bracket epiphyses of the 5th toe,HP:0010341,Abnormality of the epiphyses of the 5th toe
+HP:0100749,Chest pain,HP:0000765,Abnormality of the thorax
+UBERON:0003300,roof plate of telencephalon,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2002032,lateral ethmoid-frontal joint,UBERON:0000982,skeletal joint
+CL:0000151,secretory cell,CL:0000003,native cell
+UBERON:0000910,chyme,UBERON:0012112,ingested food
+HP:0001732,Abnormality of the pancreas,HP:0002012,Abnormality of the abdominal organs
+UBERON:0002411,clitoris,UBERON:0000062,organ
+DOID:14413,labyrinthine bilateral reactive loss,DOID:566,labyrinthine dysfunction
+UBERON:0004323,middle phalanx of manual digit 5,UBERON:0014491,middle phalanx of digit 5
+UBERON:2000401,octaval nerve sensory nucleus,UBERON:0000126,cranial nerve nucleus
+UBERON:1600008,pelvic fin distal radial element,UBERON:2100508,pelvic fin radial element
+HP:0003053,Epiphyseal deformities of tubular bones,HP:0005930,Abnormality of the epiphyses
+UBERON:4200041,aponeurosis palmaris,UBERON:0006614,aponeurosis
+UBERON:0001121,longus colli muscle,UBERON:0003830,thoracic segment muscle
+DOID:3523,brain stem infarction,DOID:3454,brain infarction
+HP:0006140,Premature fusion of phalangeal epiphyses,HP:0010656,Abnormal epiphyseal ossification
+UBERON:0007997,sesamoid bone of manus,UBERON:0011141,appendicular ossicle
+HP:0007149,Distal upper limb amyotrophy,HP:0003693,Distal amyotrophy
+CL:0002500,P enteroendocrine cell,CL:0002268,P/D1 enteroendocrine cell
+HP:0000446,Narrow nasal bridge,HP:0000422,Abnormality of the nasal bridge
+UBERON:0011951,prostate luminal epithelium,UBERON:0005156,reproductive structure
+DOID:9455,lipid storage disease,DOID:3211,lysosomal storage disease
+HP:0100752,Abnormal liver lobulation,HP:0001392,Abnormality of the liver
+HP:0011873,Abnormal platelet count,HP:0001872,Abnormality of thrombocytes
+DOID:3756,protein C deficiency,DOID:2214,inherited blood coagulation disease
+UBERON:0011979,epiphysis of distal phalanx of manus,UBERON:0004387,epiphysis of phalanx of manus
+CL:0000379,sensory processing neuron,CL:0000540,neuron
+UBERON:0004809,salivary gland epithelium,UBERON:0010371,ecto-epithelium
+UBERON:0010846,radius pre-cartilage condensation,UBERON:0015001,radius endochondral element
+UBERON:0012299,mucosa of urethra,UBERON:0004120,mesoderm-derived structure
+DOID:7502,pediatric supratentorial ependymoma,DOID:1659,supratentorial cancer
+UBERON:0013245,sinovaginal bulb,UBERON:0004120,mesoderm-derived structure
+CL:0000773,eosinophilic metamyelocyte,CL:0000772,immature eosinophil
+DOID:3318,epithelioid type angiomyolipoma,DOID:3314,angiomyolipoma
+HP:0004448,Fulminant hepatic failure,HP:0006554,Acute hepatic failure
+UBERON:0002022,insula,UBERON:0004121,ectoderm-derived structure
+UBERON:3010142,occipital arch,UBERON:0005913,zone of bone organ
+UBERON:4300013,paired fin radial skeleton,UBERON:4440008,fin radial skeleton
+DOID:4846,cauda equina intradural extramedullary astrocytoma,DOID:4847,cauda equina neoplasm
+HP:0009255,Irregular epiphysis of the distal phalanx of the 4th finger,HP:0009249,Abnormality of the epiphysis of the distal phalanx of the 4th finger
+UBERON:0014913,ventral pallium,UBERON:0002791,regional part of telencephalon
+UBERON:2002080,spina occipitalis,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009608,Complete duplication of proximal phalanx of the thumb,HP:0010002,Complete duplication of the middle phalanges of the hand
+UBERON:0006323,superior rectus extraocular muscle,UBERON:0006533,rectus extraocular muscle
+HP:0012703,Abnormality of the subarachnoid space,HP:0007319,Morphological abnormality of the central nervous system
+UBERON:2001581,ural centrum 2,UBERON:2002085,ural centrum
+HP:0005929,Synostosis involving the tibia,HP:0002992,Abnormality of the tibia
+DOID:0050042,Indian tick typhus,DOID:11104,spotted fever
+CL:1001096,kidney afferent arteriole endothelial cell,CL:1001006,kidney afferent arteriole cell
+HP:0009454,Patchy sclerosis of the proximal phalanx of the 3rd finger,HP:0009856,Patchy sclerosis of the proximal phalanges of the hand
+DOID:0050793,short QT syndrome,DOID:0050736,autosomal dominant disease
+HP:0012007,Hallucinatory auras,HP:0012002,Experiential auras
+DOID:7332,esophageal tuberculosis,DOID:404,gastrointestinal tuberculosis
+UBERON:0014643,spinoocerebellum,UBERON:0002946,regional part of cerebellum
+DOID:7429,childhood brain germinoma,DOID:2127,brain germinoma
+UBERON:0003013,alar central lobule,UBERON:0004003,cerebellum hemisphere lobule
+UBERON:0006287,radius-ulna pre-cartilage condensation,UBERON:0003327,mesenchyme of forearm
+HP:0005397,Exaggerated cellular immune processes,HP:0011840,Abnormality of T cell physiology
+CL:0002173,extraglomerular mesangial cell,CL:1001318,renal interstitial pericyte
+UBERON:0010150,duct of major vestibular gland,UBERON:0011831,duct of vestibular gland
+DOID:9589,urethral calculus,DOID:9590,lower urinary tract calculus
+HP:0100023,Recurrent hand flapping,HP:0000733,Stereotypic behavior
+DOID:5642,localized pulmonary fibrosis,DOID:3770,pulmonary fibrosis
+DOID:3652,Leigh disease,DOID:700,mitochondrial metabolism disease
+DOID:4407,phototoxic dermatitis,DOID:3159,photosensitivity disease
+HP:0012565,Premature epimetaphyseal fusion in fibula,HP:0010588,Premature epimetaphyseal fusion
+HP:0011626,Scimitar anomaly,HP:0010773,Partial anomalous pulmonary venous return
+UBERON:3010166,fringe on postaxial edge of Toe V,UBERON:3010124,toe fringes
+UBERON:0013420,groove for sigmoid sinus,UBERON:0013685,foramen of skull
+UBERON:0003408,gland of gut,UBERON:0013765,digestive system organ
+HP:0000478,Abnormality of the eye,HP:0000118,Phenotypic abnormality
+UBERON:0006694,cerebellum vasculature,UBERON:0005284,brain vasculature
+UBERON:0001738,thyroid cartilage,UBERON:0001739,laryngeal cartilage
+UBERON:1000015,skin of snout,UBERON:1000021,skin of face
+HP:0000914,Shield chest,HP:0100625,Enlarged thorax
+UBERON:2001980,vertebral element 6,UBERON:0010913,vertebral element
+HP:0001751,Vestibular dysfunction,HP:0011389,Functional abnormality of the inner ear
+UBERON:0006618,atrium auricular region,UBERON:0004120,mesoderm-derived structure
+HP:0002104,Apnea,HP:0002793,Abnormal pattern of respiration
+HP:0001696,Situs inversus totalis,HP:0011534,Abnormal spatial orientation of the cardiac segments
+UBERON:3000363,otic ligament,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:11829,degenerative myopia,DOID:9799,eye degenerative disease
+HP:0009483,Symphalangism of the proximal phalanx of the 3rd finger with the 3rd metatcarpal,HP:0005880,Metacarpophalangeal synostosis
+UBERON:2002130,caudal appendage,UBERON:0000481,multi-tissue structure
+UBERON:0010570,manual digit 1 metacarpus cartilage element,UBERON:0015043,manual digit 1 metacarpus endochondral element
+CL:0002162,internal epithelial cell of tympanic membrane,CL:0002076,endo-epithelial cell
+UBERON:4000053,vacuolated notochordal tissue,UBERON:0004120,mesoderm-derived structure
+UBERON:0001275,pubis,UBERON:0008202,bone of hip region
+UBERON:0009916,wall of ureter,UBERON:0004120,mesoderm-derived structure
+DOID:0050836,focal dystonia,DOID:543,dystonia
+HP:0001006,Hypotrichosis,HP:0011362,Abnormal hair quantity
+HP:0012472,Eclabion,HP:0000159,Abnormality of the lip
+UBERON:0015857,parotid lymph node,UBERON:0015870,lymph node of head
+HP:0200056,Macular scarring,HP:0001103,Abnormality of the macula
+HP:0009834,Abnormality of the proximal phalanges of the hand,HP:0005918,Abnormality of phalanx of finger
+UBERON:0005613,left dorsal aorta,UBERON:0003513,trunk blood vessel
+UBERON:0015019,rib endochondral element,UBERON:0010363,endochondral element
+DOID:2647,parachordoma,DOID:3350,mesenchymal cell neoplasm
+HP:0010060,Bullet-shaped phalanges of the hallux,HP:0010175,Bullet-shaped phalanges of the toes
+DOID:4539,labyrinthine disease,DOID:2952,inner ear disease
+UBERON:0001643,oculomotor nerve,UBERON:0004121,ectoderm-derived structure
+UBERON:0010507,layer of dura mater,UBERON:0004121,ectoderm-derived structure
+UBERON:0002770,posterior hypothalamic region,UBERON:0000477,anatomical cluster
+DOID:5999,apocrine adenosis of breast,DOID:5998,microglandular adenosis
+HP:0002756,Pathologic fracture,HP:0002659,Increased susceptibility to fractures
+CL:0000596,sexual spore,CL:0002369,fungal spore
+HP:0004812,Pre-B-cell acute lymphoblastic leukemia,HP:0006721,Acute lymphatic leukemia
+DOID:8302,mixed endometrial stromal and smooth muscle tumor,DOID:9460,uterine corpus cancer
+HP:0004401,Meconium ileus,HP:0010676,Mechanical ileus
+DOID:1023,borderline leprosy,DOID:1024,leprosy
+HP:0100786,Hypersomnia,HP:0002360,Sleep disturbance
+HP:0100468,Patchy sclerosis of the distal phalanx of the 4th toe,HP:0010190,Patchy sclerosis of the distal phalanges of the toes
+HP:0004446,Stomatocytosis,HP:0004447,Poikilocytosis
+HP:0001248,Short tubular bones (hand),HP:0001155,Abnormality of the hand
+HP:0006529,Abnormal pulmonary lymphatics,HP:0002088,Abnormality of the lung
+DOID:12358,patulous eustachian tube,DOID:9739,eustachian tube disease
+DOID:2222,factor X deficiency,DOID:2214,inherited blood coagulation disease
+HP:0009793,Presacral teratoma,HP:0009792,Teratoma
+HP:0004044,Pointed ulnar metaphysis,HP:0004039,Abnormality of ulnar metaphysis
+UBERON:0010576,manual digit 2 phalanx pre-cartilage condensation,UBERON:0015026,manual digit 2 phalanx endochondral element
+HP:0006048,Distal widening of metacarpals,HP:0005916,Abnormal metacarpal morphology
+UBERON:0001521,flexor carpi radialis muscle,UBERON:0004254,forelimb zeugopod muscle
+UBERON:0002079,left cardiac atrium,UBERON:0002081,cardiac atrium
+UBERON:0004443,proximal epiphysis of proximal phalanx of manual digit 5,UBERON:0011977,epiphysis of proximal phalanx of manus
+UBERON:0004729,nematode larval stage,UBERON:0000069,larval stage
+UBERON:0002352,atrioventricular node,UBERON:0004491,cardiac muscle tissue of interatrial septum
+UBERON:3010204,ventral tail fin,UBERON:3000982,tail external integument structure
+CL:0002264,type A cell of stomach,CL:0002067,type A enterocrine cell
+HP:0002330,Paroxysmal drowsiness,HP:0002329,Drowsiness
+UBERON:0000435,lateral tuberal nucleus,UBERON:0006568,hypothalamic nucleus
+UBERON:0015717,smooth muscle tissue layer of ejaculatory duct,UBERON:0001135,smooth muscle tissue
+HP:0012092,Abnormality of exocrine pancreas physiology,HP:0012091,Abnormality of pancreas physiology
+CL:0000348,choroidal cell of the eye,CL:0000293,structural cell
+DOID:0050599,abdominal tuberculosis,DOID:0050598,extrapulmonary tuberculosis
+UBERON:0006189,mesonephric connecting tubule,UBERON:0005330,mesonephric nephron epithelium
+HP:0011819,Submucous cleft soft palate,HP:0000185,Cleft soft palate
+NCBITaxon:117570,Teleostomi,NCBITaxon:7776,Gnathostomata <vertebrate>
+HP:0010376,Patchy sclerosis of the phalanges of the 4th toe,HP:0100928,Sclerosis of the phalanges of the 4th toe
+HP:0200023,Priapism,HP:0100639,Erectile abnormalities
+UBERON:0006013,interdigital region between manual digits,UBERON:0006012,interdigital region
+HP:0012167,Hair-pulling,HP:0100716,Self-injurious behavior
+UBERON:0012311,deep anterior cervical lymph node,UBERON:0004722,deep cervical lymph node
+HP:0100353,Contractures of the distal interphalangeal joint of the 3rd toe,HP:0010333,Flexion contracture of 3rd toe
+HP:0002377,Paraganglioma-related cranial nerve palsy,HP:0002864,Paraganglioma of head and neck
+HP:0003547,Shoulder girdle muscle weakness,HP:0001435,Abnormality of the shoulder girdle musculature
+HP:0009630,Broad proximal phalanx of the thumb,HP:0009618,Abnormality of the proximal phalanx of the thumb
+UBERON:0009778,pleural sac,UBERON:0005906,serous sac
+DOID:90,degenerative disc disease,DOID:0080007,bone deterioration disease
+UBERON:2000717,apical ectodermal ridge median fin fold,UBERON:0004356,apical ectodermal ridge
+UBERON:0005976,ansiform lobule crus I,UBERON:0005348,ansiform lobule
+HP:0011146,Dialeptic seizures,HP:0001250,Seizures
+DOID:8507,juvenile dermatitis herpetiformis,DOID:8505,dermatitis herpetiformis
+HP:0007215,Periodic hyperkalemic paralysis,HP:0003768,Periodic paralysis
+HP:0000822,Hypertension,HP:0011025,Abnormality of cardiovascular system physiology
+UBERON:0010065,auditory meatus epithelium,UBERON:0010371,ecto-epithelium
+DOID:0050012,chikungunya,DOID:934,viral infectious disease
+UBERON:0007614,extensor digiti minimi muscle,UBERON:0011024,extrinsic extensor muscle of manus
+UBERON:0002018,synovial membrane of synovial joint,UBERON:0007616,layer of synovial tissue
+HP:0000763,Sensory neuropathy,HP:0009830,Peripheral neuropathy
+UBERON:0008881,rostral migratory stream,UBERON:0002791,regional part of telencephalon
+HP:0006216,Single interphalangeal crease of fifth finger,HP:0006109,Absent phalangeal crease
+UBERON:0011610,ceratohyal cartilage,UBERON:0011609,ceratohyal element
+UBERON:3000364,otic plate of pterygoid,UBERON:0010313,neural crest-derived structure
+CL:0002124,CD27-positive gamma-delta T cell,CL:0000912,helper T cell
+HP:0000008,Abnormality of female internal genitalia,HP:0010460,Abnormality of the female genitalia
+UBERON:0015038,pedal digit 2 metatarsal endochondral element,UBERON:0015036,pedal digit metatarsal endochondral element
+DOID:11593,bladder lateral wall cancer,DOID:11054,urinary bladder cancer
+UBERON:0002228,rib,UBERON:0002513,endochondral bone
+HP:0000664,Synophrys,HP:0000534,Abnormality of the eyebrow
+DOID:11758,iron deficiency anemia,DOID:5113,nutritional deficiency disease
+UBERON:0013612,tooth cingulid,UBERON:0000063,organ segment
+CL:0000037,hematopoietic stem cell,CL:0000048,multi fate stem cell
+HP:0003717,Minimal subcutaneous fat,HP:0003758,Reduced subcutaneous adipose tissue
+DOID:674,cleft palate,DOID:0050567,orofacial cleft
+HP:0007911,Congenital bilateral ptosis,HP:0001488,Bilateral ptosis
+CL:0000314,milk secreting cell,CL:0000151,secretory cell
+HP:0004288,Pseudoepiphyses of hand bones,HP:0010584,Pseudoepiphyses
+DOID:10195,pleural lipoma,DOID:0050621,respiratory system benign neoplasm
+HP:0009270,Stippling of the epiphysis of the proximal phalanx of the 4th finger,HP:0009402,Stippling of the epiphyses of the 4th finger
+HP:0001713,Abnormality of cardiac ventricle,HP:0002564,Malformation of the heart and great vessels
+NCBITaxon:5151,Ophiostomatales,NCBITaxon:222544,Sordariomycetidae
+UBERON:0005681,right lung upper lobe bronchiole,UBERON:0003538,right lung bronchiole
+DOID:11382,corneal neovascularization,DOID:4677,keratitis
+HP:0009128,Aplasia/Hypoplasia involving the musculature of the extremities,HP:0009127,Abnormality of the musculature of the limbs
+UBERON:2000975,somite 13,UBERON:0002329,somite
+UBERON:0008435,vertebral arch of sacral segment,UBERON:0003828,abdominal segment bone
+HP:0010606,Hordeolum,HP:0010604,Cyst of the eyelid
+UBERON:2002260,premaxillary-maxillary joint,UBERON:2001950,inter-premaxillary joint
+UBERON:0004346,gubernaculum,UBERON:0005291,embryonic tissue
+UBERON:0003421,mesenchyme of vomeronasal organ,UBERON:0007213,mesenchyme derived from head neural crest
+HP:0011823,Chin with horizontal crease,HP:0000306,Abnormality of the chin
+DOID:4906,small intestine adenocarcinoma,DOID:4907,small intestine carcinoma
+HP:0100408,Complete duplication of the distal phalanx of the 4th toe,HP:0100399,Duplication of the distal phalanx of the 4th toe
+DOID:3480,uveal disease,DOID:5614,eye disease
+UBERON:0001366,parietal peritoneum,UBERON:0004120,mesoderm-derived structure
+HP:0005857,Cervical spina bifida,HP:0002414,Spina bifida
+HP:0004348,Abnormality of bone mineral density,HP:0003330,Abnormal bone structure
+DOID:0050521,Oropouche fever,DOID:934,viral infectious disease
+HP:0010998,Increased susceptibility to spontaneous sister chromatid exchange,HP:0003220,Abnormality of chromosome stability
+HP:0011670,Left superior vena cava draining to coronary sinus,HP:0005301,Persistent left superior vena cava
+UBERON:0009845,urogenital sinus mesenchyme,UBERON:0003104,mesenchyme
+HP:0003988,Long ulna,HP:0002997,Abnormality of the ulna
+HP:0001491,Congenital fibrosis of extraocular muscles,HP:0008049,Abnormality of the extraocular muscles
+UBERON:0001043,esophagus,UBERON:0013765,digestive system organ
+UBERON:0004001,olfactory bulb layer,UBERON:0000119,cell layer
+HP:0010593,Abnormality of fibular epiphyses,HP:0006500,Abnormality involving the epiphyses of the lower limbs
+UBERON:0000362,renal medulla,UBERON:0006554,urinary system structure
+UBERON:0002250,popliteal artery,UBERON:0001637,artery
+UBERON:0006274,tetrapod parietal bone primordium,UBERON:0001048,primordium
+DOID:2355,anemia,DOID:74,hematopoietic system disease
+DOID:1483,gingival disease,DOID:3388,periodontal disease
+DOID:14443,cholinergic urticaria,DOID:0060220,physical urticaria
+UBERON:0001189,left testicular artery,UBERON:0001187,testicular artery
+HP:0009993,Complete duplication of the proximal phalanx of the 5th finger,HP:0009986,Complete duplication of the phalanges of the 5th finger
+UBERON:0004655,zygomatic process of temporal bone,UBERON:0004120,mesoderm-derived structure
+UBERON:0012457,Ruffini nerve ending,UBERON:0012449,mechanoreceptor
+UBERON:0003436,shoulder nerve,UBERON:0001021,nerve
+DOID:13381,pernicious anemia,DOID:5113,nutritional deficiency disease
+CL:0000830,basophilic promyelocyte,CL:0000836,promyelocyte
+DOID:8533,hypopharynx cancer,DOID:0060119,pharynx cancer
+HP:0000471,Gastrointestinal angiodysplasia,HP:0004296,Abnormality of gastrointestinal vasculature
+HP:0005462,Calcification of falx cerebri,HP:0002514,Cerebral calcification
+UBERON:0002047,pontine raphe nucleus,UBERON:0006331,brainstem nucleus
+UBERON:0007167,right dome of diaphragm,UBERON:0007145,dome of diaphragm
+UBERON:2001181,epidermal intermediate stratum,UBERON:0000479,tissue
+DOID:7244,bladder urachal urothelial carcinoma,DOID:4006,bladder transitional cell carcinoma
+UBERON:0005922,inferior nasal concha,UBERON:0015212,lateral structure
+DOID:3765,pseudohermaphroditism,DOID:1923,sex differentiation disease
+HP:0004238,Lytic defects of carpal bones,HP:0001495,Carpal osteolysis
+CL:0002526,CD14-positive dermal dendritic cell,CL:0001006,dermal dendritic cell
+UBERON:0015115,distal tarsal bone 5 cartilage,UBERON:0015064,autopod cartilage
+DOID:1079,setariasis,DOID:1080,filariasis
+HP:0005989,Redundant neck skin,HP:0000464,Abnormality of the neck
+UBERON:0011383,inferior pancreaticoduodenal vein,UBERON:0004690,pancreaticoduodenal vein
+UBERON:0006435,os penis,UBERON:0007719,bone of reproductive structure
+CL:0000976,IgA short lived plasma cell,CL:0000975,short lived plasma cell
+UBERON:0002308,nucleus of brain,UBERON:0000125,neural nucleus
+DOID:0050858,Marshall-Smith syndrome,DOID:225,syndrome
+CL:0002447,CD94-negative natural killer cell,CL:0002438,NK1.1-positive natural killer cell
+HP:0002453,Abnormality of the globus pallidus,HP:0002134,Abnormality of the basal ganglia
+UBERON:0006822,proximal epiphysis of ulna,UBERON:0004386,epiphysis of ulna
+DOID:8729,milker's nodule,DOID:934,viral infectious disease
+UBERON:0006761,corneo-scleral junction,UBERON:0004121,ectoderm-derived structure
+UBERON:0005090,muscle structure,UBERON:0000061,anatomical structure
+UBERON:4200026,supraglenoid foramen,UBERON:0005744,bone foramen
+CL:0002266,type D cell of small intestine,CL:0000502,type D enteroendocrine cell
+DOID:110,lens disease,DOID:5614,eye disease
+UBERON:0004177,hemopoietic organ,UBERON:0000062,organ
+HP:0003907,Abnormality of the humeral metaphyses,HP:0003063,Abnormality of the humerus
+HP:0010134,Pseudoepiphysis of the proximal phalanx of the hallux,HP:0010126,Abnormality of the epiphysis of the proximal phalanx of the hallux
+HP:0011601,Rightward direction of ventricular apex,HP:0011600,Abnormal direction of ventricular apex
+HP:0008954,Intrinsic hand muscle atrophy,HP:0009130,Hand muscle atrophy
+HP:0010234,Ivory epiphyses of the phalanges of the hand,HP:0100899,Sclerosis of the phalanges of the hand
+UBERON:0003077,paraxial mesoderm,UBERON:0015212,lateral structure
+HP:0001773,Short foot,HP:0001769,Broad foot
+NCBITaxon:72294,Campylobacteraceae,NCBITaxon:213849,Campylobacterales
+DOID:11472,subglottis cancer,DOID:2596,larynx cancer
+UBERON:0001114,right lobe of liver,UBERON:0001113,lobe of liver
+DOID:12399,pathological gambling,DOID:10937,impulse control disorder
+UBERON:0005291,embryonic tissue,UBERON:0002050,embryonic structure
+HP:0004027,Abnormality of radial diaphysis,HP:0009808,Anomaly of the upper limb diaphyses
+DOID:121,vaginal disease,DOID:229,female reproductive system disease
+UBERON:3010242,nasolabial groove,UBERON:0006846,surface groove
+HP:0100155,Stippling of the epiphysis of the middle phalanx of the 3rd toe,HP:0100064,Stippling of the epiphyses of the 3rd toe
+HP:0000286,Epicanthus,HP:0000492,Abnormality of the eyelid
+UBERON:0014600,paraventricular nucleus of the hypothalamus magnocellular division - medial magnocellular part,UBERON:0003048,regional part of hypothalamus
+HP:0100232,Small epiphysis of the proximal phalanx of the 5th toe,HP:0100099,Abnormality of the epiphysis of the proximal phalanx of the 5th toe
+HP:0100179,Triangular epiphysis of the distal phalanx of the 4th toe,HP:0100094,Abnormality of the epiphysis of the distal phalanx of the 4th toe
+UBERON:0003560,spinal cord arachnoid mater,UBERON:0002362,arachnoid mater
+CL:0000813,memory T cell,CL:0002419,mature T cell
+HP:0010553,Oculogyric crisis,HP:0001332,Dystonia
+HP:0011206,EEG with generalized slow activity grade 1,HP:0010845,EEG with generalized slow activity
+UBERON:3010653,ramus nasalis medialis,UBERON:0004732,segmental subdivision of nervous system
+DOID:4249,Gerstmann-Straussler-Scheinker syndrome,DOID:649,prion disease
+UBERON:0004015,embryonic-extraembryonic boundary,UBERON:0000015,anatomical boundary
+CL:0000962,Bm2 B cell,CL:0000843,follicular B cell
+NCBITaxon:134742,Sigmodon alstoni,NCBITaxon:42414,Sigmodon
+HP:0006955,Olivopontocerebellar hypoplasia,HP:0001317,Abnormality of the cerebellum
+UBERON:0011120,laryngeal joint,UBERON:0002217,synovial joint
+UBERON:3010224,vertebral,UBERON:0001637,artery
+CL:0000096,mature neutrophil,CL:0000775,neutrophil
+HP:0005288,Abnormality of the nares,HP:0000366,Abnormality of the nose
+UBERON:0004801,cervix epithelium,UBERON:0006955,uterine epithelium
+UBERON:3000743,sacral condyle,UBERON:0000064,organ part
+DOID:1799,islet cell tumor,DOID:1793,pancreatic cancer
+UBERON:0005777,glomerular basement membrane,UBERON:0004120,mesoderm-derived structure
+UBERON:2000491,commissure of the caudal tuberculum,UBERON:0003931,diencephalic white matter
+HP:0001471,Aplasia/Hypoplasia of the musculature of the pelvis,HP:0001469,Abnormality of the musculature of the pelvis
+HP:0009531,Pseudoepiphysis of the proximal phalanx of the 2nd finger,HP:0009495,Pseudoepiphyses of the 2nd finger
+DOID:13533,osteopetrosis,DOID:4254,osteosclerosis
+CL:0002157,endosteal cell,CL:0002078,meso-epithelial cell
+UBERON:2001772,anal fin lepidotrichium 4,UBERON:4000176,anal fin lepidotrichium
+HP:0003403,EMG: decremental response of compound muscle action potential (CMAP) to repetitive nerve stimulation,HP:0003457,EMG abnormality
+UBERON:0004021,spongiotrophoblast layer,UBERON:0005156,reproductive structure
+UBERON:0000029,lymph node,UBERON:0000064,organ part
+UBERON:0001492,radial nerve,UBERON:0002003,peripheral nerve
+CL:0000061,cementoblast,CL:0000062,osteoblast
+UBERON:0004699,outflow tract endothelium,UBERON:0008307,heart endothelium
+DOID:9499,disseminated eosinophilic collagen disease,DOID:854,collagen disease
+UBERON:0002884,intercalated amygdaloid nuclei,UBERON:0002619,regional part of cerebral cortex
+UBERON:0001839,bony labyrinth,UBERON:0000477,anatomical cluster
+UBERON:0015014,calcaneum endochondral element,UBERON:0015050,tarsus endochondral element
+DOID:6274,malignant thyroid stimulating hormone producing neoplasm of pituitary gland,DOID:5716,hormone producing pituitary cancer
+HP:0100173,Fragmentation of the epiphysis of the distal phalanx of the 4th toe,HP:0100070,Fragmentation of the epiphyses of the 4th toe
+DOID:5876,apocrine sweat gland neoplasm,DOID:2664,sweat gland neoplasm
+HP:0002546,Incomprehensible speech,HP:0002167,Neurological speech impairment
+UBERON:0002910,posterior ascending limb of lateral sulcus,UBERON:0008334,subarachnoid sulcus
+NCBITaxon:333774,unclassified Papillomaviridae,NCBITaxon:151340,Papillomaviridae
+UBERON:0010686,manual digit phalanx cartilage element,UBERON:0005257,manual digit mesenchyme
+DOID:1382,miliaria,DOID:1383,sweat gland disease
+HP:0011709,Atrioventricular dissociation,HP:0005150,Abnormal atrioventricular conduction
+UBERON:0004175,internal genitalia,UBERON:0003133,reproductive organ
+UBERON:3000399,pars externa plectri,UBERON:0010313,neural crest-derived structure
+HP:0100724,Hypercoagulability,HP:0001928,Abnormality of coagulation
+UBERON:0001077,transverse process of vertebra,UBERON:0006061,process of vertebra
+DOID:5597,fallopian tube papillary adenocarcinoma,DOID:3706,fallopian tube adenocarcinoma
+HP:0011994,Abnormality of the atrial septum,HP:0001671,Abnormality of the cardiac septa
+UBERON:0002375,cricoid cartilage,UBERON:0001739,laryngeal cartilage
+HP:0009616,Bifid first metacarpal,HP:0009944,Partial duplication of the phalanges of the thumb
+HP:0100445,Curved middle phalanx of the 5th toe,HP:0010386,Curved phalanges of the 5th toe
+HP:0006716,Hereditary nonpolyposis colorectal carcinoma,HP:0002672,Gastrointestinal carcinoma
+UBERON:0011188,lesser tubercle of humerus,UBERON:0005813,tubercle
+UBERON:2002293,hypaxial basal fulcrum,UBERON:2002082,basal fulcrum
+DOID:3803,Crigler-Najjar syndrome,DOID:2741,bilirubin metabolic disorder
+HP:0009573,Patchy sclerosis of the middle phalanx of the 2nd finger,HP:0009848,Patchy sclerosis of the middle phalanges of the hand
+DOID:0050649,atransferrinemia,DOID:896,metal metabolism disorder
+HP:0100253,Abnormality of the medullary cavity of the long bones,HP:0000940,Abnormal diaphysis morphology
+HP:0100743,Neoplasm of the rectum,HP:0002034,Abnormality of the rectum
+CL:0002564,nucleus pulposus cell of intervertebral disc,CL:0002320,connective tissue cell
+DOID:6727,colon small cell carcinoma,DOID:1520,colon carcinoma
+CL:0000834,neutrophil progenitor cell,CL:0000763,myeloid cell
+CL:0002207,brush cell of trachea,CL:0002075,brush cell of trachebronchial tree
+DOID:3594,choriocarcinoma,DOID:2021,placenta cancer
+HP:0100804,Ungual fibroma,HP:0100803,Abnormality of the periungual region
+HP:0006722,Small intestine carcinoid,HP:0100570,Carcinoid
+UBERON:0013479,lung endothelium,UBERON:0004702,respiratory system blood vessel endothelium
+UBERON:2007030,posterior neural rod,UBERON:0005291,embryonic tissue
+UBERON:0010355,ossification center,UBERON:0005913,zone of bone organ
+UBERON:0010022,ventral part of pharyngeal pouch 1,UBERON:0005291,embryonic tissue
+UBERON:0001265,trabecula of spleen,UBERON:0000440,trabecula
+HP:0000716,Depression,HP:0100851,Abnormal emotion/affect behavior
+UBERON:0002756,anterior cingulate gyrus,UBERON:0000200,gyrus
+HP:0008905,Rhizomelia,HP:0008873,Disproportionate short-limb short stature
+HP:0008501,Median cleft lip and palate,HP:0000161,Median cleft lip
+HP:0009626,Contractures of the interphalangeal joint of the thumb,HP:0001220,Interphalangeal joint contractures (hands)
+UBERON:0000951,rotator muscle of the vertebral column,UBERON:0002324,muscle of back
+UBERON:0010365,odontoid tissue,UBERON:0004755,skeletal tissue
+UBERON:0004471,musculature of pectoral girdle,UBERON:0014793,musculature of pectoral complex
+UBERON:0004475,musculature of hip,UBERON:0014792,musculature of pelvic complex
+CL:0002590,smooth muscle cell of the brain vasculature,CL:0002319,neural cell
+HP:0004397,Ectopic anus,HP:0004378,Abnormality of the anus
+NCBITaxon:170,Leptospiraceae,NCBITaxon:136,Spirochaetales
+DOID:7315,Jewett-Marshall bladder cancer,DOID:4007,bladder carcinoma
+HP:0011155,Focal autonomic seizures with altered responsiveness,HP:0011154,Focal autonomic seizures
+DOID:2658,dermoid cyst,DOID:2660,cystic teratoma
+DOID:5353,colonic disease,DOID:5295,intestinal disease
+UBERON:0001948,regional part of spinal cord,UBERON:0000073,regional part of nervous system
+UBERON:0007711,sixth cervical dorsal root ganglion,UBERON:0002834,cervical dorsal root ganglion
+UBERON:2005022,opercular artery,UBERON:0001637,artery
+HP:0009982,Partial duplication of the middle phalanx of the 4th finger,HP:0010005,Partial duplication of the middle phalanges of the hand
+CL:0001033,hippocampal granule cell,CL:0002608,hippocampal neuron
+UBERON:0001876,amygdala,UBERON:0002420,basal ganglion
+UBERON:3010093,villosities,UBERON:0013703,integumentary projection
+UBERON:0010541,tarsus cartilage element,UBERON:0003328,mesenchyme of footplate
+CL:0000056,myoblast,CL:0000680,muscle precursor cell
+UBERON:0006568,hypothalamic nucleus,UBERON:0006569,diencephalic nucleus
+UBERON:0015230,dorsal vessel heart,UBERON:0004120,mesoderm-derived structure
+CL:0002313,endocrine-paracrine cell of prostate gland,CL:0002159,general ecto-epithelial cell
+UBERON:4300015,ventral cleithrum,UBERON:0008907,dermal bone
+UBERON:0005995,mitral valve anulus,UBERON:0010313,neural crest-derived structure
+UBERON:3000523,pterygoid process of palatoquadrate,UBERON:4100000,skeletal element projection
+UBERON:0004750,blastoderm,UBERON:0002050,embryonic structure
+DOID:12124,episcleritis periodica fugax,DOID:11343,scleral disease
+UBERON:0012313,1st arch maxillary ectoderm,UBERON:0010371,ecto-epithelium
+HP:0009144,Supernumerary bones of the axial skeleton,HP:0009121,Abnormal axial skeleton morphology
+UBERON:0015156,terminal branch of ophthalmic artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:6608,endobronchial leiomyoma,DOID:5136,lung leiomyoma
+DOID:14491,regional ureteric cancer,DOID:4939,ureter carcinoma
+UBERON:3010757,ramus superficial ophthalmic,UBERON:3010105,anterodorsal lateral line nerve (ADLLN)
+CL:0000062,osteoblast,CL:0000055,non-terminally differentiated cell
+UBERON:3000363,otic ligament,UBERON:0004121,ectoderm-derived structure
+UBERON:0010348,hyoid pre-muscle mass,UBERON:0005865,pre-muscle condensation
+UBERON:0011628,early premaxilla,UBERON:0008907,dermal bone
+UBERON:0006571,trabecula carnea of left ventricle,UBERON:0002511,trabecula carnea
+HP:0003905,Abnormality of the humeral epiphyseal plate,HP:0003891,Abnormality of the humeral epiphysis
+UBERON:0009041,superficial circumflex iliac artery,UBERON:0003520,pelvis blood vessel
+UBERON:2001856,gill ray,UBERON:0011004,pharyngeal arch cartilage
+UBERON:0000086,zona pellucida,UBERON:0000470,cell part
+UBERON:0005594,head somite,UBERON:0002329,somite
+HP:0100385,Aplasia of the proximal phalanx of the 4th toe,HP:0100388,Aplasia of the proximal phalanges of the toes
+UBERON:2001023,epaxial region somite 19,UBERON:0003900,epaxial myotome region
+HP:0005849,Diffuse cerebral calcification,HP:0002514,Cerebral calcification
+UBERON:0002566,superior precentral sulcus,UBERON:0013118,sulcus of brain
+UBERON:0006801,proximal head of humerus,UBERON:0005055,zone of long bone
+CL:1000405,epithelial cell of appendix,CL:0011108,colon epithelial cell
+NCBITaxon:9989,Rodentia,NCBITaxon:314147,Glires
+HP:0003128,Lactic acidosis,HP:0001941,Acidosis
+UBERON:2001166,supraneural 9 bone,UBERON:2000442,supraneural bone
+HP:0100077,Absent epiphyses of the 5th toe,HP:0010341,Abnormality of the epiphyses of the 5th toe
+HP:0100627,Displacement of the external urethral meatus,HP:0000795,Abnormality of the urethra
+DOID:4399,acneiform dermatitis,DOID:2723,dermatitis
+UBERON:0001777,substantia propria of cornea,UBERON:0010313,neural crest-derived structure
+UBERON:0004744,articular/anguloarticular,UBERON:0002513,endochondral bone
+HP:0009504,Cone-shaped epiphysis of the distal phalanx of the 2nd finger,HP:0009490,Cone-shaped epiphyses of the 2nd finger
+HP:0000294,Low anterior hairline,HP:0000599,Abnormality of the frontal hairline
+UBERON:0000020,sense organ,UBERON:0000062,organ
+UBERON:0001785,cranial nerve,UBERON:0015212,lateral structure
+HP:0100598,Pulmonary edema,HP:0000969,Edema
+DOID:4043,skeletal muscle cancer,DOID:4045,muscle cancer
+HP:0002925,Thyroid-stimulating hormone excess,HP:0010514,Hyperpituitarism
+CL:1000606,kidney nerve cell,CL:0000540,neuron
+DOID:10686,lactocele,DOID:10350,breast cyst
+UBERON:0001378,rectus femoris,UBERON:0001377,quadriceps femoris
+UBERON:2000422,retroarticular,UBERON:0004768,bone of lower jaw
+UBERON:0004548,left eye,UBERON:0000970,eye
+UBERON:0015129,epicardial fat,UBERON:0004120,mesoderm-derived structure
+UBERON:0002012,pulmonary artery,UBERON:0013768,great vessel of heart
+UBERON:0002998,inferior frontal gyrus,UBERON:0015593,frontal gyrus
+DOID:11285,tick paralysis,DOID:4109,tick infestation
+HP:0008371,Abnormal metatarsal ossification,HP:0010675,Abnormal foot bone ossification
+DOID:28,endocrine system disease,DOID:7,disease of anatomical entity
+UBERON:0005129,metanephric distal tubule,UBERON:0004135,distal tubule
+HP:0005105,Abnormal nasal morphology,HP:0000366,Abnormality of the nose
+UBERON:0014549,pyramidal layer of CA2,UBERON:0002619,regional part of cerebral cortex
+UBERON:0004737,metanephric collecting duct,UBERON:0001232,collecting duct of renal tubule
+UBERON:0011318,capsule of temporomandibular joint,UBERON:0001484,articular capsule
+UBERON:0015246,septal organ of Masera,UBERON:0015245,septal olfactory organ
+HP:0011034,Amyloidosis,HP:0001939,Abnormality of metabolism/homeostasis
+HP:0011850,Parotitis,HP:0000197,Abnormality of parotid gland
+DOID:0050872,large cell neuroendocrine carcinoma,DOID:4556,lung large cell carcinoma
+HP:0010774,Cor triatriatrum,HP:0005120,Abnormality of cardiac atrium
+HP:0004379,Abnormality of alkaline phosphatase activity,HP:0012379,Abnormal enzyme/coenzyme activity
+DOID:0060198,amyotrophic lateral sclerosis type 6,DOID:332,amyotrophic lateral sclerosis
+UBERON:2001200,corpuscles of Stannius,UBERON:0000479,tissue
+HP:0006161,Short metacarpals with rounded proximal ends,HP:0010049,Short metacarpal
+HP:0007943,Congenital stapes ankylosis,HP:0000381,Stapes ankylosis
+HP:0000577,Exotropia,HP:0000486,Strabismus
+HP:0002478,Progressive spastic quadriplegia,HP:0002191,Progressive spasticity
+DOID:6621,cerebral angioma,DOID:5393,brain angioma
+HP:0010234,Ivory epiphyses of the phalanges of the hand,HP:0011001,Increased bone mineral density
+HP:0001181,Adducted thumb,HP:0001172,Abnormality of the thumb
+HP:0010397,Bullet-shaped proximal phalanx of the 2nd toe,HP:0010358,Abnormality of the proximal phalanx of the 2nd toe
+UBERON:0011686,spiracularis muscle,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:13353,diffuse interstitial keratitis,DOID:9857,interstitial keratitis
+HP:0007107,Segmental peripheral demyelination,HP:0011096,Peripheral demyelination
+UBERON:0014684,Helicoprion tooth whorl,UBERON:0009679,set of lower jaw teeth
+HP:0011564,Mitral valve arcade,HP:0001633,Abnormality of the mitral valve
+NCBITaxon:41820,Culicoides <genus>,NCBITaxon:58262,Culicoidini
+UBERON:4300020,anal fin basal cartilage,UBERON:0007844,cartilage element
+HP:0000804,Xanthine nephrolithiasis,HP:0000787,Nephrolithiasis
+UBERON:0005054,dorsal nerve cord,UBERON:0005053,nerve cord
+HP:0000767,Pectus excavatum,HP:0000766,Abnormality of the sternum
+UBERON:2001797,epibranchial 1 bone uncinate process,UBERON:2001382,epibranchial bone uncinate process
+HP:0010104,Absent first metatarsal,HP:0010744,Absent metatarsal bone
+UBERON:0005576,rhombomere 4 floor plate,UBERON:0005500,rhombomere floor plate
+UBERON:0006878,decidua parietalis,UBERON:0014404,female anatomical structure
+UBERON:0000957,lamina,UBERON:0000479,tissue
+DOID:10866,total third-nerve palsy,DOID:10863,paralytic squint
+HP:0100392,Short middle phalanx of the 3rd toe,HP:0100372,Aplasia/Hypoplasia of the middle phalanx of the 3rd toe
+CL:0002491,auditory epithelial cell,CL:0000098,sensory epithelial cell
+HP:0000234,Abnormality of the head,HP:0000152,Abnormality of head and neck
+HP:0009199,Irregular epiphysis of the proximal phalanx of the 5th finger,HP:0009387,Irregular epiphyses of the 5th finger
+DOID:0060063,X-linked sideroblastic anemia,DOID:8955,sideroblastic anemia
+HP:0008484,Thoracolumbar interpediculate narrowness,HP:0008450,Narrow vertebral interpedicular distance
+UBERON:2000607,ventral rhombencephalic commissure brain stem,UBERON:2000318,brainstem and spinal white matter
+CL:1000454,kidney collecting duct epithelial cell,CL:0000072,non-branched duct epithelial cell
+CL:0002066,Feyrter cell,CL:0000165,neuroendocrine cell
+DOID:4675,uremic neuropathy,DOID:4676,uremia
+HP:0009459,Short proximal phalanx of the 3rd finger,HP:0009457,Aplasia/Hypoplasia of the proximal phalanx of the 3rd finger
+UBERON:0010251,anterior meningeal artery,UBERON:0004573,systemic artery
+UBERON:0007250,lingual tonsil,UBERON:0015212,lateral structure
+HP:0004294,Subluxation of metacarpal phalangeal joints,HP:0011911,Abnormality of metacarpophalangeal joint
+HP:0002161,Hyperlysinemia,HP:0010908,Abnormality of lysine metabolism
+DOID:9140,xeroderma of eyelid,DOID:1894,noninfectious dermatoses of eyelid
+UBERON:3000799,cartilago paraglenoidalis,UBERON:0000064,organ part
+DOID:1206,Rett syndrome,DOID:0060040,pervasive developmental disorder
+HP:0000712,Emotional lability,HP:0100852,Abnormal fear/anxiety-related behavior
+HP:0010762,Chordoma,HP:0010622,Neoplasm of the skeletal system
+UBERON:0001565,geniohyoid muscle,UBERON:0008571,suprahyoid muscle
+HP:0001596,Alopecia,HP:0011362,Abnormal hair quantity
+UBERON:0002032,areola,UBERON:0005156,reproductive structure
+DOID:2477,motor peripheral neuropathy,DOID:0060053,peripheral neuropathy
+UBERON:0000009,submucosa,UBERON:0004923,organ component layer
+UBERON:0005789,lamina rara externa,UBERON:0000476,acellular anatomical structure
+DOID:13608,biliary atresia,DOID:13580,cholestasis
+UBERON:2002130,caudal appendage,UBERON:0004120,mesoderm-derived structure
+UBERON:0002565,olivary pretectal nucleus,UBERON:0011214,nucleus of midbrain tectum
+UBERON:4200081,hypocleideum,UBERON:0004121,ectoderm-derived structure
+CL:0000777,mesangial phagocyte,CL:1000500,kidney interstitial cell
+UBERON:0004334,proximal phalanx of pedal digit 3,UBERON:0014503,proximal phalanx of digit 3
+CL:0002594,smooth muscle cell of the umbilical artery,CL:0000359,vascular associated smooth muscle cell
+DOID:905,Zellweger syndrome,DOID:906,peroxisomal disease
+DOID:5853,lateral myocardial infarction,DOID:5844,myocardial infarction
+HP:0012692,Focal T2 hyperintense thalamic lesion,HP:0012696,Abnormal thalamic MRI signal intensity
+UBERON:0002282,stria vascularis of cochlear duct,UBERON:0004121,ectoderm-derived structure
+HP:0003225,Reduced factor V activity,HP:0010990,Abnormality of the common coagulation pathway
+UBERON:0003220,metanephric mesenchyme,UBERON:0004120,mesoderm-derived structure
+HP:0012737,Small intestinal polyp,HP:0005266,Intestinal polyp
+HP:0010583,Ivory epiphyses,HP:0005930,Abnormality of the epiphyses
+UBERON:0010276,vertebral column opening,UBERON:0004120,mesoderm-derived structure
+UBERON:0006854,distal straight tubule postmacula segment,UBERON:0008408,distal tubular epithelium
+HP:0007936,Restrictive external ophthalmoplegia,HP:0000544,External ophthalmoplegia
+HP:0009197,Bracket epiphysis of the proximal phalanx of the 5th finger,HP:0009153,Abnormality of the epiphysis of the proximal phalanx of the 5th finger
+DOID:7371,superficial urinary bladder cancer,DOID:4007,bladder carcinoma
+UBERON:0006789,deep gray layer of superior colliculus,UBERON:0006785,gray matter of superior colliculus
+HP:0009209,Ivory epiphysis of the middle phalanx of the 5th finger,HP:0004224,Abnormality of the epiphysis of the middle phalanx of the 5th finger
+DOID:13687,chronic duodenal ileus,DOID:3558,duodenal obstruction
+UBERON:0006796,cephalopod optic lobe,UBERON:0006794,visual processing part of nervous system
+DOID:13409,perforation of bile duct,DOID:9741,biliary tract disease
+UBERON:4200052,crista tibiofibularis,UBERON:0004120,mesoderm-derived structure
+UBERON:0005344,peritoneal vaginal process,UBERON:0005423,developing anatomical structure
+UBERON:2001457,postcranial axial cartilage,UBERON:0007844,cartilage element
+DOID:12402,pyromania,DOID:10937,impulse control disorder
+UBERON:2001391,anterior lateral line ganglion,UBERON:2000120,lateral line ganglion
+UBERON:2002002,anterior distal serration of pectoral fin spine,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0001692,Primary atrial arrhythmia,HP:0004755,Supraventricular tachycardia
+HP:0004493,Craniofacial hyperostosis,HP:0004437,Cranial hyperostosis
+HP:0200096,Triangular-shaped open mouth,HP:0000194,Open mouth
+DOID:11874,abnormal threshold of rods,DOID:8499,night blindness
+DOID:9250,acrocallosal syndrome,DOID:225,syndrome
+HP:0010404,Aplasia/Hypoplasia of the middle phalanx of the 2nd toe,HP:0010194,Aplasia/Hypoplasia of the middle phalanges of the toes
+HP:0012159,Internal carotid artery dissection,HP:0012158,Carotid artery dissection
+DOID:2106,Thomsen disease,DOID:450,myotonic disease
+UBERON:0005874,3rd arch pharyngeal cleft,UBERON:0005879,pharyngeal cleft
+UBERON:0002616,regional part of brain,UBERON:0004121,ectoderm-derived structure
+UBERON:0007150,superior thyroid artery,UBERON:0004573,systemic artery
+HP:0012391,Hyporeflexia of upper limbs,HP:0001265,Hyporeflexia
+HP:0012229,CSF pleocytosis,HP:0002921,Abnormality of the cerebrospinal fluid
+HP:0100045,Bracket epiphyses of the 2nd toe,HP:0010163,Bracket epiphyses of the toes
+DOID:4687,mucoepidermoid thyroid carcinoma,DOID:3963,thyroid carcinoma
+HP:0009968,Partial duplication of the distal phalanx of the 3rd finger,HP:0010004,Partial duplication of the distal phalanges of the hand
+UBERON:0007186,pericardial visceral mesothelium,UBERON:0007141,visceral mesothelium
+DOID:918,liver inflammatory pseudotumor,DOID:409,liver disease
+DOID:1171,hyperlipoproteinemia type V,DOID:1168,familial hyperlipidemia
+DOID:5465,conjunctival intraepithelial neoplasm,DOID:0060071,pre-malignant neoplasm
+UBERON:0004337,distal phalanx of manual digit 1,UBERON:0014483,distal phalanx of digit 1
+UBERON:0002970,intermediate oculomotor nucleus,UBERON:0007414,nucleus of midbrain tegmentum
+CL:0000667,collagen secreting cell,CL:0000327,extracellular matrix secreting cell
+UBERON:0011384,superior pancreaticoduodenal vein,UBERON:0004690,pancreaticoduodenal vein
+UBERON:0012135,prepollex skeleton,UBERON:0004120,mesoderm-derived structure
+UBERON:0005320,mesonephric juxtaglomerular apparatus,UBERON:0002303,juxtaglomerular apparatus
+UBERON:0006563,tunica media of pulmonary trunk,UBERON:0007239,tunica media of artery
+CL:0000680,muscle precursor cell,CL:0000055,non-terminally differentiated cell
+UBERON:0005675,right lung caudal lobe endothelium,UBERON:0005640,right lung caudal lobe epithelium
+UBERON:0007314,superior external pudendal artery,UBERON:0013137,external pudendal artery
+UBERON:0005621,rhomboid,UBERON:0001630,muscle organ
+UBERON:0010215,arytenoid swellings,UBERON:0004119,endoderm-derived structure
+UBERON:3000827,margo anterior of cleithrum,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0002211,type I muscle cell,CL:0002210,red muscle cell
+UBERON:0005969,reticulum trabeculare,UBERON:0004121,ectoderm-derived structure
+HP:0003172,Abnormality of the pubic bones,HP:0003272,Abnormality of the hip bone
+HP:0010302,Spinal cord tumor,HP:0002143,Abnormality of the spinal cord
+HP:0010140,Cone-shaped epiphysis of the distal phalanx of the hallux,HP:0010115,Cone-shaped epiphyses of the hallux
+HP:0007042,Focal white matter lesions,HP:0002500,Abnormality of the cerebral white matter
+UBERON:0001600,tensor tympani,UBERON:0004112,muscle of middle ear
+UBERON:0001945,superior colliculus,UBERON:0006794,visual processing part of nervous system
+UBERON:0003655,molar tooth,UBERON:0013164,molariform tooth
+DOID:5998,microglandular adenosis,DOID:3463,breast disease
+UBERON:0001472,vaginal venous plexus,UBERON:0014404,female anatomical structure
+DOID:9504,benign mammary dysplasia,DOID:0060082,breast benign neoplasm
+UBERON:0012278,gland of nasal mucosa,UBERON:0004121,ectoderm-derived structure
+DOID:13452,scleritis,DOID:11343,scleral disease
+UBERON:2000442,supraneural bone,UBERON:0002513,endochondral bone
+DOID:6484,mediastinal melanocytic neurilemmoma,DOID:6175,mediastinal neurilemmoma
+HP:0010561,Undulate ribs,HP:0000772,Abnormality of the ribs
+UBERON:0006675,venous valve,UBERON:0004120,mesoderm-derived structure
+HP:0007754,Macular dystrophy,HP:0000608,Macular degeneration
+HP:0009839,Osteolytic defects of the distal phalanges of the hand,HP:0009832,Abnormality of the distal phalanx of finger
+HP:0010255,Stippling of the epiphyses of the distal phalanges of the hand,HP:0010243,Abnormality of the epiphyses of the distal phalanx of finger
+UBERON:0000006,islet of Langerhans,UBERON:0004119,endoderm-derived structure
+HP:0004239,Proximally placed carpal bones,HP:0001191,Abnormality of the carpal bones
+CL:0002652,endothelial cell of high endothelial venule,CL:1000414,endothelial cell of venule
+UBERON:2005119,barbel primordium,UBERON:0003102,surface structure
+HP:0007987,Progressive visual field defects,HP:0001123,Visual field defect
+HP:0002066,Gait ataxia,HP:0001288,Gait disturbance
+UBERON:0009744,lymph node medullary sinus,UBERON:0004111,anatomical conduit
+UBERON:0004399,epiphysis of fifth metatarsal bone,UBERON:0004389,epiphysis of metatarsal bone
+UBERON:0003295,pharyngeal gland,UBERON:0003408,gland of gut
+DOID:3755,antithrombin III deficiency,DOID:2214,inherited blood coagulation disease
+UBERON:0004069,accessory olfactory bulb,UBERON:0002791,regional part of telencephalon
+HP:0002879,Anisospondyly,HP:0003312,Abnormal form of the vertebral bodies
+HP:0003874,Humerus varus,HP:0003063,Abnormality of the humerus
+HP:0002098,Respiratory distress,HP:0002094,Dyspnea
+DOID:1835,mononeuritis multiplex,DOID:572,mononeuritis of upper limb and mononeuritis multiplex
+HP:0009168,Bullet-shaped middle phalanx of the 5th finger,HP:0009375,Bullet-shaped phalanges of the 5th finger
+HP:0012489,Suprasellar arachnoid cyst,HP:0100702,Arachnoid cyst
+HP:0000823,Delayed puberty,HP:0001510,Growth delay
+HP:0003451,Increased rate of premature chromosome condensation,HP:0011019,Abnormality of chromosome condensation
+UBERON:2001605,caudal scute series,UBERON:0000477,anatomical cluster
+DOID:8193,papillary pattern testicular yolk sac tumor,DOID:5344,testicular yolk sac tumor
+DOID:11712,lipoatrophic diabetes,DOID:9352,type 2 diabetes mellitus
+HP:0001863,Toe clinodactyly,HP:0001780,Abnormality of toe
+UBERON:0006097,ventral external arcuate fiber bundle,UBERON:0011215,cell part cluster of neuraxis
+HP:0012221,Pretibial blistering,HP:0011356,Regional abnormality of skin
+HP:0008817,Aplastic pubic bones,HP:0009104,Aplasia/Hypoplasia of the pubic bone
+HP:0100136,Bracket epiphysis of the distal phalanx of the 3rd toe,HP:0100056,Bracket epiphyses of the 3rd toe
+HP:0000141,Amenorrhea,HP:0000140,Abnormality of the menstrual cycle
+UBERON:0010197,trunk of common carotid artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001280,liver parenchyma,UBERON:0000353,parenchyma
+UBERON:2200936,dorsal fin distal radial cartilage,UBERON:2201672,dorsal fin radial cartilage
+HP:0001249,Intellectual disability,HP:0100543,Cognitive impairment
+HP:0005120,Abnormality of cardiac atrium,HP:0002564,Malformation of the heart and great vessels
+DOID:0050041,Astrakhan spotted fever,DOID:11104,spotted fever
+UBERON:0012416,respiratory system arterial smooth muscle,UBERON:0004297,respiratory system blood vessel smooth muscle
+DOID:1637,breast angiomatosis,DOID:1271,capillary disease
+HP:0002991,Abnormality of the fibula,HP:0002981,Abnormality of the calf
+HP:0000601,Hypotelorism,HP:0100886,Abnormality of globe location
+CL:0005014,auditory epithelial support cell,CL:0000710,neurecto-epithelial cell
+HP:0009584,Osteolytic defects of the proximal phalanx of the 2nd finger,HP:0009855,Osteolytic defects of the proximal phalanges of the hand
+HP:0001989,Fetal akinesia sequence,HP:0001558,Decreased fetal movement
+UBERON:0012312,maxillary process ectoderm,UBERON:0000490,unilaminar epithelium
+DOID:0050835,generalized dystonia,DOID:543,dystonia
+HP:0009161,Aplasia/Hypoplasia of the middle phalanx of the 5th finger,HP:0009376,Aplasia/Hypoplasia of the phalanges of the 5th finger
+UBERON:3010710,m. interscapularis,UBERON:0010891,pectoral complex muscle
+HP:0012471,Thick vermilion border,HP:0000159,Abnormality of the lip
+HP:0007249,Decreased number of small peripheral myelinated nerve fibers,HP:0003380,Decreased number of peripheral myelinated nerve fibers
+HP:0100716,Self-injurious behavior,HP:0006919,"Abnormal aggressive, impulsive or violent behavior"
+NCBITaxon:451866,Taphrinomycotina,NCBITaxon:4890,Ascomycota
+CL:0002187,basal cell of epidermis,CL:0000312,keratinocyte
+UBERON:0009573,sulcus limitans of fourth ventricle,UBERON:0002553,anatomical cavity
+HP:0001028,Hemangioma,HP:0100742,Vascular neoplasm
+UBERON:2001691,posterior cartilage of palatine,UBERON:0011004,pharyngeal arch cartilage
+HP:0002947,Cervical kyphosis,HP:0002808,Kyphosis
+HP:0010403,Duplication of the proximal phalanx of the 2nd toe,HP:0010355,Duplication of the phalanges of the 2nd toe
+HP:0004866,Impaired ADP-induced platelet aggregation,HP:0003540,Impaired platelet aggregation
+HP:0005464,Craniofacial osteosclerosis,HP:0011001,Increased bone mineral density
+DOID:9383,iridocyclitis,DOID:1407,anterior uveitis
+UBERON:0015787,upper respiratory conduit,UBERON:0004119,endoderm-derived structure
+UBERON:0005475,sigmoid sinus,UBERON:0005486,venous dural sinus
+HP:0004445,Elliptocytosis,HP:0004447,Poikilocytosis
+UBERON:0006720,pterygoid muscle,UBERON:0003681,masticatory muscle
+HP:0010004,Partial duplication of the distal phalanges of the hand,HP:0009883,Duplication of the distal phalanx of hand
+CL:0002009,macrophage dendritic cell progenitor,CL:0002032,hematopoietic oligopotent progenitor cell
+HP:0005244,Gastrointestinal infarctions,HP:0012719,Functional abnormality of the gastrointestinal tract
+HP:0009169,Broad middle phalanx of the 5th finger,HP:0004219,Abnormality of the middle phalanx of the 5th finger
+HP:0012564,Premature epimetaphyseal fusion in tibia,HP:0010588,Premature epimetaphyseal fusion
+HP:0004043,Lytic defects of ulnar metaphysis,HP:0004039,Abnormality of ulnar metaphysis
+HP:0009256,Ivory epiphysis of the distal phalanx of the 4th finger,HP:0009249,Abnormality of the epiphysis of the distal phalanx of the 4th finger
+HP:0004790,Hypoplasia of the small intestine,HP:0002244,Abnormality of the small intestine
+UBERON:0004235,mammary gland smooth muscle,UBERON:0004121,ectoderm-derived structure
+HP:0011732,Abnormality of adrenal morphology,HP:0000834,Abnormality of the adrenal glands
+HP:0001520,Large for gestational age,HP:0004324,Increased body weight
+UBERON:0001624,anterior cerebral artery,UBERON:0004449,cerebral artery
+UBERON:0004646,infraorbital artery,UBERON:0001637,artery
+UBERON:0013497,muscularis orbicularis,UBERON:0002036,striated muscle tissue
+HP:0007514,Edema of the dorsum of hands,HP:0000969,Edema
+CL:1001502,mitral cell,CL:1001434,olfactory bulb interneuron
+UBERON:0003634,pedal digit 4,UBERON:0006051,digit 4
+DOID:9911,infected hydrocele,DOID:9912,hydrocele
+HP:0011127,Perioral eczema,HP:0000964,Eczema
+HP:0009167,Irregular epiphysis of the distal phalanx of the 5th finger,HP:0009387,Irregular epiphyses of the 5th finger
+UBERON:0009552,distal segment of manual digit,UBERON:0005451,segment of manus
+HP:0100312,Cerebral germinoma,HP:0100620,Germinoma
+UBERON:0003021,central lobule,UBERON:0004070,cerebellum vermis lobule
+UBERON:0012375,subserosa,UBERON:0004923,organ component layer
+UBERON:2001531,epibranchial 4 cartilage,UBERON:2001527,epibranchial cartilage
+HP:0002757,Recurrent fractures,HP:0002659,Increased susceptibility to fractures
+UBERON:0010423,primary lymphoid nodule of tonsil,UBERON:0004119,endoderm-derived structure
+UBERON:0006343,right subhepatic recess,UBERON:0006442,subhepatic recess
+UBERON:3000894,femoral ridge,UBERON:0004120,mesoderm-derived structure
+DOID:1844,mononeuritis of upper limb,DOID:1802,mononeuritis
+HP:0011569,Cleft anterior mitral valve leaflet,HP:0001653,Mitral regurgitation
+DOID:0080023,Schwachman Diamond type metaphyseal dysplasia,DOID:26,pancreas disease
+UBERON:0005233,medial-nasal process ectoderm,UBERON:0000924,ectoderm
+UBERON:0001522,flexor carpi ulnaris muscle,UBERON:0004254,forelimb zeugopod muscle
+UBERON:2001992,branched anal fin ray,UBERON:4000176,anal fin lepidotrichium
+HP:0006461,Proximal femoral epiphysiolysis,HP:0010574,Abnormality of the epiphysis of the femoral head
+UBERON:0004728,amphibian larval stage,UBERON:0000069,larval stage
+UBERON:0010408,ocular angle artery,UBERON:0004573,systemic artery
+UBERON:3010203,dorsal tail fin,UBERON:3000982,tail external integument structure
+CL:0002040,immature NK T cell stage II,CL:0000914,immature NK T cell
+UBERON:0014762,fused metapodial bones 2-4,UBERON:0013586,fused metapodial bones 3 and 4
+UBERON:0001330,pampiniform plexus,UBERON:0001593,venous plexus
+HP:0005218,Anoperineal fistula,HP:0010447,Anal fistula
+DOID:4907,small intestine carcinoma,DOID:10154,small intestine cancer
+UBERON:0004087,vena cava,UBERON:0013768,great vessel of heart
+HP:0010078,Bullet-shaped distal phalanx of the hallux,HP:0010053,Abnormality of the distal phalanx of the hallux
+UBERON:0005309,pronephric nephron,UBERON:0004120,mesoderm-derived structure
+HP:0000059,Hypoplastic labia majora,HP:0000066,Labial hypoplasia
+UBERON:0001668,cerebellar vein,UBERON:0001638,vein
+UBERON:0015037,pedal digit 1 metatarsal endochondral element,UBERON:0015036,pedal digit metatarsal endochondral element
+UBERON:0001965,substantia nigra pars compacta,UBERON:0000064,organ part
+HP:0006143,Abnormal finger flexion creases,HP:0001167,Abnormality of finger
+UBERON:0002598,paracentral sulcus,UBERON:0013118,sulcus of brain
+HP:0006488,Bowing of the arm,HP:0006487,Bowing of the long bones
+UBERON:0011782,feather follicle,UBERON:0004121,ectoderm-derived structure
+UBERON:0004609,rib 10,UBERON:0002228,rib
+UBERON:0006597,quadrate bone,UBERON:0002513,endochondral bone
+DOID:0050291,parasitic Ichthyosporea infectious disease,DOID:1398,parasitic infectious disease
+UBERON:0001628,posterior communicating artery,UBERON:0004573,systemic artery
+UBERON:0012310,deep lateral cervical lymph node,UBERON:0004722,deep cervical lymph node
+HP:0200104,Absent fifth fingernail,HP:0001817,Absent fingernail
+UBERON:0014169,nigrostriatal tract,UBERON:0007702,tract of brain
+UBERON:0008310,nasopharyngeal gland,UBERON:0003295,pharyngeal gland
+UBERON:0001817,lacrimal gland,UBERON:0015154,lateral gland of orbital region
+UBERON:2001825,urohyal lateral process,UBERON:0004121,ectoderm-derived structure
+UBERON:0004242,bronchus smooth muscle,UBERON:0004233,lower respiratory tract smooth muscle
+DOID:7320,ovarian serous cystadenofibroma,DOID:5474,ovarian serous adenofibroma
+UBERON:3010243,ventricular musculature,UBERON:0000477,anatomical cluster
+DOID:869,cholesteatoma,DOID:161,keratosis
+UBERON:0011303,lamprey sucker,UBERON:0004121,ectoderm-derived structure
+DOID:10690,mastitis,DOID:3463,breast disease
+HP:0003955,Bone-in-a-bone appearance (forearm),HP:0002973,Abnormality of the forearm
+UBERON:3000428,perilymphatic system,UBERON:0004121,ectoderm-derived structure
+HP:0009599,Abnormality of the epiphyses of the thumb,HP:0001172,Abnormality of the thumb
+UBERON:0003495,respiratory system arteriole,UBERON:0001980,arteriole
+CL:0000135,fibrocyte,CL:0000499,stromal cell
+HP:0001761,Pes cavus,HP:0001760,Abnormality of the foot
+HP:0001712,Left ventricular hypertrophy,HP:0001711,Abnormality of the left ventricle
+UBERON:0002264,olfactory bulb,UBERON:0002791,regional part of telencephalon
+DOID:11452,perinatal jaundice due to hepatocellular damage,DOID:2383,neonatal jaundice
+HP:0009406,Patchy sclerosis of the phalanges of the 4th finger,HP:0009772,Patchy sclerosis of the phalanges of the hand
+UBERON:0011204,rectovesical pouch,UBERON:0002553,anatomical cavity
+UBERON:2000544,pectoral fin actinotrichium,UBERON:0004120,mesoderm-derived structure
+HP:0001054,Numerous nevi,HP:0003764,Nevus
+HP:0005199,Aplasia of the abdominal wall musculature,HP:0010318,Aplasia/Hypoplasia of the abdominal wall musculature
+UBERON:0004885,hilum,UBERON:0000161,orifice
+UBERON:0002891,cortical amygdaloid nucleus,UBERON:0009663,telencephalic nucleus
+DOID:8331,perineural angioma,DOID:469,deep angioma
+UBERON:0013450,simian shelf,UBERON:0004120,mesoderm-derived structure
+UBERON:3010724,levator quadrati,UBERON:0011648,jaw muscle
+UBERON:2202027,pectoral fin proximal radial cartilage 2,UBERON:2201587,pectoral fin proximal radial cartilage
+UBERON:0015023,phalanx endochondral element,UBERON:0015063,autopod endochondral element
+CL:0002125,CD27-negative gamma-delta T cell,CL:0000912,helper T cell
+DOID:3459,breast carcinoma,DOID:1612,breast cancer
+UBERON:0010012,upper beak,UBERON:0004121,ectoderm-derived structure
+UBERON:0009736,sublaminar layers S3 or S4 or S5,UBERON:0008921,substratum of layer of retina
+HP:0010225,Pseudoepiphysis of the 4th metacarpal,HP:0010224,Abnormality of the epiphysis of the 4th metacarpal
+HP:0005707,Bilateral triphalangeal thumbs,HP:0001199,Triphalangeal thumb
+UBERON:0013613,tooth cingulum,UBERON:0000063,organ segment
+UBERON:0004454,tarsal region,UBERON:0008784,lower limb segment
+UBERON:0004032,podocyte slit diaphragm,UBERON:0000470,cell part
+HP:0007901,Retinal malformation,HP:0000479,Abnormality of the retina
+UBERON:0006014,interdigital region between pedal digits,UBERON:0006012,interdigital region
+HP:0012168,Head-banging,HP:0100716,Self-injurious behavior
+UBERON:0007299,choroid plexus of tectal ventricle,UBERON:0001886,choroid plexus
+UBERON:0009129,right atrium endocardium,UBERON:0000487,simple squamous epithelium
+HP:0008770,Obsessive-compulsive trait,HP:0000722,Obsessive-compulsive behavior
+UBERON:0003632,pedal digit 2,UBERON:0006049,digit 2
+HP:0005200,Retroperitoneal fibrosis,HP:0002585,Abnormality of the peritoneum
+HP:0012717,Severe conductive hearing impairment,HP:0012712,Mild hearing impairment
+HP:0004280,Irregular ossification of hand bones,HP:0005921,Abnormal ossification of hand bones
+HP:0006265,Aplasia/Hypoplasia of fingers,HP:0005927,Aplasia/Hypoplasia involving bones of the hand
+UBERON:2002242,scale primordium,UBERON:0000479,tissue
+DOID:12900,Mikulicz disease,DOID:1400,lacrimal apparatus disease
+UBERON:0005622,right dorsal aorta,UBERON:0000947,aorta
+UBERON:2000766,granular layer valvula cerebelli,UBERON:0000479,tissue
+UBERON:0002885,accessory basal amygdaloid nucleus,UBERON:0002619,regional part of cerebral cortex
+HP:0100774,Hyperostosis,HP:0011842,Abnormality of skeletal morphology
+UBERON:0004683,parasubiculum,UBERON:0002619,regional part of cerebral cortex
+UBERON:4000105,limiting layer of elasmoid scale,UBERON:0000479,tissue
+HP:0006773,Cutaneous angiolipomas,HP:0001012,Multiple lipomas
+UBERON:0008921,substratum of layer of retina,UBERON:0004923,organ component layer
+HP:0010008,Duplication of the middle phalanx of hand,HP:0009997,Duplication of phalanx of hand
+NCBITaxon:194,Campylobacter,NCBITaxon:72294,Campylobacteraceae
+DOID:9467,nail-patella syndrome,DOID:0050736,autosomal dominant disease
+HP:0005932,Abnormal renal corticomedullary differentiation,HP:0011035,Abnormality of the renal cortex
+NCBITaxon:43733,Muscomorpha,NCBITaxon:7203,Brachycera
+UBERON:0000054,macula,UBERON:0000479,tissue
+UBERON:0008859,cardiac gastric gland,UBERON:0000414,mucous gland
+HP:0010914,Abnormality of valine metabolism,HP:0010892,Abnormality of branched chain family amino acid metabolism
+HP:0003658,Hypomethioninemia,HP:0010901,Abnormality of methionine metabolism
+DOID:0050083,Keshan disease,DOID:5113,nutritional deficiency disease
+UBERON:0003110,otic region,UBERON:0000477,anatomical cluster
+DOID:4254,osteosclerosis,DOID:0080005,bone remodeling disease
+UBERON:2000259,mandibular lateral line,UBERON:2001470,anterior lateral line
+UBERON:0012330,nasal-associated lymphoid tissue,UBERON:0001962,gut-associated lymphoid tissue
+HP:0011367,Yellow nails,HP:0100643,Abnormality of nail color
+HP:0011824,Chin with H-shaped crease,HP:0000306,Abnormality of the chin
+HP:0005916,Abnormal metacarpal morphology,HP:0001163,Abnormality of the metacarpal bones
+DOID:265,spleen angiosarcoma,DOID:254,hemangioma of intra-abdominal structure
+DOID:11049,meconium aspiration syndrome,DOID:850,lung disease
+UBERON:0010202,lateral line,UBERON:0000479,tissue
+UBERON:0009658,pancreaticoduodenal artery,UBERON:0001637,artery
+UBERON:0002259,corpora quadrigemina,UBERON:0000064,organ part
+HP:0100174,Irregular epiphysis of the distal phalanx of the 4th toe,HP:0100071,Irregular epiphyses of the 4th toe
+HP:0000061,"Ambiguous genitalia, female",HP:0000062,Ambiguous genitalia
+UBERON:0008941,pleural ganglion,UBERON:0000045,ganglion
+HP:0100323,Juvenile aseptic necrosis,HP:0010885,Aseptic necrosis
+HP:0006384,Club-shaped distal femur,HP:0002823,Abnormality of the femur
+UBERON:2002080,spina occipitalis,UBERON:0004120,mesoderm-derived structure
+UBERON:0008843,gubernaculum testis,UBERON:0004346,gubernaculum
+CL:0000150,glandular epithelial cell,CL:0000066,epithelial cell
+HP:0010098,Complete duplication of the 1st metatarsal,HP:0010100,Complete duplication of the phalanges of the hallux
+CL:0002448,Ly49H-negative natural killer cell,CL:0002438,NK1.1-positive natural killer cell
+HP:0004918,hyperchloremic metabolic acidosis,HP:0001995,Hyperchloremic acidosis
+UBERON:0006318,orbitalis muscle,UBERON:0004277,eye muscle
+HP:0006552,Fibrocystic lung disease,HP:0005948,Cystic lung disease
+HP:0007779,Anterior segment of eye aplasia,HP:0008062,Aplasia/Hypoplasia affecting the anterior segment of the eye
+UBERON:0001892,rhombomere,UBERON:0004731,neuromere
+UBERON:2001425,basal plate cartilage,UBERON:0003932,cartilage element of chondrocranium
+UBERON:0005108,metanephric epithelium,UBERON:0004819,kidney epithelium
+HP:0011392,Abnormality of the vestibular nerve,HP:0011391,Morphological abnormality of the nerves of the inner ear
+HP:0010133,Ivory epiphysis of the proximal phalanx of the hallux,HP:0010126,Abnormality of the epiphysis of the proximal phalanx of the hallux
+DOID:11634,myxedema,DOID:3141,mucinoses
+UBERON:2000058,polster,UBERON:0004120,mesoderm-derived structure
+UBERON:2001883,parapophysis + rib of vertebra 3 + rib of vertebra 4,UBERON:0002513,endochondral bone
+HP:0008399,Circumungual hyperkeratosis,HP:0000962,Hyperkeratosis
+UBERON:0006288,rib cartilage element,UBERON:0005863,cartilaginous condensation
+HP:0007221,Progressive truncal ataxia,HP:0002078,Truncal ataxia
+HP:0004370,Abnormality of temperature regulation,HP:0001939,Abnormality of metabolism/homeostasis
+UBERON:0000569,ileocecal valve,UBERON:0011185,gastrointestinal sphincter
+UBERON:0007315,internal pudendal artery,UBERON:0004573,systemic artery
+DOID:10846,angiodysplasia of intestine,DOID:5295,intestinal disease
+DOID:14287,brawny scleritis,DOID:13794,anterior scleritis
+UBERON:0005421,pectoral appendage apical ectodermal ridge,UBERON:0004356,apical ectodermal ridge
+DOID:3528,anterior cerebral artery infarction,DOID:3527,cerebral arterial disease
+UBERON:0012458,antler velvet,UBERON:0001084,skin of head
+UBERON:0015476,nose skin,UBERON:1000021,skin of face
+HP:0008803,Narrow sacroiliac notch,HP:0003185,Small sacroiliac notches
+HP:0008124,Talipes calcaneovarus,HP:0001883,Talipes
+HP:0000491,Keratitis,HP:0011495,Abnormality of corneal epithelium
+DOID:11256,typhus,DOID:0050338,primary bacterial infectious disease
+UBERON:0005080,metanephric ureteric bud,UBERON:0007497,developing epithelial placode
+UBERON:0015039,pedal digit 3 metatarsal endochondral element,UBERON:0015036,pedal digit metatarsal endochondral element
+UBERON:0006376,premacula segment of distal straight tubule,UBERON:0008408,distal tubular epithelium
+UBERON:0001859,lateral semicircular duct,UBERON:0001856,semicircular duct
+UBERON:0000366,flexor muscle,UBERON:0004120,mesoderm-derived structure
+CL:0000977,IgG short lived plasma cell,CL:0000975,short lived plasma cell
+DOID:10845,St. Louis encephalitis,DOID:934,viral infectious disease
+HP:0011207,EEG with generalized slow activity grade 2,HP:0010845,EEG with generalized slow activity
+UBERON:0009044,pudendal venous plexus,UBERON:0001593,venous plexus
+HP:0100553,Hemihypertrophy of lower limb,HP:0001528,Hemihypertrophy
+UBERON:2005270,depressor muscle,UBERON:0001134,skeletal muscle tissue
+DOID:14422,dipetalonemiasis,DOID:1080,filariasis
+DOID:5615,spinal canal intradural extramedullary neoplasm,DOID:5612,spinal cancer
+UBERON:0007390,pectoral appendage cartilage tissue,UBERON:0007389,paired limb/fin cartilage
+HP:0010815,Nevus sebaceous,HP:0010816,Epidermal nevus
+UBERON:0015791,digit connective tissue,UBERON:0003587,limb connective tissue
+UBERON:0015052,femur endochondral element,UBERON:0015022,hindlimb endochondral element
+UBERON:0006762,suspensory ligament of lens,UBERON:0004121,ectoderm-derived structure
+HP:0007517,Palmoplantar cutis laxa,HP:0000973,Cutis laxa
+HP:0009994,Partial duplication of the distal phalanx of the 5th finger,HP:0009987,Partial duplication of the phalanges of the 5th finger
+HP:0010787,Genital neoplasm,HP:0007379,Neoplasm of the genitourinary tract
+UBERON:3000744,urostyle cotyle,UBERON:0000064,organ part
+CL:0002249,primitive cardiac myocyte,CL:0000035,single fate stem cell
+DOID:6594,bladder colonic type adenocarcinoma,DOID:3711,bladder adenocarcinoma
+DOID:1802,mononeuritis,DOID:1803,neuritis
+UBERON:3010729,M. coracobrachialis longus,UBERON:0010891,pectoral complex muscle
+HP:0010542,Vestibular nystagmus,HP:0000639,Nystagmus
+UBERON:0004377,distal metaphysis,UBERON:0001438,metaphysis
+UBERON:2201818,dorsal fin proximal radial cartilage 1,UBERON:2200947,dorsal fin proximal radial cartilage
+HP:0012456,Medial arterial calcification,HP:0003207,Arterial calcification
+HP:0001853,Bifid distal phalanx of toe,HP:0009136,Duplication involving bones of the feet
+DOID:3742,bladder squamous cell carcinoma,DOID:4007,bladder carcinoma
+DOID:2239,granulomatous hepatitis,DOID:2237,hepatitis
+UBERON:0010021,dorsal part of pharyngeal pouch 1,UBERON:0005291,embryonic tissue
+HP:0010672,Abnormality of the third metatarsal bone,HP:0001832,Abnormality of the metatarsal bones
+DOID:0060220,physical urticaria,DOID:1555,urticaria
+DOID:1776,labyrinthine unilateral reactive loss,DOID:566,labyrinthine dysfunction
+DOID:6476,clear cell variant infiltrating bladder urothelial carcinoma,DOID:6477,invasive bladder transitional cell carcinoma
+UBERON:0011326,superior laryngeal nerve,UBERON:0002003,peripheral nerve
+HP:0000148,Vaginal atresia,HP:0001827,Genital tract atresia
+UBERON:0013674,ctenactinium,UBERON:0003457,head bone
+UBERON:0004176,external genitalia,UBERON:0003133,reproductive organ
+UBERON:0001646,abducens nerve,UBERON:0004121,ectoderm-derived structure
+UBERON:4200037,supinator process,UBERON:4100000,skeletal element projection
+UBERON:2000582,saccus dorsalis,UBERON:0004121,ectoderm-derived structure
+HP:0012132,Erythroid hyperplasia,HP:0012131,Abnormal number of erythroid precursors
+UBERON:0013229,eyelid gland,UBERON:0004859,eye gland
+HP:0009640,Symphalangism of the proximal phalanx of the thumb with the 1st metatcarpal,HP:0009635,Symphalangism of proximal phalanx of  thumb
+UBERON:3010392,mesonephric early proximal tubule,UBERON:0006553,renal duct
+NCBITaxon:523103,Trichophyton mentagrophytes,NCBITaxon:5550,Trichophyton
+UBERON:0002279,vestibular aqueduct,UBERON:0013685,foramen of skull
+DOID:5598,fallopian tube serous adenocarcinoma,DOID:3706,fallopian tube adenocarcinoma
+HP:0010261,Fragmentation of the epiphyses of the middle phalanges of the hand,HP:0010232,Fragmentation of the epiphyses of the phalanges of the hand
+HP:0007590,Aplasia cutis congenita over posterior parietal area,HP:0004476,Aplasia cutis congenita over parietal area
+HP:0100252,Diaphyseal dysplasia,HP:0000940,Abnormal diaphysis morphology
+UBERON:0004440,proximal epiphysis of proximal phalanx of manual digit 2,UBERON:0011977,epiphysis of proximal phalanx of manus
+HP:0100196,Irregular epiphysis of the proximal phalanx of the 4th toe,HP:0100071,Irregular epiphyses of the 4th toe
+UBERON:0003036,central lateral nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0006722,manubrium of malleus,UBERON:0005913,zone of bone organ
+UBERON:0008253,Aristotle's lantern,UBERON:0000481,multi-tissue structure
+CL:0002208,brush cell of bronchus,CL:0002075,brush cell of trachebronchial tree
+UBERON:2001167,vertebral element 1,UBERON:0010913,vertebral element
+HP:0008207,Primary adrenal insufficiency,HP:0000846,Adrenal insufficiency
+UBERON:0015853,dental pulp of median incisor tusk,UBERON:0003566,head connective tissue
+DOID:2816,malignant oculomotor nerve tumor,DOID:2817,cranial nerve III tumor
+HP:0100817,Renovascular hypertension,HP:0012211,Abnormal renal physiology
+UBERON:2001693,protractor operculi,UBERON:0002376,cranial muscle
+HP:0006919,"Abnormal aggressive, impulsive or violent behavior",HP:0100851,Abnormal emotion/affect behavior
+UBERON:2200271,radial cartilage,UBERON:0007844,cartilage element
+DOID:7729,acinar cell cystadenocarcinoma,DOID:4073,pancreatic cystadenocarcinoma
+HP:0006779,Alveolar rhabdomyosarcoma,HP:0002859,Rhabdomyosarcoma
+HP:0009558,Broad distal phalanx of the 2nd finger,HP:0009542,Abnormality of the distal phalanx of the 2nd finger
+UBERON:0005969,reticulum trabeculare,UBERON:0000479,tissue
+UBERON:0012499,serosa of uterine tube,UBERON:0005156,reproductive structure
+HP:0011700,Automatic atrial tachycardia,HP:0001692,Primary atrial arrhythmia
+UBERON:3010074,M. ileo-femoralis,UBERON:0010890,pelvic complex muscle
+UBERON:0001902,epithelium of small intestine,UBERON:0001277,intestinal epithelium
+UBERON:0000399,jejunal mucosa,UBERON:0001204,mucosa of small intestine
+UBERON:2001799,recessus lateralis,UBERON:0000464,anatomical space
+HP:0011162,Psychic auras,HP:0011157,Auras
+UBERON:0011176,oval nucleus of stria terminalis,UBERON:0009663,telencephalic nucleus
+UBERON:0004743,coracoid bone,UBERON:0002513,endochondral bone
+DOID:9834,hyperopia,DOID:9835,refractive error
+HP:0000547,Tapetoretinal degeneration,HP:0000546,Retinal degeneration
+UBERON:0004228,urinary bladder smooth muscle,UBERON:0001135,smooth muscle tissue
+UBERON:0015231,circulatory system dorsal vessel,UBERON:0004120,mesoderm-derived structure
+HP:0007851,Temporal displacement of maculae,HP:0001103,Abnormality of the macula
+HP:0009588,Vestibular Schwannoma,HP:0009591,Abnormality of the vestibulocochlear nerve
+UBERON:0003114,pharyngeal arch 3,UBERON:0002539,pharyngeal arch
+HP:0006500,Abnormality involving the epiphyses of the lower limbs,HP:0002814,Abnormality of the lower limb
+HP:0000548,Cone-rod dystrophy,HP:0000556,Retinal dystrophy
+HP:0006723,Intestinal carcinoid,HP:0100570,Carcinoid
+UBERON:0009030,left pulmonary vein,UBERON:0002016,pulmonary vein
+HP:0004230,Subluxation of the proximal interphalangeal joint of the little finger,HP:0001373,Joint dislocation
+UBERON:0001517,skin of elbow,UBERON:0002427,arm skin
+UBERON:0004901,right lung lobar bronchus mesenchyme,UBERON:0009603,right lung associated mesenchyme
+DOID:12217,Lewy body dementia,DOID:0050890,synucleinopathy
+UBERON:0005968,infundibulum of hair follicle,UBERON:0004121,ectoderm-derived structure
+DOID:10080,sparganosis,DOID:883,parasitic helminthiasis infectious disease
+NCBITaxon:147553,Pneumocystidomycetes,NCBITaxon:451866,Taphrinomycotina
+DOID:2383,neonatal jaundice,DOID:10123,pigmentation disease
+HP:0100869,Palmar telangiectasia,HP:0100585,Teleangiectasia of the skin
+UBERON:0001669,superior cerebellar vein,UBERON:0001668,cerebellar vein
+UBERON:0001380,vastus medialis,UBERON:0001377,quadriceps femoris
+DOID:0080018,dysbaric osteonecrosis,DOID:0080008,ischemic bone disease
+HP:0009294,Absent middle phalanx of 4th finger,HP:0010239,Aplasia of the middle phalanx of the hand
+UBERON:2001150,tooth 2D,UBERON:2000694,ceratobranchial 5 tooth
+UBERON:0009040,deep circumflex iliac artery,UBERON:0003520,pelvis blood vessel
+DOID:0060197,amyotrophic lateral sclerosis type 5,DOID:332,amyotrophic lateral sclerosis
+HP:0100384,Absent proximal phalanx of the 3rd toe,HP:0100388,Aplasia of the proximal phalanges of the toes
+HP:0004469,Chronic bronchitis,HP:0002788,Recurrent upper respiratory tract infections
+DOID:4075,bile duct cystadenocarcinoma,DOID:4896,bile duct adenocarcinoma
+UBERON:0011589,non-mineralized cartilage tissue,UBERON:0002418,cartilage tissue
+UBERON:0002283,nail matrix,UBERON:0004121,ectoderm-derived structure
+UBERON:4200179,manual claw,UBERON:0004120,mesoderm-derived structure
+UBERON:2001165,supraneural 5 bone,UBERON:2000442,supraneural bone
+HP:0100248,Hemiballismus,HP:0002134,Abnormality of the basal ganglia
+UBERON:0013132,penicillar arteriole,UBERON:0001980,arteriole
+DOID:5439,papillary hidradenoma,DOID:3896,hidradenoma
+DOID:4398,pustulosis of palm and sole,DOID:2723,dermatitis
+UBERON:2001771,anal fin lepidotrichium 3,UBERON:4000176,anal fin lepidotrichium
+UBERON:0007958,central carpal bone,UBERON:0001435,carpal bone
+DOID:683,motor neuritis,DOID:231,motor neuron disease
+HP:0011041,Aplasia/Hypoplasia of the cervical spine,HP:0003319,Abnormality of the cervical spine
+UBERON:0014683,parasymphisial tooth whorl,UBERON:0009679,set of lower jaw teeth
+UBERON:0012331,mesosalpinx,UBERON:0002095,mesentery
+DOID:0060187,diversion colitis,DOID:0060180,colitis
+UBERON:0010145,paraurethral gland,UBERON:0005398,female reproductive gland
+UBERON:0005982,Bachmann's bundle,UBERON:0004120,mesoderm-derived structure
+DOID:2832,geotrichosis,DOID:2473,opportunistic mycosis
+NCBITaxon:28292,Sandfly fever Sicilian virus,NCBITaxon:327794,unclassified Phlebovirus
+UBERON:0014473,precentral fissure of cerebellum,UBERON:0003980,cerebellum fissure
+HP:0011024,Abnormality of the gastrointestinal tract,HP:0002012,Abnormality of the abdominal organs
+UBERON:0003653,metatarsal bone of digit 4,UBERON:0015040,pedal digit 4 metatarsal endochondral element
+UBERON:4200167,mesial pelvic ridge,UBERON:0004529,anatomical projection
+UBERON:0001630,muscle organ,UBERON:0000062,organ
+UBERON:0004334,proximal phalanx of pedal digit 3,UBERON:0003642,pedal digit 3 phalanx
+HP:0010740,Osteopathia striata,HP:0004348,Abnormality of bone mineral density
+UBERON:0011629,supratemporal bone,UBERON:0008907,dermal bone
+DOID:14070,vestibular nystagmus,DOID:1242,globe disease
+HP:0011645,Sinus of Valsalva aneurysm,HP:0002631,Ascending aortic aneurysm
+DOID:5759,sebaceous gland neoplasm,DOID:3165,skin benign neoplasm
+UBERON:0004415,proximal epiphysis of metatarsal bone,UBERON:0004389,epiphysis of metatarsal bone
+HP:0000943,Dysostosis multiplex,HP:0011842,Abnormality of skeletal morphology
+UBERON:0013399,blood vessel layer of choroid,UBERON:0004923,organ component layer
+DOID:12857,achilles bursitis,DOID:2965,bursitis
+HP:0006206,Hypersegmentation of proximal phalanx of second finger,HP:0009544,Abnormality of the proximal phalanx of the 2nd finger
+UBERON:0004409,distal epiphysis of phalanx of manus,UBERON:0004387,epiphysis of phalanx of manus
+CL:0002250,intestinal crypt stem cell,CL:0000048,multi fate stem cell
+DOID:0050475,Weill-Marchesani syndrome,DOID:0050739,autosomal genetic disease
+UBERON:0013606,magnocellular layer of dorsal nucleus of lateral geniculate body,UBERON:0013605,layer of lateral geniculate body
+DOID:3042,allergic contact dermatitis,DOID:2773,contact dermatitis
+UBERON:0013120,eyelid submuscular connective tissue,UBERON:0003581,eyelid connective tissue
+HP:0008161,Absent leukocyte alkaline phosphatase,HP:0004852,Reduced leukocyte alkaline phosphatase
+DOID:5557,testicular germ cell cancer,DOID:2998,testicular cancer
+UBERON:0006306,ulna cartilage element,UBERON:0015003,ulna endochondral element
+UBERON:0013511,ambiens muscle,UBERON:0003663,hindlimb muscle
+DOID:2732,Rothmund-Thomson syndrome,DOID:37,skin disease
+UBERON:0002007,medulla of lymph node,UBERON:0000958,medulla of organ
+DOID:4005,endometrial transitional cell carcinoma,DOID:2871,endometrial carcinoma
+UBERON:0005290,myelencephalon,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:9768,heart aneurysm,DOID:114,heart disease
+DOID:11850,transient refractive change,DOID:9835,refractive error
+CL:0000362,epidermal cell,CL:0002159,general ecto-epithelial cell
+UBERON:0000117,respiratory tube,UBERON:0000025,tube
+HP:0007793,Macular retinal pigment epithelial mottling,HP:0008002,Abnormality of macular pigmentation
+UBERON:0004689,naso-frontal vein,UBERON:0003499,brain blood vessel
+UBERON:0005968,infundibulum of hair follicle,UBERON:0000479,tissue
+UBERON:2002051,circulus,UBERON:0006800,anatomical line
+NCBITaxon:10372,Human herpesvirus 7,NCBITaxon:40272,Roseolovirus
+HP:0002150,Hypercalciuria,HP:0011280,Abnormality of urine calcium concentration
+UBERON:0003048,regional part of hypothalamus,UBERON:0002784,regional part of diencephalon
+UBERON:2001690,anterior cartilage of palatine,UBERON:0011004,pharyngeal arch cartilage
+CL:0000502,type D enteroendocrine cell,CL:0000164,enteroendocrine cell
+HP:0012691,Focal T2 hypointense thalamic lesion,HP:0012696,Abnormal thalamic MRI signal intensity
+UBERON:2000125,mandibular lateral line neuromast,UBERON:0008904,neuromast
+UBERON:0010728,sphenoid lesser wing pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+CL:0002177,folliculostellate cell of pars distalis of adenohypophysis,CL:0000710,neurecto-epithelial cell
+DOID:0060004,autoimmune disease of central nervous system,DOID:438,autoimmune disease of the nervous system
+UBERON:0010540,tarsus pre-cartilage condensation,UBERON:0003328,mesenchyme of footplate
+UBERON:2001524,hypobranchial 1 cartilage,UBERON:2001894,hypobranchial 1 element
+UBERON:2001363,neural complex,UBERON:0000477,anatomical cluster
+UBERON:0002698,preoccipital notch,UBERON:0000464,anatomical space
+UBERON:0004198,comma-shaped body,UBERON:0010532,primitive nephron
+HP:0009188,Pseudoepiphysis of the distal phalanx of the 5th finger,HP:0010253,Pseudoepiphyses of the distal phalanges of the hand
+CL:0002293,epithelial cell of thymus,CL:0002076,endo-epithelial cell
+HP:0008451,Posterior vertebral hypoplasia,HP:0008417,Vertebral hypoplasia
+DOID:8552,chronic myeloid leukemia,DOID:8692,myeloid leukemia
+HP:0010263,Ivory epiphyses of the middle phalanges of the hand,HP:0100916,Sclerosis of the middle phalanges of the hand
+UBERON:0014772,lateral palpebral artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005983,heart layer,UBERON:0004923,organ component layer
+HP:0005769,Fifth finger distal phalanx clinodactyly,HP:0004209,Clinodactyly of the 5th finger
+UBERON:0014560,CA3 stratum lucidum,UBERON:0014567,layer of hippocampal field
+DOID:11186,allescheriosis,DOID:0050292,primary systemic mycosis
+CL:0000315,tears secreting cell,CL:0000151,secretory cell
+DOID:10361,eosinophilic meningitis,DOID:10341,chronic meningitis
+CL:0002353,fetal liver hematopoietic progenitor cell,CL:0002195,hepatic stem cell
+DOID:7608,parathyroid adenoma,DOID:0060089,endocrine organ benign neoplasm
+DOID:6482,lung acinar adenocarcinoma,DOID:3910,lung adenocarcinoma
+UBERON:0004340,allantois,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:5852,inferolateral myocardial infarct,DOID:5844,myocardial infarction
+HP:0010582,Irregular epiphyses,HP:0005930,Abnormality of the epiphyses
+HP:0003208,Fingerprint intracellular accumulation of autofluorescent lipopigment storage material,HP:0003204,Intracellular accumulation of autofluorescent lipopigment storage material
+UBERON:3000518,pseudodentary,UBERON:0002513,endochondral bone
+HP:0010612,Plantar pits,HP:0100276,Skin pits
+NCBITaxon:10114,Rattus,NCBITaxon:39107,Murinae
+UBERON:0003718,muscle spindle,UBERON:0000477,anatomical cluster
+UBERON:0006116,vagal nerve fiber bundle,UBERON:0000122,neuron projection bundle
+HP:0001892,Abnormal bleeding,HP:0001871,Abnormality of  blood and blood-forming tissues
+HP:0002105,Hemoptysis,HP:0002088,Abnormality of the lung
+UBERON:0010851,fibula cartilage element,UBERON:0010885,hindlimb cartilage element
+HP:0011515,Abnormal stereopsis,HP:0011514,Abnormality of binocular vision
+UBERON:0008338,plantar part of pes,UBERON:0008837,palmar/plantar part of autopod
+HP:0007963,Macroreticular retinal dystrophy,HP:0000556,Retinal dystrophy
+HP:0002111,Restrictive respiratory insufficiency,HP:0002091,Restrictive lung disease
+UBERON:0010183,liver trabecula,UBERON:0000440,trabecula
+DOID:8002,supraglottis neoplasm,DOID:2598,laryngeal benign neoplasm
+UBERON:4200075,fin spine,UBERON:4000172,lepidotrichium
+UBERON:0002737,lateral inferior limiting sulcus,UBERON:0008334,subarachnoid sulcus
+CL:0000312,keratinocyte,CL:0000362,epidermal cell
+DOID:0050870,in situ pulmonary adenocarcinoma,DOID:1324,lung cancer
+UBERON:0005855,lumbar spinal cord ventral column,UBERON:0002318,white matter of spinal cord
+UBERON:2001603,maxilla ascending process,UBERON:0004120,mesoderm-derived structure
+UBERON:0001189,left testicular artery,UBERON:0010192,genital artery
+CL:1001590,epididymis glandular cell,CL:0000068,duct epithelial cell
+UBERON:3000728,nucal keel,UBERON:4100000,skeletal element projection
+HP:0001642,Pulmonic stenosis,HP:0001641,Abnormality of the pulmonary valve
+HP:0009694,Small epiphyses of the thumb,HP:0010236,Small epiphyses of the phalanges of the hand
+DOID:907,liver fibroma,DOID:916,liver neoplasm
+HP:0100917,Sclerosis of the proximal phalanges of the hand,HP:0009834,Abnormality of the proximal phalanges of the hand
+HP:0000371,Acute otitis media,HP:0000388,Otitis media
+CL:0002595,smooth muscle cell of the subclavian artery,CL:0000359,vascular associated smooth muscle cell
+DOID:6059,nasal vestibule papilloma,DOID:0050621,respiratory system benign neoplasm
+HP:0009780,Iliac horns,HP:0003796,Irregular iliac crest
+HP:0005379,Severe T lymphocytopenia,HP:0005403,T lymphocytopenia
+DOID:7033,anisakiasis,DOID:883,parasitic helminthiasis infectious disease
+CL:0002175,primary follicular cell of ovary,CL:0002174,follicular cell of ovary
+HP:0100958,Narrow foramen obturatorium,HP:0003174,Abnormality of the ischium
+DOID:6419,tetralogy of Fallot,DOID:1682,congenital heart disease
+UBERON:3000226,hyolaryngeal complex,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005435,cisterna chyli,UBERON:0000063,organ segment
+HP:0010177,Osteolytic defects of the phalanges of the toes,HP:0010161,Abnormality of the phalanges of the toes
+UBERON:0001091,calcareous tooth,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:10021,duodenum cancer,DOID:10154,small intestine cancer
+UBERON:0010277,mesocardium,UBERON:0004120,mesoderm-derived structure
+HP:0000465,Webbed neck,HP:0000464,Abnormality of the neck
+DOID:11079,leech infestation,DOID:4110,parasitic ectoparasitic infectious disease
+UBERON:0007204,brachiocephalic vasculature,UBERON:0002049,vasculature
+HP:0002497,Spastic ataxia,HP:0001251,Ataxia
+UBERON:0002329,somite,UBERON:0007503,epithelial vesicle
+HP:0100701,Abnormality of the pia mater,HP:0010651,Abnormality of the meninges
+DOID:0060099,musculoskeletal system benign neoplasm,DOID:0060085,organ system benign neoplasm
+HP:0010450,Esophageal stenosis,HP:0002031,Abnormality of the esophagus
+HP:0003693,Distal amyotrophy,HP:0003202,Amyotrophy
+HP:0004246,Delayed ossification of the scaphoid,HP:0001216,Delayed ossification of carpal bones
+UBERON:0011940,arrector pili muscle of vibrissa,UBERON:0004121,ectoderm-derived structure
+UBERON:0008906,lateral line nerve,UBERON:0001785,cranial nerve
+DOID:9300,neurofibroma of the heart,DOID:962,neurofibroma
+NCBITaxon:186458,Bornavirus,NCBITaxon:178830,Bornaviridae
+UBERON:2002003,posterior dentation of dorsal fin spine 2,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0006642,muscle layer of oviduct,UBERON:0006660,muscle layer
+HP:0009968,Partial duplication of the distal phalanx of the 3rd finger,HP:0009962,Duplication of the distal phalanx of the 3rd finger
+UBERON:0014763,fused metatarsal bones 2-4,UBERON:0014762,fused metapodial bones 2-4
+HP:0100537,Fasciitis,HP:0100536,Abnormality of the fascia
+HP:0008734,Decreased testicular size,HP:0010468,Aplasia/Hypoplasia of the testes
+HP:0005476,Widely patent sagittal suture,HP:0011329,Abnormality of cranial sutures
+UBERON:0015162,superior branch of oculomotor nerve,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:7540,breast apocrine adenoma,DOID:1625,breast adenoma
+HP:0012370,Cheekbone prominence,HP:0010668,Abnormality of the zygomatic bone
+DOID:5158,pleural cancer,DOID:201,connective tissue cancer
+UBERON:2002041,parapophysis 6,UBERON:0003109,parapophysis
+UBERON:0010420,lymph node follicular corona,UBERON:0010755,secondary follicle corona
+UBERON:0011997,coelom,UBERON:0002050,embryonic structure
+UBERON:0001076,neural spine,UBERON:0006061,process of vertebra
+HP:0010267,Triangular epiphyses of the middle phalanges of the hand,HP:0010244,Abnormality of the epiphyses of the middle phalanges of the hand
+DOID:13579,kwashiorkor,DOID:11801,protein-energy malnutrition
+HP:0009124,Abnormality of adipose tissue,HP:0003549,Abnormality of connective tissue
+HP:0003574,Positive regitine blocking test,HP:0002640,Hypertension associated with pheochromocytoma
+UBERON:0002359,fibrous pericardium,UBERON:0005181,thoracic segment organ
+DOID:631,fibromyalgia,DOID:633,myositis
+UBERON:0004146,His-Purkinje system,UBERON:0002350,conducting system of heart
+HP:0005246,Giant hypertrophic gastritis,HP:0005263,Gastritis
+DOID:5128,deep leiomyoma,DOID:127,leiomyoma
+HP:0010264,Pseudoepiphyses of the middle phalanges of the hand,HP:0010235,Pseudoepiphyses of the phalanges of the hand
+UBERON:0000025,tube,UBERON:0004111,anatomical conduit
+HP:0100855,Triceps hypoplasia,HP:0009004,Hypoplasia of the musculature
+UBERON:0004564,hindlimb digital vein,UBERON:0003521,pes blood vessel
+UBERON:0001528,radio-ulnar joint,UBERON:0011139,synovial limb joint
+DOID:728,nodular episcleritis,DOID:11343,scleral disease
+HP:0010599,Abnormality of the distal humeral epiphysis,HP:0003891,Abnormality of the humeral epiphysis
+HP:0010254,Small epiphyses of the distal phalanges of the hand,HP:0010243,Abnormality of the epiphyses of the distal phalanx of finger
+CL:0000612,eosinophilic myelocyte,CL:0000772,immature eosinophil
+CL:0000069,branched duct epithelial cell,CL:0000068,duct epithelial cell
+UBERON:0011363,cranial lymph vasculature,UBERON:0002200,vasculature of head
+CL:0002653,squamous endothelial cell,CL:1000414,endothelial cell of venule
+UBERON:0007180,atretic follicle of ovary,UBERON:0001305,ovarian follicle
+DOID:2859,hemoglobin C disease,DOID:2860,hemoglobinopathy
+UBERON:0005863,cartilaginous condensation,UBERON:0005856,developing mesenchymal condensation
+UBERON:3000659,postchoanal process,UBERON:4100000,skeletal element projection
+UBERON:0000320,duodenal mucosa,UBERON:0001204,mucosa of small intestine
+UBERON:0004403,periosteum of epiphysis,UBERON:0002515,periosteum
+DOID:6263,inflammatory breast carcinoma,DOID:3458,breast adenocarcinoma
+UBERON:0005126,metanephric S1,UBERON:0004196,proximal convoluted tubule segment 1
+HP:0001488,Bilateral ptosis,HP:0000508,Ptosis
+HP:0000309,Abnormality of the midface,HP:0000271,Abnormality of the face
+UBERON:0015433,external elastic membrane,UBERON:0003614,blood vessel elastic tissue
+UBERON:0011949,endometrium luminal epithelium,UBERON:0011945,luminal layer of epithelium
+HP:0006625,Multifocal breast carcinoma,HP:0003002,Breast carcinoma
+UBERON:0002100,trunk,UBERON:0011676,subdivision of organism along main body axis
+HP:0007522,Increased number of skin folds,HP:0008067,Abnormally lax or hyperextensible skin
+HP:0009125,Lipodystrophy,HP:0009124,Abnormality of adipose tissue
+HP:0012051,Reactive hypoglycemia,HP:0001943,Hypoglycemia
+DOID:0050679,blue cone monochromacy,DOID:13911,achromatopsia
+UBERON:0005467,platysma,UBERON:0001577,facial nerve muscle
+CL:0000312,keratinocyte,CL:0000237,keratinizing barrier epithelial cell
+UBERON:0005032,mucosa of lower lip,UBERON:0003729,mouth mucosa
+UBERON:0001653,facial vein,UBERON:0003496,head blood vessel
+UBERON:2001527,epibranchial cartilage,UBERON:0011004,pharyngeal arch cartilage
+UBERON:2000376,infraorbital,UBERON:0008907,dermal bone
+DOID:4239,alveolar soft part sarcoma,DOID:4043,skeletal muscle cancer
+DOID:6606,eosinophilic variant of chromophobe renal cell carcinoma,DOID:4471,chromophobe adenocarcinoma
+HP:0003273,Hip contracture,HP:0005750,Contractures of the joints of the lower limbs
+HP:0012563,Premature epimetaphyseal fusion in foot,HP:0010588,Premature epimetaphyseal fusion
+UBERON:0013562,Brodmann (1909) area 8a,UBERON:0013529,Brodmann area
+UBERON:0001582,buccinator muscle,UBERON:0001577,facial nerve muscle
+DOID:10649,acute inferolateral myocardial infarction,DOID:9408,acute myocardial infarction
+HP:0010166,Fragmentation of the epiphyses of the toes,HP:0100168,Fragmented epiphyses
+DOID:9945,constant exophthalmos,DOID:930,orbital disease
+HP:0009196,Absent metacarpal epiphyses,HP:0010577,Absent epiphyses
+CL:0000906,"activated CD8-positive, alpha-beta T cell",CL:0000625,"CD8-positive, alpha-beta T cell"
+DOID:1629,breast myofibroblastoma,DOID:0060082,breast benign neoplasm
+UBERON:0002892,medial amygdaloid nucleus,UBERON:0009663,telencephalic nucleus
+DOID:571,median neuropathy,DOID:572,mononeuritis of upper limb and mononeuritis multiplex
+UBERON:0005021,mucosa of sphenoidal sinus,UBERON:0000344,mucosa
+UBERON:0002783,central tegmental tract of pons,UBERON:0007702,tract of brain
+HP:0009252,Cone-shaped epiphysis of the distal phalanx of the 4th finger,HP:0009395,Cone-shaped epiphyses of the 4th finger
+UBERON:0010013,lower beak,UBERON:0004121,ectoderm-derived structure
+UBERON:0011135,intervertebral cartilage,UBERON:0004120,mesoderm-derived structure
+UBERON:0004041,spleen primary B follicle,UBERON:0010422,primary nodular lymphoid tissue
+UBERON:0012313,1st arch maxillary ectoderm,UBERON:0000490,unilaminar epithelium
+UBERON:0014532,lamina of cerebral hemisphere,UBERON:0002437,cerebral hemisphere white matter
+DOID:4693,nerve plexus neoplasm,DOID:1192,peripheral nervous system neoplasm
+UBERON:0006235,foregut-midgut junction,UBERON:0007651,anatomical junction
+UBERON:0003035,regional part of cerebellar white matter,UBERON:0000073,regional part of nervous system
+HP:0009250,Absent epiphysis of the distal phalanx of the 4th finger,HP:0009393,Absent epiphyses of the 4th finger
+HP:0002069,Generalized tonic-clonic seizures,HP:0002197,Generalized seizures
+UBERON:4200094,inner digits of hand,UBERON:0005451,segment of manus
+UBERON:4200000,medial blade of ilium,UBERON:0005913,zone of bone organ
+UBERON:0001436,phalanx of manus,UBERON:0004249,manual digit bone
+UBERON:4200086,iliac neck,UBERON:0004120,mesoderm-derived structure
+UBERON:0002066,umbilical vein,UBERON:0001638,vein
+HP:0005357,Defective B cell differentiation,HP:0005372,Abnormality of B cell physiology
+HP:0005069,rhizo-meso-acromelic limb shortening,HP:0008905,Rhizomelia
+UBERON:0002397,maxilla,UBERON:0008907,dermal bone
+HP:0004444,Spherocytosis,HP:0004447,Poikilocytosis
+HP:0009168,Bullet-shaped middle phalanx of the 5th finger,HP:0004219,Abnormality of the middle phalanx of the 5th finger
+HP:0011733,Abnormality of adrenal physiology,HP:0000834,Abnormality of the adrenal glands
+HP:0007308,Extrapyramidal dyskinesia,HP:0100660,Dyskinesia
+UBERON:0010884,forelimb bone pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+UBERON:0011768,pineal gland stalk,UBERON:0000479,tissue
+UBERON:0011603,coronoid tooth,UBERON:0003268,tooth of lower jaw
+DOID:7698,non-functioning pancreatic endocrine tumor,DOID:1799,islet cell tumor
+UBERON:0002505,spiral modiolar artery,UBERON:0001637,artery
+UBERON:3000367,otic ramus of squamosal,UBERON:0010313,neural crest-derived structure
+UBERON:0005308,nephrostome,UBERON:0004120,mesoderm-derived structure
+HP:0012541,Cephalohematoma,HP:0001787,Abnormal delivery
+HP:0000841,Hyperactive renin-angiotensin system,HP:0000847,Abnormality of renin-angiotensin system
+HP:0004226,Curved distal phalanx of the 5th finger,HP:0004214,Curved phalanges of the 5th finger
+HP:0002780,Bronchomalacia,HP:0002109,Abnormality of the bronchi
+HP:0006304,Widely-spaced incisors,HP:0011062,Misalignment of incisors
+HP:0000916,Broad clavicles,HP:0000889,Abnormality of the clavicles
+HP:0009349,Enlarged epiphysis of the proximal phalanx of the 3rd finger,HP:0009413,Enlarged epiphyses of the 3rd finger
+DOID:0050120,hemophagocytic lymphohistiocytosis,DOID:75,lymphatic system disease
+UBERON:3000831,spina acromioidea,UBERON:4100000,skeletal element projection
+HP:0009559,Bullet-shaped distal phalanx of the 2nd finger,HP:0009542,Abnormality of the distal phalanx of the 2nd finger
+UBERON:0003015,anterior quadrangular lobule,UBERON:0004003,cerebellum hemisphere lobule
+UBERON:0013715,ilio-marsupialis muscle,UBERON:0001630,muscle organ
+UBERON:0008956,involucrum,UBERON:0000064,organ part
+DOID:308,early myoclonic encephalopathy,DOID:0050702,neonatal period electroclinical syndrome
+HP:0003954,Angulated forearm bones,HP:0002973,Abnormality of the forearm
+UBERON:0001423,radius bone,UBERON:0003607,forelimb long bone
+UBERON:0008609,transversus menti muscle,UBERON:0001577,facial nerve muscle
+UBERON:0015851,upper right incisor tusk,UBERON:0015212,lateral structure
+UBERON:2005276,inclinator muscle,UBERON:0001134,skeletal muscle tissue
+DOID:6903,eye lymphoma,DOID:2174,ocular cancer
+DOID:3818,photoallergic dermatitis,DOID:3042,allergic contact dermatitis
+UBERON:0005286,tela choroidea of midbrain cerebral aqueduct,UBERON:0005283,tela choroidea
+HP:0005832,Dysharmonic delayed bone age,HP:0002750,Delayed skeletal maturation
+HP:0006358,Shovel-shaped maxillary central incisors,HP:0011063,Abnormality of incisor morphology
+CL:1001578,vagina squamous cell,CL:0000076,squamous epithelial cell
+CL:0002181,mucus neck cell of gastric gland,CL:0002180,mucous cell of stomach
+HP:0002937,Hemivertebrae,HP:0003422,Vertebral segmentation defect
+HP:0100732,Pancreatic fibrosis,HP:0012090,Abnormality of pancreas morphology
+HP:0011139,Gastric duplication,HP:0002577,Abnormality of the stomach
+HP:0002686,Prenatal maternal abnormality,HP:0001197,Abnormality of prenatal development or birth
+UBERON:0006063,cartilaginous neural arch,UBERON:0010358,arch of centrum of vertebra
+UBERON:2202026,pectoral fin proximal radial cartilage 1,UBERON:2201587,pectoral fin proximal radial cartilage
+HP:0010079,Curved distal phalanx of the hallux,HP:0010053,Abnormality of the distal phalanx of the hallux
+UBERON:0012463,cloacal lumen,UBERON:0000464,anatomical space
+UBERON:2001674,infraorbital 6,UBERON:2000376,infraorbital
+HP:0000623,Supranuclear ophthalmoplegia,HP:0000602,Ophthalmoplegia
+UBERON:0004716,conceptus,UBERON:0000480,anatomical group
+UBERON:0011629,supratemporal bone,UBERON:0002514,intramembranous bone
+UBERON:3010713,m. sternoepicoracoideus,UBERON:0010891,pectoral complex muscle
+UBERON:0009735,sublaminar layers S1 or S3 or S4,UBERON:0008921,substratum of layer of retina
+HP:0001643,Patent ductus arteriosus,HP:0011603,Congenital malformation of the great arteries
+UBERON:2002092,rostral cartilage,UBERON:0003932,cartilage element of chondrocranium
+HP:0012536,Maternal anticardiolipin antibody positive,HP:0011437,Maternal autoimmune disease
+HP:0003768,Periodic paralysis,HP:0003470,Paralysis
+DOID:13787,localized anterior staphyloma,DOID:11595,scleral staphyloma
+UBERON:0004050,subarachnoid cistern,UBERON:0000315,subarachnoid space
+DOID:2725,capillary hemangioma,DOID:471,skin hemangioma
+UBERON:3010812,Dorsal tail tubercle,UBERON:3000977,body external integument structure
+UBERON:0014848,tendon of quadriceps femoris,UBERON:0003589,hindlimb connective tissue
+DOID:13134,hordeolum externum,DOID:9423,blepharitis
+UBERON:0003439,nerve of trunk region,UBERON:0001021,nerve
+HP:0009725,Bladder neoplasm,HP:0010786,Urinary tract neoplasm
+UBERON:0005134,metanephric nephron epithelium,UBERON:0005108,metanephric epithelium
+HP:0001305,Dandy-Walker malformation,HP:0005445,Widened posterior fossa
+UBERON:0012247,cervical gland,UBERON:0000414,mucous gland
+HP:0002521,Hypsarrhythmia,HP:0011198,EEG with generalized epileptiform discharges
+UBERON:0008433,lumbar vertebral arch,UBERON:0003828,abdominal segment bone
+HP:0000024,Prostatitis,HP:0008775,Abnormality of the prostate
+UBERON:0001884,phrenic nerve,UBERON:0003443,thoracic cavity nerve
+UBERON:0003216,hard palate,UBERON:0010314,structure with developmental contribution from neural crest
+NCBITaxon:10374,Gammaherpesvirinae,NCBITaxon:10292,Herpesviridae
+HP:0009808,Anomaly of the upper limb diaphyses,HP:0002817,Abnormality of the upper limb
+UBERON:0005255,pedal digit mesenchyme,UBERON:0004120,mesoderm-derived structure
+UBERON:0009662,hindbrain nucleus,UBERON:0002308,nucleus of brain
+UBERON:0001828,gingiva,UBERON:0003729,mouth mucosa
+UBERON:0003083,trunk neural crest,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:4300106,ventral limb of posttemporal,UBERON:0004121,ectoderm-derived structure
+HP:0100277,Periauricular skin pits,HP:0100276,Skin pits
+HP:0100665,Angioedema,HP:0011276,Vascular skin abnormality
+DOID:572,mononeuritis of upper limb and mononeuritis multiplex,DOID:1188,mononeuropathy
+HP:0100881,Congenital mesoblastic nephroma,HP:0011794,Embryonal renal neoplasm
+UBERON:0004713,corpus cavernosum penis,UBERON:0014403,male anatomical structure
+UBERON:0002947,frontal operculum,UBERON:0003022,cerebral cortex lobe
+CL:0000815,regulatory T cell,CL:0002419,mature T cell
+UBERON:0005278,nail bed of finger,UBERON:0005273,nail bed
+UBERON:0011195,inferior parathyroid epithelium,UBERON:0011197,parathyroid epithelium
+HP:0004859,Amegakaryocytic thrombocytopenia,HP:0001873,Thrombocytopenia
+UBERON:0010947,occipitalis,UBERON:0004120,mesoderm-derived structure
+UBERON:0013766,epicanthal fold,UBERON:0001457,skin of eyelid
+UBERON:0015488,sural nerve,UBERON:0002003,peripheral nerve
+UBERON:0004033,podocyte slit junction,UBERON:0000470,cell part
+UBERON:0004044,anterior visceral endoderm,UBERON:0000478,extraembryonic structure
+UBERON:0001836,saliva,UBERON:0000456,bodily secretion
+UBERON:0006015,webbed interdigital region,UBERON:0006012,interdigital region
+HP:0012169,Self-biting,HP:0100716,Self-injurious behavior
+UBERON:0003580,lower respiratory tract connective tissue,UBERON:0004119,endoderm-derived structure
+HP:0006392,Increased density of long bones,HP:0011001,Increased bone mineral density
+UBERON:0005641,otocyst epithelium,UBERON:0010371,ecto-epithelium
+UBERON:3000003,alary process of premaxilla,UBERON:0004120,mesoderm-derived structure
+HP:0008345,Hypoplasia of the iris dilator muscle,HP:0007676,Hypoplasia of the iris
+UBERON:2001826,urohyal median process,UBERON:0004121,ectoderm-derived structure
+UBERON:0013708,anterior superior iliac spine,UBERON:0013712,anterior iliac spine
+HP:0009991,Complete duplication of the distal phalanx of the 5th finger,HP:0009986,Complete duplication of the phalanges of the 5th finger
+HP:0009995,Partial duplication of the middle phalanx of the 5th finger,HP:0009987,Partial duplication of the phalanges of the 5th finger
+UBERON:0010534,primitive mesonephric nephron,UBERON:0000083,mesonephric tubule
+UBERON:3000745,webbing of bone,UBERON:0000064,organ part
+CL:0002095,hilus cell of ovary,CL:0000593,androgen secreting cell
+HP:0004284,Notched hand bones,HP:0005922,Abnormal hand morphology
+UBERON:4200086,iliac neck,UBERON:0005913,zone of bone organ
+DOID:4910,urethra adenocarcinoma,DOID:734,urethra cancer
+DOID:2006,preretinal fibrosis,DOID:2007,degeneration of macula and posterior pole
+UBERON:3010824,processus triangularis of palatoquadrate cartilage,UBERON:4100000,skeletal element projection
+UBERON:0001628,posterior communicating artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0009914,renal lobule,UBERON:0009911,lobule
+HP:0009669,Irregular epiphysis of the proximal phalanx of the thumb,HP:0010262,Irregular epiphyses of the middle phalanges of the hand
+UBERON:0008201,scute,UBERON:0007381,epidermal scale
+DOID:5295,intestinal disease,DOID:77,gastrointestinal system disease
+HP:0009283,Abnormality of the middle phalanx of the 4th finger,HP:0009172,Abnormality of the phalanges of the 4th finger
+UBERON:2001777,pelvic fin lepidotrichium 2,UBERON:4000173,pelvic fin lepidotrichium
+UBERON:0001732,pharyngeal tonsil,UBERON:0002372,tonsil
+UBERON:1000010,mole,UBERON:0004121,ectoderm-derived structure
+UBERON:0005475,sigmoid sinus,UBERON:0003496,head blood vessel
+DOID:2301,atrophy of prostate,DOID:47,prostate disease
+UBERON:2005384,dorsal fin proximal radial bone 7,UBERON:2105384,dorsal fin proximal radial element 7
+HP:0002459,Dysautonomia,HP:0012332,Abnormal autonomic nervous system physiology
+CL:0000882,thymic medullary macrophage,CL:0000866,thymic macrophage
+UBERON:0003057,chordal neural plate,UBERON:0005423,developing anatomical structure
+DOID:4817,ganglioneuroma,DOID:2621,autonomic nervous system neoplasm
+HP:0006473,Anterior bowing of long bones,HP:0006487,Bowing of the long bones
+HP:0009117,Aplasia/Hypoplasia of the maxilla,HP:0009116,Aplasia/Hypoplasia involving bones of the skull
+HP:0003799,Marked delay in bone age,HP:0002750,Delayed skeletal maturation
+UBERON:0005440,ductus arteriosus,UBERON:0004573,systemic artery
+HP:0003127,Hypocalciuria,HP:0011280,Abnormality of urine calcium concentration
+UBERON:0006118,lamina I of gray matter of spinal cord,UBERON:0001948,regional part of spinal cord
+CL:0002546,embryonic blood vessel endothelial progenitor cell,CL:0000222,mesodermal cell
+HP:0010019,Fragmentation of the epiphysis of the 1st metacarpal,HP:0010272,Fragmentation of the epiphyses of the proximal phalanges of the hand
+DOID:11887,ureter leiomyoma,DOID:11885,ureteral benign neoplasm
+HP:0009967,Complete duplication of the proximal phalanx of the 3rd finger,HP:0010000,Complete duplication of the proximal phalanges of the hand
+UBERON:0000928,embryonic segment,UBERON:0000914,organismal segment
+DOID:4205,cerebellum cancer,DOID:4706,infratentorial cancer
+HP:0010132,Irregular epiphysis of the proximal phalanx of the hallux,HP:0010126,Abnormality of the epiphysis of the proximal phalanx of the hallux
+UBERON:0013504,caudal vertebra pre-cartilage condensation,UBERON:0011095,vertebra pre-cartilage condensation
+DOID:2537,inflammatory and toxic neuropathy,DOID:870,neuropathy
+UBERON:0008257,radial sesamoid,UBERON:0007997,sesamoid bone of manus
+HP:0100020,Posterior capsular cataract,HP:0100017,Capsular cataract
+UBERON:0010310,nictitating membrane lamina,UBERON:0002418,cartilage tissue
+UBERON:0010376,pancreas ventral primordium,UBERON:0002365,exocrine gland
+HP:0008103,Delayed tarsal ossification,HP:0008369,Abnormal tarsal ossification
+UBERON:0003700,temporomandibular joint,UBERON:0010313,neural crest-derived structure
+DOID:10573,osteomalacia,DOID:0080005,bone remodeling disease
+CL:1000359,microfold cell of epithelium proper of appendix,CL:1000360,microfold cell of epithelium proper of large intestine
+UBERON:0006062,articular process of vertebra,UBERON:0015212,lateral structure
+HP:0009400,Pseudoepiphyses of the 4th finger,HP:0010235,Pseudoepiphyses of the phalanges of the hand
+HP:0009942,Duplication of phalanx of thumb,HP:0009602,Abnormality of the phalanges of the thumb
+UBERON:0002012,pulmonary artery,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0012216,Entrapment neuropathy of suprascapular nerve,HP:0012181,Entrapment neuropathy
+UBERON:0005660,2nd arch ectoderm,UBERON:0000924,ectoderm
+UBERON:0010213,laryngeal pre-cartilage condensation,UBERON:0004119,endoderm-derived structure
+NCBITaxon:10242,Orthopoxvirus,NCBITaxon:10241,Chordopoxvirinae
+HP:0100200,Stippling of the epiphysis of the proximal phalanx of the 4th toe,HP:0100096,Abnormality of the epiphysis of the proximal phalanx of the 4th toe
+HP:0009598,Symphalangism of the proximal phalanx of the 2nd finger with the 2nd metatcarpal,HP:0005880,Metacarpophalangeal synostosis
+CL:0002386,multinucleate macroconidium,CL:0002382,multinucleate conidium
+UBERON:0007149,inferior thyroid artery,UBERON:0004573,systemic artery
+UBERON:3010124,toe fringes,UBERON:3000981,limb external integument structure
+DOID:8362,enteric pattern testicular yolk sac tumor,DOID:5344,testicular yolk sac tumor
+HP:0001122,Aplasia/Hypoplasia of the choroid,HP:0000610,Abnormality of the choroid
+HP:0012214,Increased glomerular filtration rate,HP:0012212,Abnormal glomerular filtration rate
+UBERON:0006641,appendix epididymis,UBERON:0014403,male anatomical structure
+HP:0007962,Speckled corneal dystrophy,HP:0001131,Corneal dystrophy
+DOID:495,sclerosing hemangioma,DOID:255,hemangioma
+HP:0003871,Deformed humerus,HP:0003063,Abnormality of the humerus
+HP:0003409,Distal sensory impairment of all modalities,HP:0000763,Sensory neuropathy
+UBERON:0006294,stapes pre-cartilage condensation,UBERON:0009506,associated mesenchyme of middle ear
+UBERON:2002008,neural lamina,UBERON:0004120,mesoderm-derived structure
+DOID:1461,cholesterol embolism,DOID:178,vascular disease
+HP:0012292,Fusion of gums,HP:0000168,Abnormality of the gingiva
+UBERON:0004657,mandible condylar process,UBERON:0004120,mesoderm-derived structure
+UBERON:2001882,parapophysis + rib of vertebra 3,UBERON:0002513,endochondral bone
+DOID:10316,pneumoconiosis,DOID:3082,interstitial lung disease
+UBERON:0002835,thoracic dorsal root ganglion,UBERON:0000961,thoracic ganglion
+UBERON:0011150,pharyngeal arch derived gill,UBERON:0004119,endoderm-derived structure
+UBERON:0015873,heel skin,UBERON:0001513,skin of pes
+UBERON:0014508,distal interphalangeal joint of manual digit 3,UBERON:0007730,interphalangeal joint of manual digit 3
+CL:0000210,photoreceptor cell,CL:0000006,neuronal receptor cell
+HP:0010776,Tracheobronchmegaly,HP:0010777,Bronchomegaly
+HP:0005917,Supernumerary metacarpal bones,HP:0001163,Abnormality of the metacarpal bones
+HP:0010073,Synostosis involving the 1st metatarsal,HP:0010064,Symphalangism affecting the phalanges of the hallux
+HP:0012455,Large artery calcification,HP:0003207,Arterial calcification
+UBERON:2000171,interhyal bone,UBERON:2001892,interhyal element
+UBERON:0005081,ureter ureteric bud,UBERON:0007497,developing epithelial placode
+UBERON:0002265,olfactory tract,UBERON:0007702,tract of brain
+HP:0002576,Intussusception,HP:0002242,Abnormality of the intestine
+UBERON:2005317,pectoral fin fold,UBERON:0004121,ectoderm-derived structure
+UBERON:0005283,tela choroidea,UBERON:0004923,organ component layer
+DOID:127,leiomyoma,DOID:0060084,cell type benign neoplasm
+CL:0002071,enterocyte of epithelium of large intestine,CL:0002253,epithelial cell of large intestine
+DOID:11701,selective IgA deficiency disease,DOID:11702,dysgammaglobulinemia
+UBERON:0011256,rhinarium,UBERON:0003102,surface structure
+UBERON:0004521,vasculature of muscle organ,UBERON:0004522,vasculature of musculoskeletal system
+DOID:4784,immune-complex glomerulonephritis,DOID:2921,glomerulonephritis
+UBERON:0013450,simian shelf,UBERON:0010313,neural crest-derived structure
+HP:0007964,Degenerative vitreoretinopathy,HP:0007773,Vitreoretinal abnormalities
+UBERON:0004001,olfactory bulb layer,UBERON:0004121,ectoderm-derived structure
+UBERON:0013673,os priapium,UBERON:0003457,head bone
+UBERON:4200119,pubis-ischium contact,UBERON:0005913,zone of bone organ
+UBERON:0006684,sphenoidal fontanelle,UBERON:0002221,fontanelle
+DOID:315,synovium neoplasm,DOID:0060123,connective tissue benign neoplasm
+UBERON:0001983,crypt of Lieberkuhn,UBERON:0000333,intestinal gland
+UBERON:0002485,prostate duct,UBERON:0005904,duct of male reproductive system
+HP:0012138,Granulocytic hyperplasia,HP:0012137,Abnormal number of granulocyte precursors
+UBERON:0002380,trapezius muscle,UBERON:0010313,neural crest-derived structure
+UBERON:0010427,ciliary processes,UBERON:0000481,multi-tissue structure
+UBERON:0011845,duct of sebaceous gland,UBERON:0000058,duct
+HP:0010901,Abnormality of methionine metabolism,HP:0004339,Abnormality of sulfur amino acid metabolism
+HP:0010323,Abnormality of the epiphyses of the 2nd toe,HP:0010160,Abnormality of the epiphyses of the toes
+CL:0002393,intermediate monocyte,CL:0000576,monocyte
+DOID:3119,gastrointestinal system cancer,DOID:0050686,organ system cancer
+UBERON:0003354,epithelium of rectum,UBERON:0001278,epithelium of large intestine
+UBERON:0005148,metanephric S-shaped body,UBERON:0005330,mesonephric nephron epithelium
+UBERON:0012504,adventitia of esophagus,UBERON:0005742,adventitia
+HP:0007185,Loss of consciousness,HP:0004372,Reduced consciousness/confusion
+DOID:10128,venous insufficiency,DOID:866,vein disease
+UBERON:0004378,proximal metaphysis,UBERON:0001438,metaphysis
+HP:0009614,Bifid proximal phalanx of the thumb,HP:0009944,Partial duplication of the phalanges of the thumb
+DOID:11665,Patau syndrome,DOID:0080014,chromosomal disease
+UBERON:0007316,deep external pudendal artery,UBERON:0004573,systemic artery
+HP:0009328,Pseudoepiphysis of the middle phalanx of the 3rd finger,HP:0009334,Abnormality of the epiphysis of the middle phalanx of the 3rd finger
+HP:0010190,Patchy sclerosis of the distal phalanges of the toes,HP:0100948,Sclerosis of the distal phalanges of the toes
+CL:1001581,lateral ventricle glial cell,CL:0000125,glial cell
+HP:0009252,Cone-shaped epiphysis of the distal phalanx of the 4th finger,HP:0009249,Abnormality of the epiphysis of the distal phalanx of the 4th finger
+UBERON:2001592,claustrum bone,UBERON:0002513,endochondral bone
+HP:0004112,Midline nasal groove,HP:0004122,Midline defect of the nose
+DOID:431,myofascial pain syndrome,DOID:423,myopathy
+UBERON:0011144,adductor muscle of hip,UBERON:0011145,adductor muscle
+UBERON:0005740,tunica intima of artery,UBERON:0002523,tunica intima
+HP:0006509,Diverticulosis of trachea,HP:0002778,Abnormality of the trachea
+HP:0002398,Degeneration of anterior horn cells,HP:0006802,Abnormality of the anterior horn cell
+HP:0006783,Posterior pharyngeal cleft,HP:0000600,Abnormality of the pharynx
+CL:0005008,macular hair cell,CL:0000202,auditory hair cell
+UBERON:0015716,anal canal epithelium,UBERON:0001278,epithelium of large intestine
+HP:0011208,EEG with generalized slow activity grade 3,HP:0010845,EEG with generalized slow activity
+UBERON:4200172,neck of humerus,UBERON:0005055,zone of long bone
+UBERON:0004603,rib 3,UBERON:0002228,rib
+UBERON:2001521,ceratobranchial 5 cartilage,UBERON:2001516,ceratobranchial cartilage
+DOID:11119,Gilles de la Tourette syndrome,DOID:2769,tic disorder
+UBERON:4200036,internal trochanter,UBERON:4100000,skeletal element projection
+UBERON:0004829,urethra skeletal muscle,UBERON:0006554,urinary system structure
+HP:0011123,Inflammatory abnormality of the skin,HP:0011122,Abnormality of skin physiology
+UBERON:0000453,decidua basalis,UBERON:0005156,reproductive structure
+CL:0008007,visceral muscle cell,CL:0000187,muscle cell
+UBERON:0013139,ligament of liver,UBERON:0008845,nonskeletal ligament
+HP:0005059,arthralgia/arthritis,HP:0002829,Arthralgia
+UBERON:0001752,enamel,UBERON:0001973,substance of tooth
+DOID:1063,interstitial nephritis,DOID:10952,nephritis
+HP:0009492,Fragmentation of the epiphyses of the 2nd finger,HP:0010232,Fragmentation of the epiphyses of the phalanges of the hand
+UBERON:0001440,forelimb skeleton,UBERON:0004381,skeleton of limb
+CL:0008009,transversely striated visceral muscle cell,CL:0008008,striated visceral muscle cell
+DOID:0050616,malignant Leydig cell tumor,DOID:192,sex cord-gonadal stromal tumor
+CL:0000308,metal ion accumulating cell,CL:0000325,stuff accumulating cell
+UBERON:0003839,forelimb joint,UBERON:0003657,limb joint
+CL:0000702,R5 photoreceptor cell,CL:0000287,eye photoreceptor cell
+UBERON:2005020,central artery,UBERON:0001637,artery
+CL:0001029,common dendritic progenitor,CL:0000763,myeloid cell
+HP:0003712,Muscle hypertrophy,HP:0011805,Abnormality of muscle morphology
+UBERON:0001869,cerebral hemisphere,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003842,neural tube lumen,UBERON:0005082,tube lumen
+DOID:8104,vaginal tubulovillous adenoma,DOID:5402,vaginal adenoma
+UBERON:0000220,atlanto-occipital joint,UBERON:0002217,synovial joint
+UBERON:0001574,palatoglossus muscle,UBERON:0003682,palatal muscle
+HP:0007371,Atrophy/Degeneration of the corpus callosum,HP:0007369,Atrophy/Degeneration affecting the cerebrum
+DOID:3277,thymus cancer,DOID:0060083,immune system cancer
+UBERON:0001494,ulnar nerve,UBERON:0002003,peripheral nerve
+DOID:3301,gonadoblastoma,DOID:0060084,cell type benign neoplasm
+HP:0000092,Tubular atrophy,HP:0000091,Abnormality of the renal tubule
+HP:0003397,Generalized hypotonia due to defect at the neuromuscular junction,HP:0003398,Abnormality of the neuromuscular junction
+DOID:6873,skin tag,DOID:2053,reactive cutaneous fibrous lesion
+UBERON:2001168,vertebral element 2,UBERON:0010913,vertebral element
+UBERON:0004149,ventriculo bulbo valve,UBERON:0000946,cardial valve
+HP:0002363,Abnormality of the brainstem,HP:0012443,Abnormality of the brain
+UBERON:0004755,skeletal tissue,UBERON:0002384,connective tissue
+CL:0000712,stratum granulosum cell,CL:0000362,epidermal cell
+DOID:8336,childhood choriocarcinoma of the ovary,DOID:5550,choriocarcinoma of ovary
+UBERON:0010186,male urethral gland,UBERON:0001338,urethral gland
+HP:0004975,Erlenmeyer flask deformity of the femurs,HP:0002823,Abnormality of the femur
+UBERON:0003074,mesonephric duct,UBERON:0000083,mesonephric tubule
+HP:0004902,Congenital lactic acidosis,HP:0003128,Lactic acidosis
+HP:0003903,Broad humeral epiphyses,HP:0003891,Abnormality of the humeral epiphysis
+UBERON:0003967,cutaneous elastic tissue,UBERON:0004121,ectoderm-derived structure
+UBERON:2005052,anterior mesencephalic central artery,UBERON:2005020,central artery
+HP:0008095,Osteolysis of talus,HP:0009134,Osteolysis involving bones of the feet
+HP:0011161,Olfactory Auras,HP:0011157,Auras
+UBERON:0013240,future glans clitoris,UBERON:0013238,future glans
+DOID:4397,granulomatous dermatitis,DOID:2723,dermatitis
+UBERON:0008989,submocosal esophageal gland,UBERON:0011148,submucosal gland
+UBERON:0004441,proximal epiphysis of proximal phalanx of manual digit 3,UBERON:0011977,epiphysis of proximal phalanx of manus
+CL:0002659,glandular cell of stomach,CL:0000150,glandular epithelial cell
+UBERON:0009906,root of optic nerve,UBERON:0006843,root of cranial nerve
+NCBITaxon:186536,Ebolavirus,NCBITaxon:11266,Filoviridae
+HP:0012396,Biliary dyskinesia,HP:0012439,Abnormal biliary tract physiology
+HP:0009197,Bracket epiphysis of the proximal phalanx of the 5th finger,HP:0009383,Bracket epiphyses of the 5th finger
+UBERON:0005046,mucosa of hard palate,UBERON:0005019,mucosa of palate
+HP:0009996,Partial duplication of the proximal phalanx of the 5th finger,HP:0009990,Duplication of the proximal phalanx of the 5th finger
+UBERON:0011628,early premaxilla,UBERON:0011597,bone of upper jaw
+UBERON:0013153,arachnoid villus,UBERON:0004732,segmental subdivision of nervous system
+DOID:0060029,autoimmune disease of exocrine system,DOID:417,hypersensitivity reaction type II disease
+UBERON:0004345,trophectoderm,UBERON:0010303,extraembryonic epithelium
+HP:0003110,Abnormality of urine homeostasis,HP:0011277,Abnormality of the urinary system physiology
+UBERON:0003684,abdominal cavity,UBERON:0002323,coelemic cavity lumen
+UBERON:0015430,levator auris longus muscle,UBERON:0001577,facial nerve muscle
+UBERON:0006190,mesonephric distal tubule,UBERON:0004135,distal tubule
+UBERON:0002018,synovial membrane of synovial joint,UBERON:0006915,stratified squamous epithelium
+UBERON:3000041,Bidder's organ,UBERON:0000481,multi-tissue structure
+DOID:0050931,parotid gland adenoid cystic carcinoma,DOID:9036,parotid gland cancer
+DOID:0060196,amyotrophic lateral sclerosis type 4,DOID:332,amyotrophic lateral sclerosis
+DOID:0050908,myelodysplastic syndrome,DOID:4960,bone marrow cancer
+CL:0002148,dental pulp cell,CL:0002159,general ecto-epithelial cell
+HP:0009234,Symphalangism of the proximal phalanx of the 5th finger with the 5th metatcarpal,HP:0005880,Metacarpophalangeal synostosis
+HP:0003186,Inverted nipples,HP:0004404,Abnormality of the nipple
+HP:0012317,Sacroiliac arthritis,HP:0002758,Osteoarthritis
+HP:0009817,Aplasia involving bones of the lower limbs,HP:0009825,Aplasia involving bones of the extremities
+DOID:5048,posterior pituitary gland neoplasm,DOID:3643,sella turcica neoplasm
+HP:0000091,Abnormality of the renal tubule,HP:0012575,Abnormality of the nephron
+UBERON:0003075,neural plate,UBERON:0005291,embryonic tissue
+UBERON:2002229,presumptive atrium primitive heart tube,UBERON:0002050,embryonic structure
+CL:0002159,general ecto-epithelial cell,CL:0002077,ecto-epithelial cell
+HP:0003994,Dislocated wrist,HP:0001373,Joint dislocation
+DOID:437,myasthenia gravis,DOID:439,neuromuscular junction disease
+CL:0000255,eukaryotic cell,CL:0000003,native cell
+HP:0003974,Absent radius,HP:0009822,Aplasia involving forearm bones
+UBERON:0011087,pharyngeal arch 7,UBERON:0008896,post-hyoid pharyngeal arch
+UBERON:0014790,lingual septum,UBERON:0004121,ectoderm-derived structure
+HP:0011422,Abnormality of chloride homeostasis,HP:0003111,Abnormality of ion homeostasis
+UBERON:0005997,tricuspid valve anulus,UBERON:0010313,neural crest-derived structure
+UBERON:0015213,barnacle cement gland,UBERON:0002365,exocrine gland
+CL:1000239,anterior lateral line nerve glial cell,CL:1000050,lateral line nerve glial cell
+UBERON:2001721,caudal principal ray 9,UBERON:2001585,caudal principal ray
+UBERON:0003214,mammary gland alveolus,UBERON:0003215,alveolus
+DOID:2731,vesiculobullous skin disease,DOID:37,skin disease
+DOID:1339,Diamond-Blackfan anemia,DOID:1342,congenital hypoplastic anemia
+UBERON:0005876,undifferentiated genital tubercle,UBERON:0005423,developing anatomical structure
+UBERON:0014474,postcentral fissure of cerebellum,UBERON:0003980,cerebellum fissure
+HP:0005863,Type E brachydactyly,HP:0001156,Brachydactyly syndrome
+UBERON:0013748,ulnar metaphysis,UBERON:0004120,mesoderm-derived structure
+DOID:712,refractory hematologic cancer,DOID:2531,hematologic cancer
+UBERON:0007384,appendage lymph vessel,UBERON:0001473,lymphatic vessel
+DOID:594,panic disorder,DOID:2030,anxiety disorder
+DOID:5457,laryngeal neuroendocrine tumor,DOID:2598,laryngeal benign neoplasm
+UBERON:0007414,nucleus of midbrain tegmentum,UBERON:0009661,midbrain nucleus
+UBERON:0006813,nasal skeleton,UBERON:0010912,subdivision of skeleton
+DOID:10864,partial third-nerve palsy,DOID:10863,paralytic squint
+UBERON:3000365,otic process,UBERON:0004121,ectoderm-derived structure
+UBERON:4200091,ethomosphenoid region,UBERON:0003462,facial bone
+UBERON:3000263,lamina precerebralis,UBERON:0000064,organ part
+DOID:0050127,sinusitis,DOID:1352,paranasal sinus disease
+DOID:7179,mixed eosinophil-basophil adenoma,DOID:3829,pituitary adenoma
+UBERON:0009071,mesobronchus,UBERON:0002182,main bronchus
+UBERON:0000155,theca cell layer,UBERON:0000481,multi-tissue structure
+CL:0000530,primary neuron,CL:0000540,neuron
+UBERON:0004410,distal epiphysis of fibula,UBERON:0004388,epiphysis of fibula
+UBERON:0010062,pharyngotympanic tube epithelium,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0009775,lateral medullary reticular complex,UBERON:0007245,nuclear complex of neuraxis
+HP:0006376,Limited elbow flexion,HP:0005060,limited elbow flexion/extension
+UBERON:0004746,prootic bone,UBERON:0002513,endochondral bone
+CL:0000349,extraembryonic cell,CL:0002371,somatic cell
+HP:0006055,Ulnar deviated club hands,HP:0009487,Ulnar deviation of the hand
+HP:0007499,Recurrent staphylococcal infections,HP:0002718,Recurrent bacterial infections
+HP:0010419,Symphalangism affecting the distal phalanx of the 2nd toe,HP:0001859,Distal symphalangism (feet)
+HP:0005560,Imbalanced hemoglobin synthesis,HP:0011902,Abnormal hemoglobin
+HP:0010468,Aplasia/Hypoplasia of the testes,HP:0000035,Abnormality of the testis
+DOID:0050218,polycystic echinococcosis,DOID:1496,echinococcosis
+UBERON:0004223,vagina smooth muscle,UBERON:0001135,smooth muscle tissue
+UBERON:2201672,dorsal fin radial cartilage,UBERON:2101672,dorsal fin radial element
+CL:0001015,CD8_alpha-low Langerhans cell,CL:0000453,Langerhans cell
+UBERON:0005983,heart layer,UBERON:0004120,mesoderm-derived structure
+UBERON:2007036,hindbrain neural rod,UBERON:0005291,embryonic tissue
+CL:0002572,vertebral mesenchymal stem cell,CL:0000134,mesenchymal cell
+DOID:11190,pseudomembranous conjunctivitis,DOID:11184,acute conjunctivitis
+DOID:11029,pinguecula,DOID:10139,conjunctival degeneration
+HP:0010006,Duplication of the proximal phalanx of hand,HP:0009997,Duplication of phalanx of hand
+DOID:11875,denture stomatitis,DOID:9637,stomatitis
+HP:0002196,Myelopathy,HP:0002143,Abnormality of the spinal cord
+UBERON:0014773,medial palpebral artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0009862,ascidian cerebral ganglion,UBERON:0000064,organ part
+CL:0001021,"CD34-positive, CD38-positive common lymphoid progenitor",CL:0000051,common lymphoid progenitor
+UBERON:0005566,rhombomere 1 floor plate,UBERON:0005500,rhombomere floor plate
+HP:0012698,Cerebellar gliosis,HP:0001317,Abnormality of the cerebellum
+HP:0100649,Neoplasm of the oral cavity,HP:0000163,Abnormality of the oral cavity
+UBERON:2001904,epibranchial element,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0004097,Deviation of finger,HP:0001167,Abnormality of finger
+DOID:9598,fasciitis,DOID:65,connective tissue disease
+HP:0001317,Abnormality of the cerebellum,HP:0011283,Abnormality of the metencephalon
+UBERON:0001128,sternocleidomastoid,UBERON:0002377,muscle of neck
+UBERON:0006805,sternal end of clavicle,UBERON:0005055,zone of long bone
+HP:0012690,T2 hypointense thalamus,HP:0012696,Abnormal thalamic MRI signal intensity
+UBERON:2000508,pelvic fin radial bone,UBERON:2100508,pelvic fin radial element
+DOID:3073,brain glioblastoma multiforme,DOID:0060108,brain glioma
+HP:0007755,Juvenile epithelial corneal dystrophy,HP:0200020,Corneal erosions
+HP:0005092,Streaky metaphyseal sclerosis,HP:0004979,Metaphyseal sclerosis
+HP:0011262,Crimped helix,HP:0011039,Abnormality of the helix
+HP:0001704,Tricuspid valve prolapse,HP:0001702,Abnormality of the tricuspid valve
+HP:0002738,Hypoplastic frontal sinuses,HP:0009119,Aplasia/Hypoplasia of the frontal sinuses
+UBERON:0000711,splenius capitis,UBERON:0002377,muscle of neck
+UBERON:0013607,parvocellular layer of dorsal nucleus of lateral geniculate body,UBERON:0013605,layer of lateral geniculate body
+UBERON:0015001,radius endochondral element,UBERON:0015021,forelimb endochondral element
+UBERON:0011389,bulbospongiosus muscle,UBERON:0002379,perineal muscle
+UBERON:0014773,medial palpebral artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0013147,early mesencephalic vesicle,UBERON:0013150,future brain vesicle
+UBERON:0002662,medial pes lemniscus,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0009556,long pastern bone,UBERON:0009558,pastern bone
+UBERON:0005279,nail bed of toe,UBERON:0005273,nail bed
+UBERON:0003830,thoracic segment muscle,UBERON:0005181,thoracic segment organ
+UBERON:0002224,thoracic cavity,UBERON:0000464,anatomical space
+CL:1000285,smooth muscle cell of sigmoid colon,CL:0000540,neuron
+UBERON:0001138,superior mesenteric vein,UBERON:0005617,mesenteric vein
+UBERON:3010123,finger fringes,UBERON:3000981,limb external integument structure
+UBERON:0005586,rhombomere 7 lateral wall,UBERON:0005501,rhombomere lateral wall
+UBERON:3000707,pleurapophysis,UBERON:0000064,organ part
+CL:0000639,basophil cell of pars distalis of adenohypophysis,CL:0000637,chromophil cell of anterior pituitary gland
+UBERON:0011604,carina of sternum,UBERON:0000064,organ part
+NCBITaxon:5597,Pseudallescheria boydii,NCBITaxon:5596,Pseudallescheria
+DOID:4613,ulnar neuropathy,DOID:1188,mononeuropathy
+UBERON:0015881,internal iliac lymph node,UBERON:0015877,parietal pelvic lymph node
+HP:0005054,Metaphyseal spurs,HP:0000944,Abnormality of the metaphyses
+UBERON:0006296,subcardinal vein,UBERON:0002050,embryonic structure
+UBERON:0001258,neck of urinary bladder,UBERON:0001560,neck of organ
+UBERON:0008229,craniocervical region musculature,UBERON:0001015,musculature
+CL:0002576,perineural cell,CL:0000186,myofibroblast cell
+DOID:0050758,metabolic acidosis,DOID:3650,lactic acidosis
+HP:0001899,Increased hematocrit,HP:0001901,Polycythemia
+UBERON:4200113,predorsal scute,UBERON:2002294,fish scute
+UBERON:0001424,ulna,UBERON:0003466,forelimb zeugopod bone
+DOID:13140,suppurative uveitis,DOID:13141,uveitis
+HP:0100064,Stippling of the epiphyses of the 3rd toe,HP:0010171,Epiphyseal stippling of toe phalanges
+HP:0000952,Jaundice,HP:0001005,Dermatological manifestations of systemic disorders
+UBERON:0006115,posterior column of fornix,UBERON:0000122,neuron projection bundle
+HP:0100939,Sclerosis of the distal phalanx of the 2nd toe,HP:0010356,Abnormality of the distal phalanx of the 2nd toe
+UBERON:0010940,belly of digastric,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0003762,Uterus didelphys,HP:0000130,Abnormality of the uterus
+HP:0008115,Third toe clinodactyly,HP:0001863,Toe clinodactyly
+DOID:5742,pancreatic acinar cell adenocarcinoma,DOID:4074,pancreas adenocarcinoma
+HP:0100006,Neoplasm of the central nervous system,HP:0004375,Neoplasm of the nervous system
+CL:0000347,scleral cell,CL:0000293,structural cell
+HP:0008142,Delayed calcaneal ossification,HP:0008103,Delayed tarsal ossification
+HP:0010353,Symphalangism affecting the phalanges of the 2nd toe,HP:0010179,Symphalangism affecting the phalanges of the toes
+HP:0004297,Abnormality of the biliary system,HP:0001392,Abnormality of the liver
+UBERON:2001186,collagenous dermal stroma,UBERON:0004120,mesoderm-derived structure
+UBERON:3000727,haemal arch lamina,UBERON:4100000,skeletal element projection
+UBERON:0006954,mammary myoepithelium,UBERON:0003244,epithelium of mammary gland
+HP:0000306,Abnormality of the chin,HP:0000271,Abnormality of the face
+HP:0010093,Duplication of the proximal phalanx of the hallux,HP:0010066,Duplication of phalanx of hallux
+NCBITaxon:43735,Tabanomorpha,NCBITaxon:7203,Brachycera
+DOID:2987,familial Mediterranean fever,DOID:417,hypersensitivity reaction type II disease
+DOID:1442,Alpers syndrome,DOID:1443,cerebral degeneration
+CL:0002596,smooth muscle cell of the carotid artery,CL:0000359,vascular associated smooth muscle cell
+UBERON:0002514,intramembranous bone,UBERON:0001474,bone element
+DOID:1875,impotence,DOID:1876,sexual dysfunction
+DOID:5127,bizarre leiomyoma,DOID:127,leiomyoma
+DOID:1059,intellectual disability,DOID:0060038,specific developmental disorder
+HP:0010370,Abnormality of the proximal phalanx of the 3rd toe,HP:0010330,Abnormality of the phalanges of the 3rd toe
+CL:1001585,appendix glandular cell,CL:1001588,colon glandular cell
+DOID:5875,retroperitoneal cancer,DOID:0050686,organ system cancer
+DOID:12899,benign lymphoepithelial lesion of salivary gland,DOID:10854,salivary gland disease
+HP:0010253,Pseudoepiphyses of the distal phalanges of the hand,HP:0010243,Abnormality of the epiphyses of the distal phalanx of finger
+HP:0004821,Hypersegmentation of neutrophil nuclei,HP:0011992,Abnormality of neutrophil morphology
+HP:0100700,Abnormality of the arachnoid mater,HP:0010651,Abnormality of the meninges
+NCBITaxon:10911,Coltivirus,NCBITaxon:689831,Spinareovirinae
+DOID:2660,cystic teratoma,DOID:3307,teratoma
+HP:0007383,Congenital localized absence of skin,HP:0008065,Aplasia/Hypoplasia of the skin
+UBERON:0004117,pharyngeal pouch,UBERON:0005291,embryonic tissue
+UBERON:0006638,remnant of urachus,UBERON:0006590,vestigial embryonic structure
+UBERON:0009843,prostate epithelial cord,UBERON:0005154,epithelial cord
+UBERON:3000658,prechoanal process,UBERON:4100000,skeletal element projection
+HP:0002439,Frontolimbic dementia,HP:0000726,Dementia
+UBERON:2001604,lateral ethmoid palatine process,UBERON:0004120,mesoderm-derived structure
+UBERON:0014697,posterior choroidal artery,UBERON:0003496,head blood vessel
+HP:0006172,"Flattened, squared-off epiphyses of tubular bones",HP:0003071,Flattened epiphyses
+DOID:2615,papilloma,DOID:0060084,cell type benign neoplasm
+HP:0010822,Scintillating scotoma,HP:0000575,Scotoma
+DOID:6659,cervical large cell neuroendocrine carcinoma,DOID:2893,cervix carcinoma
+UBERON:3000381,paranasal commissure,UBERON:0003406,cartilage of respiratory system
+HP:0003872,Exostoses (humeral),HP:0003063,Abnormality of the humerus
+UBERON:0005096,descending thin limb,UBERON:0000064,organ part
+DOID:8020,glomangiomyoma,DOID:5238,benign perivascular tumor
+HP:0009563,Distal/middle symphalangism of 2nd finger,HP:0009574,Symphalangism of middle phalanx of 2nd finger
+UBERON:2005374,dorsal fin distal radial bone 3,UBERON:2105374,dorsal fin distal radial element 3
+UBERON:3000295,median symphysis,UBERON:0004121,ectoderm-derived structure
+DOID:992,Omsk hemorrhagic fever,DOID:934,viral infectious disease
+DOID:2048,autoimmune hepatitis,DOID:0060031,autoimmune disease of gastrointestinal tract
+UBERON:0004016,dermatome,UBERON:0005291,embryonic tissue
+UBERON:0001782,pigmented layer of retina,UBERON:0001781,layer of retina
+UBERON:0004448,distal epiphysis of phalanx,UBERON:0004446,epiphysis of phalanx
+UBERON:0001474,bone element,UBERON:0004765,skeletal element
+UBERON:0009007,superficial inguinal lymph node,UBERON:0001542,inguinal lymph node
+DOID:10816,duodenum adenocarcinoma,DOID:10021,duodenum cancer
+UBERON:0010361,synostosis,UBERON:0011134,nonsynovial joint
+DOID:10648,acute inferoposterior infarction,DOID:9408,acute myocardial infarction
+DOID:2382,kernicterus,DOID:936,brain disease
+UBERON:0011362,cranial blood vasculature,UBERON:0002200,vasculature of head
+UBERON:0004949,submucosa of main bronchus,UBERON:0001957,submucosa of bronchus
+CL:0000649,prickle cell,CL:0000312,keratinocyte
+UBERON:2001892,interhyal element,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009878,Cerebellar ataxia associated with quadrupedal gait,HP:0001251,Ataxia
+UBERON:0011277,nail of manual digit 5,UBERON:0009565,nail of manual digit
+UBERON:0007316,deep external pudendal artery,UBERON:0013137,external pudendal artery
+UBERON:0008338,plantar part of pes,UBERON:0005445,segment of pes
+HP:0100257,Ectrodactyly,HP:0002813,Abnormality of limb bone morphology
+UBERON:0011784,feather shaft,UBERON:0004121,ectoderm-derived structure
+UBERON:0008906,lateral line nerve,UBERON:0004121,ectoderm-derived structure
+UBERON:0011131,intermetacarpal joint,UBERON:0001489,manus joint
+UBERON:0007654,maturing nephron,UBERON:0010532,primitive nephron
+DOID:824,periodontitis,DOID:3388,periodontal disease
+HP:0007592,Aplasia/Hypoplastia of the eccrine sweat glands,HP:0011135,Aplasia/Hypoplasia of the sweat glands
+DOID:13865,facial neuralgia,DOID:1756,facial nerve disease
+DOID:7843,female breast carcinoma,DOID:3459,breast carcinoma
+HP:0003587,Insidious onset,HP:0011008,Speed of onset
+UBERON:0000989,penis,UBERON:0008811,intromittent organ
+HP:0009330,Stippling of the epiphysis of the middle phalanx of the 3rd finger,HP:0010266,Stippling of the epiphyses of the middle phalanges of the hand
+DOID:5851,posterolateral myocardial infarction,DOID:5844,myocardial infarction
+UBERON:0003891,stroma,UBERON:0002384,connective tissue
+UBERON:0001867,cartilage of external ear,UBERON:0001996,elastic cartilage tissue
+UBERON:0006669,alveolar canal,UBERON:0004121,ectoderm-derived structure
+HP:0009254,Fragmentation of the epiphysis of the distal phalanx of the 4th finger,HP:0009249,Abnormality of the epiphysis of the distal phalanx of the 4th finger
+UBERON:0001581,depressor labii inferioris,UBERON:0001577,facial nerve muscle
+HP:0100523,Liver abscess,HP:0002722,Recurrent abscess formation
+HP:0009778,Short thumb,HP:0009381,Short finger
+UBERON:0000389,lens cortex,UBERON:0001851,cortex
+HP:0000946,Hypoplastic ilia,HP:0002867,Abnormality of the ilium
+UBERON:0002893,nucleus of lateral olfactory tract,UBERON:0009663,telencephalic nucleus
+HP:0010616,Lung fibroma,HP:0100526,Neoplasm of the lungs
+DOID:7697,pancreatic ACTH hormone producing tumor,DOID:1799,islet cell tumor
+DOID:6929,retinal edema,DOID:5679,retinal disease
+UBERON:0002594,dentatothalamic tract,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0012466,extraembryonic cavities,UBERON:0000464,anatomical space
+UBERON:0014642,vestibulocerebellum,UBERON:0002946,regional part of cerebellum
+UBERON:0011136,ligament of vertebral column,UBERON:0004120,mesoderm-derived structure
+HP:0002747,Respiratory insufficiency due to muscle weakness,HP:0004347,Weakness of muscles of respiration
+UBERON:0004740,basibranchial bone,UBERON:0013746,basibranchial element
+UBERON:0012293,anal fold,UBERON:0000481,multi-tissue structure
+UBERON:0015510,body of corpus callosum,UBERON:0002791,regional part of telencephalon
+UBERON:0003005,dorsal longitudinal fasciculus of midbrain,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001683,jugal bone,UBERON:0008907,dermal bone
+HP:0010320,Abnormality of the 3rd toe,HP:0001780,Abnormality of toe
+UBERON:0002038,substantia nigra,UBERON:0015212,lateral structure
+HP:0010061,Curved phalanges of the hallux,HP:0010176,Curved phalanges of the toes
+CL:0000504,enterochromaffin-like cell,CL:0002274,histamine secreting cell
+UBERON:3010790,muscle rectus abdominis superficialis,UBERON:0002461,anterior abdominal wall muscle
+HP:0100489,Proximal/middle symphalangism of 2nd toe,HP:0010401,Symphalangism affecting the proximal phalanx of the 2nd toe
+UBERON:0006973,protonephridium,UBERON:0006972,nephridium
+UBERON:0000305,amnion,UBERON:0005631,extraembryonic membrane
+UBERON:2000978,somite 22,UBERON:0002329,somite
+CL:0000153,GAG secreting cell,CL:0000327,extracellular matrix secreting cell
+HP:0012149,Bilineage myelodysplasia,HP:0002863,Myelodysplasia
+DOID:5641,diffuse pulmonary fibrosis,DOID:3770,pulmonary fibrosis
+DOID:5591,eccrine papillary adenocarcinoma,DOID:4920,eccrine adenocarcinoma
+HP:0011573,Hypoplastic tricuspid valve,HP:0001702,Abnormality of the tricuspid valve
+HP:0007206,Hemimegalencephaly,HP:0001355,Megalencephaly
+HP:0003637,Reduced 4-Hydroxyphenylpyruvate dioxygenase activity,HP:0010996,Abnormality of monocarboxylic acid metabolism
+UBERON:0003303,roof plate of medulla oblongata,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0011379,Dilated vestibule of the inner ear,HP:0011376,Morphological abnormality of the vestibule of the inner ear
+UBERON:0012398,large intestine smooth muscle circular layer,UBERON:0012368,circular muscle layer
+UBERON:0004290,dermomyotome,UBERON:0005291,embryonic tissue
+UBERON:0004360,cauda epididymis,UBERON:0014403,male anatomical structure
+DOID:9835,refractive error,DOID:5614,eye disease
+UBERON:0008804,stylopharyngeus muscle,UBERON:0013765,digestive system organ
+UBERON:3000680,manubrium of hyale,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0007608,Abnormal palmar dermal ridges,HP:0001018,Abnormal palmar dermatoglyphics
+NCBITaxon:51290,Chlamydiae/Verrucomicrobia group,NCBITaxon:2,Bacteria
+HP:0200063,Colorectal polyps,HP:0200008,Intestinal polyposis
+DOID:4347,lymphocele,DOID:75,lymphatic system disease
+HP:0000193,Bifid uvula,HP:0000172,Abnormality of the uvula
+UBERON:0002042,lymphatic vessel endothelium,UBERON:0004852,cardiovascular system endothelium
+CL:1000505,kidney pelvis cell,CL:1000601,ureteral cell
+UBERON:0007440,stratum intermedium of tooth,UBERON:0000119,cell layer
+DOID:3117,hepatobiliary benign neoplasm,DOID:0050624,gastrointestinal system benign neoplasm
+UBERON:0007773,scrotal sweat gland,UBERON:0005399,male reproductive gland
+CL:0000883,thymic cortical macrophage,CL:0000866,thymic macrophage
+UBERON:0013236,ventral trunk,UBERON:0009569,subdivision of trunk
+HP:0010405,Broad middle phalanx of the 2nd toe,HP:0010348,Broad phalanges of the 2nd toe
+HP:0009817,Aplasia involving bones of the lower limbs,HP:0006493,Aplasia/Hypoplasia involving bones of the lower limbs
+HP:0008229,Thyroid lymphangiectasia,HP:0100763,Abnormality of the lymphatic system
+DOID:5503,spinal cord ependymoma,DOID:3185,spinal cord glioma
+HP:0001922,Vacuolated lymphocytes,HP:0004332,Abnormality of lymphocytes
+HP:0009447,Aplasia/Hypoplasia of the phalanges of the 3rd finger,HP:0009316,Abnormality of the phalanges of the 3rd finger
+CL:0000841,mature conventional dendritic cell,CL:0000766,myeloid leukocyte
+UBERON:4200087,iliac peduncle,UBERON:0004120,mesoderm-derived structure
+HP:0010266,Stippling of the epiphyses of the middle phalanges of the hand,HP:0010244,Abnormality of the epiphyses of the middle phalanges of the hand
+HP:0003953,Absent ossification/absent forearm bones,HP:0002973,Abnormality of the forearm
+DOID:7631,adult ependymoblastoma,DOID:4794,ependymoblastoma
+UBERON:0010869,calcar,UBERON:0002418,cartilage tissue
+UBERON:0009743,visceral yolk sac cavity,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:903,gastrointestinal lymphoma,DOID:3119,gastrointestinal system cancer
+DOID:3819,toxicodendron dermatitis,DOID:3042,allergic contact dermatitis
+UBERON:0005287,tela choroidea of fourth ventricle,UBERON:0005283,tela choroidea
+HP:0007346,Subcortical white matter calcifications,HP:0002500,Abnormality of the cerebral white matter
+UBERON:3000931,intercalary element of hind digit,UBERON:0004248,pedal digit bone
+CL:1001577,tonsil squamous cell,CL:0000076,squamous epithelial cell
+HP:0011423,Hyperchloremia,HP:0011422,Abnormality of chloride homeostasis
+UBERON:0011620,basihyal lingual process,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:10131,psychologic vaginismus,DOID:121,vaginal disease
+HP:0009702,Carpal synostosis,HP:0001191,Abnormality of the carpal bones
+HP:0001052,Nevus flammeus,HP:0003764,Nevus
+DOID:14555,Foster-Kennedy syndrome,DOID:146,papilledema
+HP:0011487,Increased corneal thickness,HP:0011486,Abnormality of corneal thickness
+CL:0005007,Kolmer-Agduhr neuron,CL:0011005,GABAergic interneuron
+HP:0009455,Symphalangism affecting the proximal phalanx of the 3rd finger,HP:0009857,Symphalangism affecting the proximal phalanges of the hand
+HP:0001802,Absent toenail,HP:0001798,Anonychia
+HP:0011785,Thyrotoxicosis with toxic multinodular goitre,HP:0000836,Hyperthyroidism
+HP:0012004,Mnemonic auras,HP:0012002,Experiential auras
+UBERON:3000667,pars reuniens,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003567,abdomen connective tissue,UBERON:0003838,abdominal segment connective tissue
+UBERON:0014619,cervical spinal cord lateral horn,UBERON:0004676,spinal cord lateral horn
+DOID:2648,sebaceous adenoma,DOID:5759,sebaceous gland neoplasm
+DOID:672,spleen cancer,DOID:0060073,lymphatic system cancer
+NCBITaxon:41827,Culicoidea,NCBITaxon:43786,Culicimorpha
+UBERON:0008596,mentalis,UBERON:0004121,ectoderm-derived structure
+HP:0000430,Underdeveloped nasal alae,HP:0000429,Abnormality of the nasal alae
+UBERON:0009994,secondary chorionic villus,UBERON:0007106,chorionic villus
+UBERON:0010955,trapezius pre-muscle mass,UBERON:0005865,pre-muscle condensation
+HP:0004337,Abnormality of amino acid metabolism,HP:0004354,Abnormality of carboxylic acid metabolism
+HP:0007811,Horizontal pendular nystagmus,HP:0006934,Congenital nystagmus
+UBERON:0004735,archenteron,UBERON:0002050,embryonic structure
+HP:0001340,Enhancement of the C-reflex,HP:0007377,Abnormality of somatosensory evoked potentials
+HP:0000964,Eczema,HP:0011123,Inflammatory abnormality of the skin
+HP:0008554,Cochlear malformation,HP:0000375,Abnormality of cochlea
+UBERON:0015458,mediastinal fat pad,UBERON:0003837,thoracic segment connective tissue
+UBERON:0005299,prepuce of clitoris,UBERON:0014404,female anatomical structure
+UBERON:0002849,sixth thoracic dorsal root ganglion,UBERON:0002835,thoracic dorsal root ganglion
+HP:0003113,Hypochloremia,HP:0011422,Abnormality of chloride homeostasis
+HP:0000597,Ophthalmoparesis,HP:0000496,Abnormality of eye movement
+HP:0008050,Abnormality of the palpebral fissures,HP:0000492,Abnormality of the eyelid
+UBERON:0005977,ansiform lobule crus II,UBERON:0005348,ansiform lobule
+DOID:5828,endometrioid ovary carcinoma,DOID:3713,ovary adenocarcinoma
+DOID:2597,glottis neoplasm,DOID:2598,laryngeal benign neoplasm
+UBERON:0005016,mucosa of intermediate urethra,UBERON:0012299,mucosa of urethra
+HP:0009687,Bracket epiphyses of the thumb,HP:0009599,Abnormality of the epiphyses of the thumb
+UBERON:0006565,female urethral meatus,UBERON:0012240,urethral meatus
+UBERON:0009663,telencephalic nucleus,UBERON:0002308,nucleus of brain
+HP:0008743,Coronal hypospadias,HP:0000047,Hypospadias
+HP:0009912,Abnormality of the tragus,HP:0000377,Abnormality of the pinna
+UBERON:0002478,orbitosphenoid,UBERON:0003462,facial bone
+UBERON:0010551,pedal digit 5 metatarsal pre-cartilage condensation,UBERON:0010687,pedal digit metatarsal pre-cartilage condensation
+DOID:0050879,fragile X-associated tremor/ataxia syndrome,DOID:1289,neurodegenerative disease
+HP:0003635,Loss of subcutaneous adipose tissue in limbs,HP:0008887,Adipose tissue loss
+UBERON:0000420,myoepithelium,UBERON:0000488,atypical epithelium
+UBERON:0002419,skin gland,UBERON:0003297,gland of integumental system
+UBERON:2002021,ascending process of the parasphenoid,UBERON:0004530,bony projection
+UBERON:0000305,amnion,UBERON:0004120,mesoderm-derived structure
+DOID:1554,vibratory urticaria,DOID:0060220,physical urticaria
+UBERON:0003928,digestive system duct,UBERON:0000058,duct
+CL:0000249,hatching gland cell,CL:0000151,secretory cell
+DOID:3324,mood disorder,DOID:1561,cognitive disorder
+UBERON:0015139,infundibulum of gallbladder,UBERON:0004119,endoderm-derived structure
+UBERON:0003605,eye skin gland,UBERON:0002419,skin gland
+HP:0100395,Short proximal phalanx of the 3rd toe,HP:0100375,Aplasia/Hypoplasia of the proximal phalanx of the 3rd toe
+HP:0006504,Anomaly of the limb diaphyses,HP:0000940,Abnormal diaphysis morphology
+UBERON:0008862,stomach smooth muscle inner oblique layer,UBERON:0002385,muscle tissue
+HP:0002360,Sleep disturbance,HP:0000708,Behavioural/Psychiatric Abnormality
+HP:0003900,Small humeral epiphyses,HP:0003891,Abnormality of the humeral epiphysis
+UBERON:3000512,processus zygomatico-maxillaris,UBERON:4100000,skeletal element projection
+UBERON:3000746,urostyle ridge,UBERON:0000064,organ part
+HP:0010912,Abnormality of isoleucine metabolism,HP:0010892,Abnormality of branched chain family amino acid metabolism
+UBERON:0012456,Merkel nerve ending,UBERON:0012449,mechanoreceptor
+UBERON:2002115,uroneural 3,UBERON:2000602,uroneural
+HP:0100426,Broad middle phalanx of the 4th toe,HP:0010372,Broad phalanges of the 4th toe
+UBERON:0004753,scapulocoracoid,UBERON:0004765,skeletal element
+HP:0012575,Abnormality of the nephron,HP:0012210,Abnormal renal morphology
+UBERON:0003217,neural lobe of neurohypophysis,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3000898,trochanteric crest,UBERON:0004120,mesoderm-derived structure
+HP:0009809,Abnormality of upper limb metaphysis,HP:0002817,Abnormality of the upper limb
+DOID:5743,acinic cell breast carcinoma,DOID:3458,breast adenocarcinoma
+UBERON:0002175,intermediolateral nucleus,UBERON:0000064,organ part
+DOID:7732,childhood malignant schwannoma,DOID:5940,malignant peripheral nerve sheath tumor
+HP:0005238,Discrete intestinal polyps,HP:0005266,Intestinal polyp
+HP:0012615,Cylindruria,HP:0012614,Abnormal urine cytology
+UBERON:4200021,astragalus-calcaneum unit,UBERON:0000477,anatomical cluster
+UBERON:2001776,pelvic fin lepidotrichium 1,UBERON:4000173,pelvic fin lepidotrichium
+UBERON:2202029,pectoral fin proximal radial cartilage 4,UBERON:2201587,pectoral fin proximal radial cartilage
+UBERON:0002228,rib,UBERON:0002495,long bone
+DOID:1098,fetal erythroblastosis,DOID:11252,microcytic anemia
+UBERON:0001284,renal column,UBERON:0000064,organ part
+CL:0000307,tracheal epithelial cell,CL:0002202,epithelial cell of tracheobronchial tree
+CL:1000236,posterior lateral line nerve glial cell,CL:1000050,lateral line nerve glial cell
+CL:0000878,central nervous system macrophage,CL:0000864,tissue-resident macrophage
+DOID:5561,gastric teratoma,DOID:0050624,gastrointestinal system benign neoplasm
+UBERON:0010286,midbrain neural tube,UBERON:0005291,embryonic tissue
+HP:0100152,Ivory epiphysis of the middle phalanx of the 3rd toe,HP:0100092,Abnormality of the epiphysis of the middle phalanx of the 3rd toe
+UBERON:0010882,limb bone pre-cartilage condensation,UBERON:0009749,limb mesenchyme
+UBERON:0015020,otic capsule endochondral element,UBERON:0010363,endochondral element
+HP:0012213,Decreased glomerular filtration rate,HP:0012212,Abnormal glomerular filtration rate
+UBERON:0011634,ectopterygoid bone,UBERON:0012071,palate bone
+HP:0001956,Truncal obesity,HP:0001513,Obesity
+UBERON:0011202,urachus epithelium,UBERON:0006555,excretory tube
+UBERON:0010251,anterior meningeal artery,UBERON:0003496,head blood vessel
+UBERON:0010937,salpingopharyngeus muscle,UBERON:0004119,endoderm-derived structure
+CL:0002304,non-pigmented ciliary epithelial cell,CL:0000067,ciliated epithelial cell
+HP:0008163,Decreased circulating cortisol level,HP:0011731,Abnormality of circulating cortisol level
+HP:0010487,Small hypothenar eminence,HP:0010486,Abnormality of the hypothenar eminence
+DOID:1796,pancreas sarcoma,DOID:1793,pancreatic cancer
+HP:0010131,Fragmentation of the epiphysis of the proximal phalanx of the hallux,HP:0010126,Abnormality of the epiphysis of the proximal phalanx of the hallux
+HP:0100785,Insomnia,HP:0002360,Sleep disturbance
+UBERON:0010422,primary nodular lymphoid tissue,UBERON:0000444,lymphoid follicle
+HP:0001613,Hoarse voice (caused by tumor impingement),HP:0001609,Hoarse voice
+HP:0001605,Vocal cord paralysis,HP:0001604,Vocal cord paresis
+UBERON:0006163,dorsal digital artery,UBERON:0004552,digital artery
+UBERON:0006300,supracardinal vein,UBERON:0002050,embryonic structure
+HP:0003335,Low gonadotropins (secondary hypogonadism),HP:0003117,Abnormality of circulating hormone level
+DOID:12716,newborn respiratory distress syndrome,DOID:11162,respiratory failure
+CL:1000426,chromaffin cell of adrenal gland,CL:0000150,glandular epithelial cell
+UBERON:0004910,epithelium of male gonad,UBERON:0014403,male anatomical structure
+HP:0010999,Aplasia of the optic tract,HP:0011000,Aplasia/Hypoplasia of the optic tract
+HP:0009267,Ivory epiphysis of the proximal phalanx of the 4th finger,HP:0009399,Ivory epiphyses of the 4th finger
+HP:0008800,Limited hip movement,HP:0002644,Abnormality of pelvic girdle bone morphology
+DOID:9499,disseminated eosinophilic collagen disease,DOID:999,eosinophilia
+NCBITaxon:12637,Dengue virus,NCBITaxon:11052,Dengue virus group
+UBERON:0000091,bilaminar disc,UBERON:0002050,embryonic structure
+UBERON:0000068,embryo stage,UBERON:0000105,life cycle stage
+UBERON:2000147,presumptive epidermis,UBERON:0006598,presumptive structure
+UBERON:0010289,scleral cartilage,UBERON:0003932,cartilage element of chondrocranium
+UBERON:1000011,labial commissure,UBERON:0004121,ectoderm-derived structure
+DOID:6067,ovarian mucinous neoplasm,DOID:2152,ovary epithelial cancer
+DOID:5859,periosteal chondrosarcoma,DOID:3371,chondrosarcoma
+UBERON:0003578,pedal digit connective tissue,UBERON:0003595,pes connective tissue
+UBERON:0005661,3rd arch ectoderm,UBERON:0000924,ectoderm
+UBERON:0006606,mandibular symphysis,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:0050713,fatal infantile encephalocardiomyopathy,DOID:700,mitochondrial metabolism disease
+UBERON:0000365,urothelium,UBERON:0006554,urinary system structure
+UBERON:2001972,intercostal ligament,UBERON:0008846,skeletal ligament
+CL:0005019,pancreatic epsilon cell,CL:0005018,ghrelin secreting cell
+UBERON:3010076,M. iliacus internus,UBERON:0010890,pelvic complex muscle
+UBERON:0010129,femur cartilage element,UBERON:0005254,upper leg mesenchyme
+UBERON:0005897,manus bone,UBERON:0011250,autopod bone
+UBERON:0003542,right lung respiratory bronchiole,UBERON:0002188,respiratory bronchiole
+CL:0000833,eosinophilic promyelocyte,CL:0000836,promyelocyte
+HP:0011845,Short second metatarsal,HP:0010743,Short metatarsal
+UBERON:4200081,hypocleideum,UBERON:0005913,zone of bone organ
+UBERON:0001115,left lobe of liver,UBERON:0001113,lobe of liver
+HP:0009316,Abnormality of the phalanges of the 3rd finger,HP:0004150,Abnormality of the 3rd finger
+HP:0009026,Hypoplasia of latissimus dorsi muscle,HP:0009131,Abnormality of the musculature of the thorax
+UBERON:0005483,thymus lobe,UBERON:0000064,organ part
+UBERON:0006059,falx cerebri,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:7381,lymphohistiocytoid mesothelioma,DOID:7474,malignant pleural mesothelioma
+HP:0010404,Aplasia/Hypoplasia of the middle phalanx of the 2nd toe,HP:0010325,Aplasia/Hypoplasia of the 2nd toe
+DOID:4515,thyroid sarcoma,DOID:1781,thyroid cancer
+HP:0000929,Abnormality of the skull,HP:0009121,Abnormal axial skeleton morphology
+DOID:4260,gait apraxia,DOID:0060135,apraxia
+UBERON:0001667,tibialis posterior,UBERON:0008230,tibialis
+HP:0009334,Abnormality of the epiphysis of the middle phalanx of the 3rd finger,HP:0010244,Abnormality of the epiphyses of the middle phalanges of the hand
+UBERON:0001461,elbow,UBERON:0008785,upper limb segment
+DOID:12556,acute kidney tubular necrosis,DOID:3021,acute kidney failure
+DOID:7512,localized Intraductal papillomatosis,DOID:2615,papilloma
+UBERON:0002470,autopod region,UBERON:0002529,limb segment
+HP:0100711,Abnormality of the thoracic spine,HP:0000765,Abnormality of the thorax
+HP:0002859,Rhabdomyosarcoma,HP:0009728,Neoplasm of striated muscle
+DOID:3122,gastric outlet obstruction,DOID:76,stomach disease
+DOID:4783,mesangial proliferative glomerulonephritis,DOID:2921,glomerulonephritis
+CL:1001567,lung endothelial cell,CL:0000082,epithelial cell of lung
+UBERON:0004602,rib 2,UBERON:0002228,rib
+DOID:4698,nerve root neoplasm,DOID:1192,peripheral nervous system neoplasm
+UBERON:2000040,median fin fold,UBERON:0003102,surface structure
+UBERON:0008828,presphenoid bone,UBERON:0003462,facial bone
+HP:0001662,Bradycardia,HP:0011675,Arrhythmia
+UBERON:0006657,glenoid fossa,UBERON:0004704,bone fossa
+CL:0001005,mature CD8_alpha-positive CD11b-negative dendritic cell,CL:0000841,mature conventional dendritic cell
+HP:0000769,Abnormality of the breast,HP:0000118,Phenotypic abnormality
+UBERON:0004470,musculature of pelvic girdle,UBERON:0014792,musculature of pelvic complex
+CL:0008002,skeletal muscle fiber,CL:0000188,skeletal muscle cell
+DOID:4277,penis basal cell carcinoma,DOID:3449,penis carcinoma
+UBERON:0004658,mandible head,UBERON:0004120,mesoderm-derived structure
+HP:0100618,Leydig cell neoplasia,HP:0010789,Abnormality of the Leydig cells
+CL:0000037,hematopoietic stem cell,CL:0008001,hematopoietic precursor cell
+UBERON:0000410,bronchial mucosa,UBERON:0000379,tracheal mucosa
+UBERON:0002390,hematopoietic system,UBERON:0004120,mesoderm-derived structure
+HP:0100761,Visceral angiomatosis,HP:0007461,Hemangiomatosis
+DOID:3038,submucosal invasive colon adenocarcinoma,DOID:234,colon adenocarcinoma
+UBERON:0005184,hair medulla,UBERON:0004121,ectoderm-derived structure
+HP:0008383,Slow-growing nails,HP:0001597,Abnormality of the nail
+HP:0001218,Autoamputation,HP:0002813,Abnormality of limb bone morphology
+UBERON:0007317,superficial external pudendal artery,UBERON:0004573,systemic artery
+HP:0009329,Small epiphysis of the middle phalanx of the 3rd finger,HP:0009334,Abnormality of the epiphysis of the middle phalanx of the 3rd finger
+UBERON:0006319,spinal cord reticular nucleus,UBERON:0002315,gray matter of spinal cord
+UBERON:3010589,cloacal papilla,UBERON:0000479,tissue
+HP:0009253,Enlarged epiphysis of the distal phalanx of the 4th finger,HP:0009249,Abnormality of the epiphysis of the distal phalanx of the 4th finger
+DOID:2490,congenital nervous system abnormality,DOID:0080015,physical disorder
+HP:0009313,Patchy sclerosis of the proximal phalanx of the 4th finger,HP:0009406,Patchy sclerosis of the phalanges of the 4th finger
+UBERON:4200087,iliac peduncle,UBERON:4100000,skeletal element projection
+HP:0005145,Coronary artery stenosis,HP:0001677,Coronary artery disease
+DOID:11258,cat-scratch disease,DOID:0050338,primary bacterial infectious disease
+UBERON:0009097,gravid organism,UBERON:0007023,adult organism
+UBERON:0001824,mucosa of larynx,UBERON:0004119,endoderm-derived structure
+UBERON:0006137,proper palmar digital artery,UBERON:0006141,palmar digital artery
+HP:0010760,Absent toe,HP:0001991,Aplasia/Hypoplasia of toe
+HP:0009282,Abnormality of the distal phalanx of the 4th finger,HP:0009172,Abnormality of the phalanges of the 4th finger
+DOID:7612,childhood intracortical osteosarcoma,DOID:3361,pediatric osteosarcoma
+HP:0000496,Abnormality of eye movement,HP:0012373,Abnormal eye physiology
+UBERON:0005443,filum terminale,UBERON:0004121,ectoderm-derived structure
+CL:0000233,platelet,CL:0000225,anucleate cell
+UBERON:0002883,central amygdaloid nucleus,UBERON:0002619,regional part of cerebral cortex
+UBERON:0011613,hypohyal element,UBERON:0010522,replacement element
+HP:0005021,Bilateral elbow dislocations,HP:0003042,Elbow dislocation
+UBERON:0007156,inferior thyroid vein,UBERON:0001638,vein
+HP:0009123,Mixed hypo- and hyperpigmentation of the skin,HP:0000953,Hyperpigmentation of the skin
+CL:1000433,epithelial cell of lacrimal canaliculus,CL:0000068,duct epithelial cell
+UBERON:0005806,portal system,UBERON:0002049,vasculature
+DOID:0050833,orotic aciduria,DOID:0050832,pyrimidine metabolic disorder
+HP:0011209,EEG with generalized slow activity grade 4,HP:0010845,EEG with generalized slow activity
+UBERON:0013753,distal epiphysis of metacarpal bone,UBERON:0004390,epiphysis of metacarpal bone
+DOID:7326,cranial pseudosarcomatous fasciitis,DOID:7327,pseudosarcomatous fibromatosis
+DOID:7851,pancreatic intraductal papillary-mucinous adenoma,DOID:7575,pancreatic intraductal papillary-mucinous neoplasm
+UBERON:0004941,submucosa of right hepatic duct,UBERON:0004938,submucosa of biliary tree
+UBERON:0003907,left atrioventricular canal,UBERON:0002087,atrioventricular canal
+DOID:732,urethral disease,DOID:18,urinary system disease
+UBERON:3000264,lamina superior,UBERON:0000064,organ part
+HP:0008615,Adult onset sensorineural hearing impairment,HP:0000407,Sensorineural hearing impairment
+DOID:3574,lateral sinus thrombosis,DOID:3572,intracranial sinus thrombosis
+HP:0007193,Generalized tonic-clonic seizures on awakening,HP:0002069,Generalized tonic-clonic seizures
+DOID:7460,spindle cell variant squamous cell breast carcinoma,DOID:5514,breast squamous cell carcinoma
+DOID:5612,spinal cancer,DOID:3620,central nervous system cancer
+UBERON:0001441,hindlimb skeleton,UBERON:0004381,skeleton of limb
+HP:0000387,Absent earlobe,HP:0009906,Aplasia/Hypoplasia of the earlobes
+UBERON:0010561,pedal digit 5 metatarsal cartilage element,UBERON:0010684,pedal digit 5 phalanx cartilage element
+UBERON:3010146,lacrimal,UBERON:0006813,nasal skeleton
+HP:0010580,Enlarged epiphyses,HP:0005930,Abnormality of the epiphyses
+DOID:3525,middle cerebral artery infarction,DOID:3527,cerebral arterial disease
+UBERON:0008269,nacre,UBERON:0000463,portion of organism substance
+HP:0000576,Centrocecal scotoma,HP:0000575,Scotoma
+DOID:0050780,Opitz-GBBB syndrome,DOID:0050177,monogenic disease
+NCBITaxon:1386,Bacillus <bacterium>,NCBITaxon:186817,Bacillaceae
+CL:0002419,mature T cell,CL:0000084,T cell
+UBERON:0003652,metatarsal bone of digit 3,UBERON:0015039,pedal digit 3 metatarsal endochondral element
+CL:0001029,common dendritic progenitor,CL:0001019,CD115-positive monocyte OR common dendritic progenitor
+UBERON:0008285,rumen epithelium,UBERON:0010040,stomach non-glandular epithelium
+HP:0012689,Abnormal pineal melatonin secretion,HP:0012688,Abnormality of pineal physiology
+UBERON:0004382,epiphysis of humerus,UBERON:0004120,mesoderm-derived structure
+HP:0010940,Aplasia/Hypoplasia of the nasal bone,HP:0010939,Abnormality of the nasal bone
+HP:0003771,Pulp stones,HP:0006479,Abnormality of the dental pulp
+DOID:0080027,spondyloepimetaphyseal dysplasia,DOID:2256,osteochondrodysplasia
+DOID:10784,Queensland tick typhus,DOID:11104,spotted fever
+HP:0005932,Abnormal renal corticomedullary differentiation,HP:0100957,Abnormality of the renal medulla
+HP:0008336,Complex organic aciduria,HP:0003355,Aminoaciduria
+UBERON:0010151,duct of bulbourethral gland,UBERON:0005904,duct of male reproductive system
+UBERON:0013716,branch of ilio-marsupialis muscle,UBERON:0000064,organ part
+UBERON:0013676,aproctal bone of priapium,UBERON:0003457,head bone
+HP:0008802,Hypoplasia of the femoral head,HP:0009108,Aplasia/Hypoplasia involving the femoral head and neck
+UBERON:4200039,supraacetabular buttress,UBERON:4100000,skeletal element projection
+UBERON:0011012,flexor pollicis brevis muscle,UBERON:0001500,muscle of manus
+UBERON:0006913,lip epithelium,UBERON:0003929,gut epithelium
+HP:0004901,Exercise-induced lactic acidemia,HP:0003128,Lactic acidosis
+UBERON:0001548,lateral marginal vein,UBERON:0001638,vein
+UBERON:0006841,central vein of liver,UBERON:0015796,liver blood vessel
+UBERON:0000066,fully formed stage,UBERON:0000092,post-embryonic stage
+DOID:0060195,amyotrophic lateral sclerosis type 3,DOID:332,amyotrophic lateral sclerosis
+UBERON:2001515,taenia marginalis posterior,UBERON:0003932,cartilage element of chondrocranium
+DOID:7192,hereditary conventional renal cell carcinoma,DOID:4455,hereditary renal cell carcinoma
+DOID:10138,xerophthalmia,DOID:10139,conjunctival degeneration
+HP:0011750,Neoplasm of the anterior pituitary,HP:0011747,Abnormality of the anterior pituitary
+HP:0008420,Punctate vertebral calcifications,HP:0003468,Abnormality of the vertebrae
+UBERON:0015117,lamina terminalis of cerebral hemisphere,UBERON:0014532,lamina of cerebral hemisphere
+DOID:1138,spinal meningioma,DOID:1140,spinal canal and spinal cord meningioma
+CL:0002013,GlyA-positive basophillic erythroblast,CL:0000549,basophilic erythroblast
+HP:0001986,Hypertonic dehydration,HP:0001944,Dehydration
+HP:0009307,Patchy sclerosis of the middle phalanx of the 4th finger,HP:0009283,Abnormality of the middle phalanx of the 4th finger
+HP:0009155,Cone-shaped epiphysis of the proximal phalanx of the 5th finger,HP:0010270,Cone-shaped epiphyses of the proximal phalanges of the hand
+DOID:299,adenocarcinoma,DOID:305,carcinoma
+UBERON:0001857,anterior semicircular duct,UBERON:0001856,semicircular duct
+UBERON:0011264,femoral pore,UBERON:0000161,orifice
+UBERON:2001782,pelvic fin lepidotrichium 7,UBERON:4000173,pelvic fin lepidotrichium
+UBERON:2000674,interopercle,UBERON:0008907,dermal bone
+DOID:1512,chronic gonorrhea of cervix,DOID:1513,chronic cervicitis
+HP:0007898,Exudative retinopathy,HP:0001147,Retinal exudate
+HP:0011727,Peroneal muscle weakness,HP:0009053,Distal lower limb muscle weakness
+UBERON:2001720,caudal principal ray 8,UBERON:2001585,caudal principal ray
+UBERON:0000119,cell layer,UBERON:0000479,tissue
+HP:0006224,Tapering pointed ends of distal finger phalanges,HP:0009884,Tapered distal phalanges of finger
+UBERON:0004396,epiphysis of second metatarsal bone,UBERON:0004389,epiphysis of metatarsal bone
+DOID:1713,benign shuddering attacks,DOID:481,central nervous system hereditary degenerative disease
+UBERON:0000175,pleural effusion,UBERON:0001087,pleural fluid
+UBERON:0002221,fontanelle,UBERON:0000477,anatomical cluster
+UBERON:0010187,female urethral gland,UBERON:0001338,urethral gland
+HP:0003359,Decreased urinary sulfate,HP:0012612,Abnormal urinary sulfate concentration
+DOID:9111,cutaneous leishmaniasis,DOID:9065,leishmaniasis
+UBERON:4300090,X bone,UBERON:0001076,neural spine
+UBERON:0002429,cervical lymph node,UBERON:0000029,lymph node
+UBERON:0003112,olfactory region,UBERON:0000477,anatomical cluster
+HP:0004964,Pulmonary arterial medial hypertrophy,HP:0004414,Abnormality of the pulmonary artery
+DOID:10907,microcephaly,DOID:2490,congenital nervous system abnormality
+UBERON:0011178,principal nucleus of stria terminalis,UBERON:0009663,telencephalic nucleus
+UBERON:0006239,future central tendon,UBERON:0005423,developing anatomical structure
+HP:0003729,Enteroviral dermatomyositis syndrome,HP:0002743,Recurrent enteroviral infections
+CL:0000737,striated muscle cell,CL:0000187,muscle cell
+UBERON:3000767,pelvic girdle opening,UBERON:0007832,pelvic girdle skeleton
+UBERON:0005292,extraembryonic tissue,UBERON:0000478,extraembryonic structure
+DOID:8692,myeloid leukemia,DOID:1240,leukemia
+UBERON:0001850,lacrimal duct,UBERON:0004121,ectoderm-derived structure
+HP:0001204,Distal symphalangism (hands),HP:0100263,Distal symphalangism
+NCBITaxon:186537,Marburgvirus,NCBITaxon:11266,Filoviridae
+HP:0003658,Hypomethioninemia,HP:0003112,Abnormality of serum amino acid levels
+HP:0001087,Congenital glaucoma,HP:0000501,Glaucoma
+HP:0100558,Hemiatrophy of upper limb,HP:0002817,Abnormality of the upper limb
+UBERON:0015142,falciform fat,UBERON:0005291,embryonic tissue
+NCBITaxon:12092,Hepatitis A virus,NCBITaxon:12091,Hepatovirus
+NCBITaxon:444,Legionellaceae,NCBITaxon:118969,Legionellales
+DOID:8689,anorexia nervosa,DOID:8670,eating disorder
+DOID:14199,posterior dislocation of lens,DOID:1242,globe disease
+UBERON:0012925,bronchial bud,UBERON:0005911,endo-epithelium
+UBERON:0004549,right eye,UBERON:0000970,eye
+HP:0012195,Irregular respiration,HP:0002793,Abnormal pattern of respiration
+HP:0011014,Abnormal glucose homeostasis,HP:0011013,Abnormality of carbohydrate metabolism/homeostasis
+HP:0011788,Increased serum free triiodothyronine (fT3),HP:0002926,Abnormality of thyroid physiology
+UBERON:0005390,cortical layer I,UBERON:0002301,layer of neocortex
+HP:0001468,Aplasia/Hypoplasia involving the musculature of the upper arm,HP:0001457,Abnormality of the musculature of the upper arm
+UBERON:0002160,nucleus prepositus,UBERON:0007635,nucleus of medulla oblongata
+DOID:8659,chickenpox,DOID:934,viral infectious disease
+HP:0004431,Complement deficiency,HP:0005339,Abnormality of complement system
+UBERON:2001183,dermal superficial region,UBERON:0004121,ectoderm-derived structure
+DOID:6500,cerebellar angioblastoma,DOID:4205,cerebellum cancer
+NCBITaxon:6267,Anisakidae,NCBITaxon:33256,Ascaridoidea
+UBERON:0009850,nematode larva,UBERON:0002548,larva
+UBERON:2000936,dorsal fin distal radial bone,UBERON:2001672,dorsal fin radial bone
+UBERON:0001867,cartilage of external ear,UBERON:0003566,head connective tissue
+UBERON:0001751,dentine,UBERON:0001973,substance of tooth
+HP:0100901,Sclerosis of the distal phalanx of the 3rd finger,HP:0100919,Sclerosis of the phalanges of the 3rd finger
+UBERON:2001651,pharyngobranchial 2 tooth,UBERON:0004756,dermal skeletal element
+CL:1000480,transitional myocyte of internodal tract,CL:0002096,internodal tract myocyte
+CL:0000287,eye photoreceptor cell,CL:0000210,photoreceptor cell
+DOID:4154,dentinogenesis imperfecta,DOID:1091,tooth disease
+HP:0011261,Darwin tubercle of helix,HP:0011039,Abnormality of the helix
+UBERON:0015717,smooth muscle tissue layer of ejaculatory duct,UBERON:0005156,reproductive structure
+UBERON:0010852,fibula pre-cartilage condensation,UBERON:0010886,hindlimb bone pre-cartilage condensation
+HP:0100114,Enlarged epiphysis of the middle phalanx of the 2nd toe,HP:0100047,Enlarged epiphyses of the 2nd toe
+UBERON:0005435,cisterna chyli,UBERON:0004120,mesoderm-derived structure
+UBERON:0013486,crypt of Lieberkuhn of appendix,UBERON:0013485,crypt of Lieberkuhn of colon
+UBERON:0003911,choroid plexus epithelium,UBERON:0005357,brain ependyma
+HP:0001388,Joint laxity,HP:0001382,Joint hypermobility
+HP:0100528,Pleuropulmonary blastoma,HP:0100552,Neoplasm of the tracheobronchial system
+UBERON:0006857,interrenal primordium,UBERON:0002050,embryonic structure
+UBERON:3010032,M. semitendinosus,UBERON:0010890,pelvic complex muscle
+DOID:1459,hypothyroidism,DOID:50,thyroid gland disease
+UBERON:2007035,spinal cord neural rod,UBERON:0005291,embryonic tissue
+CL:0002571,hepatic mesenchymal stem cell,CL:0000134,mesenchymal cell
+UBERON:0002939,ventral posteroinferior nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0009555,short pastern bone,UBERON:0009558,pastern bone
+HP:0009305,Distal/middle symphalangism of 4th finger,HP:0004197,Symphalangism of the 4th finger
+HP:0004490,Calvarial hyperostosis,HP:0004437,Cranial hyperostosis
+UBERON:2001833,premaxillary tooth row,UBERON:0009678,tooth row
+UBERON:0014772,lateral palpebral artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+NCBITaxon:33340,Neoptera,NCBITaxon:7496,Pterygota <winged insects>
+UBERON:0009863,ascidian ciliated funnel,UBERON:0000064,organ part
+UBERON:0003306,floor plate of neural tube,UBERON:0002050,embryonic structure
+UBERON:3000998,suprarostral cartilage,UBERON:0007844,cartilage element
+UBERON:2002223,pillar of the semicircular canal,UBERON:0004121,ectoderm-derived structure
+HP:0012698,Cerebellar gliosis,HP:0002171,Gliosis
+UBERON:0003657,limb joint,UBERON:0000982,skeletal joint
+DOID:3501,ampullary signet ring cell adenocarcinoma,DOID:3502,ampulla of Vater adenocarcinoma
+UBERON:3000374,palatine process of pars palatina of premaxilla,UBERON:0004120,mesoderm-derived structure
+UBERON:0004479,musculature of trunk,UBERON:0001015,musculature
+DOID:14269,suppurative cholangitis,DOID:9446,cholangitis
+HP:0100291,Abnormality of central somatosensory evoked potentials,HP:0007377,Abnormality of somatosensory evoked potentials
+DOID:11968,postmenopausal atrophic vaginitis,DOID:2170,vaginitis
+UBERON:0005710,lower jaw incisor epithelium,UBERON:0003236,epithelium of lower jaw
+UBERON:0007380,dermal scale,UBERON:0004121,ectoderm-derived structure
+HP:0001162,Postaxial hand polydactyly,HP:0001161,Hand polydactyly
+UBERON:0010700,phalanx pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+UBERON:0005077,neuropore,UBERON:0004121,ectoderm-derived structure
+UBERON:0004682,corona radiata,UBERON:0011299,white matter of telencephalon
+UBERON:0006806,entepicondyle of humerus,UBERON:0005055,zone of long bone
+DOID:3688,plexopathy,DOID:1289,neurodegenerative disease
+DOID:4422,malignant adenofibroma,DOID:4236,carcinosarcoma
+HP:0011160,Gustatory auras,HP:0011157,Auras
+UBERON:3000830,margo vertebralis,UBERON:0004121,ectoderm-derived structure
+CL:0002224,lens epithelial cell,CL:0002222,vertebrate lens cell
+HP:0100073,Pseudoepiphyses of the 4th toe,HP:0010169,Pseudoepiphyses of the toes
+UBERON:0009776,intermediate reticular formation,UBERON:0007245,nuclear complex of neuraxis
+HP:0001216,Delayed ossification of carpal bones,HP:0006257,Abnormality of carpal bone ossification
+HP:0003268,Argininuria,HP:0010909,Abnormality of arginine metabolism
+HP:0003260,Hydroxyprolinemia,HP:0010907,Abnormality of proline metabolism
+HP:0010016,Bracket epiphysis of the 1st metacarpal,HP:0200050,Bracket metacarpal epiphyses
+HP:0009505,Enlarged epiphysis of the distal phalanx of the 2nd finger,HP:0009491,Enlarged epiphyses of the 2nd finger
+UBERON:0000209,tetrapod frontal bone,UBERON:0002514,intramembranous bone
+HP:0009458,Aplasia of the proximal phalanx of the 3rd finger,HP:0009457,Aplasia/Hypoplasia of the proximal phalanx of the 3rd finger
+UBERON:0015002,radius-ulna endochondral element,UBERON:0015021,forelimb endochondral element
+NCBITaxon:85025,Nocardiaceae,NCBITaxon:85007,Corynebacterineae
+UBERON:0003005,dorsal longitudinal fasciculus of midbrain,UBERON:0003045,dorsal longitudinal fasciculus
+DOID:1627,intraductal papilloma,DOID:2615,papilloma
+HP:0001942,Metabolic acidosis,HP:0001941,Acidosis
+UBERON:0012286,hemisphere of embryo,UBERON:0002050,embryonic structure
+UBERON:0004486,musculature of perineum,UBERON:0004479,musculature of trunk
+DOID:0050711,aceruloplasminemia,DOID:2351,iron metabolism disease
+HP:0010891,Morbus Scheuermann,HP:0003468,Abnormality of the vertebrae
+UBERON:0009483,mesentery of foregut-midgut junction,UBERON:0002095,mesentery
+UBERON:0010270,filum terminale externum,UBERON:0000479,tissue
+UBERON:0005136,metanephric glomerular endothelium,UBERON:0004189,glomerular endothelium
+UBERON:0005581,rhombomere 5 roof plate,UBERON:0005502,rhombomere roof plate
+DOID:4555,ovarian large-cell neuroendocrine carcinoma,DOID:4001,ovarian carcinoma
+DOID:591,phobic disorder,DOID:2030,anxiety disorder
+UBERON:0015479,scrotum skin,UBERON:0005156,reproductive structure
+HP:0010141,Enlarged epiphysis of the distal phalanx of the hallux,HP:0010116,Enlarged epiphyses of the hallux
+UBERON:2000384,levator arcus palatini,UBERON:0011648,jaw muscle
+HP:0100466,Patchy sclerosis of the proximal phalanx of the 5th toe,HP:0100934,Sclerosis of the proximal phalanx of the 5th toe
+DOID:6484,mediastinal melanocytic neurilemmoma,DOID:3205,melanotic neurilemmoma
+DOID:706,mature B-cell neoplasm,DOID:707,B-cell lymphoma
+HP:0100809,Hypersensibility of scalp,HP:0001965,Abnormality of the scalp
+HP:0010960,Bronchopulmonary sequestration,HP:0002088,Abnormality of the lung
+UBERON:2001681,cornu mesial process,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010175,Bullet-shaped phalanges of the toes,HP:0010161,Abnormality of the phalanges of the toes
+HP:0000463,Anteverted nares,HP:0000429,Abnormality of the nasal alae
+DOID:8478,actinomycosis,DOID:0050339,commensal bacterial infectious disease
+UBERON:0007413,nucleus of pontine reticular formation,UBERON:0006331,brainstem nucleus
+UBERON:0008940,parietal ganglion,UBERON:0000045,ganglion
+UBERON:0002106,spleen,UBERON:0013765,digestive system organ
+HP:0012468,Chronic acidosis,HP:0001941,Acidosis
+UBERON:0002767,inferior rostral sulcus,UBERON:0003022,cerebral cortex lobe
+HP:0009351,Irregular epiphysis of the proximal phalanx of the 3rd finger,HP:0009333,Abnormality of the epiphysis of the proximal phalanx of the 3rd finger
+HP:0010246,Absent epiphyses of the distal phalanges of the hand,HP:0010228,Absent epiphyses of the phalanges of the hand
+HP:0010151,Cone-shaped epiphysis of the 1st metatarsal,HP:0010054,Abnormality of the first metatarsal
+HP:0000158,Macroglossia,HP:0003712,Muscle hypertrophy
+HP:0010397,Bullet-shaped proximal phalanx of the 2nd toe,HP:0010349,Bullet-shaped phalanges of the 2nd toe
+DOID:0050749,peripheral T-cell lymphoma,DOID:0050743,mature T-cell and NK-cell lymphoma
+UBERON:0001489,manus joint,UBERON:0003839,forelimb joint
+DOID:3360,multifocal osteogenic sarcoma,DOID:3347,osteosarcoma
+UBERON:2201416,pelvic fin distal radial cartilage 3,UBERON:1700006,paired fin radial cartilage
+UBERON:0006287,radius-ulna pre-cartilage condensation,UBERON:0010884,forelimb bone pre-cartilage condensation
+HP:0010105,Short first metatarsal,HP:0010743,Short metatarsal
+CL:0002383,conidium of conidiophore head,CL:0002381,uninucleate conidium
+UBERON:0002655,body of lateral ventricle,UBERON:0002285,telencephalic ventricle
+UBERON:0015160,supraorbital artery,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009792,Teratoma,HP:0100728,Germ cell neoplasia
+HP:0007905,Abnormal iris vasculature,HP:0000525,Abnormality of the iris
+HP:0001710,Conotruncal defect,HP:0002564,Malformation of the heart and great vessels
+HP:0011176,EEG with constitutional variants,HP:0002353,EEG abnormality
+DOID:5040,malignant granular cell esophageal tumor,DOID:5041,esophageal cancer
+UBERON:0005891,coelomic epithelium,UBERON:0005291,embryonic tissue
+DOID:14006,splenic artery aneurysm,DOID:0050828,artery disease
+UBERON:4200002,coracoid plate,UBERON:0005913,zone of bone organ
+DOID:11678,onchocerciasis,DOID:37,skin disease
+HP:0010957,Congenital posterior urethral valve,HP:0010481,Urethral valve
+UBERON:0007417,peduncle of neuraxis,UBERON:0002316,white matter
+UBERON:0012130,olecranon fossa,UBERON:0005055,zone of long bone
+DOID:2988,antiphospholipid syndrome,DOID:417,hypersensitivity reaction type II disease
+HP:0010269,Bracket epiphyses of the proximal phalanges of the hand,HP:0010245,Abnormality of the epiphyses of the proximal phalanges of the hand
+HP:0004244,Accessory scaphoid,HP:0004232,Accessory carpal bones
+UBERON:0001997,olfactory epithelium,UBERON:0006934,sensory epithelium
+UBERON:0002513,endochondral bone,UBERON:0001474,bone element
+CL:0000415,diploid cell,CL:0000003,native cell
+HP:0005556,Abnormality of the metopic suture,HP:0011329,Abnormality of cranial sutures
+UBERON:0003130,arthropod sternum,UBERON:0000061,anatomical structure
+CL:0000769,basophilic metamyelocyte,CL:0002192,metamyelocyte
+HP:0100759,Clubbing of fingers,HP:0001211,Abnormality of the fingertips
+HP:0100961,Enlarged hippocampus,HP:0002538,Abnormality of the cerebral cortex
+UBERON:0001897,dorsal plus ventral thalamus,UBERON:0015212,lateral structure
+HP:0002225,Sparse pubic hair,HP:0008070,Sparse hair
+HP:0010252,Ivory epiphyses of the distal phalanges of the hand,HP:0010243,Abnormality of the epiphyses of the distal phalanx of finger
+CL:0001014,CD1a-positive Langerhans cell,CL:0000453,Langerhans cell
+DOID:2079,eccrine mixed tumor of skin,DOID:173,eccrine sweat gland neoplasm
+UBERON:0008230,tibialis,UBERON:0000366,flexor muscle
+UBERON:3010781,pars convoluta,UBERON:0000064,organ part
+UBERON:0003512,lung blood vessel,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0001617,mental artery,UBERON:0000078,mixed ectoderm/mesoderm/endoderm-derived structure
+UBERON:0004134,proximal tubule,UBERON:0006853,renal cortex tubule
+UBERON:4100009,pedal digit 7 phalanx,UBERON:0001449,phalanx of pes
+UBERON:0011947,ureter luminal urothelium,UBERON:0011945,luminal layer of epithelium
+UBERON:0005495,midbrain lateral wall,UBERON:0005496,neural tube lateral wall
+DOID:10183,endobronchial lipoma,DOID:3906,bronchial neoplasm
+UBERON:0009006,deep inguinal lymph node,UBERON:0001542,inguinal lymph node
+UBERON:0005734,tunica adventitia of blood vessel,UBERON:0004797,blood vessel layer
+DOID:461,muscle benign neoplasm,DOID:0060099,musculoskeletal system benign neoplasm
+UBERON:0001495,pectoral muscle,UBERON:0004120,mesoderm-derived structure
+HP:0009267,Ivory epiphysis of the proximal phalanx of the 4th finger,HP:0009248,Abnormality of the epiphysis of the proximal phalanx of the 4th finger
+UBERON:0000491,solid compound organ,UBERON:0003103,compound organ
+UBERON:0005195,deferent duct vein,UBERON:0001638,vein
+UBERON:3010828,commissura terminales of hyoid apparatus,UBERON:0011004,pharyngeal arch cartilage
+DOID:12361,Graves' disease,DOID:0060005,autoimmune disease of endocrine system
+DOID:5590,aggressive digital papillary adenocarcinoma,DOID:3451,skin carcinoma
+HP:0000145,Transverse vaginal septum,HP:0001153,Septate vagina
+UBERON:0010020,tubotympanic recess epithelium,UBERON:0005911,endo-epithelium
+UBERON:0002991,supramammillary commissure,UBERON:0011590,commissure of diencephalon
+UBERON:2002185,climbing fiber,UBERON:0000479,tissue
+UBERON:2001223,basibranchial 1 bone,UBERON:2001915,basibranchial 1 element
+DOID:1649,female breast lower-inner quadrant cancer,DOID:0050671,female breast cancer
+UBERON:0002381,pectoralis major,UBERON:0001495,pectoral muscle
+UBERON:0013636,epithelium of intestinal villus,UBERON:0001902,epithelium of small intestine
+UBERON:2005031,dorsal longitudinal vein,UBERON:0003499,brain blood vessel
+UBERON:2001801,quadrate-hyomandibula joint,UBERON:0000982,skeletal joint
+NCBITaxon:5014,Dothideales,NCBITaxon:451867,Dothideomycetidae
+UBERON:0011785,ramus of feather barb,UBERON:0004121,ectoderm-derived structure
+UBERON:0002237,true rib,UBERON:0002228,rib
+HP:0000023,Inguinal hernia,HP:0004299,Hernia of the abdominal wall
+UBERON:0008198,nail plate,UBERON:0004121,ectoderm-derived structure
+UBERON:0006091,inferior horn of the lateral ventricle,UBERON:0000064,organ part
+HP:0010087,Bullet-shaped proximal phalanx of the hallux,HP:0010060,Bullet-shaped phalanges of the hallux
+DOID:3011,breast granular cell tumor,DOID:1612,breast cancer
+HP:0004362,Abnormality of the enteric ganglia,HP:0002242,Abnormality of the intestine
+CL:0002370,respiratory goblet cell,CL:0000160,goblet cell
+UBERON:0010513,strand of zigzag hair,UBERON:0010509,strand of pelage hair
+UBERON:0016374,sciatic lymph node,UBERON:0016398,lymph node of lower limb
+UBERON:0002060,femoral artery,UBERON:0001637,artery
+DOID:14121,blue toe syndrome,DOID:1461,cholesterol embolism
+UBERON:4000160,anocleithrum,UBERON:0008907,dermal bone
+DOID:13372,alpha 1-antitrypsin deficiency,DOID:2345,plasma protein metabolism disease
+UBERON:0012299,mucosa of urethra,UBERON:0000344,mucosa
+UBERON:0003610,heart elastic tissue,UBERON:0003837,thoracic segment connective tissue
+UBERON:0008271,turtle shell,UBERON:0006612,shell
+DOID:5850,inferior myocardial infarction,DOID:5844,myocardial infarction
+HP:0008114,Metatarsal diaphyseal endosteal sclerosis,HP:0100925,Sclerosis of bones of the feet
+UBERON:2001521,ceratobranchial 5 cartilage,UBERON:2001903,ceratobranchial 5 element
+UBERON:0003833,abdominal segment muscle,UBERON:0005173,abdominal segment organ
+HP:0100167,Triangular epiphysis of the proximal phalanx of the 3rd toe,HP:0100065,Triangular epiphyses of the 3rd toe
+UBERON:0010014,epigonal organ,UBERON:0005057,immune organ
+DOID:5982,kidney fibrosarcoma,DOID:4242,kidney sarcoma
+UBERON:0011606,hyomandibular bone,UBERON:0011608,hyomandibular element
+UBERON:2001893,hypobranchial element,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:7427,anthrax disease,DOID:37,skin disease
+UBERON:0004194,long nephron,UBERON:0001285,nephron
+UBERON:0002806,left occipital lobe,UBERON:0002021,occipital lobe
+UBERON:0004127,compact layer of ventricle,UBERON:0004125,myocardial compact layer
+HP:0100237,Proximal symphalangism (feet),HP:0010179,Symphalangism affecting the phalanges of the toes
+HP:0000468,Increased adipose tissue around the neck,HP:0009124,Abnormality of adipose tissue
+UBERON:0010007,placenta fetal blood space,UBERON:0002553,anatomical cavity
+UBERON:0004374,vitelline vasculature,UBERON:0002049,vasculature
+UBERON:0007809,fascia of Camper,UBERON:0014455,subcutaneous abdominal adipose tissue
+UBERON:0005933,hair root sheath,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:12667,binocular vision disease,DOID:540,strabismus
+UBERON:4000120,mineralized avascular GAG-rich matrix,UBERON:4000059,avascular GAG-rich matrix
+UBERON:0007376,outer epithelium,UBERON:0003102,surface structure
+HP:0007045,Midline brain calcifications,HP:0002514,Cerebral calcification
+UBERON:0005853,sacral spinal cord ventral column,UBERON:0002318,white matter of spinal cord
+HP:0009920,Nevus of Ota,HP:0001034,Hypermelanotic macule
+UBERON:0001701,glossopharyngeal ganglion,UBERON:0009127,epibranchial ganglion
+HP:0009439,Short middle phalanx of the 3rd finger,HP:0009461,Short 3rd finger
+UBERON:0006974,metanephridium,UBERON:0006972,nephridium
+HP:0005572,Decreased renal tubular phosphate excretion,HP:0011036,Abnormality of renal excretion
+HP:0100560,Upper limb asymmetry,HP:0100555,Asymmetric growth
+DOID:5602,T-cell adult acute lymphocytic leukemia,DOID:5604,adult acute lymphocytic leukemia
+UBERON:0001048,primordium,UBERON:0005423,developing anatomical structure
+UBERON:0001231,nephron tubule,UBERON:0009773,renal tubule
+DOID:8503,impetigo herpetiformis,DOID:8505,dermatitis herpetiformis
+HP:0012148,Multiple lineage myelodysplasia,HP:0002863,Myelodysplasia
+UBERON:0014618,middle frontal sulcus,UBERON:0003022,cerebral cortex lobe
+HP:0003906,Broad humeral epiphyseal plate,HP:0003846,Wide epiphyseal plates of the upper limbs
+UBERON:0000460,major vestibular gland,UBERON:0003297,gland of integumental system
+CL:1001576,oral mucosa squamous cell,CL:0000076,squamous epithelial cell
+DOID:9521,Laron syndrome,DOID:0050737,autosomal recessive disease
+HP:0011378,Hypoplasia of the vestibule of the inner ear,HP:0011376,Morphological abnormality of the vestibule of the inner ear
+UBERON:0006330,anterior lingual gland,UBERON:0003409,gland of tongue
+HP:0003440,Horizontal sacrum,HP:0005107,Abnormality of the sacrum
+UBERON:0010069,outer epithelial layer of tympanic membrane,UBERON:0010371,ecto-epithelium
+UBERON:2001692,median premaxilla,UBERON:0008907,dermal bone
+HP:0009501,Abnormality of the epiphysis of the proximal phalanx of the 2nd finger,HP:0009544,Abnormality of the proximal phalanx of the 2nd finger
+CL:0000908,"CD8-positive, alpha-beta cytokine secreting effector T cell",CL:0000625,"CD8-positive, alpha-beta T cell"
+CL:0002527,immature CD14-positive dermal dendritic cell,CL:0002526,CD14-positive dermal dendritic cell
+HP:0012464,Decreased transferrin saturation,HP:0011031,Abnormality of iron homeostasis
+HP:0001049,Absent dorsal skin creases over affected joints,HP:0006143,Abnormal finger flexion creases
+HP:0001180,Oligodactyly (hands),HP:0012165,Oligodactyly
+UBERON:0010732,alisphenoid pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+HP:0003910,Enlarged humeral metaphyses,HP:0003051,Enlarged metaphyses
+NCBITaxon:6231,Nematoda,NCBITaxon:1206794,Ecdysozoa
+UBERON:0015097,distal carpal bone 5 cartilage,UBERON:0010883,forelimb cartilage element
+DOID:13198,endemic goiter,DOID:12176,goiter
+DOID:2024,placental choriocarcinoma,DOID:2025,gestational choriocarcinoma
+CL:0002169,basal cell of olfactory epithelium,CL:0002167,olfactory epithelial cell
+UBERON:0013113,angular/surangular bone,UBERON:0008907,dermal bone
+NCBITaxon:10245,Vaccinia virus,NCBITaxon:10242,Orthopoxvirus
+UBERON:0001456,face,UBERON:0001444,subdivision of head
+HP:0001075,Atrophic scars,HP:0000987,Atypical scarring of skin
+UBERON:3000660,margo choanalis,UBERON:0000064,organ part
+HP:0005788,Abnormal cervical myelogram,HP:0002318,Cervical myelopathy
+HP:0012739,Agenesis of the small intestine,HP:0002244,Abnormality of the small intestine
+UBERON:0003083,trunk neural crest,UBERON:0004121,ectoderm-derived structure
+UBERON:3010006,dorsal skin texture,UBERON:3000977,body external integument structure
+UBERON:0005298,skin of clitoris,UBERON:0014404,female anatomical structure
+UBERON:4200088,iliac peduncle of the pubis,UBERON:0004120,mesoderm-derived structure
+HP:0010265,Small epiphyses of the middle phalanges of the hand,HP:0010244,Abnormality of the epiphyses of the middle phalanges of the hand
+UBERON:0002015,kidney capsule,UBERON:0003567,abdomen connective tissue
+UBERON:3000922,prehallux skeleton,UBERON:0010712,limb skeleton subdivision
+UBERON:0003505,trachea blood vessel,UBERON:0003504,respiratory system blood vessel
+HP:0010546,Muscle fibrillation,HP:0100022,Abnormality of movement
+UBERON:2001931,infranuchal scute,UBERON:2002294,fish scute
+HP:0006236,Slender metacarpals,HP:0005916,Abnormal metacarpal morphology
+UBERON:2001200,corpuscles of Stannius,UBERON:0006554,urinary system structure
+HP:0002392,EEG with polyspike wave complexes,HP:0010850,EEG with spike-wave complexes
+HP:0008178,Abnormal cartilage matrix,HP:0002763,Abnormal cartilage morphology
+UBERON:0005217,midbrain subarachnoid space,UBERON:0000315,subarachnoid space
+DOID:4024,scirrhous adenocarcinoma,DOID:299,adenocarcinoma
+UBERON:0007255,intervertebral disk of lumbar vertebra,UBERON:0001066,intervertebral disk
+HP:0009777,Absent thumb,HP:0009380,Aplasia of the fingers
+UBERON:0010886,hindlimb bone pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+CL:0000995,"CD34-positive, CD38-positive common myeloid progenitor OR CD34-positive, CD38-positive common lymphoid progenitor",CL:0001060,"hematopoietic oligopotent progenitor cell, lineage-negative"
+HP:0011786,Thyrotoxicosis with toxic single thyroid nodule,HP:0000836,Hyperthyroidism
+DOID:0060130,akinetopsia,DOID:4090,agnosia
+HP:0012003,Affective auras,HP:0012002,Experiential auras
+HP:0004934,Vascular calcification,HP:0011915,Cardiovascular calcification
+NCBITaxon:41828,Chironomoidea,NCBITaxon:43786,Culicimorpha
+DOID:3504,prostate signet ring cell adenocarcinoma,DOID:2526,prostate adenocarcinoma
+HP:0011699,Atrial reentry tachycardia,HP:0001692,Primary atrial arrhythmia
+HP:0009818,Amelia involving the lower limbs,HP:0006493,Aplasia/Hypoplasia involving bones of the lower limbs
+UBERON:0006589,round ligament of uterus,UBERON:0008845,nonskeletal ligament
+DOID:13690,acute gonococcal cystitis,DOID:13148,acute cystitis
+UBERON:0014782,allantois of embryonic urinary system,UBERON:0006554,urinary system structure
+UBERON:0006223,dorsal meso-oesophagus,UBERON:0004120,mesoderm-derived structure
+HP:0007064,Progressive language deterioration,HP:0002344,Progressive neurologic deterioration
+HP:0011944,Small vessel vasculitis,HP:0002633,Vasculitis
+UBERON:0003296,gland of diencephalon,UBERON:0004121,ectoderm-derived structure
+HP:0009688,Cone-shaped epiphyses of the thumb,HP:0009599,Abnormality of the epiphyses of the thumb
+UBERON:0006607,medial umbilical ligament,UBERON:0006591,transformed artery
+UBERON:0005288,tela choroidea of third ventricle,UBERON:0005283,tela choroidea
+UBERON:0006378,vibrissa hair,UBERON:0001037,strand of hair
+UBERON:0013560,Brodmann (1909) area 32,UBERON:0013529,Brodmann area
+HP:0011660,Anomalous origin of one pulmonary artery from ascending aorta,HP:0004414,Abnormality of the pulmonary artery
+HP:0100378,Absent distal phalanx of the 3rd toe,HP:0010645,Aplasia of the distal phalanges of the toes
+HP:0007985,Retinal arteriolar occlusion,HP:0100545,Arterial stenosis
+UBERON:0010550,pedal digit 4 metatarsal pre-cartilage condensation,UBERON:0010687,pedal digit metatarsal pre-cartilage condensation
+UBERON:0003820,prostate bud,UBERON:0012275,meso-epithelium
+UBERON:2202028,pectoral fin proximal radial cartilage 3,UBERON:2201587,pectoral fin proximal radial cartilage
+DOID:13050,corpus luteum cyst,DOID:5119,ovarian cyst
+UBERON:0006675,venous valve,UBERON:0003978,valve
+CL:0010010,cerebellar stellate cell,CL:0000122,stellate cell
+UBERON:0008813,helicotrema,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000134,mesenchymal cell,CL:0000219,motile cell
+UBERON:0012465,lumen of terminal part of digestive tract,UBERON:0000464,anatomical space
+CL:0000980,plasmablast,CL:0000946,antibody secreting cell
+DOID:13868,hypoactive sexual desire disorder,DOID:10132,psychosexual disorder
+UBERON:0015158,ophthalmotemporal branch of external ophthalmic artery,UBERON:0001622,lacrimal artery
+UBERON:0006867,anal part of perineum,UBERON:0000064,organ part
+DOID:3930,otitis interna,DOID:2952,inner ear disease
+UBERON:0009737,sublaminar layers S1 or S2 or S3 or S4,UBERON:0008921,substratum of layer of retina
+HP:0008205,Insulin-dependent but ketosis-resistant diabetes,HP:0005978,Type II diabetes mellitus
+UBERON:0009576,medulla oblongata sulcus limitans,UBERON:0005478,sulcus limitans of neural tube
+UBERON:0002533,post-anal tail bud,UBERON:0005423,developing anatomical structure
+HP:0001623,Breech presentation,HP:0001787,Abnormal delivery
+UBERON:0010881,limb cartilage element,UBERON:0009749,limb mesenchyme
+HP:0003649,Abnormality of glycoside metabolism,HP:0011013,Abnormality of carbohydrate metabolism/homeostasis
+UBERON:0002478,orbitosphenoid,UBERON:0011164,neurocranium bone
+DOID:3456,cervix erosion,DOID:2253,cervix disease
+HP:0009688,Cone-shaped epiphyses of the thumb,HP:0010230,Cone-shaped epiphyses of the phalanges of the hand
+DOID:10286,prostate carcinoma,DOID:10283,prostate cancer
+HP:0003901,Stippled calcification of the humeral epiphyses,HP:0003891,Abnormality of the humeral epiphysis
+DOID:562,third cranial nerve disease,DOID:5656,cranial nerve disease
+HP:0000161,Median cleft lip,HP:0000204,Cleft upper lip
+UBERON:0000163,embryonic cloaca,UBERON:0000162,cloaca
+DOID:10783,methemoglobinemia,DOID:2860,hemoglobinopathy
+CL:0005026,hepatoblast,CL:0000048,multi fate stem cell
+UBERON:0003416,mesenchyme of tongue,UBERON:0003104,mesenchyme
+HP:0004616,Cleft vertebral arch,HP:0008438,Vertebral arch anomaly
+HP:0007328,Impaired pain sensation,HP:0010832,Abnormality of pain sensation
+UBERON:0002176,lateral cervical nucleus,UBERON:0000064,organ part
+UBERON:0005257,manual digit mesenchyme,UBERON:0004120,mesoderm-derived structure
+UBERON:0012650,gastroduodenal junction,UBERON:0007651,anatomical junction
+UBERON:2001760,dorsal fin lepidotrichium 7,UBERON:4000177,dorsal fin lepidotrichium
+CL:0002657,glandular cell of esophagus,CL:0000150,glandular epithelial cell
+UBERON:0004365,vitelline blood vessel,UBERON:0001981,blood vessel
+UBERON:0001285,nephron,UBERON:0000064,organ part
+DOID:9076,discoid lupus erythematosus of eyelid,DOID:1894,noninfectious dermatoses of eyelid
+HP:0001640,Cardiomegaly,HP:0001627,Abnormality of cardiac morphology
+CL:0000240,stratified squamous epithelial cell,CL:0000076,squamous epithelial cell
+CL:0000711,cumulus cell,CL:0000154,protein secreting cell
+HP:0100557,Hemiatrophy of lower limb,HP:0100559,Lower limb asymmetry
+UBERON:0013475,gustatory gland,UBERON:0000409,serous gland
+UBERON:0004606,rib 6,UBERON:0002228,rib
+HP:0000574,Thick eyebrow,HP:0000534,Abnormality of the eyebrow
+UBERON:0006443,prinicipal vein of limb,UBERON:0001638,vein
+UBERON:0004942,submucosa of left hepatic duct,UBERON:0004938,submucosa of biliary tree
+UBERON:2001582,non-Weberian precaudal vertebra,UBERON:0011677,trunk vertebra
+DOID:3012,Li-Fraumeni syndrome,DOID:0050736,autosomal dominant disease
+UBERON:0009679,set of lower jaw teeth,UBERON:0010313,neural crest-derived structure
+HP:0010386,Curved phalanges of the 5th toe,HP:0010176,Curved phalanges of the toes
+HP:0000457,Flat nose,HP:0005105,Abnormal nasal morphology
+HP:0000199,Tongue nodules,HP:0000157,Abnormality of the tongue
+UBERON:0008974,apocrine gland,UBERON:0002530,gland
+DOID:873,anaerobic pneumonia,DOID:0050152,aspiration pneumonia
+DOID:7461,large cell keratinizing variant squamous cell breast carcinoma,DOID:5514,breast squamous cell carcinoma
+DOID:1795,tumor of exocrine pancreas,DOID:1793,pancreatic cancer
+HP:0008467,Thoracic hemivertebrae,HP:0002937,Hemivertebrae
+UBERON:0003111,sphenoid region,UBERON:0000477,anatomical cluster
+HP:0010719,Abnormality of hair texture,HP:0001595,Abnormality of the hair
+UBERON:0013125,left subcardinal vein,UBERON:0015212,lateral structure
+UBERON:0011660,hypoplastron,UBERON:0015212,lateral structure
+UBERON:0013679,inner canthus of right eye,UBERON:0005611,inner canthus
+HP:0001606,Vocal cord paralysis (caused by tumor impingement),HP:0001604,Vocal cord paresis
+UBERON:0000977,pleura,UBERON:0000042,serous membrane
+UBERON:0003329,submucosa of anal canal,UBERON:0001208,submucosa of large intestine
+HP:0011133,Increased sensitivity to ionizing radiation,HP:0011017,Abnormality of cell physiology
+HP:0006414,Distal tibial bowing,HP:0002982,Tibial bowing
+DOID:6293,central nervous system lipoma,DOID:0060090,central nervous system organ benign neoplasm
+HP:0003207,Arterial calcification,HP:0004934,Vascular calcification
+UBERON:0006954,mammary myoepithelium,UBERON:0000420,myoepithelium
+DOID:9498,pulmonary eosinophilia,DOID:999,eosinophilia
+UBERON:4300117,pelvic fin soft ray,UBERON:4000173,pelvic fin lepidotrichium
+UBERON:0014796,common tendinous ring,UBERON:0000481,multi-tissue structure
+HP:0009285,Curved phalanges of the 4th finger,HP:0009172,Abnormality of the phalanges of the 4th finger
+UBERON:0001241,crypt of Lieberkuhn of small intestine,UBERON:0001983,crypt of Lieberkuhn
+DOID:1364,ethmoidal sinus neoplasm,DOID:1350,paranasal sinus neoplasm
+UBERON:0012332,broad ligament of uterus,UBERON:0004120,mesoderm-derived structure
+UBERON:0005151,metanephric proximal tubule,UBERON:0004134,proximal tubule
+UBERON:1000012,nose anterior margin,UBERON:0004121,ectoderm-derived structure
+UBERON:0014455,subcutaneous abdominal adipose tissue,UBERON:0007808,adipose tissue of abdominal region
+CL:1001111,kidney loop of henle thin descending limb epithelial cell,CL:1001021,kidney loop of henle descending limb epithelial cell
+DOID:200,giant cell tumor,DOID:201,connective tissue cancer
+HP:0011560,Mitral atresia,HP:0001633,Abnormality of the mitral valve
+HP:0002066,Gait ataxia,HP:0001251,Ataxia
+HP:0008240,Secondary growth hormone deficiency,HP:0000824,Growth hormone deficiency
+UBERON:0003059,presomitic mesoderm,UBERON:0005423,developing anatomical structure
+DOID:4782,subacute glomerulonephritis,DOID:2921,glomerulonephritis
+UBERON:2001818,dorsal fin proximal radial bone 1,UBERON:2000947,dorsal fin proximal radial bone
+UBERON:0011004,pharyngeal arch cartilage,UBERON:0003933,cranial cartilage
+NCBITaxon:7496,Pterygota <winged insects>,NCBITaxon:85512,Dicondylia
+HP:0100153,Pseudoepiphysis of the middle phalanx of the 3rd toe,HP:0100092,Abnormality of the epiphysis of the middle phalanx of the 3rd toe
+HP:0009108,Aplasia/Hypoplasia involving the femoral head and neck,HP:0005613,Aplasia/hypoplasia of the femur
+UBERON:0009993,primary chorionic villus,UBERON:0007106,chorionic villus
+HP:0003869,Cortical thinning (humeral),HP:0002753,Thin bony cortex
+DOID:11748,round ligament malignant neoplasm,DOID:1725,peritoneum cancer
+UBERON:0009986,lateral epicondyle of femur,UBERON:0009978,epicondyle
+HP:0004759,Nodular calcific aortic valve disease,HP:0001646,Abnormality of the aortic valve
+UBERON:0004813,seminiferous tubule epithelium,UBERON:0004910,epithelium of male gonad
+DOID:0050266,tungiasis,DOID:37,skin disease
+DOID:7689,leptomeninges sarcoma,DOID:6086,malignant leptomeningeal tumor
+HP:0010262,Irregular epiphyses of the middle phalanges of the hand,HP:0010233,Irregular epiphyses of the phalanges of the hand
+HP:0002919,Ketonuria,HP:0012072,Aciduria
+UBERON:0002492,sagittal suture,UBERON:0003685,cranial suture
+UBERON:0007632,Barrington's nucleus,UBERON:0009662,hindbrain nucleus
+HP:0006623,Costochondral joint sclerosis,HP:0000919,Abnormality of the costochondral junction
+UBERON:3000645,corpus,UBERON:0002513,endochondral bone
+HP:0005622,Broad long bones,HP:0011314,Abnormality of long bone morphology
+UBERON:0002471,zeugopod,UBERON:0002529,limb segment
+HP:0008732,Renal hypophosphatemia,HP:0002148,Hypophosphatemia
+HP:0009373,Type C brachydactyly,HP:0001156,Brachydactyly syndrome
+HP:0100274,Gustatory lacrimation,HP:0000632,Lacrimation abnormality
+HP:0000143,Rectovaginal fistula,HP:0004320,Vaginal fistula
+DOID:2786,cerebellar disease,DOID:936,brain disease
+UBERON:0006958,great vein of heart,UBERON:0015212,lateral structure
+UBERON:0002700,subcuneiform nucleus,UBERON:0007415,nucleus of midbrain reticular formation
+HP:0010621,Cutaneous syndactyly of toes,HP:0001770,Toe syndactyly
+CL:0002315,supporting cell of cochlea,CL:0005014,auditory epithelial support cell
+UBERON:3010067,M. gracilis minor,UBERON:0010890,pelvic complex muscle
+CL:0002512,"CD11b-high, CD103-negative, langerin-negative lymph node dendritic cell",CL:0002454,"Cd4-negative, CD8_alpha-negative, CD11b-positive dendritic cell"
+DOID:3895,apocrine adenoma,DOID:5876,apocrine sweat gland neoplasm
+HP:0010786,Urinary tract neoplasm,HP:0007379,Neoplasm of the genitourinary tract
+UBERON:0009637,alisphenoid ossification center,UBERON:0010355,ossification center
+UBERON:0004659,mandible neck,UBERON:0004120,mesoderm-derived structure
+HP:0100904,Sclerosis of the middle phalanx of the 2nd finger,HP:0100918,Sclerosis of the phalanges of the 2nd finger
+UBERON:0001693,exoccipital bone,UBERON:0015051,exoccipital endochondral element
+UBERON:0005486,venous dural sinus,UBERON:0006615,venous sinus
+HP:0009100,Thick anterior alveolar ridges,HP:0009085,Alveolar ridge overgrowth
+UBERON:0011179,transverse nucleus of stria terminalis,UBERON:0009663,telencephalic nucleus
+HP:0009317,Deviation of the 3rd finger,HP:0004150,Abnormality of the 3rd finger
+UBERON:0001327,coccygeus muscle,UBERON:0015212,lateral structure
+UBERON:2001902,ceratobranchial 4 element,UBERON:2001898,ceratobranchial element
+HP:0000897,Rachitic rosary,HP:0000919,Abnormality of the costochondral junction
+UBERON:2001324,enteric musculature,UBERON:0000383,musculature of body
+UBERON:0001340,dorsal artery of penis,UBERON:0005156,reproductive structure
+UBERON:0004271,outflow tract pericardium,UBERON:0012275,meso-epithelium
+UBERON:4200115,presupracleithrum,UBERON:0007829,pectoral girdle bone
+UBERON:0002085,interatrial septum,UBERON:0002099,cardiac septum
+DOID:2012,Nezelof syndrome,DOID:11200,T cell deficiency
+UBERON:0002684,nucleus raphe obscurus,UBERON:0007635,nucleus of medulla oblongata
+DOID:9080,macroglobulinemia,DOID:2345,plasma protein metabolism disease
+HP:0008335,Renal aminoaciduria,HP:0003355,Aminoaciduria
+UBERON:0011327,deep temporal nerve,UBERON:0002003,peripheral nerve
+UBERON:0001700,geniculate ganglion,UBERON:0009127,epibranchial ganglion
+UBERON:0001622,lacrimal artery,UBERON:0004573,systemic artery
+UBERON:0003908,right atrioventricular canal,UBERON:0002087,atrioventricular canal
+DOID:7646,multiple spinal canal and spinal cord meningioma,DOID:1140,spinal canal and spinal cord meningioma
+UBERON:0004767,vomerine tooth,UBERON:0012070,palatal tooth
+UBERON:0010948,cleidooccipital muscle,UBERON:0000933,pharyngeal muscle
+HP:0004900,Severe lactic acidosis,HP:0003128,Lactic acidosis
+HP:0007565,Multiple cafe-au-lait spots,HP:0000957,Cafe-au-lait spot
+DOID:7435,polyvesicular vitelline pattern testicular yolk sac tumor,DOID:5344,testicular yolk sac tumor
+UBERON:0004196,proximal convoluted tubule segment 1,UBERON:0004120,mesoderm-derived structure
+UBERON:0005607,hyaloid vascular plexus,UBERON:0004120,mesoderm-derived structure
+HP:0004864,Refractory sideroblastic anemia,HP:0001924,Sideroblastic anemia
+HP:0001960,Hypokalemic metabolic alkalosis,HP:0200114,Metabolic alkalosis
+UBERON:0004408,distal epiphysis of ulna,UBERON:0004386,epiphysis of ulna
+DOID:11283,peripheral scars of retina,DOID:11086,chorioretinal scar
+HP:0007716,Intraocular melanoma,HP:0002861,Melanoma
+HP:0009537,Flexion contracture of the 2nd finger,HP:0004100,Abnormality of the 2nd finger
+UBERON:0005291,embryonic tissue,UBERON:0000479,tissue
+UBERON:0014570,CA1 alveus,UBERON:0002619,regional part of cerebral cortex
+HP:0006016,Delayed phalangeal epiphyseal ossification,HP:0002663,Delayed epiphyseal ossification
+DOID:0050773,paraganglioma,DOID:169,neuroendocrine tumor
+HP:0007932,Bilateral congenital mydriasis,HP:0011499,Mydriasis
+HP:0005404,Increase in B cell number,HP:0010975,Abnormality of B cell number
+UBERON:2000492,coracoradialis,UBERON:0014794,pectoral appendage muscle
+DOID:8912,tinea nigra,DOID:0050133,superficial mycosis
+CL:0000513,cardiac muscle myoblast,CL:0002494,cardiocyte
+UBERON:0003107,Meckel's cartilage,UBERON:0011004,pharyngeal arch cartilage
+UBERON:0001094,sacral vertebra,UBERON:0003828,abdominal segment bone
+UBERON:0004383,epiphysis of tibia,UBERON:0004120,mesoderm-derived structure
+UBERON:0003678,tooth apex,UBERON:0000015,anatomical boundary
+UBERON:0008115,surface of cartilage,UBERON:0006984,anatomical surface
+DOID:0080026,otospondylomegaepiphyseal dysplasia,DOID:2256,osteochondrodysplasia
+HP:0000405,Conductive hearing impairment,HP:0000365,Hearing impairment
+DOID:1626,breast duct papilloma,DOID:1628,intraductal papillary breast neoplasm
+HP:0009557,Aplasia/Hypoplasia of the distal phalanx of the 2nd finger,HP:0009542,Abnormality of the distal phalanx of the 2nd finger
+HP:0100358,Contractures of the metatarsophalangeal joint of the 4th toe,HP:0010339,Flexion contracture of the 4th toe
+HP:0100369,Aplasia/Hypoplasia of the distal phalanx of the 3rd toe,HP:0010331,Aplasia/Hypoplasia of the 3rd toe
+UBERON:0003277,skeleton of upper jaw,UBERON:0010912,subdivision of skeleton
+HP:0000842,Hyperinsulinemia,HP:0011014,Abnormal glucose homeostasis
+UBERON:0001122,scalenus medius,UBERON:0002377,muscle of neck
+UBERON:0012240,urethral meatus,UBERON:0010418,urethral opening
+DOID:1664,pineoblastoma,DOID:5032,pineal gland cancer
+UBERON:0001311,inferior vesical artery,UBERON:0003468,ureteric segment of renal artery
+UBERON:0012071,palate bone,UBERON:0003457,head bone
+HP:0009532,Small epiphysis of the proximal phalanx of the 2nd finger,HP:0009496,Small epiphyses of the 2nd finger
+HP:0011374,Incomplete partition of the cochlea type I,HP:0011373,Incomplete partition of the cochlea
+UBERON:0007643,node of ligamentum arteriosum,UBERON:0002524,mediastinal lymph node
+UBERON:0014529,lenticular fasciculus,UBERON:0005838,fasciculus of brain
+DOID:4015,spindle cell carcinoma,DOID:1749,squamous cell carcinoma
+HP:0009432,Curved middle phalanx of the 3rd finger,HP:0009846,Curved middle phalanges of the hand
+HP:0011504,Bull's eye maculopathy,HP:0008002,Abnormality of macular pigmentation
+UBERON:0001858,posterior semicircular duct,UBERON:0001856,semicircular duct
+UBERON:2001781,pelvic fin lepidotrichium 6,UBERON:4000173,pelvic fin lepidotrichium
+UBERON:3010736,ramus posterior of CN VIII,UBERON:0004529,anatomical projection
+UBERON:0001418,skin of thorax,UBERON:0001085,skin of trunk
+UBERON:0001424,ulna,UBERON:0015003,ulna endochondral element
+UBERON:0011157,cuneiform cartilage,UBERON:0001996,elastic cartilage tissue
+UBERON:0004395,epiphysis of first metatarsal bone,UBERON:0004389,epiphysis of metatarsal bone
+UBERON:0003823,hindlimb zeugopod,UBERON:0002471,zeugopod
+UBERON:0005584,rhombomere 6 roof plate,UBERON:0005502,rhombomere roof plate
+HP:0008356,Combined hyperlipidemia,HP:0003077,Hyperlipidemia
+UBERON:0009522,lateral lingual swelling epithelium,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:8036,childhood ovarian embryonal carcinoma,DOID:6084,pediatric ovarian germ cell tumor
+UBERON:0007182,muscle layer of infundibulum of uterine tube,UBERON:0005983,heart layer
+UBERON:0001549,dorsal metatarsal vein,UBERON:0001638,vein
+HP:0000010,Recurrent urinary tract infections,HP:0002719,Recurrent infections
+HP:0006426,Rudimentary to absent tibiae,HP:0005772,Aplasia/Hypoplasia of the tibia
+DOID:1942,intermittent squint,DOID:540,strabismus
+UBERON:0009139,right posterior cardinal vein,UBERON:0002065,posterior cardinal vein
+UBERON:0011242,ethmoid cartilage,UBERON:0003932,cartilage element of chondrocranium
+DOID:366,olfactory nerve neoplasm,DOID:2815,cranial nerve malignant neoplasm
+DOID:10235,Brown's tendon sheath syndrome,DOID:9306,mechanical strabismus
+DOID:9369,orbital plasma cell granuloma,DOID:633,myositis
+HP:0009326,Irregular epiphysis of the middle phalanx of the 3rd finger,HP:0009334,Abnormality of the epiphysis of the middle phalanx of the 3rd finger
+HP:0005825,Mixed sclerosis of humeral metaphyses,HP:0003918,Sclerotic humeral metaphysis
+UBERON:0006238,future brain,UBERON:0005423,developing anatomical structure
+UBERON:3000406,pars interna plectri,UBERON:0010313,neural crest-derived structure
+CL:0002014,"Kit-negative, Ly-76 high basophilic erythroblast",CL:0000549,basophilic erythroblast
+HP:0100612,Odontogenic neoplasm,HP:0000164,Abnormality of the teeth
+UBERON:0007959,falciform carpal bone,UBERON:0001435,carpal bone
+HP:0002643,Neonatal respiratory distress,HP:0002093,Respiratory insufficiency
+UBERON:0002394,bile duct,UBERON:0004119,endoderm-derived structure
+DOID:13087,Lown-Ganong-Levine syndrome,DOID:225,syndrome
+UBERON:0015130,connective tissue of prostate,UBERON:0014403,male anatomical structure
+DOID:1360,frontal sinus cancer,DOID:0050619,paranasal sinus cancer
+UBERON:0006925,digestive gland,UBERON:0002368,endocrine gland
+DOID:3178,skin papilloma,DOID:3165,skin benign neoplasm
+UBERON:0010313,neural crest-derived structure,UBERON:0004121,ectoderm-derived structure
+HP:0012196,Cheyne-Stokes respiration,HP:0002793,Abnormal pattern of respiration
+UBERON:2000712,I-YSL,UBERON:0005291,embryonic tissue
+UBERON:2007034,forebrain neural rod,UBERON:0005291,embryonic tissue
+CL:0002570,mesenchymal stem cell of adipose,CL:0000134,mesenchymal cell
+UBERON:0004104,hairline,UBERON:0000061,anatomical structure
+HP:0000376,Incomplete partition of the cochlea type II,HP:0011373,Incomplete partition of the cochlea
+DOID:12375,bronchopneumonia,DOID:552,pneumonia
+UBERON:0009692,lumen of pharyngotympanic tube,UBERON:0005082,tube lumen
+DOID:4525,mediastinum angiosarcoma,DOID:4050,mediastinum sarcoma
+DOID:5713,mediastinum liposarcoma,DOID:3382,liposarcoma
+UBERON:0003597,manual digit connective tissue,UBERON:0003598,manus connective tissue
+HP:0002215,Sparse axillary hair,HP:0100134,Abnormality of the axillary hair
+HP:0002406,Limb dysmetria,HP:0001310,Dysmetria
+UBERON:0004096,odontoid process of cervical vertebra 2,UBERON:4100000,skeletal element projection
+DOID:6312,clivus chordoma,DOID:4151,skull base chordoma
+HP:0004095,Curved fingers,HP:0001167,Abnormality of finger
+UBERON:2001256,lateral floor plate,UBERON:0004120,mesoderm-derived structure
+DOID:6869,parasagittal meningioma,DOID:6114,cerebral convexity meningioma
+DOID:11177,total internal ophthalmoplegia,DOID:238,pupil disease
+DOID:635,acquired immunodeficiency syndrome,DOID:526,Human immunodeficiency virus infectious disease
+HP:0000615,Abnormality of the pupil,HP:0000525,Abnormality of the iris
+HP:0100464,Patchy sclerosis of the proximal phalanx of the 3rd toe,HP:0010364,Patchy sclerosis of the phalanges of the 3rd toe
+UBERON:4300091,Y bone,UBERON:0001076,neural spine
+UBERON:0007315,internal pudendal artery,UBERON:0015212,lateral structure
+UBERON:0008522,nasal muscle,UBERON:0001577,facial nerve muscle
+NCBITaxon:774,Bartonella bacilliformis,NCBITaxon:773,Bartonella
+UBERON:4100004,ischial peduncle,UBERON:0004120,mesoderm-derived structure
+HP:0003065,Patellar hypoplasia,HP:0006498,Aplasia/Hypoplasia of the patella
+UBERON:0005137,metanephric capsule,UBERON:0002015,kidney capsule
+UBERON:0005422,pelvic appendage apical ectodermal ridge,UBERON:0004356,apical ectodermal ridge
+DOID:10554,meningoencephalitis,DOID:331,central nervous system disease
+UBERON:0002099,cardiac septum,UBERON:0003037,septum
+UBERON:0010954,ceratohyoideus muscle,UBERON:0000933,pharyngeal muscle
+CL:0002483,hair follicle melanocyte,CL:0002559,hair follicle cell
+UBERON:0004893,interalveolar septum,UBERON:0003037,septum
+HP:0008498,No permanent dentition,HP:0000696,Delayed eruption of permanent teeth
+HP:0010475,Cloacal exstrophy,HP:0100548,Exstrophy
+DOID:8427,retinal melanoma,DOID:4645,retinal cancer
+UBERON:0000051,fornix of vagina,UBERON:0002553,anatomical cavity
+UBERON:2001697,transverse radial,UBERON:0002513,endochondral bone
+DOID:0050859,hemorrhagic cystitis,DOID:1679,cystitis
+UBERON:0001350,coccyx,UBERON:0006076,caudal region of vertebral column
+DOID:13736,uterine inflammatory disease,DOID:345,uterine disease
+CL:0000992,immature CD11c-low plasmacytoid dendritic cell,CL:0000766,myeloid leukocyte
+UBERON:3000375,palatine process of the pars facialis of the maxilla,UBERON:0004120,mesoderm-derived structure
+UBERON:0010146,paraurethral duct,UBERON:0014404,female anatomical structure
+HP:0004425,Flat forehead,HP:0000290,Abnormality of the forehead
+UBERON:0004478,musculature of larynx,UBERON:0001015,musculature
+HP:0009215,Bracket epiphysis of the middle phalanx of the 4th finger,HP:0010258,Bracket epiphyses of the middle phalanges of the hand
+DOID:2510,Kluver-Bucy syndrome,DOID:10937,impulse control disorder
+UBERON:2001699,dorsal-fin stay,UBERON:0004376,fin bone
+UBERON:0001541,medial plantar artery,UBERON:0001637,artery
+HP:0003226,Rectilinear intracellular accumulation of autofluorescent lipopigment storage material,HP:0003204,Intracellular accumulation of autofluorescent lipopigment storage material
+UBERON:2005273,intestinal mucosal muscle,UBERON:0004221,intestine smooth muscle
+UBERON:0002562,superior frontal sulcus,UBERON:0013118,sulcus of brain
+HP:0001122,Aplasia/Hypoplasia of the choroid,HP:0008055,Aplasia/Hypoplasia affecting the uvea
+HP:0003259,Elevated serum creatinine,HP:0002157,Azotemia
+DOID:11786,splenic sequestration,DOID:2529,splenic disease
+HP:0003205,Curvilinear intracellular accumulation of autofluorescent lipopigment storage material,HP:0003204,Intracellular accumulation of autofluorescent lipopigment storage material
+UBERON:0005886,post-hyoid pharyngeal arch skeleton,UBERON:0010912,subdivision of skeleton
+UBERON:2001911,pharyngobranchial 2 element,UBERON:2001909,pharyngobranchial element
+HP:0005315,Occlusive arterial disease,HP:0004950,Peripheral arterial disease
+UBERON:0004225,respiratory system smooth muscle,UBERON:0001135,smooth muscle tissue
+HP:0008718,Unilateral renal dysplasia,HP:0000110,Renal dysplasia
+HP:0004291,Stippled calcification of hand bones,HP:0005921,Abnormal ossification of hand bones
+HP:0012218,Alveolar soft part sarcoma,HP:0100242,Sarcoma
+HP:0001770,Toe syndactyly,HP:0001159,Syndactyly
+HP:0007438,Mottled pigmentation of the trunk and proximal extremities,HP:0001070,Mottled pigmentation
+HP:0010431,Short phalanx of the 2nd toe,HP:0010746,Hypoplasia of the phalanges of the toes
+DOID:2018,hyperinsulinism,DOID:1428,endocrine pancreas disease
+UBERON:0005985,coronary vessel,UBERON:0004120,mesoderm-derived structure
+HP:0003212,Increased IgE level,HP:0010702,Hypergammaglobulinemia
+UBERON:0001887,internal capsule,UBERON:0002437,cerebral hemisphere white matter
+UBERON:0011605,supracoracoideus muscle of wing,UBERON:0008196,muscle of pectoral girdle
+HP:0001959,Polydipsia,HP:0000708,Behavioural/Psychiatric Abnormality
+UBERON:0001886,choroid plexus,UBERON:0003947,brain ventricle/choroid plexus
+UBERON:0013623,pedal autopod pad,UBERON:0001513,skin of pes
+HP:0010936,Abnormality of the lower urinary tract,HP:0000079,Abnormality of the urinary system
+HP:0010903,Abnormality of glutamine metabolism,HP:0010902,Abnormality of glutamine family amino acid metabolism
+UBERON:0001228,renal papilla,UBERON:0006554,urinary system structure
+UBERON:0006534,renal convoluted tubule,UBERON:0007685,region of nephron tubule
+UBERON:0005890,gonad germinal epithelium,UBERON:0005291,embryonic tissue
+CL:0000286,hyphal cell,CL:0000521,fungal cell
+UBERON:3010044,dorsal crest,UBERON:3000977,body external integument structure
+UBERON:0009098,gravid uterus,UBERON:0000995,uterus
+UBERON:0007381,epidermal scale,UBERON:0004121,ectoderm-derived structure
+HP:0010268,Absent epiphyses of the proximal phalanges of the hand,HP:0010245,Abnormality of the epiphyses of the proximal phalanges of the hand
+HP:0003835,Shoulder subluxation,HP:0003834,Shoulder dislocation
+UBERON:0006807,ectepicondyle of humerus,UBERON:0005055,zone of long bone
+HP:0010176,Curved phalanges of the toes,HP:0010161,Abnormality of the phalanges of the toes
+UBERON:3000831,spina acromioidea,UBERON:0004121,ectoderm-derived structure
+CL:0002384,uninucleate macroconidium,CL:0000606,macroconidium
+UBERON:2002088,interhaemal bone,UBERON:0002513,endochondral bone
+HP:0100251,Lipomas of the central neryous system,HP:0100835,Benign neoplasm of the central nervous system
+HP:0006896,Hypnopompic hallucinations,HP:0000738,Hallucinations
+UBERON:0007414,nucleus of midbrain tegmentum,UBERON:0006331,brainstem nucleus
+UBERON:0003435,pedal digit nerve,UBERON:0003445,pes nerve
+HP:0002186,Apraxia,HP:0011442,Abnormality of central motor function
+NCBITaxon:464095,Picornavirales,NCBITaxon:35278,"ssRNA positive-strand viruses, no DNA stage"
+NCBITaxon:44281,Pneumocystidaceae,NCBITaxon:37987,Pneumocystidales
+HP:0002849,Absence of lymph node germinal center,HP:0002733,Abnormality of the lymph nodes
+DOID:12897,submandibular gland disease,DOID:10854,salivary gland disease
+HP:0000742,Self-mutilation,HP:0100716,Self-injurious behavior
+HP:0009336,Bracket epiphysis of the distal phalanx of the 3rd finger,HP:0010247,Bracket epiphyses of the distal phalanges of the hand
+UBERON:0004199,S-shaped body,UBERON:0010532,primitive nephron
+HP:0009352,Ivory epiphysis of the proximal phalanx of the 3rd finger,HP:0009333,Abnormality of the epiphysis of the proximal phalanx of the 3rd finger
+DOID:5531,ovarian squamous cell carcinoma,DOID:4001,ovarian carcinoma
+UBERON:3010184,inner metatarsal tubercle,UBERON:0005813,tubercle
+UBERON:0011350,mylohyoid raphe,UBERON:0002384,connective tissue
+DOID:0070003,blastoma,DOID:0050687,cell type cancer
+DOID:3081,cystic lymphangioma,DOID:1475,lymphangioma
+DOID:0050464,Farber lipogranulomatosis,DOID:9455,lipid storage disease
+HP:0100279,Ulcerative colitis,HP:0100281,Chronic colitis
+HP:0004319,Hypoaldosteronism,HP:0008207,Primary adrenal insufficiency
+UBERON:2005073,atrioventricular ring,UBERON:2005072,endocardial ring
+HP:0010360,Broad phalanges of the 3rd toe,HP:0010174,Broad phalanx of the toes
+UBERON:2201415,pelvic fin distal radial cartilage 2,UBERON:1700006,paired fin radial cartilage
+UBERON:0015157,zygomatico-orbital artery,UBERON:0001637,artery
+UBERON:0009732,sublaminar layers S1 or S2 or S5,UBERON:0008921,substratum of layer of retina
+HP:0005404,Increase in B cell number,HP:0100827,Lymphocytosis
+UBERON:3000131,dilatatio alaris,UBERON:0004120,mesoderm-derived structure
+UBERON:0015161,inferior branch of oculomotor nerve,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005306,blastema,UBERON:0007567,regenerating anatomical structure
+UBERON:3000022,antorbital process,UBERON:0010313,neural crest-derived structure
+UBERON:0011610,ceratohyal cartilage,UBERON:0011004,pharyngeal arch cartilage
+HP:0006687,Aortic tortuosity,HP:0001679,Abnormality of the aorta
+HP:0009597,Short proximal phalanx of the 2nd finger,HP:0009580,Aplasia/Hypoplasia of the proximal phalanx of the 2nd finger
+DOID:4766,embryoma,DOID:688,embryonal cancer
+UBERON:0015083,proximal tarsal bone pre-cartilage condensation,UBERON:0015081,proximal tarsal bone endochondral element
+UBERON:0002067,dermis,UBERON:0004121,ectoderm-derived structure
+HP:0009949,Duplication of the middle phalanx of the 2nd finger,HP:0009945,Duplication of phalanx of 2nd finger
+UBERON:0000375,mandibular nerve,UBERON:0001021,nerve
+UBERON:0013220,foramen of Panizza,UBERON:0000464,anatomical space
+DOID:7047,penis basaloid carcinoma,DOID:5518,penis squamous cell carcinoma
+UBERON:0006117,accessory nerve fiber bundle,UBERON:0000122,neuron projection bundle
+UBERON:0000984,imaginal disc-derived wing,UBERON:0000023,wing
+HP:0009640,Symphalangism of the proximal phalanx of the thumb with the 1st metatcarpal,HP:0006152,Proximal symphalangism (hands)
+HP:0000280,Coarse facial features,HP:0001999,Abnormal facial shape
+DOID:0050750,splenic marginal zone lymphoma,DOID:0050748,marginal zone B-cell lymphoma
+UBERON:2005383,dorsal fin proximal radial bone 6,UBERON:2105383,dorsal fin proximal radial element 6
+UBERON:0004187,Harderian gland,UBERON:0001817,lacrimal gland
+DOID:0050891,adrenal cortical adenoma,DOID:656,adrenal adenoma
+DOID:6408,ovary papillary carcinoma,DOID:6214,ovarian papillary neoplasm
+HP:0010938,Abnormality of the external nose,HP:0000366,Abnormality of the nose
+HP:0009251,Bracket epiphysis of the distal phalanx of the 4th finger,HP:0009394,Bracket epiphyses of the 4th finger
+HP:0000842,Hyperinsulinemia,HP:0003117,Abnormality of circulating hormone level
+DOID:3842,skull base neoplasm,DOID:1863,skull cancer
+UBERON:2001188,Weberian apparatus,UBERON:0004120,mesoderm-derived structure
+DOID:1602,lymphadenitis,DOID:9942,lymph node disease
+DOID:4682,extrahepatic bile duct carcinoma,DOID:4897,bile duct carcinoma
+DOID:1467,serous labyrinthitis,DOID:1468,labyrinthitis
+HP:0006423,Peg-like central prominence of distal tibial metaphyses,HP:0006491,Abnormality of the tibial metaphysis
+HP:0011964,Intermittent painful muscle spasms,HP:0004305,Involuntary movements
+UBERON:2001698,anal-fin stay,UBERON:0004376,fin bone
+CL:1000123,metanephric nephron tubule epithelial cell,CL:1000494,epithelial cell of renal tubule
+NCBITaxon:37727,Talaromyces marneffei,NCBITaxon:5094,Talaromyces
+HP:0003134,Abnormality of peripheral nerve conduction,HP:0000759,Abnormality of the peripheral nervous system
+UBERON:0011650,epihyoidean,UBERON:0005493,hyoid muscle
+UBERON:0011925,preganglionic autonomic fiber,UBERON:0006134,nerve fiber
+UBERON:0012194,superior intercostal vein,UBERON:0012197,intercostal vein
+UBERON:0005359,spinal cord ependyma,UBERON:0004670,ependyma
+UBERON:0003224,chorion syncytiotrophoblast,UBERON:0004120,mesoderm-derived structure
+UBERON:0001005,respiratory airway,UBERON:0003103,compound organ
+DOID:6605,classic variant of chromophobe renal cell carcinoma,DOID:4471,chromophobe adenocarcinoma
+DOID:0050619,paranasal sinus cancer,DOID:0050615,respiratory system cancer
+DOID:1394,urinary schistosomiasis,DOID:1395,schistosomiasis
+UBERON:3000405,pars inferior of labyrinth,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003529,respiratory system lymphatic vessel endothelium,UBERON:0004807,respiratory system epithelium
+HP:0000080,Abnormality of genital physiology,HP:0000078,Abnormality of the genital system
+HP:0009268,Pseudoepiphysis of the proximal phalanx of the 4th finger,HP:0009248,Abnormality of the epiphysis of the proximal phalanx of the 4th finger
+UBERON:2000225,lateral crista primordium,UBERON:0003249,epithelium of otic placode
+UBERON:2001525,hypobranchial 2 cartilage,UBERON:2001895,hypobranchial 2 element
+HP:0005828,Transient pulmonary infiltrates,HP:0002113,Pulmonary infiltrates
+HP:0012557,EEG with centrotemporal focal spike waves,HP:0011197,EEG with focal spike waves
+HP:0003951,Irregular metaphyses (elbow),HP:0003850,Irregular metaphyses of the upper limbs
+DOID:1361,frontal sinus neoplasm,DOID:1350,paranasal sinus neoplasm
+DOID:11550,oculomotor nerve paralysis,DOID:562,third cranial nerve disease
+DOID:6854,ethmoid sinus ectopic meningioma,DOID:1364,ethmoidal sinus neoplasm
+UBERON:0002668,oculomotor nerve fibers,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0000439,arachnoid trabecula,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0004591,Disc-like vertebral bodies,HP:0003312,Abnormal form of the vertebral bodies
+UBERON:0002753,posterior spinocerebellar tract,UBERON:0001018,axon tract
+UBERON:0004209,renal vesicle,UBERON:0004211,nephron epithelium
+UBERON:3000833,sinus dorsalis,UBERON:0000464,anatomical space
+UBERON:0009207,geschmacksstreifen,UBERON:0000064,organ part
+UBERON:0006922,cervix squamous epithelium,UBERON:0004801,cervix epithelium
+HP:0008373,Puberty and gonadal disorders,HP:0000818,Abnormality of the endocrine system
+UBERON:0005500,rhombomere floor plate,UBERON:0004121,ectoderm-derived structure
+HP:0009695,Stippling of the epiphyses of the thumb,HP:0010237,Epiphyseal stippling of finger phalanges
+DOID:9312,chronic ethmoiditis,DOID:9507,ethmoid sinusitis
+UBERON:0005598,trunk somite,UBERON:0002329,somite
+UBERON:0013539,Brodmann (1909) area 8,UBERON:0013529,Brodmann area
+UBERON:0006844,cusp of tooth,UBERON:0000476,acellular anatomical structure
+UBERON:0008270,mollusc shell,UBERON:0006612,shell
+UBERON:0002185,bronchus,UBERON:0000117,respiratory tube
+UBERON:2001662,basibranchial 4 tooth plate,UBERON:2001647,pharyngeal tooth plate
+UBERON:0006713,foramen cecum of frontal bone,UBERON:0013685,foramen of skull
+DOID:693,dental enamel hypoplasia,DOID:214,teeth hard tissue disease
+HP:0011377,Aplasia of the vestibule,HP:0011376,Morphological abnormality of the vestibule of the inner ear
+UBERON:0002345,descending thoracic aorta,UBERON:0000063,organ segment
+DOID:2384,Wernicke encephalopathy,DOID:936,brain disease
+DOID:0050451,Brugada syndrome,DOID:10273,heart conduction disease
+DOID:5003,eunuchism,DOID:2519,testicular disease
+UBERON:0006322,inferior rectus extraocular muscle,UBERON:0006533,rectus extraocular muscle
+CL:0002414,"immature Vgamma1.1-positive, Vdelta6.3-negative thymocyte",CL:0002411,"Vgamma1.1-positive, Vdelta6.3-negative thymocyte"
+UBERON:0002496,stapes base,UBERON:0005913,zone of bone organ
+HP:0009640,Symphalangism of the proximal phalanx of the thumb with the 1st metatcarpal,HP:0005880,Metacarpophalangeal synostosis
+UBERON:2005039,anterior lateral mesoderm,UBERON:0005291,embryonic tissue
+HP:0009438,Absent middle phalanx of 3rd finger,HP:0009437,Aplasia/Hypoplasia of the middle phalanx of the 3rd finger
+UBERON:0010006,placenta intervillous maternal lacunae,UBERON:0002553,anatomical cavity
+HP:0007902,Vitreous hemorrhage,HP:0004327,Abnormality of the vitreous humor
+UBERON:2001412,epiotic,UBERON:0002513,endochondral bone
+UBERON:0001976,epithelium of esophagus,UBERON:0003350,epithelium of mucosa
+NCBITaxon:10244,Monkeypox virus,NCBITaxon:10242,Orthopoxvirus
+UBERON:0008199,chin,UBERON:0004121,ectoderm-derived structure
+HP:0011876,Abnormal platelet volume,HP:0001872,Abnormality of thrombocytes
+HP:0007601,Midline facial capillary hemangioma,HP:0000996,Facial capillary hemangioma
+DOID:7891,testicular spermatocytic seminoma,DOID:5842,testis seminoma
+HP:0100881,Congenital mesoblastic nephroma,HP:0003549,Abnormality of connective tissue
+UBERON:0002842,fifth cervical dorsal root ganglion,UBERON:0002834,cervical dorsal root ganglion
+HP:0009445,Symphalangism of the 3rd finger,HP:0009316,Abnormality of the phalanges of the 3rd finger
+HP:0000510,Retinitis pigmentosa,HP:0007703,Abnormal retinal pigmentation
+UBERON:0006715,radio-ulna,UBERON:0003466,forelimb zeugopod bone
+HP:0005542,Prolonged whole-blood clotting time,HP:0001928,Abnormality of coagulation
+UBERON:2000788,mesenchyme dorsal fin,UBERON:0003104,mesenchyme
+UBERON:0002061,truncus arteriosus,UBERON:0001637,artery
+HP:0010264,Pseudoepiphyses of the middle phalanges of the hand,HP:0010244,Abnormality of the epiphyses of the middle phalanges of the hand
+UBERON:2000495,infraorbital 5,UBERON:2000376,infraorbital
+UBERON:0010069,outer epithelial layer of tympanic membrane,UBERON:0015814,outer ear epithelium
+DOID:14764,Larsen syndrome,DOID:0050736,autosomal dominant disease
+DOID:1029,familial periodic paralysis,DOID:896,metal metabolism disorder
+HP:0008208,Parathyroid hyperplasia,HP:0011766,Abnormality of the parathyroid morphology
+DOID:2738,pseudoxanthoma elasticum,DOID:0050737,autosomal recessive disease
+DOID:13200,substernal goiter,DOID:12176,goiter
+CL:1001575,uterine cervix squamous cell,CL:0000076,squamous epithelial cell
+DOID:1475,lymphangioma,DOID:0060084,cell type benign neoplasm
+UBERON:0007254,intervertebral disk of thoracic vertebra,UBERON:0001066,intervertebral disk
+UBERON:0014738,medial pallium,UBERON:0002791,regional part of telencephalon
+UBERON:0010947,occipitalis,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009776,Adactyly,HP:0009380,Aplasia of the fingers
+CL:0000909,"CD8-positive, alpha-beta memory T cell",CL:0000625,"CD8-positive, alpha-beta T cell"
+HP:0002111,Restrictive respiratory insufficiency,HP:0002093,Respiratory insufficiency
+UBERON:0011607,hyomandibular cartilage,UBERON:0011608,hyomandibular element
+HP:0007017,Progressive forgetfulness,HP:0002354,Memory impairment
+UBERON:0002807,right occipital lobe,UBERON:0002021,occipital lobe
+UBERON:0004195,short nephron,UBERON:0001285,nephron
+UBERON:0013128,bulb of penis,UBERON:0000064,organ part
+UBERON:0005998,tricuspid valve cusp,UBERON:0005484,tricuspid valve leaflet
+UBERON:0011138,post-cranial axial skeletal system,UBERON:0004120,mesoderm-derived structure
+UBERON:0009195,anal membrane,UBERON:0002050,embryonic structure
+HP:0100480,Proximal/middle symphalangism of 3rd toe,HP:0100470,Symphalangism affecting the middle phalanx of the 3rd toe
+NCBITaxon:11018,Togaviridae,NCBITaxon:35278,"ssRNA positive-strand viruses, no DNA stage"
+UBERON:0002324,muscle of back,UBERON:0001774,muscle of trunk
+UBERON:3010792,m. rectus abdominis profundus,UBERON:0002461,anterior abdominal wall muscle
+UBERON:0015017,incus endochondral element,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010118,Irregular epiphyses of the hallux,HP:0010167,Irregular epiphyses of the toes
+NCBITaxon:12475,Hepatitis delta virus,NCBITaxon:39759,Deltavirus
+UBERON:0015145,pes hair,UBERON:0015144,autopod hair
+DOID:2531,hematologic cancer,DOID:0060083,immune system cancer
+UBERON:0009661,midbrain nucleus,UBERON:0002308,nucleus of brain
+HP:0100407,Complete duplication of the distal phalanx of the 3rd toe,HP:0100398,Duplication of the distal phalanx of the 3rd toe
+UBERON:0010868,uropropatagium,UBERON:0010858,inter limb-segment region
+UBERON:4200025,ascending process of the astragalus,UBERON:4100000,skeletal element projection
+HP:0003719,Muscle mounding,HP:0010548,Percussion myotonia
+HP:0007209,Facial paralysis,HP:0001293,Cranial nerve compression
+CL:0002528,mature CD14-positive dermal dendritic cell,CL:0002526,CD14-positive dermal dendritic cell
+DOID:8282,adult epithelioid sarcoma,DOID:6193,epithelioid sarcoma
+HP:0012465,Elevated hepatic iron concentration,HP:0011031,Abnormality of iron homeostasis
+UBERON:0005284,brain vasculature,UBERON:0006876,vasculature of organ
+UBERON:0000170,pair of lungs,UBERON:0000477,anatomical cluster
+HP:0010984,Digenic inheritance,HP:0001426,Multifactorial inheritance
+HP:0009585,Patchy sclerosis of the proximal phalanx of the 2nd finger,HP:0009856,Patchy sclerosis of the proximal phalanges of the hand
+UBERON:0005322,mesonephric nephron,UBERON:0001285,nephron
+HP:0001371,Flexion contracture,HP:0011805,Abnormality of muscle morphology
+DOID:10287,prostate squamous cell carcinoma,DOID:10286,prostate carcinoma
+UBERON:0013731,basilar papilla,UBERON:0004121,ectoderm-derived structure
+HP:0010018,Enlarged epiphysis of the 1st metacarpal,HP:0010271,Enlarged epiphyses of the proximal phalanges of the hand
+UBERON:0015229,accessory circulatory organ,UBERON:0015228,circulatory organ
+UBERON:0015170,nauplius eye,UBERON:0000970,eye
+HP:0100469,Patchy sclerosis of the distal phalanx of the 5th toe,HP:0010190,Patchy sclerosis of the distal phalanges of the toes
+UBERON:4440011,paired fin lepidotrichium,UBERON:4000172,lepidotrichium
+CL:0000087,male germ line stem cell (sensu Nematoda and Protostomia),CL:0000016,male germ line stem cell
+UBERON:0005289,tela choroidea of telencephalic ventricle,UBERON:0005283,tela choroidea
+UBERON:0004806,vas deferens epithelium,UBERON:0014403,male anatomical structure
+HP:0005912,Biliary atresia,HP:0012440,Abnormal biliary tract morphology
+HP:0100721,Mediastinal lymphadenopathy,HP:0002716,Lymphadenopathy
+UBERON:0013561,Brodmann (1909) area 43,UBERON:0013529,Brodmann area
+HP:0100010,Spinal meningioma,HP:0002858,Meningioma
+UBERON:0014438,superior pubic ramus,UBERON:0014444,pubic ramus
+DOID:9021,esophageal leukoplakia,DOID:6050,esophageal disease
+HP:0004794,Malrotation of small bowel,HP:0002244,Abnormality of the small intestine
+UBERON:0003538,right lung bronchiole,UBERON:0002186,bronchiole
+UBERON:0003425,renal lymph node,UBERON:0000029,lymph node
+UBERON:0001236,adrenal medulla,UBERON:0000958,medulla of organ
+DOID:9892,median arcuate ligament syndrome,DOID:0050828,artery disease
+DOID:3446,anal Paget's disease,DOID:3447,anus adenocarcinoma
+UBERON:0005843,sacral spinal cord,UBERON:0005844,spinal cord segment
+UBERON:2002095,third posttemporal fossa,UBERON:2001753,posttemporal fossa
+UBERON:0002400,parietal pleura,UBERON:0000977,pleura
+UBERON:0014767,left crus of diaphragm,UBERON:0015212,lateral structure
+UBERON:0011196,superior parathyroid epithelium,UBERON:0011197,parathyroid epithelium
+UBERON:0002491,lambdoid suture,UBERON:0003685,cranial suture
+HP:0100150,Fragmentation of the epiphysis of the middle phalanx of the 3rd toe,HP:0100092,Abnormality of the epiphysis of the middle phalanx of the 3rd toe
+UBERON:0010358,arch of centrum of vertebra,UBERON:0004120,mesoderm-derived structure
+CL:0002216,intermediate muscle cell,CL:0008002,skeletal muscle fiber
+HP:0100883,Chorangioma,HP:0010566,Hamartoma
+CL:1000090,pronephric nephron tubule epithelial cell,CL:1000494,epithelial cell of renal tubule
+DOID:492,acquired hemangioma,DOID:255,hemangioma
+DOID:3341,osteitis fibrosa,DOID:0080011,bone resorption disease
+DOID:0050869,villous adenoma,DOID:657,adenoma
+HP:0200057,Marcus Gunn pupil,HP:0000587,Abnormality of the optic nerve
+UBERON:0001188,right testicular artery,UBERON:0001187,testicular artery
+UBERON:0013709,anterior inferior iliac spine,UBERON:0013712,anterior iliac spine
+DOID:561,trigeminal nerve disease,DOID:5656,cranial nerve disease
+DOID:9681,cervical incompetence,DOID:2253,cervix disease
+DOID:261,transverse colon cancer,DOID:219,colon cancer
+HP:0006577,Macronodular cirrhosis,HP:0001394,Cirrhosis
+HP:0010724,Advanced pneumatization of the mastoid process,HP:0000264,Abnormality of the mastoid
+UBERON:2000976,somite 16,UBERON:0002329,somite
+HP:0009701,Metacarpal synostosis,HP:0100265,Synostosis of metacarpals/metatarsals
+UBERON:2101671,anal fin radial element,UBERON:2105225,median fin radial element
+HP:0004340,Abnormality of vitamin B metabolism,HP:0100508,Abnormality of vitamin metabolism
+HP:0009530,Ivory epiphysis of the proximal phalanx of the 2nd finger,HP:0009494,Ivory epiphyses of the 2nd finger
+UBERON:0001065,parotid duct,UBERON:0001837,duct of salivary gland
+HP:0100379,Aplasia of the distal phalanx of the 4th toe,HP:0010645,Aplasia of the distal phalanges of the toes
+HP:0010823,Ridged cranial sutures,HP:0011329,Abnormality of cranial sutures
+UBERON:0005192,deferent duct artery,UBERON:0001637,artery
+HP:0011650,Bilateral ductus arteriosus,HP:0001643,Patent ductus arteriosus
+HP:0009192,Aplasia/Hypoplasia of the proximal phalanx of the 5th finger,HP:0009150,Abnormality of the proximal phalanx of the 5th finger
+DOID:12972,intrapelvic lymph node leukemic reticuloendotheliosis,DOID:285,hairy cell leukemia
+HP:0009284,Abnormality of the proximal phalanx of the 4th finger,HP:0009172,Abnormality of the phalanges of the 4th finger
+UBERON:0006906,ala of nose,UBERON:0003102,surface structure
+UBERON:0014876,distal epiphysis of distal phalanx of pedal digit,UBERON:0013122,distal epiphysis of phalanx of pes
+DOID:0050340,opportunistic bacterial infectious disease,DOID:104,bacterial infectious disease
+HP:0000650,Reduced amplitude of pattern visual evoked potentials,HP:0000649,Abnormality of vision evoked potentials
+UBERON:0009777,intermediate reticular nucleus,UBERON:0002579,regional part of medullary reticular formation
+HP:0003371,Enlargement of the proximal femoral epiphysis,HP:0010580,Enlarged epiphyses
+UBERON:0004605,rib 5,UBERON:0002228,rib
+HP:0000819,Diabetes mellitus,HP:0011014,Abnormal glucose homeostasis
+UBERON:3000399,pars externa plectri,UBERON:0000064,organ part
+CL:0000963,Bm3-delta B cell,CL:0000844,germinal center B cell
+UBERON:0005093,cement gland,UBERON:0002530,gland
+UBERON:2001821,notochord posterior region,UBERON:0004121,ectoderm-derived structure
+DOID:0050596,taeniasis,DOID:883,parasitic helminthiasis infectious disease
+UBERON:0015839,molar epithelium,UBERON:0003843,dental epithelium
+HP:0009684,Stippling of the epiphysis of the distal phalanx of the thumb,HP:0009695,Stippling of the epiphyses of the thumb
+DOID:627,severe combined immunodeficiency,DOID:628,combined T cell and B cell immunodeficiency
+UBERON:0015178,somite border,UBERON:0007651,anatomical junction
+UBERON:0013124,left posterior cardinal vein,UBERON:0015212,lateral structure
+UBERON:0009506,associated mesenchyme of middle ear,UBERON:0007524,dense mesenchyme tissue
+CL:0002608,hippocampal neuron,CL:0002609,neuron of cerebral cortex
+HP:0009611,Bifid distal phalanx of the thumb,HP:0009944,Partial duplication of the phalanges of the thumb
+DOID:0060096,sensory organ benign neoplasm,DOID:0060115,nervous system benign neoplasm
+CL:0000943,Be1 Cell,CL:0000968,Be cell
+HP:0002599,Head titubation,HP:0002457,Abnormal head movements
+HP:0005407,Decreased number of CD4+ T cells,HP:0005403,T lymphocytopenia
+UBERON:0007656,lateral recess of fourth ventricle,UBERON:0000464,anatomical space
+UBERON:0003161,dorsal ocellus,UBERON:0000963,head sensillum
+UBERON:0010733,alisphenoid cartilage element,UBERON:0011004,pharyngeal arch cartilage
+UBERON:0012333,ovarian bursa,UBERON:0004120,mesoderm-derived structure
+UBERON:4000003,permanent cartilage,UBERON:0007844,cartilage element
+UBERON:0009975,remnant of lumen of Rathke's pouch,UBERON:0005082,tube lumen
+UBERON:3000393,pars amphibiorum,UBERON:0000479,tissue
+DOID:3968,papillary follicular thyroid adenocarcinoma,DOID:3969,papillary thyroid carcinoma
+CL:0002097,cortical cell of adrenal gland,CL:1001601,adrenal gland glandular cell
+DOID:4781,diffuse glomerulonephritis,DOID:2921,glomerulonephritis
+HP:0005872,Brachytelomesophalangy,HP:0001156,Brachydactyly syndrome
+UBERON:0001811,conjunctiva,UBERON:0000060,anatomical wall
+UBERON:0003935,mesenchyme pelvic fin,UBERON:0003104,mesenchyme
+HP:0009905,Thin ear helix,HP:0011039,Abnormality of the helix
+UBERON:0010017,spiral valve of cystic duct,UBERON:0004119,endoderm-derived structure
+HP:0007992,Lattice retinal degeneration,HP:0000546,Retinal degeneration
+HP:0003870,Crumpled humerus,HP:0003063,Abnormality of the humerus
+CL:0001003,mature CD8_alpha-negative CD11b-positive dendritic cell,CL:0000841,mature conventional dendritic cell
+DOID:1407,anterior uveitis,DOID:12030,panuveitis
+UBERON:0002847,third thoracic dorsal root ganglion,UBERON:0002835,thoracic dorsal root ganglion
+HP:0011124,Abnormality of epidermal morphology,HP:0011121,Abnormality of skin morphology
+UBERON:0010357,secondary ossification center,UBERON:0010355,ossification center
+HP:0009493,Irregular epiphyses of the 2nd finger,HP:0010233,Irregular epiphyses of the phalanges of the hand
+UBERON:0013774,diaphysis of metatarsal bone,UBERON:0004120,mesoderm-derived structure
+HP:0003691,Scapular winging,HP:0001435,Abnormality of the shoulder girdle musculature
+HP:0001343,Kernicterus,HP:0002011,Abnormality of the central nervous system
+UBERON:4000122,acellular bone tissue,UBERON:4000115,mineralized bone tissue
+CL:0000092,osteoclast,CL:0000766,myeloid leukocyte
+UBERON:2000348,exoccipital posteroventral region,UBERON:0011164,neurocranium bone
+HP:0002340,Caudate atrophy,HP:0007374,Atrophy/Degeneration involving the caudate nucleus
+UBERON:2005278,preopercle vertical limb-hyomandibula joint,UBERON:0000982,skeletal joint
+HP:0001762,Talipes equinovarus,HP:0001883,Talipes
+HP:0000528,Anophthalmia,HP:0008056,Aplasia/Hypoplasia affecting the eye
+DOID:8508,subcorneal pustular dermatosis,DOID:8502,bullous skin disease
+UBERON:4300034,antorbital cartilage,UBERON:0003932,cartilage element of chondrocranium
+HP:0009353,Pseudoepiphysis of the proximal phalanx of the 3rd finger,HP:0009333,Abnormality of the epiphysis of the proximal phalanx of the 3rd finger
+HP:0009069,Lethal infantile mitochondrial myopathy,HP:0003737,Mitochondrial myopathy
+DOID:7061,precursor B lymphoblastic lymphoma/leukemia,DOID:5600,precursor lymphoblastic lymphoma/leukemia
+HP:0004925,Chronic lactic acidosis,HP:0012468,Chronic acidosis
+DOID:6370,hepatic osteogenic sarcoma,DOID:270,liver sarcoma
+UBERON:2001520,ceratobranchial 1 cartilage,UBERON:2001516,ceratobranchial cartilage
+HP:0010952,Mild fetal ventriculomegaly,HP:0011425,Fetal ultrasound soft marker
+HP:0100658,Cellulitis,HP:0003549,Abnormality of connective tissue
+HP:0007352,Cerebellar calcifications,HP:0001317,Abnormality of the cerebellum
+HP:0003268,Argininuria,HP:0003355,Aminoaciduria
+HP:0100386,Aplasia of the proximal phalanx of the 5th toe,HP:0100364,Aplasia of the phalanges of the 5th toe
+HP:0010799,Pinealoma,HP:0100568,Neoplasm of the endocrine system
+CL:0002511,"CD11b-low, CD103-negative, langerin-negative lymph node dendritic cell",CL:0002454,"Cd4-negative, CD8_alpha-negative, CD11b-positive dendritic cell"
+NCBITaxon:34632,Rhipicephalus sanguineus,NCBITaxon:578835,Rhipicephalus sanguineus group
+HP:0010242,Aplasia of the proximal phalanges of the hand,HP:0009802,Aplasia of the phalanges of the hand
+HP:0002326,Transient ischemic attack,HP:0001297,Stroke
+HP:0006603,"Flared, irregular rib ends",HP:0000887,Cupped ribs
+UBERON:0005899,pes bone,UBERON:0011250,autopod bone
+HP:0000385,Small earlobe,HP:0009906,Aplasia/Hypoplasia of the earlobes
+UBERON:0000467,anatomical system,UBERON:0000480,anatomical group
+UBERON:0003124,chorion,UBERON:0005631,extraembryonic membrane
+HP:0010485,Hyperextensibility at elbow,HP:0001382,Joint hypermobility
+UBERON:0007798,vascular system,UBERON:0000467,anatomical system
+HP:0003375,Narrow greater sacrosciatic notches,HP:0010456,Abnormality of the greater sacrosciatic notch
+CL:0000189,slow muscle cell,CL:0008002,skeletal muscle fiber
+CL:1001005,glomerular capillary endothelial cell,CL:1000510,kidney glomerular epithelial cell
+DOID:5508,brain stem ependymoma,DOID:4202,brain stem glioma
+UBERON:0004319,distal phalanx of pedal digit 5,UBERON:0014487,distal phalanx of digit 5
+HP:0007697,Hypoplasia of the lower eyelids,HP:0011226,Aplasia/Hypoplasia affecting the eyelid
+DOID:1574,alcohol abuse,DOID:302,substance abuse
+UBERON:3000006,alveolar foramen,UBERON:0011772,lower jaw opening
+DOID:11552,Bowman's membrane folds or rupture,DOID:10124,corneal disease
+HP:0002514,Cerebral calcification,HP:0002060,Abnormality of the cerebrum
+UBERON:0001837,duct of salivary gland,UBERON:0003928,digestive system duct
+HP:0004751,Paroxysmal ventricular tachycardia,HP:0004756,Ventricular tachycardia
+CL:1000222,stomach neuroendocrine cell,CL:0002178,epithelial cell of stomach
+HP:0010169,Pseudoepiphyses of the toes,HP:0010160,Abnormality of the epiphyses of the toes
+NCBITaxon:69474,Orientia,NCBITaxon:33988,Rickettsieae
+HP:0010674,Abnormality of the curvature of the vertebral column,HP:0000925,Abnormality of the vertebral column
+UBERON:0004604,rib 4,UBERON:0002228,rib
+UBERON:3010189,ulnar protuberances,UBERON:3000981,limb external integument structure
+DOID:6705,gastric body carcinoma,DOID:5517,stomach carcinoma
+DOID:786,laryngeal disease,DOID:974,upper respiratory tract disease
+UBERON:0005047,mucosa of vocal fold,UBERON:0001824,mucosa of larynx
+UBERON:0004043,semicircular canal ampulla,UBERON:0004121,ectoderm-derived structure
+HP:0012460,Dysmorphic inferior cerebellar vermis,HP:0002334,Abnormality of the cerebellar vermis
+HP:0100046,Cone-shaped epiphyses of the 2nd toe,HP:0010164,Cone-shaped epiphyses of the toes
+HP:0001348,Brisk reflexes,HP:0001347,Hyperreflexia
+UBERON:0001753,cementum,UBERON:0001973,substance of tooth
+HP:0010137,Triangular epiphysis of the proximal phalanx of the hallux,HP:0010126,Abnormality of the epiphysis of the proximal phalanx of the hallux
+UBERON:0001167,wall of stomach,UBERON:0000328,gut wall
+DOID:4110,parasitic ectoparasitic infectious disease,DOID:1398,parasitic infectious disease
+UBERON:0010893,median external naris,UBERON:0005928,external naris
+DOID:7168,lung occult adenocarcinoma,DOID:3910,lung adenocarcinoma
+HP:0010173,Aplasia/Hypoplasia of the phalanges of the toes,HP:0010161,Abnormality of the phalanges of the toes
+UBERON:2000203,rhinosphenoid,UBERON:0002513,endochondral bone
+UBERON:3010742,interhyoideus posterior,UBERON:0011648,jaw muscle
+UBERON:2001347,stratum fibrosum et griseum superficiale,UBERON:0000479,tissue
+DOID:5166,endometrial stromal tumor,DOID:1380,endometrial cancer
+HP:0003872,Exostoses (humeral),HP:0002762,Multiple exostoses
+DOID:10139,conjunctival degeneration,DOID:4251,conjunctival disease
+HP:0007869,Peripheral retinopathy,HP:0000479,Abnormality of the retina
+UBERON:0006495,osseus cochlear canal,UBERON:0005744,bone foramen
+UBERON:2001903,ceratobranchial 5 element,UBERON:2001898,ceratobranchial element
+UBERON:0014571,CA3 alveus,UBERON:0002619,regional part of cerebral cortex
+CL:0002180,mucous cell of stomach,CL:0002659,glandular cell of stomach
+DOID:538,internuclear ophthalmoplegia,DOID:540,strabismus
+DOID:0060183,collagenous colitis,DOID:0060182,microscopic colitis
+UBERON:0002319,mesangium,UBERON:0004120,mesoderm-derived structure
+UBERON:3000599,taenia tecti marginalis,UBERON:0003932,cartilage element of chondrocranium
+UBERON:0004276,fourth ventricle choroid plexus epithelium,UBERON:0004644,fourth ventricle ependyma
+UBERON:0000451,prefrontal cortex,UBERON:0002619,regional part of cerebral cortex
+UBERON:0002708,posterior periventricular nucleus,UBERON:0006568,hypothalamic nucleus
+HP:0006671,Paroxysmal atrial tachycardia,HP:0004763,Paroxysmal supraventricular tachycardia
+UBERON:0013648,masseteric artery,UBERON:0001637,artery
+HP:0010477,Aplasia of the bladder,HP:0010476,Aplasia/Hypoplasia of the bladder
+HP:0008155,Mucopolysacchariduria,HP:0011020,Abnormality of mucopolysaccharide metabolism
+UBERON:0012078,fovea capitis of femur,UBERON:0004120,mesoderm-derived structure
+HP:0003083,Dislocated radial head,HP:0003042,Elbow dislocation
+UBERON:3000437,planum conchale,UBERON:0003933,cranial cartilage
+DOID:3052,Balkan nephropathy,DOID:1063,interstitial nephritis
+UBERON:4200043,brevis fossa,UBERON:0004704,bone fossa
+UBERON:0004197,proximal convoluted tubule segment 2,UBERON:0004120,mesoderm-derived structure
+UBERON:3000783,fovea capitis of humerus,UBERON:0004120,mesoderm-derived structure
+UBERON:3000647,crista interna,UBERON:4100000,skeletal element projection
+UBERON:0007352,stria vascularis vasculature,UBERON:0006876,vasculature of organ
+CL:0002658,glandular cell of the large intestine,CL:0000150,glandular epithelial cell
+HP:0010977,Abnormality of phagocytes,HP:0010974,Abnormality of myeloid leukocytes
+HP:0010242,Aplasia of the proximal phalanges of the hand,HP:0009851,Aplasia/Hypoplasia of the proximal phalanges of the hand
+UBERON:0006775,zone of epiphyseal plate,UBERON:0002418,cartilage tissue
+CL:0000808,DN4 thymocyte,CL:0002489,double negative thymocyte
+UBERON:0007239,tunica media of artery,UBERON:0002522,tunica media
+UBERON:0008878,palmar part of manus,UBERON:0005451,segment of manus
+HP:0010086,Broad proximal phalanx of the hallux,HP:0010059,Broad phalanges of the hallux
+UBERON:0003691,epidural space,UBERON:0000464,anatomical space
+HP:0012443,Abnormality of the brain,HP:0007319,Morphological abnormality of the central nervous system
+HP:0005473,Fusion of middle ear ossicles,HP:0100240,Synostosis of joints
+UBERON:2002119,dermal scale focus,UBERON:0004121,ectoderm-derived structure
+UBERON:0004384,epiphysis of femur,UBERON:0004120,mesoderm-derived structure
+HP:0009963,Duplication of the middle phalanx of the 3rd finger,HP:0004172,Abnormality of the middle phalanx of the 3rd finger
+CL:0000964,Bm2' B cell,CL:0000844,germinal center B cell
+CL:0011113,spiral ganglion neuron,CL:0000540,neuron
+UBERON:0007181,serosa of infundibulum of uterine tube,UBERON:0005983,heart layer
+UBERON:0005654,lower jaw molar epithelium,UBERON:0010313,neural crest-derived structure
+HP:0100552,Neoplasm of the tracheobronchial system,HP:0100526,Neoplasm of the lungs
+UBERON:3010590,amphibian cloacal gland,UBERON:0012478,cloacal gland
+UBERON:0002672,anterior subcentral sulcus,UBERON:0014639,frontal sulcus
+HP:0011686,Abnormal coronary artery course,HP:0006704,Abnormality of the coronary arteries
+DOID:12363,intermittent proptosis,DOID:930,orbital disease
+DOID:1573,communicating hydrocephalus,DOID:10908,hydrocephalus
+UBERON:3000785,trochlear groove of humerus,UBERON:0004120,mesoderm-derived structure
+HP:0011307,Splayed toes,HP:0001780,Abnormality of toe
+CL:0002406,immature Vgamma2-positive thymocyte,CL:0002405,gamma-delta thymocyte
+HP:0009327,Ivory epiphysis of the middle phalanx of the 3rd finger,HP:0009334,Abnormality of the epiphysis of the middle phalanx of the 3rd finger
+DOID:9909,hordeolum,DOID:530,eyelid disease
+HP:0012587,Macroscopic hematuria,HP:0000790,Hematuria
+DOID:3590,gestational trophoblastic neoplasm,DOID:4085,trophoblastic neoplasm
+DOID:5675,cribriform carcinoma,DOID:3459,breast carcinoma
+UBERON:0008842,suspensory ligament of testis,UBERON:0005156,reproductive structure
+UBERON:0004637,otic capsule,UBERON:0002513,endochondral bone
+HP:0009309,Triangular shaped middle phalanx of the 4th finger,HP:0009283,Abnormality of the middle phalanx of the 4th finger
+DOID:5870,eosinophilic pneumonia,DOID:552,pneumonia
+DOID:12347,osteogenesis imperfecta,DOID:2256,osteochondrodysplasia
+DOID:0050578,occult macular dystrophy,DOID:4448,macular degeneration
+HP:0010535,Sleep apnea,HP:0002360,Sleep disturbance
+DOID:0050589,inflammatory bowel disease,DOID:5295,intestinal disease
+HP:0100172,Enlarged epiphysis of the distal phalanx of the 4th toe,HP:0100094,Abnormality of the epiphysis of the distal phalanx of the 4th toe
+HP:0000025,Functional abnormality of male internal genitalia,HP:0000080,Abnormality of genital physiology
+UBERON:0015091,distal carpal bone 3 cartilage,UBERON:0010883,forelimb cartilage element
+UBERON:0014624,basis modioli,UBERON:0010313,neural crest-derived structure
+UBERON:0005724,roof plate spinal cord region,UBERON:0003298,roof plate of neural tube
+HP:0011099,Spastic hemiplegia,HP:0001257,Spasticity
+UBERON:0004398,epiphysis of fourth metatarsal bone,UBERON:0004389,epiphysis of metatarsal bone
+HP:0010244,Abnormality of the epiphyses of the middle phalanges of the hand,HP:0009833,Abnormality of the middle phalanges of the hand
+DOID:14535,malignant cardiac germ cell tumor,DOID:117,heart cancer
+DOID:11543,corneal abscess,DOID:9858,deep keratitis
+UBERON:0001608,dilatator pupillae,UBERON:0004234,iris smooth muscle
+DOID:5714,intracranial liposarcoma,DOID:3382,liposarcoma
+UBERON:0002751,inferior temporal gyrus,UBERON:0000200,gyrus
+UBERON:0002663,septal nuclear complex,UBERON:0005401,cerebral hemisphere grey matter
+UBERON:0002814,posterior superior fissure of cerebellum,UBERON:0003980,cerebellum fissure
+HP:0011863,Abnormal sternal ossification,HP:0011849,Abnormal bone ossification
+HP:0004227,Short distal phalanx of the 5th finger,HP:0009882,Short distal phalanx of finger
+UBERON:3000020,anterolateral process of frontoparietal,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0002284,type X enteroendocrine cell,CL:0005018,ghrelin secreting cell
+DOID:3542,adult choroid plexus cancer,DOID:3540,choroid plexus cancer
+UBERON:3000948,articular process,UBERON:0000072,segment of respiratory tract
+UBERON:0015146,manus hair,UBERON:0015144,autopod hair
+UBERON:0009140,right subcardinal vein,UBERON:0015212,lateral structure
+UBERON:0002022,insula,UBERON:0000064,organ part
+DOID:3421,trochlear nerve neoplasm,DOID:338,cranial nerve neoplasm
+HP:0008365,Abnormality of the talus,HP:0001850,Abnormality of the tarsal bones
+DOID:8256,olfactory neural tumor,DOID:366,olfactory nerve neoplasm
+DOID:11615,penile cancer,DOID:3856,male reproductive organ cancer
+CL:1000702,kidney pelvis smooth muscle cell,CL:1000979,ureter smooth muscle cell
+UBERON:0004224,vas deferens smooth muscle,UBERON:0001135,smooth muscle tissue
+UBERON:0011986,mucosa of infraorbital sinus,UBERON:0005030,mucosa of paranasal sinus
+CL:0002673,tongue muscle cell,CL:0008002,skeletal muscle fiber
+HP:0012259,Absent inner and outer dynein arms,HP:0012256,Absent outer dynein arms
+HP:0100237,Proximal symphalangism (feet),HP:0100235,Synostosis involving bones of the toes
+UBERON:0004259,lower arm blood vessel,UBERON:0003507,arm blood vessel
+CL:0000618,sheath cell,CL:0000075,columnar/cuboidal epithelial cell
+UBERON:0003312,mesenchyme of testis,UBERON:0003855,gonad mesenchyme
+UBERON:0011757,differentiated genital tubercle,UBERON:0005423,developing anatomical structure
+HP:0010767,Sacrococcygeal pilonidal abnormality,HP:0005107,Abnormality of the sacrum
+CL:0001056,"dendritic cell, human",CL:0000451,dendritic cell
+DOID:502,central nervous system mesenchymal non-meningothelial tumor,DOID:3620,central nervous system cancer
+UBERON:2001257,medial floor plate,UBERON:0004120,mesoderm-derived structure
+UBERON:0006801,proximal head of humerus,UBERON:0004120,mesoderm-derived structure
+DOID:14512,candidal paronychia,DOID:1508,candidiasis
+DOID:1614,male breast cancer,DOID:1612,breast cancer
+HP:0009182,Triangular shaped middle phalanx of the 5th finger,HP:0009850,Triangular shaped middle phalanges of the hand
+HP:0005458,Premature closure of fontanelles,HP:0011328,Abnormality of fontanelles
+CL:0002201,renal beta-intercalated cell,CL:0005010,renal intercalated cell
+DOID:848,arthritis,DOID:3342,bone inflammation disease
+CL:0009003,larval midgut cell,CL:0002371,somatic cell
+HP:0001002,Decreased subcutaneous fat,HP:0001001,Abnormality of subcutaneous fat tissue
+UBERON:0014439,inferior pubic ramus,UBERON:0014444,pubic ramus
+UBERON:2001910,pharyngobranchial 1 element,UBERON:2001909,pharyngobranchial element
+UBERON:0002511,trabecula carnea,UBERON:0004120,mesoderm-derived structure
+HP:0011509,Macular hyperpigmentation,HP:0008002,Abnormality of macular pigmentation
+UBERON:0004188,glomerular epithelium,UBERON:0012275,meso-epithelium
+HP:0010771,Pilonidal abscess,HP:0100838,Recurrent cutaneous abscess formation
+HP:0012426,Optic disc drusen,HP:0000587,Abnormality of the optic nerve
+HP:0011856,Pica,HP:0100738,Abnormal eating behavior
+UBERON:0005153,epithelial bud,UBERON:0005157,epithelial fold
+UBERON:2001884,accessory neural arch,UBERON:0003861,neural arch
+UBERON:0001273,ilium,UBERON:0008202,bone of hip region
+HP:0007981,Concentric narrowing of visual fields,HP:0001133,Constricted visual fields
+UBERON:0006777,tectal plate,UBERON:0005423,developing anatomical structure
+UBERON:0009731,sublaminar layers S3 or S4,UBERON:0008921,substratum of layer of retina
+CL:0000291,spore (sensu Mycetozoa),CL:0000263,vegetative cell (sensu Mycetozoa)
+HP:0010935,Abnormality of the upper urinary tract,HP:0000079,Abnormality of the urinary system
+CL:1001127,outer renal medulla vasa recta cell,CL:1001036,vasa recta cell
+DOID:13208,background diabetic retinopathy,DOID:8947,diabetic retinopathy
+UBERON:0001229,renal corpuscle,UBERON:0006554,urinary system structure
+CL:0000993,mature CD11c-low plasmacytoid dendritic cell,CL:0000766,myeloid leukocyte
+UBERON:3000384,parasagittal crest,UBERON:0004121,ectoderm-derived structure
+HP:0012002,Experiential auras,HP:0011157,Auras
+UBERON:0010756,spleen follicular dendritic cell network,UBERON:0004120,mesoderm-derived structure
+HP:0009596,Aplasia of the proximal phalanx of the 2nd finger,HP:0009580,Aplasia/Hypoplasia of the proximal phalanx of the 2nd finger
+UBERON:0002270,hyaloid artery,UBERON:0002050,embryonic structure
+UBERON:0003054,roof plate,UBERON:0005291,embryonic tissue
+UBERON:3010725,M. coracoradialis,UBERON:0010891,pectoral complex muscle
+CL:0000413,haploid cell,CL:0000003,native cell
+UBERON:2000209,lateral preglomerular nucleus,UBERON:2002226,preglomerular nucleus
+CL:0002385,blastoconidium,CL:0000606,macroconidium
+UBERON:0002379,perineal muscle,UBERON:0001325,muscle of pelvis
+UBERON:0009846,embryonic cloacal epithelium,UBERON:0005291,embryonic tissue
+UBERON:2005078,middle mesencephalic central artery,UBERON:2005020,central artery
+DOID:11787,chronic congestive splenomegaly,DOID:2529,splenic disease
+DOID:4159,skin cancer,DOID:0060122,integumentary system cancer
+UBERON:0005052,gizzard,UBERON:0000945,stomach
+UBERON:0009967,spleen venous sinus,UBERON:0006615,venous sinus
+UBERON:0010851,fibula cartilage element,UBERON:0015013,fibula endochondral element
+CL:1000333,serous cell of epithelium of lobular bronchiole,CL:1000272,lung secretory cell
+UBERON:0003838,abdominal segment connective tissue,UBERON:0003586,trunk connective tissue
+UBERON:0001315,superior gluteal artery,UBERON:0001637,artery
+DOID:3850,hemangiopericytic tumor,DOID:3316,perivascular tumor
+HP:0001696,Situs inversus totalis,HP:0003363,Abdominal situs inversus
+DOID:2018,hyperinsulinism,DOID:4194,glucose metabolism disease
+HP:0008753,Aplasia of the epiglottis,HP:0010565,Aplasia/Hypoplasia of the Epiglottis
+UBERON:0002061,truncus arteriosus,UBERON:0002050,embryonic structure
+HP:0000921,Missing ribs,HP:0006712,Aplasia/Hypoplasia of the ribs
+HP:0100734,Abnormality of the vertebral epiphyses,HP:0005930,Abnormality of the epiphyses
+UBERON:0000980,trochanter,UBERON:0004120,mesoderm-derived structure
+UBERON:0001742,epiglottic cartilage,UBERON:0001996,elastic cartilage tissue
+HP:0008953,Pectoralis major hypoplasia,HP:0011957,Abnormality of the  pectoral muscle
+HP:0000711,Restlessness,HP:0100851,Abnormal emotion/affect behavior
+HP:0007774,Hypoplasia of the ciliary body,HP:0008055,Aplasia/Hypoplasia affecting the uvea
+UBERON:0001593,venous plexus,UBERON:0005629,vascular plexus
+DOID:8438,afferent loop syndrome,DOID:8439,postgastrectomy syndrome
+UBERON:0013481,crypt of Lieberkuhn of ileum,UBERON:0001241,crypt of Lieberkuhn of small intestine
+HP:0100781,Abnormality of the sacroiliac joint,HP:0005107,Abnormality of the sacrum
+DOID:3541,cerebral ventricle cancer,DOID:368,cerebrum cancer
+HP:0000054,Micropenis,HP:0008736,Hypoplasia of penis
+UBERON:0005561,telencephalon lateral wall,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0009854,digestive tract diverticulum,UBERON:0009856,sac
+DOID:4681,bile duct mucoepidermoid carcinoma,DOID:4897,bile duct carcinoma
+UBERON:0010744,sacral vertebra pre-cartilage condensation,UBERON:0011095,vertebra pre-cartilage condensation
+HP:0000843,Hyperparathyroidism,HP:0011767,Abnormality of the parathyroid physiology
+HP:0005240,Esophageal obstruction,HP:0004796,Gastrointestinal obstruction
+UBERON:0001776,optic choroid,UBERON:0002203,vasculature of eye
+UBERON:0006608,corpus cavernosum clitoridis,UBERON:0014404,female anatomical structure
+HP:0008041,Late onset congenital glaucoma,HP:0001087,Congenital glaucoma
+HP:0009948,Duplication of the distal phalanx of the 2nd finger,HP:0009945,Duplication of phalanx of 2nd finger
+HP:0100387,Aplasia of the middle phalanges of the toes,HP:0010745,Aplasia of the phalanges of the toes
+HP:0010752,Cleft mandible,HP:0010753,Midline defect of mandible
+HP:0001615,Hoarse cry,HP:0001609,Hoarse voice
+HP:0010872,EKG: T-wave inversion,HP:0005135,EKG: T-wave abnormalities
+UBERON:0010129,femur cartilage element,UBERON:0010881,limb cartilage element
+UBERON:0012150,skeleton of digitopodium,UBERON:0004120,mesoderm-derived structure
+HP:0009265,Fragmentation of the epiphysis of the proximal phalanx of the 4th finger,HP:0009248,Abnormality of the epiphysis of the proximal phalanx of the 4th finger
+UBERON:3010584,mandibular arch neural crest,UBERON:0004121,ectoderm-derived structure
+HP:0012318,Occipital neuralgia,HP:0002315,Headache
+DOID:2773,contact dermatitis,DOID:2723,dermatitis
+DOID:1625,breast adenoma,DOID:0060082,breast benign neoplasm
+UBERON:0002043,dorsal raphe nucleus,UBERON:0007415,nucleus of midbrain reticular formation
+DOID:14049,phaeohyphomycosis,DOID:0050292,primary systemic mycosis
+CL:0002152,columnar cell of endocervix,CL:0002149,epithelial cell of uterus
+DOID:4534,Hallermann-Streiff syndrome,DOID:225,syndrome
+UBERON:0009471,dorsum of tongue,UBERON:0000064,organ part
+DOID:10575,calcium metabolism disease,DOID:0050032,mineral metabolism disease
+DOID:1647,female breast upper-inner quadrant cancer,DOID:0050671,female breast cancer
+HP:0008715,Testicular dysgenesis,HP:0000035,Abnormality of the testis
+HP:0010404,Aplasia/Hypoplasia of the middle phalanx of the 2nd toe,HP:0010347,Aplasia/Hypoplasia of the phalanges of the 2nd toe
+UBERON:0010706,parenchyma of caudate lobe of liver,UBERON:0005222,liver left lobe parenchyma
+UBERON:2001649,basihyal tooth,UBERON:0001091,calcareous tooth
+DOID:7223,breast giant fibroadenoma,DOID:1618,breast fibroadenoma
+HP:0010937,Abnormality of the nasal skeleton,HP:0000366,Abnormality of the nose
+UBERON:0003081,lateral plate mesoderm,UBERON:0004120,mesoderm-derived structure
+DOID:3633,beta-mannosidosis,DOID:3211,lysosomal storage disease
+HP:0009550,Osteolytic defects of the phalanges of the 2nd finger,HP:0009541,Abnormality of the phalanges of the 2nd finger
+UBERON:0009653,trachea basement membrane,UBERON:0015329,respiratory system basement membrane
+UBERON:0010848,radius-ulna cartilage element,UBERON:0015002,radius-ulna endochondral element
+UBERON:0005599,common dorsal aorta,UBERON:0003513,trunk blood vessel
+DOID:6948,malignant gastric teratoma,DOID:4716,malignant gastric germ cell tumor
+DOID:396,Loeffler endocarditis,DOID:397,restrictive cardiomyopathy
+HP:0009304,Patchy sclerosis of the distal phalanx of the 4th finger,HP:0009840,Patchy sclerosis of the distal phalanges of the hand
+UBERON:0002270,hyaloid artery,UBERON:0003496,head blood vessel
+DOID:9790,toxocariasis,DOID:883,parasitic helminthiasis infectious disease
+DOID:9643,babesiosis,DOID:2789,parasitic protozoa infectious disease
+HP:0003855,Spurred metaphyses of the upper limbs,HP:0005054,Metaphyseal spurs
+UBERON:0002279,vestibular aqueduct,UBERON:0004120,mesoderm-derived structure
+UBERON:0004361,stylohyoid ligament,UBERON:0010313,neural crest-derived structure
+UBERON:0006842,lymphatic capillary,UBERON:0001473,lymphatic vessel
+HP:0004841,Reduced factor XII activity,HP:0010989,Abnormality of the intrinsic pathway
+CL:1001588,colon glandular cell,CL:0011108,colon epithelial cell
+UBERON:0012314,embryonic facial prominence,UBERON:0005423,developing anatomical structure
+HP:0011296,EEG with temporal sharp waves,HP:0011196,EEG with focal sharp waves
+UBERON:0002488,helix,UBERON:0001444,subdivision of head
+HP:0100069,Enlarged epiphyses of the 4th toe,HP:0010335,Abnormality of the epiphyses of the 4th toe
+CL:0002413,"mature Vgamma1.1-positive, Vdelta6.3-negative thymocyte",CL:0002411,"Vgamma1.1-positive, Vdelta6.3-negative thymocyte"
+UBERON:2002021,ascending process of the parasphenoid,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0008480,Cervical spondylosis,HP:0003319,Abnormality of the cervical spine
+UBERON:0007317,superficial external pudendal artery,UBERON:0013137,external pudendal artery
+HP:0000962,Hyperkeratosis,HP:0011368,Epidermal thickening
+HP:0009541,Abnormality of the phalanges of the 2nd finger,HP:0009774,Triangular shaped phalanges of the hand
+UBERON:0011132,intercarpal joint,UBERON:0001489,manus joint
+DOID:5766,pulmonary sclerosing hemangioma,DOID:495,sclerosing hemangioma
+UBERON:3000828,margo posterior of cleithrum,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:4258,Weissenbacher-Zweymüller syndrome,DOID:2256,osteochondrodysplasia
+HP:0009101,Submucous cleft lip,HP:0000204,Cleft upper lip
+UBERON:2001607,basipterygoid process of parasphenoid,UBERON:0004120,mesoderm-derived structure
+UBERON:0013764,common crus of semicircular duct,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0011892,anterior uvea,UBERON:0000481,multi-tissue structure
+HP:0100149,Enlarged epiphysis of the middle phalanx of the 3rd toe,HP:0100058,Enlarged epiphyses of the 3rd toe
+CL:0002038,T follicular helper cell,CL:0000492,CD4-positive helper T cell
+HP:0000492,Abnormality of the eyelid,HP:0000606,Abnormality of the periorbital region
+UBERON:0009629,coccygeal nerve,UBERON:0015212,lateral structure
+UBERON:0007521,smooth muscle sphincter,UBERON:0001135,smooth muscle tissue
+HP:0010001,Complete duplication of the distal phalanges of the hand,HP:0009883,Duplication of the distal phalanx of hand
+UBERON:0001038,chordotonal organ,UBERON:0000020,sense organ
+UBERON:0005397,brain arachnoid mater,UBERON:0003547,brain meninx
+HP:0000463,Anteverted nares,HP:0005105,Abnormal nasal morphology
+HP:0001300,Parkinsonism,HP:0002071,Abnormality of extrapyramidal motor function
+UBERON:0003868,proximal phalanx of pes,UBERON:0004302,proximal phalanx
+UBERON:0001342,mesovarium,UBERON:0005156,reproductive structure
+UBERON:0010022,ventral part of pharyngeal pouch 1,UBERON:0005911,endo-epithelium
+DOID:529,blepharospasm,DOID:0050836,focal dystonia
+DOID:3302,chordoma,DOID:3303,notochordal cancer
+HP:0011875,Abnormal platelet morphology,HP:0001872,Abnormality of thrombocytes
+DOID:3184,spinal cord oligodendroglioma,DOID:3185,spinal cord glioma
+HP:0002027,Abdominal pain,HP:0011458,Abdominal symptom
+UBERON:2007003,ventro-caudal cluster,UBERON:0001891,midbrain
+DOID:0060068,marantic endocarditis,DOID:10314,endocarditis
+UBERON:0001798,vitreous body,UBERON:0003566,head connective tissue
+HP:0009446,Triangular shaped phalanges of the 3rd finger,HP:0009316,Abnormality of the phalanges of the 3rd finger
+CL:0002495,fetal cardiomyocyte,CL:0000746,cardiac muscle cell
+UBERON:0005012,mucosa of left uterine tube,UBERON:0005048,mucosa of uterine tube
+HP:0002754,Osteomyelitis,HP:0011843,Abnormality of skeletal physiology
+HP:0010263,Ivory epiphyses of the middle phalanges of the hand,HP:0010244,Abnormality of the epiphyses of the middle phalanges of the hand
+DOID:10817,sexual sadism,DOID:0060043,sexual disorder
+UBERON:2000977,somite 19,UBERON:0002329,somite
+DOID:0060033,autoimmune disease of peripheral nervous system,DOID:438,autoimmune disease of the nervous system
+UBERON:0002186,bronchiole,UBERON:0000117,respiratory tube
+UBERON:0001523,flexor digitorum profundus,UBERON:0004255,forelimb stylopod muscle
+HP:0012055,Ciliary body melanoma,HP:0007716,Intraocular melanoma
+UBERON:0004797,blood vessel layer,UBERON:0004120,mesoderm-derived structure
+HP:0010983,Oligogenic inheritance,HP:0001426,Multifactorial inheritance
+CL:0000048,multi fate stem cell,CL:0000723,somatic stem cell
+HP:0012094,Abnormal pancreas size,HP:0012090,Abnormality of pancreas morphology
+UBERON:0013129,bulb of vestibule,UBERON:0000064,organ part
+HP:0012407,Scissor gait,HP:0001288,Gait disturbance
+HP:0009816,Lower limb undergrowth,HP:0006493,Aplasia/Hypoplasia involving bones of the lower limbs
+UBERON:0010368,pulmonary lobule,UBERON:0009911,lobule
+UBERON:0012335,navicular bursa of manus,UBERON:0012334,navicular bursa
+UBERON:2005104,presumptive dorsal fin fold,UBERON:2005102,presumptive median fin fold
+DOID:8505,dermatitis herpetiformis,DOID:0060039,autoimmune disease of skin and connective tissue
+UBERON:0012297,male urethral crest,UBERON:0012296,urethral crest
+NCBITaxon:147545,Eurotiomycetes,NCBITaxon:716546,leotiomyceta
+UBERON:0002843,seventh cervical dorsal root ganglion,UBERON:0002834,cervical dorsal root ganglion
+HP:0009959,Duplication of phalanx of 3rd finger,HP:0009997,Duplication of phalanx of hand
+DOID:6931,papillary extrahepatic bile duct adenocarcinoma,DOID:3495,extrahepatic bile duct adenocarcinoma
+UBERON:0004167,orbitofrontal cortex,UBERON:0002619,regional part of cerebral cortex
+HP:0009205,Cone-shaped epiphysis of the middle phalanx of the 5th finger,HP:0009384,Cone-shaped epiphyses of the 5th finger
+DOID:9305,splenic tuberculosis,DOID:0050599,abdominal tuberculosis
+CL:1000448,epithelial cell of sweat gland,CL:0002308,epithelial cell of skin gland
+HP:0009686,Absent epiphyses of the thumb,HP:0009599,Abnormality of the epiphyses of the thumb
+UBERON:0005339,outflow tract pulmonary component,UBERON:0004145,outflow tract
+UBERON:0013153,arachnoid villus,UBERON:0004121,ectoderm-derived structure
+DOID:6687,Achenbach syndrome,DOID:37,skin disease
+HP:0012567,Premature epimetaphyseal fusion in ulna,HP:0010588,Premature epimetaphyseal fusion
+DOID:4078,tricuspid valve stenosis,DOID:0050826,tricuspid valve disease
+UBERON:0002108,small intestine,UBERON:0013765,digestive system organ
+CL:0002396,"CD14-low, CD16-positive monocyte",CL:0002397,"CD14-positive, CD16-positive monocyte"
+UBERON:0005623,semi-lunar valve,UBERON:0000946,cardial valve
+DOID:5923,distal biliary tract carcinoma,DOID:4897,bile duct carcinoma
+UBERON:0001627,middle cerebral artery,UBERON:0004449,cerebral artery
+HP:0010507,Foot asymmetry,HP:0001760,Abnormality of the foot
+DOID:5639,rete testis neoplasm,DOID:3856,male reproductive organ cancer
+CL:0000623,natural killer cell,CL:0000542,lymphocyte
+UBERON:1000010,mole,UBERON:0004120,mesoderm-derived structure
+HP:0002173,Hypoglycemic seizures,HP:0001943,Hypoglycemia
+UBERON:0005083,nipple sheath,UBERON:0001003,skin epidermis
+UBERON:0014766,right crus of diaphragm,UBERON:0015212,lateral structure
+HP:0000291,Abnormality of facial adipose tissue,HP:0011799,Abnormality of facial soft tissue
+HP:0006247,Enlarged interphalangeal joints,HP:0003037,Enlarged joints
+HP:0006067,Multiple carpal ossification centers,HP:0005921,Abnormal ossification of hand bones
+HP:0009389,Pseudoepiphyses of the 5th finger,HP:0010235,Pseudoepiphyses of the phalanges of the hand
+HP:0010667,Aplasia of the maxilla,HP:0009117,Aplasia/Hypoplasia of the maxilla
+UBERON:0009995,tertiary chorionic villus,UBERON:0007106,chorionic villus
+DOID:874,bacterial pneumonia,DOID:552,pneumonia
+HP:0100882,Fibrous hamartoma,HP:0010566,Hamartoma
+UBERON:0010855,skin of forelimb wing,UBERON:0003531,forelimb skin
+UBERON:0011139,synovial limb joint,UBERON:0002217,synovial joint
+HP:0000593,Abnormality of the anterior chamber,HP:0004328,Abnormality of the anterior segment of the eye
+DOID:1130,pituitary infarct,DOID:3646,necrosis of pituitary
+UBERON:3000264,lamina superior,UBERON:0010313,neural crest-derived structure
+DOID:0050868,hepatocellular adenoma,DOID:657,adenoma
+UBERON:0000458,endocervix,UBERON:0005156,reproductive structure
+UBERON:0010272,hyoid apparatus,UBERON:0000075,subdivision of skeletal system
+DOID:560,jaw-winking syndrome,DOID:5656,cranial nerve disease
+DOID:10691,fat necrosis of breast,DOID:3463,breast disease
+UBERON:0015018,malleus endochondral element,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:2433,epidermal appendage tumor,DOID:3165,skin benign neoplasm
+UBERON:0004333,proximal phalanx of pedal digit 2,UBERON:0014502,proximal phalanx of digit 2
+UBERON:0004187,Harderian gland,UBERON:0015153,medial gland of orbital region
+HP:0005001,Recurrent patellar dislocation,HP:0002999,Patellar dislocation
+HP:0000113,Polycystic kidney dysplasia,HP:0000107,Renal cyst
+UBERON:0006763,epithelium of conjunctiva,UBERON:0010304,non-keratinized stratified squamous epithelium
+HP:0004309,Ventricular preexcitation,HP:0004308,Ventricular arrhythmia
+UBERON:0011638,pharyngeal arch 8,UBERON:0008896,post-hyoid pharyngeal arch
+UBERON:0007257,intervertebral disk of sacral vertebra,UBERON:0001066,intervertebral disk
+UBERON:0003714,neural tissue,UBERON:0000479,tissue
+UBERON:0003539,left lung bronchiole,UBERON:0002186,bronchiole
+CL:0000984,IgA plasmablast,CL:0000980,plasmablast
+HP:0002544,Retrocollis,HP:0000473,Torticollis
+UBERON:0007630,septohippocampal nucleus,UBERON:0009663,telencephalic nucleus
+UBERON:4200028,adductor blade,UBERON:4100000,skeletal element projection
+HP:0100169,Absent epiphysis of the distal phalanx of the 4th toe,HP:0100066,Absent epiphyses of the 4th toe
+CL:0000716,lymph gland crystal cell,CL:0000392,crystal cell
+HP:0100850,Neoplasia of the penis,HP:0100848,Neoplasia of the male external genitalia
+DOID:2862,glucosephosphate dehydrogenase deficiency,DOID:2978,carbohydrate metabolic disorder
+UBERON:0008437,posterior arch of atlas,UBERON:0005814,arch of atlas
+UBERON:0007486,fluid-based anatomical entity,UBERON:0000481,multi-tissue structure
+HP:0008790,Widened proximal femoral metaphyses,HP:0006417,Broad femoral metaphyses
+UBERON:0008442,webbed pes,UBERON:0002387,pes
+UBERON:0001067,vertebral arch joint,UBERON:0004120,mesoderm-derived structure
+UBERON:2000210,gigantocellular part of magnocellular preoptic nucleus,UBERON:0004121,ectoderm-derived structure
+HP:0009549,Curved phalanges of the 2nd finger,HP:0009770,Curved phalanges of the hand
+UBERON:0010852,fibula pre-cartilage condensation,UBERON:0005259,lower leg mesenchyme
+UBERON:0011370,transverse process of atlas,UBERON:0001077,transverse process of vertebra
+UBERON:0001075,vertebral centrum,UBERON:0004765,skeletal element
+UBERON:0002490,frontal suture,UBERON:0003685,cranial suture
+HP:0100663,Synotia,HP:0000357,Abnormal location of ears
+HP:0003320,C1-C2 subluxation,HP:0003308,Cervical subluxation
+UBERON:0006562,pharynx,UBERON:0004921,subdivision of digestive tract
+HP:0100416,Partial duplication of the distal phalanx of the 3rd toe,HP:0100398,Duplication of the distal phalanx of the 3rd toe
+HP:0002036,Hiatus hernia,HP:0002577,Abnormality of the stomach
+HP:0010106,Aplasia of the proximal phalanx of the hallux,HP:0010085,Aplasia/Hypoplasia of the proximal phalanx of the hallux
+UBERON:3000020,anterolateral process of frontoparietal,UBERON:0004530,bony projection
+UBERON:0003110,otic region,UBERON:0004120,mesoderm-derived structure
+UBERON:0006215,rhombic lip,UBERON:0001048,primordium
+HP:0005306,Capillary hemangiomas,HP:0001028,Hemangioma
+DOID:7081,lung mixed small cell and squamous cell carcinoma,DOID:5410,pulmonary neuroendocrine tumor
+HP:0010651,Abnormality of the meninges,HP:0007319,Morphological abnormality of the central nervous system
+HP:0100309,Subdural hemorrhage,HP:0002170,Intracranial hemorrhage
+HP:0010776,Tracheobronchmegaly,HP:0010778,Tracheomegaly
+DOID:3763,hermaphroditism,DOID:1923,sex differentiation disease
+HP:0009323,Cone-shaped epiphysis of the middle phalanx of the 3rd finger,HP:0009412,Cone-shaped epiphyses of the 3rd finger
+UBERON:0010209,plica semilunaris of conjunctiva,UBERON:0004121,ectoderm-derived structure
+HP:0005725,Nonopposable triphalangeal thumb,HP:0001199,Triphalangeal thumb
+UBERON:0003276,skeleton of embryo,UBERON:0002050,embryonic structure
+CL:0002333,neural crest derived fat cell,CL:0000136,fat cell
+HP:0000384,Preauricular skin tag,HP:0010609,Skin tags
+UBERON:0002401,visceral pleura,UBERON:0000977,pleura
+CL:0000669,pericyte cell,CL:0000630,supportive cell
+DOID:4780,anti-basement membrane glomerulonephritis,DOID:2921,glomerulonephritis
+HP:0100151,Irregular epiphysis of the middle phalanx of the 3rd toe,HP:0100092,Abnormality of the epiphysis of the middle phalanx of the 3rd toe
+UBERON:0014765,crus of diaphragm,UBERON:0004120,mesoderm-derived structure
+UBERON:0003654,metatarsal bone of digit 5,UBERON:0015041,pedal digit 5 metatarsal endochondral element
+HP:0001579,Primary hypercorticolism,HP:0001578,Hypercortisolism
+UBERON:0015150,dorsal hair,UBERON:0001037,strand of hair
+HP:0008663,Renal sarcoma,HP:0100242,Sarcoma
+UBERON:0009075,membrana tympaniformis,UBERON:0000060,anatomical wall
+HP:0100222,Stippling of the epiphysis of the middle phalanx of the 5th toe,HP:0100086,Stippling of the epiphyses of the 5th toe
+HP:0001289,Confusion,HP:0004372,Reduced consciousness/confusion
+CL:0000516,perineuronal satellite cell,CL:0000243,glial cell (sensu Vertebrata)
+UBERON:0004520,striated muscle tissue of prostate,UBERON:0001134,skeletal muscle tissue
+UBERON:0009505,associated mesenchyme of trachea,UBERON:0007524,dense mesenchyme tissue
+HP:0003321,Biconcave flattened vertebrae,HP:0000926,Platyspondyly
+DOID:10908,hydrocephalus,DOID:9428,intracranial hypertension
+DOID:4138,bile duct disease,DOID:9741,biliary tract disease
+HP:0009260,Triangular epiphysis of the distal phalanx of the 4th finger,HP:0009249,Abnormality of the epiphysis of the distal phalanx of the 4th finger
+UBERON:0005385,nasal cavity respiratory epithelium,UBERON:0005384,nasal cavity epithelium
+CL:1000411,endothelial cell of peyer's patch,CL:0002254,epithelial cell of small intestine
+UBERON:0011183,corpus spongiosum of penis,UBERON:0008324,erectile tissue
+UBERON:0004622,sacral vertebra 1,UBERON:0001094,sacral vertebra
+HP:0009292,Broad distal phalanx of the 4th finger,HP:0009404,Broad phalanges of the 4th finger
+UBERON:0006959,mandible angular process,UBERON:4100000,skeletal element projection
+HP:0011348,Abnormality of the sixth cranial nerve,HP:0001291,Abnormality of the cranial nerves
+UBERON:0009974,lumen of Rathke's pouch,UBERON:0005082,tube lumen
+UBERON:2001073,axial vasculature,UBERON:0002049,vasculature
+UBERON:2005093,nasal vein,UBERON:0003496,head blood vessel
+DOID:3856,male reproductive organ cancer,DOID:193,reproductive organ cancer
+HP:0010959,Congenital cystic adenomatoid malformation of the lung,HP:0005948,Cystic lung disease
+DOID:6370,hepatic osteogenic sarcoma,DOID:3357,extraosseous osteosarcoma
+HP:0002948,Vertebral fusion,HP:0003468,Abnormality of the vertebrae
+DOID:8596,scarlet fever,DOID:974,upper respiratory tract disease
+NCBITaxon:31957,Propionibacteriaceae,NCBITaxon:85009,Propionibacterineae
+HP:0011248,Everted antitragus,HP:0009896,Abnormality of the antitragus
+DOID:3211,lysosomal storage disease,DOID:655,inherited metabolic disorder
+UBERON:0003934,mesenchyme pectoral fin,UBERON:0003104,mesenchyme
+HP:0009904,Prominent ear helix,HP:0011039,Abnormality of the helix
+DOID:26,pancreas disease,DOID:28,endocrine system disease
+UBERON:0006115,posterior column of fornix,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0003947,Delayed elbow epiphyseal ossification,HP:0003946,Abnormality of the epiphyses of the elbow
+CL:0001002,mature CD8_alpha-negative CD11b-negative dendritic cell,CL:0000841,mature conventional dendritic cell
+UBERON:0002848,fifth thoracic dorsal root ganglion,UBERON:0002835,thoracic dorsal root ganglion
+HP:0001969,Tubulointerstitial abnormality,HP:0000091,Abnormality of the renal tubule
+HP:0010364,Patchy sclerosis of the phalanges of the 3rd toe,HP:0100927,Sclerosis of the phalanges of the 3rd toe
+CL:0002510,"CD103-negative, langerin-positive lymph node dendritic cell",CL:0002454,"Cd4-negative, CD8_alpha-negative, CD11b-positive dendritic cell"
+UBERON:0010356,primary ossification center,UBERON:0010355,ossification center
+UBERON:0001310,umbilical artery,UBERON:0010260,umbilical blood vessel
+HP:0010908,Abnormality of lysine metabolism,HP:0010899,Abnormality of aspartate family amino acid metabolism
+UBERON:0003610,heart elastic tissue,UBERON:0003613,cardiovascular system elastic tissue
+UBERON:0005298,skin of clitoris,UBERON:0000014,zone of skin
+UBERON:0003961,cingulum of brain,UBERON:0004121,ectoderm-derived structure
+HP:0011604,Aortopulmonary window,HP:0011603,Congenital malformation of the great arteries
+HP:0100373,Aplasia/Hypoplasia of the middle phalanx of the 4th toe,HP:0010381,Abnormality of the middle phalanx of the 4th toe
+UBERON:0006250,infundibular recess of 3rd ventricle,UBERON:0012275,meso-epithelium
+HP:0100135,Absent epiphysis of the distal phalanx of the 3rd toe,HP:0100055,Absent epiphyses of the 3rd toe
+UBERON:0003551,midbrain pia mater,UBERON:0003549,brain pia mater
+CL:0000944,Be2 cell,CL:0000968,Be cell
+UBERON:0004865,actinopterygian parietal bone,UBERON:0011164,neurocranium bone
+HP:0003781,Excessive salivation,HP:0100755,Abnormality of salivation
+UBERON:0008460,superior articular process of thoracic vertebra,UBERON:0001079,superior articular process of vertebra
+UBERON:0008588,procerus,UBERON:0008522,nasal muscle
+HP:0008772,Aplasia/Hypoplasia of the external ear,HP:0008771,Aplasia/Hypoplasia of the ear
+NCBITaxon:172148,Alkhumra hemorrhagic fever virus,NCBITaxon:33743,Kyasanur forest disease virus
+HP:0012113,Abnormality of creatine metabolism,HP:0004337,Abnormality of amino acid metabolism
+HP:0010081,Patchy sclerosis of the distal phalanx of the hallux,HP:0010190,Patchy sclerosis of the distal phalanges of the toes
+HP:0011075,Green teeth,HP:0011073,Abnormality of dental color
+HP:0100543,Cognitive impairment,HP:0011446,Abnormality of higher mental function
+HP:0010418,Patchy sclerosis of the distal phalanx of the 2nd toe,HP:0100939,Sclerosis of the distal phalanx of the 2nd toe
+HP:0007824,Total ophthalmoplegia,HP:0000602,Ophthalmoplegia
+CL:0000565,fat body cell,CL:0000181,metabolising cell
+HP:0003071,Flattened epiphyses,HP:0005930,Abnormality of the epiphyses
+DOID:9210,geniculate herpes zoster,DOID:934,viral infectious disease
+DOID:2089,constipation,DOID:5353,colonic disease
+DOID:14268,sclerosing cholangitis,DOID:9446,cholangitis
+UBERON:0012651,mucosa of gastroduodenal junction,UBERON:0001199,mucosa of stomach
+CL:1000441,epithelial cell of viscerocranial mucosa,CL:0002371,somatic cell
+DOID:6016,adult central nervous system mature teratoma,DOID:6015,adult central nervous system teratoma
+DOID:11446,Sciatic Neuropathy,DOID:12528,lesion of sciatic nerve
+HP:0010136,Stippling of the epiphysis of the proximal phalanx of the hallux,HP:0010126,Abnormality of the epiphysis of the proximal phalanx of the hallux
+UBERON:0003543,left lung respiratory bronchiole,UBERON:0002188,respiratory bronchiole
+HP:0007521,Irregular hyperpigmentation of back,HP:0007400,Irregular hyperpigmentation
+UBERON:3000408,pars media plectri,UBERON:0010313,neural crest-derived structure
+HP:0011766,Abnormality of the parathyroid morphology,HP:0000828,Abnormality of the parathyroid gland
+HP:0000953,Hyperpigmentation of the skin,HP:0001000,Abnormality of skin pigmentation
+HP:0000498,Blepharitis,HP:0000492,Abnormality of the eyelid
+DOID:1897,sigmoid disease,DOID:5353,colonic disease
+UBERON:0002197,median eminence of neurohypophysis,UBERON:0004120,mesoderm-derived structure
+HP:0004568,Beaking of vertebral bodies,HP:0003312,Abnormal form of the vertebral bodies
+UBERON:0002016,pulmonary vein,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0002432,"CD24-positive, CD4 single-positive thymocyte",CL:0000810,"CD4-positive, alpha-beta thymocyte"
+UBERON:3000601,tectum nasi,UBERON:0010313,neural crest-derived structure
+UBERON:0002160,nucleus prepositus,UBERON:0002680,regional part of metencephalon
+HP:0005207,Gastric hypertrophy,HP:0002577,Abnormality of the stomach
+UBERON:0004553,forelimb digital artery,UBERON:0004552,digital artery
+UBERON:0002767,inferior rostral sulcus,UBERON:0013118,sulcus of brain
+CL:0000371,protoplast,CL:0000578,experimentally modified cell in vitro
+UBERON:0011095,vertebra pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+HP:0001538,Protuberant abdomen,HP:0003270,Abdominal distention
+HP:0005037,Proximal radio-ulnar synostosis,HP:0002974,Radioulnar synostosis
+UBERON:0003998,hyoid bone lesser horn,UBERON:0010273,zone of hyoid bone
+CL:2000000,epidermal melanocyte,CL:1000458,melanocyte of skin
+UBERON:0015129,epicardial fat,UBERON:0003837,thoracic segment connective tissue
+HP:0000960,Sacral dimple,HP:0010767,Sacrococcygeal pilonidal abnormality
+HP:0010150,Bracket epiphysis of the 1st metatarsal,HP:0010114,Bracket epiphyses of the hallux
+DOID:10615,acute gonococcal cervicitis,DOID:10616,acute cervicitis
+HP:0009331,Triangular epiphysis of the middle phalanx of the 3rd finger,HP:0009420,Triangular epiphyses of the 3rd finger
+UBERON:2002107,medullary command nucleus,UBERON:0002616,regional part of brain
+HP:0100074,Small epiphyses of the 4th toe,HP:0010170,Small epiphyses of the toes
+HP:0009161,Aplasia/Hypoplasia of the middle phalanx of the 5th finger,HP:0004219,Abnormality of the middle phalanx of the 5th finger
+UBERON:0000412,dermal papilla,UBERON:0000479,tissue
+HP:0003384,Peripheral axonal atrophy,HP:0000764,Peripheral axonal degeneration
+HP:0007030,Nonprogressive encephalopathy,HP:0001298,Encephalopathy
+HP:0005722,Hyperextensible thumb,HP:0005639,Hyperextensible hand joints
+CL:1001509,glycinergic neuron,CL:0000540,neuron
+UBERON:0002372,tonsil,UBERON:0001962,gut-associated lymphoid tissue
+HP:0010174,Broad phalanx of the toes,HP:0010161,Abnormality of the phalanges of the toes
+UBERON:0010921,thyrohyoid ligament,UBERON:0008845,nonskeletal ligament
+UBERON:0008124,joint articular surface,UBERON:0008115,surface of cartilage
+UBERON:0010270,filum terminale externum,UBERON:0004121,ectoderm-derived structure
+DOID:482,hemangioma of peripheral nerve,DOID:255,hemangioma
+UBERON:0012248,cervical mucosa,UBERON:0000344,mucosa
+HP:0011636,Abnormal origin of the coronary arteries,HP:0006704,Abnormality of the coronary arteries
+DOID:0060184,lymphocytic colitis,DOID:0060182,microscopic colitis
+HP:0006485,Agenesis of incisor,HP:0001592,Selective tooth agenesis
+CL:1000353,microfold cell of epithelium of small intestine,CL:0000682,M cell of gut
+HP:0009173,Curved middle phalanx of the 5th finger,HP:0004214,Curved phalanges of the 5th finger
+DOID:6276,malignant ACTH producing neoplasm of pituitary gland,DOID:5716,hormone producing pituitary cancer
+UBERON:2000408,periventricular nucleus of caudal tuberculum,UBERON:0006569,diencephalic nucleus
+UBERON:0001305,ovarian follicle,UBERON:0000064,organ part
+HP:0006477,Abnormality of the alveolar ridges,HP:0000163,Abnormality of the oral cavity
+HP:0003653,Cellular metachromasia,HP:0011020,Abnormality of mucopolysaccharide metabolism
+HP:0002257,Chronic rhinitis,HP:0012384,Rhinitis
+UBERON:0012474,hepatic cecum,UBERON:0009854,digestive tract diverticulum
+HP:0012183,Hyperplastic colonic polyposis,HP:0200008,Intestinal polyposis
+HP:0002561,Absent nipples,HP:0006709,Aplasia/Hypoplasia of the nipples
+HP:0008551,Microtia,HP:0000377,Abnormality of the pinna
+HP:0008703,Gonadal calcification,HP:0010766,Ectopic calcification
+HP:0010883,Aortic valve atresia,HP:0001646,Abnormality of the aortic valve
+HP:0100157,Absent epiphysis of the proximal phalanx of the 3rd toe,HP:0100055,Absent epiphyses of the 3rd toe
+HP:0100830,Round ear,HP:0000377,Abnormality of the pinna
+HP:0009994,Partial duplication of the distal phalanx of the 5th finger,HP:0009988,Duplication of the distal phalanx of the 5th finger
+HP:0100820,Glomerulopathy,HP:0000095,Abnormality of the glomerulus
+UBERON:0002346,neurectoderm,UBERON:0004121,ectoderm-derived structure
+HP:0009574,Symphalangism of middle phalanx of 2nd finger,HP:0009545,Symphalangism of the 2nd finger
+UBERON:0011106,cruciate ligament of atlas,UBERON:0004267,back connective tissue
+CL:0008003,somatic muscle myotube,CL:0008004,somatic muscle cell
+DOID:9476,Sheehan syndrome,DOID:9406,hypopituitarism
+UBERON:3000784,ulnar condyle,UBERON:0004120,mesoderm-derived structure
+HP:0010967,Abnormality of carnitine metabolism,HP:0010966,Abnormality of fatty-acid anion metabolism
+UBERON:0002952,intermediate acoustic stria,UBERON:0014891,brainstem white matter
+HP:0009324,Enlarged epiphysis of the middle phalanx of the 3rd finger,HP:0009334,Abnormality of the epiphysis of the middle phalanx of the 3rd finger
+HP:0005213,Pancreatic calcification,HP:0012090,Abnormality of pancreas morphology
+CL:0000989,CD11c-low plasmacytoid dendritic cell,CL:0000784,plasmacytoid dendritic cell
+DOID:9235,pyriform sinus cancer,DOID:8533,hypopharynx cancer
+HP:0009751,Aplasia of the pectoralis major muscle,HP:0100854,Aplasia of the musculature
+HP:0009264,Enlarged epiphysis of the proximal phalanx of the 4th finger,HP:0009248,Abnormality of the epiphysis of the proximal phalanx of the 4th finger
+HP:0012170,Nail-biting,HP:0012169,Self-biting
+UBERON:0003609,aorta elastic tissue,UBERON:0003614,blood vessel elastic tissue
+HP:0012001,EEG with generalized polyspikes,HP:0011198,EEG with generalized epileptiform discharges
+UBERON:2000419,pterosphenoid,UBERON:0002513,endochondral bone
+UBERON:0010935,tensor tympani pre-muscle condensation,UBERON:0009506,associated mesenchyme of middle ear
+UBERON:0003216,hard palate,UBERON:0000477,anatomical cluster
+HP:0011475,Persistent stapedial artery,HP:0008609,Morphological abnormality of the middle ear
+CL:0000807,DN3 thymocyte,CL:0002489,double negative thymocyte
+HP:0100606,Neoplasm of the respiratory system,HP:0011793,Neoplasm by anatomical site
+HP:0009258,Small epiphysis of the distal phalanx of the 4th finger,HP:0010254,Small epiphyses of the distal phalanges of the hand
+HP:0001187,Hyperextensibility of the finger joints,HP:0001382,Joint hypermobility
+UBERON:2001312,dorsal anterior lateral line ganglion,UBERON:2001391,anterior lateral line ganglion
+HP:0011895,Anemia due to reduced life span of red cells,HP:0001903,Anemia
+UBERON:0006650,tunica vaginalis testis,UBERON:0000158,membranous layer
+UBERON:0008281,tooth bud,UBERON:0007499,epithelial sac
+UBERON:0001705,nail,UBERON:0009564,distal limb integumentary appendage
+HP:0002403,Positive Romberg sign,HP:0010831,Impaired proprioception
+HP:0004468,Anomalous tracheal cartilage,HP:0002778,Abnormality of the trachea
+UBERON:0009042,prostatic venous plexus,UBERON:0001593,venous plexus
+UBERON:0004385,epiphysis of radius,UBERON:0004120,mesoderm-derived structure
+UBERON:2002174,octaval nerve motor nucleus,UBERON:0000126,cranial nerve nucleus
+DOID:14397,protozoal dysentery,DOID:12384,dysentery
+CL:0000965,Bm3 B cell,CL:0000844,germinal center B cell
+UBERON:0001607,sphincter pupillae,UBERON:0004234,iris smooth muscle
+UBERON:3010758,M. coccygeocutaneus,UBERON:0010890,pelvic complex muscle
+DOID:4927,Klatskin's tumor,DOID:4928,intrahepatic cholangiocarcinoma
+CL:0000576,monocyte,CL:0000766,myeloid leukocyte
+HP:0000952,Jaundice,HP:0001396,Cholestasis
+HP:0009528,Fragmentation of the epiphysis of the proximal phalanx of the 2nd finger,HP:0009492,Fragmentation of the epiphyses of the 2nd finger
+HP:0004288,Pseudoepiphyses of hand bones,HP:0005924,Abnormality of the epiphyses of the hand
+HP:0011308,Slender toe,HP:0001780,Abnormality of toe
+UBERON:0005013,mucosa of male urethra,UBERON:0012299,mucosa of urethra
+UBERON:0004355,podocyte foot process,UBERON:0000470,cell part
+DOID:1657,ventricular septal defect,DOID:1681,heart septal defect
+HP:0008364,Abnormality of the calcaneus,HP:0001850,Abnormality of the tarsal bones
+HP:0002867,Abnormality of the ilium,HP:0003272,Abnormality of the hip bone
+DOID:2457,giant papillary conjunctivitis,DOID:2456,blepharoconjunctivitis
+HP:0009308,Symphalangism of middle phalanx of 4th finger,HP:0009283,Abnormality of the middle phalanx of the 4th finger
+HP:0004222,Cone-shaped epiphysis of the distal phalanx of the 5th finger,HP:0009198,Abnormality of the epiphysis of the distal phalanx of the 5th finger
+DOID:3609,breast mucinous cystadenocarcinoma,DOID:3610,breast mucinous carcinoma
+DOID:5559,mediastinal cancer,DOID:5093,thoracic cancer
+DOID:4787,cerebellopontine angle primitive neuroectodermal,DOID:3200,cerebellopontine angle tumor
+DOID:6383,childhood brain stem glioma,DOID:4206,childhood brain stem neoplasm
+UBERON:2001900,ceratobranchial 2 element,UBERON:2001898,ceratobranchial element
+HP:0100115,Fragmentation of the epiphysis of the middle phalanx of the 2nd toe,HP:0100048,Fragmentation of the epiphyses of the 2nd toe
+DOID:9553,adrenal gland disease,DOID:28,endocrine system disease
+HP:0011327,Posterior plagiocephaly,HP:0001357,Plagiocephaly
+UBERON:0011163,supraoccipital pre-cartilage condensation,UBERON:0015015,supraoccipital endochondral element
+HP:0010186,Broad distal phalanx of the toes,HP:0010174,Broad phalanx of the toes
+UBERON:0001197,ileocolic artery,UBERON:0004573,systemic artery
+UBERON:0003998,hyoid bone lesser horn,UBERON:0015212,lateral structure
+UBERON:0015062,bone condensation,UBERON:0005856,developing mesenchymal condensation
+DOID:9856,congenital syphilis,DOID:4166,syphilis
+UBERON:0002161,gracile nucleus,UBERON:0007635,nucleus of medulla oblongata
+UBERON:0001665,triceps surae,UBERON:0004256,hindlimb zeugopod muscle
+UBERON:0004397,epiphysis of third metatarsal bone,UBERON:0004389,epiphysis of metatarsal bone
+HP:0006463,Rickets of the lower limbs,HP:0002814,Abnormality of the lower limb
+UBERON:0015786,respiratory segment of nasal mucosa,UBERON:0001826,nasal cavity mucosa
+HP:0000308,Microretrognathia,HP:0000347,Micrognathia
+UBERON:0002815,horizontal fissure of cerebellum,UBERON:0003980,cerebellum fissure
+DOID:9588,encephalitis,DOID:936,brain disease
+HP:0010994,Abnormality of the striatum,HP:0002134,Abnormality of the basal ganglia
+DOID:7633,macular holes,DOID:5679,retinal disease
+DOID:914,peliosis hepatis,DOID:272,hepatic vascular disease
+HP:0009204,Bracket epiphysis of the middle phalanx of the 5th finger,HP:0009383,Bracket epiphyses of the 5th finger
+HP:0004610,Lumbar spinal canal stenosis,HP:0003416,Spinal canal stenosis
+UBERON:0013516,uterine tube magnum,UBERON:0013515,subdivision of uterine tube
+HP:0100105,Irregular epiphysis of the distal phalanx of the 2nd toe,HP:0100049,Irregular epiphyses of the 2nd toe
+HP:0007250,Recurrent external ophthalmoplegia,HP:0000544,External ophthalmoplegia
+UBERON:0003510,eyelid blood vessel,UBERON:0003496,head blood vessel
+CL:0000421,coelomocyte,CL:0000080,circulating cell
+CL:0002407,mature Vgamma2-positive thymocyte,CL:0002405,gamma-delta thymocyte
+UBERON:0000377,maxillary nerve,UBERON:0001021,nerve
+UBERON:0014401,renal venous blood vessel,UBERON:0003517,kidney blood vessel
+UBERON:0005884,hyoid arch skeleton,UBERON:0010912,subdivision of skeleton
+NCBITaxon:36734,Unikaryonidae,NCBITaxon:6032,Apansporoblastina
+HP:0001166,Arachnodactyly,HP:0010511,Long toe
+HP:0100173,Fragmentation of the epiphysis of the distal phalanx of the 4th toe,HP:0100094,Abnormality of the epiphysis of the distal phalanx of the 4th toe
+UBERON:0009952,dentate gyrus subgranular zone,UBERON:0000119,cell layer
+HP:0011399,Tibialis atrophy,HP:0008944,Distal lower limb amyotrophy
+DOID:7438,ovarian clear cell cystadenocarcinoma,DOID:3605,ovarian cystadenocarcinoma
+DOID:0050733,methylmalonic aciduria and homocystinuria type cblG,DOID:14749,methylmalonic acidemia
+HP:0000532,Chorioretinal abnormality,HP:0000610,Abnormality of the choroid
+HP:0012185,Constrictive median neuropathy,HP:0012181,Entrapment neuropathy
+UBERON:0002784,regional part of diencephalon,UBERON:0002780,regional part of forebrain
+DOID:8619,recurrent hypersomnia,DOID:535,sleep disorder
+UBERON:0000104,life cycle,UBERON:0000105,life cycle stage
+HP:0200021,Down-sloping shoulders,HP:0003043,Abnormality of the shoulder
+DOID:13207,proliferative diabetic retinopathy,DOID:8947,diabetic retinopathy
+DOID:293,lacrimal gland carcinoma,DOID:294,lacrimal gland cancer
+CL:0000129,microglial cell,CL:0000878,central nervous system macrophage
+UBERON:0006802,acetabular rim,UBERON:0004120,mesoderm-derived structure
+UBERON:0004572,arterial system,UBERON:0007798,vascular system
+HP:0001634,Mitral valve prolapse,HP:0001633,Abnormality of the mitral valve
+HP:0012755,Enlarged brainstem,HP:0002363,Abnormality of the brainstem
+UBERON:0002280,otolith,UBERON:0004121,ectoderm-derived structure
+HP:0007763,Retinal telangiectasia,HP:0008046,Abnormality of the retinal vasculature
+UBERON:2201819,dorsal fin proximal radial cartilage 2,UBERON:2200947,dorsal fin proximal radial cartilage
+UBERON:0014538,subdivision of spinal cord central canal,UBERON:0004121,ectoderm-derived structure
+HP:0012249,Abnormal ST segment,HP:0003115,Abnormal EKG
+DOID:0050696,fetal alcohol spectrum disorder,DOID:0060038,specific developmental disorder
+DOID:13214,hole retinal cyst,DOID:2007,degeneration of macula and posterior pole
+CL:0000811,"CD8-positive, alpha-beta thymocyte",CL:0000893,thymocyte
+CL:0000704,endothelial tip cell,CL:0000071,blood vessel endothelial cell
+DOID:0050490,parenchymatous neurosyphilis,DOID:9988,tertiary neurosyphilis
+HP:0010913,Hyperisoleucinemia,HP:0010912,Abnormality of isoleucine metabolism
+UBERON:2000630,caudal parvocellular preoptic nucleus,UBERON:0007251,preoptic nucleus
+HP:0009350,Fragmentation of the epiphysis of the proximal phalanx of the 3rd finger,HP:0009333,Abnormality of the epiphysis of the proximal phalanx of the 3rd finger
+HP:0010985,Gonosomal inheritance,HP:0000005,Mode of inheritance
+CL:0002107,IgD-negative CD38-positive IgG memory B cell,CL:0002105,CD38-positive IgG memory B cell
+UBERON:0004409,distal epiphysis of phalanx of manus,UBERON:0004448,distal epiphysis of phalanx
+DOID:4743,mixed testicular germ cell tumor,DOID:5556,testicular malignant germ cell cancer
+CL:0002503,adventitial cell,CL:0002320,connective tissue cell
+DOID:10017,Wermer syndrome,DOID:0050736,autosomal dominant disease
+DOID:12197,punctate epithelial keratoconjunctivitis,DOID:12196,superficial keratitis
+HP:0008452,Wafer-thin platyspondyly,HP:0004565,Severe platyspondyly
+HP:0012552,Increased neutrophil nuclear projections,HP:0011992,Abnormality of neutrophil morphology
+CL:1001126,inner renal medulla vasa recta cell,CL:1001036,vasa recta cell
+HP:0100394,Short middle phalanx of the 5th toe,HP:0100374,Aplasia/Hypoplasia of the middle phalanx of the 5th toe
+DOID:849,rheumatoid lung disease,DOID:417,hypersensitivity reaction type II disease
+DOID:8029,sporadic breast cancer,DOID:3459,breast carcinoma
+UBERON:0004546,cribriform plate,UBERON:0004120,mesoderm-derived structure
+HP:0002744,Bilateral cleft lip and palate,HP:0100336,Bilateral cleft lip
+UBERON:2001678,mesethmoid-frontal joint,UBERON:0000982,skeletal joint
+HP:0007443,Partial albinism,HP:0001010,Hypopigmentation of the skin
+CL:0009004,retinal cell,CL:0002371,somatic cell
+HP:0001803,Nail pits,HP:0002164,Nail dysplasia
+UBERON:0010852,fibula pre-cartilage condensation,UBERON:0015013,fibula endochondral element
+UBERON:0014406,nauplius stage,UBERON:0000069,larval stage
+UBERON:0003837,thoracic segment connective tissue,UBERON:0003586,trunk connective tissue
+UBERON:0007298,pronephric proximal convoluted tubule,UBERON:0001287,proximal convoluted tubule
+UBERON:0004730,instar larval stage,UBERON:0000069,larval stage
+HP:0007792,Microsaccadic pursuit,HP:0001152,Saccadic smooth pursuit
+HP:0003348,Hyperalaninemia,HP:0003112,Abnormality of serum amino acid levels
+UBERON:0002801,stratum zonale of thalamus,UBERON:0003931,diencephalic white matter
+DOID:0050155,sensory system disease,DOID:863,nervous system disease
+UBERON:0011273,nail of manual digit 1,UBERON:0009565,nail of manual digit
+UBERON:0006726,outer canthus,UBERON:0006742,canthus
+HP:0012752,Focal T2 hypointense basal ganglia lesion,HP:0012751,Abnormal basal ganglia MRI signal intensity
+DOID:14261,fragile X syndrome,DOID:1289,neurodegenerative disease
+DOID:62,aortic valve disease,DOID:4079,heart valve disease
+UBERON:0001463,manual digit 1,UBERON:0002389,manual digit
+UBERON:0001741,corniculate cartilage,UBERON:0001996,elastic cartilage tissue
+HP:0002728,Chronic mucocutaneous candidiasis,HP:0002841,Recurrent fungal infections
+UBERON:0001775,ciliary body,UBERON:0004121,ectoderm-derived structure
+UBERON:0001282,intralobular bile duct,UBERON:0003704,intrahepatic bile duct
+UBERON:3000903,tibial crest,UBERON:4100000,skeletal element projection
+UBERON:0013482,crypt of Lieberkuhn of duodenum,UBERON:0001241,crypt of Lieberkuhn of small intestine
+UBERON:2000677,segmental intercostal artery,UBERON:0005612,intercostal artery
+HP:0100230,Ivory epiphysis of the proximal phalanx of the 5th toe,HP:0100083,Ivory epiphyses of the 5th toe
+DOID:3893,hidrocystoma,DOID:5876,apocrine sweat gland neoplasm
+UBERON:0007418,decussation of neuraxis,UBERON:0002316,white matter
+UBERON:0003690,sacrum,UBERON:0008001,irregular bone
+UBERON:0006295,sternebral bone pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+DOID:7333,nephrogenic adenoma of urinary bladder,DOID:0050623,bladder benign neoplasm
+UBERON:3010523,M. plantaris longus,UBERON:0010890,pelvic complex muscle
+UBERON:2005079,posterior mesencephalic central artery,UBERON:2005020,central artery
+DOID:2736,Hajdu-Cheney syndrome,DOID:0050736,autosomal dominant disease
+DOID:2219,Glanzmann's thrombasthenia,DOID:2214,inherited blood coagulation disease
+HP:0003716,Generalized muscular appearance from birth,HP:0011805,Abnormality of muscle morphology
+HP:0009266,Irregular epiphysis of the proximal phalanx of the 4th finger,HP:0009248,Abnormality of the epiphysis of the proximal phalanx of the 4th finger
+HP:0100068,Cone-shaped epiphyses of the 4th toe,HP:0010335,Abnormality of the epiphyses of the 4th toe
+NCBITaxon:151340,Papillomaviridae,NCBITaxon:35237,"dsDNA viruses, no RNA stage"
+UBERON:3010186,outer metatarsal tubercle,UBERON:0005813,tubercle
+HP:0009539,Contracture of the metacarpophalangeal joint of the 2nd finger,HP:0009537,Flexion contracture of the 2nd finger
+HP:0008220,Hypocortisolemia,HP:0008207,Primary adrenal insufficiency
+CL:0000690,R2 photoreceptor cell,CL:0000488,visible light photoreceptor cell
+HP:0005598,Facial telangiectasia in butterfly midface distribution,HP:0007380,Facial telangiectasia
+UBERON:2000666,filamental artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+CL:0000367,sheath cell (sensu Nematoda),CL:0000619,support cell (sensu Nematoda)
+UBERON:0003235,epithelium of upper jaw,UBERON:0000490,unilaminar epithelium
+HP:0010302,Spinal cord tumor,HP:0100006,Neoplasm of the central nervous system
+UBERON:0002666,mesencephalic tract of trigeminal nerve,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2201417,pelvic fin distal radial cartilage 1,UBERON:1700006,paired fin radial cartilage
+HP:0000837,Gonadotropin excess,HP:0010514,Hyperpituitarism
+UBERON:0000437,arachnoid barrier layer,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002333,pulmonary trunk,UBERON:0001637,artery
+HP:0009560,Curved distal phalanx of the 2nd finger,HP:0009549,Curved phalanges of the 2nd finger
+HP:0100755,Abnormality of salivation,HP:0000163,Abnormality of the oral cavity
+UBERON:0009987,medial epicondyle of femur,UBERON:0009978,epicondyle
+HP:0008655,Aplasia/Hypoplasia of the fallopian tube,HP:0011027,Abnormality of the fallopian tube
+UBERON:4000030,oropharyngeal papilla,UBERON:0001763,odontogenic papilla
+UBERON:2002042,parapophysis 5,UBERON:0003109,parapophysis
+HP:0009331,Triangular epiphysis of the middle phalanx of the 3rd finger,HP:0010267,Triangular epiphyses of the middle phalanges of the hand
+UBERON:0004670,ependyma,UBERON:0007601,ciliated epithelium
+HP:0100470,Symphalangism affecting the middle phalanx of the 3rd toe,HP:0010365,Symphalangism affecting the phalanges of the 3rd toe
+HP:0100274,Gustatory lacrimation,HP:0001291,Abnormality of the cranial nerves
+HP:0100899,Sclerosis of the phalanges of the hand,HP:0005918,Abnormality of phalanx of finger
+DOID:3089,granulomatous orchitis,DOID:2519,testicular disease
+DOID:14069,cerebral malaria,DOID:12365,malaria
+HP:0007332,Hemifacial seizures,HP:0002266,Focal clonic seizures
+UBERON:0005037,mucosa of lobar bronchus,UBERON:0000410,bronchial mucosa
+UBERON:0003260,endoderm of hindgut,UBERON:0000925,endoderm
+UBERON:0005194,thoracic vein,UBERON:0001638,vein
+HP:0100197,Ivory epiphysis of the proximal phalanx of the 4th toe,HP:0100072,Ivory epiphyses of the 4th toe
+HP:0005906,Delayed pneumatization of the mastoid process,HP:0000264,Abnormality of the mastoid
+HP:0009989,Duplication of the middle phalanx of the 5th finger,HP:0010008,Duplication of the middle phalanx of hand
+HP:0010513,Pituitary calcification,HP:0011747,Abnormality of the anterior pituitary
+UBERON:0010021,dorsal part of pharyngeal pouch 1,UBERON:0005911,endo-epithelium
+DOID:0050645,arterial tortuosity syndrome,DOID:65,connective tissue disease
+UBERON:0001171,portal lobule,UBERON:0000064,organ part
+UBERON:0004946,submucosa of ileum,UBERON:0001205,submucosa of small intestine
+UBERON:3000829,margo scapularis,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3000141,endolymphatic system,UBERON:0004121,ectoderm-derived structure
+UBERON:2001186,collagenous dermal stroma,UBERON:0004121,ectoderm-derived structure
+UBERON:0002840,third cervical dorsal root ganglion,UBERON:0002834,cervical dorsal root ganglion
+HP:0003568,Decreased glucosephosphate isomerase activity,HP:0004366,Abnormality of glycolysis
+HP:0011180,Partial beta-EEG,HP:0011179,Beta-EEG
+UBERON:0004332,proximal phalanx of pedal digit 1,UBERON:0014501,proximal phalanx of digit 1
+UBERON:2002291,fulcrum,UBERON:0008907,dermal bone
+UBERON:2000663,extrascapula,UBERON:0007829,pectoral girdle bone
+DOID:0060214,FTDALS2,DOID:332,amyotrophic lateral sclerosis
+DOID:10154,small intestine cancer,DOID:10155,intestinal cancer
+DOID:0050821,first-degree atrioventricular block,DOID:0050820,atrioventricular block
+UBERON:0002987,anterior spinocerebellar tract,UBERON:0007702,tract of brain
+UBERON:3000031,ascending process of palatoquadrate,UBERON:4100000,skeletal element projection
+UBERON:0003550,forebrain pia mater,UBERON:0003548,forebrain meninges
+UBERON:0013398,choroidal gland,UBERON:0004121,ectoderm-derived structure
+CL:0002266,type D cell of small intestine,CL:1001598,small intestine glandular cell
+UBERON:0002633,motor nucleus of trigeminal nerve,UBERON:0002680,regional part of metencephalon
+HP:0000468,Increased adipose tissue around the neck,HP:0000464,Abnormality of the neck
+HP:0100192,Bracket epiphysis of the proximal phalanx of the 4th toe,HP:0100096,Abnormality of the epiphysis of the proximal phalanx of the 4th toe
+UBERON:3010240,Nobelian rod,UBERON:0014403,male anatomical structure
+UBERON:0011877,margin of tongue,UBERON:0006800,anatomical line
+UBERON:0010934,panniculus carnosus,UBERON:0002036,striated muscle tissue
+UBERON:0002613,globose nucleus,UBERON:0008995,nucleus of cerebellar nuclear complex
+UBERON:0006594,chorda gubernaculum,UBERON:0002050,embryonic structure
+UBERON:0006833,lumen of trachea,UBERON:0000464,anatomical space
+UBERON:0000166,oral opening,UBERON:0004121,ectoderm-derived structure
+UBERON:0002990,mammillothalamic tract of hypothalamus,UBERON:0011591,tract of diencephalon
+UBERON:0005751,visceral layer of glomerular capsule,UBERON:0004211,nephron epithelium
+UBERON:0015094,distal carpal bone 4 cartilage,UBERON:0010883,forelimb cartilage element
+UBERON:2002065,ural centrum 1,UBERON:2002085,ural centrum
+UBERON:0001231,nephron tubule,UBERON:0004211,nephron epithelium
+UBERON:0007374,incus cartilage element,UBERON:0015017,incus endochondral element
+DOID:5804,discrete subaortic stenosis,DOID:5805,subvalvular aortic stenosis
+DOID:7907,mixed astrocytoma-ependymoma,DOID:5076,mixed glioma
+UBERON:0009570,spinal cord sulcus limitans,UBERON:0005478,sulcus limitans of neural tube
+HP:0000588,Optic nerve coloboma,HP:0000587,Abnormality of the optic nerve
+UBERON:3010606,limb glands,UBERON:3000981,limb external integument structure
+HP:0002038,Protein avoidance,HP:0011458,Abdominal symptom
+UBERON:0000988,pons,UBERON:0002680,regional part of metencephalon
+DOID:6334,anterior optic tract meningioma,DOID:3419,optic nerve neoplasm
+HP:0000399,Prelingual sensorineural hearing impairment,HP:0011474,Childhood onset sensorineural hearing impairment
+HP:0009442,Curved phalanges of the 3rd finger,HP:0004095,Curved fingers
+DOID:10176,neuroretinitis,DOID:10175,optic papillitis
+DOID:8195,hepatoid pattern testicular yolk sac tumor,DOID:5344,testicular yolk sac tumor
+HP:0012197,Insulinoma,HP:0008261,Pancreatic islet cell adenoma
+DOID:13732,panophthalmitis,DOID:9724,purulent endophthalmitis
+HP:0001995,Hyperchloremic acidosis,HP:0001941,Acidosis
+DOID:10629,microphthalmia,DOID:5614,eye disease
+HP:0010271,Enlarged epiphyses of the proximal phalanges of the hand,HP:0010231,Enlarged epiphyses of the phalanges of the hand
+UBERON:4300111,lateral ethmoid element,UBERON:0010363,endochondral element
+DOID:14265,pulmonary valve insufficiency,DOID:5749,pulmonary valve disease
+DOID:6210,bladder diffuse clear cell adenocarcinoma,DOID:5306,bladder clear cell adenocarcinoma
+CL:0000098,sensory epithelial cell,CL:0000197,receptor cell
+UBERON:0002819,apex of cochlea,UBERON:0004120,mesoderm-derived structure
+UBERON:0005966,outflow part of left atrium,UBERON:0005946,outflow tract of atrium
+UBERON:0004800,bronchus basal lamina,UBERON:0004799,trachea basal lamina
+HP:0200042,Skin ulcer,HP:0011355,Localized skin lesion
+HP:0002398,Degeneration of anterior horn cells,HP:0002127,Upper motor neuron abnormality
+UBERON:0005323,mesonephric mesenchyme,UBERON:0004120,mesoderm-derived structure
+UBERON:0009913,renal lobe,UBERON:0009912,anatomical lobe
+DOID:9392,tracheitis,DOID:3225,tracheal disease
+NCBITaxon:66225,Phaeoannellomyces,NCBITaxon:36051,mitosporic Chaetothyriales
+HP:0012054,Choroidal melanoma,HP:0007716,Intraocular melanoma
+DOID:12134,factor VIII deficiency,DOID:0050735,X-linked disease
+CL:0000060,odontoblast,CL:0002159,general ecto-epithelial cell
+UBERON:0004124,myocardium trabecular layer,UBERON:0004123,myocardial layer
+UBERON:0006921,stomach squamous epithelium,UBERON:0000487,simple squamous epithelium
+UBERON:0005135,metanephric glomerular epithelium,UBERON:0005134,metanephric nephron epithelium
+HP:0012463,Elevated transferrin saturation,HP:0011031,Abnormality of iron homeostasis
+UBERON:2001869,supraneural 2 cartilage,UBERON:4300036,supraneural cartilage
+UBERON:0003023,pontine tegmentum,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005387,olfactory glomerulus,UBERON:0001047,neural glomerulus
+CL:0000762,nucleated thrombocyte,CL:0000763,myeloid cell
+HP:0000009,Functional abnormality of the bladder,HP:0000014,Abnormality of the bladder
+HP:0000698,Conical tooth,HP:0006482,Abnormality of dental morphology
+UBERON:0004766,cranial bone,UBERON:0003457,head bone
+CL:1001045,kidney cortex artery cell,CL:1000891,kidney arterial blood vessel cell
+HP:0008668,"Gonadal dysgenesis, male",HP:0000133,Gonadal dysgenesis
+DOID:0050590,severe congenital neutropenia,DOID:1227,neutropenia
+UBERON:2005103,presumptive ventral fin fold,UBERON:2005102,presumptive median fin fold
+UBERON:0003685,cranial suture,UBERON:0009198,craniofacial suture
+UBERON:2001579,ural vertebra 2,UBERON:2002162,ural vertebra
+HP:0005170,Complete heart block with broad RS complexes,HP:0001709,Third degree atrioventricular block
+UBERON:0012298,female urethral crest,UBERON:0012296,urethral crest
+UBERON:0009652,bronchus basement membrane,UBERON:0015329,respiratory system basement membrane
+DOID:8506,bullous pemphigoid,DOID:0060039,autoimmune disease of skin and connective tissue
+UBERON:0010952,frontalis,UBERON:0010938,muscle belly
+UBERON:0002895,secondary olfactory cortex,UBERON:0002619,regional part of cerebral cortex
+HP:0011701,Multifocal atrial tachycardia,HP:0001692,Primary atrial arrhythmia
+UBERON:0003976,saccule duct,UBERON:0010314,structure with developmental contribution from neural crest
+NCBITaxon:140564,Ornithodoros parkeri,NCBITaxon:6937,Ornithodoros
+UBERON:0009709,ventral pancreas,UBERON:0005177,trunk organ
+UBERON:0003029,stria terminalis,UBERON:0002316,white matter
+UBERON:0014870,inferior orbital fissure,UBERON:0006271,orbital fissure
+DOID:260,hepatic flexure cancer,DOID:218,ascending colon cancer
+UBERON:0005308,nephrostome,UBERON:0006554,urinary system structure
+HP:0000575,Scotoma,HP:0001123,Visual field defect
+UBERON:3010404,capillary system of liver,UBERON:0001982,capillary
+UBERON:0008447,intertarsal joint,UBERON:0001487,pes joint
+CL:0002511,"CD11b-low, CD103-negative, langerin-negative lymph node dendritic cell",CL:0002508,"langerin-negative, CD103-negative lymph node dendritic cell"
+CL:0002386,multinucleate macroconidium,CL:0000606,macroconidium
+DOID:0060090,central nervous system organ benign neoplasm,DOID:0060115,nervous system benign neoplasm
+UBERON:0011316,nerve to stylohyoid from facial nerve,UBERON:0002003,peripheral nerve
+UBERON:2005022,opercular artery,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000983,IgM plasmablast,CL:0000980,plasmablast
+HP:0006608,Midclavicular hypoplasia,HP:0000894,Short clavicles
+UBERON:0004623,sacral vertebra 2,UBERON:0001094,sacral vertebra
+HP:0008608,Hypertrophic auricular cartilage,HP:0000356,Abnormality of the outer ear
+UBERON:4200179,manual claw,UBERON:0009564,distal limb integumentary appendage
+DOID:5825,adult lymphoma,DOID:0060058,lymphoma
+UBERON:0003849,mesencephalic neural crest,UBERON:0002342,neural crest
+HP:0008209,Premature ovarian failure,HP:0000137,Abnormality of the ovary
+UBERON:0010697,pedal digit metatarsal cartilage element,UBERON:0003860,hindlimb mesenchyme
+DOID:7984,sclerosing breast papilloma,DOID:1626,breast duct papilloma
+NCBITaxon:29907,Sporothrix,NCBITaxon:117573,mitosporic Ophiostomataceae
+HP:0010433,Short distal phalanx of the 2nd toe,HP:0010413,Aplasia/Hypoplasia of the distal phalanx of the 2nd toe
+UBERON:0009734,sublaminar layers S2 or S3 or S4,UBERON:0008921,substratum of layer of retina
+UBERON:0003009,dorsal tegmental decussation,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100517,Neoplasm of the urethra,HP:0010786,Urinary tract neoplasm
+HP:0007773,Vitreoretinal abnormalities,HP:0004327,Abnormality of the vitreous humor
+UBERON:0011601,gingiva of upper jaw,UBERON:0001828,gingiva
+HP:0009345,Triangular epiphysis of the distal phalanx of the 3rd finger,HP:0010256,Triangular epiphyses of the distal phalanges of the hand
+HP:0008846,Severe intrauterine growth retardation,HP:0001511,Intrauterine growth retardation
+UBERON:0002922,olfactory trigone,UBERON:0002791,regional part of telencephalon
+DOID:13788,equatorial staphyloma,DOID:11595,scleral staphyloma
+UBERON:2001118,urogenital papilla,UBERON:0005156,reproductive structure
+UBERON:0014888,iliotibialis muscle,UBERON:0003663,hindlimb muscle
+HP:0009689,Enlarged epiphyses of the thumb,HP:0010231,Enlarged epiphyses of the phalanges of the hand
+UBERON:0000459,uterine wall,UBERON:0005156,reproductive structure
+UBERON:0011612,hypohyal cartilage,UBERON:0011004,pharyngeal arch cartilage
+CL:0000601,outer hair cell,CL:0000202,auditory hair cell
+UBERON:0002267,laterodorsal tegmental nucleus,UBERON:0006331,brainstem nucleus
+HP:0006693,Myocardial steatosis,HP:0001713,Abnormality of cardiac ventricle
+DOID:2351,iron metabolism disease,DOID:0050032,mineral metabolism disease
+DOID:9590,lower urinary tract calculus,DOID:18,urinary system disease
+HP:0008696,Renal hamartoma,HP:0009726,Renal neoplasm
+UBERON:0007707,superior cerebellar peduncle of midbrain,UBERON:0002635,regional part of midbrain tegmentum
+HP:0007462,Bitot spots of the conjunctiva,HP:0000502,Abnormality of the conjunctiva
+HP:0003234,Decreased plasma carnitine,HP:0010967,Abnormality of carnitine metabolism
+HP:0010723,Cystic lesions of the pinnae,HP:0000377,Abnormality of the pinna
+UBERON:0004867,orbital cavity,UBERON:0002553,anatomical cavity
+UBERON:4200027,supraglenoid buttress,UBERON:4100000,skeletal element projection
+DOID:6925,peroneal nerve paralysis,DOID:574,peripheral nervous system disease
+HP:0100328,Carpometacarpal synostosis,HP:0009701,Metacarpal synostosis
+UBERON:0001937,lateral hypothalamic nucleus,UBERON:0002785,regional part of lateral hypothalamic region
+HP:0002695,"Symmetrical, oval parietal bone defects",HP:0002696,Abnormality of the parietal bone
+UBERON:0005912,transitional epithelium of major calyx,UBERON:0003350,epithelium of mucosa
+CL:0000336,adrenal medulla chromaffin cell,CL:1000426,chromaffin cell of adrenal gland
+UBERON:0006038,interdigital region between pedal digits 1 and 2,UBERON:0006014,interdigital region between pedal digits
+UBERON:0001198,superior suprarenal artery,UBERON:0004573,systemic artery
+HP:0004916,Generalized distal tubular acidosis,HP:0008341,Distal renal tubular acidosis
+HP:0002353,EEG abnormality,HP:0001311,Abnormal nervous system electrophysiology
+DOID:2814,malignant neoplasm of acoustic nerve,DOID:2815,cranial nerve malignant neoplasm
+UBERON:0002443,choroidal blood vessel,UBERON:0003496,head blood vessel
+HP:0003946,Abnormality of the epiphyses of the elbow,HP:0003839,Abnormality involving the epiphyses of the upper limbs
+UBERON:0008716,hilum of kidney,UBERON:0006554,urinary system structure
+UBERON:0009885,interlobar artery,UBERON:0001637,artery
+DOID:14559,anaerobic meningitis,DOID:9470,bacterial meningitis
+HP:0009499,Abnormality of the epiphysis of the distal phalanx of the 2nd finger,HP:0006263,Abnormality of the epiphyses of the 2nd finger
+UBERON:0011793,flight feather,UBERON:0008297,pennaceous feather
+HP:0001928,Abnormality of coagulation,HP:0001871,Abnormality of  blood and blood-forming tissues
+HP:0012225,Oligodontia of primary teeth,HP:0000677,Oligodontia
+CL:0000150,glandular epithelial cell,CL:0002371,somatic cell
+DOID:6932,urinary bladder inverted papilloma,DOID:6933,bladder transitional cell papilloma
+HP:0009443,Osteolytic defects of the phalanges of the 3rd finger,HP:0009316,Abnormality of the phalanges of the 3rd finger
+HP:0009996,Partial duplication of the proximal phalanx of the 5th finger,HP:0009987,Partial duplication of the phalanges of the 5th finger
+HP:0010262,Irregular epiphyses of the middle phalanges of the hand,HP:0010244,Abnormality of the epiphyses of the middle phalanges of the hand
+UBERON:0003111,sphenoid region,UBERON:0004120,mesoderm-derived structure
+HP:0009648,Triangular shaped distal phalanx of the thumb,HP:0009875,Triangular shaped distal phalanges of the hand
+DOID:314,tenosynovial giant cell tumor,DOID:200,giant cell tumor
+HP:0001964,Aplasia/Hypoplasia of metatarsal bones,HP:0006494,Aplasia/Hypoplasia involving bones of the feet
+HP:0100891,Bifid xiphoid process,HP:0100892,Abnormality of the xiphoid process
+DOID:5275,gallbladder leiomyosarcoma,DOID:4058,gallbladder sarcoma
+UBERON:0010749,middle pharyngeal constrictor,UBERON:0001569,constrictor muscle of pharynx
+HP:0010330,Abnormality of the phalanges of the 3rd toe,HP:0010161,Abnormality of the phalanges of the toes
+UBERON:0005821,gracile fasciculus,UBERON:0001018,axon tract
+UBERON:0004337,distal phalanx of manual digit 1,UBERON:0003865,distal phalanx of manus
+CL:0002535,epithelial cell of cervix,CL:0002371,somatic cell
+HP:0011520,Deuteranomoly,HP:0011519,Anomalous trichromacy
+HP:0009430,Broad middle phalanx of the 3rd finger,HP:0009844,Broad middle phalanx of finger
+HP:0006771,Duodenal carcinoma,HP:0100833,Neoplasm of the small intestine
+UBERON:4000164,caudal fin,UBERON:4000162,median fin
+HP:0008330,Reduced von Willebrand factor activity,HP:0012146,Abnormality of  von Willebrand factor
+HP:0003553,Cellulitis due to immunodeficiency,HP:0100658,Cellulitis
+HP:0002515,Waddling gait,HP:0001288,Gait disturbance
+UBERON:2001699,dorsal-fin stay,UBERON:0002513,endochondral bone
+UBERON:3010090,M. tibialis anticus brevis,UBERON:0010890,pelvic complex muscle
+HP:0005563,Decreased numbers of nephrons,HP:0012575,Abnormality of the nephron
+UBERON:2002021,ascending process of the parasphenoid,UBERON:0004120,mesoderm-derived structure
+HP:0006765,Chondrosarcoma,HP:0010622,Neoplasm of the skeletal system
+UBERON:0006008,fibrous ring of heart,UBERON:0006444,annulus fibrosus
+NCBITaxon:400053,Sylvaemus group,NCBITaxon:10128,Apodemus
+CL:0002123,B220-low CD38-positive IgG-negative class switched memory B cell,CL:0002122,B220-positive CD38-positive IgG-negative class switched memory B cell
+UBERON:0002845,first thoracic dorsal root ganglion,UBERON:0002835,thoracic dorsal root ganglion
+NCBITaxon:543769,Rhizaria,NCBITaxon:2759,Eukaryota
+HP:0100821,Urethrocele,HP:0000795,Abnormality of the urethra
+UBERON:0002371,bone marrow,UBERON:0012429,hemopoietic tissue
+DOID:12573,neonatal thyrotoxicosis,DOID:7997,thyrotoxicosis
+UBERON:0004276,fourth ventricle choroid plexus epithelium,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001116,quadrate lobe of liver,UBERON:0001114,right lobe of liver
+UBERON:4300108,lepidotrichial segment,UBERON:0005913,zone of bone organ
+HP:0003645,Prolonged partial thromboplastin time,HP:0001928,Abnormality of coagulation
+UBERON:0012119,vinculum tendon of wing,UBERON:0003588,forelimb connective tissue
+UBERON:0001266,splenic cord,UBERON:0000064,organ part
+CL:1000309,epicardial adipocyte,CL:0000136,fat cell
+HP:0005700,Increased bone density with cystic changes,HP:0011001,Increased bone mineral density
+UBERON:0010892,mesethmoid element,UBERON:0004120,mesoderm-derived structure
+CL:0000109,adrenergic neuron,CL:0000540,neuron
+UBERON:4200127,suprascapula foramen,UBERON:0005744,bone foramen
+UBERON:0014399,sinusoidal space,UBERON:0010161,lumen of blood vessel
+DOID:1623,breast leiomyoma,DOID:0060082,breast benign neoplasm
+HP:0009293,Broad middle phalanx of the 4th finger,HP:0009404,Broad phalanges of the 4th finger
+UBERON:0006438,principal artery to hindlimb,UBERON:0007718,principal artery to limb
+UBERON:0007412,midbrain raphe nuclei,UBERON:0002635,regional part of midbrain tegmentum
+HP:0002700,Large foramen magnum,HP:0002699,Abnormality of the foramen magnum
+UBERON:0002122,capsule of thymus,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:4090,agnosia,DOID:2033,communication disorder
+HP:0009326,Irregular epiphysis of the middle phalanx of the 3rd finger,HP:0009415,Irregular epiphyses of the 3rd finger
+UBERON:4000105,limiting layer of elasmoid scale,UBERON:0004120,mesoderm-derived structure
+HP:0011249,Absent antitragus,HP:0009896,Abnormality of the antitragus
+CL:0000555,neuronal brush cell,CL:0000117,CNS neuron (sensu Vertebrata)
+HP:0001507,Growth abnormality,HP:0000118,Phenotypic abnormality
+CL:0000961,Bm1 B cell,CL:0000843,follicular B cell
+UBERON:4200112,prepectoral space,UBERON:0005055,zone of long bone
+DOID:3172,papillary adenoma,DOID:2615,papilloma
+UBERON:3000263,lamina precerebralis,UBERON:0010313,neural crest-derived structure
+UBERON:0006116,vagal nerve fiber bundle,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:9649,congenital nystagmus,DOID:9650,pathologic nystagmus
+HP:0010758,Abnormality of the premaxilla,HP:0000326,Abnormality of the maxilla
+UBERON:0003973,nasal concha of ethmoid bone,UBERON:0010313,neural crest-derived structure
+UBERON:0012449,mechanoreceptor,UBERON:0012451,sensory receptor
+UBERON:0003890,Mullerian duct,UBERON:0004120,mesoderm-derived structure
+UBERON:0002576,temporal pole,UBERON:0009899,pole of cerebral hemisphere
+DOID:599,specific phobia,DOID:591,phobic disorder
+UBERON:4300038,facet,UBERON:0006984,anatomical surface
+UBERON:0011661,xiphiplastron,UBERON:0015212,lateral structure
+HP:0011943,Increased urinary thiosulfate,HP:0003110,Abnormality of urine homeostasis
+DOID:4929,tubular adenocarcinoma,DOID:299,adenocarcinoma
+UBERON:2001352,stratum periventriculare,UBERON:0004121,ectoderm-derived structure
+CL:0002558,fibroblast of villous mesenchyme,CL:0000057,fibroblast
+HP:0001717,Coronary artery calcification,HP:0006704,Abnormality of the coronary arteries
+UBERON:0008589,depressor septi nasi,UBERON:0008522,nasal muscle
+HP:0008773,Aplasia/Hypoplasia of the middle ear,HP:0008771,Aplasia/Hypoplasia of the ear
+UBERON:3000395,pars basilaris,UBERON:0000479,tissue
+HP:0005354,Absent cellular immunity,HP:0011840,Abnormality of T cell physiology
+UBERON:0003604,trachea cartilage,UBERON:0003571,trachea connective tissue
+UBERON:2000729,epaxial region somite 3,UBERON:0003900,epaxial myotome region
+UBERON:0002833,medial nucleus of trapezoid body,UBERON:0007633,nucleus of trapezoid body
+CL:0002357,fetal derived definitive erythrocyte,CL:0000595,enucleate erythrocyte
+HP:0010167,Irregular epiphyses of the toes,HP:0010160,Abnormality of the epiphyses of the toes
+HP:0005339,Abnormality of complement system,HP:0005368,Abnormality of humoral immunity
+CL:0008010,cranial somatomotor neuron,CL:0005024,somatomotor neuron
+HP:0012486,Myelitis,HP:0002143,Abnormality of the spinal cord
+UBERON:0011626,tympanohyoid cartilage,UBERON:0011004,pharyngeal arch cartilage
+HP:0100156,Triangular epiphysis of the middle phalanx of the 3rd toe,HP:0100092,Abnormality of the epiphysis of the middle phalanx of the 3rd toe
+UBERON:0003997,hyoid bone greater horn,UBERON:0010273,zone of hyoid bone
+HP:0001533,Slender build,HP:0004325,Decreased body weight
+CL:0000731,urothelial cell,CL:0000244,transitional epithelial cell
+HP:0002375,Hypokinesia,HP:0002374,Diminished movement
+UBERON:3010068,M. semimembranosus,UBERON:0010890,pelvic complex muscle
+DOID:6682,spondylolisthesis,DOID:0080010,bone structure disease
+UBERON:0010030,ventral part of pharyngeal pouch 5,UBERON:0005291,embryonic tissue
+UBERON:0009470,postsphenoidal bone,UBERON:0002513,endochondral bone
+HP:0003085,Long fibula,HP:0002991,Abnormality of the fibula
+UBERON:4300087,mesopterygium bone,UBERON:4300081,mesopterygium element
+UBERON:0009638,orbitosphenoid ossification center,UBERON:0010355,ossification center
+HP:0010135,Small epiphysis of the proximal phalanx of the hallux,HP:0010126,Abnormality of the epiphysis of the proximal phalanx of the hallux
+HP:0009287,Curved middle phalanx of the 4th finger,HP:0009846,Curved middle phalanges of the hand
+HP:0002605,Hepatic necrosis,HP:0001392,Abnormality of the liver
+UBERON:0013249,paroophoron,UBERON:0012275,meso-epithelium
+HP:0007768,Central retinal vessel vascular tortuosity,HP:0008046,Abnormality of the retinal vasculature
+UBERON:0006868,seminal fluid secreting gland,UBERON:0005399,male reproductive gland
+UBERON:0011865,corneal stroma collagen fibril,UBERON:0010313,neural crest-derived structure
+UBERON:0012292,embryonic cloacal fold,UBERON:0000481,multi-tissue structure
+NCBITaxon:11039,Western equine encephalomyelitis virus,NCBITaxon:177874,WEEV complex
+UBERON:0003707,sinus of Valsalva,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0010360,pharyngeal arch mesenchyme from head mesenchyme,UBERON:0003104,mesenchyme
+UBERON:2001901,ceratobranchial 3 element,UBERON:2001898,ceratobranchial element
+DOID:0060181,ischemic colitis,DOID:0060180,colitis
+DOID:9270,alkaptonuria,DOID:0060159,organic acidemia
+UBERON:2001397,post-Weberian supraneural,UBERON:2000442,supraneural bone
+UBERON:0002198,neurohypophysis,UBERON:0004120,mesoderm-derived structure
+UBERON:0002787,decussation of trochlear nerve,UBERON:0007418,decussation of neuraxis
+HP:0000140,Abnormality of the menstrual cycle,HP:0000008,Abnormality of female internal genitalia
+CL:0002433,"CD69-positive, CD4-positive single-positive thymocyte",CL:0000810,"CD4-positive, alpha-beta thymocyte"
+UBERON:2000106,extension,UBERON:0002050,embryonic structure
+DOID:3527,cerebral arterial disease,DOID:13089,intracranial arterial disease
+HP:0100270,Abnormality of dorsoventral patterning of the limbs,HP:0001760,Abnormality of the foot
+HP:0005356,Decreased serum complement factor I,HP:0004431,Complement deficiency
+HP:0006495,Aplasia/Hypoplasia of the ulna,HP:0006503,Aplasia/Hypoplasia involving forearm bones
+UBERON:0004554,hindlimb digital artery,UBERON:0004552,digital artery
+DOID:176,cardiovascular cancer,DOID:0050686,organ system cancer
+UBERON:0010311,scleral sesamoid bone,UBERON:0010290,scleral ossicle
+HP:0000008,Abnormality of female internal genitalia,HP:0000812,Abnormal internal genitalia
+HP:0006149,Increased laxity of fingers,HP:0006094,Finger joint hypermobility
+CL:0000149,visual pigment cell,CL:0000147,pigment cell
+UBERON:0002816,prepyramidal fissure of cerebellum,UBERON:0003980,cerebellum fissure
+HP:0012461,Bacteriuria,HP:0003110,Abnormality of urine homeostasis
+UBERON:0002107,liver,UBERON:0006925,digestive gland
+HP:0007058,Generalized cerebral atrophy/hypoplasia,HP:0002059,Cerebral atrophy
+HP:0001483,Eye poking,HP:0000733,Stereotypic behavior
+HP:0004785,Malrotation of colon,HP:0002250,Abnormality of the large intestine
+HP:0100366,Short phalanx of the 3rd toe,HP:0010331,Aplasia/Hypoplasia of the 3rd toe
+CL:0007021,alarm substance cell,CL:0000473,defensive cell
+UBERON:0000348,ophthalmic nerve,UBERON:0002003,peripheral nerve
+UBERON:0008989,submocosal esophageal gland,UBERON:0005181,thoracic segment organ
+UBERON:0002046,thyroid gland,UBERON:0002368,endocrine gland
+HP:0100580,Barrett esophagus,HP:0100751,Esophageal neoplasm
+UBERON:2001740,posterior cranial fontanel,UBERON:0002221,fontanelle
+UBERON:0010713,paired fin skeleton,UBERON:0011582,paired limb/fin skeleton
+DOID:0050617,malignant Sertoli cell tumor,DOID:192,sex cord-gonadal stromal tumor
+HP:0009816,Lower limb undergrowth,HP:0009826,Limb undergrowth
+CL:0002494,cardiocyte,CL:0000548,animal cell
+UBERON:0014765,crus of diaphragm,UBERON:0000064,organ part
+UBERON:0004745,parasphenoid,UBERON:0002514,intramembranous bone
+HP:0011388,Enlarged cochlear aqueduct,HP:0000375,Abnormality of cochlea
+UBERON:0004179,prostate glandular acinus,UBERON:0005156,reproductive structure
+HP:0010492,Osseous finger syndactyly,HP:0006101,Finger syndactyly
+UBERON:0009920,optic neural crest,UBERON:0007530,migrating mesenchyme population
+HP:0004598,Supernumerary vertebral ossification centers,HP:0000926,Platyspondyly
+HP:0000925,Abnormality of the vertebral column,HP:0009121,Abnormal axial skeleton morphology
+UBERON:0001610,lingual artery,UBERON:0015212,lateral structure
+UBERON:0000059,large intestine,UBERON:0013765,digestive system organ
+HP:0009333,Abnormality of the epiphysis of the proximal phalanx of the 3rd finger,HP:0010245,Abnormality of the epiphyses of the proximal phalanges of the hand
+HP:0001409,Portal hypertension,HP:0000822,Hypertension
+UBERON:0005292,extraembryonic tissue,UBERON:0000479,tissue
+HP:0012000,EEG with generalized spikes,HP:0011198,EEG with generalized epileptiform discharges
+HP:0100554,Hemihypertrophy of upper limb,HP:0002817,Abnormality of the upper limb
+CL:0000806,DN2 thymocyte,CL:0002489,double negative thymocyte
+UBERON:0001844,cochlea,UBERON:0000477,anatomical cluster
+HP:0009260,Triangular epiphysis of the distal phalanx of the 4th finger,HP:0010256,Triangular epiphyses of the distal phalanges of the hand
+DOID:8681,paraneoplastic polyneuropathy,DOID:2537,inflammatory and toxic neuropathy
+UBERON:0001826,nasal cavity mucosa,UBERON:0004121,ectoderm-derived structure
+DOID:9513,plasmacytic leukemia,DOID:1037,lymphoblastic leukemia
+UBERON:0001306,cumulus oophorus,UBERON:0000064,organ part
+HP:0012325,Chronic myelomonocytic leukemia,HP:0012324,Myeloid leukemia
+DOID:3449,penis carcinoma,DOID:11615,penile cancer
+HP:0005745,Congenital foot contractures,HP:0005750,Contractures of the joints of the lower limbs
+HP:0011469,Nasal regurgitation,HP:0008872,Feeding difficulties in infancy
+UBERON:0001366,parietal peritoneum,UBERON:0000064,organ part
+HP:0008887,Adipose tissue loss,HP:0003758,Reduced subcutaneous adipose tissue
+UBERON:0011963,talocalcaneonavicular joint,UBERON:0003698,subtalar joint
+UBERON:2000336,preopercle vertical limb,UBERON:0008907,dermal bone
+HP:0010289,Alveolar ridge cleft,HP:0006477,Abnormality of the alveolar ridges
+UBERON:0003097,dorsal fin,UBERON:0008897,fin
+UBERON:0002397,maxilla,UBERON:0015212,lateral structure
+UBERON:0002641,oral pulvinar nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0009048,deep external pudendal vein,UBERON:0009029,pudendal vein
+CL:0000821,B-1b B cell,CL:0000819,B-1 B cell
+UBERON:0015006,coccygeal vertebra endochondral element,UBERON:0010363,endochondral element
+DOID:768,retinoblastoma,DOID:771,retinal cell cancer
+HP:0009325,Fragmentation of the epiphysis of the middle phalanx of the 3rd finger,HP:0009334,Abnormality of the epiphysis of the middle phalanx of the 3rd finger
+UBERON:0010564,manual digit 1 mesenchyme,UBERON:0005257,manual digit mesenchyme
+UBERON:2001349,stratum opticum,UBERON:0000479,tissue
+DOID:7427,anthrax disease,DOID:0050338,primary bacterial infectious disease
+UBERON:0014805,inferior nuchal line,UBERON:0014801,nuchal line
+UBERON:2002132,hypural 7,UBERON:2000364,hypural
+UBERON:0010299,scleral mesenchyme,UBERON:0003104,mesenchyme
+DOID:12900,Mikulicz disease,DOID:417,hypersensitivity reaction type II disease
+CL:0000237,keratinizing barrier epithelial cell,CL:0000311,keratin accumulating cell
+HP:0011326,Anterior plagiocephaly,HP:0001357,Plagiocephaly
+UBERON:0002943,lingual gyrus,UBERON:0003022,cerebral cortex lobe
+CL:0002569,mesenchymal stem cell of umbilical cord,CL:0000349,extraembryonic cell
+DOID:6000,congestive heart failure,DOID:114,heart disease
+UBERON:3010735,ramus anterior of CN VIII,UBERON:0004529,anatomical projection
+HP:0100170,Bracket epiphysis of the distal phalanx of the 4th toe,HP:0100094,Abnormality of the epiphysis of the distal phalanx of the 4th toe
+UBERON:0002306,nasal mucus,UBERON:0000912,mucus
+UBERON:0003997,hyoid bone greater horn,UBERON:0015212,lateral structure
+DOID:4679,breast mucoepidermoid carcinoma,DOID:4680,breast metaplastic carcinoma
+HP:0011080,Abnormality of premolar morphology,HP:0011076,Abnormality of premolar
+UBERON:0008805,gingival groove,UBERON:0006800,anatomical line
+HP:0009139,Osteolysis involving bones of the lower limbs,HP:0002814,Abnormality of the lower limb
+HP:0011545,Abnormal connection of the cardiac segments,HP:0002564,Malformation of the heart and great vessels
+UBERON:0006664,greater palatine artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:6868,mediastinal malignant lymphoma,DOID:5559,mediastinal cancer
+UBERON:2002221,pericardial muscle,UBERON:0001774,muscle of trunk
+UBERON:0000144,trochlea of humerus,UBERON:0005055,zone of long bone
+HP:0100686,Enthesitis,HP:0100685,Abnormality of Sharpey fibers
+UBERON:0003267,tooth of upper jaw,UBERON:0013765,digestive system organ
+UBERON:0010387,Peyer's patch T cell area,UBERON:0010393,T cell domain
+UBERON:0001123,scalenus posterior,UBERON:0002377,muscle of neck
+UBERON:0006140,palmar digital vein,UBERON:0004563,forelimb digital vein
+UBERON:3000649,anterior process of vomer,UBERON:4100000,skeletal element projection
+DOID:4773,congenital mesoblastic nephroma,DOID:3675,childhood kidney neoplasm
+UBERON:3000830,margo vertebralis,UBERON:0004120,mesoderm-derived structure
+UBERON:0005363,inferior vagus X ganglion,UBERON:0005362,vagus X ganglion
+DOID:3407,carotid artery disease,DOID:6713,cerebrovascular disease
+HP:0008363,Aplasia/Hypoplasia of the tarsal bones,HP:0001850,Abnormality of the tarsal bones
+UBERON:2000627,posterior ceratohyal,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:14702,branchiootorenal syndrome,DOID:0050736,autosomal dominant disease
+UBERON:2002099,lateral line scale series,UBERON:0000477,anatomical cluster
+UBERON:0013192,ovarian medulla,UBERON:0014404,female anatomical structure
+UBERON:0015233,nucleus of dorsal thalamus,UBERON:0007692,nucleus of thalamus
+DOID:13326,chronic follicular conjunctivitis,DOID:2475,chronic conjunctivitis
+HP:0010114,Bracket epiphyses of the hallux,HP:0010056,Abnormality of the epiphyses of the hallux
+HP:0004913,Intermittent lactic acidemia,HP:0003128,Lactic acidosis
+CL:0000622,acinar cell,CL:0000150,glandular epithelial cell
+DOID:12594,Potter's syndrome,DOID:12215,oligohydramnios
+UBERON:0011162,supraoccipital cartilage element,UBERON:0015015,supraoccipital endochondral element
+DOID:12733,hypercementosis,DOID:214,teeth hard tissue disease
+UBERON:2002282,preopercle-opercle joint,UBERON:0000982,skeletal joint
+UBERON:2001052,primordial hindbrain channel,UBERON:0003496,head blood vessel
+HP:0012747,Abnormal brainstem MRI signal intensity,HP:0002363,Abnormality of the brainstem
+UBERON:0003693,retroperitoneal space,UBERON:0000464,anatomical space
+HP:0012098,Edema of the dorsum of feet,HP:0000969,Edema
+UBERON:0005925,ethmoidal process of inferior nasal concha,UBERON:0004120,mesoderm-derived structure
+DOID:0050732,methylmalonic aciduria and homocystinuria type cblE,DOID:14749,methylmalonic acidemia
+UBERON:0004386,epiphysis of ulna,UBERON:0004120,mesoderm-derived structure
+UBERON:0001098,incisor tooth,UBERON:0001091,calcareous tooth
+CL:0000966,Bm4 B cell,CL:0000844,germinal center B cell
+UBERON:3010219,internal carotid,UBERON:3010217,carotid
+HP:0007360,Aplasia/Hypoplasia of the cerebellum,HP:0002977,Aplasia/Hypoplasia involving the central nervous system
+UBERON:0003543,left lung respiratory bronchiole,UBERON:0003539,left lung bronchiole
+UBERON:0006640,crus of clitoris,UBERON:0014404,female anatomical structure
+HP:0100404,Duplication of the proximal phalanx of the 3rd toe,HP:0010370,Abnormality of the proximal phalanx of the 3rd toe
+UBERON:2002149,vertebral element 9,UBERON:0010913,vertebral element
+DOID:0060199,amyotrophic lateral sclerosis type 7,DOID:332,amyotrophic lateral sclerosis
+UBERON:0007692,nucleus of thalamus,UBERON:0006569,diencephalic nucleus
+HP:0011002,Osteopetrosis,HP:0011001,Increased bone mineral density
+UBERON:0010063,tympanic cavity epithelium,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3000787,collum antibrachii,UBERON:0004120,mesoderm-derived structure
+HP:0010422,Complete duplication of the proximal phalanx of the 2nd toe,HP:0010403,Duplication of the proximal phalanx of the 2nd toe
+DOID:8778,Crohn's disease,DOID:0050589,inflammatory bowel disease
+UBERON:0003511,iris blood vessel,UBERON:0003496,head blood vessel
+HP:0012248,Prolonged PR interval,HP:0003115,Abnormal EKG
+CL:0002408,immature Vgamma2-negative thymocyte,CL:0002405,gamma-delta thymocyte
+CL:0009001,compound eye retinal cell,CL:0002371,somatic cell
+UBERON:0002070,superior pancreaticoduodenal artery,UBERON:0004573,systemic artery
+HP:0100743,Neoplasm of the rectum,HP:0100834,Neoplasm of the large intestine
+HP:0003022,Hypoplasia of the ulna,HP:0006495,Aplasia/Hypoplasia of the ulna
+UBERON:4440009,pectoral fin radial skeleton,UBERON:4300013,paired fin radial skeleton
+UBERON:0002259,corpora quadrigemina,UBERON:0004121,ectoderm-derived structure
+HP:0009500,Abnormality of the epiphysis of the middle phalanx of the 2nd finger,HP:0009543,Abnormality of the middle phalanx of the 2nd finger
+UBERON:0003914,epithelial tube,UBERON:0000483,epithelium
+UBERON:0002792,lumbar spinal cord,UBERON:0005844,spinal cord segment
+UBERON:0010262,operculum of brain,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009405,Bullet-shaped phalanges of the 4th finger,HP:0009769,Bullet-shaped phalanges of the hand
+DOID:6004,aleukemic leukemia,DOID:1240,leukemia
+CL:0002645,endo-epithelial cell of pharyngotympanic part of viscerocranial mucosa,CL:0002261,endothelial cell of viscerocranial mucosa
+HP:0001131,Corneal dystrophy,HP:0000481,Abnormality of the cornea
+UBERON:2001698,anal-fin stay,UBERON:0002513,endochondral bone
+CL:0000257,Mycetozoan cell,CL:0000255,eukaryotic cell
+HP:0000041,Chordee,HP:0000036,Abnormality of the penis
+UBERON:3010031,ventral glands,UBERON:3010603,body gland
+HP:0004713,Reversible renal failure,HP:0000083,Renal insufficiency
+DOID:12668,abnormal retinal correspondence,DOID:12667,binocular vision disease
+HP:0012320,Absent pigmentation of the limbs,HP:0200098,Absent skin pigmentation
+CL:0002063,type II pneumocyte,CL:0000322,pneumocyte
+UBERON:0004571,systemic arterial system,UBERON:0007798,vascular system
+CL:0000908,"CD8-positive, alpha-beta cytokine secreting effector T cell",CL:0000912,helper T cell
+DOID:2228,thrombocytosis,DOID:2218,blood platelet disease
+UBERON:0003541,left lung terminal bronchiole,UBERON:0002187,terminal bronchiole
+UBERON:0001423,radius bone,UBERON:0003466,forelimb zeugopod bone
+HP:0001094,Iridocyclitis,HP:0012122,Anterior uveitis
+HP:0010282,Thin lower lip vermilion,HP:0000178,Abnormality of lower lip
+HP:0100442,Bullet-shaped distal phalanx of the 5th toe,HP:0010385,Bullet-shaped phalanges of the 5th toe
+HP:0011333,Asymmetric crying face,HP:0000324,Facial asymmetry
+UBERON:0002196,adenohypophysis,UBERON:0000064,organ part
+HP:0000635,Blue irides,HP:0008034,Abnormal iris pigmentation
+CL:0000810,"CD4-positive, alpha-beta thymocyte",CL:0000893,thymocyte
+UBERON:0014405,nymph stage,UBERON:0000069,larval stage
+UBERON:0001313,iliolumbar artery,UBERON:0001637,artery
+UBERON:0006077,subdivision of vertebral column,UBERON:0000075,subdivision of skeletal system
+CL:0000745,horizontal cell,CL:0000099,interneuron
+UBERON:0002723,mammillary princeps fasciculus,UBERON:0002316,white matter
+UBERON:0000445,habenular trigone,UBERON:0002757,regional part of epithalamus
+CL:0002106,IgD-positive CD38-positive IgG memory B cell,CL:0002105,CD38-positive IgG memory B cell
+UBERON:3000798,presacral shield,UBERON:0000064,organ part
+HP:0009285,Curved phalanges of the 4th finger,HP:0004095,Curved fingers
+UBERON:0002771,middle temporal gyrus,UBERON:0000200,gyrus
+HP:0012551,Absent neutrophil specific granules,HP:0011992,Abnormality of neutrophil morphology
+UBERON:0002831,posteroventral cochlear nucleus,UBERON:0001720,cochlear nucleus
+HP:0009459,Short proximal phalanx of the 3rd finger,HP:0009461,Short 3rd finger
+HP:0012186,Entrapment neuropathy of the ulnar nerve at elbow,HP:0012181,Entrapment neuropathy
+HP:0009159,Small epiphysis of the proximal phalanx of the 5th finger,HP:0009390,Small epiphyses of the 5th finger
+HP:0009531,Pseudoepiphysis of the proximal phalanx of the 2nd finger,HP:0010275,Pseudoepiphyses of the proximal phalanges of the hand
+DOID:8337,appendicitis,DOID:1518,cecal disease
+HP:0002891,Uterine leiomyosarcoma,HP:0100243,Leiomyosarcoma
+UBERON:0006803,obturator foramen,UBERON:0004120,mesoderm-derived structure
+HP:0004943,Accelerated atherosclerosis,HP:0002621,Atherosclerosis
+DOID:6548,angiomatous meningioma,DOID:3565,meningioma
+HP:0002281,Gray matter heterotopias,HP:0002282,Heterotopia
+UBERON:0009708,dorsal pancreas,UBERON:0005177,trunk organ
+UBERON:0013720,dartos muscle of labia majora,UBERON:0005156,reproductive structure
+UBERON:0003419,mesenchyme of parotid,UBERON:0009891,facial mesenchyme
+HP:0100905,Sclerosis of the middle phalanx of the 3rd finger,HP:0100919,Sclerosis of the phalanges of the 3rd finger
+DOID:10124,corneal disease,DOID:5614,eye disease
+DOID:5421,lung combined type small cell carcinoma,DOID:5409,lung small cell carcinoma
+UBERON:0002281,vestibular membrane of cochlear duct,UBERON:0004121,ectoderm-derived structure
+DOID:1307,dementia,DOID:1561,cognitive disorder
+UBERON:2001677,mesethmoid-nasal joint,UBERON:0000982,skeletal joint
+DOID:5550,choriocarcinoma of ovary,DOID:3594,choriocarcinoma
+UBERON:0004367,Descemet's membrane,UBERON:0005769,basement membrane of epithelium
+CL:1000597,papillary tips cell,CL:1000505,kidney pelvis cell
+HP:0003365,Arthralgia of the hip,HP:0003272,Abnormality of the hip bone
+UBERON:0010540,tarsus pre-cartilage condensation,UBERON:0015050,tarsus endochondral element
+UBERON:0004316,distal phalanx of pedal digit 2,UBERON:0003641,pedal digit 2 phalanx
+HP:0100600,Penoscrotal transposition,HP:0000045,Abnormality of the scrotum
+HP:0009538,Contracture of the distal interphalangeal joint of the 2nd finger,HP:0009537,Flexion contracture of the 2nd finger
+UBERON:0006666,great cerebral vein,UBERON:0001663,cerebral vein
+HP:0001923,Reticulocytosis,HP:0004312,Abnormality of reticulocytes
+HP:0012629,Phacodonesis,HP:0000517,Abnormality of the lens
+UBERON:0005988,atrium myocardial trabecula,UBERON:0004120,mesoderm-derived structure
+UBERON:0003092,ultimobranchial body,UBERON:0004119,endoderm-derived structure
+UBERON:0007252,intervertebral disk of cervical vertebra,UBERON:2001457,postcranial axial cartilage
+UBERON:0009733,sublaminar layers S1 or S2 or S3,UBERON:0008921,substratum of layer of retina
+DOID:1260,parametritis,DOID:1003,pelvic inflammatory disease
+HP:0012473,Tongue atrophy,HP:0000157,Abnormality of the tongue
+DOID:6407,ovarian surface papilloma,DOID:6214,ovarian papillary neoplasm
+UBERON:0016410,male breast,UBERON:0014403,male anatomical structure
+HP:0008504,Moderate sensorineural hearing impairment,HP:0000407,Sensorineural hearing impairment
+DOID:6166,prostatic urethra urothelial carcinoma,DOID:6167,prostatic urethral cancer
+CL:1000398,endothelial cell of hepatic sinusoid,CL:0002262,endothelial cell of sinusoid
+DOID:0050860,colorectal adenoma,DOID:4610,intestinal benign neoplasm
+NCBITaxon:11086,Louping ill virus,NCBITaxon:29263,tick-borne encephalitis virus group
+HP:0200129,Calcific mitral stenosis,HP:0001718,Mitral stenosis
+UBERON:0012074,bony part of hard palate,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:12506,Bell's palsy,DOID:13934,facial paralysis
+DOID:986,alopecia areata,DOID:417,hypersensitivity reaction type II disease
+HP:0000140,Abnormality of the menstrual cycle,HP:0008373,Puberty and gonadal disorders
+HP:0008628,Abnormality of the stapes,HP:0004452,Abnormality of the middle ear ossicles
+UBERON:4200070,median fin spine,UBERON:4200075,fin spine
+DOID:13515,tuberous sclerosis,DOID:0050736,autosomal dominant disease
+UBERON:0006294,stapes pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+HP:0002028,Chronic diarrhea,HP:0002014,Diarrhea
+UBERON:0002775,olivocochlear bundle,UBERON:0003544,brain white matter
+UBERON:0010404,lateral ventricle subependymal layer,UBERON:0000119,cell layer
+DOID:5638,malignant giant cell tumor of soft parts,DOID:1907,malignant fibroxanthoma
+UBERON:0004271,outflow tract pericardium,UBERON:0005983,heart layer
+CL:0002307,brush border cell of the proximal tubule,CL:0002306,epithelial cell of proximal tubule
+HP:0010328,Polydactyly affecting the 2nd toe,HP:0010112,Mesoaxial foot polydactyly
+UBERON:0010146,paraurethral duct,UBERON:0005156,reproductive structure
+UBERON:0005036,mucosa of main bronchus,UBERON:0000410,bronchial mucosa
+DOID:6943,vulvar inverted follicular keratosis,DOID:6944,vulvar seborrheic keratosis
+UBERON:0005294,genital ridge,UBERON:0005423,developing anatomical structure
+HP:0010081,Patchy sclerosis of the distal phalanx of the hallux,HP:0100944,Sclerosis of the distal phalanx of the hallux
+HP:0007808,Bilateral retinal coloboma,HP:0000480,Retinal coloboma
+HP:0003455,Elevated long chain fatty acids,HP:0010964,Abnormality of long-chain fatty-acid metabolism
+DOID:5604,adult acute lymphocytic leukemia,DOID:9952,acute lymphocytic leukemia
+UBERON:3000828,margo posterior of cleithrum,UBERON:0004121,ectoderm-derived structure
+HP:0100067,Bracket epiphyses of the 4th toe,HP:0010335,Abnormality of the epiphyses of the 4th toe
+DOID:4812,adult brainstem gliosarcoma,DOID:4813,adult brain stem glioma
+UBERON:0001903,thalamic reticular nucleus,UBERON:0015234,nucleus of ventral thalamus
+UBERON:0011274,nail of manual digit 2,UBERON:0009565,nail of manual digit
+UBERON:0003236,epithelium of lower jaw,UBERON:0000490,unilaminar epithelium
+DOID:0060167,seasonal affective disorder,DOID:1596,mental depression
+DOID:5207,monodermal teratoma,DOID:5567,ovarian germ cell teratoma
+DOID:3766,leukorrhea,DOID:3767,vaginal discharge
+UBERON:0013483,crypt of Lieberkuhn of jejunum,UBERON:0001241,crypt of Lieberkuhn of small intestine
+UBERON:0005387,olfactory glomerulus,UBERON:0010314,structure with developmental contribution from neural crest
+NCBITaxon:29185,Rotaliida,NCBITaxon:29178,Foraminifera
+UBERON:0003125,vitelline membrane,UBERON:0000470,cell part
+UBERON:2001909,pharyngobranchial element,UBERON:0010314,structure with developmental contribution from neural crest
+NCBITaxon:40005,Yellow fever virus group,NCBITaxon:11051,Flavivirus
+UBERON:0015121,left outer canthus,UBERON:0015212,lateral structure
+HP:0007661,Chorioretinal hypopigmentation and hyperpigmentation,HP:0000532,Chorioretinal abnormality
+UBERON:0013538,Brodmann (1909) area 7,UBERON:0013529,Brodmann area
+UBERON:4300018,ventral marginal cartilage,UBERON:0014403,male anatomical structure
+DOID:2934,aleutian mink disease,DOID:934,viral infectious disease
+HP:0004863,Compensated hemolytic anemia,HP:0001878,Hemolytic anemia
+UBERON:0002290,choroid plexus of fourth ventricle,UBERON:0006694,cerebellum vasculature
+UBERON:0001580,levator labii superioris,UBERON:0001577,facial nerve muscle
+UBERON:0011199,prostatic utricle,UBERON:0000064,organ part
+UBERON:0003261,thyroid primordium endoderm,UBERON:0000925,endoderm
+UBERON:0010534,primitive mesonephric nephron,UBERON:0005322,mesonephric nephron
+HP:0010514,Hyperpituitarism,HP:0011747,Abnormality of the anterior pituitary
+HP:0000283,Broad face,HP:0001999,Abnormal facial shape
+CL:0000884,mucosa-associated lymphoid tissue macrophage,CL:0000867,secondary lymphoid organ macrophage
+HP:0100524,Limb duplication,HP:0002813,Abnormality of limb bone morphology
+NCBITaxon:39759,Deltavirus,NCBITaxon:10239,Viruses
+HP:0004835,Microspherocytosis,HP:0004444,Spherocytosis
+UBERON:0007653,capillary loop nephron,UBERON:0010532,primitive nephron
+DOID:1822,secondary lacrimal atrophy,DOID:1400,lacrimal apparatus disease
+DOID:13789,staphyloma posticum,DOID:11595,scleral staphyloma
+UBERON:0004930,submucosa of transverse colon,UBERON:0003331,submucosa of colon
+DOID:6514,polyvesicular vitelline pattern ovarian yolk sac tumor,DOID:5350,ovarian endodermal sinus tumor
+HP:0003524,Decreased methionine synthase activity,HP:0010901,Abnormality of methionine metabolism
+HP:0100119,Small epiphysis of the middle phalanx of the 2nd toe,HP:0100052,Small epiphyses of the 2nd toe
+UBERON:0006877,vasculature of liver,UBERON:0004119,endoderm-derived structure
+DOID:9938,dacryocystitis,DOID:6970,acute inflammation of lacrimal passage
+HP:0002078,Truncal ataxia,HP:0001251,Ataxia
+UBERON:3000982,tail external integument structure,UBERON:3000961,external integument structure
+CL:0001004,immature CD8_alpha-positive CD11b-negative dendritic cell,CL:0001000,CD8_alpha-positive CD11b-negative dendritic cell
+DOID:0060213,FTDALS1,DOID:332,amyotrophic lateral sclerosis
+DOID:0050822,second-degree atrioventricular block,DOID:0050820,atrioventricular block
+DOID:3033,colon signet ring adenocarcinoma,DOID:234,colon adenocarcinoma
+UBERON:2007051,ventral interhyoideus,UBERON:0005493,hyoid muscle
+DOID:7039,Borst-Jadassohn intraepidermal carcinoma,DOID:3451,skin carcinoma
+DOID:4934,apocrine sweat gland cancer,DOID:2095,sweat gland cancer
+UBERON:0002748,medial lemniscus of medulla,UBERON:0003002,medial lemniscus
+HP:0011767,Abnormality of the parathyroid physiology,HP:0000828,Abnormality of the parathyroid gland
+HP:0010256,Triangular epiphyses of the distal phalanges of the hand,HP:0010243,Abnormality of the epiphyses of the distal phalanx of finger
+HP:0005235,Jejunal atresia,HP:0005265,Abnormality of the jejunum
+UBERON:0004114,tympanic cavity,UBERON:0010064,open anatomical space
+UBERON:0010882,limb bone pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+HP:0006203,Decreased movement range in interphalangeal joints,HP:0006135,Decreased finger mobility
+UBERON:0006832,lumen of open tracheal system trachea,UBERON:0000464,anatomical space
+UBERON:0011252,scent gland,UBERON:0002530,gland
+UBERON:2007001,dorso-rostral cluster,UBERON:0004121,ectoderm-derived structure
+HP:0005263,Gastritis,HP:0004295,Abnormality of the gastric mucosa
+CL:0000790,immature alpha-beta T cell,CL:0002420,immature T cell
+DOID:1699,congenital ichthyosiform erythroderma,DOID:0050737,autosomal recessive disease
+HP:0006739,Squamous cell carcinoma of the skin,HP:0002860,Squamous cell carcinoma
+UBERON:0002892,medial amygdaloid nucleus,UBERON:0002619,regional part of cerebral cortex
+HP:0009393,Absent epiphyses of the 4th finger,HP:0010228,Absent epiphyses of the phalanges of the hand
+UBERON:0002841,fourth cervical dorsal root ganglion,UBERON:0002834,cervical dorsal root ganglion
+CL:0000043,mature basophil,CL:0002274,histamine secreting cell
+DOID:6335,bilateral meningioma of optic nerve,DOID:3419,optic nerve neoplasm
+DOID:6019,central nervous system immature teratoma,DOID:3640,central nervous system teratoma
+UBERON:2001753,posttemporal fossa,UBERON:0004704,bone fossa
+HP:0008511,Central posterior corneal opacity,HP:0011493,Central opacification of the cornea
+UBERON:0000023,wing,UBERON:0000026,appendage
+UBERON:0001284,renal column,UBERON:0006554,urinary system structure
+UBERON:0002670,anterior ascending limb of lateral sulcus,UBERON:0014639,frontal sulcus
+UBERON:3000022,antorbital process,UBERON:0004530,bony projection
+UBERON:0004166,superior reticular formation,UBERON:0002579,regional part of medullary reticular formation
+HP:0008388,Abnormality of the toenail,HP:0001597,Abnormality of the nail
+UBERON:0001067,vertebral arch joint,UBERON:0002217,synovial joint
+UBERON:0013399,blood vessel layer of choroid,UBERON:0004121,ectoderm-derived structure
+UBERON:0005965,outflow part of right atrium,UBERON:0005946,outflow tract of atrium
+HP:0010579,Cone-shaped epiphysis,HP:0005930,Abnormality of the epiphyses
+HP:0005248,Intrahepatic biliary atresia,HP:0005912,Biliary atresia
+UBERON:3010659,subarcualis rectus I,UBERON:3000224,hyobranchial muscle
+HP:0100193,Cone-shaped epiphysis of the proximal phalanx of the 4th toe,HP:0100096,Abnormality of the epiphysis of the proximal phalanx of the 4th toe
+CL:0000571,leucophore,CL:0000147,pigment cell
+UBERON:0005324,mesonephric macula densa,UBERON:0004120,mesoderm-derived structure
+HP:0000187,Broad alveolar ridges,HP:0006477,Abnormality of the alveolar ridges
+UBERON:0002763,accessory medullary lamina of globus pallidus,UBERON:0014532,lamina of cerebral hemisphere
+HP:0010992,Stress urinary incontinence,HP:0000020,Urinary incontinence
+UBERON:0009918,retrotrapezoid nucleus,UBERON:0007635,nucleus of medulla oblongata
+UBERON:0010332,epithelium of handplate,UBERON:0005291,embryonic tissue
+HP:0012504,Abnormal size of pituitary gland,HP:0012503,Abnormality of the pituitary gland
+UBERON:0006912,urinary bladder muscularis mucosa,UBERON:0004228,urinary bladder smooth muscle
+UBERON:0010414,omental fat pad,UBERON:0010411,retroperitoneal fat pad
+UBERON:0011415,cutaneous trunci muscle,UBERON:0006821,cutaneous muscle
+HP:0100516,Neoplasm of the ureter,HP:0010786,Urinary tract neoplasm
+UBERON:0005017,mucosa of lacrimal sac,UBERON:0004121,ectoderm-derived structure
+UBERON:0009202,vasa recta descending limb,UBERON:0000064,organ part
+HP:0011812,Agraphesthesia,HP:0011730,Abnormality of central sensory function
+HP:0011685,Infra-aortic superior vena cava,HP:0005345,Abnormality of the vena cava
+DOID:5579,gastric gastrinoma,DOID:10534,stomach cancer
+UBERON:0002028,hindbrain,UBERON:0002616,regional part of brain
+UBERON:0010938,muscle belly,UBERON:0000064,organ part
+HP:0008269,Increased red cell hemolysis by shear stress,HP:0001878,Hemolytic anemia
+UBERON:0004909,epithelium of gonad,UBERON:0012275,meso-epithelium
+UBERON:0015016,stapes endochondral element,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100461,Patchy sclerosis of the middle phalanx of the 3rd toe,HP:0010364,Patchy sclerosis of the phalanges of the 3rd toe
+UBERON:0001085,skin of trunk,UBERON:0000014,zone of skin
+UBERON:0005206,choroid plexus stroma,UBERON:0004121,ectoderm-derived structure
+UBERON:2000241,midline column,UBERON:0000477,anatomical cluster
+CL:0002512,"CD11b-high, CD103-negative, langerin-negative lymph node dendritic cell",CL:0002508,"langerin-negative, CD103-negative lymph node dendritic cell"
+HP:0011052,Agenesis of maxillary premolar,HP:0011051,Agenesis of premolar
+UBERON:0005454,internal oblique,UBERON:0002461,anterior abdominal wall muscle
+CL:0002387,arthroconidium,CL:0000606,macroconidium
+UBERON:0004363,aortic arch,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0011315,digastric branch of facial nerve,UBERON:0002003,peripheral nerve
+CL:0000982,IgG plasmablast,CL:0000980,plasmablast
+UBERON:0009090,outer medulla vasa recta descending limb,UBERON:0006554,urinary system structure
+UBERON:0004624,sacral vertebra 3,UBERON:0001094,sacral vertebra
+HP:0003457,EMG abnormality,HP:0011804,Abnormality of muscle physiology
+HP:0003940,Osteoarthritis of the elbow,HP:0002758,Osteoarthritis
+UBERON:2001898,ceratobranchial element,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010430,Aplasia of the phalanges of the 2nd toe,HP:0010745,Aplasia of the phalanges of the toes
+DOID:4325,Ebola hemorrhagic fever,DOID:934,viral infectious disease
+DOID:0050824,sinoatrial node disease,DOID:10273,heart conduction disease
+UBERON:0007718,principal artery to limb,UBERON:0001637,artery
+HP:0002383,Encephalitis,HP:0011450,CNS infection
+UBERON:2205226,median fin proximal radial cartilage,UBERON:2205225,median fin radial cartilage
+HP:0010432,Absent distal phalanx of the 2nd toe,HP:0010413,Aplasia/Hypoplasia of the distal phalanx of the 2nd toe
+UBERON:0002293,costochondral joint,UBERON:0002215,synchondrosis
+HP:0000867,Secondary hyperparathyroidism,HP:0000843,Hyperparathyroidism
+DOID:9365,vesiculitis,DOID:48,male reproductive system disease
+UBERON:0006234,femur pre-cartilage condensation,UBERON:0010882,limb bone pre-cartilage condensation
+HP:0011877,Increased mean platelet volume,HP:0011876,Abnormal platelet volume
+HP:0002680,J-shaped sella turcica,HP:0002681,Deformed sella turcica
+HP:0100170,Bracket epiphysis of the distal phalanx of the 4th toe,HP:0100067,Bracket epiphyses of the 4th toe
+UBERON:0010759,equine distal sesamoid,UBERON:0011250,autopod bone
+HP:0012328,Cementoma,HP:0100612,Odontogenic neoplasm
+DOID:1428,endocrine pancreas disease,DOID:26,pancreas disease
+CL:0002169,basal cell of olfactory epithelium,CL:0002319,neural cell
+UBERON:0015871,facial lymph node,UBERON:0015870,lymph node of head
+CL:0000232,erythrocyte,CL:0000329,oxygen accumulating cell
+UBERON:0002453,ethmoid sinus,UBERON:0001825,paranasal sinus
+UBERON:0010066,tympanic plate,UBERON:0010313,neural crest-derived structure
+DOID:1725,peritoneum cancer,DOID:0050686,organ system cancer
+HP:0011461,Fetal onset,HP:0003577,Congenital onset
+UBERON:2001661,basibranchial tooth plate,UBERON:2001647,pharyngeal tooth plate
+DOID:5286,vulvar leiomyosarcoma,DOID:2096,vulvar sarcoma
+DOID:12217,Lewy body dementia,DOID:1307,dementia
+HP:0007341,Diffuse swelling of cerebral white matter,HP:0002500,Abnormality of the cerebral white matter
+HP:0012524,Abnormal platelet shape,HP:0011875,Abnormal platelet morphology
+HP:0010259,Cone-shaped epiphyses of the middle phalanges of the hand,HP:0010230,Cone-shaped epiphyses of the phalanges of the hand
+HP:0006872,Cerebral hypoplasia,HP:0007364,Aplasia/Hypoplasia of the cerebrum
+NCBITaxon:203691,Spirochaetes,NCBITaxon:2,Bacteria
+HP:0010722,Asymmetry of the ears,HP:0000377,Abnormality of the pinna
+HP:0004607,Anterior beaking of lower thoracic vertebrae,HP:0004568,Beaking of vertebral bodies
+UBERON:0015814,outer ear epithelium,UBERON:0015807,ear epithelium
+UBERON:0014534,external medullary lamina of thalamus,UBERON:0014533,medullary lamina of thalamus
+UBERON:0005022,mucosa of nasopharynx,UBERON:0000379,tracheal mucosa
+DOID:14654,prostatitis,DOID:47,prostate disease
+HP:0007418,Alopecia totalis,HP:0001596,Alopecia
+UBERON:4000163,anal fin,UBERON:4000162,median fin
+CL:1001099,kidney efferent arteriole endothelial cell,CL:1001009,kidney efferent arteriole cell
+DOID:14096,infertility due to extratesticular cause,DOID:12336,male infertility
+UBERON:0006065,hemal arch,UBERON:0010358,arch of centrum of vertebra
+UBERON:0005463,marginal sinus of lymph node,UBERON:0001638,vein
+UBERON:0001936,tuberomammillary nucleus,UBERON:0002785,regional part of lateral hypothalamic region
+UBERON:0009500,associated mesenchyme of otocyst,UBERON:0007213,mesenchyme derived from head neural crest
+HP:0009031,Amyotrophy of ankle musculature,HP:0001436,Abnormality of the foot musculature
+UBERON:0010015,ventral patch of Leydig's organ,UBERON:0004120,mesoderm-derived structure
+UBERON:0002065,posterior cardinal vein,UBERON:0003513,trunk blood vessel
+CL:0013000,forebrain radial glial cell,CL:0000681,radial glial cell
+HP:0008773,Aplasia/Hypoplasia of the middle ear,HP:0008609,Morphological abnormality of the middle ear
+HP:0005543,Reduced protein C activity,HP:0003256,Abnormality of the coagulation cascade
+DOID:14547,sphenoid sinus squamous cell carcinoma,DOID:14546,sphenoidal sinus cancer
+HP:0011041,Aplasia/Hypoplasia of the cervical spine,HP:0008518,Aplasia/Hypoplasia involving the vertebral column
+UBERON:0000086,zona pellucida,UBERON:0014404,female anatomical structure
+HP:0009647,Proximal/distal symphalangism of thumb,HP:0009635,Symphalangism of proximal phalanx of  thumb
+HP:0010261,Fragmentation of the epiphyses of the middle phalanges of the hand,HP:0010244,Abnormality of the epiphyses of the middle phalanges of the hand
+UBERON:0013503,caudal vertebra cartilage element,UBERON:0011094,vertebra cartilage element
+UBERON:2002085,ural centrum,UBERON:0002513,endochondral bone
+HP:0004315,IgG deficiency,HP:0004313,Hypogammaglobulinemia
+HP:0200041,Skin erosion,HP:0011355,Localized skin lesion
+UBERON:2001993,branched pectoral fin ray,UBERON:4000175,pectoral fin lepidotrichium
+UBERON:0002580,brachium of superior colliculus,UBERON:0006786,white matter of superior colliculus
+UBERON:0001495,pectoral muscle,UBERON:0003830,thoracic segment muscle
+HP:0010267,Triangular epiphyses of the middle phalanges of the hand,HP:0010238,Triangular epiphyses of the phalanges of the hand
+UBERON:0000019,camera-type eye,UBERON:0004121,ectoderm-derived structure
+HP:0003496,Increased IgM level,HP:0010702,Hypergammaglobulinemia
+DOID:7735,pancreatic colloid cystadenoma,DOID:3918,pancreatic cystadenoma
+HP:0002575,Tracheoesophageal fistula,HP:0002778,Abnormality of the trachea
+HP:0010139,Bracket epiphysis of the distal phalanx of the hallux,HP:0010114,Bracket epiphyses of the hallux
+CL:1000436,epithelial cell of lacrimal sac,CL:0000068,duct epithelial cell
+DOID:4971,myelofibrosis,DOID:0070004,myeloma
+DOID:0060030,"autoimmune disease of eyes, ear, nose and throat",DOID:417,hypersensitivity reaction type II disease
+DOID:1583,laryngeal tuberculosis,DOID:3437,laryngitis
+UBERON:3000837,crista medialis humeri,UBERON:4100000,skeletal element projection
+CL:0005012,multi-ciliated epithelial cell,CL:0000064,ciliated cell
+DOID:0050025,human granulocytic anaplasmosis,DOID:10242,ehrlichiosis
+UBERON:0002846,second thoracic dorsal root ganglion,UBERON:0002835,thoracic dorsal root ganglion
+DOID:7206,melanomatosis,DOID:1909,melanoma
+HP:0100383,Aplasia of the middle phalanx of the 5th toe,HP:0100364,Aplasia of the phalanges of the 5th toe
+HP:0009199,Irregular epiphysis of the proximal phalanx of the 5th finger,HP:0010273,Irregular epiphyses of the proximal phalanges of the hand
+UBERON:0001279,portal triad,UBERON:0004119,endoderm-derived structure
+HP:0010400,Patchy sclerosis of the proximal phalanx of the 2nd toe,HP:0010352,Patchy sclerosis of the phalanges of the 2nd toe
+DOID:746,adenomatoid tumor,DOID:2645,benign mesothelioma
+HP:0010119,Ivory epiphyses of the hallux,HP:0010168,Ivory epiphyses of the toes
+UBERON:0003112,olfactory region,UBERON:0004120,mesoderm-derived structure
+HP:0010866,Abdominal wall defect,HP:0004298,Abnormality of the abdominal wall
+UBERON:2101672,dorsal fin radial element,UBERON:2105225,median fin radial element
+UBERON:0013505,cervical vertebra cartilage element,UBERON:0011094,vertebra cartilage element
+UBERON:0005867,mandibular prominence,UBERON:0012314,embryonic facial prominence
+DOID:10533,viral pneumonia,DOID:552,pneumonia
+UBERON:0011948,ureter subluminal urothelium,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0011264,Discontinuous ascending root of helix,HP:0011039,Abnormality of the helix
+HP:0100012,Neoplasm of the eye,HP:0011793,Neoplasm by anatomical site
+CL:0002126,"CD25-positive, CD27-positive immature gamma-delta T cell",CL:0000893,thymocyte
+UBERON:2001650,pharyngobranchial 2 tooth plate,UBERON:2002015,pharyngobranchial tooth plate
+CL:0000108,cholinergic neuron,CL:0000540,neuron
+CL:0000913,"effector memory CD8-positive, alpha-beta T cell",CL:0000909,"CD8-positive, alpha-beta memory T cell"
+UBERON:0000067,embryo stage part,UBERON:0000105,life cycle stage
+HP:0000452,Choanal stenosis,HP:0000415,Abnormality of the choanae
+UBERON:0003482,vein of trabecular bone,UBERON:0001638,vein
+CL:0000797,alpha-beta intraepithelial T cell,CL:0000791,mature alpha-beta T cell
+CL:0000227,binucleate cell,CL:0000228,multinucleate cell
+HP:0010112,Mesoaxial foot polydactyly,HP:0100260,Mesoaxial polydactyly
+UBERON:0009548,hepatic sinusoid of left of lobe of liver,UBERON:0001281,hepatic sinusoid
+HP:0100235,Synostosis involving bones of the toes,HP:0009140,Synostosis involving bones of the feet
+DOID:193,reproductive organ cancer,DOID:0050686,organ system cancer
+DOID:3507,dermatofibrosarcoma protuberans,DOID:3355,fibrosarcoma
+UBERON:0000453,decidua basalis,UBERON:0000478,extraembryonic structure
+UBERON:3010831,occipito-petrosal,UBERON:0004765,skeletal element
+UBERON:0011948,ureter subluminal urothelium,UBERON:0011946,subluminal layer of epithelium
+HP:0009965,Complete duplication of the distal phalanx of the 3rd finger,HP:0010001,Complete duplication of the distal phalanges of the hand
+UBERON:0015445,anterior lingual gland duct,UBERON:0001837,duct of salivary gland
+DOID:14262,oral candidiasis,DOID:1508,candidiasis
+HP:0010991,Abnormality of the abdominal musculature,HP:0004298,Abnormality of the abdominal wall
+UBERON:0003309,floor plate of diencephalon,UBERON:0003306,floor plate of neural tube
+UBERON:0002172,alveolar atrium,UBERON:0000064,organ part
+UBERON:0013126,vein of abdomen,UBERON:0003497,abdomen blood vessel
+HP:0010329,Abnormality of the epiphyses of the 3rd toe,HP:0010320,Abnormality of the 3rd toe
+UBERON:2001396,parapophysis + rib of vertebra 4,UBERON:0004120,mesoderm-derived structure
+CL:0002557,fibroblast of pulmonary artery,CL:0000057,fibroblast
+HP:0004850,Recurrent deep vein thrombosis,HP:0002625,Deep venous thrombosis
+HP:0007866,Focal retinal infarction,HP:0000479,Abnormality of the retina
+DOID:543,dystonia,DOID:480,movement disease
+DOID:5527,ampulla of Vater squamous cell carcinoma,DOID:4932,ampulla of Vater carcinoma
+NCBITaxon:10066,Muridae,NCBITaxon:337687,Muroidea
+UBERON:0001520,pronator teres,UBERON:0003662,forelimb muscle
+DOID:3713,ovary adenocarcinoma,DOID:4001,ovarian carcinoma
+HP:0000237,Small anterior fontanelle,HP:0000236,Abnormality of the anterior fontanelle
+UBERON:0015480,proper hepatic artery,UBERON:0001193,hepatic artery
+NCBITaxon:10298,Human herpesvirus 1,NCBITaxon:10294,Simplexvirus
+HP:0011840,Abnormality of T cell physiology,HP:0002843,Abnormality of T cells
+UBERON:0004062,neural tube marginal layer,UBERON:0000119,cell layer
+HP:0010068,Broad first metatarsal,HP:0010059,Broad phalanges of the hallux
+UBERON:2001930,accessory vomerine tooth plate,UBERON:0008907,dermal bone
+DOID:0050797,peroxisomal acyl-CoA oxidase deficiency,DOID:906,peroxisomal disease
+HP:0011040,Abnormality of the intrahepatic bile duct,HP:0012440,Abnormal biliary tract morphology
+UBERON:0002832,ventral nucleus of trapezoid body,UBERON:0007633,nucleus of trapezoid body
+DOID:0050892,adrenal gland pheochromocytoma,DOID:5719,adrenal medulla cancer
+HP:0002283,Global brain atrophy,HP:0002977,Aplasia/Hypoplasia involving the central nervous system
+DOID:11243,anemia of prematurity,DOID:11244,neonatal anemia
+HP:0009458,Aplasia of the proximal phalanx of the 3rd finger,HP:0009460,Aplasia of the 3rd finger
+UBERON:3000394,pars articularis of mandibular arch,UBERON:0000064,organ part
+CL:0007006,chordamesodermal cell,CL:0000222,mesodermal cell
+CL:1000477,cardiac pacemaker cell of sinoatrial node,CL:1000409,myocyte of sinoatrial node
+DOID:11245,transient neonatal neutropenia,DOID:1227,neutropenia
+HP:0100354,Contractures of the distal interphalangeal joint of the 4th toe,HP:0010339,Flexion contracture of the 4th toe
+UBERON:4200034,cnemial crest,UBERON:4100000,skeletal element projection
+DOID:0050754,ataxia with oculomotor apraxia type 1,DOID:0050753,cerebellar ataxia
+UBERON:0014732,compound cell cluster organ,UBERON:0010000,multicellular anatomical structure
+UBERON:0013129,bulb of vestibule,UBERON:0015212,lateral structure
+DOID:13431,bejel,DOID:0050338,primary bacterial infectious disease
+DOID:12835,quadriplegia,DOID:331,central nervous system disease
+DOID:8503,impetigo herpetiformis,DOID:8504,impetigo
+HP:0001769,Broad foot,HP:0001760,Abnormality of the foot
+UBERON:0002169,alveolar sac,UBERON:0000115,lung epithelium
+UBERON:3000580,stylus of pars media plectri,UBERON:0000064,organ part
+HP:0002509,Limb hypertonia,HP:0002813,Abnormality of limb bone morphology
+UBERON:0006010,hyaloid canal,UBERON:0000078,mixed ectoderm/mesoderm/endoderm-derived structure
+DOID:4114,uterine body mixed cancer,DOID:9460,uterine corpus cancer
+UBERON:0001488,ankle joint,UBERON:0011139,synovial limb joint
+UBERON:0002363,dura mater,UBERON:0002360,meninx
+HP:0012616,Leukocyte cylindruria,HP:0012615,Cylindruria
+HP:0009356,Triangular epiphysis of the proximal phalanx of the 3rd finger,HP:0009333,Abnormality of the epiphysis of the proximal phalanx of the 3rd finger
+DOID:0060182,microscopic colitis,DOID:0060180,colitis
+UBERON:0007157,superior thyroid vein,UBERON:0001638,vein
+UBERON:4400000,metapterygium cartilage,UBERON:4300082,metapterygium element
+UBERON:3000162,fenestra endonarina communis,UBERON:3000316,nasal opening
+UBERON:0013585,metapodium bone 5,UBERON:0003821,metapodium bone
+UBERON:0002242,nucleus pulposus,UBERON:0004120,mesoderm-derived structure
+CL:0000744,columnar chondrocyte,CL:0000138,chondrocyte
+CL:0002405,gamma-delta thymocyte,CL:0000798,gamma-delta T cell
+DOID:0080028,"spondyloepimetaphyseal dysplasia, Strudwick type",DOID:0080027,spondyloepimetaphyseal dysplasia
+HP:0010168,Ivory epiphyses of the toes,HP:0010160,Abnormality of the epiphyses of the toes
+CL:0002009,macrophage dendritic cell progenitor,CL:0000763,myeloid cell
+DOID:5117,dermoid cyst of ovary,DOID:2658,dermoid cyst
+HP:0003842,Irregular epiphyses of the upper limbs,HP:0010582,Irregular epiphyses
+UBERON:0014626,base of cochlear canal,UBERON:0010313,neural crest-derived structure
+UBERON:0008878,palmar part of manus,UBERON:0008837,palmar/plantar part of autopod
+HP:0001043,Prominent scalp veins,HP:0001015,Prominent superficial veins
+UBERON:0003134,female reproductive organ,UBERON:0003133,reproductive organ
+HP:0100040,Broad 2nd toe,HP:0010319,Abnormality of the 2nd toe
+HP:0000795,Abnormality of the urethra,HP:0010936,Abnormality of the lower urinary tract
+UBERON:1500005,ischial cartilage,UBERON:0007844,cartilage element
+DOID:1659,supratentorial cancer,DOID:1319,brain cancer
+CL:0000148,melanocyte,CL:0000147,pigment cell
+UBERON:0002817,secondary fissure of cerebellum,UBERON:0003980,cerebellum fissure
+UBERON:0003987,Hassall's corpuscle,UBERON:0000064,organ part
+DOID:0050799,guanidinoacetate methyltransferase deficiency,DOID:0050798,cerebral creatine deficiency syndrome
+NCBITaxon:127007,Rhipicephalus pumilio,NCBITaxon:426455,Rhipicephalus <subgenus>
+HP:0000133,Gonadal dysgenesis,HP:0000812,Abnormal internal genitalia
+HP:0012492,Cerebral artery stenosis,HP:0009145,Abnormality of cerebral artery
+HP:0004904,Maturity-onset diabetes of the young,HP:0000819,Diabetes mellitus
+UBERON:0002392,nasolacrimal duct,UBERON:0000058,duct
+UBERON:0001749,parenchyma of parathyroid gland,UBERON:0000353,parenchyma
+HP:0004528,Generalized hypotrichosis,HP:0001006,Hypotrichosis
+HP:0001854,Gout (feet),HP:0001760,Abnormality of the foot
+DOID:3593,epithelioid trophoblastic tumor,DOID:4085,trophoblastic neoplasm
+UBERON:2001348,stratum marginale,UBERON:0000479,tissue
+DOID:9908,internal hordeolum,DOID:9909,hordeolum
+CL:1000143,lung goblet cell,CL:0002370,respiratory goblet cell
+UBERON:0003864,middle phalanx of manus,UBERON:0004301,middle phalanx
+HP:0001283,Bulbar palsy,HP:0002363,Abnormality of the brainstem
+DOID:0050169,cutaneous lupus erythematosus,DOID:37,skin disease
+HP:0100604,Neoplasm of the lip,HP:0011793,Neoplasm by anatomical site
+HP:0100642,Neoplasm of the adrenal medulla,HP:0100631,Neoplasm of the adrenal gland
+CL:0002257,epithelial cell of thyroid gland,CL:0000150,glandular epithelial cell
+UBERON:0011622,thyrohyoid bone,UBERON:0002513,endochondral bone
+HP:0100403,Duplication of the middle phalanx of the 5th toe,HP:0010391,Duplication of the phalanges of the 5th toe
+CL:0000447,carbohydrate secreting cell,CL:0000151,secretory cell
+DOID:297,pleomorphic adenoma carcinoma,DOID:8850,salivary gland cancer
+UBERON:3000438,planum internasale,UBERON:0003933,cranial cartilage
+UBERON:0002061,truncus arteriosus,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0000941,cranial nerve II,UBERON:0002464,nerve trunk
+UBERON:0007179,basal cell layer of urothelium,UBERON:0006554,urinary system structure
+UBERON:0002182,main bronchus,UBERON:0002185,bronchus
+DOID:1519,cecum carcinoma,DOID:1521,cecum cancer
+NCBITaxon:169495,This,NCBITaxon:169455,Coelopellini
+UBERON:0004500,skeletal muscle tissue of deltoid,UBERON:0001134,skeletal muscle tissue
+CL:0001004,immature CD8_alpha-positive CD11b-negative dendritic cell,CL:0000840,immature conventional dendritic cell
+UBERON:0005659,primary palate epithelium,UBERON:0010313,neural crest-derived structure
+UBERON:0009049,superficial external pudendal vein,UBERON:0009029,pudendal vein
+HP:0100900,Sclerosis of the distal phalanx of the 2nd finger,HP:0100918,Sclerosis of the phalanges of the 2nd finger
+DOID:12360,lateral displacement of eye,DOID:930,orbital disease
+DOID:5849,subendocardial myocardial infarction,DOID:5844,myocardial infarction
+DOID:0050618,malignant Sertoli-Leydig cell tumor,DOID:192,sex cord-gonadal stromal tumor
+UBERON:0015005,vertebra endochondral element,UBERON:0010363,endochondral element
+UBERON:0003597,manual digit connective tissue,UBERON:0015791,digit connective tissue
+UBERON:0005259,lower leg mesenchyme,UBERON:0003860,hindlimb mesenchyme
+UBERON:0014804,median nuchal line,UBERON:0014801,nuchal line
+DOID:4437,skull base meningioma,DOID:3842,skull base neoplasm
+DOID:1293,labia minora carcinoma,DOID:1243,labia minora cancer
+UBERON:0002280,otolith,UBERON:0000476,acellular anatomical structure
+HP:0010241,Short proximal phalanx of finger,HP:0009851,Aplasia/Hypoplasia of the proximal phalanges of the hand
+DOID:3767,vaginal discharge,DOID:121,vaginal disease
+UBERON:0005451,segment of manus,UBERON:0012139,segment of autopod
+HP:0001775,Tarsal osteovalgus,HP:0008365,Abnormality of the talus
+UBERON:0010426,oropharyngeal choana,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000559,promonocyte,CL:0000763,myeloid cell
+UBERON:0015808,eye epithelium,UBERON:0007625,pigment epithelium of eye
+HP:0009910,Aplasia of the middle ear ossicles,HP:0004452,Abnormality of the middle ear ossicles
+UBERON:4200117,pubic boot,UBERON:0005913,zone of bone organ
+DOID:6511,glandular pattern ovarian yolk sac tumor,DOID:5350,ovarian endodermal sinus tumor
+UBERON:0009073,dorsobronchus,UBERON:0002183,lobar bronchus
+DOID:3817,cranial nerve palsy,DOID:5656,cranial nerve disease
+UBERON:2005372,dorsal fin distal radial bone 1,UBERON:2105372,dorsal fin distal radial element 1
+DOID:1798,pancreatic endocrine carcinoma,DOID:1799,islet cell tumor
+DOID:14717,centronuclear myopathy,DOID:423,myopathy
+DOID:13042,persistent fetal circulation syndrome,DOID:6432,pulmonary hypertension
+UBERON:3000648,crista praeopercularis,UBERON:4100000,skeletal element projection
+UBERON:0000401,mandibular ramus,UBERON:0010313,neural crest-derived structure
+UBERON:0005364,superior vagus X ganglion,UBERON:0005362,vagus X ganglion
+HP:0006371,Broad long bone diaphyses,HP:0006504,Anomaly of the limb diaphyses
+HP:0100072,Ivory epiphyses of the 4th toe,HP:0010168,Ivory epiphyses of the toes
+NCBITaxon:11250,Human respiratory syncytial virus,NCBITaxon:11245,Pneumovirus
+UBERON:0012126,fibulare,UBERON:0011679,proximal tarsal bone
+UBERON:2002098,hemal spine series,UBERON:0000477,anatomical cluster
+UBERON:0002588,decussation of superior cerebellar peduncle,UBERON:0007418,decussation of neuraxis
+HP:0010113,Absent epiphyses of the hallux,HP:0010056,Abnormality of the epiphyses of the hallux
+UBERON:0008886,pulmonary vascular system,UBERON:0007798,vascular system
+CL:0000090,female germ line stem cell (sensu Vertebrata),CL:0000022,female germ line stem cell
+HP:0100760,Clubbing of toes,HP:0001217,Clubbing
+DOID:7389,pulmonary artery leiomyosarcoma,DOID:175,vascular cancer
+HP:0100171,Cone-shaped epiphysis of the distal phalanx of the 4th toe,HP:0100094,Abnormality of the epiphysis of the distal phalanx of the 4th toe
+UBERON:0015095,distal carpal bone 4 pre-cartilage condensation,UBERON:0015093,distal carpal bone 4 endochondral element
+CL:0002423,DN2a thymocyte,CL:0000806,DN2 thymocyte
+HP:0000270,Delayed cranial suture closure,HP:0011329,Abnormality of cranial sutures
+CL:0000743,hypertrophic chondrocyte,CL:0000138,chondrocyte
+UBERON:0006286,radius cartilage element,UBERON:0010883,forelimb cartilage element
+HP:0011304,Broad thumb,HP:0009768,Broad phalanges of the hand
+HP:0100590,Rectal fistula,HP:0002034,Abnormality of the rectum
+UBERON:0003306,floor plate of neural tube,UBERON:0004120,mesoderm-derived structure
+DOID:7522,pediatric infratentorial ependymoblastoma,DOID:4207,childhood infratentorial neoplasm
+UBERON:0004193,loop of Henle ascending limb thin segment,UBERON:0008408,distal tubular epithelium
+DOID:4362,cervical cancer,DOID:120,female reproductive organ cancer
+HP:0100491,Abnormality of the joints of the lower limbs,HP:0002814,Abnormality of the lower limb
+UBERON:0006650,tunica vaginalis testis,UBERON:0005156,reproductive structure
+HP:0006463,Rickets of the lower limbs,HP:0002748,Rickets
+HP:0001140,Epibulbar dermoid,HP:0000502,Abnormality of the conjunctiva
+HP:0007469,Palmoplantar cutis gyrata,HP:0007477,Abnormal dermatoglyphics
+CL:0002062,type I pneumocyte,CL:0000322,pneumocyte
+HP:0100047,Enlarged epiphyses of the 2nd toe,HP:0010165,Enlarged epiphyses of the toes
+UBERON:0006768,epiphyseal line,UBERON:0010361,synostosis
+UBERON:0008436,thoracic vertebral arch,UBERON:0003827,thoracic segment bone
+CL:0005024,somatomotor neuron,CL:0000108,cholinergic neuron
+UBERON:0004675,hypoglossal nerve root,UBERON:0011215,cell part cluster of neuraxis
+DOID:0050873,follicular lymphoma,DOID:0060060,non-Hodgkin lymphoma
+UBERON:3000831,spina acromioidea,UBERON:0004120,mesoderm-derived structure
+NCBITaxon:37962,Bayou virus,NCBITaxon:11598,Hantavirus
+HP:0006558,Decreased mitochondrial complex III activity in liver tissue,HP:0001392,Abnormality of the liver
+DOID:14735,hereditary angioedema,DOID:1558,angioedema
+CL:1000454,kidney collecting duct epithelial cell,CL:1001225,kidney collecting duct cell
+UBERON:4000175,pectoral fin lepidotrichium,UBERON:0010741,bone of pectoral complex
+UBERON:0006190,mesonephric distal tubule,UBERON:0000083,mesonephric tubule
+UBERON:0016393,deep parotid lymph node,UBERON:0015918,deep lymph node
+UBERON:0001896,medulla oblongata,UBERON:0000064,organ part
+UBERON:0002198,neurohypophysis,UBERON:0010134,secretory circumventricular organ
+HP:0012006,Jamais vu,HP:0012004,Mnemonic auras
+CL:0000418,arcade cell,CL:0000066,epithelial cell
+HP:0000040,Enlarged penis,HP:0000036,Abnormality of the penis
+UBERON:0011949,endometrium luminal epithelium,UBERON:0005156,reproductive structure
+DOID:14243,chronic perichondritis of pinna,DOID:222,perichondritis of auricle
+UBERON:0001987,placenta,UBERON:0000062,organ
+UBERON:0009526,maxillary process mesenchyme,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:9024,intestine carcinoma in situ,DOID:8719,in situ carcinoma
+HP:0011068,Odontoma,HP:0100612,Odontogenic neoplasm
+DOID:11206,opioid abuse,DOID:302,substance abuse
+DOID:3545,childhood choroid plexus cancer,DOID:3540,choroid plexus cancer
+DOID:1453,atrophic glossitis,DOID:1456,glossitis
+HP:0010423,Partial duplication of the proximal phalanx of the 2nd toe,HP:0010403,Duplication of the proximal phalanx of the 2nd toe
+UBERON:0005647,manual digit 4 epithelium,UBERON:0005227,manual digit epithelium
+HP:0010281,Cleft lower lip,HP:0000178,Abnormality of lower lip
+HP:0011332,Hemifacial hypoplasia,HP:0000324,Facial asymmetry
+HP:0009322,Bracket epiphysis of the middle phalanx of the 3rd finger,HP:0009334,Abnormality of the epiphysis of the middle phalanx of the 3rd finger
+CL:0009002,inflammatory cell,CL:0002371,somatic cell
+UBERON:0002764,inferior precentral sulcus,UBERON:0003022,cerebral cortex lobe
+HP:0010247,Bracket epiphyses of the distal phalanges of the hand,HP:0010229,Bracket epiphyses of the phalanges of the hand
+HP:0200135,Macrocephaly due to hydrocephalus,HP:0000256,Macrocephaly
+DOID:12475,pes anserinus tendinitis or bursitis,DOID:204,enthesopathy
+UBERON:0002830,anteroventral cochlear nucleus,UBERON:0001720,cochlear nucleus
+UBERON:3000704,anterior intervertebral notch,UBERON:0000464,anatomical space
+UBERON:0007140,parietal mesothelium,UBERON:0001136,mesothelium
+HP:0000214,Lip telangiectasia,HP:0000228,Oral cavity teleangiectasia
+DOID:8927,learning disability,DOID:0060038,specific developmental disorder
+HP:0007665,Curly eyelashes,HP:0000499,Abnormality of the eyelashes
+UBERON:0001188,right testicular artery,UBERON:0010192,genital artery
+HP:0100539,Periorbital edema,HP:0000282,Facial edema
+HP:0004254,Delayed ossification of the trapezium,HP:0001216,Delayed ossification of carpal bones
+DOID:3458,breast adenocarcinoma,DOID:3459,breast carcinoma
+UBERON:0004931,submucosa of descending colon,UBERON:0003331,submucosa of colon
+HP:0012025,Abnormality of ornithine metabolism,HP:0004337,Abnormality of amino acid metabolism
+HP:0100428,Broad proximal phalanx of the 3rd toe,HP:0010360,Broad phalanges of the 3rd toe
+HP:0004295,Abnormality of the gastric mucosa,HP:0002577,Abnormality of the stomach
+UBERON:0007732,interphalangeal joint of manual digit 5,UBERON:0007722,interphalangeal joint of manus
+UBERON:0000158,membranous layer,UBERON:0004923,organ component layer
+HP:0012480,Abnormality of cerebral veins,HP:0100659,Abnormality of the cerebral vasculature
+HP:0100007,Neoplasm of the peripheral nervous system,HP:0000759,Abnormality of the peripheral nervous system
+UBERON:0011582,paired limb/fin skeleton,UBERON:0004120,mesoderm-derived structure
+DOID:0050823,third-degree atrioventricular block,DOID:0050820,atrioventricular block
+UBERON:0003314,eye mesenchyme,UBERON:0007213,mesenchyme derived from head neural crest
+NCBITaxon:11077,Kunjin virus,NCBITaxon:11082,West Nile virus
+UBERON:0002604,ventral nucleus of lateral lemniscus,UBERON:0006840,nucleus of lateral lemniscus
+UBERON:0004731,neuromere,UBERON:0004732,segmental subdivision of nervous system
+UBERON:4100008,pedal claws,UBERON:0004120,mesoderm-derived structure
+UBERON:0007100,primary circulatory organ,UBERON:0015228,circulatory organ
+DOID:2455,angular blepharoconjunctivitis,DOID:2456,blepharoconjunctivitis
+UBERON:2000685,superficial abductor,UBERON:0006845,abductor muscle
+CL:0002268,P/D1 enteroendocrine cell,CL:0000164,enteroendocrine cell
+UBERON:0006906,ala of nose,UBERON:0004121,ectoderm-derived structure
+UBERON:0001314,obturator artery,UBERON:0001637,artery
+HP:0001951,Episodic ammonia intoxication,HP:0004364,Abnormality of nitrogen compound homeostasis
+HP:0003318,Cervical spine hypermobility,HP:0003319,Abnormality of the cervical spine
+HP:0005894,Double first metacarpals,HP:0005917,Supernumerary metacarpal bones
+CL:0010008,cardiac endothelial cell,CL:0002494,cardiocyte
+UBERON:0010207,nictitating membrane,UBERON:0001711,eyelid
+UBERON:0001232,collecting duct of renal tubule,UBERON:0006555,excretory tube
+UBERON:2001727,caudal principal ray 15,UBERON:2001585,caudal principal ray
+NCBITaxon:29031,Phlebotomus papatasi,NCBITaxon:44556,Phlebotomus <subgenus>
+UBERON:0002460,vesical vein,UBERON:0001638,vein
+HP:0005789,Generalized osteosclerosis,HP:0011001,Increased bone mineral density
+HP:0100595,Camptocormia,HP:0010674,Abnormality of the curvature of the vertebral column
+UBERON:0006285,pubic pre-cartilage condensation,UBERON:0015055,pubic endochondral element
+UBERON:0005687,orbitosphenoid cartilage element,UBERON:0009891,facial mesenchyme
+HP:0000032,Abnormality of male external genitalia,HP:0010461,Abnormality of the male genitalia
+UBERON:0008290,afterfeather,UBERON:0000064,organ part
+UBERON:0006806,entepicondyle of humerus,UBERON:0004120,mesoderm-derived structure
+UBERON:0011641,odontogenic mesenchyme of molar,UBERON:0003856,odontogenic mesenchyme
+HP:0002987,Elbow flexion contracture,HP:0002996,Limited elbow movement
+DOID:1612,breast cancer,DOID:5093,thoracic cancer
+HP:0004938,Tortuous cerebral arteries,HP:0005116,Arterial tortuosity
+DOID:1460,atheroembolism of kidney,DOID:1461,cholesterol embolism
+HP:0001017,Anemic pallor,HP:0000980,Pallor
+HP:0002891,Uterine leiomyosarcoma,HP:0010784,Uterine neoplasm
+HP:0004382,Mitral valve calcification,HP:0001633,Abnormality of the mitral valve
+UBERON:0012081,patella pre-cartilage condensation,UBERON:0010886,hindlimb bone pre-cartilage condensation
+HP:0005875,Increased dermatoglyphic whorls,HP:0001018,Abnormal palmar dermatoglyphics
+UBERON:0005638,anterior chamber epithelium,UBERON:0015808,eye epithelium
+UBERON:0010541,tarsus cartilage element,UBERON:0015050,tarsus endochondral element
+HP:0003194,Short nasal bridge,HP:0000422,Abnormality of the nasal bridge
+UBERON:3000829,margo scapularis,UBERON:0004121,ectoderm-derived structure
+UBERON:0006065,hemal arch,UBERON:0002513,endochondral bone
+UBERON:0002180,ventral funiculus,UBERON:0015212,lateral structure
+HP:0010358,Abnormality of the proximal phalanx of the 2nd toe,HP:0010184,Abnormality of the proximal phalanges of the toes
+CL:0002057,"CD14-positive, CD16-negative classical monocyte",CL:0000860,classical monocyte
+UBERON:2001822,epibranchial 3 bone uncinate process,UBERON:2001382,epibranchial bone uncinate process
+DOID:2772,irritant dermatitis,DOID:2773,contact dermatitis
+HP:0001947,Renal tubular acidosis,HP:0000124,Renal tubular dysfunction
+UBERON:0002234,proximal phalanx of manus,UBERON:0004302,proximal phalanx
+UBERON:0004731,neuromere,UBERON:0004121,ectoderm-derived structure
+UBERON:0011275,nail of manual digit 3,UBERON:0009565,nail of manual digit
+UBERON:0010752,exoccipital cartilage element,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:1383,sweat gland disease,DOID:37,skin disease
+HP:0002761,Generalized joint laxity,HP:0001382,Joint hypermobility
+UBERON:0000379,tracheal mucosa,UBERON:0004785,respiratory system mucosa
+DOID:8022,liver fibrosarcoma,DOID:270,liver sarcoma
+DOID:12474,capillariasis,DOID:883,parasitic helminthiasis infectious disease
+UBERON:0014283,piriform cortex layer 3,UBERON:0002791,regional part of telencephalon
+HP:0010907,Abnormality of proline metabolism,HP:0010902,Abnormality of glutamine family amino acid metabolism
+UBERON:0004189,glomerular endothelium,UBERON:0004188,glomerular epithelium
+HP:0010354,Triangular shaped phalanges of the 2nd toe,HP:0010180,Triangular shaped phalanges of the toes
+HP:0006637,Sternal punctate calcifications,HP:0010766,Ectopic calcification
+UBERON:0015120,right outer canthus,UBERON:0015212,lateral structure
+HP:0006375,Dumbbell-shaped femur,HP:0002823,Abnormality of the femur
+HP:0003696,Absent epiphysis of the distal phalanx of the 5th finger,HP:0009382,Absent epiphyses of the 5th finger
+HP:0006208,Metaphyseal cupping of proximal phalanges,HP:0003021,Metaphyseal cupping
+HP:0011178,Alpha-EEG,HP:0011176,EEG with constitutional variants
+HP:0002075,Dysdiadochokinesis,HP:0001251,Ataxia
+UBERON:0010065,auditory meatus epithelium,UBERON:0015814,outer ear epithelium
+DOID:1660,malignant pineal area germ cell neoplasm,DOID:5032,pineal gland cancer
+HP:0000319,Smooth philtrum,HP:0000288,Abnormality of the philtrum
+UBERON:0013228,sweat gland of eyelid,UBERON:0000382,apocrine sweat gland
+HP:0001363,Craniosynostosis,HP:0011329,Abnormality of cranial sutures
+NCBITaxon:11572,Orthobunyavirus,NCBITaxon:11571,Bunyaviridae
+HP:0006780,Parathyroid carcinoma,HP:0100733,Neoplasm of the parathyroid gland
+UBERON:0009720,oral siphon,UBERON:0009719,tunicate siphon
+HP:0009569,Broad middle phalanx of the 2nd finger,HP:0009844,Broad middle phalanx of finger
+HP:0009306,Triangular shaped distal phalanx of the 4th finger,HP:0009282,Abnormality of the distal phalanx of the 4th finger
+UBERON:4200160,mesomere (fin),UBERON:0010912,subdivision of skeleton
+DOID:4840,sebaceous carcinoma,DOID:4159,skin cancer
+UBERON:2002057,gill opening,UBERON:0000464,anatomical space
+UBERON:0015234,nucleus of ventral thalamus,UBERON:0007692,nucleus of thalamus
+HP:0010259,Cone-shaped epiphyses of the middle phalanges of the hand,HP:0010244,Abnormality of the epiphyses of the middle phalanges of the hand
+UBERON:0013777,skin of palm of manus,UBERON:0001519,skin of manus
+CL:0002028,basophil mast progenitor cell,CL:0002191,granulocytopoietic cell
+HP:0011489,Abnormal migration of corneal endothelium,HP:0011488,Abnormality of corneal endothelium
+UBERON:0014763,fused metatarsal bones 2-4,UBERON:0013588,fused metatarsal bones 3 and 4
+CL:0000708,leptomeningeal cell,CL:0000327,extracellular matrix secreting cell
+DOID:1184,nephrotic syndrome,DOID:2527,nephrosis
+HP:0002249,Melena,HP:0002239,Gastrointestinal hemorrhage
+HP:0003517,Birth length greater than 97th percentile,HP:0000098,Tall stature
+UBERON:0004737,metanephric collecting duct,UBERON:0004120,mesoderm-derived structure
+UBERON:0004781,gall bladder lamina propria,UBERON:0004119,endoderm-derived structure
+DOID:11217,chronic tympanitis,DOID:5782,tympanic membrane disease
+HP:0012172,Stereotypical body rocking,HP:0000733,Stereotypic behavior
+HP:0002443,Abnormality of the hypothalamus,HP:0010662,Abnormality of the diencephalon
+HP:0000734,Disinhibition,HP:0000719,Inappropriate behavior
+CL:0010010,cerebellar stellate cell,CL:1001611,cerebellar neuron
+UBERON:4300101,dorsal fin ceratotrichial spine,UBERON:4400001,ceratotrichium
+HP:0007039,Symmetric lesions of the basal ganglia,HP:0002134,Abnormality of the basal ganglia
+UBERON:0006222,future diencephalon,UBERON:0000481,multi-tissue structure
+HP:0001706,Endocardial fibroelastosis,HP:0004306,Abnormality of the endocardium
+UBERON:3000877,intumescentia bilateralis inferior,UBERON:0000064,organ part
+HP:0001927,Acanthocytosis,HP:0004447,Poikilocytosis
+HP:0000997,Axillary freckling,HP:0001480,Freckling
+UBERON:0010677,manual digit 3 phalanx cartilage element,UBERON:0005693,manual digit 3 mesenchyme
+DOID:12465,secondary hyperparathyroidism of renal origin,DOID:11705,impaired renal function disease
+UBERON:0005641,otocyst epithelium,UBERON:0005291,embryonic tissue
+HP:0009206,Enlarged epiphysis of the middle phalanx of the 5th finger,HP:0009385,Enlarged epiphyses of the 5th finger
+CL:0002075,brush cell of trachebronchial tree,CL:0002202,epithelial cell of tracheobronchial tree
+UBERON:0011962,transverse tarsal joint,UBERON:0001487,pes joint
+UBERON:2007052,hyohyoideus,UBERON:0005493,hyoid muscle
+UBERON:0005039,mucosa of bronchiole,UBERON:0000410,bronchial mucosa
+HP:0009246,Aplasia of the distal phalanx of the 5th finger,HP:0009239,Aplasia/Hypoplasia of the distal phalanx of the 5th finger
+UBERON:0003083,trunk neural crest,UBERON:0005291,embryonic tissue
+HP:0008483,Cervical vertebral bodies with decreased anteroposterior diameter,HP:0003319,Abnormality of the cervical spine
+HP:0005295,Pseudocoarctation of the aorta,HP:0012303,Abnormality of the aortic arch
+HP:0009677,Cone-shaped epiphysis of the distal phalanx of the thumb,HP:0010248,Cone-shaped epiphyses of the distal phalanges of the hand
+HP:0000860,Parathyroid hypoplasia,HP:0011768,Parathyroid dysgenesis
+UBERON:2000517,glossopharyngeal lobe,UBERON:0002678,regional part of medulla oblongata
+UBERON:0004713,corpus cavernosum penis,UBERON:0006609,corpus cavernosum
+HP:0004180,Short distal phalanx of the 3rd finger,HP:0009421,Aplasia/Hypoplasia of the distal phalanx of the 3rd finger
+UBERON:0009978,epicondyle,UBERON:0005913,zone of bone organ
+UBERON:2000864,epaxial region somite 1,UBERON:0003900,epaxial myotome region
+HP:0005522,Pyridoxine-responsive sideroblastic anemia,HP:0001924,Sideroblastic anemia
+HP:0100000,Early onset of sexual maturation,HP:0008373,Puberty and gonadal disorders
+UBERON:2000739,epaxial region somite 11,UBERON:0003900,epaxial myotome region
+HP:0006453,Lateral displacement of the femoral head,HP:0003368,Abnormality of the femoral head
+UBERON:0012450,Meissner's corpuscle,UBERON:0012449,mechanoreceptor
+UBERON:0001285,nephron,UBERON:0006554,urinary system structure
+UBERON:0006216,cervical sinus,UBERON:0002050,embryonic structure
+DOID:2217,Bernard-Soulier syndrome,DOID:2214,inherited blood coagulation disease
+UBERON:0011854,acinus of areolar gland,UBERON:0011856,acinus of lactiferous gland
+UBERON:0005145,metanephric comma-shaped body,UBERON:0004198,comma-shaped body
+UBERON:0010010,basal nucleus of telencephalon,UBERON:0009663,telencephalic nucleus
+UBERON:3000387,subotic alae,UBERON:4100000,skeletal element projection
+HP:0100113,Cone-shaped epiphysis of the middle phalanx of the 2nd toe,HP:0100046,Cone-shaped epiphyses of the 2nd toe
+CL:0002010,pre-conventional dendritic cell,CL:0000763,myeloid cell
+HP:0002227,White eyelashes,HP:0009887,Abnormality of hair pigmentation
+DOID:5410,pulmonary neuroendocrine tumor,DOID:1324,lung cancer
+DOID:5823,pediatric lymphoma,DOID:0060058,lymphoma
+UBERON:0010202,lateral line,UBERON:0004121,ectoderm-derived structure
+DOID:13866,multiple cranial nerve palsy,DOID:3418,glossopharyngeal nerve disease
+CL:0000781,mononuclear odontoclast,CL:0000588,odontoclast
+UBERON:2007027,forebrain midbrain boundary neural keel,UBERON:0006800,anatomical line
+CL:0000706,choroid plexus epithelial cell,CL:0000065,ependymal cell
+UBERON:0007094,visceral muculature,UBERON:0000383,musculature of body
+HP:0003704,Scapuloperoneal weakness,HP:0001324,Muscle weakness
+UBERON:0001701,glossopharyngeal ganglion,UBERON:0010313,neural crest-derived structure
+HP:0011811,Impaired touch localization,HP:0011730,Abnormality of central sensory function
+DOID:0050204,Epstein-Barr virus hepatitis,DOID:37,skin disease
+HP:0002394,Walking on tiptoes,HP:0001288,Gait disturbance
+DOID:4505,pediatric angiosarcoma,DOID:0001816,angiosarcoma
+HP:0010385,Bullet-shaped phalanges of the 5th toe,HP:0010175,Bullet-shaped phalanges of the toes
+CL:1000443,ciliary muscle cell,CL:0000359,vascular associated smooth muscle cell
+UBERON:0002175,intermediolateral nucleus,UBERON:0004121,ectoderm-derived structure
+UBERON:0013535,Brodmann (1909) area 4,UBERON:0013529,Brodmann area
+HP:0010489,Absent palmar crease,HP:0010488,Aplasia/Hypoplasia of the palmar creases
+UBERON:2000311,adductor mandibulae complex,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001365,sacro-iliac joint,UBERON:0011107,synovial joint of pelvic girdle
+DOID:13714,anodontia,DOID:1091,tooth disease
+HP:0012074,Tonic pupil,HP:0007686,Abnormal pupillary function
+UBERON:0005218,diencephalon subarachnoid space,UBERON:0000315,subarachnoid space
+UBERON:0015813,middle ear epithelium,UBERON:0015807,ear epithelium
+UBERON:0000322,cerebral lobe,UBERON:0002619,regional part of cerebral cortex
+CL:0000062,osteoblast,CL:0002320,connective tissue cell
+HP:0011821,Abnormality of facial skeleton,HP:0000929,Abnormality of the skull
+UBERON:0007414,nucleus of midbrain tegmentum,UBERON:0002635,regional part of midbrain tegmentum
+UBERON:2000319,branchiostegal membrane,UBERON:0000479,tissue
+UBERON:4200095,infraspinous process,UBERON:4100000,skeletal element projection
+UBERON:0001447,tarsal bone,UBERON:0003656,mesopodium bone
+UBERON:0005355,malleus neck,UBERON:0001560,neck of organ
+DOID:2559,opiate dependence,DOID:9974,drug dependence
+UBERON:0002064,common cardinal vein,UBERON:0003513,trunk blood vessel
+UBERON:0009887,interlobar vein,UBERON:0001638,vein
+HP:0009497,Stippling of the epiphyses of the 2nd finger,HP:0006263,Abnormality of the epiphyses of the 2nd finger
+HP:0004976,Knee dislocation,HP:0001373,Joint dislocation
+HP:0100858,Celiac artery aneurysm,HP:0002636,Aneurysm of an abdominal artery
+CL:1001596,salivary gland glandular cell,CL:0002251,epithelial cell of alimentary canal
+HP:0012365,Hypophosphaturia,HP:0012599,Abnormal urine phosphate concentration
+HP:0100221,Small epiphysis of the middle phalanx of the 5th toe,HP:0100085,Small epiphyses of the 5th toe
+DOID:120,female reproductive organ cancer,DOID:193,reproductive organ cancer
+UBERON:0005945,neurocranial trabecula,UBERON:0000440,trabecula
+DOID:6759,bone lymphoma,DOID:184,bone cancer
+HP:0005954,Pulmonary capillary hemangiomatosis,HP:0007461,Hemangiomatosis
+DOID:11669,hypertrichosis of eyelid,DOID:420,hypertrichosis
+HP:0010260,Enlarged epiphyses of the middle phalanges of the hand,HP:0010244,Abnormality of the epiphyses of the middle phalanges of the hand
+HP:0011460,Embryonal onset,HP:0003577,Congenital onset
+HP:0006770,Clear cell renal cell carcinoma,HP:0005584,Renal cell carcinoma
+HP:0006742,Congenital neuroblastoma,HP:0003006,Neuroblastoma
+UBERON:0002677,regional part of medullary raphe nuclear complex,UBERON:0002678,regional part of medulla oblongata
+HP:0011053,Agenesis of mandibular premolar,HP:0011051,Agenesis of premolar
+UBERON:0002946,regional part of cerebellum,UBERON:0002680,regional part of metencephalon
+HP:0009603,Deviation/Displacement of the thumb,HP:0001172,Abnormality of the thumb
+UBERON:0010586,manual digit phalanx pre-cartilage condensation,UBERON:0010700,phalanx pre-cartilage condensation
+UBERON:3000515,pseudoangular,UBERON:0002513,endochondral bone
+UBERON:0011622,thyrohyoid bone,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009975,Duplication of the distal phalanx of the 4th finger,HP:0009883,Duplication of the distal phalanx of hand
+CL:0000715,embryonic crystal cell,CL:0000392,crystal cell
+UBERON:0004625,sacral vertebra 4,UBERON:0001094,sacral vertebra
+HP:0009746,Thick nasal septum,HP:0000419,Abnormality of the nasal septum
+CL:0000386,attachment cell,CL:0000630,supportive cell
+DOID:3222,causalgia,DOID:3223,complex regional pain syndrome
+DOID:2491,sensory peripheral neuropathy,DOID:0060053,peripheral neuropathy
+HP:0002790,Neonatal breathing dysregulation,HP:0005957,Breathing dysregulation
+HP:0008114,Metatarsal diaphyseal endosteal sclerosis,HP:0001832,Abnormality of the metatarsal bones
+DOID:7848,interdigitating dendritic cell sarcoma,DOID:3405,histiocytosis
+UBERON:0003652,metatarsal bone of digit 3,UBERON:0001448,metatarsal bone
+HP:0005656,Positional foot deformity,HP:0001760,Abnormality of the foot
+UBERON:0005818,cephalic flexure,UBERON:0002050,embryonic structure
+HP:0100912,Sclerosis of the distal phalanx of the thumb,HP:0100915,Sclerosis of the distal phalanges of the hand
+UBERON:3000815,sternal head of coracoid,UBERON:0005913,zone of bone organ
+UBERON:0001779,iris stroma,UBERON:0004121,ectoderm-derived structure
+HP:0005341,Autonomic bladder dysfunction,HP:0002459,Dysautonomia
+UBERON:3000836,crista lateralis humeri,UBERON:4100000,skeletal element projection
+DOID:13454,gonococcal synovitis,DOID:2703,synovitis
+UBERON:2001263,ovarian follicle stage I,UBERON:0001305,ovarian follicle
+NCBITaxon:35268,Retro-transcribing viruses,NCBITaxon:10239,Viruses
+HP:0100425,Broad middle phalanx of the 3rd toe,HP:0010360,Broad phalanges of the 3rd toe
+CL:0008000,non-striated muscle cell,CL:0000187,muscle cell
+CL:0002199,oxyphil cell of parathyroid gland,CL:0002198,oncocyte
+HP:0001993,Ketoacidosis,HP:0001941,Acidosis
+DOID:6703,gastric pylorus carcinoma,DOID:5517,stomach carcinoma
+HP:0004846,Prolonged bleeding after surgery,HP:0011890,Prolonged bleeding following procedure
+HP:0100804,Ungual fibroma,HP:0010614,Fibroma
+UBERON:0001953,presubiculum,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0007160,inferior petrosal sinus,UBERON:0003499,brain blood vessel
+HP:0009689,Enlarged epiphyses of the thumb,HP:0009599,Abnormality of the epiphyses of the thumb
+HP:0200040,Epidermoid cyst,HP:0011355,Localized skin lesion
+UBERON:0011947,ureter luminal urothelium,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0003371,Enlargement of the proximal femoral epiphysis,HP:0010574,Abnormality of the epiphysis of the femoral head
+HP:0007503,Generalized ichthyosis,HP:0008064,Ichthyosis
+DOID:5437,intrahepatic bile duct adenoma,DOID:5381,bile duct adenoma
+DOID:8580,malignant histiocytosis,DOID:3405,histiocytosis
+UBERON:0015097,distal carpal bone 5 cartilage,UBERON:0015096,distal carpal bone 5 endochondral element
+UBERON:0004314,distal phalanx of manual digit 5,UBERON:0014487,distal phalanx of digit 5
+UBERON:0011623,horn of thyroid cartilage,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0014649,white matter of medulla oblongata,UBERON:0014891,brainstem white matter
+UBERON:0013588,fused metatarsal bones 3 and 4,UBERON:0001448,metatarsal bone
+CL:0000107,autonomic neuron,CL:0000540,neuron
+CL:0001048,"activated CD4-positive, CD25-positive, CCR4-positive, alpha-beta regulatory T cell, human",CL:0001047,"CD4-positive, CD25-positive, CCR4-positive, alpha-beta regulatory T cell"
+UBERON:0000423,eccrine sweat gland,UBERON:0010243,merocrine gland
+UBERON:0006436,principal artery to forelimb,UBERON:0007718,principal artery to limb
+DOID:9663,aphthous stomatitis,DOID:9637,stomatitis
+UBERON:0009501,mesenchyme of fronto-nasal process,UBERON:0007213,mesenchyme derived from head neural crest
+UBERON:0006254,ischial cartilage element,UBERON:0007844,cartilage element
+UBERON:0010018,spiral valve of conus arteriosus,UBERON:0004120,mesoderm-derived structure
+UBERON:0005626,ventral mesogastrium,UBERON:0003281,mesentery of stomach
+DOID:2816,malignant oculomotor nerve tumor,DOID:2815,cranial nerve malignant neoplasm
+UBERON:0001700,geniculate ganglion,UBERON:0010313,neural crest-derived structure
+CL:0000936,early lymphoid progenitor,CL:0000837,hematopoietic multipotent progenitor cell
+HP:0012520,Perivascular spaces,HP:0100659,Abnormality of the cerebral vasculature
+UBERON:3000020,anterolateral process of frontoparietal,UBERON:0004120,mesoderm-derived structure
+HP:0008005,Congenital corneal dystrophy,HP:0001131,Corneal dystrophy
+HP:0002509,Limb hypertonia,HP:0001276,Hypertonia
+HP:0006595,Scapulohumeral synostosis,HP:0000782,Abnormality of the scapula
+UBERON:3000177,flange of quadratojugal,UBERON:0010313,neural crest-derived structure
+DOID:0050026,human monocytic ehrlichiosis,DOID:10242,ehrlichiosis
+CL:0002188,glomerular endothelial cell,CL:1000746,glomerular cell
+UBERON:0009647,tympanic membrane epithelium,UBERON:0015813,middle ear epithelium
+HP:0010628,Facial palsy,HP:0006824,Cranial nerve paralysis
+HP:0100005,Testicular mesothelioma,HP:0010788,Testicular neoplasm
+HP:0001824,Weight loss,HP:0004325,Decreased body weight
+NCBITaxon:10310,Human herpesvirus 2,NCBITaxon:10294,Simplexvirus
+HP:0009484,Deviation of the hand or of fingers of the hand,HP:0001155,Abnormality of the hand
+UBERON:4300002,palatine prong,UBERON:0004120,mesoderm-derived structure
+DOID:3701,cervical mucinous adenocarcinoma,DOID:3702,cervical adenocarcinoma
+UBERON:0015469,splenic lymph node,UBERON:0000029,lymph node
+HP:0011158,Auditory auras,HP:0011157,Auras
+UBERON:2005319,intersegmental lymph vessel,UBERON:0004536,lymph vasculature
+HP:0006994,Diffuse leukoencephalopathy,HP:0002352,Leukoencephalopathy
+HP:0000866,Euthyroid multinodular goiter,HP:0009798,Euthyroid goiter
+UBERON:0003308,floor plate of telencephalon,UBERON:0003306,floor plate of neural tube
+HP:0001258,Spastic paraplegia,HP:0002061,Lower limb spasticity
+UBERON:3010069,intermedium (fore),UBERON:0000064,organ part
+CL:0000650,mesangial cell,CL:0000669,pericyte cell
+DOID:754,bladder tuberculosis,DOID:2149,urogenital tuberculosis
+DOID:10174,lacrimal passage granuloma,DOID:1400,lacrimal apparatus disease
+CL:0000941,thymic conventional dendritic cell,CL:0000990,conventional dendritic cell
+HP:0004877,respiratory failure in infancy,HP:0002093,Respiratory insufficiency
+CL:0002556,fibroblast of periodontium,CL:0000057,fibroblast
+UBERON:0003846,thymus epithelium,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0100066,Absent epiphyses of the 4th toe,HP:0010335,Abnormality of the epiphyses of the 4th toe
+DOID:7841,pediatric cerebral ependymoblastoma,DOID:4794,ependymoblastoma
+HP:0100692,Increased corneal curvature,HP:0100691,Abnormality of the curvature of the cornea
+HP:0005943,Respiratory arrest,HP:0002093,Respiratory insufficiency
+UBERON:0005673,left lung endothelium,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0001859,Distal symphalangism (feet),HP:0100235,Synostosis involving bones of the toes
+HP:0003320,C1-C2 subluxation,HP:0008440,C1-C2 vertebral abnormality
+UBERON:0006170,mesonephric capsule,UBERON:0004120,mesoderm-derived structure
+HP:0100154,Small epiphysis of the middle phalanx of the 3rd toe,HP:0100092,Abnormality of the epiphysis of the middle phalanx of the 3rd toe
+CL:0000418,arcade cell,CL:0002371,somatic cell
+DOID:0060031,autoimmune disease of gastrointestinal tract,DOID:417,hypersensitivity reaction type II disease
+UBERON:0002083,ductus venosus,UBERON:0001638,vein
+UBERON:0011653,diapophysis of rib,UBERON:0004120,mesoderm-derived structure
+UBERON:0001869,cerebral hemisphere,UBERON:0015212,lateral structure
+CL:0002584,renal cortical epithelial cell,CL:0002518,kidney epithelial cell
+UBERON:3000486,processus ascendens plectri,UBERON:0010313,neural crest-derived structure
+DOID:2722,acrodermatitis,DOID:2723,dermatitis
+HP:0007704,Paroxysmal involuntary eye movements,HP:0012547,Abnormal involuntary eye movements
+HP:0010232,Fragmentation of the epiphyses of the phalanges of the hand,HP:0003841,Fragmented epiphyses of the upper limbs
+DOID:6838,rete ovarii cystadenofibroma,DOID:4895,rete ovarii neoplasm
+UBERON:0011186,Krause's gland,UBERON:0013226,accessory lacrimal gland
+DOID:13585,alveolar periostitis,DOID:9957,periostitis
+UBERON:0003550,forebrain pia mater,UBERON:0003549,brain pia mater
+UBERON:0003719,Pacinian corpuscle,UBERON:0004121,ectoderm-derived structure
+UBERON:0004128,optic vesicle,UBERON:0004121,ectoderm-derived structure
+UBERON:0004866,actinopterygian frontal bone,UBERON:0011164,neurocranium bone
+UBERON:0003659,pedal digit muscle,UBERON:0001498,muscle of pes
+UBERON:0002331,umbilical cord,UBERON:0004120,mesoderm-derived structure
+UBERON:0014733,dorsal ventricular ridge of pallium,UBERON:0002791,regional part of telencephalon
+HP:0009431,Bullet-shaped middle phalanx of the 3rd finger,HP:0009845,Bullet-shaped middle phalanges of the hand
+DOID:6517,clivus meningioma,DOID:4437,skull base meningioma
+CL:0000095,neuron associated cell,CL:0002319,neural cell
+DOID:4048,central nervous system rhabdomyosarcoma,DOID:2133,central nervous system sarcoma
+UBERON:2005316,fin fold pectoral fin bud,UBERON:0004121,ectoderm-derived structure
+HP:0000453,Choanal atresia,HP:0000415,Abnormality of the choanae
+HP:0004558,Cervical platyspondyly,HP:0003319,Abnormality of the cervical spine
+UBERON:2000691,supraorbital bone,UBERON:0003462,facial bone
+HP:0009170,Osteolytic defects of the middle phalanx of the 5th finger,HP:0004216,Osteolytic defects of the phalanges of the 5th finger
+UBERON:0002124,medulla of thymus,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0002764,inferior precentral sulcus,UBERON:0013118,sulcus of brain
+UBERON:0009549,hepatic sinusoid of right of lobe of liver,UBERON:0001281,hepatic sinusoid
+UBERON:2001819,dorsal fin proximal radial bone 2,UBERON:2000947,dorsal fin proximal radial bone
+DOID:11175,enophthalmos,DOID:930,orbital disease
+UBERON:3000380,palatoquadrate articular process,UBERON:0004121,ectoderm-derived structure
+HP:0009269,Small epiphysis of the proximal phalanx of the 4th finger,HP:0009401,Small epiphyses of the 4th finger
+UBERON:0002938,parvocellular part of red nucleus,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004788,kidney pelvis urothelium,UBERON:0001254,urothelium of ureter
+UBERON:0005620,primary palate,UBERON:0004120,mesoderm-derived structure
+HP:0009778,Short thumb,HP:0009601,Aplasia/Hypoplasia of the thumb
+DOID:0050135,subcutaneous mycosis,DOID:1564,fungal infectious disease
+CL:0002312,somatotroph,CL:0000295,somatotropin secreting cell
+HP:0009978,Complete duplication of the distal phalanx of the 4th finger,HP:0009975,Duplication of the distal phalanx of the 4th finger
+UBERON:0008790,rugal fold,UBERON:0000061,anatomical structure
+HP:0003203,Negative nitroblue tetrazolium (NBT) reduction test,HP:0011993,Impaired neutrophil bactericidal activity
+UBERON:0003058,hypochord,UBERON:0005291,embryonic tissue
+HP:0008417,Vertebral hypoplasia,HP:0008515,Aplasia/Hypoplasia of the vertebrae
+UBERON:2000957,hypaxial region somite 19,UBERON:0003895,hypaxial myotome region
+HP:0009207,Fragmentation of the epiphysis of the middle phalanx of the 5th finger,HP:0009386,Fragmentation of the epiphyses of the 5th finger
+UBERON:0001811,conjunctiva,UBERON:0004121,ectoderm-derived structure
+HP:0100773,Cartilage destruction,HP:0002763,Abnormal cartilage morphology
+UBERON:0003526,respiratory system capillary,UBERON:0001982,capillary
+UBERON:2001889,supraneural 1 cartilage,UBERON:4300036,supraneural cartilage
+HP:0001162,Postaxial hand polydactyly,HP:0004207,Abnormality of the 5th finger
+CL:0000256,uric acid accumulating cell,CL:0000325,stuff accumulating cell
+HP:0200133,Lumbosacral meningocele,HP:0100712,Abnormality of the lumbar spine
+DOID:5524,adenoid squamous cell carcinoma,DOID:1749,squamous cell carcinoma
+CL:0002148,dental pulp cell,CL:0002320,connective tissue cell
+DOID:6867,mediastinal gray zone lymphoma,DOID:5822,gray zone lymphoma
+UBERON:0008993,habenular nucleus,UBERON:0000445,habenular trigone
+UBERON:0005272,peritubular capillary,UBERON:0003527,kidney capillary
+HP:0001320,Cerebellar vermis hypoplasia,HP:0006817,Aplasia/Hypoplasia of the  cerebellar vermis
+UBERON:0001489,manus joint,UBERON:0011139,synovial limb joint
+HP:0009335,Absent epiphysis of the distal phalanx of the 3rd finger,HP:0010246,Absent epiphyses of the distal phalanges of the hand
+HP:0006595,Scapulohumeral synostosis,HP:0100238,Synostosis involving bones of the upper limbs
+UBERON:2000293,synencephalon,UBERON:0002784,regional part of diencephalon
+HP:0012617,Erythrocyte cylindruria,HP:0012615,Cylindruria
+DOID:4386,myofibroma,DOID:201,connective tissue cancer
+DOID:470,verrucous keratotic hemangioma,DOID:471,skin hemangioma
+UBERON:0015481,left hepatic artery,UBERON:0001193,hepatic artery
+UBERON:0015043,manual digit 1 metacarpus endochondral element,UBERON:0015042,manual digit metacarpus endochondral element
+HP:0009259,Stippling of the epiphysis of the distal phalanx of the 4th finger,HP:0010255,Stippling of the epiphyses of the distal phalanges of the hand
+UBERON:0002472,stylopod,UBERON:0002529,limb segment
+UBERON:0013584,metapodium bone 4,UBERON:0003821,metapodium bone
+DOID:6994,malignant iris melanoma,DOID:3478,iris cancer
+DOID:0060053,peripheral neuropathy,DOID:870,neuropathy
+UBERON:0002714,rubrospinal tract,UBERON:0007702,tract of brain
+UBERON:0003135,male reproductive organ,UBERON:0003133,reproductive organ
+UBERON:0003081,lateral plate mesoderm,UBERON:0007524,dense mesenchyme tissue
+DOID:961,neurofibroma of the esophagus,DOID:962,neurofibroma
+HP:0001929,Reduced factor XI activity,HP:0010989,Abnormality of the intrinsic pathway
+HP:0009464,Ulnar deviation of the 2nd finger,HP:0009468,Deviation of the 2nd finger
+UBERON:0003999,hyoid bone body,UBERON:0010273,zone of hyoid bone
+UBERON:0005587,rhombomere 7 roof plate,UBERON:0005502,rhombomere roof plate
+UBERON:0003675,tooth crown,UBERON:0000063,organ segment
+NCBITaxon:6960,Hexapoda,NCBITaxon:197562,Pancrustacea
+UBERON:2202277,pectoral fin distal radial cartilage 1,UBERON:2201588,pectoral fin distal radial cartilage
+UBERON:0016408,corona of glans penis,UBERON:0005156,reproductive structure
+UBERON:0009635,parachordal cartilage,UBERON:0003932,cartilage element of chondrocranium
+NCBITaxon:34353,Dipodascaceae,NCBITaxon:4892,Saccharomycetales
+CL:0000273,prestalk AB cell,CL:0000269,prestalk cell
+UBERON:0014394,uterine fat pad,UBERON:0014404,female anatomical structure
+HP:0011450,CNS infection,HP:0002011,Abnormality of the central nervous system
+CL:1000312,bronchial goblet cell,CL:0002328,bronchial epithelial cell
+CL:1000432,conjunctival epithelial cell,CL:0002371,somatic cell
+HP:0009991,Complete duplication of the distal phalanx of the 5th finger,HP:0009988,Duplication of the distal phalanx of the 5th finger
+HP:0009995,Partial duplication of the middle phalanx of the 5th finger,HP:0009989,Duplication of the middle phalanx of the 5th finger
+UBERON:0007731,interphalangeal joint of manual digit 4,UBERON:0007722,interphalangeal joint of manus
+DOID:0050755,ataxia with oculomotor apraxia type 2,DOID:0050753,cerebellar ataxia
+UBERON:0002338,lamina propria of bronchus,UBERON:0004119,endoderm-derived structure
+HP:0009173,Curved middle phalanx of the 5th finger,HP:0009846,Curved middle phalanges of the hand
+UBERON:0002068,urachus,UBERON:0000481,multi-tissue structure
+HP:0009514,Bracket epiphysis of the middle phalanx of the 2nd finger,HP:0009489,Bracket epiphyses of the 2nd finger
+HP:0009171,Triangular epiphyses of the metacarpals,HP:0010587,Triangular epiphyses
+HP:0009533,Stippling of the epiphysis of the proximal phalanx of the 2nd finger,HP:0009497,Stippling of the epiphyses of the 2nd finger
+HP:0011571,Parachute mitral valve,HP:0001718,Mitral stenosis
+DOID:7930,glandular-alveolar pattern testicular yolk sac tumor,DOID:5344,testicular yolk sac tumor
+DOID:9230,dyshidrosis,DOID:1383,sweat gland disease
+UBERON:0004357,paired limb/fin bud,UBERON:0003102,surface structure
+HP:0009311,Bullet-shaped proximal phalanx of the 4th finger,HP:0009405,Bullet-shaped phalanges of the 4th finger
+DOID:1064,cystinosis,DOID:3211,lysosomal storage disease
+CL:1001064,kidney artery smooth muscle cell,CL:1000891,kidney arterial blood vessel cell
+UBERON:0005212,Leydig cell region of testis,UBERON:0005156,reproductive structure
+DOID:471,skin hemangioma,DOID:3165,skin benign neoplasm
+UBERON:2001780,pelvic fin lepidotrichium 5,UBERON:4000173,pelvic fin lepidotrichium
+CL:0000584,enterocyte,CL:0000677,gut absorptive cell
+HP:0000142,Abnormality of the vagina,HP:0000008,Abnormality of female internal genitalia
+HP:0100641,Neoplasm of the adrenal cortex,HP:0100631,Neoplasm of the adrenal gland
+UBERON:0014385,aryepiglottic fold,UBERON:0004119,endoderm-derived structure
+HP:0100400,Duplication of the distal phalanx of the 5th toe,HP:0010392,Abnormality of the distal phalanx of the 5th toe
+UBERON:0014629,terminal part of the cochlear canal,UBERON:0010313,neural crest-derived structure
+UBERON:0012109,zygomatic process of frontal bone,UBERON:0004121,ectoderm-derived structure
+UBERON:0002183,lobar bronchus,UBERON:0002185,bronchus
+UBERON:0002818,posterolateral fissure of cerebellum,UBERON:0003980,cerebellum fissure
+HP:0010059,Broad phalanges of the hallux,HP:0010174,Broad phalanx of the toes
+UBERON:0003278,skeleton of lower jaw,UBERON:0010912,subdivision of skeleton
+UBERON:0002450,decidua,UBERON:0005156,reproductive structure
+UBERON:4200141,prehallical element,UBERON:0015050,tarsus endochondral element
+DOID:8031,pineal region meningioma,DOID:5032,pineal gland cancer
+UBERON:0007106,chorionic villus,UBERON:0004120,mesoderm-derived structure
+UBERON:4200021,astragalus-calcaneum unit,UBERON:0004120,mesoderm-derived structure
+DOID:4658,benign mastocytoma,DOID:0060084,cell type benign neoplasm
+DOID:13799,female breast central part cancer,DOID:0050671,female breast cancer
+HP:0010717,Osseous syndactyly of toes,HP:0001770,Toe syndactyly
+UBERON:0009132,peroneus,UBERON:0004256,hindlimb zeugopod muscle
+UBERON:0013216,udder,UBERON:0000481,multi-tissue structure
+DOID:2550,tactile epilepsy,DOID:2548,reflex epilepsy
+UBERON:0000471,compound organ component,UBERON:0000481,multi-tissue structure
+CL:0000043,mature basophil,CL:0002242,nucleate cell
+DOID:4424,juvenile xanthogranuloma,DOID:4330,non-langerhans-cell histiocytosis
+UBERON:0002925,trigeminal nucleus,UBERON:0002308,nucleus of brain
+HP:0007112,Temporal cortical atrophy,HP:0002120,Cerebral cortical atrophy
+DOID:9726,vitreous detachment,DOID:5614,eye disease
+DOID:10131,psychologic vaginismus,DOID:10132,psychosexual disorder
+CL:0000687,R1 photoreceptor cell,CL:0000287,eye photoreceptor cell
+DOID:13550,angle-closure glaucoma,DOID:1686,glaucoma
+UBERON:0001319,vaginal vein,UBERON:0001638,vein
+CL:0005021,mesenchymal lymphangioblast,CL:0000134,mesenchymal cell
+HP:0007956,Bilateral choroid coloboma,HP:0000611,Choroid coloboma
+HP:0011610,Type IV truncus arteriosus,HP:0001660,Truncus arteriosus
+UBERON:0011921,connecting stalk blood islands,UBERON:0007503,epithelial vesicle
+HP:0003698,Difficulty standing,HP:0004302,Functional motor problems.
+UBERON:0001846,internal ear,UBERON:0000477,anatomical cluster
+HP:0012259,Absent inner and outer dynein arms,HP:0012257,Absent inner dynein arms
+HP:0010769,Pilonidal sinus,HP:0010767,Sacrococcygeal pilonidal abnormality
+DOID:10932,obsessive-compulsive personality disorder,DOID:1510,personality disorder
+UBERON:2002088,interhaemal bone,UBERON:0004120,mesoderm-derived structure
+HP:0005584,Renal cell carcinoma,HP:0009726,Renal neoplasm
+UBERON:2001181,epidermal intermediate stratum,UBERON:0004121,ectoderm-derived structure
+UBERON:0002391,lymph,UBERON:0000179,haemolymphatic fluid
+UBERON:0003541,left lung terminal bronchiole,UBERON:0003539,left lung bronchiole
+UBERON:0006284,early prosencephalic vesicle,UBERON:0013150,future brain vesicle
+UBERON:0010970,intercostal pre-muscle mass,UBERON:0004120,mesoderm-derived structure
+UBERON:0009207,geschmacksstreifen,UBERON:0004121,ectoderm-derived structure
+DOID:7522,pediatric infratentorial ependymoblastoma,DOID:4794,ependymoblastoma
+HP:0009598,Symphalangism of the proximal phalanx of the 2nd finger with the 2nd metatcarpal,HP:0009586,Symphalangism affecting the proximal phalanx of the 2nd finger
+HP:0010445,Primum atrial septal defect,HP:0001631,Defect in the atrial septum
+UBERON:0015227,peristaltic circulatory vessel,UBERON:0007100,primary circulatory organ
+DOID:3308,embryonal carcinoma,DOID:688,embryonal cancer
+DOID:6809,vaginal tubular adenoma,DOID:5402,vaginal adenoma
+UBERON:0008812,hemipenis,UBERON:0008811,intromittent organ
+UBERON:0005014,mucosa of female urethra,UBERON:0012299,mucosa of urethra
+UBERON:0015008,thoracic vertebra endochondral element,UBERON:0010363,endochondral element
+UBERON:0003910,splenic sinusoid,UBERON:0003497,abdomen blood vessel
+UBERON:0002820,zona arcuata of basilar membrane of cochlea,UBERON:0004121,ectoderm-derived structure
+HP:0003900,Small humeral epiphyses,HP:0003844,Small epiphyses of the upper limbs
+HP:0002205,Recurrent respiratory infections,HP:0002719,Recurrent infections
+HP:0004223,Ivory epiphysis of the distal phalanx of the 5th finger,HP:0009198,Abnormality of the epiphysis of the distal phalanx of the 5th finger
+HP:0010396,Broad proximal phalanx of the 2nd toe,HP:0010358,Abnormality of the proximal phalanx of the 2nd toe
+DOID:5146,appendix leiomyoma,DOID:127,leiomyoma
+UBERON:0007389,paired limb/fin cartilage,UBERON:0002418,cartilage tissue
+DOID:0050604,acrocapitofemoral dysplasia,DOID:2256,osteochondrodysplasia
+NCBITaxon:32523,Tetrapoda,NCBITaxon:8287,Sarcopterygii
+NCBITaxon:813,Chlamydia trachomatis,NCBITaxon:810,Chlamydia
+UBERON:0001294,inner medulla of kidney,UBERON:0006554,urinary system structure
+HP:0003715,Myofibrillar myopathy,HP:0003198,Myopathy
+HP:0003296,Hyperthreoninuria,HP:0003355,Aminoaciduria
+CL:0002424,DN2b thymocyte,CL:0000806,DN2 thymocyte
+HP:0100878,Enlarged uterus,HP:0000130,Abnormality of the uterus
+CL:0000350,amnioserosal cell,CL:0000349,extraembryonic cell
+UBERON:3010079,upper eyelid protuberances,UBERON:3000972,head external integument structure
+HP:0009294,Absent middle phalanx of 4th finger,HP:0009281,Aplasia of the 4th finger
+NCBITaxon:5970,Exophiala dermatitidis,NCBITaxon:5583,Exophiala
+UBERON:0006651,appendix testis,UBERON:0005156,reproductive structure
+HP:0006670,Impaired myocardial contractility,HP:0006673,Reduced systolic function
+HP:0003436,Prolonged miniature endplate currents,HP:0003398,Abnormality of the neuromuscular junction
+UBERON:0008323,dorsal artery of clitoris,UBERON:0004573,systemic artery
+HP:0008486,Lumbar interpedicular narrowing,HP:0008457,Caudal interpedicular narrowing
+UBERON:0004674,facial nerve root,UBERON:0011215,cell part cluster of neuraxis
+UBERON:0000164,primitive urogenital sinus,UBERON:0005423,developing anatomical structure
+UBERON:3000832,anterior lamina recurvata,UBERON:0004120,mesoderm-derived structure
+HP:0012383,Bidirectional shunt,HP:0001693,Cardiac shunt
+UBERON:2001747,lateral mesethmoid wing,UBERON:0004120,mesoderm-derived structure
+HP:0011331,Hemifacial atrophy,HP:0000324,Facial asymmetry
+UBERON:0005402,philtrum,UBERON:0006846,surface groove
+DOID:11491,acquired night blindness,DOID:5113,nutritional deficiency disease
+HP:0006559,Hepatic calcification,HP:0001392,Abnormality of the liver
+DOID:5712,cutaneous liposarcoma,DOID:2687,skin sarcoma
+HP:0005164,Dysplastic pulmonary valve,HP:0001641,Abnormality of the pulmonary valve
+DOID:4252,Alexander disease,DOID:10579,leukodystrophy
+UBERON:0011149,Marshall's gland,UBERON:0006554,urinary system structure
+HP:0000725,Psychotic episodes,HP:0000709,Psychosis
+UBERON:4300104,ectocoracoid bone,UBERON:0008907,dermal bone
+UBERON:0002548,larva,UBERON:0000468,multi-cellular organism
+HP:0004492,Widely patent fontanelles and sutures,HP:0010537,Wide cranial sutures
+DOID:0050523,adult T-cell leukemia,DOID:715,T-cell leukemia
+DOID:13450,coccidioidomycosis,DOID:0050292,primary systemic mycosis
+HP:0012447,Abnormal myelination,HP:0007319,Morphological abnormality of the central nervous system
+UBERON:0003230,epithelium of carpal region,UBERON:0000490,unilaminar epithelium
+UBERON:0013643,lophophore,UBERON:0013642,ring of oral cilia
+UBERON:0012256,digestive syncytial vacuole,UBERON:0000470,cell part
+UBERON:2001237,ceratobranchial 1 bone,UBERON:2001899,ceratobranchial 1 element
+UBERON:0006035,interdigital region between manual digits 4 and 5,UBERON:0006025,interdigital region between digits 4 and 5
+UBERON:0010173,sinotubular junction,UBERON:0000477,anatomical cluster
+UBERON:0004388,epiphysis of fibula,UBERON:0004120,mesoderm-derived structure
+DOID:8632,Kaposi's sarcoma,DOID:201,connective tissue cancer
+UBERON:0005583,rhombomere 6 lateral wall,UBERON:0005501,rhombomere lateral wall
+DOID:8646,substance-induced psychosis,DOID:2468,psychotic disorder
+DOID:5848,apical myocardial infarction,DOID:5844,myocardial infarction
+HP:0012306,Abnormal rib ossification,HP:0000772,Abnormality of the ribs
+HP:0009529,Irregular epiphysis of the proximal phalanx of the 2nd finger,HP:0009493,Irregular epiphyses of the 2nd finger
+DOID:3263,piebaldism,DOID:0050736,autosomal dominant disease
+UBERON:0010389,pterygoid bone,UBERON:0003462,facial bone
+UBERON:0005646,manual digit 3 epithelium,UBERON:0005227,manual digit epithelium
+UBERON:0004017,periocular mesenchyme,UBERON:0004121,ectoderm-derived structure
+HP:0009323,Cone-shaped epiphysis of the middle phalanx of the 3rd finger,HP:0009334,Abnormality of the epiphysis of the middle phalanx of the 3rd finger
+HP:0010578,Bracket epiphyses,HP:0005930,Abnormality of the epiphyses
+UBERON:3010821,hyoquadrate process,UBERON:0004752,palatoquadrate cartilage
+UBERON:0014875,distal epiphysis of distal phalanx of pedal digit 5,UBERON:0014876,distal epiphysis of distal phalanx of pedal digit
+HP:0010930,Abnormality of monovalent inorganic cation homeostasis,HP:0010929,Abnormality of cation homeostasis
+DOID:0060218,CREST syndrome,DOID:225,syndrome
+HP:0009269,Small epiphysis of the proximal phalanx of the 4th finger,HP:0009248,Abnormality of the epiphysis of the proximal phalanx of the 4th finger
+CL:0000114,surface ectodermal cell,CL:0000221,ectodermal cell
+UBERON:2001069,ventral fin fold,UBERON:0000481,multi-tissue structure
+UBERON:2000930,myotome somite 24,UBERON:0003082,myotome
+HP:0006273,Pancreatic lymphangiectasis,HP:0012090,Abnormality of pancreas morphology
+HP:0002595,Ileus,HP:0002242,Abnormality of the intestine
+UBERON:0007254,intervertebral disk of thoracic vertebra,UBERON:0005174,dorsal region organ
+DOID:6680,Capgras syndrome,DOID:778,delusional disorder
+UBERON:0004141,heart tube,UBERON:0012275,meso-epithelium
+UBERON:2001726,caudal principal ray 14,UBERON:2001585,caudal principal ray
+DOID:61,mitral valve disease,DOID:4079,heart valve disease
+DOID:6270,gastric cardia carcinoma,DOID:5517,stomach carcinoma
+UBERON:0012142,pedal digitopodium region,UBERON:0005445,segment of pes
+DOID:3429,inclusion body myositis,DOID:633,myositis
+UBERON:2000479,caudal mesencephalo-cerebellar tract,UBERON:0000073,regional part of nervous system
+UBERON:0002187,terminal bronchiole,UBERON:0002186,bronchiole
+UBERON:0013753,distal epiphysis of metacarpal bone,UBERON:0004379,distal epiphysis
+DOID:10873,Kuhnt-Junius degeneration,DOID:2007,degeneration of macula and posterior pole
+HP:0001845,Overlapping toe,HP:0001780,Abnormality of toe
+UBERON:0004932,submucosa of sigmoid colon,UBERON:0003331,submucosa of colon
+DOID:8151,appendiceal L-cell glucagon-like peptide producing tumor,DOID:11239,appendix cancer
+UBERON:0003669,fascia lata,UBERON:0011236,deep fascia
+NCBITaxon:11084,Tick-borne encephalitis virus,NCBITaxon:29263,tick-borne encephalitis virus group
+HP:0010733,Naevus flammeus of the eyelid,HP:0001052,Nevus flammeus
+UBERON:0002295,scala media,UBERON:0013685,foramen of skull
+HP:0100806,Sepsis,HP:0010978,Abnormality of immune system physiology
+UBERON:0011583,stylopodial skeleton,UBERON:0004120,mesoderm-derived structure
+HP:0100467,Patchy sclerosis of the distal phalanx of the 3rd toe,HP:0010364,Patchy sclerosis of the phalanges of the 3rd toe
+DOID:5254,central nervous system leiomyosarcoma,DOID:502,central nervous system mesenchymal non-meningothelial tumor
+UBERON:0011895,endomysium,UBERON:0006804,reticular tissue
+HP:0008369,Abnormal tarsal ossification,HP:0001850,Abnormality of the tarsal bones
+HP:0009483,Symphalangism of the proximal phalanx of the 3rd finger with the 3rd metatcarpal,HP:0009706,Synostosis involving the 3rd metacarpal
+UBERON:0006633,coracoid process of scapula,UBERON:0005913,zone of bone organ
+HP:0004437,Cranial hyperostosis,HP:0100774,Hyperostosis
+HP:0010881,Abnormality of the umbilical cord,HP:0001194,Abnormalities of placenta and umbilical cord
+CL:0000038,erythroid progenitor cell,CL:0000764,erythroid lineage cell
+UBERON:0005053,nerve cord,UBERON:0000479,tissue
+HP:0005681,Juvenile rheumatoid arthritis,HP:0001370,Rheumatoid arthritis
+HP:0010425,Partial duplication of the distal phalanx of the 2nd toe,HP:0010421,Duplication of the distal phalanx of the 2nd toe
+DOID:14686,Axenfeld-Rieger syndrome,DOID:0050736,autosomal dominant disease
+DOID:11514,fissured tongue,DOID:10944,tongue disease
+UBERON:0014717,mucous acinus,UBERON:0011858,acinus of exocrine gland
+DOID:4023,linitis plastica,DOID:6217,gastric diffuse adenocarcinoma
+DOID:481,central nervous system hereditary degenerative disease,DOID:440,neuromuscular disease
+UBERON:0001540,peroneal artery,UBERON:0003516,hindlimb blood vessel
+UBERON:0011592,future upper lip,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0004009,Medially sloping radial epiphyses,HP:0004008,Sloping radial epiphyses
+UBERON:0001483,skin of shoulder,UBERON:0000014,zone of skin
+HP:0001727,Thromboembolic stroke,HP:0001907,Thromboembolism
+CL:0000617,GABAergic neuron,CL:0000540,neuron
+UBERON:2001607,basipterygoid process of parasphenoid,UBERON:0004121,ectoderm-derived structure
+HP:0000778,Hypoplasia of the thymus,HP:0010515,Aplasia/Hypoplasia of the thymus
+HP:0010355,Duplication of the phalanges of the 2nd toe,HP:0010181,Duplication of phalanx of toe
+HP:0010388,Patchy sclerosis of the phalanges of the 5th toe,HP:0010178,Patchy sclerosis of the phalanges of the toes
+HP:0012367,Extra fontanelles,HP:0011328,Abnormality of fontanelles
+HP:0000205,Pursed lips,HP:0011338,Abnormality of mouth shape
+UBERON:0010683,pedal digit 4 phalanx cartilage element,UBERON:0005698,pedal digit 4 mesenchyme
+HP:0006934,Congenital nystagmus,HP:0000639,Nystagmus
+HP:0011177,EEG with 4-5/second background activity,HP:0011176,EEG with constitutional variants
+UBERON:0007641,trigeminal nuclear complex,UBERON:0007245,nuclear complex of neuraxis
+DOID:12930,dilated cardiomyopathy,DOID:0060036,intrinsic cardiomyopathy
+DOID:9794,hereditary choroidal atrophy,DOID:980,choroidal sclerosis
+HP:0100628,Esophageal diverticulum,HP:0002031,Abnormality of the esophagus
+UBERON:2001679,mesethmoid-lateral ethmoid joint,UBERON:0000982,skeletal joint
+UBERON:2001816,anterior nuchal plate,UBERON:0002513,endochondral bone
+UBERON:0005821,gracile fasciculus,UBERON:0001019,nerve fasciculus
+CL:0000207,olfactory receptor cell,CL:0000206,chemoreceptor cell
+HP:0011540,Congenitally corrected transposition of the great arteries,HP:0011603,Congenital malformation of the great arteries
+HP:0100022,Abnormality of movement,HP:0012638,Abnormality of nervous system physiology
+HP:0010726,Prominent corneal nerve fibers,HP:0011492,Abnormality of corneal stroma
+HP:0001134,Anterior polar cataract,HP:0010696,Polar cataract
+HP:0010096,Complete duplication of the distal phalanx of the hallux,HP:0010084,Duplication of the distal phalanx of the hallux
+UBERON:0003369,fossa ovalis of heart,UBERON:0006984,anatomical surface
+UBERON:2001823,epibranchial 4 bone uncinate process,UBERON:2001382,epibranchial bone uncinate process
+UBERON:0007722,interphalangeal joint of manus,UBERON:0001489,manus joint
+HP:0005817,Postaxial polysyndactyly of foot,HP:0001830,Postaxial foot polydactyly
+HP:0003034,Diaphyseal sclerosis,HP:0000940,Abnormal diaphysis morphology
+HP:0008695,Transient nephrotic syndrome,HP:0000100,Nephrotic syndrome
+UBERON:0006780,zonal layer of superior colliculus,UBERON:0006785,gray matter of superior colliculus
+UBERON:0006742,canthus,UBERON:0007651,anatomical junction
+NCBITaxon:11080,St. Louis encephalitis virus,NCBITaxon:11071,Japanese encephalitis virus group
+HP:0007572,Hyperpigmented streaks,HP:0007400,Irregular hyperpigmentation
+DOID:6425,eyelid carcinoma,DOID:3451,skin carcinoma
+UBERON:2001366,tract of the postoptic commissure,UBERON:0003931,diencephalic white matter
+UBERON:0011896,smooth muscle endomysium,UBERON:0011895,endomysium
+UBERON:0001276,epithelium of stomach,UBERON:0004808,gastrointestinal system epithelium
+HP:0005540,Red blood cell keratocytosis,HP:0004447,Poikilocytosis
+UBERON:2001040,epaxial region somite 24,UBERON:0003900,epaxial myotome region
+UBERON:0006340,fourth ventricle choroid plexus stroma,UBERON:0005206,choroid plexus stroma
+DOID:5059,childhood cerebellar neoplasm,DOID:4205,cerebellum cancer
+UBERON:0006270,optic pit,UBERON:0004121,ectoderm-derived structure
+CL:0002261,endothelial cell of viscerocranial mucosa,CL:0002076,endo-epithelial cell
+DOID:6512,hepatoid pattern ovarian yolk sac tumor,DOID:5350,ovarian endodermal sinus tumor
+UBERON:0011250,autopod bone,UBERON:0002428,limb bone
+UBERON:0006807,ectepicondyle of humerus,UBERON:0004120,mesoderm-derived structure
+UBERON:3000290,medial inferior prenasal cartilage,UBERON:0003406,cartilage of respiratory system
+UBERON:0007777,umbilical vein endothelium,UBERON:0001919,endothelium of vein
+UBERON:0005079,eggshell,UBERON:0004120,mesoderm-derived structure
+UBERON:0002147,reticulotegmental nucleus,UBERON:0009662,hindbrain nucleus
+UBERON:0002597,principal sensory nucleus of trigeminal nerve,UBERON:0002680,regional part of metencephalon
+DOID:0060212,amyotrophic lateral sclerosis type 21,DOID:332,amyotrophic lateral sclerosis
+NCBITaxon:6035,Encephalitozoon cuniculi,NCBITaxon:6033,Encephalitozoon
+HP:0002140,Ischemic stroke,HP:0002637,Cerebral ischemia
+UBERON:0001804,capsule of lens,UBERON:0005769,basement membrane of epithelium
+HP:0010757,Aplasia of the premaxilla,HP:0010756,Aplasia/Hypoplasia of the premaxilla
+DOID:0050902,medulloblastoma,DOID:4706,infratentorial cancer
+HP:0006716,Hereditary nonpolyposis colorectal carcinoma,HP:0100834,Neoplasm of the large intestine
+HP:0006544,Extrapulmonary sequestrum,HP:0100632,Pulmonary sequestration
+HP:0010763,Low insertion of columella,HP:0009929,Abnormality of the columella
+UBERON:0002873,interpolar part of spinal trigeminal nucleus,UBERON:0003528,brain grey matter
+UBERON:0005038,mucosa of segmental bronchus,UBERON:0000410,bronchial mucosa
+HP:0100380,Aplasia of the distal phalanx of the 5th toe,HP:0010645,Aplasia of the distal phalanges of the toes
+HP:0010258,Bracket epiphyses of the middle phalanges of the hand,HP:0010244,Abnormality of the epiphyses of the middle phalanges of the hand
+UBERON:0001739,laryngeal cartilage,UBERON:0003406,cartilage of respiratory system
+UBERON:0015004,tibia endochondral element,UBERON:0015022,hindlimb endochondral element
+UBERON:0004905,articulation,UBERON:0000477,anatomical cluster
+UBERON:0008818,superior mediastinum,UBERON:0002224,thoracic cavity
+UBERON:0002517,basicranium,UBERON:0004120,mesoderm-derived structure
+HP:0008640,Congenital macroorchidism,HP:0000053,Macroorchidism
+HP:0011425,Fetal ultrasound soft marker,HP:0001197,Abnormality of prenatal development or birth
+HP:0008447,Hypoplastic coccygeal vertebrae,HP:0008417,Vertebral hypoplasia
+HP:0002248,Hematemesis,HP:0002239,Gastrointestinal hemorrhage
+HP:0003554,Type 2 muscle fiber atrophy,HP:0100295,Muscle fiber atrophy
+UBERON:0004738,metanephric juxtaglomerular apparatus,UBERON:0004120,mesoderm-derived structure
+UBERON:0011276,nail of manual digit 4,UBERON:0009565,nail of manual digit
+HP:0010185,Aplasia/Hypoplasia of the distal phalanges of the toes,HP:0010173,Aplasia/Hypoplasia of the phalanges of the toes
+HP:0010849,EEG with spike-wave complexes (>3.5 Hz),HP:0010850,EEG with spike-wave complexes
+HP:0012171,Stereotypical hand wringing,HP:0000733,Stereotypic behavior
+UBERON:0005943,hair root sheath matrix,UBERON:0000479,tissue
+HP:0006353,Hypoplasia of the tooth germ,HP:0000685,Hypoplasia of teeth
+CL:0005006,ionocyte,CL:0000066,epithelial cell
+UBERON:3010103,vocal sac glands,UBERON:3010604,cranial glands
+UBERON:0014284,endopiriform nucleus,UBERON:0002791,regional part of telencephalon
+DOID:13767,clonorchiasis,DOID:883,parasitic helminthiasis infectious disease
+UBERON:0000915,thoracic segment of trunk,UBERON:0009569,subdivision of trunk
+UBERON:0004721,crista ampullaris,UBERON:0000020,sense organ
+DOID:0050648,atelosteogenesis,DOID:2256,osteochondrodysplasia
+DOID:6017,central nervous system mature teratoma,DOID:3640,central nervous system teratoma
+HP:0010117,Fragmentation of the epiphyses of the hallux,HP:0010166,Fragmentation of the epiphyses of the toes
+UBERON:0014463,cardiac ganglion,UBERON:0001808,parasympathetic ganglion
+HP:0009434,Patchy sclerosis of the middle phalanx of the 3rd finger,HP:0009444,Patchy sclerosis of the phalanges of the 3rd finger
+HP:0008386,Aplasia/Hypoplasia of the nails,HP:0001597,Abnormality of the nail
+UBERON:2000268,anal fin proximal radial bone,UBERON:2100268,anal fin proximal radial element
+HP:0007495,Prematurely aged appearance,HP:0011354,Generalized abnormality of skin
+UBERON:0013106,elapid venom,UBERON:0013076,snake venom
+UBERON:2000284,subopercle,UBERON:0008907,dermal bone
+DOID:2216,factor V deficiency,DOID:2214,inherited blood coagulation disease
+UBERON:3010657,subhyoideus,UBERON:3000224,hyobranchial muscle
+HP:0003797,Limb-girdle muscle atrophy,HP:0003202,Amyotrophy
+HP:0100191,Absent epiphysis of the proximal phalanx of the 4th toe,HP:0100096,Abnormality of the epiphysis of the proximal phalanx of the 4th toe
+UBERON:3000386,cultriform process,UBERON:4100000,skeletal element projection
+DOID:3749,urethral verrucous carcinoma,DOID:3750,urethra squamous cell carcinoma
+HP:0008605,Unilateral external ear deformity,HP:0000356,Abnormality of the outer ear
+UBERON:2002240,Purkinje cell layer corpus cerebelli,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0008576,thyro-arytenoid,UBERON:0006328,laryngeal intrinsic muscle
+UBERON:0003082,myotome,UBERON:0005291,embryonic tissue
+DOID:3070,malignant glioma,DOID:0050687,cell type cancer
+UBERON:0010584,pedal digit 5 phalanx pre-cartilage condensation,UBERON:0015035,pedal digit 5 phalanx endochondral element
+DOID:1949,cholecystitis,DOID:9446,cholangitis
+HP:0009045,Exercise-induced rhabdomyolysis,HP:0003201,Rhabdomyolysis
+UBERON:0001735,tonsillar ring,UBERON:0001962,gut-associated lymphoid tissue
+HP:0011810,Impaired two-point discrimination,HP:0011730,Abnormality of central sensory function
+UBERON:0001335,prostatic urethra,UBERON:0014403,male anatomical structure
+UBERON:0014466,subarachnoid fissure,UBERON:0000464,anatomical space
+UBERON:2001635,pharyngobranchial 1 bone,UBERON:2001910,pharyngobranchial 1 element
+UBERON:0014898,lamina terminalis of ischium,UBERON:0005913,zone of bone organ
+UBERON:0012302,male membranous urethra,UBERON:0014403,male anatomical structure
+CL:0000840,immature conventional dendritic cell,CL:0000766,myeloid leukocyte
+HP:0003484,Upper limb muscle weakness,HP:0003690,Limb muscle weakness
+DOID:657,adenoma,DOID:0060084,cell type benign neoplasm
+UBERON:0010338,1st arch maxillary mesenchyme from head mesenchyme,UBERON:0010341,1st arch mesenchyme from head mesenchyme
+DOID:0050594,glycogen storage disease IX,DOID:2747,glycogen storage disease
+UBERON:0006217,cloacal membrane,UBERON:0002050,embryonic structure
+HP:0011942,Increased urinary sulfite,HP:0003110,Abnormality of urine homeostasis
+HP:0009972,Duplication of phalanx of 4th finger,HP:0009971,Polydactyly affecting the 4th finger
+UBERON:0001737,larynx,UBERON:0004119,endoderm-derived structure
+UBERON:0002607,superior rostral sulcus,UBERON:0013118,sulcus of brain
+UBERON:2007053,dorsal adductor hyomandibulae,UBERON:0005493,hyoid muscle
+HP:0005946,Ventilator dependence with inability to wean,HP:0004887,Respiratory failure requiring assisted ventilation
+HP:0012543,Hemosiderinuria,HP:0003110,Abnormality of urine homeostasis
+DOID:10802,acute gonococcal epididymo-orchitis,DOID:9401,epididymo-orchitis
+UBERON:0001037,strand of hair,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001960,periarterial lymphatic sheath,UBERON:0004120,mesoderm-derived structure
+CL:0000780,multinuclear odontoclast,CL:0000588,odontoclast
+DOID:0050646,distal arthrogryposis,DOID:66,muscle tissue disease
+UBERON:2007042,spinal cord neural tube,UBERON:0004121,ectoderm-derived structure
+UBERON:2002019,pterotic-posttemporal-supracleithrum,UBERON:0008907,dermal bone
+UBERON:0015157,zygomatico-orbital artery,UBERON:0003496,head blood vessel
+UBERON:0010234,palatopharyngeus muscle,UBERON:0000933,pharyngeal muscle
+CL:0000492,CD4-positive helper T cell,CL:0000912,helper T cell
+HP:0000033,"Ambiguous genitalia, male",HP:0000032,Abnormality of male external genitalia
+UBERON:0004238,spleen smooth muscle,UBERON:0001135,smooth muscle tissue
+DOID:439,neuromuscular junction disease,DOID:440,neuromuscular disease
+DOID:4647,trilateral retinoblastoma,DOID:768,retinoblastoma
+HP:0009526,Cone-shaped epiphysis of the proximal phalanx of the 2nd finger,HP:0009501,Abnormality of the epiphysis of the proximal phalanx of the 2nd finger
+HP:0003401,Paresthesia,HP:0000763,Sensory neuropathy
+HP:0012272,J wave,HP:0003115,Abnormal EKG
+DOID:11984,hypertrophic cardiomyopathy,DOID:0060036,intrinsic cardiomyopathy
+UBERON:0002176,lateral cervical nucleus,UBERON:0004121,ectoderm-derived structure
+HP:0010145,Pseudoepiphysis of the distal phalanx of the hallux,HP:0010120,Pseudoepiphyses of the hallux
+DOID:5193,nodular ganglioneuroblastoma,DOID:4163,ganglioneuroblastoma
+UBERON:0004523,papillary muscle of right ventricle,UBERON:0002494,papillary muscle of heart
+UBERON:0006695,mammillary axonal complex,UBERON:0000477,anatomical cluster
+UBERON:0000472,simple organ,UBERON:0000481,multi-tissue structure
+HP:0009613,Duplication of the proximal phalanx of the thumb,HP:0009942,Duplication of phalanx of thumb
+DOID:182,calcinosis,DOID:10575,calcium metabolism disease
+UBERON:0010092,future metencephalon,UBERON:0005423,developing anatomical structure
+UBERON:0004771,posterior nasal aperture,UBERON:0010425,internal naris
+HP:0003359,Decreased urinary sulfate,HP:0004369,Decreased purine levels
+HP:0009266,Irregular epiphysis of the proximal phalanx of the 4th finger,HP:0009398,Irregular epiphyses of the 4th finger
+DOID:13922,eosinophilic esophagitis,DOID:11963,esophagitis
+HP:0009596,Aplasia of the proximal phalanx of the 2nd finger,HP:0009535,Aplasia of the 2nd finger
+HP:0008229,Thyroid lymphangiectasia,HP:0011772,Abnormality of thyroid morphology
+HP:0009322,Bracket epiphysis of the middle phalanx of the 3rd finger,HP:0009411,Bracket epiphyses of the 3rd finger
+UBERON:0002765,lateral medullary lamina of globus pallidus,UBERON:0014532,lamina of cerebral hemisphere
+UBERON:0009203,internasal suture,UBERON:0011160,nasal suture
+UBERON:0001346,vaginal hymen,UBERON:0005156,reproductive structure
+DOID:10541,microinvasive gastric cancer,DOID:3717,gastric adenocarcinoma
+DOID:3892,insulinoma,DOID:657,adenoma
+UBERON:0015784,duct of olfactory gland,UBERON:0000117,respiratory tube
+UBERON:0005310,pronephric nephron tubule,UBERON:0001231,nephron tubule
+UBERON:0004726,vasa recta,UBERON:0001140,renal vein
+UBERON:0007095,somatic musculature,UBERON:0000383,musculature of body
+HP:0007859,Congenital horizontal nystagmus,HP:0006934,Congenital nystagmus
+UBERON:0015082,proximal tarsal cartilage,UBERON:0015064,autopod cartilage
+UBERON:0000929,pharyngeal branch of vagus nerve,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001244,internal anal sphincter,UBERON:0004231,anal region smooth muscle
+HP:0010554,Cutaneous finger syndactyly,HP:0006101,Finger syndactyly
+HP:0100117,Ivory epiphysis of the middle phalanx of the 2nd toe,HP:0100050,Ivory epiphyses of the 2nd toe
+CL:0000021,female germ cell,CL:0000586,germ cell
+DOID:2068,Bartholin's gland neoplasm,DOID:0060088,vestibular gland benign neoplasm
+DOID:3086,gingival overgrowth,DOID:1483,gingival disease
+HP:0008812,Flattened femoral head,HP:0003368,Abnormality of the femoral head
+DOID:4352,ciliary body cancer,DOID:3479,uveal cancer
+HP:0010433,Short distal phalanx of the 2nd toe,HP:0010431,Short phalanx of the 2nd toe
+UBERON:0009191,sphenoid bone pre-cartilage condensation,UBERON:0000481,multi-tissue structure
+UBERON:2001871,Weberian ossicle set,UBERON:0004120,mesoderm-derived structure
+UBERON:2001333,sublingual dorsal and ventral fused,UBERON:2001275,sublingual
+HP:0011801,Enlargement of parotid gland,HP:0000197,Abnormality of parotid gland
+UBERON:0005868,maxillary prominence,UBERON:0005423,developing anatomical structure
+UBERON:2000462,abductor hyohyoid,UBERON:0005493,hyoid muscle
+NCBITaxon:565995,Bundibugyo ebolavirus,NCBITaxon:186536,Ebolavirus
+UBERON:0011317,nerve to stylopharyngeus from glossopharyngeal nerve,UBERON:0002003,peripheral nerve
+HP:0011916,Toe extensor amyotrophy,HP:0001436,Abnormality of the foot musculature
+HP:0003370,Flat capital femoral epiphysis,HP:0010574,Abnormality of the epiphysis of the femoral head
+HP:0006042,Y-shaped metacarpals,HP:0005916,Abnormal metacarpal morphology
+UBERON:0005219,hindbrain subarachnoid space,UBERON:0000315,subarachnoid space
+UBERON:3000707,pleurapophysis,UBERON:0004120,mesoderm-derived structure
+UBERON:0011859,internal acoustic meatus,UBERON:0004111,anatomical conduit
+UBERON:0005334,oral lamina propria,UBERON:0004121,ectoderm-derived structure
+DOID:5670,comedo carcinoma,DOID:8791,breast carcinoma in situ
+CL:0000325,stuff accumulating cell,CL:0000003,native cell
+HP:0010235,Pseudoepiphyses of the phalanges of the hand,HP:0004288,Pseudoepiphyses of hand bones
+DOID:137,vagina squamous papilloma,DOID:138,vaginal squamous tumor
+HP:0003146,Hypocholesterolemia,HP:0003107,Abnormality of cholesterol metabolism
+HP:0008736,Hypoplasia of penis,HP:0000050,Hypoplastic genitalia
+UBERON:0001767,posterior chamber of eyeball,UBERON:0006311,chamber of eyeball
+UBERON:0010887,tragus,UBERON:0001444,subdivision of head
+UBERON:0010034,copula linguae,UBERON:0005423,developing anatomical structure
+DOID:4327,Marburg hemorrhagic fever,DOID:934,viral infectious disease
+HP:0003978,Fractured radius,HP:0003961,Fractured forearm bones
+DOID:3901,vulvitis,DOID:2059,vulvar disease
+UBERON:0002516,epiphyseal plate,UBERON:0001994,hyaline cartilage tissue
+UBERON:0001817,lacrimal gland,UBERON:0004859,eye gland
+HP:0009443,Osteolytic defects of the phalanges of the 3rd finger,HP:0009771,Osteolytic defects of the phalanges of the hand
+UBERON:3000396,pars dentalis of maxilla,UBERON:0000064,organ part
+HP:0010226,Abnormality of the epiphysis of the 5th metacarpal,HP:0010013,Abnormality of the 5th metacarpal
+HP:0009498,Triangular epiphyses of the 2nd finger,HP:0006263,Abnormality of the epiphyses of the 2nd finger
+HP:0006491,Abnormality of the tibial metaphysis,HP:0002992,Abnormality of the tibia
+UBERON:0002258,dorsal funiculus,UBERON:0006127,funiculus of spinal cord
+DOID:4147,gastrointestinal adenoma,DOID:3119,gastrointestinal system cancer
+UBERON:0010677,manual digit 3 phalanx cartilage element,UBERON:0010686,manual digit phalanx cartilage element
+HP:0011299,Partial absence of finger,HP:0005918,Abnormality of phalanx of finger
+UBERON:3000569,solum nasi,UBERON:0000064,organ part
+HP:0001943,Hypoglycemia,HP:0011015,Abnormality of blood glucose concentration
+UBERON:0008786,third trochanter,UBERON:0000980,trochanter
+NCBITaxon:29120,Oligoryzomys,NCBITaxon:40141,Sigmodontinae
+UBERON:2000364,hypural,UBERON:2001364,hemal spine
+HP:0006283,Multiple unerupted teeth,HP:0000706,Unerupted tooth
+HP:0004132,Dimple on nasal tip,HP:0000436,Abnormality of the nasal tip
+CL:1000223,lung neuroendocrine cell,CL:1000272,lung secretory cell
+UBERON:0003527,kidney capillary,UBERON:0001982,capillary
+UBERON:3010746,T-shaped terminal phalanx,UBERON:0004300,distal phalanx
+HP:0005220,Multiple intestinal neurofibromatosis,HP:0001067,Neurofibromas
+UBERON:0004911,epithelium of female gonad,UBERON:0014404,female anatomical structure
+HP:0000337,Broad forehead,HP:0000290,Abnormality of the forehead
+UBERON:0008254,styliform cartilage,UBERON:0010883,forelimb cartilage element
+CL:0000106,unipolar neuron,CL:0000540,neuron
+DOID:5822,gray zone lymphoma,DOID:0060058,lymphoma
+UBERON:0011875,ligament of sternoclavicular joint,UBERON:0008846,skeletal ligament
+UBERON:2001536,pharyngobranchial 2 cartilage,UBERON:2001533,pharyngobranchial cartilage
+UBERON:0011967,costotransverse joint,UBERON:0002292,costovertebral joint
+HP:0001177,Preaxial hand polydactyly,HP:0001172,Abnormality of the thumb
+HP:0002898,Embryonal neoplasm,HP:0011792,Neoplasm by histology
+UBERON:2005320,dorsal longitudinal lymphatic vessel,UBERON:0004536,lymph vasculature
+UBERON:2002249,ctenius,UBERON:0004121,ectoderm-derived structure
+UBERON:0005672,right lung endothelium,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0003653,metatarsal bone of digit 4,UBERON:0001448,metatarsal bone
+UBERON:0005819,cervical flexure,UBERON:0002050,embryonic structure
+HP:0011711,Left anterior fascicular block,HP:0011713,Left bundle branch block
+HP:0000890,Long clavicles,HP:0000889,Abnormality of the clavicles
+DOID:1205,hypersensitivity reaction type I disease,DOID:0060056,hypersensitivity reaction disease
+UBERON:0001481,distal carpal bone,UBERON:0015068,distal carpal endochondral element
+HP:0001702,Abnormality of the tricuspid valve,HP:0006705,Abnormality of the atrioventricular valves
+UBERON:0005281,ventricular system of central nervous system,UBERON:0000467,anatomical system
+UBERON:0009980,condyle of femur,UBERON:0009979,condyle
+HP:0004727,Impaired renal concentrating ability,HP:0011038,Abnormality of renal resorption
+HP:0006679,Granulomatous coronary arteritis,HP:0006704,Abnormality of the coronary arteries
+HP:0002622,Dissecting aortic aneurysm,HP:0002647,Aortic dissection
+DOID:743,dermatographia,DOID:0060220,physical urticaria
+HP:0010755,Asymmetry of the maxilla,HP:0000326,Abnormality of the maxilla
+HP:0005913,Abnormality of metacarpal epiphyses,HP:0005924,Abnormality of the epiphyses of the hand
+UBERON:0016418,nasion,UBERON:0006983,anatomical point
+HP:0010407,Curved middle phalanx of the 2nd toe,HP:0010350,Curved phalanges of the 2nd toe
+UBERON:0006558,lymphatic part of lymphoid system,UBERON:0000477,anatomical cluster
+DOID:1455,geographic tongue,DOID:1453,atrophic glossitis
+HP:0009334,Abnormality of the epiphysis of the middle phalanx of the 3rd finger,HP:0004172,Abnormality of the middle phalanx of the 3rd finger
+CL:0002047,Fraction B precursor B cell,CL:0002400,Fraction B/C precursor B cell
+HP:0000422,Abnormality of the nasal bridge,HP:0000366,Abnormality of the nose
+UBERON:0005411,bony otic capsule,UBERON:0004637,otic capsule
+UBERON:0015098,distal carpal bone 5 pre-cartilage condensation,UBERON:0015096,distal carpal bone 5 endochondral element
+HP:0011849,Abnormal bone ossification,HP:0003330,Abnormal bone structure
+HP:0004878,Respiratory failure due to intercostal muscle and diaphragm involvement,HP:0002093,Respiratory insufficiency
+CL:0002555,fibroblast of mammary gland,CL:0000057,fibroblast
+UBERON:3000688,prominentia apicalis dorsalis,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0002048,Renal cortical atrophy,HP:0011035,Abnormality of the renal cortex
+UBERON:0002310,hippocampus fimbria,UBERON:0004121,ectoderm-derived structure
+CL:1000838,kidney proximal convoluted tubule epithelial cell,CL:0002306,epithelial cell of proximal tubule
+UBERON:0000470,cell part,UBERON:0000061,anatomical structure
+HP:0006825,Pallor of dorsal columns of the spinal cord,HP:0011397,Abnormality of the dorsal column of the spinal cord
+HP:0009023,Abdominal wall muscle weakness,HP:0001324,Muscle weakness
+CL:1001575,uterine cervix squamous cell,CL:0002535,epithelial cell of cervix
+UBERON:0002123,cortex of thymus,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0000976,Eczematoid dermatitis,HP:0000964,Eczema
+HP:0003795,Short middle phalanx of toe,HP:0001831,Short toe
+CL:0000635,Deiter's cell,CL:0002165,phalangeal cell
+DOID:7244,bladder urachal urothelial carcinoma,DOID:5958,bladder urachal carcinoma
+HP:0000775,Abnormality of the diaphragm,HP:0001438,Abnormality of the abdomen
+HP:0010245,Abnormality of the epiphyses of the proximal phalanges of the hand,HP:0009834,Abnormality of the proximal phalanges of the hand
+DOID:0060032,autoimmune disease of musculoskeletal system,DOID:417,hypersensitivity reaction type II disease
+DOID:0050160,inhalation anthrax,DOID:7427,anthrax disease
+UBERON:3000839,crista radii,UBERON:4100000,skeletal element projection
+UBERON:0002184,segmental bronchus,UBERON:0002185,bronchus
+UBERON:0002188,respiratory bronchiole,UBERON:0002186,bronchiole
+UBERON:0000220,atlanto-occipital joint,UBERON:0004120,mesoderm-derived structure
+CL:0000140,odontocyte,CL:0002320,connective tissue cell
+DOID:0050134,cutaneous mycosis,DOID:1564,fungal infectious disease
+DOID:2770,diaper rash,DOID:2772,irritant dermatitis
+HP:0011266,"Microtia, first degree",HP:0008551,Microtia
+UBERON:0005658,secondary palatal shelf epithelium,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100522,Thymoma,HP:0100521,Neoplasm of the thymus
+DOID:6712,anterior spinal artery syndrome,DOID:6713,cerebrovascular disease
+UBERON:0013507,thoracic vertebra cartilage element,UBERON:0011094,vertebra cartilage element
+HP:0100750,Atelectasis,HP:0002088,Abnormality of the lung
+HP:0004255,Small trapezium,HP:0001498,Carpal bone hypoplasia
+NCBITaxon:134362,Capnodiales,NCBITaxon:451867,Dothideomycetidae
+DOID:5350,ovarian endodermal sinus tumor,DOID:5351,ovarian primitive germ cell tumor
+UBERON:0014606,infundibular stem,UBERON:0004120,mesoderm-derived structure
+HP:0100921,Sclerosis of the phalanges of the 5th finger,HP:0004213,Abnormality of the phalanges of the 5th finger
+HP:0006756,Diffuse leiomyomatosis,HP:0011793,Neoplasm by anatomical site
+HP:0009354,Small epiphysis of the proximal phalanx of the 3rd finger,HP:0009333,Abnormality of the epiphysis of the proximal phalanx of the 3rd finger
+HP:0009560,Curved distal phalanx of the 2nd finger,HP:0009838,Curved distal phalanges of the hand
+UBERON:3000160,fenestra dorsalis nasi,UBERON:3000316,nasal opening
+DOID:9306,mechanical strabismus,DOID:540,strabismus
+HP:0000400,Macrotia,HP:0000377,Abnormality of the pinna
+NCBITaxon:53551,Sabethes,NCBITaxon:53549,Sabethini
+UBERON:0006780,zonal layer of superior colliculus,UBERON:0006791,superficial layer of superior colliculus
+CL:1000478,transitional myocyte of sinoatrial node,CL:0002073,transitional myocyte
+HP:0100155,Stippling of the epiphysis of the middle phalanx of the 3rd toe,HP:0100092,Abnormality of the epiphysis of the middle phalanx of the 3rd toe
+UBERON:3000814,glenoid head of coracoid,UBERON:0005913,zone of bone organ
+UBERON:0007391,pelvic appendage cartilage tissue,UBERON:0007389,paired limb/fin cartilage
+NCBITaxon:291484,Hepeviridae,NCBITaxon:35278,"ssRNA positive-strand viruses, no DNA stage"
+UBERON:0004055,primitive pit,UBERON:0002050,embryonic structure
+HP:0012494,Anterior cerebral artery stenosis,HP:0012492,Cerebral artery stenosis
+UBERON:0010012,upper beak,UBERON:0003102,surface structure
+UBERON:0005621,rhomboid,UBERON:0004120,mesoderm-derived structure
+CL:1000323,pylroric gastric gland goblet cell,CL:1000313,gastric goblet cell
+HP:0004969,Peripheral pulmonary artery stenosis,HP:0004415,Pulmonary artery stenosis
+UBERON:4300108,lepidotrichial segment,UBERON:0004121,ectoderm-derived structure
+UBERON:2000195,dorsal depressor,UBERON:2005270,depressor muscle
+DOID:13689,prostate calculus,DOID:9590,lower urinary tract calculus
+UBERON:2000580,rostral preglomerular nucleus,UBERON:2002226,preglomerular nucleus
+HP:0012482,Frontal venous angioma,HP:0012481,Cerebral venous angioma
+UBERON:0009016,ciliary stroma,UBERON:0003891,stroma
+HP:0007813,Nongranulomatous uveitis,HP:0000554,Uveitis
+HP:0012573,Global proximal tubulopathy,HP:0000114,Proximal tubulopathy
+HP:0012613,Increased urinary sulfate,HP:0012612,Abnormal urinary sulfate concentration
+DOID:4905,pancreatic carcinoma,DOID:1793,pancreatic cancer
+DOID:6880,small bowel fibrosarcoma,DOID:5272,small intestinal sarcoma
+UBERON:0015482,right hepatic artery,UBERON:0001193,hepatic artery
+UBERON:0013494,keratin-coated spine,UBERON:0008260,spine appendage
+UBERON:0015044,manual digit 2 metacarpus endochondral element,UBERON:0015042,manual digit metacarpus endochondral element
+UBERON:0003081,lateral plate mesoderm,UBERON:0005291,embryonic tissue
+DOID:7615,sarcomatosis,DOID:1115,sarcoma
+NCBITaxon:11244,Pneumovirinae,NCBITaxon:11158,Paramyxoviridae
+HP:0007483,Depigmentation/hyperpigmentation of skin,HP:0001000,Abnormality of skin pigmentation
+UBERON:0008804,stylopharyngeus muscle,UBERON:0015212,lateral structure
+UBERON:2002031,orbital foramen,UBERON:0005744,bone foramen
+UBERON:0011966,manubriosternal joint,UBERON:0002216,symphysis
+HP:0000682,Abnormality of dental enamel,HP:0011061,Abnormality of dental structure
+UBERON:0011205,carpometacarpus,UBERON:0005897,manus bone
+HP:0007643,Peripheral traction retinal detachment,HP:0007917,Tractional retinal detachment
+UBERON:0016409,base of glans penis,UBERON:0005156,reproductive structure
+HP:0001739,Abnormality of the nasopharynx,HP:0000366,Abnormality of the nose
+UBERON:0005067,amphid sensory organ,UBERON:0000020,sense organ
+UBERON:0002573,pontine reticular formation,UBERON:0015827,brainstem reticular formation
+HP:0011984,Atretic gallbladder,HP:0011466,Aplasia/Hypoplasia of the gallbladder
+UBERON:0003614,blood vessel elastic tissue,UBERON:0003613,cardiovascular system elastic tissue
+UBERON:0010063,tympanic cavity epithelium,UBERON:0015813,middle ear epithelium
+UBERON:3011120,early proximal tubule,UBERON:0006554,urinary system structure
+UBERON:0009882,anal column,UBERON:0004121,ectoderm-derived structure
+HP:0002764,Stippled chondral calcification,HP:0002832,Calcific stippling
+CL:0000097,mast cell,CL:0000766,myeloid leukocyte
+HP:0000026,Male hypogonadism,HP:0000022,Abnormality of male internal genitalia
+UBERON:0007713,fourth sacral spinal ganglion,UBERON:0002837,sacral dorsal root ganglion
+HP:0100360,Contractures of the joints of the upper limbs,HP:0003121,Limb joint contracture
+UBERON:0000116,lung saccule,UBERON:0000064,organ part
+HP:0009300,Aplasia/Hypoplasia of the proximal phalanx of the 4th finger,HP:0009284,Abnormality of the proximal phalanx of the 4th finger
+DOID:0050469,Costello syndrome,DOID:0050736,autosomal dominant disease
+UBERON:0001404,radial artery,UBERON:0001637,artery
+UBERON:0001316,external iliac vein,UBERON:0001638,vein
+HP:0000223,Abnormality of taste sensation,HP:0000759,Abnormality of the peripheral nervous system
+UBERON:0015472,tracheobronchial lymph node,UBERON:0004119,endoderm-derived structure
+UBERON:0003480,vein of clitoris,UBERON:0001638,vein
+HP:0003059,Abnormality of the radioulnar joints,HP:0002973,Abnormality of the forearm
+CL:0010022,cardiac neuron,CL:0000540,neuron
+HP:0100374,Aplasia/Hypoplasia of the middle phalanx of the 5th toe,HP:0010194,Aplasia/Hypoplasia of the middle phalanges of the toes
+DOID:5637,adenosquamous pancreas carcinoma,DOID:3498,pancreatic ductal adenocarcinoma
+UBERON:0014628,vestibular fissure of the cochlear canal,UBERON:0010313,neural crest-derived structure
+HP:0001836,Camptodactyly (feet),HP:0100492,Joint contractures involving the joints of the feet
+HP:0001305,Dandy-Walker malformation,HP:0002350,Cerebellar cyst
+HP:0005313,Arterial fibromuscular dysplasia,HP:0011004,Abnormality of the systemic arterial tree
+HP:0002909,Generalized aminoaciduria,HP:0003355,Aminoaciduria
+HP:0011706,Second degree atrioventricular block,HP:0001678,Atrioventricular block
+UBERON:2002291,fulcrum,UBERON:0004376,fin bone
+HP:0003025,Metaphyseal irregularity,HP:0000944,Abnormality of the metaphyses
+HP:0011541,Criss-cross atrioventricular valves,HP:0011534,Abnormal spatial orientation of the cardiac segments
+HP:0010103,Short distal phalanx of hallux,HP:0010076,Aplasia/Hypoplasia of the distal phalanx of the hallux
+HP:0011517,Cone monochromacy,HP:0007803,Monochromacy
+UBERON:0011022,flexor hallucis brevis muscle,UBERON:0000366,flexor muscle
+UBERON:0005835,cuneate fasciculus of spinal cord,UBERON:0007699,tract of spinal cord
+HP:0005867,Fused fourth and fifth metacarpals,HP:0009707,Synostosis involving the 4th metacarpal
+DOID:11760,Kohler's disease,DOID:8125,osteochondrosis
+HP:0004617,Butterfly vertebral arch,HP:0008438,Vertebral arch anomaly
+UBERON:0011667,pleural plate of carapace,UBERON:0015212,lateral structure
+DOID:1570,ectropion,DOID:530,eyelid disease
+DOID:8216,parapharyngeal meningioma,DOID:3565,meningioma
+UBERON:0011214,nucleus of midbrain tectum,UBERON:0009661,midbrain nucleus
+DOID:11342,arcus senilis,DOID:1237,corneal degeneration
+UBERON:0011774,utriculosaccular duct,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:9778,irritable bowel syndrome,DOID:225,syndrome
+UBERON:0003020,subcallosal area,UBERON:0011300,gray matter of telencephalon
+UBERON:0006240,future forebrain,UBERON:0006598,presumptive structure
+HP:0004971,Pulmonary artery hypoplasia,HP:0004414,Abnormality of the pulmonary artery
+UBERON:0000403,scalp,UBERON:0000477,anatomical cluster
+UBERON:0003307,floor plate of midbrain,UBERON:0002950,regional part of midbrain
+UBERON:0015154,lateral gland of orbital region,UBERON:0015212,lateral structure
+UBERON:0003866,middle phalanx of pes,UBERON:0004301,middle phalanx
+DOID:4227,uterine corpus endometrial stromal sarcoma,DOID:5165,uterine corpus sarcoma
+HP:0001071,Angiokeratoma corporis diffusum,HP:0001014,Angiokeratoma
+UBERON:0007606,ciliated stratified columnar epithelium,UBERON:0007602,stratified columnar epithelium
+UBERON:0000487,simple squamous epithelium,UBERON:0006914,squamous epithelium
+UBERON:0005412,optic fissure,UBERON:0004121,ectoderm-derived structure
+DOID:10931,dependent personality disorder,DOID:1510,personality disorder
+UBERON:0002827,auditory ganglion,UBERON:0001714,cranial ganglion
+HP:0000407,Sensorineural hearing impairment,HP:0000365,Hearing impairment
+HP:0010662,Abnormality of the diencephalon,HP:0100547,Abnormality of the forebrain
+DOID:2749,glycogen storage disease I,DOID:2747,glycogen storage disease
+UBERON:0004502,skeletal muscle tissue of biceps brachii,UBERON:0001134,skeletal muscle tissue
+CL:0002371,somatic cell,CL:0000003,native cell
+CL:1001597,seminal vesicle glandular cell,CL:0000068,duct epithelial cell
+CL:0000486,garland cell,CL:0000519,phagocyte (sensu Nematoda and Protostomia)
+DOID:0050290,trichosporonosis,DOID:2473,opportunistic mycosis
+CL:0000174,steroid hormone secreting cell,CL:0000163,endocrine cell
+DOID:4716,malignant gastric germ cell tumor,DOID:10534,stomach cancer
+CL:1001598,small intestine glandular cell,CL:0002254,epithelial cell of small intestine
+UBERON:3010728,otic opercular element,UBERON:0007844,cartilage element
+HP:0009590,Unilateral vestibular Schwannoma,HP:0009588,Vestibular Schwannoma
+CL:0000681,radial glial cell,CL:0000243,glial cell (sensu Vertebrata)
+HP:0004625,Biconvex vertebral bodies,HP:0003312,Abnormal form of the vertebral bodies
+UBERON:0001581,depressor labii inferioris,UBERON:0015212,lateral structure
+UBERON:0003430,neck nerve,UBERON:0001021,nerve
+NCBITaxon:163158,Xenopsylla,NCBITaxon:476427,Xenopsyllinae
+UBERON:0002107,liver,UBERON:0002365,exocrine gland
+UBERON:0004733,segmental subdivision of hindbrain,UBERON:0004732,segmental subdivision of nervous system
+UBERON:0015007,cervical vertebra endochondral element,UBERON:0010363,endochondral element
+HP:0005150,Abnormal atrioventricular conduction,HP:0011675,Arrhythmia
+HP:0010395,Aplasia/Hypoplasia of the proximal phalanx of the 2nd toe,HP:0010358,Abnormality of the proximal phalanx of the 2nd toe
+DOID:0050603,acheiropody,DOID:2256,osteochondrodysplasia
+NCBITaxon:6943,Amblyomma americanum,NCBITaxon:6942,Amblyomma
+UBERON:3000002,alary cartilage,UBERON:0003933,cranial cartilage
+UBERON:0003082,myotome,UBERON:0000490,unilaminar epithelium
+CL:0000067,ciliated epithelial cell,CL:0000064,ciliated cell
+UBERON:0009624,lumbar nerve,UBERON:0001780,spinal nerve
+UBERON:0001766,anterior chamber of eyeball,UBERON:0006311,chamber of eyeball
+HP:0009212,Stippling of the epiphysis of the middle phalanx of the 5th finger,HP:0010266,Stippling of the epiphyses of the middle phalanges of the hand
+HP:0000897,Rachitic rosary,HP:0000766,Abnormality of the sternum
+HP:0009955,Partial duplication of the proximal phalanx of the 2nd finger,HP:0009956,Partial duplication of the phalanges of the 2nd finger
+UBERON:0006960,ovary stroma,UBERON:0014404,female anatomical structure
+CL:0002644,endo-epithelial cell of tympanic part of viscerocranial mucosa,CL:0002261,endothelial cell of viscerocranial mucosa
+HP:0003116,Abnormal echocardiogram,HP:0011025,Abnormality of cardiovascular system physiology
+DOID:3262,phagocyte bactericidal dysfunction,DOID:612,primary immunodeficiency disease
+UBERON:2000404,paracommissural nucleus,UBERON:0006569,diencephalic nucleus
+UBERON:0004772,eyelid tarsus,UBERON:0004121,ectoderm-derived structure
+HP:0006159,Mesoaxial hand polydactyly,HP:0100260,Mesoaxial polydactyly
+DOID:0080006,bone development disease,DOID:0080001,bone disease
+UBERON:0008904,neuromast,UBERON:0004121,ectoderm-derived structure
+DOID:9477,pulmonary embolism,DOID:0050828,artery disease
+DOID:4762,vasculogenic impotence,DOID:1875,impotence
+UBERON:3010218,external carotid,UBERON:3010217,carotid
+UBERON:0010676,manual digit 2 phalanx cartilage element,UBERON:0010686,manual digit phalanx cartilage element
+HP:0010510,Hypermobility of toe joints,HP:0001780,Abnormality of toe
+DOID:6587,invasive tubular breast carcinoma,DOID:3458,breast adenocarcinoma
+UBERON:0004678,apex of spinal cord dorsal horn,UBERON:0002315,gray matter of spinal cord
+DOID:5199,ureteral obstruction,DOID:5200,urinary tract obstruction
+UBERON:0003268,tooth of lower jaw,UBERON:0013765,digestive system organ
+UBERON:0001687,stapes bone,UBERON:0001686,auditory ossicle
+UBERON:0010032,anterior part of tongue,UBERON:0000064,organ part
+UBERON:0002342,neural crest,UBERON:0004121,ectoderm-derived structure
+HP:0002744,Bilateral cleft lip and palate,HP:0100337,Bilateral cleft palate
+DOID:5655,chiasmal syndrome,DOID:5656,cranial nerve disease
+UBERON:2005066,bulbus arteriosus outer layer,UBERON:0005291,embryonic tissue
+UBERON:3010818,hepatic peritoneum,UBERON:0002358,peritoneum
+UBERON:0002264,olfactory bulb,UBERON:0015212,lateral structure
+UBERON:0002632,medial part of medial mammillary nucleus,UBERON:0003528,brain grey matter
+UBERON:0009024,adrenal gland X zone,UBERON:0009753,adrenal gland cortex zone
+UBERON:0011655,interclavicle,UBERON:0007829,pectoral girdle bone
+HP:0000240,Abnormality of skull size,HP:0000929,Abnormality of the skull
+HP:0007787,Posterior subcapsular cataract,HP:0000523,Subcapsular cataract
+HP:0008461,Cervical vertebral facet hypoplasia,HP:0011041,Aplasia/Hypoplasia of the cervical spine
+HP:0011792,Neoplasm by histology,HP:0002664,Neoplasm
+UBERON:0005139,metanephric long descending thin limb,UBERON:0005134,metanephric nephron epithelium
+HP:0004532,Sacral hypertrichosis,HP:0000998,Hypertrichosis
+UBERON:0005384,nasal cavity epithelium,UBERON:0010371,ecto-epithelium
+DOID:2841,asthma,DOID:2320,obstructive lung disease
+UBERON:0004733,segmental subdivision of hindbrain,UBERON:0004121,ectoderm-derived structure
+HP:0000876,Oligomenorrhea,HP:0000140,Abnormality of the menstrual cycle
+UBERON:0010172,bulb of aorta,UBERON:0000477,anatomical cluster
+UBERON:0004389,epiphysis of metatarsal bone,UBERON:0004120,mesoderm-derived structure
+HP:0012724,Upper eyelid edema,HP:0100540,Palpebral edema
+UBERON:0013192,ovarian medulla,UBERON:0000958,medulla of organ
+DOID:3428,granulomatous myositis,DOID:633,myositis
+UBERON:0002067,dermis,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0007979,Gaze-evoked horizontal nystagmus,HP:0000666,Horizontal nystagmus
+HP:0011068,Odontoma,HP:0010566,Hamartoma
+UBERON:0002891,cortical amygdaloid nucleus,UBERON:0002619,regional part of cerebral cortex
+UBERON:0006652,muscular layer of vagina,UBERON:0005156,reproductive structure
+UBERON:0000416,subdural space,UBERON:0000464,anatomical space
+HP:0010500,Hyperextensibility of the knee,HP:0002815,Abnormality of the knees
+UBERON:0003283,mesentery of oesophagus,UBERON:0001975,serosa of esophagus
+HP:0010239,Aplasia of the middle phalanx of the hand,HP:0009380,Aplasia of the fingers
+DOID:5847,posterior myocardial infarction,DOID:5844,myocardial infarction
+UBERON:0006291,scapula pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+HP:0006006,Hypotrophy of the small hand muscles,HP:0001421,Abnormality of the musculature of the hand
+CL:1000483,purkinje myocyte of internodal tract,CL:0002096,internodal tract myocyte
+UBERON:0009836,fronto-orbital gyrus,UBERON:0007193,orbital gyrus
+HP:0008368,Tarsal synostosis,HP:0001850,Abnormality of the tarsal bones
+UBERON:0001234,left adrenal gland,UBERON:0002369,adrenal gland
+HP:0010577,Absent epiphyses,HP:0005930,Abnormality of the epiphyses
+UBERON:2005000,basal communicating artery,UBERON:0003496,head blood vessel
+DOID:4435,cavernous sinus meningioma,DOID:3842,skull base neoplasm
+UBERON:0003645,metacarpal bone of digit 1,UBERON:0013581,metapodium bone 1
+DOID:13902,white piedra,DOID:0050133,superficial mycosis
+UBERON:0006250,infundibular recess of 3rd ventricle,UBERON:0005291,embryonic tissue
+HP:0006866,Midline central nervous system lipomas,HP:0100251,Lipomas of the central neryous system
+UBERON:0004058,biliary ductule,UBERON:0000025,tube
+UBERON:0003244,epithelium of mammary gland,UBERON:0014404,female anatomical structure
+DOID:0050771,phaeochromocytoma,DOID:0060084,cell type benign neoplasm
+HP:0010424,Complete duplication of the distal phalanx of the 2nd toe,HP:0010421,Duplication of the distal phalanx of the 2nd toe
+HP:0009005,Weakness of the intrinsic hand muscles,HP:0001421,Abnormality of the musculature of the hand
+UBERON:0006192,mesonephric proximal tubule,UBERON:0000083,mesonephric tubule
+UBERON:0001837,duct of salivary gland,UBERON:0014719,intralobular duct
+UBERON:0002325,epithelium of urethra,UBERON:0003914,epithelial tube
+DOID:4751,striatonigral degeneration,DOID:4752,multiple system atrophy
+UBERON:0003315,mesenchyme of ovary,UBERON:0003855,gonad mesenchyme
+UBERON:0009641,ansa lenticularis,UBERON:0002784,regional part of diencephalon
+HP:0011950,Bronchiolitis,HP:0011948,Acute respiratory tract infection
+HP:0005422,Absence of CD8+ T cells,HP:0005415,Decreased number of CD8+ T cells
+HP:0008391,Dystrophic fingernails,HP:0001231,Abnormality of the fingernails
+UBERON:0014711,carapacial ridge mesenchyme,UBERON:0003104,mesenchyme
+UBERON:0004366,extraembryonic ectoderm,UBERON:0000478,extraembryonic structure
+HP:0010026,Aplasia/Hypoplasia of the 1st metacarpal,HP:0010009,Abnormality of the 1st metacarpal
+UBERON:0005362,vagus X ganglion,UBERON:0009127,epibranchial ganglion
+HP:0002086,Abnormality of the respiratory system,HP:0000118,Phenotypic abnormality
+DOID:0050620,infiltrating renal pelvis transitional cell carcinoma,DOID:5974,renal pelvis transitional cell carcinoma
+HP:0011572,Supramitral ring,HP:0001718,Mitral stenosis
+HP:0000531,Corneal crystals,HP:0007759,Opacification of the corneal stroma
+UBERON:2000931,myotome somite 27,UBERON:0003082,myotome
+HP:0003546,Exercise intolerance,HP:0004302,Functional motor problems.
+HP:0006276,Hyperechogenic pancreas,HP:0012090,Abnormality of pancreas morphology
+DOID:2712,phimosis,DOID:1529,penile disease
+UBERON:0004060,neural tube ventricular layer,UBERON:0000119,cell layer
+UBERON:0004245,oviduct smooth muscle,UBERON:0014404,female anatomical structure
+UBERON:0007255,intervertebral disk of lumbar vertebra,UBERON:0005174,dorsal region organ
+UBERON:0011163,supraoccipital pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+UBERON:0006655,septum of scrotum,UBERON:0014403,male anatomical structure
+UBERON:3010790,muscle rectus abdominis superficialis,UBERON:0004120,mesoderm-derived structure
+CL:0001057,"myeloid dendritic cell, human",CL:0000782,myeloid dendritic cell
+HP:0006156,Ulnar deviation of thumb,HP:0009465,Ulnar deviation of finger
+HP:0012118,Laryngeal carcinoma,HP:0100605,Neoplasm of the larynx
+UBERON:0010151,duct of bulbourethral gland,UBERON:0006555,excretory tube
+DOID:0050730,coenzyme Q10 deficiency disease,DOID:700,mitochondrial metabolism disease
+HP:0009494,Ivory epiphyses of the 2nd finger,HP:0006263,Abnormality of the epiphyses of the 2nd finger
+UBERON:0000398,cartilage tissue of sternum,UBERON:0003837,thoracic segment connective tissue
+UBERON:0002177,right main bronchus,UBERON:0002182,main bronchus
+HP:0008314,Decreased activity of mitochondrial complex II,HP:0008972,Decreased activity of mitochondrial respiratory chain
+DOID:9942,lymph node disease,DOID:75,lymphatic system disease
+HP:0011899,Hyperfibrinogenemia,HP:0011898,Abnormality of circulating fibrinogen
+HP:0003553,Cellulitis due to immunodeficiency,HP:0002721,Immunodeficiency
+DOID:10301,parotitis,DOID:10302,parotid disease
+HP:0012589,Multidrug-resistant nephrotic syndrome,HP:0000100,Nephrotic syndrome
+UBERON:0016452,upper secondary premolar tooth,UBERON:0003268,tooth of lower jaw
+HP:0006769,Myxoid subcutaneous tumors,HP:0008069,Neoplasm of the skin
+HP:0012091,Abnormality of pancreas physiology,HP:0001732,Abnormality of the pancreas
+HP:0012618,Urachal cyst,HP:0010478,Abnormality of the urachus
+UBERON:0011584,zeugopodial skeleton,UBERON:0004120,mesoderm-derived structure
+UBERON:0004361,stylohyoid ligament,UBERON:0008846,skeletal ligament
+DOID:3193,peripheral nerve sheath neoplasm,DOID:1192,peripheral nervous system neoplasm
+HP:0010067,Aplasia/Hypoplasia of the 1st metatarsal,HP:0010203,Aplasia/Hypoplasia of the proximal phalanges of the toes
+HP:0009534,Triangular epiphysis of the proximal phalanx of the 2nd finger,HP:0009498,Triangular epiphyses of the 2nd finger
+HP:0011446,Abnormality of higher mental function,HP:0012638,Abnormality of nervous system physiology
+CL:0000208,pH receptor cell,CL:0000206,chemoreceptor cell
+DOID:6933,bladder transitional cell papilloma,DOID:5432,bladder papillary transitional cell neoplasm
+HP:0010257,Absent epiphyses of the middle phalanges of the hand,HP:0010244,Abnormality of the epiphyses of the middle phalanges of the hand
+UBERON:0004761,cartilaginous neurocranium,UBERON:0000075,subdivision of skeletal system
+CL:0002573,Schwann cell,CL:0000243,glial cell (sensu Vertebrata)
+HP:0010097,Partial duplication of the distal phalanx of the hallux,HP:0010084,Duplication of the distal phalanx of the hallux
+UBERON:0012360,bone of jaw,UBERON:0013765,digestive system organ
+UBERON:0002420,basal ganglion,UBERON:0003528,brain grey matter
+UBERON:3010780,pars recta,UBERON:0000064,organ part
+HP:0010848,EEG with spike-wave complexes (2.5-3.5 Hz),HP:0010850,EEG with spike-wave complexes
+UBERON:2001729,caudal principal ray 17,UBERON:2001585,caudal principal ray
+UBERON:3010104,pectoral glands,UBERON:3010603,body gland
+UBERON:0001488,ankle joint,UBERON:0003840,hindlimb joint
+HP:0011063,Abnormality of incisor morphology,HP:0006482,Abnormality of dental morphology
+DOID:1432,blindness,DOID:5679,retinal disease
+UBERON:0015847,upper left incisor tooth,UBERON:0003450,upper jaw incisor
+HP:0012312,Monocytopenia,HP:0012310,Abnormal monocyte count
+HP:0000207,Triangular mouth,HP:0011338,Abnormality of mouth shape
+UBERON:0012301,female membranous urethra,UBERON:0014404,female anatomical structure
+HP:0010436,Aplasia of the proximal phalanx of the 2nd toe,HP:0010430,Aplasia of the phalanges of the 2nd toe
+UBERON:0013397,stratum argenteum of choroid,UBERON:0000479,tissue
+HP:0012344,Morphea,HP:0001072,Thickened skin
+UBERON:0007277,presumptive hindbrain,UBERON:0006598,presumptive structure
+UBERON:0002943,lingual gyrus,UBERON:0000064,organ part
+HP:0011214,EEG with photoparoxysmal response grade IV,HP:0010852,EEG with photoparoxysmal response
+UBERON:0004835,epididymis smooth muscle,UBERON:0005156,reproductive structure
+HP:0008108,Advanced tarsal ossification,HP:0008369,Abnormal tarsal ossification
+HP:0200043,Verrucae,HP:0012740,Papilloma
+UBERON:0015219,middle nasal meatus,UBERON:0015216,nasal meatus
+DOID:0050047,Flinders Island spotted fever,DOID:11104,spotted fever
+HP:0004599,Absent or minimally ossified vertebral bodies,HP:0100569,Abnormal vertebral ossification
+DOID:13137,Werdnig-Hoffmann disease,DOID:0060160,survival motor neuron spinal muscular atrophy
+DOID:1673,pneumothorax,DOID:1532,pleural disease
+UBERON:0002631,cerebral crus,UBERON:0015212,lateral structure
+HP:0007911,Congenital bilateral ptosis,HP:0007970,Congenital ptosis
+HP:0000690,Agenesis of maxillary lateral incisor,HP:0006485,Agenesis of incisor
+CL:0000351,trophoblast cell,CL:0000349,extraembryonic cell
+HP:0002724,Recurrent Aspergillus infections,HP:0002841,Recurrent fungal infections
+UBERON:0005082,tube lumen,UBERON:0000464,anatomical space
+UBERON:0001277,intestinal epithelium,UBERON:0004808,gastrointestinal system epithelium
+HP:0010909,Abnormality of arginine metabolism,HP:0010902,Abnormality of glutamine family amino acid metabolism
+HP:0004608,Anteriorly placed odontoid process,HP:0003310,Abnormality of the odontoid process
+CL:1000313,gastric goblet cell,CL:0000160,goblet cell
+DOID:5922,adult brainstem astrocytoma,DOID:4813,adult brain stem glioma
+DOID:14780,KBG syndrome,DOID:225,syndrome
+UBERON:0010047,oral gland,UBERON:0004121,ectoderm-derived structure
+DOID:5042,malignant granular cell myoblastoma,DOID:4159,skin cancer
+UBERON:0002148,locus ceruleus,UBERON:0009662,hindbrain nucleus
+UBERON:3000981,limb external integument structure,UBERON:3000961,external integument structure
+HP:0005210,Hypoplastic colon,HP:0100811,Aplasia/Hypoplasia of the colon
+HP:0010889,Morbus Kienboeck,HP:0100323,Juvenile aseptic necrosis
+CL:0002061,T-helper 9 cell,CL:0000492,CD4-positive helper T cell
+DOID:893,Wilson disease,DOID:896,metal metabolism disorder
+HP:0012562,Premature epimetaphyseal fusion in hand,HP:0010588,Premature epimetaphyseal fusion
+DOID:4548,extraskeletal mesenchymal chondrosarcoma,DOID:4545,mesenchymal chondrosarcoma
+UBERON:0003297,gland of integumental system,UBERON:0002530,gland
+UBERON:0008779,subclavius,UBERON:0001495,pectoral muscle
+CL:0000508,type G enteroendocrine cell,CL:0002180,mucous cell of stomach
+DOID:3448,penis Paget's disease,DOID:3449,penis carcinoma
+HP:0001973,Autoimmune thrombocytopenia,HP:0001873,Thrombocytopenia
+UBERON:0000450,corpus albicans,UBERON:0003982,mature ovarian follicle
+UBERON:0001375,semitendinosus,UBERON:0003663,hindlimb muscle
+DOID:14445,chronic closed-angle glaucoma,DOID:1405,primary angle-closure glaucoma
+HP:0100887,Abnormality of globe size,HP:0000315,Abnormality of the orbital region
+CL:0000794,"CD8-positive, alpha-beta cytotoxic T cell",CL:0000625,"CD8-positive, alpha-beta T cell"
+UBERON:0009005,femorotibial joint,UBERON:0011139,synovial limb joint
+HP:0007375,Abnormality of the septum pellucidum,HP:0002060,Abnormality of the cerebrum
+UBERON:0003360,epithelium of parotid gland,UBERON:0003236,epithelium of lower jaw
+DOID:11713,diabetic angiopathy,DOID:341,peripheral vascular disease
+UBERON:3010538,pars nervosa,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0004031,Broad radial diaphysis,HP:0004027,Abnormality of radial diaphysis
+HP:0011955,Hepatic granulomatosis,HP:0001392,Abnormality of the liver
+UBERON:0007318,saphenous vein,UBERON:0001638,vein
+HP:0009388,Ivory epiphyses of the 5th finger,HP:0010234,Ivory epiphyses of the phalanges of the hand
+UBERON:0003291,meninx of hindbrain,UBERON:0003547,brain meninx
+DOID:4659,extracutaneous mastocytoma,DOID:349,systemic mastocytosis
+UBERON:0004680,body of fornix,UBERON:0002791,regional part of telencephalon
+DOID:4137,common bile duct disease,DOID:4138,bile duct disease
+UBERON:0003389,mesothelium of diaphragm,UBERON:0004807,respiratory system epithelium
+UBERON:3000879,incisura terminalis,UBERON:0000064,organ part
+DOID:5393,brain angioma,DOID:2517,intracranial structure hemangioma
+HP:0100118,Pseudoepiphysis of the middle phalanx of the 2nd toe,HP:0100051,Pseudoepiphyses of the 2nd toe
+UBERON:0005011,mucosa of right uterine tube,UBERON:0005048,mucosa of uterine tube
+UBERON:2002281,retractor posttemporalis,UBERON:0002376,cranial muscle
+UBERON:0008861,pyloric gastric gland,UBERON:0000414,mucous gland
+HP:0002170,Intracranial hemorrhage,HP:0011029,Internal hemorrhage
+UBERON:0013533,Brodmann (1909) area 2,UBERON:0013529,Brodmann area
+HP:0003076,Glycosuria,HP:0011016,Abnormality of urine glucose concentration
+DOID:14140,pulp erosion,DOID:2498,tooth erosion
+HP:0001278,Orthostatic hypotension,HP:0002615,Hypotension
+UBERON:0010408,ocular angle artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0003741,Congenital muscular dystrophy,HP:0003560,Muscular dystrophy
+UBERON:0004796,prostate gland secretion,UBERON:0006530,seminal fluid
+HP:0007373,Atrophy/Degeneration involving motor neurons,HP:0007367,Atrophy/Degeneration affecting the central nervous system
+UBERON:0013518,coccygeal vertebra pre-cartilage condensation,UBERON:0015006,coccygeal vertebra endochondral element
+HP:0008122,Calcaneonavicular fusion,HP:0008368,Tarsal synostosis
+UBERON:2002241,Purkinje cell layer valvula cerebelli,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0003349,Low cholesterol esterification rates,HP:0003107,Abnormality of cholesterol metabolism
+UBERON:0002131,anterior lobe of cerebellum,UBERON:0005293,cerebellum lobe
+UBERON:2007043,hindbrain neural tube,UBERON:0004121,ectoderm-derived structure
+DOID:11589,Riley-Day syndrome,DOID:0050548,hereditary sensory neuropathy
+HP:0010075,Duplication of the 1st metatarsal,HP:0001449,Duplication of metatarsal bones
+UBERON:3010328,equatorial belt,UBERON:0000470,cell part
+NCBITaxon:54292,Apodemus flavicollis,NCBITaxon:400053,Sylvaemus group
+HP:0011185,EEG with focal epileptiform discharges,HP:0011182,Epileptiform EEG discharges
+UBERON:0013676,aproctal bone of priapium,UBERON:0007719,bone of reproductive structure
+UBERON:2000866,epaxial region somite 15,UBERON:0003900,epaxial myotome region
+HP:0100148,Cone-shaped epiphysis of the middle phalanx of the 3rd toe,HP:0100057,Cone-shaped epiphyses of the 3rd toe
+HP:0009527,Enlarged epiphysis of the proximal phalanx of the 2nd finger,HP:0009501,Abnormality of the epiphysis of the proximal phalanx of the 2nd finger
+HP:0007346,Subcortical white matter calcifications,HP:0002514,Cerebral calcification
+HP:0003731,Quadriceps muscle weakness,HP:0008994,Proximal muscle weakness in lower limbs
+UBERON:0000444,lymphoid follicle,UBERON:0001744,lymphoid tissue
+UBERON:0011247,procoracoid cartilage,UBERON:0007844,cartilage element
+DOID:10652,Alzheimer's disease,DOID:1307,dementia
+HP:0002073,Progressive cerebellar ataxia,HP:0001251,Ataxia
+UBERON:2002055,vertebra 6 - vertebra 7 joint,UBERON:0000982,skeletal joint
+UBERON:0006376,premacula segment of distal straight tubule,UBERON:0007685,region of nephron tubule
+DOID:1389,polyneuropathy,DOID:574,peripheral nervous system disease
+UBERON:0006637,coeliac trunk,UBERON:0004120,mesoderm-derived structure
+HP:0100196,Irregular epiphysis of the proximal phalanx of the 4th toe,HP:0100096,Abnormality of the epiphysis of the proximal phalanx of the 4th toe
+HP:0011718,Abnormality of the pulmonary veins,HP:0004930,Abnormality of the pulmonary vasculature
+UBERON:0002444,lens fiber,UBERON:0004121,ectoderm-derived structure
+HP:0006659,Internally rotated shoulders,HP:0003043,Abnormality of the shoulder
+UBERON:0016425,epiphyseal plate of radius,UBERON:0007390,pectoral appendage cartilage tissue
+UBERON:0005604,hepatic duct extrahepatic part,UBERON:0003914,epithelial tube
+DOID:13501,Mobius syndrome,DOID:1756,facial nerve disease
+HP:0002119,Ventriculomegaly,HP:0002118,Abnormality of the cerebral ventricles
+HP:0001520,Large for gestational age,HP:0001548,Overgrowth
+CL:0000384,ligament cell,CL:0000630,supportive cell
+HP:0006008,Unilateral brachydactyly,HP:0001156,Brachydactyly syndrome
+HP:0010228,Absent epiphyses of the phalanges of the hand,HP:0010577,Absent epiphyses
+UBERON:0010372,uncinate process of ethmoid,UBERON:0004120,mesoderm-derived structure
+HP:0004990,Epiphyseal streaking,HP:0005930,Abnormality of the epiphyses
+UBERON:0003650,metatarsal bone of digit 1,UBERON:0001448,metatarsal bone
+CL:0000551,unimodal nocireceptor,CL:0000198,pain receptor cell
+DOID:4690,childhood mediastinal neurogenic tumor,DOID:1192,peripheral nervous system neoplasm
+UBERON:0001956,cartilage of bronchus,UBERON:0003592,bronchus connective tissue
+DOID:13474,progressive peripheral pterygium,DOID:10526,conjunctival pterygium
+CL:0000633,Hensen cell,CL:0002490,organ of Corti supporting cell
+UBERON:0008883,osteoid,UBERON:0007475,matrix-based tissue
+UBERON:0006275,pericardio-peritoneal canal,UBERON:0004120,mesoderm-derived structure
+DOID:10964,cholesteatoma of middle ear,DOID:869,cholesteatoma
+HP:0009924,Aplasia/Hypoplasia involving the nose,HP:0005105,Abnormal nasal morphology
+HP:0000271,Abnormality of the face,HP:0000234,Abnormality of the head
+UBERON:0005106,metanephric tubule,UBERON:0006555,excretory tube
+UBERON:0004524,papillary muscle of left ventricle,UBERON:0002494,papillary muscle of heart
+CL:0000488,visible light photoreceptor cell,CL:0000210,photoreceptor cell
+UBERON:0001518,skin of wrist,UBERON:0001519,skin of manus
+CL:0000687,R1 photoreceptor cell,CL:0000488,visible light photoreceptor cell
+UBERON:0001957,submucosa of bronchus,UBERON:0004119,endoderm-derived structure
+DOID:13560,subserous uterine fibroid,DOID:13223,uterine fibroid
+DOID:11782,astigmatism,DOID:9835,refractive error
+DOID:6115,lateral ventricle meningioma,DOID:3772,intraventricular meningioma
+HP:0003561,Birth length <3rd percentile,HP:0004322,Short stature
+NCBITaxon:37987,Pneumocystidales,NCBITaxon:147553,Pneumocystidomycetes
+UBERON:0001638,vein,UBERON:0003920,venous blood vessel
+DOID:11838,penis sarcoma,DOID:11615,penile cancer
+DOID:11042,Felty's syndrome,DOID:225,syndrome
+UBERON:0003917,arthropod fat body,UBERON:0001013,adipose tissue
+UBERON:0010029,dorsal part of pharyngeal pouch 5,UBERON:0005911,endo-epithelium
+UBERON:0011609,ceratohyal element,UBERON:0010522,replacement element
+HP:0012505,Enlarged pituitary gland,HP:0012504,Abnormal size of pituitary gland
+UBERON:0007237,1st arch mandibular component,UBERON:0005423,developing anatomical structure
+UBERON:0010995,deep part of masseter muscle,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:10520,acute infection of pinna,DOID:9463,otitis externa
+HP:0007373,Atrophy/Degeneration involving motor neurons,HP:0002450,Abnormality of the motor neurons
+UBERON:3000397,pars dentalis of premaxilla,UBERON:0000064,organ part
+DOID:2834,acquired polycythemia,DOID:8432,polycythemia
+HP:0010020,Irregular epiphysis of the 1st metacarpal,HP:0009190,Irregular epiphyses of the metacarpals
+HP:0100490,Camptodactyly of finger,HP:0012385,Camptodactyly
+UBERON:0005844,spinal cord segment,UBERON:0001948,regional part of spinal cord
+DOID:4876,trachea carcinoma,DOID:11920,tracheal cancer
+HP:0004027,Abnormality of radial diaphysis,HP:0002818,Abnormality of the radius
+HP:0100380,Aplasia of the distal phalanx of the 5th toe,HP:0100364,Aplasia of the phalanges of the 5th toe
+DOID:3087,gingivitis,DOID:1483,gingival disease
+HP:0006557,Polycystic liver disease,HP:0006706,Cystic liver disease
+DOID:14175,von Hippel-Lindau disease,DOID:5241,hemangioblastoma
+HP:0004268,Osteoarthritis of the small joints of the hand,HP:0006261,Abnormality of phalangeal joints of the hand
+HP:0010107,Short proximal phalanx of hallux,HP:0010085,Aplasia/Hypoplasia of the proximal phalanx of the hallux
+HP:0003563,Hypobetalipoproteinemia,HP:0010981,Hypolipoproteinemia
+UBERON:0009670,rectal lumen,UBERON:0000464,anatomical space
+UBERON:0014612,substantia gelatinosa of thoracic spinal cord dorsal horn,UBERON:0002181,substantia gelatinosa
+CL:0000089,male germ line stem cell (sensu Vertebrata),CL:0000016,male germ line stem cell
+UBERON:0010947,occipitalis,UBERON:0010938,muscle belly
+DOID:7951,Schwannian stroma-rich and stroma-poor composite ganglioneuroblastoma,DOID:5193,nodular ganglioneuroblastoma
+HP:0011632,Partial right sided absence of pericardium,HP:0011628,Congenital defect of the pericardium
+HP:0009170,Osteolytic defects of the middle phalanx of the 5th finger,HP:0004219,Abnormality of the middle phalanx of the 5th finger
+HP:0002047,Malignant hyperthermia,HP:0004370,Abnormality of temperature regulation
+DOID:3240,aspiration pneumonitis,DOID:552,pneumonia
+UBERON:0016405,pulmonary capillary,UBERON:0003526,respiratory system capillary
+UBERON:2002019,pterotic-posttemporal-supracleithrum,UBERON:0002513,endochondral bone
+UBERON:0008999,hoof lamina,UBERON:0004121,ectoderm-derived structure
+DOID:10970,spastic quadriplegia,DOID:0050669,spastic cerebral palsy
+UBERON:0011148,submucosal gland,UBERON:0000414,mucous gland
+CL:0000694,R3 photoreceptor cell,CL:0000488,visible light photoreceptor cell
+UBERON:0008265,echinopluteus larva,UBERON:0002548,larva
+UBERON:0005317,pulmonary artery endothelium,UBERON:0005911,endo-epithelium
+DOID:2314,malt worker's lung,DOID:841,extrinsic allergic alveolitis
+HP:0000750,Delayed speech and language development,HP:0100543,Cognitive impairment
+DOID:14392,thrombophlebitis migrans,DOID:3875,thrombophlebitis
+HP:0009298,Aplasia of the proximal phalanx of the 4th finger,HP:0009281,Aplasia of the 4th finger
+CL:0002210,red muscle cell,CL:0008002,skeletal muscle fiber
+HP:0005352,Severe T-cell immunodeficiency,HP:0005374,Cellular immunodeficiency
+NCBITaxon:7511,Pulicidae,NCBITaxon:129369,Pulicoidea
+UBERON:0003902,retinal neural layer,UBERON:0001781,layer of retina
+UBERON:3000003,alary process of premaxilla,UBERON:0004530,bony projection
+UBERON:0000381,urinary bladder detrusor smooth muscle,UBERON:0004228,urinary bladder smooth muscle
+UBERON:3000752,pars acromialis,UBERON:0000479,tissue
+HP:0100048,Fragmentation of the epiphyses of the 2nd toe,HP:0010166,Fragmentation of the epiphyses of the toes
+UBERON:0002302,myocardium of atrium,UBERON:0002349,myocardium
+UBERON:3011121,late distal segment,UBERON:0006554,urinary system structure
+UBERON:0004328,proximal phalanx of manual digit 2,UBERON:0002234,proximal phalanx of manus
+CL:0000059,ameloblast,CL:0000151,secretory cell
+UBERON:2005227,protoneuromast,UBERON:0000477,anatomical cluster
+HP:0002884,Hepatoblastoma,HP:0002896,Neoplasm of the liver
+HP:0001083,Ectopia lentis,HP:0000517,Abnormality of the lens
+HP:0009538,Contracture of the distal interphalangeal joint of the 2nd finger,HP:0009697,Contractures of the distal interphalangeal joints of the fingers
+DOID:8529,ulcer of lower limbs,DOID:8549,chronic ulcer of skin
+DOID:174,acanthoma,DOID:3168,squamous cell neoplasm
+CL:1000850,macula densa epithelial cell,CL:0002305,epithelial cell of distal tubule
+DOID:2916,hypersensitivity reaction type IV disease,DOID:0060056,hypersensitivity reaction disease
+UBERON:0010937,salpingopharyngeus muscle,UBERON:0013765,digestive system organ
+HP:0007892,Hypoplasia of the lacrimal puncta,HP:0011479,Abnormality of the lacrimal punctum
+UBERON:3000689,prominentia apicalis ventralis,UBERON:0010314,structure with developmental contribution from neural crest
+CL:1001224,interlobulary vein smooth muscle cell,CL:1001068,kidney venous system smooth muscle cell
+UBERON:0008848,cranial suspensory ligament,UBERON:0008841,suspensory ligament
+DOID:10443,hypopyon,DOID:9383,iridocyclitis
+UBERON:0013234,violet gland,UBERON:0011252,scent gland
+HP:0011902,Abnormal hemoglobin,HP:0001877,Abnormality of erythrocytes
+UBERON:3010458,suprarostral ala,UBERON:0000064,organ part
+UBERON:3000022,antorbital process,UBERON:0004120,mesoderm-derived structure
+DOID:8335,microglandular adenosis of breast,DOID:5998,microglandular adenosis
+HP:0010772,Anomalous pulmonary venous return,HP:0011718,Abnormality of the pulmonary veins
+HP:0011001,Increased bone mineral density,HP:0004348,Abnormality of bone mineral density
+UBERON:0002493,uterine artery,UBERON:0005156,reproductive structure
+HP:0100171,Cone-shaped epiphysis of the distal phalanx of the 4th toe,HP:0100068,Cone-shaped epiphyses of the 4th toe
+CL:0002377,immature Schwann cell,CL:0002573,Schwann cell
+UBERON:0004763,endochondral bone tissue,UBERON:0002481,bone tissue
+DOID:0050133,superficial mycosis,DOID:1564,fungal infectious disease
+CL:0002310,mammosomatotroph,CL:0000295,somatotropin secreting cell
+DOID:1996,rectum adenocarcinoma,DOID:1993,rectum cancer
+HP:0011267,"Microtia, third degree",HP:0008551,Microtia
+UBERON:0015104,distal tarsal bone 1 pre-cartilage condensation,UBERON:0015102,distal tarsal bone 1 endochondral element
+DOID:2001,neuroma,DOID:0060115,nervous system benign neoplasm
+HP:0008095,Osteolysis of talus,HP:0008365,Abnormality of the talus
+HP:0009601,Aplasia/Hypoplasia of the thumb,HP:0001172,Abnormality of the thumb
+UBERON:0008824,duct of epididymis,UBERON:0005904,duct of male reproductive system
+UBERON:0005239,basal plate metencephalon,UBERON:0004064,neural tube basal plate
+UBERON:0001487,pes joint,UBERON:0011139,synovial limb joint
+UBERON:0003906,cardiac jelly,UBERON:0000479,tissue
+DOID:14545,seminal vesicle adenocarcinoma,DOID:3856,male reproductive organ cancer
+CL:1000839,kidney proximal straight tubule epithelial cell,CL:0002306,epithelial cell of proximal tubule
+HP:0009938,Sunken cheeks,HP:0004426,Abnormality of the cheeks
+UBERON:0004061,neural tube mantle layer,UBERON:0000119,cell layer
+UBERON:2000481,caudal preglomerular nucleus,UBERON:2002226,preglomerular nucleus
+DOID:2361,macrocytic anemia,DOID:2355,anemia
+HP:0010290,Short hard palate,HP:0100737,Abnormality of the hard palate
+HP:0009745,Spinalarachnoid cyst,HP:0010303,Abnormality of the spinal meninges
+UBERON:0007639,hippocampus alveus,UBERON:0002305,layer of hippocampus
+CL:0002469,MHC-II-negative classical monocyte,CL:0002395,Gr1-high classical monocyte
+UBERON:2002021,ascending process of the parasphenoid,UBERON:0004121,ectoderm-derived structure
+UBERON:0001621,coronary artery,UBERON:0004573,systemic artery
+DOID:3025,acinar cell carcinoma,DOID:305,carcinoma
+HP:0012495,Posterior cerebral artery stenosis,HP:0012492,Cerebral artery stenosis
+DOID:0050430,Sipple syndrome,DOID:0050736,autosomal dominant disease
+HP:0100390,Short distal phalanx of the 4th toe,HP:0100370,Aplasia/Hypoplasia of the distal phalanx of the 4th toe
+HP:0010653,Abnormality of the falx cerebri,HP:0010652,Abnormality of the dura mater
+UBERON:0006011,hyaloid vein,UBERON:0005492,hyaloid vessel
+CL:0000271,prestalk A cell,CL:0000269,prestalk cell
+HP:0009243,Patchy sclerosis of the distal phalanx of the 5th finger,HP:0100903,Sclerosis of the distal phalanx of the 5th finger
+UBERON:0011216,organ system subdivision,UBERON:0000477,anatomical cluster
+UBERON:0005427,corneal primordium,UBERON:0001048,primordium
+UBERON:0011580,platypus crural gland,UBERON:0011579,venom gland
+UBERON:0005600,crus commune,UBERON:0004121,ectoderm-derived structure
+UBERON:0011756,male genital swelling,UBERON:0011754,genital swelling
+HP:0002751,Kyphoscoliosis,HP:0002808,Kyphosis
+HP:0000114,Proximal tubulopathy,HP:0000091,Abnormality of the renal tubule
+DOID:4480,achondroplasia,DOID:2256,osteochondrodysplasia
+HP:0009355,Stippling of the epiphysis of the proximal phalanx of the 3rd finger,HP:0009333,Abnormality of the epiphysis of the proximal phalanx of the 3rd finger
+UBERON:0009551,distal segment of digit,UBERON:0002529,limb segment
+HP:0003037,Enlarged joints,HP:0001367,Abnormal joint morphology
+CL:0001046,memory CCR4-positive regulatory T cell,CL:0001047,"CD4-positive, CD25-positive, CCR4-positive, alpha-beta regulatory T cell"
+DOID:2544,extratemporal epilepsy,DOID:1826,epilepsy syndrome
+UBERON:3000161,fenestra endochoanalis,UBERON:3000316,nasal opening
+DOID:12132,Wegener's granulomatosis,DOID:417,hypersensitivity reaction type II disease
+HP:0008529,Absence of acoustic reflex,HP:0004454,Abnormal middle ear reflexes
+UBERON:0006070,coccygeal vertebra,UBERON:0015006,coccygeal vertebra endochondral element
+HP:0009678,Enlarged epiphysis of the distal phalanx of the thumb,HP:0010249,Enlarged epiphyses of the distal phalanges of the hand
+DOID:11864,peripheral focal chorioretinitis,DOID:1979,focal chorioretinitis
+UBERON:0013165,epiglottic vallecula,UBERON:0000064,organ part
+DOID:0050940,endocervical adenocarcinoma,DOID:7519,endocervical carcinoma
+UBERON:4000105,limiting layer of elasmoid scale,UBERON:0004121,ectoderm-derived structure
+HP:0008986,Agenesis of the diaphragm,HP:0010315,Aplasia/Hypoplasia of the diaphragm
+HP:0011540,Congenitally corrected transposition of the great arteries,HP:0011534,Abnormal spatial orientation of the cardiac segments
+UBERON:0003601,neck cartilage,UBERON:0002418,cartilage tissue
+UBERON:0009741,tailbud stage,UBERON:0000068,embryo stage
+UBERON:0003946,placenta labyrinth,UBERON:0005156,reproductive structure
+CL:0002678,memory regulatory T cell,CL:0000792,"CD4-positive, CD25-positive, alpha-beta regulatory T cell"
+UBERON:0002501,oval window,UBERON:0000161,orifice
+HP:0005176,Dysplastic aortic valve,HP:0001646,Abnormality of the aortic valve
+HP:0000421,Epistaxis,HP:0000366,Abnormality of the nose
+HP:0010715,2-5 toe syndactyly,HP:0001770,Toe syndactyly
+DOID:8645,subacute delirium,DOID:8646,substance-induced psychosis
+HP:0009212,Stippling of the epiphysis of the middle phalanx of the 5th finger,HP:0009391,Stippling of the epiphyses of the 5th finger
+DOID:4488,sarcomatoid mesothelioma,DOID:1790,malignant mesothelioma
+HP:0012283,Small distal femoral epiphysis,HP:0010590,Abnormality of the distal femoral epiphysis
+HP:0100437,Bullet-shaped proximal phalanx of the 3rd toe,HP:0010205,Bullet-shaped proximal phalanges of the toes
+DOID:10337,glaucomatous atrophy of optic disc,DOID:5723,optic atrophy
+UBERON:0005410,cartilaginous otic capsule,UBERON:0004637,otic capsule
+DOID:0050729,neutral lipid storage disease,DOID:9455,lipid storage disease
+UBERON:0010254,2nd arch mesenchyme from neural crest,UBERON:0010258,mesenchyme from rhombencephalic neural crest
+UBERON:0002070,superior pancreaticoduodenal artery,UBERON:0009658,pancreaticoduodenal artery
+CL:0002554,fibroblast of lymphatic vessel,CL:0000057,fibroblast
+DOID:6943,vulvar inverted follicular keratosis,DOID:6945,inverted follicular keratosis
+UBERON:0001317,internal iliac vein,UBERON:0001638,vein
+UBERON:3010726,ramus muscularis of glossopharyngeus nerve,UBERON:0000479,tissue
+DOID:0050457,Sertoli cell-only syndrome,DOID:12336,male infertility
+UBERON:4200051,cotyloid notch,UBERON:0005913,zone of bone organ
+UBERON:0003481,tail vein,UBERON:0001638,vein
+HP:0011542,Criss-cross atrioventricular valves with superior-inferior ventricles,HP:0011541,Criss-cross atrioventricular valves
+UBERON:0015045,manual digit 3 metacarpus endochondral element,UBERON:0015042,manual digit metacarpus endochondral element
+UBERON:0013586,fused metapodial bones 3 and 4,UBERON:0003821,metapodium bone
+HP:0006302,Dagger-shaped pulp calcifications,HP:0006479,Abnormality of the dental pulp
+HP:0007494,Discrete 2 to 5-mm hyper- and hypopigmented macules,HP:0007441,Hyperpigmented/hypopigmented macules
+DOID:10930,borderline personality disorder,DOID:1510,personality disorder
+UBERON:0010290,scleral ossicle,UBERON:0010296,scleral skeletal element
+HP:0002006,Facial cleft,HP:0000271,Abnormality of the face
+HP:0100148,Cone-shaped epiphysis of the middle phalanx of the 3rd toe,HP:0100092,Abnormality of the epiphysis of the middle phalanx of the 3rd toe
+HP:0011705,First degree atrioventricular block,HP:0001678,Atrioventricular block
+UBERON:0003677,tooth root,UBERON:0000063,organ segment
+UBERON:0004501,skeletal muscle tissue of teres major,UBERON:0001134,skeletal muscle tissue
+HP:0002916,Abnormality of chromosome segregation,HP:0011017,Abnormality of cell physiology
+UBERON:0002701,anterior median oculomotor nucleus,UBERON:0007414,nucleus of midbrain tegmentum
+DOID:5273,cutaneous leiomyosarcoma,DOID:2687,skin sarcoma
+HP:0011516,Rod monochromacy,HP:0007803,Monochromacy
+UBERON:2202279,pectoral fin distal radial cartilage 2,UBERON:2201588,pectoral fin distal radial cartilage
+UBERON:0001785,cranial nerve,UBERON:0001021,nerve
+NCBITaxon:173087,Human papillomavirus types,NCBITaxon:333774,unclassified Papillomaviridae
+UBERON:0003500,corneal blood vessel,UBERON:0010313,neural crest-derived structure
+HP:0100438,Bullet-shaped proximal phalanx of the 4th toe,HP:0010205,Bullet-shaped proximal phalanges of the toes
+HP:0010171,Epiphyseal stippling of toe phalanges,HP:0010160,Abnormality of the epiphyses of the toes
+UBERON:2001530,epibranchial 2 cartilage,UBERON:2001906,epibranchial 2 element
+DOID:4838,myoepithelial carcinoma,DOID:305,carcinoma
+UBERON:0008450,psoas muscle,UBERON:0008549,prevertebral muscle of neck
+UBERON:4100006,parasternal process,UBERON:0011655,interclavicle
+DOID:0050651,atrioventricular septal defect,DOID:1681,heart septal defect
+UBERON:0010304,non-keratinized stratified squamous epithelium,UBERON:0006915,stratified squamous epithelium
+HP:0012736,Profound global developmental delay,HP:0001263,Global developmental delay
+HP:0011717,AV nodal reentry tachycardia,HP:0011687,AV nodal tachycardia
+HP:0010525,Finger agnosia,HP:0010524,Agnosia
+HP:0009950,Complete duplication of the distal phalanx of the 2nd finger,HP:0009957,Complete duplication of the phalanges of the 2nd finger
+DOID:1607,hypoglycemic coma,DOID:1428,endocrine pancreas disease
+CL:0000564,neutrophilic promyelocyte,CL:0000834,neutrophil progenitor cell
+UBERON:0002493,uterine artery,UBERON:0014404,female anatomical structure
+NCBITaxon:6202,Taenia,NCBITaxon:6208,Taeniidae
+UBERON:0013148,early midbrain vesicle,UBERON:0013150,future brain vesicle
+DOID:9640,sarcocystosis,DOID:2113,coccidiosis
+DOID:1760,facial nerve neoplasm,DOID:338,cranial nerve neoplasm
+UBERON:0012128,nose tip,UBERON:0006983,anatomical point
+HP:0004485,Cessation of head growth,HP:0005484,Postnatal microcephaly
+HP:0200130,Congestive cardiomyopathy,HP:0001638,Cardiomyopathy
+HP:0002853,Increased proportion of HLA DR+ and CD57+ T cells,HP:0011839,Abnormality of T cell number
+HP:0010089,Osteolytic defects of the proximal phalanx of the hallux,HP:0010062,Osteolytic defects of the phalanges of the hallux
+UBERON:0000964,cornea,UBERON:0003102,surface structure
+HP:0100869,Palmar telangiectasia,HP:0100871,Abnormality of the palm
+HP:0100374,Aplasia/Hypoplasia of the middle phalanx of the 5th toe,HP:0010383,Aplasia/Hypoplasia of the phalanges of the 5th toe
+UBERON:0004027,chorionic plate,UBERON:0004120,mesoderm-derived structure
+UBERON:0002319,mesangium,UBERON:0003567,abdomen connective tissue
+UBERON:0011775,vagus nerve nucleus,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000404,electrically signaling cell,CL:0000211,electrically active cell
+CL:0001032,cortical granule cell,CL:0002609,neuron of cerebral cortex
+UBERON:0009625,sacral nerve,UBERON:0001780,spinal nerve
+UBERON:0003865,distal phalanx of manus,UBERON:0004300,distal phalanx
+UBERON:0010269,filum terminale internum,UBERON:0004121,ectoderm-derived structure
+DOID:7388,pulmonary vein leiomyosarcoma,DOID:175,vascular cancer
+HP:0001707,Abnormality of the right ventricle,HP:0001713,Abnormality of cardiac ventricle
+HP:0000327,Hypoplasia of the maxilla,HP:0009117,Aplasia/Hypoplasia of the maxilla
+HP:0006202,Osteolysis of scaphoids,HP:0009699,Osteolytic defects of the hand bones
+HP:0001194,Abnormalities of placenta and umbilical cord,HP:0001197,Abnormality of prenatal development or birth
+UBERON:2000647,dorsal caudal thalamic nucleus,UBERON:0015233,nucleus of dorsal thalamus
+DOID:1895,allergic contact dermatitis of eyelid,DOID:1894,noninfectious dermatoses of eyelid
+NCBITaxon:1750,Propionibacterium propionicum,NCBITaxon:1743,Propionibacterium
+UBERON:0007132,head kidney,UBERON:0003103,compound organ
+UBERON:0010675,manual digit 1 phalanx cartilage element,UBERON:0010686,manual digit phalanx cartilage element
+HP:0100902,Sclerosis of the distal phalanx of the 4th finger,HP:0100920,Sclerosis of the phalanges of the 4th finger
+DOID:5044,cardiac granular cell neoplasm,DOID:0060091,cardiovascular organ benign neoplasm
+CL:0001001,immature CD8_alpha-negative CD11b-negative dendritic cell,CL:0000840,immature conventional dendritic cell
+HP:0012137,Abnormal number of granulocyte precursors,HP:0012135,Abnormality of cells of the granulocytic lineage
+HP:0003655,Reduced activity of N-acetylglucosaminyltransferase II,HP:0004367,Abnormality of glycoprotein metabolism
+CL:0000469,ganglion mother cell,CL:0000468,neuroglioblast
+UBERON:0002213,cartilaginous joint,UBERON:0011134,nonsynovial joint
+HP:0010408,Osteolytic defects of the middle phalanx of the 2nd toe,HP:0010351,Osteolytic defects of the phalanges of the 2nd toe
+DOID:7436,sarcomatoid uterine corpus endometrioid adenocarcinoma,DOID:2870,endometrial adenocarcinoma
+HP:0005369,Decreased serum complement factor H,HP:0004431,Complement deficiency
+UBERON:2000956,sclerotome somite 20,UBERON:0003089,sclerotome
+DOID:5846,septal myocardial infarction,DOID:5844,myocardial infarction
+HP:0006881,Diffuse peripheral demyelination,HP:0011096,Peripheral demyelination
+UBERON:0002633,motor nucleus of trigeminal nerve,UBERON:0003528,brain grey matter
+UBERON:0012377,muscle layer of jejunum,UBERON:0011201,muscle layer of small intestine
+UBERON:0010285,midbrain basal plate,UBERON:0002050,embryonic structure
+HP:0009321,Absent epiphysis of the middle phalanx of the 3rd finger,HP:0009334,Abnormality of the epiphysis of the middle phalanx of the 3rd finger
+UBERON:0006821,cutaneous muscle,UBERON:0002385,muscle tissue
+UBERON:0002822,macula lutea proper,UBERON:0004121,ectoderm-derived structure
+UBERON:0006866,terminal part of digestive tract,UBERON:0004921,subdivision of digestive tract
+CL:0000209,taste receptor cell,CL:0000206,chemoreceptor cell
+DOID:849,rheumatoid lung disease,DOID:850,lung disease
+UBERON:0015165,multi-unit eye,UBERON:0000970,eye
+HP:0005864,Pseudoarthrosis,HP:0011314,Abnormality of long bone morphology
+CL:0000105,pseudounipolar neuron,CL:0000540,neuron
+HP:0009889,Localized hirsutism,HP:0001007,Hirsutism
+HP:0002593,Intestinal lymphangiectasia,HP:0002242,Abnormality of the intestine
+HP:0000722,Obsessive-compulsive behavior,HP:0000708,Behavioural/Psychiatric Abnormality
+UBERON:0002267,laterodorsal tegmental nucleus,UBERON:0009662,hindbrain nucleus
+HP:0008056,Aplasia/Hypoplasia affecting the eye,HP:0012374,Abnormality of the globe
+HP:0004635,Cervical vertebrae fusion (C5/C6),HP:0002949,Fused cervical vertebrae
+UBERON:0001846,internal ear,UBERON:0004121,ectoderm-derived structure
+HP:0010856,EEG with periodic complexes,HP:0010857,EEG with periodic abnormalities
+UBERON:0006782,stratum lemnisci of superior colliculus,UBERON:0006785,gray matter of superior colliculus
+DOID:6567,uterine corpus myxoid leiomyosarcoma,DOID:5289,uterus leiomyosarcoma
+HP:0009327,Ivory epiphysis of the middle phalanx of the 3rd finger,HP:0009416,Ivory epiphyses of the 3rd finger
+DOID:1852,intrahepatic cholestasis,DOID:409,liver disease
+HP:0011239,Underdeveloped inferior crus of antihelix,HP:0011243,Abnormality of inferior crus of antihelix
+HP:0001304,Torsion dystonia,HP:0001332,Dystonia
+UBERON:0006653,glans clitoris,UBERON:0005156,reproductive structure
+DOID:5948,angiokeratoma of mibelli,DOID:479,angiokeratoma
+DOID:3255,botryoid rhabdomyosarcoma,DOID:3246,embryonal rhabdomyosarcoma
+HP:0012390,Anal fissure,HP:0004378,Abnormality of the anus
+HP:0010501,Limitation of knee mobility,HP:0002815,Abnormality of the knees
+UBERON:0010033,posterior part of tongue,UBERON:0000064,organ part
+UBERON:0010181,straight venules of kidney,UBERON:0006544,kidney vasculature
+UBERON:0002556,corticotectal tract,UBERON:0003544,brain white matter
+DOID:3544,atypical choroid plexus papilloma,DOID:3540,choroid plexus cancer
+DOID:13794,anterior scleritis,DOID:13452,scleritis
+UBERON:3000834,posterior lamina recurvata,UBERON:0004120,mesoderm-derived structure
+NCBITaxon:186538,Zaire ebolavirus,NCBITaxon:186536,Ebolavirus
+CL:0000041,mature eosinophil,CL:0002242,nucleate cell
+DOID:4676,uremia,DOID:1074,kidney failure
+DOID:4902,appendix carcinoma,DOID:11239,appendix cancer
+UBERON:0010369,secondary pulmonary lobule,UBERON:0010368,pulmonary lobule
+DOID:9775,diastolic heart failure,DOID:6000,congestive heart failure
+HP:0002676,Cloverleaf skull,HP:0002648,Abnormality of calvarial morphology
+HP:0007372,Atrophy/Degeneration involving the corticospinal tracts,HP:0007367,Atrophy/Degeneration affecting the central nervous system
+HP:0000470,Short neck,HP:0003319,Abnormality of the cervical spine
+UBERON:0006921,stomach squamous epithelium,UBERON:0001276,epithelium of stomach
+HP:0006202,Osteolysis of scaphoids,HP:0004243,Abnormality of the scaphoid
+HP:0012421,Congenital absence of foreskin,HP:0100587,Abnormality of the preputium
+UBERON:0009589,mesenchyme of interdigital region between manual digits 4 and 5,UBERON:0009599,mesenchyme of interdigital region between digits 4 and 5
+DOID:7441,chronic metabolic polyneuropathy,DOID:5221,chronic polyneuropathy
+UBERON:0013546,Brodmann (1909) area 15,UBERON:0013529,Brodmann area
+UBERON:0004179,prostate glandular acinus,UBERON:0014403,male anatomical structure
+HP:0100492,Joint contractures involving the joints of the feet,HP:0001371,Flexion contracture
+HP:0010421,Duplication of the distal phalanx of the 2nd toe,HP:0010193,Duplication of distal phalanx of toe
+UBERON:0011278,nail of pedal digit 1,UBERON:0009567,nail of pedal digit
+NCBITaxon:35792,Rickettsia parkeri,NCBITaxon:114277,spotted fever group
+UBERON:3000856,intercalary element of fore digit,UBERON:0004249,manual digit bone
+HP:0100209,Pseudoepiphysis of the distal phalanx of the 5th toe,HP:0100097,Abnormality of the epiphysis of the distal phalanx of the 5th toe
+CL:0002325,mammary alveolar cell,CL:1001586,mammary gland glandular cell
+UBERON:0005091,left horn of sinus venosus,UBERON:0004120,mesoderm-derived structure
+HP:0006263,Abnormality of the epiphyses of the 2nd finger,HP:0004100,Abnormality of the 2nd finger
+HP:0002289,Alopecia universalis,HP:0001596,Alopecia
+HP:0100617,Testicular seminoma,HP:0100620,Germinoma
+UBERON:0010020,tubotympanic recess epithelium,UBERON:0005423,developing anatomical structure
+HP:0009524,Absent epiphysis of the proximal phalanx of the 2nd finger,HP:0009501,Abnormality of the epiphysis of the proximal phalanx of the 2nd finger
+CL:0002111,CD38-negative unswitched memory B cell,CL:0000970,unswitched memory B cell
+HP:0002171,Gliosis,HP:0100705,Abnormality of the glial cells
+DOID:409,liver disease,DOID:3118,hepatobiliary disease
+UBERON:0005648,manual digit 5 epithelium,UBERON:0005227,manual digit epithelium
+HP:0009615,Complete duplication of the first metacarpal,HP:0009943,Complete duplication of the phalanges of the thumb
+CL:0009005,salivary gland cell,CL:0002371,somatic cell
+DOID:12836,senile entropion,DOID:12397,entropion
+DOID:0050059,oropharyngeal anthrax,DOID:13386,gastrointestinal anthrax
+HP:0001088,Brushfield spots,HP:0008034,Abnormal iris pigmentation
+UBERON:0002276,lamina of spiral limbus,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0012644,Increased caudate lactate level,HP:0002339,Abnormality of the caudate nucleus
+DOID:10507,Dressler's syndrome,DOID:1787,pericarditis
+UBERON:0002255,vomeronasal organ,UBERON:0004121,ectoderm-derived structure
+HP:0007863,Retinal lesions,HP:0000479,Abnormality of the retina
+UBERON:0004869,parietal organ,UBERON:0004121,ectoderm-derived structure
+UBERON:0011874,amphiarthrosis,UBERON:0000982,skeletal joint
+UBERON:4200153,metatarsal bone of digit 6,UBERON:4200154,metapodium bone 6
+UBERON:2000534,lateral longitudinal fasciculus,UBERON:0014649,white matter of medulla oblongata
+UBERON:0002813,right cerebral hemisphere,UBERON:0001869,cerebral hemisphere
+HP:0005593,"Macular hypopigmented whorls, streaks, and patches",HP:0001053,Hypopigmented skin patches
+DOID:116,pericardium cancer,DOID:117,heart cancer
+UBERON:3000934,foramen perforans tarsi,UBERON:0004111,anatomical conduit
+UBERON:2001747,lateral mesethmoid wing,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004323,middle phalanx of manual digit 5,UBERON:0003639,manual digit 5 phalanx
+UBERON:2001728,caudal principal ray 16,UBERON:2001585,caudal principal ray
+UBERON:0007141,visceral mesothelium,UBERON:0001136,mesothelium
+UBERON:0010305,region of conjunctiva,UBERON:0000064,organ part
+DOID:11885,ureteral benign neoplasm,DOID:731,urinary system benign neoplasm
+DOID:0050524,maturity-onset diabetes of the young,DOID:630,genetic disease
+DOID:0080005,bone remodeling disease,DOID:0080001,bone disease
+DOID:14449,mixed gonadal dysgenesis,DOID:3491,Turner syndrome
+HP:0009495,Pseudoepiphyses of the 2nd finger,HP:0006263,Abnormality of the epiphyses of the 2nd finger
+UBERON:0002178,left main bronchus,UBERON:0002182,main bronchus
+UBERON:0013217,zygomatic plate,UBERON:0010313,neural crest-derived structure
+UBERON:0002992,paratenial nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0003061,blood island,UBERON:0005423,developing anatomical structure
+HP:0005619,Thoracolumbar kyphosis,HP:0002942,Thoracic kyphosis
+DOID:0050566,X-linked nonsyndromic deafness,DOID:0050563,nonsyndromic deafness
+HP:0012588,Steroid-resistant nephrotic syndrome,HP:0000100,Nephrotic syndrome
+UBERON:0003578,pedal digit connective tissue,UBERON:0015791,digit connective tissue
+UBERON:0002415,tail,UBERON:0011676,subdivision of organism along main body axis
+HP:0012090,Abnormality of pancreas morphology,HP:0001732,Abnormality of the pancreas
+HP:0010027,Broad 1st metacarpal,HP:0010009,Abnormality of the 1st metacarpal
+UBERON:0003056,pre-chordal neural plate,UBERON:0005291,embryonic tissue
+DOID:2339,Crouzon syndrome,DOID:2340,craniosynostosis
+DOID:467,venous hemangioma,DOID:255,hemangioma
+HP:0001401,Intrahepatic biliary dysgenesis,HP:0011040,Abnormality of the intrahepatic bile duct
+DOID:4998,trichorhinophalangeal syndrome type II,DOID:203,exostosis
+HP:0006893,Severely dysplastic cerebellum,HP:0007033,Cerebellar dysplasia
+UBERON:0005674,right lung cranial lobe endothelium,UBERON:0005672,right lung endothelium
+UBERON:0016393,deep parotid lymph node,UBERON:0015857,parotid lymph node
+UBERON:3000825,crista longitudinalis scapula,UBERON:4100000,skeletal element projection
+DOID:0050445,X-linked hypophosphatemia,DOID:896,metal metabolism disorder
+CL:0000087,male germ line stem cell (sensu Nematoda and Protostomia),CL:0000086,germ line stem cell (sensu Nematoda and Protostomia)
+CL:0000734,embryonic gland plasmatocyte,CL:0000394,plasmatocyte
+CL:0002188,glomerular endothelial cell,CL:0000666,fenestrated cell
+DOID:0080000,muscular disease,DOID:17,musculoskeletal system disease
+HP:0000891,Cervical ribs,HP:0005815,Supernumerary ribs
+DOID:10457,Legionnaires' disease,DOID:10458,legionellosis
+CL:0002602,annulus pulposus cell,CL:0002320,connective tissue cell
+DOID:0050046,Far Eastern spotted fever,DOID:11104,spotted fever
+HP:0001716,Wolff-Parkinson-White syndrome,HP:0004309,Ventricular preexcitation
+UBERON:2001983,centrum 1,UBERON:0001075,vertebral centrum
+CL:0000609,vestibular hair cell,CL:0002374,ear hair cell
+UBERON:2000576,pterotic,UBERON:0011164,neurocranium bone
+DOID:13477,balanitis xerotica obliterans,DOID:13033,balanitis
+HP:0007133,Progressive peripheral neuropathy,HP:0009830,Peripheral neuropathy
+HP:0010871,Sensory ataxia,HP:0010831,Impaired proprioception
+CL:0000200,touch receptor cell,CL:0000199,mechanoreceptor cell
+HP:0010847,EEG with spike-wave complexes (<2.5 Hz),HP:0010850,EEG with spike-wave complexes
+UBERON:0005353,spleen perifollicular zone,UBERON:0004120,mesoderm-derived structure
+UBERON:2005292,distal late tubule,UBERON:0006553,renal duct
+HP:0012484,Abnormal dense granules,HP:0011883,Abnormal platelet granules
+UBERON:0003670,smegma,UBERON:0000456,bodily secretion
+UBERON:0008855,placenta metrial gland,UBERON:0005398,female reproductive gland
+HP:0011928,Short proximal phalanx of toe,HP:0001831,Short toe
+DOID:5921,adult brainstem mixed glioma,DOID:4813,adult brain stem glioma
+UBERON:0002428,limb bone,UBERON:0002513,endochondral bone
+DOID:13662,ulcer of anus and rectum,DOID:1285,rectal disease
+HP:0012311,Monocytosis,HP:0012310,Abnormal monocyte count
+UBERON:0003866,middle phalanx of pes,UBERON:0001449,phalanx of pes
+UBERON:0009749,limb mesenchyme,UBERON:0003104,mesenchyme
+UBERON:0010054,malleus cartilage element,UBERON:0005863,cartilaginous condensation
+CL:0000508,type G enteroendocrine cell,CL:0000164,enteroendocrine cell
+UBERON:0008806,buccal funnel,UBERON:0000166,oral opening
+UBERON:3000500,processus posterior of maxilla,UBERON:0004120,mesoderm-derived structure
+NCBITaxon:118968,Coxiellaceae,NCBITaxon:118969,Legionellales
+HP:0011213,EEG with photoparoxysmal response grade III,HP:0010852,EEG with photoparoxysmal response
+DOID:10493,adrenal cortical hypofunction,DOID:3952,adrenal cortex disease
+HP:0010888,Morbus Koehler,HP:0100323,Juvenile aseptic necrosis
+HP:0000509,Conjunctivitis,HP:0100533,Inflammatory abnormality of the eye
+DOID:3947,adrenal gland hyperfunction,DOID:3952,adrenal cortex disease
+HP:0001269,Hemiparesis,HP:0004374,Hemiplegia/hemiparesis
+UBERON:3000259,lamina inferior,UBERON:4100000,skeletal element projection
+UBERON:0007329,pancreatic duct,UBERON:0004119,endoderm-derived structure
+UBERON:0007150,superior thyroid artery,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:1233,transvestism,DOID:1235,fetishism
+UBERON:2000373,dorsal fin actinotrichium,UBERON:0005174,dorsal region organ
+UBERON:0003296,gland of diencephalon,UBERON:0002530,gland
+UBERON:0006820,body of sternum,UBERON:0000064,organ part
+HP:0010779,Large pelvis,HP:0002644,Abnormality of pelvic girdle bone morphology
+UBERON:0001999,iliopsoas,UBERON:0000477,anatomical cluster
+HP:0004053,Dysharmonic maturation of the hand bones,HP:0005921,Abnormal ossification of hand bones
+HP:0100886,Abnormality of globe location,HP:0000315,Abnormality of the orbital region
+HP:0004598,Supernumerary vertebral ossification centers,HP:0100569,Abnormal vertebral ossification
+UBERON:0002263,lentiform nucleus,UBERON:0009663,telencephalic nucleus
+UBERON:2001623,type 1 odontode,UBERON:0004120,mesoderm-derived structure
+UBERON:0002942,ventral posterolateral nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0008231,dorsal thoracic segment of trunk,UBERON:0000475,organism subdivision
+UBERON:0008437,posterior arch of atlas,UBERON:0008434,cervical vertebral arch
+UBERON:2000311,adductor mandibulae complex,UBERON:0004120,mesoderm-derived structure
+HP:0100406,Duplication of the proximal phalanx of the 5th toe,HP:0010394,Abnormality of the proximal phalanx of the 5th toe
+HP:0001065,Striae distensae,HP:0100679,Lack of skin elasticity
+UBERON:0009215,pharyngeal membrane of 2nd arch,UBERON:0009210,pharyngeal membrane
+CL:0000218,myelinating Schwann cell,CL:0000328,myelin accumulating cell
+HP:0010547,Muscle flaccidity,HP:0001324,Muscle weakness
+UBERON:0001487,pes joint,UBERON:0003841,autopod joint
+DOID:0050709,Ohtahara syndrome,DOID:0050702,neonatal period electroclinical syndrome
+DOID:4524,prostate angiosarcoma,DOID:0001816,angiosarcoma
+UBERON:0005277,dorsal skin of toe,UBERON:0003530,pedal digit skin
+HP:0007067,Distal peripheral sensory neuropathy,HP:0000763,Sensory neuropathy
+DOID:6018,adult central nervous system immature teratoma,DOID:6015,adult central nervous system teratoma
+DOID:5751,pancreatic serous cystadenocarcinoma,DOID:4073,pancreatic cystadenocarcinoma
+HP:0001438,Abnormality of the abdomen,HP:0000118,Phenotypic abnormality
+UBERON:3000756,crista dorsalis humeri,UBERON:4100000,skeletal element projection
+DOID:5733,salpingitis,DOID:1962,fallopian tube disease
+HP:0009297,Osteolytic defects of the middle phalanx of the 4th finger,HP:0009847,Osteolytic defects of the middle phalanges of the hand
+UBERON:0010541,tarsus cartilage element,UBERON:0010695,mesenchyme of tarsal region
+HP:0006525,Lung segmentation defects,HP:0002088,Abnormality of the lung
+HP:0100066,Absent epiphyses of the 4th toe,HP:0010162,Absent epiphyses of the toes
+HP:0009991,Complete duplication of the distal phalanx of the 5th finger,HP:0010001,Complete duplication of the distal phalanges of the hand
+UBERON:0009721,atrial siphon,UBERON:0009719,tunicate siphon
+DOID:4547,adult mesenchymal chondrosarcoma,DOID:4545,mesenchymal chondrosarcoma
+UBERON:2001528,epibranchial 1 cartilage,UBERON:2001527,epibranchial cartilage
+UBERON:0002348,epicardium,UBERON:0000064,organ part
+HP:0009652,Bullet-shaped phalanges of the thumb,HP:0009769,Bullet-shaped phalanges of the hand
+HP:0100577,Urinary bladder inflammation,HP:0000014,Abnormality of the bladder
+DOID:2150,ovarian lymphoma,DOID:2394,ovarian cancer
+UBERON:0000398,cartilage tissue of sternum,UBERON:0002418,cartilage tissue
+UBERON:0009007,superficial inguinal lymph node,UBERON:0015917,superficial lymph node
+HP:0010357,Abnormality of the middle phalanx of the 2nd toe,HP:0010183,Abnormality of the middle phalanges of the toes
+HP:0010567,Y-shaped metatarsals,HP:0001832,Abnormality of the metatarsal bones
+UBERON:0001013,adipose tissue,UBERON:0002384,connective tissue
+HP:0004845,Acute monocytic leukemia,HP:0002488,Acute leukemia
+DOID:3431,cerebritis,DOID:936,brain disease
+CL:0002274,histamine secreting cell,CL:0000457,biogenic amine secreting cell
+HP:0009668,Fragmentation of the epiphysis of the proximal phalanx of the thumb,HP:0009690,Fragmentation of the epiphyses of the thumb
+UBERON:2000582,saccus dorsalis,UBERON:0000479,tissue
+HP:0010948,Abnormality of the fetal cardiovascular system,HP:0001626,Abnormality of the cardiovascular system
+UBERON:2105373,dorsal fin distal radial element 2,UBERON:2100936,dorsal fin distal radial element
+HP:0010144,Ivory epiphysis of the distal phalanx of the hallux,HP:0010119,Ivory epiphyses of the hallux
+UBERON:0012287,Rathkes pouch epithelium,UBERON:0007499,epithelial sac
+HP:0003745,Sporadic,HP:0000005,Mode of inheritance
+UBERON:0009979,condyle,UBERON:0005913,zone of bone organ
+DOID:0050673,mixed cerebral palsy,DOID:1969,cerebral palsy
+UBERON:0007762,metatarsophalangeal joint of pedal digit 5,UBERON:0003696,metatarsophalangeal joint
+HP:0100651,Type I diabetes mellitus,HP:0000819,Diabetes mellitus
+UBERON:0010714,iliac cartilage element,UBERON:0005863,cartilaginous condensation
+UBERON:0001775,ciliary body,UBERON:0000481,multi-tissue structure
+DOID:3278,encapsulated thymoma,DOID:3275,thymoma
+HP:0009613,Duplication of the proximal phalanx of the thumb,HP:0010008,Duplication of the middle phalanx of hand
+HP:0002226,White eyebrow,HP:0009887,Abnormality of hair pigmentation
+UBERON:0013517,coccygeal vertebra cartilage element,UBERON:0015006,coccygeal vertebra endochondral element
+CL:0000795,"CD8-positive, alpha-beta regulatory T cell",CL:0000625,"CD8-positive, alpha-beta T cell"
+DOID:11200,T cell deficiency,DOID:612,primary immunodeficiency disease
+UBERON:0012241,male urethral meatus,UBERON:0012240,urethral meatus
+HP:0012037,Pectoralis amyotrophy,HP:0003202,Amyotrophy
+DOID:10376,amblyopia,DOID:5614,eye disease
+HP:0004454,Abnormal middle ear reflexes,HP:0011452,Functional abnormality of the middle ear
+DOID:4236,carcinosarcoma,DOID:154,mixed cell type cancer
+HP:0004355,Abnormality of proteoglycan metabolism,HP:0004367,Abnormality of glycoprotein metabolism
+UBERON:2200268,anal fin proximal radial cartilage,UBERON:2100268,anal fin proximal radial element
+DOID:8310,sclerosing adenosis of breast,DOID:5998,microglandular adenosis
+UBERON:0009194,basisphenoid cartilage condenstion,UBERON:0006904,head mesenchyme from mesoderm
+UBERON:0003002,medial lemniscus,UBERON:0003544,brain white matter
+NCBITaxon:10508,Adenoviridae,NCBITaxon:35237,"dsDNA viruses, no RNA stage"
+UBERON:0001337,spongiose part of urethra,UBERON:0014403,male anatomical structure
+DOID:7528,acute endometritis,DOID:1002,endometritis
+UBERON:0006956,buccal mucosa,UBERON:0003729,mouth mucosa
+UBERON:2000865,epaxial region somite 12,UBERON:0003900,epaxial myotome region
+UBERON:0003977,utricle duct,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0015884,presymphysial lymph node,UBERON:0015877,parietal pelvic lymph node
+UBERON:0001578,orbicularis oculi,UBERON:0003660,eyelid muscle
+UBERON:0006469,first cervical spinal cord segment,UBERON:0007714,cervical subsegment of spinal cord
+UBERON:2002054,vertebra 5-vertebra 6 joint,UBERON:0000982,skeletal joint
+DOID:2426,gangliocytoma,DOID:0050687,cell type cancer
+DOID:6700,gastric fundus carcinoma,DOID:5517,stomach carcinoma
+HP:0005172,Left postterior fascicular block,HP:0011713,Left bundle branch block
+UBERON:0006245,humerus cartilage element,UBERON:0015053,humerus endochondral element
+UBERON:0001739,laryngeal cartilage,UBERON:0004119,endoderm-derived structure
+DOID:6788,vagina botryoid rhabdomyosarcoma,DOID:1901,vagina sarcoma
+UBERON:0011792,feather muscle,UBERON:0004253,skin muscle
+UBERON:0004803,penis epithelium,UBERON:0014403,male anatomical structure
+UBERON:0001919,endothelium of vein,UBERON:0004701,venous system endothelium
+HP:0010761,Broad columella,HP:0009929,Abnormality of the columella
+HP:0002562,Low-set nipples,HP:0004404,Abnormality of the nipple
+UBERON:2000657,entopterygoid,UBERON:0008907,dermal bone
+UBERON:0003946,placenta labyrinth,UBERON:0014404,female anatomical structure
+HP:0001991,Aplasia/Hypoplasia of toe,HP:0006494,Aplasia/Hypoplasia involving bones of the feet
+HP:0008734,Decreased testicular size,HP:0000050,Hypoplastic genitalia
+UBERON:0004765,skeletal element,UBERON:0000062,organ
+UBERON:0002027,stratum corneum of epidermis,UBERON:0003055,periderm
+NCBITaxon:222543,Hypocreomycetidae,NCBITaxon:147550,Sordariomycetes
+UBERON:0001220,quadratus lumborum,UBERON:0003897,axial muscle
+HP:0011268,Absent tragus,HP:0009913,Aplasia/Hypoplasia of the tragus
+DOID:4890,juvenile myoclonic epilepsy,DOID:0050705,adolescence-adult electroclinical syndrome
+CL:0002567,light melanocyte,CL:0000148,melanocyte
+UBERON:0003546,distal convoluted tubule macula densa,UBERON:0004120,mesoderm-derived structure
+HP:0010453,Pelvic asymmetry,HP:0002644,Abnormality of pelvic girdle bone morphology
+UBERON:3010100,mental glands,UBERON:3010604,cranial glands
+HP:0009496,Small epiphyses of the 2nd finger,HP:0006263,Abnormality of the epiphyses of the 2nd finger
+UBERON:0009618,trunk paraxial mesoderm,UBERON:0004120,mesoderm-derived structure
+UBERON:2005415,inner ear foramen,UBERON:0004121,ectoderm-derived structure
+CL:1000333,serous cell of epithelium of lobular bronchiole,CL:1000331,serous cell of epithelium of bronchus
+HP:0010942,Echogenic intracardiac focus,HP:0010948,Abnormality of the fetal cardiovascular system
+HP:0011405,Childhood onset short-limb short stature,HP:0008873,Disproportionate short-limb short stature
+HP:0100471,Symphalangism affecting the middle phalanx of the 4th toe,HP:0010377,Symphalangism affecting the phalanges of the 4th toe
+DOID:6015,adult central nervous system teratoma,DOID:3640,central nervous system teratoma
+UBERON:0002796,motor root of trigeminal nerve,UBERON:0004673,trigeminal nerve root
+UBERON:0007825,reticular membrane of spiral organ,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010270,Cone-shaped epiphyses of the proximal phalanges of the hand,HP:0010230,Cone-shaped epiphyses of the phalanges of the hand
+HP:0003765,Psoriasis,HP:0011123,Inflammatory abnormality of the skin
+HP:0007581,"Mediosternal, longitudinal streak of hypopigmentation",HP:0007535,Hypopigmented streaks
+UBERON:0010585,pedal digit phalanx pre-cartilage condensation,UBERON:0010700,phalanx pre-cartilage condensation
+DOID:2218,blood platelet disease,DOID:2213,hemorrhagic disease
+DOID:9255,frontotemporal dementia,DOID:679,basal ganglia disease
+HP:0100197,Ivory epiphysis of the proximal phalanx of the 4th toe,HP:0100096,Abnormality of the epiphysis of the proximal phalanx of the 4th toe
+UBERON:0006681,interthalamic adhesion,UBERON:0001020,nervous system commissure
+HP:0009667,Enlarged epiphysis of the proximal phalanx of the thumb,HP:0010260,Enlarged epiphyses of the middle phalanges of the hand
+HP:0010452,Ectopia of the spleen,HP:0001743,Abnormality of the spleen
+HP:0007502,Follicular hyperkeratosis,HP:0000962,Hyperkeratosis
+HP:0011521,Deuteranopia,HP:0011518,Dichromacy
+HP:0003541,Urinary glycosaminoglycan excretion,HP:0004371,Abnormality of glycosaminoglycan metabolism
+CL:0002394,CD141-positive myeloid dendritic cell,CL:0000782,myeloid dendritic cell
+DOID:7231,pediatric CNS embryonal cell carcinoma,DOID:6052,central nervous system childhood germ cell tumor
+HP:0000525,Abnormality of the iris,HP:0004328,Abnormality of the anterior segment of the eye
+UBERON:0003916,fat pad,UBERON:0001013,adipose tissue
+HP:0003837,Soft-tissue ossification around the shoulders,HP:0011986,Ectopic ossification
+UBERON:0010028,ventral part of pharyngeal pouch 4,UBERON:0005911,endo-epithelium
+UBERON:0004164,branchiomeric muscle,UBERON:0004120,mesoderm-derived structure
+UBERON:0005139,metanephric long descending thin limb,UBERON:0005100,long descending thin limb
+HP:0005652,Cortical sclerosis,HP:0011001,Increased bone mineral density
+HP:0005715,Flattened knee epiphyses,HP:0002815,Abnormality of the knees
+UBERON:0011199,prostatic utricle,UBERON:0005156,reproductive structure
+UBERON:0003651,metatarsal bone of digit 2,UBERON:0001448,metatarsal bone
+DOID:14374,norwegian scabies,DOID:8295,scabies
+CL:0000897,"CD4-positive, alpha-beta memory T cell",CL:0000624,"CD4-positive, alpha-beta T cell"
+DOID:5104,testicular infarct,DOID:2519,testicular disease
+UBERON:0011898,skeletal muscle endomysium,UBERON:0011895,endomysium
+UBERON:0001446,fibula,UBERON:0003608,hindlimb long bone
+UBERON:0005169,interstitial tissue,UBERON:0003891,stroma
+UBERON:0013673,os priapium,UBERON:0007719,bone of reproductive structure
+HP:0001844,Abnormality of the hallux,HP:0001780,Abnormality of toe
+UBERON:0002052,capsule of adrenal gland,UBERON:0004120,mesoderm-derived structure
+UBERON:0008936,gastropod genital pore,UBERON:0000161,orifice
+DOID:7491,vulvar proximal-type epithelioid sarcoma,DOID:7492,central epithelioid sarcoma
+HP:0006579,Prolonged neonatal jaundice,HP:0000952,Jaundice
+DOID:7302,endodermal sinus pattern testicular yolk sac tumor,DOID:5344,testicular yolk sac tumor
+UBERON:2000264,preopercle,UBERON:0008907,dermal bone
+HP:0007453,Flexural lichenification,HP:0100725,Lichenification
+UBERON:0007300,pectoral appendage blood vessel,UBERON:0007301,appendage blood vessel
+HP:0002579,Gastrointestinal dysmotility,HP:0012719,Functional abnormality of the gastrointestinal tract
+UBERON:0005208,right atrium valve,UBERON:0003978,valve
+HP:0009935,Aplasia/Hypoplasia of the nasal septum,HP:0009924,Aplasia/Hypoplasia involving the nose
+DOID:13711,dental fluorosis,DOID:1091,tooth disease
+HP:0006655,Rib segmentation abnormalities,HP:0000772,Abnormality of the ribs
+HP:0008776,Abnormality of the renal artery,HP:0011004,Abnormality of the systemic arterial tree
+HP:0000524,Conjunctival telangiectasia,HP:0008054,Abnormality of the vasculature of the conjunctiva
+UBERON:0004290,dermomyotome,UBERON:0000486,multilaminar epithelium
+HP:0006598,Irregular ossification at anterior rib ends,HP:0011849,Abnormal bone ossification
+HP:0002313,Spastic paraparesis,HP:0002385,Paraparesis
+UBERON:0013114,compressor glandulae muscle,UBERON:0010959,craniocervical muscle
+HP:0000363,Abnormality of earlobe,HP:0000377,Abnormality of the pinna
+DOID:11839,glans penis cancer,DOID:11615,penile cancer
+HP:0009585,Patchy sclerosis of the proximal phalanx of the 2nd finger,HP:0100908,Sclerosis of the proximal phalanx of the 2nd finger
+DOID:0050766,chorea-acanthocytosis,DOID:0050765,neuroacanthocytosis
+UBERON:2005380,dorsal fin proximal radial bone 3,UBERON:2000947,dorsal fin proximal radial bone
+DOID:7614,meninges sarcoma,DOID:3565,meningioma
+HP:0012506,Small pituitary gland,HP:0012504,Abnormal size of pituitary gland
+UBERON:0005438,coronary sinus,UBERON:0003920,venous blood vessel
+HP:0200085,Limb tremor,HP:0001337,Tremor
+UBERON:2001934,rostral plate,UBERON:0008907,dermal bone
+DOID:0050820,atrioventricular block,DOID:10273,heart conduction disease
+CL:0002367,trabecular meshwork cell,CL:0000115,endothelial cell
+DOID:3055,paratyphoid fever,DOID:0050338,primary bacterial infectious disease
+UBERON:0013166,vallecula of cerebellum,UBERON:0000064,organ part
+UBERON:0001570,inferior pharyngeal constrictor,UBERON:0001569,constrictor muscle of pharynx
+UBERON:0004851,aorta endothelium,UBERON:0004700,arterial system endothelium
+CL:0002376,non-myelinating Schwann cell,CL:0002573,Schwann cell
+UBERON:0010679,manual digit 5 phalanx cartilage element,UBERON:0010686,manual digit phalanx cartilage element
+UBERON:0001448,metatarsal bone,UBERON:0003608,hindlimb long bone
+HP:0004947,Arteriovenous fistula,HP:0100026,Arteriovenous malformation
+UBERON:3000871,fossula tuberis superioris,UBERON:0000064,organ part
+HP:0001829,Foot polydactyly,HP:0010442,Polydactyly
+UBERON:0003236,epithelium of lower jaw,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0004855,Reduced protein S activity,HP:0003256,Abnormality of the coagulation cascade
+HP:0002590,Paralytic ileus,HP:0002595,Ileus
+HP:0006698,Ventricular aneurysm,HP:0001713,Abnormality of cardiac ventricle
+CL:1001503,olfactory bulb tufted cell,CL:0000540,neuron
+HP:0001069,Episodic hyperhidrosis,HP:0000975,Hyperhidrosis
+HP:0003228,Hypernatremia,HP:0010931,Abnormality of sodium homeostasis
+HP:0011633,Complete left sided absence of pericardium,HP:0011628,Congenital defect of the pericardium
+UBERON:0005337,outflow tract of ventricle,UBERON:0004145,outflow tract
+HP:0200013,Neoplasm of fatty tissue,HP:0011793,Neoplasm by anatomical site
+HP:0002024,Malabsorption,HP:0002242,Abnormality of the intestine
+HP:0012071,Abnormality of acetylcarnitine metabolism,HP:0010967,Abnormality of carnitine metabolism
+DOID:104,bacterial infectious disease,DOID:0050117,disease by infectious agent
+HP:0005956,Anteroposteriorly shortened larynx,HP:0001600,Abnormality of the larynx
+HP:0001177,Preaxial hand polydactyly,HP:0100258,Preaxial polydactyly
+HP:0009676,Bracket epiphysis of the distal phalanx of the thumb,HP:0010247,Bracket epiphyses of the distal phalanges of the hand
+UBERON:2001472,anterior lateral line neuromast,UBERON:0008904,neuromast
+HP:0009953,Partial duplication of the middle phalanx of the 2nd finger,HP:0009956,Partial duplication of the phalanges of the 2nd finger
+UBERON:3000178,footplate of pars media plectri,UBERON:0010313,neural crest-derived structure
+UBERON:0000042,serous membrane,UBERON:0004457,cavity lining
+DOID:5308,ampulla of Vater clear cell adenocarcinoma,DOID:3502,ampulla of Vater adenocarcinoma
+UBERON:2001266,ovarian follicle stage III,UBERON:0001305,ovarian follicle
+HP:0100585,Teleangiectasia of the skin,HP:0001009,Telangiectasia
+HP:0006782,Malignant eosinophil proliferation,HP:0004377,Hematological neoplasm
+DOID:1995,rectum sarcoma,DOID:1993,rectum cancer
+UBERON:2005048,primitive prosencephalic artery,UBERON:0001637,artery
+HP:0009681,Ivory epiphysis of the distal phalanx of the thumb,HP:0009692,Ivory epiphyses of the thumb
+CL:0000621,fusion competent myoblast,CL:0000056,myoblast
+UBERON:0013248,paradidymis,UBERON:0012275,meso-epithelium
+DOID:0050304,aniseikonia,DOID:9835,refractive error
+UBERON:0006211,buccopharyngeal membrane,UBERON:0002050,embryonic structure
+UBERON:3000994,longitudinal dorsal folds,UBERON:3000991,dorsal folds
+HP:0100894,Broad xiphoid process,HP:0100892,Abnormality of the xiphoid process
+HP:0009602,Abnormality of the phalanges of the thumb,HP:0001172,Abnormality of the thumb
+HP:0003031,Ulnar bowing,HP:0003956,Bowed forearm bones
+UBERON:0003907,left atrioventricular canal,UBERON:0015212,lateral structure
+DOID:12325,kyphoscoliotic heart disease,DOID:12326,chronic pulmonary heart disease
+DOID:12899,benign lymphoepithelial lesion of salivary gland,DOID:417,hypersensitivity reaction type II disease
+UBERON:0015096,distal carpal bone 5 endochondral element,UBERON:0015049,carpus endochondral element
+UBERON:0003661,limb muscle,UBERON:0001630,muscle organ
+CL:0001045,naive CCR4-positive regulatory T cell,CL:0001047,"CD4-positive, CD25-positive, CCR4-positive, alpha-beta regulatory T cell"
+HP:0010874,Tendon xanthomatosis,HP:0100261,Abnormal tendon morphology
+HP:0006490,Abnormality of lower-limb metaphyses,HP:0002814,Abnormality of the lower limb
+HP:0006566,Neonatal cholestatic liver disease,HP:0002611,Cholestatic liver disease
+UBERON:0003948,blood-air barrier,UBERON:0004119,endoderm-derived structure
+HP:0003810,Late-onset distal muscle weakness,HP:0002460,Distal muscle weakness
+UBERON:0011850,acinus of salivary gland,UBERON:0004121,ectoderm-derived structure
+HP:0003414,Atlantoaxial dislocation,HP:0003413,Atlantoaxial abnormality
+HP:0002333,Motor deterioration,HP:0001268,Mental deterioration
+HP:0009744,Abnormality of the spinal dura mater,HP:0010303,Abnormality of the spinal meninges
+UBERON:0002719,spino-olivary tract,UBERON:0007702,tract of brain
+UBERON:0001810,nerve plexus,UBERON:0003714,neural tissue
+NCBITaxon:34622,Haemaphysalis,NCBITaxon:426439,Haemaphysalinae
+UBERON:3000031,ascending process of palatoquadrate,UBERON:0004121,ectoderm-derived structure
+UBERON:0014446,acetabular notch,UBERON:0005744,bone foramen
+CL:0000719,posterior cone cell (sensu Endopterygota),CL:0000718,cone cell (sensu Endopterygota)
+UBERON:0005356,Rathke's pouch,UBERON:0007499,epithelial sac
+UBERON:0001747,parenchyma of thyroid gland,UBERON:0004119,endoderm-derived structure
+HP:0009653,Curved phalanges of the thumb,HP:0009770,Curved phalanges of the hand
+HP:0008696,Renal hamartoma,HP:0010566,Hamartoma
+DOID:12662,paracoccidioidomycosis,DOID:0050292,primary systemic mycosis
+DOID:5553,pineal region choriocarcinoma,DOID:1660,malignant pineal area germ cell neoplasm
+UBERON:0004764,intramembranous bone tissue,UBERON:0002481,bone tissue
+UBERON:0006117,accessory nerve fiber bundle,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:4200091,ethomosphenoid region,UBERON:0011164,neurocranium bone
+HP:0009777,Absent thumb,HP:0009601,Aplasia/Hypoplasia of the thumb
+CL:0002677,naive regulatory T cell,CL:0000792,"CD4-positive, CD25-positive, alpha-beta regulatory T cell"
+HP:0004267,Narrow small joints of the hand,HP:0006261,Abnormality of phalangeal joints of the hand
+UBERON:0005070,anterior neuropore,UBERON:0005077,neuropore
+UBERON:4300007,medial pelvic process,UBERON:0004120,mesoderm-derived structure
+UBERON:0011755,female labial swelling,UBERON:0011754,genital swelling
+HP:0100500,Fibular deviation of toes,HP:0100498,Deviation of toes
+UBERON:0013509,lumbar vertebra cartilage element,UBERON:0011094,vertebra cartilage element
+UBERON:2001817,middle nuchal plate,UBERON:0002513,endochondral bone
+NCBITaxon:92860,Pleosporales,NCBITaxon:451868,Pleosporomycetidae
+DOID:7679,sphenoid sinus Schneiderian papilloma,DOID:6947,sphenoidal sinus neoplasm
+UBERON:0005255,pedal digit mesenchyme,UBERON:0003860,hindlimb mesenchyme
+DOID:956,peripheral nerve schwannoma,DOID:3192,neurilemmoma
+CL:0000187,muscle cell,CL:0000393,electrically responsive cell
+UBERON:0002104,visual system,UBERON:0001032,sensory system
+DOID:14701,propionic acidemia,DOID:0060159,organic acidemia
+DOID:3557,superior mesenteric artery syndrome,DOID:3558,duodenal obstruction
+HP:0100399,Duplication of the distal phalanx of the 4th toe,HP:0010380,Abnormality of the distal phalanx of the 4th toe
+DOID:5100,middle ear disease,DOID:2742,auditory system disease
+UBERON:0009495,extrahepatic part of biliary bud,UBERON:0007499,epithelial sac
+HP:0002207,Diffuse reticular or finely nodular infiltrations,HP:0002088,Abnormality of the lung
+UBERON:2001985,centrum 3,UBERON:0001075,vertebral centrum
+UBERON:0001000,vas deferens,UBERON:0005904,duct of male reproductive system
+UBERON:2000348,exoccipital posteroventral region,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000660,glycocalyx secreting cell,CL:0000327,extracellular matrix secreting cell
+UBERON:0001783,optic disc,UBERON:0000064,organ part
+HP:0100372,Aplasia/Hypoplasia of the middle phalanx of the 3rd toe,HP:0010194,Aplasia/Hypoplasia of the middle phalanges of the toes
+CL:0000676,cap cell,CL:0000378,support cell (sensu Nematoda and Protostomia)
+UBERON:2000406,parvocellular superficial pretectal nucleus,UBERON:0006569,diencephalic nucleus
+UBERON:0001153,caecum,UBERON:0009854,digestive tract diverticulum
+HP:0003075,Hypoproteinemia,HP:0010876,Abnormality of circulating protein level
+UBERON:0004341,primitive streak,UBERON:0007497,developing epithelial placode
+HP:0008436,Absent/hypoplastic coccyx,HP:0008517,Aplasia/Hypoplasia of the sacrum
+UBERON:0012088,lateroobronchus,UBERON:0002185,bronchus
+UBERON:2001826,urohyal median process,UBERON:4100000,skeletal element projection
+UBERON:0009636,prechordal cartilage,UBERON:0003932,cartilage element of chondrocranium
+UBERON:0010152,skin mucus,UBERON:0000456,bodily secretion
+HP:0100519,Anuria,HP:0011037,Decreased urine output
+CL:0000819,B-1 B cell,CL:0000785,mature B cell
+HP:0010233,Irregular epiphyses of the phalanges of the hand,HP:0003842,Irregular epiphyses of the upper limbs
+HP:0100369,Aplasia/Hypoplasia of the distal phalanx of the 3rd toe,HP:0010359,Aplasia/Hypoplasia of the phalanges of the 3rd toe
+CL:0000581,peritoneal macrophage,CL:0000864,tissue-resident macrophage
+DOID:14504,Niemann-Pick disease,DOID:4330,non-langerhans-cell histiocytosis
+HP:0010716,3-5 toe syndactyly,HP:0001770,Toe syndactyly
+DOID:4489,malignant epithelial mesothelioma,DOID:1790,malignant mesothelioma
+UBERON:0005483,thymus lobe,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0003562,Abnormal metaphyseal vascular invasion,HP:0000944,Abnormality of the metaphyses
+UBERON:0003261,thyroid primordium endoderm,UBERON:0004119,endoderm-derived structure
+DOID:4423,sea-blue histiocyte syndrome,DOID:4330,non-langerhans-cell histiocytosis
+HP:0006501,Aplasia/Hypoplasia of the radius,HP:0006503,Aplasia/Hypoplasia involving forearm bones
+HP:0100243,Leiomyosarcoma,HP:0100242,Sarcoma
+HP:0009705,Synostosis involving the 2nd metacarpal,HP:0009701,Metacarpal synostosis
+CL:0002553,fibroblast of lung,CL:0000057,fibroblast
+UBERON:0005980,pectinate muscle,UBERON:0000064,organ part
+HP:0100151,Irregular epiphysis of the middle phalanx of the 3rd toe,HP:0100060,Irregular epiphyses of the 3rd toe
+HP:0003168,Dibasicaminoaciduria,HP:0003355,Aminoaciduria
+UBERON:0004868,tapetum lucidum of camera-type eye,UBERON:0004121,ectoderm-derived structure
+HP:0009264,Enlarged epiphysis of the proximal phalanx of the 4th finger,HP:0010271,Enlarged epiphyses of the proximal phalanges of the hand
+HP:0001574,Abnormality of the integument,HP:0000118,Phenotypic abnormality
+UBERON:0009015,upper back skin,UBERON:0001068,skin of back
+UBERON:0015046,manual digit 4 metacarpus endochondral element,UBERON:0015042,manual digit metacarpus endochondral element
+CL:1000618,juxtaglomerular complex cell,CL:0002681,kidney cortical cell
+HP:0009404,Broad phalanges of the 4th finger,HP:0009768,Broad phalanges of the hand
+UBERON:0002629,triangular part of inferior frontal gyrus,UBERON:0000064,organ part
+UBERON:0006783,layer of superior colliculus,UBERON:0004121,ectoderm-derived structure
+DOID:3367,bone leiomyosarcoma,DOID:3347,osteosarcoma
+UBERON:0012179,bone of pelvis,UBERON:0003828,abdominal segment bone
+HP:0100149,Enlarged epiphysis of the middle phalanx of the 3rd toe,HP:0100092,Abnormality of the epiphysis of the middle phalanx of the 3rd toe
+NCBITaxon:7776,Gnathostomata <vertebrate>,NCBITaxon:7742,Vertebrata <Metazoa>
+UBERON:0003306,floor plate of neural tube,UBERON:0004121,ectoderm-derived structure
+HP:0004249,Accessory lunate,HP:0004248,Abnormality of the lunate bone
+DOID:3177,verrucous papilloma,DOID:2615,papilloma
+CL:0000664,closable valve cell,CL:0000185,myoepithelial cell
+UBERON:0000127,facial nucleus,UBERON:0000126,cranial nerve nucleus
+DOID:0050565,autosomal recessive nonsyndromic deafness,DOID:0050563,nonsyndromic deafness
+UBERON:0010684,pedal digit 5 phalanx cartilage element,UBERON:0005699,pedal digit 5 mesenchyme
+UBERON:0002502,round window of inner ear,UBERON:0000161,orifice
+DOID:0060194,amyotrophic lateral sclerosis type 2,DOID:332,amyotrophic lateral sclerosis
+UBERON:4000013,mineralized tissue,UBERON:0004755,skeletal tissue
+DOID:3010,lobular neoplasia,DOID:8791,breast carcinoma in situ
+UBERON:3000323,nasopremaxilla,UBERON:0011597,bone of upper jaw
+UBERON:0000312,inner cambium layer of periosteum,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100439,Bullet-shaped proximal phalanx of the 5th toe,HP:0010205,Bullet-shaped proximal phalanges of the toes
+HP:0011671,Interrupted inferior vena cava with azygous continuation,HP:0005345,Abnormality of the vena cava
+HP:0010172,Triangular epiphyses of the toes,HP:0010160,Abnormality of the epiphyses of the toes
+DOID:14188,frozen shoulder,DOID:65,connective tissue disease
+HP:0002716,Lymphadenopathy,HP:0002733,Abnormality of the lymph nodes
+HP:0006699,Ectopic supraventricular rhythms,HP:0005115,Supraventricular arrhythmia
+UBERON:0013727,notochordal fluid,UBERON:0007779,transduate
+UBERON:0001002,cuticle,UBERON:0000476,acellular anatomical structure
+UBERON:0000993,oviduct,UBERON:0000025,tube
+HP:0009325,Fragmentation of the epiphysis of the middle phalanx of the 3rd finger,HP:0009414,Fragmentation of the epiphyses of the 3rd finger
+HP:0100677,Vaginal varicocele,HP:0100672,Vaginal hernia
+UBERON:3000166,fenestra nasobasalis,UBERON:3000316,nasal opening
+UBERON:0005223,pancreas body parenchyma,UBERON:0000353,parenchyma
+DOID:10887,lepromatous leprosy,DOID:1024,leprosy
+UBERON:0006256,knee joint primordium,UBERON:0001048,primordium
+UBERON:0010879,tusk,UBERON:0001091,calcareous tooth
+UBERON:4200150,accessory foramina,UBERON:0005744,bone foramen
+HP:0002573,Hematochezia,HP:0002239,Gastrointestinal hemorrhage
+UBERON:0013149,hindbrain vesicle,UBERON:0013150,future brain vesicle
+HP:0011842,Abnormality of skeletal morphology,HP:0000924,Abnormality of the skeletal system
+UBERON:0002506,iris epithelium,UBERON:0015808,eye epithelium
+UBERON:0007684,uriniferous tubule,UBERON:0003914,epithelial tube
+HP:0002025,Anal stenosis,HP:0004378,Abnormality of the anus
+UBERON:0002410,autonomic nervous system,UBERON:0011216,organ system subdivision
+CL:0000700,dopaminergic neuron,CL:0000540,neuron
+UBERON:0005580,rhombomere 5 lateral wall,UBERON:0005501,rhombomere lateral wall
+HP:0009530,Ivory epiphysis of the proximal phalanx of the 2nd finger,HP:0010274,Ivory epiphyses of the proximal phalanges of the hand
+DOID:8058,pituitary stalk meningioma,DOID:3643,sella turcica neoplasm
+DOID:9098,sebaceous gland disease,DOID:37,skin disease
+HP:0003041,Humeroradial synostosis,HP:0003063,Abnormality of the humerus
+DOID:6585,oncocytic breast carcinoma,DOID:3458,breast adenocarcinoma
+UBERON:2005089,swim bladder artery,UBERON:0001637,artery
+HP:0006077,Absent proximal finger flexion creases,HP:0006109,Absent phalangeal crease
+HP:0012136,Dysplastic granulopoesis,HP:0012135,Abnormality of cells of the granulocytic lineage
+HP:0100569,Abnormal vertebral ossification,HP:0003468,Abnormality of the vertebrae
+HP:0009992,Complete duplication of the middle phalanx of the 5th finger,HP:0009989,Duplication of the middle phalanx of the 5th finger
+UBERON:0004544,epididymis epithelium,UBERON:0000485,simple columnar epithelium
+HP:0010527,Astereognosia,HP:0011730,Abnormality of central sensory function
+DOID:4624,Ollier disease,DOID:225,syndrome
+CL:0008005,obliquely striated somatic muscle cell,CL:0008004,somatic muscle cell
+HP:0009945,Duplication of phalanx of 2nd finger,HP:0009946,Polydactyly affecting the 2nd finger
+DOID:10153,ileum cancer,DOID:10154,small intestine cancer
+UBERON:0006749,superior parathyroid gland,UBERON:0015212,lateral structure
+DOID:5551,choriocarcinoma of the testis,DOID:3594,choriocarcinoma
+UBERON:2000581,rostral tuberal nucleus,UBERON:0006568,hypothalamic nucleus
+DOID:955,benign neurilemmoma,DOID:3192,neurilemmoma
+HP:0009102,Anterior open-bite malocclusion,HP:0000689,Dental malocclusion
+HP:0004283,Narrow palm,HP:0100871,Abnormality of the palm
+UBERON:0006924,stomach glandular epithelium,UBERON:0001276,epithelium of stomach
+DOID:6696,synchronous multifocal osteogenic sarcoma,DOID:3360,multifocal osteogenic sarcoma
+HP:0100942,Sclerosis of the distal phalanx of the 5th toe,HP:0100948,Sclerosis of the distal phalanges of the toes
+HP:0003051,Enlarged metaphyses,HP:0000944,Abnormality of the metaphyses
+UBERON:0007825,reticular membrane of spiral organ,UBERON:0001967,reticular lamina of epithelium
+HP:0011037,Decreased urine output,HP:0012590,Abnormal urine output
+UBERON:0006610,tunica albuginea,UBERON:0005156,reproductive structure
+HP:0007439,Generalized keratosis follicularis,HP:0011368,Epidermal thickening
+UBERON:2000691,supraorbital bone,UBERON:0008907,dermal bone
+CL:0000843,follicular B cell,CL:0000822,B-2 B cell
+HP:0009311,Bullet-shaped proximal phalanx of the 4th finger,HP:0009853,Bullet-shaped proximal phalanges of the hand
+UBERON:0001172,hepatic acinus,UBERON:0011858,acinus of exocrine gland
+DOID:3963,thyroid carcinoma,DOID:1781,thyroid cancer
+UBERON:3000280,margo mandibularis of pterygoid,UBERON:0010313,neural crest-derived structure
+UBERON:0004522,vasculature of musculoskeletal system,UBERON:0002049,vasculature
+CL:1000432,conjunctival epithelial cell,CL:0000066,epithelial cell
+UBERON:3000291,medial orbitonasal foramen,UBERON:3000316,nasal opening
+UBERON:3000434,planum antorbitale,UBERON:0003933,cranial cartilage
+HP:0008909,Lethal short-limbed short stature,HP:0008873,Disproportionate short-limb short stature
+HP:0001878,Hemolytic anemia,HP:0011895,Anemia due to reduced life span of red cells
+UBERON:0002976,preolivary nucleus,UBERON:0007247,superior olivary nucleus
+UBERON:0004504,skeletal muscle tissue of mylohyoid,UBERON:0001134,skeletal muscle tissue
+HP:0010058,Aplasia/Hypoplasia of the phalanges of the hallux,HP:0010173,Aplasia/Hypoplasia of the phalanges of the toes
+UBERON:0003037,septum,UBERON:0000061,anatomical structure
+UBERON:0007619,limiting membrane of retina,UBERON:0003902,retinal neural layer
+UBERON:0009957,ciliated pit,UBERON:0006846,surface groove
+HP:0000150,Gonadoblastoma,HP:0100728,Germ cell neoplasia
+UBERON:0006575,mantle,UBERON:0000475,organism subdivision
+UBERON:0003601,neck cartilage,UBERON:0003568,neck connective tissue
+UBERON:3000190,foramen orbitonasale mediale,UBERON:3000316,nasal opening
+DOID:12364,pulsating exophthalmos,DOID:930,orbital disease
+HP:0004433,Secretory IgA deficiency,HP:0002720,IgA deficiency
+UBERON:0010014,epigonal organ,UBERON:0015212,lateral structure
+UBERON:0003556,forebrain arachnoid mater,UBERON:0003548,forebrain meninges
+UBERON:0015009,lumbar vertebra endochondral element,UBERON:0010363,endochondral element
+HP:0012382,Left-to-right shunt,HP:0001693,Cardiac shunt
+HP:0007089,Facial-lingual fasciculations,HP:0002380,Fasciculations
+UBERON:0001059,pars intercerebralis,UBERON:0011215,cell part cluster of neuraxis
+UBERON:0013116,venom gland musculature,UBERON:0004461,musculature of head
+UBERON:0014391,palmar/plantar sweat gland,UBERON:0000423,eccrine sweat gland
+CL:0000104,multipolar neuron,CL:0000540,neuron
+UBERON:0006230,extrinsic ocular pre-muscle mass,UBERON:0003314,eye mesenchyme
+UBERON:0003886,body cavity precursor,UBERON:0000464,anatomical space
+UBERON:0000347,myelin sheath,UBERON:0000470,cell part
+NCBITaxon:53549,Sabethini,NCBITaxon:43817,Culicinae
+DOID:13641,exfoliation syndrome,DOID:240,iris disease
+UBERON:3000527,quadrate process of palatoquadrate,UBERON:4100000,skeletal element projection
+DOID:11432,endometriosis of ovary,DOID:289,endometriosis
+HP:0004232,Accessory carpal bones,HP:0004275,Duplication of hand bones
+UBERON:0010891,pectoral complex muscle,UBERON:0001630,muscle organ
+UBERON:0001839,bony labyrinth,UBERON:0004120,mesoderm-derived structure
+UBERON:0003011,facial motor nucleus,UBERON:0000127,facial nucleus
+HP:0011065,Conical incisor,HP:0011063,Abnormality of incisor morphology
+UBERON:4100014,posterior dorsal fin,UBERON:0003097,dorsal fin
+HP:0005954,Pulmonary capillary hemangiomatosis,HP:0002088,Abnormality of the lung
+UBERON:2001723,caudal principal ray 11,UBERON:2001585,caudal principal ray
+UBERON:0002550,anterior hypothalamic region,UBERON:0000477,anatomical cluster
+UBERON:0001308,external iliac artery,UBERON:0005609,iliac artery
+UBERON:0005341,ventral commissure,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:9072,lethal midline granuloma,DOID:2825,nose disease
+UBERON:0003828,abdominal segment bone,UBERON:0005173,abdominal segment organ
+UBERON:0003710,vasa vasorum,UBERON:0001981,blood vessel
+UBERON:3010097,M. tarsalis posticus,UBERON:0010890,pelvic complex muscle
+UBERON:0015012,tarsometatarsus endochondral element,UBERON:0015063,autopod endochondral element
+CL:0000006,neuronal receptor cell,CL:0000197,receptor cell
+HP:0005307,Postural hypotension with compensatory tachycardia,HP:0001278,Orthostatic hypotension
+HP:0010898,Abnormality of sarcosine metabolism,HP:0010895,Abnormality of glycine metabolism
+DOID:10835,chylocele of tunica vaginalis,DOID:48,male reproductive system disease
+UBERON:0006642,muscle layer of oviduct,UBERON:0005156,reproductive structure
+NCBITaxon:11083,Powassan virus,NCBITaxon:29263,tick-borne encephalitis virus group
+UBERON:2002086,pelvic axillary process,UBERON:0010742,bone of pelvic complex
+HP:0003264,Deficiency of N-acetylglucosamine-1-phosphotransferase,HP:0004356,Abnormality of lysosomal metabolism
+UBERON:0004109,cortex of humerus,UBERON:0004269,upper arm connective tissue
+UBERON:0001689,malleus bone,UBERON:0001686,auditory ossicle
+HP:0006850,Hypoplasia of the ventral pons,HP:0007361,Abnormality of the pons
+UBERON:2005054,inner optic circle,UBERON:0002203,vasculature of eye
+UBERON:0010360,pharyngeal arch mesenchyme from head mesenchyme,UBERON:0005291,embryonic tissue
+UBERON:0002005,enteric nervous system,UBERON:0002410,autonomic nervous system
+HP:0005914,Aplasia/Hypoplasia involving the metacarpal bones,HP:0005916,Abnormal metacarpal morphology
+CL:1000699,kidney resident dendritic cell,CL:1000500,kidney interstitial cell
+UBERON:0014605,fundus striati,UBERON:0002791,regional part of telencephalon
+UBERON:0010562,pedal digit 1 mesenchyme,UBERON:0005255,pedal digit mesenchyme
+HP:0003999,Abnormality of radial epiphyses,HP:0003839,Abnormality involving the epiphyses of the upper limbs
+UBERON:0004672,posterior horn lateral ventricle,UBERON:0002285,telencephalic ventricle
+UBERON:0001044,salivary gland,UBERON:0003294,gland of foregut
+HP:0007862,Retinal calcification,HP:0000479,Abnormality of the retina
+UBERON:0001961,mucosa-associated lymphoid tissue,UBERON:0012069,epithelium-associated lymphoid tissue
+UBERON:0011873,synarthrosis,UBERON:0000982,skeletal joint
+UBERON:0012249,ectocervix,UBERON:0014404,female anatomical structure
+DOID:9767,myocardial stunning,DOID:5844,myocardial infarction
+UBERON:0013547,Brodmann (1909) area 16,UBERON:0013529,Brodmann area
+DOID:14239,gastrointestinal tularemia,DOID:2123,tularemia
+DOID:367,olfactory nerve disease,DOID:3418,glossopharyngeal nerve disease
+UBERON:0011279,nail of pedal digit 2,UBERON:0009567,nail of pedal digit
+UBERON:2001322,dorsoventral diencephalic tract,UBERON:0003931,diencephalic white matter
+HP:0009295,Short middle phalanx of the 4th finger,HP:0009280,Short 4th finger
+HP:0008082,Medial deviation of the foot,HP:0001760,Abnormality of the foot
+UBERON:0005092,right horn of sinus venosus,UBERON:0004120,mesoderm-derived structure
+DOID:0050546,congenital adrenal insufficiency,DOID:9553,adrenal gland disease
+HP:0007597,Congenital palmoplantar keratodermia,HP:0000982,Palmoplantar keratoderma
+UBERON:0002331,umbilical cord,UBERON:0000478,extraembryonic structure
+UBERON:0007223,osseus cochlea,UBERON:0000477,anatomical cluster
+HP:0009525,Bracket epiphysis of the proximal phalanx of the 2nd finger,HP:0009501,Abnormality of the epiphysis of the proximal phalanx of the 2nd finger
+UBERON:0002254,thyroglossal duct,UBERON:0000025,tube
+UBERON:0007214,mesenchyme derived from trunk neural crest,UBERON:0005256,trunk mesenchyme
+HP:0002015,Dysphagia,HP:0012638,Abnormality of nervous system physiology
+HP:0009647,Proximal/distal symphalangism of thumb,HP:0009656,Symphalangism of the thumb
+UBERON:0003086,caudal artery,UBERON:0001637,artery
+UBERON:2001630,supratemporal sensory canal,UBERON:2001612,sensory canal
+DOID:12309,urticaria pigmentosa,DOID:3663,cutaneous mastocytosis
+HP:0001500,Broad finger,HP:0001167,Abnormality of finger
+UBERON:0015112,distal tarsal bone 4 cartilage,UBERON:0015111,distal tarsal bone 4 endochondral element
+HP:0000255,Acute sinusitis,HP:0000246,Sinusitis
+UBERON:0015003,ulna endochondral element,UBERON:0015021,forelimb endochondral element
+DOID:2215,factor VII deficiency,DOID:2214,inherited blood coagulation disease
+HP:0009499,Abnormality of the epiphysis of the distal phalanx of the 2nd finger,HP:0010243,Abnormality of the epiphyses of the distal phalanx of finger
+HP:0005973,Fructose intolerance,HP:0011033,Impairment of fructose metabolism
+DOID:0050876,Caroli disease,DOID:4138,bile duct disease
+DOID:7736,retinal telangiectasia,DOID:2462,retinal vascular disease
+UBERON:0004029,canal of Schlemm,UBERON:0003499,brain blood vessel
+HP:0009823,Aplasia involving bones of the upper limbs,HP:0006496,Aplasia/Hypoplasia involving bones of the upper limbs
+DOID:0050459,hyperphosphatemia,DOID:2485,phosphorus metabolism disease
+HP:0006489,Abnormality of the femoral metaphysis,HP:0002823,Abnormality of the femur
+HP:0009654,Osteolytic defects of the phalanges of the thumb,HP:0009699,Osteolytic defects of the hand bones
+UBERON:2000643,rostral cerebellar tract,UBERON:0002316,white matter
+HP:0005508,Waldenstrom macroglobulinemia,HP:0010701,Abnormal immunoglobulin level
+HP:0006264,Aplasia/Hypoplasia of the 2nd finger,HP:0004100,Abnormality of the 2nd finger
+CL:0002260,epithelial cell of parathyroid gland,CL:0002076,endo-epithelial cell
+CL:0000328,myelin accumulating cell,CL:0000325,stuff accumulating cell
+UBERON:0009191,sphenoid bone pre-cartilage condensation,UBERON:0015060,sphenoid endochondral element
+HP:0010028,Bullet-shaped 1st metacarpal,HP:0010009,Abnormality of the 1st metacarpal
+HP:0002722,Recurrent abscess formation,HP:0002719,Recurrent infections
+UBERON:3000389,paries nasi,UBERON:0003406,cartilage of respiratory system
+HP:0011030,Abnormality of transition element cation homeostasis,HP:0010929,Abnormality of cation homeostasis
+HP:0003348,Hyperalaninemia,HP:0010916,Abnormality of alanine metabolism
+HP:0002750,Delayed skeletal maturation,HP:0000927,Abnormality of skeletal maturation
+UBERON:0009198,craniofacial suture,UBERON:0002209,fibrous joint
+NCBITaxon:1279,Staphylococcus,NCBITaxon:90964,Staphylococcaceae
+HP:0011212,EEG with photoparoxysmal response grade II,HP:0010852,EEG with photoparoxysmal response
+HP:0003796,Irregular iliac crest,HP:0002867,Abnormality of the ilium
+CL:0000088,female germ line stem cell (sensu Nematoda and Protostomia),CL:0000086,germ line stem cell (sensu Nematoda and Protostomia)
+HP:0003118,Increased circulating cortisol level,HP:0011731,Abnormality of circulating cortisol level
+CL:0000619,support cell (sensu Nematoda),CL:0000124,glial cell (sensu Nematoda and Protostomia)
+UBERON:2005067,bulbus arteriosus middle layer,UBERON:0002050,embryonic structure
+DOID:3883,Lynch syndrome,DOID:0050736,autosomal dominant disease
+UBERON:2001089,myoseptum,UBERON:0002050,embryonic structure
+UBERON:0000014,zone of skin,UBERON:0004121,ectoderm-derived structure
+HP:0012246,Oculomotor nerve palsy,HP:0000597,Ophthalmoparesis
+DOID:1343,urethritis,DOID:732,urethral disease
+HP:0007501,Streaks of hyperkeratosis along each finger onto the palm,HP:0000962,Hyperkeratosis
+HP:0006278,Ectopic pancreatic tissue,HP:0012090,Abnormality of pancreas morphology
+DOID:14223,ochronosis,DOID:65,connective tissue disease
+HP:0004052,Delayed ossification of the hand bones,HP:0005921,Abnormal ossification of hand bones
+UBERON:3010243,ventricular musculature,UBERON:0004120,mesoderm-derived structure
+UBERON:2001984,centrum 2,UBERON:0001075,vertebral centrum
+UBERON:0010027,dorsal part of pharyngeal pouch 4,UBERON:0005911,endo-epithelium
+CL:0000206,chemoreceptor cell,CL:0000006,neuronal receptor cell
+DOID:4118,colon neuroendocrine neoplasm,DOID:235,colonic benign neoplasm
+HP:0000758,Impaired use of nonverbal behaviors,HP:0000735,Impaired social interactions
+UBERON:0007257,intervertebral disk of sacral vertebra,UBERON:0005174,dorsal region organ
+CL:1000486,basal cell of urothelium,CL:0000646,basal cell
+UBERON:3010792,m. rectus abdominis profundus,UBERON:0004120,mesoderm-derived structure
+HP:0012483,Abnormal alpha granules,HP:0011883,Abnormal platelet granules
+DOID:14264,benign neonatal seizures,DOID:0050702,neonatal period electroclinical syndrome
+CL:0001027,CD7-negative lymphoid progenitor cell,CL:0000051,common lymphoid progenitor
+UBERON:2000887,floor plate neural rod,UBERON:0003079,floor plate
+UBERON:0011897,cardiac endomysium,UBERON:0011895,endomysium
+HP:0007942,Internal ophthalmoplegia,HP:0000602,Ophthalmoplegia
+UBERON:0009468,basiotic bone,UBERON:0002050,embryonic structure
+UBERON:2000868,epaxial region somite 20,UBERON:0003900,epaxial myotome region
+UBERON:0003867,distal phalanx of pes,UBERON:0001449,phalanx of pes
+HP:0011596,Left aortic arch with right descending aorta and right ductus arteriosus,HP:0011587,Abnormal branching pattern of the aortic arch
+HP:0009394,Bracket epiphyses of the 4th finger,HP:0010229,Bracket epiphyses of the phalanges of the hand
+DOID:1681,heart septal defect,DOID:1682,congenital heart disease
+UBERON:0002171,lower lobe of right lung,UBERON:0008949,lower lobe of lung
+DOID:2530,splenic abscess,DOID:2529,splenic disease
+CL:0002020,GlyA-positive reticulocytes,CL:0002422,enucleated reticulocyte
+CL:0000831,mast cell progenitor,CL:0000839,myeloid lineage restricted progenitor cell
+UBERON:0010540,tarsus pre-cartilage condensation,UBERON:0010695,mesenchyme of tarsal region
+CL:1000698,kidney resident macrophage,CL:1000500,kidney interstitial cell
+CL:0002063,type II pneumocyte,CL:1000272,lung secretory cell
+HP:0008131,Tarsal stippling,HP:0100925,Sclerosis of bones of the feet
+CL:0002640,amniotic epithelial stem cell,CL:0000036,epithelial fate stem cell
+DOID:4546,pediatric mesenchymal chondrosarcoma,DOID:4545,mesenchymal chondrosarcoma
+HP:0004987,Mesomelic leg shortening,HP:0003027,Mesomelia
+UBERON:0006508,interosseous muscle,UBERON:0003661,limb muscle
+UBERON:2001036,sclerotome somite 10,UBERON:0003089,sclerotome
+UBERON:0004315,distal phalanx of pedal digit 1,UBERON:0003640,pedal digit 1 phalanx
+UBERON:0008819,inferior mediastinum,UBERON:0002224,thoracic cavity
+DOID:3579,testicular gonadoblastoma,DOID:0060087,male reproductive organ benign neoplasm
+HP:0008445,Cervical spinal canal stenosis,HP:0003416,Spinal canal stenosis
+NCBITaxon:32008,Burkholderia,NCBITaxon:119060,Burkholderiaceae
+UBERON:0009842,acinus,UBERON:0000064,organ part
+DOID:440,neuromuscular disease,DOID:870,neuropathy
+DOID:4288,external ear carcinoma,DOID:5665,external ear cancer
+UBERON:0015925,superficial intraparotid lymph node,UBERON:0015870,lymph node of head
+UBERON:0011298,submucosa of uterine tube,UBERON:0000009,submucosa
+UBERON:0007304,appendage vasculature,UBERON:0002049,vasculature
+UBERON:0009216,pharyngeal membrane of 3rd arch,UBERON:0009210,pharyngeal membrane
+DOID:3985,ostertagiasis,DOID:1255,trichostrongyloidiasis
+CL:0000237,keratinizing barrier epithelial cell,CL:0000240,stratified squamous epithelial cell
+UBERON:0003821,metapodium bone,UBERON:0012357,digitopodium bone
+UBERON:0000916,abdomen,UBERON:0009569,subdivision of trunk
+UBERON:0010040,stomach non-glandular epithelium,UBERON:0011952,non-glandular epithelium
+UBERON:0001524,extensor carpi radialis longus muscle,UBERON:0011867,extensor carpi radialis muscle
+HP:0009195,Epiphyseal stippling of the metacarpals,HP:0010655,Epiphyseal stippling
+UBERON:2001634,pharyngobranchial 1 cartilage,UBERON:2001910,pharyngobranchial 1 element
+UBERON:0009074,syrinx organ,UBERON:0000062,organ
+HP:0100645,Cystocele,HP:0100672,Vaginal hernia
+UBERON:0002694,anterior hypothalamic commissure,UBERON:0011590,commissure of diencephalon
+UBERON:0005243,interventricular septum endocardium,UBERON:0002165,endocardium
+DOID:1786,adrenal rest tumor,DOID:0060089,endocrine organ benign neoplasm
+UBERON:0005945,neurocranial trabecula,UBERON:0003932,cartilage element of chondrocranium
+DOID:7148,rheumatoid arthritis,DOID:848,arthritis
+DOID:3876,colonic pseudo-obstruction,DOID:3878,intestinal pseudo-obstruction
+HP:0008710,Small external genitalia,HP:0000811,Abnormal external genitalia
+UBERON:0001687,stapes bone,UBERON:0002513,endochondral bone
+CL:0000682,M cell of gut,CL:0002251,epithelial cell of alimentary canal
+DOID:8125,osteochondrosis,DOID:0080008,ischemic bone disease
+HP:0004779,Brittle scalp hair,HP:0002299,Brittle hair
+UBERON:3000898,trochanteric crest,UBERON:4100000,skeletal element projection
+HP:0008683,Enlarged labia minora,HP:0000065,Labial hypertrophy
+DOID:862,diplegia of upper limb,DOID:863,nervous system disease
+HP:0001452,Autosomal dominant contiguous gene syndrome,HP:0000006,Autosomal dominant inheritance
+CL:0000393,electrically responsive cell,CL:0000211,electrically active cell
+DOID:5387,middle ear adenoma,DOID:0060096,sensory organ benign neoplasm
+UBERON:0012111,diastema,UBERON:0000464,anatomical space
+HP:0000766,Abnormality of the sternum,HP:0000765,Abnormality of the thorax
+UBERON:4200182,lateral tubercle of astragalus,UBERON:0005813,tubercle
+HP:0009579,Proximal/middle symphalangism of the 2nd finger,HP:0006152,Proximal symphalangism (hands)
+HP:0001053,Hypopigmented skin patches,HP:0001010,Hypopigmentation of the skin
+HP:0001042,High axial triradius,HP:0001018,Abnormal palmar dermatoglyphics
+UBERON:0001773,sclera,UBERON:0004121,ectoderm-derived structure
+HP:0006062,5th finger camptodactyly,HP:0100490,Camptodactyly of finger
+UBERON:2105374,dorsal fin distal radial element 3,UBERON:2100936,dorsal fin distal radial element
+DOID:5634,adenosquamous prostate carcinoma,DOID:10286,prostate carcinoma
+UBERON:0004809,salivary gland epithelium,UBERON:0015833,foregut epithelium
+DOID:4525,mediastinum angiosarcoma,DOID:0001816,angiosarcoma
+UBERON:0014782,allantois of embryonic urinary system,UBERON:0002050,embryonic structure
+UBERON:0001845,perilymph,UBERON:0006586,otolymph
+UBERON:0010676,manual digit 2 phalanx cartilage element,UBERON:0005692,manual digit 2 mesenchyme
+DOID:4337,tinea capitis,DOID:8913,dermatophytosis
+UBERON:0000963,head sensillum,UBERON:0002536,arthropod sensillum
+DOID:0050744,anaplastic large cell lymphoma,DOID:0060060,non-Hodgkin lymphoma
+HP:0012597,Heavy proteinuria,HP:0000093,Proteinuria
+HP:0009433,Osteolytic defects of the middle phalanx of the 3rd finger,HP:0009443,Osteolytic defects of the phalanges of the 3rd finger
+UBERON:0010339,1st arch mandibular mesenchyme from head mesenchyme,UBERON:0010341,1st arch mesenchyme from head mesenchyme
+DOID:4379,nut allergic reaction,DOID:3044,food allergy
+UBERON:0001962,gut-associated lymphoid tissue,UBERON:0001961,mucosa-associated lymphoid tissue
+UBERON:0008434,cervical vertebral arch,UBERON:0003458,neck bone
+HP:0012277,Hypoglycinemia,HP:0010895,Abnormality of glycine metabolism
+HP:0100194,Enlarged epiphysis of the proximal phalanx of the 4th toe,HP:0100096,Abnormality of the epiphysis of the proximal phalanx of the 4th toe
+UBERON:2001529,epibranchial 3 cartilage,UBERON:2001527,epibranchial cartilage
+UBERON:0013115,pterygoideus glandulae muscle,UBERON:0010959,craniocervical muscle
+DOID:3279,spindle cell thymoma,DOID:3275,thymoma
+UBERON:0007268,upper esophageal sphincter,UBERON:0007522,striated muscle sphincter
+UBERON:0001377,quadriceps femoris,UBERON:0003663,hindlimb muscle
+UBERON:0010695,mesenchyme of tarsal region,UBERON:0003860,hindlimb mesenchyme
+UBERON:0008577,vocalis muscle,UBERON:0006328,laryngeal intrinsic muscle
+HP:0012036,Sternocleidomastoid amyotrophy,HP:0003202,Amyotrophy
+UBERON:0000926,mesoderm,UBERON:0000923,germ layer
+UBERON:2001389,regeneration epithelium of fin/limb,UBERON:0000483,epithelium
+HP:0006338,Malformation of mandibular premolar,HP:0011080,Abnormality of premolar morphology
+DOID:6195,conjunctivitis,DOID:4251,conjunctival disease
+HP:0100751,Esophageal neoplasm,HP:0007378,Neoplasm of the gastrointestinal tract
+UBERON:0002330,exocrine system,UBERON:0000467,anatomical system
+UBERON:0004692,external naris epithelium,UBERON:0010371,ecto-epithelium
+UBERON:0009537,vascular element of right lung,UBERON:0000102,lung vasculature
+DOID:9461,exposure keratitis,DOID:9368,keratoconjunctivitis
+UBERON:0013161,left lateral ventricle,UBERON:0015212,lateral structure
+HP:0000394,Lop ear,HP:0000377,Abnormality of the pinna
+UBERON:0009989,condyle of tibia,UBERON:0009979,condyle
+UBERON:0011151,jaw depressor muscle,UBERON:0005493,hyoid muscle
+DOID:295,eye carcinoma,DOID:2174,ocular cancer
+HP:0010209,Symphalangism affecting the proximal phalanges of the toes,HP:0010179,Symphalangism affecting the phalanges of the toes
+UBERON:3000873,pars cylindriformis ilei,UBERON:0000064,organ part
+HP:0009875,Triangular shaped distal phalanges of the hand,HP:0009774,Triangular shaped phalanges of the hand
+UBERON:0015883,gluteal lymph node,UBERON:0015877,parietal pelvic lymph node
+UBERON:0015009,lumbar vertebra endochondral element,UBERON:0005173,abdominal segment organ
+CL:0008004,somatic muscle cell,CL:0000187,muscle cell
+HP:0100378,Absent distal phalanx of the 3rd toe,HP:0100369,Aplasia/Hypoplasia of the distal phalanx of the 3rd toe
+UBERON:0010038,fundic gastric gland,UBERON:0000414,mucous gland
+UBERON:2000315,asteriscus,UBERON:0010313,neural crest-derived structure
+HP:0006502,Aplasia/Hypoplasia involving the carpal bones,HP:0001191,Abnormality of the carpal bones
+DOID:2430,skin glomus tumor,DOID:2431,glomus tumor
+HP:0008588,Slit-like opening of the exterior auditory meatus,HP:0000402,Stenosis of the external auditory canal
+HP:0009612,Duplication of the distal phalanx of the thumb,HP:0009942,Duplication of phalanx of thumb
+HP:0000518,Cataract,HP:0000517,Abnormality of the lens
+UBERON:0005338,outflow tract aortic component,UBERON:0004145,outflow tract
+HP:0004018,Flared radial metaphyses,HP:0003849,Flared metaphyses of the upper limbs
+UBERON:0001918,endothelium of venule,UBERON:0004701,venous system endothelium
+UBERON:0010253,1st arch maxillary mesenchyme from neural crest,UBERON:0010259,1st arch mesenchyme from neural crest
+HP:0100016,Abnormality of the mesentery,HP:0001438,Abnormality of the abdomen
+UBERON:0007641,trigeminal nuclear complex,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010451,Aplasia/Hypoplasia of the spleen,HP:0001743,Abnormality of the spleen
+DOID:2999,granulosa cell tumor,DOID:192,sex cord-gonadal stromal tumor
+HP:0006858,Impaired distal proprioception,HP:0002936,Distal sensory impairment
+UBERON:0014477,thoracic skeleton,UBERON:0004120,mesoderm-derived structure
+DOID:14789,spondyloepiphyseal dysplasia congenita,DOID:0080027,spondyloepimetaphyseal dysplasia
+HP:0009234,Symphalangism of the proximal phalanx of the 5th finger with the 5th metatcarpal,HP:0009232,Symphalangism affecting the proximal phalanx of the 5th finger
+HP:0012067,Glycopeptiduria,HP:0011013,Abnormality of carbohydrate metabolism/homeostasis
+HP:0100087,Triangular epiphyses of the 5th toe,HP:0010341,Abnormality of the epiphyses of the 5th toe
+UBERON:3010503,oviduct artery,UBERON:0004573,systemic artery
+HP:0000872,Hashimoto thyroiditis,HP:0002960,Autoimmunity
+HP:0006069,Severe carpal ossification delay,HP:0001216,Delayed ossification of carpal bones
+HP:0002929,Leydig cell insensitivity to gonadotropin,HP:0008373,Puberty and gonadal disorders
+UBERON:0008923,sublaminar layer S2,UBERON:0008928,sublaminar layers S2 or S3
+CL:0002566,dark melanocyte,CL:0000148,melanocyte
+DOID:8465,retinoschisis,DOID:8466,retinal degeneration
+DOID:0060048,nosophobia,DOID:599,specific phobia
+DOID:11747,uterine adnexa cancer,DOID:363,uterine cancer
+DOID:9958,hemometra,DOID:345,uterine disease
+UBERON:0003979,utricle valve,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002980,opercular part of inferior frontal gyrus,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:6998,gallbladder mucinous carcinoma,DOID:3500,gallbladder adenocarcinoma
+UBERON:0003323,mesenchyme of upper jaw,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:0060222,Scheie syndrome,DOID:12798,mucopolysaccharidosis
+UBERON:0010892,mesethmoid element,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004338,proximal phalanx of manual digit 1,UBERON:0014501,proximal phalanx of digit 1
+UBERON:0004943,submucosa of urinary bladder,UBERON:0004120,mesoderm-derived structure
+UBERON:0010426,oropharyngeal choana,UBERON:0010425,internal naris
+HP:0008796,Externally rotated hips,HP:0003783,Externally rotated/abducted legs
+DOID:4486,malignant biphasic mesothelioma,DOID:1790,malignant mesothelioma
+UBERON:2002215,otic vesicle protrusion,UBERON:0005291,embryonic tissue
+UBERON:0002169,alveolar sac,UBERON:0000117,respiratory tube
+UBERON:0005675,right lung caudal lobe endothelium,UBERON:0005672,right lung endothelium
+UBERON:0014382,collection of hairs on head or neck,UBERON:0010164,collection of hairs
+HP:0002045,Hypothermia,HP:0004370,Abnormality of temperature regulation
+UBERON:2007023,posterior neural keel,UBERON:0000479,tissue
+HP:0008517,Aplasia/Hypoplasia of the sacrum,HP:0008518,Aplasia/Hypoplasia involving the vertebral column
+HP:0011522,Protanopia,HP:0011518,Dichromacy
+UBERON:0002242,nucleus pulposus,UBERON:0002384,connective tissue
+HP:0010480,Urethral fistula,HP:0100589,Urogenital fistula
+UBERON:0004219,urethra smooth muscle,UBERON:0006554,urinary system structure
+UBERON:0003901,horizontal septum,UBERON:0003037,septum
+DOID:4226,endometrial stromal sarcoma,DOID:5166,endometrial stromal tumor
+DOID:1192,peripheral nervous system neoplasm,DOID:3093,nervous system cancer
+DOID:9754,ganglion or cyst of synovium/tendon/bursa,DOID:381,arthropathy
+DOID:8947,diabetic retinopathy,DOID:2462,retinal vascular disease
+HP:0000824,Growth hormone deficiency,HP:0003117,Abnormality of circulating hormone level
+UBERON:0004235,mammary gland smooth muscle,UBERON:0001135,smooth muscle tissue
+DOID:6839,breast intraductal proliferative lesion,DOID:3013,intraductal breast neoplasm
+UBERON:0010678,manual digit 4 phalanx cartilage element,UBERON:0010686,manual digit phalanx cartilage element
+UBERON:2001995,papilla,UBERON:0003102,surface structure
+UBERON:0004787,urethra urothelium,UBERON:0002325,epithelium of urethra
+UBERON:0010013,lower beak,UBERON:0003102,surface structure
+HP:0012112,Abnormality of circulating corticosterone level,HP:0012111,Abnormality of circulating glucocorticoid level
+UBERON:0003868,proximal phalanx of pes,UBERON:0001449,phalanx of pes
+CL:0000652,pinealocyte,CL:0000163,endocrine cell
+DOID:339,accessory nerve disease,DOID:3418,glossopharyngeal nerve disease
+UBERON:0011658,epiplastron,UBERON:0011657,dermal element of plastron
+UBERON:0008787,fourth trochanter,UBERON:0000980,trochanter
+HP:0004249,Accessory lunate,HP:0004232,Accessory carpal bones
+CL:0000477,follicle cell,CL:0000075,columnar/cuboidal epithelial cell
+UBERON:0003016,postcommissural fornix,UBERON:0000052,fornix of brain
+UBERON:0006325,laryngeal intrinsic ligament,UBERON:0001743,ligament of larynx
+UBERON:3000017,anterior process of pars palatina of maxilla,UBERON:4100000,skeletal element projection
+HP:0011282,Abnormality of the hindbrain,HP:0012443,Abnormality of the brain
+UBERON:4300106,ventral limb of posttemporal,UBERON:0005913,zone of bone organ
+UBERON:0007324,pancreatic lobe,UBERON:0004119,endoderm-derived structure
+HP:0012569,Delayed menarche,HP:0000823,Delayed puberty
+UBERON:3010417,posterior palatine artery,UBERON:0001637,artery
+UBERON:0012327,pearly penile papule,UBERON:0005156,reproductive structure
+UBERON:3000687,processus confluens,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003361,epithelium of sublingual gland,UBERON:0010371,ecto-epithelium
+UBERON:2007048,ventral intermandibularis posterior,UBERON:0001630,muscle organ
+HP:0002296,Progressive hypotrichosis,HP:0001006,Hypotrichosis
+HP:0002697,Parietal foramina,HP:0002696,Abnormality of the parietal bone
+UBERON:2007047,midbrain hindbrain boundary neural tube,UBERON:0006800,anatomical line
+NCBITaxon:5598,Alternaria,NCBITaxon:117568,mitosporic Pleosporaceae
+UBERON:0015155,conjunctival space,UBERON:0000464,anatomical space
+UBERON:0010131,conducting tissue of heart,UBERON:0001133,cardiac muscle tissue
+DOID:813,septic arthritis,DOID:848,arthritis
+HP:0002492,Abnormality of the corticospinal tract,HP:0002062,Abnormality of the pyramidal tracts
+DOID:5747,uterine ligament serous adenocarcinoma,DOID:3700,uterine ligament adenocarcinoma
+HP:0009612,Duplication of the distal phalanx of the thumb,HP:0009883,Duplication of the distal phalanx of hand
+UBERON:0003326,mesenchyme of mammary gland,UBERON:0014404,female anatomical structure
+HP:0007305,CNS demyelination,HP:0011400,Abnormal CNS myelination
+UBERON:0013674,ctenactinium,UBERON:0007719,bone of reproductive structure
+UBERON:0002169,alveolar sac,UBERON:0007499,epithelial sac
+UBERON:3000872,collum ilei,UBERON:0000064,organ part
+UBERON:2001634,pharyngobranchial 1 cartilage,UBERON:2001533,pharyngobranchial cartilage
+CL:1000597,papillary tips cell,CL:1000617,kidney inner medulla cell
+HP:0003921,Laterally sloping humeral metaphysis,HP:0003920,Sloping humeral metaphysis
+UBERON:0002156,nucleus raphe magnus,UBERON:0002677,regional part of medullary raphe nuclear complex
+UBERON:0004048,pontine cistern,UBERON:0005219,hindbrain subarachnoid space
+UBERON:2002166,pseudourostyle,UBERON:4100000,skeletal element projection
+DOID:1060,Hartnup disease,DOID:9252,amino acid metabolic disorder
+UBERON:0003060,pronephric duct,UBERON:0012275,meso-epithelium
+HP:0010524,Agnosia,HP:0011446,Abnormality of higher mental function
+UBERON:0009881,anterior lateral plate mesoderm,UBERON:0004120,mesoderm-derived structure
+HP:0100130,Small epiphysis of the proximal phalanx of the 2nd toe,HP:0100052,Small epiphyses of the 2nd toe
+UBERON:2000465,adductor operculi,UBERON:0005493,hyoid muscle
+HP:0100893,Prominent xiphoid process,HP:0100892,Abnormality of the xiphoid process
+HP:0011634,Partial left sided absence of pericardium,HP:0011628,Congenital defect of the pericardium
+DOID:10914,amnestic disorder,DOID:1561,cognitive disorder
+UBERON:0010256,4th arch mesenchyme from neural crest,UBERON:0010258,mesenchyme from rhombencephalic neural crest
+UBERON:0001485,knee joint,UBERON:0011139,synovial limb joint
+UBERON:0005981,vena cava sinus,UBERON:0002553,anatomical cavity
+UBERON:0003254,amniotic ectoderm,UBERON:0012275,meso-epithelium
+HP:0011054,Agenesis of molar,HP:0001592,Selective tooth agenesis
+UBERON:0009894,siphon primordium,UBERON:0005423,developing anatomical structure
+UBERON:0009992,cranial sensory ganglion,UBERON:0001800,sensory ganglion
+HP:0008187,Absence of secondary sex characteristics,HP:0008373,Puberty and gonadal disorders
+DOID:4517,skin angiosarcoma,DOID:2687,skin sarcoma
+HP:0007737,Bony spicule pigmentary retinopathy,HP:0000580,Pigmentary retinopathy
+UBERON:0015047,manual digit 5 metacarpus endochondral element,UBERON:0015042,manual digit metacarpus endochondral element
+HP:0010495,Amniotic constriction rings of legs,HP:0009775,Amniotic constriction ring
+HP:0005185,Global systolic dysfunction,HP:0006673,Reduced systolic function
+DOID:3665,diffuse cutaneous mastocytosis,DOID:3663,cutaneous mastocytosis
+HP:0004230,Subluxation of the proximal interphalangeal joint of the little finger,HP:0004207,Abnormality of the 5th finger
+CL:0002318,periperhal blood mesothelial cell,CL:0000081,blood cell
+NCBITaxon:33342,Paraneoptera,NCBITaxon:33340,Neoptera
+UBERON:0002718,solitary tract,UBERON:0007702,tract of brain
+HP:0100027,Recurrent pancreatitis,HP:0001733,Pancreatitis
+HP:0012327,Celiac artery compression,HP:0012326,Abnormality of the celiac artery
+UBERON:3000101,hyale,UBERON:0004529,anatomical projection
+HP:0008079,Absent fifth metatarsal,HP:0010744,Absent metatarsal bone
+UBERON:0001746,fibrous capsule of thyroid gland,UBERON:0004119,endoderm-derived structure
+CL:0000748,retinal bipolar neuron,CL:0009004,retinal cell
+HP:0012309,Cutaneous amyloidosis,HP:0011034,Amyloidosis
+DOID:13135,exophthalmic ophthalmoplegia,DOID:539,ophthalmoplegia
+UBERON:0005725,olfactory system,UBERON:0005726,chemosensory system
+UBERON:2005049,prosencephalic artery,UBERON:0001637,artery
+HP:0010434,Aplasia of the middle phalanx of the 2nd toe,HP:0010430,Aplasia of the phalanges of the 2nd toe
+CL:0002024,Kit-positive megakaryocyte progenitor cell,CL:0000553,megakaryocyte progenitor cell
+DOID:9640,sarcocystosis,DOID:37,skin disease
+DOID:9637,stomatitis,DOID:403,mouth disease
+UBERON:0013247,male paramesonephric duct,UBERON:0012275,meso-epithelium
+UBERON:0004100,renal collecting system,UBERON:0000467,anatomical system
+DOID:4989,pancreatitis,DOID:26,pancreas disease
+HP:0001611,Nasal speech,HP:0001608,Abnormality of the voice
+HP:0200012,Short corpus callosum,HP:0200011,Abnormal length of corpus callosum
+UBERON:0005254,upper leg mesenchyme,UBERON:0003860,hindlimb mesenchyme
+UBERON:0015113,distal tarsal bone 4 pre-cartilage condensation,UBERON:0015111,distal tarsal bone 4 endochondral element
+UBERON:0014397,lateral process of malleus,UBERON:0010313,neural crest-derived structure
+DOID:3603,mucinous cystadenocarcinoma,DOID:3111,cystadenocarcinoma
+HP:0004019,Irregular radial metaphysis,HP:0004015,Abnormality of radial metaphyses
+UBERON:0001981,blood vessel,UBERON:0000055,vessel
+UBERON:0003660,eyelid muscle,UBERON:0001630,muscle organ
+CL:0002362,granule cell precursor,CL:0000337,neuroblast (sensu Vertebrata)
+UBERON:0006251,interparietal bone primordium,UBERON:0001048,primordium
+UBERON:0006032,interdigital region between manual digits 3 and 4,UBERON:0006013,interdigital region between manual digits
+HP:0100400,Duplication of the distal phalanx of the 5th toe,HP:0010391,Duplication of the phalanges of the 5th toe
+DOID:5381,bile duct adenoma,DOID:0050625,biliary tract neoplasm
+DOID:6610,bone epithelioid hemangioma,DOID:0060094,bone benign neoplasm
+HP:0002500,Abnormality of the cerebral white matter,HP:0010993,Abnormality of the cerebral subcortex
+HP:0011238,Prominent inferior crus of antihelix,HP:0011243,Abnormality of inferior crus of antihelix
+UBERON:0010537,mesonephric nephron progenitor,UBERON:0004120,mesoderm-derived structure
+DOID:8696,subacute monocytic leukemia,DOID:8527,monocytic leukemia
+UBERON:2001825,urohyal lateral process,UBERON:4100000,skeletal element projection
+DOID:3369,peripheral primitive neuroectodermal tumor,DOID:184,bone cancer
+HP:0004257,Delayed ossification of the trapezoid bone,HP:0001216,Delayed ossification of carpal bones
+HP:0100465,Patchy sclerosis of the proximal phalanx of the 4th toe,HP:0010208,Patchy sclerosis of the proximal phalanges of the toes
+HP:0010029,Curved 1st metacarpal,HP:0010009,Abnormality of the 1st metacarpal
+DOID:11653,conjunctival deposit,DOID:4251,conjunctival disease
+UBERON:0002051,epithelium of bronchiole,UBERON:0000115,lung epithelium
+DOID:4140,biliary dyskinesia,DOID:0000000,gallbladder disease
+DOID:593,agoraphobia,DOID:591,phobic disorder
+UBERON:0006212,bulbo-ventricular groove,UBERON:0002050,embryonic structure
+HP:0007052,Multifocal cerebral white matter abnormalities,HP:0002500,Abnormality of the cerebral white matter
+UBERON:0011187,greater tubercle of humerus,UBERON:0005813,tubercle
+HP:0001342,Cerebral hemorrhage,HP:0002170,Intracranial hemorrhage
+DOID:7678,sphenoid sinus inverted papilloma,DOID:6947,sphenoidal sinus neoplasm
+UBERON:0001819,palpebral fissure,UBERON:0000161,orifice
+HP:0002719,Recurrent infections,HP:0010978,Abnormality of immune system physiology
+UBERON:2005068,bulbus arteriosus inner layer,UBERON:0002050,embryonic structure
+CL:0002552,fibroblast of gingiva,CL:0000057,fibroblast
+UBERON:0009496,intrahepatic part of biliary bud,UBERON:0007499,epithelial sac
+UBERON:2001986,centrum 4,UBERON:0001075,vertebral centrum
+UBERON:0003903,bursa of Fabricius,UBERON:0013765,digestive system organ
+CL:0005018,ghrelin secreting cell,CL:0000167,peptide hormone secreting cell
+UBERON:0009014,lower back skin,UBERON:0001068,skin of back
+UBERON:0011119,carpometacarpal joint,UBERON:0001489,manus joint
+UBERON:0004062,neural tube marginal layer,UBERON:0005291,embryonic tissue
+HP:0011329,Abnormality of cranial sutures,HP:0000235,Abnormality of the fontanelles and cranial sutures
+UBERON:0010230,eyeball of camera-type eye,UBERON:0000020,sense organ
+HP:0010077,Broad distal phalanx of the hallux,HP:0010186,Broad distal phalanx of the toes
+DOID:10936,schizoid personality disorder,DOID:1510,personality disorder
+UBERON:0007312,pudendal artery,UBERON:0001637,artery
+UBERON:2005339,nucleus of the lateral recess,UBERON:0006568,hypothalamic nucleus
+HP:0100146,Absent epiphysis of the middle phalanx of the 3rd toe,HP:0100092,Abnormality of the epiphysis of the middle phalanx of the 3rd toe
+DOID:10656,colon leiomyoma,DOID:5143,large bowel leiomyoma
+DOID:6752,internal auditory canal lipoma,DOID:833,auditory system cancer
+HP:0011575,Imperforate tricuspid valve,HP:0011574,Imperforate atrioventricular valve
+DOID:13801,pharyngoconjunctival fever,DOID:934,viral infectious disease
+HP:0002287,Progressive alopecia,HP:0001596,Alopecia
+DOID:13378,Kawasaki disease,DOID:1602,lymphadenitis
+HP:0001081,Cholelithiasis,HP:0012437,Abnormal gallbladder morphology
+DOID:0060193,amyotrophic lateral sclerosis type 1,DOID:332,amyotrophic lateral sclerosis
+HP:0000282,Facial edema,HP:0011799,Abnormality of facial soft tissue
+DOID:11613,hyperandrogenism,DOID:1923,sex differentiation disease
+DOID:14115,toxic shock syndrome,DOID:0050339,commensal bacterial infectious disease
+HP:0100616,Testicular teratoma,HP:0010788,Testicular neoplasm
+UBERON:0008243,upper back muscle,UBERON:0002324,muscle of back
+UBERON:0005071,posterior neuropore,UBERON:0005077,neuropore
+UBERON:0003554,hindbrain pia mater,UBERON:0003549,brain pia mater
+HP:0010070,Curved 1st metatarsal,HP:0010206,Curved proximal phalanges of the toes
+UBERON:0009958,bladder lumen,UBERON:0000464,anatomical space
+UBERON:2001188,Weberian apparatus,UBERON:0000477,anatomical cluster
+UBERON:0014803,superior nuchal line,UBERON:0014801,nuchal line
+NCBITaxon:138950,Human enterovirus C,NCBITaxon:12059,Enterovirus
+HP:0003720,Generalized muscle hypertrophy,HP:0003712,Muscle hypertrophy
+UBERON:0009768,distal interphalangeal joint,UBERON:0006658,interphalangeal joint
+HP:0100244,Fibrosarcoma,HP:0100242,Sarcoma
+HP:0002231,Sparse body hair,HP:0008070,Sparse hair
+UBERON:0003709,circle of Willis,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002127,inferior olivary complex,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0011013,spinalis muscle,UBERON:0004518,muscle of vertebral column
+DOID:5784,esophageal neuroendocrine tumor,DOID:5041,esophageal cancer
+HP:0010455,Steep acetabular roof,HP:0003170,Abnormality of the acetabulum
+UBERON:0003607,forelimb long bone,UBERON:0003606,limb long bone
+DOID:9675,pulmonary emphysema,DOID:3083,chronic obstructive pulmonary disease
+NCBITaxon:114292,typhus group,NCBITaxon:780,Rickettsia
+HP:0005520,Chronic disseminated intravascular coagulation,HP:0005521,Disseminated intravascular coagulation
+NCBITaxon:11019,Alphavirus,NCBITaxon:11018,Togaviridae
+HP:0100373,Aplasia/Hypoplasia of the middle phalanx of the 4th toe,HP:0010194,Aplasia/Hypoplasia of the middle phalanges of the toes
+UBERON:0003931,diencephalic white matter,UBERON:0003544,brain white matter
+DOID:0060221,Maffucci syndrome,DOID:225,syndrome
+HP:0007710,Peripheral vitreous opacities,HP:0004327,Abnormality of the vitreous humor
+UBERON:0001309,internal iliac artery,UBERON:0005609,iliac artery
+DOID:14544,rete testis adenocarcinoma,DOID:5639,rete testis neoplasm
+UBERON:0008922,sublaminar layer S1,UBERON:0008927,sublaminar layers S1 or S2
+UBERON:0002804,left limbic lobe,UBERON:0002600,limbic lobe
+HP:0000685,Hypoplasia of teeth,HP:0011061,Abnormality of dental structure
+HP:0012165,Oligodactyly,HP:0011297,Abnormality of the digits
+UBERON:0002323,coelemic cavity lumen,UBERON:0002553,anatomical cavity
+UBERON:0001533,subclavian artery,UBERON:0004573,systemic artery
+DOID:3187,brain oligodendroglioma,DOID:0060108,brain glioma
+HP:0100531,Wind-swept deformity of the knees,HP:0002857,Genu valgum
+DOID:9097,erythematosquamous dermatosis,DOID:37,skin disease
+DOID:1188,mononeuropathy,DOID:870,neuropathy
+UBERON:0001324,common fibular nerve,UBERON:0002003,peripheral nerve
+UBERON:0001525,extensor carpi radialis brevis muscle,UBERON:0011867,extensor carpi radialis muscle
+DOID:0050564,autosomal dominant nonsyndromic deafness,DOID:0050563,nonsyndromic deafness
+DOID:8712,neurofibromatosis,DOID:0050736,autosomal dominant disease
+UBERON:0015833,foregut epithelium,UBERON:0003929,gut epithelium
+HP:0000892,Bifid ribs,HP:0000772,Abnormality of the ribs
+UBERON:2005027,posterior cerebral vein,UBERON:0009141,craniocervical region vein
+UBERON:0012245,silk,UBERON:0000463,portion of organism substance
+DOID:11184,acute conjunctivitis,DOID:6195,conjunctivitis
+UBERON:0001829,major salivary gland,UBERON:0010047,oral gland
+HP:0100676,Vaginal lymphocele,HP:0100672,Vaginal hernia
+UBERON:0004783,gall bladder serosa,UBERON:0000042,serous membrane
+DOID:12759,choroid cancer,DOID:3479,uveal cancer
+HP:0011016,Abnormality of urine glucose concentration,HP:0011014,Abnormal glucose homeostasis
+HP:0011843,Abnormality of skeletal physiology,HP:0000924,Abnormality of the skeletal system
+DOID:1893,eczematous dermatitis of eyelid,DOID:1894,noninfectious dermatoses of eyelid
+UBERON:2000411,posterior crista primordium,UBERON:0003249,epithelium of otic placode
+DOID:3500,gallbladder adenocarcinoma,DOID:4948,gallbladder carcinoma
+HP:0010630,Abnormality of metatarsal epiphysis,HP:0010631,Abnormality of the epiphyses of the feet
+HP:0009783,Biceps aplasia,HP:0009782,Aplasia/Hypoplasia of the biceps
+UBERON:0004503,skeletal muscle tissue of digastric,UBERON:0001134,skeletal muscle tissue
+UBERON:0011314,anterior subdivision of masseter,UBERON:0000064,organ part
+DOID:535,sleep disorder,DOID:150,disease of mental health
+DOID:263,kidney cancer,DOID:3996,urinary system cancer
+UBERON:0004361,stylohyoid ligament,UBERON:0004119,endoderm-derived structure
+HP:0003527,Hyperprostaglandinuria,HP:0011023,Abnormality of prostaglandin metabolism
+CL:0008005,obliquely striated somatic muscle cell,CL:0000444,obliquely striated muscle cell
+UBERON:0002534,paired fin,UBERON:0004708,paired limb/fin
+UBERON:0006308,vagal X nerve trunk,UBERON:0002464,nerve trunk
+UBERON:0004758,salt gland,UBERON:0002530,gland
+HP:0006827,Atrophy of the spinal cord,HP:0007344,Atrophy/Degeneration involving the spinal cord
+UBERON:0011972,medial ligament of ankle joint,UBERON:0003589,hindlimb connective tissue
+DOID:9439,chronic cholangitis,DOID:9446,cholangitis
+UBERON:0000055,vessel,UBERON:0004111,anatomical conduit
+CL:1000147,heart valve cell,CL:0000663,valve cell
+HP:0100494,Abnormality of mast cells,HP:0003549,Abnormality of connective tissue
+HP:0001978,Extramedullary hematopoiesis,HP:0001871,Abnormality of  blood and blood-forming tissues
+HP:0010527,Astereognosia,HP:0010524,Agnosia
+UBERON:3000167,fenestra nasolateralis,UBERON:3000316,nasal opening
+DOID:0050624,gastrointestinal system benign neoplasm,DOID:0060085,organ system benign neoplasm
+DOID:6996,intermediate cell type choroid melanoma,DOID:6438,malignant choroid melanoma
+UBERON:0013721,deep inguinal ring,UBERON:0006674,inguinal ring
+UBERON:0006196,mesonephric sinus,UBERON:0006171,renal sinus
+CL:0002302,type A synovial cell,CL:0000214,synovial cell
+UBERON:0001346,vaginal hymen,UBERON:0000063,organ segment
+UBERON:2001722,caudal principal ray 10,UBERON:2001585,caudal principal ray
+DOID:11917,tinea cruris,DOID:8913,dermatophytosis
+CL:0000071,blood vessel endothelial cell,CL:0000076,squamous epithelial cell
+UBERON:0015024,manual digit phalanx endochondral element,UBERON:0015023,phalanx endochondral element
+HP:0009635,Symphalangism of proximal phalanx of  thumb,HP:0009849,Symphalangism of middle phalanx of finger
+HP:0008705,Ureteral triplication,HP:0000073,Ureteral duplication
+CL:0000146,simple columnar epithelial cell,CL:0000075,columnar/cuboidal epithelial cell
+UBERON:0010091,future hindbrain meninges,UBERON:0002616,regional part of brain
+HP:0005211,Midgut malrotation,HP:0002566,Intestinal malrotation
+CL:0000098,sensory epithelial cell,CL:0000066,epithelial cell
+HP:0003526,Orotic acid crystalluria,HP:0010928,Abnormality of orotic acid metabolism
+UBERON:4200025,ascending process of the astragalus,UBERON:0004120,mesoderm-derived structure
+CL:0000391,podocyte (sensu Diptera),CL:0000387,hemocyte (sensu Nematoda and Protostomia)
+HP:0009997,Duplication of phalanx of hand,HP:0005918,Abnormality of phalanx of finger
+HP:0002897,Parathyroid adenoma,HP:0100733,Neoplasm of the parathyroid gland
+HP:0010713,1-5 toe syndactyly,HP:0001770,Toe syndactyly
+UBERON:3010819,gastrointestinal peritoneum,UBERON:0002358,peritoneum
+HP:0100682,Tracheal atresia,HP:0002777,Tracheal stenosis
+UBERON:0006337,distal early tubule,UBERON:0007685,region of nephron tubule
+UBERON:0003356,epithelium of nasal septum,UBERON:0004807,respiratory system epithelium
+DOID:6697,asynchronous multifocal osteogenic sarcoma,DOID:3360,multifocal osteogenic sarcoma
+DOID:11028,pseudopterygium,DOID:10124,corneal disease
+UBERON:0008571,suprahyoid muscle,UBERON:0005493,hyoid muscle
+HP:0100950,Long chain 3 hydroxyacyl coA dehydrogenase deficiency,HP:0003287,Abnormality of mitochondrial metabolism
+DOID:424,pulmonary immaturity,DOID:850,lung disease
+UBERON:0003867,distal phalanx of pes,UBERON:0004300,distal phalanx
+HP:0009110,Diaphragmatic eventration,HP:0000775,Abnormality of the diaphragm
+UBERON:0013544,Brodmann (1909) area 13,UBERON:0013529,Brodmann area
+UBERON:0008845,nonskeletal ligament,UBERON:0000211,ligament
+DOID:14427,abnormality of glucagon secretion,DOID:1428,endocrine pancreas disease
+DOID:11431,endometriosis of rectovaginal septum and vagina,DOID:289,endometriosis
+HP:0004385,Protracted diarrhea,HP:0002014,Diarrhea
+UBERON:0013075,venom gland duct,UBERON:0000058,duct
+UBERON:0006203,conchal part of pinna,UBERON:0000064,organ part
+CL:1000334,enterocyte of epithelium of small intestine,CL:0002254,epithelial cell of small intestine
+DOID:8519,barbiturate abuse,DOID:302,substance abuse
+HP:0100207,Irregular epiphysis of the distal phalanx of the 5th toe,HP:0100097,Abnormality of the epiphysis of the distal phalanx of the 5th toe
+UBERON:0009293,embryonic frontal process,UBERON:0012314,embryonic facial prominence
+UBERON:0014567,layer of hippocampal field,UBERON:0004121,ectoderm-derived structure
+UBERON:0004864,vasculature of retina,UBERON:0002203,vasculature of eye
+HP:0009997,Duplication of phalanx of hand,HP:0001167,Abnormality of finger
+HP:0002092,Pulmonary hypertension,HP:0004890,Elevated pulmonary artery pressure
+UBERON:0009773,renal tubule,UBERON:0003914,epithelial tube
+DOID:576,proteinuria,DOID:557,kidney disease
+HP:0000434,Nasal mucosa telangiectasia,HP:0000433,Abnormality of the nasal mucosa
+UBERON:2205379,dorsal fin distal radial cartilage 8,UBERON:2105379,dorsal fin distal radial element 8
+UBERON:0001688,incus bone,UBERON:0001686,auditory ossicle
+UBERON:0002699,supraopticohypophysial tract,UBERON:0011591,tract of diencephalon
+HP:0002070,Limb ataxia,HP:0001251,Ataxia
+DOID:13141,uveitis,DOID:3480,uveal disease
+UBERON:2000958,sclerotome somite 23,UBERON:0003089,sclerotome
+CL:0002179,foveolar cell of stomach,CL:0002178,epithelial cell of stomach
+HP:0100382,Aplasia of the middle phalanx of the 4th toe,HP:0100363,Aplasia of the phalanges of the 4th toe
+HP:0011625,Multiple muscular ventricular septal defects,HP:0011623,Muscular ventricular septal defect
+DOID:8574,lichen disease,DOID:37,skin disease
+UBERON:4200015,inner digits of foot,UBERON:0005445,segment of pes
+UBERON:0001353,anal region,UBERON:0000477,anatomical cluster
+HP:0007452,Midface capillary hemangioma,HP:0000996,Facial capillary hemangioma
+NCBITaxon:5794,Apicomplexa,NCBITaxon:33630,Alveolata
+HP:0009690,Fragmentation of the epiphyses of the thumb,HP:0009599,Abnormality of the epiphyses of the thumb
+CL:1000484,purkinje myocyte of atrioventricular bundle,CL:0010005,atrioventricular bundle cell
+UBERON:0001220,quadratus lumborum,UBERON:0002378,muscle of abdomen
+HP:0004535,Anterior cervical hypertrichosis,HP:0000998,Hypertrichosis
+UBERON:4300031,fin web,UBERON:0000014,zone of skin
+NCBITaxon:10128,Apodemus,NCBITaxon:39107,Murinae
+UBERON:0011348,raphe of soft palate,UBERON:0011346,palatine raphe
+HP:0006732,Papillary renal cell carcinoma type 2,HP:0006766,Papillary renal cell carcinoma
+UBERON:0002945,ventral posteromedial nucleus of thalamus,UBERON:0015233,nucleus of dorsal thalamus
+DOID:11249,vitamin K deficiency hemorrhagic disease,DOID:5113,nutritional deficiency disease
+UBERON:0013119,haemal node,UBERON:0005057,immune organ
+UBERON:0006287,radius-ulna pre-cartilage condensation,UBERON:0015002,radius-ulna endochondral element
+HP:0100636,Pulmonary paraglioma,HP:0100526,Neoplasm of the lungs
+UBERON:0005108,metanephric epithelium,UBERON:0012275,meso-epithelium
+UBERON:0001485,knee joint,UBERON:0003840,hindlimb joint
+UBERON:0012441,endothelium of peritubular capillary,UBERON:0004819,kidney epithelium
+UBERON:0001489,manus joint,UBERON:0003841,autopod joint
+HP:0002423,Long-tract signs,HP:0002143,Abnormality of the spinal cord
+UBERON:0001609,isthmus of thyroid gland,UBERON:0004119,endoderm-derived structure
+UBERON:0001677,sphenoid bone,UBERON:0015060,sphenoid endochondral element
+HP:0007163,Corticospinal tract disease in lower limbs,HP:0002493,Corticospinal tract dysfunction
+HP:0002140,Ischemic stroke,HP:0001297,Stroke
+DOID:0050867,Jensen syndrome,DOID:225,syndrome
+DOID:3316,perivascular tumor,DOID:175,vascular cancer
+HP:0012693,Abnormal thalamic size,HP:0010663,Abnormality of the thalamus
+HP:0004461,Congenital earlobe sinuses,HP:0000363,Abnormality of earlobe
+UBERON:0006518,right lung lobe,UBERON:0000101,lobe of lung
+DOID:6053,pediatric germ cell cancer,DOID:2994,germ cell cancer
+UBERON:3000836,crista lateralis humeri,UBERON:0004120,mesoderm-derived structure
+DOID:7356,rectum sarcomatoid carcinoma,DOID:1993,rectum cancer
+CL:0000089,male germ line stem cell (sensu Vertebrata),CL:0000085,germ line stem cell (sensu Vertebrata)
+HP:0008768,Inappropriate sexual behavior,HP:0000719,Inappropriate behavior
+UBERON:0010254,2nd arch mesenchyme from neural crest,UBERON:0005689,2nd arch mesenchyme
+DOID:2685,ossifying fibromyxoid tumor,DOID:3350,mesenchymal cell neoplasm
+UBERON:0008816,embryonic head,UBERON:0000033,head
+HP:0002678,Skull asymmetry,HP:0002648,Abnormality of calvarial morphology
+UBERON:0002283,nail matrix,UBERON:0000479,tissue
+HP:0012745,Short palpebral fissure,HP:0200007,Abnormal size of the palpebral fissures
+HP:0008921,Neonatal short-limb short stature,HP:0008873,Disproportionate short-limb short stature
+CL:0002140,acinar cell of sebaceous gland,CL:0000622,acinar cell
+CL:0000782,myeloid dendritic cell,CL:0000990,conventional dendritic cell
+DOID:8538,reticulosarcoma,DOID:0060073,lymphatic system cancer
+UBERON:0001978,parenchyma of pancreas,UBERON:0000353,parenchyma
+HP:0009824,Upper limb undergrowth,HP:0006496,Aplasia/Hypoplasia involving bones of the upper limbs
+DOID:2176,carbuncle,DOID:4223,pyoderma
+CL:0000851,neuromast mantle cell,CL:0000151,secretory cell
+DOID:13929,lacrimal duct obstruction,DOID:1400,lacrimal apparatus disease
+UBERON:0014280,piriform cortex layer 2,UBERON:0002791,regional part of telencephalon
+HP:0005178,Complete heart block with narrow QRS complexes,HP:0001709,Third degree atrioventricular block
+HP:0004795,Hamartomatous stomach polyps,HP:0006753,Neoplasm of the stomach
+UBERON:0005282,ventricular system of brain,UBERON:0000467,anatomical system
+HP:0011595,Left aortic arch with retroesophageal right subclavian artery,HP:0011587,Abnormal branching pattern of the aortic arch
+HP:0006433,Dysplastic radii,HP:0002818,Abnormality of the radius
+DOID:2441,frontal sinus squamous cell carcinoma,DOID:1360,frontal sinus cancer
+HP:0009160,Absent epiphysis of the proximal phalanx of the 5th finger,HP:0010268,Absent epiphyses of the proximal phalanges of the hand
+HP:0100462,Patchy sclerosis of the middle phalanx of the 4th toe,HP:0010376,Patchy sclerosis of the phalanges of the 4th toe
+DOID:0060170,generalized epilepsy with febrile seizures plus,DOID:1827,idiopathic generalized epilepsy
+HP:0007431,Congenital ichthyosiform erythroderma,HP:0008064,Ichthyosis
+UBERON:0003846,thymus epithelium,UBERON:0005911,endo-epithelium
+DOID:8352,aortic malignant tumor,DOID:175,vascular cancer
+HP:0011211,EEG with photoparoxysmal response grade I,HP:0010852,EEG with photoparoxysmal response
+DOID:9694,toxic myocarditis,DOID:3951,acute myocarditis
+UBERON:0000976,humerus,UBERON:0015053,humerus endochondral element
+HP:0005242,Extrahepatic biliary duct atresia,HP:0005912,Biliary atresia
+HP:0009504,Cone-shaped epiphysis of the distal phalanx of the 2nd finger,HP:0010248,Cone-shaped epiphyses of the distal phalanges of the hand
+HP:0002737,Thick skull base,HP:0002693,Abnormality of the skull base
+HP:0009315,Triangular shaped proximal phalanx of the 4th finger,HP:0009407,Triangular shaped phalanges of the 4th finger
+HP:0011702,Abnormal electrophysiology of sinoatrial node origin,HP:0011675,Arrhythmia
+UBERON:0008894,pharyngeal gill precursor,UBERON:0001048,primordium
+UBERON:0012357,digitopodium bone,UBERON:0011250,autopod bone
+UBERON:0015764,dense regular elastic tissue,UBERON:0007845,regular connective tissue
+HP:0100112,Bracket epiphysis of the middle phalanx of the 2nd toe,HP:0100045,Bracket epiphyses of the 2nd toe
+HP:0004383,Hypoplastic left heart,HP:0001961,Hypoplastic heart
+HP:0004051,Advanced ossification of the hand bones,HP:0005921,Abnormal ossification of hand bones
+DOID:3706,fallopian tube adenocarcinoma,DOID:1963,fallopian tube carcinoma
+DOID:480,movement disease,DOID:936,brain disease
+CL:0000205,thermoreceptor cell,CL:0000006,neuronal receptor cell
+DOID:361,cervix endometriosis,DOID:2253,cervix disease
+HP:0001090,Large eyes,HP:0100887,Abnormality of globe size
+UBERON:0006656,deep dorsal vein of penis,UBERON:0014403,male anatomical structure
+NCBITaxon:12058,Picornaviridae,NCBITaxon:464095,Picornavirales
+HP:0002229,Alopecia areata,HP:0001596,Alopecia
+HP:0008311,Spinal cord posterior columns myelin loss,HP:0002143,Abnormality of the spinal cord
+UBERON:0012059,right lung lower lobe bronchiole,UBERON:0003538,right lung bronchiole
+NCBITaxon:43750,Sciomyzoidea,NCBITaxon:43741,Acalyptratae
+HP:0100514,Abnormality of vitamin E metabolism,HP:0100508,Abnormality of vitamin metabolism
+CL:1000360,microfold cell of epithelium proper of large intestine,CL:0002253,epithelial cell of large intestine
+UBERON:0003063,prechordal plate,UBERON:0005423,developing anatomical structure
+UBERON:0008949,lower lobe of lung,UBERON:0000101,lobe of lung
+HP:0006507,Aplasia/Hypoplasia of the humerus,HP:0006496,Aplasia/Hypoplasia involving bones of the upper limbs
+UBERON:2000867,epaxial region somite 18,UBERON:0003900,epaxial myotome region
+HP:0006677,Prolonged QRS complex,HP:0003115,Abnormal EKG
+CL:0000365,zygote,CL:0000007,early embryonic cell
+CL:0002172,interdental cell of cochlea,CL:0002315,supporting cell of cochlea
+UBERON:0007635,nucleus of medulla oblongata,UBERON:0002678,regional part of medulla oblongata
+UBERON:0016453,lower secondary premolar tooth,UBERON:0003268,tooth of lower jaw
+UBERON:0001295,endometrium,UBERON:0014404,female anatomical structure
+UBERON:0001299,glans penis,UBERON:0014403,male anatomical structure
+UBERON:0010986,serratus ventralis pre-muscle mass,UBERON:0005865,pre-muscle condensation
+HP:0002731,Defective lymphocyte apoptosis,HP:0004332,Abnormality of lymphocytes
+HP:0003235,Hypermethioninemia,HP:0010901,Abnormality of methionine metabolism
+UBERON:2001649,basihyal tooth,UBERON:0004756,dermal skeletal element
+CL:1000697,kidney interstitial suppressor macrophage,CL:1000500,kidney interstitial cell
+UBERON:0005177,trunk organ,UBERON:0000062,organ
+HP:0009993,Complete duplication of the proximal phalanx of the 5th finger,HP:0010000,Complete duplication of the proximal phalanges of the hand
+HP:0000289,Broad philtrum,HP:0000288,Abnormality of the philtrum
+UBERON:0001917,endothelium of artery,UBERON:0004700,arterial system endothelium
+UBERON:0000457,cavernous artery,UBERON:0001637,artery
+UBERON:0011320,ligament of temporomandibular joint,UBERON:0008846,skeletal ligament
+UBERON:0014708,costal plate of carapace,UBERON:0011665,carapace bone
+HP:0100885,Lateral venous anomaly,HP:0001015,Prominent superficial veins
+HP:0012146,Abnormality of  von Willebrand factor,HP:0003256,Abnormality of the coagulation cascade
+DOID:12849,autistic disorder,DOID:0060041,autism spectrum disorder
+DOID:14557,primary pulmonary hypertension,DOID:12326,chronic pulmonary heart disease
+UBERON:0010371,ecto-epithelium,UBERON:0004121,ectoderm-derived structure
+DOID:12270,coloboma,DOID:5614,eye disease
+HP:0006153,Disharmonious carpal bone,HP:0006014,Abnormally shaped carpal bones
+HP:0012243,Abnormal genital system morphology,HP:0000078,Abnormality of the genital system
+UBERON:4200100,latissimus dorsi process,UBERON:0004529,anatomical projection
+HP:0100014,Epiretinal membrane,HP:0001103,Abnormality of the macula
+HP:0000037,Male pseudohermaphroditism,HP:0000032,Abnormality of male external genitalia
+HP:0009623,Proximal placement of thumb,HP:0009603,Deviation/Displacement of the thumb
+UBERON:0005777,glomerular basement membrane,UBERON:0006554,urinary system structure
+CL:0001028,CD7-positive lymphoid progenitor cell,CL:0000051,common lymphoid progenitor
+UBERON:0006173,pronephric proximal tubule,UBERON:0004134,proximal tubule
+UBERON:0004193,loop of Henle ascending limb thin segment,UBERON:0007685,region of nephron tubule
+DOID:5501,Pediculus humanus capitis infestation,DOID:5502,lice infestation
+DOID:2495,senile angioma,DOID:3165,skin benign neoplasm
+DOID:0050436,mulibrey nanism,DOID:0050737,autosomal recessive disease
+UBERON:0004421,proximal epiphysis of phalanx of manual digit 5,UBERON:0004414,proximal epiphysis of phalanx of manus
+UBERON:0006333,snout,UBERON:0000475,organism subdivision
+DOID:2485,phosphorus metabolism disease,DOID:0050032,mineral metabolism disease
+UBERON:0013222,otic notch,UBERON:0005913,zone of bone organ
+UBERON:0000941,cranial nerve II,UBERON:0004904,nerve connecting eye with brain
+UBERON:3010690,fetal tooth,UBERON:0001091,calcareous tooth
+UBERON:3000571,specialized connective tissue,UBERON:0002384,connective tissue
+UBERON:0015060,sphenoid endochondral element,UBERON:0010313,neural crest-derived structure
+UBERON:0013640,internal cheek pouch,UBERON:0008802,cheek pouch
+UBERON:0013513,anal pterya,UBERON:0013512,row of feathers
+UBERON:0013397,stratum argenteum of choroid,UBERON:0004121,ectoderm-derived structure
+CL:0000730,leading edge cell,CL:0000066,epithelial cell
+UBERON:0007499,epithelial sac,UBERON:0003914,epithelial tube
+UBERON:0010096,future myelencephalon,UBERON:0005423,developing anatomical structure
+CL:0000517,macrophage derived foam cell,CL:0000891,foam cell
+DOID:10159,osteonecrosis,DOID:0080008,ischemic bone disease
+HP:0010209,Symphalangism affecting the proximal phalanges of the toes,HP:0010184,Abnormality of the proximal phalanges of the toes
+UBERON:2000637,claustrum cartilage,UBERON:2001457,postcranial axial cartilage
+UBERON:2001037,sclerotome somite 13,UBERON:0003089,sclerotome
+HP:0200114,Metabolic alkalosis,HP:0001948,Alkalosis
+HP:0011092,Mulberry molar,HP:0011070,Abnormality of molar morphology
+HP:0007939,Blue cone monochromacy,HP:0011517,Cone monochromacy
+UBERON:0005913,zone of bone organ,UBERON:0000064,organ part
+UBERON:3010042,protogynous hermaphroditic organism,UBERON:0010895,sequential hermaphroditic organism
+UBERON:0005331,mesonephric renal vesicle,UBERON:0004209,renal vesicle
+UBERON:2001935,oral disk,UBERON:0001833,lip
+UBERON:0015926,cranial deep lymph node,UBERON:0015870,lymph node of head
+HP:0011954,Nodular regenerative hyperplasia of liver,HP:0001392,Abnormality of the liver
+HP:0100481,Proximal/middle symphalangism of 4th toe,HP:0100471,Symphalangism affecting the middle phalanx of the 4th toe
+DOID:1394,urinary schistosomiasis,DOID:18,urinary system disease
+UBERON:0003552,telencephalon pia mater,UBERON:0003550,forebrain pia mater
+UBERON:0004988,mucosa of cystic duct,UBERON:0004999,mucosa of biliary tree
+HP:0200023,Priapism,HP:0000056,Abnormality of the clitoris
+UBERON:0008883,osteoid,UBERON:0002481,bone tissue
+UBERON:0009192,basisphenoid pre-cartilage condensation,UBERON:0006904,head mesenchyme from mesoderm
+UBERON:0010155,parietomastoid suture,UBERON:0003685,cranial suture
+NCBITaxon:85512,Dicondylia,NCBITaxon:50557,Insecta
+DOID:327,syringomyelia,DOID:319,spinal cord disease
+UBERON:0003218,ovary septum,UBERON:0003037,septum
+HP:0100218,Irregular epiphysis of the middle phalanx of the 5th toe,HP:0100082,Irregular epiphyses of the 5th toe
+UBERON:0004795,pancreas secretion,UBERON:0000456,bodily secretion
+HP:0100248,Hemiballismus,HP:0004305,Involuntary movements
+HP:0010437,Short proximal phalanx of the 2nd toe,HP:0010431,Short phalanx of the 2nd toe
+NCBITaxon:942,Anaplasmataceae,NCBITaxon:766,Rickettsiales
+DOID:7280,congenital epulis,DOID:5337,epulis
+DOID:3699,uterine ligament mucinous adenocarcinoma,DOID:3700,uterine ligament adenocarcinoma
+UBERON:0004897,right lung accessory lobe lobar bronchus mesenchyme,UBERON:0004901,right lung lobar bronchus mesenchyme
+UBERON:2000424,opercular lateral line,UBERON:2001470,anterior lateral line
+HP:0005793,Shortening of all distal phalanges of the toes,HP:0001857,Short distal phalanx of toe
+DOID:4640,axillary adenitis,DOID:1602,lymphadenitis
+HP:0100190,Triangular epiphysis of the middle phalanx of the 4th toe,HP:0100095,Abnormality of the epiphysis of the middle phalanx of the 4th toe
+HP:0010853,EEG with periodic lateralized epileptiform discharges,HP:0011186,Focal epileptiform discharges with limited propagation to contralateral hemisphere
+UBERON:0007121,dermatome segment of skin,UBERON:0000014,zone of skin
+HP:0010170,Small epiphyses of the toes,HP:0010585,Small epiphyses
+HP:0005420,Recurrent gram-negative bacterial infections,HP:0002718,Recurrent bacterial infections
+UBERON:2002052,prootic depression,UBERON:0000464,anatomical space
+HP:0006380,Knee flexion contracture,HP:0005750,Contractures of the joints of the lower limbs
+HP:0010698,Nuclear pulverulent cataract,HP:0010693,Pulverulent Cataract
+HP:0010965,Abnormality of phytanic acid metabolism,HP:0010964,Abnormality of long-chain fatty-acid metabolism
+HP:0010558,Abnormality of the clivus,HP:0000932,Abnormality of the posterior cranial fossa
+UBERON:0009077,membrana tympaniformis medialis,UBERON:0009075,membrana tympaniformis
+UBERON:0002393,pharyngotympanic tube,UBERON:0000062,organ
+UBERON:0015215,median arcuate ligament,UBERON:0015214,arcuate ligament
+UBERON:0006643,tunica albuginea of testis,UBERON:0007475,matrix-based tissue
+HP:0008797,Early ossification of capital femoral epiphyses,HP:0010574,Abnormality of the epiphysis of the femoral head
+UBERON:0007364,reticulorumen,UBERON:0004921,subdivision of digestive tract
+CL:0000204,acceleration receptive cell,CL:0000006,neuronal receptor cell
+HP:0100813,Testicular torsion,HP:0000035,Abnormality of the testis
+HP:0100086,Stippling of the epiphyses of the 5th toe,HP:0010341,Abnormality of the epiphyses of the 5th toe
+UBERON:2002080,spina occipitalis,UBERON:4100000,skeletal element projection
+HP:0009313,Patchy sclerosis of the proximal phalanx of the 4th finger,HP:0009856,Patchy sclerosis of the proximal phalanges of the hand
+UBERON:0000927,mesectoderm,UBERON:0000923,germ layer
+UBERON:0002110,gallbladder,UBERON:0002075,viscus
+DOID:3319,lymphangioleiomyomatosis,DOID:850,lung disease
+UBERON:2000315,asteriscus,UBERON:0004120,mesoderm-derived structure
+UBERON:0015238,pineal complex,UBERON:0004121,ectoderm-derived structure
+DOID:7867,adult central nervous system germinoma,DOID:4438,central nervous system germinoma
+UBERON:0015133,terminal lactiferous duct,UBERON:0001765,mammary duct
+CL:1000482,myocardial endocrine cell of interventricular septum,CL:0002074,myocardial endocrine cell
+UBERON:3000079,cartilago retronarina,UBERON:0003406,cartilage of respiratory system
+CL:0001062,"effector memory CD8-positive, alpha-beta T cell, terminally differentiated",CL:0000625,"CD8-positive, alpha-beta T cell"
+UBERON:0006360,intermolar eminence,UBERON:0004121,ectoderm-derived structure
+DOID:6657,breast large cell neuroendocrine carcinoma,DOID:1612,breast cancer
+DOID:11111,hydronephrosis,DOID:5200,urinary tract obstruction
+HP:0003044,Shoulder flexion contracture,HP:0100360,Contractures of the joints of the upper limbs
+DOID:5806,stork bite,DOID:2725,capillary hemangioma
+HP:0002684,Thickened calvaria,HP:0002683,Abnormality of the calvaria
+UBERON:0010984,pectoral pre-muscle mass,UBERON:0005865,pre-muscle condensation
+DOID:14221,metabolic syndrome X,DOID:654,overnutrition
+HP:0010900,Abnormality of threonine metabolism,HP:0010899,Abnormality of aspartate family amino acid metabolism
+UBERON:2000573,internal cellular layer,UBERON:0004121,ectoderm-derived structure
+HP:0010886,Osteochondrosis dissecans,HP:0100323,Juvenile aseptic necrosis
+UBERON:0009967,spleen venous sinus,UBERON:0003497,abdomen blood vessel
+HP:0008358,Hyperprolinemia,HP:0010907,Abnormality of proline metabolism
+UBERON:0001812,palpebral conjunctiva,UBERON:0010305,region of conjunctiva
+HP:0000666,Horizontal nystagmus,HP:0000639,Nystagmus
+HP:0002829,Arthralgia,HP:0001367,Abnormal joint morphology
+DOID:6113,intracerebral cystic meningioma,DOID:6112,cerebral meningioma
+HP:0100195,Fragmentation of the epiphysis of the proximal phalanx of the 4th toe,HP:0100096,Abnormality of the epiphysis of the proximal phalanx of the 4th toe
+NCBITaxon:10379,Rhadinovirus,NCBITaxon:10374,Gammaherpesvirinae
+DOID:11465,autonomic nervous system disease,DOID:574,peripheral nervous system disease
+DOID:3121,gallbladder cancer,DOID:4607,biliary tract cancer
+UBERON:0005205,vagina stroma,UBERON:0005156,reproductive structure
+DOID:8757,gastric mucosal hypertrophy,DOID:4029,gastritis
+HP:0009687,Bracket epiphyses of the thumb,HP:0010229,Bracket epiphyses of the phalanges of the hand
+UBERON:0005216,optic eminence surface ectoderm,UBERON:0000076,external ectoderm
+HP:0009355,Stippling of the epiphysis of the proximal phalanx of the 3rd finger,HP:0009419,Stippling of the epiphyses of the 3rd finger
+HP:0009245,Triangular shaped distal phalanx of the 5th finger,HP:0009378,Triangular shaped phalanges of the 5th finger
+UBERON:0003461,shoulder bone,UBERON:0007829,pectoral girdle bone
+UBERON:2000662,external pharyngoclavicularis,UBERON:0000933,pharyngeal muscle
+UBERON:0006280,polar trophectoderm,UBERON:0000478,extraembryonic structure
+UBERON:0016413,medullary cavity of long bone,UBERON:0002553,anatomical cavity
+UBERON:0002370,thymus,UBERON:0005057,immune organ
+UBERON:0004664,aorta tunica adventitia,UBERON:0005734,tunica adventitia of blood vessel
+DOID:8792,eye carcinoma in situ,DOID:8719,in situ carcinoma
+CL:1000001,retrotrapezoid nucleus neuron,CL:0000540,neuron
+UBERON:0003089,sclerotome,UBERON:0004120,mesoderm-derived structure
+HP:0003021,Metaphyseal cupping,HP:0000944,Abnormality of the metaphyses
+HP:0005329,Fixed facial expression,HP:0004673,Decreased facial expression
+UBERON:0014437,iliac crest,UBERON:0005913,zone of bone organ
+HP:0005886,Aphalangy of the hands,HP:0009767,Aplasia/Hypoplasia of the phalanges of the hand
+DOID:5752,cervical serous adenocarcinoma,DOID:3702,cervical adenocarcinoma
+HP:0012497,Reduced maximal expiratory pressure,HP:0004347,Weakness of muscles of respiration
+UBERON:0003324,mesenchyme of lower jaw,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3000828,margo posterior of cleithrum,UBERON:0000064,organ part
+UBERON:0005248,bulbus cordis myocardium,UBERON:0002349,myocardium
+UBERON:0005676,right lung accessory lobe endothelium,UBERON:0005672,right lung endothelium
+DOID:891,progressive myoclonus epilepsy,DOID:0050706,variable age at onset electroclinical syndrome
+UBERON:0001247,falciform ligament,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:4100007,pectoral articular facet,UBERON:4100003,articular surface
+CL:0002124,CD27-positive gamma-delta T cell,CL:0000800,mature gamma-delta T cell
+HP:0006297,Hypoplasia of dental enamel,HP:0000685,Hypoplasia of teeth
+UBERON:0011947,ureter luminal urothelium,UBERON:0006554,urinary system structure
+CL:0000907,"central memory CD8-positive, alpha-beta T cell",CL:0000909,"CD8-positive, alpha-beta memory T cell"
+DOID:4674,androgen insensitivity syndrome,DOID:2519,testicular disease
+HP:0010554,Cutaneous finger syndactyly,HP:0012725,Cutaneous syndactyly
+UBERON:0004461,musculature of head,UBERON:0008229,craniocervical region musculature
+HP:0009588,Vestibular Schwannoma,HP:0100008,Schwannoma
+HP:0002689,Absent paranasal sinuses,HP:0005453,Absent/hypoplastic paranasal sinuses
+UBERON:0007238,1st arch maxillary component,UBERON:0005423,developing anatomical structure
+UBERON:0011347,raphe of hard palate,UBERON:0011346,palatine raphe
+DOID:6458,cerebellar liponeurocytoma,DOID:4205,cerebellum cancer
+CL:0000696,PP cell,CL:0000167,peptide hormone secreting cell
+UBERON:0011599,lenticular process of incus,UBERON:0010313,neural crest-derived structure
+UBERON:0008924,sublaminar layer S3,UBERON:0008928,sublaminar layers S2 or S3
+DOID:6841,flat ductal epithelial atypia,DOID:6839,breast intraductal proliferative lesion
+UBERON:0002297,cerumen,UBERON:0001089,sweat
+UBERON:0008817,thymus primordium endoderm,UBERON:0000925,endoderm
+UBERON:0006755,inferior parathyroid gland,UBERON:0001132,parathyroid gland
+HP:0003743,Genetic anticipation,HP:0000005,Mode of inheritance
+UBERON:0013469,external occipital protuberance,UBERON:0005913,zone of bone organ
+HP:0100049,Irregular epiphyses of the 2nd toe,HP:0010167,Irregular epiphyses of the toes
+HP:0000093,Proteinuria,HP:0003110,Abnormality of urine homeostasis
+NCBITaxon:1301,Streptococcus,NCBITaxon:1300,Streptococcaceae
+UBERON:0011659,entoplastron,UBERON:0011657,dermal element of plastron
+HP:0005146,Cardiac valve calcification,HP:0011915,Cardiovascular calcification
+HP:0004936,Venous thrombosis,HP:0001977,Abnormal thrombosis
+HP:0002046,Heat intolerance,HP:0004370,Abnormality of temperature regulation
+UBERON:0012328,penile spine,UBERON:0005156,reproductive structure
+HP:0001256,"Intellectual disability, mild",HP:0001249,Intellectual disability
+HP:0003187,Breast hypoplasia,HP:0010311,Aplasia/Hypoplasia of the breasts
+HP:0001387,Joint stiffness,HP:0001376,Limitation of joint mobility
+HP:0002634,Arteriosclerosis,HP:0002597,Abnormality of the vasculature
+UBERON:0005299,prepuce of clitoris,UBERON:0011374,prepuce
+HP:0009951,Partial duplication of the distal phalanx of the 2nd finger,HP:0009956,Partial duplication of the phalanges of the 2nd finger
+HP:0009959,Duplication of phalanx of 3rd finger,HP:0009958,Polydactyly affecting the 3rd finger
+UBERON:2007046,midbrain hindbrain boundary neural rod,UBERON:0006800,anatomical line
+HP:0002512,Brain stem compression,HP:0002363,Abnormality of the brainstem
+HP:0010162,Absent epiphyses of the toes,HP:0010160,Abnormality of the epiphyses of the toes
+HP:0001648,Cor pulmonale,HP:0001707,Abnormality of the right ventricle
+HP:0010665,Bilateral coxa valga,HP:0002673,Coxa valga
+DOID:6211,mixed epithelial tumor of ovary,DOID:0060112,ovarian benign neoplasm
+HP:0006159,Mesoaxial hand polydactyly,HP:0001161,Hand polydactyly
+UBERON:2100271,radial element,UBERON:0010363,endochondral element
+UBERON:0002608,caudal part of ventral lateral nucleus,UBERON:0003528,brain grey matter
+UBERON:0009217,pharyngeal membrane of 4th arch,UBERON:0009210,pharyngeal membrane
+UBERON:0015848,incisor tusk,UBERON:0010879,tusk
+UBERON:0005696,pedal digit 2 mesenchyme,UBERON:0005255,pedal digit mesenchyme
+HP:0100161,Fragmentation of the epiphysis of the proximal phalanx of the 3rd toe,HP:0100059,Fragmentation of the epiphyses of the 3rd toe
+UBERON:3000753,pars glenoidalis of scapula,UBERON:0000479,tissue
+HP:0009606,Complete duplication of distal phalanx of the thumb,HP:0009612,Duplication of the distal phalanx of the thumb
+UBERON:0006430,xiphoid cartilage,UBERON:0002236,costal cartilage
+UBERON:0004329,proximal phalanx of manual digit 3,UBERON:0002234,proximal phalanx of manus
+HP:0006703,Aplasia/Hypoplasia of the lungs,HP:0002088,Abnormality of the lung
+HP:0003196,Short nose,HP:0005105,Abnormal nasal morphology
+HP:0009600,Flexion contracture of thumb,HP:0001172,Abnormality of the thumb
+UBERON:0008860,intermediate gastric gland,UBERON:0010038,fundic gastric gland
+UBERON:0001275,pubis,UBERON:0015055,pubic endochondral element
+DOID:6457,Cowden disease,DOID:0050736,autosomal dominant disease
+DOID:6284,epicardium lipoma,DOID:6285,heart lipoma
+HP:0000081,Duplicated collecting system,HP:0000073,Ureteral duplication
+UBERON:0010255,3rd arch mesenchyme from neural crest,UBERON:0010258,mesenchyme from rhombencephalic neural crest
+HP:0004018,Flared radial metaphyses,HP:0004015,Abnormality of radial metaphyses
+HP:0005743,Avascular necrosis of the capital femoral epiphysis,HP:0010574,Abnormality of the epiphysis of the femoral head
+HP:0010229,Bracket epiphyses of the phalanges of the hand,HP:0010578,Bracket epiphyses
+DOID:10264,mumps,DOID:934,viral infectious disease
+UBERON:0010929,stapedius pre-muscle condensation,UBERON:0009506,associated mesenchyme of middle ear
+DOID:8791,breast carcinoma in situ,DOID:8719,in situ carcinoma
+UBERON:0010148,mating plug,UBERON:0000463,portion of organism substance
+DOID:2092,transient arthritis,DOID:381,arthropathy
+HP:0000232,Everted lower lip vermilion,HP:0012472,Eclabion
+HP:0009422,Broad distal phalanx of the 3rd finger,HP:0009836,Broad distal phalanx of finger
+HP:0010654,Aplasia of the falx cerebri,HP:0010653,Abnormality of the falx cerebri
+HP:0000083,Renal insufficiency,HP:0012211,Abnormal renal physiology
+UBERON:3000565,skeletal support for eminentia olfactoria,UBERON:0000064,organ part
+HP:0006595,Scapulohumeral synostosis,HP:0003043,Abnormality of the shoulder
+CL:1000343,paneth cell of epithelium of small intestine,CL:1001598,small intestine glandular cell
+UBERON:0012468,anal tooth,UBERON:0003913,tooth-like structure
+CL:0002023,"CD34-positive, CD41-positive, CD42-positive megakaryocyte progenitor cell",CL:0000553,megakaryocyte progenitor cell
+UBERON:0008895,splanchnocranium,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100624,Corpus cavernosum sclerosis,HP:0100623,Abnormality of corpus cavernosum
+DOID:8170,fibroepithelial polyp of the anus,DOID:6873,skin tag
+HP:0011635,Partial diaphragmatic absence of pericardium,HP:0011628,Congenital defect of the pericardium
+UBERON:0006213,carpus cartilage element,UBERON:0003319,mesenchyme of carpal region
+UBERON:2002089,gular plate,UBERON:0008907,dermal bone
+HP:0009996,Partial duplication of the proximal phalanx of the 5th finger,HP:0010003,Partial duplication of the proximal phalanges of the hand
+CL:0000385,prohemocyte (sensu Nematoda and Protostomia),CL:0000390,blood cell (sensu Nematoda and Protostomia)
+UBERON:0011879,mesorchium,UBERON:0014403,male anatomical structure
+DOID:2703,synovitis,DOID:65,connective tissue disease
+HP:0200068,Nonprogressive visual loss,HP:0000572,Visual loss
+UBERON:0005701,lower jaw molar odontogenic papilla,UBERON:0009891,facial mesenchyme
+UBERON:0000210,tetrapod parietal bone,UBERON:0011164,neurocranium bone
+HP:0100847,Palmoplantar pustules,HP:0011356,Regional abnormality of skin
+DOID:11430,endometriosis in scar of skin,DOID:289,endometriosis
+HP:0010190,Patchy sclerosis of the distal phalanges of the toes,HP:0010178,Patchy sclerosis of the phalanges of the toes
+DOID:10849,sexual masochism,DOID:0060043,sexual disorder
+HP:0011328,Abnormality of fontanelles,HP:0000235,Abnormality of the fontanelles and cranial sutures
+UBERON:2001929,epioccipital posterior process,UBERON:0010313,neural crest-derived structure
+HP:0009187,Bracket epiphysis of the distal phalanx of the 5th finger,HP:0009383,Bracket epiphyses of the 5th finger
+UBERON:0007617,synovial cavity of joint,UBERON:0002553,anatomical cavity
+DOID:1557,hypersensitivity reaction type III disease,DOID:0060056,hypersensitivity reaction disease
+HP:0011237,Broad inferior crus of antihelix,HP:0011243,Abnormality of inferior crus of antihelix
+UBERON:0005299,prepuce of clitoris,UBERON:0004121,ectoderm-derived structure
+HP:0012324,Myeloid leukemia,HP:0001909,Leukemia
+DOID:4057,gallbladder rhabdomyosarcoma,DOID:4058,gallbladder sarcoma
+HP:0100466,Patchy sclerosis of the proximal phalanx of the 5th toe,HP:0010208,Patchy sclerosis of the proximal phalanges of the toes
+UBERON:0002417,abdominal segment of trunk,UBERON:0011676,subdivision of organism along main body axis
+DOID:784,chronic kidney failure,DOID:1074,kidney failure
+UBERON:0001747,parenchyma of thyroid gland,UBERON:0000353,parenchyma
+UBERON:2005245,inter-parietal joint,UBERON:0002209,fibrous joint
+DOID:1210,optic neuritis,DOID:1891,optic nerve disease
+UBERON:0008242,lower back muscle,UBERON:0002324,muscle of back
+HP:0009003,Increased subcutaneous truncal adipose tissue,HP:0009126,Increased adipose tissue
+UBERON:2001850,ceratohyal-branchiostegal ray joint,UBERON:0000982,skeletal joint
+HP:0004986,Rudimentary to absent fibulae,HP:0002990,Fibular aplasia
+HP:0001612,Weak cry,HP:0001608,Abnormality of the voice
+HP:0007384,Aberrant melanosome maturation,HP:0011125,Abnormality of dermal melanosomes
+HP:0100071,Irregular epiphyses of the 4th toe,HP:0010167,Irregular epiphyses of the toes
+DOID:9378,glaucomatocyclitic crisis,DOID:9383,iridocyclitis
+HP:0009796,Branchial cyst,HP:0009794,Branchial anomaly
+UBERON:3010194,mediale,UBERON:0004120,mesoderm-derived structure
+HP:0006657,Hypoplasia of first ribs,HP:0000773,Short ribs
+UBERON:0001782,pigmented layer of retina,UBERON:0015808,eye epithelium
+HP:0000222,Gingival hyperkeratosis,HP:0000962,Hyperkeratosis
+HP:0004944,Cerebral aneurysm,HP:0002617,Aneurysm
+HP:0005739,Posterior subluxation of radial head,HP:0003048,Radial head subluxation
+HP:0009703,Synostosis involving the 1st metacarpal,HP:0009701,Metacarpal synostosis
+CL:0000951,IgE short lived plasma cell,CL:0000975,short lived plasma cell
+HP:0010916,Abnormality of alanine metabolism,HP:0010915,Abnormality of pyruvate family amino acid metabolism
+UBERON:0014371,future telencephalon,UBERON:0004121,ectoderm-derived structure
+UBERON:0008271,turtle shell,UBERON:0000075,subdivision of skeletal system
+HP:0010749,Blepharochalasis,HP:0100540,Palpebral edema
+HP:0001031,Subcutaneous lipoma,HP:0001001,Abnormality of subcutaneous fat tissue
+UBERON:0012276,endometrium glandular epithelium,UBERON:0006799,glandular epithelium
+DOID:13359,Ehlers-Danlos syndrome,DOID:854,collagen disease
+DOID:0050834,CHARGE syndrome,DOID:225,syndrome
+UBERON:0005988,atrium myocardial trabecula,UBERON:0000440,trabecula
+HP:0006660,Aplastic clavicles,HP:0006710,Aplasia/Hypoplasia of the clavicles
+UBERON:2001932,sensory canal tubular ossicle,UBERON:0008907,dermal bone
+UBERON:0007255,intervertebral disk of lumbar vertebra,UBERON:0005173,abdominal segment organ
+UBERON:0002095,mesentery,UBERON:0000042,serous membrane
+UBERON:0005445,segment of pes,UBERON:0012139,segment of autopod
+UBERON:0004061,neural tube mantle layer,UBERON:0005291,embryonic tissue
+UBERON:3000282,margo orbitalis of pterygoid,UBERON:0010313,neural crest-derived structure
+DOID:3309,neurodermatitis,DOID:2723,dermatitis
+UBERON:0000951,rotator muscle of the vertebral column,UBERON:0004518,muscle of vertebral column
+HP:0009900,Unilateral deafness,HP:0000365,Hearing impairment
+DOID:14737,craniofrontonasal syndrome,DOID:0050735,X-linked disease
+HP:0100147,Bracket epiphysis of the middle phalanx of the 3rd toe,HP:0100092,Abnormality of the epiphysis of the middle phalanx of the 3rd toe
+HP:0006643,Fused sternal ossification centers,HP:0011863,Abnormal sternal ossification
+UBERON:0003542,right lung respiratory bronchiole,UBERON:0003538,right lung bronchiole
+HP:0007776,Sparse lower eyelashes,HP:0000653,Sparse eyelashes
+UBERON:0006231,facial bone primordium,UBERON:0002050,embryonic structure
+HP:0005558,Chronic leukemia,HP:0001909,Leukemia
+HP:0009685,Triangular epiphysis of the distal phalanx of the thumb,HP:0009696,Triangular epiphyses of the thumb
+HP:0006646,Costal cartilage calcification,HP:0012306,Abnormal rib ossification
+HP:0100617,Testicular seminoma,HP:0010788,Testicular neoplasm
+UBERON:0000941,cranial nerve II,UBERON:0004121,ectoderm-derived structure
+UBERON:0014668,distal interphalangeal joint of manual digit 2,UBERON:0014677,distal interphalangeal joint of digit 2
+DOID:0050259,baylisascariasis,DOID:883,parasitic helminthiasis infectious disease
+HP:0010990,Abnormality of the common coagulation pathway,HP:0003256,Abnormality of the coagulation cascade
+UBERON:0014802,highest nuchal line,UBERON:0014801,nuchal line
+UBERON:0009767,proximal interphalangeal joint,UBERON:0006658,interphalangeal joint
+NCBITaxon:138951,Human enterovirus D,NCBITaxon:12059,Enterovirus
+HP:0009649,Aplasia of the distal phalanx of the thumb,HP:0009881,Aplasia of the distal phalanges of the hand
+UBERON:2001957,epibranchial 2 bone proximal cartilage,UBERON:0011004,pharyngeal arch cartilage
+DOID:484,vascular hemostatic disease,DOID:2213,hemorrhagic disease
+HP:0010454,Acetabular spurs,HP:0003170,Abnormality of the acetabulum
+UBERON:0009076,membrana tympaniformis lateralis,UBERON:0009075,membrana tympaniformis
+CL:1001221,arcuate vein smooth muscle cell,CL:1001068,kidney venous system smooth muscle cell
+UBERON:2001987,centrum 5,UBERON:0001075,vertebral centrum
+HP:0100675,Vaginal pyocele,HP:0100672,Vaginal hernia
+UBERON:0009615,midbrain hindbrain boundary neural plate,UBERON:0007281,presumptive midbrain hindbrain boundary
+NCBITaxon:197,Campylobacter jejuni,NCBITaxon:194,Campylobacter
+HP:0008838,Stippled calcification proximal humeral epiphyses,HP:0003901,Stippled calcification of the humeral epiphyses
+UBERON:3000164,fenestra lateralis nasi,UBERON:3000316,nasal opening
+DOID:2493,gastric antral vascular ectasia,DOID:1271,capillary disease
+UBERON:0002780,regional part of forebrain,UBERON:0002616,regional part of brain
+HP:0007159,Fluctuations in consciousness,HP:0004372,Reduced consciousness/confusion
+DOID:5384,bile duct cystadenoma,DOID:0050625,biliary tract neoplasm
+HP:0000573,Retinal hemorrhage,HP:0011885,Hemorrhage of the eye
+UBERON:0011618,basihyal bone,UBERON:0011614,basihyal element
+HP:0002023,Anal atresia,HP:0004378,Abnormality of the anus
+UBERON:0000127,facial nucleus,UBERON:0006331,brainstem nucleus
+HP:0003973,Wide radioulnar joints,HP:0003037,Enlarged joints
+HP:0000071,Ureteral stenosis,HP:0006000,Ureteral obstruction
+UBERON:0001323,tibial nerve,UBERON:0002003,peripheral nerve
+DOID:1474,aggressive periodontitis,DOID:824,periodontitis
+DOID:11014,anorectal stricture,DOID:3128,anus disease
+HP:0011898,Abnormality of circulating fibrinogen,HP:0010990,Abnormality of the common coagulation pathway
+DOID:6733,intrahepatic bile duct cystadenoma,DOID:5384,bile duct cystadenoma
+UBERON:3000515,pseudoangular,UBERON:0004768,bone of lower jaw
+UBERON:2002086,pelvic axillary process,UBERON:0004376,fin bone
+HP:0009406,Patchy sclerosis of the phalanges of the 4th finger,HP:0100920,Sclerosis of the phalanges of the 4th finger
+UBERON:2000959,sclerotome somite 26,UBERON:0003089,sclerotome
+CL:1000458,melanocyte of skin,CL:0000148,melanocyte
+HP:0009208,Irregular epiphysis of the middle phalanx of the 5th finger,HP:0009387,Irregular epiphyses of the 5th finger
+HP:0009200,Pseudoepiphysis of the proximal phalanx of the 5th finger,HP:0009389,Pseudoepiphyses of the 5th finger
+HP:0011373,Incomplete partition of the cochlea,HP:0008554,Cochlear malformation
+HP:0006962,"Gait instability, worse in the dark",HP:0002317,Unsteady gait
+HP:0006957,Loss of ability to walk,HP:0002505,Progressive inability to walk
+DOID:5521,keratinizing squamous cell carcinoma,DOID:1749,squamous cell carcinoma
+HP:0000265,Mastoiditis,HP:0000264,Abnormality of the mastoid
+UBERON:2005026,primary head sinus,UBERON:0009141,craniocervical region vein
+NCBITaxon:693995,Coronavirinae,NCBITaxon:11118,Coronaviridae
+HP:0000996,Facial capillary hemangioma,HP:0005306,Capillary hemangiomas
+HP:0006094,Finger joint hypermobility,HP:0006256,Abnormality of hand joint mobility
+HP:0001697,Abnormality of the pericardium,HP:0002564,Malformation of the heart and great vessels
+UBERON:0003520,pelvis blood vessel,UBERON:0003835,abdominal segment blood vessel
+UBERON:0002128,superior olivary complex,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0009712,endocardium of right ventricle,UBERON:0001081,endocardium of ventricle
+UBERON:0002347,thoracic vertebra,UBERON:0003827,thoracic segment bone
+UBERON:0014458,female bulbospongiosus muscle,UBERON:0005156,reproductive structure
+UBERON:0003608,hindlimb long bone,UBERON:0003606,limb long bone
+UBERON:0009652,bronchus basement membrane,UBERON:0003592,bronchus connective tissue
+UBERON:0005450,greater sac cavity,UBERON:0000464,anatomical space
+UBERON:0001074,pericardial cavity,UBERON:0002323,coelemic cavity lumen
+HP:0011015,Abnormality of blood glucose concentration,HP:0011014,Abnormal glucose homeostasis
+DOID:12720,cerebral atherosclerosis,DOID:1936,atherosclerosis
+CL:0002301,type B synovial cell,CL:0000214,synovial cell
+UBERON:0010549,pedal digit 3 metatarsal pre-cartilage condensation,UBERON:0010582,pedal digit 3 phalanx pre-cartilage condensation
+UBERON:4200184,ulnar tuberosity,UBERON:0005813,tubercle
+HP:0100661,Trigeminal neuralgia,HP:0010824,Abnormality of the fifth cranial nerve
+DOID:10428,stable condition keratoconus,DOID:10126,keratoconus
+HP:0011770,Tertiary hyperparathyroidism,HP:0000843,Hyperparathyroidism
+HP:0009654,Osteolytic defects of the phalanges of the thumb,HP:0009771,Osteolytic defects of the phalanges of the hand
+UBERON:0000991,gonad,UBERON:0003133,reproductive organ
+HP:0100865,Broad ischia,HP:0003174,Abnormality of the ischium
+DOID:3179,inverted papilloma,DOID:2615,papilloma
+CL:0000799,immature gamma-delta T cell,CL:0002420,immature T cell
+CL:0002481,peritubular myoid cell,CL:0000185,myoepithelial cell
+UBERON:0003219,shell septum,UBERON:0003037,septum
+UBERON:0008772,proximal epiphysis of tibia,UBERON:0004383,epiphysis of tibia
+HP:0008422,Vertebral wedging,HP:0003312,Abnormal form of the vertebral bodies
+UBERON:0010681,pedal digit 2 phalanx cartilage element,UBERON:0005696,pedal digit 2 mesenchyme
+HP:0010409,Patchy sclerosis of the middle phalanx of the 2nd toe,HP:0010352,Patchy sclerosis of the phalanges of the 2nd toe
+UBERON:0005154,epithelial cord,UBERON:0000486,multilaminar epithelium
+UBERON:0010557,pedal digit 1 metatarsal cartilage element,UBERON:0015037,pedal digit 1 metatarsal endochondral element
+UBERON:0008320,common penile artery,UBERON:0004573,systemic artery
+DOID:1686,glaucoma,DOID:8466,retinal degeneration
+HP:0005482,Abnormality of the alternate complement pathway,HP:0005339,Abnormality of complement system
+UBERON:2000585,kinethmoid cartilage,UBERON:0003932,cartilage element of chondrocranium
+UBERON:0003467,sesamoid bone of gastrocnemius,UBERON:0004251,hindlimb zeugopod bone
+HP:0006830,Severe neonatal hypotonia in males,HP:0001319,Neonatal hypotonia
+HP:0000511,Vertical supranuclear gaze palsy,HP:0000605,Supranuclear gaze palsy
+NCBITaxon:12455,Borna disease virus,NCBITaxon:186458,Bornavirus
+DOID:1392,pseudopapilledema,DOID:1393,visual pathway disease
+UBERON:2000499,dorsal arrector,UBERON:2002147,arrector muscle
+DOID:10024,migraine with aura,DOID:6364,migraine
+UBERON:2002207,medial motor nucleus of vagal nerve,UBERON:2000297,vagal lobe
+CL:0000453,Langerhans cell,CL:0000766,myeloid leukocyte
+UBERON:0010358,arch of centrum of vertebra,UBERON:0004765,skeletal element
+CL:0011107,Muller cell,CL:0009004,retinal cell
+HP:0003100,Slender long bone,HP:0011314,Abnormality of long bone morphology
+CL:0002256,supporting cell of carotid body,CL:0000630,supportive cell
+UBERON:0012475,skeleton of pectoral complex,UBERON:0010912,subdivision of skeleton
+CL:0000102,polymodal neuron,CL:0000540,neuron
+UBERON:2001817,middle nuchal plate,UBERON:2001815,nuchal plate
+HP:0001977,Abnormal thrombosis,HP:0001871,Abnormality of  blood and blood-forming tissues
+DOID:2679,dysembryoplastic neuroepithelial tumor,DOID:0060090,central nervous system organ benign neoplasm
+DOID:0050909,MALT lymphoma,DOID:0060060,non-Hodgkin lymphoma
+DOID:2959,hyperimmunoglobulin syndrome,DOID:2115,B cell deficiency
+HP:0001934,Persistent bleeding after trauma,HP:0001892,Abnormal bleeding
+HP:0100194,Enlarged epiphysis of the proximal phalanx of the 4th toe,HP:0100069,Enlarged epiphyses of the 4th toe
+UBERON:0006195,renal sinus of left kidney,UBERON:0006171,renal sinus
+UBERON:0005172,abdomen organ,UBERON:0005173,abdominal segment organ
+DOID:8549,chronic ulcer of skin,DOID:37,skin disease
+DOID:0060144,mirror agnosia,DOID:4090,agnosia
+UBERON:0003103,compound organ,UBERON:0010000,multicellular anatomical structure
+UBERON:0009292,embryonic nasal process,UBERON:0012314,embryonic facial prominence
+HP:0007437,Multiple cutaneous leiomyomas,HP:0008069,Neoplasm of the skin
+HP:0010400,Patchy sclerosis of the proximal phalanx of the 2nd toe,HP:0100931,Sclerosis of the proximal phalanx of the 2nd toe
+UBERON:0010172,bulb of aorta,UBERON:0004120,mesoderm-derived structure
+HP:0100002,Pleural mesothelioma,HP:0100527,Neoplasia of the pleura
+UBERON:2000751,epaxial region somite 8,UBERON:0003900,epaxial myotome region
+CL:0002064,pancreatic acinar cell,CL:0000622,acinar cell
+DOID:224,transient cerebral ischemia,DOID:2316,brain ischemia
+UBERON:0002517,basicranium,UBERON:0000075,subdivision of skeletal system
+UBERON:0005919,supreme nasal concha,UBERON:0003973,nasal concha of ethmoid bone
+UBERON:0010092,future metencephalon,UBERON:0002616,regional part of brain
+HP:0004601,Spina bifida occulta at L5,HP:0003298,Spina bifida occulta
+DOID:10149,long bones of lower limb cancer,DOID:184,bone cancer
+HP:0000049,Shawl scrotum,HP:0000045,Abnormality of the scrotum
+HP:0001195,Single umbilical artery,HP:0010948,Abnormality of the fetal cardiovascular system
+UBERON:0010050,infralabial gland,UBERON:0010047,oral gland
+HP:0010714,2-4 toe syndactyly,HP:0001770,Toe syndactyly
+UBERON:0005328,mesonephric comma-shaped body,UBERON:0010534,primitive mesonephric nephron
+HP:0003689,Multiple mitochondrial DNA deletions,HP:0009141,Depletion of mitochondrial DNA in muscle tissue
+HP:0000713,Agitation,HP:0000711,Restlessness
+UBERON:0005475,sigmoid sinus,UBERON:0003502,neck blood vessel
+UBERON:3000866,agger limitans anterior of ilium,UBERON:0005913,zone of bone organ
+CL:0000740,retinal ganglion cell,CL:0000117,CNS neuron (sensu Vertebrata)
+HP:0001287,Meningitis,HP:0011450,CNS infection
+HP:0100944,Sclerosis of the distal phalanx of the hallux,HP:0100948,Sclerosis of the distal phalanges of the toes
+HP:0010628,Facial palsy,HP:0001324,Muscle weakness
+HP:0009425,Patchy sclerosis of the distal phalanx of the 3rd finger,HP:0009840,Patchy sclerosis of the distal phalanges of the hand
+HP:0004271,Cortical thickening of hand bones,HP:0100039,Thickened cortex of bones
+UBERON:0006924,stomach glandular epithelium,UBERON:0006929,glandular columnar epithelium
+DOID:1362,paranasal sinus sarcoma,DOID:0050619,paranasal sinus cancer
+HP:0010528,Prosopagnosia,HP:0010524,Agnosia
+UBERON:0004368,Reichert's cartilage,UBERON:0004119,endoderm-derived structure
+UBERON:0013545,Brodmann (1909) area 14,UBERON:0013529,Brodmann area
+HP:0000117,Renal phosphate wasting,HP:0012599,Abnormal urine phosphate concentration
+HP:0004758,Effort-induced polymorphic ventricular tachycardias,HP:0004756,Ventricular tachycardia
+DOID:2392,glandular cystitis,DOID:1680,chronic cystitis
+DOID:613,T lymphocyte deficiency,DOID:11200,T cell deficiency
+UBERON:0001042,chordate pharynx,UBERON:0006562,pharynx
+HP:0004950,Peripheral arterial disease,HP:0100545,Arterial stenosis
+HP:0100208,Ivory epiphysis of the distal phalanx of the 5th toe,HP:0100097,Abnormality of the epiphysis of the distal phalanx of the 5th toe
+UBERON:0005383,caudate-putamen,UBERON:0002791,regional part of telencephalon
+HP:0008155,Mucopolysacchariduria,HP:0003541,Urinary glycosaminoglycan excretion
+HP:0000533,Chorioretinal atrophy,HP:0000532,Chorioretinal abnormality
+UBERON:0011325,pharyngeal nerve plexus,UBERON:0001816,autonomic nerve plexus
+UBERON:0005309,pronephric nephron,UBERON:0001285,nephron
+HP:0010356,Abnormality of the distal phalanx of the 2nd toe,HP:0010182,Abnormality of the distal phalanges of the toes
+DOID:5662,pleomorphic carcinoma,DOID:305,carcinoma
+DOID:7181,benign dermal neurilemmoma,DOID:3165,skin benign neoplasm
+UBERON:0010326,optic pedicel,UBERON:0003932,cartilage element of chondrocranium
+UBERON:4200028,adductor blade,UBERON:0004120,mesoderm-derived structure
+CL:0002200,oxyphil cell of thyroid,CL:0002257,epithelial cell of thyroid gland
+DOID:4377,egg allergy,DOID:3044,food allergy
+HP:0011624,Apical muscular ventricular septal defect,HP:0011623,Muscular ventricular septal defect
+UBERON:0001017,central nervous system,UBERON:0011216,organ system subdivision
+DOID:5623,adenosquamous breast carcinoma,DOID:4680,breast metaplastic carcinoma
+HP:0009691,Irregular epiphyses of the thumb,HP:0009599,Abnormality of the epiphyses of the thumb
+HP:0100780,Conjunctival hamartoma,HP:0010568,Hamartoma of the eye
+HP:0006493,Aplasia/Hypoplasia involving bones of the lower limbs,HP:0002814,Abnormality of the lower limb
+NCBITaxon:6935,Ixodida,NCBITaxon:6934,Parasitiformes
+HP:0000893,Bulging of the costochondral junction,HP:0000766,Abnormality of the sternum
+UBERON:0002266,anterior olfactory nucleus,UBERON:0009663,telencephalic nucleus
+UBERON:2001977,pad,UBERON:0003102,surface structure
+HP:0003382,Hypertrophic nerve changes,HP:0000759,Abnormality of the peripheral nervous system
+UBERON:2001725,caudal principal ray 13,UBERON:2001585,caudal principal ray
+CL:0001020,mature CD8_alpha-low Langerhans cell,CL:0001015,CD8_alpha-low Langerhans cell
+UBERON:2000098,proliferative region,UBERON:0000477,anatomical cluster
+HP:0000588,Optic nerve coloboma,HP:0000589,Coloboma
+UBERON:0006820,body of sternum,UBERON:0004120,mesoderm-derived structure
+CL:0000238,non keratinizing barrier epithelial cell,CL:0000240,stratified squamous epithelial cell
+DOID:6275,TSH producing pituitary tumor,DOID:5395,functioning pituitary adenoma
+UBERON:0003843,dental epithelium,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100903,Sclerosis of the distal phalanx of the 5th finger,HP:0100921,Sclerosis of the phalanges of the 5th finger
+UBERON:0010898,gastralium,UBERON:0005172,abdomen organ
+UBERON:0010349,otic capsule pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+UBERON:0011774,utriculosaccular duct,UBERON:0004121,ectoderm-derived structure
+HP:0006681,Absent atrioventricular node,HP:0001678,Atrioventricular block
+HP:0000940,Abnormal diaphysis morphology,HP:0011314,Abnormality of long bone morphology
+HP:0009189,Fragmentation of the metacarpal epiphyses,HP:0003841,Fragmented epiphyses of the upper limbs
+DOID:2444,hyperpituitarism,DOID:53,pituitary gland disease
+UBERON:2001404,preethmoid bone,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002370,thymus,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0005456,jugular foramen,UBERON:0004120,mesoderm-derived structure
+NCBITaxon:59848,Chrysopsini,NCBITaxon:43920,Chrysopsinae
+UBERON:0003922,pancreatic bud,UBERON:0007499,epithelial sac
+UBERON:3000827,margo anterior of cleithrum,UBERON:0004121,ectoderm-derived structure
+UBERON:0004292,cardiac skeleton,UBERON:0004120,mesoderm-derived structure
+CL:0000673,Kenyon cell,CL:0000028,CNS neuron (sensu Nematoda and Protostomia)
+UBERON:0002812,left cerebral hemisphere,UBERON:0001869,cerebral hemisphere
+UBERON:2005340,nucleus of the posterior recess,UBERON:0006568,hypothalamic nucleus
+DOID:3910,lung adenocarcinoma,DOID:3908,non-small cell lung carcinoma
+DOID:10608,celiac disease,DOID:0060031,autoimmune disease of gastrointestinal tract
+CL:1001569,hippocampal interneuron,CL:0000402,CNS interneuron
+UBERON:0015850,upper left incisor tusk,UBERON:0015847,upper left incisor tooth
+UBERON:0004330,proximal phalanx of manual digit 4,UBERON:0003638,manual digit 4 phalanx
+UBERON:2001806,intracranial diverticulum of swimbladder,UBERON:3010717,diverticulum
+HP:0004264,Narrow carpal joint spaces,HP:0001191,Abnormality of the carpal bones
+DOID:869,cholesteatoma,DOID:5100,middle ear disease
+UBERON:0010057,hypopharyngeal eminence,UBERON:0010188,protuberance
+UBERON:2000493,decussation of medial funicular nucleus,UBERON:0014649,white matter of medulla oblongata
+HP:0002056,Abnormality of the glabella,HP:0000290,Abnormality of the forehead
+UBERON:0003700,temporomandibular joint,UBERON:0011171,jaw joint
+DOID:8443,brachial plexus lesion,DOID:3690,brachial plexus neuropathy
+HP:0007179,Absent smooth pursuit,HP:0007772,Impaired smooth pursuit
+UBERON:0014912,thalamic eminence,UBERON:0002784,regional part of diencephalon
+HP:0008711,Benign prostatic hyperplasia,HP:0008775,Abnormality of the prostate
+HP:0005004,Flattened proximal radial epiphyses,HP:0004002,Flattened radial epiphyses
+UBERON:0005697,pedal digit 3 mesenchyme,UBERON:0005255,pedal digit mesenchyme
+DOID:3918,pancreatic cystadenoma,DOID:0050624,gastrointestinal system benign neoplasm
+UBERON:2001820,posterior nuchal plate,UBERON:0004376,fin bone
+HP:0007103,Hypointensity of cerebral white matter on MRI,HP:0002500,Abnormality of the cerebral white matter
+UBERON:0004939,submucosa of common bile duct,UBERON:0004938,submucosa of biliary tree
+DOID:4549,extraosseous chondrosarcoma,DOID:3371,chondrosarcoma
+HP:0009781,Lester's sign,HP:0001100,Heterochromia iridis
+UBERON:0004673,trigeminal nerve root,UBERON:0011215,cell part cluster of neuraxis
+UBERON:0001349,vestibule,UBERON:0002553,anatomical cavity
+CL:1000696,kidney interstitial inflammatory macrophage,CL:1000500,kidney interstitial cell
+UBERON:3000837,crista medialis humeri,UBERON:0004120,mesoderm-derived structure
+DOID:0050722,PHGDH deficiency,DOID:0050721,serine deficiency
+UBERON:0006539,mammary gland fluid/secretion,UBERON:0000456,bodily secretion
+HP:0006948,Progressive infantile encephalopathy,HP:0002448,Progressive encephalopathy
+HP:0000828,Abnormality of the parathyroid gland,HP:0000818,Abnormality of the endocrine system
+CL:0000733,lymph gland plasmatocyte,CL:0000394,plasmatocyte
+UBERON:0001018,axon tract,UBERON:0011215,cell part cluster of neuraxis
+UBERON:3000951,anterior radial,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000428,yolk cell,CL:0000349,extraembryonic cell
+HP:0005309,Peripheral vascular insufficiency,HP:0004950,Peripheral arterial disease
+HP:0000920,Enlargement of the costochondral junction,HP:0000919,Abnormality of the costochondral junction
+DOID:3770,pulmonary fibrosis,DOID:3082,interstitial lung disease
+UBERON:0003268,tooth of lower jaw,UBERON:0010313,neural crest-derived structure
+UBERON:0001047,neural glomerulus,UBERON:0002606,neuropil
+UBERON:3010558,quadrato-ethmoid ligament,UBERON:0011648,jaw muscle
+UBERON:0009689,anterior inferior cerebellar artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0004060,neural tube ventricular layer,UBERON:0005291,embryonic tissue
+CL:0000700,dopaminergic neuron,CL:0000151,secretory cell
+HP:0009328,Pseudoepiphysis of the middle phalanx of the 3rd finger,HP:0009417,Pseudoepiphyses of the 3rd finger
+DOID:0050437,Danon disease,DOID:3211,lysosomal storage disease
+HP:0008392,Subungual hyperkeratosis,HP:0009723,Abnormality of the subungual region
+HP:0009622,Distally placed thumb,HP:0009603,Deviation/Displacement of the thumb
+HP:0100910,Sclerosis of the proximal phalanx of the 4th finger,HP:0100917,Sclerosis of the proximal phalanges of the hand
+UBERON:0013750,metaphysis of tibia,UBERON:0001438,metaphysis
+HP:0100369,Aplasia/Hypoplasia of the distal phalanx of the 3rd toe,HP:0010368,Abnormality of the distal phalanx of the 3rd toe
+HP:0002837,Recurrent bronchitis,HP:0002788,Recurrent upper respiratory tract infections
+HP:0010387,Osteolytic defects of the phalanges of the 5th toe,HP:0010177,Osteolytic defects of the phalanges of the toes
+HP:0007770,Retinal hypoplasia,HP:0008061,Aplasia/Hypoplasia affecting the retina
+UBERON:0002938,parvocellular part of red nucleus,UBERON:0003528,brain grey matter
+UBERON:0004420,proximal epiphysis of phalanx of manual digit 4,UBERON:0004414,proximal epiphysis of phalanx of manus
+UBERON:0015007,cervical vertebra endochondral element,UBERON:0005174,dorsal region organ
+CL:0002242,nucleate cell,CL:0000003,native cell
+CL:0002409,mature Vgamma2-negative thymocyte,CL:0002405,gamma-delta thymocyte
+DOID:14798,Blount's disease,DOID:2256,osteochondrodysplasia
+UBERON:0010985,rhomboid pre-muscle mass,UBERON:0005865,pre-muscle condensation
+UBERON:0006532,oblique extraocular muscle,UBERON:0006531,oculomotor muscle
+HP:0006599,Medial widening of clavicles,HP:0000889,Abnormality of the clavicles
+UBERON:0005649,pedal digit 2 epithelium,UBERON:0005226,pedal digit epithelium
+UBERON:0015062,bone condensation,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0007199,Progressive spastic paraparesis,HP:0002313,Spastic paraparesis
+HP:0004258,Small trapezoid bone,HP:0001498,Carpal bone hypoplasia
+HP:0001446,Abnormality of the musculature of the upper limbs,HP:0009127,Abnormality of the musculature of the limbs
+UBERON:3010654,rectus cervicis,UBERON:3000224,hyobranchial muscle
+UBERON:0007827,external nose,UBERON:0003102,surface structure
+HP:0000194,Open mouth,HP:0011338,Abnormality of mouth shape
+UBERON:0003323,mesenchyme of upper jaw,UBERON:0009891,facial mesenchyme
+UBERON:0010316,germ layer / neural crest,UBERON:0005291,embryonic tissue
+DOID:5940,malignant peripheral nerve sheath tumor,DOID:3193,peripheral nerve sheath neoplasm
+DOID:11076,Brucella suis brucellosis,DOID:11077,brucellosis
+DOID:0050600,ABCD syndrome,DOID:0050737,autosomal recessive disease
+UBERON:0005096,descending thin limb,UBERON:0006554,urinary system structure
+UBERON:0002079,left cardiac atrium,UBERON:0015212,lateral structure
+UBERON:0001731,cavity of pharynx,UBERON:0000464,anatomical space
+HP:0002018,Nausea,HP:0002017,Nausea and vomiting
+UBERON:2105372,dorsal fin distal radial element 1,UBERON:2100936,dorsal fin distal radial element
+HP:0012599,Abnormal urine phosphate concentration,HP:0012591,Abnormal urinary electrolyte concentration
+UBERON:0006292,shoulder joint primordium,UBERON:0003322,mesenchyme of shoulder
+UBERON:2001623,type 1 odontode,UBERON:2001622,odontode
+UBERON:0001393,auditory cortex,UBERON:0002619,regional part of cerebral cortex
+DOID:6271,gastric cardia adenocarcinoma,DOID:3717,gastric adenocarcinoma
+HP:0003752,Episodic flaccid weakness,HP:0010547,Muscle flaccidity
+UBERON:0007249,dorsal accessory inferior olivary nucleus,UBERON:0007244,inferior olivary nucleus
+HP:0007057,Poor hand-eye coordination,HP:0002370,Poor coordination
+DOID:8418,congenital fibrosarcoma,DOID:3520,pediatric fibrosarcoma
+UBERON:0009970,epithelium of pancreatic duct,UBERON:0010371,ecto-epithelium
+CL:0001005,mature CD8_alpha-positive CD11b-negative dendritic cell,CL:0001000,CD8_alpha-positive CD11b-negative dendritic cell
+UBERON:0007390,pectoral appendage cartilage tissue,UBERON:0004120,mesoderm-derived structure
+HP:0012595,Mild proteinuria,HP:0000093,Proteinuria
+HP:0000252,Microcephaly,HP:0007364,Aplasia/Hypoplasia of the cerebrum
+UBERON:2001794,orbitosphenoid-prootic joint,UBERON:0000982,skeletal joint
+UBERON:2002086,pelvic axillary process,UBERON:0008907,dermal bone
+UBERON:0013164,molariform tooth,UBERON:0001091,calcareous tooth
+CL:0002636,nonkeratinized epithelial cell of inferior part of anal canal,CL:0002635,nonkeratinized epithelial cell of anal column
+UBERON:2005371,dorsal fin pterygiophore 8,UBERON:2001419,dorsal fin pterygiophore
+DOID:154,mixed cell type cancer,DOID:0050687,cell type cancer
+UBERON:0004882,eponychium,UBERON:0004923,organ component layer
+UBERON:3000538,recessus fenestrae ovalis,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003065,ciliary marginal zone,UBERON:0004121,ectoderm-derived structure
+UBERON:0009849,tadpole stage,UBERON:0000069,larval stage
+HP:0009636,Triangular shaped proximal phalanx of the thumb,HP:0009850,Triangular shaped middle phalanges of the hand
+UBERON:0004637,otic capsule,UBERON:0011164,neurocranium bone
+UBERON:0015132,extralobar lactiferous duct,UBERON:0001765,mammary duct
+HP:0001580,Pigmented micronodular adrenocortical disease,HP:0000849,Adrenocortical abnormality
+UBERON:0005120,metanephric late distal convoluted tubule,UBERON:0005102,late distal convoluted tubule
+HP:0100814,Blue nevus,HP:0003764,Nevus
+UBERON:0005432,aortic sac,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010764,Short eyelashes,HP:0000499,Abnormality of the eyelashes
+UBERON:0005455,interventricular groove,UBERON:0004111,anatomical conduit
+HP:0000486,Strabismus,HP:0000549,Abnormal conjugate eye movement
+UBERON:2000468,anterior crista primordium,UBERON:0001048,primordium
+HP:0004323,Abnormality of body weight,HP:0001507,Growth abnormality
+UBERON:0002869,diffuse reticular nucleus,UBERON:0009662,hindbrain nucleus
+UBERON:0003577,knee connective tissue,UBERON:0003569,leg connective tissue
+HP:0005275,Cartilaginous ossification of nose,HP:0000429,Abnormality of the nasal alae
+UBERON:0007134,trunk ganglion,UBERON:0000045,ganglion
+UBERON:0002462,erector spinae muscle group,UBERON:0004120,mesoderm-derived structure
+UBERON:0015231,circulatory system dorsal vessel,UBERON:0000055,vessel
+DOID:0050432,Asperger syndrome,DOID:0060041,autism spectrum disorder
+DOID:9847,peripheral vertigo,DOID:3426,vestibular disease
+HP:0001454,Abnormality of the upper arm,HP:0002817,Abnormality of the upper limb
+HP:0006496,Aplasia/Hypoplasia involving bones of the upper limbs,HP:0009815,Aplasia/Hypoplasia of the extremities
+HP:0007831,Nonprogressive restrictive external ophthalmoplegia,HP:0000544,External ophthalmoplegia
+UBERON:3000561,septum semicircularium laterale,UBERON:0003037,septum
+UBERON:0001689,malleus bone,UBERON:0002513,endochondral bone
+UBERON:0002728,entorhinal area,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009123,Mixed hypo- and hyperpigmentation of the skin,HP:0001010,Hypopigmentation of the skin
+HP:0007980,Absent retinal pigment epithelium,HP:0008051,Abnormality of the retinal pigment epithelium
+UBERON:0004894,alveolar wall,UBERON:0000060,anatomical wall
+HP:0100502,Vitamin B12 deficiency,HP:0004341,Abnormality of the vitamin B12 metabolism
+HP:0100506,Vitamin B8 deficiency,HP:0004340,Abnormality of vitamin B metabolism
+UBERON:0003604,trachea cartilage,UBERON:0003603,lower respiratory tract cartilage
+HP:0009296,Bullet-shaped middle phalanx of the 4th finger,HP:0009405,Bullet-shaped phalanges of the 4th finger
+DOID:0050043,Israeli tick typhus,DOID:11104,spotted fever
+UBERON:0007684,uriniferous tubule,UBERON:0006555,excretory tube
+UBERON:0003265,chorionic mesenchyme,UBERON:0005292,extraembryonic tissue
+HP:0100085,Small epiphyses of the 5th toe,HP:0010341,Abnormality of the epiphyses of the 5th toe
+HP:0000816,Abnormality of Krebs cycle metabolism,HP:0001939,Abnormality of metabolism/homeostasis
+HP:0002318,Cervical myelopathy,HP:0002196,Myelopathy
+UBERON:0006194,renal sinus of right kidney,UBERON:0006171,renal sinus
+HP:0003391,Gower sign,HP:0003701,Proximal muscle weakness
+CL:0002476,bone marrow macrophage,CL:0000864,tissue-resident macrophage
+HP:0009638,Short proximal phalanx of thumb,HP:0005819,Short middle phalanx of finger
+CL:0001025,"Kit-positive, Sca1-positive common lymphoid progenitor",CL:0000051,common lymphoid progenitor
+UBERON:0001044,salivary gland,UBERON:0010047,oral gland
+HP:0010817,Linear nevus sebaceous,HP:0010815,Nevus sebaceous
+HP:0100590,Rectal fistula,HP:0100819,Intestinal fistula
+UBERON:0002293,costochondral joint,UBERON:0002001,joint of rib
+HP:0010901,Abnormality of methionine metabolism,HP:0010899,Abnormality of aspartate family amino acid metabolism
+UBERON:0001995,fibrocartilage,UBERON:0002418,cartilage tissue
+UBERON:0007679,intersomitic vein,UBERON:0001638,vein
+DOID:14332,postencephalitic Parkinson disease,DOID:13548,secondary Parkinson disease
+DOID:0050242,primary amebic meningoencephalitis,DOID:2789,parasitic protozoa infectious disease
+DOID:9746,hemorrhoid,DOID:9742,pelvic varices
+DOID:0050466,Loeys-Dietz syndrome,DOID:0050736,autosomal dominant disease
+HP:0009520,Pseudoepiphysis of the middle phalanx of the 2nd finger,HP:0010264,Pseudoepiphyses of the middle phalanges of the hand
+DOID:7139,endometrial small cell carcinoma,DOID:2871,endometrial carcinoma
+NCBITaxon:86661,Bacillus cereus group,NCBITaxon:1386,Bacillus <bacterium>
+UBERON:0005224,pancreas tail parenchyma,UBERON:0000353,parenchyma
+NCBITaxon:222544,Sordariomycetidae,NCBITaxon:147550,Sordariomycetes
+UBERON:0012378,muscle layer of urinary bladder,UBERON:0006554,urinary system structure
+HP:0002632,Low-to-normal blood pressure,HP:0002615,Hypotension
+HP:0100598,Pulmonary edema,HP:0002088,Abnormality of the lung
+NCBITaxon:34625,Hyalomma,NCBITaxon:426438,Hyalomminae
+DOID:3069,astrocytoma,DOID:3070,malignant glioma
+UBERON:0012105,baleen plate,UBERON:0004121,ectoderm-derived structure
+UBERON:0009477,associated mesenchyme of otic placode,UBERON:0007213,mesenchyme derived from head neural crest
+NCBITaxon:4751,Fungi,NCBITaxon:33154,Opisthokonta
+HP:0002057,Prominent glabella,HP:0002056,Abnormality of the glabella
+HP:0012496,Reduced maximal inspiratory pressure,HP:0004347,Weakness of muscles of respiration
+UBERON:3000518,pseudodentary,UBERON:0004768,bone of lower jaw
+HP:0001435,Abnormality of the shoulder girdle musculature,HP:0001446,Abnormality of the musculature of the upper limbs
+UBERON:0003382,cardiac muscle of left ventricle,UBERON:0001133,cardiac muscle tissue
+UBERON:0004647,liver lobule,UBERON:0004119,endoderm-derived structure
+UBERON:3000829,margo scapularis,UBERON:0000064,organ part
+UBERON:0011253,gland of anal sac,UBERON:0002365,exocrine gland
+UBERON:0013141,capillary bed,UBERON:0006914,squamous epithelium
+UBERON:0006599,presumptive hypochord,UBERON:0006598,presumptive structure
+UBERON:3000792,anterior ramus of cleithrum,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0002125,CD27-negative gamma-delta T cell,CL:0000800,mature gamma-delta T cell
+UBERON:0009955,neurogenic placode,UBERON:0002546,cranial placode
+DOID:9063,Ritter's disease,DOID:37,skin disease
+UBERON:0010259,1st arch mesenchyme from neural crest,UBERON:0010258,mesenchyme from rhombencephalic neural crest
+DOID:6114,cerebral convexity meningioma,DOID:6112,cerebral meningioma
+HP:0002203,Respiratory paralysis,HP:0004347,Weakness of muscles of respiration
+DOID:14145,malignant anus melanoma,DOID:14110,anus cancer
+HP:0009136,Duplication involving bones of the feet,HP:0001760,Abnormality of the foot
+HP:0009434,Patchy sclerosis of the middle phalanx of the 3rd finger,HP:0100905,Sclerosis of the middle phalanx of the 3rd finger
+UBERON:0011375,skin of prepuce of clitoris,UBERON:0005298,skin of clitoris
+HP:0009324,Enlarged epiphysis of the middle phalanx of the 3rd finger,HP:0009413,Enlarged epiphyses of the 3rd finger
+HP:0002223,Absent eyebrow,HP:0002298,Absent hair
+DOID:13112,mechanical entropion,DOID:12397,entropion
+UBERON:0011856,acinus of lactiferous gland,UBERON:0005156,reproductive structure
+UBERON:0015092,distal carpal bone 3 pre-cartilage condensation,UBERON:0015090,distal carpal bone 3 endochondral element
+DOID:12234,cascade stomach,DOID:76,stomach disease
+HP:0010031,Patchy sclerosis of the 1st metacarpal,HP:0009655,Patchy sclerosis of the phalanges of the thumb
+UBERON:0004752,palatoquadrate cartilage,UBERON:0011004,pharyngeal arch cartilage
+UBERON:0002356,perineum,UBERON:0009569,subdivision of trunk
+UBERON:0001992,papillary layer of dermis,UBERON:0004923,organ component layer
+CL:0002177,folliculostellate cell of pars distalis of adenohypophysis,CL:0000642,folliculostellate cell
+CL:1000278,smooth muscle fiber of ileum,CL:1000275,smooth muscle cell of small intestine
+CL:0002188,glomerular endothelial cell,CL:0000115,endothelial cell
+CL:0002319,neural cell,CL:0002371,somatic cell
+DOID:1091,tooth disease,DOID:403,mouth disease
+HP:0005293,Venous insufficiency,HP:0002624,Venous abnormality
+UBERON:2005410,pars inferior ear,UBERON:0004121,ectoderm-derived structure
+HP:0004686,Short third metatarsal,HP:0010743,Short metatarsal
+DOID:4049,mediastinum rhabdomyosarcoma,DOID:4050,mediastinum sarcoma
+NCBITaxon:6157,Platyhelminthes,NCBITaxon:33213,Bilateria
+DOID:10747,lymphoid leukemia,DOID:1037,lymphoblastic leukemia
+HP:0004428,Elfin facies,HP:0001999,Abnormal facial shape
+CL:0000357,stratified epithelial stem cell,CL:0000036,epithelial fate stem cell
+HP:0006390,Anterior tibial bowing,HP:0002982,Tibial bowing
+UBERON:0004804,oviduct epithelium,UBERON:0014404,female anatomical structure
+HP:0000263,Oxycephaly,HP:0000262,Turricephaly
+HP:0002202,Pleural effusion,HP:0002103,Abnormality of the pleura
+UBERON:0011948,ureter subluminal urothelium,UBERON:0006554,urinary system structure
+UBERON:2007025,midbrain neural keel,UBERON:0000479,tissue
+HP:0011885,Hemorrhage of the eye,HP:0012373,Abnormal eye physiology
+UBERON:0012131,centrale,UBERON:0015067,centrale endochondral element
+HP:0002766,Relatively short spine,HP:0008518,Aplasia/Hypoplasia involving the vertebral column
+DOID:0050426,Stevens-Johnson syndrome,DOID:37,skin disease
+DOID:14761,Greig cephalopolysyndactyly syndrome,DOID:12960,acrocephalosyndactylia
+HP:0002633,Vasculitis,HP:0002597,Abnormality of the vasculature
+HP:0007841,Amyloid deposition in the vitreous humor,HP:0004327,Abnormality of the vitreous humor
+HP:0012533,Allodynia,HP:0012531,Pain
+HP:0100084,Pseudoepiphyses of the 5th toe,HP:0010169,Pseudoepiphyses of the toes
+HP:0011269,Bifid tragus,HP:0009912,Abnormality of the tragus
+UBERON:0000312,inner cambium layer of periosteum,UBERON:0000158,membranous layer
+UBERON:0001786,fovea centralis,UBERON:0000064,organ part
+UBERON:0003654,metatarsal bone of digit 5,UBERON:0001448,metatarsal bone
+UBERON:0001840,semicircular canal,UBERON:0004121,ectoderm-derived structure
+UBERON:0010952,frontalis,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0003473,Fatigable weakness,HP:0003398,Abnormality of the neuromuscular junction
+UBERON:0002489,coronal suture,UBERON:0003685,cranial suture
+UBERON:0004237,blood vessel smooth muscle,UBERON:0001135,smooth muscle tissue
+UBERON:2001265,ovarian follicle stage II,UBERON:0001305,ovarian follicle
+HP:0005060,limited elbow flexion/extension,HP:0001377,Limited elbow extension
+UBERON:0002729,claustral amygdaloid area,UBERON:0005401,cerebral hemisphere grey matter
+CL:1000355,microfold cell of epithelium proper of small intestine,CL:1000353,microfold cell of epithelium of small intestine
+HP:0010432,Absent distal phalanx of the 2nd toe,HP:0010430,Aplasia of the phalanges of the 2nd toe
+UBERON:0007759,metatarsophalangeal joint of pedal digit 4,UBERON:0003696,metatarsophalangeal joint
+HP:0004287,Pointed hand bones,HP:0005922,Abnormal hand morphology
+UBERON:0012310,deep lateral cervical lymph node,UBERON:0012306,lateral cervical lymph node
+HP:0001029,Poikiloderma,HP:0011121,Abnormality of skin morphology
+DOID:3646,necrosis of pituitary,DOID:53,pituitary gland disease
+UBERON:0001113,lobe of liver,UBERON:0004119,endoderm-derived structure
+HP:0004017,Exostoses of the radial metaphysis,HP:0004015,Abnormality of radial metaphyses
+HP:0100626,Chronic hepatic failure,HP:0001399,Hepatic failure
+HP:0003358,Elevated intracellular cystine,HP:0010918,Abnormality of cysteine metabolism
+HP:0008166,Decreased beta-galactosidase activity,HP:0004342,Abnormality of galactoside metabolism
+UBERON:0013765,digestive system organ,UBERON:0000062,organ
+UBERON:0009564,distal limb integumentary appendage,UBERON:0004121,ectoderm-derived structure
+DOID:3698,bile duct mucinous adenocarcinoma,DOID:4896,bile duct adenocarcinoma
+UBERON:0000978,leg,UBERON:0006058,multi-limb segment region
+UBERON:0005342,malleus head,UBERON:0010313,neural crest-derived structure
+UBERON:0012456,Merkel nerve ending,UBERON:0000470,cell part
+UBERON:0003290,meninx of diencephalon,UBERON:0003548,forebrain meninges
+HP:0009892,Anotia,HP:0008772,Aplasia/Hypoplasia of the external ear
+UBERON:0002240,spinal cord,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009293,Broad middle phalanx of the 4th finger,HP:0009283,Abnormality of the middle phalanx of the 4th finger
+UBERON:0015849,canine tusk,UBERON:0010879,tusk
+CL:0002541,chorionic membrane mesenchymal stem cell,CL:0000134,mesenchymal cell
+HP:0007149,Distal upper limb amyotrophy,HP:0009129,Upper limb amyotrophy
+UBERON:0006645,adventitia of epididymis,UBERON:0005156,reproductive structure
+UBERON:0004714,septum pellucidum,UBERON:0000477,anatomical cluster
+UBERON:4200152,os sesamoides tarsale,UBERON:0008000,sesamoid bone of pes
+DOID:5874,retroperitoneal germ cell neoplasm,DOID:5875,retroperitoneal cancer
+UBERON:0014836,levator arcuum muscle,UBERON:0004164,branchiomeric muscle
+UBERON:2002087,pectoral axillary process,UBERON:0004376,fin bone
+UBERON:3000516,pseudobasal process,UBERON:4100000,skeletal element projection
+UBERON:0012168,umbilical cord blood,UBERON:0000178,blood
+DOID:2120,focal dermal hypoplasia,DOID:0050735,X-linked disease
+CL:0002271,type EC1 enteroendocrine cell,CL:0000505,substance P secreting cell
+HP:0006946,Recurrent meningitis,HP:0011450,CNS infection
+UBERON:3000995,transversal dorsal folds,UBERON:3000991,dorsal folds
+UBERON:3000453,posterolateral vomerine process,UBERON:4100000,skeletal element projection
+DOID:5522,basaloid squamous cell carcinoma,DOID:1749,squamous cell carcinoma
+UBERON:0003908,right atrioventricular canal,UBERON:0015212,lateral structure
+NCBITaxon:10376,Human herpesvirus 4,NCBITaxon:10375,Lymphocryptovirus
+HP:0009708,Synostosis involving the 5th metacarpal,HP:0009701,Metacarpal synostosis
+NCBITaxon:39744,Rubulavirus,NCBITaxon:11159,Paramyxovirinae
+UBERON:0010577,manual digit 3 phalanx pre-cartilage condensation,UBERON:0005693,manual digit 3 mesenchyme
+UBERON:0006919,tongue squamous epithelium,UBERON:0003357,epithelium of tongue
+UBERON:0003607,forelimb long bone,UBERON:0008962,forelimb bone
+DOID:1748,conjunctiva squamous cell carcinoma,DOID:5467,conjunctival cancer
+HP:0009248,Abnormality of the epiphysis of the proximal phalanx of the 4th finger,HP:0009174,Abnormality of the epiphyses of the 4th finger
+UBERON:0004786,gastrointestinal system mucosa,UBERON:0000344,mucosa
+HP:0011689,Supraventricular tachycardia with a concealed accessory connection,HP:0011688,Supraventricular tachycardia with an accessory connection mediated pathway
+UBERON:0010752,exoccipital cartilage element,UBERON:0005863,cartilaginous condensation
+HP:0001896,Reticulocytopenia,HP:0004312,Abnormality of reticulocytes
+HP:0100574,Biliary tract neoplasm,HP:0012440,Abnormal biliary tract morphology
+UBERON:0013201,olfactory pathway,UBERON:0011215,cell part cluster of neuraxis
+HP:0100205,Enlarged epiphysis of the distal phalanx of the 5th toe,HP:0100097,Abnormality of the epiphysis of the distal phalanx of the 5th toe
+HP:0009395,Cone-shaped epiphyses of the 4th finger,HP:0010230,Cone-shaped epiphyses of the phalanges of the hand
+HP:0001904,Autoimmune neutropenia,HP:0002960,Autoimmunity
+UBERON:0002002,interchondral joint,UBERON:0002210,syndesmosis
+UBERON:0001381,semimembranosus muscle,UBERON:0002463,hamstring muscle
+DOID:2436,glomangioma,DOID:5238,benign perivascular tumor
+CL:0002275,pancreatic PP cell,CL:0000696,PP cell
+DOID:3216,jejunal somatostatinoma,DOID:13499,jejunal cancer
+DOID:2044,drug-induced hepatitis,DOID:2237,hepatitis
+UBERON:2001220,basibranchial copula,UBERON:0011004,pharyngeal arch cartilage
+UBERON:0003591,lobar bronchus connective tissue,UBERON:0000114,lung connective tissue
+UBERON:0010558,pedal digit 2 metatarsal cartilage element,UBERON:0010697,pedal digit metatarsal cartilage element
+UBERON:3010636,egg capsules,UBERON:0000478,extraembryonic structure
+DOID:1312,focal segmental glomerulosclerosis,DOID:0050851,glomerulosclerosis
+UBERON:0014795,pelvic appendage muscle,UBERON:0010890,pelvic complex muscle
+DOID:9531,latent syphilis,DOID:4166,syphilis
+CL:1001106,kidney loop of henle thick ascending limb epithelial cell,CL:1001016,kidney loop of henle ascending limb epithelial cell
+UBERON:0001988,feces,UBERON:0000174,excreta
+UBERON:0003269,skeletal muscle tissue of eye,UBERON:0004121,ectoderm-derived structure
+HP:0002206,Pulmonary fibrosis,HP:0002088,Abnormality of the lung
+UBERON:0010075,sacral neural crest,UBERON:0004121,ectoderm-derived structure
+DOID:12756,lacrimal duct cancer,DOID:292,lacrimal system cancer
+UBERON:0004903,bronchoalveolar duct junction,UBERON:0007651,anatomical junction
+UBERON:0000018,compound eye,UBERON:0015165,multi-unit eye
+HP:0008331,Elevated creatine kinase after exercise,HP:0003236,Elevated serum creatine phosphokinase
+UBERON:0007719,bone of reproductive structure,UBERON:0001474,bone element
+UBERON:0002824,vestibular ganglion,UBERON:0001714,cranial ganglion
+DOID:6132,bronchitis,DOID:2320,obstructive lung disease
+HP:0009655,Patchy sclerosis of the phalanges of the thumb,HP:0009772,Patchy sclerosis of the phalanges of the hand
+HP:0006642,Large sternal ossification centers,HP:0011863,Abnormal sternal ossification
+UBERON:0002790,dorsal acoustic stria,UBERON:0002316,white matter
+UBERON:2005380,dorsal fin proximal radial bone 3,UBERON:2105380,dorsal fin proximal radial element 3
+UBERON:2005084,metencephalic artery,UBERON:0001637,artery
+UBERON:0015203,non-connected functional system,UBERON:0000467,anatomical system
+HP:0006239,Shortening of all middle phalanges of the toes,HP:0003795,Short middle phalanx of toe
+UBERON:0001297,serosa of uterus,UBERON:0014404,female anatomical structure
+DOID:5532,ovarian squamous cell neoplasm,DOID:2152,ovary epithelial cancer
+HP:0011039,Abnormality of the helix,HP:0000377,Abnormality of the pinna
+DOID:9042,polyp of corpus uteri,DOID:345,uterine disease
+HP:0009685,Triangular epiphysis of the distal phalanx of the thumb,HP:0009662,Abnormality of the epiphysis of the distal phalanx of the thumb
+HP:0001407,Hepatic cysts,HP:0006706,Cystic liver disease
+UBERON:0006853,renal cortex tubule,UBERON:0007685,region of nephron tubule
+DOID:7241,uterine corpus apoplectic leiomyoma,DOID:7242,uterine corpus cellular leiomyoma
+UBERON:2001956,epibranchial 1 bone proximal cartilage,UBERON:0011004,pharyngeal arch cartilage
+DOID:0050728,glycogen metabolism disorder,DOID:2978,carbohydrate metabolic disorder
+UBERON:0009629,coccygeal nerve,UBERON:0001780,spinal nerve
+UBERON:0011800,dermal pulp of feather shaft,UBERON:0004120,mesoderm-derived structure
+UBERON:2001988,centrum 6,UBERON:0001075,vertebral centrum
+DOID:5026,sclerosing hepatic carcinoma,DOID:684,hepatocellular carcinoma
+DOID:74,hematopoietic system disease,DOID:2914,immune system disease
+DOID:10582,Refsum disease,DOID:3146,lipid metabolism disorder
+HP:0008059,Aplasia/Hypoplasia of the macula,HP:0001103,Abnormality of the macula
+CL:0012001,neuron of the forebrain,CL:0000117,CNS neuron (sensu Vertebrata)
+DOID:1237,corneal degeneration,DOID:10124,corneal disease
+UBERON:3010098,M. plantaris profundus,UBERON:0010890,pelvic complex muscle
+HP:0008063,Aplasia/Hypoplasia of the lens,HP:0008062,Aplasia/Hypoplasia affecting the anterior segment of the eye
+HP:0004871,Perineal fistula,HP:0100589,Urogenital fistula
+UBERON:0002106,spleen,UBERON:0004177,hemopoietic organ
+UBERON:0006232,facio-acoustic VII-VIII preganglion complex,UBERON:0002050,embryonic structure
+HP:0100468,Patchy sclerosis of the distal phalanx of the 4th toe,HP:0010376,Patchy sclerosis of the phalanges of the 4th toe
+CL:1000434,epithelial cell of external acoustic meatus,CL:0002371,somatic cell
+UBERON:3000936,zonal element,UBERON:0000477,anatomical cluster
+UBERON:0002019,accessory XI nerve,UBERON:0001785,cranial nerve
+HP:0010116,Enlarged epiphyses of the hallux,HP:0010165,Enlarged epiphyses of the toes
+HP:0100618,Leydig cell neoplasia,HP:0010788,Testicular neoplasm
+HP:0009943,Complete duplication of the phalanges of the thumb,HP:0009942,Duplication of phalanx of thumb
+HP:0005148,Pulmonary valve defects,HP:0001641,Abnormality of the pulmonary valve
+UBERON:0009472,axilla,UBERON:0000475,organism subdivision
+UBERON:0000163,embryonic cloaca,UBERON:0002050,embryonic structure
+UBERON:0009713,endocardium of left ventricle,UBERON:0001081,endocardium of ventricle
+HP:0011073,Abnormality of dental color,HP:0011061,Abnormality of dental structure
+HP:0009289,Aplasia/Hypoplasia of the distal phalanx of the 4th finger,HP:0009408,Aplasia/Hypoplasia of the phalanges of the 4th finger
+HP:0005974,Episodic ketoacidosis,HP:0001993,Ketoacidosis
+DOID:0050622,reproductive organ benign neoplasm,DOID:0060085,organ system benign neoplasm
+HP:0001337,Tremor,HP:0100022,Abnormality of movement
+DOID:5396,prolactin producing pituitary tumor,DOID:5716,hormone producing pituitary cancer
+HP:0010465,Precocious puberty in females,HP:0000826,Precocious puberty
+UBERON:3000773,ilial ridge,UBERON:0004530,bony projection
+HP:0000138,Ovarian cysts,HP:0000137,Abnormality of the ovary
+HP:0001972,Macrocytic anemia,HP:0010972,Anemia of inadequate production
+UBERON:0002883,central amygdaloid nucleus,UBERON:0009663,telencephalic nucleus
+UBERON:0003281,mesentery of stomach,UBERON:0004854,gastrointestinal system mesentery
+DOID:4856,gliofibroma,DOID:3069,astrocytoma
+DOID:14118,familial lipoprotein lipase deficiency,DOID:1168,familial hyperlipidemia
+HP:0011544,L-looping of the right ventricle,HP:0011534,Abnormal spatial orientation of the cardiac segments
+DOID:7650,pulmonary type ovarian small cell carcinoma,DOID:6179,ovarian small cell carcinoma
+UBERON:0011592,future upper lip,UBERON:0003235,epithelium of upper jaw
+HP:0100391,Short distal phalanx of the 5th toe,HP:0100371,Aplasia/Hypoplasia of the distal phalanx of the 5th toe
+DOID:12145,detrusor sphincter dyssynergia,DOID:365,bladder disease
+NCBITaxon:34608,Amblyomma hebraeum,NCBITaxon:6942,Amblyomma
+UBERON:4200032,clavicle blade,UBERON:0005055,zone of long bone
+DOID:1869,chronic rheumatic pericarditis,DOID:1787,pericarditis
+UBERON:0008321,deep artery of penis,UBERON:0004573,systemic artery
+HP:0012330,Pyelonephritis,HP:0000123,Nephritis
+HP:0000375,Abnormality of cochlea,HP:0011390,Morphological abnormality of the inner ear
+UBERON:0005787,lamina densa of glomerular basement membrane,UBERON:0006554,urinary system structure
+DOID:14176,selective IgG deficiency disease,DOID:11702,dysgammaglobulinemia
+HP:0100535,Tibiofibular diastasis,HP:0002991,Abnormality of the fibula
+UBERON:0005564,gonad primordium,UBERON:0005156,reproductive structure
+CL:0000586,germ cell,CL:0000039,germ line cell
+CL:0002550,fibroblast of the conjuctiva,CL:0000057,fibroblast
+UBERON:0012476,skeleton of pelvic complex,UBERON:0010912,subdivision of skeleton
+CL:0002315,supporting cell of cochlea,CL:0001035,bone cell
+UBERON:2000946,hypaxial region somite 16,UBERON:0003895,hypaxial myotome region
+HP:0001933,Subcutaneous hemorrhage,HP:0001892,Abnormal bleeding
+DOID:8913,dermatophytosis,DOID:0050134,cutaneous mycosis
+HP:0002826,Halberd-shaped pelvis,HP:0002644,Abnormality of pelvic girdle bone morphology
+UBERON:3000281,margo orbitalis of maxilla,UBERON:0010313,neural crest-derived structure
+DOID:0060143,integrative agnosia,DOID:4090,agnosia
+UBERON:0005340,dorsal telencephalic commissure,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0015135,primary lactiferous duct,UBERON:0001765,mammary duct
+HP:0009219,Irregular epiphysis of the middle phalanx of the 4th finger,HP:0009247,Abnormality of the epiphysis of the middle phalanx of the 4th finger
+DOID:9249,Beemer-Langer syndrome,DOID:225,syndrome
+UBERON:0005728,extraembryonic mesoderm,UBERON:0007524,dense mesenchyme tissue
+UBERON:0010173,sinotubular junction,UBERON:0004120,mesoderm-derived structure
+UBERON:0014606,infundibular stem,UBERON:0002784,regional part of diencephalon
+UBERON:0002633,motor nucleus of trigeminal nerve,UBERON:0002925,trigeminal nucleus
+DOID:11705,impaired renal function disease,DOID:557,kidney disease
+DOID:13160,scrotum melanoma,DOID:518,scrotum neoplasm
+HP:0007009,Central nervous system degeneration,HP:0007367,Atrophy/Degeneration affecting the central nervous system
+DOID:6016,adult central nervous system mature teratoma,DOID:6017,central nervous system mature teratoma
+HP:0000048,Bifid scrotum,HP:0000045,Abnormality of the scrotum
+HP:0007213,Late-onset form of familial Alzheimer disease,HP:0002511,Alzheimer disease
+HP:0000047,Hypospadias,HP:0100627,Displacement of the external urethral meatus
+DOID:0050353,wound botulism,DOID:11976,botulism
+HP:0012415,Abnormal blood gas level,HP:0002795,Functional respiratory abnormality
+HP:0010179,Symphalangism affecting the phalanges of the toes,HP:0010161,Abnormality of the phalanges of the toes
+HP:0008132,Medial rotation of the medial malleolus,HP:0001760,Abnormality of the foot
+DOID:9842,total circumpapillary dystrophy of choroid,DOID:9794,hereditary choroidal atrophy
+UBERON:0011969,mesotarsal joint,UBERON:0001487,pes joint
+HP:0011194,EEG with series of focal spikes,HP:0011193,EEG with focal spikes
+DOID:12359,endocrine exophthalmos,DOID:930,orbital disease
+HP:0005116,Arterial tortuosity,HP:0004948,Vascular tortuosity
+UBERON:0000392,longissimus muscle,UBERON:0004518,muscle of vertebral column
+DOID:0050159,lymphoid interstitial pneumonia,DOID:2797,idiopathic interstitial pneumonia
+UBERON:0014729,striated duct of salivary gland,UBERON:0001837,duct of salivary gland
+UBERON:0007840,spinal cord dorsal white commissure,UBERON:0007838,spinal cord white commissure
+HP:0008742,Prominent prostate median bar,HP:0008775,Abnormality of the prostate
+HP:0003089,Hamstring contractures,HP:0005750,Contractures of the joints of the lower limbs
+HP:0009954,Complete duplication of the proximal phalanx of the 2nd finger,HP:0009957,Complete duplication of the phalanges of the 2nd finger
+HP:0006386,Hypoplastic distal radial epiphyses,HP:0010597,Abnormality of the distal radial epiphysis
+HP:0001636,Tetralogy of Fallot,HP:0001710,Conotruncal defect
+UBERON:2001724,caudal principal ray 12,UBERON:2001585,caudal principal ray
+HP:0009551,Patchy sclerosis of the phalanges of the 2nd finger,HP:0009772,Patchy sclerosis of the phalanges of the hand
+CL:0000562,nucleate erythrocyte,CL:0002242,nucleate cell
+HP:0012400,Abnormal aldolase level,HP:0012379,Abnormal enzyme/coenzyme activity
+UBERON:0009569,subdivision of trunk,UBERON:0000475,organism subdivision
+UBERON:3000111,crista dentalis of maxilla,UBERON:0010313,neural crest-derived structure
+UBERON:0001944,pretectal region,UBERON:0003528,brain grey matter
+HP:0011311,Sydney crease,HP:0010490,Abnormality of the palmar creases
+UBERON:2002062,branched caudal fin ray,UBERON:4000174,caudal fin lepidotrichium
+UBERON:0006197,auricular vein,UBERON:0003496,head blood vessel
+HP:0000875,Episodic hypertension,HP:0000822,Hypertension
+NCBITaxon:34104,Streptobacillus,NCBITaxon:1129771,Leptotrichiaceae
+DOID:11914,gastroparesis,DOID:1159,functional gastric disease
+DOID:218,ascending colon cancer,DOID:219,colon cancer
+UBERON:0008603,helicis major,UBERON:0001596,intrinsic auricular muscle
+HP:0004860,Thiamine-responsive megaloblastic anemia,HP:0001889,Megaloblastic anemia
+HP:0000357,Abnormal location of ears,HP:0000356,Abnormality of the outer ear
+UBERON:0001233,right adrenal gland,UBERON:0002369,adrenal gland
+DOID:3312,bipolar disorder,DOID:3324,mood disorder
+UBERON:3000141,endolymphatic system,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2000371,internal pharyngoclavicularis,UBERON:0000933,pharyngeal muscle
+UBERON:0006905,mandibular process mesenchyme,UBERON:0004121,ectoderm-derived structure
+HP:0009337,Cone-shaped epiphysis of the distal phalanx of the 3rd finger,HP:0010248,Cone-shaped epiphyses of the distal phalanges of the hand
+DOID:1788,peritoneal mesothelioma,DOID:1725,peritoneum cancer
+HP:0002587,Projectile vomiting,HP:0002013,Vomiting
+UBERON:3010673,m. rhomboideus anterior,UBERON:0010891,pectoral complex muscle
+UBERON:0008440,webbed autopod,UBERON:0002470,autopod region
+UBERON:0006205,pectineal ligament,UBERON:0000064,organ part
+DOID:3740,vulva verrucous carcinoma,DOID:2101,vulva squamous cell carcinoma
+UBERON:0000424,gastric pit,UBERON:0002553,anatomical cavity
+UBERON:0003853,spinal cord neural crest,UBERON:0002342,neural crest
+UBERON:3000692,pedicel,UBERON:0004120,mesoderm-derived structure
+DOID:3307,teratoma,DOID:3095,germ cell and embryonal cancer
+CL:1000547,kidney inner medulla collecting duct epithelial cell,CL:1000546,kidney medulla collecting duct epithelial cell
+UBERON:0003884,CA4 field of hippocampus,UBERON:0003876,subdivision of hippocampus
+HP:0011593,Left aortic arch with retroesophageal diverticulum of Kommerell,HP:0011587,Abnormal branching pattern of the aortic arch
+UBERON:3000685,foramen nervi hypoglossi,UBERON:3000681,hyoid apparatus opening
+UBERON:2001229,pharyngeal arch 7 skeleton,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0006858,adrenal/interrenal gland,UBERON:0005172,abdomen organ
+DOID:5700,gastric liposarcoma,DOID:10534,stomach cancer
+DOID:3082,interstitial lung disease,DOID:850,lung disease
+DOID:0050764,Armfield syndrome,DOID:225,syndrome
+HP:0100575,Neoplasm of the gallbladder,HP:0100574,Biliary tract neoplasm
+UBERON:0006297,sublingual gland primordium,UBERON:0001048,primordium
+UBERON:0009099,typhlosole,UBERON:0005423,developing anatomical structure
+HP:0011530,Retinal hole,HP:0011958,Retinal perforation
+NCBITaxon:121225,Pediculus humanus,NCBITaxon:121222,Pediculus
+DOID:6936,ureter urothelial papilloma,DOID:11885,ureteral benign neoplasm
+UBERON:0005787,lamina densa of glomerular basement membrane,UBERON:0004120,mesoderm-derived structure
+HP:0003982,Absent ulna,HP:0003953,Absent ossification/absent forearm bones
+UBERON:0013492,prevertebral cervical fascia,UBERON:0004923,organ component layer
+UBERON:0010024,ventral part of pharyngeal pouch 2,UBERON:0005911,endo-epithelium
+UBERON:0004130,cerebellar layer,UBERON:0003528,brain grey matter
+DOID:4837,Gorham's disease,DOID:225,syndrome
+HP:0009090,Facial diplegic appearance,HP:0001349,Facial diplegia
+DOID:11656,cicatricial pemphigoid,DOID:8502,bullous skin disease
+HP:0011409,Abnormality of placental membranes,HP:0001194,Abnormalities of placenta and umbilical cord
+DOID:6707,malignant triton tumor,DOID:5940,malignant peripheral nerve sheath tumor
+UBERON:0001487,pes joint,UBERON:0003840,hindlimb joint
+DOID:8440,ileus,DOID:8437,intestinal obstruction
+UBERON:0010739,distal carpal bone 5,UBERON:0015096,distal carpal bone 5 endochondral element
+DOID:8410,childhood kidney angiomyolipoma,DOID:3675,childhood kidney neoplasm
+UBERON:0014478,rib skeletal system,UBERON:0000075,subdivision of skeletal system
+DOID:3265,chronic granulomatous disease,DOID:3262,phagocyte bactericidal dysfunction
+HP:0001279,Syncope,HP:0011025,Abnormality of cardiovascular system physiology
+HP:0002152,Hyperproteinemia,HP:0010876,Abnormality of circulating protein level
+UBERON:0002748,medial lemniscus of medulla,UBERON:0014649,white matter of medulla oblongata
+HP:0008820,Absent ossification of capital femoral epiphysis,HP:0009107,Abnormal ossification involving the femoral head and neck
+NCBITaxon:5500,Coccidioides,NCBITaxon:34383,mitosporic Onygenales
+UBERON:0015010,sacral vertebra endochondral element,UBERON:0010363,endochondral element
+DOID:0050723,PSAT deficiency,DOID:0050721,serine deficiency
+HP:0009178,Symphalangism of middle phalanx of 5th finger,HP:0004218,Symphalangism of the 5th finger
+UBERON:0004899,right lung cranial lobe lobar bronchus mesenchyme,UBERON:0004901,right lung lobar bronchus mesenchyme
+DOID:10081,syphilitic encephalitis,DOID:9588,encephalitis
+HP:0000931,Thinning and bulging of the posterior fossa bones,HP:0000932,Abnormality of the posterior cranial fossa
+HP:0002377,Paraganglioma-related cranial nerve palsy,HP:0006824,Cranial nerve paralysis
+DOID:1254,trichostrongylosis,DOID:1255,trichostrongyloidiasis
+UBERON:0005368,hippocampus molecular layer,UBERON:0002305,layer of hippocampus
+HP:0005977,Hypochloremic metabolic alkalosis,HP:0001948,Alkalosis
+HP:0009382,Absent epiphyses of the 5th finger,HP:0009152,Abnormality of the epiphyses of the 5th finger
+DOID:0060117,peritoneal benign neoplasm,DOID:0060085,organ system benign neoplasm
+UBERON:0013554,Brodmann (1909) area 23,UBERON:0013529,Brodmann area
+HP:0003610,Fibroblast metachromasia,HP:0003653,Cellular metachromasia
+HP:0001578,Hypercortisolism,HP:0002717,Adrenal overactivity
+CL:0005015,inner phalangeal cell,CL:0002165,phalangeal cell
+DOID:7613,sarcomatosis of the meninges,DOID:7614,meninges sarcoma
+UBERON:0014844,pubioischiofemoralis externus muscle,UBERON:0014842,pubioischiofemoralis muscle
+UBERON:3010144,odontoids,UBERON:0000064,organ part
+UBERON:3000999,dorsal pouch,UBERON:3000977,body external integument structure
+HP:0002965,Cutaneous anergy,HP:0002963,Abnormal delayed hypersensitivity skin test
+UBERON:0010402,epidermis suprabasal layer,UBERON:0004923,organ component layer
+CL:0002098,regular cardiac myocyte,CL:0000746,cardiac muscle cell
+UBERON:4100000,skeletal element projection,UBERON:0004529,anatomical projection
+HP:0003150,Glutaric aciduria,HP:0003215,Dicarboxylic aciduria
+DOID:5550,choriocarcinoma of ovary,DOID:2155,malignant ovarian germ cell neoplasm
+HP:0100914,Sclerosis of the 1st metacarpal,HP:0100922,Sclerosis of the phalanges of the thumb
+UBERON:0003593,thoracic cavity connective tissue,UBERON:0002384,connective tissue
+HP:0007550,Hypohidrosis/hyperhidrosis,HP:0000971,Abnormality of the sweat gland
+UBERON:0005192,deferent duct artery,UBERON:0006554,urinary system structure
+HP:0007782,Peripheral retinal cone degeneration,HP:0007769,Peripheral retinal degeneration
+HP:0100051,Pseudoepiphyses of the 2nd toe,HP:0010169,Pseudoepiphyses of the toes
+UBERON:0015008,thoracic vertebra endochondral element,UBERON:0005174,dorsal region organ
+HP:0011179,Beta-EEG,HP:0011176,EEG with constitutional variants
+HP:0009527,Enlarged epiphysis of the proximal phalanx of the 2nd finger,HP:0009491,Enlarged epiphyses of the 2nd finger
+CL:0010011,cerebral cortex GABAergic interneuron,CL:0000617,GABAergic neuron
+HP:0003397,Generalized hypotonia due to defect at the neuromuscular junction,HP:0001290,Generalized hypotonia
+HP:0100384,Absent proximal phalanx of the 3rd toe,HP:0100362,Aplasia of the phalanges of the 3rd toe
+HP:0009810,Abnormality of the joints of the upper limbs,HP:0002817,Abnormality of the upper limb
+DOID:10354,breast fibrocystic disease,DOID:0060082,breast benign neoplasm
+UBERON:0014680,distal interphalangeal joint of digit 5,UBERON:0009768,distal interphalangeal joint
+HP:0003850,Irregular metaphyses of the upper limbs,HP:0009809,Abnormality of upper limb metaphysis
+UBERON:3000952,posterior radial,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0009743,visceral yolk sac cavity,UBERON:0000464,anatomical space
+DOID:5746,ovarian serous cystadenocarcinoma,DOID:3605,ovarian cystadenocarcinoma
+NCBITaxon:64895,Borrelia burgdorferi group,NCBITaxon:138,Borrelia
+UBERON:0005497,non-neural ectoderm,UBERON:0000479,tissue
+UBERON:0002078,right cardiac atrium,UBERON:0015212,lateral structure
+UBERON:0007842,membrane bone,UBERON:0001474,bone element
+DOID:7953,nipple duct carcinoma,DOID:6629,nipple carcinoma
+UBERON:0015181,neck of tooth,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001706,nasal septum,UBERON:0010313,neural crest-derived structure
+DOID:13034,relapsing fever,DOID:0050338,primary bacterial infectious disease
+NCBITaxon:11082,West Nile virus,NCBITaxon:11071,Japanese encephalitis virus group
+UBERON:0013751,metaphysis of radius,UBERON:0001438,metaphysis
+UBERON:0001835,lower lip,UBERON:0001833,lip
+UBERON:0011390,pudendal nerve,UBERON:0015212,lateral structure
+UBERON:0005462,lower back,UBERON:0009569,subdivision of trunk
+UBERON:2000869,epaxial region somite 23,UBERON:0003900,epaxial myotome region
+UBERON:0001505,coracobrachialis muscle,UBERON:0004255,forelimb stylopod muscle
+UBERON:0010988,teres major pre-muscle mass,UBERON:0005865,pre-muscle condensation
+DOID:0050743,mature T-cell and NK-cell lymphoma,DOID:0060060,non-Hodgkin lymphoma
+UBERON:0007391,pelvic appendage cartilage tissue,UBERON:0004120,mesoderm-derived structure
+HP:0012596,Moderate proteinuria,HP:0000093,Proteinuria
+UBERON:0001735,tonsillar ring,UBERON:0004119,endoderm-derived structure
+UBERON:0007330,rhamphotheca,UBERON:0004121,ectoderm-derived structure
+UBERON:3000560,septum semicircularium anterior,UBERON:0003037,septum
+HP:0012278,Abnormality of serine metabolism,HP:0010894,Abnormality of serine family amino acid metabolism
+UBERON:0001167,wall of stomach,UBERON:0009034,stomach region
+DOID:4008,fallopian tube transitional cell carcinoma,DOID:1963,fallopian tube carcinoma
+DOID:2796,desquamative interstitial pneumonia,DOID:2797,idiopathic interstitial pneumonia
+HP:0010208,Patchy sclerosis of the proximal phalanges of the toes,HP:0100946,Sclerosis of the proximal phalanges of the toes
+UBERON:1000007,forehead protuberance,UBERON:0001444,subdivision of head
+DOID:11165,common wart,DOID:934,viral infectious disease
+HP:0007649,Congenital hypertrophy of retinal pigment epithelium,HP:0011512,Hyperpigmentation of the fundus
+DOID:5916,uterine corpus leiomyomatosis,DOID:0060095,uterine benign neoplasm
+DOID:14766,renal agenesis,DOID:557,kidney disease
+DOID:5169,ovarian endometrioid stromal sarcoma,DOID:2146,ovary sarcoma
+DOID:9906,frontalis acne,DOID:6543,acne
+HP:0002990,Fibular aplasia,HP:0006492,Aplasia/Hypoplasia of the fibula
+UBERON:4200183,bicipital tuberosity,UBERON:0005813,tubercle
+UBERON:0005659,primary palate epithelium,UBERON:0012275,meso-epithelium
+CL:0002338,"CD56-positive, CD161-positive immature natural killer cell",CL:0000823,immature natural killer cell
+NCBITaxon:4753,Pneumocystis,NCBITaxon:44281,Pneumocystidaceae
+UBERON:2001624,type 2 odontode,UBERON:2001622,odontode
+DOID:7566,eccrine porocarcinoma,DOID:4921,eccrine sweat gland cancer
+HP:0002058,Myopathic facies,HP:0004673,Decreased facial expression
+DOID:931,monieziasis,DOID:883,parasitic helminthiasis infectious disease
+HP:0003328,Abnormal hair laboratory examination,HP:0001595,Abnormality of the hair
+DOID:7037,childhood immature teratoma of ovary,DOID:6230,childhood teratoma of the ovary
+UBERON:0011824,fibrous connective tissue,UBERON:0011822,dense irregular connective tissue
+UBERON:0003862,pedal digit 4 phalanx,UBERON:0001449,phalanx of pes
+UBERON:0011799,cavity of feather shaft,UBERON:0002553,anatomical cavity
+UBERON:0002697,dorsal supraoptic decussation,UBERON:0011590,commissure of diencephalon
+HP:0003080,Hydroxyprolinuria,HP:0003355,Aminoaciduria
+UBERON:0007194,vesicular gland,UBERON:0010147,male accessory sex gland
+UBERON:0006904,head mesenchyme from mesoderm,UBERON:0005253,head mesenchyme
+DOID:4378,peanut allergic reaction,DOID:3044,food allergy
+DOID:13371,scrub typhus,DOID:11256,typhus
+UBERON:0002228,rib,UBERON:0015212,lateral structure
+UBERON:0001688,incus bone,UBERON:0002513,endochondral bone
+HP:0011476,Profound sensorineural hearing impairment,HP:0012715,Profound hearing impairment
+UBERON:0009120,gill filament,UBERON:0000479,tissue
+UBERON:0004641,spleen capsule,UBERON:0004120,mesoderm-derived structure
+HP:0000871,Panhypopituitarism,HP:0000830,Anterior hypopituitarism
+UBERON:0006289,rib pre-cartilage condensation,UBERON:0015019,rib endochondral element
+NCBITaxon:11036,Venezuelan equine encephalitis virus,NCBITaxon:177872,VEEV complex
+HP:0008047,Abnormality of the vasculature of the eye,HP:0002597,Abnormality of the vasculature
+UBERON:0003679,mouth floor,UBERON:0001444,subdivision of head
+DOID:1679,cystitis,DOID:365,bladder disease
+UBERON:2000698,tripus,UBERON:0002513,endochondral bone
+UBERON:0006721,alisphenoid bone,UBERON:0011164,neurocranium bone
+HP:0003458,EMG: myopathic abnormalities,HP:0003198,Myopathy
+DOID:4953,poliomyelitis,DOID:934,viral infectious disease
+HP:0004886,Congenital laryngeal stridor,HP:0005348,Inspiratory stridor
+CL:0000697,R4 photoreceptor cell,CL:0000488,visible light photoreceptor cell
+UBERON:2001690,anterior cartilage of palatine,UBERON:0004121,ectoderm-derived structure
+HP:0003470,Paralysis,HP:0011442,Abnormality of central motor function
+NCBITaxon:1817,Nocardia,NCBITaxon:85025,Nocardiaceae
+HP:0100125,Enlarged epiphysis of the proximal phalanx of the 2nd toe,HP:0100047,Enlarged epiphyses of the 2nd toe
+HP:0005327,Loss of facial expression,HP:0004673,Decreased facial expression
+NCBITaxon:476427,Xenopsyllinae,NCBITaxon:7511,Pulicidae
+UBERON:0001664,inferior cerebral vein,UBERON:0001663,cerebral vein
+NCBITaxon:7711,Chordata,NCBITaxon:33511,Deuterostomia
+UBERON:0002292,costovertebral joint,UBERON:0002001,joint of rib
+CL:0002049,Fraction C precursor B cell,CL:0002400,Fraction B/C precursor B cell
+CL:0000578,experimentally modified cell in vitro,CL:0001034,cell in vitro
+UBERON:0001963,bronchial-associated lymphoid tissue,UBERON:0001961,mucosa-associated lymphoid tissue
+UBERON:0008835,hepatic diverticulum,UBERON:0004185,endodermal part of digestive tract
+HP:0004240,Sclerotic foci within carpal bones,HP:0004054,Sclerosis of hand bones
+DOID:6460,large intestine lipoma,DOID:4610,intestinal benign neoplasm
+UBERON:2001699,dorsal-fin stay,UBERON:0004247,bone of dorsum
+DOID:1278,tolosa-hunt syndrome,DOID:1279,ocular motility disease
+HP:0005588,Patchy palmoplantar keratoderma,HP:0000982,Palmoplantar keratoderma
+DOID:2497,enamel erosion,DOID:2498,tooth erosion
+HP:0000789,Infertility,HP:0000144,Decreased fertility
+HP:0009338,Enlarged epiphysis of the distal phalanx of the 3rd finger,HP:0010249,Enlarged epiphyses of the distal phalanges of the hand
+DOID:6627,cervical adenoma malignum,DOID:3701,cervical mucinous adenocarcinoma
+UBERON:0015091,distal carpal bone 3 cartilage,UBERON:0015090,distal carpal bone 3 endochondral element
+HP:0009200,Pseudoepiphysis of the proximal phalanx of the 5th finger,HP:0010275,Pseudoepiphyses of the proximal phalanges of the hand
+CL:0000654,primary oocyte,CL:0000023,oocyte
+HP:0100553,Hemihypertrophy of lower limb,HP:0100559,Lower limb asymmetry
+HP:0200022,Choroid plexus papilloma,HP:0007376,Abnormality of the choroid plexus
+HP:0012591,Abnormal urinary electrolyte concentration,HP:0003110,Abnormality of urine homeostasis
+DOID:2368,gangliosidosis,DOID:1443,cerebral degeneration
+HP:0007656,Lacrimal gland aplasia,HP:0008038,Aplastic/hypoplastic lacrimal glands
+HP:0004438,Hyperostosis frontalis interna,HP:0004437,Cranial hyperostosis
+HP:0009976,Duplication of the middle phalanx of the 4th finger,HP:0010008,Duplication of the middle phalanx of hand
+HP:0003133,Abnormality of the spinocerebellar tracts,HP:0002143,Abnormality of the spinal cord
+UBERON:0012106,baleen plate bristle,UBERON:0004121,ectoderm-derived structure
+UBERON:0009650,cortical arch of kidney,UBERON:0006554,urinary system structure
+DOID:5325,Roberts syndrome,DOID:0050737,autosomal recessive disease
+UBERON:0013162,right lateral ventricle,UBERON:0015212,lateral structure
+UBERON:0007769,medial preoptic region,UBERON:0003048,regional part of hypothalamus
+NCBITaxon:3193,Embryophyta,NCBITaxon:131221,Streptophytina
+HP:0010295,Aplasia/Hypoplasia of the tongue,HP:0000157,Abnormality of the tongue
+UBERON:3000333,olfactory foramen,UBERON:3000316,nasal opening
+HP:0007553,Congenital symmetrical palmoplantar keratosis,HP:0000972,Palmoplantar hyperkeratosis
+HP:0009808,Anomaly of the upper limb diaphyses,HP:0006504,Anomaly of the limb diaphyses
+HP:0009528,Fragmentation of the epiphysis of the proximal phalanx of the 2nd finger,HP:0009501,Abnormality of the epiphysis of the proximal phalanx of the 2nd finger
+UBERON:0001754,dental pulp,UBERON:0011825,loose connective tissue
+HP:0009683,Small epiphysis of the distal phalanx of the thumb,HP:0009694,Small epiphyses of the thumb
+UBERON:0003381,cardiac muscle of right ventricle,UBERON:0001133,cardiac muscle tissue
+HP:0009301,Short proximal phalanx of the 4th finger,HP:0009300,Aplasia/Hypoplasia of the proximal phalanx of the 4th finger
+HP:0011277,Abnormality of the urinary system physiology,HP:0000079,Abnormality of the urinary system
+UBERON:3001008,body wart,UBERON:3000977,body external integument structure
+UBERON:0003904,bursal plica,UBERON:0004120,mesoderm-derived structure
+UBERON:0002219,subfornical organ,UBERON:0010135,sensory circumventricular organ
+UBERON:4200006,infraglenoid buttress,UBERON:4100000,skeletal element projection
+UBERON:0006838,anterior ramus of spinal nerve,UBERON:0001021,nerve
+UBERON:0000985,axillary vein,UBERON:0001638,vein
+UBERON:2001534,pharyngobranchial 3 cartilage,UBERON:2001533,pharyngobranchial cartilage
+DOID:13113,cicatricial entropion,DOID:12397,entropion
+HP:0004570,Increased vertebral height,HP:0003312,Abnormal form of the vertebral bodies
+HP:0012532,Chronic pain,HP:0012531,Pain
+UBERON:0000127,facial nucleus,UBERON:0002680,regional part of metencephalon
+HP:0002908,Conjugated hyperbilirubinemia,HP:0002904,Hyperbilirubinemia
+UBERON:0006035,interdigital region between manual digits 4 and 5,UBERON:0006013,interdigital region between manual digits
+HP:0005679,Dupuytren contracture,HP:0009473,Joint contracture of the hand
+CL:1000277,smooth muscle fiber of jejunum,CL:1000275,smooth muscle cell of small intestine
+DOID:3001,female reproductive endometrioid cancer,DOID:120,female reproductive organ cancer
+CL:1001577,tonsil squamous cell,CL:0002251,epithelial cell of alimentary canal
+HP:0006771,Duodenal carcinoma,HP:0002672,Gastrointestinal carcinoma
+UBERON:0002236,costal cartilage,UBERON:0002418,cartilage tissue
+UBERON:0008823,neural tube derived brain,UBERON:0000489,cavitated compound organ
+DOID:9698,gonococcal endophthalmia,DOID:4692,endophthalmitis
+DOID:10022,ampulla of vater neoplasm,DOID:1737,duodenal benign neoplasm
+HP:0001696,Situs inversus totalis,HP:0001651,Dextrocardia
+DOID:227,ankylosis,DOID:381,arthropathy
+UBERON:0008465,abductor pollicis brevis muscle,UBERON:0011534,abductor pollicis muscle
+HP:0009976,Duplication of the middle phalanx of the 4th finger,HP:0009972,Duplication of phalanx of 4th finger
+UBERON:2000530,lapillus,UBERON:0002280,otolith
+HP:0001695,Cardiac arrest,HP:0011675,Arrhythmia
+HP:0010435,Short middle phalanx of the 2nd toe,HP:0010431,Short phalanx of the 2nd toe
+DOID:4203,brain stem cancer,DOID:4706,infratentorial cancer
+UBERON:2000525,intercalarium,UBERON:2000461,Weberian ossicle
+HP:0009202,Fragmentation of the epiphysis of the proximal phalanx of the 5th finger,HP:0009386,Fragmentation of the epiphyses of the 5th finger
+HP:0001139,Choroideremia,HP:0000610,Abnormality of the choroid
+UBERON:3000018,anterior ramus of pterygoid,UBERON:4100000,skeletal element projection
+UBERON:0003981,primordial ovarian follicle,UBERON:0001305,ovarian follicle
+DOID:4359,amelanotic melanoma,DOID:1909,melanoma
+UBERON:0002279,vestibular aqueduct,UBERON:0010313,neural crest-derived structure
+HP:0004467,Preauricular pit,HP:0100277,Periauricular skin pits
+UBERON:2007024,anterior neural keel,UBERON:0000479,tissue
+HP:0008424,Hypoplastic 5th lumbar vertebrae,HP:0008417,Vertebral hypoplasia
+HP:0004016,Cupped radial metaphyses,HP:0004015,Abnormality of radial metaphyses
+UBERON:3010131,orbital cartilages,UBERON:0004120,mesoderm-derived structure
+HP:0009256,Ivory epiphysis of the distal phalanx of the 4th finger,HP:0010252,Ivory epiphyses of the distal phalanges of the hand
+HP:0100084,Pseudoepiphyses of the 5th toe,HP:0010341,Abnormality of the epiphyses of the 5th toe
+HP:0011782,Thyroid crisis,HP:0000836,Hyperthyroidism
+UBERON:0010377,mesenchyme from somatopleure,UBERON:0004120,mesoderm-derived structure
+DOID:5537,squamous cell bile duct carcinoma,DOID:4897,bile duct carcinoma
+HP:0010201,Triangular shaped middle phalanges of the toes,HP:0010180,Triangular shaped phalanges of the toes
+UBERON:0000002,uterine cervix,UBERON:0005156,reproductive structure
+HP:0100403,Duplication of the middle phalanx of the 5th toe,HP:0010393,Abnormality of the middle phalanx of the 5th toe
+HP:0011614,Interrupted aortic arch type C,HP:0011611,Interrupted aortic arch
+CL:0000931,activated type II NK T cell,CL:0000922,type II NK T cell
+HP:0009988,Duplication of the distal phalanx of the 5th finger,HP:0009883,Duplication of the distal phalanx of hand
+HP:0002946,Supernumerary vertebrae,HP:0003468,Abnormality of the vertebrae
+DOID:5510,pineal dysgerminoma,DOID:1660,malignant pineal area germ cell neoplasm
+HP:0010224,Abnormality of the epiphysis of the 4th metacarpal,HP:0010012,Abnormality of the 4th metacarpal
+UBERON:2005411,common crus,UBERON:0004121,ectoderm-derived structure
+UBERON:0001482,muscle of shoulder,UBERON:0010891,pectoral complex muscle
+CL:1000354,microfold cell of epithelium of intestinal villus,CL:1000353,microfold cell of epithelium of small intestine
+UBERON:0005120,metanephric late distal convoluted tubule,UBERON:0005134,metanephric nephron epithelium
+UBERON:0015103,distal tarsal bone 1 cartilage,UBERON:0015102,distal tarsal bone 1 endochondral element
+HP:0012560,Decreased T3/T4 ratio,HP:0012558,Abnormal T3/T4 ratio
+CL:0000024,oogonial cell,CL:0000021,female germ cell
+HP:0000086,Ectopic kidney,HP:0100542,Abnormal localization of kidney
+NCBITaxon:28314,Aleutian mink disease virus,NCBITaxon:310911,Amdovirus
+HP:0011070,Abnormality of molar morphology,HP:0006482,Abnormality of dental morphology
+HP:0008952,Shoulder muscle hypoplasia,HP:0001464,Aplasia/Hypoplasia involving the shoulder musculature
+UBERON:2002087,pectoral axillary process,UBERON:0008907,dermal bone
+HP:0009378,Triangular shaped phalanges of the 5th finger,HP:0004213,Abnormality of the phalanges of the 5th finger
+HP:0005335,Sleepy facial expression,HP:0005324,Disturbance of facial expression
+UBERON:0011142,axial ossicle,UBERON:0010911,ossicle
+HP:0009234,Symphalangism of the proximal phalanx of the 5th finger with the 5th metatcarpal,HP:0009708,Synostosis involving the 5th metacarpal
+UBERON:0000955,brain,UBERON:0000062,organ
+UBERON:0007799,mixed dentition,UBERON:0003672,dentition
+DOID:2914,immune system disease,DOID:7,disease of anatomical entity
+DOID:0050461,aspartylglucosaminuria,DOID:3211,lysosomal storage disease
+UBERON:0004785,respiratory system mucosa,UBERON:0000344,mucosa
+HP:0008969,Leg muscle stiffness,HP:0003552,Muscle stiffness
+DOID:0060122,integumentary system cancer,DOID:0050686,organ system cancer
+UBERON:0009050,nucleus of solitary tract,UBERON:0011775,vagus nerve nucleus
+UBERON:0010397,efferent lymphatic vessel,UBERON:0001473,lymphatic vessel
+HP:0009616,Bifid first metacarpal,HP:0009609,Duplication of the 1st metacarpal
+UBERON:0010944,posterior belly of digastric,UBERON:0010940,belly of digastric
+HP:0012470,Setting-sun eye phenomenon,HP:0000597,Ophthalmoparesis
+CL:0002540,mesenchymal stem cell of the bone marrow,CL:0000134,mesenchymal cell
+UBERON:0013658,corpus cavernosum maxillaris,UBERON:0003103,compound organ
+UBERON:0006646,muscle layer of epididymis,UBERON:0005156,reproductive structure
+UBERON:0009202,vasa recta descending limb,UBERON:0004120,mesoderm-derived structure
+UBERON:0001838,sublingual duct,UBERON:0001837,duct of salivary gland
+UBERON:0002157,nucleus raphe pallidus,UBERON:0002677,regional part of medullary raphe nuclear complex
+UBERON:0002534,paired fin,UBERON:0008897,fin
+UBERON:3010661,ramus nasalis internus,UBERON:0000348,ophthalmic nerve
+UBERON:0010557,pedal digit 1 metatarsal cartilage element,UBERON:0010697,pedal digit metatarsal cartilage element
+UBERON:0003695,metacarpophalangeal joint,UBERON:0001489,manus joint
+HP:0010880,Increased nuchal translucency,HP:0000969,Edema
+UBERON:0010257,6th arch mesenchyme from neural crest,UBERON:0010258,mesenchyme from rhombencephalic neural crest
+HP:0003881,Humeral sclerosis,HP:0006392,Increased density of long bones
+DOID:13198,endemic goiter,DOID:5113,nutritional deficiency disease
+UBERON:0002506,iris epithelium,UBERON:0000488,atypical epithelium
+HP:0007334,Bilateral convulsive seizures,HP:0011153,Focal motor seizures
+NCBITaxon:11552,Influenza C virus,NCBITaxon:197913,Influenzavirus C
+HP:0009247,Abnormality of the epiphysis of the middle phalanx of the 4th finger,HP:0009174,Abnormality of the epiphyses of the 4th finger
+HP:0012659,Prefrontal hypometabolism in FDG PET,HP:0012658,Abnormal brain FDG positron emission tomography
+UBERON:3000756,crista dorsalis humeri,UBERON:0004120,mesoderm-derived structure
+UBERON:0011648,jaw muscle,UBERON:0002376,cranial muscle
+UBERON:0003620,manual digit 1 phalanx,UBERON:0015025,manual digit 1 phalanx endochondral element
+HP:0100206,Fragmentation of the epiphysis of the distal phalanx of the 5th toe,HP:0100097,Abnormality of the epiphysis of the distal phalanx of the 5th toe
+DOID:0080031,fibrous dysplasia,DOID:0080005,bone remodeling disease
+CL:0000841,mature conventional dendritic cell,CL:0000990,conventional dendritic cell
+HP:0002927,Histidinuria,HP:0003355,Aminoaciduria
+UBERON:0003540,right lung terminal bronchiole,UBERON:0003538,right lung bronchiole
+DOID:4413,cervix melanoma,DOID:4362,cervical cancer
+UBERON:0003915,endothelial tube,UBERON:0001986,endothelium
+NCBITaxon:34609,Amblyomma maculatum,NCBITaxon:6942,Amblyomma
+HP:0010090,Patchy sclerosis of the proximal phalanx of the hallux,HP:0010063,Patchy sclerosis of the phalanges of the hallux
+UBERON:2001783,supraoccipital crest,UBERON:4100000,skeletal element projection
+HP:0002872,"Apneic episodes precipitated by illness, fatigue, stress",HP:0002104,Apnea
+HP:0002970,Genu varum,HP:0002815,Abnormality of the knees
+HP:0009702,Carpal synostosis,HP:0100266,Synostosis of carpals/tarsals
+HP:0011913,Lumbar hypertrichosis,HP:0000998,Hypertrichosis
+UBERON:0012236,intercostal lymph node,UBERON:0007644,thoracic lymph node
+DOID:4333,parovarian cyst,DOID:229,female reproductive system disease
+HP:0011064,Abnormal number of incisors,HP:0000676,Abnormality of the incisor
+UBERON:0010718,pubic cartilage element,UBERON:0005863,cartilaginous condensation
+UBERON:0004133,salivatory nucleus,UBERON:0009662,hindbrain nucleus
+UBERON:0000083,mesonephric tubule,UBERON:0005103,mesonephric epithelium
+HP:0008469,Cervical vertebral dysplasia,HP:0003319,Abnormality of the cervical spine
+UBERON:0003049,collagen and cuticulin-based cuticle,UBERON:0001002,cuticle
+UBERON:2002125,caudal-fin organ,UBERON:0003103,compound organ
+UBERON:0016425,epiphyseal plate of radius,UBERON:0004268,lower arm connective tissue
+DOID:5533,endometrial squamous cell carcinoma,DOID:2871,endometrial carcinoma
+HP:0009702,Carpal synostosis,HP:0004278,Synostosis involving bones of the hand
+DOID:4385,papillary squamous carcinoma,DOID:1749,squamous cell carcinoma
+UBERON:4300098,anal fin spine 2,UBERON:2002262,anal fin spine
+HP:0100911,Sclerosis of the proximal phalanx of the 5th finger,HP:0100917,Sclerosis of the proximal phalanges of the hand
+CL:0002000,Kit-positive erythroid progenitor cell,CL:0000038,erythroid progenitor cell
+HP:0012712,Mild hearing impairment,HP:0000365,Hearing impairment
+HP:0010252,Ivory epiphyses of the distal phalanges of the hand,HP:0100915,Sclerosis of the distal phalanges of the hand
+HP:0100497,Vitamin B3 deficiency,HP:0100496,Abnormality of the vitamin B3 metabolism
+DOID:2746,glycogen storage disease V,DOID:2747,glycogen storage disease
+DOID:1229,paranoid schizophrenia,DOID:5419,schizophrenia
+HP:0006136,Bilateral postaxial polydactyly,HP:0001162,Postaxial hand polydactyly
+DOID:6581,breast apocrine carcinoma,DOID:3458,breast adenocarcinoma
+UBERON:2005085,nasal artery,UBERON:0001637,artery
+HP:0010229,Bracket epiphyses of the phalanges of the hand,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+UBERON:3000957,basihyal,UBERON:0002513,endochondral bone
+DOID:6179,ovarian small cell carcinoma,DOID:4001,ovarian carcinoma
+UBERON:2200268,anal fin proximal radial cartilage,UBERON:2201671,anal fin radial cartilage
+HP:0000366,Abnormality of the nose,HP:0000271,Abnormality of the face
+HP:0006144,Shortening of all proximal phalanges of the fingers,HP:0010241,Short proximal phalanx of finger
+HP:0009649,Aplasia of the distal phalanx of the thumb,HP:0009641,Aplasia/Hypoplasia of the distal phalanx of the thumb
+HP:0009505,Enlarged epiphysis of the distal phalanx of the 2nd finger,HP:0010249,Enlarged epiphyses of the distal phalanges of the hand
+UBERON:0005432,aortic sac,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0009959,lumen of oropharynx,UBERON:0000464,anatomical space
+HP:0011570,Congenital mitral stenosis,HP:0001718,Mitral stenosis
+UBERON:2000449,torus longitudinalis,UBERON:0002966,regional part of midbrain tectum
+HP:0012723,Sinoatrial block,HP:0012722,Heart block
+UBERON:2001171,os suspensorium,UBERON:0002513,endochondral bone
+UBERON:0003351,pharyngeal epithelium,UBERON:0004807,respiratory system epithelium
+HP:0002300,Mutism,HP:0002167,Neurological speech impairment
+UBERON:0002126,solitary tract nuclear complex,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010780,Hyperacusis,HP:0000364,Hearing abnormality
+HP:0003778,Short mandibular rami,HP:0000347,Micrognathia
+UBERON:0002524,mediastinal lymph node,UBERON:0007644,thoracic lymph node
+HP:0000573,Retinal hemorrhage,HP:0008046,Abnormality of the retinal vasculature
+HP:0001112,Leber optic atrophy,HP:0000479,Abnormality of the retina
+UBERON:0005056,external female genitalia,UBERON:0003134,female reproductive organ
+UBERON:0002565,olivary pretectal nucleus,UBERON:0014450,pretectal nucleus
+UBERON:0008946,lung parenchyma,UBERON:0000353,parenchyma
+HP:0008883,Mild intrauterine growth retardation,HP:0001511,Intrauterine growth retardation
+UBERON:0001134,skeletal muscle tissue,UBERON:0002036,striated muscle tissue
+UBERON:3000284,margo tympanicus of pterygoid,UBERON:0010313,neural crest-derived structure
+UBERON:0005967,conotruncal ridge,UBERON:0009751,cardiac mesenchyme
+UBERON:0008923,sublaminar layer S2,UBERON:0008927,sublaminar layers S1 or S2
+DOID:3002,ovary neuroendocrine neoplasm,DOID:2394,ovarian cancer
+UBERON:2005030,dorsal ciliary vein,UBERON:0003496,head blood vessel
+DOID:6496,extraskeletal myxoid chondrosarcoma,DOID:4549,extraosseous chondrosarcoma
+HP:0011349,Abducens palsy,HP:0011348,Abnormality of the sixth cranial nerve
+HP:0009445,Symphalangism of the 3rd finger,HP:0009773,Symphalangism affecting the phalanges of the hand
+UBERON:0013490,deep cervical fascia,UBERON:0004923,organ component layer
+UBERON:3000917,apophysis distalis of tibiale fibulare,UBERON:0004120,mesoderm-derived structure
+HP:0100622,Maternal seizures,HP:0002686,Prenatal maternal abnormality
+HP:0003161,4-Hydroxyphenylpyruvic aciduria,HP:0010996,Abnormality of monocarboxylic acid metabolism
+UBERON:3010576,prenasal,UBERON:0008907,dermal bone
+NCBITaxon:33988,Rickettsieae,NCBITaxon:775,Rickettsiaceae
+UBERON:0005380,olfactory bulb subependymal zone,UBERON:0004001,olfactory bulb layer
+HP:0010864,"Intellectual disability, severe",HP:0001249,Intellectual disability
+HP:0009295,Short middle phalanx of the 4th finger,HP:0005819,Short middle phalanx of finger
+HP:0000947,Dumbbell-shaped long bone,HP:0011314,Abnormality of long bone morphology
+HP:0010863,Receptive language delay,HP:0000750,Delayed speech and language development
+DOID:0050477,Liddle syndrome,DOID:447,renal tubular transport disease
+HP:0100619,Sertoli cell neoplasm,HP:0010788,Testicular neoplasm
+DOID:5349,central nervous system adult germ cell tumor,DOID:4439,central nervous system germ cell tumor
+UBERON:0010372,uncinate process of ethmoid,UBERON:4100000,skeletal element projection
+HP:0100371,Aplasia/Hypoplasia of the distal phalanx of the 5th toe,HP:0010383,Aplasia/Hypoplasia of the phalanges of the 5th toe
+UBERON:0004079,cerebellum vermis lobule V,UBERON:0004070,cerebellum vermis lobule
+DOID:11759,hypochromic anemia,DOID:2355,anemia
+UBERON:2001680,mesethmoid-vomer joint,UBERON:0000982,skeletal joint
+CL:0002197,inactive chief cell of parathyoid gland,CL:0000446,chief cell of parathyroid gland
+UBERON:0011175,fusiform nucleus of stria terminalis,UBERON:0009663,telencephalic nucleus
+HP:0012674,Aplasia of the lower vagina,HP:0003250,Aplasia of the vagina
+UBERON:0011346,palatine raphe,UBERON:0003566,head connective tissue
+UBERON:0005222,liver left lobe parenchyma,UBERON:0001280,liver parenchyma
+UBERON:2001959,ceratobranchial 4 bone proximal cartilage,UBERON:0011004,pharyngeal arch cartilage
+HP:0003041,Humeroradial synostosis,HP:0003938,Synostosis involving the elbow
+UBERON:0001803,epithelium of lens,UBERON:0015808,eye epithelium
+UBERON:0011801,dermal condensation of feather follicle,UBERON:0004120,mesoderm-derived structure
+UBERON:0006918,parakeratinized epithelium of tongue,UBERON:0003357,epithelium of tongue
+DOID:8838,"Hodgkin's lymphoma, nodular sclerosis",DOID:8567,Hodgkin's lymphoma
+UBERON:0001821,sebaceous gland,UBERON:0012344,holocrine gland
+DOID:0050621,respiratory system benign neoplasm,DOID:0060085,organ system benign neoplasm
+DOID:3857,large cell medulloblastoma,DOID:0050902,medulloblastoma
+DOID:6691,Aagenaes syndrome,DOID:225,syndrome
+DOID:75,lymphatic system disease,DOID:2914,immune system disease
+HP:0002414,Spina bifida,HP:0010301,Spinal dysraphism
+UBERON:0002285,telencephalic ventricle,UBERON:0004086,brain ventricle
+UBERON:3010164,ulnar fold,UBERON:3000981,limb external integument structure
+HP:0002461,Dense calcifications in the cerebellar dentate nucleus,HP:0007352,Cerebellar calcifications
+UBERON:2001431,primitive olfactory epithelium,UBERON:0005291,embryonic tissue
+DOID:6938,pediatric Intraocular retinoblastoma,DOID:4653,intraocular retinoblastoma
+UBERON:0005944,axial skeleton plus cranial skeleton,UBERON:0010912,subdivision of skeleton
+DOID:530,eyelid disease,DOID:0050815,adnexa disease
+HP:0008026,Horizontal opticokinetic nystagmus,HP:0000666,Horizontal nystagmus
+HP:0006927,Unilateral polymicrogyria,HP:0002126,Polymicrogyria
+HP:0006378,Osteolysis of patellae,HP:0003045,Abnormality of the patella
+HP:0011543,Superior-inferior ventricles without criss-cross atrioventricular valves,HP:0011534,Abnormal spatial orientation of the cardiac segments
+HP:0000687,Widely spaced teeth,HP:0000692,Misalignment of teeth
+DOID:7651,hypercalcemic type ovarian small cell carcinoma,DOID:6179,ovarian small cell carcinoma
+UBERON:0013491,cervical fascia,UBERON:0008982,fascia
+UBERON:0001287,proximal convoluted tubule,UBERON:0004134,proximal tubule
+DOID:12144,low compliance bladder,DOID:365,bladder disease
+UBERON:0004676,spinal cord lateral horn,UBERON:0002315,gray matter of spinal cord
+HP:0100276,Skin pits,HP:0011355,Localized skin lesion
+UBERON:0004108,clivus of occipital bone,UBERON:0005913,zone of bone organ
+HP:0003573,Increased total bilirubin,HP:0002904,Hyperbilirubinemia
+UBERON:0002639,midbrain reticular formation,UBERON:0002635,regional part of midbrain tegmentum
+DOID:0050561,Lennox-Gastaut syndrome,DOID:0050704,childhood electroclinical syndrome
+DOID:7224,spinal meninges cancer,DOID:5612,spinal cancer
+UBERON:0009102,supraneural body,UBERON:0005057,immune organ
+HP:0100762,Hemobilia,HP:0012439,Abnormal biliary tract physiology
+DOID:0050352,foodborne botulism,DOID:11976,botulism
+UBERON:0005788,lamina rara interna,UBERON:0006554,urinary system structure
+NCBITaxon:36831,Clostridium botulinum F,NCBITaxon:1491,Clostridium botulinum
+HP:0006323,Premature loss of primary teeth,HP:0006480,Premature loss of teeth
+DOID:9234,kidney carcinoma in situ,DOID:8719,in situ carcinoma
+DOID:214,teeth hard tissue disease,DOID:1091,tooth disease
+NCBITaxon:121222,Pediculus,NCBITaxon:121221,Pediculidae
+HP:0002454,Eye of the tiger anomaly of globus pallidus,HP:0002453,Abnormality of the globus pallidus
+UBERON:0000460,major vestibular gland,UBERON:0002365,exocrine gland
+HP:0100195,Fragmentation of the epiphysis of the proximal phalanx of the 4th toe,HP:0100070,Fragmentation of the epiphyses of the 4th toe
+UBERON:0001203,muscularis mucosae of stomach,UBERON:0004222,stomach smooth muscle
+UBERON:0002888,lateral part of basal amygdaloid nucleus,UBERON:0005401,cerebral hemisphere grey matter
+HP:0004292,Undermodelled hand bones,HP:0005922,Abnormal hand morphology
+DOID:115,cardiac tamponade,DOID:118,pericardial effusion
+HP:0003297,Hyperlysinuria,HP:0003355,Aminoaciduria
+UBERON:0009568,trunk region of vertebral column,UBERON:0006077,subdivision of vertebral column
+UBERON:0003692,acromioclavicular joint,UBERON:0011108,synovial joint of pectoral girdle
+HP:0200029,Vasculitis in the skin,HP:0002633,Vasculitis
+HP:0002851,Increased number of CD4-/CD8- T cells expressing alpha/beta T-cell receptors,HP:0100828,Increase in T cell number
+UBERON:0009002,placental membrane,UBERON:0005156,reproductive structure
+HP:0100877,Renal diverticulum,HP:0000107,Renal cyst
+DOID:12960,acrocephalosyndactylia,DOID:11971,synostosis
+UBERON:0005854,cervical spinal cord ventral column,UBERON:0014614,cervical spinal cord white matter
+CL:1000497,kidney cell,CL:0000548,animal cell
+CL:0000490,photopic photoreceptor cell,CL:0000488,visible light photoreceptor cell
+UBERON:0010019,spiracle,UBERON:0003102,surface structure
+HP:0012228,Tension-type headache,HP:0002315,Headache
+DOID:13448,posterior corneal pigmentation,DOID:11547,corneal deposit
+UBERON:2000576,pterotic,UBERON:0008907,dermal bone
+DOID:5660,lymphoepithelioma-like carcinoma,DOID:305,carcinoma
+UBERON:2000226,lateral ethmoid bone,UBERON:0002513,endochondral bone
+UBERON:0010756,spleen follicular dendritic cell network,UBERON:0001744,lymphoid tissue
+HP:0000051,Perineal hypospadias,HP:0000047,Hypospadias
+UBERON:0008322,deep artery of clitoris,UBERON:0004573,systemic artery
+HP:0008119,Deformed tarsal bones,HP:0001850,Abnormality of the tarsal bones
+UBERON:0007837,thoracic spinal cord ventral commissure,UBERON:0004170,spinal cord ventral commissure
+HP:0001171,Split hand,HP:0001155,Abnormality of the hand
+DOID:0050724,PSPH deficiency,DOID:0050721,serine deficiency
+DOID:2743,pyeloureteritis cystica,DOID:782,renal infectious disease
+HP:0009540,Contracture of the proximal interphalangeal joint of the 2nd finger,HP:0009698,Contractures of the proximal interphalangeal joints of the fingers
+NCBITaxon:11593,Crimean-Congo hemorrhagic fever virus,NCBITaxon:11592,Nairovirus
+HP:0012614,Abnormal urine cytology,HP:0003110,Abnormality of urine homeostasis
+UBERON:0005094,beak,UBERON:0003102,surface structure
+HP:0000460,Narrow nose,HP:0005105,Abnormal nasal morphology
+NCBITaxon:6945,Ixodes scapularis,NCBITaxon:6944,Ixodes
+HP:0010618,Ovarian fibroma,HP:0100615,Ovarian neoplasm
+DOID:6249,mediastinum seminoma,DOID:5559,mediastinal cancer
+UBERON:0008846,skeletal ligament,UBERON:0000211,ligament
+UBERON:0011220,mastoid process of temporal bone,UBERON:0010313,neural crest-derived structure
+HP:0100343,Tibial deviation of the 3rd toe,HP:0010332,Deviation/Displacement of the 3rd toe
+UBERON:0006496,external acoustic meatus osseus part,UBERON:0004121,ectoderm-derived structure
+HP:0001278,Orthostatic hypotension,HP:0012332,Abnormal autonomic nervous system physiology
+UBERON:0004789,larynx mucous gland,UBERON:0004119,endoderm-derived structure
+DOID:0060146,phonagnosia,DOID:4090,agnosia
+UBERON:0003852,rhombencephalon neural crest,UBERON:0002342,neural crest
+HP:0010735,Polyostotic fibrous dysplasia,HP:0010734,Fibrous dysplasia of the bones
+DOID:0080008,ischemic bone disease,DOID:0080001,bone disease
+UBERON:0010174,Schweigger-Seidel sheath,UBERON:0004120,mesoderm-derived structure
+HP:0006108,Tapered metacarpals,HP:0005916,Abnormal metacarpal morphology
+UBERON:3000110,crista contacta,UBERON:0010313,neural crest-derived structure
+HP:0002240,Hepatomegaly,HP:0003271,Visceromegaly
+UBERON:0003064,intermediate mesoderm,UBERON:0005423,developing anatomical structure
+UBERON:3010827,anterior prenasal cartilage,UBERON:0003933,cranial cartilage
+HP:0009510,Small epiphysis of the distal phalanx of the 2nd finger,HP:0009496,Small epiphyses of the 2nd finger
+HP:0009956,Partial duplication of the phalanges of the 2nd finger,HP:0009999,Partial duplication of the phalanx of hand
+DOID:4688,laryngeal mucoepidermoid carcinoma,DOID:2600,laryngeal carcinoma
+UBERON:2005044,optic artery,UBERON:0001637,artery
+UBERON:0003051,ear vesicle,UBERON:0005291,embryonic tissue
+UBERON:2000551,nucleus lateralis valvulae,UBERON:0007635,nucleus of medulla oblongata
+HP:0000654,Decreased electroretinogram (ERG) amplitude,HP:0000512,Abnormal electroretinogram
+UBERON:0006077,subdivision of vertebral column,UBERON:0004120,mesoderm-derived structure
+HP:0008285,Transient hypophosphatemia,HP:0002148,Hypophosphatemia
+HP:0100129,Pseudoepiphysis of the proximal phalanx of the 2nd toe,HP:0100051,Pseudoepiphyses of the 2nd toe
+CL:0002652,endothelial cell of high endothelial venule,CL:0000075,columnar/cuboidal epithelial cell
+UBERON:2000984,superior reticular formation tegmentum,UBERON:0007414,nucleus of midbrain tegmentum
+UBERON:0001682,palatine bone,UBERON:0012071,palate bone
+HP:0012699,Anomaly of lower limb diaphyses,HP:0006504,Anomaly of the limb diaphyses
+HP:0010481,Urethral valve,HP:0000796,Urethral obstruction
+UBERON:0004430,proximal epiphysis of fourth metatarsal bone,UBERON:0004398,epiphysis of fourth metatarsal bone
+HP:0100849,Neoplasia of the scrotum,HP:0100848,Neoplasia of the male external genitalia
+NCBITaxon:12086,Human poliovirus 3,NCBITaxon:138950,Human enterovirus C
+DOID:4282,pigmented basal cell carcinoma,DOID:2513,basal cell carcinoma
+UBERON:0004515,smooth muscle tissue of bronchiole,UBERON:0004242,bronchus smooth muscle
+UBERON:0002503,greater trochanter,UBERON:0000980,trochanter
+HP:0006355,Agenesis of mandibular central incisor,HP:0006289,Agenesis of central incisor
+HP:0010502,Fibular bowing,HP:0002979,Bowing of the legs
+HP:0003979,Lytic defects of the radius,HP:0003963,Lytic defects of the forearm bones
+CL:0002639,amniotic stem cell,CL:0000134,mesenchymal cell
+HP:0004262,Abnormality of the capitate bone,HP:0001191,Abnormality of the carpal bones
+DOID:6039,uveal melanoma,DOID:3479,uveal cancer
+NCBITaxon:803,Bartonella quintana,NCBITaxon:773,Bartonella
+UBERON:0003937,sex gland,UBERON:0002530,gland
+DOID:7656,adult infiltrating astrocytic neoplasm,DOID:3076,adult astrocytic tumour
+UBERON:0000391,leptomeninx,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000323,lysozyme secreting cell,CL:0000154,protein secreting cell
+HP:0002483,Bulbar signs,HP:0002363,Abnormality of the brainstem
+HP:0100953,Enlarged interhemispheric fissure,HP:0002119,Ventriculomegaly
+HP:0003750,Increased muscle fatiguability,HP:0011804,Abnormality of muscle physiology
+UBERON:0006192,mesonephric proximal tubule,UBERON:0004134,proximal tubule
+UBERON:4200034,cnemial crest,UBERON:0004530,bony projection
+CL:1000548,kidney outer medulla collecting duct epithelial cell,CL:1000546,kidney medulla collecting duct epithelial cell
+CL:0000360,morula cell,CL:0000007,early embryonic cell
+HP:0011592,Left aortic arch with isolated subclavian artery,HP:0011587,Abnormal branching pattern of the aortic arch
+DOID:235,colonic benign neoplasm,DOID:4610,intestinal benign neoplasm
+UBERON:0004063,spinal cord alar plate,UBERON:0005882,neural tube alar plate
+UBERON:0013758,cervical os,UBERON:0014404,female anatomical structure
+HP:0008783,Wide proximal femoral metaphysis,HP:0006489,Abnormality of the femoral metaphysis
+UBERON:0003616,bronchus elastic tissue,UBERON:0003611,respiratory system elastic tissue
+UBERON:0001419,skin of limb,UBERON:0000014,zone of skin
+UBERON:0003050,olfactory placode,UBERON:0007497,developing epithelial placode
+HP:0003596,Middle age onset,HP:0003581,Adult onset
+HP:0012428,Prominent calcaneus,HP:0008364,Abnormality of the calcaneus
+HP:0011975,Aminoglycoside-induced hearing loss,HP:0000365,Hearing impairment
+UBERON:0004534,right testis,UBERON:0000473,testis
+HP:0100245,Desmoid tumors,HP:0010614,Fibroma
+UBERON:2001854,postcleithrum 3,UBERON:2000410,postcleithrum
+UBERON:0005788,lamina rara interna,UBERON:0004120,mesoderm-derived structure
+UBERON:2000358,granular layer corpus cerebelli,UBERON:0000479,tissue
+DOID:10273,heart conduction disease,DOID:1287,cardiovascular system disease
+HP:0005381,Recurrent meningococcal disease,HP:0005430,Recurrent Neisserial infections
+UBERON:2000452,urohyal,UBERON:0008907,dermal bone
+UBERON:1500000,scapular blade,UBERON:0005913,zone of bone organ
+UBERON:0014843,pubioischiofemoralis internus muscle,UBERON:0014842,pubioischiofemoralis muscle
+UBERON:0002624,orbital part of inferior frontal gyrus,UBERON:0000064,organ part
+HP:0010076,Aplasia/Hypoplasia of the distal phalanx of the hallux,HP:0010185,Aplasia/Hypoplasia of the distal phalanges of the toes
+HP:0004389,Intestinal pseudo-obstruction,HP:0002242,Abnormality of the intestine
+UBERON:0006286,radius cartilage element,UBERON:0015001,radius endochondral element
+UBERON:0004064,neural tube basal plate,UBERON:0004121,ectoderm-derived structure
+HP:0012037,Pectoralis amyotrophy,HP:0011957,Abnormality of the  pectoral muscle
+UBERON:0014742,central nucleus of pallium,UBERON:0002791,regional part of telencephalon
+HP:0009387,Irregular epiphyses of the 5th finger,HP:0010233,Irregular epiphyses of the phalanges of the hand
+DOID:251,alcohol-induced mental disorder,DOID:8646,substance-induced psychosis
+UBERON:0002828,ventral cochlear nucleus,UBERON:0001720,cochlear nucleus
+HP:0100923,Clavicular sclerosis,HP:0000889,Abnormality of the clavicles
+HP:0000311,Round face,HP:0001999,Abnormal facial shape
+HP:0006267,Large placenta,HP:0100767,Abnormality of the placenta
+HP:0005574,Non-acidotic proximal tubulopathy,HP:0000114,Proximal tubulopathy
+DOID:4879,Bartholin's gland adenoid cystic carcinoma,DOID:3999,Bartholin's gland carcinoma
+CL:1000272,lung secretory cell,CL:0000151,secretory cell
+HP:0010089,Osteolytic defects of the proximal phalanx of the hallux,HP:0010198,Osteolytic defects of the middle phalanges of the toes
+HP:0001930,Nonspherocytic hemolytic anemia,HP:0001878,Hemolytic anemia
+UBERON:0002603,paraterminal gyrus,UBERON:0002665,supracallosal gyrus
+UBERON:0000003,naris,UBERON:0000161,orifice
+HP:0100377,Aplasia/Hypoplasia of the proximal phalanx of the 5th toe,HP:0010203,Aplasia/Hypoplasia of the proximal phalanges of the toes
+DOID:14067,Plasmodium falciparum malaria,DOID:12365,malaria
+UBERON:0002205,manubrium of sternum,UBERON:0010363,endochondral element
+HP:0004322,Short stature,HP:0001510,Growth delay
+UBERON:0001647,facial nerve,UBERON:0011779,nerve of head region
+UBERON:0005367,hippocampus granule cell layer,UBERON:0002305,layer of hippocampus
+UBERON:3000894,femoral ridge,UBERON:4100000,skeletal element projection
+HP:0009695,Stippling of the epiphyses of the thumb,HP:0009599,Abnormality of the epiphyses of the thumb
+UBERON:3000880,crista hypertrophica ischium,UBERON:0004120,mesoderm-derived structure
+DOID:0050158,respiratory bronchiolitis-associated interstitial lung disease,DOID:2797,idiopathic interstitial pneumonia
+UBERON:0011199,prostatic utricle,UBERON:0014403,male anatomical structure
+CL:0000333,migratory neural crest cell,CL:0002321,embryonic cell
+HP:0200147,Neuronal loss in basal ganglia,HP:0002134,Abnormality of the basal ganglia
+UBERON:0012359,pedal digitopodium bone,UBERON:0012357,digitopodium bone
+HP:0005101,High-frequency hearing impairment,HP:0000365,Hearing impairment
+DOID:820,myocarditis,DOID:3978,extrinsic cardiomyopathy
+UBERON:0001972,submucosa of esophagus,UBERON:0000009,submucosa
+DOID:12961,Poland syndrome,DOID:0080015,physical disorder
+UBERON:0001296,myometrium,UBERON:0014404,female anatomical structure
+HP:0100414,Complete duplication of the proximal phalanx of the 4th toe,HP:0100405,Duplication of the proximal phalanx of the 4th toe
+DOID:896,metal metabolism disorder,DOID:655,inherited metabolic disorder
+CL:1000329,tracheal goblet cell,CL:0002370,respiratory goblet cell
+HP:0006174,Metacarpal diaphyseal endosteal sclerosis,HP:0005916,Abnormal metacarpal morphology
+UBERON:3000839,crista radii,UBERON:0004120,mesoderm-derived structure
+UBERON:2001658,upper pharyngeal tooth plate,UBERON:2001647,pharyngeal tooth plate
+HP:0010167,Irregular epiphyses of the toes,HP:0010582,Irregular epiphyses
+HP:0009831,Mononeuropathy,HP:0009830,Peripheral neuropathy
+HP:0009686,Absent epiphyses of the thumb,HP:0010228,Absent epiphyses of the phalanges of the hand
+HP:0001919,Acute kidney injury,HP:0000083,Renal insufficiency
+UBERON:0002889,medial part of basal amygdaloid nucleus,UBERON:0005401,cerebral hemisphere grey matter
+DOID:2211,factor XIII deficiency,DOID:2214,inherited blood coagulation disease
+DOID:3482,plague,DOID:0050338,primary bacterial infectious disease
+NCBITaxon:279271,Leptotrombidium,NCBITaxon:92251,Trombiculidae
+DOID:6139,uterine corpus epithelioid leiomyosarcoma,DOID:5289,uterus leiomyosarcoma
+HP:0000974,Hyperextensible skin,HP:0008067,Abnormally lax or hyperextensible skin
+DOID:731,urinary system benign neoplasm,DOID:0060085,organ system benign neoplasm
+HP:0008096,Medially deviated second toe,HP:0100498,Deviation of toes
+UBERON:0004447,proximal epiphysis of phalanx,UBERON:0004380,proximal epiphysis
+UBERON:0009484,dorsal mesentery of mesentery of foregut-midgut junction,UBERON:0009483,mesentery of foregut-midgut junction
+DOID:12663,blastomycosis,DOID:0050292,primary systemic mycosis
+HP:0010794,Impaired visuospatial constructive cognition,HP:0001328,Specific learning disability
+DOID:13768,opisthorchiasis,DOID:883,parasitic helminthiasis infectious disease
+CL:0000340,glioblast (sensu Nematoda and Protostomia),CL:0000030,glioblast
+HP:0011664,Non-compaction cardiomyopathy,HP:0001638,Cardiomyopathy
+HP:0100216,Enlarged epiphysis of the middle phalanx of the 5th toe,HP:0100080,Enlarged epiphyses of the 5th toe
+UBERON:0002434,pituitary stalk,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0015009,lumbar vertebra endochondral element,UBERON:0005174,dorsal region organ
+UBERON:0010987,sterno-mastoid pre-muscle mass,UBERON:0005865,pre-muscle condensation
+DOID:14218,dihydropyrimidine dehydrogenase deficiency,DOID:653,purine-pyrimidine metabolic disorder
+DOID:9801,tuberculous peritonitis,DOID:404,gastrointestinal tuberculosis
+DOID:0050763,ARC syndrome,DOID:225,syndrome
+HP:0002090,Pneumonia,HP:0011947,Respiratory tract infection
+UBERON:0013503,caudal vertebra cartilage element,UBERON:0005174,dorsal region organ
+UBERON:3001009,body spicule,UBERON:3000977,body external integument structure
+DOID:5374,pilomatrixoma,DOID:5375,hair follicle neoplasm
+DOID:10955,strongyloidiasis,DOID:883,parasitic helminthiasis infectious disease
+UBERON:2001840,tip,UBERON:0006983,anatomical point
+HP:0009988,Duplication of the distal phalanx of the 5th finger,HP:0004225,Abnormality of the distal phalanx of the 5th finger
+CL:1001579,cerebral cortex glial cell,CL:0000125,glial cell
+UBERON:0015049,carpus endochondral element,UBERON:0015063,autopod endochondral element
+UBERON:0006288,rib cartilage element,UBERON:0015019,rib endochondral element
+HP:0005994,Nodular goiter,HP:0000853,Goiter
+HP:0100504,Vitamin B2 deficiency,HP:0004340,Abnormality of vitamin B metabolism
+DOID:7041,choroid epithelioid cell melanoma,DOID:6438,malignant choroid melanoma
+DOID:0050602,triple-A syndrome,DOID:0050737,autosomal recessive disease
+DOID:5983,kidney osteogenic sarcoma,DOID:4242,kidney sarcoma
+UBERON:0010023,dorsal part of pharyngeal pouch 2,UBERON:0005911,endo-epithelium
+HP:0001238,Slender finger,HP:0001167,Abnormality of finger
+NCBITaxon:6270,Pseudoterranova,NCBITaxon:6267,Anisakidae
+UBERON:2007041,forebrain neural tube,UBERON:0004121,ectoderm-derived structure
+UBERON:2005144,ampullary nerve,UBERON:0001021,nerve
+CL:0000203,gravity sensitive cell,CL:0000199,mechanoreceptor cell
+HP:0001116,Macular coloboma,HP:0000480,Retinal coloboma
+DOID:1906,malignant skin fibrous histiocytoma,DOID:5274,malignant dermis tumor
+HP:0003787,Type 1 and type 2 muscle fiber minicore regions,HP:0003789,Minicore (multicore) myopathy
+UBERON:0001001,chitin-based cuticle,UBERON:0004121,ectoderm-derived structure
+DOID:2876,laryngeal squamous cell carcinoma,DOID:2600,laryngeal carcinoma
+HP:0002885,Medulloblastoma,HP:0100836,Malignant neoplasm of the central nervous system
+DOID:0050439,Usher syndrome,DOID:0050737,autosomal recessive disease
+UBERON:0004495,skeletal muscle tissue of diaphragm,UBERON:0004830,respiratory system skeletal muscle
+UBERON:0003035,regional part of cerebellar white matter,UBERON:0004121,ectoderm-derived structure
+UBERON:0003863,pedal digit 5 phalanx,UBERON:0001449,phalanx of pes
+HP:0012648,Decreased inflammatory response,HP:0012647,Abnormal inflammatory response
+HP:0009977,Duplication of the proximal phalanx of the 4th finger,HP:0009972,Duplication of phalanx of 4th finger
+DOID:5434,scrapie,DOID:649,prion disease
+DOID:12225,Plica syndrome,DOID:381,arthropathy
+CL:0002498,secondary trophoblast giant cell,CL:0002488,trophoblast giant cell
+CL:1001569,hippocampal interneuron,CL:0002608,hippocampal neuron
+HP:0003130,Abnormal peripheral myelination,HP:0000759,Abnormality of the peripheral nervous system
+HP:0000857,Neonatal insulin-dependent diabetes mellitus,HP:0000831,Insulin-resistant diabetes mellitus
+UBERON:0006905,mandibular process mesenchyme,UBERON:0005253,head mesenchyme
+HP:0006190,Radially deviated wrists,HP:0009486,Radial deviation of the hand
+DOID:4813,adult brain stem glioma,DOID:4202,brain stem glioma
+CL:0000173,pancreatic D cell,CL:0000502,type D enteroendocrine cell
+UBERON:2001654,upper pharyngeal 4 tooth plate,UBERON:2001647,pharyngeal tooth plate
+HP:0005855,Multiple prenatal fractures,HP:0002659,Increased susceptibility to fractures
+HP:0004848,Ph-positive acute lymphoblastic leukemia,HP:0006721,Acute lymphatic leukemia
+UBERON:0005305,thyroid follicle,UBERON:0000064,organ part
+UBERON:0002868,commissural nucleus of vagus nerve,UBERON:0011775,vagus nerve nucleus
+HP:0003858,Cortical diaphyseal irregularity of the upper limbs,HP:0009808,Anomaly of the upper limb diaphyses
+UBERON:0010569,manual digit 5 metacarpus pre-cartilage condensation,UBERON:0015047,manual digit 5 metacarpus endochondral element
+DOID:4607,biliary tract cancer,DOID:3119,gastrointestinal system cancer
+HP:0005881,Spinal instability,HP:0000925,Abnormality of the vertebral column
+UBERON:4200083,postaxial centrale,UBERON:0012131,centrale
+UBERON:0005441,external intercostal muscle,UBERON:0001111,intercostal muscle
+UBERON:0004823,intrahepatic bile duct epithelium,UBERON:0004820,bile duct epithelium
+UBERON:0002474,cerebellar peduncular complex,UBERON:0002616,regional part of brain
+UBERON:0008243,upper back muscle,UBERON:0003830,thoracic segment muscle
+CL:0001059,"common myeloid progenitor, CD34-positive",CL:0000049,common myeloid progenitor
+DOID:5624,adenosquamous bile duct carcinoma,DOID:4897,bile duct carcinoma
+DOID:1998,Lutembacher's syndrome,DOID:1882,atrial heart septal defect
+UBERON:0015134,main lactiferous duct,UBERON:0001765,mammary duct
+HP:0009196,Absent metacarpal epiphyses,HP:0005913,Abnormality of metacarpal epiphyses
+HP:0004392,Prune belly,HP:0004298,Abnormality of the abdominal wall
+HP:0002510,Spastic tetraplegia,HP:0001257,Spasticity
+UBERON:0002671,pallidotegmental fasciculus,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0000150,Gonadoblastoma,HP:0000812,Abnormal internal genitalia
+UBERON:0010698,manual digit metacarpus pre-cartilage condensation,UBERON:0015042,manual digit metacarpus endochondral element
+DOID:438,autoimmune disease of the nervous system,DOID:417,hypersensitivity reaction type II disease
+UBERON:3000505,processus pterygoideus of maxilla,UBERON:0004120,mesoderm-derived structure
+HP:0009513,Absent epiphysis of the middle phalanx of the 2nd finger,HP:0009488,Absent epiphyses of the 2nd finger
+DOID:5697,liposarcoma of the ovary,DOID:2146,ovary sarcoma
+UBERON:2001611,quadrate posterodorsal process,UBERON:4100000,skeletal element projection
+UBERON:0012428,proximal convoluted tubule brush border,UBERON:0012424,brush border layer
+UBERON:0002980,opercular part of inferior frontal gyrus,UBERON:0000064,organ part
+HP:0001339,Lissencephaly,HP:0002536,Abnormal cortical gyration
+UBERON:0007332,mandibular rhamphotheca,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0006938,Impaired vibration sensation at ankles,HP:0006886,Impaired distal vibration sensation
+HP:0010165,Enlarged epiphyses of the toes,HP:0010580,Enlarged epiphyses
+DOID:0050737,autosomal recessive disease,DOID:0050739,autosomal genetic disease
+UBERON:0016481,bronchial lymph node,UBERON:0004119,endoderm-derived structure
+HP:0009134,Osteolysis involving bones of the feet,HP:0001760,Abnormality of the foot
+HP:0004912,Hypophosphatemic rickets,HP:0002148,Hypophosphatemia
+UBERON:2001096,immature anterior macula,UBERON:2001095,immature macula
+HP:0009675,Absent epiphysis of the distal phalanx of the thumb,HP:0010246,Absent epiphyses of the distal phalanges of the hand
+UBERON:0009859,endosteum,UBERON:0000158,membranous layer
+DOID:1579,respiratory system disease,DOID:7,disease of anatomical entity
+UBERON:0013647,lateral pterygoid nerve,UBERON:0001021,nerve
+HP:0009819,Lower limb phocomelia,HP:0006493,Aplasia/Hypoplasia involving bones of the lower limbs
+CL:1000276,smooth muscle fiber of duodenum,CL:1000275,smooth muscle cell of small intestine
+HP:0000036,Abnormality of the penis,HP:0000032,Abnormality of male external genitalia
+DOID:2367,neuroaxonal dystrophy,DOID:1443,cerebral degeneration
+HP:0100635,Carotid paraganglioma,HP:0002864,Paraganglioma of head and neck
+HP:0006725,Pancreatic adenocarcinoma,HP:0002894,Neoplasm of the pancreas
+DOID:65,connective tissue disease,DOID:17,musculoskeletal system disease
+HP:0010066,Duplication of phalanx of hallux,HP:0010181,Duplication of phalanx of toe
+HP:0011731,Abnormality of circulating cortisol level,HP:0012111,Abnormality of circulating glucocorticoid level
+UBERON:3010092,basitrabecular process,UBERON:4100000,skeletal element projection
+DOID:9655,oral mucosa leukoplakia,DOID:403,mouth disease
+HP:0100158,Bracket epiphysis of the proximal phalanx of the 3rd toe,HP:0100056,Bracket epiphyses of the 3rd toe
+HP:0009529,Irregular epiphysis of the proximal phalanx of the 2nd finger,HP:0009501,Abnormality of the epiphysis of the proximal phalanx of the 2nd finger
+HP:0002971,Absent microvilli on the surface of peripheral blood lymphocytes,HP:0004332,Abnormality of lymphocytes
+UBERON:0011112,tibiofibular joint,UBERON:0003840,hindlimb joint
+HP:0012376,Microphakia,HP:0008063,Aplasia/Hypoplasia of the lens
+UBERON:0008913,perichondral bone,UBERON:0007842,membrane bone
+HP:0001683,Ectopia cordis,HP:0004307,Abnormal anatomic location of the heart
+UBERON:0001818,tarsal gland,UBERON:0013231,sebaceous gland of eyelid
+HP:0011630,Complete diaphragmatic absence of pericardium,HP:0011628,Congenital defect of the pericardium
+HP:0010336,Abnormality of the phalanges of the 4th toe,HP:0010161,Abnormality of the phalanges of the toes
+UBERON:0003043,posterior part of anterior commissure,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0012417,Hypocapnia,HP:0012415,Abnormal blood gas level
+HP:0100198,Pseudoepiphysis of the proximal phalanx of the 4th toe,HP:0100096,Abnormality of the epiphysis of the proximal phalanx of the 4th toe
+HP:0009177,Proximal/middle symphalangism of 5th finger,HP:0006152,Proximal symphalangism (hands)
+UBERON:0006839,posterior ramus of spinal nerve,UBERON:0001021,nerve
+HP:0007968,Persistent hyperplastic primary vitreous,HP:0004327,Abnormality of the vitreous humor
+UBERON:3000645,corpus,UBERON:0012360,bone of jaw
+UBERON:0002762,internal medullary lamina of thalamus,UBERON:0014533,medullary lamina of thalamus
+HP:0012630,Abnormality of the trabecular meshwork,HP:0000593,Abnormality of the anterior chamber
+UBERON:0011271,caudal-sacral region of vertebral column,UBERON:0006077,subdivision of vertebral column
+HP:0100398,Duplication of the distal phalanx of the 3rd toe,HP:0010367,Duplication of phalanx of the 3rd toe
+HP:0006691,Pulmonic valve myxoma,HP:0001641,Abnormality of the pulmonary valve
+UBERON:0006957,submandibular gland primordium epithelium,UBERON:0004809,salivary gland epithelium
+UBERON:0002039,inferior phrenic vein,UBERON:0012193,phrenic vein
+UBERON:0004659,mandible neck,UBERON:0001560,neck of organ
+DOID:4788,intracranial primitive neuroectodermal tumor,DOID:0060103,central nervous system primitive neuroectodermal neoplasm
+HP:0100703,Tongue thrusting,HP:0000733,Stereotypic behavior
+CL:0002340,luminal cell of prostate epithelium,CL:0002231,epithelial cell of prostate
+UBERON:3000911,foramen nutritium exterius,UBERON:0004120,mesoderm-derived structure
+HP:0000326,Abnormality of the maxilla,HP:0011821,Abnormality of facial skeleton
+CL:0000541,melanoblast,CL:0000055,non-terminally differentiated cell
+UBERON:0009651,nephron tubule basement membrane,UBERON:0006554,urinary system structure
+UBERON:0002499,cochlear labyrinth,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3010431,archenteron floor,UBERON:0002050,embryonic structure
+DOID:6196,reactive arthritis,DOID:848,arthritis
+HP:0009268,Pseudoepiphysis of the proximal phalanx of the 4th finger,HP:0009400,Pseudoepiphyses of the 4th finger
+UBERON:0003699,pubic symphysis,UBERON:0002216,symphysis
+CL:0002057,"CD14-positive, CD16-negative classical monocyte",CL:0001054,CD14-positive monocyte
+DOID:0050670,ataxic cerebral palsy,DOID:1969,cerebral palsy
+UBERON:0004401,bone tissue of distal epiphysis,UBERON:0004400,bone tissue of epiphysis
+HP:0010512,Adrenal calcification,HP:0010766,Ectopic calcification
+UBERON:0010513,strand of zigzag hair,UBERON:0016447,hair of trunk
+CL:0002048,late pro-B cell,CL:0000817,precursor B cell
+HP:0001885,Short 2nd toe,HP:0001831,Short toe
+UBERON:3000586,superior prenasal cartilage,UBERON:0003406,cartilage of respiratory system
+HP:0001076,Glabellar hemangioma,HP:0001028,Hemangioma
+HP:0000085,Horseshoe kidney,HP:0100542,Abnormal localization of kidney
+HP:0004285,Overmodelled hand bones,HP:0005922,Abnormal hand morphology
+UBERON:0009210,pharyngeal membrane,UBERON:0002050,embryonic structure
+UBERON:0003905,bursal follicle,UBERON:0004120,mesoderm-derived structure
+HP:0004363,Abnormality of calcium homeostasis,HP:0010927,Abnormality of divalent inorganic cation homeostasis
+UBERON:0003982,mature ovarian follicle,UBERON:0001305,ovarian follicle
+DOID:6755,amyloid tumor,DOID:3350,mesenchymal cell neoplasm
+DOID:3202,neurilemmoma of the fifth cranial nerve,DOID:1201,trigeminal nerve neoplasm
+HP:0100188,Small epiphysis of the middle phalanx of the 4th toe,HP:0100074,Small epiphyses of the 4th toe
+HP:0006282,Generalized hypoplasia of dental enamel,HP:0006297,Hypoplasia of dental enamel
+HP:0010478,Abnormality of the urachus,HP:0000014,Abnormality of the bladder
+HP:0004459,Exostosis of the external auditory canal,HP:0100777,Exostoses
+UBERON:0011801,dermal condensation of feather follicle,UBERON:0011585,cell condensation
+HP:0100131,Stippling of the epiphysis of the proximal phalanx of the 2nd toe,HP:0100090,Abnormality of the epiphysis of the proximal phalanx of the 2nd toe
+HP:0100083,Ivory epiphyses of the 5th toe,HP:0010341,Abnormality of the epiphyses of the 5th toe
+UBERON:0001698,foramen ovale of skull,UBERON:0013685,foramen of skull
+UBERON:0004554,hindlimb digital artery,UBERON:0003516,hindlimb blood vessel
+HP:0011613,Interrupted aortic arch type B,HP:0011611,Interrupted aortic arch
+HP:0003026,Short long bones,HP:0011314,Abnormality of long bone morphology
+HP:0003916,Normal-density transverse bands (humerus),HP:0003852,Normal density transverse bands in metaphyses of the upper limbs
+CL:0000932,type II NK T cell secreting interferon-gamma,CL:0000922,type II NK T cell
+DOID:10444,ring corneal ulcer,DOID:8463,corneal ulcer
+HP:0009279,Radial deviation of the 4th finger,HP:0009466,Radial deviation of finger
+HP:0009615,Complete duplication of the first metacarpal,HP:0009609,Duplication of the 1st metacarpal
+DOID:11031,bullous keratopathy,DOID:11030,corneal edema
+HP:0010456,Abnormality of the greater sacrosciatic notch,HP:0002644,Abnormality of pelvic girdle bone morphology
+DOID:11612,polycystic ovary syndrome,DOID:225,syndrome
+DOID:447,renal tubular transport disease,DOID:557,kidney disease
+UBERON:0008789,cranial fossa,UBERON:0004704,bone fossa
+UBERON:0001449,phalanx of pes,UBERON:0003608,hindlimb long bone
+UBERON:0010720,hindlimb zeugopod skeleton,UBERON:0011584,zeugopodial skeleton
+DOID:5426,premature ovarian failure,DOID:1100,ovarian disease
+HP:0001084,Corneal arcus,HP:0008011,Peripheral opacification of the cornea
+HP:0001875,Neutropenia,HP:0011991,Abnormal neutrophil cell number
+UBERON:0000939,imaginal disc,UBERON:0000481,multi-tissue structure
+CL:0000023,oocyte,CL:0000021,female germ cell
+HP:0100298,Motheaten muscle fibers,HP:0004303,Abnormality of muscle fibers
+UBERON:0007224,medial entorhinal cortex,UBERON:0004121,ectoderm-derived structure
+HP:0010569,Elevated 7-dehydrocholesterol,HP:0003107,Abnormality of cholesterol metabolism
+CL:0000520,prokaryotic cell,CL:0000003,native cell
+HP:0002370,Poor coordination,HP:0002311,Incoordination
+HP:0000746,Delusions,HP:0000708,Behavioural/Psychiatric Abnormality
+HP:0009706,Synostosis involving the 3rd metacarpal,HP:0009701,Metacarpal synostosis
+UBERON:0010521,electroreceptor organ,UBERON:0000020,sense organ
+HP:0012411,Premature pubarche,HP:0000826,Precocious puberty
+HP:0006597,Diaphragmatic paralysis,HP:0009113,Diaphragmatic weakness
+UBERON:0005687,orbitosphenoid cartilage element,UBERON:0015059,orbitosphenoid endochondral element
+DOID:573,nerve compression syndrome,DOID:574,peripheral nervous system disease
+UBERON:0011267,quadratojugal bone,UBERON:0008907,dermal bone
+UBERON:0002504,lesser trochanter,UBERON:0000980,trochanter
+UBERON:2005316,fin fold pectoral fin bud,UBERON:0002050,embryonic structure
+UBERON:0006688,sublingual caruncle,UBERON:0000064,organ part
+HP:0011783,Thyrotoxicosis from ectopic thyroid tissue,HP:0000836,Hyperthyroidism
+UBERON:0010378,mesenchyme from splanchnopleure,UBERON:0004120,mesoderm-derived structure
+UBERON:0012110,frontal process of zygomatic bone,UBERON:0005913,zone of bone organ
+HP:0010165,Enlarged epiphyses of the toes,HP:0010160,Abnormality of the epiphyses of the toes
+DOID:0080015,physical disorder,DOID:4,disease
+UBERON:0006779,superficial white layer of superior colliculus,UBERON:0006786,white matter of superior colliculus
+UBERON:0013646,buccal nerve,UBERON:0001021,nerve
+UBERON:0010396,afferent lymphatic vessel,UBERON:0001473,lymphatic vessel
+HP:0100203,Bracket epiphysis of the distal phalanx of the 5th toe,HP:0100097,Abnormality of the epiphysis of the distal phalanx of the 5th toe
+UBERON:0007637,hippocampus stratum lucidum,UBERON:0002305,layer of hippocampus
+UBERON:0010943,anterior belly of digastric,UBERON:0010940,belly of digastric
+UBERON:0005519,rhombomere 6,UBERON:0001892,rhombomere
+CL:0000840,immature conventional dendritic cell,CL:0000990,conventional dendritic cell
+UBERON:0007379,egg,UBERON:0002050,embryonic structure
+UBERON:0004830,respiratory system skeletal muscle,UBERON:0001134,skeletal muscle tissue
+HP:0012651,Abasia,HP:0002066,Gait ataxia
+HP:0003896,Irregular humeral epiphyses,HP:0003842,Irregular epiphyses of the upper limbs
+UBERON:0004275,third ventricle choroid plexus epithelium,UBERON:0003911,choroid plexus epithelium
+UBERON:0012287,Rathkes pouch epithelium,UBERON:0009854,digestive tract diverticulum
+DOID:204,enthesopathy,DOID:65,connective tissue disease
+UBERON:0002623,cerebral peduncle,UBERON:0003544,brain white matter
+HP:0010238,Triangular epiphyses of the phalanges of the hand,HP:0010587,Triangular epiphyses
+HP:0011063,Abnormality of incisor morphology,HP:0000676,Abnormality of the incisor
+UBERON:0001274,ischium,UBERON:0015056,ischial endochondral element
+DOID:1271,capillary disease,DOID:178,vascular disease
+HP:0006400,Absent knee epiphyses,HP:0002815,Abnormality of the knees
+HP:0002221,Absent axillary hair,HP:0002298,Absent hair
+HP:0000454,Flared nostrils,HP:0000429,Abnormality of the nasal alae
+UBERON:0004031,ectomesenchyme,UBERON:0007213,mesenchyme derived from head neural crest
+UBERON:2001691,posterior cartilage of palatine,UBERON:0004121,ectoderm-derived structure
+HP:0012550,Colonic varices,HP:0002250,Abnormality of the large intestine
+UBERON:4200003,archipterygial fin,UBERON:0000151,pectoral fin
+DOID:225,syndrome,DOID:4,disease
+UBERON:0002292,costovertebral joint,UBERON:0002217,synovial joint
+DOID:12179,tinea corporis,DOID:37,skin disease
+UBERON:0007294,presumptive rhombomere 7,UBERON:0006598,presumptive structure
+UBERON:2005082,dorsal branch nasal ciliary artery,UBERON:0001637,artery
+HP:0011283,Abnormality of the metencephalon,HP:0011282,Abnormality of the hindbrain
+HP:0010228,Absent epiphyses of the phalanges of the hand,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+HP:0009602,Abnormality of the phalanges of the thumb,HP:0005918,Abnormality of phalanx of finger
+UBERON:0006647,adventitia of ductus deferens,UBERON:0005156,reproductive structure
+UBERON:0002561,neuraxis cavity,UBERON:0002558,organ cavity
+HP:0100366,Short phalanx of the 3rd toe,HP:0010359,Aplasia/Hypoplasia of the phalanges of the 3rd toe
+HP:0003577,Congenital onset,HP:0011007,Age of onset
+HP:0002871,Central apnea,HP:0002104,Apnea
+HP:0012593,Nephrotic range proteinuria,HP:0000093,Proteinuria
+UBERON:2002193,dorsolateral septum,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0007458,Focal hyperextensible skin,HP:0000974,Hyperextensible skin
+UBERON:0005789,lamina rara externa,UBERON:0006554,urinary system structure
+HP:0012719,Functional abnormality of the gastrointestinal tract,HP:0011024,Abnormality of the gastrointestinal tract
+HP:0001602,Laryngeal stenosis,HP:0001600,Abnormality of the larynx
+UBERON:0010883,forelimb cartilage element,UBERON:0015021,forelimb endochondral element
+HP:0000749,Paroxysmal bursts of laughter,HP:0000748,Inappropriate laughter
+UBERON:0014626,base of cochlear canal,UBERON:0005913,zone of bone organ
+HP:0009387,Irregular epiphyses of the 5th finger,HP:0009152,Abnormality of the epiphyses of the 5th finger
+HP:0009795,Branchial fistula,HP:0009794,Branchial anomaly
+UBERON:0006214,carpus pre-cartilage condensation,UBERON:0009523,mesenchyme of handplate
+UBERON:0013719,dartos muscle of scrotum,UBERON:0014403,male anatomical structure
+UBERON:2000634,caudal zone of median tuberal portion of hypothalamus,UBERON:0003048,regional part of hypothalamus
+CL:0002530,immature CD1a-positive dermal dendritic cell,CL:0001009,immature dermal dendritic cell
+UBERON:0001600,tensor tympani,UBERON:0004113,muscle of auditory ossicle
+DOID:8368,chordoid meningioma,DOID:4210,clear cell meningioma
+UBERON:0015238,pineal complex,UBERON:0000477,anatomical cluster
+DOID:9119,acute myeloid leukemia,DOID:8692,myeloid leukemia
+UBERON:0002778,ventral pallidum,UBERON:0005401,cerebral hemisphere grey matter
+DOID:4281,metatypical basal cell carcinoma,DOID:2513,basal cell carcinoma
+UBERON:0001133,cardiac muscle tissue,UBERON:0002036,striated muscle tissue
+DOID:6774,polyembryoma of the ovary,DOID:5351,ovarian primitive germ cell tumor
+HP:0009465,Ulnar deviation of finger,HP:0001193,Ulnar deviation of the hand or of fingers of the hand
+UBERON:0011773,upper jaw opening,UBERON:0000464,anatomical space
+UBERON:3000283,margo orbitalis of squamosal,UBERON:0010313,neural crest-derived structure
+HP:0009879,Cortical gyral simplification,HP:0002536,Abnormal cortical gyration
+UBERON:0004220,large intestine smooth muscle,UBERON:0004221,intestine smooth muscle
+UBERON:0004756,dermal skeletal element,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0003926,Abnormality of the humeral diaphysis,HP:0003063,Abnormality of the humerus
+HP:0007188,Congenital facial diplegia,HP:0001349,Facial diplegia
+HP:0100546,Carotid artery stenosis,HP:0100545,Arterial stenosis
+UBERON:0011203,urachus mesenchyme,UBERON:0006554,urinary system structure
+UBERON:0005693,manual digit 3 mesenchyme,UBERON:0005257,manual digit mesenchyme
+DOID:11337,Lemierre's syndrome,DOID:0050339,commensal bacterial infectious disease
+HP:0012139,Granulocytic hypoplasia,HP:0012137,Abnormal number of granulocyte precursors
+HP:0012568,Lower eyelid edema,HP:0100540,Palpebral edema
+DOID:9277,primary cerebellar degeneration,DOID:2478,spinocerebellar degeneration
+CL:1000042,forebrain neuroblast,CL:0000031,neuroblast
+UBERON:0006071,caudal region,UBERON:0011676,subdivision of organism along main body axis
+UBERON:0008596,mentalis,UBERON:0015212,lateral structure
+HP:0011914,Thoracic hypertrichosis,HP:0000998,Hypertrichosis
+UBERON:3010541,median pars intermedia,UBERON:0004121,ectoderm-derived structure
+UBERON:0006099,Brodmann (1909) area 1,UBERON:0013529,Brodmann area
+DOID:6898,ovary mixed epithelial carcinoma,DOID:4001,ovarian carcinoma
+HP:0002764,Stippled chondral calcification,HP:0100593,Calcification of cartilage
+DOID:11247,disseminated intravascular coagulation,DOID:2452,thrombophilia
+UBERON:0010576,manual digit 2 phalanx pre-cartilage condensation,UBERON:0005692,manual digit 2 mesenchyme
+UBERON:2000439,superficial pelvic abductor,UBERON:0006845,abductor muscle
+HP:0001335,Bimanual synkinesia,HP:0100022,Abnormality of movement
+UBERON:0002291,central canal of spinal cord,UBERON:0004111,anatomical conduit
+HP:0011628,Congenital defect of the pericardium,HP:0001697,Abnormality of the pericardium
+UBERON:3010163,metacarpal fold,UBERON:3000981,limb external integument structure
+HP:0009329,Small epiphysis of the middle phalanx of the 3rd finger,HP:0009418,Small epiphyses of the 3rd finger
+UBERON:0008267,left supracardinal vein,UBERON:0006300,supracardinal vein
+CL:1001610,bone marrow hematopoietic cell,CL:0000988,hematopoietic cell
+DOID:288,endometriosis of uterus,DOID:289,endometriosis
+DOID:2748,glycogen storage disease III,DOID:2747,glycogen storage disease
+UBERON:0002496,stapes base,UBERON:0010313,neural crest-derived structure
+DOID:4217,malignant ovarian Brenner tumor,DOID:2151,malignant ovarian surface epithelial-stromal neoplasm
+UBERON:0003603,lower respiratory tract cartilage,UBERON:0002418,cartilage tissue
+UBERON:0007182,muscle layer of infundibulum of uterine tube,UBERON:0006660,muscle layer
+DOID:12143,neurogenic bladder,DOID:365,bladder disease
+HP:0003088,Premature osteoarthritis,HP:0002758,Osteoarthritis
+CL:0000567,polymodal nocireceptor,CL:0000198,pain receptor cell
+CL:0000395,procrystal cell,CL:0000387,hemocyte (sensu Nematoda and Protostomia)
+HP:0011384,Abnormality of the internal auditory canal,HP:0011390,Morphological abnormality of the inner ear
+UBERON:0013504,caudal vertebra pre-cartilage condensation,UBERON:0005174,dorsal region organ
+UBERON:0004078,cerebellum vermis lobule IX,UBERON:0004070,cerebellum vermis lobule
+CL:0000637,chromophil cell of anterior pituitary gland,CL:2000004,pituitary gland cell
+HP:0001357,Plagiocephaly,HP:0002648,Abnormality of calvarial morphology
+DOID:2253,cervix disease,DOID:345,uterine disease
+UBERON:0005466,paravertebral ganglia,UBERON:0001806,sympathetic ganglion
+HP:0009668,Fragmentation of the epiphysis of the proximal phalanx of the thumb,HP:0010261,Fragmentation of the epiphyses of the middle phalanges of the hand
+UBERON:0003477,vein of upper lip,UBERON:0013136,vein of lip
+HP:0002501,Spasticity of pharyngeal muscles,HP:0001257,Spasticity
+DOID:9108,uterus carcinoma in situ,DOID:8719,in situ carcinoma
+UBERON:2001958,ceratobranchial 3 bone distal cartilage,UBERON:0011004,pharyngeal arch cartilage
+HP:0011168,Eyelid myoclonias,HP:0011166,Focal myoclonic seizures
+UBERON:0013195,parakeratinized epithelium of gingiva,UBERON:0013193,parakeratinized epithelium
+DOID:4606,bile duct cancer,DOID:4607,biliary tract cancer
+UBERON:0007182,muscle layer of infundibulum of uterine tube,UBERON:0014404,female anatomical structure
+HP:0012638,Abnormality of nervous system physiology,HP:0000707,Abnormality of the nervous system
+HP:0005086,Knee osteoarthritis,HP:0002758,Osteoarthritis
+CL:0002584,renal cortical epithelial cell,CL:0002681,kidney cortical cell
+CL:0001058,"plasmacytoid dendritic cell, human",CL:0000784,plasmacytoid dendritic cell
+HP:0009217,Enlarged epiphysis of the middle phalanx of the 4th finger,HP:0009247,Abnormality of the epiphysis of the middle phalanx of the 4th finger
+DOID:734,urethra cancer,DOID:3996,urinary system cancer
+UBERON:0011177,posterior division of bed nuclei of stria terminalis,UBERON:0002791,regional part of telencephalon
+HP:0003423,Thoracolumbar kyphoscoliosis,HP:0005619,Thoracolumbar kyphosis
+HP:0100544,Neoplasm of the heart,HP:0001627,Abnormality of cardiac morphology
+DOID:4468,clear cell adenocarcinoma,DOID:299,adenocarcinoma
+UBERON:3000938,postzonal element,UBERON:0000477,anatomical cluster
+UBERON:0013719,dartos muscle of scrotum,UBERON:0005156,reproductive structure
+UBERON:0010755,secondary follicle corona,UBERON:0001744,lymphoid tissue
+DOID:1571,spastic ectropion,DOID:1570,ectropion
+UBERON:0007632,Barrington's nucleus,UBERON:0006331,brainstem nucleus
+UBERON:0002585,central tegmental tract of midbrain,UBERON:0014891,brainstem white matter
+UBERON:0007836,cervical spinal cord ventral commissure,UBERON:0004170,spinal cord ventral commissure
+HP:0002570,Steatorrhea,HP:0002630,Fat malabsorption
+NCBITaxon:36830,Clostridium botulinum E,NCBITaxon:1491,Clostridium botulinum
+DOID:917,liver leiomyoma,DOID:916,liver neoplasm
+DOID:11577,Cauda equina syndrome,DOID:574,peripheral nervous system disease
+NCBITaxon:451864,Dikarya,NCBITaxon:4751,Fungi
+CL:0000215,barrier cell,CL:0000003,native cell
+UBERON:0011905,plantaris,UBERON:0004256,hindlimb zeugopod muscle
+UBERON:0003547,brain meninx,UBERON:0002360,meninx
+HP:0003551,Difficulty climbing stairs,HP:0004302,Functional motor problems.
+DOID:11211,buphthalmos,DOID:11212,hydrophthalmos
+HP:0003102,Increased carrying angle,HP:0009811,Abnormality of the elbow
+HP:0100531,Wind-swept deformity of the knees,HP:0002970,Genu varum
+UBERON:0002478,orbitosphenoid,UBERON:0002513,endochondral bone
+UBERON:0014727,intercalated duct of salivary gland,UBERON:0001837,duct of salivary gland
+HP:0002979,Bowing of the legs,HP:0006487,Bowing of the long bones
+HP:0009952,Complete duplication of the middle phalanx of the 2nd finger,HP:0009957,Complete duplication of the phalanges of the 2nd finger
+DOID:7138,cystitis cystica,DOID:1679,cystitis
+UBERON:0010890,pelvic complex muscle,UBERON:0001630,muscle organ
+UBERON:0013686,anatomical conduit space,UBERON:0000464,anatomical space
+HP:0011111,Abnormality of immune serum protein physiology,HP:0010978,Abnormality of immune system physiology
+UBERON:0007693,caroticotympanic artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0012594,Microalbuminuria,HP:0012592,Albuminuria
+DOID:2861,congenital nonspherocytic hemolytic anemia,DOID:589,congenital hemolytic anemia
+UBERON:2001228,pharyngeal arch 3 skeleton,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:1241,luxation of globe,DOID:1242,globe disease
+UBERON:0007119,neck of femur,UBERON:0005055,zone of long bone
+HP:0007441,Hyperpigmented/hypopigmented macules,HP:0009123,Mixed hypo- and hyperpigmentation of the skin
+HP:0009978,Complete duplication of the distal phalanx of the 4th finger,HP:0009973,Complete duplication of the phalanges of the 4th finger
+UBERON:0014615,accessory nerve root,UBERON:0002211,nerve root
+UBERON:0005942,hair outer root sheath,UBERON:0005933,hair root sheath
+UBERON:0003050,olfactory placode,UBERON:0005291,embryonic tissue
+HP:0002341,Cervical cord compression,HP:0002176,Spinal cord compression
+DOID:6969,acute canaliculitis,DOID:6970,acute inflammation of lacrimal passage
+HP:0011181,Low voltage EEG,HP:0011176,EEG with constitutional variants
+HP:0009577,Short middle phalanx of the 2nd finger,HP:0009536,Short 2nd finger
+HP:0002064,Spastic gait,HP:0001257,Spasticity
+HP:0001409,Portal hypertension,HP:0006707,Abnormality of the hepatic vasculature
+HP:0100484,Symphalangism of the proximal phalanx of the 3rd toe with the 3rd metatarsal,HP:0100473,Symphalangism affecting the proximal phalanx of the 3rd toe
+UBERON:0011209,lateral migration pathway NC-derived mesenchyme,UBERON:0011210,migration pathway NC-derived mesenchyme
+DOID:6432,pulmonary hypertension,DOID:10763,hypertension
+UBERON:0002319,mesangium,UBERON:0003891,stroma
+HP:0200098,Absent skin pigmentation,HP:0001010,Hypopigmentation of the skin
+HP:0011793,Neoplasm by anatomical site,HP:0002664,Neoplasm
+UBERON:2001028,hypurapophysis,UBERON:4100000,skeletal element projection
+DOID:1363,ethmoid sinus cancer,DOID:0050619,paranasal sinus cancer
+UBERON:2001097,immature posterior macula,UBERON:2001095,immature macula
+DOID:2789,parasitic protozoa infectious disease,DOID:1398,parasitic infectious disease
+UBERON:2001541,pelvic radial 2 cartilage,UBERON:2001538,pelvic radial cartilage
+HP:0005510,Transient erythroblastopenia,HP:0001903,Anemia
+HP:0000127,Renal salt wasting,HP:0012591,Abnormal urinary electrolyte concentration
+DOID:6003,aleukemic leukemia cutis,DOID:6004,aleukemic leukemia
+HP:0001566,Widely-spaced maxillary central incisors,HP:0006304,Widely-spaced incisors
+HP:0100342,Fibular deviation of the 3rd toe,HP:0010332,Deviation/Displacement of the 3rd toe
+HP:0011612,Interrupted aortic arch type A,HP:0011611,Interrupted aortic arch
+DOID:0060145,pain agnosia,DOID:4090,agnosia
+NCBITaxon:35790,Rickettsia japonica,NCBITaxon:114277,spotted fever group
+HP:0010736,Monostotic fibrous dysplasia,HP:0010734,Fibrous dysplasia of the bones
+HP:0000245,Abnormality of the sinuses,HP:0011821,Abnormality of facial skeleton
+DOID:3305,teratocarcinoma,DOID:3095,germ cell and embryonal cancer
+HP:0100952,Enlarged sylvian cistern,HP:0002119,Ventriculomegaly
+DOID:7071,spinal cord dermoid cyst,DOID:5612,spinal cancer
+HP:0002638,Superficial thrombophlebitis,HP:0004418,Thrombophlebitis
+UBERON:0007616,layer of synovial tissue,UBERON:0002384,connective tissue
+DOID:1803,neuritis,DOID:870,neuropathy
+HP:0010696,Polar cataract,HP:0000518,Cataract
+HP:0010687,Low intestinal alkaline phosphatase,HP:0003282,Low alkaline phosphatase
+DOID:6777,villoglandular endometrial endometrioid adenocarcinoma,DOID:2870,endometrial adenocarcinoma
+CL:0000261,anterior cell,CL:0000263,vegetative cell (sensu Mycetozoa)
+HP:0011591,Left aortic arch with cervical origin of the right subclavian artery,HP:0011587,Abnormal branching pattern of the aortic arch
+DOID:4855,diencephalic astrocytomas,DOID:3843,diencephalic neoplasm
+DOID:12510,retinal ischemia,DOID:5679,retinal disease
+DOID:139,squamous cell papilloma,DOID:2615,papilloma
+UBERON:3000652,fossa maxillaris,UBERON:0004704,bone fossa
+HP:0100139,Fragmentation of the epiphysis of the distal phalanx of the 3rd toe,HP:0100059,Fragmentation of the epiphyses of the 3rd toe
+HP:0007417,Discoid lupus erythematosus,HP:0001005,Dermatological manifestations of systemic disorders
+UBERON:0005728,extraembryonic mesoderm,UBERON:0005292,extraembryonic tissue
+UBERON:0005078,lamina terminalis of neural tube,UBERON:0010371,ecto-epithelium
+DOID:0060045,Munchausen by proxy,DOID:1766,factitious disorder
+HP:0005070,Proximal radial head dislocation,HP:0003083,Dislocated radial head
+CL:0002081,type II cell of carotid body,CL:0002256,supporting cell of carotid body
+CL:1000337,enterocyte of epithelium of duodenal gland,CL:0002254,epithelial cell of small intestine
+UBERON:0006604,lamina orbitonasalis,UBERON:0004120,mesoderm-derived structure
+HP:0012075,Personality disorder,HP:0000708,Behavioural/Psychiatric Abnormality
+UBERON:0003428,gonadal fat pad,UBERON:0005156,reproductive structure
+UBERON:3000113,crista intermedia,UBERON:0010313,neural crest-derived structure
+UBERON:3010432,archenteron roof,UBERON:0002050,embryonic structure
+UBERON:3010061,anterior quadratocranial commissure,UBERON:0004121,ectoderm-derived structure
+HP:0003510,Severe short stature,HP:0003508,Proportionate short stature
+HP:0010371,Aplasia/Hypoplasia of the phalanges of the 4th toe,HP:0010173,Aplasia/Hypoplasia of the phalanges of the toes
+CL:0000390,blood cell (sensu Nematoda and Protostomia),CL:0000081,blood cell
+CL:0000361,gastrula cell,CL:0000007,early embryonic cell
+UBERON:0001507,biceps brachii,UBERON:0004255,forelimb stylopod muscle
+CL:0000946,antibody secreting cell,CL:0000945,lymphocyte of B lineage
+UBERON:0010558,pedal digit 2 metatarsal cartilage element,UBERON:0015038,pedal digit 2 metatarsal endochondral element
+HP:0009177,Proximal/middle symphalangism of 5th finger,HP:0009178,Symphalangism of middle phalanx of 5th finger
+UBERON:0003615,lung elastic tissue,UBERON:0003611,respiratory system elastic tissue
+UBERON:0003380,cardiac muscle of left atrium,UBERON:0004490,cardiac muscle tissue of atrium
+HP:0001898,Increased red blood cell mass,HP:0001901,Polycythemia
+CL:0000103,bipolar neuron,CL:0000099,interneuron
+HP:0009723,Abnormality of the subungual region,HP:0001597,Abnormality of the nail
+UBERON:0013519,uterine tube isthmus,UBERON:0013515,subdivision of uterine tube
+UBERON:0008605,tragicus muscle,UBERON:0001596,intrinsic auricular muscle
+UBERON:0012240,urethral meatus,UBERON:0004120,mesoderm-derived structure
+HP:0008648,Anteriorly displaced urethral meatus,HP:0100627,Displacement of the external urethral meatus
+DOID:8861,pulmonary subvalvular stenosis,DOID:6420,pulmonary valve stenosis
+UBERON:0004533,left testis,UBERON:0000473,testis
+HP:0100376,Aplasia/Hypoplasia of the proximal phalanx of the 4th toe,HP:0010203,Aplasia/Hypoplasia of the proximal phalanges of the toes
+DOID:9740,postcholecystectomy syndrome,DOID:9741,biliary tract disease
+UBERON:2001853,postcleithrum 2,UBERON:2000410,postcleithrum
+NCBITaxon:6936,Argasidae,NCBITaxon:297308,Ixodoidea
+HP:0009742,Stiff shoulders,HP:0001387,Joint stiffness
+DOID:10190,liver lipoma,DOID:409,liver disease
+DOID:0060115,nervous system benign neoplasm,DOID:0060085,organ system benign neoplasm
+DOID:0050339,commensal bacterial infectious disease,DOID:104,bacterial infectious disease
+UBERON:0011804,"feather bud, epidermal component",UBERON:0010371,ecto-epithelium
+UBERON:2000221,internal levator,UBERON:0000933,pharyngeal muscle
+UBERON:0013552,Brodmann (1909) area 21,UBERON:0013529,Brodmann area
+DOID:3141,mucinoses,DOID:65,connective tissue disease
+UBERON:0012321,deep cervical artery,UBERON:0012320,cervical artery
+HP:0009132,Abnormal tarsal bone mineral density,HP:0001850,Abnormality of the tarsal bones
+UBERON:2000673,hypobranchial artery,UBERON:0001637,artery
+UBERON:0005257,manual digit mesenchyme,UBERON:0010702,digit mesenchyme
+HP:0004940,Generalized arterial calcification,HP:0003207,Arterial calcification
+UBERON:0016426,proximal interphalangeal joint of little finger,UBERON:0007732,interphalangeal joint of manual digit 5
+CL:0002043,"CD34-positive, CD38-negative multipotent progenitor cell",CL:0000837,hematopoietic multipotent progenitor cell
+UBERON:0004545,external capsule,UBERON:0002437,cerebral hemisphere white matter
+UBERON:3000694,atlantal cotyle,UBERON:0004120,mesoderm-derived structure
+UBERON:0006279,pleuroperitoneal canal,UBERON:0003914,epithelial tube
+HP:0001980,Megaloblastic bone marrow,HP:0012145,Abnormality of multiple cell lineages in the bone marrow
+UBERON:4200068,prepubic element,UBERON:0007844,cartilage element
+HP:0100217,Fragmentation of the epiphysis of the middle phalanx of the 5th toe,HP:0100081,Fragmentation of the epiphyses of the 5th toe
+HP:0006266,Small placenta,HP:0100767,Abnormality of the placenta
+HP:0000046,Scrotal hypoplasia,HP:0000045,Abnormality of the scrotum
+UBERON:0002502,round window of inner ear,UBERON:0010313,neural crest-derived structure
+UBERON:0003051,ear vesicle,UBERON:0007497,developing epithelial placode
+HP:0010987,Abnormality of cellular immune system,HP:0002715,Abnormality of the immune system
+DOID:2913,acute pancreatitis,DOID:4989,pancreatitis
+UBERON:2002252,epural 1,UBERON:2000660,epural
+UBERON:0010222,anatomical line between pupils,UBERON:0006800,anatomical line
+HP:0002135,Basal ganglia calcification,HP:0002134,Abnormality of the basal ganglia
+UBERON:0002361,pia mater,UBERON:0000391,leptomeninx
+DOID:14068,blackwater fever,DOID:12365,malaria
+DOID:0050881,inclusion body myopathy with Paget disease of bone and frontotemporal dementia,DOID:225,syndrome
+HP:0003368,Abnormality of the femoral head,HP:0003366,Abnormality of the femoral neck and head region
+UBERON:0005789,lamina rara externa,UBERON:0004120,mesoderm-derived structure
+UBERON:0004462,musculature of body wall,UBERON:0004479,musculature of trunk
+HP:0008251,Congenital goiter,HP:0000853,Goiter
+UBERON:3000950,os triangulare,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0002079,Hypoplasia of the corpus callosum,HP:0007370,Aplasia/Hypoplasia of the corpus callosum
+CL:0002139,endothelial cell of vascular tree,CL:0000115,endothelial cell
+NCBITaxon:12089,Human coxsackievirus A24,NCBITaxon:138950,Human enterovirus C
+UBERON:0002706,posterior nucleus of hypothalamus,UBERON:0002789,regional part of posterior hypothalamic region
+CL:0000576,monocyte,CL:0002087,nongranular leukocyte
+DOID:0050157,cryptogenic organizing pneumonia,DOID:2797,idiopathic interstitial pneumonia
+HP:0010663,Abnormality of the thalamus,HP:0010662,Abnormality of the diencephalon
+HP:0011485,Corneolenticular adhesion,HP:0000593,Abnormality of the anterior chamber
+UBERON:0010026,ventral part of pharyngeal pouch 3,UBERON:0005911,endo-epithelium
+UBERON:0008950,azygous lobe of lung,UBERON:0004890,right lung accessory lobe
+HP:0009312,Osteolytic defects of the proximal phalanx of the 4th finger,HP:0009855,Osteolytic defects of the proximal phalanges of the hand
+UBERON:0012358,manual digitopodium bone,UBERON:0012357,digitopodium bone
+UBERON:0011973,epiphysis of phalanx of pes,UBERON:0001437,epiphysis
+HP:0001912,Abnormality of basophils,HP:0001911,Abnormality of granulocytes
+HP:0000743,Frontal release signs,HP:0100022,Abnormality of movement
+UBERON:0009213,pharyngeal membrane of 1st arch,UBERON:0009210,pharyngeal membrane
+UBERON:0000301,amniotic cavity,UBERON:0012467,enclosed anatomical space
+HP:0002690,Large sella turcica,HP:0002679,Abnormality of the sella turcica
+HP:0009290,Short distal phalanx of the 4th finger,HP:0009280,Short 4th finger
+UBERON:0010335,maxillary process mesenchyme from head mesenchyme,UBERON:0009526,maxillary process mesenchyme
+UBERON:2002225,posterior pronephric duct,UBERON:0004120,mesoderm-derived structure
+HP:0010054,Abnormality of the first metatarsal,HP:0001832,Abnormality of the metatarsal bones
+UBERON:0004360,cauda epididymis,UBERON:0000064,organ part
+HP:0012598,Abnormal urine potassium concentration,HP:0012591,Abnormal urinary electrolyte concentration
+UBERON:0001224,renal pelvis,UBERON:0006554,urinary system structure
+UBERON:0013203,hypogastrium,UBERON:0009569,subdivision of trunk
+DOID:4522,superior vena cava angiosarcoma,DOID:0001816,angiosarcoma
+UBERON:0010699,manual digit metacarpus cartilage element,UBERON:0015042,manual digit metacarpus endochondral element
+UBERON:3000917,apophysis distalis of tibiale fibulare,UBERON:0000064,organ part
+HP:0000466,Limited neck range of motion,HP:0005986,Limitation of neck motion
+DOID:13389,labia majora carcinoma,DOID:11905,labium majus cancer
+UBERON:0011564,adductor pollicis muscle of prepollex,UBERON:0011145,adductor muscle
+UBERON:0006121,hemispheric lobule VIII,UBERON:0014648,hemisphere part of cerebellar posterior lobe
+UBERON:0004353,female inguinal canal,UBERON:0005156,reproductive structure
+UBERON:0012352,mesangial matrix,UBERON:0000463,portion of organism substance
+DOID:10763,hypertension,DOID:0050828,artery disease
+UBERON:3010061,anterior quadratocranial commissure,UBERON:0013765,digestive system organ
+UBERON:0001692,basioccipital bone,UBERON:0015048,basioccipital endochondral element
+UBERON:0006234,femur pre-cartilage condensation,UBERON:0005254,upper leg mesenchyme
+DOID:1022,pinta disease,DOID:0050338,primary bacterial infectious disease
+DOID:8738,leukoplakia of penis,DOID:1529,penile disease
+UBERON:1000005,external ear margin,UBERON:0001444,subdivision of head
+HP:0009696,Triangular epiphyses of the thumb,HP:0009599,Abnormality of the epiphyses of the thumb
+UBERON:0006331,brainstem nucleus,UBERON:0002308,nucleus of brain
+HP:0009384,Cone-shaped epiphyses of the 5th finger,HP:0009152,Abnormality of the epiphyses of the 5th finger
+CL:0002516,interrenal chromaffin cell,CL:0000166,chromaffin cell
+UBERON:0013688,tonsil germinal center,UBERON:0004119,endoderm-derived structure
+UBERON:0012139,segment of autopod,UBERON:0002529,limb segment
+DOID:3659,sialuria,DOID:3211,lysosomal storage disease
+HP:0003207,Arterial calcification,HP:0011004,Abnormality of the systemic arterial tree
+HP:0007820,Atretic lacrimal puncta,HP:0011479,Abnormality of the lacrimal punctum
+UBERON:0005461,levator scapulae muscle,UBERON:0001482,muscle of shoulder
+UBERON:0001770,lacrimal canaliculus,UBERON:0004121,ectoderm-derived structure
+HP:0007285,Facial palsy secondary to cranial hyperostosis,HP:0005465,Facial hyperostosis
+DOID:6043,ciliary body spindle cell melanoma,DOID:6524,malignant ciliary body melanoma
+CL:1000409,myocyte of sinoatrial node,CL:0002072,nodal myocyte
+HP:0007546,Linear hyperpigmentation,HP:0007400,Irregular hyperpigmentation
+HP:0011665,Takotsubo cardiomyopathy,HP:0001638,Cardiomyopathy
+CL:0002497,primary trophoblast giant cell,CL:0002488,trophoblast giant cell
+UBERON:0006304,future trigeminal ganglion,UBERON:0005423,developing anatomical structure
+CL:0007012,non-terminally differentiated odontoblast,CL:0000060,odontoblast
+UBERON:0011210,migration pathway NC-derived mesenchyme,UBERON:0007214,mesenchyme derived from trunk neural crest
+HP:0008767,Self-mutilation of tongue and lips due to involuntary movements,HP:0004305,Involuntary movements
+UBERON:2000912,mesenchyme median fin fold,UBERON:0003104,mesenchyme
+DOID:2425,cutaneous ganglioneuroma,DOID:3165,skin benign neoplasm
+UBERON:0006098,basal nuclear complex,UBERON:0002780,regional part of forebrain
+HP:0006493,Aplasia/Hypoplasia involving bones of the lower limbs,HP:0009815,Aplasia/Hypoplasia of the extremities
+UBERON:0013626,medial metatarsal pad,UBERON:0008840,plantar pad
+HP:0012360,Decreased fucosylation of O-linked protein glycosylation,HP:0012359,Abnormal fucosylation of O-linked protein glycosylation
+UBERON:0013675,toxactinium,UBERON:0005156,reproductive structure
+HP:0003911,Flared humeral metaphysis,HP:0003849,Flared metaphyses of the upper limbs
+HP:0100748,Muscular edema,HP:0011805,Abnormality of muscle morphology
+UBERON:2005370,dorsal fin pterygiophore 7,UBERON:2001419,dorsal fin pterygiophore
+UBERON:2002034,prootic-exoccipital joint,UBERON:0000982,skeletal joint
+HP:0100262,Synostosis involving digits,HP:0100240,Synostosis of joints
+HP:0100505,Vitamin B5 deficiency,HP:0004340,Abnormality of vitamin B metabolism
+UBERON:0006976,peptonephridium,UBERON:0005181,thoracic segment organ
+HP:0003454,Platelet antibody positive,HP:0002960,Autoimmunity
+HP:0008537,Cleft at the superior portion of the pinna,HP:0009902,Cleft helix
+UBERON:0003262,amniotic mesoderm,UBERON:0005292,extraembryonic tissue
+DOID:450,myotonic disease,DOID:9884,muscular dystrophy
+UBERON:0009122,adenohypophyseal placode,UBERON:0011814,non-neurogenic ectodermal placode
+UBERON:2000318,brainstem and spinal white matter,UBERON:0002316,white matter
+UBERON:0004822,extrahepatic bile duct epithelium,UBERON:0004820,bile duct epithelium
+HP:0004991,Rhizomelic arm shortening,HP:0008905,Rhizomelia
+UBERON:0011584,zeugopodial skeleton,UBERON:0010712,limb skeleton subdivision
+UBERON:0016455,upper lateral secondary incisor tooth,UBERON:0003450,upper jaw incisor
+CL:0002153,corneocyte,CL:0000311,keratin accumulating cell
+HP:0005790,Short mandibular condyles,HP:0003778,Short mandibular rami
+UBERON:0009988,condyle of humerus,UBERON:0009979,condyle
+DOID:5435,variant Creutzfeldt-Jakob disease,DOID:649,prion disease
+HP:0009147,Enlarged epiphysis of the distal phalanx of the 5th finger,HP:0010249,Enlarged epiphyses of the distal phalanges of the hand
+HP:0010241,Short proximal phalanx of finger,HP:0009803,Short phalanx of finger
+UBERON:0014709,carapace primordium,UBERON:0002050,embryonic structure
+UBERON:0014569,dorsal tegmental nucleus pars ventralis,UBERON:0002635,regional part of midbrain tegmentum
+UBERON:2001610,quadrate dorsal process,UBERON:4100000,skeletal element projection
+UBERON:0013238,future glans,UBERON:0005423,developing anatomical structure
+UBERON:3000012,angulosplenial coronoid process,UBERON:4100000,skeletal element projection
+UBERON:0002068,urachus,UBERON:0006554,urinary system structure
+UBERON:3000562,septum semircularium posterior,UBERON:0003037,septum
+DOID:14699,thrombocytopenia-absent radius syndrome,DOID:0080014,chromosomal disease
+DOID:0050736,autosomal dominant disease,DOID:0050739,autosomal genetic disease
+DOID:12108,bullous retinoschisis,DOID:8465,retinoschisis
+UBERON:1000009,midline crest,UBERON:0001444,subdivision of head
+UBERON:2001816,anterior nuchal plate,UBERON:2001815,nuchal plate
+UBERON:0002020,gray matter of neuraxis,UBERON:0011215,cell part cluster of neuraxis
+UBERON:0006715,radio-ulna,UBERON:0015002,radius-ulna endochondral element
+HP:0003536,Decreased fumarate hydratase activity,HP:0000816,Abnormality of Krebs cycle metabolism
+HP:0000718,Aggressive behavior,HP:0006919,"Abnormal aggressive, impulsive or violent behavior"
+UBERON:4000020,mineralized extracellular matrix,UBERON:0000479,tissue
+UBERON:0003993,interventricular foramen of CNS,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000084,T cell,CL:0000542,lymphocyte
+HP:0009195,Epiphyseal stippling of the metacarpals,HP:0005913,Abnormality of metacarpal epiphyses
+HP:0012162,Common carotid artery dissection,HP:0012158,Carotid artery dissection
+UBERON:0012322,ascending cervical artery,UBERON:0004573,systemic artery
+DOID:4331,burning mouth syndrome,DOID:403,mouth disease
+HP:0100864,Short femoral neck,HP:0009108,Aplasia/Hypoplasia involving the femoral head and neck
+HP:0012649,Increased inflammatory response,HP:0012647,Abnormal inflammatory response
+UBERON:0001726,papilla of tongue,UBERON:0004121,ectoderm-derived structure
+DOID:13169,spermatic cord cancer,DOID:3856,male reproductive organ cancer
+UBERON:0001994,hyaline cartilage tissue,UBERON:0002418,cartilage tissue
+HP:0011774,Thyroid follicular adenoma,HP:0000854,Thyroid adenoma
+UBERON:0002201,vasculature of trunk,UBERON:0002049,vasculature
+UBERON:0013614,fasciculus aberans,UBERON:0002473,intercerebral commissure
+HP:0002886,Vagal paraganglioma,HP:0002864,Paraganglioma of head and neck
+CL:0000453,Langerhans cell,CL:0000990,conventional dendritic cell
+UBERON:0011043,obturator muscle,UBERON:0002000,gluteal muscle
+UBERON:0002443,choroidal blood vessel,UBERON:0004121,ectoderm-derived structure
+DOID:3284,thymic carcinoma,DOID:3277,thymus cancer
+DOID:5304,ovarian clear cell adenocarcinoma,DOID:3713,ovary adenocarcinoma
+UBERON:0010221,laryngeal associated mesenchyme,UBERON:0007524,dense mesenchyme tissue
+HP:0007875,Congenital blindness,HP:0000618,Blindness
+HP:0100547,Abnormality of the forebrain,HP:0012443,Abnormality of the brain
+HP:0100529,Abnormality of phosphate homeostasis,HP:0003111,Abnormality of ion homeostasis
+HP:0007961,Rarefaction of retinal pigmentation,HP:0007894,Hypopigmentation of the fundus
+UBERON:0013634,intertrochanteric line,UBERON:0006800,anatomical line
+UBERON:2000373,dorsal fin actinotrichium,UBERON:2000089,actinotrichium
+DOID:8310,sclerosing adenosis of breast,DOID:3274,proliferative type fibrocystic change of breast
+CL:0000647,multinucleated giant cell,CL:0000766,myeloid leukocyte
+DOID:7042,ciliary body epithelioid cell melanoma,DOID:7040,uveal epithelioid cell melanoma
+DOID:2316,brain ischemia,DOID:326,ischemia
+CL:0007009,prechondroblast,CL:0000055,non-terminally differentiated cell
+UBERON:2002274,transforming ctenoid scale,UBERON:2002273,ctenoid scale
+UBERON:0001959,white pulp of spleen,UBERON:1000023,spleen pulp
+UBERON:0009653,trachea basement membrane,UBERON:0004119,endoderm-derived structure
+UBERON:0012430,tunica fibrosa of eyeball,UBERON:0004121,ectoderm-derived structure
+UBERON:0004999,mucosa of biliary tree,UBERON:0000344,mucosa
+HP:0009974,Partial duplication of the phalanges of the 4th finger,HP:0009972,Duplication of phalanx of 4th finger
+UBERON:3000428,perilymphatic system,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0006092,cuneus cortex,UBERON:0003022,cerebral cortex lobe
+UBERON:1600006,paired fin radial element,UBERON:0004120,mesoderm-derived structure
+HP:0002846,Abnormality of B cells,HP:0004332,Abnormality of lymphocytes
+UBERON:0001368,obturator externus,UBERON:0011043,obturator muscle
+UBERON:0000948,heart,UBERON:0005181,thoracic segment organ
+UBERON:2001221,anterior copula,UBERON:2001220,basibranchial copula
+UBERON:0014381,whorl of hair,UBERON:0010164,collection of hairs
+DOID:7969,nested variant infiltrating bladder urothelial carcinoma,DOID:6477,invasive bladder transitional cell carcinoma
+HP:0001259,Coma,HP:0004372,Reduced consciousness/confusion
+HP:0006965,Acute necrotizing encephalopathy,HP:0006846,Acute encephalopathy
+DOID:6975,bladder urothelial papillary carcinoma,DOID:4006,bladder transitional cell carcinoma
+UBERON:0003073,lens placode,UBERON:0002546,cranial placode
+UBERON:2002185,climbing fiber,UBERON:0004121,ectoderm-derived structure
+HP:0012416,Hypercapnia,HP:0012415,Abnormal blood gas level
+HP:0009716,Subependymal nodules,HP:0002118,Abnormality of the cerebral ventricles
+HP:0010026,Aplasia/Hypoplasia of the 1st metacarpal,HP:0009658,Aplasia/Hypoplasia of the phalanges of the thumb
+UBERON:0007642,ligamentum arteriosum,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:5789,mixed hepatoblastoma,DOID:687,hepatoblastoma
+HP:0100130,Small epiphysis of the proximal phalanx of the 2nd toe,HP:0100090,Abnormality of the epiphysis of the proximal phalanx of the 2nd toe
+HP:0100082,Irregular epiphyses of the 5th toe,HP:0010341,Abnormality of the epiphyses of the 5th toe
+UBERON:0001344,epithelium of vagina,UBERON:0004804,oviduct epithelium
+UBERON:0010578,manual digit 4 phalanx pre-cartilage condensation,UBERON:0015028,manual digit 4 phalanx endochondral element
+DOID:9505,cannabis abuse,DOID:302,substance abuse
+HP:0002566,Intestinal malrotation,HP:0002242,Abnormality of the intestine
+HP:0000464,Abnormality of the neck,HP:0000152,Abnormality of head and neck
+DOID:10441,marginal corneal ulcer,DOID:8463,corneal ulcer
+CL:0002341,basal cell of prostate epithelium,CL:0002231,epithelial cell of prostate
+HP:0100733,Neoplasm of the parathyroid gland,HP:0011766,Abnormality of the parathyroid morphology
+CL:1000742,glomerular mesangial cell,CL:0000650,mesangial cell
+HP:0010345,Flexion contracture of the 5th toe,HP:0005830,Flexion contracture of toe
+DOID:4871,cutaneous adenocystic carcinoma,DOID:3451,skin carcinoma
+UBERON:0000992,female gonad,UBERON:0003134,female reproductive organ
+UBERON:0002088,lateral thoracic vein,UBERON:0001638,vein
+DOID:9283,borderline glaucoma,DOID:1686,glaucoma
+UBERON:2202280,pectoral fin distal radial cartilage 3,UBERON:2201588,pectoral fin distal radial cartilage
+HP:0010128,Bracket epiphysis of the proximal phalanx of the hallux,HP:0010114,Bracket epiphyses of the hallux
+CL:1000356,microfold cell of epithelium proper of duodenum,CL:1000354,microfold cell of epithelium of intestinal villus
+DOID:9880,cardiovascular syphilis,DOID:8200,tertiary syphilis
+HP:0006265,Aplasia/Hypoplasia of fingers,HP:0001167,Abnormality of finger
+UBERON:0002151,pontine nuclear group,UBERON:0009662,hindbrain nucleus
+HP:0001159,Syndactyly,HP:0011297,Abnormality of the digits
+CL:0000022,female germ line stem cell,CL:0000021,female germ cell
+CL:0000489,scotopic photoreceptor cell,CL:0000210,photoreceptor cell
+HP:0001917,Renal amyloidosis,HP:0012210,Abnormal renal morphology
+DOID:0050136,systemic mycosis,DOID:1564,fungal infectious disease
+DOID:2517,intracranial structure hemangioma,DOID:255,hemangioma
+DOID:11302,cercarial dermatitis,DOID:1395,schistosomiasis
+HP:0007457,Prominent veins on trunk,HP:0001015,Prominent superficial veins
+UBERON:0003906,cardiac jelly,UBERON:0004120,mesoderm-derived structure
+HP:0011631,Complete right sided absence of pericardium,HP:0011628,Congenital defect of the pericardium
+DOID:2474,vernal conjunctivitis,DOID:2475,chronic conjunctivitis
+DOID:9346,Taylor's syndrome,DOID:345,uterine disease
+HP:0009399,Ivory epiphyses of the 4th finger,HP:0100920,Sclerosis of the phalanges of the 4th finger
+HP:0009376,Aplasia/Hypoplasia of the phalanges of the 5th finger,HP:0004213,Abnormality of the phalanges of the 5th finger
+UBERON:2001852,postcleithrum 1,UBERON:2000410,postcleithrum
+HP:0100199,Small epiphysis of the proximal phalanx of the 4th toe,HP:0100096,Abnormality of the epiphysis of the proximal phalanx of the 4th toe
+DOID:7880,luteoma,DOID:1100,ovarian disease
+UBERON:0014398,respiratory muscle,UBERON:0003831,respiratory system muscle
+HP:0009521,Small epiphysis of the middle phalanx of the 2nd finger,HP:0010265,Small epiphyses of the middle phalanges of the hand
+CL:0000615,basidiospore,CL:0000596,sexual spore
+UBERON:0007361,ruminant reticulum,UBERON:0011954,stomach non-glandular region
+HP:0009492,Fragmentation of the epiphyses of the 2nd finger,HP:0006263,Abnormality of the epiphyses of the 2nd finger
+UBERON:0007838,spinal cord white commissure,UBERON:0008882,spinal cord commissure
+HP:0005036,Unilateral ulnar hypoplasia,HP:0003022,Hypoplasia of the ulna
+UBERON:0002370,thymus,UBERON:0005058,hemolymphoid system gland
+UBERON:3010664,m. intertransversarius capitus superior,UBERON:0004465,musculature of neck
+UBERON:0003437,eyelid nerve,UBERON:0004121,ectoderm-derived structure
+UBERON:0004800,bronchus basal lamina,UBERON:0004119,endoderm-derived structure
+HP:0009396,Enlarged epiphyses of the 4th finger,HP:0010231,Enlarged epiphyses of the phalanges of the hand
+CL:0002097,cortical cell of adrenal gland,CL:0002078,meso-epithelial cell
+UBERON:0006032,interdigital region between manual digits 3 and 4,UBERON:0006022,interdigital region between digits 3 and 4
+DOID:2321,dyspepsia,DOID:1159,functional gastric disease
+UBERON:0002398,manus,UBERON:0002470,autopod region
+DOID:11032,secondary corneal edema,DOID:11030,corneal edema
+UBERON:0001021,nerve,UBERON:0000122,neuron projection bundle
+HP:0009429,Aplasia of the distal phalanx of the 3rd finger,HP:0009421,Aplasia/Hypoplasia of the distal phalanx of the 3rd finger
+DOID:7515,lumbar spinal canal and spinal cord meningioma,DOID:1140,spinal canal and spinal cord meningioma
+UBERON:2001245,epibranchial 4 bone,UBERON:2001908,epibranchial 4 element
+UBERON:0008549,prevertebral muscle of neck,UBERON:0004518,muscle of vertebral column
+UBERON:0011738,quadrate lobe hepatic sinusoids,UBERON:0009549,hepatic sinusoid of right of lobe of liver
+HP:0003218,Oroticaciduria,HP:0001941,Acidosis
+DOID:12718,chronic gonococcal salpingitis,DOID:5731,chronic salpingitis
+UBERON:0001479,sesamoid bone,UBERON:0013631,sesamoid element
+DOID:910,occipital lobe neoplasm,DOID:368,cerebrum cancer
+UBERON:0010682,pedal digit 3 phalanx cartilage element,UBERON:0005697,pedal digit 3 mesenchyme
+HP:0008245,Pituitary hypothyroidism,HP:0011787,Central hypothyroidism
+UBERON:0007618,synovial cavity of hip joint,UBERON:0007617,synovial cavity of joint
+CL:0000339,glioblast (sensu Vertebrata),CL:0000123,neuron associated cell (sensu Vertebrata)
+HP:0009325,Fragmentation of the epiphysis of the middle phalanx of the 3rd finger,HP:0010261,Fragmentation of the epiphyses of the middle phalanges of the hand
+UBERON:0002270,hyaloid artery,UBERON:0003499,brain blood vessel
+CL:0000583,alveolar macrophage,CL:0000864,tissue-resident macrophage
+UBERON:3000824,tenuitas cristaeformis,UBERON:0000064,organ part
+UBERON:0007657,anular ligament of radius,UBERON:0003574,elbow connective tissue
+UBERON:0007225,lateral entorhinal cortex,UBERON:0004121,ectoderm-derived structure
+DOID:11816,vitreous syneresis,DOID:9720,vitreous disease
+HP:0012389,Appendicular hypotonia,HP:0001252,Muscular hypotonia
+UBERON:3010502,duodeno-hepatic artery,UBERON:0001637,artery
+CL:1001509,glycinergic neuron,CL:0000151,secretory cell
+HP:0009707,Synostosis involving the 4th metacarpal,HP:0009701,Metacarpal synostosis
+HP:0005716,Lethal skeletal dysplasia,HP:0002652,Skeletal dysplasia
+DOID:4501,orofaciodigital syndrome,DOID:630,genetic disease
+HP:0100727,Histiocytosis,HP:0004311,Abnormality of macrophages
+HP:0006213,Thin proximal phalanges with broad epiphyses,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+HP:0012499,Descending aortic dissection,HP:0002647,Aortic dissection
+HP:0008504,Moderate sensorineural hearing impairment,HP:0012713,Moderate hearing impairment
+UBERON:0009858,outer fibrous layer of periosteum,UBERON:0000158,membranous layer
+HP:0011784,Thyrotoxicosis with diffuse goiter,HP:0000836,Hyperthyroidism
+HP:0012434,Delayed social development,HP:0012433,Abnormal social behavior
+DOID:10939,antisocial personality disorder,DOID:1510,personality disorder
+UBERON:2000225,lateral crista primordium,UBERON:0003240,epithelium of lateral semicircular canal
+CL:0000933,type II NK T cell secreting interleukin-4,CL:0000922,type II NK T cell
+UBERON:2005032,optic vein,UBERON:0003496,head blood vessel
+HP:0100204,Cone-shaped epiphysis of the distal phalanx of the 5th toe,HP:0100097,Abnormality of the epiphysis of the distal phalanx of the 5th toe
+UBERON:0013195,parakeratinized epithelium of gingiva,UBERON:0001949,gingival epithelium
+DOID:294,lacrimal gland cancer,DOID:292,lacrimal system cancer
+UBERON:0015025,manual digit 1 phalanx endochondral element,UBERON:0015024,manual digit phalanx endochondral element
+HP:0006855,Cerebellar vermis atrophy,HP:0002334,Abnormality of the cerebellar vermis
+UBERON:0011311,hyoepiglottic ligament,UBERON:0001730,extrinsic ligament of larynx
+DOID:5134,anus leiomyoma,DOID:0050624,gastrointestinal system benign neoplasm
+HP:0000436,Abnormality of the nasal tip,HP:0010938,Abnormality of the external nose
+CL:0000027,smooth muscle cell neural crest derived,CL:0000192,smooth muscle cell
+UBERON:0002668,oculomotor nerve fibers,UBERON:0011215,cell part cluster of neuraxis
+HP:0009636,Triangular shaped proximal phalanx of the thumb,HP:0009618,Abnormality of the proximal phalanx of the thumb
+UBERON:0004274,lateral ventricle choroid plexus epithelium,UBERON:0003911,choroid plexus epithelium
+UBERON:0009708,dorsal pancreas,UBERON:0002365,exocrine gland
+UBERON:0006690,deep dorsal vein of clitoris,UBERON:0003480,vein of clitoris
+HP:0005556,Abnormality of the metopic suture,HP:0000290,Abnormality of the forehead
+DOID:14159,obstructive hydrocephalus,DOID:10908,hydrocephalus
+CL:1001106,kidney loop of henle thick ascending limb epithelial cell,CL:1000504,kidney medulla cell
+UBERON:0009116,thymoid,UBERON:0010313,neural crest-derived structure
+HP:0009435,Symphalangism of middle phalanx of 3rd finger,HP:0009445,Symphalangism of the 3rd finger
+UBERON:0004034,cutaneous microfibril,UBERON:0004121,ectoderm-derived structure
+HP:0012718,Morphological abnormality of the gastrointestinal tract,HP:0011024,Abnormality of the gastrointestinal tract
+NCBITaxon:310911,Amdovirus,NCBITaxon:40119,Parvovirinae
+UBERON:0005434,cervical region,UBERON:0011676,subdivision of organism along main body axis
+HP:0011062,Misalignment of incisors,HP:0000676,Abnormality of the incisor
+UBERON:0002202,submucosa of trachea,UBERON:0004119,endoderm-derived structure
+UBERON:3010747,submentalis,UBERON:0011648,jaw muscle
+DOID:10352,breast fibroadenosis,DOID:0060082,breast benign neoplasm
+HP:0100344,Fibular deviation of the 2nd toe,HP:0010326,Deviation/Displacement of the 2nd toe
+HP:0100348,Contractures of the proximal interphalangeal joint of the 2nd toe,HP:0010327,Flexion contracture of the 2nd toe
+HP:0012612,Abnormal urinary sulfate concentration,HP:0003110,Abnormality of urine homeostasis
+UBERON:0001756,middle ear,UBERON:0000477,anatomical cluster
+UBERON:0001213,intestinal villus,UBERON:0004923,organ component layer
+UBERON:4200090,fibular facet of the astragalus,UBERON:4100003,articular surface
+HP:0010166,Fragmentation of the epiphyses of the toes,HP:0010160,Abnormality of the epiphyses of the toes
+UBERON:3000801,caput glenoidale,UBERON:0004120,mesoderm-derived structure
+HP:0010362,Curved phalanges of the 3rd toe,HP:0010176,Curved phalanges of the toes
+UBERON:0003697,abdominal wall,UBERON:0000060,anatomical wall
+UBERON:0002050,embryonic structure,UBERON:0005423,developing anatomical structure
+NCBITaxon:782,Rickettsia prowazekii,NCBITaxon:114292,typhus group
+UBERON:2005087,pectoral vein,UBERON:0001638,vein
+UBERON:2005083,ventral branch nasal ciliary artery,UBERON:0001637,artery
+DOID:8481,rheumatic myocarditis,DOID:820,myocarditis
+UBERON:0005709,upper jaw incisor epithelium,UBERON:0003235,epithelium of upper jaw
+UBERON:0005692,manual digit 2 mesenchyme,UBERON:0005257,manual digit mesenchyme
+DOID:7465,chronic NK-cell lymphocytosis,DOID:2916,hypersensitivity reaction type IV disease
+UBERON:0003881,CA1 field of hippocampus,UBERON:0003876,subdivision of hippocampus
+UBERON:0006648,adventitia of seminal vesicle,UBERON:0005156,reproductive structure
+UBERON:0002954,dorsal hypothalamic area,UBERON:0004121,ectoderm-derived structure
+UBERON:0012252,endocervical epithelium,UBERON:0012250,cervix glandular epithelium
+HP:0012334,Extrahepatic cholestasis,HP:0001396,Cholestasis
+DOID:9771,transient neonatal thrombocytopenia,DOID:11245,transient neonatal neutropenia
+HP:0002019,Constipation,HP:0011458,Abdominal symptom
+UBERON:0010559,pedal digit 3 metatarsal cartilage element,UBERON:0010697,pedal digit metatarsal cartilage element
+UBERON:0006096,posterior transverse termporal area 42,UBERON:0013529,Brodmann area
+DOID:6083,childhood ovarian endodermal sinus tumor,DOID:5350,ovarian endodermal sinus tumor
+HP:0001601,Laryngomalacia,HP:0001600,Abnormality of the larynx
+HP:0006951,Retrocerebellar cyst,HP:0002350,Cerebellar cyst
+HP:0009386,Fragmentation of the epiphyses of the 5th finger,HP:0009152,Abnormality of the epiphyses of the 5th finger
+UBERON:4200131,trochanteric shelf,UBERON:4100000,skeletal element projection
+UBERON:0000389,lens cortex,UBERON:0004121,ectoderm-derived structure
+UBERON:0000059,large intestine,UBERON:0004921,subdivision of digestive tract
+UBERON:0006269,optic foramen,UBERON:0005423,developing anatomical structure
+UBERON:0007150,superior thyroid artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:1510,personality disorder,DOID:150,disease of mental health
+DOID:12156,arachnoiditis,DOID:9471,meningitis
+UBERON:0002930,tectopontine tract,UBERON:0007702,tract of brain
+DOID:4280,nodular basal cell carcinoma,DOID:2513,basal cell carcinoma
+HP:0009249,Abnormality of the epiphysis of the distal phalanx of the 4th finger,HP:0009174,Abnormality of the epiphyses of the 4th finger
+HP:0007807,Optic nerve compression,HP:0000587,Abnormality of the optic nerve
+HP:0010462,Aplasia/Hypoplasia of the ovary,HP:0000137,Abnormality of the ovary
+HP:0000235,Abnormality of the fontanelles and cranial sutures,HP:0002683,Abnormality of the calvaria
+UBERON:0002149,superior salivatory nucleus,UBERON:0007635,nucleus of medulla oblongata
+UBERON:0001869,cerebral hemisphere,UBERON:0000064,organ part
+UBERON:0001530,common carotid artery plus branches,UBERON:0004573,systemic artery
+HP:0000361,Pulsatile tinnitus (tympanic paraganglioma),HP:0002864,Paraganglioma of head and neck
+DOID:5351,ovarian primitive germ cell tumor,DOID:2155,malignant ovarian germ cell neoplasm
+UBERON:0006728,liver left medial lobe,UBERON:0001115,left lobe of liver
+UBERON:0001122,scalenus medius,UBERON:0004518,muscle of vertebral column
+HP:0009655,Patchy sclerosis of the phalanges of the thumb,HP:0100922,Sclerosis of the phalanges of the thumb
+DOID:0060126,alpha chain disease,DOID:0060125,heavy chain disease
+UBERON:0002646,dorsal longitudinal fasciculus of medulla,UBERON:0003045,dorsal longitudinal fasciculus
+HP:0000798,Oligospermia,HP:0008669,Abnormal spermatogenesis
+CL:0002674,H minus,CL:0000521,fungal cell
+UBERON:0010141,primitive sex cord of indifferent gonad,UBERON:0004909,epithelium of gonad
+UBERON:0007756,metatarsophalangeal joint of pedal digit 3,UBERON:0003696,metatarsophalangeal joint
+DOID:9669,senile cataract,DOID:83,cataract
+HP:0011025,Abnormality of cardiovascular system physiology,HP:0001626,Abnormality of the cardiovascular system
+UBERON:0004077,cerebellum vermis lobule IV,UBERON:0004070,cerebellum vermis lobule
+UBERON:0011233,synovial membrane of synovial tendon sheath,UBERON:0007616,layer of synovial tissue
+UBERON:0010884,forelimb bone pre-cartilage condensation,UBERON:0015021,forelimb endochondral element
+CL:0000034,stem cell,CL:0000003,native cell
+UBERON:0014629,terminal part of the cochlear canal,UBERON:0005913,zone of bone organ
+UBERON:2001747,lateral mesethmoid wing,UBERON:4100000,skeletal element projection
+CL:0000849,crypt olfactory receptor neuron,CL:0000207,olfactory receptor cell
+UBERON:0003680,posterior cruciate ligament of knee joint,UBERON:0006659,cruciate ligament of knee
+UBERON:0010401,spleen central arteriole,UBERON:0001980,arteriole
+HP:0009637,Absent proximal phalanx of thumb,HP:0009659,Partial absence of thumb
+HP:0004260,Large hamate bone,HP:0004259,Abnormality of the hamate bone
+DOID:6227,articular cartilage disease,DOID:381,arthropathy
+UBERON:0014730,osteon,UBERON:0000064,organ part
+UBERON:0008844,gubernaculum (female),UBERON:0004346,gubernaculum
+UBERON:0007803,preen oil,UBERON:0000456,bodily secretion
+HP:0012746,Thin toenail,HP:0008388,Abnormality of the toenail
+UBERON:0004562,digital vein,UBERON:0001638,vein
+HP:0008967,Exercise-induced muscle stiffness,HP:0003552,Muscle stiffness
+UBERON:2000947,dorsal fin proximal radial bone,UBERON:2100947,dorsal fin proximal radial element
+DOID:0060148,simultanagnosia,DOID:4090,agnosia
+UBERON:0015060,sphenoid endochondral element,UBERON:0010363,endochondral element
+DOID:4113,uterine corpus adenosarcoma,DOID:4114,uterine body mixed cancer
+UBERON:0016440,glabella,UBERON:0004121,ectoderm-derived structure
+UBERON:0008268,right supracardinal vein,UBERON:0006300,supracardinal vein
+UBERON:0004877,visceral endoderm,UBERON:0005292,extraembryonic tissue
+HP:0100587,Abnormality of the preputium,HP:0000036,Abnormality of the penis
+HP:0100493,Hypoammonemia,HP:0004364,Abnormality of nitrogen compound homeostasis
+UBERON:0015010,sacral vertebra endochondral element,UBERON:0005179,pelvic region organ
+UBERON:3000937,prezonal element,UBERON:0000477,anatomical cluster
+UBERON:0008882,spinal cord commissure,UBERON:0001020,nervous system commissure
+UBERON:0012648,ampulla of uterine tube,UBERON:0000064,organ part
+DOID:2435,skin glomangioma,DOID:2436,glomangioma
+HP:0000612,Iris coloboma,HP:0000525,Abnormality of the iris
+HP:0002843,Abnormality of T cells,HP:0004332,Abnormality of lymphocytes
+UBERON:0006247,iliac pre-cartilage condensation,UBERON:0015054,iliac endochondral element
+DOID:1703,Richter's syndrome,DOID:1040,chronic lymphocytic leukemia
+HP:0005461,Craniofacial disproportion,HP:0001999,Abnormal facial shape
+UBERON:2000291,medial octavolateralis nucleus,UBERON:2000381,lateral line sensory nucleus
+CL:0000506,enkephalin secreting cell,CL:0000507,endorphin secreting cell
+UBERON:0005678,right lung cranial lobe segmental bronchus,UBERON:0002184,segmental bronchus
+UBERON:0001785,cranial nerve,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100940,Sclerosis of the distal phalanx of the 3rd toe,HP:0100948,Sclerosis of the distal phalanges of the toes
+UBERON:0007181,serosa of infundibulum of uterine tube,UBERON:0014404,female anatomical structure
+HP:0100230,Ivory epiphysis of the proximal phalanx of the 5th toe,HP:0100099,Abnormality of the epiphysis of the proximal phalanx of the 5th toe
+UBERON:3010624,subarticular sesamoid,UBERON:0011141,appendicular ossicle
+HP:0012639,Abnormality of nervous system morphology,HP:0000707,Abnormality of the nervous system
+HP:0001905,Congenital thrombocytopenia,HP:0001873,Thrombocytopenia
+HP:0003736,Autophagic vacuoles,HP:0004303,Abnormality of muscle fibers
+UBERON:0005125,metanephric proximal straight tubule,UBERON:0001290,proximal straight tubule
+UBERON:0000388,epiglottis,UBERON:0000477,anatomical cluster
+HP:0012735,Cough,HP:0002795,Functional respiratory abnormality
+NCBITaxon:5592,Microascales,NCBITaxon:222543,Hypocreomycetidae
+UBERON:2000322,caudal octaval nerve sensory nucleus,UBERON:2000401,octaval nerve sensory nucleus
+HP:0008442,Vertebral hyperostosis,HP:0003468,Abnormality of the vertebrae
+DOID:298,lacrimal gland adenocarcinoma,DOID:293,lacrimal gland carcinoma
+HP:0004787,Fulminant hepatitis,HP:0004448,Fulminant hepatic failure
+UBERON:0001252,adventitia of ureter,UBERON:0005742,adventitia
+UBERON:2000484,celiacomesenteric artery,UBERON:0001637,artery
+UBERON:0003673,ligamentum flavum,UBERON:0000211,ligament
+NCBITaxon:34607,Amblyomma cajennense,NCBITaxon:6942,Amblyomma
+UBERON:0006953,ejaculatory duct epithelium,UBERON:0005156,reproductive structure
+HP:0004979,Metaphyseal sclerosis,HP:0000944,Abnormality of the metaphyses
+HP:0009213,Triangular epiphysis of the middle phalanx of the 5th finger,HP:0009392,Triangular epiphyses of the 5th finger
+HP:0012224,Circulating immune complexes,HP:0005368,Abnormality of humoral immunity
+HP:0010071,Osteolytic defects of the 1st metatarsal,HP:0010207,Osteolytic defects of the proximal phalanges of the toes
+DOID:11231,orbital periostitis,DOID:9957,periostitis
+HP:0004387,Enterocolitis,HP:0100282,Acute colitis
+CL:0000925,activated CD4-positive type I NK T cell,CL:0000912,helper T cell
+HP:0007641,Dyschromatopsia,HP:0000551,Abnormality of color vision
+UBERON:0014442,superior ischial ramus,UBERON:0014441,ischial ramus
+UBERON:0011208,medial migration pathway NC-derived mesenchyme,UBERON:0011210,migration pathway NC-derived mesenchyme
+HP:0009653,Curved phalanges of the thumb,HP:0004095,Curved fingers
+HP:0001890,Autoimmune hemolytic anemia,HP:0001878,Hemolytic anemia
+UBERON:0006904,head mesenchyme from mesoderm,UBERON:0004120,mesoderm-derived structure
+UBERON:0011803,"feather bud, dermal component",UBERON:0004120,mesoderm-derived structure
+HP:0006045,Short pointed phalanges,HP:0009803,Short phalanx of finger
+UBERON:0015704,sagittal sinus,UBERON:0005486,venous dural sinus
+HP:0006398,Flat distal femoral epiphysis,HP:0010590,Abnormality of the distal femoral epiphysis
+UBERON:0011104,epiphysis of fifth metacarpal bone,UBERON:0004390,epiphysis of metacarpal bone
+UBERON:0011772,lower jaw opening,UBERON:0000464,anatomical space
+UBERON:0003719,Pacinian corpuscle,UBERON:0012449,mechanoreceptor
+UBERON:0012315,incisive foramen,UBERON:0000464,anatomical space
+UBERON:0007135,neural keel,UBERON:0000479,tissue
+UBERON:0003214,mammary gland alveolus,UBERON:0014404,female anatomical structure
+UBERON:0011149,Marshall's gland,UBERON:0002365,exocrine gland
+HP:0009218,Fragmentation of the epiphysis of the middle phalanx of the 4th finger,HP:0009247,Abnormality of the epiphysis of the middle phalanx of the 4th finger
+HP:0012656,Reduced CSF dopamine level,HP:0012654,Abnormal CSF dopamine level
+UBERON:0006815,areolar connective tissue,UBERON:0011825,loose connective tissue
+UBERON:0013493,abdominal fascia,UBERON:0008982,fascia
+DOID:606,Brown-Sequard syndrome,DOID:607,paraplegia
+DOID:2860,hemoglobinopathy,DOID:589,congenital hemolytic anemia
+DOID:2667,benign mesenchymoma,DOID:2668,mesenchymoma
+UBERON:2100268,anal fin proximal radial element,UBERON:2101671,anal fin radial element
+UBERON:0005941,hair inner root sheath,UBERON:0005933,hair root sheath
+UBERON:2002086,pelvic axillary process,UBERON:0004375,bone of free limb or fin
+UBERON:0010008,mammalian cotyledon,UBERON:0014404,female anatomical structure
+DOID:3134,facial dermatosis,DOID:37,skin disease
+UBERON:0009709,ventral pancreas,UBERON:0002365,exocrine gland
+UBERON:0014847,vastus intermedius,UBERON:0001377,quadriceps femoris
+DOID:0050769,N syndrome,DOID:225,syndrome
+HP:0000358,Posteriorly rotated ears,HP:0000357,Abnormal location of ears
+HP:0010793,Bifid nail,HP:0002164,Nail dysplasia
+HP:0002301,Hemiplegia,HP:0004374,Hemiplegia/hemiparesis
+HP:0006157,Prominent palmar flexion creases,HP:0010490,Abnormality of the palmar creases
+HP:0002538,Abnormality of the cerebral cortex,HP:0002060,Abnormality of the cerebrum
+UBERON:0009291,cartilaginous vertebral centrum,UBERON:0001075,vertebral centrum
+HP:0012107,Increased fibular diameter,HP:0002991,Abnormality of the fibula
+UBERON:0001223,left ureter,UBERON:0000056,ureter
+UBERON:0005944,axial skeleton plus cranial skeleton,UBERON:0004120,mesoderm-derived structure
+HP:0003453,Antineutrophil antibody positivity,HP:0002960,Autoimmunity
+HP:0012156,Hemophagocytosis,HP:0004311,Abnormality of macrophages
+UBERON:2001542,pelvic radial 1 cartilage,UBERON:2001538,pelvic radial cartilage
+HP:0012368,Flat face,HP:0001999,Abnormal facial shape
+DOID:664,angiokeratoma of Fordyce,DOID:3165,skin benign neoplasm
+UBERON:2002240,Purkinje cell layer corpus cerebelli,UBERON:0004121,ectoderm-derived structure
+UBERON:2000523,inferior reticular formation,UBERON:0007635,nucleus of medulla oblongata
+CL:1000434,epithelial cell of external acoustic meatus,CL:0000066,epithelial cell
+DOID:3229,gastric dilatation,DOID:76,stomach disease
+DOID:8931,Evans' syndrome,DOID:8925,primary thrombocytopenia
+UBERON:2001544,sublingual cartilage,UBERON:0011004,pharyngeal arch cartilage
+HP:0100951,Enlarged fossa interpeduncularis,HP:0002119,Ventriculomegaly
+DOID:0050708,early onset absence epilepsy,DOID:0050704,childhood electroclinical syndrome
+HP:0004415,Pulmonary artery stenosis,HP:0004414,Abnormality of the pulmonary artery
+UBERON:0008278,nematocyst,UBERON:0008277,cnida
+HP:0011590,Double aortic arch,HP:0011587,Abnormal branching pattern of the aortic arch
+HP:0011310,Bridged palmar crease,HP:0010490,Abnormality of the palmar creases
+UBERON:0002623,cerebral peduncle,UBERON:0007417,peduncle of neuraxis
+HP:0009979,Complete duplication of the middle phalanx of the 4th finger,HP:0009973,Complete duplication of the phalanges of the 4th finger
+DOID:4074,pancreas adenocarcinoma,DOID:4905,pancreatic carcinoma
+HP:0100465,Patchy sclerosis of the proximal phalanx of the 4th toe,HP:0010376,Patchy sclerosis of the phalanges of the 4th toe
+UBERON:0011662,plastron-carapace bridge,UBERON:0000075,subdivision of skeletal system
+UBERON:0002890,anterior amygdaloid area,UBERON:0005401,cerebral hemisphere grey matter
+CL:0000394,plasmatocyte,CL:0000387,hemocyte (sensu Nematoda and Protostomia)
+HP:0012529,Abnormal dense granule content,HP:0012484,Abnormal dense granules
+DOID:4545,mesenchymal chondrosarcoma,DOID:3371,chondrosarcoma
+HP:0003763,Bruxism,HP:0002360,Sleep disturbance
+HP:0100297,Increased endomysial connective tissue,HP:0004303,Abnormality of muscle fibers
+HP:0010801,Underdeveloped nasolabial fold,HP:0005289,Abnormality of the nasolabial region
+UBERON:0008604,helicis minor,UBERON:0001596,intrinsic auricular muscle
+UBERON:2002024,mental barbel,UBERON:2000622,barbel
+HP:0008400,Onycholysis of distal fingernails,HP:0001806,Onycholysis
+HP:0004905,Vitamin A deficiency,HP:0008372,Abnormality of vitamin A metabolism
+HP:0001440,Synostosis involving metatarsal bones,HP:0100265,Synostosis of metacarpals/metatarsals
+HP:0008956,Proximal lower limb amyotrophy,HP:0007126,Proximal amyotrophy
+UBERON:0000468,multi-cellular organism,UBERON:0000061,anatomical structure
+UBERON:2002277,pectoral fin distal radial bone 1,UBERON:2001588,pectoral fin distal radial bone
+HP:0005979,Metabolic ketoacidosis,HP:0001993,Ketoacidosis
+UBERON:0014649,white matter of medulla oblongata,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:479,angiokeratoma,DOID:471,skin hemangioma
+HP:0010306,Short thorax,HP:0000765,Abnormality of the thorax
+UBERON:3010829,sulcus intermedius,UBERON:0006846,surface groove
+UBERON:0004215,back nerve,UBERON:0001021,nerve
+HP:0001032,Absent distal interphalangeal creases,HP:0006109,Absent phalangeal crease
+HP:0010574,Abnormality of the epiphysis of the femoral head,HP:0006499,Abnormality of femoral epiphyses
+HP:0100887,Abnormality of globe size,HP:0000284,Abnormality of the ocular region
+UBERON:3000832,anterior lamina recurvata,UBERON:0000064,organ part
+UBERON:0002211,nerve root,UBERON:0000122,neuron projection bundle
+HP:0006417,Broad femoral metaphyses,HP:0006489,Abnormality of the femoral metaphysis
+UBERON:3000112,crista dentalis of premaxilla,UBERON:0010313,neural crest-derived structure
+HP:0009553,Abnormality of the hairline,HP:0011361,Congenital abnormal hair pattern
+DOID:5463,cochlear disease,DOID:4539,labyrinthine disease
+HP:0011297,Abnormality of the digits,HP:0002813,Abnormality of limb bone morphology
+HP:0011600,Abnormal direction of ventricular apex,HP:0004307,Abnormal anatomic location of the heart
+UBERON:0002037,cerebellum,UBERON:0002680,regional part of metencephalon
+UBERON:0010096,future myelencephalon,UBERON:0002616,regional part of brain
+HP:0100033,Tics,HP:0100022,Abnormality of movement
+UBERON:0010989,transverospinalis pre-muscle mass,UBERON:0005865,pre-muscle condensation
+UBERON:0005185,renal medulla collecting duct,UBERON:0001232,collecting duct of renal tubule
+UBERON:0002501,oval window,UBERON:0010313,neural crest-derived structure
+UBERON:0001110,thyrohyoid muscle,UBERON:0008523,infrahyoid muscle
+UBERON:0001103,diaphragm,UBERON:0004120,mesoderm-derived structure
+NCBITaxon:439488,ssRNA viruses,NCBITaxon:10239,Viruses
+UBERON:0015886,root of nail,UBERON:0000479,tissue
+HP:0003367,Abnormality of the femoral neck,HP:0003366,Abnormality of the femoral neck and head region
+UBERON:2005106,longitudinal lateral lymphatic vessel,UBERON:0004536,lymph vasculature
+DOID:9828,neonatal abstinence syndrome,DOID:0060001,withdrawal disorder
+UBERON:0014530,lamina of neuraxis,UBERON:0002316,white matter
+DOID:0050156,idiopathic pulmonary fibrosis,DOID:2797,idiopathic interstitial pneumonia
+UBERON:0001255,urinary bladder,UBERON:0002075,viscus
+UBERON:0011866,condylar joint,UBERON:0002217,synovial joint
+HP:0001726,Increased prevalence of valvular disease,HP:0001654,Abnormality of the heart valves
+HP:0003277,Constricted iliac wings,HP:0011867,Abnormality of the wing of the ilium
+UBERON:0010025,dorsal part of pharyngeal pouch 3,UBERON:0005911,endo-epithelium
+HP:0010576,Intracranial cystic lesion,HP:0007319,Morphological abnormality of the central nervous system
+CL:0002252,epithelial cell of esophagus,CL:0002251,epithelial cell of alimentary canal
+UBERON:0003963,otic ganglion,UBERON:0001808,parasympathetic ganglion
+UBERON:0010722,accessory bone,UBERON:0001474,bone element
+DOID:2742,auditory system disease,DOID:0050155,sensory system disease
+UBERON:2000480,caudal octavolateralis nucleus,UBERON:2000381,lateral line sensory nucleus
+HP:0012280,Hepatic amyloidosis,HP:0011034,Amyloidosis
+DOID:4389,soft tissue peripheral neuroepithelioma,DOID:4232,extraosseous Ewing's sarcoma
+HP:0009202,Fragmentation of the epiphysis of the proximal phalanx of the 5th finger,HP:0010272,Fragmentation of the epiphyses of the proximal phalanges of the hand
+DOID:3361,pediatric osteosarcoma,DOID:3347,osteosarcoma
+UBERON:0006605,tectum synoticum,UBERON:0004120,mesoderm-derived structure
+UBERON:0002066,umbilical vein,UBERON:0010260,umbilical blood vessel
+DOID:9503,Loeffler syndrome,DOID:9498,pulmonary eosinophilia
+DOID:14444,sclerosing keratitis,DOID:13794,anterior scleritis
+HP:0100490,Camptodactyly of finger,HP:0009473,Joint contracture of the hand
+CL:1001592,gall bladder glandular cell,CL:1000415,epithelial cell of gall bladder
+DOID:8130,breast columnar cell mucinous carcinoma,DOID:3610,breast mucinous carcinoma
+UBERON:4200036,internal trochanter,UBERON:0004530,bony projection
+UBERON:0002243,cutaneous vein,UBERON:0001638,vein
+UBERON:0006311,chamber of eyeball,UBERON:0004121,ectoderm-derived structure
+UBERON:0011921,connecting stalk blood islands,UBERON:0010303,extraembryonic epithelium
+UBERON:0012242,internal urethral orifice,UBERON:0010418,urethral opening
+CL:0000903,natural T-regulatory cell,CL:0000792,"CD4-positive, CD25-positive, alpha-beta regulatory T cell"
+UBERON:2001656,upper pharyngeal 5 tooth plate,UBERON:2001647,pharyngeal tooth plate
+DOID:5684,"spondyloepimetaphyseal dysplasia, Sponastrime type",DOID:0080027,spondyloepimetaphyseal dysplasia
+HP:0011581,Double outlet left ventricle,HP:0001711,Abnormality of the left ventricle
+UBERON:0011915,cerebellar glomerulus,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:8439,postgastrectomy syndrome,DOID:1159,functional gastric disease
+UBERON:0008245,pennate muscle,UBERON:0001630,muscle organ
+HP:0009383,Bracket epiphyses of the 5th finger,HP:0009152,Abnormality of the epiphyses of the 5th finger
+HP:0100925,Sclerosis of bones of the feet,HP:0011001,Increased bone mineral density
+UBERON:0013553,Brodmann (1909) area 22,UBERON:0013529,Brodmann area
+UBERON:0013230,gland of nictitating membrane,UBERON:0015153,medial gland of orbital region
+HP:0100080,Enlarged epiphyses of the 5th toe,HP:0010341,Abnormality of the epiphyses of the 5th toe
+HP:0002373,Febrile seizures,HP:0001250,Seizures
+HP:0002522,Areflexia of lower limbs,HP:0001284,Areflexia
+UBERON:0015008,thoracic vertebra endochondral element,UBERON:0005181,thoracic segment organ
+UBERON:0002487,tooth cavity,UBERON:0002558,organ cavity
+UBERON:0005624,suprarenal artery,UBERON:0001637,artery
+HP:0008432,Anterior wedging of L1,HP:0008422,Vertebral wedging
+UBERON:0015079,proximal carpal cartilage,UBERON:0015064,autopod cartilage
+HP:0006862,Intermittent cerebellar ataxia,HP:0001251,Ataxia
+UBERON:0012472,hepatoduodenal ligament,UBERON:0008845,nonskeletal ligament
+UBERON:0010334,maxillary process mesenchyme from neural crest,UBERON:0009526,maxillary process mesenchyme
+UBERON:0001834,upper lip,UBERON:0001833,lip
+DOID:3891,placental insufficiency,DOID:780,placenta disease
+HP:0009532,Small epiphysis of the proximal phalanx of the 2nd finger,HP:0010276,Small epiphyses of the proximal phalanges of the hand
+UBERON:0001225,cortex of kidney,UBERON:0006554,urinary system structure
+UBERON:0008948,upper lobe of lung,UBERON:0000101,lobe of lung
+HP:0011710,Bundle branch block,HP:0005150,Abnormal atrioventricular conduction
+CL:0000746,cardiac muscle cell,CL:0000737,striated muscle cell
+DOID:6420,pulmonary valve stenosis,DOID:5749,pulmonary valve disease
+UBERON:0004162,pulmonary myocardium,UBERON:0002036,striated muscle tissue
+UBERON:0009193,sphenoid cartilage element,UBERON:0015060,sphenoid endochondral element
+UBERON:0006303,tracheal diverticulum,UBERON:0005423,developing anatomical structure
+HP:0012696,Abnormal thalamic MRI signal intensity,HP:0010663,Abnormality of the thalamus
+DOID:0060211,amyotrophic lateral sclerosis type 20,DOID:332,amyotrophic lateral sclerosis
+DOID:10762,portal hypertension,DOID:272,hepatic vascular disease
+HP:0004437,Cranial hyperostosis,HP:0002683,Abnormality of the calvaria
+DOID:7599,lymphoepithelioma-like thymic carcinoma,DOID:3284,thymic carcinoma
+CL:0002451,mammary stem cell,CL:0000048,multi fate stem cell
+UBERON:0004354,male inguinal canal,UBERON:0005156,reproductive structure
+DOID:8483,retinal artery occlusion,DOID:1729,retinal vascular occlusion
+NCBITaxon:114277,spotted fever group,NCBITaxon:780,Rickettsia
+HP:0001950,Respiratory alkalosis,HP:0001948,Alkalosis
+UBERON:0002362,arachnoid mater,UBERON:0000391,leptomeninx
+HP:0004464,Posterior auricular pit,HP:0100277,Periauricular skin pits
+HP:0011771,Autoimmune hypoparathyroidism,HP:0000829,Hypoparathyroidism
+UBERON:0011876,body of tongue,UBERON:0004121,ectoderm-derived structure
+HP:0012395,Seasonal allergy,HP:0012393,Allergy
+HP:0012184,Hyperalphalipoproteinemia,HP:0010980,Hyperlipoproteinemia
+DOID:5781,atrophic flaccid tympanic membrane,DOID:5782,tympanic membrane disease
+CL:0000336,adrenal medulla chromaffin cell,CL:0000457,biogenic amine secreting cell
+UBERON:0001765,mammary duct,UBERON:0003244,epithelium of mammary gland
+HP:0000110,Renal dysplasia,HP:0012210,Abnormal renal morphology
+UBERON:3000882,interilial region,UBERON:0004120,mesoderm-derived structure
+HP:0003185,Small sacroiliac notches,HP:0002867,Abnormality of the ilium
+UBERON:1500007,mesopterygium cartilage,UBERON:2201587,pectoral fin proximal radial cartilage
+HP:0002726,Recurrent Staphylococcus aureus infections,HP:0007499,Recurrent staphylococcal infections
+HP:0012179,Craniofacial dystonia,HP:0004373,Focal dystonia
+UBERON:0004783,gall bladder serosa,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0012301,Type II transferrin isoform profile,HP:0003160,Abnormal isoelectric focusing of serum transferrin
+HP:0004799,Jejunoileal diverticula,HP:0002256,Small bowel diverticula
+HP:0003575,Increased intracellular sodium,HP:0010931,Abnormality of sodium homeostasis
+HP:0001913,Granulocytopenia,HP:0001911,Abnormality of granulocytes
+UBERON:3010712,levator mandibulae externus profundus,UBERON:0011648,jaw muscle
+UBERON:2002154,opercular cavity,UBERON:0000464,anatomical space
+UBERON:3000711,procoelous,UBERON:0001075,vertebral centrum
+DOID:8445,intestinal volvulus,DOID:8437,intestinal obstruction
+DOID:14111,median rhomboid glossitis,DOID:1456,glossitis
+UBERON:2000461,Weberian ossicle,UBERON:0004765,skeletal element
+HP:0009719,Hypomelanotic macules,HP:0012733,Macule
+HP:0003445,EMG: neuropathic changes,HP:0003457,EMG abnormality
+DOID:12386,balantidiasis,DOID:2789,parasitic protozoa infectious disease
+HP:0005430,Recurrent Neisserial infections,HP:0005420,Recurrent gram-negative bacterial infections
+DOID:10035,asymptomatic neurosyphilis,DOID:9988,tertiary neurosyphilis
+UBERON:2001795,ceratohyal foramen,UBERON:0005744,bone foramen
+HP:0006740,Transitional cell carcinoma of the bladder,HP:0002862,Bladder carcinoma
+HP:0006489,Abnormality of the femoral metaphysis,HP:0006490,Abnormality of lower-limb metaphyses
+HP:0006286,Yellow-brown discoloration of the teeth,HP:0011073,Abnormality of dental color
+HP:0100495,Mastocytosis,HP:0100494,Abnormality of mast cells
+HP:0002118,Abnormality of the cerebral ventricles,HP:0007319,Morphological abnormality of the central nervous system
+UBERON:0014568,dorsal tegmental nucleus pars dorsalis,UBERON:0002635,regional part of midbrain tegmentum
+UBERON:0000437,arachnoid barrier layer,UBERON:0004923,organ component layer
+UBERON:0012423,layer of microvilli,UBERON:0005162,multi cell component structure
+UBERON:0009752,pancreas mesenchyme,UBERON:0003104,mesenchyme
+HP:0000831,Insulin-resistant diabetes mellitus,HP:0000819,Diabetes mellitus
+HP:0009421,Aplasia/Hypoplasia of the distal phalanx of the 3rd finger,HP:0009357,Abnormality of the distal phalanx of the 3rd finger
+HP:0005298,Atrioventricular canal defect with right ventricle aorta and pulmonary atresia,HP:0006695,Atrioventricular canal defect
+UBERON:3000955,ceratobranchial I,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:5719,adrenal medulla cancer,DOID:3953,adrenal gland cancer
+DOID:0050032,mineral metabolism disease,DOID:0060158,acquired metabolic disease
+UBERON:3000884,epipubis,UBERON:0004120,mesoderm-derived structure
+HP:0000782,Abnormality of the scapula,HP:0000765,Abnormality of the thorax
+DOID:0050338,primary bacterial infectious disease,DOID:104,bacterial infectious disease
+HP:0002286,Fair hair,HP:0011358,Generalized hypopigmentation of hair
+HP:0006334,Hypoplasia of the primary teeth,HP:0000685,Hypoplasia of teeth
+CL:0002202,epithelial cell of tracheobronchial tree,CL:0002632,epithelial cell of lower respiratory tract
+UBERON:0003554,hindbrain pia mater,UBERON:0003291,meninx of hindbrain
+HP:0010237,Epiphyseal stippling of finger phalanges,HP:0010655,Epiphyseal stippling
+HP:0002636,Aneurysm of an abdominal artery,HP:0002617,Aneurysm
+DOID:14004,thoracic aortic aneurysm,DOID:3627,aortic aneurysm
+UBERON:4200062,epichordal lepidotrichium,UBERON:4000174,caudal fin lepidotrichium
+UBERON:0005471,right umbilical vein,UBERON:0015212,lateral structure
+DOID:10293,monocular esotropia,DOID:9840,esotropia
+UBERON:0011190,lunule of nail,UBERON:0004121,ectoderm-derived structure
+HP:0100126,Fragmentation of the epiphysis of the proximal phalanx of the 2nd toe,HP:0100048,Fragmentation of the epiphyses of the 2nd toe
+UBERON:0002089,thoracodorsal vein,UBERON:0001638,vein
+CL:0002499,spongiotrophoblast cell,CL:0000351,trophoblast cell
+UBERON:0008909,perichordal bone,UBERON:0012075,replacement bone
+DOID:0050672,dyskinetic cerebral palsy,DOID:1969,cerebral palsy
+CL:0000480,secretin stimulating hormone secreting cell,CL:0000167,peptide hormone secreting cell
+HP:0000359,Abnormality of the inner ear,HP:0000598,Abnormality of the ear
+HP:0000176,Submucous cleft hard palate,HP:0100737,Abnormality of the hard palate
+UBERON:0010733,alisphenoid cartilage element,UBERON:0003932,cartilage element of chondrocranium
+UBERON:0006561,non-lymphatic part of lymphoid system,UBERON:0000477,anatomical cluster
+UBERON:0013674,ctenactinium,UBERON:0014403,male anatomical structure
+DOID:1485,cystic fibrosis,DOID:0050737,autosomal recessive disease
+DOID:14495,dumping syndrome,DOID:8439,postgastrectomy syndrome
+HP:0002895,Papillary thyroid carcinoma,HP:0002890,Thyroid carcinoma
+UBERON:0006699,foramen cecum of tongue,UBERON:0004119,endoderm-derived structure
+HP:0002884,Hepatoblastoma,HP:0002898,Embryonal neoplasm
+UBERON:2000716,afferent branchial artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0006522,Repeated pneumothoraces,HP:0002107,Pneumothorax
+UBERON:0013627,lateral metatarsal pad,UBERON:0008840,plantar pad
+UBERON:0002200,vasculature of head,UBERON:0002049,vasculature
+HP:0001582,Redundant skin,HP:0000973,Cutis laxa
+HP:0005928,Synostosis involving the fibula,HP:0002991,Abnormality of the fibula
+UBERON:0013232,serous acinus,UBERON:0011858,acinus of exocrine gland
+HP:0011143,Age-related cortical cataract,HP:0011141,Age-related cataract
+DOID:0050880,Koolen de Vries syndrome,DOID:225,syndrome
+UBERON:0010137,polarized epithelium,UBERON:0000483,epithelium
+UBERON:1000008,left part of face,UBERON:0001444,subdivision of head
+HP:0008046,Abnormality of the retinal vasculature,HP:0000479,Abnormality of the retina
+UBERON:0004638,blood vessel endothelium,UBERON:0004852,cardiovascular system endothelium
+HP:0012102,Abnormal mitochondrial number,HP:0008322,Abnormal mitochondrial morphology
+DOID:11168,anogenital venereal wart,DOID:934,viral infectious disease
+HP:0001162,Postaxial hand polydactyly,HP:0100259,Postaxial polydactyly
+HP:0009113,Diaphragmatic weakness,HP:0000775,Abnormality of the diaphragm
+HP:0000189,Narrow palate,HP:0000174,Abnormality of the palate
+UBERON:3000155,extremitas anterior,UBERON:0004120,mesoderm-derived structure
+UBERON:0013633,intertrochanteric crest,UBERON:0006800,anatomical line
+CL:1000332,serous cell of epithelium of terminal bronchiole,CL:1000333,serous cell of epithelium of lobular bronchiole
+DOID:7731,childhood malignant hemangiopericytoma,DOID:264,hemangiopericytoma
+HP:0000996,Facial capillary hemangioma,HP:0000329,Facial hemangioma
+UBERON:3000141,endolymphatic system,UBERON:0000467,anatomical system
+UBERON:0011248,procoracoid element,UBERON:0004765,skeletal element
+HP:0004029,Lytic defects of radial diaphysis,HP:0004027,Abnormality of radial diaphysis
+HP:0100863,Aplasia of the femoral neck,HP:0009108,Aplasia/Hypoplasia involving the femoral head and neck
+HP:0005792,Short humerus,HP:0006507,Aplasia/Hypoplasia of the humerus
+CL:0001008,Kit and Sca1-positive hematopoietic stem cell,CL:0000037,hematopoietic stem cell
+HP:0005617,Bilateral camptodactyly,HP:0100490,Camptodactyly of finger
+UBERON:0001391,popliteus muscle,UBERON:0001383,muscle of leg
+UBERON:0003317,odontogenic papilla of incisor,UBERON:0015846,incisor mesenchyme
+UBERON:0003488,abdominal mammary gland,UBERON:0005172,abdomen organ
+DOID:1712,aortic valve stenosis,DOID:62,aortic valve disease
+UBERON:0002106,spleen,UBERON:0005172,abdomen organ
+UBERON:0005174,dorsal region organ,UBERON:0000062,organ
+HP:0009385,Enlarged epiphyses of the 5th finger,HP:0009152,Abnormality of the epiphyses of the 5th finger
+HP:0007325,Generalized dystonia,HP:0001332,Dystonia
+UBERON:0006268,notochordal process,UBERON:0005423,developing anatomical structure
+DOID:13921,bacterial esophagitis,DOID:11963,esophagitis
+HP:0010971,Absence of Lutheran antigen on erythrocytes,HP:0010970,Blood group antigen abnormality
+DOID:6297,viral esophagitis,DOID:11963,esophagitis
+UBERON:0007768,ventral premammillary nucleus,UBERON:0002712,premammillary nucleus
+UBERON:0013249,paroophoron,UBERON:0003914,epithelial tube
+UBERON:0011118,tarsometatarsal joint,UBERON:0001487,pes joint
+NCBITaxon:578835,Rhipicephalus sanguineus group,NCBITaxon:426455,Rhipicephalus <subgenus>
+DOID:7541,mixed epithelial/mesenchymal metaplastic breast carcinoma,DOID:4680,breast metaplastic carcinoma
+UBERON:0009116,thymoid,UBERON:0004177,hemopoietic organ
+UBERON:0005820,pontine flexure,UBERON:0005817,neuraxis flexure
+DOID:7041,choroid epithelioid cell melanoma,DOID:7040,uveal epithelioid cell melanoma
+CL:1001576,oral mucosa squamous cell,CL:0002251,epithelial cell of alimentary canal
+UBERON:0003202,endocuticle,UBERON:0000476,acellular anatomical structure
+UBERON:0006727,liver left lateral lobe,UBERON:0001115,left lobe of liver
+CL:1000606,kidney nerve cell,CL:1000500,kidney interstitial cell
+UBERON:0003078,epibranchial placode,UBERON:0007497,developing epithelial placode
+DOID:14501,Sjogren-Larsson syndrome,DOID:0050737,autosomal recessive disease
+DOID:9500,leukocyte disease,DOID:74,hematopoietic system disease
+DOID:13417,alexia,DOID:4090,agnosia
+HP:0004757,Paroxysmal atrial fibrillation,HP:0005110,Atrial fibrillation
+UBERON:0006093,precuneus cortex,UBERON:0003022,cerebral cortex lobe
+UBERON:0000359,preputial gland,UBERON:0015251,modified sebaceous gland
+UBERON:2000068,proneural cluster,UBERON:0004121,ectoderm-derived structure
+HP:0200117,Recurrent upper and lower respiratory tract infections,HP:0002788,Recurrent upper respiratory tract infections
+UBERON:3001007,body granules,UBERON:3000977,body external integument structure
+DOID:341,peripheral vascular disease,DOID:178,vascular disease
+UBERON:2000157,somite 30,UBERON:0002329,somite
+HP:0002926,Abnormality of thyroid physiology,HP:0000820,Abnormality of the thyroid gland
+HP:0007576,Palmar neurofibromas,HP:0001067,Neurofibromas
+UBERON:0001681,nasal bone,UBERON:0002514,intramembranous bone
+UBERON:0005704,secondary palatal shelf mesenchyme,UBERON:0003323,mesenchyme of upper jaw
+DOID:4739,testicular Brenner tumor,DOID:2998,testicular cancer
+HP:0009374,Broad phalanges of the 5th finger,HP:0004213,Abnormality of the phalanges of the 5th finger
+DOID:10261,discharging ear,DOID:2742,auditory system disease
+UBERON:0007221,neonate stage,UBERON:0000105,life cycle stage
+UBERON:0011697,right extraembryonic umbilical artery,UBERON:0011693,extraembryonic portion of umbilical artery
+UBERON:0004438,proximal epiphysis of middle phalanx of manual digit 4,UBERON:0011978,epiphysis of middle phalanx of manus
+HP:0009886,Trichorrhexis nodosa,HP:0003328,Abnormal hair laboratory examination
+CL:0000569,cardiac mesenchymal cell,CL:0000134,mesenchymal cell
+HP:0006389,Limited knee flexion,HP:0005085,limited knee flexion/extension
+UBERON:2000214,hypobranchial vessel,UBERON:0003498,heart blood vessel
+HP:0007786,Lacunar retinal depigmentation,HP:0007894,Hypopigmentation of the fundus
+HP:0007971,Lamellar cataract,HP:0010920,Zonular cataract
+UBERON:0010296,scleral skeletal element,UBERON:0010321,skeletal element of eye region
+HP:0100081,Fragmentation of the epiphyses of the 5th toe,HP:0010341,Abnormality of the epiphyses of the 5th toe
+HP:0007759,Opacification of the corneal stroma,HP:0011492,Abnormality of corneal stroma
+UBERON:2007045,midbrain hindbrain boundary neural keel,UBERON:0006800,anatomical line
+HP:0000057,Clitoromegaly,HP:0000056,Abnormality of the clitoris
+DOID:0050802,Ehlers-Danlos syndrome progeroid type,DOID:13359,Ehlers-Danlos syndrome
+HP:0009549,Curved phalanges of the 2nd finger,HP:0004095,Curved fingers
+UBERON:0006293,spleen primordium,UBERON:0004120,mesoderm-derived structure
+DOID:10442,hypopyon ulcer,DOID:8463,corneal ulcer
+DOID:9987,orbit sarcoma,DOID:4143,orbital cancer
+HP:0200102,Sparse/absent eyelashes,HP:0000499,Abnormality of the eyelashes
+HP:0005193,Restricted large joint movement,HP:0001376,Limitation of joint mobility
+UBERON:0002003,peripheral nerve,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009669,Irregular epiphysis of the proximal phalanx of the thumb,HP:0009691,Irregular epiphyses of the thumb
+UBERON:0007295,presumptive rhombomere 8,UBERON:0006598,presumptive structure
+HP:0000980,Pallor,HP:0011121,Abnormality of skin morphology
+HP:0003137,Prolinuria,HP:0003355,Aminoaciduria
+UBERON:0006260,lingual swellings,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001122,scalenus medius,UBERON:0003897,axial muscle
+HP:0009975,Duplication of the distal phalanx of the 4th finger,HP:0009972,Duplication of phalanx of 4th finger
+HP:0001019,Erythroderma,HP:0011123,Inflammatory abnormality of the skin
+UBERON:2002087,pectoral axillary process,UBERON:0004375,bone of free limb or fin
+HP:0008420,Punctate vertebral calcifications,HP:0010766,Ectopic calcification
+UBERON:0011301,manubrium sternum pre-cartilage condensation,UBERON:0004120,mesoderm-derived structure
+HP:0009682,Pseudoepiphysis of the distal phalanx of the thumb,HP:0009693,Pseudoepiphyses of the thumb
+UBERON:2000440,superior raphe nucleus,UBERON:0009662,hindbrain nucleus
+UBERON:0006345,stapedial artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0005720,hindbrain venous system,UBERON:0004582,venous system
+HP:0002973,Abnormality of the forearm,HP:0002817,Abnormality of the upper limb
+HP:0010352,Patchy sclerosis of the phalanges of the 2nd toe,HP:0010324,Abnormality of phalanx of the 2nd toe
+UBERON:4200001,postpubis,UBERON:4100000,skeletal element projection
+CL:1000495,small intestine goblet cell,CL:0000160,goblet cell
+HP:0008801,Hypoplasia of the lesser trochanter,HP:0003366,Abnormality of the femoral neck and head region
+DOID:8867,molluscum contagiosum,DOID:934,viral infectious disease
+HP:0100725,Lichenification,HP:0011121,Abnormality of skin morphology
+HP:0009375,Bullet-shaped phalanges of the 5th finger,HP:0004213,Abnormality of the phalanges of the 5th finger
+DOID:7222,gallbladder pleomorphic giant cell adenocarcinoma,DOID:3500,gallbladder adenocarcinoma
+UBERON:0007362,omasum,UBERON:0011954,stomach non-glandular region
+UBERON:2001241,ceratobranchial 3 bone,UBERON:2000488,ceratobranchial bone
+UBERON:0005608,hyoid artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0009493,Irregular epiphyses of the 2nd finger,HP:0006263,Abnormality of the epiphyses of the 2nd finger
+HP:0004372,Reduced consciousness/confusion,HP:0011446,Abnormality of higher mental function
+HP:0012658,Abnormal brain FDG positron emission tomography,HP:0012657,Abnormal brain positron emission tomography
+UBERON:0002779,lateral superior olivary nucleus,UBERON:0007247,superior olivary nucleus
+HP:0010163,Bracket epiphyses of the toes,HP:0010160,Abnormality of the epiphyses of the toes
+UBERON:2000419,pterosphenoid,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0010551,pedal digit 5 metatarsal pre-cartilage condensation,UBERON:0010584,pedal digit 5 phalanx pre-cartilage condensation
+DOID:10938,paranoid personality disorder,DOID:1510,personality disorder
+UBERON:0003438,iris nerve,UBERON:0004121,ectoderm-derived structure
+HP:0012444,Brain atrophy,HP:0007367,Atrophy/Degeneration affecting the central nervous system
+DOID:4947,cholangiocarcinoma,DOID:4896,bile duct adenocarcinoma
+HP:0100369,Aplasia/Hypoplasia of the distal phalanx of the 3rd toe,HP:0010185,Aplasia/Hypoplasia of the distal phalanges of the toes
+UBERON:0007176,superior angle of scapula,UBERON:0007172,angle of scapula
+HP:0012161,External carotid artery dissection,HP:0012158,Carotid artery dissection
+DOID:8498,hereditary night blindness,DOID:8499,night blindness
+UBERON:0011737,caudate lobe hepatic sinusoids,UBERON:0009549,hepatic sinusoid of right of lobe of liver
+HP:0009634,Patchy sclerosis of the proximal phalanx of the thumb,HP:0009848,Patchy sclerosis of the middle phalanges of the hand
+UBERON:0001660,maxillary vein,UBERON:0003496,head blood vessel
+HP:0009635,Symphalangism of proximal phalanx of  thumb,HP:0009618,Abnormality of the proximal phalanx of the thumb
+HP:0006743,Embryonal rhabdomyosarcoma,HP:0002859,Rhabdomyosarcoma
+UBERON:0014468,ansoparamedian fissure of cerebellum,UBERON:0003980,cerebellum fissure
+UBERON:0003386,smooth muscle of eye,UBERON:0001135,smooth muscle tissue
+UBERON:0003622,manual digit 2,UBERON:0006049,digit 2
+UBERON:0006081,fundus of gallbladder,UBERON:0004119,endoderm-derived structure
+UBERON:0005386,olfactory segment of nasal mucosa,UBERON:0001826,nasal cavity mucosa
+DOID:9159,gas gangrene,DOID:37,skin disease
+UBERON:0013620,lower primary molar tooth,UBERON:0003667,lower jaw molar
+HP:0010203,Aplasia/Hypoplasia of the proximal phalanges of the toes,HP:0010184,Abnormality of the proximal phalanges of the toes
+DOID:8805,intermediate coronary syndrome,DOID:3393,coronary artery disease
+UBERON:0008275,carapace,UBERON:0000075,subdivision of skeletal system
+HP:0006721,Acute lymphatic leukemia,HP:0002488,Acute leukemia
+DOID:9540,vascular skin disease,DOID:37,skin disease
+DOID:1203,drug-induced mental disorder,DOID:8646,substance-induced psychosis
+CL:0002085,tanycyte,CL:0000683,ependymoglial cell
+HP:0010080,Osteolytic defects of the distal phalanx of the hallux,HP:0010053,Abnormality of the distal phalanx of the hallux
+UBERON:0010565,manual digit 1 metacarpus pre-cartilage condensation,UBERON:0010698,manual digit metacarpus pre-cartilage condensation
+CL:0000564,neutrophilic promyelocyte,CL:0000836,promyelocyte
+DOID:4985,extraosseous Ewings sarcoma-primitive neuroepithelial tumor,DOID:4232,extraosseous Ewing's sarcoma
+UBERON:0009966,internodal tract,UBERON:0002385,muscle tissue
+DOID:1540,parathyroid carcinoma,DOID:170,endocrine gland cancer
+HP:0000362,Otosclerosis,HP:0008628,Abnormality of the stapes
+UBERON:0006721,alisphenoid bone,UBERON:0002513,endochondral bone
+DOID:4699,epicardium cancer,DOID:116,pericardium cancer
+UBERON:2000006,ball,UBERON:0002050,embryonic structure
+UBERON:0008408,distal tubular epithelium,UBERON:0004810,nephron tubule epithelium
+HP:0002904,Hyperbilirubinemia,HP:0001939,Abnormality of metabolism/homeostasis
+UBERON:2000732,somite 3,UBERON:0002329,somite
+UBERON:0003929,gut epithelium,UBERON:0000483,epithelium
+UBERON:0008611,scalene muscle,UBERON:0004518,muscle of vertebral column
+HP:0003272,Abnormality of the hip bone,HP:0002644,Abnormality of pelvic girdle bone morphology
+DOID:12445,conjugate gaze palsy,DOID:540,strabismus
+UBERON:0015026,manual digit 2 phalanx endochondral element,UBERON:0015024,manual digit phalanx endochondral element
+HP:0010787,Genital neoplasm,HP:0000078,Abnormality of the genital system
+CL:0000909,"CD8-positive, alpha-beta memory T cell",CL:0000813,memory T cell
+UBERON:0005501,rhombomere lateral wall,UBERON:0005496,neural tube lateral wall
+UBERON:0003606,limb long bone,UBERON:0002495,long bone
+CL:0000456,mineralocorticoid secreting cell,CL:0000174,steroid hormone secreting cell
+UBERON:0005594,head somite,UBERON:0005291,embryonic tissue
+NCBITaxon:89593,Craniata <chordata>,NCBITaxon:7711,Chordata
+DOID:3096,stenosis of lacrimal sac,DOID:1400,lacrimal apparatus disease
+DOID:296,mixed lacrimal gland cancer,DOID:294,lacrimal gland cancer
+CL:0002653,squamous endothelial cell,CL:0000076,squamous epithelial cell
+UBERON:0013121,proximal epiphysis of phalanx of pes,UBERON:0004447,proximal epiphysis of phalanx
+UBERON:3010195,lateral appendix,UBERON:0000064,organ part
+HP:0011957,Abnormality of the  pectoral muscle,HP:0009131,Abnormality of the musculature of the thorax
+UBERON:0011349,pterygomandibular raphe,UBERON:0003566,head connective tissue
+HP:0007448,Hyperkeratosis over edematous areas,HP:0000969,Edema
+HP:0100345,Tibial deviation of the 2nd toe,HP:0010326,Deviation/Displacement of the 2nd toe
+CL:0000068,duct epithelial cell,CL:0000066,epithelial cell
+CL:0000431,iridophore,CL:0000147,pigment cell
+HP:0009257,Pseudoepiphysis of the distal phalanx of the 4th finger,HP:0010253,Pseudoepiphyses of the distal phalanges of the hand
+DOID:2377,multiple sclerosis,DOID:3213,demyelinating disease
+DOID:5022,aflatoxins-related hepatocellular carcinoma,DOID:684,hepatocellular carcinoma
+UBERON:0006358,vasa hyaloidea propria,UBERON:0002050,embryonic structure
+CL:0002486,strial intermediate cell,CL:0000148,melanocyte
+HP:0004626,Lumbar scoliosis,HP:0002944,Thoracolumbar scoliosis
+HP:0000694,Shell teeth,HP:0000703,Dentinogenesis imperfecta
+DOID:13037,mechanical lagophthalmos,DOID:12959,lagophthalmos
+UBERON:0001708,jaw skeleton,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100482,Proximal/middle symphalangism of 5th toe,HP:0100472,Symphalangism affecting the middle phalanx of the 5th toe
+UBERON:0011615,basihyal cartilage,UBERON:0011614,basihyal element
+HP:0012521,Optic nerve aplasia,HP:0008058,Aplasia/Hypoplasia of the optic nerve
+DOID:5694,esophagus liposarcoma,DOID:1114,esophagus sarcoma
+UBERON:0010001,cell cluster organ,UBERON:0010000,multicellular anatomical structure
+UBERON:0000359,preputial gland,UBERON:0003937,sex gland
+DOID:0050452,mevalonic aciduria,DOID:906,peroxisomal disease
+UBERON:0007741,metacarpophalangeal joint of manual digit 3,UBERON:0003695,metacarpophalangeal joint
+HP:0008798,"Widened, small sacrosciatic notches",HP:0003185,Small sacroiliac notches
+HP:0008730,Female external genitalia in males,HP:0000032,Abnormality of male external genitalia
+UBERON:0000007,pituitary gland,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0010171,strand of hair of face,UBERON:0016446,hair of head
+UBERON:3000954,hypobranchial I,UBERON:0002513,endochondral bone
+HP:0000944,Abnormality of the metaphyses,HP:0011314,Abnormality of long bone morphology
+UBERON:2001612,sensory canal,UBERON:0000073,regional part of nervous system
+UBERON:0001885,dentate gyrus of hippocampal formation,UBERON:0000200,gyrus
+UBERON:0005109,metanephric smooth muscle tissue,UBERON:0006554,urinary system structure
+HP:0012727,Thoracic aortic aneurysm,HP:0004942,Aortic aneurysm
+HP:0009599,Abnormality of the epiphyses of the thumb,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+UBERON:0011828,areolar tubercle,UBERON:0005813,tubercle
+UBERON:0001286,Bowman's space,UBERON:0000464,anatomical space
+DOID:481,central nervous system hereditary degenerative disease,DOID:331,central nervous system disease
+UBERON:0008835,hepatic diverticulum,UBERON:0007499,epithelial sac
+UBERON:2001515,taenia marginalis posterior,UBERON:0004120,mesoderm-derived structure
+UBERON:3000759,omosternum,UBERON:0004120,mesoderm-derived structure
+UBERON:2000520,horizontal commissure,UBERON:0003931,diencephalic white matter
+UBERON:2002043,posterior limb of parapophysis 4,UBERON:0004120,mesoderm-derived structure
+UBERON:3000802,fossa glenoidalis,UBERON:0004120,mesoderm-derived structure
+HP:0011795,Intralobar nephroblastomatosis,HP:0008643,Nephroblastomatosis
+HP:0100478,Symphalangism affecting the distal phalanx of the 5th toe,HP:0010389,Symphalangism affecting the phalanges of the 5th toe
+HP:0009297,Osteolytic defects of the middle phalanx of the 4th finger,HP:0009283,Abnormality of the middle phalanx of the 4th finger
+HP:0008820,Absent ossification of capital femoral epiphysis,HP:0005003,Aplasia/Hypoplasia of the capital femoral epiphysis
+HP:0005318,Cerebral vasculitis,HP:0002633,Vasculitis
+UBERON:2002214,os suspensorium medial flange,UBERON:2000461,Weberian ossicle
+UBERON:0004056,primitive groove,UBERON:0002050,embryonic structure
+DOID:1678,chronic interstitial cystitis,DOID:65,connective tissue disease
+HP:0000069,Abnormality of the ureter,HP:0010935,Abnormality of the upper urinary tract
+HP:0010895,Abnormality of glycine metabolism,HP:0010894,Abnormality of serine family amino acid metabolism
+UBERON:0004794,esophagus secretion,UBERON:0000456,bodily secretion
+UBERON:0009852,border of sublaminar layers S2 and S3,UBERON:0009740,border between sublaminar layers
+UBERON:0010045,1st arch maxillary mesenchyme,UBERON:0010042,1st arch mesenchyme
+HP:0012209,Juvenile myelomonocytic leukemia,HP:0012324,Myeloid leukemia
+DOID:5936,ovarian mixed germ cell neoplasm,DOID:5351,ovarian primitive germ cell tumor
+UBERON:0004076,cerebellum vermis lobule III,UBERON:0004070,cerebellum vermis lobule
+UBERON:0003524,tail blood vessel,UBERON:0001981,blood vessel
+UBERON:0002689,supraoptic crest,UBERON:0003048,regional part of hypothalamus
+HP:0012673,Aplasia of the upper vagina,HP:0003250,Aplasia of the vagina
+UBERON:0014628,vestibular fissure of the cochlear canal,UBERON:0005913,zone of bone organ
+HP:0009389,Pseudoepiphyses of the 5th finger,HP:0009152,Abnormality of the epiphyses of the 5th finger
+HP:0100535,Tibiofibular diastasis,HP:0002992,Abnormality of the tibia
+CL:0002269,vasoactive intestinal peptide secreting cell,CL:0000167,peptide hormone secreting cell
+DOID:0050476,Barth syndrome,DOID:3146,lipid metabolism disorder
+UBERON:0002103,hindlimb,UBERON:0004709,pelvic appendage
+HP:0009853,Bullet-shaped proximal phalanges of the hand,HP:0009769,Bullet-shaped phalanges of the hand
+UBERON:0011141,appendicular ossicle,UBERON:0010911,ossicle
+UBERON:3000290,medial inferior prenasal cartilage,UBERON:0003933,cranial cartilage
+UBERON:2000139,immature otolith,UBERON:0003103,compound organ
+UBERON:0002029,epithelium of gall bladder,UBERON:0005911,endo-epithelium
+UBERON:4200109,outer digits of pes,UBERON:0005445,segment of pes
+UBERON:0005220,pancreas head parenchyma,UBERON:0000353,parenchyma
+HP:0011997,Postprandial hyperlactemia,HP:0002151,Increased serum lactate
+CL:1000143,lung goblet cell,CL:1000272,lung secretory cell
+HP:0100193,Cone-shaped epiphysis of the proximal phalanx of the 4th toe,HP:0100068,Cone-shaped epiphyses of the 4th toe
+HP:0001276,Hypertonia,HP:0007256,Abnormality of pyramidal motor function
+CL:0002022,Ly-76 high positive erythrocyte,CL:0000595,enucleate erythrocyte
+UBERON:0004064,neural tube basal plate,UBERON:0005291,embryonic tissue
+DOID:1285,rectal disease,DOID:5295,intestinal disease
+HP:0000550,Abolished electroretinogram (ERG),HP:0000512,Abnormal electroretinogram
+UBERON:0012441,endothelium of peritubular capillary,UBERON:0001915,endothelium of capillary
+DOID:0060147,semantic agnosia,DOID:4090,agnosia
+DOID:10609,rickets,DOID:0080005,bone remodeling disease
+HP:0007465,Honeycomb palmoplantar keratoderma,HP:0000982,Palmoplantar keratoderma
+HP:0009215,Bracket epiphysis of the middle phalanx of the 4th finger,HP:0009247,Abnormality of the epiphysis of the middle phalanx of the 4th finger
+HP:0100914,Sclerosis of the 1st metacarpal,HP:0100917,Sclerosis of the proximal phalanges of the hand
+HP:0000795,Abnormality of the urethra,HP:0000032,Abnormality of male external genitalia
+DOID:4085,trophoblastic neoplasm,DOID:3095,germ cell and embryonal cancer
+UBERON:0005695,manual digit 5 mesenchyme,UBERON:0005257,manual digit mesenchyme
+HP:0003894,Delayed humeral epiphyseal ossification,HP:0003840,Delayed upper limb epiphyseal ossification
+DOID:8109,nephrogenic adenoma of the urethra,DOID:730,urethral benign neoplasm
+HP:0011125,Abnormality of dermal melanosomes,HP:0001000,Abnormality of skin pigmentation
+HP:0002839,Urinary bladder sphincter dysfunction,HP:0000009,Functional abnormality of the bladder
+HP:0009004,Hypoplasia of the musculature,HP:0001460,Aplasia/Hypoplasia involving the musculature
+HP:0007024,Pseudobulbar paralysis,HP:0001618,Dysphonia
+HP:0007327,Mixed demyelinating and axonal polyneuropathy,HP:0009830,Peripheral neuropathy
+UBERON:0011970,talofibular ligament,UBERON:0003589,hindlimb connective tissue
+NCBITaxon:6200,Eucestoda,NCBITaxon:6199,Cestoda
+UBERON:0002129,cerebellar cortex,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002147,reticulotegmental nucleus,UBERON:0006331,brainstem nucleus
+HP:0100941,Sclerosis of the distal phalanx of the 4th toe,HP:0100948,Sclerosis of the distal phalanges of the toes
+HP:0009420,Triangular epiphyses of the 3rd finger,HP:0009320,Abnormality of the epiphyses of the 3rd finger
+HP:0010637,Conjunctival amyloidosis,HP:0011034,Amyloidosis
+HP:0002595,Ileus,HP:0002579,Gastrointestinal dysmotility
+HP:0001193,Ulnar deviation of the hand or of fingers of the hand,HP:0009484,Deviation of the hand or of fingers of the hand
+HP:0002280,Enlarged cisterna magna,HP:0002119,Ventriculomegaly
+DOID:1781,thyroid cancer,DOID:170,endocrine gland cancer
+HP:0005541,Congenital agranulocytosis,HP:0012234,Agranulocytosis
+HP:0006583,Fatal liver failure in infancy,HP:0001399,Hepatic failure
+UBERON:0010065,auditory meatus epithelium,UBERON:0003914,epithelial tube
+DOID:8991,cervix uteri carcinoma in situ,DOID:8719,in situ carcinoma
+UBERON:3010604,cranial glands,UBERON:3000972,head external integument structure
+DOID:6015,adult central nervous system teratoma,DOID:5349,central nervous system adult germ cell tumor
+HP:0003210,Decreased methylmalonyl-CoA mutase activity,HP:0000816,Abnormality of Krebs cycle metabolism
+UBERON:0011964,calcaneocuboid joint,UBERON:0011969,mesotarsal joint
+DOID:5327,retinal detachment,DOID:5679,retinal disease
+UBERON:0001057,corpus allatum,UBERON:0002368,endocrine gland
+HP:0004861,refractory macrocytic anemia,HP:0001972,Macrocytic anemia
+HP:0001608,Abnormality of the voice,HP:0001600,Abnormality of the larynx
+HP:0100430,Broad proximal phalanx of the 5th toe,HP:0010384,Broad phalanges of the 5th toe
+CL:0000408,male gamete,CL:0000300,gamete
+UBERON:0004637,otic capsule,UBERON:0015020,otic capsule endochondral element
+UBERON:2002275,Jakubowski's organ,UBERON:0000477,anatomical cluster
+DOID:4639,suppurative lymphadenitis,DOID:1602,lymphadenitis
+UBERON:0005679,right lung caudal lobe segmental bronchus,UBERON:0002184,segmental bronchus
+HP:0002615,Hypotension,HP:0011025,Abnormality of cardiovascular system physiology
+UBERON:0002271,periventricular zone of hypothalamus,UBERON:0004121,ectoderm-derived structure
+HP:0000526,Aniridia,HP:0008053,Aplasia/Hypoplasia of the iris
+UBERON:2001013,myotome somite 10,UBERON:0003082,myotome
+UBERON:0003701,calcaneal tendon,UBERON:0008846,skeletal ligament
+UBERON:0007997,sesamoid bone of manus,UBERON:0001479,sesamoid bone
+UBERON:0012443,row of scales,UBERON:0000477,anatomical cluster
+UBERON:0012416,respiratory system arterial smooth muscle,UBERON:0004695,arterial system smooth muscle
+HP:0007834,Progressive cataract,HP:0000518,Cataract
+HP:0010458,Female pseudohermaphroditism,HP:0000055,Abnormality of female external genitalia
+DOID:0050438,Frasier syndrome,DOID:0050736,autosomal dominant disease
+NCBITaxon:7174,Culex <genus>,NCBITaxon:53550,Culicini
+UBERON:2001548,intercalarium ascending process,UBERON:0004120,mesoderm-derived structure
+UBERON:3000292,medial ramus of pterygoid,UBERON:0004120,mesoderm-derived structure
+CL:1000742,glomerular mesangial cell,CL:1000500,kidney interstitial cell
+DOID:8420,malignant glandular tumor of peripheral nerve sheath,DOID:5940,malignant peripheral nerve sheath tumor
+UBERON:0007376,outer epithelium,UBERON:0010371,ecto-epithelium
+HP:0007402,Areas of hypopigmentation and hyperpigmentation that do not follow Blaschko lines,HP:0009123,Mixed hypo- and hyperpigmentation of the skin
+DOID:783,end stage renal failure,DOID:784,chronic kidney failure
+UBERON:0006293,spleen primordium,UBERON:0001048,primordium
+HP:0011309,Tapered toe,HP:0001780,Abnormality of toe
+HP:0200073,Respiratory insufficiency due to defective ciliary clearance,HP:0012261,Abnormal respiratory motile cilium physiology
+UBERON:0006214,carpus pre-cartilage condensation,UBERON:0003319,mesenchyme of carpal region
+HP:0100256,Senile plaques,HP:0007367,Atrophy/Degeneration affecting the central nervous system
+CL:0002460,CD8alpha-negative thymic conventional dendritic cell,CL:0000941,thymic conventional dendritic cell
+CL:0002001,"CD34-positive, CD38-positive granulocyte monocyte progenitor",CL:0000557,granulocyte monocyte progenitor cell
+UBERON:4200118,pubic peduncle,UBERON:4100000,skeletal element projection
+DOID:9749,internal hemorrhoid,DOID:9746,hemorrhoid
+HP:0001234,Hitchhiker thumb,HP:0009603,Deviation/Displacement of the thumb
+UBERON:3000193,foramen perilymphaticum accessorium,UBERON:0005744,bone foramen
+UBERON:0001222,right ureter,UBERON:0000056,ureter
+HP:0009903,Conjunctival nodule,HP:0000502,Abnormality of the conjunctiva
+NCBITaxon:12083,Human poliovirus 2,NCBITaxon:138950,Human enterovirus C
+HP:0012009,EEG with central focal spike waves,HP:0011197,EEG with focal spike waves
+UBERON:0009089,inner medulla vasa recta descending limb,UBERON:0006554,urinary system structure
+HP:0006683,Abnormal ventricular filling,HP:0001713,Abnormality of cardiac ventricle
+DOID:1532,pleural disease,DOID:0050161,lower respiratory tract disease
+UBERON:0005700,upper jaw molar odontogenic papilla,UBERON:0015844,molar dental papilla
+DOID:10126,keratoconus,DOID:10124,corneal disease
+UBERON:0007497,developing epithelial placode,UBERON:0000485,simple columnar epithelium
+UBERON:0000346,myelin membrane,UBERON:0000470,cell part
+HP:0000502,Abnormality of the conjunctiva,HP:0012372,Abnormal eye morphology
+UBERON:0002346,neurectoderm,UBERON:0000923,germ layer
+UBERON:0009840,lower rhombic lip,UBERON:0002616,regional part of brain
+UBERON:0010990,transversospinales muscle,UBERON:0004120,mesoderm-derived structure
+HP:0009292,Broad distal phalanx of the 4th finger,HP:0009282,Abnormality of the distal phalanx of the 4th finger
+DOID:10871,age related macular degeneration,DOID:2007,degeneration of macula and posterior pole
+HP:0010539,Thin calvarium,HP:0002683,Abnormality of the calvaria
+UBERON:0008279,spirocyst,UBERON:0008277,cnida
+DOID:1752,ocular melanoma,DOID:2174,ocular cancer
+DOID:7340,pediatric ovarian dysgerminoma,DOID:6084,pediatric ovarian germ cell tumor
+UBERON:0004412,proximal epiphysis of femur,UBERON:0004380,proximal epiphysis
+HP:0010876,Abnormality of circulating protein level,HP:0001939,Abnormality of metabolism/homeostasis
+UBERON:0010586,manual digit phalanx pre-cartilage condensation,UBERON:0005257,manual digit mesenchyme
+HP:0000524,Conjunctival telangiectasia,HP:0100579,Mucosal telangiectasiae
+DOID:2273,vulvovaginitis,DOID:229,female reproductive system disease
+DOID:7350,thymic dysplasia,DOID:533,thymus gland disease
+HP:0010798,Lip freckle,HP:0000159,Abnormality of the lip
+HP:0100296,Perifascicular muscle fiber atrophy,HP:0004303,Abnormality of muscle fibers
+CL:0002609,neuron of cerebral cortex,CL:0012001,neuron of the forebrain
+CL:0002605,astrocyte of the cerebral cortex,CL:0012000,astrocyte of the forebrain
+DOID:7046,cervical basaloid squamous cell carcinoma,DOID:3744,cervical squamous cell carcinoma
+HP:0004060,Trident hand,HP:0001167,Abnormality of finger
+HP:0007958,Optic atrophy from cranial nerve compression,HP:0000648,Optic atrophy
+HP:0011069,Increased number of teeth,HP:0006483,Abnormal number of teeth
+HP:0006112,Expanded phalanges with widened medullary cavities,HP:0009768,Broad phalanges of the hand
+UBERON:0003485,vagina sebaceous gland,UBERON:0005398,female reproductive gland
+HP:0001953,Diabetic ketoacidosis,HP:0001993,Ketoacidosis
+UBERON:0005705,primary palate mesenchyme,UBERON:0003323,mesenchyme of upper jaw
+DOID:1024,leprosy,DOID:0050338,primary bacterial infectious disease
+UBERON:2000611,visceromotor column,UBERON:0004121,ectoderm-derived structure
+HP:0011120,Saddle nose,HP:0011119,Abnormality of the nasal dorsum
+UBERON:0010848,radius-ulna cartilage element,UBERON:0003327,mesenchyme of forearm
+HP:0100704,Cortical visual impairment,HP:0000505,Visual impairment
+UBERON:0011143,upper urinary tract,UBERON:0006554,urinary system structure
+UBERON:0005136,metanephric glomerular endothelium,UBERON:0005135,metanephric glomerular epithelium
+UBERON:0004294,glomerular capillary endothelium,UBERON:0001915,endothelium of capillary
+UBERON:0005945,neurocranial trabecula,UBERON:0004120,mesoderm-derived structure
+HP:0007086,Social and occupational deterioration,HP:0001268,Mental deterioration
+DOID:4164,cerebral neuroblastoma,DOID:1319,brain cancer
+UBERON:0003962,pterygopalatine ganglion,UBERON:0001808,parasympathetic ganglion
+CL:0000216,Sertoli cell,CL:0000511,androgen binding protein secreting cell
+DOID:12934,Kearns-Sayre syndrome,DOID:12558,chronic progressive external ophthalmoplegia
+UBERON:0000121,perineurium,UBERON:0002384,connective tissue
+UBERON:0013180,bursal cartilage,UBERON:0007844,cartilage element
+DOID:974,upper respiratory tract disease,DOID:1579,respiratory system disease
+HP:0007988,Macular hypopigmentation,HP:0008002,Abnormality of macular pigmentation
+DOID:6489,periosteal osteogenic sarcoma,DOID:3374,peripheral osteosarcoma
+DOID:13976,peptic esophagitis,DOID:11963,esophagitis
+HP:0005039,Multiple long-bone exostoses,HP:0002762,Multiple exostoses
+DOID:867,maxillary sinus cholesteatoma,DOID:1352,paranasal sinus disease
+UBERON:0013701,main body axis,UBERON:0000475,organism subdivision
+HP:0010448,Colonic atresia,HP:0011100,Intestinal atresia
+CL:0011006,lugaro cell,CL:0011005,GABAergic interneuron
+UBERON:3000800,intercotylar space,UBERON:0000464,anatomical space
+UBERON:0006306,ulna cartilage element,UBERON:0005423,developing anatomical structure
+DOID:4618,maxillary neoplasm,DOID:1862,jaw cancer
+DOID:1962,fallopian tube disease,DOID:229,female reproductive system disease
+HP:0000495,Recurrent corneal erosions,HP:0200020,Corneal erosions
+UBERON:0005376,olfactory bulb external plexiform layer,UBERON:0009950,olfactory bulb plexiform layer
+DOID:0050169,cutaneous lupus erythematosus,DOID:8857,lupus erythematosus
+DOID:4638,postauricular lymphadenitis,DOID:1602,lymphadenitis
+UBERON:0013523,lateral vaginal canal,UBERON:0000996,vagina
+HP:0008472,Prominent protruding coccyx,HP:0008519,Abnormality of the coccyx
+UBERON:2000932,myotome somite 3,UBERON:0003082,myotome
+UBERON:0010685,pedal digit phalanx cartilage element,UBERON:0015030,pedal digit phalanx endochondral element
+DOID:6148,nasal cavity carcinoma in situ,DOID:8719,in situ carcinoma
+HP:0007210,Lower limb amyotrophy,HP:0003202,Amyotrophy
+HP:0009692,Ivory epiphyses of the thumb,HP:0009599,Abnormality of the epiphyses of the thumb
+CL:0002637,keratinized epithelial cell of the anal canal,CL:0000237,keratinizing barrier epithelial cell
+HP:0006494,Aplasia/Hypoplasia involving bones of the feet,HP:0001760,Abnormality of the foot
+HP:0008981,Calf muscle hypertrophy,HP:0001430,Abnormality of the calf musculature
+HP:0011527,Lentiglobus,HP:0011526,Abnormality of lens shape
+HP:0005308,Pulmonary artery vasoconstriction,HP:0004414,Abnormality of the pulmonary artery
+UBERON:0006318,orbitalis muscle,UBERON:0003660,eyelid muscle
+UBERON:0002397,maxilla,UBERON:0008193,pneumatized bone
+HP:0000830,Anterior hypopituitarism,HP:0011747,Abnormality of the anterior pituitary
+UBERON:0005382,dorsal striatum,UBERON:0011300,gray matter of telencephalon
+UBERON:0014641,terminal nerve root,UBERON:0006843,root of cranial nerve
+DOID:248,trachea leiomyoma,DOID:0050621,respiratory system benign neoplasm
+DOID:5057,papillary meningioma of the cerebellum,DOID:4205,cerebellum cancer
+HP:0007680,Depigmented fundus,HP:0001487,Hypopigmented fundi
+DOID:5658,lipid-rich carcinoma,DOID:3459,breast carcinoma
+CL:1001107,kidney loop of henle thin ascending limb epithelial cell,CL:1000617,kidney inner medulla cell
+UBERON:0001509,triceps brachii,UBERON:0004255,forelimb stylopod muscle
+HP:0007913,Reticular retinal dystrophy,HP:0000556,Retinal dystrophy
+DOID:3168,squamous cell neoplasm,DOID:0060084,cell type benign neoplasm
+UBERON:0010946,occipitofrontalis muscle,UBERON:0001577,facial nerve muscle
+HP:0100705,Abnormality of the glial cells,HP:0007319,Morphological abnormality of the central nervous system
+UBERON:0003617,trachea elastic tissue,UBERON:0003611,respiratory system elastic tissue
+UBERON:0001990,middle cervical ganglion,UBERON:0001991,cervical ganglion
+DOID:0060210,amyotrophic lateral sclerosis type 19,DOID:332,amyotrophic lateral sclerosis
+HP:0002708,Prominent median palatal raphe,HP:0000174,Abnormality of the palate
+UBERON:0006594,chorda gubernaculum,UBERON:0005156,reproductive structure
+HP:0009646,Patchy sclerosis of the distal phalanx of the thumb,HP:0009655,Patchy sclerosis of the phalanges of the thumb
+UBERON:0001543,popliteal lymph node,UBERON:0003968,peripheral lymph node
+HP:0005048,Synostosis of carpal bones,HP:0009702,Carpal synostosis
+UBERON:0008607,transverse muscle of auricle,UBERON:0001596,intrinsic auricular muscle
+UBERON:0012242,internal urethral orifice,UBERON:0004120,mesoderm-derived structure
+CL:0000902,induced T-regulatory cell,CL:0000792,"CD4-positive, CD25-positive, alpha-beta regulatory T cell"
+UBERON:0003510,eyelid blood vessel,UBERON:0004121,ectoderm-derived structure
+DOID:146,papilledema,DOID:1891,optic nerve disease
+UBERON:0013743,base of crypt of lieberkuhn of small intestine,UBERON:0013739,base of crypt of lieberkuhn
+DOID:8006,skin meningioma,DOID:3165,skin benign neoplasm
+HP:0004257,Delayed ossification of the trapezoid bone,HP:0004256,Abnormality of the trapezoid bone
+UBERON:0005912,transitional epithelium of major calyx,UBERON:0004788,kidney pelvis urothelium
+HP:0009694,Small epiphyses of the thumb,HP:0009599,Abnormality of the epiphyses of the thumb
+UBERON:0015147,pinna hair,UBERON:0016446,hair of head
+DOID:10941,intracranial aneurysm,DOID:3527,cerebral arterial disease
+DOID:0050601,ADULT syndrome,DOID:0050736,autosomal dominant disease
+HP:0012481,Cerebral venous angioma,HP:0012480,Abnormality of cerebral veins
+UBERON:3010092,basitrabecular process,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001344,epithelium of vagina,UBERON:0000486,multilaminar epithelium
+HP:0000607,Periorbital wrinkles,HP:0100678,Premature skin wrinkling
+DOID:14489,ureteral lymphoma,DOID:11819,ureter cancer
+UBERON:0000325,gastric gland,UBERON:0002365,exocrine gland
+UBERON:0002420,basal ganglion,UBERON:0007245,nuclear complex of neuraxis
+CL:0007007,notochordal sheath cell,CL:0007005,notochordal cell
+HP:0000973,Cutis laxa,HP:0008067,Abnormally lax or hyperextensible skin
+UBERON:0002555,intermediate hypothalamic region,UBERON:0000477,anatomical cluster
+UBERON:0012471,hepatogastric ligament,UBERON:0008845,nonskeletal ligament
+HP:0004224,Abnormality of the epiphysis of the middle phalanx of the 5th finger,HP:0009152,Abnormality of the epiphyses of the 5th finger
+HP:0009785,Triceps aplasia,HP:0009784,Aplasia/Hypoplasia of the triceps
+UBERON:0002680,regional part of metencephalon,UBERON:0000477,anatomical cluster
+UBERON:0003581,eyelid connective tissue,UBERON:0004121,ectoderm-derived structure
+DOID:3151,skin squamous cell carcinoma,DOID:3451,skin carcinoma
+CL:0001009,immature dermal dendritic cell,CL:0000840,immature conventional dendritic cell
+UBERON:2002030,ventral keel of coracoid,UBERON:4100000,skeletal element projection
+CL:0001026,"CD34-positive, CD38-positive common myeloid progenitor",CL:0001059,"common myeloid progenitor, CD34-positive"
+HP:0012035,Steatocystoma multiplex,HP:0008069,Neoplasm of the skin
+UBERON:0011924,postganglionic autonomic fiber,UBERON:0006134,nerve fiber
+HP:0004788,Intestinal lymphedema,HP:0005225,Intestinal edema
+UBERON:3010524,bronchial tube,UBERON:0000489,cavitated compound organ
+CL:1000426,chromaffin cell of adrenal gland,CL:0000166,chromaffin cell
+UBERON:0004434,proximal epiphysis of distal phalanx of manual digit 4,UBERON:0011979,epiphysis of distal phalanx of manus
+DOID:5718,adrenal neuroblastoma,DOID:3953,adrenal gland cancer
+HP:0007471,Axillary and groin hyperpigmentation and hypopigmentation,HP:0009123,Mixed hypo- and hyperpigmentation of the skin
+UBERON:0016476,primary incisor tooth,UBERON:0007115,deciduous tooth
+UBERON:3000883,recessus coccygealis,UBERON:0004120,mesoderm-derived structure
+DOID:13543,hyperparathyroidism,DOID:11201,parathyroid gland disease
+UBERON:0003209,blood nerve barrier,UBERON:0000119,cell layer
+CL:0000485,mucosal type mast cell,CL:0000097,mast cell
+HP:0001908,Hypoplastic anemia,HP:0010972,Anemia of inadequate production
+UBERON:0005069,neural fold hinge point,UBERON:0002050,embryonic structure
+DOID:10881,"hand, foot and mouth disease",DOID:37,skin disease
+HP:0002421,Poor head control,HP:0001324,Muscle weakness
+DOID:5648,choroid plexus carcinoma,DOID:3540,choroid plexus cancer
+DOID:0050685,small cell carcinoma,DOID:305,carcinoma
+HP:0100571,Cardiac diverticulum,HP:0001713,Abnormality of cardiac ventricle
+HP:0003853,Sclerosis with transverse striations in metaphyses of the upper limbs,HP:0003854,Sclerosis of metaphyses of the upper limbs
+UBERON:3010260,intromittent organ (Ascaphus type),UBERON:0008811,intromittent organ
+HP:0006748,Adrenal pheochromocytoma,HP:0002666,Pheochromocytoma
+HP:0010412,Duplication of the middle phalanx of the 2nd toe,HP:0010355,Duplication of the phalanges of the 2nd toe
+DOID:3540,choroid plexus cancer,DOID:3541,cerebral ventricle cancer
+UBERON:0003563,telencephalon dura mater,UBERON:0003561,forebrain dura mater
+UBERON:0013673,os priapium,UBERON:0014403,male anatomical structure
+UBERON:0002455,common plantar digital arteries,UBERON:0006138,plantar digital artery
+HP:0009477,Proximal/middle symphalangism of 4th finger,HP:0006152,Proximal symphalangism (hands)
+UBERON:0002639,midbrain reticular formation,UBERON:0015827,brainstem reticular formation
+UBERON:0011199,prostatic utricle,UBERON:0006554,urinary system structure
+HP:0009178,Symphalangism of middle phalanx of 5th finger,HP:0004219,Abnormality of the middle phalanx of the 5th finger
+HP:0009422,Broad distal phalanx of the 3rd finger,HP:0009357,Abnormality of the distal phalanx of the 3rd finger
+UBERON:0004756,dermal skeletal element,UBERON:0004120,mesoderm-derived structure
+HP:0010958,Bilateral renal agenesis,HP:0000104,Renal agenesis
+HP:0002009,Potter facies,HP:0011334,Facial shape deformation
+UBERON:0013550,Brodmann (1909) area 19,UBERON:0013529,Brodmann area
+DOID:10383,amyotrophic neuralgia,DOID:3690,brachial plexus neuropathy
+UBERON:0006056,posterior surface of head,UBERON:0000015,anatomical boundary
+UBERON:2002241,Purkinje cell layer valvula cerebelli,UBERON:0004121,ectoderm-derived structure
+UBERON:2001156,posterior lateral line placode,UBERON:0003067,dorsolateral placode
+UBERON:0005255,pedal digit mesenchyme,UBERON:0010702,digit mesenchyme
+DOID:6448,vulvar apocrine adenocarcinoma,DOID:2098,vulva adenocarcinoma
+UBERON:2002229,presumptive atrium primitive heart tube,UBERON:0004120,mesoderm-derived structure
+UBERON:3000712,opisthocoelous,UBERON:0001075,vertebral centrum
+DOID:7095,pediatric epithelioid sarcoma,DOID:6193,epithelioid sarcoma
+HP:0100862,Aplasia of the femoral head,HP:0009108,Aplasia/Hypoplasia involving the femoral head and neck
+CL:1000435,epithelial cell of lacrimal duct,CL:0000072,non-branched duct epithelial cell
+CL:0000300,gamete,CL:0000586,germ cell
+HP:0100615,Ovarian neoplasm,HP:0010785,Gonadal neoplasm
+UBERON:0001147,trunk of peripheral nerve,UBERON:0002464,nerve trunk
+HP:0011448,Ankle clonus,HP:0003028,Abnormality of the ankles
+HP:0010522,Dyslexia,HP:0001328,Specific learning disability
+UBERON:0006530,seminal fluid,UBERON:0000456,bodily secretion
+CL:0002369,fungal spore,CL:0000521,fungal cell
+HP:0011144,Age-related posterior subcapsular cataract,HP:0011141,Age-related cataract
+UBERON:3000956,hypobranchial II,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0010136,epithelial sheet,UBERON:0000483,epithelium
+DOID:12700,hyperprolactinemia,DOID:0060158,acquired metabolic disease
+UBERON:2201671,anal fin radial cartilage,UBERON:2101671,anal fin radial element
+CL:0001043,"activated CD4-positive, alpha-beta T cell, human",CL:0000896,"activated CD4-positive, alpha-beta T cell"
+UBERON:0014507,distal interphalangeal joint of pedal digit 3,UBERON:0007726,interphalangeal joint of pedal digit 3
+UBERON:0001202,pyloric sphincter,UBERON:0011185,gastrointestinal sphincter
+DOID:7575,pancreatic intraductal papillary-mucinous neoplasm,DOID:1795,tumor of exocrine pancreas
+HP:0100134,Abnormality of the axillary hair,HP:0009888,Abnormality of secondary sexual hair
+UBERON:0013581,metapodium bone 1,UBERON:0003821,metapodium bone
+UBERON:0002146,pulmonary valve,UBERON:0005623,semi-lunar valve
+UBERON:0002274,perifornical nucleus,UBERON:0006568,hypothalamic nucleus
+UBERON:0002989,anconeus muscle,UBERON:0004255,forelimb stylopod muscle
+HP:0009286,Curved distal phalanx of the 4th finger,HP:0009838,Curved distal phalanges of the hand
+HP:0010162,Absent epiphyses of the toes,HP:0010577,Absent epiphyses
+HP:0002300,Mutism,HP:0100851,Abnormal emotion/affect behavior
+UBERON:0009002,placental membrane,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0004189,glomerular endothelium,UBERON:0004852,cardiovascular system endothelium
+CL:0000166,chromaffin cell,CL:0000568,APUD cell
+HP:0004028,Spurs of radial diaphysis,HP:0004027,Abnormality of radial diaphysis
+UBERON:0014619,cervical spinal cord lateral horn,UBERON:0014613,cervical spinal cord gray matter
+UBERON:0001595,auricular muscle,UBERON:0010959,craniocervical muscle
+HP:0002949,Fused cervical vertebrae,HP:0002948,Vertebral fusion
+UBERON:0004777,respiratory system submucosa,UBERON:0000009,submucosa
+UBERON:0001687,stapes bone,UBERON:0004119,endoderm-derived structure
+UBERON:0002747,neodentate part of dentate nucleus,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100038,Slow-growing scalp hair,HP:0100037,Abnormality of the scalp hair
+UBERON:0014840,supracoracoideus muscle,UBERON:0008196,muscle of pectoral girdle
+HP:0001593,Maxillary lateral incisor microdontia,HP:0011063,Abnormality of incisor morphology
+UBERON:0002107,liver,UBERON:0005172,abdomen organ
+DOID:3013,intraductal breast neoplasm,DOID:0060082,breast benign neoplasm
+HP:0009552,Aplasia/Hypoplasia of the phalanges of the 2nd finger,HP:0009767,Aplasia/Hypoplasia of the phalanges of the hand
+HP:0008320,Impaired collagen-induced platelet aggregation,HP:0003540,Impaired platelet aggregation
+UBERON:0003569,leg connective tissue,UBERON:0003589,hindlimb connective tissue
+DOID:7967,lipid-cell variant infiltrating bladder urothelial carcinoma,DOID:6477,invasive bladder transitional cell carcinoma
+CL:0002306,epithelial cell of proximal tubule,CL:0000239,brush border epithelial cell
+UBERON:0005226,pedal digit epithelium,UBERON:0000490,unilaminar epithelium
+UBERON:0007005,cardiac mesoderm,UBERON:0005291,embryonic tissue
+HP:0001688,Sinus bradycardia,HP:0001662,Bradycardia
+HP:0008830,Hypoplastic pubic rami,HP:0003173,Hypoplastic pubic bones
+DOID:252,alcoholic psychosis,DOID:251,alcohol-induced mental disorder
+UBERON:3000363,otic ligament,UBERON:0008846,skeletal ligament
+HP:0000677,Oligodontia,HP:0009804,Reduced number of teeth
+UBERON:0013508,thoracic vertebra pre-cartilage condensation,UBERON:0015008,thoracic vertebra endochondral element
+UBERON:0007767,dorsal premammillary nucleus,UBERON:0002712,premammillary nucleus
+DOID:3149,keratoacanthoma,DOID:3151,skin squamous cell carcinoma
+HP:0100083,Ivory epiphyses of the 5th toe,HP:0010168,Ivory epiphyses of the toes
+UBERON:3010802,courtship gland,UBERON:3010604,cranial glands
+DOID:9946,steroid-induced glaucoma,DOID:1686,glaucoma
+DOID:13014,shipyard eye,DOID:9368,keratoconjunctivitis
+HP:0011963,Pretesticular azoospermia,HP:0000027,Azoospermia
+DOID:10519,chronic fungal otitis externa,DOID:0050147,otomycosis
+UBERON:0006175,pronephric distal tubule,UBERON:0004135,distal tubule
+UBERON:0006097,ventral external arcuate fiber bundle,UBERON:0000122,neuron projection bundle
+CL:0000759,type 7 cone bipolar cell (sensu Mus),CL:0000752,cone retinal bipolar cell
+HP:0005794,Arterial disease of legs,HP:0004950,Peripheral arterial disease
+UBERON:0003346,mucosa of rectum,UBERON:0001207,mucosa of large intestine
+HP:0009957,Complete duplication of the phalanges of the 2nd finger,HP:0009998,Complete duplication of phalanx of hand
+UBERON:0014537,periamygdaloid cortex,UBERON:0002619,regional part of cerebral cortex
+UBERON:0001392,flexor hallucis longus,UBERON:0001383,muscle of leg
+DOID:5760,sebaceous breast carcinoma,DOID:3459,breast carcinoma
+HP:0000611,Choroid coloboma,HP:0000610,Abnormality of the choroid
+UBERON:0008429,cervical vertebral foramen,UBERON:0001131,vertebral foramen
+UBERON:0011332,extrinsic tongue pre-muscle mass,UBERON:0003416,mesenchyme of tongue
+UBERON:2000352,external cellular layer,UBERON:0004121,ectoderm-derived structure
+UBERON:0009751,cardiac mesenchyme,UBERON:0003104,mesenchyme
+UBERON:0010252,1st arch mandibular mesenchyme from neural crest,UBERON:0009584,1st arch mandibular mesenchyme
+HP:0009815,Aplasia/Hypoplasia of the extremities,HP:0009115,Aplasia/Hypoplasia involving the skeleton
+HP:0006763,Anal canal squamous carcinoma,HP:0100743,Neoplasm of the rectum
+UBERON:0008810,nasopalatine nerve,UBERON:0001021,nerve
+DOID:6115,lateral ventricle meningioma,DOID:6112,cerebral meningioma
+HP:0011867,Abnormality of the wing of the ilium,HP:0002867,Abnormality of the ilium
+DOID:6634,adult central nervous system choriocarcinoma,DOID:3594,choriocarcinoma
+UBERON:0004439,proximal epiphysis of middle phalanx of manual digit 5,UBERON:0011978,epiphysis of middle phalanx of manus
+HP:0100503,Vitamin B1 deficiency,HP:0004340,Abnormality of vitamin B metabolism
+HP:0006979,Sleep-wake cycle disturbance,HP:0002360,Sleep disturbance
+CL:0002039,immature NK T cell stage I,CL:0000914,immature NK T cell
+HP:0007295,Chaotic rapid conjugate ocular movements,HP:0012547,Abnormal involuntary eye movements
+DOID:10138,xerophthalmia,DOID:10140,dry eye syndrome
+HP:0006692,Short chordae tendineae of the tricuspid valve,HP:0001702,Abnormality of the tricuspid valve
+CL:0000178,Leydig cell,CL:0000177,testosterone secreting cell
+HP:0200024,Premature chromatid separation,HP:0002916,Abnormality of chromosome segregation
+HP:0000525,Abnormality of the iris,HP:0000553,Abnormality of the uvea
+DOID:11823,hepatorenal syndrome,DOID:3021,acute kidney failure
+DOID:7289,secretory uterine corpus endometrioid adenocarcinoma,DOID:2870,endometrial adenocarcinoma
+HP:0005890,Hyperostosis cranialis interna,HP:0004437,Cranial hyperostosis
+UBERON:2000375,anal fin actinotrichium,UBERON:2000089,actinotrichium
+HP:0100646,Thyroiditis,HP:0011772,Abnormality of thyroid morphology
+HP:0001180,Oligodactyly (hands),HP:0009380,Aplasia of the fingers
+HP:0012031,Lipomatous tumor,HP:0200013,Neoplasm of fatty tissue
+HP:0005592,Giant melanosomes in melanocytes,HP:0011125,Abnormality of dermal melanosomes
+HP:0000594,Shallow anterior chamber,HP:0000593,Abnormality of the anterior chamber
+HP:0002185,Neurofibrillary tangles,HP:0100314,Cerebral inclusion bodies
+HP:0011712,Right bundle branch block,HP:0011710,Bundle branch block
+UBERON:0007830,pelvic girdle bone/zone,UBERON:0010742,bone of pelvic complex
+UBERON:0007175,inferior angle of scapula,UBERON:0007172,angle of scapula
+HP:0007476,Anhidrotic ectodermal dysplasia,HP:0000968,Ectodermal dysplasia
+UBERON:0007296,presumptive rhombomere 2,UBERON:0006598,presumptive structure
+DOID:2231,factor XII deficiency,DOID:0050739,autosomal genetic disease
+DOID:10516,malignant otitis externa,DOID:9463,otitis externa
+DOID:14172,rheumatic congestive heart failure,DOID:6000,congestive heart failure
+UBERON:2000356,gill raker,UBERON:0008907,dermal bone
+UBERON:0004402,bone tissue of proximal epiphysis,UBERON:0004400,bone tissue of epiphysis
+HP:0001010,Hypopigmentation of the skin,HP:0011121,Abnormality of skin morphology
+UBERON:0006094,superior parietal cortex,UBERON:0003022,cerebral cortex lobe
+CL:1000494,epithelial cell of renal tubule,CL:1000449,epithelial cell of nephron
+DOID:8634,prostate carcinoma in situ,DOID:8719,in situ carcinoma
+UBERON:0001136,mesothelium,UBERON:0000487,simple squamous epithelium
+HP:0010351,Osteolytic defects of the phalanges of the 2nd toe,HP:0010324,Abnormality of phalanx of the 2nd toe
+DOID:12105,inflammatory spondylopathy,DOID:6590,spondylitis
+HP:0008176,Neonatal unconjugated hyperbilirubinemia,HP:0002904,Hyperbilirubinemia
+CL:0002268,P/D1 enteroendocrine cell,CL:0002269,vasoactive intestinal peptide secreting cell
+UBERON:2105379,dorsal fin distal radial element 8,UBERON:2100936,dorsal fin distal radial element
+DOID:6126,anal canal carcinoma,DOID:0050688,anal canal cancer
+DOID:7221,gallbladder papillary carcinoma,DOID:3500,gallbladder adenocarcinoma
+HP:0003888,Flattened humeral heads,HP:0003887,Abnormality of the humeral heads
+UBERON:2001240,ceratobranchial 4 bone,UBERON:2000488,ceratobranchial bone
+UBERON:0007179,basal cell layer of urothelium,UBERON:0000119,cell layer
+DOID:1934,dysostosis,DOID:0080006,bone development disease
+HP:0100132,Triangular epiphysis of the proximal phalanx of the 2nd toe,HP:0100090,Abnormality of the epiphysis of the proximal phalanx of the 2nd toe
+HP:0007344,Atrophy/Degeneration involving the spinal cord,HP:0002143,Abnormality of the spinal cord
+UBERON:0003885,mesometrium,UBERON:0002095,mesentery
+HP:0009118,Aplasia/Hypoplasia of the mandible,HP:0000277,Abnormality of the mandible
+DOID:161,keratosis,DOID:37,skin disease
+UBERON:0003558,diencephalon arachnoid mater,UBERON:0003290,meninx of diencephalon
+HP:0010562,Keloids,HP:0000987,Atypical scarring of skin
+HP:0011796,Perilobar nephroblastomatosis,HP:0008643,Nephroblastomatosis
+UBERON:0008280,cnidarian venom,UBERON:0007113,venom
+DOID:5063,basosquamous carcinoma,DOID:2513,basal cell carcinoma
+DOID:12311,stromal corneal pigmentation,DOID:10123,pigmentation disease
+UBERON:0009659,spermatic artery,UBERON:0010192,genital artery
+UBERON:0000395,cochlear ganglion,UBERON:0010313,neural crest-derived structure
+HP:0001897,Normocytic anemia,HP:0010972,Anemia of inadequate production
+UBERON:0011972,medial ligament of ankle joint,UBERON:0008846,skeletal ligament
+HP:0009646,Patchy sclerosis of the distal phalanx of the thumb,HP:0009840,Patchy sclerosis of the distal phalanges of the hand
+UBERON:3000524,pterygoquadrate,UBERON:0000064,organ part
+UBERON:0015829,forebrain ventricular layer,UBERON:0000119,cell layer
+HP:0006984,Distal sensory loss of all modalities,HP:0003409,Distal sensory impairment of all modalities
+UBERON:0011958,acetabular labrum,UBERON:0007844,cartilage element
+HP:0009634,Patchy sclerosis of the proximal phalanx of the thumb,HP:0009618,Abnormality of the proximal phalanx of the thumb
+UBERON:0005453,inferior mesenteric ganglion,UBERON:0003964,prevertebral ganglion
+DOID:11718,antidepressant type abuse,DOID:302,substance abuse
+HP:0008247,Euthyroid hyperthyroxinemia,HP:0002926,Abnormality of thyroid physiology
+CL:0000356,hair matrix stem cell,CL:0000035,single fate stem cell
+UBERON:3000727,haemal arch lamina,UBERON:0004120,mesoderm-derived structure
+HP:0006321,Multiple non-erupting secondary teeth,HP:0000696,Delayed eruption of permanent teeth
+CL:0002636,nonkeratinized epithelial cell of inferior part of anal canal,CL:1000438,epithelial cell of wall of inferior part of anal canal
+HP:0004686,Short third metatarsal,HP:0010672,Abnormality of the third metatarsal bone
+HP:0010335,Abnormality of the epiphyses of the 4th toe,HP:0010160,Abnormality of the epiphyses of the toes
+UBERON:0002967,cingulate gyrus,UBERON:0003022,cerebral cortex lobe
+UBERON:0005451,segment of manus,UBERON:0008785,upper limb segment
+DOID:10350,breast cyst,DOID:0060082,breast benign neoplasm
+UBERON:0014510,omasal lamina,UBERON:0009034,stomach region
+UBERON:0002416,integumental system,UBERON:0000467,anatomical system
+HP:0012610,Abnormality of urinary uric acid concentration,HP:0003110,Abnormality of urine homeostasis
+CL:0000549,basophilic erythroblast,CL:0000765,erythroblast
+UBERON:4200120,puboischiadic plate,UBERON:0004120,mesoderm-derived structure
+UBERON:0001238,lamina propria of small intestine,UBERON:0004780,gastrointestinal system lamina propria
+HP:0100512,Vitamin D deficiency,HP:0100511,Abnormality of vitamin D metabolism
+DOID:0060041,autism spectrum disorder,DOID:0060040,pervasive developmental disorder
+HP:0009210,Pseudoepiphysis of the middle phalanx of the 5th finger,HP:0010264,Pseudoepiphyses of the middle phalanges of the hand
+CL:1000547,kidney inner medulla collecting duct epithelial cell,CL:1000617,kidney inner medulla cell
+HP:0001477,Compensatory chin elevation,HP:0000496,Abnormality of eye movement
+UBERON:0013471,retromolar space,UBERON:0000464,anatomical space
+HP:0010164,Cone-shaped epiphyses of the toes,HP:0010160,Abnormality of the epiphyses of the toes
+UBERON:2000596,pelvic fin actinotrichium,UBERON:2000089,actinotrichium
+HP:0200115,Scalp hair loss,HP:0002234,Early balding
+HP:0010803,Everted upper lip vermilion,HP:0011339,Abnormality of upper lip vermillion
+HP:0005599,Hypopigmentation of hair,HP:0009887,Abnormality of hair pigmentation
+UBERON:0000443,left testicular vein,UBERON:0001144,testicular vein
+CL:1001573,nasopharyngeal epithelial cell,CL:0002251,epithelial cell of alimentary canal
+DOID:0050148,laryngotracheitis,DOID:974,upper respiratory tract disease
+UBERON:0002954,dorsal hypothalamic area,UBERON:0000477,anatomical cluster
+HP:0100464,Patchy sclerosis of the proximal phalanx of the 3rd toe,HP:0010208,Patchy sclerosis of the proximal phalanges of the toes
+UBERON:0001081,endocardium of ventricle,UBERON:0002165,endocardium
+UBERON:0005480,superior orbital fissure,UBERON:0006271,orbital fissure
+UBERON:0002987,anterior spinocerebellar tract,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:11104,spotted fever,DOID:0050338,primary bacterial infectious disease
+HP:0004754,Permanent atrial fibrillation,HP:0005110,Atrial fibrillation
+UBERON:2000319,branchiostegal membrane,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:6048,telangiectatic glomangioma,DOID:2435,skin glomangioma
+HP:0007099,Arnold-Chiari type I malformation,HP:0002308,Arnold-Chiari malformation
+HP:0012592,Albuminuria,HP:0000093,Proteinuria
+HP:0002017,Nausea and vomiting,HP:0011458,Abdominal symptom
+HP:0007460,Autoamputation of digits,HP:0001218,Autoamputation
+HP:0003613,Antiphospholipid antibody positivity,HP:0002960,Autoimmunity
+DOID:13268,porphyria,DOID:655,inherited metabolic disorder
+HP:0001649,Tachycardia,HP:0011675,Arrhythmia
+HP:0005439,Maxillozygomatic hypoplasia,HP:0000327,Hypoplasia of the maxilla
+UBERON:3000696,posterior intervertebral notch,UBERON:0000464,anatomical space
+UBERON:0001865,cartilaginous external acoustic tube,UBERON:0000477,anatomical cluster
+HP:0004942,Aortic aneurysm,HP:0002617,Aneurysm
+HP:0009088,Speech articulation difficulties,HP:0001608,Abnormality of the voice
+CL:0000752,cone retinal bipolar cell,CL:0000748,retinal bipolar neuron
+HP:0007705,Corneal degeneration,HP:0000481,Abnormality of the cornea
+CL:0000430,xanthophore,CL:0000147,pigment cell
+DOID:528,hydrarthrosis,DOID:381,arthropathy
+UBERON:0011162,supraoccipital cartilage element,UBERON:0003932,cartilage element of chondrocranium
+DOID:0050429,Hailey-Hailey disease,DOID:37,skin disease
+DOID:0050573,2-hydroxyglutaric aciduria,DOID:9252,amino acid metabolic disorder
+UBERON:0008276,plastron,UBERON:0000075,subdivision of skeletal system
+HP:0009231,Patchy sclerosis of the proximal phalanx of the 5th finger,HP:0009377,Patchy sclerosis of the phalanges of the 5th finger
+DOID:5713,mediastinum liposarcoma,DOID:4050,mediastinum sarcoma
+UBERON:0001723,tongue,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0007482,Generalized papillary lesions,HP:0011354,Generalized abnormality of skin
+DOID:7936,precursor T-lymphoblastic lymphoma/leukemia refractory,DOID:5599,precursor T-lymphoblastic lymphoma/leukemia
+HP:0010085,Aplasia/Hypoplasia of the proximal phalanx of the hallux,HP:0010052,Abnormality of the proximal phalanx of the hallux
+CL:0002485,retinal melanocyte,CL:0000148,melanocyte
+CL:0007017,Stiftchenzellen,CL:0000206,chemoreceptor cell
+HP:0002174,Postural tremor,HP:0001337,Tremor
+UBERON:3000375,palatine process of the pars facialis of the maxilla,UBERON:4100000,skeletal element projection
+DOID:13038,cicatricial lagophthalmos,DOID:12959,lagophthalmos
+CL:0002585,retinal blood vessel endothelial cell,CL:0000071,blood vessel endothelial cell
+UBERON:0003998,hyoid bone lesser horn,UBERON:0010313,neural crest-derived structure
+UBERON:0010354,Reichert's cartilage pre-cartilage condensation,UBERON:0010258,mesenchyme from rhombencephalic neural crest
+DOID:12566,ulceration of vulva,DOID:2059,vulvar disease
+UBERON:0004725,piriform cortex,UBERON:0002791,regional part of telencephalon
+UBERON:0009892,ascidian anterior sensory vesicle,UBERON:0000020,sense organ
+UBERON:2000733,somite 7,UBERON:0002329,somite
+HP:0008059,Aplasia/Hypoplasia of the macula,HP:0008061,Aplasia/Hypoplasia affecting the retina
+UBERON:0003102,surface structure,UBERON:0000481,multi-tissue structure
+UBERON:0012279,paraganglion,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:5585,Ferguson-Smith tumor,DOID:3149,keratoacanthoma
+UBERON:0004276,fourth ventricle choroid plexus epithelium,UBERON:0003911,choroid plexus epithelium
+HP:0012192,Cutaneous T-cell lymphoma,HP:0012190,T-cell lymphoma
+CL:0002025,"CD34-positive, CD41-positive, CD42-negative megakaryocyte progenitor cell",CL:0000553,megakaryocyte progenitor cell
+DOID:1168,familial hyperlipidemia,DOID:3146,lipid metabolism disorder
+HP:0009174,Abnormality of the epiphyses of the 4th finger,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+UBERON:0001175,common hepatic duct,UBERON:0003703,extrahepatic bile duct
+UBERON:0014624,basis modioli,UBERON:0004120,mesoderm-derived structure
+UBERON:0004075,cerebellum vermis lobule II,UBERON:0004070,cerebellum vermis lobule
+DOID:811,lipodystrophy,DOID:37,skin disease
+UBERON:0012494,muscularis mucosae of duodenum,UBERON:0001210,muscularis mucosae of small intestine
+UBERON:0002272,medial zone of hypothalamus,UBERON:0004121,ectoderm-derived structure
+UBERON:0011651,ventral head of rib,UBERON:0002230,head of rib
+UBERON:0010912,subdivision of skeleton,UBERON:0011216,organ system subdivision
+HP:0009490,Cone-shaped epiphyses of the 2nd finger,HP:0006263,Abnormality of the epiphyses of the 2nd finger
+HP:0100324,Scleroderma,HP:0001072,Thickened skin
+HP:0010852,EEG with photoparoxysmal response,HP:0002353,EEG abnormality
+UBERON:0013618,secondary molar tooth,UBERON:0007775,secondary tooth
+UBERON:0003914,epithelial tube,UBERON:0000025,tube
+UBERON:2002044,anterior limb of parapophysis 4,UBERON:0004120,mesoderm-derived structure
+UBERON:3000803,sulcus articularis lateralis,UBERON:0004120,mesoderm-derived structure
+HP:0003891,Abnormality of the humeral epiphysis,HP:0003063,Abnormality of the humerus
+NCBITaxon:11709,Human immunodeficiency virus 2,NCBITaxon:11652,Primate lentivirus group
+UBERON:0004060,neural tube ventricular layer,UBERON:0004121,ectoderm-derived structure
+DOID:14059,paraurethral gland cancer,DOID:120,female reproductive organ cancer
+DOID:6683,Aarskog-Scott syndrome,DOID:0050736,autosomal dominant disease
+HP:0009296,Bullet-shaped middle phalanx of the 4th finger,HP:0009283,Abnormality of the middle phalanx of the 4th finger
+UBERON:0005971,amniotic fold,UBERON:0004120,mesoderm-derived structure
+UBERON:0003240,epithelium of lateral semicircular canal,UBERON:0006937,inner ear epithelium
+UBERON:0004184,prostate gland stroma,UBERON:0015130,connective tissue of prostate
+UBERON:0005694,manual digit 4 mesenchyme,UBERON:0005257,manual digit mesenchyme
+UBERON:0001329,prostate gland anterior lobe,UBERON:0001328,lobe of prostate
+DOID:14762,calcaneonavicular coalition,DOID:11971,synostosis
+DOID:2978,carbohydrate metabolic disorder,DOID:655,inherited metabolic disorder
+UBERON:0014626,base of cochlear canal,UBERON:0004120,mesoderm-derived structure
+HP:0006323,Premature loss of primary teeth,HP:0006481,Abnormality of primary teeth
+DOID:782,renal infectious disease,DOID:557,kidney disease
+HP:0009388,Ivory epiphyses of the 5th finger,HP:0009152,Abnormality of the epiphyses of the 5th finger
+HP:0008065,Aplasia/Hypoplasia of the skin,HP:0011355,Localized skin lesion
+UBERON:0005148,metanephric S-shaped body,UBERON:0010535,primitive metanephric nephron
+UBERON:0004450,gastric vein,UBERON:0001638,vein
+HP:0009243,Patchy sclerosis of the distal phalanx of the 5th finger,HP:0009840,Patchy sclerosis of the distal phalanges of the hand
+UBERON:0003725,cervical plexus,UBERON:0001813,somatic nerve plexus
+UBERON:0009586,mesenchyme of interdigital region between manual digits 1 and 2,UBERON:0009596,mesenchyme of interdigital region between digits 1 and 2
+UBERON:2002192,dorsolateral motor nucleus of vagal nerve,UBERON:2000297,vagal lobe
+UBERON:0003941,cerebellum anterior vermis,UBERON:0004720,cerebellar vermis
+HP:0002169,Clonus,HP:0100022,Abnormality of movement
+CL:0002021,GlyA-positive erythrocyte,CL:0000595,enucleate erythrocyte
+HP:0100202,Absent epiphysis of the distal phalanx of the 5th toe,HP:0100097,Abnormality of the epiphysis of the distal phalanx of the 5th toe
+DOID:10223,dermatomyositis,DOID:633,myositis
+DOID:10141,asthenopia,DOID:5614,eye disease
+HP:0009291,Aplasia of the distal phalanx of the 4th finger,HP:0009281,Aplasia of the 4th finger
+UBERON:0011926,postganglionic sympathetic fiber,UBERON:0011924,postganglionic autonomic fiber
+HP:0100526,Neoplasm of the lungs,HP:0002088,Abnormality of the lung
+HP:0001230,Broad metacarpals,HP:0005916,Abnormal metacarpal morphology
+HP:0010055,Broad hallux,HP:0001837,Broad toe
+HP:0008366,Contractures involving the joints of the feet,HP:0005750,Contractures of the joints of the lower limbs
+HP:0002955,Granulomatosis,HP:0004311,Abnormality of macrophages
+HP:0003363,Abdominal situs inversus,HP:0011620,Abnormality of abdominal situs
+UBERON:0001815,lumbosacral nerve plexus,UBERON:0001813,somatic nerve plexus
+UBERON:0004163,anterior ectodermal midgut,UBERON:0000479,tissue
+UBERON:0002329,somite,UBERON:0005423,developing anatomical structure
+UBERON:0001435,carpal bone,UBERON:0015049,carpus endochondral element
+UBERON:0001056,corpus cardiacum,UBERON:0002368,endocrine gland
+DOID:12809,chronic lacrimal gland enlargement,DOID:950,dacryoadenitis
+HP:0000329,Facial hemangioma,HP:0011799,Abnormality of facial soft tissue
+CL:0000212,absorptive cell,CL:0000003,native cell
+UBERON:2002279,pectoral fin distal radial bone 2,UBERON:2001588,pectoral fin distal radial bone
+DOID:1838,Menkes disease,DOID:421,hair disease
+UBERON:0003478,vein of lower lip,UBERON:0013136,vein of lip
+UBERON:4200157,metatarsal bone of digit 7,UBERON:4200155,metapodium bone 7
+HP:0005273,Absent nasal septal cartilage,HP:0009935,Aplasia/Hypoplasia of the nasal septum
+UBERON:0004782,gastrointestinal system serosa,UBERON:0000042,serous membrane
+CL:0002109,B220-positive CD38-positive naive B cell,CL:0002101,CD38-positive naive B cell
+DOID:7235,pancreatic mucinous cystadenoma,DOID:3918,pancreatic cystadenoma
+HP:0002072,Chorea,HP:0004305,Involuntary movements
+HP:0009425,Patchy sclerosis of the distal phalanx of the 3rd finger,HP:0100901,Sclerosis of the distal phalanx of the 3rd finger
+UBERON:4000173,pelvic fin lepidotrichium,UBERON:0010742,bone of pelvic complex
+UBERON:0001762,nasal concha,UBERON:0005913,zone of bone organ
+UBERON:0011535,chondroglossus muscle,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0000614,Abnormality of the nasolacrimal system,HP:0012372,Abnormal eye morphology
+HP:0009216,Cone-shaped epiphysis of the middle phalanx of the 4th finger,HP:0009247,Abnormality of the epiphysis of the middle phalanx of the 4th finger
+UBERON:0001281,hepatic sinusoid,UBERON:0005911,endo-epithelium
+UBERON:3000115,crista lateralis of premaxilla,UBERON:0010313,neural crest-derived structure
+UBERON:0013702,body proper,UBERON:0000475,organism subdivision
+HP:0003657,Granular osmiophilic deposits (GROD) in cells,HP:0004356,Abnormality of lysosomal metabolism
+UBERON:0005323,mesonephric mesenchyme,UBERON:0003104,mesenchyme
+UBERON:0011313,posterior subdivision of masseter,UBERON:0000064,organ part
+UBERON:0009674,accessory XI nerve spinal component,UBERON:0001780,spinal nerve
+DOID:11336,rhinoscleroma,DOID:0050338,primary bacterial infectious disease
+UBERON:0008464,abductor hallucis muscle,UBERON:0001498,muscle of pes
+HP:0009175,Patchy sclerosis of the middle phalanx of the 5th finger,HP:0009377,Patchy sclerosis of the phalanges of the 5th finger
+DOID:6050,esophageal disease,DOID:77,gastrointestinal system disease
+HP:0011703,Sinus tachycardia,HP:0011702,Abnormal electrophysiology of sinoatrial node origin
+HP:0008829,Delayed femoral head ossification,HP:0009107,Abnormal ossification involving the femoral head and neck
+DOID:0050398,Carrion's Disease,DOID:0050338,primary bacterial infectious disease
+UBERON:3010010,ventral skin texture,UBERON:3000977,body external integument structure
+HP:0001618,Dysphonia,HP:0001608,Abnormality of the voice
+HP:0001607,Subglottic stenosis,HP:0001600,Abnormality of the larynx
+CL:0001039,terminally differentiated osteoblast,CL:0000062,osteoblast
+HP:0004997,Multicentric ossification of proximal humeral epiphyses,HP:0003897,Irregular ossification of the humeral epiphyses
+UBERON:2000997,medial funicular nucleus trigeminal nuclei,UBERON:0004132,trigeminal sensory nucleus
+UBERON:3000780,incisura coracoidea,UBERON:0000464,anatomical space
+UBERON:0013191,ovarian cortex,UBERON:0014404,female anatomical structure
+UBERON:2001076,intestinal bulb,UBERON:0000481,multi-tissue structure
+UBERON:0002148,locus ceruleus,UBERON:0006331,brainstem nucleus
+HP:0012611,Increased urinary urate,HP:0012610,Abnormality of urinary uric acid concentration
+UBERON:0004621,lumbar vertebra 5,UBERON:0002414,lumbar vertebra
+HP:0010931,Abnormality of sodium homeostasis,HP:0010930,Abnormality of monovalent inorganic cation homeostasis
+UBERON:2001540,pelvic radial 3 cartilage,UBERON:2001538,pelvic radial cartilage
+HP:0005456,Absent ethmoidal sinuses,HP:0009120,Aplasia/Hypoplasia involving the sinuses
+HP:0010751,Chin dimple,HP:0000306,Abnormality of the chin
+HP:0011704,Sick sinus syndrome,HP:0012722,Heart block
+HP:0010974,Abnormality of myeloid leukocytes,HP:0001881,Abnormality of leukocytes
+UBERON:0013159,epithalamus mantle layer,UBERON:0004022,embryonic neuroepithelium
+UBERON:0009648,eyelid subcutaneous connective tissue,UBERON:0003581,eyelid connective tissue
+CL:1000480,transitional myocyte of internodal tract,CL:0002073,transitional myocyte
+UBERON:4200042,brevis shelf,UBERON:0004120,mesoderm-derived structure
+UBERON:0003949,tubal tonsil,UBERON:0002372,tonsil
+UBERON:0015051,exoccipital endochondral element,UBERON:0004120,mesoderm-derived structure
+HP:0003642,Type I transferrin isoform profile,HP:0003160,Abnormal isoelectric focusing of serum transferrin
+HP:0011836,Delayed talus ossification,HP:0008365,Abnormality of the talus
+UBERON:0014540,lamina of cerebellum,UBERON:0003544,brain white matter
+HP:0010115,Cone-shaped epiphyses of the hallux,HP:0010164,Cone-shaped epiphyses of the toes
+HP:0005441,Sclerotic cranial sutures,HP:0011329,Abnormality of cranial sutures
+HP:0100295,Muscle fiber atrophy,HP:0004303,Abnormality of muscle fibers
+CL:0005025,visceromotor neuron,CL:0000100,motor neuron
+HP:0003473,Fatigable weakness,HP:0001324,Muscle weakness
+CL:0002002,Kit-positive granulocyte monocyte progenitor,CL:0000557,granulocyte monocyte progenitor cell
+HP:0006595,Scapulohumeral synostosis,HP:0001376,Limitation of joint mobility
+UBERON:2000660,epural,UBERON:0001076,neural spine
+DOID:7269,cribriform variant testicular seminoma,DOID:5842,testis seminoma
+UBERON:0012319,posterior ethmoidal artery,UBERON:0005193,ethmoidal artery
+DOID:5605,breast medullary carcinoma,DOID:3458,breast adenocarcinoma
+UBERON:0001849,membranous labyrinth,UBERON:0004121,ectoderm-derived structure
+HP:0100090,Abnormality of the epiphysis of the proximal phalanx of the 2nd toe,HP:0010323,Abnormality of the epiphyses of the 2nd toe
+UBERON:0010262,operculum of brain,UBERON:0004121,ectoderm-derived structure
+UBERON:0003519,thoracic cavity blood vessel,UBERON:0001981,blood vessel
+HP:0100005,Testicular mesothelioma,HP:0100001,Malignant mesothelioma
+UBERON:0001027,sensory nerve,UBERON:0001021,nerve
+DOID:82,myotonic cataract,DOID:83,cataract
+UBERON:0009841,upper rhombic lip,UBERON:0002616,regional part of brain
+HP:0009822,Aplasia involving forearm bones,HP:0006503,Aplasia/Hypoplasia involving forearm bones
+UBERON:2000237,medial forebrain bundle diencephalon,UBERON:0003931,diencephalic white matter
+HP:0002235,Pili canaliculi,HP:0003328,Abnormal hair laboratory examination
+CL:0000996,mature CD11c-negative plasmacytoid dendritic cell,CL:0000991,CD11c-negative plasmacytoid dendritic cell
+HP:0010631,Abnormality of the epiphyses of the feet,HP:0006500,Abnormality involving the epiphyses of the lower limbs
+DOID:13722,neuroschistosomiasis,DOID:1395,schistosomiasis
+HP:0001544,Prominent umbilicus,HP:0001551,Abnormality of the umbilicus
+UBERON:3000344,orbitonasal foramen,UBERON:3000051,braincase and otic capsule opening
+HP:0010389,Symphalangism affecting the phalanges of the 5th toe,HP:0010179,Symphalangism affecting the phalanges of the toes
+HP:0100527,Neoplasia of the pleura,HP:0002103,Abnormality of the pleura
+UBERON:3000634,vomerine canal,UBERON:0004120,mesoderm-derived structure
+UBERON:0003883,CA3 field of hippocampus,UBERON:0003876,subdivision of hippocampus
+HP:0003997,Hypoplastic radial head,HP:0003995,Abnormality of the radial head
+UBERON:0002383,supraspinatus muscle,UBERON:0001482,muscle of shoulder
+HP:0001096,Keratoconjunctivitis,HP:0000491,Keratitis
+DOID:5433,urinary tract papillary transitional cell benign neoplasm,DOID:731,urinary system benign neoplasm
+UBERON:0004413,proximal epiphysis of radius,UBERON:0004380,proximal epiphysis
+HP:0007023,Antenatal intracerebral hemorrhage,HP:0001342,Cerebral hemorrhage
+UBERON:0001849,membranous labyrinth,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0200109,Absent/shortened outer dynein arms,HP:0200108,Shortened outer dynein arms
+DOID:10937,impulse control disorder,DOID:150,disease of mental health
+UBERON:0002588,decussation of superior cerebellar peduncle,UBERON:0014891,brainstem white matter
+HP:0002545,Patchy demyelination of subcortical white matter,HP:0007305,CNS demyelination
+HP:0004794,Malrotation of small bowel,HP:0002566,Intestinal malrotation
+HP:0100871,Abnormality of the palm,HP:0001155,Abnormality of the hand
+NCBITaxon:621,Shigella boydii,NCBITaxon:620,Shigella
+HP:0008664,Urethral sphincter sclerosis,HP:0008661,Urethral stenosis
+HP:0004529,"Atrophic, patchy alopecia",HP:0002232,Patchy alopecia
+UBERON:0001954,Ammon's horn,UBERON:0002619,regional part of cerebral cortex
+HP:0009213,Triangular epiphysis of the middle phalanx of the 5th finger,HP:0010267,Triangular epiphyses of the middle phalanges of the hand
+HP:0010664,Fusion of the left and right thalami,HP:0010663,Abnormality of the thalamus
+UBERON:0013070,prepatagium,UBERON:0010858,inter limb-segment region
+HP:0002694,Sclerosis of skull base,HP:0002693,Abnormality of the skull base
+DOID:9174,rectum carcinoma in situ,DOID:8719,in situ carcinoma
+UBERON:0008852,visceral yolk sac,UBERON:0001040,yolk sac
+UBERON:0006864,distal metaphysis of femur,UBERON:0004377,distal metaphysis
+HP:0008038,Aplastic/hypoplastic lacrimal glands,HP:0011482,Abnormality of the lacrimal gland
+HP:0009974,Partial duplication of the phalanges of the 4th finger,HP:0009999,Partial duplication of the phalanx of hand
+HP:0005502,Increased red cell osmotic fragility,HP:0001877,Abnormality of erythrocytes
+UBERON:0016440,glabella,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:3112,papillary adenocarcinoma,DOID:299,adenocarcinoma
+UBERON:0002668,oculomotor nerve fibers,UBERON:0006843,root of cranial nerve
+HP:0002329,Drowsiness,HP:0004372,Reduced consciousness/confusion
+HP:0002365,Hypoplasia of the brainstem,HP:0007362,Aplasia/Hypoplasia of the brainstem
+HP:0002381,Aphasia,HP:0002167,Neurological speech impairment
+HP:0006895,Lower limb hypertonia,HP:0002814,Abnormality of the lower limb
+HP:0002616,Aortic root dilatation,HP:0005111,Dilatation of the ascending aorta
+HP:0002061,Lower limb spasticity,HP:0001257,Spasticity
+HP:0001985,Hypoketotic hypoglycemia,HP:0001943,Hypoglycemia
+DOID:5345,testicular non-seminomatous germ cell cancer,DOID:5556,testicular malignant germ cell cancer
+HP:0009526,Cone-shaped epiphysis of the proximal phalanx of the 2nd finger,HP:0009490,Cone-shaped epiphyses of the 2nd finger
+UBERON:3000563,seydels palatal process,UBERON:4100000,skeletal element projection
+UBERON:3001003,cloacal fold,UBERON:3000977,body external integument structure
+UBERON:0008606,antitragicus muscle,UBERON:0001596,intrinsic auricular muscle
+HP:0100381,Absent middle phalanx of the 3rd toe,HP:0100362,Aplasia of the phalanges of the 3rd toe
+HP:0100385,Aplasia of the proximal phalanx of the 4th toe,HP:0100363,Aplasia of the phalanges of the 4th toe
+HP:0012326,Abnormality of the celiac artery,HP:0005114,Abnormalities of the peripheral arteries
+HP:0011794,Embryonal renal neoplasm,HP:0009726,Renal neoplasm
+HP:0006146,Broad metacarpal epiphyses,HP:0005913,Abnormality of metacarpal epiphyses
+UBERON:0005402,philtrum,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:4637,cervical adenitis,DOID:1602,lymphadenitis
+HP:0009847,Osteolytic defects of the middle phalanges of the hand,HP:0009771,Osteolytic defects of the phalanges of the hand
+HP:0100482,Proximal/middle symphalangism of 5th toe,HP:0010366,Triangular shaped phalanges of the 3rd toe
+HP:0009693,Pseudoepiphyses of the thumb,HP:0009599,Abnormality of the epiphyses of the thumb
+UBERON:0001091,calcareous tooth,UBERON:0003913,tooth-like structure
+UBERON:0006968,keratin sheath of horn,UBERON:0000061,anatomical structure
+HP:0100923,Clavicular sclerosis,HP:0011001,Increased bone mineral density
+UBERON:0013551,Brodmann (1909) area 20,UBERON:0013529,Brodmann area
+HP:0100398,Duplication of the distal phalanx of the 3rd toe,HP:0010368,Abnormality of the distal phalanx of the 3rd toe
+UBERON:0005639,right lung cranial lobe epithelium,UBERON:0003364,epithelium of right lung
+HP:0003297,Hyperlysinuria,HP:0010908,Abnormality of lysine metabolism
+HP:0008165,Reduced circulating T-helper cells,HP:0005403,T lymphocytopenia
+HP:0009650,Short distal phalanx of the thumb,HP:0009660,Short phalanx of the thumb
+UBERON:0003575,wrist connective tissue,UBERON:0003598,manus connective tissue
+DOID:8515,Cor pulmonale,DOID:6000,congestive heart failure
+DOID:9827,radioulnar synostosis,DOID:0080015,physical disorder
+UBERON:0000307,blastula,UBERON:0000922,embryo
+UBERON:0001581,depressor labii inferioris,UBERON:0013765,digestive system organ
+CL:0009000,sensory neuron of spinal nerve,CL:0000101,sensory neuron
+UBERON:0003451,lower jaw incisor,UBERON:0003268,tooth of lower jaw
+UBERON:0001340,dorsal artery of penis,UBERON:0004573,systemic artery
+DOID:5056,adult cerebellar neoplasm,DOID:4205,cerebellum cancer
+DOID:14775,type VI Ehlers-Danlos syndrome,DOID:13359,Ehlers-Danlos syndrome
+DOID:1768,conversion disorder,DOID:4737,somatoform disorder
+HP:0003366,Abnormality of the femoral neck and head region,HP:0002823,Abnormality of the femur
+DOID:3218,jejunal neoplasm,DOID:7505,small intestine neoplasm
+UBERON:0013676,aproctal bone of priapium,UBERON:0014403,male anatomical structure
+HP:0010113,Absent epiphyses of the hallux,HP:0010162,Absent epiphyses of the toes
+UBERON:0013637,prostate gland lateral lobe,UBERON:0001328,lobe of prostate
+HP:0000568,Microphthalmos,HP:0008056,Aplasia/Hypoplasia affecting the eye
+UBERON:0011079,angular bone,UBERON:0004768,bone of lower jaw
+UBERON:0009968,primitive superior sagittal sinus,UBERON:0003499,brain blood vessel
+UBERON:0003511,iris blood vessel,UBERON:0004121,ectoderm-derived structure
+HP:0008182,Adrenocortical hypoplasia,HP:0000849,Adrenocortical abnormality
+HP:0004399,Congenital pyloric atresia,HP:0004400,Abnormality of the pylorus
+HP:0004373,Focal dystonia,HP:0001332,Dystonia
+HP:0011408,Moderate intrauterine growth retardation,HP:0001511,Intrauterine growth retardation
+HP:0003041,Humeroradial synostosis,HP:0002818,Abnormality of the radius
+CL:1000425,chromaffin cell of paraganglion,CL:0000166,chromaffin cell
+DOID:5274,malignant dermis tumor,DOID:4159,skin cancer
+DOID:5124,fallopian tube leiomyoma,DOID:0060111,fallopian tube benign neoplasm
+HP:0001992,Organic aciduria,HP:0012072,Aciduria
+UBERON:2000933,myotome somite 5,UBERON:0003082,myotome
+CL:1001068,kidney venous system smooth muscle cell,CL:1000893,kidney venous blood vessel cell
+UBERON:0014430,sciatic notch,UBERON:0004120,mesoderm-derived structure
+HP:0004258,Small trapezoid bone,HP:0004256,Abnormality of the trapezoid bone
+UBERON:1000002,cranial midline area,UBERON:0001444,subdivision of head
+UBERON:0001276,epithelium of stomach,UBERON:0015833,foregut epithelium
+HP:0009454,Patchy sclerosis of the proximal phalanx of the 3rd finger,HP:0100909,Sclerosis of the proximal phalanx of the 3rd finger
+DOID:5667,sweat gland carcinoma,DOID:2095,sweat gland cancer
+HP:0009246,Aplasia of the distal phalanx of the 5th finger,HP:0009238,Aplasia of the 5th finger
+NCBITaxon:10240,Poxviridae,NCBITaxon:35237,"dsDNA viruses, no RNA stage"
+UBERON:0004921,subdivision of digestive tract,UBERON:0013522,subdivision of tube
+UBERON:0010583,pedal digit 4 phalanx pre-cartilage condensation,UBERON:0015034,pedal digit 4 phalanx endochondral element
+UBERON:0002025,stratum basale of epidermis,UBERON:0013754,integumentary system layer
+HP:0003119,Abnormality of lipid metabolism,HP:0001939,Abnormality of metabolism/homeostasis
+HP:0009656,Symphalangism of the thumb,HP:0009773,Symphalangism affecting the phalanges of the hand
+CL:0000319,mucus secreting cell,CL:0000159,seromucus secreting cell
+HP:0004563,increased spinal bone density,HP:0011001,Increased bone mineral density
+HP:0009558,Broad distal phalanx of the 2nd finger,HP:0009547,Broad phalanges of the 2nd finger
+UBERON:0001759,vagus nerve,UBERON:0001785,cranial nerve
+HP:0001849,Oligodactyly (feet),HP:0012165,Oligodactyly
+DOID:12546,atrophic nonflaccid tympanic membrane,DOID:5782,tympanic membrane disease
+DOID:5715,functionless pituitary adenoma,DOID:3829,pituitary adenoma
+HP:0001442,Somatic mosaicism,HP:0001428,Somatic mutation
+UBERON:0007380,dermal scale,UBERON:0002542,scale
+HP:0010419,Symphalangism affecting the distal phalanx of the 2nd toe,HP:0010353,Symphalangism affecting the phalanges of the 2nd toe
+HP:0009324,Enlarged epiphysis of the middle phalanx of the 3rd finger,HP:0010260,Enlarged epiphyses of the middle phalanges of the hand
+HP:0003218,Oroticaciduria,HP:0010928,Abnormality of orotic acid metabolism
+DOID:7207,lung combined large cell neuroendocrine carcinoma,DOID:6658,pulmonary large cell neuroendocrine carcinoma
+UBERON:0005847,thoracic spinal cord lateral column,UBERON:0014637,thoracic spinal cord white matter
+HP:0008697,Hypoplasia of the fallopian tube,HP:0008655,Aplasia/Hypoplasia of the fallopian tube
+DOID:5170,vaginal endometrial stromal sarcoma,DOID:1901,vagina sarcoma
+UBERON:0005708,lower jaw incisor odontogenic papilla,UBERON:0003324,mesenchyme of lower jaw
+UBERON:0004435,proximal epiphysis of distal phalanx of manual digit 5,UBERON:0011979,epiphysis of distal phalanx of manus
+UBERON:3000953,ceratobranchials II--IV,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:3381,liposarcoma of bone,DOID:3347,osteosarcoma
+UBERON:0004247,bone of dorsum,UBERON:0005174,dorsal region organ
+DOID:10983,Alport syndrome,DOID:0050737,autosomal recessive disease
+UBERON:0006764,anterior communicating artery,UBERON:0004573,systemic artery
+HP:0011356,Regional abnormality of skin,HP:0000951,Abnormality of the skin
+DOID:10934,multiple personality disorder,DOID:10935,dissociative disorder
+CL:0007008,notochordal vacuole cell,CL:0007005,notochordal cell
+UBERON:2001895,hypobranchial 2 element,UBERON:2001893,hypobranchial element
+HP:0007731,Chorioretinal dysplasia,HP:0000532,Chorioretinal abnormality
+NCBITaxon:314147,Glires,NCBITaxon:314146,Euarchontoglires
+UBERON:0005465,obturator nerve,UBERON:0001021,nerve
+UBERON:0015479,scrotum skin,UBERON:0014403,male anatomical structure
+UBERON:0001131,vertebral foramen,UBERON:0010276,vertebral column opening
+DOID:12918,thromboangiitis obliterans,DOID:341,peripheral vascular disease
+UBERON:0005610,iliac vein,UBERON:0003520,pelvis blood vessel
+DOID:11758,iron deficiency anemia,DOID:11252,microcytic anemia
+UBERON:0005446,foramen rotundum,UBERON:0013685,foramen of skull
+UBERON:0003564,diencephalon dura mater,UBERON:0003561,forebrain dura mater
+UBERON:2000960,sclerotome somite 29,UBERON:0003089,sclerotome
+HP:0001133,Constricted visual fields,HP:0001123,Visual field defect
+HP:0200072,Episodic quadriplegia,HP:0002445,Tetraplegia
+UBERON:3010073,centrale 2,UBERON:0015050,tarsus endochondral element
+UBERON:2001516,ceratobranchial cartilage,UBERON:0011004,pharyngeal arch cartilage
+DOID:970,tenosynovitis,DOID:971,tendinitis
+UBERON:0004057,skeletal muscle fiber triad,UBERON:0001134,skeletal muscle tissue
+HP:0011473,Villous atrophy,HP:0011472,Abnormality of small intestinal villus morphology
+HP:0100660,Dyskinesia,HP:0100022,Abnormality of movement
+UBERON:2001685,lateral ethmoid-ectopterygoid ligament,UBERON:0008846,skeletal ligament
+UBERON:0014385,aryepiglottic fold,UBERON:0000481,multi-tissue structure
+DOID:0060074,ductal carcinoma in situ,DOID:8791,breast carcinoma in situ
+UBERON:0015827,brainstem reticular formation,UBERON:0002275,reticular formation
+UBERON:4000070,elasmoid scale,UBERON:0007380,dermal scale
+NCBITaxon:6843,Chelicerata,NCBITaxon:6656,Arthropoda
+UBERON:3010007,pit organ,UBERON:0000477,anatomical cluster
+HP:0005726,Thumbs hypoplastic with bulbous tips,HP:0009778,Short thumb
+UBERON:0010036,anterior tegmental nucleus,UBERON:0009661,midbrain nucleus
+HP:0009408,Aplasia/Hypoplasia of the phalanges of the 4th finger,HP:0009767,Aplasia/Hypoplasia of the phalanges of the hand
+HP:0005655,Multiple digital exostoses,HP:0002762,Multiple exostoses
+UBERON:2002242,scale primordium,UBERON:0004121,ectoderm-derived structure
+HP:0011131,Perianal rash,HP:0004378,Abnormality of the anus
+DOID:7765,Coats disease,DOID:7736,retinal telangiectasia
+HP:0012650,Perisylvian polymicrogyria,HP:0002126,Polymicrogyria
+HP:0003472,Hypocalcemic tetany,HP:0002901,Hypocalcemia
+UBERON:0003703,extrahepatic bile duct,UBERON:0002394,bile duct
+UBERON:0005295,sex cord,UBERON:0012275,meso-epithelium
+HP:0002866,Hypoplastic iliac wings,HP:0000946,Hypoplastic ilia
+UBERON:3000713,epichordal,UBERON:0001075,vertebral centrum
+UBERON:1000006,collection of hair on forehead,UBERON:0010165,collection of hair on face
+UBERON:0015784,duct of olfactory gland,UBERON:0000058,duct
+HP:0010298,Smooth tongue,HP:0000157,Abnormality of the tongue
+UBERON:2001157,posterior lateral line primordium,UBERON:2000228,lateral line primordium
+HP:0010146,Small epiphysis of the distal phalanx of the hallux,HP:0010121,Small epiphyses of the hallux
+UBERON:0002062,endocardial cushion,UBERON:0005256,trunk mesenchyme
+UBERON:0006008,fibrous ring of heart,UBERON:0003837,thoracic segment connective tissue
+UBERON:3000808,parasagittal processes,UBERON:4100000,skeletal element projection
+UBERON:0004370,anterior limiting lamina of cornea,UBERON:0005769,basement membrane of epithelium
+HP:0009064,Generalized lipodystrophy,HP:0009125,Lipodystrophy
+DOID:0050536,SC phocomelia syndrome,DOID:0050737,autosomal recessive disease
+UBERON:0005485,valve of inferior vena cava,UBERON:0000946,cardial valve
+HP:0003855,Spurred metaphyses of the upper limbs,HP:0009809,Abnormality of upper limb metaphysis
+HP:0010766,Ectopic calcification,HP:0000924,Abnormality of the skeletal system
+UBERON:0002086,sinoatrial valve,UBERON:0002050,embryonic structure
+UBERON:3000886,ypsiloid cartilage,UBERON:0004120,mesoderm-derived structure
+CL:0000324,metanephric mesenchyme stem cell,CL:0000134,mesenchymal cell
+UBERON:0013247,male paramesonephric duct,UBERON:0003914,epithelial tube
+DOID:10556,supine hypotensive syndrome,DOID:178,vascular disease
+HP:0010966,Abnormality of fatty-acid anion metabolism,HP:0004359,Abnormality of fatty-acid metabolism
+UBERON:0008333,hilum of inferior olivary complex,UBERON:0014649,white matter of medulla oblongata
+DOID:12858,Huntington's disease,DOID:0050736,autosomal dominant disease
+HP:0011962,Obstructive azoospermia,HP:0000027,Azoospermia
+UBERON:0015061,limb endochondral element,UBERON:0010363,endochondral element
+UBERON:0000317,colonic mucosa,UBERON:0001207,mucosa of large intestine
+CL:1001124,kidney cortex peritubular capillary cell,CL:1001033,peritubular capillary endothelial cell
+UBERON:0012103,suspensory ligament of breast,UBERON:0004121,ectoderm-derived structure
+CL:0002003,"CD34-positive, GlyA-negative erythroid progenitor cell",CL:0000038,erythroid progenitor cell
+HP:0012715,Profound hearing impairment,HP:0000365,Hearing impairment
+UBERON:4300037,bony fin ray,UBERON:4400005,fin ray
+UBERON:0003068,axial mesoderm,UBERON:0005423,developing anatomical structure
+HP:0006311,Generalized microdontia,HP:0000691,Microdontia
+UBERON:0000460,major vestibular gland,UBERON:0011826,vestibular gland
+UBERON:2000699,entopterygoid vertical strut,UBERON:0004120,mesoderm-derived structure
+HP:0000233,Thin vermilion border,HP:0000159,Abnormality of the lip
+UBERON:0006305,tunica vasculosa lentis,UBERON:0004120,mesoderm-derived structure
+UBERON:0006635,anterior abdominal wall,UBERON:0000475,organism subdivision
+DOID:624,transient hypogammaglobulinemia of infancy,DOID:625,transient hypogammaglobulinemia
+UBERON:0003379,cardiac muscle of right atrium,UBERON:0004490,cardiac muscle tissue of atrium
+UBERON:3000827,margo anterior of cleithrum,UBERON:0000064,organ part
+UBERON:3001005,dorsolateral fold,UBERON:3000977,body external integument structure
+DOID:476,breast hemangioma,DOID:0060082,breast benign neoplasm
+NCBITaxon:186677,Hepevirus,NCBITaxon:291484,Hepeviridae
+UBERON:0006246,humerus pre-cartilage condensation,UBERON:0015053,humerus endochondral element
+HP:0004381,Supravalvular aortic stenosis,HP:0001650,Aortic valve stenosis
+UBERON:0002569,transverse temporal sulcus,UBERON:0003022,cerebral cortex lobe
+HP:0010021,Ivory epiphysis of the 1st metacarpal,HP:0010274,Ivory epiphyses of the proximal phalanges of the hand
+HP:0004241,Stippled calcification in carpal bones,HP:0004054,Sclerosis of hand bones
+HP:0007663,Decreased central vision,HP:0000505,Visual impairment
+UBERON:0008778,epaxial musclulature,UBERON:0004479,musculature of trunk
+UBERON:0005227,manual digit epithelium,UBERON:0000490,unilaminar epithelium
+UBERON:2000987,hypaxial region somite 3,UBERON:0003895,hypaxial myotome region
+UBERON:0015859,hepatic lymph node,UBERON:0015860,visceral abdominal lymph node
+DOID:5241,hemangioblastoma,DOID:255,hemangioma
+UBERON:0004436,proximal epiphysis of middle phalanx of manual digit 2,UBERON:0011978,epiphysis of middle phalanx of manus
+HP:0002213,Fine hair,HP:0010719,Abnormality of hair texture
+DOID:2297,leptospirosis,DOID:0050338,primary bacterial infectious disease
+HP:0003215,Dicarboxylic aciduria,HP:0001992,Organic aciduria
+HP:0009940,Asymmetry of the mandible,HP:0000277,Abnormality of the mandible
+HP:0003070,Elbow ankylosis,HP:0001376,Limitation of joint mobility
+UBERON:0005333,mammary bud,UBERON:0005153,epithelial bud
+HP:0005134,Absence of the pulmonary valve,HP:0001641,Abnormality of the pulmonary valve
+UBERON:0010568,manual digit 4 metacarpus pre-cartilage condensation,UBERON:0010698,manual digit metacarpus pre-cartilage condensation
+UBERON:0001369,iliacus muscle,UBERON:0001497,muscle of pelvic girdle
+HP:0100110,Triangular epiphysis of the distal phalanx of the 2nd toe,HP:0100088,Abnormality of the epiphysis of the distal phalanx of the 2nd toe
+UBERON:0015048,basioccipital endochondral element,UBERON:0010363,endochondral element
+DOID:3690,brachial plexus neuropathy,DOID:3688,plexopathy
+UBERON:0004234,iris smooth muscle,UBERON:0003386,smooth muscle of eye
+UBERON:0001049,neural tube,UBERON:0010371,ecto-epithelium
+UBERON:0014622,apex of cervical spinal cord dorsal horn,UBERON:0006983,anatomical point
+HP:0009973,Complete duplication of the phalanges of the 4th finger,HP:0009972,Duplication of phalanx of 4th finger
+CL:1000290,myocyte of middle internodal tract,CL:0002096,internodal tract myocyte
+UBERON:0014395,proximal mesopodial bone,UBERON:0003656,mesopodium bone
+HP:0011065,Conical incisor,HP:0000698,Conical tooth
+DOID:13809,familial combined hyperlipidemia,DOID:1168,familial hyperlipidemia
+CL:0002467,Gr1-high myeloid suppressor cell,CL:0000889,myeloid suppressor cell
+DOID:13134,hordeolum externum,DOID:9909,hordeolum
+DOID:7968,plasmacytoid variant infiltrating bladder urothelial carcinoma,DOID:6477,invasive bladder transitional cell carcinoma
+UBERON:0005145,metanephric comma-shaped body,UBERON:0010535,primitive metanephric nephron
+UBERON:0003258,endoderm of foregut,UBERON:0000925,endoderm
+UBERON:0006254,ischial cartilage element,UBERON:0005863,cartilaginous condensation
+DOID:0050756,Batten disease,DOID:14503,neuronal ceroid lipofuscinosis
+HP:0009522,Stippling of the epiphysis of the middle phalanx of the 2nd finger,HP:0010266,Stippling of the epiphyses of the middle phalanges of the hand
+UBERON:0001980,arteriole,UBERON:0003509,arterial blood vessel
+UBERON:0010091,future hindbrain meninges,UBERON:0007524,dense mesenchyme tissue
+HP:0009353,Pseudoepiphysis of the proximal phalanx of the 3rd finger,HP:0010275,Pseudoepiphyses of the proximal phalanges of the hand
+UBERON:3010413,left channel of ventral aorta,UBERON:0004573,systemic artery
+UBERON:3000110,crista contacta,UBERON:0004120,mesoderm-derived structure
+HP:0005384,Defective B cell activation,HP:0005372,Abnormality of B cell physiology
+UBERON:3010168,tarsal fringe,UBERON:3000981,limb external integument structure
+DOID:0050807,Kahrizi syndrome,DOID:0050737,autosomal recessive disease
+UBERON:0002978,oral part of ventral lateral nucleus,UBERON:0003528,brain grey matter
+CL:0002457,epidermal Langerhans cell,CL:0000453,Langerhans cell
+HP:0010867,Dyssynergia,HP:0001251,Ataxia
+UBERON:0001877,medial septal nucleus,UBERON:0009663,telencephalic nucleus
+UBERON:0000482,basal lamina of epithelium,UBERON:0005764,acellular membrane
+DOID:14323,Marfan syndrome,DOID:0050736,autosomal dominant disease
+HP:0100446,Curved proximal phalanx of the 3rd toe,HP:0010362,Curved phalanges of the 3rd toe
+HP:0006768,Localized neuroblastoma,HP:0003006,Neuroblastoma
+UBERON:0012437,epithelial-mesenchymal boundary,UBERON:0006800,anatomical line
+HP:0009633,Osteolytic defects of the proximal phalanx of the thumb,HP:0009618,Abnormality of the proximal phalanx of the thumb
+HP:0002451,Limb dystonia,HP:0001332,Dystonia
+UBERON:0011985,infraorbital sinus,UBERON:0001825,paranasal sinus
+HP:0003739,Myoclonic spasms,HP:0001336,Myoclonus
+UBERON:2001899,ceratobranchial 1 element,UBERON:2001898,ceratobranchial element
+UBERON:0002526,lumbar lymph node,UBERON:0002507,abdominal lymph node
+UBERON:0006095,anterior transverse termporal area 41,UBERON:0003022,cerebral cortex lobe
+UBERON:3000509,processus suprafenestralis,UBERON:0004120,mesoderm-derived structure
+UBERON:2001222,posterior copula,UBERON:2001220,basibranchial copula
+DOID:3352,malignant fibrous histiocytoma of bone,DOID:1907,malignant fibroxanthoma
+HP:0004646,Hypoplasia of the nasal bone,HP:0010940,Aplasia/Hypoplasia of the nasal bone
+UBERON:0001981,blood vessel,UBERON:0004120,mesoderm-derived structure
+UBERON:3010501,duodeno-pancreatic artery,UBERON:0001637,artery
+UBERON:0001603,lateral rectus extra-ocular muscle,UBERON:0006533,rectus extraocular muscle
+DOID:5136,lung leiomyoma,DOID:3683,lung benign neoplasm
+DOID:12929,endocardial fibroelastosis,DOID:0050825,endocardium disease
+HP:0001305,Dandy-Walker malformation,HP:0002198,Dilated fourth ventricle
+UBERON:3000237,infrarostral cartilage,UBERON:0004121,ectoderm-derived structure
+UBERON:2000611,visceromotor column,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0002459,langerin-negative dermal dendritic cell,CL:0001006,dermal dendritic cell
+UBERON:3010717,diverticulum,UBERON:0002050,embryonic structure
+UBERON:0002254,thyroglossal duct,UBERON:0004119,endoderm-derived structure
+HP:0001903,Anemia,HP:0001877,Abnormality of erythrocytes
+HP:0006520,Progressive pulmonary function impairment,HP:0005952,Decreased pulmonary function
+UBERON:2005039,anterior lateral mesoderm,UBERON:0004120,mesoderm-derived structure
+DOID:4527,ovarian angiosarcoma,DOID:0001816,angiosarcoma
+UBERON:0006295,sternebral bone pre-cartilage condensation,UBERON:0004120,mesoderm-derived structure
+UBERON:3000590,supraorbital flange,UBERON:0004121,ectoderm-derived structure
+UBERON:0004738,metanephric juxtaglomerular apparatus,UBERON:0002303,juxtaglomerular apparatus
+UBERON:2102280,pectoral fin distal radial element 3,UBERON:2101588,pectoral fin distal radial element
+HP:0011008,Speed of onset,HP:0003674,Onset
+CL:0001019,CD115-positive monocyte OR common dendritic progenitor,CL:0002031,hematopoietic lineage restricted progenitor cell
+UBERON:0014917,pouch sphincter,UBERON:0004590,sphincter muscle
+UBERON:0007297,presumptive pronephric mesoderm,UBERON:0006598,presumptive structure
+HP:0009153,Abnormality of the epiphysis of the proximal phalanx of the 5th finger,HP:0009152,Abnormality of the epiphyses of the 5th finger
+DOID:13270,erythropoietic protoporphyria,DOID:3133,acute porphyria
+UBERON:0015082,proximal tarsal cartilage,UBERON:0015081,proximal tarsal bone endochondral element
+UBERON:3000728,nucal keel,UBERON:0004120,mesoderm-derived structure
+HP:0100368,Short phalanx of the 5th toe,HP:0010383,Aplasia/Hypoplasia of the phalanges of the 5th toe
+HP:0007207,Photosensitive tonic-clonic seizures,HP:0002069,Generalized tonic-clonic seizures
+DOID:14247,chronic purulent otitis media,DOID:11506,suppurative otitis media
+HP:0010409,Patchy sclerosis of the middle phalanx of the 2nd toe,HP:0010357,Abnormality of the middle phalanx of the 2nd toe
+DOID:5698,fibroblastic liposarcoma,DOID:3382,liposarcoma
+DOID:10348,blepharophimosis,DOID:530,eyelid disease
+UBERON:0005086,hair follicle placode,UBERON:0011817,follicle placode
+HP:0010014,Abnormality of the epiphysis of the 1st metacarpal,HP:0010245,Abnormality of the epiphyses of the proximal phalanges of the hand
+HP:0009958,Polydactyly affecting the 3rd finger,HP:0006159,Mesoaxial hand polydactyly
+UBERON:2002097,sensory canal pore series,UBERON:0000477,anatomical cluster
+UBERON:0015790,autopod skin,UBERON:0001419,skin of limb
+HP:0006899,Fusion of the cerebellar hemispheres,HP:0001317,Abnormality of the cerebellum
+HP:0008213,Gonadotropin deficiency,HP:0000830,Anterior hypopituitarism
+DOID:1235,fetishism,DOID:0060044,paraphilia disorder
+UBERON:0013507,thoracic vertebra cartilage element,UBERON:0015008,thoracic vertebra endochondral element
+UBERON:0001357,inferior rectal artery,UBERON:0015212,lateral structure
+HP:0004851,Folate-responsive megaloblastic anemia,HP:0001889,Megaloblastic anemia
+HP:0011230,Laterally extended eyebrow,HP:0000534,Abnormality of the eyebrow
+DOID:9113,granuloma inguinale,DOID:0050338,primary bacterial infectious disease
+HP:0200144,Anaphylactoid purpura,HP:0000979,Purpura
+UBERON:0010907,parafibula,UBERON:0004251,hindlimb zeugopod bone
+UBERON:0001666,flexor digitorum longus,UBERON:0001383,muscle of leg
+UBERON:0001214,pancreatic tributary of splenic vein,UBERON:0002017,portal vein
+HP:0010804,Tented upper lip vermilion,HP:0011339,Abnormality of upper lip vermillion
+HP:0009241,Bullet-shaped distal phalanx of the 5th finger,HP:0009837,Bullet-shaped distal phalanges of the hand
+CL:0000758,type 6 cone bipolar cell (sensu Mus),CL:0000752,cone retinal bipolar cell
+UBERON:0008775,proximal epiphysis of fibula,UBERON:0004380,proximal epiphysis
+UBERON:0005399,male reproductive gland,UBERON:0014403,male anatomical structure
+DOID:3728,acute allergic sanguinous otitis media,DOID:3696,acute sanguinous otitis media
+UBERON:0000930,stomodeum,UBERON:0002050,embryonic structure
+HP:0000067,"Urethral atresia, female",HP:0000055,Abnormality of female external genitalia
+UBERON:0001969,blood plasma,UBERON:0000179,haemolymphatic fluid
+HP:0009165,Stippling of the epiphysis of the distal phalanx of the 5th finger,HP:0010255,Stippling of the epiphyses of the distal phalanges of the hand
+HP:0008019,Superior lens subluxation,HP:0001132,Lens subluxation
+UBERON:0001864,scala tympani,UBERON:0000477,anatomical cluster
+UBERON:0013190,entotympanic bone,UBERON:0005913,zone of bone organ
+HP:0003164,Hypothalamic gonadotropin-releasing hormone (GNRH) deficiency,HP:0012285,Abnormal hypothalamus physiology
+UBERON:0003956,aqueous drainage system,UBERON:0004121,ectoderm-derived structure
+CL:0005006,ionocyte,CL:0002371,somatic cell
+CL:0005009,renal principal cell,CL:0000075,columnar/cuboidal epithelial cell
+UBERON:0010377,mesenchyme from somatopleure,UBERON:0007524,dense mesenchyme tissue
+HP:0100265,Synostosis of metacarpals/metatarsals,HP:0100240,Synostosis of joints
+HP:0006394,Limited pronation/supination of forearm,HP:0002996,Limited elbow movement
+UBERON:0002303,juxtaglomerular apparatus,UBERON:0000477,anatomical cluster
+HP:0012232,Shortened QT interval,HP:0003115,Abnormal EKG
+UBERON:2000692,symplectic,UBERON:0002513,endochondral bone
+DOID:11374,anal spasm,DOID:3128,anus disease
+DOID:0050129,secretory diarrhea,DOID:13250,diarrhea
+HP:0003495,GM2-ganglioside accumulation,HP:0004345,Abnormality of ganglioside metabolism
+UBERON:0003650,metatarsal bone of digit 1,UBERON:0013581,metapodium bone 1
+HP:0001684,Secundum atrial septal defect,HP:0001631,Defect in the atrial septum
+UBERON:0000569,ileocecal valve,UBERON:0003978,valve
+DOID:6217,gastric diffuse adenocarcinoma,DOID:3717,gastric adenocarcinoma
+UBERON:0006079,subdivision of spinal cord dorsal column,UBERON:0006080,segment of white matter of spinal cord
+UBERON:0005352,spermatic cord,UBERON:0005156,reproductive structure
+UBERON:0003414,mesenchyme of mandible,UBERON:0010258,mesenchyme from rhombencephalic neural crest
+UBERON:3000374,palatine process of pars palatina of premaxilla,UBERON:4100000,skeletal element projection
+DOID:369,olfactory neuroblastoma,DOID:366,olfactory nerve neoplasm
+UBERON:0013525,stomach lumen,UBERON:0000464,anatomical space
+UBERON:0002111,artery smooth muscle tissue,UBERON:0004695,arterial system smooth muscle
+UBERON:0005333,mammary bud,UBERON:0010371,ecto-epithelium
+UBERON:0010213,laryngeal pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+UBERON:0012109,zygomatic process of frontal bone,UBERON:0004120,mesoderm-derived structure
+UBERON:0010238,torus pylorus,UBERON:0009034,stomach region
+UBERON:0007772,scrotal sweat,UBERON:0001089,sweat
+DOID:0050761,paramyloidosis,DOID:9120,amyloidosis
+UBERON:3000911,foramen nutritium exterius,UBERON:0005744,bone foramen
+UBERON:0007491,chitin-based acellular structure,UBERON:0000476,acellular anatomical structure
+DOID:0050863,arteritic anterior ischemic optic neuropathy,DOID:12010,anterior ischemic optic neuropathy
+UBERON:0000117,respiratory tube,UBERON:0004119,endoderm-derived structure
+UBERON:0001399,deep brachial artery,UBERON:0003507,arm blood vessel
+UBERON:0012200,anterior intercostal vein,UBERON:0012197,intercostal vein
+UBERON:0013150,future brain vesicle,UBERON:0010064,open anatomical space
+UBERON:0004074,cerebellum vermis lobule I,UBERON:0004070,cerebellum vermis lobule
+DOID:13656,gastrin secretion abnormality,DOID:1428,endocrine pancreas disease
+HP:0008631,Ureteral dysgenesis,HP:0000069,Abnormality of the ureter
+UBERON:2001463,melanophore stripe,UBERON:2002284,body marking
+UBERON:0004405,distal epiphysis of tibia,UBERON:0004379,distal epiphysis
+UBERON:0010333,extraembryonic membrane mesenchyme,UBERON:0003104,mesenchyme
+HP:0002743,Recurrent enteroviral infections,HP:0004429,Recurrent viral infections
+DOID:0050875,small cell neuroendocrine carcinoma,DOID:5409,lung small cell carcinoma
+UBERON:0009558,pastern bone,UBERON:0003221,phalanx
+HP:0006313,Widely spaced primary teeth,HP:0000687,Widely spaced teeth
+UBERON:0002273,lateral zone of hypothalamus,UBERON:0004121,ectoderm-derived structure
+UBERON:3010138,trabecular horn,UBERON:0004120,mesoderm-derived structure
+HP:0003167,Carnosinuria,HP:0003355,Aminoaciduria
+HP:0009491,Enlarged epiphyses of the 2nd finger,HP:0006263,Abnormality of the epiphyses of the 2nd finger
+UBERON:0005301,male preputial gland,UBERON:0010147,male accessory sex gland
+NCBITaxon:10293,Alphaherpesvirinae,NCBITaxon:10292,Herpesviridae
+CL:1001430,urethra urothelial cell,CL:0000731,urothelial cell
+UBERON:2002200,hypobranchial muscle,UBERON:0002376,cranial muscle
+HP:0100124,Cone-shaped epiphysis of the proximal phalanx of the 2nd toe,HP:0100046,Cone-shaped epiphyses of the 2nd toe
+UBERON:0006569,diencephalic nucleus,UBERON:0002308,nucleus of brain
+DOID:2879,nodular degeneration of cornea,DOID:1237,corneal degeneration
+UBERON:0006207,aortico-pulmonary spiral septum,UBERON:0010313,neural crest-derived structure
+UBERON:0009893,ascidian ocellus,UBERON:0000020,sense organ
+UBERON:0002015,kidney capsule,UBERON:0006554,urinary system structure
+UBERON:0001105,clavicle,UBERON:0003461,shoulder bone
+UBERON:3000118,crista supraorbitalis,UBERON:0010313,neural crest-derived structure
+DOID:0050936,extra-adrenal pheochromocytoma,DOID:5719,adrenal medulla cancer
+DOID:9095,esophagus carcinoma in situ,DOID:8719,in situ carcinoma
+NCBITaxon:11598,Hantavirus,NCBITaxon:11571,Bunyaviridae
+UBERON:3000956,hypobranchial II,UBERON:0002513,endochondral bone
+UBERON:0015418,urethra mesenchymal layer,UBERON:0003104,mesenchyme
+DOID:14759,autosomal recessive type IV Ehlers-Danlos syndrome,DOID:13359,Ehlers-Danlos syndrome
+HP:0012201,Reduced prothrombin activity,HP:0012200,Abnormality of prothrombin
+UBERON:0001176,right hepatic duct,UBERON:0003703,extrahepatic bile duct
+UBERON:0010581,pedal digit 2 phalanx pre-cartilage condensation,UBERON:0010585,pedal digit phalanx pre-cartilage condensation
+UBERON:0004346,gubernaculum,UBERON:0008845,nonskeletal ligament
+UBERON:0005709,upper jaw incisor epithelium,UBERON:0003843,dental epithelium
+CL:0000211,electrically active cell,CL:0000003,native cell
+UBERON:0004694,Harderian gland epithelium,UBERON:0004817,lacrimal gland epithelium
+DOID:6024,selective IgE deficiency disease,DOID:11702,dysgammaglobulinemia
+UBERON:3000195,foramen perilymphaticus inferius,UBERON:0005744,bone foramen
+UBERON:0010994,coronoid process of ulna,UBERON:4100000,skeletal element projection
+DOID:7305,astroblastoma,DOID:3069,astrocytoma
+CL:1000768,kidney connecting tubule epithelial cell,CL:1000615,kidney cortex tubule cell
+UBERON:0011652,dorsal head of rib,UBERON:0002230,head of rib
+UBERON:0013531,retrosplenial region,UBERON:0002619,regional part of cerebral cortex
+HP:0012072,Aciduria,HP:0003110,Abnormality of urine homeostasis
+DOID:727,premenstrual tension,DOID:229,female reproductive system disease
+UBERON:0002034,suprachiasmatic nucleus,UBERON:0007251,preoptic nucleus
+UBERON:0001720,cochlear nucleus,UBERON:0000126,cranial nerve nucleus
+DOID:682,compartment syndrome,DOID:326,ischemia
+HP:0001031,Subcutaneous lipoma,HP:0008069,Neoplasm of the skin
+UBERON:0010577,manual digit 3 phalanx pre-cartilage condensation,UBERON:0015027,manual digit 3 phalanx endochondral element
+UBERON:0003701,calcaneal tendon,UBERON:0000043,tendon
+UBERON:3000804,sulcus articularis medialis,UBERON:0004120,mesoderm-derived structure
+DOID:2568,cervicitis,DOID:2253,cervix disease
+DOID:170,endocrine gland cancer,DOID:0050686,organ system cancer
+HP:0001440,Synostosis involving metatarsal bones,HP:0009140,Synostosis involving bones of the feet
+HP:0008775,Abnormality of the prostate,HP:0000022,Abnormality of male internal genitalia
+DOID:1883,hepatitis C,DOID:934,viral infectious disease
+UBERON:0008311,penile bulb artery,UBERON:0003520,pelvis blood vessel
+DOID:13839,extrapyramidal and movement disease,DOID:481,central nervous system hereditary degenerative disease
+UBERON:0000442,right testicular vein,UBERON:0001144,testicular vein
+UBERON:2000372,interpeduncular nucleus medulla oblongata,UBERON:0007635,nucleus of medulla oblongata
+HP:0009299,Aplasia/Hypoplasia of the middle phalanx of the 4th finger,HP:0009283,Abnormality of the middle phalanx of the 4th finger
+HP:0006990,Myelin-dependent gliosis,HP:0002171,Gliosis
+DOID:11105,fundus albipunctatus,DOID:8501,fundus dystrophy
+UBERON:0010538,paired limb/fin segment,UBERON:0010758,subdivision of organism along appendicular axis
+HP:0100681,Esophageal duplication,HP:0011140,Gastrointestinal duplication
+UBERON:0002658,medial lemniscus of midbrain,UBERON:0003002,medial lemniscus
+DOID:2354,myelophthisic anemia,DOID:0070004,myeloma
+UBERON:0014891,brainstem white matter,UBERON:0003544,brain white matter
+NCBITaxon:42414,Sigmodon,NCBITaxon:40141,Sigmodontinae
+UBERON:0009889,secondary heart field,UBERON:0004120,mesoderm-derived structure
+HP:0004931,Arteriosclerosis of small cerebral arteries,HP:0002634,Arteriosclerosis
+NCBITaxon:62323,funestus subgroup,NCBITaxon:59142,funestus group
+UBERON:0005928,external naris,UBERON:0000003,naris
+UBERON:0004620,lumbar vertebra 4,UBERON:0002414,lumbar vertebra
+UBERON:0007795,ascitic fluid,UBERON:0001268,peritoneal fluid
+UBERON:0005943,hair root sheath matrix,UBERON:0004121,ectoderm-derived structure
+UBERON:2001807,preepiotic fossa,UBERON:0004704,bone fossa
+UBERON:2002007,supraneural 4 bone,UBERON:2000442,supraneural bone
+DOID:0060149,social emotional agnosia,DOID:4090,agnosia
+HP:0000868,Decreased fertility in females,HP:0000144,Decreased fertility
+UBERON:0002508,celiac lymph node,UBERON:0015860,visceral abdominal lymph node
+UBERON:0002486,glottis,UBERON:0000477,anatomical cluster
+HP:0011335,Frontal hirsutism,HP:0000290,Abnormality of the forehead
+DOID:3159,photosensitivity disease,DOID:2723,dermatitis
+UBERON:0013422,infratemporal fossa,UBERON:0004704,bone fossa
+UBERON:0013411,cranial cavity,UBERON:0002553,anatomical cavity
+UBERON:0003599,tail connective tissue,UBERON:0002384,connective tissue
+HP:0012397,Aortic atherosclerosis,HP:0001679,Abnormality of the aorta
+HP:0200049,Upper limb hypertonia,HP:0002817,Abnormality of the upper limb
+HP:0003238,Hyperpepsinogenemia I,HP:0010876,Abnormality of circulating protein level
+UBERON:3010717,diverticulum,UBERON:0004119,endoderm-derived structure
+HP:0009575,Triangular shaped middle phalanx of the 2nd finger,HP:0009850,Triangular shaped middle phalanges of the hand
+HP:0011704,Sick sinus syndrome,HP:0011702,Abnormal electrophysiology of sinoatrial node origin
+DOID:11277,Plummer's disease,DOID:7998,hyperthyroidism
+HP:0001232,Nail bed telangiectasia,HP:0001009,Telangiectasia
+UBERON:3010529,ovisac,UBERON:0002384,connective tissue
+UBERON:0006095,anterior transverse termporal area 41,UBERON:0013529,Brodmann area
+HP:0000198,Absence of Stensen duct,HP:0000197,Abnormality of parotid gland
+UBERON:0001909,habenular commissure,UBERON:0005341,ventral commissure
+UBERON:0002554,regional part of superior colliculus,UBERON:0002966,regional part of midbrain tectum
+UBERON:4200165,basal scute,UBERON:0008201,scute
+HP:0011445,Athetoid cerebral palsy,HP:0002071,Abnormality of extrapyramidal motor function
+UBERON:0001392,flexor hallucis longus,UBERON:0000366,flexor muscle
+DOID:0060000,infective endocarditis,DOID:10314,endocarditis
+UBERON:2002162,ural vertebra,UBERON:0004376,fin bone
+UBERON:0008426,transverse foramen of atlas,UBERON:0000130,transverse foramen
+HP:0100004,Pericardial mesothelioma,HP:0100001,Malignant mesothelioma
+HP:0007265,Absent mesencephalon,HP:0002418,Abnormality of the midbrain
+UBERON:3010167,metatarsal fold,UBERON:3000981,limb external integument structure
+UBERON:0001562,digastric muscle,UBERON:0008571,suprahyoid muscle
+UBERON:0004443,proximal epiphysis of proximal phalanx of manual digit 5,UBERON:0004421,proximal epiphysis of phalanx of manual digit 5
+CL:1000481,transitional myocyte of atrioventricular bundle,CL:0002073,transitional myocyte
+UBERON:2000000,Brachet's cleft,UBERON:0002050,embryonic structure
+UBERON:0003672,dentition,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2000248,magnocellular preoptic nucleus,UBERON:0007251,preoptic nucleus
+UBERON:2002174,octaval nerve motor nucleus,UBERON:0007635,nucleus of medulla oblongata
+HP:0004253,Absent trapezium/absent ossification of the trapezium,HP:0006257,Abnormality of carpal bone ossification
+HP:0000989,Pruritus,HP:0011122,Abnormality of skin physiology
+HP:0007413,Nevus flammeus of the forehead,HP:0001052,Nevus flammeus
+UBERON:0010498,pseudostratified columnar epithelium,UBERON:0000485,simple columnar epithelium
+HP:0003996,Flattened radial head,HP:0003995,Abnormality of the radial head
+UBERON:0004103,alveolar ridge,UBERON:0005913,zone of bone organ
+DOID:381,arthropathy,DOID:3342,bone inflammation disease
+HP:0009511,Stippling of the epiphysis of the distal phalanx of the 2nd finger,HP:0009497,Stippling of the epiphyses of the 2nd finger
+NCBITaxon:203490,Fusobacteriia,NCBITaxon:32066,Fusobacteria
+UBERON:2001456,pectoral fin endoskeletal disc,UBERON:0007390,pectoral appendage cartilage tissue
+HP:0005442,Widely patent coronal suture,HP:0011329,Abnormality of cranial sutures
+HP:0010088,Curved proximal phalanx of the hallux,HP:0010197,Curved middle phalanges of the toes
+CL:0000049,common myeloid progenitor,CL:0002032,hematopoietic oligopotent progenitor cell
+UBERON:0001342,mesovarium,UBERON:0002095,mesentery
+HP:0010350,Curved phalanges of the 2nd toe,HP:0010324,Abnormality of phalanx of the 2nd toe
+UBERON:0010499,pseudostratified ciliated columnar epithelium,UBERON:0010498,pseudostratified columnar epithelium
+UBERON:0011577,flexural organ,UBERON:0004121,ectoderm-derived structure
+HP:0100308,Cerebral cortical hemiatrophy,HP:0002120,Cerebral cortical atrophy
+UBERON:0012318,anterior ethmoidal artery,UBERON:0005193,ethmoidal artery
+UBERON:0011049,uterovesical pouch,UBERON:0004120,mesoderm-derived structure
+CL:0000757,type 5 cone bipolar cell (sensu Mus),CL:0000749,ON-bipolar cell
+NCBITaxon:724,Haemophilus,NCBITaxon:712,Pasteurellaceae
+DOID:8687,skin carcinoma in situ,DOID:8719,in situ carcinoma
+UBERON:0011806,dermis of feather follicle,UBERON:0004120,mesoderm-derived structure
+HP:0000683,Grayish enamel,HP:0011073,Abnormality of dental color
+HP:0001119,Keratoglobus,HP:0100692,Increased corneal curvature
+HP:0000474,Thickened nuchal skin fold,HP:0011425,Fetal ultrasound soft marker
+HP:0009821,Forearm undergrowth,HP:0006503,Aplasia/Hypoplasia involving forearm bones
+UBERON:0001218,middle colic vein,UBERON:0002017,portal vein
+HP:0100886,Abnormality of globe location,HP:0000284,Abnormality of the ocular region
+UBERON:0010858,inter limb-segment region,UBERON:0000475,organism subdivision
+HP:0009386,Fragmentation of the epiphyses of the 5th finger,HP:0010232,Fragmentation of the epiphyses of the phalanges of the hand
+DOID:0050569,Seckel syndrome,DOID:0050737,autosomal recessive disease
+UBERON:0000159,anal canal,UBERON:0004121,ectoderm-derived structure
+UBERON:2001102,immature anterior otolith,UBERON:2000139,immature otolith
+HP:0004180,Short distal phalanx of the 3rd finger,HP:0009882,Short distal phalanx of finger
+UBERON:0003882,CA2 field of hippocampus,UBERON:0003876,subdivision of hippocampus
+HP:0000053,Macroorchidism,HP:0000035,Abnormality of the testis
+UBERON:3000683,sinus nervi hypoglossi,UBERON:3000681,hyoid apparatus opening
+UBERON:3000294,median prenasal process,UBERON:0004120,mesoderm-derived structure
+UBERON:0009046,inferior external pudendal vein,UBERON:0009029,pudendal vein
+UBERON:0014705,median lingual swelling epithelium,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100942,Sclerosis of the distal phalanx of the 5th toe,HP:0100929,Sclerosis of the phalanges of the 5th toe
+DOID:9809,hypersensitivity vasculitis,DOID:1557,hypersensitivity reaction type III disease
+DOID:2704,malignant giant cell tumor of the tendon sheath,DOID:2706,synovium cancer
+NCBITaxon:206351,Neisseriales,NCBITaxon:28216,Betaproteobacteria
+DOID:0050682,Athabaskan brainstem dysgenesis syndrome,DOID:0050737,autosomal recessive disease
+UBERON:0001870,frontal cortex,UBERON:0004121,ectoderm-derived structure
+HP:0012654,Abnormal CSF dopamine level,HP:0002921,Abnormality of the cerebrospinal fluid
+HP:0003288,Mitochondrial propionyl-CoA carboxylase (PCC) defect,HP:0003287,Abnormality of mitochondrial metabolism
+DOID:0050885,IMAGe syndrome,DOID:225,syndrome
+UBERON:0004538,left kidney,UBERON:0002113,kidney
+DOID:14089,root caries,DOID:216,dental caries
+HP:0009554,Projection of scalp hair onto lateral cheek,HP:0009553,Abnormality of the hairline
+HP:0004510,Pancreatic islet-cell hypertrophy,HP:0006476,Abnormality of the pancreatic islet cells
+HP:0011319,Bilambdoid synostosis,HP:0004443,Lambdoidal craniosynostosis
+HP:0008237,Hypothalamic hypothyroidism,HP:0012285,Abnormal hypothalamus physiology
+CL:0000014,germ line stem cell,CL:0000034,stem cell
+UBERON:0013119,haemal node,UBERON:0004177,hemopoietic organ
+UBERON:0005048,mucosa of uterine tube,UBERON:0005156,reproductive structure
+CL:0000658,cuticle secreting cell,CL:0000327,extracellular matrix secreting cell
+UBERON:0008853,parietal yolk sac,UBERON:0001040,yolk sac
+HP:0008089,Abnormality of the fifth metatarsal bone,HP:0001832,Abnormality of the metatarsal bones
+UBERON:2000451,upper oral valve,UBERON:0000479,tissue
+UBERON:0004061,neural tube mantle layer,UBERON:0004121,ectoderm-derived structure
+DOID:2768,transient tic disorder,DOID:2769,tic disorder
+UBERON:0014751,P1 area of pallium (Myxiniformes),UBERON:0002791,regional part of telencephalon
+HP:0009657,Triangular shaped phalanges of the thumb,HP:0009774,Triangular shaped phalanges of the hand
+HP:0012433,Abnormal social behavior,HP:0100851,Abnormal emotion/affect behavior
+DOID:4521,cervix endometrial stromal tumor,DOID:4362,cervical cancer
+UBERON:0013174,sigmoid process of tympanic bone,UBERON:0004530,bony projection
+HP:0010200,Symphalangism affecting the middle phalanges of the toes,HP:0010179,Symphalangism affecting the phalanges of the toes
+HP:0007874,Almond-shaped palpebral fissure,HP:0200005,Abnormal shape of the palpebral fissure
+DOID:3111,cystadenocarcinoma,DOID:299,adenocarcinoma
+HP:0004223,Ivory epiphysis of the distal phalanx of the 5th finger,HP:0010252,Ivory epiphyses of the distal phalanges of the hand
+UBERON:0000962,nerve of cervical vertebra,UBERON:0001780,spinal nerve
+CL:0002178,epithelial cell of stomach,CL:0002251,epithelial cell of alimentary canal
+HP:0100415,Complete duplication of the proximal phalanx of the 5th toe,HP:0100406,Duplication of the proximal phalanx of the 5th toe
+DOID:0050562,West syndrome,DOID:0050703,infancy electroclinical syndrome
+UBERON:2000962,sclerotome somite 7,UBERON:0003089,sclerotome
+HP:0001920,Renal artery stenosis,HP:0008776,Abnormality of the renal artery
+HP:0100480,Proximal/middle symphalangism of 3rd toe,HP:0100473,Symphalangism affecting the proximal phalanx of the 3rd toe
+UBERON:0005707,upper jaw incisor odontogenic papilla,UBERON:0003323,mesenchyme of upper jaw
+UBERON:0003549,brain pia mater,UBERON:0002361,pia mater
+NCBITaxon:622,Shigella dysenteriae,NCBITaxon:620,Shigella
+UBERON:0013741,base of crypt of lieberkuhn of large intestine,UBERON:0013739,base of crypt of lieberkuhn
+CL:0002136,type II cell of adrenal cortex,CL:0000460,glucocorticoid secreting cell
+DOID:3317,hepatic angiomyolipoma,DOID:916,liver neoplasm
+UBERON:2001293,posterior kidney,UBERON:0004120,mesoderm-derived structure
+UBERON:0012363,thyroid follicle epithelium,UBERON:0000484,simple cuboidal epithelium
+CL:0002484,epithelial melanocyte,CL:0000148,melanocyte
+UBERON:0000123,endoneurium,UBERON:0002384,connective tissue
+UBERON:0000024,forelimb wing,UBERON:0002102,forelimb
+UBERON:2001277,anterior chamber swim bladder,UBERON:0000481,multi-tissue structure
+UBERON:0004067,lateral nasal prominence,UBERON:0009292,embryonic nasal process
+DOID:0050856,oppositional defiant disorder,DOID:0060038,specific developmental disorder
+HP:0006200,Widened distal phalanges,HP:0006009,Broad phalanx
+UBERON:0009844,urogenital sinus lumen,UBERON:0000464,anatomical space
+UBERON:0002750,medial longitudinal fasciculus of medulla,UBERON:0002309,medial longitudinal fasciculus
+HP:0100912,Sclerosis of the distal phalanx of the thumb,HP:0100922,Sclerosis of the phalanges of the thumb
+HP:0009533,Stippling of the epiphysis of the proximal phalanx of the 2nd finger,HP:0010277,Stippling of the epiphyses of the proximal phalanges of the hand
+UBERON:0013219,parotoid gland,UBERON:0002530,gland
+UBERON:0000929,pharyngeal branch of vagus nerve,UBERON:0001021,nerve
+HP:0007519,Lack of subcutaneous fatty tissue,HP:0001002,Decreased subcutaneous fat
+UBERON:3010743,M. flexor antibrachii lateralis superficialis,UBERON:0010891,pectoral complex muscle
+UBERON:0011822,dense irregular connective tissue,UBERON:0011821,irregular connective tissue
+UBERON:0011465,longissimus atlantis muscle,UBERON:0000392,longissimus muscle
+HP:0012430,Cerebral white matter hypoplasia,HP:0012429,Aplasia/Hypoplasia of the cerebral white matter
+HP:0008277,Abnormality of zinc homeostasis,HP:0011030,Abnormality of transition element cation homeostasis
+UBERON:0001635,superior cerebellar artery,UBERON:0004573,systemic artery
+UBERON:0000116,lung saccule,UBERON:0004119,endoderm-derived structure
+UBERON:0001080,inferior articular process of vertebra,UBERON:0006062,articular process of vertebra
+CL:0002670,type 1 otic fibrocyte,CL:0002665,otic fibrocyte
+UBERON:0003893,capsule,UBERON:0000158,membranous layer
+HP:0004356,Abnormality of lysosomal metabolism,HP:0011017,Abnormality of cell physiology
+HP:0007513,Generalized hypopigmentation,HP:0001010,Hypopigmentation of the skin
+UBERON:0000313,tibial cartilage tissue,UBERON:0007391,pelvic appendage cartilage tissue
+UBERON:0014608,inferior occipital gyrus,UBERON:0014640,occipital gyrus
+UBERON:0006082,fundus of urinary bladder,UBERON:0006554,urinary system structure
+UBERON:0005062,neural fold,UBERON:0005291,embryonic tissue
+CL:1000424,chromaffin cell of paraaortic body,CL:0000166,chromaffin cell
+HP:0010061,Curved phalanges of the hallux,HP:0010057,Abnormality of the phalanges of the hallux
+HP:0012394,Iodine contrast allergy,HP:0012393,Allergy
+HP:0009776,Adactyly,HP:0010760,Absent toe
+UBERON:0004432,proximal epiphysis of distal phalanx of manual digit 2,UBERON:0011979,epiphysis of distal phalanx of manus
+UBERON:2000934,myotome somite 8,UBERON:0003082,myotome
+HP:0003548,Subsarcolemmal accumulations of abnormally shaped mitochondria,HP:0003800,Muscle abnormality related to mitochondrial dysfunction
+UBERON:0003859,forelimb mesenchyme,UBERON:0009749,limb mesenchyme
+HP:0009525,Bracket epiphysis of the proximal phalanx of the 2nd finger,HP:0010269,Bracket epiphyses of the proximal phalanges of the hand
+UBERON:0010753,lymph node secondary follicle,UBERON:0010748,lymph node follicle
+UBERON:0003890,Mullerian duct,UBERON:0000025,tube
+UBERON:2000201,dorsal transverse,UBERON:0000933,pharyngeal muscle
+HP:0004857,Hyperchromic macrocytic anemia,HP:0001972,Macrocytic anemia
+CL:0010006,cardiac blood vessel endothelial cell,CL:0000071,blood vessel endothelial cell
+HP:0011254,Type II cryptotia,HP:0011252,Cryptotia
+HP:0012590,Abnormal urine output,HP:0011036,Abnormality of renal excretion
+HP:0010493,Long metacarpals,HP:0005916,Abnormal metacarpal morphology
+UBERON:0003318,mesenchyme of elbow,UBERON:0003859,forelimb mesenchyme
+UBERON:2001894,hypobranchial 1 element,UBERON:2001893,hypobranchial element
+UBERON:0006863,proximal metaphysis of femur,UBERON:0004378,proximal metaphysis
+HP:0002762,Multiple exostoses,HP:0100777,Exostoses
+UBERON:0012055,left lung lower lobe bronchiole,UBERON:0003539,left lung bronchiole
+UBERON:0001120,left lobe of thyroid gland,UBERON:0001118,lobe of thyroid gland
+UBERON:2001144,tooth 2V,UBERON:2000694,ceratobranchial 5 tooth
+DOID:8442,paralytic ileus,DOID:8437,intestinal obstruction
+UBERON:0003822,forelimb stylopod,UBERON:0008785,upper limb segment
+DOID:5182,blastema predominant kidney Wilms' tumor,DOID:2154,nephroblastoma
+NCBITaxon:1760,Actinobacteria <class>,NCBITaxon:201174,Actinobacteria <phylum>
+UBERON:0000931,proctodeum,UBERON:0002050,embryonic structure
+HP:0007815,Abnormal distribution of retinal arterioles and venules,HP:0008046,Abnormality of the retinal vasculature
+UBERON:0003412,pelvic appendage bud mesenchyme,UBERON:0010329,paired limb/fin bud mesenchyme
+UBERON:0005674,right lung cranial lobe endothelium,UBERON:0005639,right lung cranial lobe epithelium
+CL:0000918,Tc2 cell,CL:0001052,"CD8-positive, CXCR3-negative, CCR6-negative, alpha-beta T cell"
+UBERON:3010262,capitulum of radio-ulna,UBERON:0004120,mesoderm-derived structure
+UBERON:0001454,distal tarsal bone 3,UBERON:0015108,distal tarsal bone 3 endochondral element
+UBERON:0000220,atlanto-occipital joint,UBERON:0015212,lateral structure
+HP:0000917,Superior pectus carinatum,HP:0000768,Pectus carinatum
+HP:0002732,Lymph node hypoplasia,HP:0002733,Abnormality of the lymph nodes
+HP:0011395,Aplasia/Hypoplasia of the cochlea,HP:0000375,Abnormality of cochlea
+DOID:7733,signet ring cell intrahepatic cholangiocarcinoma,DOID:4928,intrahepatic cholangiocarcinoma
+HP:0006996,Dysgenesis of corpus callosum,HP:0001273,Abnormality of the corpus callosum
+HP:0006107,Fingerpad telangiectases,HP:0100585,Teleangiectasia of the skin
+UBERON:3010711,levator mandibulae externus superficialis,UBERON:0011648,jaw muscle
+HP:0009664,Absent epiphysis of the proximal phalanx of the thumb,HP:0010257,Absent epiphyses of the middle phalanges of the hand
+HP:0003623,Neonatal onset,HP:0011007,Age of onset
+UBERON:0001401,longissimus thoracis muscle,UBERON:0000392,longissimus muscle
+HP:0010297,Bifid tongue,HP:0000157,Abnormality of the tongue
+UBERON:2000766,granular layer valvula cerebelli,UBERON:0004121,ectoderm-derived structure
+UBERON:0011173,anterior division of bed nuclei of stria terminalis,UBERON:0002791,regional part of telencephalon
+UBERON:0004690,pancreaticoduodenal vein,UBERON:0001214,pancreatic tributary of splenic vein
+HP:0000356,Abnormality of the outer ear,HP:0000598,Abnormality of the ear
+HP:0001344,Absent speech,HP:0000750,Delayed speech and language development
+DOID:0050690,brachyolmia,DOID:2256,osteochondrodysplasia
+HP:0004699,Osteoporotic metatarsal,HP:0001832,Abnormality of the metatarsal bones
+UBERON:2000961,sclerotome somite 4,UBERON:0003089,sclerotome
+UBERON:0007633,nucleus of trapezoid body,UBERON:0007247,superior olivary nucleus
+UBERON:0009523,mesenchyme of handplate,UBERON:0010377,mesenchyme from somatopleure
+DOID:11555,Fuchs' endothelial dystrophy,DOID:2566,corneal dystrophy
+HP:0006059,Cone-shaped metacarpal epiphyses,HP:0005913,Abnormality of metacarpal epiphyses
+UBERON:0003259,endoderm of midgut,UBERON:0000925,endoderm
+UBERON:0002691,ventral tegmental area,UBERON:0002635,regional part of midbrain tegmentum
+DOID:10534,stomach cancer,DOID:3119,gastrointestinal system cancer
+UBERON:3000954,hypobranchial I,UBERON:0010314,structure with developmental contribution from neural crest
+CL:1000692,kidney interstitial fibroblast,CL:0000057,fibroblast
+HP:0002847,Impaired memory B-cell generation,HP:0005372,Abnormality of B cell physiology
+CL:0000451,dendritic cell,CL:0000738,leukocyte
+DOID:2071,vulvar squamous papilloma,DOID:2072,vulvar squamous tumor
+UBERON:0003101,male organism,UBERON:0000468,multi-cellular organism
+HP:0000598,Abnormality of the ear,HP:0000118,Phenotypic abnormality
+UBERON:2000392,median tuberal portion,UBERON:0003048,regional part of hypothalamus
+HP:0003606,Absent urinary urothione,HP:0003110,Abnormality of urine homeostasis
+UBERON:0001527,abductor pollicis longus,UBERON:0011534,abductor pollicis muscle
+UBERON:0005472,right vitelline vein,UBERON:0015212,lateral structure
+UBERON:2001803,quadrate-metapterygoid joint,UBERON:0000982,skeletal joint
+HP:0100593,Calcification of cartilage,HP:0010766,Ectopic calcification
+UBERON:0004319,distal phalanx of pedal digit 5,UBERON:0003863,pedal digit 5 phalanx
+UBERON:0002428,limb bone,UBERON:0015061,limb endochondral element
+HP:0008398,Hypoplastic fifth fingernail,HP:0011937,Hypoplastic fifth toenail
+UBERON:0003704,intrahepatic bile duct,UBERON:0002394,bile duct
+HP:0009442,Curved phalanges of the 3rd finger,HP:0009770,Curved phalanges of the hand
+UBERON:2000730,somite 23,UBERON:0002329,somite
+HP:0007511,Mottled pigmentation of photoexposed areas,HP:0001070,Mottled pigmentation
+HP:0012124,Intermediate uveitis,HP:0000554,Uveitis
+HP:0012714,Severe hearing impairment,HP:0000365,Hearing impairment
+UBERON:0006120,superior colliculus superficial gray layer,UBERON:0006791,superficial layer of superior colliculus
+CL:0011104,interplexiform cell,CL:0000099,interneuron
+HP:0010750,Dermatochalasis,HP:0000492,Abnormality of the eyelid
+HP:0007833,Anterior chamber synechiae,HP:0000593,Abnormality of the anterior chamber
+CL:0002624,paneth cell of the appendix,CL:1001585,appendix glandular cell
+UBERON:0001807,paravertebral ganglion,UBERON:0007134,trunk ganglion
+CL:0000172,somatostatin secreting cell,CL:0000167,peptide hormone secreting cell
+UBERON:0002744,hilum of dentate nucleus,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0013675,toxactinium,UBERON:0014403,male anatomical structure
+UBERON:0010417,lymph node T cell domain,UBERON:0010393,T cell domain
+HP:0007379,Neoplasm of the genitourinary tract,HP:0011793,Neoplasm by anatomical site
+UBERON:0003832,esophagus muscle,UBERON:0013765,digestive system organ
+HP:0002077,Migraine with aura,HP:0002076,Migraine
+UBERON:3000209,frontoparietal fontanelle,UBERON:3000051,braincase and otic capsule opening
+HP:0004780,Elbow hypertrichosis,HP:0000998,Hypertrichosis
+UBERON:2001759,dorsal fin lepidotrichium 6,UBERON:4000177,dorsal fin lepidotrichium
+DOID:4419,benign deep fibrous histiocytoma,DOID:0060092,immune system organ benign neoplasm
+UBERON:0010707,appendage girdle complex,UBERON:0015212,lateral structure
+HP:0002627,Right aortic arch with mirror image branching,HP:0012020,Right aortic arch
+HP:0009606,Complete duplication of distal phalanx of the thumb,HP:0010001,Complete duplication of the distal phalanges of the hand
+DOID:8043,chest wall parachordoma,DOID:2647,parachordoma
+HP:0002585,Abnormality of the peritoneum,HP:0002012,Abnormality of the abdominal organs
+DOID:10122,hyperpigmentation of eyelid,DOID:10120,eyelid degenerative disease
+UBERON:0013248,paradidymis,UBERON:0003914,epithelial tube
+HP:0000058,Abnormality of the labia,HP:0000055,Abnormality of female external genitalia
+HP:0011961,Non-obstructive azoospermia,HP:0000027,Azoospermia
+UBERON:0004089,midface,UBERON:0000061,anatomical structure
+DOID:10445,perforated corneal ulcer,DOID:8463,corneal ulcer
+CL:0002477,adipose macrophage,CL:0000864,tissue-resident macrophage
+UBERON:0002296,dorsal mesentery,UBERON:0002050,embryonic structure
+UBERON:3000714,perichordal,UBERON:0001075,vertebral centrum
+HP:0005625,Osteoporosis of vertebrae,HP:0003468,Abnormality of the vertebrae
+HP:0011838,Sclerodactyly,HP:0001072,Thickened skin
+UBERON:0005114,metanephric ascending thin limb,UBERON:0004193,loop of Henle ascending limb thin segment
+HP:0011594,Right aortic arch with retroesophageal diverticulum of Kommerell,HP:0012020,Right aortic arch
+NCBITaxon:526525,Erysipelotrichales,NCBITaxon:526524,Erysipelotrichi
+UBERON:0006373,perihilar interstitium,UBERON:0006554,urinary system structure
+UBERON:0006170,mesonephric capsule,UBERON:0002015,kidney capsule
+HP:0008301,Dermatan sulfate excretion in urine,HP:0008155,Mucopolysacchariduria
+HP:0002963,Abnormal delayed hypersensitivity skin test,HP:0011840,Abnormality of T cell physiology
+HP:0000026,Male hypogonadism,HP:0000025,Functional abnormality of male internal genitalia
+UBERON:0004441,proximal epiphysis of proximal phalanx of manual digit 3,UBERON:0004419,proximal epiphysis of phalanx of manual digit 3
+UBERON:2000156,somite 20,UBERON:0002329,somite
+DOID:583,hemolytic anemia,DOID:720,normocytic anemia
+UBERON:2002038,basioccipital-exoccipital joint,UBERON:0000982,skeletal joint
+UBERON:0008777,hypaxial musclulature,UBERON:0004479,musculature of trunk
+HP:0009225,Aplasia of the proximal phalanx of the 5th finger,HP:0009238,Aplasia of the 5th finger
+DOID:7049,basaloid squamous cell skin carcinoma,DOID:3151,skin squamous cell carcinoma
+UBERON:0013621,lower secondary molar tooth,UBERON:0003667,lower jaw molar
+UBERON:2000986,hypaxial region somite 27,UBERON:0003895,hypaxial myotome region
+HP:0000118,Phenotypic abnormality,HP:0000001,All
+HP:0012222,Arachnoid hemangiomatosis,HP:0001028,Hemangioma
+HP:0003856,Upper limb metaphyseal widening,HP:0009809,Abnormality of upper limb metaphysis
+UBERON:0004437,proximal epiphysis of middle phalanx of manual digit 3,UBERON:0011978,epiphysis of middle phalanx of manus
+HP:0002445,Tetraplegia,HP:0010549,Paralysis due to lesions of the principle motor tracts
+CL:1001287,outer medulla vasa recta descending limb cell,CL:1001127,outer renal medulla vasa recta cell
+UBERON:0002087,atrioventricular canal,UBERON:0002050,embryonic structure
+HP:0100011,Scleral schwannoma,HP:0100008,Schwannoma
+DOID:6379,diffuse meningeal melanocytosis,DOID:4955,central nervous system melanocytic neoplasm
+UBERON:0013583,metapodium bone 3,UBERON:0003821,metapodium bone
+UBERON:0010567,manual digit 3 metacarpus pre-cartilage condensation,UBERON:0010698,manual digit metacarpus pre-cartilage condensation
+UBERON:2000475,paraventricular organ,UBERON:0006569,diencephalic nucleus
+HP:0011355,Localized skin lesion,HP:0000951,Abnormality of the skin
+HP:0001691,Muscular subvalvular aortic stenosis,HP:0001682,Subaortic stenosis
+HP:0003915,Lytic defects of the humeral metaphsis,HP:0003851,Lytic defects in metaphyses of the upper limbs
+CL:0000998,CD8_alpha-negative CD11b-negative dendritic cell,CL:0000990,conventional dendritic cell
+HP:0009450,Broad proximal phalanx of the 3rd finger,HP:0009440,Broad phalanges of the 3rd finger
+UBERON:3010669,trunk maxillary-mandibularis,UBERON:0002003,peripheral nerve
+HP:0007990,Hypoplastic iris stroma,HP:0007676,Hypoplasia of the iris
+UBERON:0001390,sural artery,UBERON:0001637,artery
+UBERON:0010332,epithelium of handplate,UBERON:0000490,unilaminar epithelium
+UBERON:0008202,bone of hip region,UBERON:0001474,bone element
+HP:0011357,Abnormality of hair density,HP:0001595,Abnormality of the hair
+DOID:0050854,Muckle-Wells syndrome,DOID:0050736,autosomal dominant disease
+UBERON:0000941,cranial nerve II,UBERON:0001785,cranial nerve
+UBERON:0015010,sacral vertebra endochondral element,UBERON:0005174,dorsal region organ
+HP:0009187,Bracket epiphysis of the distal phalanx of the 5th finger,HP:0010247,Bracket epiphyses of the distal phalanges of the hand
+HP:0002613,Biliary cirrhosis,HP:0012440,Abnormal biliary tract morphology
+UBERON:0011215,cell part cluster of neuraxis,UBERON:0005162,multi cell component structure
+CL:0002096,internodal tract myocyte,CL:0002086,specialized cardiac myocyte
+HP:0003538,Increased serum iduronate sulfatase activity,HP:0004355,Abnormality of proteoglycan metabolism
+DOID:5267,anus leiomyosarcoma,DOID:4067,anus sarcoma
+CL:0002468,Gr1-low myeloid suppressor cell,CL:0000889,myeloid suppressor cell
+UBERON:0001729,oropharynx,UBERON:0004119,endoderm-derived structure
+UBERON:0011850,acinus of salivary gland,UBERON:0011858,acinus of exocrine gland
+UBERON:0001374,biceps femoris,UBERON:0002463,hamstring muscle
+UBERON:2105377,dorsal fin distal radial element 6,UBERON:2100936,dorsal fin distal radial element
+UBERON:3010559,retroarticular process of the palatoquadrate,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0015109,distal tarsal bone 3 cartilage,UBERON:0015064,autopod cartilage
+CL:0002671,endothelial stalk cell,CL:0000071,blood vessel endothelial cell
+UBERON:0002919,anterior parolfactory sulcus,UBERON:0008334,subarachnoid sulcus
+HP:0010025,Triangular epiphysis of the 1st metacarpal,HP:0010014,Abnormality of the epiphysis of the 1st metacarpal
+UBERON:0013506,cervical vertebra pre-cartilage condensation,UBERON:0015007,cervical vertebra endochondral element
+HP:0010649,Flat nasal alae,HP:0000429,Abnormality of the nasal alae
+DOID:0050757,deafness dystonia syndrome,DOID:700,mitochondrial metabolism disease
+CL:0000683,ependymoglial cell,CL:0000127,astrocyte
+UBERON:3000111,crista dentalis of maxilla,UBERON:0004120,mesoderm-derived structure
+UBERON:3000388,parasphenoid tooth,UBERON:0001091,calcareous tooth
+UBERON:0006594,chorda gubernaculum,UBERON:0014403,male anatomical structure
+HP:0009581,Broad proximal phalanx of the 2nd finger,HP:0009547,Broad phalanges of the 2nd finger
+HP:0012611,Increased urinary urate,HP:0004369,Decreased purine levels
+DOID:9986,orbit lymphoma,DOID:4143,orbital cancer
+HP:0004005,Large radial epiphyses,HP:0010580,Enlarged epiphyses
+HP:0009858,Triangular shaped proximal phalanges of the hand,HP:0009774,Triangular shaped phalanges of the hand
+HP:0100250,Meningeal calcification,HP:0010651,Abnormality of the meninges
+UBERON:0001878,septofimbrial nucleus,UBERON:0009663,telencephalic nucleus
+HP:0000643,Blepharospasm,HP:0000492,Abnormality of the eyelid
+UBERON:0013717,superficial inguinal ring,UBERON:0006674,inguinal ring
+DOID:3814,extraskeletal chondroma,DOID:0060123,connective tissue benign neoplasm
+HP:0009461,Short 3rd finger,HP:0009381,Short finger
+HP:0009718,Subependymal giant-cell astrocytoma,HP:0009592,Astrocytoma
+DOID:5890,malignant adult ependymoma,DOID:5074,malignant ependymoma
+UBERON:3010205,postminimus,UBERON:0015064,autopod cartilage
+UBERON:2001431,primitive olfactory epithelium,UBERON:0010371,ecto-epithelium
+DOID:7230,postgerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma,DOID:6354,CLL/SLL
+CL:0000669,pericyte cell,CL:0000183,contractile cell
+UBERON:0011158,primary subdivision of skull,UBERON:0000075,subdivision of skeletal system
+HP:0100040,Broad 2nd toe,HP:0001837,Broad toe
+HP:0011003,Severe Myopia,HP:0000545,Myopia
+DOID:12211,filarial elephantiasis,DOID:1080,filariasis
+CL:1000291,myocyte of posterior internodal tract,CL:0002096,internodal tract myocyte
+UBERON:0002527,pancreatic lymph node,UBERON:0002507,abdominal lymph node
+DOID:4885,Colorado tick fever,DOID:934,viral infectious disease
+UBERON:0010090,future falx cerebri,UBERON:0005423,developing anatomical structure
+UBERON:0012290,fused carpals 2 and 3,UBERON:0001481,distal carpal bone
+HP:0005107,Abnormality of the sacrum,HP:0000925,Abnormality of the vertebral column
+UBERON:0013179,posterior dorsal bursa,UBERON:0013177,dorsal bursa
+HP:0010408,Osteolytic defects of the middle phalanx of the 2nd toe,HP:0010357,Abnormality of the middle phalanx of the 2nd toe
+NCBITaxon:178830,Bornaviridae,NCBITaxon:11157,Mononegavirales
+UBERON:0003044,uncinate fasciculus,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005721,pronephric mesoderm,UBERON:0004120,mesoderm-derived structure
+UBERON:2001041,sclerotome somite 21,UBERON:0003089,sclerotome
+HP:0001871,Abnormality of  blood and blood-forming tissues,HP:0000118,Phenotypic abnormality
+UBERON:0002894,olfactory cortex,UBERON:0002791,regional part of telencephalon
+UBERON:0009040,deep circumflex iliac artery,UBERON:0004573,systemic artery
+CL:0002458,langerin-positive dermal dendritic cell,CL:0001006,dermal dendritic cell
+UBERON:0001028,diaphysis of radius,UBERON:0004120,mesoderm-derived structure
+UBERON:0004324,middle phalanx of pedal digit 2,UBERON:0003641,pedal digit 2 phalanx
+UBERON:0003142,prepupa,UBERON:0000468,multi-cellular organism
+HP:0002901,Hypocalcemia,HP:0004363,Abnormality of calcium homeostasis
+CL:1001123,kidney outer medulla peritubular capillary cell,CL:1001033,peritubular capillary endothelial cell
+NCBITaxon:785,Rickettsia typhi,NCBITaxon:114292,typhus group
+UBERON:0007819,minor alar cartilage,UBERON:0001823,nasal cartilage
+DOID:12451,sulfhemoglobinemia,DOID:620,blood protein disease
+CL:0000175,luteal cell,CL:0002132,stromal cell of ovary
+UBERON:0003701,calcaneal tendon,UBERON:0004270,lower leg connective tissue
+HP:0008804,Broad femoral head,HP:0003368,Abnormality of the femoral head
+DOID:2745,narcissistic personality disorder,DOID:1510,personality disorder
+HP:0010092,Triangular shaped proximal phalanx of the hallux,HP:0010201,Triangular shaped middle phalanges of the toes
+UBERON:2002058,Weberian complex centrum,UBERON:0001075,vertebral centrum
+HP:0001010,Hypopigmentation of the skin,HP:0001000,Abnormality of skin pigmentation
+UBERON:0004649,sphenoid bone pterygoid process,UBERON:0004120,mesoderm-derived structure
+DOID:5699,kidney liposarcoma,DOID:3382,liposarcoma
+UBERON:0004539,right kidney,UBERON:0002113,kidney
+HP:0002148,Hypophosphatemia,HP:0100529,Abnormality of phosphate homeostasis
+UBERON:0005569,rhombomere 2,UBERON:0001892,rhombomere
+UBERON:2002096,bony plate series,UBERON:0000477,anatomical cluster
+UBERON:0005389,transparent eye structure,UBERON:0000064,organ part
+HP:0012016,EEG with occipital focal spikes,HP:0011193,EEG with focal spikes
+UBERON:2001242,ceratobranchial 2 bone,UBERON:2000488,ceratobranchial bone
+UBERON:0002350,conducting system of heart,UBERON:0004493,cardiac muscle tissue of myocardium
+DOID:14075,geniculate ganglionitis,DOID:1756,facial nerve disease
+HP:0009711,Retinal hemangioblastoma,HP:0001028,Hemangioma
+CL:0002465,CD11b-positive dendritic cell,CL:0000990,conventional dendritic cell
+UBERON:0004773,superior eyelid tarsus,UBERON:0004772,eyelid tarsus
+UBERON:0010566,manual digit 2 metacarpus pre-cartilage condensation,UBERON:0010698,manual digit metacarpus pre-cartilage condensation
+HP:0002494,Abnormal rapid eye movement (REM) sleep,HP:0002360,Sleep disturbance
+HP:0007667,Cystic retinal degeneration,HP:0000546,Retinal degeneration
+NCBITaxon:136,Spirochaetales,NCBITaxon:203692,Spirochaetia
+UBERON:4200107,obturator process of ischium,UBERON:4100000,skeletal element projection
+UBERON:0003512,lung blood vessel,UBERON:0003834,thoracic segment blood vessel
+UBERON:0002819,apex of cochlea,UBERON:0000477,anatomical cluster
+UBERON:2000731,somite 27,UBERON:0002329,somite
+CL:0000757,type 5 cone bipolar cell (sensu Mus),CL:0000752,cone retinal bipolar cell
+CL:0000182,hepatocyte,CL:0000181,metabolising cell
+HP:0002361,Psychomotor deterioration,HP:0001268,Mental deterioration
+HP:0009174,Abnormality of the epiphyses of the 4th finger,HP:0004188,Abnormality of the 4th finger
+UBERON:0012287,Rathkes pouch epithelium,UBERON:0004906,ectodermal part of digestive tract
+UBERON:0013526,otocyst lumen,UBERON:0007473,lumen of epithelial sac
+UBERON:0003067,dorsolateral placode,UBERON:0009955,neurogenic placode
+UBERON:0007490,keratin-based acellular structure,UBERON:0000476,acellular anatomical structure
+DOID:1789,benign peritoneal mesothelioma,DOID:0060117,peritoneal benign neoplasm
+UBERON:0005500,rhombomere floor plate,UBERON:0000073,regional part of nervous system
+HP:0008670,Partial vaginal septum,HP:0001153,Septate vagina
+UBERON:0003959,rete testis,UBERON:0002050,embryonic structure
+UBERON:0000485,simple columnar epithelium,UBERON:0012274,columnar epithelium
+DOID:11488,idiopathic peripheral autonomic neuropathy,DOID:11465,autonomic nervous system disease
+CL:0002359,placental hematopoietic stem cell,CL:0002352,gestational hematopoietic stem cell
+UBERON:0004404,distal epiphysis of humerus,UBERON:0004379,distal epiphysis
+UBERON:0002969,inferior temporal sulcus,UBERON:0003022,cerebral cortex lobe
+UBERON:2000694,ceratobranchial 5 tooth,UBERON:0001091,calcareous tooth
+HP:0010202,Duplication of middle phalanx of toe,HP:0010183,Abnormality of the middle phalanges of the toes
+UBERON:0003957,Bruch's membrane,UBERON:0004121,ectoderm-derived structure
+UBERON:0001236,adrenal medulla,UBERON:0010313,neural crest-derived structure
+HP:0000316,Hypertelorism,HP:0100886,Abnormality of globe location
+HP:0007949,Progressive macular scarring,HP:0200056,Macular scarring
+HP:0100266,Synostosis of carpals/tarsals,HP:0100240,Synostosis of joints
+CL:0000566,angioblastic mesenchymal cell,CL:0000134,mesenchymal cell
+DOID:5296,liver leiomyosarcoma,DOID:270,liver sarcoma
+UBERON:0009877,metapodium region,UBERON:0002529,limb segment
+HP:0200008,Intestinal polyposis,HP:0005266,Intestinal polyp
+NCBITaxon:526524,Erysipelotrichi,NCBITaxon:1239,Firmicutes
+UBERON:0006078,subdivision of spinal cord lateral column,UBERON:0006080,segment of white matter of spinal cord
+UBERON:0010699,manual digit metacarpus cartilage element,UBERON:0010686,manual digit phalanx cartilage element
+UBERON:3000916,apophysis proximalis,UBERON:0004120,mesoderm-derived structure
+HP:0100913,Sclerosis of the proximal phalanx of the thumb,HP:0100916,Sclerosis of the middle phalanges of the hand
+UBERON:0010283,oblique pericardial sinus,UBERON:0010279,pericardial sinus
+HP:0007530,Punctate palmoplantar hyperkeratosis,HP:0000972,Palmoplantar hyperkeratosis
+UBERON:0006209,basioccipital cartilage element,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002005,enteric nervous system,UBERON:0010313,neural crest-derived structure
+DOID:2839,erythropoietin polycythemia,DOID:2834,acquired polycythemia
+UBERON:0010233,stroma of thyroid gland,UBERON:0003891,stroma
+HP:0007011,Fourth cranial nerve palsy,HP:0006824,Cranial nerve paralysis
+UBERON:0006312,ocular refractive media,UBERON:0000463,portion of organism substance
+UBERON:0011576,supra-orbital ridge,UBERON:0008001,irregular bone
+HP:0009092,Progressive alveolar ridge hypertropy,HP:0006477,Abnormality of the alveolar ridges
+UBERON:0000461,minor vestibular gland,UBERON:0011826,vestibular gland
+NCBITaxon:6937,Ornithodoros,NCBITaxon:352061,Ornithodorinae
+UBERON:3000955,ceratobranchial I,UBERON:0002513,endochondral bone
+HP:0009054,Scapuloperoneal myopathy,HP:0001465,Amyotrophy involving the shoulder musculature
+UBERON:0014633,substantia gelatinosa of lumbar spinal cord dorsal horn,UBERON:0002181,substantia gelatinosa
+DOID:0050864,non-arteritic anterior ischemic optic neuropathy,DOID:12010,anterior ischemic optic neuropathy
+HP:0001700,Myocardial necrosis,HP:0001637,Abnormality of the myocardium
+UBERON:0007645,future meninx,UBERON:0005423,developing anatomical structure
+HP:0012208,Nonmotile sperm,HP:0012206,Abnormal sperm motility
+UBERON:0010580,pedal digit 1 phalanx pre-cartilage condensation,UBERON:0010585,pedal digit phalanx pre-cartilage condensation
+UBERON:3000820,margo posterior of scapula,UBERON:0000064,organ part
+HP:0011402,Demyelinating sensory neuropathy,HP:0007108,Demyelinating peripheral neuropathy
+CL:0002375,Schwann cell precursor,CL:0000030,glioblast
+HP:0100726,Kaposi's sarcoma,HP:0008069,Neoplasm of the skin
+UBERON:0006616,right external ear,UBERON:0001691,external ear
+HP:0009810,Abnormality of the joints of the upper limbs,HP:0001367,Abnormal joint morphology
+UBERON:0002092,brain dura mater,UBERON:0002363,dura mater
+HP:0009175,Patchy sclerosis of the middle phalanx of the 5th finger,HP:0004219,Abnormality of the middle phalanx of the 5th finger
+DOID:14524,senile degeneration of brain,DOID:1443,cerebral degeneration
+UBERON:0010332,epithelium of handplate,UBERON:0010371,ecto-epithelium
+DOID:5975,renal pelvis papillary tumor,DOID:5977,renal pelvis neoplasm
+HP:0000079,Abnormality of the urinary system,HP:0000119,Abnormality of the genitourinary system
+DOID:0060178,familial hemiplegic migraine,DOID:10024,migraine with aura
+DOID:9460,uterine corpus cancer,DOID:363,uterine cancer
+HP:0011580,Short chordae tendineae of the mitral valve,HP:0001633,Abnormality of the mitral valve
+HP:0003166,Increased urinary taurine,HP:0003355,Aminoaciduria
+HP:0002040,Esophageal varix,HP:0002031,Abnormality of the esophagus
+HP:0001810,Dystrophic toenail,HP:0008404,Nail dystrophy
+UBERON:0001941,lateral habenular nucleus,UBERON:0002757,regional part of epithalamus
+HP:0002661,Painless fractures due to injury,HP:0002659,Increased susceptibility to fractures
+UBERON:0009960,esophagus smooth muscle circular layer,UBERON:0012368,circular muscle layer
+HP:0008090,Ankylosis of feet small joints,HP:0001376,Limitation of joint mobility
+NCBITaxon:5600,Phialophora,NCBITaxon:126331,mitosporic Magnaporthaceae
+HP:0100477,Symphalangism affecting the distal phalanx of the 4th toe,HP:0100471,Symphalangism affecting the middle phalanx of the 4th toe
+DOID:11656,cicatricial pemphigoid,DOID:0060039,autoimmune disease of skin and connective tissue
+HP:0100656,Thoracoabdominal wall defects,HP:0010866,Abdominal wall defect
+HP:0001895,Normochromic anemia,HP:0010972,Anemia of inadequate production
+UBERON:0001901,epithelium of trachea,UBERON:0004815,lower respiratory tract epithelium
+HP:0011514,Abnormality of binocular vision,HP:0000504,Abnormality of vision
+UBERON:0000083,mesonephric tubule,UBERON:0003914,epithelial tube
+CL:0000234,phagocyte,CL:0000325,stuff accumulating cell
+NCBITaxon:715962,dothideomyceta,NCBITaxon:716546,leotiomyceta
+UBERON:0006614,aponeurosis,UBERON:0000158,membranous layer
+UBERON:0002024,internal carotid nerve plexus,UBERON:0001816,autonomic nerve plexus
+HP:0008035,Retinitis pigmentosa inversa,HP:0000510,Retinitis pigmentosa
+CL:0000233,platelet,CL:0000081,blood cell
+UBERON:0004030,aqueous vein,UBERON:0004121,ectoderm-derived structure
+UBERON:0002571,external nucleus of inferior colliculus,UBERON:0003528,brain grey matter
+DOID:5764,lung meningioma,DOID:1324,lung cancer
+UBERON:0001998,sternocostal joint,UBERON:0002001,joint of rib
+UBERON:0002140,parabigeminal nucleus,UBERON:0011214,nucleus of midbrain tectum
+HP:0100379,Aplasia of the distal phalanx of the 4th toe,HP:0100363,Aplasia of the phalanges of the 4th toe
+UBERON:2001788,pelvic splint,UBERON:0010742,bone of pelvic complex
+DOID:960,esophagus leiomyoma,DOID:0050624,gastrointestinal system benign neoplasm
+HP:0011142,Age-related nuclear cataract,HP:0011141,Age-related cataract
+HP:0010339,Flexion contracture of the 4th toe,HP:0010321,Abnormality of the 4th toe
+DOID:1234,gender identity disorder,DOID:150,disease of mental health
+DOID:14308,skin epithelioid hemangioma,DOID:471,skin hemangioma
+HP:0012073,Abnormal urinary acylglycine profile,HP:0003110,Abnormality of urine homeostasis
+UBERON:0002035,medial preoptic nucleus,UBERON:0007251,preoptic nucleus
+UBERON:0005701,lower jaw molar odontogenic papilla,UBERON:0015844,molar dental papilla
+HP:0004332,Abnormality of lymphocytes,HP:0001881,Abnormality of leukocytes
+UBERON:0001778,ciliary epithelium,UBERON:0015808,eye epithelium
+HP:0003031,Ulnar bowing,HP:0002997,Abnormality of the ulna
+CL:0001021,"CD34-positive, CD38-positive common lymphoid progenitor",CL:0000995,"CD34-positive, CD38-positive common myeloid progenitor OR CD34-positive, CD38-positive common lymphoid progenitor"
+HP:0009482,Proximal/middle symphalangism of 3rd finger,HP:0009455,Symphalangism affecting the proximal phalanx of the 3rd finger
+CL:1000742,glomerular mesangial cell,CL:1001318,renal interstitial pericyte
+UBERON:0002303,juxtaglomerular apparatus,UBERON:0006554,urinary system structure
+UBERON:3000805,carina proximalis,UBERON:0004120,mesoderm-derived structure
+UBERON:0015794,left lung lobar bronchus epithelium,UBERON:0002339,epithelium of lobar bronchus
+HP:0100329,Tarsometatarsal synostosis,HP:0001440,Synostosis involving metatarsal bones
+HP:0009214,Absent epiphysis of the middle phalanx of the 4th finger,HP:0009247,Abnormality of the epiphysis of the middle phalanx of the 4th finger
+HP:0000419,Abnormality of the nasal septum,HP:0000366,Abnormality of the nose
+UBERON:2000358,granular layer corpus cerebelli,UBERON:0004121,ectoderm-derived structure
+UBERON:0010188,protuberance,UBERON:0003102,surface structure
+DOID:2127,brain germinoma,DOID:1319,brain cancer
+UBERON:0000428,prostate epithelium,UBERON:0012275,meso-epithelium
+CL:0000064,ciliated cell,CL:0000003,native cell
+UBERON:0006615,venous sinus,UBERON:0003920,venous blood vessel
+HP:0002577,Abnormality of the stomach,HP:0012718,Morphological abnormality of the gastrointestinal tract
+UBERON:0014628,vestibular fissure of the cochlear canal,UBERON:0004120,mesoderm-derived structure
+DOID:8162,thyroid hurthle cell adenoma,DOID:6204,follicular adenoma
+HP:0009598,Symphalangism of the proximal phalanx of the 2nd finger with the 2nd metatcarpal,HP:0009705,Synostosis involving the 2nd metacarpal
+UBERON:0004346,gubernaculum,UBERON:0005156,reproductive structure
+HP:0002922,Increased CSF protein,HP:0002921,Abnormality of the cerebrospinal fluid
+UBERON:0001573,styloglossus,UBERON:0001575,extrinsic muscle of tongue
+UBERON:0001283,bile canaliculus,UBERON:0000464,anatomical space
+UBERON:0009660,adrenal vein,UBERON:0001638,vein
+DOID:1081,mansonelliasis,DOID:1080,filariasis
+HP:0100359,Contractures of the metatarsophalangeal joint of the 5th toe,HP:0010345,Flexion contracture of the 5th toe
+HP:0007712,Choroidal dystrophy,HP:0000610,Abnormality of the choroid
+NCBITaxon:69034,Rotaliidae,NCBITaxon:203397,Rotaliacea
+UBERON:0008449,trochlear notch,UBERON:0004120,mesoderm-derived structure
+HP:0001670,Asymmetric septal hypertrophy,HP:0001639,Hypertrophic cardiomyopathy
+UBERON:0006263,Meckel's cartilage pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+UBERON:0006829,remnant of left anterior vena cava,UBERON:0003498,heart blood vessel
+HP:0009312,Osteolytic defects of the proximal phalanx of the 4th finger,HP:0004195,Osteolytic defects of the phalanges of the 4th finger
+UBERON:0005732,paired limb/fin field,UBERON:0001048,primordium
+UBERON:3010801,ramus lateral,UBERON:3010115,posterior lateral line nerve (PLLN)
+UBERON:0012328,penile spine,UBERON:0014403,male anatomical structure
+HP:0100475,Symphalangism affecting the proximal phalanx of the 5th toe,HP:0010389,Symphalangism affecting the phalanges of the 5th toe
+UBERON:0002509,mesenteric lymph node,UBERON:0015860,visceral abdominal lymph node
+HP:0003707,Calf muscle pseudohypertrophy,HP:0001430,Abnormality of the calf musculature
+DOID:13351,pedophilia,DOID:0060044,paraphilia disorder
+UBERON:0003131,arthropod tibia,UBERON:0000475,organism subdivision
+HP:0008063,Aplasia/Hypoplasia of the lens,HP:0000517,Abnormality of the lens
+UBERON:0005879,pharyngeal cleft,UBERON:0010371,ecto-epithelium
+UBERON:0006721,alisphenoid bone,UBERON:0015212,lateral structure
+UBERON:2001228,pharyngeal arch 3 skeleton,UBERON:0010912,subdivision of skeleton
+DOID:7868,maxillary sinus inverted papilloma,DOID:1358,maxillary sinus neoplasm
+CL:0000398,polygonal cell,CL:0000387,hemocyte (sensu Nematoda and Protostomia)
+CL:1000345,paneth cell of epithelium of crypt of lieberkuhn of small intestine,CL:1000343,paneth cell of epithelium of small intestine
+DOID:14423,glossopharyngeal neuralgia,DOID:3418,glossopharyngeal nerve disease
+UBERON:0003289,meninx of telencephalon,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0014624,basis modioli,UBERON:0005913,zone of bone organ
+HP:0004333,Bone-marrow foam cells,HP:0004311,Abnormality of macrophages
+CL:1001210,outer medulla vasa recta ascending limb cell,CL:1001131,vasa recta ascending limb cell
+UBERON:0003915,endothelial tube,UBERON:0003914,epithelial tube
+UBERON:0003107,Meckel's cartilage,UBERON:0013765,digestive system organ
+HP:0011076,Abnormality of premolar,HP:0000164,Abnormality of the teeth
+HP:0007400,Irregular hyperpigmentation,HP:0000953,Hyperpigmentation of the skin
+HP:0100003,Peritoneal mesothelioma,HP:0100001,Malignant mesothelioma
+HP:0009237,Short 5th finger,HP:0006262,Aplasia/Hypoplasia of the 5th finger
+HP:0009970,Partial duplication of the proximal phalanx of the 3rd finger,HP:0009961,Partial duplication of the phalanges of the 3rd finger
+HP:0003910,Enlarged humeral metaphyses,HP:0003907,Abnormality of the humeral metaphyses
+HP:0200097,Oral mucusa blisters,HP:0008066,Abnormal blistering of the skin
+CL:0000994,immature CD11c-negative plasmacytoid dendritic cell,CL:0000991,CD11c-negative plasmacytoid dendritic cell
+HP:0011970,Cerebral amyloid angiopathy,HP:0011034,Amyloidosis
+HP:0010031,Patchy sclerosis of the 1st metacarpal,HP:0100914,Sclerosis of the 1st metacarpal
+UBERON:3000117,crista subnasalis,UBERON:0010313,neural crest-derived structure
+HP:0010372,Broad phalanges of the 4th toe,HP:0010174,Broad phalanx of the toes
+DOID:11338,tetanus,DOID:0050338,primary bacterial infectious disease
+UBERON:0002149,superior salivatory nucleus,UBERON:0000126,cranial nerve nucleus
+HP:0007819,Presenile cataracts,HP:0000518,Cataract
+UBERON:0001020,nervous system commissure,UBERON:0001018,axon tract
+DOID:10935,dissociative disorder,DOID:150,disease of mental health
+UBERON:0011015,iliac fossa,UBERON:0005913,zone of bone organ
+UBERON:0010886,hindlimb bone pre-cartilage condensation,UBERON:0015022,hindlimb endochondral element
+HP:0007688,Absent rod-and cone-mediated responses on ERG,HP:0008323,Abnormal rod and cone electroretinograms
+CL:0000758,type 6 cone bipolar cell (sensu Mus),CL:0000749,ON-bipolar cell
+DOID:0060217,Cogan-Reese syndrome,DOID:5614,eye disease
+HP:0005328,Progeroid facial appearance,HP:0007495,Prematurely aged appearance
+DOID:12129,bulimia nervosa,DOID:8670,eating disorder
+UBERON:0001679,ethmoid bone,UBERON:0011164,neurocranium bone
+UBERON:4300092,mesocoracoid element,UBERON:0010363,endochondral element
+UBERON:3010624,subarticular sesamoid,UBERON:0001479,sesamoid bone
+HP:0012069,Keratan sulfate excretion in urine,HP:0008155,Mucopolysacchariduria
+UBERON:0008427,transverse foramen of axis,UBERON:0000130,transverse foramen
+UBERON:0009020,left uterine horn,UBERON:0002247,uterine horn
+UBERON:2002015,pharyngobranchial tooth plate,UBERON:0008907,dermal bone
+HP:0004977,Bilateral radial aplasia,HP:0003974,Absent radius
+UBERON:0014452,gustatory epithelium of tongue,UBERON:0003357,epithelium of tongue
+UBERON:0001217,ileal vein,UBERON:0002017,portal vein
+DOID:9348,carotid artery dissection,DOID:3407,carotid artery disease
+UBERON:0002027,stratum corneum of epidermis,UBERON:0013754,integumentary system layer
+HP:0004037,Abnormality of the ulnar epiphyses,HP:0003839,Abnormality involving the epiphyses of the upper limbs
+UBERON:0005659,primary palate epithelium,UBERON:0003235,epithelium of upper jaw
+UBERON:2000001,Kupffer's vesicle,UBERON:0002050,embryonic structure
+UBERON:0002675,diagonal sulcus,UBERON:0013118,sulcus of brain
+HP:0011197,EEG with focal spike waves,HP:0011185,EEG with focal epileptiform discharges
+CL:1000308,fibrocyte of adventitia of ureter,CL:1000708,ureter adventitial cell
+HP:0010688,Low placental alkaline phosphatase,HP:0003282,Low alkaline phosphatase
+HP:0000157,Abnormality of the tongue,HP:0000163,Abnormality of the oral cavity
+DOID:11195,acute laryngopharyngitis,DOID:974,upper respiratory tract disease
+UBERON:0009047,superior external pudendal vein,UBERON:0009029,pudendal vein
+HP:0007910,Nonprogressive congenital retinal dystrophy,HP:0000556,Retinal dystrophy
+HP:0004856,Normochromic microcytic anemia,HP:0001935,Microcytic anemia
+UBERON:0000979,tibia,UBERON:0004251,hindlimb zeugopod bone
+DOID:5123,mediastinum leiomyoma,DOID:127,leiomyoma
+UBERON:0003616,bronchus elastic tissue,UBERON:0003592,bronchus connective tissue
+UBERON:0003088,caudal vein,UBERON:0001638,vein
+UBERON:0007602,stratified columnar epithelium,UBERON:0012274,columnar epithelium
+UBERON:0008322,deep artery of clitoris,UBERON:0014404,female anatomical structure
+UBERON:0003970,placental labyrinth vasculature,UBERON:0006876,vasculature of organ
+HP:0010169,Pseudoepiphyses of the toes,HP:0010584,Pseudoepiphyses
+HP:0006201,Hypermobility of distal interphalangeal joints,HP:0005620,Hypermobility of interphalangeal joints
+DOID:13867,focal labyrinthitis,DOID:1468,labyrinthitis
+UBERON:0010540,tarsus pre-cartilage condensation,UBERON:0010886,hindlimb bone pre-cartilage condensation
+UBERON:2002167,stegural,UBERON:2000602,uroneural
+UBERON:0004317,distal phalanx of pedal digit 3,UBERON:0003642,pedal digit 3 phalanx
+HP:0007795,Anterior cortical cataract,HP:0100019,Cortical cataract
+UBERON:0005049,mucosa of infundibulum of uterine tube,UBERON:0005156,reproductive structure
+CL:0000659,eggshell secreting cell,CL:0000327,extracellular matrix secreting cell
+HP:0004831,Recurrent thromboembolism,HP:0001907,Thromboembolism
+HP:0004328,Abnormality of the anterior segment of the eye,HP:0012374,Abnormality of the globe
+UBERON:0003218,ovary septum,UBERON:0014404,female anatomical structure
+UBERON:0010993,subscapularis pre-muscle mass,UBERON:0004120,mesoderm-derived structure
+UBERON:0004062,neural tube marginal layer,UBERON:0004121,ectoderm-derived structure
+HP:0004814,Fava bean-induced hemolytic anemia,HP:0001878,Hemolytic anemia
+UBERON:0004066,frontonasal prominence,UBERON:0009292,embryonic nasal process
+UBERON:2001060,basidorsal,UBERON:2001457,postcranial axial cartilage
+DOID:6713,cerebrovascular disease,DOID:0050828,artery disease
+UBERON:0002871,hypoglossal nucleus,UBERON:0007635,nucleus of medulla oblongata
+HP:0010207,Osteolytic defects of the proximal phalanges of the toes,HP:0010177,Osteolytic defects of the phalanges of the toes
+UBERON:2000594,supracleithrum,UBERON:0008907,dermal bone
+DOID:2106,Thomsen disease,DOID:1289,neurodegenerative disease
+HP:0010235,Pseudoepiphyses of the phalanges of the hand,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+UBERON:0003706,laryngeal vocal fold,UBERON:0000062,organ
+HP:0009754,Fibrous syngnathia,HP:0000277,Abnormality of the mandible
+CL:0007013,terminally differentiated odontoblast,CL:0000060,odontoblast
+UBERON:0004415,proximal epiphysis of metatarsal bone,UBERON:0004380,proximal epiphysis
+NCBITaxon:716545,saccharomyceta,NCBITaxon:4890,Ascomycota
+HP:0000617,Abnormality of ocular smooth pursuit,HP:0000496,Abnormality of eye movement
+HP:0006859,Posterior leukoencephalopathy,HP:0002352,Leukoencephalopathy
+DOID:8943,lattice corneal dystrophy,DOID:2566,corneal dystrophy
+HP:0007429,Few cafe-au-lait spots,HP:0000957,Cafe-au-lait spot
+DOID:774,retina lymphoma,DOID:4645,retinal cancer
+CL:0000412,polyploid cell,CL:0000003,native cell
+UBERON:0010718,pubic cartilage element,UBERON:0007844,cartilage element
+HP:0003305,Block vertebrae,HP:0003312,Abnormal form of the vertebral bodies
+NCBITaxon:623,Shigella flexneri,NCBITaxon:620,Shigella
+DOID:0050887,Townes-Brocks syndrome,DOID:0050736,autosomal dominant disease
+UBERON:0004231,anal region smooth muscle,UBERON:0001135,smooth muscle tissue
+UBERON:3010404,capillary system of liver,UBERON:0015796,liver blood vessel
+HP:0009342,Pseudoepiphysis of the distal phalanx of the 3rd finger,HP:0009417,Pseudoepiphyses of the 3rd finger
+UBERON:0006172,rectal diverticulum,UBERON:0000061,anatomical structure
+HP:0006264,Aplasia/Hypoplasia of the 2nd finger,HP:0006265,Aplasia/Hypoplasia of fingers
+UBERON:0010413,parametrial fat pad,UBERON:0015143,mesenteric fat pad
+HP:0011019,Abnormality of chromosome condensation,HP:0011017,Abnormality of cell physiology
+UBERON:0009846,embryonic cloacal epithelium,UBERON:0000490,unilaminar epithelium
+UBERON:0011767,vagus X nerve right recurrent laryngeal branch,UBERON:0003716,recurrent laryngeal nerve
+UBERON:2001278,posterior chamber swim bladder,UBERON:0000481,multi-tissue structure
+UBERON:0014752,P2 area of pallium (Myxiniformes),UBERON:0002791,regional part of telencephalon
+UBERON:0008870,pulmonary alveolar parenchyma,UBERON:0008946,lung parenchyma
+UBERON:0009866,Hatschek's nephridium,UBERON:0000062,organ
+HP:0005944,Bilateral lung agenesis,HP:0006703,Aplasia/Hypoplasia of the lungs
+HP:0010979,Abnormality of the level of lipoprotein cholesterol,HP:0003107,Abnormality of cholesterol metabolism
+HP:0009630,Broad proximal phalanx of the thumb,HP:0011304,Broad thumb
+CL:0002453,oligodendrocyte precursor cell,CL:0000123,neuron associated cell (sensu Vertebrata)
+UBERON:0010175,nutrient foramen vein,UBERON:0001638,vein
+HP:0010319,Abnormality of the 2nd toe,HP:0001780,Abnormality of toe
+HP:0001537,Umbilical hernia,HP:0001551,Abnormality of the umbilicus
+HP:0200106,Absent/shortened dynein arms,HP:0012255,Dynein arm defect of motile cilia
+DOID:365,bladder disease,DOID:18,urinary system disease
+UBERON:0011826,vestibular gland,UBERON:0005398,female reproductive gland
+UBERON:0002593,orbital operculum,UBERON:0003022,cerebral cortex lobe
+UBERON:0005809,cortex of manus bone,UBERON:0003598,manus connective tissue
+HP:0100263,Distal symphalangism,HP:0100262,Synostosis involving digits
+HP:0010372,Broad phalanges of the 4th toe,HP:0010336,Abnormality of the phalanges of the 4th toe
+HP:0010413,Aplasia/Hypoplasia of the distal phalanx of the 2nd toe,HP:0010356,Abnormality of the distal phalanx of the 2nd toe
+UBERON:0001780,spinal nerve,UBERON:0001021,nerve
+UBERON:2001865,basibranchial 4 cartilage,UBERON:0013747,basibranchial cartilage
+HP:0010890,Morbus Osgood-Schlatter,HP:0002992,Abnormality of the tibia
+DOID:5343,central nervous system endodermal sinus tumor,DOID:4439,central nervous system germ cell tumor
+UBERON:0005379,olfactory bulb internal plexiform layer,UBERON:0009950,olfactory bulb plexiform layer
+HP:0002707,Palate telangiectasia,HP:0000174,Abnormality of the palate
+DOID:1106,esophagus lymphoma,DOID:5041,esophageal cancer
+UBERON:0008608,oblique muscle of auricle,UBERON:0001596,intrinsic auricular muscle
+UBERON:2000168,anterior macula,UBERON:0000054,macula
+UBERON:0013524,median vaginal canal,UBERON:0000996,vagina
+HP:0010206,Curved proximal phalanges of the toes,HP:0010184,Abnormality of the proximal phalanges of the toes
+DOID:4686,mucoepidermoid esophageal carcinoma,DOID:1107,esophageal carcinoma
+DOID:10773,bubonic plague,DOID:3482,plague
+UBERON:0004433,proximal epiphysis of distal phalanx of manual digit 3,UBERON:0011979,epiphysis of distal phalanx of manus
+HP:0100141,Ivory epiphysis of the distal phalanx of the 3rd toe,HP:0100061,Ivory epiphyses of the 3rd toe
+UBERON:0011831,duct of vestibular gland,UBERON:0005156,reproductive structure
+DOID:1929,supravalvular aortic stenosis,DOID:1712,aortic valve stenosis
+HP:0009419,Stippling of the epiphyses of the 3rd finger,HP:0009320,Abnormality of the epiphyses of the 3rd finger
+CL:0002399,CD1c-positive myeloid dendritic cell,CL:0000782,myeloid dendritic cell
+CL:0000484,connective tissue type mast cell,CL:0000097,mast cell
+UBERON:0009970,epithelium of pancreatic duct,UBERON:0013697,exocrine pancreas epithelium
+UBERON:0016454,upper central secondary incisor tooth,UBERON:0003450,upper jaw incisor
+UBERON:3010235,nuchal groove,UBERON:3000972,head external integument structure
+DOID:100,intestinal infectious disease,DOID:5295,intestinal disease
+HP:0100889,Abnormality of the ductus choledochus,HP:0012440,Abnormal biliary tract morphology
+UBERON:0001541,medial plantar artery,UBERON:0003516,hindlimb blood vessel
+UBERON:0000124,epineurium,UBERON:0002384,connective tissue
+UBERON:0003319,mesenchyme of carpal region,UBERON:0003859,forelimb mesenchyme
+UBERON:2000635,central pretectal nucleus,UBERON:0014450,pretectal nucleus
+UBERON:0012056,left lung upper lobe bronchiole,UBERON:0003539,left lung bronchiole
+HP:0008416,Six lumbar vertebrae,HP:0002946,Supernumerary vertebrae
+UBERON:0010211,granulation tissue,UBERON:0002384,connective tissue
+UBERON:2001143,tooth 4V,UBERON:2000694,ceratobranchial 5 tooth
+CL:0000078,peridermal cell,CL:0000076,squamous epithelial cell
+HP:0100913,Sclerosis of the proximal phalanx of the thumb,HP:0100922,Sclerosis of the phalanges of the thumb
+UBERON:2002065,ural centrum 1,UBERON:0004247,bone of dorsum
+HP:0005914,Aplasia/Hypoplasia involving the metacarpal bones,HP:0005927,Aplasia/Hypoplasia involving bones of the hand
+HP:0100110,Triangular epiphysis of the distal phalanx of the 2nd toe,HP:0100054,Triangular epiphyses of the 2nd toe
+HP:0000894,Short clavicles,HP:0006710,Aplasia/Hypoplasia of the clavicles
+UBERON:0011821,irregular connective tissue,UBERON:0002384,connective tissue
+HP:0009893,Telangiectasia of the ear,HP:0000356,Abnormality of the outer ear
+UBERON:0003214,mammary gland alveolus,UBERON:0005156,reproductive structure
+DOID:5183,hereditary Wilms' tumor,DOID:2154,nephroblastoma
+UBERON:0001997,olfactory epithelium,UBERON:0010499,pseudostratified ciliated columnar epithelium
+UBERON:0005645,manual digit 2 epithelium,UBERON:0005227,manual digit epithelium
+HP:0000011,Neurogenic bladder,HP:0000009,Functional abnormality of the bladder
+HP:0002758,Osteoarthritis,HP:0001369,Arthritis
+UBERON:0015214,arcuate ligament,UBERON:0004120,mesoderm-derived structure
+UBERON:0000110,neurula stage,UBERON:0000067,embryo stage part
+UBERON:2001528,epibranchial 1 cartilage,UBERON:2001905,epibranchial 1 element
+HP:0006370,Distal ulnar epiphyseal stippling,HP:0010655,Epiphyseal stippling
+DOID:7971,microcystic variant infiltrating bladder urothelial carcinoma,DOID:6477,invasive bladder transitional cell carcinoma
+CL:0002462,adipose dendritic cell,CL:0002320,connective tissue cell
+DOID:14130,lateral cystocele,DOID:1284,prolapse of female genital organ
+UBERON:0005849,cervical spinal cord lateral column,UBERON:0006078,subdivision of spinal cord lateral column
+HP:0005546,Increased red cell osmotic resistance,HP:0001877,Abnormality of erythrocytes
+DOID:14435,chronic tubotympanic suppurative otitis media,DOID:11506,suppurative otitis media
+DOID:3118,hepatobiliary disease,DOID:77,gastrointestinal system disease
+HP:0010163,Bracket epiphyses of the toes,HP:0010578,Bracket epiphyses
+CL:0000997,immature CD8_alpha-negative CD11b-positive dendritic cell,CL:0000840,immature conventional dendritic cell
+HP:0012260,Abnormal central microtubular pair morphology of motile cilia,HP:0005938,Abnormal respiratory motile cilium morphology
+HP:0012123,Posterior uveitis,HP:0000554,Uveitis
+UBERON:0009663,telencephalic nucleus,UBERON:0002791,regional part of telencephalon
+HP:0002693,Abnormality of the skull base,HP:0000929,Abnormality of the skull
+DOID:3200,cerebellopontine angle tumor,DOID:4203,brain stem cancer
+HP:0010296,Ankyloglossia,HP:0000157,Abnormality of the tongue
+UBERON:0003584,mammary gland connective tissue,UBERON:0004121,ectoderm-derived structure
+HP:0006349,Agenesis of permanent teeth,HP:0009804,Reduced number of teeth
+DOID:7054,multiple skull base meningioma,DOID:4437,skull base meningioma
+HP:0005151,Preductal coarctation of the aorta,HP:0012305,Coarctation of the descending aortic arch
+DOID:12053,cryptococcosis,DOID:2473,opportunistic mycosis
+HP:0003969,Slender forearm bones,HP:0002973,Abnormality of the forearm
+DOID:9297,lip disease,DOID:403,mouth disease
+UBERON:0001700,geniculate ganglion,UBERON:0001800,sensory ganglion
+HP:0003833,Laterally deficient tibial plateaux,HP:0003832,Abnormality of the tibial plateaux
+HP:0007378,Neoplasm of the gastrointestinal tract,HP:0011793,Neoplasm by anatomical site
+HP:0009820,Lower limb peromelia,HP:0009828,Peromelia
+HP:0009645,Osteolytic defects of the distal phalanx of the thumb,HP:0009654,Osteolytic defects of the phalanges of the thumb
+UBERON:0003413,pectoral appendage bud mesenchyme,UBERON:0010329,paired limb/fin bud mesenchyme
+DOID:11554,Chandler syndrome,DOID:2566,corneal dystrophy
+HP:0005819,Short middle phalanx of finger,HP:0009381,Short finger
+HP:0011778,Thyroid atypical adenoma,HP:0000854,Thyroid adenoma
+UBERON:0006689,frenulum of tongue,UBERON:0005020,mucosa of tongue
+HP:0012513,Upper limb pain,HP:0009763,Limb pain
+UBERON:0006212,bulbo-ventricular groove,UBERON:0004120,mesoderm-derived structure
+UBERON:2002283,melanophore spot,UBERON:2002284,body marking
+UBERON:0007190,paracentral gyrus,UBERON:0000200,gyrus
+DOID:6993,iris mixed cell melanoma,DOID:6994,malignant iris melanoma
+UBERON:0011079,angular bone,UBERON:0015212,lateral structure
+HP:0001651,Dextrocardia,HP:0004307,Abnormal anatomic location of the heart
+UBERON:0001743,ligament of larynx,UBERON:0008845,nonskeletal ligament
+UBERON:0002133,atrioventricular valve,UBERON:0000946,cardial valve
+UBERON:0015246,septal organ of Masera,UBERON:0004119,endoderm-derived structure
+UBERON:0001695,squamous part of temporal bone,UBERON:0003462,facial bone
+DOID:1443,cerebral degeneration,DOID:936,brain disease
+HP:0000396,Overfolded helix,HP:0008544,Abnormally folded helix
+UBERON:2002216,otic vesicle ventral protrusion,UBERON:2002215,otic vesicle protrusion
+HP:0009947,Duplication of the proximal phalanx of the 2nd finger,HP:0009544,Abnormality of the proximal phalanx of the 2nd finger
+UBERON:4200004,intertrochanteric fossa,UBERON:0004704,bone fossa
+UBERON:0000355,pharyngeal mucosa,UBERON:0004785,respiratory system mucosa
+HP:0010964,Abnormality of long-chain fatty-acid metabolism,HP:0004359,Abnormality of fatty-acid metabolism
+UBERON:0000924,ectoderm,UBERON:0000923,germ layer
+CL:0000058,chondroblast,CL:0000055,non-terminally differentiated cell
+HP:0009587,Triangular shaped proximal phalanx of the 2nd finger,HP:0009546,Triangular shaped phalanges of the 2nd finger
+UBERON:2001897,hypobranchial 4 element,UBERON:2001893,hypobranchial element
+HP:0007354,Amyotrophic lateral sclerosis,HP:0007373,Atrophy/Degeneration involving motor neurons
+UBERON:0000043,tendon,UBERON:0007846,dense regular connective tissue
+CL:0002126,"CD25-positive, CD27-positive immature gamma-delta T cell",CL:0000799,immature gamma-delta T cell
+UBERON:2000985,ventral rhombencephalic commissure medulla oblongata,UBERON:0014649,white matter of medulla oblongata
+HP:0004993,Slender long bones with narrow diaphyses,HP:0000940,Abnormal diaphysis morphology
+HP:0009183,Joint contractures of the 5th finger,HP:0004207,Abnormality of the 5th finger
+UBERON:0009002,placental membrane,UBERON:0000478,extraembryonic structure
+HP:0012713,Moderate hearing impairment,HP:0000365,Hearing impairment
+UBERON:0001402,longissimus cervicis muscle,UBERON:0000392,longissimus muscle
+UBERON:0010760,supraglenoid tubercle,UBERON:4100000,skeletal element projection
+HP:0010127,Absent epiphysis of the proximal phalanx of the hallux,HP:0010113,Absent epiphyses of the hallux
+UBERON:0001723,tongue,UBERON:0004121,ectoderm-derived structure
+UBERON:2005066,bulbus arteriosus outer layer,UBERON:0004120,mesoderm-derived structure
+HP:0011480,Unilateral microphthalmos,HP:0000568,Microphthalmos
+UBERON:0001982,capillary,UBERON:0010523,microcirculatory vessel
+UBERON:0004525,cardiac muscle tissue of trabecula carnea of right ventricle,UBERON:0003452,trabecula carnea cardiac muscle tissue
+UBERON:0001542,inguinal lymph node,UBERON:0003968,peripheral lymph node
+DOID:7411,ovarian endometrioid cystadenofibroma,DOID:5480,ovarian endometrioid adenofibroma
+UBERON:0004476,musculature of shoulder,UBERON:0014793,musculature of pectoral complex
+HP:0007713,Juvenile zonular cataracts,HP:0001118,Juvenile cataract
+HP:0100810,Pointed helix,HP:0011039,Abnormality of the helix
+UBERON:2001758,dorsal fin lepidotrichium 5,UBERON:4000177,dorsal fin lepidotrichium
+CL:0011111,gonadotropin releasing neuron,CL:0011112,magnocellular neurosecretory cell
+HP:0100860,Inferior mesenteric artery aneurysm,HP:0011934,Mesenteric artery aneurysm
+UBERON:0011197,parathyroid epithelium,UBERON:0006799,glandular epithelium
+HP:0010060,Bullet-shaped phalanges of the hallux,HP:0010057,Abnormality of the phalanges of the hallux
+UBERON:0001872,parietal lobe,UBERON:0000064,organ part
+UBERON:2001687,interopercular-mandibular ligament,UBERON:0008846,skeletal ligament
+CL:0000129,microglial cell,CL:0000243,glial cell (sensu Vertebrata)
+HP:0010437,Short proximal phalanx of the 2nd toe,HP:0010395,Aplasia/Hypoplasia of the proximal phalanx of the 2nd toe
+HP:0010597,Abnormality of the distal radial epiphysis,HP:0003999,Abnormality of radial epiphyses
+UBERON:0003672,dentition,UBERON:0000477,anatomical cluster
+DOID:8150,pancreatic invasive intraductal papillary-mucinous carcinoma,DOID:7574,pancreatic intraductal papillary-colloid carcinoma
+HP:0003220,Abnormality of chromosome stability,HP:0011017,Abnormality of cell physiology
+HP:0010189,Osteolytic defects of the distal phalanges of the toes,HP:0010177,Osteolytic defects of the phalanges of the toes
+UBERON:3000701,intervertebral space,UBERON:0010276,vertebral column opening
+DOID:3825,Shwartzman phenomenon,DOID:484,vascular hemostatic disease
+UBERON:0011678,hindlimb intermedium,UBERON:0011679,proximal tarsal bone
+UBERON:0008925,sublaminar layer S4,UBERON:0008929,sublaminar layers S4 or S5
+UBERON:0005135,metanephric glomerular epithelium,UBERON:0004188,glomerular epithelium
+UBERON:3000715,heterocoelous,UBERON:0001075,vertebral centrum
+HP:0002644,Abnormality of pelvic girdle bone morphology,HP:0011844,Abnormal appendicular skeleton morphology
+UBERON:0005973,blood-inner ear barrier,UBERON:0003496,head blood vessel
+UBERON:0009616,presumptive midbrain,UBERON:0006598,presumptive structure
+DOID:7840,pancreatic non-functioning delta cell tumor,DOID:4433,pancreatic delta cell neoplasm
+UBERON:0006374,part of afferent arteriole forming the juxtaglomerular complex,UBERON:0006554,urinary system structure
+HP:0012440,Abnormal biliary tract morphology,HP:0001080,Biliary tract abnormality
+CL:0002547,fibroblast of the aortic adventitia,CL:1000306,fibroblast of tunica adventitia of artery
+UBERON:0004103,alveolar ridge,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010120,Pseudoepiphyses of the hallux,HP:0010169,Pseudoepiphyses of the toes
+HP:0005423,Dysfunctional alternative complement pathway,HP:0005482,Abnormality of the alternate complement pathway
+HP:0000934,Chondrocalcinosis,HP:0001367,Abnormal joint morphology
+HP:0001937,Microangiopathic hemolytic anemia,HP:0001878,Hemolytic anemia
+DOID:217,enamel caries,DOID:216,dental caries
+UBERON:0013675,toxactinium,UBERON:0000062,organ
+UBERON:0001728,nasopharynx,UBERON:0004119,endoderm-derived structure
+HP:0009992,Complete duplication of the middle phalanx of the 5th finger,HP:0010002,Complete duplication of the middle phalanges of the hand
+UBERON:0001911,mammary gland,UBERON:0005398,female reproductive gland
+DOID:6162,childhood embryonal testis carcinoma,DOID:5680,embryonal testis carcinoma
+HP:0009425,Patchy sclerosis of the distal phalanx of the 3rd finger,HP:0009357,Abnormality of the distal phalanx of the 3rd finger
+DOID:4266,intravascular angioleiomyoma,DOID:4265,angiomyoma
+UBERON:2002210,mossy fiber,UBERON:0000479,tissue
+HP:0010024,Epiphyseal stippling of the first metacarpal,HP:0010014,Abnormality of the epiphysis of the 1st metacarpal
+UBERON:0012355,manual acropodium region,UBERON:0005451,segment of manus
+UBERON:0005986,left branch of atrioventricular bundle,UBERON:0010131,conducting tissue of heart
+UBERON:0013505,cervical vertebra cartilage element,UBERON:0015007,cervical vertebra endochondral element
+UBERON:2000350,epipleural,UBERON:2000526,intermuscular bone
+UBERON:0011374,prepuce,UBERON:0005156,reproductive structure
+UBERON:0011060,perilymphatic channel,UBERON:0004121,ectoderm-derived structure
+UBERON:0013582,metapodium bone 2,UBERON:0003821,metapodium bone
+UBERON:0007247,superior olivary nucleus,UBERON:0006331,brainstem nucleus
+HP:0002371,Loss of speech,HP:0002167,Neurological speech impairment
+UBERON:3000178,footplate of pars media plectri,UBERON:0000064,organ part
+UBERON:0002948,superior occipital gyrus,UBERON:0014640,occipital gyrus
+UBERON:0009526,maxillary process mesenchyme,UBERON:0003104,mesenchyme
+NCBITaxon:1300,Streptococcaceae,NCBITaxon:186826,Lactobacillales
+HP:0011354,Generalized abnormality of skin,HP:0000951,Abnormality of the skin
+UBERON:0010406,cholinergic enteric nerve,UBERON:0010380,enteric nerve
+HP:0010378,Triangular shaped phalanges of the 4th toe,HP:0010180,Triangular shaped phalanges of the toes
+HP:0011417,Long umbilical cord,HP:0010881,Abnormality of the umbilical cord
+HP:0009774,Triangular shaped phalanges of the hand,HP:0005918,Abnormality of phalanx of finger
+UBERON:0005296,ovary sex cord,UBERON:0004911,epithelium of female gonad
+UBERON:3000068,cartilago ectochoanalis,UBERON:0003933,cranial cartilage
+HP:0100892,Abnormality of the xiphoid process,HP:0000766,Abnormality of the sternum
+HP:0000537,Epicanthus inversus,HP:0000492,Abnormality of the eyelid
+DOID:4866,salivary gland adenoid cystic carcinoma,DOID:0050904,salivary gland carcinoma
+UBERON:0003361,epithelium of sublingual gland,UBERON:0003929,gut epithelium
+HP:0007182,Peripheral hypomyelination,HP:0003130,Abnormal peripheral myelination
+HP:0100219,Ivory epiphysis of the middle phalanx of the 5th toe,HP:0100083,Ivory epiphyses of the 5th toe
+CL:0000763,myeloid cell,CL:0000988,hematopoietic cell
+UBERON:0009600,mesenchyme of interdigital region of manus,UBERON:0009585,interdigital region mesenchyme
+UBERON:0006307,urogenital membrane,UBERON:0004120,mesoderm-derived structure
+UBERON:3000364,otic plate of pterygoid,UBERON:0000064,organ part
+HP:0100954,Open operculum,HP:0002538,Abnormality of the cerebral cortex
+UBERON:0004270,lower leg connective tissue,UBERON:0003569,leg connective tissue
+HP:0100827,Lymphocytosis,HP:0004332,Abnormality of lymphocytes
+UBERON:0003889,fallopian tube,UBERON:0005156,reproductive structure
+UBERON:0009119,branchial basket,UBERON:0010313,neural crest-derived structure
+HP:0000204,Cleft upper lip,HP:0000177,Abnormality of upper lip
+UBERON:0013178,anterior dorsal bursa,UBERON:0013177,dorsal bursa
+UBERON:0009564,distal limb integumentary appendage,UBERON:0013703,integumentary projection
+HP:0011777,Thyroid papillary adenoma,HP:0000854,Thyroid adenoma
+UBERON:3010636,egg capsules,UBERON:0000476,acellular anatomical structure
+UBERON:0003989,medulla oblongata anterior median fissure,UBERON:0000464,anatomical space
+UBERON:2000989,hypaxial region somite 8,UBERON:0003895,hypaxial myotome region
+UBERON:2105378,dorsal fin distal radial element 7,UBERON:2100936,dorsal fin distal radial element
+HP:0010070,Curved 1st metatarsal,HP:0010061,Curved phalanges of the hallux
+UBERON:3010736,ramus posterior of CN VIII,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0014451,tongue taste bud,UBERON:0001727,taste bud
+HP:0001528,Hemihypertrophy,HP:0002813,Abnormality of limb bone morphology
+HP:0010084,Duplication of the distal phalanx of the hallux,HP:0010053,Abnormality of the distal phalanx of the hallux
+HP:0001901,Polycythemia,HP:0001877,Abnormality of erythrocytes
+HP:0008053,Aplasia/Hypoplasia of the iris,HP:0000525,Abnormality of the iris
+HP:0010361,Bullet-shaped phalanges of the 3rd toe,HP:0010175,Bullet-shaped phalanges of the toes
+HP:0012610,Abnormality of urinary uric acid concentration,HP:0004369,Decreased purine levels
+UBERON:4200045,articular surface for the astragalus on the calcaneum,UBERON:4100003,articular surface
+HP:0006152,Proximal symphalangism (hands),HP:0100264,Proximal symphalangism
+HP:0011007,Age of onset,HP:0003674,Onset
+HP:0002227,White eyelashes,HP:0000499,Abnormality of the eyelashes
+HP:0000825,Hyperinsulinemic hypoglycemia,HP:0000842,Hyperinsulinemia
+UBERON:0008828,presphenoid bone,UBERON:0011164,neurocranium bone
+CL:0002604,astrocyte of the hippocampus,CL:1001580,hippocampus glial cell
+HP:0012153,Hypotriglyceridemia,HP:0003119,Abnormality of lipid metabolism
+HP:0002199,Hypocalcemic seizures,HP:0011145,Symptomatic seizures
+DOID:12328,marasmus,DOID:11801,protein-energy malnutrition
+UBERON:0009494,pharyngeal arch mesenchymal region,UBERON:0005253,head mesenchyme
+UBERON:3000433,pineal foramen,UBERON:0004120,mesoderm-derived structure
+HP:0100486,Symphalangism of the proximal phalanx of the 5th toe with the 5th metatarsal,HP:0010378,Triangular shaped phalanges of the 4th toe
+HP:0010403,Duplication of the proximal phalanx of the 2nd toe,HP:0010358,Abnormality of the proximal phalanx of the 2nd toe
+HP:0010407,Curved middle phalanx of the 2nd toe,HP:0010357,Abnormality of the middle phalanx of the 2nd toe
+DOID:2098,vulva adenocarcinoma,DOID:1294,vulva carcinoma
+DOID:0050428,nonepidermolytic palmoplantar keratoderma,DOID:3390,palmoplantar keratosis
+HP:0012419,Hyperoxemia,HP:0012415,Abnormal blood gas level
+DOID:0050140,acute diarrhea,DOID:13250,diarrhea
+HP:0000709,Psychosis,HP:0000708,Behavioural/Psychiatric Abnormality
+UBERON:0009041,superficial circumflex iliac artery,UBERON:0004573,systemic artery
+UBERON:3010730,pterygoideus,UBERON:0011648,jaw muscle
+HP:0001902,Giant platelets,HP:0011877,Increased mean platelet volume
+UBERON:0009644,trachea non-cartilage connective tissue,UBERON:0003571,trachea connective tissue
+NCBITaxon:117573,mitosporic Ophiostomataceae,NCBITaxon:5152,Ophiostomataceae
+CL:0000138,chondrocyte,CL:0000667,collagen secreting cell
+HP:0001239,Wrist flexion contracture,HP:0003019,Abnormality of the wrist
+UBERON:3000112,crista dentalis of premaxilla,UBERON:0004120,mesoderm-derived structure
+UBERON:0000361,red bone marrow,UBERON:0002371,bone marrow
+HP:0011018,Abnormality of the cell cycle,HP:0011017,Abnormality of cell physiology
+UBERON:2002013,ascending limb of ceratobranchial 5 bone,UBERON:0004530,bony projection
+UBERON:0002552,vestibulocerebellar tract,UBERON:0007702,tract of brain
+UBERON:2001275,sublingual,UBERON:0002513,endochondral bone
+HP:0000042,Absent external genitalia,HP:0000032,Abnormality of male external genitalia
+UBERON:0009000,ischial spine,UBERON:0004120,mesoderm-derived structure
+UBERON:2102029,pectoral fin proximal radial element 4,UBERON:2101587,pectoral fin proximal radial element
+CL:0000651,mucous neck cell,CL:0000150,glandular epithelial cell
+HP:0010557,Overlapping fingers,HP:0004097,Deviation of finger
+CL:0000756,type 4 cone bipolar cell (sensu Mus),CL:0000752,cone retinal bipolar cell
+UBERON:2001675,mesethmoid cornu,UBERON:0004120,mesoderm-derived structure
+DOID:8461,Aicardi syndrome,DOID:225,syndrome
+UBERON:2000461,Weberian ossicle,UBERON:0000491,solid compound organ
+UBERON:0007108,vernix caseosa,UBERON:0000456,bodily secretion
+CL:0010005,atrioventricular bundle cell,CL:0010007,His-Purkinje system cell
+UBERON:0002282,stria vascularis of cochlear duct,UBERON:0000064,organ part
+UBERON:0011159,primary subdivision of cranial skeletal system,UBERON:0000075,subdivision of skeletal system
+UBERON:3000950,os triangulare,UBERON:0002513,endochondral bone
+UBERON:0011318,capsule of temporomandibular joint,UBERON:0013765,digestive system organ
+CL:1001602,cerebral cortex endothelial cell,CL:0002319,neural cell
+HP:0011050,Agenesis of permanent maxillary lateral incisor,HP:0000690,Agenesis of maxillary lateral incisor
+UBERON:0005253,head mesenchyme,UBERON:0003104,mesenchyme
+HP:0009436,Triangular shaped middle phalanx of the 3rd finger,HP:0009446,Triangular shaped phalanges of the 3rd finger
+HP:0005108,Abnormality of the intervertebral disk,HP:0000925,Abnormality of the vertebral column
+UBERON:0015227,peristaltic circulatory vessel,UBERON:0000055,vessel
+UBERON:0005490,posterior interventricular sulcus,UBERON:0005455,interventricular groove
+UBERON:0002380,trapezius muscle,UBERON:0004120,mesoderm-derived structure
+UBERON:0006805,sternal end of clavicle,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0005203,Spontaneous esophageal perforation,HP:0002031,Abnormality of the esophagus
+HP:0012114,Endometrial carcinoma,HP:0010784,Uterine neoplasm
+HP:0012017,EEG with parietal focal spikes,HP:0011193,EEG with focal spikes
+HP:0001982,Sea-blue histiocytosis,HP:0004311,Abnormality of macrophages
+DOID:2352,hemochromatosis,DOID:896,metal metabolism disorder
+DOID:7933,childhood precursor T-lymphoblastic lymphoma/leukemia,DOID:5599,precursor T-lymphoblastic lymphoma/leukemia
+CL:0002389,uninucleate arthroconidium,CL:0002384,uninucleate macroconidium
+UBERON:0006263,Meckel's cartilage pre-cartilage condensation,UBERON:0014387,mesenchyme derived from neural crest
+UBERON:0007415,nucleus of midbrain reticular formation,UBERON:0007414,nucleus of midbrain tegmentum
+UBERON:0004774,inferior eyelid tarsus,UBERON:0004772,eyelid tarsus
+DOID:0060103,central nervous system primitive neuroectodermal neoplasm,DOID:3620,central nervous system cancer
+UBERON:0002218,tympanic ring,UBERON:0003457,head bone
+UBERON:0000310,breast,UBERON:0000475,organism subdivision
+UBERON:0002899,hippocampal sulcus,UBERON:0008334,subarachnoid sulcus
+HP:0007946,Unilateral narrow palpebral fissure,HP:0000581,Blepharophimosis
+UBERON:0001331,skin of penis,UBERON:0000014,zone of skin
+UBERON:0006713,foramen cecum of frontal bone,UBERON:0004120,mesoderm-derived structure
+UBERON:0001583,extrinsic auricular muscle,UBERON:0001595,auricular muscle
+CL:1001433,epithelial cell of exocrine pancreas,CL:0000083,epithelial cell of pancreas
+HP:0001659,Aortic regurgitation,HP:0001646,Abnormality of the aortic valve
+HP:0011804,Abnormality of muscle physiology,HP:0003011,Abnormality of the musculature
+DOID:11033,idiopathic corneal edema,DOID:11030,corneal edema
+HP:0009444,Patchy sclerosis of the phalanges of the 3rd finger,HP:0009772,Patchy sclerosis of the phalanges of the hand
+DOID:14687,diastrophic dysplasia,DOID:2256,osteochondrodysplasia
+UBERON:0011959,glenoid labrum of scapula,UBERON:0007844,cartilage element
+UBERON:2001548,intercalarium ascending process,UBERON:4100000,skeletal element projection
+HP:0009762,Facial wrinkling,HP:0100678,Premature skin wrinkling
+DOID:6906,glomangiomatosis,DOID:5238,benign perivascular tumor
+HP:0009789,Perianal abscess,HP:0004378,Abnormality of the anus
+DOID:10973,acute salpingitis,DOID:5733,salpingitis
+UBERON:0005656,lens vesicle epithelium,UBERON:0010371,ecto-epithelium
+HP:0010356,Abnormality of the distal phalanx of the 2nd toe,HP:0010324,Abnormality of phalanx of the 2nd toe
+DOID:0060223,agraphia,DOID:0060047,writing disorder
+UBERON:0010885,hindlimb cartilage element,UBERON:0015022,hindlimb endochondral element
+UBERON:0000936,posterior commissure,UBERON:0011590,commissure of diencephalon
+DOID:0050214,Lambert-Eaton myasthenic syndrome,DOID:439,neuromuscular junction disease
+UBERON:0003448,manus nerve,UBERON:0003441,forelimb nerve
+DOID:3479,uveal cancer,DOID:2174,ocular cancer
+UBERON:0012497,muscularis mucosae of rectum,UBERON:0001239,muscularis mucosae of large intestine
+DOID:3444,scrotum Paget's disease,DOID:3445,scrotal carcinoma
+UBERON:0002351,sinoatrial node,UBERON:0004493,cardiac muscle tissue of myocardium
+CL:0000569,cardiac mesenchymal cell,CL:0002494,cardiocyte
+HP:0006456,Irregular proximal tibial epiphyses,HP:0010591,Abnormality of the proximal tibial epiphysis
+UBERON:0001216,jejunal vein,UBERON:0002017,portal vein
+HP:0000224,Decreased taste sensation,HP:0000223,Abnormality of taste sensation
+UBERON:0010507,layer of dura mater,UBERON:0004923,organ component layer
+DOID:0050725,tyrosinemia type II,DOID:37,skin disease
+UBERON:0007716,lumbar subsegment of spinal cord,UBERON:0002792,lumbar spinal cord
+HP:0009922,Persistence of the hyaloid artery,HP:0004327,Abnormality of the vitreous humor
+HP:0009190,Irregular epiphyses of the metacarpals,HP:0005913,Abnormality of metacarpal epiphyses
+CL:0000632,hepatic stellate cell,CL:0000057,fibroblast
+DOID:14757,type III Ehlers-Danlos syndrome,DOID:13359,Ehlers-Danlos syndrome
+UBERON:0001318,inferior vesical vein,UBERON:0002460,vesical vein
+UBERON:0001174,common bile duct,UBERON:0003703,extrahepatic bile duct
+DOID:9957,periostitis,DOID:65,connective tissue disease
+UBERON:3000821,margo suprascapularis,UBERON:0000064,organ part
+UBERON:0006617,left external ear,UBERON:0001691,external ear
+UBERON:0002093,spinal dura mater,UBERON:0002363,dura mater
+HP:0010402,Triangular shaped proximal phalanx of the 2nd toe,HP:0010358,Abnormality of the proximal phalanx of the 2nd toe
+HP:0000800,Cystic renal dysplasia,HP:0000107,Renal cyst
+HP:0009517,Fragmentation of the epiphysis of the middle phalanx of the 2nd finger,HP:0009492,Fragmentation of the epiphyses of the 2nd finger
+UBERON:0001246,interlobular bile duct,UBERON:0003704,intrahepatic bile duct
+HP:0010338,Deviation/Displacement of the 4th toe,HP:0010321,Abnormality of the 4th toe
+UBERON:0004817,lacrimal gland epithelium,UBERON:0010313,neural crest-derived structure
+UBERON:2000673,hypobranchial artery,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0002943,Thoracic scoliosis,HP:0002650,Scoliosis
+DOID:5564,fallopian tube teratoma,DOID:5324,fallopian tube germ cell cancer
+HP:0100945,Sclerosis of the 1st metatarsal,HP:0100946,Sclerosis of the proximal phalanges of the toes
+HP:0100029,Lingual thyroid,HP:0100028,Ectopic thyroid
+HP:0011937,Hypoplastic fifth toenail,HP:0001800,Hypoplastic toenails
+UBERON:4200158,metatarsal bone of digit 8,UBERON:4200156,metapodium bone 8
+HP:0009211,Small epiphysis of the middle phalanx of the 5th finger,HP:0010265,Small epiphyses of the middle phalanges of the hand
+DOID:14695,galactokinase deficiency,DOID:9870,galactosemia
+HP:0011077,Abnormality of molar,HP:0000164,Abnormality of the teeth
+UBERON:0002206,mammillary body,UBERON:0004121,ectoderm-derived structure
+UBERON:3000036,basal process of palatoquadrate,UBERON:0004121,ectoderm-derived structure
+UBERON:0015177,helicine artery,UBERON:0001637,artery
+NCBITaxon:121752,Lacazia loboi,NCBITaxon:121739,Lacazia
+UBERON:0001942,medial habenular nucleus,UBERON:0002757,regional part of epithalamus
+HP:0001047,Atopic dermatitis,HP:0011123,Inflammatory abnormality of the skin
+HP:0010413,Aplasia/Hypoplasia of the distal phalanx of the 2nd toe,HP:0010185,Aplasia/Hypoplasia of the distal phalanges of the toes
+HP:0000253,Progressive microcephaly,HP:0000252,Microcephaly
+HP:0100866,Short iliac bones,HP:0000946,Hypoplastic ilia
+UBERON:0002539,pharyngeal arch,UBERON:0010188,protuberance
+UBERON:0013622,manual autopod pad,UBERON:0012348,autopod pad
+CL:0000930,"CD4-negative, CD8-negative type I NK T cell secreting interleukin-4",CL:0000924,"CD4-negative, CD8-negative type I NK T cell"
+UBERON:4300097,anal fin spine 1,UBERON:2002262,anal fin spine
+UBERON:2000902,hypural musculature,UBERON:0001630,muscle organ
+HP:0006696,Polymorphic and polytopic ventricular extrasystoles,HP:0004308,Ventricular arrhythmia
+UBERON:0011157,cuneiform cartilage,UBERON:0001739,laryngeal cartilage
+HP:0003276,Pelvic exostoses,HP:0002644,Abnormality of pelvic girdle bone morphology
+DOID:10834,voyeurism,DOID:0060044,paraphilia disorder
+UBERON:0001148,median nerve,UBERON:0003433,arm nerve
+UBERON:0002227,spiral organ of cochlea,UBERON:0000020,sense organ
+HP:0000298,Mask-like facies,HP:0004673,Decreased facial expression
+CL:0000558,reticulocyte,CL:0000764,erythroid lineage cell
+UBERON:0001814,brachial nerve plexus,UBERON:0001813,somatic nerve plexus
+HP:0012193,Anaplastic large-cell lymphoma,HP:0012190,T-cell lymphoma
+CL:0000657,secondary spermatocyte,CL:0000413,haploid cell
+HP:0002932,Aldehyde oxidase deficiency,HP:0004354,Abnormality of carboxylic acid metabolism
+UBERON:0004643,lateral ventricle ependyma,UBERON:0005357,brain ependyma
+UBERON:0002572,principal pretectal nucleus,UBERON:0003528,brain grey matter
+UBERON:0013680,inner canthus of left eye,UBERON:0005611,inner canthus
+UBERON:0010326,optic pedicel,UBERON:0010321,skeletal element of eye region
+DOID:1142,alternating exotropia,DOID:1143,exotropia
+HP:0006191,Deep palmar crease,HP:0010490,Abnormality of the palmar creases
+UBERON:0011143,upper urinary tract,UBERON:0015212,lateral structure
+UBERON:4200025,ascending process of the astragalus,UBERON:0004530,bony projection
+UBERON:0005221,liver right lobe parenchyma,UBERON:0001280,liver parenchyma
+CL:0000759,type 7 cone bipolar cell (sensu Mus),CL:0000749,ON-bipolar cell
+DOID:0060042,atypical autism,DOID:0060041,autism spectrum disorder
+HP:0007902,Vitreous hemorrhage,HP:0011885,Hemorrhage of the eye
+HP:0100674,Vaginal hematocele,HP:0100672,Vaginal hernia
+UBERON:0003459,chest bone,UBERON:0003827,thoracic segment bone
+HP:0002215,Sparse axillary hair,HP:0008070,Sparse hair
+UBERON:0006262,malleus pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+HP:0007618,Subcutaneous calcification,HP:0011354,Generalized abnormality of skin
+UBERON:0003304,mesoderm blood island,UBERON:0007497,developing epithelial placode
+HP:0001350,Slurred speech,HP:0011443,Abnormality of coordination
+UBERON:2001922,inter-frontal joint,UBERON:0000982,skeletal joint
+UBERON:0010583,pedal digit 4 phalanx pre-cartilage condensation,UBERON:0010585,pedal digit phalanx pre-cartilage condensation
+UBERON:0014629,terminal part of the cochlear canal,UBERON:0004120,mesoderm-derived structure
+HP:0000926,Platyspondyly,HP:0003312,Abnormal form of the vertebral bodies
+UBERON:4200114,prepubic process,UBERON:4100000,skeletal element projection
+UBERON:0003644,kidney arterial blood vessel,UBERON:0003517,kidney blood vessel
+HP:0009565,Aplasia of the distal phalanx of the 2nd finger,HP:0009535,Aplasia of the 2nd finger
+HP:0005425,Recurrent sinopulmonary infections,HP:0002205,Recurrent respiratory infections
+UBERON:0010963,trunk and cervical myotome group,UBERON:0003082,myotome
+CL:0000397,ganglion interneuron,CL:0000099,interneuron
+UBERON:0005144,metanephric glomerular capillary,UBERON:0004212,glomerular capillary
+DOID:404,gastrointestinal tuberculosis,DOID:0050599,abdominal tuberculosis
+HP:0009523,Triangular epiphysis of the middle phalanx of the 2nd finger,HP:0010267,Triangular epiphyses of the middle phalanges of the hand
+HP:0008818,Large iliac wings,HP:0011867,Abnormality of the wing of the ilium
+NCBITaxon:128827,Erysipelotrichaceae,NCBITaxon:526525,Erysipelotrichales
+UBERON:0012325,retrocerebral complex,UBERON:0002368,endocrine gland
+HP:0100002,Pleural mesothelioma,HP:0100001,Malignant mesothelioma
+HP:0009483,Symphalangism of the proximal phalanx of the 3rd finger with the 3rd metatcarpal,HP:0009455,Symphalangism affecting the proximal phalanx of the 3rd finger
+DOID:6692,Barre-Lieou syndrome,DOID:225,syndrome
+UBERON:3000806,carina medialis,UBERON:0004120,mesoderm-derived structure
+UBERON:0002339,epithelium of lobar bronchus,UBERON:0002031,epithelium of bronchus
+UBERON:0004160,proepicardium,UBERON:0003104,mesenchyme
+HP:0100406,Duplication of the proximal phalanx of the 5th toe,HP:0010391,Duplication of the phalanges of the 5th toe
+UBERON:0015795,right lung lobar bronchus epitheium,UBERON:0002339,epithelium of lobar bronchus
+NCBITaxon:10404,Hepadnaviridae,NCBITaxon:35268,Retro-transcribing viruses
+UBERON:0012327,pearly penile papule,UBERON:0014403,male anatomical structure
+UBERON:0001764,maxillary sinus,UBERON:0001825,paranasal sinus
+UBERON:0011929,postganglionic parasympathetic fiber,UBERON:0011924,postganglionic autonomic fiber
+DOID:2838,stress polycythemia,DOID:2834,acquired polycythemia
+HP:0100271,Hyponasal speech,HP:0001608,Abnormality of the voice
+UBERON:2002273,ctenoid scale,UBERON:0007380,dermal scale
+UBERON:0007352,stria vascularis vasculature,UBERON:0002200,vasculature of head
+DOID:5844,myocardial infarction,DOID:3393,coronary artery disease
+DOID:913,atrophic muscular disease,DOID:440,neuromuscular disease
+UBERON:0014892,skeletal muscle organ,UBERON:0001630,muscle organ
+HP:0011137,Non-pruritic urticaria,HP:0011276,Vascular skin abnormality
+UBERON:0001417,skin of neck,UBERON:0012180,head or neck skin
+UBERON:3010021,dorsal glands,UBERON:3010603,body gland
+HP:0005225,Intestinal edema,HP:0002242,Abnormality of the intestine
+DOID:5189,epithelial predominant Wilms' tumor,DOID:2154,nephroblastoma
+DOID:0060056,hypersensitivity reaction disease,DOID:2914,immune system disease
+HP:0008828,Delayed proximal femoral epiphyseal ossification,HP:0009107,Abnormal ossification involving the femoral head and neck
+UBERON:0006326,base of arytenoid,UBERON:0001994,hyaline cartilage tissue
+DOID:4283,anal margin basal cell carcinoma,DOID:4284,anal margin carcinoma
+UBERON:0010190,pair of dorsal aortae,UBERON:0000481,multi-tissue structure
+UBERON:0001581,depressor labii inferioris,UBERON:0004121,ectoderm-derived structure
+HP:0004377,Hematological neoplasm,HP:0011793,Neoplasm by anatomical site
+DOID:5744,ovary serous adenocarcinoma,DOID:3713,ovary adenocarcinoma
+DOID:4870,lacrimal gland adenoid cystic carcinoma,DOID:298,lacrimal gland adenocarcinoma
+DOID:0060216,Cogan syndrome,DOID:5614,eye disease
+HP:0005941,Intermittent hyperpnea at rest,HP:0004879,intermittent hyperventilation
+HP:0003388,Easy fatigability,HP:0012638,Abnormality of nervous system physiology
+HP:0002283,Global brain atrophy,HP:0012444,Brain atrophy
+HP:0001549,Abnormality of the ileum,HP:0002244,Abnormality of the small intestine
+UBERON:0003943,fourth lumbar dorsal root ganglion,UBERON:0002836,lumbar dorsal root ganglion
+UBERON:0002305,layer of hippocampus,UBERON:0004923,organ component layer
+HP:0000969,Edema,HP:0011032,Abnormality of fluid regulation
+UBERON:0010744,sacral vertebra pre-cartilage condensation,UBERON:0015010,sacral vertebra endochondral element
+HP:0010443,Bifid femur,HP:0002823,Abnormality of the femur
+UBERON:0005654,lower jaw molar epithelium,UBERON:0003236,epithelium of lower jaw
+UBERON:0005658,secondary palatal shelf epithelium,UBERON:0003235,epithelium of upper jaw
+HP:0000567,Chorioretinal coloboma,HP:0000532,Chorioretinal abnormality
+UBERON:3000716,acoelous,UBERON:0001075,vertebral centrum
+UBERON:3000341,optic fenestra,UBERON:3000051,braincase and otic capsule opening
+UBERON:0003726,thoracic nerve,UBERON:0001780,spinal nerve
+HP:0010090,Patchy sclerosis of the proximal phalanx of the hallux,HP:0010199,Patchy sclerosis of the middle phalanges of the toes
+UBERON:0003841,autopod joint,UBERON:0003657,limb joint
+DOID:1866,giant cell reparative granuloma,DOID:4305,bone giant cell tumor
+UBERON:0014899,anterolateral ligament of knee,UBERON:0011088,ligament of knee joint
+UBERON:2000803,myotome somite 18,UBERON:0003082,myotome
+DOID:6209,malignant mediastinum hemangiopericytoma,DOID:264,hemangiopericytoma
+HP:0001153,Septate vagina,HP:0000142,Abnormality of the vagina
+DOID:12128,pica disease,DOID:8670,eating disorder
+HP:0100501,Recurrent bronchiolitis,HP:0002837,Recurrent bronchitis
+UBERON:0001826,nasal cavity mucosa,UBERON:0000379,tracheal mucosa
+DOID:8857,lupus erythematosus,DOID:417,hypersensitivity reaction type II disease
+HP:0010381,Abnormality of the middle phalanx of the 4th toe,HP:0010183,Abnormality of the middle phalanges of the toes
+HP:0009238,Aplasia of the 5th finger,HP:0006262,Aplasia/Hypoplasia of the 5th finger
+HP:0010686,Low alkaline phosphatase of hepatic origin,HP:0010683,Low tissue non-specific alkaline phosphatase
+HP:0003911,Flared humeral metaphysis,HP:0003907,Abnormality of the humeral metaphyses
+HP:0009323,Cone-shaped epiphysis of the middle phalanx of the 3rd finger,HP:0010259,Cone-shaped epiphyses of the middle phalanges of the hand
+DOID:1785,pituitary cancer,DOID:170,endocrine gland cancer
+HP:0010071,Osteolytic defects of the 1st metatarsal,HP:0001473,Metatarsal osteolysis
+CL:0002605,astrocyte of the cerebral cortex,CL:1001579,cerebral cortex glial cell
+UBERON:0006606,mandibular symphysis,UBERON:0004121,ectoderm-derived structure
+HP:0006233,Osteoarthritis of the distal interphalangeal joint,HP:0004268,Osteoarthritis of the small joints of the hand
+UBERON:0001564,mylohyoid muscle,UBERON:0008571,suprahyoid muscle
+HP:0012155,Decreased corneal sensation,HP:0000481,Abnormality of the cornea
+UBERON:2007034,forebrain neural rod,UBERON:0004121,ectoderm-derived structure
+CL:0005010,renal intercalated cell,CL:0002078,meso-epithelial cell
+HP:0010511,Long toe,HP:0001780,Abnormality of toe
+HP:0100127,Irregular epiphysis of the proximal phalanx of the 2nd toe,HP:0100049,Irregular epiphyses of the 2nd toe
+HP:0003250,Aplasia of the vagina,HP:0011026,Aplasia/Hypoplasia of the vagina
+HP:0009155,Cone-shaped epiphysis of the proximal phalanx of the 5th finger,HP:0009153,Abnormality of the epiphysis of the proximal phalanx of the 5th finger
+HP:0012581,Solitary renal cyst,HP:0000107,Renal cyst
+HP:0000534,Abnormality of the eyebrow,HP:0000606,Abnormality of the periorbital region
+UBERON:0010902,tibiotarsus cartilage element,UBERON:0015011,tibiotarsus endochondral element
+UBERON:0001552,kidney arcuate artery,UBERON:0001637,artery
+HP:0010092,Triangular shaped proximal phalanx of the hallux,HP:0010065,Triangular shaped phalanges of the hallux
+UBERON:3010130,taenia tecti transversalis,UBERON:0003932,cartilage element of chondrocranium
+HP:0012477,Vocal tremor,HP:0001337,Tremor
+UBERON:0010046,entire pharyngeal arch associated mesenchyme,UBERON:0007524,dense mesenchyme tissue
+UBERON:0003939,transverse gyrus of Heschl,UBERON:0000200,gyrus
+UBERON:0001029,neuromuscular junction,UBERON:0000477,anatomical cluster
+UBERON:0011246,procoracoid bone,UBERON:0002513,endochondral bone
+DOID:5696,larynx liposarcoma,DOID:3382,liposarcoma
+UBERON:2001520,ceratobranchial 1 cartilage,UBERON:2001899,ceratobranchial 1 element
+UBERON:0013166,vallecula of cerebellum,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002006,cortex of lymph node,UBERON:0001851,cortex
+HP:0006471,Fixed elbow flexion,HP:0005060,limited elbow flexion/extension
+UBERON:0003012,flocculonodular lobe,UBERON:0005293,cerebellum lobe
+UBERON:0010028,ventral part of pharyngeal pouch 4,UBERON:0000490,unilaminar epithelium
+HP:0006118,Shortening of all distal phalanges of the fingers,HP:0009882,Short distal phalanx of finger
+HP:0100158,Bracket epiphysis of the proximal phalanx of the 3rd toe,HP:0100093,Abnormality of the epiphysis of the proximal phalanx of the 3rd toe
+HP:0011742,Ectopic adrenal gland,HP:0011732,Abnormality of adrenal morphology
+UBERON:0011770,mentomeckelian,UBERON:0002513,endochondral bone
+UBERON:0012326,gubernacular bulb,UBERON:0005423,developing anatomical structure
+UBERON:2002127,myorhabdoid bone,UBERON:2000526,intermuscular bone
+HP:0005632,Absent forearm,HP:0003953,Absent ossification/absent forearm bones
+UBERON:0010210,blood clot,UBERON:0000463,portion of organism substance
+HP:0010038,Short 2nd metacarpal,HP:0010036,Aplasia/Hypoplasia of the 2nd metacarpal
+UBERON:0002870,dorsal motor nucleus of vagus nerve,UBERON:0007635,nucleus of medulla oblongata
+UBERON:0009919,ureter smooth muscle,UBERON:0006554,urinary system structure
+HP:0000484,Hyperopic astigmatism,HP:0000483,Astigmatism
+HP:0010234,Ivory epiphyses of the phalanges of the hand,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+UBERON:0015054,iliac endochondral element,UBERON:0004120,mesoderm-derived structure
+UBERON:0003342,mucosa of anal canal,UBERON:0001207,mucosa of large intestine
+DOID:730,urethral benign neoplasm,DOID:731,urinary system benign neoplasm
+DOID:2365,West Nile encephalitis,DOID:934,viral infectious disease
+HP:0001730,Progressive hearing impairment,HP:0000365,Hearing impairment
+DOID:3137,multiple symmetrical lipomatosis,DOID:37,skin disease
+HP:0009168,Bullet-shaped middle phalanx of the 5th finger,HP:0009845,Bullet-shaped middle phalanges of the hand
+UBERON:0000412,dermal papilla,UBERON:0004121,ectoderm-derived structure
+UBERON:0004326,middle phalanx of pedal digit 4,UBERON:0003862,pedal digit 4 phalanx
+DOID:0050684,Bowen-Conradi syndrome,DOID:0050737,autosomal recessive disease
+HP:0010274,Ivory epiphyses of the proximal phalanges of the hand,HP:0010234,Ivory epiphyses of the phalanges of the hand
+HP:0100142,Pseudoepiphysis of the distal phalanx of the 3rd toe,HP:0100062,Pseudoepiphyses of the 3rd toe
+HP:0010744,Absent metatarsal bone,HP:0001964,Aplasia/Hypoplasia of metatarsal bones
+HP:0006467,Limited shoulder movement,HP:0001376,Limitation of joint mobility
+CL:1001586,mammary gland glandular cell,CL:0002327,mammary gland epithelial cell
+HP:0001586,Vesicovaginal fistula,HP:0004320,Vaginal fistula
+HP:0004329,Abnormality of the posterior segment of the eye,HP:0012374,Abnormality of the globe
+UBERON:2000646,anal fin distal radial bone,UBERON:2100646,anal fin distal radial element
+UBERON:0000201,endothelial blood brain barrier,UBERON:0000120,blood brain barrier
+DOID:1176,bronchial disease,DOID:0050161,lower respiratory tract disease
+UBERON:0003679,mouth floor,UBERON:0004121,ectoderm-derived structure
+UBERON:0003579,shoulder connective tissue,UBERON:0002384,connective tissue
+HP:0000721,Lack of spontaneous play,HP:0100851,Abnormal emotion/affect behavior
+UBERON:0010994,coronoid process of ulna,UBERON:0004120,mesoderm-derived structure
+HP:0007509,Patchy hypo- and hyperpigmentation,HP:0009123,Mixed hypo- and hyperpigmentation of the skin
+UBERON:0003010,lateral pes lemniscus,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0014753,P3 area of pallium (Myxiniformes),UBERON:0002791,regional part of telencephalon
+HP:0007035,Anterior encephalocele,HP:0002084,Encephalocele
+CL:0000077,mesothelial cell,CL:0000076,squamous epithelial cell
+DOID:501,central nervous system hemangioma,DOID:502,central nervous system mesenchymal non-meningothelial tumor
+HP:0010660,Abnormal hand bone ossification,HP:0011849,Abnormal bone ossification
+UBERON:0004861,right lung alveolus,UBERON:0002299,alveolus of lung
+DOID:0050775,schneckenbecken dysplasia,DOID:2256,osteochondrodysplasia
+UBERON:0014783,cloacal muscle,UBERON:0001630,muscle organ
+UBERON:0014951,proisocortex,UBERON:0002619,regional part of cerebral cortex
+HP:0100264,Proximal symphalangism,HP:0100262,Synostosis involving digits
+HP:0010371,Aplasia/Hypoplasia of the phalanges of the 4th toe,HP:0010336,Abnormality of the phalanges of the 4th toe
+UBERON:4200053,diphycercal tail,UBERON:4000164,caudal fin
+UBERON:0004416,proximal epiphysis of metacarpal bone,UBERON:0004380,proximal epiphysis
+HP:0008694,Hypertrophic labia minora,HP:0000058,Abnormality of the labia
+HP:0002021,Pyloric stenosis,HP:0004400,Abnormality of the pylorus
+HP:0008401,Onychogryposis of toenails,HP:0001805,Thick nail
+DOID:13223,uterine fibroid,DOID:0060095,uterine benign neoplasm
+NCBITaxon:624,Shigella sonnei,NCBITaxon:620,Shigella
+DOID:3664,mast cell neoplasm,DOID:2531,hematologic cancer
+UBERON:0004756,dermal skeletal element,UBERON:0004121,ectoderm-derived structure
+UBERON:0003702,inguinal canal,UBERON:0004111,anatomical conduit
+UBERON:3010796,ramus supraotic,UBERON:3010126,middle lateral line nerve (MLLN)
+DOID:1357,maxillary sinus cancer,DOID:0050619,paranasal sinus cancer
+UBERON:0004734,gastrula,UBERON:0000922,embryo
+HP:0003341,Junctional split,HP:0008066,Abnormal blistering of the skin
+DOID:0050628,advanced sleep phase syndrome,DOID:535,sleep disorder
+UBERON:0005411,bony otic capsule,UBERON:0002481,bone tissue
+UBERON:4200102,median dorsal plate,UBERON:0008907,dermal bone
+UBERON:0001804,capsule of lens,UBERON:0003893,capsule
+UBERON:0002026,stratum spinosum of epidermis,UBERON:0013754,integumentary system layer
+UBERON:0006652,muscular layer of vagina,UBERON:0006660,muscle layer
+HP:0007166,Paroxysmal dyskinesia,HP:0004305,Involuntary movements
+HP:0003785,Decreased CSF homovanillic acid (HVA),HP:0002921,Abnormality of the cerebrospinal fluid
+DOID:3896,hidradenoma,DOID:2664,sweat gland neoplasm
+UBERON:0011255,Eimer's organ,UBERON:0004120,mesoderm-derived structure
+UBERON:3000051,braincase and otic capsule opening,UBERON:3000050,braincase and auditory apparatus
+CL:0000217,insulating cell,CL:0000215,barrier cell
+UBERON:0011827,areolar gland,UBERON:0005398,female reproductive gland
+UBERON:0010544,metacarpus skeleton,UBERON:0015042,manual digit metacarpus endochondral element
+HP:0009381,Short finger,HP:0011927,Short digit
+UBERON:0007266,intervertebral disk of atlas,UBERON:0007252,intervertebral disk of cervical vertebra
+HP:0001533,Slender build,HP:0000098,Tall stature
+UBERON:2001866,basibranchial 5 cartilage,UBERON:0013747,basibranchial cartilage
+HP:0010147,Stippling of the epiphysis of the distal phalanx of the hallux,HP:0010122,Stippling of the epiphyses of the hallux
+DOID:6959,rectal cloacogenic carcinoma,DOID:5528,rectum squamous cell carcinoma
+HP:0008392,Subungual hyperkeratosis,HP:0000962,Hyperkeratosis
+HP:0012549,Conjunctival lipoma,HP:0000502,Abnormality of the conjunctiva
+HP:0000012,Urinary urgency,HP:0000009,Functional abnormality of the bladder
+CL:0002285,type III taste bud cell,CL:0000209,taste receptor cell
+UBERON:3000663,parahyoid,UBERON:0002513,endochondral bone
+UBERON:0005452,hepatic cord,UBERON:0004119,endoderm-derived structure
+NCBITaxon:565302,Human adenovirus B1,NCBITaxon:108098,Human adenovirus B
+HP:0005684,Distal arthrogryposis,HP:0002803,Congenital contracture
+UBERON:0005114,metanephric ascending thin limb,UBERON:0005146,metanephric nephron tubule
+HP:0001560,Abnormality of the amniotic fluid,HP:0001197,Abnormality of prenatal development or birth
+DOID:12424,thyrocalcitonin secretion disease,DOID:50,thyroid gland disease
+HP:0010207,Osteolytic defects of the proximal phalanges of the toes,HP:0010184,Abnormality of the proximal phalanges of the toes
+UBERON:0004893,interalveolar septum,UBERON:0004119,endoderm-derived structure
+UBERON:0010215,arytenoid swellings,UBERON:0005856,developing mesenchymal condensation
+HP:0012182,Oropharyngeal squamous cell carcinoma,HP:0002860,Squamous cell carcinoma
+HP:0002529,Neuronal loss in central nervous system,HP:0007367,Atrophy/Degeneration affecting the central nervous system
+UBERON:0006857,interrenal primordium,UBERON:0001048,primordium
+DOID:7972,lymphoma-like variant infiltrating bladder urothelial carcinoma,DOID:6477,invasive bladder transitional cell carcinoma
+UBERON:3010827,anterior prenasal cartilage,UBERON:0010313,neural crest-derived structure
+UBERON:0015851,upper right incisor tusk,UBERON:0015848,incisor tusk
+HP:0005621,Trapezoidal shaped vertebral bodies,HP:0003312,Abnormal form of the vertebral bodies
+UBERON:2001896,hypobranchial 3 element,UBERON:2001893,hypobranchial element
+HP:0012634,Iris pigment dispersion,HP:0008034,Abnormal iris pigmentation
+HP:0009926,Increased lacrimation,HP:0000632,Lacrimation abnormality
+DOID:13919,irregular astigmatism,DOID:11782,astigmatism
+UBERON:0003585,dermis connective tissue,UBERON:0010313,neural crest-derived structure
+UBERON:0005515,rhombomere 5,UBERON:0001892,rhombomere
+UBERON:2001146,tooth 1MD,UBERON:2000694,ceratobranchial 5 tooth
+HP:0012122,Anterior uveitis,HP:0000554,Uveitis
+DOID:6386,childhood brainstem astrocytoma,DOID:6383,childhood brain stem glioma
+UBERON:0006314,bodily fluid,UBERON:0000463,portion of organism substance
+UBERON:0002207,xiphoid process,UBERON:4100000,skeletal element projection
+UBERON:0005334,oral lamina propria,UBERON:0000030,lamina propria
+UBERON:0007381,epidermal scale,UBERON:0002542,scale
+DOID:2533,splenic infarction,DOID:2529,splenic disease
+UBERON:0004335,proximal phalanx of pedal digit 4,UBERON:0014504,proximal phalanx of digit 4
+HP:0000067,"Urethral atresia, female",HP:0000068,Urethral atresia
+CL:1000347,vacuolar absorptive cell of epithelium of colon,CL:0011108,colon epithelial cell
+HP:0010720,Abnormal hair pattern,HP:0001595,Abnormality of the hair
+HP:0007293,Anterior sacral meningocele,HP:0005765,Sacral meningocele
+HP:0008114,Metatarsal diaphyseal endosteal sclerosis,HP:0000940,Abnormal diaphysis morphology
+UBERON:0001650,hypoglossal nerve,UBERON:0001785,cranial nerve
+HP:0002815,Abnormality of the knees,HP:0100491,Abnormality of the joints of the lower limbs
+HP:0004218,Symphalangism of the 5th finger,HP:0009700,Synostosis involving bones of the fingers
+UBERON:0003257,yolk sac endoderm,UBERON:0000478,extraembryonic structure
+HP:0012514,Lower limb pain,HP:0009763,Limb pain
+UBERON:0004408,distal epiphysis of ulna,UBERON:0004379,distal epiphysis
+CL:0000408,male gamete,CL:0000015,male germ cell
+HP:0100481,Proximal/middle symphalangism of 4th toe,HP:0100474,Symphalangism affecting the proximal phalanx of the 4th toe
+HP:0000659,Peters anomaly,HP:0007700,Anterior segment dysgenesis
+UBERON:0002335,macula densa,UBERON:0006554,urinary system structure
+HP:0012731,Ectopic anterior pituitary gland,HP:0011747,Abnormality of the anterior pituitary
+CL:0011110,histaminergic neuron,CL:0011112,magnocellular neurosecretory cell
+UBERON:0006127,funiculus of spinal cord,UBERON:0006080,segment of white matter of spinal cord
+HP:0010596,Abnormality of the proximal radial epiphysis,HP:0003999,Abnormality of radial epiphyses
+HP:0011067,Mesiodens,HP:0011069,Increased number of teeth
+HP:0010655,Epiphyseal stippling,HP:0005930,Abnormality of the epiphyses
+HP:0100670,Rough bone trabeculation,HP:0100671,Abnormal trabecular bone morphology
+UBERON:0007308,pronephric distal early tubule,UBERON:0006337,distal early tubule
+DOID:14131,midline cystocele,DOID:1284,prolapse of female genital organ
+UBERON:0000925,endoderm,UBERON:0000923,germ layer
+UBERON:0003329,submucosa of anal canal,UBERON:0004121,ectoderm-derived structure
+DOID:12577,urethral obstruction,DOID:732,urethral disease
+HP:0000056,Abnormality of the clitoris,HP:0000055,Abnormality of female external genitalia
+UBERON:0007196,tracheobronchial tree,UBERON:0004119,endoderm-derived structure
+CL:0002583,subcutaneous preadipocyte,CL:0002334,preadipocyte
+UBERON:0011590,commissure of diencephalon,UBERON:0011591,tract of diencephalon
+DOID:12704,ataxia telangiectasia,DOID:0050737,autosomal recessive disease
+HP:0009260,Triangular epiphysis of the distal phalanx of the 4th finger,HP:0009403,Triangular epiphyses of the 4th finger
+NCBITaxon:862507,"Mus <mouse, subgenus>",NCBITaxon:10088,"Mus <mouse, genus>"
+HP:0009451,Bullet-shaped proximal phalanx of the 3rd finger,HP:0009441,Bullet-shaped phalanges of the 3rd finger
+HP:0012321,D-2-hydroxyglutaric aciduria,HP:0003215,Dicarboxylic aciduria
+UBERON:0001403,longissimus capitis,UBERON:0000392,longissimus muscle
+HP:0002753,Thin bony cortex,HP:0003103,Abnormal cortical bone morphology
+HP:0010624,Aplastic/hypoplastic toenail,HP:0008386,Aplasia/Hypoplasia of the nails
+HP:0010065,Triangular shaped phalanges of the hallux,HP:0010180,Triangular shaped phalanges of the toes
+UBERON:0015119,scolex,UBERON:0000062,organ
+HP:0001874,Abnormality of neutrophils,HP:0001911,Abnormality of granulocytes
+HP:0005157,Concentric hypertrophic cardiomyopathy,HP:0001639,Hypertrophic cardiomyopathy
+DOID:6054,frontal sinus Schneiderian papilloma,DOID:1361,frontal sinus neoplasm
+UBERON:0004427,proximal epiphysis of first metatarsal bone,UBERON:0004415,proximal epiphysis of metatarsal bone
+HP:0002650,Scoliosis,HP:0010674,Abnormality of the curvature of the vertebral column
+DOID:10567,late yaws,DOID:37,skin disease
+HP:0011090,Fused teeth,HP:0011089,Double tooth
+UBERON:2005067,bulbus arteriosus middle layer,UBERON:0004120,mesoderm-derived structure
+UBERON:0006859,swim bladder bud,UBERON:0005423,developing anatomical structure
+DOID:12721,multiple epiphyseal dysplasia,DOID:2256,osteochondrodysplasia
+DOID:12286,testicular leukemia,DOID:2998,testicular cancer
+UBERON:0001684,mandible,UBERON:0002514,intramembranous bone
+DOID:9207,periodic limb movement disorder,DOID:535,sleep disorder
+UBERON:0004324,middle phalanx of pedal digit 2,UBERON:0003866,middle phalanx of pes
+UBERON:0010252,1st arch mandibular mesenchyme from neural crest,UBERON:0010259,1st arch mesenchyme from neural crest
+DOID:5370,breast hemangiopericytoma,DOID:3017,breast sarcoma
+HP:0010436,Aplasia of the proximal phalanx of the 2nd toe,HP:0010395,Aplasia/Hypoplasia of the proximal phalanx of the 2nd toe
+HP:0100374,Aplasia/Hypoplasia of the middle phalanx of the 5th toe,HP:0010343,Aplasia/Hypoplasia of the 5th toe
+DOID:13593,eclampsia,DOID:10591,pre-eclampsia
+HP:0000812,Abnormal internal genitalia,HP:0012243,Abnormal genital system morphology
+HP:0001949,Hypokalemic alkalosis,HP:0001948,Alkalosis
+DOID:2479,central nervous system origin vertigo,DOID:3426,vestibular disease
+CL:0002546,embryonic blood vessel endothelial progenitor cell,CL:0002371,somatic cell
+UBERON:3000792,anterior ramus of cleithrum,UBERON:4100000,skeletal element projection
+HP:0010379,Duplication of phalanx of the 4th toe,HP:0010181,Duplication of phalanx of toe
+DOID:709,splenic manifestation of hairy cell leukemia,DOID:710,splenic manifestation of leukemia
+HP:0004453,Overfolding of the superior helices,HP:0000396,Overfolded helix
+UBERON:0005565,facio-acoustic neural crest,UBERON:0007530,migrating mesenchyme population
+UBERON:0003201,exocuticle,UBERON:0000476,acellular anatomical structure
+DOID:8448,intestinal impaction,DOID:8437,intestinal obstruction
+DOID:9840,esotropia,DOID:540,strabismus
+CL:0002164,external pillar cell of cochlea,CL:1000191,pillar cell
+DOID:10590,mild pre-eclampsia,DOID:10591,pre-eclampsia
+HP:0002200,Pseudobulbar signs,HP:0002011,Abnormality of the central nervous system
+DOID:0050383,typhoidal tularemia,DOID:2123,tularemia
+UBERON:0005454,internal oblique,UBERON:0003897,axial muscle
+UBERON:0004526,cardiac muscle tissue of trabecula carnea of left ventricle,UBERON:0003452,trabecula carnea cardiac muscle tissue
+UBERON:0004503,skeletal muscle tissue of digastric,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002966,regional part of midbrain tectum,UBERON:0002950,regional part of midbrain
+UBERON:0006920,esophagus squamous epithelium,UBERON:0001976,epithelium of esophagus
+HP:0009426,Distal/middle symphalangism of 3rd finger,HP:0009357,Abnormality of the distal phalanx of the 3rd finger
+UBERON:0015130,connective tissue of prostate,UBERON:0005156,reproductive structure
+UBERON:0004789,larynx mucous gland,UBERON:0000414,mucous gland
+HP:0010023,Small epiphysis of the 1st metacarpal,HP:0010014,Abnormality of the epiphysis of the 1st metacarpal
+UBERON:0007522,striated muscle sphincter,UBERON:0002036,striated muscle tissue
+UBERON:4000109,mineralized hyaline cartilage tissue,UBERON:4000088,mineralized cartilage tissue
+UBERON:0003559,hindbrain arachnoid mater,UBERON:0003291,meninx of hindbrain
+UBERON:0005173,abdominal segment organ,UBERON:0005177,trunk organ
+UBERON:0002373,palatine tonsil,UBERON:0002372,tonsil
+DOID:501,central nervous system hemangioma,DOID:255,hemangioma
+CL:0000662,neuroglioblast (sensu Nematoda),CL:0000468,neuroglioblast
+UBERON:0008926,sublaminar layer S5,UBERON:0008929,sublaminar layers S4 or S5
+HP:0009278,Ulnar deviation of the 4th finger,HP:0009465,Ulnar deviation of finger
+UBERON:0011187,greater tubercle of humerus,UBERON:0004120,mesoderm-derived structure
+HP:0003213,Deficient excision of UV-induced pyrimidine dimers in DNA,HP:0003254,Abnormality of DNA repair
+CL:0002076,endo-epithelial cell,CL:0000066,epithelial cell
+CL:0001055,"CD14-positive, CD16-low monocyte",CL:0002393,intermediate monocyte
+HP:0005512,Impaired neutrophil killing of staphylococci,HP:0011993,Impaired neutrophil bactericidal activity
+HP:0003621,Juvenile onset,HP:0011007,Age of onset
+HP:0005528,Bone marrow hypocellularity,HP:0012145,Abnormality of multiple cell lineages in the bone marrow
+HP:0009154,Triangular epiphysis of the proximal phalanx of the 5th finger,HP:0009153,Abnormality of the epiphysis of the proximal phalanx of the 5th finger
+UBERON:0009601,mesenchyme of interdigital region of pes,UBERON:0009585,interdigital region mesenchyme
+HP:0100044,Absent epiphyses of the 2nd toe,HP:0010162,Absent epiphyses of the toes
+CL:0007018,epidermal ciliary cell,CL:0002321,embryonic cell
+HP:0002974,Radioulnar synostosis,HP:0002818,Abnormality of the radius
+UBERON:0002495,long bone,UBERON:0001474,bone element
+UBERON:0004804,oviduct epithelium,UBERON:0012275,meso-epithelium
+DOID:5260,colon sarcoma,DOID:219,colon cancer
+HP:0010406,Bullet-shaped middle phalanx of the 2nd toe,HP:0010357,Abnormality of the middle phalanx of the 2nd toe
+UBERON:0004046,anterior definitive endoderm,UBERON:0000089,hypoblast (generic)
+HP:0002461,Dense calcifications in the cerebellar dentate nucleus,HP:0100321,Abnormality of the dentate nucleus
+UBERON:2000988,hypaxial region somite 5,UBERON:0003895,hypaxial myotome region
+UBERON:0011696,left extraembryonic umbilical artery,UBERON:0011693,extraembryonic portion of umbilical artery
+HP:0007899,Retinal nonattachment,HP:0000541,Retinal detachment
+CL:0002099,type I cell of adrenal cortex,CL:0002097,cortical cell of adrenal gland
+UBERON:0003598,manus connective tissue,UBERON:0003588,forelimb connective tissue
+UBERON:0005199,cervical mammary gland,UBERON:0001911,mammary gland
+UBERON:0012343,navicular bursa of pes,UBERON:0012334,navicular bursa
+UBERON:0010569,manual digit 5 metacarpus pre-cartilage condensation,UBERON:0010698,manual digit metacarpus pre-cartilage condensation
+UBERON:0010582,pedal digit 3 phalanx pre-cartilage condensation,UBERON:0015033,pedal digit 3 phalanx endochondral element
+UBERON:2100646,anal fin distal radial element,UBERON:2101671,anal fin radial element
+HP:0010364,Patchy sclerosis of the phalanges of the 3rd toe,HP:0010178,Patchy sclerosis of the phalanges of the toes
+HP:0006487,Bowing of the long bones,HP:0011314,Abnormality of long bone morphology
+UBERON:0004344,cardinal vein,UBERON:0002050,embryonic structure
+HP:0009534,Triangular epiphysis of the proximal phalanx of the 2nd finger,HP:0010278,Triangular epiphyses of the proximal phalanges of the hand
+HP:0000487,Congenital strabismus,HP:0000486,Strabismus
+UBERON:2002199,hindbrain commissure,UBERON:0003544,brain white matter
+DOID:6871,spinal cord neuroblastoma,DOID:6872,spinal cord primitive neuroectodermal neoplasm
+HP:0008828,Delayed proximal femoral epiphyseal ossification,HP:0002663,Delayed epiphyseal ossification
+HP:0100463,Patchy sclerosis of the middle phalanx of the 5th toe,HP:0100938,Sclerosis of the middle phalanx of the 5th toe
+CL:0000170,glucagon secreting cell,CL:0000167,peptide hormone secreting cell
+UBERON:0003923,dorsal pancreatic bud,UBERON:0003922,pancreatic bud
+DOID:3007,breast ductal carcinoma,DOID:3459,breast carcinoma
+HP:0009130,Hand muscle atrophy,HP:0001421,Abnormality of the musculature of the hand
+UBERON:3000822,pars suprascapularis,UBERON:0000064,organ part
+DOID:3355,fibrosarcoma,DOID:201,connective tissue cancer
+HP:0003694,Late-onset proximal muscle weakness,HP:0003701,Proximal muscle weakness
+UBERON:0013672,priapium,UBERON:0008811,intromittent organ
+UBERON:0014591,anterior nucleus of hypothalamus posterior part,UBERON:0002784,regional part of diencephalon
+UBERON:0003463,trunk bone,UBERON:0001474,bone element
+HP:0012418,Hypoxemia,HP:0012415,Abnormal blood gas level
+UBERON:0006217,cloacal membrane,UBERON:0006554,urinary system structure
+HP:0011501,Anterior lenticonus,HP:0001142,Lenticonus
+HP:0010743,Short metatarsal,HP:0001964,Aplasia/Hypoplasia of metatarsal bones
+HP:0100267,Lip pit,HP:0100276,Skin pits
+UBERON:0003832,esophagus muscle,UBERON:0003830,thoracic segment muscle
+UBERON:0005565,facio-acoustic neural crest,UBERON:0007213,mesenchyme derived from head neural crest
+HP:0100037,Abnormality of the scalp hair,HP:0001595,Abnormality of the hair
+UBERON:0006262,malleus pre-cartilage condensation,UBERON:0014387,mesenchyme derived from neural crest
+UBERON:0013616,primary molar tooth,UBERON:0007115,deciduous tooth
+UBERON:0005429,dorsal pancreatic duct,UBERON:0007329,pancreatic duct
+HP:0009339,Fragmentation of the epiphysis of the distal phalanx of the 3rd finger,HP:0010250,Fragmentation of the epiphyses of the distal phalanges of the hand
+UBERON:0003505,trachea blood vessel,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0006647,Congenital microthorax,HP:0005257,Thoracic hypoplasia
+UBERON:0002692,medullary raphe nuclear complex,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:6721,littre gland carcinoma,DOID:3856,male reproductive organ cancer
+UBERON:0005127,metanephric thick ascending limb,UBERON:0001291,thick ascending limb of loop of Henle
+UBERON:2102028,pectoral fin proximal radial element 3,UBERON:2101587,pectoral fin proximal radial element
+DOID:13404,uveoparotid fever,DOID:11335,sarcoidosis
+CL:0000755,type 3 cone bipolar cell (sensu Mus),CL:0000752,cone retinal bipolar cell
+HP:0011456,Absent stapes,HP:0008628,Abnormality of the stapes
+CL:0001050,"effector CD8-positive, alpha-beta T cell",CL:0000911,effector T cell
+HP:0000211,Trismus,HP:0000277,Abnormality of the mandible
+HP:0005219,Absence of intrinsic factor,HP:0002577,Abnormality of the stomach
+UBERON:3000779,pectoral fenestra,UBERON:3000755,pectoral girdle opening
+HP:0011979,Elevated urinary dopamine,HP:0011976,Elevated urinary catecholamines
+UBERON:0013277,remnant of processus vaginalis,UBERON:0005156,reproductive structure
+UBERON:2001688,palatine cartilage,UBERON:0011004,pharyngeal arch cartilage
+HP:0002751,Kyphoscoliosis,HP:0002650,Scoliosis
+DOID:10972,salpingo-oophoritis,DOID:5733,salpingitis
+UBERON:0010929,stapedius pre-muscle condensation,UBERON:0005865,pre-muscle condensation
+HP:0100299,Muscle fiber inclusion bodies,HP:0004303,Abnormality of muscle fibers
+HP:0009211,Small epiphysis of the middle phalanx of the 5th finger,HP:0009390,Small epiphyses of the 5th finger
+UBERON:0009478,associated mesenchyme of midgut,UBERON:0007524,dense mesenchyme tissue
+CL:0002421,nucleated reticulocyte,CL:0002242,nucleate cell
+HP:0011159,Epigastric auras,HP:0011157,Auras
+HP:0003103,Abnormal cortical bone morphology,HP:0003330,Abnormal bone structure
+HP:0200029,Vasculitis in the skin,HP:0011276,Vascular skin abnormality
+UBERON:0010745,sacral vertebra cartilage element,UBERON:2001457,postcranial axial cartilage
+HP:0010204,Broad proximal phalanges of the toes,HP:0010184,Abnormality of the proximal phalanges of the toes
+HP:0012288,Neoplasm of head and neck,HP:0011793,Neoplasm by anatomical site
+UBERON:4200027,supraglenoid buttress,UBERON:0004530,bony projection
+UBERON:0015350,saphenous artery,UBERON:0001637,artery
+UBERON:0006640,crus of clitoris,UBERON:0000064,organ part
+UBERON:0004877,visceral endoderm,UBERON:0004119,endoderm-derived structure
+HP:0002629,Gastrointestinal arteriovenous malformation,HP:0100026,Arteriovenous malformation
+UBERON:0002446,patella,UBERON:0005893,leg bone
+UBERON:2007040,forebrain midbrain boundary neural tube,UBERON:0006800,anatomical line
+HP:0100192,Bracket epiphysis of the proximal phalanx of the 4th toe,HP:0100067,Bracket epiphyses of the 4th toe
+UBERON:3000115,crista lateralis of premaxilla,UBERON:0004120,mesoderm-derived structure
+UBERON:0004871,somatic layer of lateral plate mesoderm,UBERON:0005423,developing anatomical structure
+HP:0011805,Abnormality of muscle morphology,HP:0003011,Abnormality of the musculature
+DOID:11034,contact lens corneal edema,DOID:11030,corneal edema
+UBERON:0007688,anlage,UBERON:0000479,tissue
+UBERON:3000451,posterior ramus of pterygoid,UBERON:0005913,zone of bone organ
+HP:0001976,Reduced antithrombin III activity,HP:0003256,Abnormality of the coagulation cascade
+UBERON:0004179,prostate glandular acinus,UBERON:0009842,acinus
+UBERON:0007378,egg yolk,UBERON:0002050,embryonic structure
+HP:0009633,Osteolytic defects of the proximal phalanx of the thumb,HP:0009847,Osteolytic defects of the middle phalanges of the hand
+HP:0100349,Contractures of the proximal interphalangeal joint of the 3rd toe,HP:0010333,Flexion contracture of 3rd toe
+HP:0006758,Malignant genitourinary tract tumor,HP:0007379,Neoplasm of the genitourinary tract
+UBERON:0002678,regional part of medulla oblongata,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0000041,odontode scale,UBERON:0007380,dermal scale
+HP:0011091,Gemination,HP:0011089,Double tooth
+HP:0001862,Acral ulceration and osteomyelitis leading to autoamputation of the digits (feet),HP:0001868,Autoamputation (feet)
+UBERON:2002232,presumptive cardiac ventricle primitive heart tube,UBERON:0000481,multi-tissue structure
+HP:0010355,Duplication of the phalanges of the 2nd toe,HP:0010324,Abnormality of phalanx of the 2nd toe
+HP:0004581,Increased anterior vertebral height,HP:0004570,Increased vertebral height
+UBERON:0003249,epithelium of otic placode,UBERON:0005291,embryonic tissue
+DOID:4257,Caffey disease,DOID:3342,bone inflammation disease
+HP:0009173,Curved middle phalanx of the 5th finger,HP:0004219,Abnormality of the middle phalanx of the 5th finger
+UBERON:0005492,hyaloid vessel,UBERON:0003496,head blood vessel
+UBERON:0005310,pronephric nephron tubule,UBERON:0012275,meso-epithelium
+UBERON:0012081,patella pre-cartilage condensation,UBERON:0010882,limb bone pre-cartilage condensation
+HP:0009729,Cardiac rhabdomyoma,HP:0009730,Rhabdomyoma
+UBERON:0002704,metathalamus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0015432,accessory olfactory bulb mitral cell layer,UBERON:0004001,olfactory bulb layer
+UBERON:0002352,atrioventricular node,UBERON:0004493,cardiac muscle tissue of myocardium
+HP:0011608,Type II truncus arteriosus,HP:0001660,Truncus arteriosus
+UBERON:0011770,mentomeckelian,UBERON:0004768,bone of lower jaw
+NCBITaxon:10294,Simplexvirus,NCBITaxon:10293,Alphaherpesvirinae
+HP:0007950,Peripapillary chorioretinal atrophy,HP:0000533,Chorioretinal atrophy
+HP:0005505,Refractory anemia,HP:0001903,Anemia
+UBERON:0004906,ectodermal part of digestive tract,UBERON:0004121,ectoderm-derived structure
+DOID:1414,ovarian dysfunction,DOID:1100,ovarian disease
+UBERON:2001589,propterygium cartilage,UBERON:4300083,propterygium element
+UBERON:0011984,pedal digit 6,UBERON:0001466,pedal digit
+DOID:6559,ethmoid sinus Schneiderian papilloma,DOID:1364,ethmoidal sinus neoplasm
+HP:0008249,Thyroid hyperplasia,HP:0011772,Abnormality of thyroid morphology
+UBERON:4200044,articular surface for the calcaneum on the astragalus,UBERON:4100003,articular surface
+DOID:5207,monodermal teratoma,DOID:5563,malignant teratoma
+UBERON:0004601,rib 1,UBERON:0002228,rib
+UBERON:2000362,hypaxialis,UBERON:0001774,muscle of trunk
+HP:0100594,Esophageal web,HP:0002031,Abnormality of the esophagus
+UBERON:0007367,surface of tongue,UBERON:0006984,anatomical surface
+UBERON:0002781,caudal part of ventral posterolateral nucleus of thalamus,UBERON:0003528,brain grey matter
+HP:0003275,Narrow pelvis,HP:0002644,Abnormality of pelvic girdle bone morphology
+DOID:0050702,neonatal period electroclinical syndrome,DOID:0050701,electroclinical syndrome
+UBERON:0002595,orbital sulcus,UBERON:0003022,cerebral cortex lobe
+HP:0012619,Multiple bladder diverticula,HP:0000015,Bladder diverticulum
+DOID:13453,gonococcal bursitis,DOID:2965,bursitis
+UBERON:0004642,third ventricle ependyma,UBERON:0005357,brain ependyma
+UBERON:0006496,external acoustic meatus osseus part,UBERON:0000477,anatomical cluster
+UBERON:0004406,distal epiphysis of femur,UBERON:0004379,distal epiphysis
+UBERON:0014712,carapacial ridge ectoderm,UBERON:0010371,ecto-epithelium
+CL:0000847,ciliated olfactory receptor neuron,CL:0000207,olfactory receptor cell
+UBERON:0010378,mesenchyme from splanchnopleure,UBERON:0007524,dense mesenchyme tissue
+HP:0010337,Aplasia/Hypoplasia of the 4th toe,HP:0010321,Abnormality of the 4th toe
+UBERON:3000774,ilial shaft,UBERON:0004120,mesoderm-derived structure
+DOID:13072,acquired hyperkeratosis,DOID:161,keratosis
+UBERON:4200124,sternal trabecula,UBERON:0004120,mesoderm-derived structure
+HP:0006944,Abolished vibration sense,HP:0002495,Impaired vibratory sensation
+HP:0100673,Vaginal hydrocele,HP:0100672,Vaginal hernia
+HP:0012056,Cutaneous melanoma,HP:0002861,Melanoma
+HP:0011224,Ablepharon,HP:0011226,Aplasia/Hypoplasia affecting the eyelid
+HP:0007281,Developmental stagnation,HP:0002376,Developmental regression
+HP:0000050,Hypoplastic genitalia,HP:0003241,Genital hypoplasia
+DOID:10518,beach ear,DOID:9463,otitis externa
+UBERON:0002080,heart right ventricle,UBERON:0015212,lateral structure
+HP:0009165,Stippling of the epiphysis of the distal phalanx of the 5th finger,HP:0009391,Stippling of the epiphyses of the 5th finger
+UBERON:0015280,pancreas left lobe,UBERON:0007324,pancreatic lobe
+DOID:11100,Q fever,DOID:0050338,primary bacterial infectious disease
+HP:0008929,Asymmetric short stature,HP:0004322,Short stature
+UBERON:0011308,pars reflexa of masseter,UBERON:0004120,mesoderm-derived structure
+UBERON:3010557,triangular process,UBERON:0004529,anatomical projection
+DOID:13403,cerebral sarcoidosis,DOID:936,brain disease
+UBERON:0010582,pedal digit 3 phalanx pre-cartilage condensation,UBERON:0010585,pedal digit phalanx pre-cartilage condensation
+UBERON:3000646,margo libera,UBERON:0000064,organ part
+HP:0011245,Abnormality of superior crus of antihelix,HP:0009738,Abnormality of the antihelix
+UBERON:0010515,brille,UBERON:1000021,skin of face
+DOID:6256,malignant growth hormone secreting neoplasm of pituitary,DOID:5716,hormone producing pituitary cancer
+HP:0010962,Extralobar sequestration,HP:0010960,Bronchopulmonary sequestration
+UBERON:0005122,metanephric macula densa,UBERON:0002335,macula densa
+HP:0009557,Aplasia/Hypoplasia of the distal phalanx of the 2nd finger,HP:0009552,Aplasia/Hypoplasia of the phalanges of the 2nd finger
+UBERON:4200126,supraacetabular rim,UBERON:0004120,mesoderm-derived structure
+HP:0012014,EEG with central focal spikes,HP:0011193,EEG with focal spikes
+UBERON:0004253,skin muscle,UBERON:0001630,muscle organ
+DOID:3342,bone inflammation disease,DOID:0080001,bone disease
+DOID:6827,pancreatic solid pseudopapillary carcinoma,DOID:4905,pancreatic carcinoma
+DOID:14768,Saethre-Chotzen syndrome,DOID:12960,acrocephalosyndactylia
+DOID:4895,rete ovarii neoplasm,DOID:0060086,female reproductive organ benign neoplasm
+HP:0006529,Abnormal pulmonary lymphatics,HP:0100763,Abnormality of the lymphatic system
+UBERON:0015796,liver blood vessel,UBERON:0003497,abdomen blood vessel
+HP:0004408,Abnormality of the sense of smell,HP:0000759,Abnormality of the peripheral nervous system
+HP:0008353,Neutral hyperaminoaciduria,HP:0003355,Aminoaciduria
+NCBITaxon:2037,Actinomycetales,NCBITaxon:85003,Actinobacteridae
+DOID:2135,temporal lobe neoplasm,DOID:368,cerebrum cancer
+UBERON:0004687,lieno-renal ligament,UBERON:0008845,nonskeletal ligament
+HP:0100831,Abnormality of vitamin K metabolism,HP:0100508,Abnormality of vitamin metabolism
+HP:0100696,Bone cysts,HP:0011842,Abnormality of skeletal morphology
+HP:0009172,Abnormality of the phalanges of the 4th finger,HP:0004188,Abnormality of the 4th finger
+HP:0009228,Bullet-shaped proximal phalanx of the 5th finger,HP:0009375,Bullet-shaped phalanges of the 5th finger
+HP:0010652,Abnormality of the dura mater,HP:0010651,Abnormality of the meninges
+CL:0000625,"CD8-positive, alpha-beta T cell",CL:0000791,mature alpha-beta T cell
+DOID:326,ischemia,DOID:178,vascular disease
+UBERON:3000793,anomocoelous,UBERON:0001075,vertebral centrum
+UBERON:0003551,midbrain pia mater,UBERON:0003288,meninx of midbrain
+CL:0000674,interfollicle cell,CL:0000075,columnar/cuboidal epithelial cell
+UBERON:0003230,epithelium of carpal region,UBERON:0010371,ecto-epithelium
+UBERON:0001296,myometrium,UBERON:0001135,smooth muscle tissue
+CL:0002238,male gonocyte,CL:0000670,primordial germ cell
+UBERON:0008320,common penile artery,UBERON:0014403,male anatomical structure
+NCBITaxon:6946,Acariformes,NCBITaxon:6933,Acari
+DOID:11294,arteriovenous malformation,DOID:255,hemangioma
+HP:0010200,Symphalangism affecting the middle phalanges of the toes,HP:0010183,Abnormality of the middle phalanges of the toes
+DOID:3578,ovarian gonadoblastoma,DOID:0060112,ovarian benign neoplasm
+UBERON:0001406,ulnar artery,UBERON:0001637,artery
+CL:0002577,placental epithelial cell,CL:0000066,epithelial cell
+DOID:7048,vulvar basaloid squamous cell carcinoma,DOID:2101,vulva squamous cell carcinoma
+UBERON:0003639,manual digit 5 phalanx,UBERON:0001436,phalanx of manus
+DOID:7017,lumbosacral lipoma,DOID:0060094,bone benign neoplasm
+CL:0000856,neuromast hair cell,CL:0000855,sensory hair cell
+UBERON:0000999,ejaculatory duct,UBERON:0015212,lateral structure
+HP:0100159,Cone-shaped epiphysis of the proximal phalanx of the 3rd toe,HP:0100093,Abnormality of the epiphysis of the proximal phalanx of the 3rd toe
+UBERON:3000807,carina distalis,UBERON:0004120,mesoderm-derived structure
+DOID:5299,endometrial clear cell adenocarcinoma,DOID:2870,endometrial adenocarcinoma
+DOID:9164,achalasia,DOID:6050,esophageal disease
+DOID:8743,erythema infectiosum,DOID:8672,viral exanthem
+DOID:12557,Duane retraction syndrome,DOID:540,strabismus
+HP:0008293,Long-chain dicarboxylic aciduria,HP:0003215,Dicarboxylic aciduria
+UBERON:2001239,ceratobranchial 5 bone,UBERON:2001903,ceratobranchial 5 element
+DOID:2142,urethra leiomyoma,DOID:730,urethral benign neoplasm
+DOID:5877,endocardium cancer,DOID:117,heart cancer
+HP:0012345,Abnormal glycosylation,HP:0011013,Abnormality of carbohydrate metabolism/homeostasis
+CL:1000379,type 1 vestibular sensory cell of epithelium of macula of utricle of membranous labyrinth,CL:0002070,type I vestibular sensory cell
+DOID:2129,atypical teratoid rhabdoid tumor,DOID:1319,brain cancer
+DOID:14793,hypohidrotic ectodermal dysplasia,DOID:0050177,monogenic disease
+DOID:8618,oral cavity cancer,DOID:3119,gastrointestinal system cancer
+DOID:14756,autosomal dominant type IV Ehlers-Danlos syndrome,DOID:13359,Ehlers-Danlos syndrome
+DOID:11241,appendix lymphoma,DOID:11239,appendix cancer
+CL:0000165,neuroendocrine cell,CL:0000393,electrically responsive cell
+DOID:7160,rectum leiomyoma,DOID:5143,large bowel leiomyoma
+HP:0009700,Synostosis involving bones of the fingers,HP:0100262,Synostosis involving digits
+HP:0003093,Limited hip extension,HP:0008800,Limited hip movement
+DOID:701,dentin dysplasia,DOID:214,teeth hard tissue disease
+HP:0001518,Small for gestational age,HP:0004325,Decreased body weight
+UBERON:3000448,posterior maxillary process,UBERON:0004529,anatomical projection
+UBERON:0002956,granular layer of cerebellar cortex,UBERON:0004130,cerebellar layer
+UBERON:0012424,brush border layer,UBERON:0012423,layer of microvilli
+UBERON:0006514,pallidum,UBERON:0003528,brain grey matter
+UBERON:0002205,manubrium of sternum,UBERON:0005181,thoracic segment organ
+UBERON:2105375,dorsal fin distal radial element 4,UBERON:2100936,dorsal fin distal radial element
+CL:0000680,muscle precursor cell,CL:0002371,somatic cell
+DOID:11504,autonomic neuropathy,DOID:11465,autonomic nervous system disease
+HP:0009852,Broad proximal phalanges of the hand,HP:0009768,Broad phalanges of the hand
+UBERON:2002021,ascending process of the parasphenoid,UBERON:4100000,skeletal element projection
+DOID:0050674,congenital bile acid synthesis defect,DOID:1701,steroid inherited metabolic disorder
+UBERON:0010403,cortical marginal zone,UBERON:0002301,layer of neocortex
+UBERON:2005114,middle lateral line system,UBERON:0002540,lateral line system
+DOID:4022,ureterocele,DOID:1426,ureteral disease
+DOID:3393,coronary artery disease,DOID:0050828,artery disease
+UBERON:0001658,middle temporal vein,UBERON:0001671,temporal vein
+HP:0000591,Abnormality of the sclera,HP:0012374,Abnormality of the globe
+CL:0005014,auditory epithelial support cell,CL:0000630,supportive cell
+HP:0009350,Fragmentation of the epiphysis of the proximal phalanx of the 3rd finger,HP:0009414,Fragmentation of the epiphyses of the 3rd finger
+UBERON:0001107,sternohyoid muscle,UBERON:0003897,axial muscle
+UBERON:2001749,dentary-anguloarticular joint,UBERON:0000982,skeletal joint
+HP:0001338,Partial agenesis of the corpus callosum,HP:0001274,Agenesis of corpus callosum
+UBERON:3000717,amphicoelous,UBERON:0001075,vertebral centrum
+CL:1001224,interlobulary vein smooth muscle cell,CL:1001145,interlobular vein cell
+HP:0011195,EEG with focal sharp slow waves,HP:0011185,EEG with focal epileptiform discharges
+HP:0004872,Incisional hernia,HP:0004299,Hernia of the abdominal wall
+UBERON:0002301,layer of neocortex,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2000185,"commissura rostral, pars ventralis",UBERON:0002437,cerebral hemisphere white matter
+DOID:9396,acute laryngitis,DOID:3437,laryngitis
+UBERON:0014930,perivascular space,UBERON:0000464,anatomical space
+DOID:14099,acquired gastric outlet stenosis,DOID:12639,pyloric stenosis
+CL:0000788,naive B cell,CL:0000785,mature B cell
+HP:0010146,Small epiphysis of the distal phalanx of the hallux,HP:0010124,Abnormality of the epiphysis of the distal phalanx of the hallux
+UBERON:0007198,hermaphrodite anatomical structure,UBERON:0000061,anatomical structure
+HP:0008008,Progressive central visual loss,HP:0000529,Progressive visual loss
+DOID:361,cervix endometriosis,DOID:288,endometriosis of uterus
+HP:0009437,Aplasia/Hypoplasia of the middle phalanx of the 3rd finger,HP:0009447,Aplasia/Hypoplasia of the phalanges of the 3rd finger
+UBERON:0003840,hindlimb joint,UBERON:0003657,limb joint
+HP:0100433,Broad distal phalanx of the 5th toe,HP:0010384,Broad phalanges of the 5th toe
+UBERON:2000804,myotome somite 20,UBERON:0003082,myotome
+UBERON:0013778,skin of sole of pes,UBERON:0001513,skin of pes
+HP:0012127,Uraciluria,HP:0004353,Abnormality of pyrimidine metabolism
+HP:0006152,Proximal symphalangism (hands),HP:0009773,Symphalangism affecting the phalanges of the hand
+UBERON:0010847,ulna pre-cartilage condensation,UBERON:0003327,mesenchyme of forearm
+DOID:8295,scabies,DOID:7894,mite infestation
+UBERON:0015593,frontal gyrus,UBERON:0000200,gyrus
+HP:0010349,Bullet-shaped phalanges of the 2nd toe,HP:0010175,Bullet-shaped phalanges of the toes
+UBERON:0010027,dorsal part of pharyngeal pouch 4,UBERON:0000490,unilaminar epithelium
+HP:0003461,Increased urinary O-linked sialopeptides,HP:0012067,Glycopeptiduria
+HP:0200083,Severe limb shortening,HP:0002983,Micromelia
+UBERON:0001479,sesamoid bone,UBERON:0001474,bone element
+HP:0010685,Low alkaline phosphatase of renal origin,HP:0010683,Low tissue non-specific alkaline phosphatase
+HP:0003912,Frayed humeral metaphyses,HP:0003907,Abnormality of the humeral metaphyses
+HP:0006600,Progressive calcification of costochondral cartilage,HP:0100593,Calcification of cartilage
+HP:0004760,Congenital septal defect,HP:0001671,Abnormality of the cardiac septa
+UBERON:3000830,margo vertebralis,UBERON:0000064,organ part
+UBERON:0010745,sacral vertebra cartilage element,UBERON:0015010,sacral vertebra endochondral element
+UBERON:0004684,raphe nuclei,UBERON:0000073,regional part of nervous system
+UBERON:0013280,diaphysis of tibia,UBERON:0004769,diaphysis
+HP:0010037,Aplasia of the 2nd metacarpal,HP:0010036,Aplasia/Hypoplasia of the 2nd metacarpal
+UBERON:2000576,pterotic,UBERON:0010313,neural crest-derived structure
+HP:0000377,Abnormality of the pinna,HP:0000356,Abnormality of the outer ear
+HP:0006491,Abnormality of the tibial metaphysis,HP:0006490,Abnormality of lower-limb metaphyses
+HP:0010233,Irregular epiphyses of the phalanges of the hand,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+DOID:5678,nerve fibre bundle defect,DOID:1393,visual pathway disease
+CL:1000682,kidney medulla interstitial cell,CL:1000504,kidney medulla cell
+UBERON:3000539,recessus marsupiatus of premaxilla,UBERON:0000464,anatomical space
+DOID:3136,scalp dermatosis,DOID:37,skin disease
+UBERON:0003727,intercostal nerve,UBERON:0001780,spinal nerve
+HP:0005815,Supernumerary ribs,HP:0000772,Abnormality of the ribs
+HP:0012637,Renal calcium wasting,HP:0004363,Abnormality of calcium homeostasis
+UBERON:0010300,epithelial scleral papilla layer,UBERON:0000483,epithelium
+UBERON:0012247,cervical gland,UBERON:0005398,female reproductive gland
+HP:0004439,Craniofacial dysostosis,HP:0000271,Abnormality of the face
+NCBITaxon:91493,Exserohilum,NCBITaxon:117568,mitosporic Pleosporaceae
+DOID:5697,liposarcoma of the ovary,DOID:3382,liposarcoma
+CL:0000508,type G enteroendocrine cell,CL:0000506,enkephalin secreting cell
+UBERON:0005236,osseus labyrinth vestibule,UBERON:0000064,organ part
+DOID:11254,Brill-Zinsser disease,DOID:0050480,epidemic typhus
+UBERON:0014896,transversely striated somatic muscle,UBERON:0014895,somatic muscle
+DOID:2945,severe acute respiratory syndrome,DOID:934,viral infectious disease
+UBERON:0010029,dorsal part of pharyngeal pouch 5,UBERON:0000490,unilaminar epithelium
+UBERON:0012312,maxillary process ectoderm,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0002797,Osteolysis,HP:0003330,Abnormal bone structure
+CL:0000381,neurosecretory neuron,CL:0000527,efferent neuron
+UBERON:0009022,right uterine horn,UBERON:0002247,uterine horn
+UBERON:0004425,proximal epiphysis of fourth metacarpal bone,UBERON:0004394,epiphysis of fourth metacarpal bone
+HP:0006262,Aplasia/Hypoplasia of the 5th finger,HP:0006265,Aplasia/Hypoplasia of fingers
+DOID:1089,tethered spinal cord syndrome,DOID:319,spinal cord disease
+UBERON:0001219,ileocolic vein,UBERON:0002017,portal vein
+UBERON:0008802,cheek pouch,UBERON:0008803,skin of cheek
+UBERON:2007035,spinal cord neural rod,UBERON:0004121,ectoderm-derived structure
+HP:0009561,Osteolytic defects of the distal phalanx of the 2nd finger,HP:0009542,Abnormality of the distal phalanx of the 2nd finger
+UBERON:0009758,abdominal ganglion,UBERON:0007134,trunk ganglion
+UBERON:0002105,vestibulo-auditory system,UBERON:0007037,mechanosensory system
+HP:0005400,Reduction of neutrophil motility,HP:0011990,Abnormality of neutrophil physiology
+UBERON:0015455,accessory hepatic vein,UBERON:0001143,hepatic vein
+CL:1001108,kidney loop of henle medullary thick ascending limb epithelial cell,CL:1000616,kidney outer medulla cell
+HP:0007403,Hypertrophy of skin of soles,HP:0100872,Abnormality of the plantar skin of foot
+UBERON:0003967,cutaneous elastic tissue,UBERON:0002521,elastic tissue
+UBERON:0015055,pubic endochondral element,UBERON:0004120,mesoderm-derived structure
+UBERON:0010903,tibiotarsus pre-cartilage condensation,UBERON:0015011,tibiotarsus endochondral element
+DOID:2366,West Nile fever,DOID:934,viral infectious disease
+UBERON:2001684,ossified transcapular ligament,UBERON:0007842,membrane bone
+HP:0100941,Sclerosis of the distal phalanx of the 4th toe,HP:0100928,Sclerosis of the phalanges of the 4th toe
+UBERON:0000428,prostate epithelium,UBERON:0014403,male anatomical structure
+HP:0007780,Cortical pulverulent cataract,HP:0010693,Pulverulent Cataract
+DOID:11219,conjunctival folliculosis,DOID:11184,acute conjunctivitis
+HP:0010084,Duplication of the distal phalanx of the hallux,HP:0010066,Duplication of phalanx of hallux
+DOID:11990,ulceroglandular tularemia,DOID:2123,tularemia
+HP:0010945,Fetal pyelectasis,HP:0010946,Dilatation of the renal pelvis
+HP:0009434,Patchy sclerosis of the middle phalanx of the 3rd finger,HP:0009848,Patchy sclerosis of the middle phalanges of the hand
+UBERON:0003372,pectoral appendage bud ectoderm,UBERON:0005291,embryonic tissue
+UBERON:0003970,placental labyrinth vasculature,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0005162,multi cell component structure,UBERON:0000477,anatomical cluster
+UBERON:3010721,limb villosities,UBERON:3000981,limb external integument structure
+UBERON:0014664,nucleus recessus posterioris,UBERON:0006568,hypothalamic nucleus
+HP:0100751,Esophageal neoplasm,HP:0002031,Abnormality of the esophagus
+UBERON:0001256,wall of urinary bladder,UBERON:0000060,anatomical wall
+UBERON:0003120,aortic arch 3,UBERON:0004363,aortic arch
+HP:0100187,Pseudoepiphysis of the middle phalanx of the 4th toe,HP:0100073,Pseudoepiphyses of the 4th toe
+UBERON:0000207,compound eye corneal lens,UBERON:0000476,acellular anatomical structure
+HP:0009417,Pseudoepiphyses of the 3rd finger,HP:0009320,Abnormality of the epiphyses of the 3rd finger
+HP:0002823,Abnormality of the femur,HP:0002814,Abnormality of the lower limb
+HP:0012057,Superficial spreading melanoma,HP:0012056,Cutaneous melanoma
+UBERON:0001481,distal carpal bone,UBERON:0001435,carpal bone
+HP:0100695,Lipedema,HP:0000969,Edema
+UBERON:2001019,myotome somite 28,UBERON:0003082,myotome
+DOID:12191,splenic flexure cancer,DOID:12190,descending colon cancer
+HP:0012076,Borderline personality disorder,HP:0012075,Personality disorder
+UBERON:0010995,deep part of masseter muscle,UBERON:0004120,mesoderm-derived structure
+HP:0012337,Abnormal homeostasis,HP:0001939,Abnormality of metabolism/homeostasis
+DOID:1733,cryptosporidiosis,DOID:2113,coccidiosis
+UBERON:0003490,respiratory system reticular lamina,UBERON:0001967,reticular lamina of epithelium
+CL:0012000,astrocyte of the forebrain,CL:2000005,brain macroglial cell
+CL:0002104,IgG-negative double negative memory B cell,CL:0000981,double negative memory B cell
+DOID:0050605,acrodermatitis enteropathica,DOID:896,metal metabolism disorder
+DOID:9445,cervix squamous papilloma,DOID:0060110,cervical benign neoplasm
+DOID:0050597,intestinal schistosomiasis,DOID:1395,schistosomiasis
+HP:0006298,Prolonged bleeding after dental extraction,HP:0011890,Prolonged bleeding following procedure
+UBERON:0016477,zygomatic process of maxilla,UBERON:0004529,anatomical projection
+HP:0008739,Labial pseudohypertrophy,HP:0000065,Labial hypertrophy
+DOID:4449,macular retinal edema,DOID:6929,retinal edema
+UBERON:0013588,fused metatarsal bones 3 and 4,UBERON:0013586,fused metapodial bones 3 and 4
+HP:0008117,Shortening of the talar neck,HP:0008365,Abnormality of the talus
+CL:0002290,Y chromosome-bearing sperm cell,CL:0000019,sperm
+CL:0000588,odontoclast,CL:0000092,osteoclast
+UBERON:0001869,cerebral hemisphere,UBERON:0004121,ectoderm-derived structure
+CL:0000822,B-2 B cell,CL:0000785,mature B cell
+HP:0005387,Combined immunodeficiency,HP:0002721,Immunodeficiency
+CL:1000481,transitional myocyte of atrioventricular bundle,CL:0010005,atrioventricular bundle cell
+DOID:11729,Lyme disease,DOID:37,skin disease
+DOID:11905,labium majus cancer,DOID:1245,vulva cancer
+HP:0011253,Type I cryptotia,HP:0011252,Cryptotia
+UBERON:2002242,scale primordium,UBERON:0004120,mesoderm-derived structure
+DOID:203,exostosis,DOID:205,hyperostosis
+DOID:13654,stenosis of lacrimal passage,DOID:530,eyelid disease
+UBERON:0011664,posterior plastron-carapace bridge,UBERON:0011662,plastron-carapace bridge
+DOID:6501,brain stem angioblastoma,DOID:4203,brain stem cancer
+HP:0002664,Neoplasm,HP:0000118,Phenotypic abnormality
+HP:0001760,Abnormality of the foot,HP:0002814,Abnormality of the lower limb
+HP:0004817,Drug-sensitive hemolytic anemia,HP:0001878,Hemolytic anemia
+NCBITaxon:8287,Sarcopterygii,NCBITaxon:117571,Euteleostomi
+HP:0012121,Panuveitis,HP:0000554,Uveitis
+DOID:135,benign vaginal carcinosarcoma,DOID:0060114,vaginal benign neoplasm
+UBERON:0009907,sensory root of trigeminal nerve,UBERON:0010313,neural crest-derived structure
+UBERON:0010183,liver trabecula,UBERON:0004119,endoderm-derived structure
+UBERON:0006630,left atrium auricular region,UBERON:0006618,atrium auricular region
+UBERON:3000052,braincase and otic capsule skeleton,UBERON:3000050,braincase and auditory apparatus
+HP:0008845,Mesomelic short stature,HP:0008873,Disproportionate short-limb short stature
+DOID:11299,vertebral artery occlusion,DOID:5976,occlusion precerebral artery
+HP:0004689,Short fourth metatarsal,HP:0010743,Short metatarsal
+UBERON:3010013,larval chondrocranium,UBERON:0010323,cranial skeletal system
+DOID:8353,epithelioid malignant peripheral nerve sheath tumor,DOID:5940,malignant peripheral nerve sheath tumor
+UBERON:3010744,M. flexor antibrachii lateralis profundus,UBERON:0010891,pectoral complex muscle
+UBERON:0002249,median artery,UBERON:0001637,artery
+DOID:13619,extrahepatic cholestasis,DOID:13580,cholestasis
+NCBITaxon:37296,Human herpesvirus 8,NCBITaxon:10379,Rhadinovirus
+UBERON:0007690,early pharyngeal endoderm,UBERON:0000925,endoderm
+DOID:9841,hypotropia,DOID:540,strabismus
+CL:0000473,defensive cell,CL:0000003,native cell
+UBERON:0004277,eye muscle,UBERON:0004121,ectoderm-derived structure
+DOID:11320,Kyasanur forest disease,DOID:934,viral infectious disease
+CL:0002286,type II taste cell,CL:0000209,taste receptor cell
+UBERON:2001783,supraoccipital crest,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010921,Coralliform cataract,HP:0010920,Zonular cataract
+UBERON:2000614,abductor profundus,UBERON:0014794,pectoral appendage muscle
+CL:0000915,"CD8-alpha-alpha-positive, alpha-beta intraepithelial T cell",CL:0000797,alpha-beta intraepithelial T cell
+UBERON:0004892,lobar bronchus alveolar system,UBERON:0004119,endoderm-derived structure
+HP:0003851,Lytic defects in metaphyses of the upper limbs,HP:0009809,Abnormality of upper limb metaphysis
+DOID:7045,basaloid lung carcinoma,DOID:3907,lung squamous cell carcinoma
+HP:0002110,Bronchiectasis,HP:0002109,Abnormality of the bronchi
+UBERON:0001555,digestive tract,UBERON:0000025,tube
+UBERON:2001999,posterior cleithral process,UBERON:4100000,skeletal element projection
+HP:0100127,Irregular epiphysis of the proximal phalanx of the 2nd toe,HP:0100090,Abnormality of the epiphysis of the proximal phalanx of the 2nd toe
+DOID:305,carcinoma,DOID:0050687,cell type cancer
+HP:0009314,Symphalangism affecting the proximal phalanx of the 4th finger,HP:0009857,Symphalangism affecting the proximal phalanges of the hand
+CL:0002462,adipose dendritic cell,CL:0000990,conventional dendritic cell
+UBERON:1500005,ischial cartilage,UBERON:0004120,mesoderm-derived structure
+UBERON:0004552,digital artery,UBERON:0003514,limb blood vessel
+UBERON:0000333,intestinal gland,UBERON:0003408,gland of gut
+UBERON:3000654,pars jugalis,UBERON:0000064,organ part
+DOID:9088,parapsoriasis,DOID:8893,psoriasis
+HP:0000740,Anxiety (with pheochromocytoma),HP:0000739,Anxiety
+UBERON:2001145,tooth 3V,UBERON:2000694,ceratobranchial 5 tooth
+UBERON:0002795,frontal pole,UBERON:0009899,pole of cerebral hemisphere
+CL:0000754,type 2 cone bipolar cell (sensu Mus),CL:0000752,cone retinal bipolar cell
+DOID:2817,cranial nerve III tumor,DOID:562,third cranial nerve disease
+HP:0002094,Dyspnea,HP:0002093,Respiratory insufficiency
+HP:0004876,Spontaneous neonatal pneumothorax,HP:0002108,Spontaneous pneumothorax
+UBERON:0011823,dense connective tissue,UBERON:0002384,connective tissue
+UBERON:0005129,metanephric distal tubule,UBERON:0005146,metanephric nephron tubule
+UBERON:2005248,trans-choroid plexus branch,UBERON:0001638,vein
+HP:0002984,Hypoplasia of the radius,HP:0009821,Forearm undergrowth
+HP:0000622,Blurred vision,HP:0000505,Visual impairment
+CL:1001505,parvocellular neurosecretory cell,CL:0011112,magnocellular neurosecretory cell
+UBERON:0010940,belly of digastric,UBERON:0010938,muscle belly
+UBERON:0002325,epithelium of urethra,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0004407,distal epiphysis of radius,UBERON:0004379,distal epiphysis
+DOID:8207,hilar lung carcinoma,DOID:3905,lung carcinoma
+NCBITaxon:1314,Streptococcus pyogenes,NCBITaxon:1301,Streptococcus
+HP:0009285,Curved phalanges of the 4th finger,HP:0009770,Curved phalanges of the hand
+HP:0100049,Irregular epiphyses of the 2nd toe,HP:0010323,Abnormality of the epiphyses of the 2nd toe
+UBERON:0015179,somite boundary epithelium,UBERON:0012275,meso-epithelium
+UBERON:0013487,epidermal ridge of digit,UBERON:0003102,surface structure
+HP:0100875,Hemimacroglossia,HP:0000158,Macroglossia
+HP:0009352,Ivory epiphysis of the proximal phalanx of the 3rd finger,HP:0010274,Ivory epiphyses of the proximal phalanges of the hand
+UBERON:0003513,trunk blood vessel,UBERON:0001981,blood vessel
+HP:0100008,Schwannoma,HP:0100007,Neoplasm of the peripheral nervous system
+DOID:6255,growth hormone secreting pituitary adenoma,DOID:5395,functioning pituitary adenoma
+DOID:2277,gonadal disease,DOID:28,endocrine system disease
+UBERON:0015852,narwhal tusk,UBERON:0015848,incisor tusk
+UBERON:0001357,inferior rectal artery,UBERON:0004121,ectoderm-derived structure
+CL:0002582,visceral preadipocyte,CL:0002334,preadipocyte
+HP:0012652,Exercise-induced asthma,HP:0002099,Asthma
+UBERON:0001711,eyelid,UBERON:0000064,organ part
+UBERON:0012253,cervical squamo-columnar junction,UBERON:0004801,cervix epithelium
+CL:0002119,CD38-positive IgG-negative class switched memory B cell,CL:0002117,IgG-negative class switched memory B cell
+UBERON:0010062,pharyngotympanic tube epithelium,UBERON:0003914,epithelial tube
+UBERON:0001779,iris stroma,UBERON:0003566,head connective tissue
+UBERON:0002676,ventral supraoptic decussation,UBERON:0011590,commissure of diencephalon
+HP:0003131,Cystinuria,HP:0003355,Aminoaciduria
+HP:0012173,Orthostatic tachycardia,HP:0012332,Abnormal autonomic nervous system physiology
+HP:0008428,Vertebral clefting,HP:0003312,Abnormal form of the vertebral bodies
+UBERON:0011241,ethmoid region,UBERON:0000477,anatomical cluster
+UBERON:0010993,subscapularis pre-muscle mass,UBERON:0005865,pre-muscle condensation
+UBERON:0011901,hair matrix,UBERON:0000021,cutaneous appendage
+HP:0010014,Abnormality of the epiphysis of the 1st metacarpal,HP:0009599,Abnormality of the epiphyses of the thumb
+CL:0002325,mammary alveolar cell,CL:0000314,milk secreting cell
+HP:0001254,Lethargy,HP:0004372,Reduced consciousness/confusion
+HP:0003856,Upper limb metaphyseal widening,HP:0003016,Metaphyseal widening
+HP:0012034,Liposarcoma,HP:0012031,Lipomatous tumor
+UBERON:2000410,postcleithrum,UBERON:0008907,dermal bone
+HP:0009423,Bullet-shaped distal phalanx of the 3rd finger,HP:0009357,Abnormality of the distal phalanx of the 3rd finger
+UBERON:2201417,pelvic fin distal radial cartilage 1,UBERON:2101417,pelvic fin distal radial element 1
+UBERON:3000957,basihyal,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:0050468,yellow nail syndrome,DOID:225,syndrome
+HP:0009915,Corneal asymmetry,HP:0001120,Abnormality of corneal size
+UBERON:0009899,pole of cerebral hemisphere,UBERON:0000477,anatomical cluster
+HP:0010022,Pseudoepiphysis of the 1st metacarpal,HP:0010014,Abnormality of the epiphysis of the 1st metacarpal
+HP:0006207,Partial fusion of carpals,HP:0009702,Carpal synostosis
+HP:0000811,Abnormal external genitalia,HP:0012243,Abnormal genital system morphology
+UBERON:2001923,aortic canal,UBERON:0005744,bone foramen
+HP:0007856,Punctate opacification of the cornea,HP:0007759,Opacification of the corneal stroma
+CL:0000670,primordial germ cell,CL:0000219,motile cell
+HP:0004219,Abnormality of the middle phalanx of the 5th finger,HP:0004213,Abnormality of the phalanges of the 5th finger
+HP:0009087,Posteriorly placed tongue,HP:0000157,Abnormality of the tongue
+UBERON:2001293,posterior kidney,UBERON:0006554,urinary system structure
+UBERON:0002001,joint of rib,UBERON:0000982,skeletal joint
+UBERON:0006230,extrinsic ocular pre-muscle mass,UBERON:0005865,pre-muscle condensation
+HP:0010536,Central sleep apnea,HP:0010535,Sleep apnea
+UBERON:0007174,medial border of scapula,UBERON:0007171,border of scapula
+UBERON:2005068,bulbus arteriosus inner layer,UBERON:0004120,mesoderm-derived structure
+UBERON:0004660,mandible coronoid process,UBERON:0004120,mesoderm-derived structure
+UBERON:0010416,lymph node B cell domain,UBERON:0010392,B cell domain
+UBERON:0001300,scrotum,UBERON:0000475,organism subdivision
+DOID:0050382,glandular tularemia,DOID:2123,tularemia
+UBERON:0001420,subscapular vein,UBERON:0001638,vein
+UBERON:0007440,stratum intermedium of tooth,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003304,mesoderm blood island,UBERON:0007503,epithelial vesicle
+HP:0009682,Pseudoepiphysis of the distal phalanx of the thumb,HP:0009662,Abnormality of the epiphysis of the distal phalanx of the thumb
+UBERON:0011653,diapophysis of rib,UBERON:4100000,skeletal element projection
+DOID:12196,superficial keratitis,DOID:4677,keratitis
+UBERON:0005477,stomach fundus epithelium,UBERON:0001276,epithelium of stomach
+DOID:5977,renal pelvis neoplasm,DOID:3116,kidney benign neoplasm
+UBERON:0001319,vaginal vein,UBERON:0005156,reproductive structure
+HP:0006633,Glenoid fossa hypoplasia,HP:0011912,Abnormality of the glenoid fossa
+UBERON:0004122,genitourinary system,UBERON:0004120,mesoderm-derived structure
+HP:0011941,Anterior wedging of L2,HP:0008422,Vertebral wedging
+HP:0011605,Congenitally corrected transposition of the great arteries with ventricular septal defect,HP:0011540,Congenitally corrected transposition of the great arteries
+DOID:1896,sigmoid neoplasm,DOID:235,colonic benign neoplasm
+HP:0002250,Abnormality of the large intestine,HP:0002242,Abnormality of the intestine
+UBERON:0006486,Brodmann (1909) area 52,UBERON:0013529,Brodmann area
+DOID:3602,toxic encephalopathy,DOID:863,nervous system disease
+UBERON:0002736,lateral nuclear group of thalamus,UBERON:0003528,brain grey matter
+HP:0000430,Underdeveloped nasal alae,HP:0009924,Aplasia/Hypoplasia involving the nose
+UBERON:0001686,auditory ossicle,UBERON:0003457,head bone
+UBERON:0010394,lymphocyte domain,UBERON:0000477,anatomical cluster
+UBERON:0012283,femoral fat pad,UBERON:0003916,fat pad
+HP:0009528,Fragmentation of the epiphysis of the proximal phalanx of the 2nd finger,HP:0010272,Fragmentation of the epiphyses of the proximal phalanges of the hand
+UBERON:0003108,suspensorium,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3000527,quadrate process of palatoquadrate,UBERON:0004121,ectoderm-derived structure
+HP:0001199,Triphalangeal thumb,HP:0009619,Accessory phalanx of the thumb
+UBERON:0004390,epiphysis of metacarpal bone,UBERON:0001437,epiphysis
+UBERON:0005749,glomerular tuft,UBERON:0000064,organ part
+HP:0009941,Asymmetry of the mouth,HP:0011338,Abnormality of mouth shape
+HP:0006548,Pulmonary arteriovenous malformation,HP:0002088,Abnormality of the lung
+UBERON:0004440,proximal epiphysis of proximal phalanx of manual digit 2,UBERON:0004418,proximal epiphysis of phalanx of manual digit 2
+UBERON:0004504,skeletal muscle tissue of mylohyoid,UBERON:0010314,structure with developmental contribution from neural crest
+NCBITaxon:121759,Paracoccidioides brasiliensis,NCBITaxon:38946,Paracoccidioides
+UBERON:0004803,penis epithelium,UBERON:0012275,meso-epithelium
+HP:0010405,Broad middle phalanx of the 2nd toe,HP:0010357,Abnormality of the middle phalanx of the 2nd toe
+UBERON:0001375,semitendinosus,UBERON:0002463,hamstring muscle
+HP:0010250,Fragmentation of the epiphyses of the distal phalanges of the hand,HP:0010232,Fragmentation of the epiphyses of the phalanges of the hand
+UBERON:0005404,frontonasal suture,UBERON:0009198,craniofacial suture
+CL:0002659,glandular cell of stomach,CL:0002178,epithelial cell of stomach
+UBERON:2000006,ball,UBERON:0000475,organism subdivision
+UBERON:3000642,maxillopalatine tooth,UBERON:0003267,tooth of upper jaw
+UBERON:0002353,atrioventricular bundle,UBERON:0004493,cardiac muscle tissue of myocardium
+HP:0010566,Hamartoma,HP:0011792,Neoplasm by histology
+CL:1000548,kidney outer medulla collecting duct epithelial cell,CL:1000616,kidney outer medulla cell
+UBERON:0004002,posterior lobe of cerebellum,UBERON:0005293,cerebellum lobe
+UBERON:0007334,nidopallium,UBERON:0002791,regional part of telencephalon
+HP:0010491,Digital constriction ring,HP:0009775,Amniotic constriction ring
+DOID:9265,histidine metabolism disease,DOID:9252,amino acid metabolic disorder
+CL:0000032,neuroplacodal cell,CL:0002321,embryonic cell
+UBERON:0001468,intervertebral joint,UBERON:0002216,symphysis
+UBERON:0011188,lesser tubercle of humerus,UBERON:0004120,mesoderm-derived structure
+DOID:3865,adult central nervous system primitive neuroectodermal neoplasm,DOID:0060103,central nervous system primitive neuroectodermal neoplasm
+UBERON:0001777,substantia propria of cornea,UBERON:0003566,head connective tissue
+HP:0100908,Sclerosis of the proximal phalanx of the 2nd finger,HP:0100917,Sclerosis of the proximal phalanges of the hand
+HP:0009787,Aplasia/Hypoplasia of the quadriceps,HP:0009786,Aplasia/Hypoplasia of the musculature of the thigh
+UBERON:0001254,urothelium of ureter,UBERON:0012275,meso-epithelium
+UBERON:0007818,major alar cartilage,UBERON:0001823,nasal cartilage
+HP:0004459,Exostosis of the external auditory canal,HP:0000372,Abnormality of the auditory canal
+DOID:3946,pituitary-dependent Cushing's disease,DOID:2444,hyperpituitarism
+UBERON:0007603,stratified cuboidal epithelium,UBERON:0010077,cuboidal epithelium
+DOID:5165,uterine corpus sarcoma,DOID:9460,uterine corpus cancer
+UBERON:0014590,anterior nucleus of hypothalamus central part,UBERON:0002784,regional part of diencephalon
+UBERON:0001004,respiratory system,UBERON:0000467,anatomical system
+DOID:303,substance-related disorder,DOID:150,disease of mental health
+UBERON:0012080,patella cartilage element,UBERON:0010881,limb cartilage element
+HP:0003338,Focal necrosis of right ventricular muscle cells,HP:0001627,Abnormality of cardiac morphology
+HP:0010304,Spinal meningeal diverticulum,HP:0010303,Abnormality of the spinal meninges
+HP:0011502,Posterior lenticonus,HP:0001142,Lenticonus
+UBERON:0012193,phrenic vein,UBERON:0001638,vein
+UBERON:0001430,distal carpal bone 1,UBERON:0015084,distal carpal bone 1 endochondral element
+UBERON:0000168,segment of colon,UBERON:0000063,organ segment
+UBERON:0006051,digit 4,UBERON:0002544,digit
+UBERON:0009113,thymic region,UBERON:0000475,organism subdivision
+UBERON:2005017,primordial midbrain channel,UBERON:0003496,head blood vessel
+HP:0100225,Bracket epiphysis of the proximal phalanx of the 5th toe,HP:0100099,Abnormality of the epiphysis of the proximal phalanx of the 5th toe
+UBERON:0011049,uterovesical pouch,UBERON:0000158,membranous layer
+UBERON:0001605,ciliary muscle,UBERON:0003386,smooth muscle of eye
+DOID:0060086,female reproductive organ benign neoplasm,DOID:0050622,reproductive organ benign neoplasm
+UBERON:0001577,facial nerve muscle,UBERON:0015789,cranial or facial muscle
+UBERON:0005373,spinal cord dorsal column,UBERON:0002318,white matter of spinal cord
+UBERON:0002619,regional part of cerebral cortex,UBERON:0002791,regional part of telencephalon
+UBERON:0014464,renal fat pad,UBERON:0003427,abdominal fat pad
+DOID:8144,pregerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma,DOID:6354,CLL/SLL
+HP:0011715,Trifascicular block,HP:0011710,Bundle branch block
+UBERON:0013763,sensory epithelium of spiral organ,UBERON:0001967,reticular lamina of epithelium
+HP:0009423,Bullet-shaped distal phalanx of the 3rd finger,HP:0009837,Bullet-shaped distal phalanges of the hand
+HP:0006628,Absent sternal ossification,HP:0006714,Aplasia/Hypoplasia of the sternum
+DOID:11101,trench fever,DOID:0050338,primary bacterial infectious disease
+UBERON:0001655,submental vein,UBERON:0004121,ectoderm-derived structure
+UBERON:0004759,salt gland of cranial region,UBERON:0004758,salt gland
+UBERON:0008962,forelimb bone,UBERON:0002428,limb bone
+DOID:6333,adult intracranial malignant hemangiopericytoma,DOID:201,connective tissue cancer
+DOID:37,skin disease,DOID:16,integumentary system disease
+HP:0010354,Triangular shaped phalanges of the 2nd toe,HP:0010324,Abnormality of phalanx of the 2nd toe
+HP:0002518,Abnormality of the periventricular white matter,HP:0002352,Leukoencephalopathy
+CL:1000746,glomerular cell,CL:1000612,kidney corpuscule cell
+HP:0009098,Chronic oral candidiasis,HP:0002728,Chronic mucocutaneous candidiasis
+DOID:11813,bladder trigone cancer,DOID:11054,urinary bladder cancer
+HP:0012459,Hypnic headache,HP:0002315,Headache
+HP:0003223,Decreased methylcobalamin,HP:0004341,Abnormality of the vitamin B12 metabolism
+UBERON:0012304,nasal diverticulum,UBERON:1000021,skin of face
+UBERON:0002101,limb,UBERON:0004708,paired limb/fin
+UBERON:4200028,adductor blade,UBERON:0004530,bony projection
+DOID:14523,Argyll Robertson pupil,DOID:11518,abnormal pupillary function
+NCBITaxon:693766,Anemiaceae,NCBITaxon:693762,Schizaeales
+DOID:8517,acute cor pulmonale,DOID:8514,acute pulmonary heart disease
+HP:0002380,Fasciculations,HP:0004305,Involuntary movements
+UBERON:0003252,thoracic rib cage,UBERON:0010912,subdivision of skeleton
+UBERON:0008885,right putamen,UBERON:0001874,putamen
+HP:0011881,Decreased platelet glycoprotein VI,HP:0011878,Abnormal platelet membrane protein expression
+UBERON:0003553,diencephalon pia mater,UBERON:0003290,meninx of diencephalon
+UBERON:0003143,pupa,UBERON:0000468,multi-cellular organism
+UBERON:0004318,distal phalanx of pedal digit 4,UBERON:0003862,pedal digit 4 phalanx
+HP:0009624,Contractures of the carpometacarpal joint of the thumb,HP:0009600,Flexion contracture of thumb
+UBERON:4000115,mineralized bone tissue,UBERON:0002481,bone tissue
+HP:0009562,Patchy sclerosis of the distal phalanx of the 2nd finger,HP:0009542,Abnormality of the distal phalanx of the 2nd finger
+HP:0003177,Squared iliac bones,HP:0002867,Abnormality of the ilium
+HP:0009559,Bullet-shaped distal phalanx of the 2nd finger,HP:0009548,Bullet-shaped phalanges of the 2nd finger
+UBERON:0001678,temporal bone,UBERON:0008193,pneumatized bone
+HP:0100449,Curved distal phalanx of the 3rd toe,HP:0010362,Curved phalanges of the 3rd toe
+UBERON:0013278,canal of Nuck,UBERON:0005156,reproductive structure
+UBERON:2000829,sclerotome somite 11,UBERON:0003089,sclerotome
+HP:0100483,Symphalangism of the proximal phalanx of the 2nd toe with the 2nd metatarsal,HP:0010401,Symphalangism affecting the proximal phalanx of the 2nd toe
+UBERON:3000952,posterior radial,UBERON:0002513,endochondral bone
+UBERON:3000234,inferior prenasal cartilage,UBERON:0003406,cartilage of respiratory system
+UBERON:4200188,manual toe disc,UBERON:4200151,toe disc
+HP:0007209,Facial paralysis,HP:0000301,Abnormality of facial musculature
+UBERON:0006431,xiphoid process bone,UBERON:0002481,bone tissue
+UBERON:0003248,epithelium of footplate,UBERON:0005291,embryonic tissue
+HP:0005627,Type D brachydactyly,HP:0001156,Brachydactyly syndrome
+HP:0005421,Decreased serum complement C3,HP:0004431,Complement deficiency
+HP:0010201,Triangular shaped middle phalanges of the toes,HP:0010183,Abnormality of the middle phalanges of the toes
+UBERON:3000773,ilial ridge,UBERON:0004120,mesoderm-derived structure
+UBERON:0002382,rectus abdominis muscle,UBERON:0004120,mesoderm-derived structure
+HP:0009739,Hypoplasia of the antihelix,HP:0009738,Abnormality of the antihelix
+UBERON:0012278,gland of nasal mucosa,UBERON:0004119,endoderm-derived structure
+UBERON:2000687,superficial pretectum,UBERON:0003047,regional part of pretectal region
+UBERON:0002705,midline nuclear group,UBERON:0015233,nucleus of dorsal thalamus
+CL:1000344,paneth cell of epithelium proper of small intestine,CL:1000343,paneth cell of epithelium of small intestine
+HP:0010161,Abnormality of the phalanges of the toes,HP:0001780,Abnormality of toe
+DOID:10265,hairy cell leukemia of spleen,DOID:285,hairy cell leukemia
+HP:0002204,Pulmonary embolism,HP:0002088,Abnormality of the lung
+HP:0011609,Type III truncus arteriosus,HP:0001660,Truncus arteriosus
+HP:0010082,Symphalangism affecting the distal phalanx of the hallux,HP:0010053,Abnormality of the distal phalanx of the hallux
+UBERON:2001789,dorsal fin spine 1,UBERON:2002261,dorsal fin spine
+HP:0009321,Absent epiphysis of the middle phalanx of the 3rd finger,HP:0010257,Absent epiphyses of the middle phalanges of the hand
+DOID:11246,DIC in newborn,DOID:11247,disseminated intravascular coagulation
+DOID:4630,inverted transitional papilloma,DOID:3179,inverted papilloma
+UBERON:0005168,interlobular vein,UBERON:0005269,renal cortex vein
+UBERON:0016409,base of glans penis,UBERON:0014403,male anatomical structure
+UBERON:0002917,regional part of inferior colliculus,UBERON:0002966,regional part of midbrain tectum
+UBERON:2201416,pelvic fin distal radial cartilage 3,UBERON:2101416,pelvic fin distal radial element 3
+UBERON:0008529,piriformis muscle,UBERON:0002000,gluteal muscle
+UBERON:0003450,upper jaw incisor,UBERON:0003267,tooth of upper jaw
+DOID:0050703,infancy electroclinical syndrome,DOID:0050701,electroclinical syndrome
+CL:0000659,eggshell secreting cell,CL:0000500,follicular epithelial cell
+DOID:1844,mononeuritis of upper limb,DOID:572,mononeuritis of upper limb and mononeuritis multiplex
+UBERON:0001128,sternocleidomastoid,UBERON:0003897,axial muscle
+UBERON:0003047,regional part of pretectal region,UBERON:0002616,regional part of brain
+HP:0008890,Severe short-limb dwarfism,HP:0008873,Disproportionate short-limb short stature
+HP:0100364,Aplasia of the phalanges of the 5th toe,HP:0010383,Aplasia/Hypoplasia of the phalanges of the 5th toe
+DOID:3704,fallopian tube mucinous adenocarcinoma,DOID:3706,fallopian tube adenocarcinoma
+HP:0009683,Small epiphysis of the distal phalanx of the thumb,HP:0009662,Abnormality of the epiphysis of the distal phalanx of the thumb
+HP:0008440,C1-C2 vertebral abnormality,HP:0003319,Abnormality of the cervical spine
+CL:0002354,yolk sac hematopoietic stem cell,CL:0002352,gestational hematopoietic stem cell
+UBERON:2001817,middle nuchal plate,UBERON:0004376,fin bone
+UBERON:2000549,posttemporal,UBERON:0007829,pectoral girdle bone
+UBERON:2002090,pro-otic fossa,UBERON:0004704,bone fossa
+HP:0006607,Precocious costochondral ossification,HP:0012306,Abnormal rib ossification
+CL:0000848,microvillous olfactory receptor neuron,CL:0000207,olfactory receptor cell
+HP:0010961,Intralobar sequestration,HP:0010960,Bronchopulmonary sequestration
+HP:0006799,Basal ganglia cysts,HP:0010576,Intracranial cystic lesion
+UBERON:4200125,supraacetabular crest,UBERON:0004120,mesoderm-derived structure
+HP:0100405,Duplication of the proximal phalanx of the 4th toe,HP:0010382,Abnormality of the proximal phalanx of the 4th toe
+UBERON:0009587,mesenchyme of interdigital region between manual digits 2 and 3,UBERON:0009597,mesenchyme of interdigital region between digits 2 and 3
+DOID:9717,hydrops of gallbladder,DOID:0000000,gallbladder disease
+CL:0000094,granulocyte,CL:0000081,blood cell
+DOID:10073,syphilitic meningitis,DOID:9470,bacterial meningitis
+HP:0100807,Long fingers,HP:0001167,Abnormality of finger
+DOID:7293,mucin-rich endometrial endometrioid adenocarcinoma,DOID:2870,endometrial adenocarcinoma
+UBERON:0012429,hemopoietic tissue,UBERON:0000479,tissue
+HP:0003013,Bulging epiphyses,HP:0010580,Enlarged epiphyses
+CL:0002569,mesenchymal stem cell of umbilical cord,CL:0000134,mesenchymal cell
+CL:1000469,myoepithelial cell of main lactiferous duct,CL:0000185,myoepithelial cell
+UBERON:0006717,autopodial skeleton,UBERON:0004120,mesoderm-derived structure
+HP:0010800,Absent cupid's bow,HP:0011339,Abnormality of upper lip vermillion
+UBERON:2002119,dermal scale focus,UBERON:0004120,mesoderm-derived structure
+UBERON:0004686,gastro-splenic ligament,UBERON:0008845,nonskeletal ligament
+CL:0002118,CD38-negative IgG-negative class switched memory B cell,CL:0002117,IgG-negative class switched memory B cell
+UBERON:2000633,caudal tuberculum,UBERON:0002784,regional part of diencephalon
+DOID:13403,cerebral sarcoidosis,DOID:11335,sarcoidosis
+HP:0011119,Abnormality of the nasal dorsum,HP:0010938,Abnormality of the external nose
+HP:0012751,Abnormal basal ganglia MRI signal intensity,HP:0002134,Abnormality of the basal ganglia
+UBERON:0001746,fibrous capsule of thyroid gland,UBERON:0003893,capsule
+HP:0004408,Abnormality of the sense of smell,HP:0000366,Abnormality of the nose
+HP:0012068,Aspartylglucosaminuria,HP:0012067,Glycopeptiduria
+HP:0006192,Tapered phalanx of finger,HP:0005918,Abnormality of phalanx of finger
+CL:0000624,"CD4-positive, alpha-beta T cell",CL:0000791,mature alpha-beta T cell
+CL:0002675,H plus,CL:0000521,fungal cell
+CL:0000251,extramedullary cell,CL:0000101,sensory neuron
+HP:0003593,Infantile onset,HP:0011007,Age of onset
+HP:0012022,Congenital portosystemic venous shunt,HP:0010948,Abnormality of the fetal cardiovascular system
+UBERON:0011309,body of mandible,UBERON:0004120,mesoderm-derived structure
+UBERON:0004330,proximal phalanx of manual digit 4,UBERON:0002234,proximal phalanx of manus
+CL:0000232,erythrocyte,CL:0000081,blood cell
+HP:0002779,Tracheomalacia,HP:0002778,Abnormality of the trachea
+HP:0100328,Carpometacarpal synostosis,HP:0009702,Carpal synostosis
+UBERON:0004139,cardiogenic plate,UBERON:0005423,developing anatomical structure
+HP:0011244,Abnormality of stem of antihelix,HP:0009738,Abnormality of the antihelix
+NCBITaxon:203491,Fusobacteriales,NCBITaxon:203490,Fusobacteriia
+UBERON:2001183,dermal superficial region,UBERON:0000481,multi-tissue structure
+HP:0001837,Broad toe,HP:0001780,Abnormality of toe
+HP:0012015,EEG with frontal focal spikes,HP:0011193,EEG with focal spikes
+HP:0000696,Delayed eruption of permanent teeth,HP:0000684,Delayed eruption of teeth
+HP:0001780,Abnormality of toe,HP:0011297,Abnormality of the digits
+HP:0100235,Synostosis involving bones of the toes,HP:0100262,Synostosis involving digits
+CL:0000675,female gamete,CL:0000021,female germ cell
+UBERON:0006447,fifth lumbar spinal cord segment,UBERON:0007716,lumbar subsegment of spinal cord
+UBERON:0002450,decidua,UBERON:0014404,female anatomical structure
+UBERON:0013196,strand of wool,UBERON:0010509,strand of pelage hair
+UBERON:2000235,magnocellular superficial pretectal nucleus,UBERON:0006569,diencephalic nucleus
+HP:0008465,Absent vertebrae,HP:0008515,Aplasia/Hypoplasia of the vertebrae
+HP:0010286,Abnormality of the salivary glands,HP:0000163,Abnormality of the oral cavity
+HP:0012050,Anasarca,HP:0007430,Generalized edema
+DOID:711,refractory hairy cell leukemia,DOID:712,refractory hematologic cancer
+UBERON:0014477,thoracic skeleton,UBERON:0010912,subdivision of skeleton
+CL:1000322,pancreatic goblet cell,CL:0000069,branched duct epithelial cell
+DOID:1577,limited scleroderma,DOID:418,systemic scleroderma
+UBERON:0013135,interdental plate,UBERON:0004121,ectoderm-derived structure
+CL:0000613,basophil progenitor cell,CL:0000763,myeloid cell
+UBERON:0004122,genitourinary system,UBERON:0000467,anatomical system
+UBERON:3000786,fossa cubitalis ventralis,UBERON:0004704,bone fossa
+UBERON:0003292,meninx of spinal cord,UBERON:0002360,meninx
+UBERON:0001235,adrenal cortex,UBERON:0004120,mesoderm-derived structure
+DOID:13629,dentine erosion,DOID:2498,tooth erosion
+UBERON:0013237,genital papilla of vulva,UBERON:0005156,reproductive structure
+UBERON:0005109,metanephric smooth muscle tissue,UBERON:0001135,smooth muscle tissue
+UBERON:0010402,epidermis suprabasal layer,UBERON:0004121,ectoderm-derived structure
+HP:0004375,Neoplasm of the nervous system,HP:0011793,Neoplasm by anatomical site
+HP:0100378,Absent distal phalanx of the 3rd toe,HP:0100362,Aplasia of the phalanges of the 3rd toe
+UBERON:0001220,quadratus lumborum,UBERON:0004518,muscle of vertebral column
+UBERON:3000459,prearticular coronoid process,UBERON:4100000,skeletal element projection
+UBERON:3010423,larval aorta,UBERON:0000947,aorta
+HP:0007685,Peripheral retinal avascularization,HP:0008046,Abnormality of the retinal vasculature
+UBERON:0008286,feather calamus,UBERON:0004121,ectoderm-derived structure
+UBERON:3000998,suprarostral cartilage,UBERON:0004121,ectoderm-derived structure
+DOID:752,peptic ulcer perforation,DOID:750,peptic ulcer disease
+DOID:1082,dirofilariasis,DOID:1080,filariasis
+NCBITaxon:208897,New world arenaviruses,NCBITaxon:11618,Arenavirus
+UBERON:2001171,os suspensorium,UBERON:2000461,Weberian ossicle
+HP:0002536,Abnormal cortical gyration,HP:0002538,Abnormality of the cerebral cortex
+UBERON:0004289,radula,UBERON:0000062,organ
+UBERON:2002124,nuptial tubercle,UBERON:0003102,surface structure
+HP:0000609,Optic nerve hypoplasia,HP:0008058,Aplasia/Hypoplasia of the optic nerve
+HP:0000564,Lacrimal duct atresia,HP:0011481,Abnormality of the lacrimal duct
+HP:0000662,Night blindness,HP:0000504,Abnormality of vision
+DOID:11156,anhidrosis,DOID:1383,sweat gland disease
+CL:0002337,keratinocyte stem cell,CL:1000428,stem cell of epidermis
+CL:0000442,follicular dendritic cell,CL:0000473,defensive cell
+HP:0011252,Cryptotia,HP:0000377,Abnormality of the pinna
+HP:0011951,Aspiration pneumonia,HP:0002090,Pneumonia
+UBERON:0001682,palatine bone,UBERON:0003462,facial bone
+CL:0000733,lymph gland plasmatocyte,CL:0000735,lymph gland hemocyte
+DOID:10919,transsexualism,DOID:1234,gender identity disorder
+CL:0002364,cortical thymic epithelial cell,CL:0002293,epithelial cell of thymus
+HP:0011459,Esophageal carcinoma,HP:0100751,Esophageal neoplasm
+UBERON:3000794,displasiocoelous,UBERON:0001075,vertebral centrum
+UBERON:0002633,motor nucleus of trigeminal nerve,UBERON:0006331,brainstem nucleus
+UBERON:0004336,proximal phalanx of pedal digit 5,UBERON:0014505,proximal phalanx of digit 5
+HP:0010145,Pseudoepiphysis of the distal phalanx of the hallux,HP:0010124,Abnormality of the epiphysis of the distal phalanx of the hallux
+CL:1000347,vacuolar absorptive cell of epithelium of colon,CL:0002071,enterocyte of epithelium of large intestine
+UBERON:0003231,epithelium of hip,UBERON:0010371,ecto-epithelium
+UBERON:0007806,connecting stalk,UBERON:0000478,extraembryonic structure
+UBERON:3000449,posterior maxillary process dorsal process,UBERON:0004529,anatomical projection
+HP:0010181,Duplication of phalanx of toe,HP:0010161,Abnormality of the phalanges of the toes
+UBERON:2000228,lateral line primordium,UBERON:0000479,tissue
+HP:0012702,Tenesmus,HP:0012700,Abnormal large intestine physiology
+UBERON:0010746,iliac blade,UBERON:0004120,mesoderm-derived structure
+DOID:7146,Langerhans cell sarcoma,DOID:5621,histiocytic and dendritic cell cancer
+HP:0001380,Ligamentous laxity,HP:0001382,Joint hypermobility
+NCBITaxon:43801,Ceratopogoninae,NCBITaxon:41819,Ceratopogonidae
+HP:0010253,Pseudoepiphyses of the distal phalanges of the hand,HP:0010235,Pseudoepiphyses of the phalanges of the hand
+UBERON:0005343,cortical plate,UBERON:0014950,layer of developing cerebral cortex
+HP:0000641,Dysmetric saccades,HP:0000570,Abnormality of saccadic eye movements
+HP:0003354,Hyperthreoninemia,HP:0010900,Abnormality of threonine metabolism
+UBERON:2105376,dorsal fin distal radial element 5,UBERON:2100936,dorsal fin distal radial element
+HP:0010336,Abnormality of the phalanges of the 4th toe,HP:0010321,Abnormality of the 4th toe
+DOID:9973,substance dependence,DOID:303,substance-related disorder
+UBERON:0015094,distal carpal bone 4 cartilage,UBERON:0015093,distal carpal bone 4 endochondral element
+HP:0007917,Tractional retinal detachment,HP:0000541,Retinal detachment
+HP:0010075,Duplication of the 1st metatarsal,HP:0010054,Abnormality of the first metatarsal
+UBERON:0009890,anterior intestinal portal,UBERON:0004111,anatomical conduit
+UBERON:0001657,superficial temporal vein,UBERON:0001671,temporal vein
+DOID:718,autoimmune hemolytic anemia,DOID:0060050,autoimmune disease of blood
+HP:0010684,Low alkaline phosphatase of bone origin,HP:0010683,Low tissue non-specific alkaline phosphatase
+DOID:229,female reproductive system disease,DOID:15,reproductive system disease
+UBERON:3000991,dorsal folds,UBERON:3000977,body external integument structure
+UBERON:0008952,upper lobe of left lung,UBERON:0008951,left lung lobe
+UBERON:0009623,spinal nerve root,UBERON:0002211,nerve root
+CL:1001210,outer medulla vasa recta ascending limb cell,CL:1001127,outer renal medulla vasa recta cell
+HP:0011967,Hypocupremia,HP:0010836,Abnormality of copper homeostasis
+HP:0008606,Supraauricular pit,HP:0100277,Periauricular skin pits
+UBERON:0011136,ligament of vertebral column,UBERON:0008846,skeletal ligament
+DOID:9258,Waardenburg's syndrome,DOID:0050736,autosomal dominant disease
+HP:0002155,Hypertriglyceridemia,HP:0003077,Hyperlipidemia
+HP:0010195,Broad middle phalanges of the toes,HP:0010174,Broad phalanx of the toes
+CL:1001223,interlobulary vein endothelial cell,CL:1001145,interlobular vein cell
+UBERON:0001082,epicardium of ventricle,UBERON:0002348,epicardium
+UBERON:0000430,ventral intermediate nucleus of thalamus,UBERON:0015234,nucleus of ventral thalamus
+UBERON:0006555,excretory tube,UBERON:0000025,tube
+UBERON:0003060,pronephric duct,UBERON:0009201,nephric duct
+DOID:13732,panophthalmitis,DOID:13452,scleritis
+DOID:12449,aplastic anemia,DOID:4961,bone marrow disease
+CL:0002220,interstitial cell of pineal gland,CL:0000710,neurecto-epithelial cell
+HP:0009643,Bullet-shaped distal phalanx of the thumb,HP:0009652,Bullet-shaped phalanges of the thumb
+UBERON:0004044,anterior visceral endoderm,UBERON:0004119,endoderm-derived structure
+UBERON:2001967,orbit,UBERON:0000464,anatomical space
+UBERON:0004928,submucosa of appendix,UBERON:0004927,submucosa of cecum
+UBERON:0008461,inferior articular process of lumbar vertebra,UBERON:0001080,inferior articular process of vertebra
+UBERON:0009897,right auditory cortex,UBERON:0001393,auditory cortex
+DOID:13972,female breast lower-outer quadrant cancer,DOID:0050671,female breast cancer
+UBERON:0003124,chorion,UBERON:0004120,mesoderm-derived structure
+HP:0009840,Patchy sclerosis of the distal phalanges of the hand,HP:0009772,Patchy sclerosis of the phalanges of the hand
+HP:0001166,Arachnodactyly,HP:0100807,Long fingers
+UBERON:0010846,radius pre-cartilage condensation,UBERON:0003327,mesenchyme of forearm
+UBERON:0010198,carotid duct,UBERON:0004573,systemic artery
+UBERON:2000033,intermediate cell mass of mesoderm,UBERON:0000479,tissue
+DOID:4289,micronodular basal cell carcinoma,DOID:2513,basal cell carcinoma
+HP:0100302,Muscle fiber tubuloreticular inclusions,HP:0100303,Muscle fiber cytoplasmatic inclusion bodies
+DOID:10966,lipoid nephrosis,DOID:1184,nephrotic syndrome
+UBERON:0002382,rectus abdominis muscle,UBERON:0002461,anterior abdominal wall muscle
+HP:0001827,Genital tract atresia,HP:0012243,Abnormal genital system morphology
+DOID:0050657,Bannayan-Riley-Ruvalcaba syndrome,DOID:0050736,autosomal dominant disease
+UBERON:2000341,dorsal flexor,UBERON:0000366,flexor muscle
+HP:0009977,Duplication of the proximal phalanx of the 4th finger,HP:0010006,Duplication of the proximal phalanx of hand
+UBERON:3000718,ectochordal,UBERON:0001075,vertebral centrum
+HP:0011196,EEG with focal sharp waves,HP:0011185,EEG with focal epileptiform discharges
+UBERON:0015122,anatomical line between outer canthi,UBERON:0006800,anatomical line
+DOID:1426,ureteral disease,DOID:18,urinary system disease
+HP:0010232,Fragmentation of the epiphyses of the phalanges of the hand,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+HP:0011936,Decreased plasma total carnitine,HP:0003234,Decreased plasma carnitine
+UBERON:0001105,clavicle,UBERON:0015212,lateral structure
+CL:0002320,connective tissue cell,CL:0002371,somatic cell
+UBERON:0010517,cephalic clasper,UBERON:0010516,clasper
+CL:0000115,endothelial cell,CL:0002078,meso-epithelial cell
+UBERON:0002268,main olfactory organ,UBERON:0000020,sense organ
+HP:0004043,Lytic defects of ulnar metaphysis,HP:0002797,Osteolysis
+HP:0010114,Bracket epiphyses of the hallux,HP:0010163,Bracket epiphyses of the toes
+UBERON:0001955,epithelium of respiratory bronchiole,UBERON:0002051,epithelium of bronchiole
+CL:0002019,Ly-76 high reticulocyte,CL:0002422,enucleated reticulocyte
+DOID:11193,syndactyly,DOID:11971,synostosis
+DOID:6204,follicular adenoma,DOID:2891,thyroid adenoma
+UBERON:0003371,pelvic appendage bud ectoderm,UBERON:0005291,embryonic tissue
+UBERON:2000805,myotome somite 23,UBERON:0003082,myotome
+UBERON:0008323,dorsal artery of clitoris,UBERON:0014404,female anatomical structure
+UBERON:0014663,nucleus recessus lateralis,UBERON:0006568,hypothalamic nucleus
+DOID:8500,hereditary retinal dystrophy,DOID:8501,fundus dystrophy
+HP:0100943,Sclerosis of the proximal phalanx of the hallux,HP:0100947,Sclerosis of the middle phalanges of the toes
+HP:0007313,Cerebral degeneration,HP:0007369,Atrophy/Degeneration affecting the cerebrum
+DOID:13862,acute closed-angle glaucoma,DOID:1405,primary angle-closure glaucoma
+DOID:1607,hypoglycemic coma,DOID:936,brain disease
+DOID:0080040,fibrogenesis imperfecta ossium,DOID:225,syndrome
+UBERON:2007036,hindbrain neural rod,UBERON:0004121,ectoderm-derived structure
+UBERON:0013152,interventricular foramen of heart,UBERON:0004111,anatomical conduit
+HP:0001082,Cholecystitis,HP:0012438,Abnormal gallbladder physiology
+UBERON:0016422,compact bone of long bone,UBERON:0005808,bone tissue of long bone
+UBERON:0007173,lateral border of scapula,UBERON:0007171,border of scapula
+HP:0002631,Ascending aortic aneurysm,HP:0005111,Dilatation of the ascending aorta
+UBERON:0008263,inter-ambulacral area,UBERON:0000475,organism subdivision
+UBERON:0002994,nucleus of pretectal area,UBERON:0011214,nucleus of midbrain tectum
+HP:0003251,Male infertility,HP:0000789,Infertility
+UBERON:3010328,equatorial belt,UBERON:0000479,tissue
+UBERON:3010132,taenia tecti medialis,UBERON:0003932,cartilage element of chondrocranium
+UBERON:0001148,median nerve,UBERON:0002003,peripheral nerve
+UBERON:0012195,left superior intercostal vein,UBERON:0012194,superior intercostal vein
+HP:0009518,Irregular epiphysis of the middle phalanx of the 2nd finger,HP:0010262,Irregular epiphyses of the middle phalanges of the hand
+HP:0100795,Abnormally straight spine,HP:0010674,Abnormality of the curvature of the vertebral column
+HP:0001384,Abnormality of the hip joint,HP:0003272,Abnormality of the hip bone
+NCBITaxon:39087,Arvicolinae,NCBITaxon:337677,Cricetidae
+HP:0010109,Short hallux,HP:0001831,Short toe
+UBERON:0001480,proximal carpal bone,UBERON:0001435,carpal bone
+DOID:7489,Osgood-Schlatter's disease,DOID:3342,bone inflammation disease
+HP:0009172,Abnormality of the phalanges of the 4th finger,HP:0005918,Abnormality of phalanx of finger
+HP:0012077,Histrionic personality disorder,HP:0012075,Personality disorder
+UBERON:0011766,vagus X nerve left recurrent laryngeal branch,UBERON:0003716,recurrent laryngeal nerve
+DOID:13913,lumbosacral plexus lesion,DOID:574,peripheral nervous system disease
+UBERON:0002363,dura mater,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005297,testis sex cord,UBERON:0004910,epithelium of male gonad
+CL:0000076,squamous epithelial cell,CL:0000066,epithelial cell
+UBERON:3011048,genital system,UBERON:0000467,anatomical system
+UBERON:0009780,cardiac muscle tissue of left auricle,UBERON:0003378,cardiac muscle of auricular region
+UBERON:0001901,epithelium of trachea,UBERON:0000485,simple columnar epithelium
+UBERON:0015056,ischial endochondral element,UBERON:0004120,mesoderm-derived structure
+UBERON:0013760,external cervical os,UBERON:0013758,cervical os
+HP:0008757,Unilateral vocal cord paralysis,HP:0001604,Vocal cord paresis
+UBERON:2001864,basibranchial 1 cartilage,UBERON:0013747,basibranchial cartilage
+UBERON:0011932,pilosebaceous unit,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0011579,venom gland,UBERON:0002365,exocrine gland
+HP:0001178,Ulnar claw,HP:0001155,Abnormality of the hand
+UBERON:0001221,transversus abdominis muscle,UBERON:0002461,anterior abdominal wall muscle
+HP:0005345,Abnormality of the vena cava,HP:0002597,Abnormality of the vasculature
+UBERON:0001008,renal system,UBERON:0000467,anatomical system
+HP:0012517,Reduced catalase activity,HP:0012379,Abnormal enzyme/coenzyme activity
+HP:0010205,Bullet-shaped proximal phalanges of the toes,HP:0010184,Abnormality of the proximal phalanges of the toes
+HP:0001669,Transposition of the great arteries,HP:0011563,Abnormal ventriculo-arterial connection
+UBERON:3011121,late distal segment,UBERON:0000479,tissue
+CL:0011001,spinal cord motor neuron,CL:0000100,motor neuron
+UBERON:0004232,lymphatic vessel smooth muscle,UBERON:0001135,smooth muscle tissue
+HP:0009418,Small epiphyses of the 3rd finger,HP:0009320,Abnormality of the epiphyses of the 3rd finger
+DOID:0050460,Wolf-Hirschhorn syndrome,DOID:0080014,chromosomal disease
+DOID:4442,cervical alveolar soft part sarcoma,DOID:4362,cervical cancer
+HP:0001080,Biliary tract abnormality,HP:0004297,Abnormality of the biliary system
+UBERON:0008921,substratum of layer of retina,UBERON:0004121,ectoderm-derived structure
+UBERON:0011663,anterior plastron-carapace bridge,UBERON:0011662,plastron-carapace bridge
+DOID:13653,stenosis of lacrimal punctum,DOID:530,eyelid disease
+HP:0009147,Enlarged epiphysis of the distal phalanx of the 5th finger,HP:0009385,Enlarged epiphyses of the 5th finger
+UBERON:0006929,glandular columnar epithelium,UBERON:0006799,glandular epithelium
+UBERON:0003253,neck of rib,UBERON:0001560,neck of organ
+DOID:12603,acute leukemia,DOID:1240,leukemia
+UBERON:0006631,right atrium auricular region,UBERON:0006618,atrium auricular region
+HP:0011022,Abnormality of unsaturated fatty acid metabolism,HP:0004359,Abnormality of fatty-acid metabolism
+HP:0006316,Irregularly spaced teeth,HP:0000692,Misalignment of teeth
+UBERON:3000639,zygomatic ramus of squamosal,UBERON:0004120,mesoderm-derived structure
+UBERON:3000757,zonal area,UBERON:0000477,anatomical cluster
+DOID:1678,chronic interstitial cystitis,DOID:1680,chronic cystitis
+UBERON:0000130,transverse foramen,UBERON:0010276,vertebral column opening
+CL:2000006,tonsil germinal center B cell,CL:0000844,germinal center B cell
+UBERON:4200055,homocercal tail,UBERON:4000164,caudal fin
+HP:0012744,Femoral aplasia,HP:0005613,Aplasia/hypoplasia of the femur
+UBERON:0010344,3rd arch mesenchyme from head mesenchyme,UBERON:0006904,head mesenchyme from mesoderm
+UBERON:2000412,posterior semicircular canal primordium,UBERON:2002215,otic vesicle protrusion
+DOID:771,retinal cell cancer,DOID:4645,retinal cancer
+HP:0100596,Absent nares,HP:0005288,Abnormality of the nares
+HP:0005877,Multiple small vertebral fractures,HP:0003468,Abnormality of the vertebrae
+HP:0000349,Widow's peak,HP:0009890,High anterior hairline
+HP:0100546,Carotid artery stenosis,HP:0005344,Abnormality of the carotid arteries
+UBERON:2001755,dorsal fin lepidotrichium 2,UBERON:4000177,dorsal fin lepidotrichium
+HP:0010053,Abnormality of the distal phalanx of the hallux,HP:0010057,Abnormality of the phalanges of the hallux
+HP:0011887,Choroid hemorrhage,HP:0011885,Hemorrhage of the eye
+DOID:4997,Camurati-Engelmann disease,DOID:4254,osteosclerosis
+CL:0000065,ependymal cell,CL:0000067,ciliated epithelial cell
+HP:0009343,Small epiphysis of the distal phalanx of the 3rd finger,HP:0009418,Small epiphyses of the 3rd finger
+UBERON:0008341,columella nasi,UBERON:0003102,surface structure
+UBERON:0005987,right branch of atrioventricular bundle,UBERON:0010131,conducting tissue of heart
+UBERON:3010094,quadratoethmoid process,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010096,Complete duplication of the distal phalanx of the hallux,HP:0010100,Complete duplication of the phalanges of the hallux
+HP:0100126,Fragmentation of the epiphysis of the proximal phalanx of the 2nd toe,HP:0100090,Abnormality of the epiphysis of the proximal phalanx of the 2nd toe
+UBERON:0001279,portal triad,UBERON:0000064,organ part
+HP:0100082,Irregular epiphyses of the 5th toe,HP:0010167,Irregular epiphyses of the toes
+UBERON:0012102,buccal salivary gland,UBERON:0001830,minor salivary gland
+CL:0002461,CD103-positive dendritic cell,CL:0000990,conventional dendritic cell
+HP:0002062,Abnormality of the pyramidal tracts,HP:0007319,Morphological abnormality of the central nervous system
+HP:0010212,Flexion contracture of the hallux,HP:0005830,Flexion contracture of toe
+CL:0002581,perirenal preadipocyte,CL:0002334,preadipocyte
+CL:0000425,pore cell,CL:0000658,cuticle secreting cell
+CL:0000753,type 1 cone bipolar cell (sensu Mus),CL:0000752,cone retinal bipolar cell
+UBERON:0011253,gland of anal sac,UBERON:0004121,ectoderm-derived structure
+CL:0000134,mesenchymal cell,CL:0000048,multi fate stem cell
+HP:0012294,Abnormality of the occipital bone,HP:0000929,Abnormality of the skull
+UBERON:0011512,puborectalis muscle,UBERON:0001325,muscle of pelvis
+UBERON:0006135,myelinated nerve fiber,UBERON:0006134,nerve fiber
+UBERON:0005097,renal connecting tubule,UBERON:0012275,meso-epithelium
+UBERON:0010585,pedal digit phalanx pre-cartilage condensation,UBERON:0005255,pedal digit mesenchyme
+UBERON:0010062,pharyngotympanic tube epithelium,UBERON:0005911,endo-epithelium
+HP:0012525,Abnormal alpha granule distribution,HP:0012483,Abnormal alpha granules
+UBERON:0000930,stomodeum,UBERON:0000481,multi-tissue structure
+UBERON:0012109,zygomatic process of frontal bone,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:0050580,hereditary lymphedema,DOID:4977,lymphedema
+NCBITaxon:40141,Sigmodontinae,NCBITaxon:337677,Cricetidae
+UBERON:0000111,organogenesis stage,UBERON:0000067,embryo stage part
+UBERON:0011565,lumen of gastrointestinal system,UBERON:0002553,anatomical cavity
+HP:0009247,Abnormality of the epiphysis of the middle phalanx of the 4th finger,HP:0009283,Abnormality of the middle phalanx of the 4th finger
+HP:0003852,Normal density transverse bands in metaphyses of the upper limbs,HP:0009809,Abnormality of upper limb metaphysis
+HP:0000966,Hypohidrosis,HP:0000971,Abnormality of the sweat gland
+CL:0000634,Claudius cell,CL:0002315,supporting cell of cochlea
+UBERON:2005275,hyomandibular foramen,UBERON:0005744,bone foramen
+DOID:10823,malignant essential hypertension,DOID:10825,essential hypertension
+UBERON:0004422,proximal epiphysis of first metacarpal bone,UBERON:0004391,epiphysis of first metacarpal bone
+HP:0003913,Irregular humeral metaphyses,HP:0003907,Abnormality of the humeral metaphyses
+HP:0004218,Symphalangism of the 5th finger,HP:0004213,Abnormality of the phalanges of the 5th finger
+HP:0005798,Posterior radial head dislocation,HP:0003083,Dislocated radial head
+HP:0007811,Horizontal pendular nystagmus,HP:0012043,Pendular nystagmus
+HP:0012653,Status Asthmaticus,HP:0002099,Asthma
+DOID:3870,childhood central nervous system primitive neuroectodermal neoplasm,DOID:0060103,central nervous system primitive neuroectodermal neoplasm
+HP:0010457,Widening of the sacrosciatic notch,HP:0010456,Abnormality of the greater sacrosciatic notch
+UBERON:0005225,upper leg epithelium,UBERON:0010371,ecto-epithelium
+DOID:13994,cleidocranial dysplasia,DOID:2256,osteochondrodysplasia
+HP:0005368,Abnormality of humoral immunity,HP:0010978,Abnormality of immune system physiology
+DOID:8446,intussusception,DOID:8437,intestinal obstruction
+DOID:11177,total internal ophthalmoplegia,DOID:10034,eye accommodation disease
+HP:0010063,Patchy sclerosis of the phalanges of the hallux,HP:0100930,Sclerosis of the phalanges of the hallux
+NCBITaxon:1763,Mycobacterium,NCBITaxon:1762,Mycobacteriaceae
+CL:0002103,IgG-positive double negative memory B cell,CL:0000981,double negative memory B cell
+DOID:5391,bronchus adenoma,DOID:5386,lung adenoma
+HP:0003839,Abnormality involving the epiphyses of the upper limbs,HP:0006505,Abnormality involving the epiphyses of the limbs
+UBERON:0010900,tarsometatarsus cartilage element,UBERON:0015012,tarsometatarsus endochondral element
+HP:0000634,Impaired ocular abduction,HP:0011347,Abnormality of ocular abduction
+HP:0000538,Pseudopapilledema,HP:0000479,Abnormality of the retina
+HP:0000175,Cleft palate,HP:0000202,Oral cleft
+DOID:0050889,non-syndromic intellectual disability,DOID:1059,intellectual disability
+HP:0004981,prominent ulnar styloid process,HP:0004035,Abnormality of the styloid process
+DOID:14681,Silver-Russell syndrome,DOID:0080014,chromosomal disease
+HP:0004380,Aortic valve calcification,HP:0005146,Cardiac valve calcification
+UBERON:3000012,angulosplenial coronoid process,UBERON:0004530,bony projection
+HP:0000506,Telecanthus,HP:0000492,Abnormality of the eyelid
+UBERON:3010618,constrictor laryngis externus,UBERON:3000224,hyobranchial muscle
+HP:0012701,Bowel urgency,HP:0012700,Abnormal large intestine physiology
+CL:0000513,cardiac muscle myoblast,CL:0010021,cardiac myoblast
+UBERON:0005424,presumptive retinal pigmented epithelium,UBERON:0006598,presumptive structure
+HP:0008802,Hypoplasia of the femoral head,HP:0003368,Abnormality of the femoral head
+UBERON:3010506,postcaval vein,UBERON:0001638,vein
+HP:0009424,Osteolytic defects of the distal phalanx of the 3rd finger,HP:0009357,Abnormality of the distal phalanx of the 3rd finger
+UBERON:0013488,panniculus adiposus,UBERON:0002190,subcutaneous adipose tissue
+UBERON:0001087,pleural fluid,UBERON:0007794,serous fluid
+HP:0002212,Curly hair,HP:0010719,Abnormality of hair texture
+HP:0004222,Cone-shaped epiphysis of the distal phalanx of the 5th finger,HP:0010248,Cone-shaped epiphyses of the distal phalanges of the hand
+HP:0010021,Ivory epiphysis of the 1st metacarpal,HP:0010014,Abnormality of the epiphysis of the 1st metacarpal
+UBERON:0015247,bifurcation of trachea,UBERON:0004119,endoderm-derived structure
+DOID:7232,central nervous system embryonal carcinoma,DOID:4439,central nervous system germ cell tumor
+UBERON:0002726,cervical spinal cord,UBERON:0005844,spinal cord segment
+HP:0012722,Heart block,HP:0011675,Arrhythmia
+DOID:13005,intra-abdominal lymph node mast cell malignancy,DOID:10619,lymph node cancer
+HP:0200150,increased serum bile acid concentration during pregnancy,HP:0012202,increased serum bile acid concentration
+UBERON:1000000,chin ventral margin,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0001583,Rotary nystagmus,HP:0000639,Nystagmus
+HP:0007270,Atypical absence seizures,HP:0002121,Absence seizures
+UBERON:0005374,spinal cord lateral column,UBERON:0002318,white matter of spinal cord
+CL:0000022,female germ line stem cell,CL:0000014,germ line stem cell
+CL:0000777,mesangial phagocyte,CL:0000864,tissue-resident macrophage
+DOID:1790,malignant mesothelioma,DOID:0050687,cell type cancer
+UBERON:0009536,vascular element of left lung,UBERON:0000102,lung vasculature
+UBERON:0003215,alveolus,UBERON:0000064,organ part
+HP:0100405,Duplication of the proximal phalanx of the 4th toe,HP:0010379,Duplication of phalanx of the 4th toe
+UBERON:2001313,ventral anterior lateral line ganglion,UBERON:2001391,anterior lateral line ganglion
+UBERON:0013589,koniocortex,UBERON:0002619,regional part of cerebral cortex
+UBERON:0011319,disk of temporomandibular joint,UBERON:0013765,digestive system organ
+HP:0009979,Complete duplication of the middle phalanx of the 4th finger,HP:0010002,Complete duplication of the middle phalanges of the hand
+CL:0002203,Brush cell of epithelium proper of large intestine,CL:0002253,epithelial cell of large intestine
+UBERON:0001254,urothelium of ureter,UBERON:0000365,urothelium
+HP:0001513,Obesity,HP:0004324,Increased body weight
+UBERON:0009118,marsupial pouch,UBERON:0005156,reproductive structure
+HP:0011813,Increased cerebral lipofuscin,HP:0007367,Atrophy/Degeneration affecting the central nervous system
+HP:0010404,Aplasia/Hypoplasia of the middle phalanx of the 2nd toe,HP:0010357,Abnormality of the middle phalanx of the 2nd toe
+DOID:13189,gout,DOID:848,arthritis
+HP:0010098,Complete duplication of the 1st metatarsal,HP:0010075,Duplication of the 1st metatarsal
+UBERON:0004326,middle phalanx of pedal digit 4,UBERON:0003866,middle phalanx of pes
+UBERON:0009052,medial nucleus of solitary tract,UBERON:0009050,nucleus of solitary tract
+HP:0005322,Prominent nasal septum,HP:0000419,Abnormality of the nasal septum
+HP:0001883,Talipes,HP:0005656,Positional foot deformity
+CL:0000547,proerythroblast,CL:0000764,erythroid lineage cell
+DOID:5895,clear cell cystadenofibroma,DOID:5482,cystadenofibroma
+HP:0002197,Generalized seizures,HP:0001250,Seizures
+UBERON:0005354,malleus processus brevis,UBERON:4100000,skeletal element projection
+HP:0010170,Small epiphyses of the toes,HP:0010160,Abnormality of the epiphyses of the toes
+UBERON:0001105,clavicle,UBERON:0002495,long bone
+HP:0003844,Small epiphyses of the upper limbs,HP:0010585,Small epiphyses
+UBERON:2101586,pectoral fin radial element,UBERON:1600006,paired fin radial element
+HP:0009246,Aplasia of the distal phalanx of the 5th finger,HP:0009881,Aplasia of the distal phalanges of the hand
+CL:0000895,"naive thymus-derived CD4-positive, alpha-beta T cell",CL:0000624,"CD4-positive, alpha-beta T cell"
+UBERON:0013684,right dorsal thalamus,UBERON:0004703,dorsal thalamus
+UBERON:3000069,cartilago infranarina,UBERON:0003933,cranial cartilage
+UBERON:0005203,trachea gland,UBERON:0002530,gland
+UBERON:0005384,nasal cavity epithelium,UBERON:0004814,upper respiratory tract epithelium
+DOID:1642,breast adenomyoepithelioma,DOID:3004,breast myoepithelial neoplasm
+HP:0009788,Quadriceps aplasia,HP:0009787,Aplasia/Hypoplasia of the quadriceps
+DOID:2224,hemorrhagic thrombocythemia,DOID:2226,chronic myeloproliferative disease
+HP:0009227,Broad proximal phalanx of the 5th finger,HP:0009374,Broad phalanges of the 5th finger
+UBERON:3000492,processus infrafenestralis,UBERON:0004120,mesoderm-derived structure
+UBERON:0005133,metanephric glomerulus vasculature,UBERON:0004190,renal glomerulus vasculature
+UBERON:0004661,mandible temporal crest,UBERON:0004120,mesoderm-derived structure
+UBERON:0006499,dorsal pes interosseous muscle,UBERON:0006497,interosseous muscle of pes
+CL:0000054,bone matrix secreting cell,CL:0000151,secretory cell
+HP:0002507,Semilobar holoprosencephaly,HP:0001360,Holoprosencephaly
+NCBITaxon:775,Rickettsiaceae,NCBITaxon:766,Rickettsiales
+UBERON:0004547,decidua capsularis,UBERON:0014404,female anatomical structure
+UBERON:3000875,spina pelvis posterior,UBERON:4100000,skeletal element projection
+HP:0100649,Neoplasm of the oral cavity,HP:0011793,Neoplasm by anatomical site
+HP:0002472,Small cerebral cortex,HP:0002538,Abnormality of the cerebral cortex
+UBERON:0003951,ocular fundus,UBERON:0004121,ectoderm-derived structure
+DOID:8601,upper gum cancer,DOID:8602,gum cancer
+HP:0011088,Dens in dente,HP:0011063,Abnormality of incisor morphology
+UBERON:3010735,ramus anterior of CN VIII,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002354,purkinje fiber,UBERON:0004493,cardiac muscle tissue of myocardium
+HP:0010083,Triangular shaped distal phalanx of the hallux,HP:0010053,Abnormality of the distal phalanx of the hallux
+HP:0011126,Nephroptosis,HP:0100542,Abnormal localization of kidney
+UBERON:0004029,canal of Schlemm,UBERON:0003496,head blood vessel
+UBERON:0004442,proximal epiphysis of proximal phalanx of manual digit 4,UBERON:0004420,proximal epiphysis of phalanx of manual digit 4
+HP:0100909,Sclerosis of the proximal phalanx of the 3rd finger,HP:0100917,Sclerosis of the proximal phalanges of the hand
+UBERON:2000321,caudal levator,UBERON:0000933,pharyngeal muscle
+HP:0005766,Disproportionate shortening of the tibia,HP:0005736,Short tibia
+DOID:13498,urethral syndrome,DOID:732,urethral disease
+UBERON:0012621,muscle of Aristotle's lantern,UBERON:0010959,craniocervical muscle
+UBERON:2000685,superficial abductor,UBERON:0014794,pectoral appendage muscle
+HP:0002877,Nocturnal hypoventilation,HP:0002791,Hypoventilation
+HP:0006549,Unilateral primary pulmonary dysgenesis,HP:0002088,Abnormality of the lung
+DOID:4875,trachea adenoid cystic carcinoma,DOID:4876,trachea carcinoma
+HP:0009951,Partial duplication of the distal phalanx of the 2nd finger,HP:0009948,Duplication of the distal phalanx of the 2nd finger
+DOID:5958,bladder urachal carcinoma,DOID:4007,bladder carcinoma
+HP:0004321,Bladder fistula,HP:0000014,Abnormality of the bladder
+HP:0011132,Chronic furunculosis,HP:0005406,Recurrent bacterial skin infections
+UBERON:0000376,hindlimb stylopod,UBERON:0002472,stylopod
+UBERON:0012080,patella cartilage element,UBERON:0003860,hindlimb mesenchyme
+UBERON:0006332,nasal capsule,UBERON:0001823,nasal cartilage
+HP:0008689,Bilateral cryptorchidism,HP:0000028,Cryptorchidism
+UBERON:0001602,medial rectus extraocular muscle,UBERON:0006533,rectus extraocular muscle
+UBERON:0015042,manual digit metacarpus endochondral element,UBERON:0015063,autopod endochondral element
+NCBITaxon:10375,Lymphocryptovirus,NCBITaxon:10374,Gammaherpesvirinae
+HP:0005402,Primary T-lymphocyte immune abnormalities,HP:0011840,Abnormality of T cell physiology
+NCBITaxon:201174,Actinobacteria <phylum>,NCBITaxon:2,Bacteria
+UBERON:0000428,prostate epithelium,UBERON:0000485,simple columnar epithelium
+UBERON:0006772,long bone epiphyseal plate hypertrophic zone,UBERON:0006775,zone of epiphyseal plate
+HP:0005772,Aplasia/Hypoplasia of the tibia,HP:0006493,Aplasia/Hypoplasia involving bones of the lower limbs
+HP:0007889,Iridescent posterior subcapsular cataract,HP:0007787,Posterior subcapsular cataract
+UBERON:0006050,digit 3,UBERON:0002544,digit
+UBERON:0005017,mucosa of lacrimal sac,UBERON:0000344,mucosa
+HP:0007756,Slitlike anterior chamber angles in children,HP:0000594,Shallow anterior chamber
+HP:0002894,Neoplasm of the pancreas,HP:0011793,Neoplasm by anatomical site
+HP:0100226,Cone-shaped epiphysis of the proximal phalanx of the 5th toe,HP:0100099,Abnormality of the epiphysis of the proximal phalanx of the 5th toe
+UBERON:0008884,left putamen,UBERON:0001874,putamen
+HP:0003049,Ulnar deviation of the wrist,HP:0003019,Abnormality of the wrist
+DOID:0060087,male reproductive organ benign neoplasm,DOID:0050622,reproductive organ benign neoplasm
+CL:0002153,corneocyte,CL:0000225,anucleate cell
+UBERON:0001635,superior cerebellar artery,UBERON:0003472,cerebellar artery
+UBERON:0011270,dorsal trunk,UBERON:0009569,subdivision of trunk
+UBERON:0014726,intercalated duct of pancreas,UBERON:0014725,intercalated duct
+UBERON:0001697,orbital region,UBERON:0000477,anatomical cluster
+HP:0100123,Bracket epiphysis of the proximal phalanx of the 2nd toe,HP:0100045,Bracket epiphyses of the 2nd toe
+HP:0007390,Hyperkeratosis with erythema,HP:0000962,Hyperkeratosis
+UBERON:0015281,pancreas right lobe,UBERON:0007324,pancreatic lobe
+UBERON:0001434,skeletal system,UBERON:0000467,anatomical system
+HP:0009428,Curved distal phalanx of the 3rd finger,HP:0009442,Curved phalanges of the 3rd finger
+DOID:5425,ovarian hyperstimulation syndrome,DOID:1100,ovarian disease
+DOID:12355,prostatocystitis,DOID:1679,cystitis
+UBERON:3000951,anterior radial,UBERON:0002513,endochondral bone
+UBERON:0004087,vena cava,UBERON:0003479,thoracic cavity vein
+UBERON:3010458,suprarostral ala,UBERON:0004121,ectoderm-derived structure
+HP:0000563,Keratoconus,HP:0100692,Increased corneal curvature
+UBERON:0011265,carpometacarpal joint of digit 1,UBERON:0011119,carpometacarpal joint
+HP:0010353,Symphalangism affecting the phalanges of the 2nd toe,HP:0010324,Abnormality of phalanx of the 2nd toe
+UBERON:3010194,mediale,UBERON:0000064,organ part
+DOID:11814,urinary bladder anterior wall cancer,DOID:11054,urinary bladder cancer
+DOID:9470,bacterial meningitis,DOID:9471,meningitis
+UBERON:0001007,digestive system,UBERON:0000467,anatomical system
+UBERON:0009746,head fold of embryonic disc,UBERON:0005291,embryonic tissue
+HP:0100924,Sclerosis of the phalanges of the toes,HP:0010161,Abnormality of the phalanges of the toes
+DOID:9459,isthmus cancer,DOID:9460,uterine corpus cancer
+UBERON:0004183,labyrinthine layer blood vessel,UBERON:0001981,blood vessel
+UBERON:2000305,ventral sulcus,UBERON:0006846,surface groove
+DOID:8516,pulmonary embolism and infarction,DOID:8514,acute pulmonary heart disease
+UBERON:0011893,endoneurial fluid,UBERON:0007794,serous fluid
+UBERON:3010500,gastrico-linealis,UBERON:0003509,arterial blood vessel
+HP:0010030,Osteolytic defects of the 1st metacarpal,HP:0009654,Osteolytic defects of the phalanges of the thumb
+HP:0006344,Abnormality of primary molar morphology,HP:0011070,Abnormality of molar morphology
+UBERON:4000119,non-mineralized avascular GAG-rich matrix,UBERON:4000059,avascular GAG-rich matrix
+DOID:986,alopecia areata,DOID:987,alopecia
+DOID:4306,radiculopathy,DOID:4307,polyradiculopathy
+UBERON:0013750,metaphysis of tibia,UBERON:0004120,mesoderm-derived structure
+HP:0009563,Distal/middle symphalangism of 2nd finger,HP:0009542,Abnormality of the distal phalanx of the 2nd finger
+UBERON:0001677,sphenoid bone,UBERON:0008193,pneumatized bone
+UBERON:0002871,hypoglossal nucleus,UBERON:0000126,cranial nerve nucleus
+UBERON:0004429,proximal epiphysis of third metatarsal bone,UBERON:0004415,proximal epiphysis of metatarsal bone
+HP:0011000,Aplasia/Hypoplasia of the optic tract,HP:0002977,Aplasia/Hypoplasia involving the central nervous system
+CL:1000444,mesothelial cell of anterior chamber of eye,CL:0000077,mesothelial cell
+UBERON:3010303,fasciculated network of fibrils,UBERON:0000478,extraembryonic structure
+UBERON:0001305,ovarian follicle,UBERON:0014404,female anatomical structure
+HP:0007277,Paucity of anterior horn motor neurons,HP:0002450,Abnormality of the motor neurons
+UBERON:2000388,medial caudal lobe,UBERON:0002946,regional part of cerebellum
+UBERON:0003434,wrist nerve,UBERON:0003448,manus nerve
+UBERON:2005074,central cardiac conduction system,UBERON:0002350,conducting system of heart
+HP:0004852,Reduced leukocyte alkaline phosphatase,HP:0003282,Low alkaline phosphatase
+UBERON:0002061,truncus arteriosus,UBERON:0003498,heart blood vessel
+UBERON:0001950,neocortex,UBERON:0002619,regional part of cerebral cortex
+UBERON:0003304,mesoderm blood island,UBERON:0005291,embryonic tissue
+HP:0009268,Pseudoepiphysis of the proximal phalanx of the 4th finger,HP:0010275,Pseudoepiphyses of the proximal phalanges of the hand
+HP:0009126,Increased adipose tissue,HP:0009025,Increased connective tissue
+DOID:0060006,artemis deficiency,DOID:627,severe combined immunodeficiency
+HP:0012268,Myxoid liposarcoma,HP:0012034,Liposarcoma
+UBERON:1600010,pelvic fin middle radial element,UBERON:2100508,pelvic fin radial element
+DOID:2122,pneumonic tularemia,DOID:2123,tularemia
+UBERON:0003033,suprageniculate nucleus,UBERON:0002308,nucleus of brain
+HP:0012275,Autosomal dominant inheritance with maternal imprinting,HP:0000006,Autosomal dominant inheritance
+UBERON:0004662,vertebra lamina,UBERON:0000063,organ segment
+HP:0007240,Progressive gait ataxia,HP:0002066,Gait ataxia
+UBERON:2001293,posterior kidney,UBERON:0005172,abdomen organ
+HP:0009973,Complete duplication of the phalanges of the 4th finger,HP:0009998,Complete duplication of phalanx of hand
+HP:0009240,Broad distal phalanx of the 5th finger,HP:0009836,Broad distal phalanx of finger
+UBERON:0016408,corona of glans penis,UBERON:0014403,male anatomical structure
+HP:0001367,Abnormal joint morphology,HP:0011842,Abnormality of skeletal morphology
+HP:0009273,Deviation of the 4th finger,HP:0004097,Deviation of finger
+UBERON:0001824,mucosa of larynx,UBERON:0000379,tracheal mucosa
+HP:0000774,Narrow chest,HP:0005257,Thoracic hypoplasia
+UBERON:0004411,proximal epiphysis of humerus,UBERON:0004382,epiphysis of humerus
+UBERON:0013201,olfactory pathway,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:6846,familial melanoma,DOID:1909,melanoma
+CL:0000387,hemocyte (sensu Nematoda and Protostomia),CL:0000519,phagocyte (sensu Nematoda and Protostomia)
+UBERON:0003900,epaxial myotome region,UBERON:0005291,embryonic tissue
+UBERON:0011602,gingiva of lower jaw,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:1838,Menkes disease,DOID:896,metal metabolism disorder
+UBERON:0003951,ocular fundus,UBERON:0000064,organ part
+HP:0009684,Stippling of the epiphysis of the distal phalanx of the thumb,HP:0009662,Abnormality of the epiphysis of the distal phalanx of the thumb
+HP:0004226,Curved distal phalanx of the 5th finger,HP:0004225,Abnormality of the distal phalanx of the 5th finger
+HP:0010182,Abnormality of the distal phalanges of the toes,HP:0010161,Abnormality of the phalanges of the toes
+HP:0009197,Bracket epiphysis of the proximal phalanx of the 5th finger,HP:0010269,Bracket epiphyses of the proximal phalanges of the hand
+UBERON:0002057,phrenic artery,UBERON:0004573,systemic artery
+UBERON:0013155,1st arch mandibular ectoderm,UBERON:0010371,ecto-epithelium
+HP:0011243,Abnormality of inferior crus of antihelix,HP:0009738,Abnormality of the antihelix
+HP:0001199,Triphalangeal thumb,HP:0001172,Abnormality of the thumb
+DOID:0060164,pain disorder,DOID:4737,somatoform disorder
+DOID:4029,gastritis,DOID:76,stomach disease
+DOID:5429,bladder flat intraepithelial lesion,DOID:0050623,bladder benign neoplasm
+HP:0003540,Impaired platelet aggregation,HP:0011869,Abnormal platelet function
+HP:0011861,Bilateral trilobed lungs,HP:0002101,Abnormal lung lobation
+DOID:13402,skin sarcoidosis,DOID:11335,sarcoidosis
+UBERON:0002571,external nucleus of inferior colliculus,UBERON:0002917,regional part of inferior colliculus
+HP:0003090,Hypoplasia of the capital femoral epiphysis,HP:0005003,Aplasia/Hypoplasia of the capital femoral epiphysis
+UBERON:2001688,palatine cartilage,UBERON:0004121,ectoderm-derived structure
+UBERON:0011970,talofibular ligament,UBERON:0008846,skeletal ligament
+DOID:0050704,childhood electroclinical syndrome,DOID:0050701,electroclinical syndrome
+HP:0006949,Episodic peripheral neuropathy,HP:0009830,Peripheral neuropathy
+UBERON:2001909,pharyngobranchial element,UBERON:0010363,endochondral element
+UBERON:0006831,pre-tracheal muscle,UBERON:0000933,pharyngeal muscle
+UBERON:0006435,os penis,UBERON:0014403,male anatomical structure
+UBERON:0004757,rectal gland,UBERON:0004758,salt gland
+UBERON:0004644,fourth ventricle ependyma,UBERON:0005357,brain ependyma
+UBERON:0001177,left hepatic duct,UBERON:0003703,extrahepatic bile duct
+CL:0002100,regular interventricular cardiac myocyte,CL:0002098,regular cardiac myocyte
+DOID:10972,salpingo-oophoritis,DOID:10974,oophoritis
+HP:0000519,Congenital cataract,HP:0000518,Cataract
+HP:0006684,Ventricular preexcitation with multiple accessory pathways,HP:0004309,Ventricular preexcitation
+DOID:9534,tuberculous pneumothorax,DOID:1673,pneumothorax
+UBERON:3000316,nasal opening,UBERON:0006332,nasal capsule
+UBERON:0001436,phalanx of manus,UBERON:0003221,phalanx
+UBERON:0004894,alveolar wall,UBERON:0004119,endoderm-derived structure
+UBERON:4200122,pubotibialis,UBERON:0001325,muscle of pelvis
+HP:0009524,Absent epiphysis of the proximal phalanx of the 2nd finger,HP:0010268,Absent epiphyses of the proximal phalanges of the hand
+UBERON:0010220,arytenoid pre-cartilage condensation,UBERON:0010213,laryngeal pre-cartilage condensation
+CL:0000126,macroglial cell,CL:0000243,glial cell (sensu Vertebrata)
+HP:0004879,intermittent hyperventilation,HP:0002883,Hyperventilation
+CL:0000242,Merkel cell,CL:0000312,keratinocyte
+DOID:12637,perineocele,DOID:1284,prolapse of female genital organ
+UBERON:2005010,mid cerebral vein,UBERON:0003496,head blood vessel
+UBERON:0013623,pedal autopod pad,UBERON:0012348,autopod pad
+DOID:0050658,Bart-Pumphrey syndrome,DOID:0050736,autosomal dominant disease
+CL:0000075,columnar/cuboidal epithelial cell,CL:0000066,epithelial cell
+UBERON:0002090,postcranial axial skeleton,UBERON:0010912,subdivision of skeleton
+DOID:2835,polycythemia due to hypoxia,DOID:2834,acquired polycythemia
+HP:0010975,Abnormality of B cell number,HP:0002846,Abnormality of B cells
+DOID:2140,urethral urothelial papilloma,DOID:730,urethral benign neoplasm
+DOID:1578,pulmonary systemic sclerosis,DOID:418,systemic scleroderma
+DOID:4115,ovarian mesodermal adenosarcoma,DOID:6170,ovarian carcinosarcoma
+HP:0100635,Carotid paraganglioma,HP:0005344,Abnormality of the carotid arteries
+UBERON:2005304,caudal fin blood vessel,UBERON:0007301,appendage blood vessel
+HP:0000052,"Urethral atresia, male",HP:0000036,Abnormality of the penis
+UBERON:0001236,adrenal medulla,UBERON:0004120,mesoderm-derived structure
+UBERON:0010584,pedal digit 5 phalanx pre-cartilage condensation,UBERON:0010585,pedal digit phalanx pre-cartilage condensation
+DOID:10206,lipoma of spermatic cord,DOID:10207,paratesticular lipoma
+DOID:13100,intracranial vasospasm,DOID:6713,cerebrovascular disease
+DOID:1970,fallopian tube carcinosarcoma,DOID:1964,fallopian tube cancer
+HP:0001631,Defect in the atrial septum,HP:0005120,Abnormality of cardiac atrium
+UBERON:0003592,bronchus connective tissue,UBERON:0003580,lower respiratory tract connective tissue
+DOID:175,vascular cancer,DOID:176,cardiovascular cancer
+CL:0002303,pigmented ciliary epithelial cell,CL:0005012,multi-ciliated epithelial cell
+HP:0009120,Aplasia/Hypoplasia involving the sinuses,HP:0000245,Abnormality of the sinuses
+HP:0003902,Epiphyseal stippling of the humerus,HP:0010655,Epiphyseal stippling
+HP:0001964,Aplasia/Hypoplasia of metatarsal bones,HP:0001832,Abnormality of the metatarsal bones
+UBERON:3010538,pars nervosa,UBERON:0004121,ectoderm-derived structure
+HP:0006948,Progressive infantile encephalopathy,HP:0007105,Infantile encephalopathy
+DOID:5213,chronic inflammatory demyelinating polyradiculoneuropathy,DOID:5214,demyelinating polyneuropathy
+UBERON:0002205,manubrium of sternum,UBERON:0004120,mesoderm-derived structure
+DOID:12384,dysentery,DOID:100,intestinal infectious disease
+DOID:5339,cyclic hematopoiesis,DOID:1227,neutropenia
+UBERON:0004161,septum transversum,UBERON:0003104,mesenchyme
+HP:0010080,Osteolytic defects of the distal phalanx of the hallux,HP:0010189,Osteolytic defects of the distal phalanges of the toes
+CL:0001053,IgD-negative memory B cell,CL:0000787,memory B cell
+DOID:12323,cough variant asthma,DOID:2841,asthma
+UBERON:0008811,intromittent organ,UBERON:0003135,male reproductive organ
+HP:0004349,Reduced bone mineral density,HP:0004348,Abnormality of bone mineral density
+DOID:3927,pelvic lipomatosis,DOID:3153,lipomatosis
+HP:0002410,Aqueductal stenosis,HP:0002118,Abnormality of the cerebral ventricles
+HP:0011193,EEG with focal spikes,HP:0011185,EEG with focal epileptiform discharges
+HP:0010279,Hyperplasia of the maxilla,HP:0000326,Abnormality of the maxilla
+UBERON:0001683,jugal bone,UBERON:0003462,facial bone
+CL:0002365,medullary thymic epithelial cell,CL:0002293,epithelial cell of thymus
+HP:0010144,Ivory epiphysis of the distal phalanx of the hallux,HP:0010124,Abnormality of the epiphysis of the distal phalanx of the hallux
+HP:0003756,Skeletal myopathy,HP:0003198,Myopathy
+HP:0001821,Broad nail,HP:0002164,Nail dysplasia
+UBERON:0003232,epithelium of knee,UBERON:0010371,ecto-epithelium
+UBERON:0014527,posterior limb of internal capsule,UBERON:0014525,subdivision of internal capsule
+UBERON:0007835,sacral spinal cord ventral commissure,UBERON:0004170,spinal cord ventral commissure
+HP:0011981,Pigment gallstones,HP:0001081,Cholelithiasis
+HP:0008060,Aplasia/Hypoplasia of the fovea,HP:0000493,Abnormality of the fovea
+HP:0010069,Bullet-shaped 1st metatarsal,HP:0010060,Bullet-shaped phalanges of the hallux
+HP:0010335,Abnormality of the epiphyses of the 4th toe,HP:0010321,Abnormality of the 4th toe
+UBERON:0009659,spermatic artery,UBERON:0001187,testicular artery
+HP:0006813,Hemiclonic seizures,HP:0002266,Focal clonic seizures
+UBERON:0008287,feather vane,UBERON:0004121,ectoderm-derived structure
+HP:0009849,Symphalangism of middle phalanx of finger,HP:0009773,Symphalangism affecting the phalanges of the hand
+HP:0005876,Progressive flexion contractures,HP:0001371,Flexion contracture
+UBERON:0002207,xiphoid process,UBERON:0004120,mesoderm-derived structure
+DOID:0060176,gamma-amino butyric acid metabolism disorder,DOID:9252,amino acid metabolic disorder
+DOID:9263,homocystinuria,DOID:9252,amino acid metabolic disorder
+HP:0010074,Triangular shaped 1st metatarsal,HP:0010054,Abnormality of the first metatarsal
+HP:0001332,Dystonia,HP:0100022,Abnormality of movement
+UBERON:0002457,intersomitic artery,UBERON:0014907,intersomitic vessel
+HP:0000155,Oral ulcer,HP:0011830,Abnormality of oral mucosa
+UBERON:0004873,splanchnopleure,UBERON:0005423,developing anatomical structure
+HP:0009700,Synostosis involving bones of the fingers,HP:0004278,Synostosis involving bones of the hand
+HP:0000415,Abnormality of the choanae,HP:0000366,Abnormality of the nose
+UBERON:0010496,teres minor muscle,UBERON:0010467,teres muscle
+HP:0003935,Wide humeral diaphysis,HP:0003861,Broad diaphyses of the upper limbs
+DOID:11736,odontoclasia,DOID:216,dental caries
+HP:0010231,Enlarged epiphyses of the phalanges of the hand,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+HP:0002390,Spinal arteriovenous malformation,HP:0100026,Arteriovenous malformation
+DOID:4932,ampulla of Vater carcinoma,DOID:10020,ampulla of Vater cancer
+HP:0001988,Recurrent hypoglycemia,HP:0001943,Hypoglycemia
+DOID:14021,Tietze's syndrome,DOID:1222,cartilage disease
+HP:0009595,Occasional neurofibromas,HP:0001067,Neurofibromas
+UBERON:0014397,lateral process of malleus,UBERON:4100000,skeletal element projection
+HP:0200025,Mandibular pain,HP:0000277,Abnormality of the mandible
+UBERON:0010747,body of ilium,UBERON:0004120,mesoderm-derived structure
+NCBITaxon:11245,Pneumovirus,NCBITaxon:11244,Pneumovirinae
+DOID:3044,food allergy,DOID:1205,hypersensitivity reaction type I disease
+UBERON:0002642,cuneate fasciculus of medulla,UBERON:0007702,tract of brain
+NCBITaxon:82104,mitosporic Herpotrichiellaceae,NCBITaxon:43219,Herpotrichiellaceae
+UBERON:0008462,inferior articular process of cervical vertebra,UBERON:0001080,inferior articular process of vertebra
+UBERON:0009898,left auditory cortex,UBERON:0001393,auditory cortex
+DOID:5031,adult pineal parenchymal tumor,DOID:5032,pineal gland cancer
+DOID:4007,bladder carcinoma,DOID:11054,urinary bladder cancer
+CL:0000597,microconidium,CL:0002381,uninucleate conidium
+HP:0004368,Increased purine levels,HP:0004352,Abnormality of purine metabolism
+UBERON:0009980,condyle of femur,UBERON:0004120,mesoderm-derived structure
+HP:0100355,Contractures of the distal interphalangeal joint of the 5th toe,HP:0010345,Flexion contracture of the 5th toe
+DOID:1561,cognitive disorder,DOID:150,disease of mental health
+HP:0006476,Abnormality of the pancreatic islet cells,HP:0012093,Abnormality of endocrine pancreas physiology
+HP:0003224,Increased cellular sensitivity to UV light,HP:0011017,Abnormality of cell physiology
+HP:0005243,Partial abdominal muscle agenesis,HP:0010318,Aplasia/Hypoplasia of the abdominal wall musculature
+DOID:1406,iritis,DOID:240,iris disease
+UBERON:0003155,arthropod occiput,UBERON:0006056,posterior surface of head
+UBERON:0003463,trunk bone,UBERON:0005177,trunk organ
+UBERON:0001109,sternothyroid muscle,UBERON:0003897,axial muscle
+UBERON:3010708,levator mandibulae articularis,UBERON:0011648,jaw muscle
+UBERON:0003299,roof plate of midbrain,UBERON:0003298,roof plate of neural tube
+UBERON:3000719,holochordal,UBERON:0001075,vertebral centrum
+DOID:10810,tibialis tendinitis,DOID:971,tendinitis
+HP:0009072,Decreased Achilles reflex,HP:0002600,Hyporeflexia of lower limbs
+HP:0007599,Generalized reticulate brown pigmentation,HP:0007440,Generalized hyperpigmentation
+DOID:5683,hereditary breast ovarian cancer,DOID:0050736,autosomal dominant disease
+HP:0010376,Patchy sclerosis of the phalanges of the 4th toe,HP:0010336,Abnormality of the phalanges of the 4th toe
+HP:0006344,Abnormality of primary molar morphology,HP:0006481,Abnormality of primary teeth
+UBERON:0010842,calcaneum cartilage element,UBERON:0015064,autopod cartilage
+UBERON:0007196,tracheobronchial tree,UBERON:0000062,organ
+HP:0011488,Abnormality of corneal endothelium,HP:0000481,Abnormality of the cornea
+DOID:10079,cysticercosis,DOID:0050596,taeniasis
+UBERON:3000572,sphenethmoid,UBERON:0002513,endochondral bone
+HP:0011922,Abnormal activity of mitochondrial respiratory chain,HP:0003287,Abnormality of mitochondrial metabolism
+HP:0012101,Decreased serum creatinine,HP:0012100,Abnormal circulating creatinine level
+HP:0009226,Short proximal phalanx of the 5th finger,HP:0009237,Short 5th finger
+NCBITaxon:7203,Brachycera,NCBITaxon:7147,Diptera
+HP:0012317,Sacroiliac arthritis,HP:0100781,Abnormality of the sacroiliac joint
+HP:0009415,Irregular epiphyses of the 3rd finger,HP:0009320,Abnormality of the epiphyses of the 3rd finger
+UBERON:0004907,lower digestive tract,UBERON:0004921,subdivision of digestive tract
+DOID:2101,vulva squamous cell carcinoma,DOID:1294,vulva carcinoma
+NCBITaxon:208896,Old world arenaviruses,NCBITaxon:11618,Arenavirus
+HP:0011100,Intestinal atresia,HP:0002242,Abnormality of the intestine
+HP:0006434,Hypoplasia of proximal radius,HP:0002984,Hypoplasia of the radius
+UBERON:0014886,distal epiphysis of distal phalanx of manual digit,UBERON:0004409,distal epiphysis of phalanx of manus
+UBERON:0000345,myelin,UBERON:0000061,anatomical structure
+HP:0007733,Laterally curved eyebrow,HP:0000534,Abnormality of the eyebrow
+UBERON:0011215,cell part cluster of neuraxis,UBERON:0004121,ectoderm-derived structure
+UBERON:0009714,intermaxillary process,UBERON:0009292,embryonic nasal process
+CL:0000516,perineuronal satellite cell,CL:0000123,neuron associated cell (sensu Vertebrata)
+UBERON:2001103,immature posterior otolith,UBERON:2000139,immature otolith
+UBERON:0006119,subbrachial nucleus,UBERON:0011214,nucleus of midbrain tectum
+UBERON:2001975,suprabranchial artery,UBERON:0001637,artery
+UBERON:0016452,upper secondary premolar tooth,UBERON:0007120,premolar tooth
+HP:0100246,Osteoma,HP:0010622,Neoplasm of the skeletal system
+DOID:7849,dendritic cell sarcoma,DOID:5621,histiocytic and dendritic cell cancer
+HP:0001191,Abnormality of the carpal bones,HP:0001155,Abnormality of the hand
+UBERON:0010518,pelvic fin clasper,UBERON:0010516,clasper
+UBERON:0001551,vein of hindlimb zeugopod,UBERON:0001638,vein
+DOID:2621,autonomic nervous system neoplasm,DOID:1192,peripheral nervous system neoplasm
+UBERON:3010200,cutaneous vasculature,UBERON:0003504,respiratory system blood vessel
+HP:0002041,Intractable diarrhea,HP:0002014,Diarrhea
+DOID:9299,myocardium cancer,DOID:117,heart cancer
+UBERON:0006634,lingual vein,UBERON:0001638,vein
+HP:0001385,Hip dysplasia,HP:0003272,Abnormality of the hip bone
+UBERON:0010718,pubic cartilage element,UBERON:0015055,pubic endochondral element
+CL:0002543,vein endothelial cell,CL:0000071,blood vessel endothelial cell
+DOID:8858,tonsil cancer,DOID:8557,oropharynx cancer
+HP:0008368,Tarsal synostosis,HP:0009140,Synostosis involving bones of the feet
+UBERON:2001913,pharyngobranchial 4 element,UBERON:2001909,pharyngobranchial element
+UBERON:0004449,cerebral artery,UBERON:0004573,systemic artery
+HP:0008935,Generalized neonatal hypotonia,HP:0001319,Neonatal hypotonia
+UBERON:0007622,pecten oculi,UBERON:0002203,vasculature of eye
+UBERON:1000000,chin ventral margin,UBERON:0001444,subdivision of head
+UBERON:0015100,distal tarsal cartilage,UBERON:0015099,distal tarsal bone endochondral element
+UBERON:0009654,alveolar artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005744,bone foramen,UBERON:0004111,anatomical conduit
+UBERON:0008785,upper limb segment,UBERON:0002529,limb segment
+UBERON:0000202,glial blood brain barrier,UBERON:0000120,blood brain barrier
+UBERON:0001351,lacrimal sac,UBERON:0004121,ectoderm-derived structure
+UBERON:0009634,root of coccygeal nerve,UBERON:0009623,spinal nerve root
+UBERON:0008443,webbed digit,UBERON:0002544,digit
+DOID:5766,pulmonary sclerosing hemangioma,DOID:490,hemangioma of lung
+UBERON:4200048,bicipital crest,UBERON:0004120,mesoderm-derived structure
+DOID:10631,partial optic atrophy,DOID:5723,optic atrophy
+UBERON:0003677,tooth root,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100338,Non-midline cleft palate,HP:0000175,Cleft palate
+UBERON:0004862,left lung alveolus,UBERON:0002299,alveolus of lung
+UBERON:0002537,hermaphrodite gonad,UBERON:0000991,gonad
+UBERON:2000052,dorsal actinotrichium,UBERON:2000089,actinotrichium
+UBERON:0002654,parvicellular part of medial dorsal nucleus,UBERON:0003528,brain grey matter
+HP:0009644,Curved distal phalanx of the thumb,HP:0009617,Abnormality of the distal phalanx of the thumb
+HP:0007677,Vitelliform maculopathy,HP:0001103,Abnormality of the macula
+HP:0011474,Childhood onset sensorineural hearing impairment,HP:0000407,Sensorineural hearing impairment
+DOID:5893,childhood malignant mesenchymoma,DOID:5758,malignant mesenchymoma
+UBERON:4200093,guard scale,UBERON:0002542,scale
+UBERON:0004655,zygomatic process of temporal bone,UBERON:0010313,neural crest-derived structure
+UBERON:0011847,acinus of parotid gland,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0007220,late embryonic stage,UBERON:0000067,embryo stage part
+HP:0010148,Triangular epiphysis of the distal phalanx of the hallux,HP:0010123,Triangular epiphyses of the hallux
+UBERON:0010303,extraembryonic epithelium,UBERON:0000483,epithelium
+UBERON:0000454,cerebral subcortex,UBERON:0004121,ectoderm-derived structure
+DOID:5282,prostate leiomyosarcoma,DOID:4054,prostate sarcoma
+UBERON:0003972,placenta junctional zone,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0100482,Proximal/middle symphalangism of 5th toe,HP:0100475,Symphalangism affecting the proximal phalanx of the 5th toe
+UBERON:0014666,nucleus recessus preopticus,UBERON:0006568,hypothalamic nucleus
+HP:0100861,Vertebral body sclerosis,HP:0003468,Abnormality of the vertebrae
+UBERON:0004884,lobar bronchus mesenchyme,UBERON:0004883,lung mesenchyme
+DOID:8886,chorioretinitis,DOID:5614,eye disease
+HP:0001361,Nystagmus-induced head nodding,HP:0000639,Nystagmus
+UBERON:0015180,neck of talus,UBERON:0001560,neck of organ
+HP:0002229,Alopecia areata,HP:0011360,Acquired abnormal hair pattern
+HP:0100301,Muscle fiber tubular inclusions,HP:0100303,Muscle fiber cytoplasmatic inclusion bodies
+DOID:5915,uterus intravascular leiomyomatosis,DOID:5916,uterine corpus leiomyomatosis
+CL:0002480,nasal mucosa goblet cell,CL:0000160,goblet cell
+DOID:4691,malignant mediastinal neurogenic neoplasm,DOID:5559,mediastinal cancer
+UBERON:0013501,cloacal sphincter,UBERON:0004590,sphincter muscle
+UBERON:0007273,pelvic appendage skeleton,UBERON:0011582,paired limb/fin skeleton
+UBERON:0002364,tympanic membrane,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0001012,Multiple lipomas,HP:0012031,Lipomatous tumor
+UBERON:0004790,skin mucous gland,UBERON:0002419,skin gland
+HP:0001315,Reduced tendon reflexes,HP:0012638,Abnormality of nervous system physiology
+CL:0000835,myeloblast,CL:0002191,granulocytopoietic cell
+DOID:5445,syringocystadenoma papilliferum,DOID:5876,apocrine sweat gland neoplasm
+UBERON:0001118,lobe of thyroid gland,UBERON:0000064,organ part
+UBERON:0006083,perirhinal cortex,UBERON:0002619,regional part of cerebral cortex
+HP:0009512,Triangular epiphysis of the distal phalanx of the 2nd finger,HP:0009499,Abnormality of the epiphysis of the distal phalanx of the 2nd finger
+UBERON:4200054,heterocercal tail,UBERON:4000164,caudal fin
+HP:0006454,Severely delayed patellae ossification,HP:0003045,Abnormality of the patella
+HP:0010275,Pseudoepiphyses of the proximal phalanges of the hand,HP:0010235,Pseudoepiphyses of the phalanges of the hand
+HP:0001909,Leukemia,HP:0001881,Abnormality of leukocytes
+UBERON:0012426,short microvillus layer,UBERON:0012423,layer of microvilli
+UBERON:0013237,genital papilla of vulva,UBERON:0000064,organ part
+DOID:4737,somatoform disorder,DOID:150,disease of mental health
+DOID:1209,nutritional optic neuropathy,DOID:1210,optic neuritis
+UBERON:2001754,dorsal fin lepidotrichium 1,UBERON:4000177,dorsal fin lepidotrichium
+HP:0010052,Abnormality of the proximal phalanx of the hallux,HP:0010057,Abnormality of the phalanges of the hallux
+HP:0011886,Hyphema,HP:0011885,Hemorrhage of the eye
+HP:0004404,Abnormality of the nipple,HP:0000769,Abnormality of the breast
+CL:1001286,inner medulla vasa recta descending limb cell,CL:1001126,inner renal medulla vasa recta cell
+HP:0002010,Narrow maxilla,HP:0000326,Abnormality of the maxilla
+UBERON:2000460,adipose fin actinotrichium,UBERON:2000089,actinotrichium
+HP:0004434,C8 deficiency,HP:0004431,Complement deficiency
+DOID:10155,intestinal cancer,DOID:3119,gastrointestinal system cancer
+UBERON:0015850,upper left incisor tusk,UBERON:0015848,incisor tusk
+CL:0002580,preadipocyte of the breast,CL:0002334,preadipocyte
+UBERON:0013146,venous system of brain,UBERON:0007798,vascular system
+DOID:1700,X-linked ichthyosis,DOID:0050735,X-linked disease
+DOID:2741,bilirubin metabolic disorder,DOID:655,inherited metabolic disorder
+UBERON:0002197,median eminence of neurohypophysis,UBERON:0005408,circumventricular organ
+UBERON:0013515,subdivision of uterine tube,UBERON:0014404,female anatomical structure
+UBERON:0001128,sternocleidomastoid,UBERON:0011364,cleidocephalicus muscle
+DOID:137,vagina squamous papilloma,DOID:0060114,vaginal benign neoplasm
+UBERON:0006949,cervical loop,UBERON:0003843,dental epithelium
+HP:0006495,Aplasia/Hypoplasia of the ulna,HP:0002997,Abnormality of the ulna
+HP:0009890,High anterior hairline,HP:0000599,Abnormality of the frontal hairline
+UBERON:0008262,ambulacral area,UBERON:0000475,organism subdivision
+UBERON:0006136,unmyelinated nerve fiber,UBERON:0006134,nerve fiber
+DOID:1080,filariasis,DOID:883,parasitic helminthiasis infectious disease
+HP:0006035,Cone-shaped epiphyses of phalanges 2 to 5,HP:0010230,Cone-shaped epiphyses of the phalanges of the hand
+UBERON:0010345,4th arch mesenchyme from head mesenchyme,UBERON:0006904,head mesenchyme from mesoderm
+HP:0010074,Triangular shaped 1st metatarsal,HP:0010065,Triangular shaped phalanges of the hallux
+HP:0009471,Contracture of the proximal interphalangeal joint of the 3rd finger,HP:0009698,Contractures of the proximal interphalangeal joints of the fingers
+HP:0100422,Partial duplication of the proximal phalanx of the 3rd toe,HP:0100404,Duplication of the proximal phalanx of the 3rd toe
+UBERON:0005871,palatine process of maxilla,UBERON:4100000,skeletal element projection
+UBERON:0012250,cervix glandular epithelium,UBERON:0006799,glandular epithelium
+UBERON:2000616,adductor profundus,UBERON:0014794,pectoral appendage muscle
+UBERON:4400005,fin ray,UBERON:0004765,skeletal element
+UBERON:0006120,superior colliculus superficial gray layer,UBERON:0006785,gray matter of superior colliculus
+HP:0100371,Aplasia/Hypoplasia of the distal phalanx of the 5th toe,HP:0010343,Aplasia/Hypoplasia of the 5th toe
+HP:0010020,Irregular epiphysis of the 1st metacarpal,HP:0010014,Abnormality of the epiphysis of the 1st metacarpal
+CL:0002058,Gr1-low non-classical monocyte,CL:0000875,non-classical monocyte
+HP:0002656,Epiphyseal dysplasia,HP:0005930,Abnormality of the epiphyses
+HP:0100129,Pseudoepiphysis of the proximal phalanx of the 2nd toe,HP:0100090,Abnormality of the epiphysis of the proximal phalanx of the 2nd toe
+HP:0008944,Distal lower limb amyotrophy,HP:0003693,Distal amyotrophy
+HP:0010112,Mesoaxial foot polydactyly,HP:0001829,Foot polydactyly
+HP:0007814,Salt and pepper retinopathy,HP:0011512,Hyperpigmentation of the fundus
+UBERON:3010239,subocular groove,UBERON:3000972,head external integument structure
+HP:0003914,Irregular ossification of humeral metaphyses,HP:0003907,Abnormality of the humeral metaphyses
+HP:0001562,Oligohydramnios,HP:0001560,Abnormality of the amniotic fluid
+HP:0001241,Capitate-hamate fusion,HP:0004262,Abnormality of the capitate bone
+HP:0009119,Aplasia/Hypoplasia of the frontal sinuses,HP:0002687,Abnormality of the frontal sinuses
+DOID:9978,acute female pelvic peritonitis,DOID:1003,pelvic inflammatory disease
+HP:0100447,Curved proximal phalanx of the 4th toe,HP:0010374,Curved phalanges of the 4th toe
+HP:0009194,Small epiphyses of the metacarpals,HP:0005913,Abnormality of metacarpal epiphyses
+UBERON:0008823,neural tube derived brain,UBERON:0000955,brain
+DOID:3162,malignant spindle cell melanoma,DOID:1909,melanoma
+CL:0000213,lining cell,CL:0000215,barrier cell
+DOID:6380,adult brain medulloblastoma,DOID:0060105,brain medulloblastoma
+UBERON:0013774,diaphysis of metatarsal bone,UBERON:0004769,diaphysis
+UBERON:0000062,organ,UBERON:0000061,anatomical structure
+UBERON:0004428,proximal epiphysis of second metatarsal bone,UBERON:0004415,proximal epiphysis of metatarsal bone
+NCBITaxon:11592,Nairovirus,NCBITaxon:11571,Bunyaviridae
+UBERON:3000859,foramen perforans carpi,UBERON:0004120,mesoderm-derived structure
+HP:0000172,Abnormality of the uvula,HP:0100736,Abnormality of the soft palate
+CL:0002163,internal pillar cell of cochlea,CL:1000191,pillar cell
+HP:0011998,Postprandial hyperglycemia,HP:0003074,Hyperglycemia
+HP:0008824,Hypoplastic iliac body,HP:0000946,Hypoplastic ilia
+UBERON:0004368,Reichert's cartilage,UBERON:0003570,respiratory system connective tissue
+UBERON:0005838,fasciculus of brain,UBERON:0011215,cell part cluster of neuraxis
+UBERON:0003218,ovary septum,UBERON:0005156,reproductive structure
+UBERON:0001300,scrotum,UBERON:0014403,male anatomical structure
+HP:0010087,Bullet-shaped proximal phalanx of the hallux,HP:0010196,Bullet-shaped middle phalanges of the toes
+UBERON:0014526,anterior limb of internal capsule,UBERON:0014525,subdivision of internal capsule
+DOID:7051,esophageal basaloid squamous cell carcinoma,DOID:3748,esophagus squamous cell carcinoma
+DOID:9909,hordeolum,DOID:37,skin disease
+HP:0009680,Irregular epiphysis of the distal phalanx of the thumb,HP:0009662,Abnormality of the epiphysis of the distal phalanx of the thumb
+DOID:0050697,chorioamnionitis,DOID:780,placenta disease
+UBERON:0005494,intermediate mesenchyme,UBERON:0007524,dense mesenchyme tissue
+HP:0000473,Torticollis,HP:0011006,Abnormality of the musculature of the neck
+UBERON:0005425,presumptive neural retina,UBERON:0006598,presumptive structure
+DOID:1073,renal hypertension,DOID:11130,secondary hypertension
+HP:0010640,Abnormality of the nasal cavity,HP:0000366,Abnormality of the nose
+UBERON:3010507,precaval vein,UBERON:0001638,vein
+HP:0007464,Sparse facial hair,HP:0008070,Sparse hair
+UBERON:0004325,middle phalanx of pedal digit 3,UBERON:0003866,middle phalanx of pes
+DOID:2892,exocervical carcinoma,DOID:2893,cervix carcinoma
+HP:0001149,Lattice corneal dystrophy,HP:0001131,Corneal dystrophy
+CL:0000131,gut endothelial cell,CL:0000115,endothelial cell
+UBERON:0004770,articular system,UBERON:0000467,anatomical system
+UBERON:2001948,anal-fin hook,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003964,prevertebral ganglion,UBERON:0001806,sympathetic ganglion
+UBERON:0010581,pedal digit 2 phalanx pre-cartilage condensation,UBERON:0015032,pedal digit 2 phalanx endochondral element
+DOID:0050593,primary congenital glaucoma,DOID:1686,glaucoma
+DOID:0050853,chronic venous insufficiency,DOID:10128,venous insufficiency
+HP:0005605,Large cafe-au-lait macules with irregular margins,HP:0001034,Hypermelanotic macule
+UBERON:0001610,lingual artery,UBERON:0004121,ectoderm-derived structure
+UBERON:0000428,prostate epithelium,UBERON:0005911,endo-epithelium
+UBERON:0010901,tarsometatarsus pre-cartilage condensation,UBERON:0015012,tarsometatarsus endochondral element
+DOID:5482,cystadenofibroma,DOID:2683,adenofibroma
+DOID:483,cavernous hemangioma,DOID:484,vascular hemostatic disease
+UBERON:1000020,collection of hair on snout,UBERON:0010165,collection of hair on face
+HP:0000534,Abnormality of the eyebrow,HP:0001595,Abnormality of the hair
+UBERON:0006913,lip epithelium,UBERON:0010371,ecto-epithelium
+DOID:6510,lung occult squamous cell carcinoma,DOID:3907,lung squamous cell carcinoma
+UBERON:3000874,crista ischii,UBERON:4100000,skeletal element projection
+UBERON:4000086,secondary cartilage tissue,UBERON:0002418,cartilage tissue
+HP:0010099,Partial duplication of the 1st metatarsal,HP:0010075,Duplication of the 1st metatarsal
+DOID:5293,extrahepatic bile duct leiomyosarcoma,DOID:4064,bile duct sarcoma
+HP:0003200,Ragged-red muscle fibers,HP:0004303,Abnormality of muscle fibers
+HP:0008661,Urethral stenosis,HP:0000796,Urethral obstruction
+UBERON:0005200,thoracic mammary gland,UBERON:0001911,mammary gland
+HP:0005413,Increased alpha-globulin,HP:0010702,Hypergammaglobulinemia
+HP:0004820,Acute myelomonocytic leukemia,HP:0002488,Acute leukemia
+UBERON:0000341,throat,UBERON:0000475,organism subdivision
+HP:0009465,Ulnar deviation of finger,HP:0004097,Deviation of finger
+NCBITaxon:11021,Eastern equine encephalitis virus,NCBITaxon:177873,EEEV complex
+NCBITaxon:11029,Ross River virus,NCBITaxon:177875,SFV complex
+DOID:12680,pseudobulbar palsy,DOID:231,motor neuron disease
+HP:0004622,Progressive intervertebral space narrowing,HP:0002945,Intervertebral space narrowing
+UBERON:0002865,arcuate nucleus of medulla,UBERON:0007635,nucleus of medulla oblongata
+HP:0007208,Irregular loops and focal folding of myelin sheaths,HP:0004336,Myelin outfoldings
+UBERON:2002017,anterior limb of ceratobranchial 5 bone,UBERON:0004530,bony projection
+HP:0002816,Genu recurvatum,HP:0002815,Abnormality of the knees
+UBERON:0013683,left dorsal thalamus,UBERON:0004703,dorsal thalamus
+HP:0100478,Symphalangism affecting the distal phalanx of the 5th toe,HP:0100472,Symphalangism affecting the middle phalanx of the 5th toe
+DOID:8536,herpes zoster,DOID:934,viral infectious disease
+UBERON:0009597,mesenchyme of interdigital region between digits 2 and 3,UBERON:0009585,interdigital region mesenchyme
+UBERON:0010537,mesonephric nephron progenitor,UBERON:0006554,urinary system structure
+HP:0100160,Enlarged epiphysis of the proximal phalanx of the 3rd toe,HP:0100058,Enlarged epiphyses of the 3rd toe
+HP:0100827,Lymphocytosis,HP:0012140,Abnormality of cells of the lymphoid lineage
+DOID:9736,blue drum syndrome,DOID:3697,acute transudative otitis media
+HP:0001268,Mental deterioration,HP:0100543,Cognitive impairment
+NCBITaxon:10509,Mastadenovirus,NCBITaxon:10508,Adenoviridae
+UBERON:0004662,vertebra lamina,UBERON:0004120,mesoderm-derived structure
+HP:0009950,Complete duplication of the distal phalanx of the 2nd finger,HP:0009948,Duplication of the distal phalanx of the 2nd finger
+UBERON:3010126,middle lateral line nerve (MLLN),UBERON:0008906,lateral line nerve
+HP:0100255,Metaphyseal dysplasia,HP:0002652,Skeletal dysplasia
+DOID:0060058,lymphoma,DOID:2531,hematologic cancer
+UBERON:0010714,iliac cartilage element,UBERON:0007844,cartilage element
+CL:0000709,R8 photoreceptor cell,CL:0000287,eye photoreceptor cell
+DOID:9165,neurotic excoriation,DOID:2723,dermatitis
+DOID:3642,empty sella syndrome,DOID:53,pituitary gland disease
+HP:0100538,Abnormality of the supraorbital ridges,HP:0000315,Abnormality of the orbital region
+HP:0000171,Microglossia,HP:0010295,Aplasia/Hypoplasia of the tongue
+HP:0003309,Ovoid thoracolumbar vertebrae,HP:0003300,Ovoid vertebral bodies
+HP:0008361,Corticospinal tract pallor,HP:0002492,Abnormality of the corticospinal tract
+UBERON:2005075,peripheral cardiac conduction system,UBERON:0002350,conducting system of heart
+UBERON:2001683,transcapular ligament,UBERON:0008846,skeletal ligament
+DOID:1964,fallopian tube cancer,DOID:120,female reproductive organ cancer
+UBERON:0001096,wall of esophagus,UBERON:0000328,gut wall
+DOID:5997,non-proliferative fibrocystic change of the breast,DOID:10354,breast fibrocystic disease
+UBERON:0002426,chest muscle,UBERON:0003830,thoracic segment muscle
+HP:0004057,Mitten deformity,HP:0005922,Abnormal hand morphology
+HP:0005939,Multiple bilateral pneumothoraces,HP:0002107,Pneumothorax
+HP:0008049,Abnormality of the extraocular muscles,HP:0012372,Abnormal eye morphology
+DOID:3529,central core myopathy,DOID:422,congenital structural myopathy
+UBERON:0003100,female organism,UBERON:0000468,multi-cellular organism
+HP:0006431,Metaphyseal abnormalities of distal and proximal femurs,HP:0006489,Abnormality of the femoral metaphysis
+UBERON:0002464,nerve trunk,UBERON:0004732,segmental subdivision of nervous system
+CL:0000896,"activated CD4-positive, alpha-beta T cell",CL:0000624,"CD4-positive, alpha-beta T cell"
+HP:0009558,Broad distal phalanx of the 2nd finger,HP:0009836,Broad distal phalanx of finger
+HP:0100304,Muscle fiber intranuclear inclusion bodies,HP:0100299,Muscle fiber inclusion bodies
+UBERON:0010737,distal tarsal bone 4,UBERON:0010721,distal tarsal bone
+CL:0000652,pinealocyte,CL:0000710,neurecto-epithelial cell
+UBERON:0014538,subdivision of spinal cord central canal,UBERON:0004111,anatomical conduit
+UBERON:0012118,infraspinatus tendon,UBERON:0003579,shoulder connective tissue
+HP:0011713,Left bundle branch block,HP:0011710,Bundle branch block
+DOID:4111,cervical adenosarcoma,DOID:4112,cervical carcinosarcoma
+UBERON:3000694,atlantal cotyle,UBERON:0000064,organ part
+CL:0000828,thromboblast,CL:0000226,single nucleate cell
+HP:0002924,Decreased circulating aldosterone level,HP:0000847,Abnormality of renin-angiotensin system
+UBERON:3010094,quadratoethmoid process,UBERON:4100000,skeletal element projection
+UBERON:0003353,epithelium of hindgut,UBERON:0003929,gut epithelium
+CL:0000611,eosinophil progenitor cell,CL:0000763,myeloid cell
+DOID:6523,ciliary body mixed cell melanoma,DOID:6524,malignant ciliary body melanoma
+UBERON:0003924,ventral pancreatic bud,UBERON:0003922,pancreatic bud
+HP:0010417,Osteolytic defects of the distal phalanx of the 2nd toe,HP:0010356,Abnormality of the distal phalanx of the 2nd toe
+DOID:6547,heart lymphoma,DOID:117,heart cancer
+HP:0005450,Calvarial osteosclerosis,HP:0011001,Increased bone mineral density
+HP:0009326,Irregular epiphysis of the middle phalanx of the 3rd finger,HP:0010262,Irregular epiphyses of the middle phalanges of the hand
+DOID:0050888,syndromic intellectual disability,DOID:1059,intellectual disability
+UBERON:0007352,stria vascularis vasculature,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004138,somitomeric trunk muscle,UBERON:0001134,skeletal muscle tissue
+HP:0007387,Hypoplastic sweat glands,HP:0011135,Aplasia/Hypoplasia of the sweat glands
+UBERON:0005904,duct of male reproductive system,UBERON:0014403,male anatomical structure
+HP:0006152,Proximal symphalangism (hands),HP:0009700,Synostosis involving bones of the fingers
+HP:0010461,Abnormality of the male genitalia,HP:0012243,Abnormal genital system morphology
+UBERON:0012351,urachal lumen,UBERON:0000464,anatomical space
+UBERON:0002687,area X of ventral lateral nucleus,UBERON:0003528,brain grey matter
+HP:0000104,Renal agenesis,HP:0008678,Renal hypoplasia/aplasia
+DOID:3798,pleural empyema,DOID:1532,pleural disease
+HP:0100801,Pancreatic aplasia,HP:0100800,Aplasia/Hypoplasia of the pancreas
+UBERON:0006771,long bone epiphyseal plate proliferative zone,UBERON:0006775,zone of epiphyseal plate
+UBERON:0010242,anterior buccal gland,UBERON:0012102,buccal salivary gland
+UBERON:0009899,pole of cerebral hemisphere,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0000154,Wide mouth,HP:0011337,Abnormality of mouth size
+HP:0010785,Gonadal neoplasm,HP:0010787,Genital neoplasm
+DOID:9267,urea cycle disorder,DOID:9252,amino acid metabolic disorder
+HP:0012561,Unicuspid aortic valve,HP:0001646,Abnormality of the aortic valve
+HP:0009562,Patchy sclerosis of the distal phalanx of the 2nd finger,HP:0009551,Patchy sclerosis of the phalanges of the 2nd finger
+DOID:505,hobnail hemangioma,DOID:255,hemangioma
+HP:0009770,Curved phalanges of the hand,HP:0005918,Abnormality of phalanx of finger
+HP:0100906,Sclerosis of the middle phalanx of the 4th finger,HP:0100916,Sclerosis of the middle phalanges of the hand
+DOID:9483,ulcerative blepharitis,DOID:9423,blepharitis
+UBERON:0010961,erector spinae pre-muscle mass,UBERON:0005865,pre-muscle condensation
+UBERON:4300088,metapterygium bone,UBERON:4300082,metapterygium element
+UBERON:0002109,pair of nares,UBERON:0000477,anatomical cluster
+UBERON:0003107,Meckel's cartilage,UBERON:0010313,neural crest-derived structure
+UBERON:0007356,crop,UBERON:0013765,digestive system organ
+DOID:14192,bicipital tenosynovitis,DOID:970,tenosynovitis
+UBERON:0014719,intralobular duct,UBERON:0000058,duct
+UBERON:0002041,terminal bronchus,UBERON:0002185,bronchus
+UBERON:2001855,hyomandibular condyle for the opercle,UBERON:0009979,condyle
+HP:0011554,Double inlet atrioventricular connection,HP:0011546,Abnormal atrioventricular connection
+DOID:12211,filarial elephantiasis,DOID:37,skin disease
+UBERON:0006953,ejaculatory duct epithelium,UBERON:0012275,meso-epithelium
+DOID:7559,asymmetric motor neuropathy,DOID:683,motor neuritis
+UBERON:0010697,pedal digit metatarsal cartilage element,UBERON:0015036,pedal digit metatarsal endochondral element
+UBERON:0006595,presumptive endoderm,UBERON:0006598,presumptive structure
+HP:0006533,Bronchodysplasia,HP:0002109,Abnormality of the bronchi
+UBERON:2000648,dorsal fin musculature,UBERON:0004469,musculature of back
+UBERON:0004648,esophagus muscularis mucosa,UBERON:0002112,smooth muscle of esophagus
+UBERON:0001641,transverse sinus,UBERON:0003496,head blood vessel
+HP:0100270,Abnormality of dorsoventral patterning of the limbs,HP:0001155,Abnormality of the hand
+UBERON:0006189,mesonephric connecting tubule,UBERON:0000083,mesonephric tubule
+UBERON:0008837,palmar/plantar part of autopod,UBERON:0002529,limb segment
+HP:0004389,Intestinal pseudo-obstruction,HP:0002579,Gastrointestinal dysmotility
+HP:0008061,Aplasia/Hypoplasia affecting the retina,HP:0000479,Abnormality of the retina
+HP:0010415,Bullet-shaped distal phalanx of the 2nd toe,HP:0010349,Bullet-shaped phalanges of the 2nd toe
+UBERON:0014549,pyramidal layer of CA2,UBERON:0014567,layer of hippocampal field
+UBERON:0006484,Brodmann (1909) area 47,UBERON:0013529,Brodmann area
+DOID:518,scrotum neoplasm,DOID:3856,male reproductive organ cancer
+UBERON:0010561,pedal digit 5 metatarsal cartilage element,UBERON:0010697,pedal digit metatarsal cartilage element
+UBERON:0014507,distal interphalangeal joint of pedal digit 3,UBERON:0014506,distal interphalangeal joint of digit 3
+CL:0000860,classical monocyte,CL:0000576,monocyte
+CL:1001209,inner medulla vasa recta ascending limb cell,CL:1001126,inner renal medulla vasa recta cell
+CL:0002310,mammosomatotroph,CL:0000638,acidophil cell of pars distalis of adenohypophysis
+CL:0000033,apocrine cell,CL:0000151,secretory cell
+UBERON:0003890,Mullerian duct,UBERON:0002050,embryonic structure
+UBERON:0010742,bone of pelvic complex,UBERON:0010740,bone of appendage girdle complex
+HP:0100370,Aplasia/Hypoplasia of the distal phalanx of the 4th toe,HP:0010380,Abnormality of the distal phalanx of the 4th toe
+UBERON:0013475,gustatory gland,UBERON:0001044,salivary gland
+DOID:6847,adult botryoid rhabdomyosarcoma,DOID:3255,botryoid rhabdomyosarcoma
+DOID:1641,benign breast adenomyoepithelioma,DOID:0060082,breast benign neoplasm
+UBERON:0008546,iliocostalis cervicis muscle,UBERON:0002251,iliocostalis muscle
+HP:0000651,Diplopia,HP:0011514,Abnormality of binocular vision
+UBERON:0002151,pontine nuclear group,UBERON:0006331,brainstem nucleus
+HP:0006277,Pancreatic hyperplasia,HP:0012094,Abnormal pancreas size
+UBERON:2000230,longitudinal hypochordal,UBERON:0001630,muscle organ
+UBERON:0004878,distal visceral endoderm,UBERON:0004119,endoderm-derived structure
+HP:0002703,Abnormality of skull ossification,HP:0000929,Abnormality of the skull
+CL:0002586,retinal pigment epithelial cell,CL:0000149,visual pigment cell
+DOID:0060007,CD3zeta deficiency,DOID:627,severe combined immunodeficiency
+UBERON:2000199,dorsal periventricular hypothalamus,UBERON:0003048,regional part of hypothalamus
+UBERON:2000226,lateral ethmoid bone,UBERON:4300111,lateral ethmoid element
+HP:0012274,Autosomal dominant inheritance with paternal imprinting,HP:0000006,Autosomal dominant inheritance
+DOID:10782,mesenteric lymphadenitis,DOID:1602,lymphadenitis
+HP:0001719,Double outlet right ventricle,HP:0011723,Congenital malformation of the right heart
+UBERON:0013751,metaphysis of radius,UBERON:0004120,mesoderm-derived structure
+HP:0011323,Cleft of chin,HP:0000306,Abnormality of the chin
+UBERON:0006334,posterior lateral line,UBERON:0010202,lateral line
+HP:0007027,Poorly formed metencephalon,HP:0011283,Abnormality of the metencephalon
+UBERON:0002738,isthmus of cingulate gyrus,UBERON:0004121,ectoderm-derived structure
+DOID:605,flying phobia,DOID:599,specific phobia
+UBERON:0001691,external ear,UBERON:0001444,subdivision of head
+HP:0010508,Metatarsus valgus,HP:0001832,Abnormality of the metatarsal bones
+DOID:12571,phacogenic glaucoma,DOID:1686,glaucoma
+UBERON:0012271,major duodenal papilla,UBERON:0004914,duodenal papilla
+UBERON:0003233,epithelium of shoulder,UBERON:0010371,ecto-epithelium
+UBERON:0014697,posterior choroidal artery,UBERON:0004573,systemic artery
+CL:0000128,oligodendrocyte,CL:0000126,macroglial cell
+HP:0002777,Tracheal stenosis,HP:0002778,Abnormality of the trachea
+DOID:1835,mononeuritis multiplex,DOID:1802,mononeuritis
+HP:0001857,Short distal phalanx of toe,HP:0001831,Short toe
+UBERON:0005728,extraembryonic mesoderm,UBERON:0004120,mesoderm-derived structure
+UBERON:4200121,puboischiotibialis,UBERON:0001325,muscle of pelvis
+DOID:0060163,body dysmorphic disorder,DOID:4737,somatoform disorder
+HP:0000751,Personality changes,HP:0000708,Behavioural/Psychiatric Abnormality
+UBERON:0005895,insect leg,UBERON:0000026,appendage
+CL:1000352,basal cell of epithelium of lobular bronchiole,CL:0000082,epithelial cell of lung
+HP:0001586,Vesicovaginal fistula,HP:0004321,Bladder fistula
+CL:0000793,"CD4-positive, alpha-beta intraepithelial T cell",CL:0000797,alpha-beta intraepithelial T cell
+CL:0000050,megakaryocyte-erythroid progenitor cell,CL:0000763,myeloid cell
+HP:0003555,Muscle fiber splitting,HP:0004303,Abnormality of muscle fibers
+CL:0000019,sperm,CL:0000219,motile cell
+UBERON:0003558,diencephalon arachnoid mater,UBERON:0003556,forebrain arachnoid mater
+DOID:5204,"fructose-1,6-bisphosphatase deficiency",DOID:2978,carbohydrate metabolic disorder
+DOID:0050705,adolescence-adult electroclinical syndrome,DOID:0050701,electroclinical syndrome
+UBERON:1000010,mole,UBERON:0000479,tissue
+UBERON:0000429,enteric plexus,UBERON:0010313,neural crest-derived structure
+UBERON:0002450,decidua,UBERON:0000478,extraembryonic structure
+UBERON:0006253,embryonic intraretinal space,UBERON:0012467,enclosed anatomical space
+UBERON:0013619,upper secondary molar tooth,UBERON:0013618,secondary molar tooth
+DOID:272,hepatic vascular disease,DOID:178,vascular disease
+CL:0000797,alpha-beta intraepithelial T cell,CL:0002496,intraepithelial lymphocyte
+HP:0010018,Enlarged epiphysis of the 1st metacarpal,HP:0006134,Enlarged metacarpal epiphyses
+HP:0008003,Jerky ocular pursuit movements,HP:0000617,Abnormality of ocular smooth pursuit
+DOID:10146,thymus lymphoma,DOID:3277,thymus cancer
+DOID:2653,benign fibrous mesothelioma,DOID:2645,benign mesothelioma
+DOID:7014,infiltrating lipoma,DOID:3315,lipoma
+UBERON:0002114,duodenum,UBERON:0004921,subdivision of digestive tract
+UBERON:0013509,lumbar vertebra cartilage element,UBERON:0015009,lumbar vertebra endochondral element
+UBERON:0002051,epithelium of bronchiole,UBERON:0002031,epithelium of bronchus
+HP:0100520,Oliguria,HP:0011037,Decreased urine output
+UBERON:0002797,dorsal trigeminal tract,UBERON:0004171,trigeminothalamic tract
+HP:0002837,Recurrent bronchitis,HP:0002109,Abnormality of the bronchi
+HP:0100630,Neoplasia of the nasopharynx,HP:0001739,Abnormality of the nasopharynx
+HP:0009550,Osteolytic defects of the phalanges of the 2nd finger,HP:0009771,Osteolytic defects of the phalanges of the hand
+UBERON:2001333,sublingual dorsal and ventral fused,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010129,Cone-shaped epiphysis of the proximal phalanx of the hallux,HP:0010115,Cone-shaped epiphyses of the hallux
+UBERON:0016478,liver stroma,UBERON:0004119,endoderm-derived structure
+DOID:10963,cholesteatoma of attic,DOID:10964,cholesteatoma of middle ear
+UBERON:0011784,feather shaft,UBERON:0000025,tube
+UBERON:0002091,appendicular skeleton,UBERON:0010912,subdivision of skeleton
+UBERON:0001748,capsule of parathyroid gland,UBERON:0003893,capsule
+HP:0007569,Generalized seborrheic dermatitis,HP:0001051,Seborrheic dermatitis
+CL:0000663,valve cell,CL:0000003,native cell
+UBERON:0003894,liver primordium,UBERON:0007497,developing epithelial placode
+DOID:0060127,gamma heavy chain disease,DOID:0060125,heavy chain disease
+UBERON:0013637,prostate gland lateral lobe,UBERON:0015212,lateral structure
+UBERON:0002287,optic recess of third ventricle,UBERON:0002553,anatomical cavity
+HP:0000301,Abnormality of facial musculature,HP:0003011,Abnormality of the musculature
+CL:0000582,neutrophilic metamyelocyte,CL:0000776,immature neutrophil
+HP:0010143,Irregular epiphysis of the distal phalanx of the hallux,HP:0010124,Abnormality of the epiphysis of the distal phalanx of the hallux
+DOID:10921,Siberian tick typhus,DOID:11104,spotted fever
+NCBITaxon:33213,Bilateria,NCBITaxon:6072,Eumetazoa
+DOID:6225,Cronkhite-Canada syndrome,DOID:76,stomach disease
+UBERON:0008320,common penile artery,UBERON:0005156,reproductive structure
+UBERON:0003824,nerve of thoracic segment,UBERON:0003439,nerve of trunk region
+UBERON:0000057,urethra,UBERON:0006554,urinary system structure
+UBERON:0004003,cerebellum hemisphere lobule,UBERON:0004004,cerebellum lobule
+UBERON:0008321,deep artery of penis,UBERON:0014403,male anatomical structure
+HP:0005314,Anomalous branches of internal carotid artery,HP:0005344,Abnormality of the carotid arteries
+UBERON:0010047,oral gland,UBERON:0003408,gland of gut
+UBERON:0001572,hyoglossus muscle,UBERON:0001575,extrinsic muscle of tongue
+DOID:4872,lung adenoid cystic carcinoma,DOID:3905,lung carcinoma
+DOID:0060038,specific developmental disorder,DOID:0060037,developmental disorder of mental health
+HP:0010073,Synostosis involving the 1st metatarsal,HP:0010054,Abnormality of the first metatarsal
+HP:0007395,Postnatal-onset ichthyosiform erythroderma,HP:0008064,Ichthyosis
+UBERON:2002061,predorsal vertebra,UBERON:0002412,vertebra
+DOID:11482,hemopericardium,DOID:118,pericardial effusion
+UBERON:0002389,manual digit,UBERON:0002544,digit
+UBERON:0008835,hepatic diverticulum,UBERON:0009854,digestive tract diverticulum
+DOID:342,subclavian artery aneurysm,DOID:0050828,artery disease
+DOID:7187,subacute lymphocytic thyroiditis,DOID:7166,thyroiditis
+UBERON:0002084,heart left ventricle,UBERON:0015212,lateral structure
+HP:0004195,Osteolytic defects of the phalanges of the 4th finger,HP:0009172,Abnormality of the phalanges of the 4th finger
+HP:0009180,Ulnar deviation of the 5th finger,HP:0009465,Ulnar deviation of finger
+DOID:1575,rheumatic disease,DOID:417,hypersensitivity reaction type II disease
+HP:0012733,Macule,HP:0011355,Localized skin lesion
+CL:1000378,type 1 vestibular sensory cell of stato-acoustic epithelium,CL:0002070,type I vestibular sensory cell
+DOID:5119,ovarian cyst,DOID:1100,ovarian disease
+DOID:2481,infantile epileptic encephalopathy,DOID:1827,idiopathic generalized epilepsy
+UBERON:0006664,greater palatine artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2000651,dorsal pelvic arrector,UBERON:2002147,arrector muscle
+UBERON:2001229,pharyngeal arch 7 skeleton,UBERON:0010912,subdivision of skeleton
+UBERON:4300014,dorsal cleithrum,UBERON:0007829,pectoral girdle bone
+HP:0006347,Microdontia of primary teeth,HP:0006481,Abnormality of primary teeth
+DOID:5075,myxopapillary ependymoma,DOID:4844,benign ependymoma
+UBERON:2001672,dorsal fin radial bone,UBERON:0004247,bone of dorsum
+UBERON:0003452,trabecula carnea cardiac muscle tissue,UBERON:0001133,cardiac muscle tissue
+HP:0010434,Aplasia of the middle phalanx of the 2nd toe,HP:0010404,Aplasia/Hypoplasia of the middle phalanx of the 2nd toe
+UBERON:0014386,vertebral endplate,UBERON:0004120,mesoderm-derived structure
+UBERON:0012425,striated border microvillus layer,UBERON:0012423,layer of microvilli
+UBERON:0011820,atrioventricular region,UBERON:0004120,mesoderm-derived structure
+UBERON:0014443,inferior ischial ramus,UBERON:0014441,ischial ramus
+UBERON:0001861,ductus reuniens,UBERON:0000025,tube
+DOID:5411,lung oat cell carcinoma,DOID:5409,lung small cell carcinoma
+UBERON:0004164,branchiomeric muscle,UBERON:0001630,muscle organ
+UBERON:0002208,sternebra,UBERON:0004120,mesoderm-derived structure
+HP:0002539,Cortical dysplasia,HP:0002538,Abnormality of the cerebral cortex
+UBERON:0005332,mesonephric S-shaped body,UBERON:0004199,S-shaped body
+DOID:7807,choroid necrotic melanoma,DOID:6438,malignant choroid melanoma
+UBERON:0003262,amniotic mesoderm,UBERON:0007524,dense mesenchyme tissue
+UBERON:0004872,splanchnic layer of lateral plate mesoderm,UBERON:0005423,developing anatomical structure
+HP:0009701,Metacarpal synostosis,HP:0004278,Synostosis involving bones of the hand
+UBERON:0015716,anal canal epithelium,UBERON:0014703,anal membrane ectodermal component
+UBERON:0003921,pancreas primordium,UBERON:0001048,primordium
+CL:0002116,B220-low CD38-positive unswitched memory B cell,CL:0002115,B220-positive CD38-positive unswitched memory B cell
+DOID:3928,adiposis dolorosa,DOID:3153,lipomatosis
+UBERON:0010697,pedal digit metatarsal cartilage element,UBERON:0005863,cartilaginous condensation
+HP:0009050,Quadriceps muscle atrophy,HP:0008956,Proximal lower limb amyotrophy
+HP:0008162,Asymptomatic hyperammonemia,HP:0001987,Hyperammonemia
+HP:0010230,Cone-shaped epiphyses of the phalanges of the hand,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+DOID:4848,cerebellar astrocytoma,DOID:4205,cerebellum cancer
+HP:0004209,Clinodactyly of the 5th finger,HP:0009466,Radial deviation of finger
+HP:0002503,Spinocerebellar tract degeneration,HP:0003133,Abnormality of the spinocerebellar tracts
+HP:0001001,Abnormality of subcutaneous fat tissue,HP:0009124,Abnormality of adipose tissue
+HP:0009169,Broad middle phalanx of the 5th finger,HP:0009844,Broad middle phalanx of finger
+UBERON:3000688,prominentia apicalis dorsalis,UBERON:0011769,cartilaginous projection
+HP:0009215,Bracket epiphysis of the middle phalanx of the 4th finger,HP:0009394,Bracket epiphyses of the 4th finger
+HP:0010325,Aplasia/Hypoplasia of the 2nd toe,HP:0010319,Abnormality of the 2nd toe
+UBERON:0009777,intermediate reticular nucleus,UBERON:0007635,nucleus of medulla oblongata
+HP:0008336,Complex organic aciduria,HP:0001992,Organic aciduria
+UBERON:0003410,oropharyngeal gland,UBERON:0003295,pharyngeal gland
+CL:1000720,kidney papillary duct intercalated cell,CL:1000550,kidney papillary duct principal epithelial cell
+HP:0009209,Ivory epiphysis of the middle phalanx of the 5th finger,HP:0010263,Ivory epiphyses of the middle phalanges of the hand
+UBERON:2002284,body marking,UBERON:0003102,surface structure
+UBERON:0008622,scalenus anterior,UBERON:0008611,scalene muscle
+DOID:4329,Erdheim-Chester disease,DOID:4330,non-langerhans-cell histiocytosis
+UBERON:0003009,dorsal tegmental decussation,UBERON:0014891,brainstem white matter
+UBERON:2000651,dorsal pelvic arrector,UBERON:0014795,pelvic appendage muscle
+UBERON:2001990,epibranchial arborescent organ,UBERON:0000477,anatomical cluster
+HP:0011104,Abnormality of blood volume homeostasis,HP:0011028,Abnormality of blood circulation
+UBERON:0007160,inferior petrosal sinus,UBERON:0001638,vein
+HP:0100166,Stippling of the epiphysis of the proximal phalanx of the 3rd toe,HP:0100093,Abnormality of the epiphysis of the proximal phalanx of the 3rd toe
+UBERON:0006190,mesonephric distal tubule,UBERON:0005330,mesonephric nephron epithelium
+HP:0009660,Short phalanx of the thumb,HP:0009778,Short thumb
+HP:0100697,Neurofibrosarcoma,HP:0100242,Sarcoma
+UBERON:2001934,rostral plate,UBERON:0011164,neurocranium bone
+HP:0005042,"Irregular, rachitic-like metaphyses",HP:0003025,Metaphyseal irregularity
+UBERON:3010709,levator mandibulae lateralis,UBERON:0011648,jaw muscle
+UBERON:2001233,hypobranchial 1 bone,UBERON:2001894,hypobranchial 1 element
+DOID:13918,somatization disorder,DOID:4737,somatoform disorder
+HP:0000134,Female hypogonadism,HP:0000137,Abnormality of the ovary
+UBERON:0001760,frontal sinus,UBERON:0001825,paranasal sinus
+DOID:2833,dehydration polycythemia,DOID:2834,acquired polycythemia
+UBERON:0006544,kidney vasculature,UBERON:0002201,vasculature of trunk
+DOID:9442,cervical mullerian papilloma,DOID:0060110,cervical benign neoplasm
+UBERON:0009916,wall of ureter,UBERON:0000060,anatomical wall
+UBERON:0004544,epididymis epithelium,UBERON:0012275,meso-epithelium
+DOID:7848,interdigitating dendritic cell sarcoma,DOID:5621,histiocytic and dendritic cell cancer
+HP:0008225,Thyroid follicular hyperplasia,HP:0008249,Thyroid hyperplasia
+UBERON:0000432,endopeduncular nucleus,UBERON:0015234,nucleus of ventral thalamus
+UBERON:0004341,primitive streak,UBERON:0005291,embryonic tissue
+HP:0010375,Osteolytic defects of the phalanges of the 4th toe,HP:0010336,Abnormality of the phalanges of the 4th toe
+UBERON:0003552,telencephalon pia mater,UBERON:0003289,meninx of telencephalon
+HP:0002247,Duodenal atresia,HP:0002246,Abnormality of the duodenum
+UBERON:0001945,superior colliculus,UBERON:0015212,lateral structure
+DOID:0050598,extrapulmonary tuberculosis,DOID:399,tuberculosis
+HP:0009717,Cortical tubers,HP:0002538,Abnormality of the cerebral cortex
+UBERON:0001247,falciform ligament,UBERON:0005291,embryonic tissue
+UBERON:0004445,proximal epiphysis of proximal phalanx of manual digit 1,UBERON:0004417,proximal epiphysis of phalanx of manual digit 1
+UBERON:0015251,modified sebaceous gland,UBERON:0001821,sebaceous gland
+UBERON:0008463,inferior articular process of thoracic vertebra,UBERON:0001080,inferior articular process of vertebra
+DOID:13401,angioid streaks,DOID:5679,retinal disease
+UBERON:0001140,renal vein,UBERON:0001638,vein
+UBERON:2000348,exoccipital posteroventral region,UBERON:0002513,endochondral bone
+HP:0004369,Decreased purine levels,HP:0004352,Abnormality of purine metabolism
+DOID:13359,Ehlers-Danlos syndrome,DOID:0050177,monogenic disease
+HP:0009636,Triangular shaped proximal phalanx of the thumb,HP:0009657,Triangular shaped phalanges of the thumb
+UBERON:0006937,inner ear epithelium,UBERON:0010371,ecto-epithelium
+UBERON:2001800,cephalic rib,UBERON:2001798,epicentral bone
+HP:0009728,Neoplasm of striated muscle,HP:0011793,Neoplasm by anatomical site
+UBERON:0004906,ectodermal part of digestive tract,UBERON:0004921,subdivision of digestive tract
+UBERON:3010625,embryonic hypochord,UBERON:0002050,embryonic structure
+UBERON:0012103,suspensory ligament of breast,UBERON:0005156,reproductive structure
+DOID:4141,intraorbital meningioma,DOID:4143,orbital cancer
+CL:1000487,smooth muscle cell of prostate,CL:0000192,smooth muscle cell
+UBERON:2001783,supraoccipital crest,UBERON:0004120,mesoderm-derived structure
+UBERON:3000037,basicranial fenestra,UBERON:3000051,braincase and otic capsule opening
+HP:0002154,Hyperglycinemia,HP:0003112,Abnormality of serum amino acid levels
+HP:0009560,Curved distal phalanx of the 2nd finger,HP:0009542,Abnormality of the distal phalanx of the 2nd finger
+HP:0002464,Spastic dysarthria,HP:0001257,Spasticity
+DOID:11432,endometriosis of ovary,DOID:1100,ovarian disease
+DOID:13306,diphtheritic cystitis,DOID:1679,cystitis
+UBERON:3010741,M. ulnocarpalis,UBERON:0010891,pectoral complex muscle
+DOID:332,amyotrophic lateral sclerosis,DOID:231,motor neuron disease
+HP:0005144,Left ventricular septal hypertrophy,HP:0010438,Abnormality of the ventricular septum
+HP:0004945,Extracranial internal carotid artery dissection,HP:0005294,Arterial dissection
+DOID:0050688,anal canal cancer,DOID:5672,large intestine cancer
+UBERON:0002558,organ cavity,UBERON:0002553,anatomical cavity
+CL:2000001,peripheral blood mononuclear cell,CL:0000842,mononuclear cell
+UBERON:0001304,germinal epithelium of ovary,UBERON:0004911,epithelium of female gonad
+DOID:14504,Niemann-Pick disease,DOID:1927,sphingolipidosis
+DOID:990,congenital heart block,DOID:0050820,atrioventricular block
+HP:0003991,Osteosclerosis of the ulna,HP:0006392,Increased density of long bones
+UBERON:0003958,long bone epiphyseal ossification zone,UBERON:0000061,anatomical structure
+UBERON:0007834,lumbar spinal cord ventral commissure,UBERON:0004170,spinal cord ventral commissure
+UBERON:0001833,lip,UBERON:0003102,surface structure
+DOID:6209,malignant mediastinum hemangiopericytoma,DOID:4050,mediastinum sarcoma
+UBERON:0005723,floor plate spinal cord region,UBERON:0003306,floor plate of neural tube
+HP:0001467,Aplasia/Hypoplasia involving the musculature of the upper limbs,HP:0009128,Aplasia/Hypoplasia involving the musculature of the extremities
+UBERON:0006062,articular process of vertebra,UBERON:0006061,process of vertebra
+UBERON:0014665,nucleus preopticus,UBERON:0006568,hypothalamic nucleus
+DOID:13375,temporal arteritis,DOID:525,central nervous system vasculitis
+UBERON:2001912,pharyngobranchial 3 element,UBERON:2001909,pharyngobranchial element
+HP:0007812,Herpetiform corneal ulceration,HP:0011495,Abnormality of corneal epithelium
+UBERON:0014897,obliquely striated somatic muscle,UBERON:0014895,somatic muscle
+NCBITaxon:90010,unclassified Enterovirus,NCBITaxon:12059,Enterovirus
+HP:0009416,Ivory epiphyses of the 3rd finger,HP:0009320,Abnormality of the epiphyses of the 3rd finger
+UBERON:0015101,distal tarsal bone pre-cartilage condensation,UBERON:0015099,distal tarsal bone endochondral element
+HP:0000587,Abnormality of the optic nerve,HP:0001098,Abnormality of the fundus
+UBERON:0004641,spleen capsule,UBERON:0003893,capsule
+HP:0008985,Increased intramuscular fat,HP:0009126,Increased adipose tissue
+HP:0001055,Erysipelas,HP:0011123,Inflammatory abnormality of the skin
+UBERON:0005311,mammary placode,UBERON:0011814,non-neurogenic ectodermal placode
+UBERON:0004424,proximal epiphysis of third metacarpal bone,UBERON:0004393,epiphysis of third metacarpal bone
+UBERON:0003323,mesenchyme of upper jaw,UBERON:0004121,ectoderm-derived structure
+UBERON:0001607,sphincter pupillae,UBERON:0001606,muscle of iris
+HP:0006167,Prominent proximal interphalangeal joints,HP:0006237,Prominent interphalangeal joints
+UBERON:0012422,secretion of crop,UBERON:0000463,portion of organism substance
+UBERON:4300002,palatine prong,UBERON:0004530,bony projection
+UBERON:3000689,prominentia apicalis ventralis,UBERON:4100000,skeletal element projection
+DOID:11624,penile neoplasm,DOID:0060087,male reproductive organ benign neoplasm
+UBERON:0002405,immune system,UBERON:0000467,anatomical system
+UBERON:2007030,posterior neural rod,UBERON:0004121,ectoderm-derived structure
+UBERON:2001142,tooth 5V,UBERON:2000694,ceratobranchial 5 tooth
+DOID:9036,parotid gland cancer,DOID:8850,salivary gland cancer
+HP:0003193,Allergic rhinitis,HP:0012384,Rhinitis
+DOID:1518,cecal disease,DOID:5295,intestinal disease
+UBERON:0002996,nucleus of optic tract,UBERON:0011214,nucleus of midbrain tectum
+UBERON:0016453,lower secondary premolar tooth,UBERON:0007120,premolar tooth
+HP:0004755,Supraventricular tachycardia,HP:0001649,Tachycardia
+DOID:5809,childhood parosteal osteogenic sarcoma,DOID:3361,pediatric osteosarcoma
+HP:0009643,Bullet-shaped distal phalanx of the thumb,HP:0009617,Abnormality of the distal phalanx of the thumb
+UBERON:0006965,vascular cord,UBERON:0005423,developing anatomical structure
+HP:0005871,Metaphyseal chondrodysplasia,HP:0100255,Metaphyseal dysplasia
+UBERON:0004654,temporal process of zygomatic bone,UBERON:0010313,neural crest-derived structure
+HP:0100128,Ivory epiphysis of the proximal phalanx of the 2nd toe,HP:0100050,Ivory epiphyses of the 2nd toe
+DOID:1107,esophageal carcinoma,DOID:5041,esophageal cancer
+CL:0000127,astrocyte,CL:0000126,macroglial cell
+HP:0008009,Three rows of eyelashes,HP:0008496,Multiple rows of eyelashes
+CL:0000727,primary pigment cell,CL:0001658,visual pigment cell (sensu Nematoda and Protostomia)
+HP:0100926,Sclerosis of the phalanges of the 2nd toe,HP:0100924,Sclerosis of the phalanges of the toes
+DOID:853,polymyalgia rheumatica,DOID:423,myopathy
+HP:0010168,Ivory epiphyses of the toes,HP:0010583,Ivory epiphyses
+UBERON:0005438,coronary sinus,UBERON:0003498,heart blood vessel
+UBERON:2002218,parallel fiber,UBERON:0000479,tissue
+HP:0010178,Patchy sclerosis of the phalanges of the toes,HP:0005686,Patchy osteosclerosis
+DOID:57,aortic valve insufficiency,DOID:62,aortic valve disease
+HP:0002936,Distal sensory impairment,HP:0003474,Sensory impairment
+UBERON:0015181,neck of tooth,UBERON:0001560,neck of organ
+UBERON:0014783,cloacal muscle,UBERON:0013765,digestive system organ
+HP:0010094,Complete duplication of the proximal phalanx of the hallux,HP:0010100,Complete duplication of the phalanges of the hallux
+HP:0004039,Abnormality of ulnar metaphysis,HP:0009809,Abnormality of upper limb metaphysis
+HP:0007260,Type II lissencephaly,HP:0001339,Lissencephaly
+HP:0100300,Desmin bodies,HP:0100303,Muscle fiber cytoplasmatic inclusion bodies
+UBERON:0003869,presumptive ganglion,UBERON:0006598,presumptive structure
+UBERON:0005498,primitive heart tube,UBERON:0000481,multi-tissue structure
+UBERON:0010952,frontalis,UBERON:0004120,mesoderm-derived structure
+UBERON:0003056,pre-chordal neural plate,UBERON:0004121,ectoderm-derived structure
+HP:0000338,Hypomimic face,HP:0000301,Abnormality of facial musculature
+UBERON:2000503,dorsal oblique branchial muscle,UBERON:0000933,pharyngeal muscle
+HP:0000045,Abnormality of the scrotum,HP:0000032,Abnormality of male external genitalia
+UBERON:0012649,anococcygeus muscle,UBERON:0004231,anal region smooth muscle
+DOID:738,female urethral cancer,DOID:734,urethra cancer
+UBERON:0000125,neural nucleus,UBERON:0004121,ectoderm-derived structure
+HP:0100940,Sclerosis of the distal phalanx of the 3rd toe,HP:0100927,Sclerosis of the phalanges of the 3rd toe
+UBERON:0007278,presumptive sinus venosus,UBERON:0006598,presumptive structure
+NCBITaxon:62324,Anopheles funestus,NCBITaxon:62323,funestus subgroup
+UBERON:3000015,anterior maxillary process,UBERON:0004530,bony projection
+DOID:9188,vestibule of mouth cancer,DOID:8618,oral cavity cancer
+HP:0100137,Cone-shaped epiphysis of the distal phalanx of the 3rd toe,HP:0100057,Cone-shaped epiphyses of the 3rd toe
+DOID:1108,esophagus melanoma,DOID:5041,esophageal cancer
+NCBITaxon:11071,Japanese encephalitis virus group,NCBITaxon:11051,Flavivirus
+HP:0003300,Ovoid vertebral bodies,HP:0003312,Abnormal form of the vertebral bodies
+UBERON:2000300,ventral hypohyal bone,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:0060062,familial juvenile hyperuricemic nephropathy,DOID:557,kidney disease
+UBERON:0002271,periventricular zone of hypothalamus,UBERON:0000064,organ part
+NCBITaxon:445,Legionella,NCBITaxon:444,Legionellaceae
+UBERON:0009130,dorsal meso-duodenum,UBERON:0004120,mesoderm-derived structure
+HP:0000060,Clitoral hypoplasia,HP:0000056,Abnormality of the clitoris
+UBERON:0003675,tooth crown,UBERON:0004121,ectoderm-derived structure
+HP:0006308,Atrophy of alveolar ridges,HP:0006477,Abnormality of the alveolar ridges
+DOID:4863,spinal cord astrocytoma,DOID:3185,spinal cord glioma
+UBERON:0006658,interphalangeal joint,UBERON:0011139,synovial limb joint
+UBERON:0006841,central vein of liver,UBERON:0013126,vein of abdomen
+NCBITaxon:186820,Listeriaceae,NCBITaxon:1385,Bacillales
+CL:0000836,promyelocyte,CL:0002191,granulocytopoietic cell
+UBERON:0011202,urachus epithelium,UBERON:0012275,meso-epithelium
+UBERON:0003071,eye primordium,UBERON:0007497,developing epithelial placode
+UBERON:2005272,immature gonad,UBERON:0000481,multi-tissue structure
+UBERON:0002245,cerebellar hemisphere,UBERON:0015212,lateral structure
+HP:0007534,Congenital posterior occipital alopecia,HP:0011361,Congenital abnormal hair pattern
+UBERON:0015102,distal tarsal bone 1 endochondral element,UBERON:0015050,tarsus endochondral element
+UBERON:0002298,brainstem,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0011587,Abnormal branching pattern of the aortic arch,HP:0012303,Abnormality of the aortic arch
+CL:0002663,myocardial endocrine cell of atrium,CL:0002074,myocardial endocrine cell
+HP:0005050,Anterolateral radial head dislocation,HP:0003083,Dislocated radial head
+UBERON:2001757,dorsal fin lepidotrichium 4,UBERON:4000177,dorsal fin lepidotrichium
+UBERON:0013249,paroophoron,UBERON:0014404,female anatomical structure
+HP:0006615,Absent in utero rib ossification,HP:0011849,Abnormal bone ossification
+UBERON:0004752,palatoquadrate cartilage,UBERON:0004121,ectoderm-derived structure
+UBERON:0011953,stomach glandular region,UBERON:0009034,stomach region
+HP:0007181,Interosseus muscle atrophy,HP:0003693,Distal amyotrophy
+HP:0011481,Abnormality of the lacrimal duct,HP:0000614,Abnormality of the nasolacrimal system
+UBERON:0005366,olfactory lobe,UBERON:0002791,regional part of telencephalon
+HP:0100128,Ivory epiphysis of the proximal phalanx of the 2nd toe,HP:0100090,Abnormality of the epiphysis of the proximal phalanx of the 2nd toe
+DOID:8187,gestational uterine corpus choriocarcinoma,DOID:2025,gestational choriocarcinoma
+HP:0001563,Fetal polyuria,HP:0001560,Abnormality of the amniotic fluid
+UBERON:0013498,vestibulo-cochlear VIII ganglion complex,UBERON:0001714,cranial ganglion
+CL:0000580,neutrophilic myelocyte,CL:0002087,nongranular leukocyte
+CL:1000892,kidney capillary endothelial cell,CL:0000071,blood vessel endothelial cell
+HP:0008488,Anterior rounding of vertebral bodies,HP:0003300,Ovoid vertebral bodies
+HP:0009193,Pseudoepiphyses of the metacarpals,HP:0005913,Abnormality of metacarpal epiphyses
+UBERON:0011255,Eimer's organ,UBERON:0004121,ectoderm-derived structure
+UBERON:0000966,retina,UBERON:0004121,ectoderm-derived structure
+UBERON:0008961,parabronchus,UBERON:0002184,segmental bronchus
+HP:0003865,Bowed humerus,HP:0003063,Abnormality of the humerus
+DOID:1731,histoplasmosis,DOID:0050292,primary systemic mycosis
+DOID:7591,gestational ovarian choriocarcinoma,DOID:5550,choriocarcinoma of ovary
+DOID:654,overnutrition,DOID:374,nutrition disease
+UBERON:0001621,coronary artery,UBERON:0003498,heart blood vessel
+CL:0002606,astrocyte of the spinal cord,CL:0000128,oligodendrocyte
+HP:0007266,Cerebral dysmyelination,HP:0011400,Abnormal CNS myelination
+UBERON:0005837,fasciculus of spinal cord,UBERON:0011215,cell part cluster of neuraxis
+CL:0000846,vestibular dark cell,CL:0002371,somatic cell
+HP:0007371,Atrophy/Degeneration of the corpus callosum,HP:0001273,Abnormality of the corpus callosum
+HP:0003759,Hypoplasia of lymphatic vessels,HP:0100766,Abnormality of the lymphatic vessels
+HP:0000514,Slow saccadic eye movements,HP:0000570,Abnormality of saccadic eye movements
+HP:0010039,Aplasia/Hypoplasia of the 3rd metacarpal,HP:0005914,Aplasia/Hypoplasia involving the metacarpal bones
+UBERON:0003280,endothelium of main bronchus,UBERON:0002340,epithelium of main bronchus
+UBERON:0000431,ventral medial complex of thalamus,UBERON:0010009,aggregate regional part of brain
+UBERON:1500006,paired fin radial bone,UBERON:0004375,bone of free limb or fin
+UBERON:0014794,pectoral appendage muscle,UBERON:0010891,pectoral complex muscle
+HP:0010251,Irregular epiphyses of the distal phalanges of the hand,HP:0010233,Irregular epiphyses of the phalanges of the hand
+HP:0006440,Increased density of long bone diaphyses,HP:0006504,Anomaly of the limb diaphyses
+UBERON:0007151,mitral valve leaflet,UBERON:0011741,cardiac valve leaflet
+NCBITaxon:629,Yersinia <bacteria>,NCBITaxon:543,Enterobacteriaceae
+UBERON:0004043,semicircular canal ampulla,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0003854,Sclerosis of metaphyses of the upper limbs,HP:0009809,Abnormality of upper limb metaphysis
+UBERON:2001748,superficial ophthalmic nerve foramen,UBERON:0005744,bone foramen
+HP:0011940,Anterior wedging of T12,HP:0008422,Vertebral wedging
+UBERON:0007693,caroticotympanic artery,UBERON:0004573,systemic artery
+HP:0100489,Proximal/middle symphalangism of 2nd toe,HP:0100237,Proximal symphalangism (feet)
+HP:0003938,Synostosis involving the elbow,HP:0009811,Abnormality of the elbow
+DOID:11572,Listeria meningitis,DOID:9470,bacterial meningitis
+HP:0003915,Lytic defects of the humeral metaphsis,HP:0003907,Abnormality of the humeral metaphyses
+HP:0010928,Abnormality of orotic acid metabolism,HP:0010996,Abnormality of monocarboxylic acid metabolism
+UBERON:0002864,accessory cuneate nucleus,UBERON:0007635,nucleus of medulla oblongata
+UBERON:0012334,navicular bursa,UBERON:0003668,synovial bursa
+HP:0009771,Osteolytic defects of the phalanges of the hand,HP:0005918,Abnormality of phalanx of finger
+UBERON:0004008,cerebellar plate,UBERON:0000490,unilaminar epithelium
+UBERON:0014597,paraventricular nucleus of the hypothalamus descending division - lateral parvicellular part,UBERON:0003048,regional part of hypothalamus
+UBERON:0011939,vibrissa outer root sheath,UBERON:0005942,hair outer root sheath
+CL:0000115,endothelial cell,CL:0000213,lining cell
+UBERON:0013250,vesicular appendage of epoophoron,UBERON:0006590,vestigial embryonic structure
+UBERON:0005511,rhombomere 4,UBERON:0001892,rhombomere
+CL:1000456,mesothelial cell of parietal peritoneum,CL:1000490,mesothelial cell of peritoneum
+HP:0010388,Patchy sclerosis of the phalanges of the 5th toe,HP:0100929,Sclerosis of the phalanges of the 5th toe
+HP:0001459,1-3 toe syndactyly,HP:0001770,Toe syndactyly
+CL:1000413,endothelial cell of artery,CL:0000071,blood vessel endothelial cell
+UBERON:0010910,opisthotic,UBERON:0005913,zone of bone organ
+UBERON:0002366,bulbo-urethral gland,UBERON:0006868,seminal fluid secreting gland
+HP:0005214,Intestinal obstruction,HP:0004796,Gastrointestinal obstruction
+HP:0005396,Susceptibility to coronavirus 229e,HP:0004429,Recurrent viral infections
+HP:0009944,Partial duplication of the phalanges of the thumb,HP:0009942,Duplication of phalanx of thumb
+UBERON:0003378,cardiac muscle of auricular region,UBERON:0004490,cardiac muscle tissue of atrium
+HP:0009681,Ivory epiphysis of the distal phalanx of the thumb,HP:0009662,Abnormality of the epiphysis of the distal phalanx of the thumb
+HP:0010091,Symphalangism affecting the proximal phalanx of the hallux,HP:0010200,Symphalangism affecting the middle phalanges of the toes
+UBERON:0006217,cloacal membrane,UBERON:0004120,mesoderm-derived structure
+DOID:12965,subleukemic leukemia,DOID:1240,leukemia
+HP:0010090,Patchy sclerosis of the proximal phalanx of the hallux,HP:0100943,Sclerosis of the proximal phalanx of the hallux
+UBERON:0014437,iliac crest,UBERON:0004120,mesoderm-derived structure
+UBERON:2001949,caudal-fin hook,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0006605,tectum synoticum,UBERON:0003932,cartilage element of chondrocranium
+HP:0009466,Radial deviation of finger,HP:0004097,Deviation of finger
+UBERON:0006485,Brodmann (1909) area 48,UBERON:0013529,Brodmann area
+UBERON:0001352,external acoustic meatus,UBERON:0004121,ectoderm-derived structure
+UBERON:4200091,ethomosphenoid region,UBERON:0002513,endochondral bone
+HP:0007650,Progressive ophthalmoplegia,HP:0000602,Ophthalmoplegia
+HP:0100303,Muscle fiber cytoplasmatic inclusion bodies,HP:0100299,Muscle fiber inclusion bodies
+CL:0000575,corneal epithelial cell,CL:0002159,general ecto-epithelial cell
+HP:0100656,Thoracoabdominal wall defects,HP:0000765,Abnormality of the thorax
+UBERON:0012282,mammary fat pad,UBERON:0003916,fat pad
+UBERON:0014769,palpebral vein,UBERON:0003496,head blood vessel
+UBERON:0008951,left lung lobe,UBERON:0000101,lobe of lung
+HP:0001879,Abnormality of eosinophils,HP:0001911,Abnormality of granulocytes
+DOID:7483,cervical keratinizing squamous cell carcinoma,DOID:3744,cervical squamous cell carcinoma
+UBERON:0004870,superficial cervical lymph node,UBERON:0002429,cervical lymph node
+UBERON:0007352,stria vascularis vasculature,UBERON:0004121,ectoderm-derived structure
+CL:0002664,cardioblast,CL:0000048,multi fate stem cell
+CL:1000854,kidney blood vessel cell,CL:1000504,kidney medulla cell
+HP:0002647,Aortic dissection,HP:0001679,Abnormality of the aorta
+HP:0009953,Partial duplication of the middle phalanx of the 2nd finger,HP:0009949,Duplication of the middle phalanx of the 2nd finger
+HP:0010460,Abnormality of the female genitalia,HP:0012243,Abnormal genital system morphology
+UBERON:0000390,lens nucleus,UBERON:0000064,organ part
+DOID:14203,childhood type dermatomyositis,DOID:10223,dermatomyositis
+UBERON:0010276,vertebral column opening,UBERON:0005744,bone foramen
+CL:1000284,smooth muscle fiber of descending colon,CL:1000280,smooth muscle cell of colon
+HP:0011021,Abnormality of circulating enzyme level,HP:0010876,Abnormality of circulating protein level
+DOID:10651,acute anterolateral myocardial infarction,DOID:9408,acute myocardial infarction
+DOID:4908,anal carcinoma,DOID:14110,anus cancer
+HP:0100143,Small epiphysis of the distal phalanx of the 3rd toe,HP:0100063,Small epiphyses of the 3rd toe
+HP:0009784,Aplasia/Hypoplasia of the triceps,HP:0001468,Aplasia/Hypoplasia involving the musculature of the upper arm
+DOID:9446,cholangitis,DOID:4138,bile duct disease
+UBERON:0010034,copula linguae,UBERON:0010188,protuberance
+DOID:6239,non-invasive bladder papillary urothelial neoplasm,DOID:5432,bladder papillary transitional cell neoplasm
+HP:0012329,Tufted angioma,HP:0001028,Hemangioma
+UBERON:0001750,lacrimal apparatus,UBERON:0000477,anatomical cluster
+DOID:0060008,janus kinase-3 deficiency,DOID:627,severe combined immunodeficiency
+DOID:9266,cystinuria,DOID:9252,amino acid metabolic disorder
+HP:0004244,Accessory scaphoid,HP:0004243,Abnormality of the scaphoid
+HP:0001374,Congenital hip dislocation,HP:0002827,Hip dislocation
+UBERON:4000053,vacuolated notochordal tissue,UBERON:0004121,ectoderm-derived structure
+HP:0009452,Curved proximal phalanx of the 3rd finger,HP:0009442,Curved phalanges of the 3rd finger
+UBERON:0011079,angular bone,UBERON:0008907,dermal bone
+UBERON:3000869,ilial protuberance,UBERON:4100000,skeletal element projection
+UBERON:0009598,mesenchyme of interdigital region between digits 3 and 4,UBERON:0009585,interdigital region mesenchyme
+HP:0001676,Palpitations (with pheochromocytoma),HP:0001675,Rhythm disturbances associated with pheochromocytoma
+CL:0011108,colon epithelial cell,CL:0002253,epithelial cell of large intestine
+DOID:8108,fibroepithelial polyp of urethra,DOID:732,urethral disease
+UBERON:3000494,processus lingualis of pterygoid,UBERON:0004120,mesoderm-derived structure
+HP:0007392,Excessive wrinkled skin,HP:0008067,Abnormally lax or hyperextensible skin
+HP:0010416,Curved distal phalanx of the 2nd toe,HP:0010356,Abnormality of the distal phalanx of the 2nd toe
+UBERON:0004663,aorta wall,UBERON:0004120,mesoderm-derived structure
+HP:0000503,Tortuosity of conjunctival vessels,HP:0008054,Abnormality of the vasculature of the conjunctiva
+UBERON:2001616,lateral ethmoid wing,UBERON:4100000,skeletal element projection
+UBERON:0005672,right lung endothelium,UBERON:0003364,epithelium of right lung
+HP:0008729,Absence of labia majora,HP:0000058,Abnormality of the labia
+HP:0002601,Paresis of extensor muscles of the big toe,HP:0002460,Distal muscle weakness
+DOID:5701,breast liposarcoma,DOID:3017,breast sarcoma
+UBERON:0002742,lamina of septum pellucidum,UBERON:0002437,cerebral hemisphere white matter
+CL:0011107,Muller cell,CL:0000681,radial glial cell
+UBERON:0001091,calcareous tooth,UBERON:0004121,ectoderm-derived structure
+CL:0002030,Fc-epsilon RIalpha-high basophil progenitor cell,CL:0000613,basophil progenitor cell
+HP:0000853,Goiter,HP:0011772,Abnormality of thyroid morphology
+UBERON:2001379,pharyngeal ectoderm,UBERON:0000924,ectoderm
+UBERON:0014548,pyramidal layer of CA1,UBERON:0014567,layer of hippocampal field
+UBERON:0002663,septal nuclear complex,UBERON:0007245,nuclear complex of neuraxis
+HP:0010784,Uterine neoplasm,HP:0010787,Genital neoplasm
+UBERON:0002022,insula,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0010560,pedal digit 4 metatarsal cartilage element,UBERON:0010697,pedal digit metatarsal cartilage element
+DOID:4195,hyperglycemia,DOID:4194,glucose metabolism disease
+UBERON:0015069,distal carpal cartilage,UBERON:0010883,forelimb cartilage element
+HP:0005375,Partial cellular immunodeficiency,HP:0005374,Cellular immunodeficiency
+DOID:1883,hepatitis C,DOID:37,skin disease
+UBERON:0005795,embryonic uterus,UBERON:0002050,embryonic structure
+HP:0012613,Increased urinary sulfate,HP:0004369,Decreased purine levels
+UBERON:0010738,distal tarsal bone 5,UBERON:0010721,distal tarsal bone
+HP:0100907,Sclerosis of the middle phalanx of the 5th finger,HP:0100916,Sclerosis of the middle phalanges of the hand
+HP:0001072,Thickened skin,HP:0011121,Abnormality of skin morphology
+DOID:11155,hypohidrosis,DOID:1383,sweat gland disease
+HP:0004976,Knee dislocation,HP:0002815,Abnormality of the knees
+DOID:13760,Pthirus pubis infestation,DOID:5502,lice infestation
+UBERON:2201415,pelvic fin distal radial cartilage 2,UBERON:2101415,pelvic fin distal radial element 2
+HP:0002442,Dyscalculia,HP:0001328,Specific learning disability
+DOID:0050706,variable age at onset electroclinical syndrome,DOID:0050701,electroclinical syndrome
+UBERON:0004456,entire sense organ system,UBERON:0000467,anatomical system
+UBERON:3000804,sulcus articularis medialis,UBERON:0000064,organ part
+HP:0001041,Facial erythema,HP:0010783,Erythema
+HP:0010636,Schizencephaly,HP:0002060,Abnormality of the cerebrum
+UBERON:0013710,posterior superior iliac spine,UBERON:0013713,posterior iliac spine
+NCBITaxon:139,Borrelia burgdorferi,NCBITaxon:64895,Borrelia burgdorferi group
+UBERON:0006338,lateral ventricle choroid plexus stroma,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0002221,Absent axillary hair,HP:0100134,Abnormality of the axillary hair
+UBERON:0001889,trunk of phrenic nerve,UBERON:0001147,trunk of peripheral nerve
+UBERON:0002349,myocardium,UBERON:0005983,heart layer
+UBERON:0002748,medial lemniscus of medulla,UBERON:0002678,regional part of medulla oblongata
+UBERON:2002242,scale primordium,UBERON:0001048,primordium
+HP:0000132,Menorrhagia,HP:0000140,Abnormality of the menstrual cycle
+HP:0011559,Double inlet to single ventricle with two atrioventricular valves,HP:0011557,Double inlet to single ventricle of indeterminate morphology
+DOID:8482,transient retinal arterial occlusion,DOID:8483,retinal artery occlusion
+UBERON:0006596,presumptive blood,UBERON:0006598,presumptive structure
+UBERON:0012167,buccal fat pad,UBERON:0003566,head connective tissue
+UBERON:0006915,stratified squamous epithelium,UBERON:0000486,multilaminar epithelium
+UBERON:0004640,efferent arteriole,UBERON:0003644,kidney arterial blood vessel
+HP:0100758,Gangrene,HP:0001939,Abnormality of metabolism/homeostasis
+UBERON:0001160,fundus of stomach,UBERON:0009870,zone of stomach
+CL:0000900,"naive thymus-derived CD8-positive, alpha-beta T cell",CL:0000625,"CD8-positive, alpha-beta T cell"
+UBERON:0010064,open anatomical space,UBERON:0000464,anatomical space
+DOID:5528,rectum squamous cell carcinoma,DOID:1993,rectum cancer
+UBERON:0006052,digit 5,UBERON:0002544,digit
+DOID:0050529,adult spinal muscular atrophy,DOID:12377,spinal muscular atrophy
+HP:0001182,Tapered finger,HP:0001167,Abnormality of finger
+CL:0002565,iris pigment epithelial cell,CL:0000342,pigment cell (sensu Vertebrata)
+HP:0011035,Abnormality of the renal cortex,HP:0012210,Abnormal renal morphology
+DOID:2073,perinatal intestinal perforation,DOID:2074,intestinal perforation
+UBERON:0002242,nucleus pulposus,UBERON:0004121,ectoderm-derived structure
+DOID:12161,peripheral retinal degeneration,DOID:8466,retinal degeneration
+HP:0006158,Finger joint hyperextensibility,HP:0006094,Finger joint hypermobility
+DOID:857,multiple carboxylase deficiency,DOID:9252,amino acid metabolic disorder
+UBERON:0014508,distal interphalangeal joint of manual digit 3,UBERON:0014506,distal interphalangeal joint of digit 3
+UBERON:0011155,sylvian cistern,UBERON:0004050,subarachnoid cistern
+CL:0001022,CD115-positive monocyte,CL:0001019,CD115-positive monocyte OR common dendritic progenitor
+UBERON:0014835,serratus muscle,UBERON:0001630,muscle organ
+DOID:8717,decubitus ulcer,DOID:8549,chronic ulcer of skin
+UBERON:0011320,ligament of temporomandibular joint,UBERON:0004120,mesoderm-derived structure
+DOID:8850,salivary gland cancer,DOID:8618,oral cavity cancer
+UBERON:0001823,nasal cartilage,UBERON:0002418,cartilage tissue
+UBERON:0001566,cricothyroid muscle,UBERON:0006328,laryngeal intrinsic muscle
+UBERON:0005323,mesonephric mesenchyme,UBERON:0006554,urinary system structure
+UBERON:3000059,capsular process,UBERON:0004529,anatomical projection
+DOID:5444,spiradenoma,DOID:5876,apocrine sweat gland neoplasm
+UBERON:0006947,male genital duct,UBERON:0005904,duct of male reproductive system
+UBERON:0005809,cortex of manus bone,UBERON:0001439,compact bone tissue
+HP:0005326,Hypoplastic philtrum,HP:0000288,Abnormality of the philtrum
+UBERON:0005256,trunk mesenchyme,UBERON:0003104,mesenchyme
+UBERON:0005321,mesonephric smooth muscle tissue,UBERON:0006554,urinary system structure
+UBERON:0007223,osseus cochlea,UBERON:0004120,mesoderm-derived structure
+HP:0009338,Enlarged epiphysis of the distal phalanx of the 3rd finger,HP:0009332,Abnormality of the epiphysis of the distal phalanx of the 3rd finger
+UBERON:0011623,horn of thyroid cartilage,UBERON:0004119,endoderm-derived structure
+DOID:2479,central nervous system origin vertigo,DOID:936,brain disease
+DOID:14692,Smith-Lemli-Opitz syndrome,DOID:3146,lipid metabolism disorder
+HP:0010160,Abnormality of the epiphyses of the toes,HP:0001780,Abnormality of toe
+CL:0002520,nephrocyte,CL:0002522,renal filtration cell
+UBERON:0002203,vasculature of eye,UBERON:0004121,ectoderm-derived structure
+HP:0003447,Axonal loss,HP:0000764,Peripheral axonal degeneration
+HP:0009971,Polydactyly affecting the 4th finger,HP:0006159,Mesoaxial hand polydactyly
+HP:0009315,Triangular shaped proximal phalanx of the 4th finger,HP:0009858,Triangular shaped proximal phalanges of the hand
+HP:0000022,Abnormality of male internal genitalia,HP:0000812,Abnormal internal genitalia
+UBERON:0007354,cartilage of pharyngotympanic tube,UBERON:0002418,cartilage tissue
+UBERON:3010538,pars nervosa,UBERON:0000064,organ part
+HP:0010826,Abnormality of the twelfth cranial nerve,HP:0001291,Abnormality of the cranial nerves
+UBERON:0013752,diaphysis of metacarpal bone,UBERON:0004120,mesoderm-derived structure
+UBERON:0005953,outflow part of right ventricle,UBERON:0005337,outflow tract of ventricle
+CL:0002311,mammotroph,CL:0000638,acidophil cell of pars distalis of adenohypophysis
+UBERON:0002123,cortex of thymus,UBERON:0001851,cortex
+HP:0001877,Abnormality of erythrocytes,HP:0001871,Abnormality of  blood and blood-forming tissues
+HP:0012640,Abnormality of intracranial pressure,HP:0012638,Abnormality of nervous system physiology
+UBERON:0006266,nasolacrimal groove,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:6110,jugular foramen meningioma,DOID:3565,meningioma
+HP:0003549,Abnormality of connective tissue,HP:0000118,Phenotypic abnormality
+HP:0009105,Abnormal ossification of the pubic bone,HP:0009106,Abnormal pelvis bone ossification
+UBERON:0005023,mucosa of oropharynx,UBERON:0000355,pharyngeal mucosa
+UBERON:0001307,capsule of ovary,UBERON:0014404,female anatomical structure
+DOID:11771,spontaneous ocular nystagmus,DOID:9650,pathologic nystagmus
+UBERON:0012272,minor duodenal papilla,UBERON:0004914,duodenal papilla
+UBERON:0006241,future spinal cord,UBERON:0005423,developing anatomical structure
+CL:0002353,fetal liver hematopoietic progenitor cell,CL:0002352,gestational hematopoietic stem cell
+HP:0009994,Partial duplication of the distal phalanx of the 5th finger,HP:0010004,Partial duplication of the distal phalanges of the hand
+UBERON:0000983,metatarsus region,UBERON:0009877,metapodium region
+HP:0011108,Recurrent sinusitis,HP:0002788,Recurrent upper respiratory tract infections
+UBERON:0001409,semispinalis capitis,UBERON:0011017,semispinalis muscle
+HP:0010656,Abnormal epiphyseal ossification,HP:0011849,Abnormal bone ossification
+CL:0000760,type 8 cone bipolar cell (sensu Mus),CL:0000749,ON-bipolar cell
+UBERON:0007804,sclerotic ring,UBERON:0010290,scleral ossicle
+HP:0009851,Aplasia/Hypoplasia of the proximal phalanges of the hand,HP:0009767,Aplasia/Hypoplasia of the phalanges of the hand
+HP:0002944,Thoracolumbar scoliosis,HP:0002650,Scoliosis
+UBERON:0005342,malleus head,UBERON:0005913,zone of bone organ
+NCBITaxon:10258,Orf virus,NCBITaxon:10257,Parapoxvirus
+DOID:2303,stereotypic movement disorder,DOID:0060038,specific developmental disorder
+HP:0100224,Absent epiphysis of the proximal phalanx of the 5th toe,HP:0100099,Abnormality of the epiphysis of the proximal phalanx of the 5th toe
+UBERON:0002997,nucleus of medial eminence,UBERON:0002308,nucleus of brain
+HP:0002923,Rheumatoid factor positive,HP:0002960,Autoimmunity
+UBERON:0000378,tongue muscle,UBERON:0013765,digestive system organ
+UBERON:0005484,tricuspid valve leaflet,UBERON:0011741,cardiac valve leaflet
+HP:0009805,Low-output congestive heart failure,HP:0001635,Congestive heart failure
+HP:0100884,Compensatory scoliosis,HP:0002650,Scoliosis
+CL:0000073,barrier epithelial cell,CL:0000066,epithelial cell
+CL:0002217,intermediate trophoblast cell,CL:0000351,trophoblast cell
+HP:0012631,Pigment deposition in the trabecular meshwork,HP:0012630,Abnormality of the trabecular meshwork
+HP:0002154,Hyperglycinemia,HP:0010895,Abnormality of glycine metabolism
+UBERON:0009622,pronephric proximal straight tubule,UBERON:0005310,pronephric nephron tubule
+HP:0000670,Carious teeth,HP:0011061,Abnormality of dental structure
+HP:0011553,Discordant atrioventricular connection,HP:0011546,Abnormal atrioventricular connection
+UBERON:0004331,proximal phalanx of manual digit 5,UBERON:0014505,proximal phalanx of digit 5
+UBERON:0001944,pretectal region,UBERON:0007245,nuclear complex of neuraxis
+CL:0002273,type ECL enteroendocrine cell,CL:0002274,histamine secreting cell
+HP:0004234,Bone-in-a-bone appearance of carpal bones,HP:0009164,Abnormal calcification of the carpal bones
+CL:0002613,striatum neuron,CL:0012001,neuron of the forebrain
+HP:0000660,Lipemia retinalis,HP:0000479,Abnormality of the retina
+UBERON:0010191,aortic system,UBERON:0000480,anatomical group
+HP:0001679,Abnormality of the aorta,HP:0011004,Abnormality of the systemic arterial tree
+UBERON:0001763,odontogenic papilla,UBERON:0003856,odontogenic mesenchyme
+HP:0100838,Recurrent cutaneous abscess formation,HP:0002722,Recurrent abscess formation
+HP:0005773,Short forearm,HP:0009821,Forearm undergrowth
+HP:0011340,Incomplete cleft of the upper lip,HP:0000204,Cleft upper lip
+UBERON:0005892,mesonephric early distal tubule,UBERON:0000083,mesonephric tubule
+UBERON:0001250,red pulp of spleen,UBERON:1000023,spleen pulp
+UBERON:0001448,metatarsal bone,UBERON:0015036,pedal digit metatarsal endochondral element
+DOID:2744,pyelitis,DOID:557,kidney disease
+UBERON:3000834,posterior lamina recurvata,UBERON:0005913,zone of bone organ
+DOID:4047,liver rhabdomyosarcoma,DOID:270,liver sarcoma
+UBERON:0010519,tail electric organ,UBERON:0006869,electric organ
+HP:0010160,Abnormality of the epiphyses of the toes,HP:0010631,Abnormality of the epiphyses of the feet
+UBERON:0001862,vestibular labyrinth,UBERON:0000064,organ part
+DOID:2548,reflex epilepsy,DOID:0050706,variable age at onset electroclinical syndrome
+UBERON:0009553,distal segment of pedal digit,UBERON:0005445,segment of pes
+UBERON:0002656,periamygdaloid area,UBERON:0005401,cerebral hemisphere grey matter
+HP:0001104,Macular hypoplasia,HP:0008059,Aplasia/Hypoplasia of the macula
+DOID:0060128,mu chain disease,DOID:0060125,heavy chain disease
+UBERON:0004918,internal urethral sphincter,UBERON:0004917,urethral sphincter
+HP:0012200,Abnormality of prothrombin,HP:0003256,Abnormality of the coagulation cascade
+HP:0007082,DIlated third ventricle,HP:0002119,Ventriculomegaly
+UBERON:0009014,lower back skin,UBERON:0003836,abdominal segment skin
+UBERON:0012621,muscle of Aristotle's lantern,UBERON:0013765,digestive system organ
+HP:0100120,Stippling of the epiphysis of the middle phalanx of the 2nd toe,HP:0100053,Stippling of the epiphyses of the 2nd toe
+HP:0002623,Overriding aorta,HP:0001679,Abnormality of the aorta
+HP:0009418,Small epiphyses of the 3rd finger,HP:0010236,Small epiphyses of the phalanges of the hand
+UBERON:0012472,hepatoduodenal ligament,UBERON:0003567,abdomen connective tissue
+UBERON:0008321,deep artery of penis,UBERON:0005156,reproductive structure
+NCBITaxon:12461,Hepatitis E virus,NCBITaxon:186677,Hepevirus
+UBERON:2001527,epibranchial cartilage,UBERON:2001904,epibranchial element
+DOID:8883,lower lip cancer,DOID:8564,lip cancer
+HP:0004336,Myelin outfoldings,HP:0003130,Abnormal peripheral myelination
+HP:0003084,Fractures of the long bones,HP:0011314,Abnormality of long bone morphology
+DOID:4388,bone peripheral neuroepithelioma,DOID:3368,bone Ewing's sarcoma
+CL:0000552,orthochromatic erythroblast,CL:0000765,erythroblast
+UBERON:0014732,compound cell cluster organ,UBERON:0000062,organ
+UBERON:0001676,occipital bone,UBERON:0011164,neurocranium bone
+DOID:2841,asthma,DOID:1176,bronchial disease
+HP:0006960,Choroid plexus calcification,HP:0002514,Cerebral calcification
+UBERON:0010023,dorsal part of pharyngeal pouch 2,UBERON:0000490,unilaminar epithelium
+UBERON:0001916,endothelium of arteriole,UBERON:0001917,endothelium of artery
+UBERON:0002102,forelimb,UBERON:0004710,pectoral appendage
+HP:0010072,Patchy sclerosis of the 1st metatarsal,HP:0010054,Abnormality of the first metatarsal
+HP:0011568,Double orifice mitral valve,HP:0001633,Abnormality of the mitral valve
+HP:0009322,Bracket epiphysis of the middle phalanx of the 3rd finger,HP:0010258,Bracket epiphyses of the middle phalanges of the hand
+HP:0008636,Lobular glomerulopathy,HP:0000095,Abnormality of the glomerulus
+HP:0100388,Aplasia of the proximal phalanges of the toes,HP:0010745,Aplasia of the phalanges of the toes
+UBERON:0010250,middle meningeal artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0011692,enameloid,UBERON:0010365,odontoid tissue
+UBERON:0004410,distal epiphysis of fibula,UBERON:0004379,distal epiphysis
+HP:0001593,Maxillary lateral incisor microdontia,HP:0000691,Microdontia
+UBERON:0009206,lateral nasal process surface ectoderm,UBERON:0014702,frontonasal process epithelium
+HP:0100698,Subcutaneous neurofibromas,HP:0001067,Neurofibromas
+UBERON:0013704,notochordal canal,UBERON:0004121,ectoderm-derived structure
+UBERON:0014445,acetabular fossa,UBERON:0004704,bone fossa
+UBERON:0011608,hyomandibular element,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003645,metacarpal bone of digit 1,UBERON:0015043,manual digit 1 metacarpus endochondral element
+HP:0010435,Short middle phalanx of the 2nd toe,HP:0010404,Aplasia/Hypoplasia of the middle phalanx of the 2nd toe
+CL:0002677,naive regulatory T cell,CL:0000898,naive T cell
+UBERON:0007807,connecting stalk blood vessel,UBERON:0000478,extraembryonic structure
+HP:0010180,Triangular shaped phalanges of the toes,HP:0010161,Abnormality of the phalanges of the toes
+UBERON:2002110,metapterygoid-quadrate fenestra,UBERON:0005744,bone foramen
+DOID:11134,prolapse of lacrimal gland,DOID:1400,lacrimal apparatus disease
+UBERON:3010346,globe,UBERON:0000481,multi-tissue structure
+DOID:6789,vulvar childhood botryoid-type embryonal rhabdomyosarcoma,DOID:2096,vulvar sarcoma
+HP:0003466,Paradoxical increased cortisol secretion on dexamethasone suppression test,HP:0011731,Abnormality of circulating cortisol level
+UBERON:0005922,inferior nasal concha,UBERON:0011164,neurocranium bone
+HP:0001392,Abnormality of the liver,HP:0002012,Abnormality of the abdominal organs
+UBERON:0001860,endolymphatic duct,UBERON:0000025,tube
+CL:0000083,epithelial cell of pancreas,CL:0002371,somatic cell
+UBERON:0007214,mesenchyme derived from trunk neural crest,UBERON:0014387,mesenchyme derived from neural crest
+HP:0009073,Progressive proximal muscle weakness,HP:0003701,Proximal muscle weakness
+DOID:4286,sebaceous basal cell carcinoma,DOID:2513,basal cell carcinoma
+UBERON:2001014,myotome somite 13,UBERON:0003082,myotome
+HP:0008020,Progressive cone degeneration,HP:0000546,Retinal degeneration
+UBERON:0008808,prostate gland dorsolateral lobe,UBERON:0001328,lobe of prostate
+HP:0012202,increased serum bile acid concentration,HP:0010996,Abnormality of monocarboxylic acid metabolism
+UBERON:0006554,urinary system structure,UBERON:0000061,anatomical structure
+UBERON:0002062,endocardial cushion,UBERON:0009751,cardiac mesenchyme
+HP:0000720,Mood swings,HP:0100852,Abnormal fear/anxiety-related behavior
+UBERON:2001236,hypobranchial 2 bone,UBERON:2001895,hypobranchial 2 element
+DOID:7188,autoimmune thyroiditis,DOID:7166,thyroiditis
+HP:0004691,2-3 toe syndactyly,HP:0001770,Toe syndactyly
+UBERON:0007270,pelvic appendage musculature,UBERON:0014792,musculature of pelvic complex
+HP:0002487,Hyperkinesis,HP:0100022,Abnormality of movement
+DOID:4071,duodenogastric reflux,DOID:4072,duodenal disease
+HP:0000704,Periodontitis,HP:0000168,Abnormality of the gingiva
+HP:0010374,Curved phalanges of the 4th toe,HP:0010336,Abnormality of the phalanges of the 4th toe
+HP:0009490,Cone-shaped epiphyses of the 2nd finger,HP:0010230,Cone-shaped epiphyses of the phalanges of the hand
+UBERON:4300015,ventral cleithrum,UBERON:0007829,pectoral girdle bone
+UBERON:0004657,mandible condylar process,UBERON:0010313,neural crest-derived structure
+UBERON:3000689,prominentia apicalis ventralis,UBERON:0011769,cartilaginous projection
+DOID:3362,coronary aneurysm,DOID:9768,heart aneurysm
+UBERON:0002538,hatching gland,UBERON:0002530,gland
+UBERON:0004444,proximal epiphysis of distal phalanx of manual digit 1,UBERON:0004417,proximal epiphysis of phalanx of manual digit 1
+UBERON:2005346,extrapancreatic duct,UBERON:0003928,digestive system duct
+UBERON:2001929,epioccipital posterior process,UBERON:4100000,skeletal element projection
+HP:0000817,Poor eye contact,HP:0000735,Impaired social interactions
+UBERON:0014480,blood feather,UBERON:0000022,feather
+UBERON:0001758,periodontium,UBERON:0000479,tissue
+HP:0100167,Triangular epiphysis of the proximal phalanx of the 3rd toe,HP:0100093,Abnormality of the epiphysis of the proximal phalanx of the 3rd toe
+UBERON:0001251,marginal zone of spleen,UBERON:0000466,immaterial anatomical entity
+UBERON:4200060,ectepicondylar foramen,UBERON:0004120,mesoderm-derived structure
+HP:0008087,Nonossified fifth metatarsal,HP:0008371,Abnormal metatarsal ossification
+UBERON:0001787,photoreceptor layer of retina,UBERON:0003902,retinal neural layer
+NCBITaxon:36087,Trichuris trichiura,NCBITaxon:36086,Trichuris
+UBERON:0003265,chorionic mesenchyme,UBERON:0007524,dense mesenchyme tissue
+UBERON:0004875,nephrogenic cord,UBERON:0005423,developing anatomical structure
+DOID:5593,gastric papillary adenocarcinoma,DOID:3717,gastric adenocarcinoma
+UBERON:3000650,processus frontalis of maxilla,UBERON:0004120,mesoderm-derived structure
+UBERON:0000180,lateral lumbar region of abdomen,UBERON:0000475,organism subdivision
+UBERON:0005118,metanephric early distal convoluted tubule,UBERON:0005101,early distal convoluted tubule
+UBERON:0005979,crista terminalis,UBERON:0004120,mesoderm-derived structure
+DOID:3878,intestinal pseudo-obstruction,DOID:8440,ileus
+UBERON:0002610,cochlear nuclear complex,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001207,mucosa of large intestine,UBERON:0001242,intestinal mucosa
+UBERON:0006569,diencephalic nucleus,UBERON:0002784,regional part of diencephalon
+UBERON:0003664,manual digit muscle,UBERON:0001500,muscle of manus
+HP:0010326,Deviation/Displacement of the 2nd toe,HP:0010319,Abnormality of the 2nd toe
+UBERON:2001676,mesethmoid-premaxillary joint,UBERON:2001950,inter-premaxillary joint
+UBERON:0000094,membrane organ,UBERON:0000062,organ
+HP:0000708,Behavioural/Psychiatric Abnormality,HP:0011446,Abnormality of higher mental function
+DOID:0050125,dengue shock syndrome,DOID:12205,dengue disease
+HP:0100590,Rectal fistula,HP:0100589,Urogenital fistula
+CL:0002149,epithelial cell of uterus,CL:0002076,endo-epithelial cell
+UBERON:0003441,forelimb nerve,UBERON:0003440,limb nerve
+UBERON:0001571,genioglossus muscle,UBERON:0001575,extrinsic muscle of tongue
+UBERON:0002272,medial zone of hypothalamus,UBERON:0000064,organ part
+HP:0002156,Homocystinuria,HP:0010919,Abnormality of homocysteine metabolism
+UBERON:0004865,actinopterygian parietal bone,UBERON:0002514,intramembranous bone
+UBERON:0014288,dorsal accessory olive,UBERON:0007702,tract of brain
+UBERON:0005970,brain commissure,UBERON:0007702,tract of brain
+UBERON:0010404,lateral ventricle subependymal layer,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002136,hilus of dentate gyrus,UBERON:0003022,cerebral cortex lobe
+UBERON:0006862,diaphysis of femur,UBERON:0004769,diaphysis
+DOID:11516,hypertensive heart disease,DOID:10763,hypertension
+HP:0009699,Osteolytic defects of the hand bones,HP:0002797,Osteolysis
+DOID:5711,vulvar liposarcoma,DOID:3382,liposarcoma
+HP:0006930,Frontoparietal cortical dysplasia,HP:0002539,Cortical dysplasia
+UBERON:0005258,upper arm mesenchyme,UBERON:0003859,forelimb mesenchyme
+UBERON:0011379,male external urethral sphincter,UBERON:0014403,male anatomical structure
+DOID:6316,Bartholin's gland adenocarcinoma,DOID:2098,vulva adenocarcinoma
+UBERON:0009553,distal segment of pedal digit,UBERON:0009551,distal segment of digit
+HP:0006150,Swan neck-like deformities of the fingers,HP:0001167,Abnormality of finger
+UBERON:3000433,pineal foramen,UBERON:0005744,bone foramen
+UBERON:2000698,tripus,UBERON:2000461,Weberian ossicle
+UBERON:0003675,tooth crown,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0008423,Spinal dysplasia,HP:0000925,Abnormality of the vertebral column
+HP:0200146,Cystic medial necrosis of the aorta,HP:0002597,Abnormality of the vasculature
+UBERON:0002305,layer of hippocampus,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:7694,bladder urachal adenocarcinoma,DOID:5958,bladder urachal carcinoma
+HP:0100350,Contractures of the proximal interphalangeal joint of the 4th toe,HP:0010339,Flexion contracture of the 4th toe
+HP:0100319,Cerebral hyaline bodies,HP:0100314,Cerebral inclusion bodies
+HP:0100050,Ivory epiphyses of the 2nd toe,HP:0010168,Ivory epiphyses of the toes
+UBERON:0010889,ectethmoid,UBERON:0005913,zone of bone organ
+UBERON:0001723,tongue,UBERON:0013765,digestive system organ
+DOID:1350,paranasal sinus neoplasm,DOID:0050621,respiratory system benign neoplasm
+HP:0009214,Absent epiphysis of the middle phalanx of the 4th finger,HP:0009393,Absent epiphyses of the 4th finger
+DOID:10310,viral meningitis,DOID:9471,meningitis
+DOID:6208,mediastinal osteogenic sarcoma,DOID:4050,mediastinum sarcoma
+HP:0001525,Severe failure to thrive,HP:0001508,Failure to thrive
+CL:0000247,Rohon-Beard neuron,CL:0000531,primary sensory neuron
+DOID:11547,corneal deposit,DOID:10124,corneal disease
+CL:0000521,fungal cell,CL:0000255,eukaryotic cell
+UBERON:4000055,polypteroid scale,UBERON:4000052,ganoid scale
+CL:1001595,rectum glandular cell,CL:0002658,glandular cell of the large intestine
+DOID:4897,bile duct carcinoma,DOID:4606,bile duct cancer
+CL:0001031,cerebellar granule cell,CL:1001611,cerebellar neuron
+DOID:2173,eyelid neoplasm,DOID:3165,skin benign neoplasm
+HP:0010097,Partial duplication of the distal phalanx of the hallux,HP:0010101,Partial duplication of the phalanges of the hallux
+HP:0100123,Bracket epiphysis of the proximal phalanx of the 2nd toe,HP:0100090,Abnormality of the epiphysis of the proximal phalanx of the 2nd toe
+UBERON:0004223,vagina smooth muscle,UBERON:0014404,female anatomical structure
+UBERON:0015800,taenia tectum of brain,UBERON:0013199,stria of neuraxis
+UBERON:0003091,thyroid primordium,UBERON:0004119,endoderm-derived structure
+UBERON:0003324,mesenchyme of lower jaw,UBERON:0004121,ectoderm-derived structure
+UBERON:0002262,celiac ganglion,UBERON:0003964,prevertebral ganglion
+UBERON:0009015,upper back skin,UBERON:0001418,skin of thorax
+UBERON:0002961,archicortex,UBERON:0014734,allocortex
+UBERON:0007272,pectoral appendage skeleton,UBERON:0011582,paired limb/fin skeleton
+HP:0100376,Aplasia/Hypoplasia of the proximal phalanx of the 4th toe,HP:0010337,Aplasia/Hypoplasia of the 4th toe
+DOID:8023,myxoid liposarcoma of the ovary,DOID:5697,liposarcoma of the ovary
+DOID:0050656,pseudo-TORCH syndrome,DOID:0050737,autosomal recessive disease
+UBERON:3000688,prominentia apicalis dorsalis,UBERON:4100000,skeletal element projection
+UBERON:0001397,subscapular artery,UBERON:0001637,artery
+UBERON:2001141,tooth 1V,UBERON:2000694,ceratobranchial 5 tooth
+UBERON:0006117,accessory nerve fiber bundle,UBERON:0011215,cell part cluster of neuraxis
+UBERON:0011256,rhinarium,UBERON:0004121,ectoderm-derived structure
+HP:0000107,Renal cyst,HP:0012210,Abnormal renal morphology
+HP:0012554,Absent thumbnail,HP:0001817,Absent fingernail
+UBERON:0000975,sternum,UBERON:0004120,mesoderm-derived structure
+DOID:0050650,familial atrial fibrillation,DOID:10273,heart conduction disease
+HP:0007001,Loss of Purkinje cells in the cerebellar vermis,HP:0002334,Abnormality of the cerebellar vermis
+UBERON:0006851,renal cortex peritubular capillary,UBERON:0005272,peritubular capillary
+UBERON:0011320,ligament of temporomandibular joint,UBERON:0003566,head connective tissue
+UBERON:0006089,dorsal external arcuate fiber bundle,UBERON:0011215,cell part cluster of neuraxis
+HP:0002223,Absent eyebrow,HP:0100840,Aplasia/Hypoplasia of the eyebrow
+UBERON:0000100,blastopore,UBERON:0002050,embryonic structure
+CL:1000416,myoepithelial cell of lactiferous gland,CL:0000185,myoepithelial cell
+DOID:7762,childhood multilocular cystic kidney neoplasm,DOID:3116,kidney benign neoplasm
+UBERON:0014372,fibroelastic membrane of larynx,UBERON:0000094,membrane organ
+CL:0000661,distal tip cell (sensu Nematoda),CL:0000422,mitogenic signaling cell
+HP:0100927,Sclerosis of the phalanges of the 3rd toe,HP:0100924,Sclerosis of the phalanges of the toes
+CL:0000396,lamellocyte,CL:0000394,plasmatocyte
+UBERON:0001009,circulatory system,UBERON:0000467,anatomical system
+CL:0000508,type G enteroendocrine cell,CL:0000509,gastrin secreting cell
+UBERON:0007136,rectouterine fold,UBERON:0000063,organ segment
+HP:0011087,Talon cusp,HP:0011063,Abnormality of incisor morphology
+DOID:6322,tibial adamantinoma,DOID:2775,long bone adamantinoma
+HP:0009763,Limb pain,HP:0011843,Abnormality of skeletal physiology
+UBERON:0000979,tibia,UBERON:0015004,tibia endochondral element
+HP:0003214,Prolonged G2 phase of cell cycle,HP:0011018,Abnormality of the cell cycle
+HP:0010955,Dilatation of the bladder,HP:0000014,Abnormality of the bladder
+UBERON:3000486,processus ascendens plectri,UBERON:4100000,skeletal element projection
+UBERON:0006029,interdigital region between manual digits 2 and 3,UBERON:0006019,interdigital region between digits 2 and 3
+DOID:12215,oligohydramnios,DOID:780,placenta disease
+HP:0008708,Partial development of the penile shaft,HP:0000036,Abnormality of the penis
+UBERON:0002462,erector spinae muscle group,UBERON:0004518,muscle of vertebral column
+DOID:9410,panhypopituitarism,DOID:9406,hypopituitarism
+CL:0002361,primitive erythroid progenitor,CL:0002417,primitive erythroid lineage cell
+HP:0000679,Taurodontia,HP:0006479,Abnormality of the dental pulp
+UBERON:2007031,anterior neural rod,UBERON:0004121,ectoderm-derived structure
+HP:0002199,Hypocalcemic seizures,HP:0002901,Hypocalcemia
+HP:0004756,Ventricular tachycardia,HP:0001649,Tachycardia
+NCBITaxon:10090,Mus musculus,NCBITaxon:862507,"Mus <mouse, subgenus>"
+HP:0009664,Absent epiphysis of the proximal phalanx of the thumb,HP:0009686,Absent epiphyses of the thumb
+HP:0002493,Corticospinal tract dysfunction,HP:0007256,Abnormality of pyramidal motor function
+UBERON:0015059,orbitosphenoid endochondral element,UBERON:0004120,mesoderm-derived structure
+CL:0002327,mammary gland epithelial cell,CL:0002371,somatic cell
+HP:0011476,Profound sensorineural hearing impairment,HP:0000407,Sensorineural hearing impairment
+DOID:8866,actinic keratosis,DOID:0060071,pre-malignant neoplasm
+UBERON:0001519,skin of manus,UBERON:0015790,autopod skin
+HP:0000787,Nephrolithiasis,HP:0012210,Abnormal renal morphology
+UBERON:0010343,2nd arch mesenchyme from head mesenchyme,UBERON:0006904,head mesenchyme from mesoderm
+HP:0002322,Resting tremor,HP:0001337,Tremor
+HP:0009736,Tibial pseudoarthrosis,HP:0005864,Pseudoarthrosis
+UBERON:0004362,pharyngeal arch 1,UBERON:0002539,pharyngeal arch
+DOID:2112,cystoisosporiasis,DOID:2113,coccidiosis
+HP:0002536,Abnormal cortical gyration,HP:0002269,Abnormality of neuronal migration
+HP:0011486,Abnormality of corneal thickness,HP:0000481,Abnormality of the cornea
+HP:0007289,Limb fasciculations,HP:0002380,Fasciculations
+HP:0009320,Abnormality of the epiphyses of the 3rd finger,HP:0004150,Abnormality of the 3rd finger
+UBERON:2000238,medial olfactory tract,UBERON:2000597,telencephalic tracts
+UBERON:0007010,cleaving embryo,UBERON:0000922,embryo
+UBERON:0005612,intercostal artery,UBERON:0004573,systemic artery
+CL:0000728,secondary pigment cell,CL:0001658,visual pigment cell (sensu Nematoda and Protostomia)
+CL:0000689,myoendocrine cell,CL:0000163,endocrine cell
+HP:0005300,Nodular inflammatory vasculitis,HP:0002633,Vasculitis
+UBERON:0003362,epithelium of endolymphatic duct,UBERON:0006937,inner ear epithelium
+DOID:6198,corneal intraepithelial neoplasm,DOID:0060071,pre-malignant neoplasm
+DOID:900,hepatopulmonary syndrome,DOID:409,liver disease
+NCBITaxon:12090,Human enterovirus 70,NCBITaxon:138951,Human enterovirus D
+HP:0004407,Bony paranasal bossing,HP:0005105,Abnormal nasal morphology
+HP:0001911,Abnormality of granulocytes,HP:0010974,Abnormality of myeloid leukocytes
+DOID:0050765,neuroacanthocytosis,DOID:1289,neurodegenerative disease
+HP:0001782,Bulbous tips of toes,HP:0001780,Abnormality of toe
+DOID:14693,Clouston syndrome,DOID:0050736,autosomal dominant disease
+DOID:5917,uterine corpus diffuse leiomyomatosis,DOID:5916,uterine corpus leiomyomatosis
+HP:0200006,Slanting of the palpebral fissure,HP:0008050,Abnormality of the palpebral fissures
+UBERON:0006264,mouth-foregut junction,UBERON:0007651,anatomical junction
+UBERON:0011583,stylopodial skeleton,UBERON:0010712,limb skeleton subdivision
+UBERON:0011011,brachioradialis,UBERON:0001499,muscle of arm
+UBERON:0013250,vesicular appendage of epoophoron,UBERON:0005156,reproductive structure
+UBERON:0004711,jugular vein,UBERON:0003502,neck blood vessel
+UBERON:2001157,posterior lateral line primordium,UBERON:0004121,ectoderm-derived structure
+HP:0000957,Cafe-au-lait spot,HP:0011355,Localized skin lesion
+HP:0012667,Regional left ventricular wall motion abnormality,HP:0003116,Abnormal echocardiogram
+UBERON:0004212,glomerular capillary,UBERON:0003527,kidney capillary
+UBERON:0011825,loose connective tissue,UBERON:0011821,irregular connective tissue
+UBERON:0012132,intercuneiform joint,UBERON:0000982,skeletal joint
+HP:0011051,Agenesis of premolar,HP:0011076,Abnormality of premolar
+HP:0004439,Craniofacial dysostosis,HP:0000929,Abnormality of the skull
+UBERON:4200056,hypocercal tail,UBERON:4000164,caudal fin
+NCBITaxon:11089,Yellow fever virus,NCBITaxon:40005,Yellow fever virus group
+HP:0010878,Fetal cystic hygroma,HP:0010880,Increased nuchal translucency
+UBERON:0007279,presumptive atrioventricular canal,UBERON:0006598,presumptive structure
+DOID:4364,malignant breast melanoma,DOID:1612,breast cancer
+DOID:0050681,Borjeson-Forssman-Lehmann syndrome,DOID:0050735,X-linked disease
+UBERON:0006553,renal duct,UBERON:0000058,duct
+HP:0001467,Aplasia/Hypoplasia involving the musculature of the upper limbs,HP:0001446,Abnormality of the musculature of the upper limbs
+UBERON:2001756,dorsal fin lepidotrichium 3,UBERON:4000177,dorsal fin lepidotrichium
+UBERON:2002269,interarcual cartilage,UBERON:0011004,pharyngeal arch cartilage
+UBERON:0001870,frontal cortex,UBERON:0000064,organ part
+UBERON:2000542,medial column,UBERON:0004121,ectoderm-derived structure
+UBERON:0011954,stomach non-glandular region,UBERON:0009034,stomach region
+HP:0007761,Pericentral scotoma,HP:0000575,Scotoma
+UBERON:0001911,mammary gland,UBERON:0002365,exocrine gland
+UBERON:0005606,hyaloid cavity,UBERON:0012467,enclosed anatomical space
+UBERON:0005452,hepatic cord,UBERON:0004923,organ component layer
+HP:0010363,Osteolytic defects of the phalanges of the 3rd toe,HP:0010177,Osteolytic defects of the phalanges of the toes
+UBERON:2000826,central nucleus torus semicircularis,UBERON:0011214,nucleus of midbrain tectum
+HP:0005600,Congenital giant melanocytic nevus,HP:0000995,Melanocytic nevus
+HP:0002132,Porencephaly,HP:0002060,Abnormality of the cerebrum
+UBERON:0004692,external naris epithelium,UBERON:0004807,respiratory system epithelium
+HP:0003866,Coarse trabeculae (humeral),HP:0003063,Abnormality of the humerus
+DOID:7297,childhood extraosseous osteosarcoma,DOID:3357,extraosseous osteosarcoma
+HP:0009642,Broad distal phalanx of the thumb,HP:0009617,Abnormality of the distal phalanx of the thumb
+CL:0000772,immature eosinophil,CL:0000771,eosinophil
+DOID:980,choroidal sclerosis,DOID:9799,eye degenerative disease
+NCBITaxon:632,Yersinia pestis,NCBITaxon:629,Yersinia <bacteria>
+DOID:8736,smallpox,DOID:934,viral infectious disease
+UBERON:0013776,skin of palmar/plantar part of autopod,UBERON:0015790,autopod skin
+HP:0012219,Erythema nodosum,HP:0011123,Inflammatory abnormality of the skin
+UBERON:2001371,pancreatic system,UBERON:0000467,anatomical system
+UBERON:0013248,paradidymis,UBERON:0014403,male anatomical structure
+UBERON:0013176,phonic lip,UBERON:0000481,multi-tissue structure
+HP:0007659,Decreased retinal pigmentation with dispersion,HP:0007894,Hypopigmentation of the fundus
+HP:0008017,Depigmented lesions of the retinal pigment epithelium,HP:0007894,Hypopigmentation of the fundus
+UBERON:0004673,trigeminal nerve root,UBERON:0006843,root of cranial nerve
+HP:0011482,Abnormality of the lacrimal gland,HP:0000614,Abnormality of the nasolacrimal system
+UBERON:0006604,lamina orbitonasalis,UBERON:0003932,cartilage element of chondrocranium
+HP:0000402,Stenosis of the external auditory canal,HP:0000372,Abnormality of the auditory canal
+HP:0003916,Normal-density transverse bands (humerus),HP:0003907,Abnormality of the humeral metaphyses
+HP:0010138,Absent epiphysis of the distal phalanx of the hallux,HP:0010113,Absent epiphyses of the hallux
+UBERON:2002206,macula communis,UBERON:0006937,inner ear epithelium
+DOID:3982,Meige syndrome,DOID:0050845,cranio-facial dystonia
+UBERON:0001640,celiac artery,UBERON:0001194,splenic artery
+HP:0005317,Increased pulmonary vascular resistance,HP:0004930,Abnormality of the pulmonary vasculature
+UBERON:0014596,paraventricular nucleus of the hypothalamus descending division - dorsal parvicellular part,UBERON:0003048,regional part of hypothalamus
+CL:1001566,bronchioalveolar stem cells,CL:0000034,stem cell
+DOID:4001,ovarian carcinoma,DOID:2151,malignant ovarian surface epithelial-stromal neoplasm
+UBERON:0005176,tooth enamel organ,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2002066,auditory fenestra,UBERON:0005744,bone foramen
+UBERON:0000064,organ part,UBERON:0000061,anatomical structure
+HP:0001967,Diffuse mesangial sclerosis,HP:0001966,Mesangial abnormality
+HP:0009510,Small epiphysis of the distal phalanx of the 2nd finger,HP:0009499,Abnormality of the epiphysis of the distal phalanx of the 2nd finger
+UBERON:0008977,pes anserinus of tibia,UBERON:0001630,muscle organ
+DOID:0050825,endocardium disease,DOID:114,heart disease
+HP:0005850,Congenital talipes calcaneovalgus,HP:0001884,Talipes calcaneovalgus
+HP:0009952,Complete duplication of the middle phalanx of the 2nd finger,HP:0009949,Duplication of the middle phalanx of the 2nd finger
+UBERON:2000913,molecular layer valvula cerebelli,UBERON:0004121,ectoderm-derived structure
+HP:0005235,Jejunal atresia,HP:0011100,Intestinal atresia
+HP:0006518,Pulmonary venoocclusive disease,HP:0002088,Abnormality of the lung
+HP:0003641,Hemoglobinuria,HP:0003110,Abnormality of urine homeostasis
+UBERON:0003930,atrioventricular canal endocardium,UBERON:0002165,endocardium
+UBERON:0015160,supraorbital artery,UBERON:0004573,systemic artery
+HP:0007000,Morning myoclonic jerks,HP:0001336,Myoclonus
+CL:0002192,metamyelocyte,CL:0002191,granulocytopoietic cell
+HP:0000112,Nephropathy,HP:0012211,Abnormal renal physiology
+UBERON:0001254,urothelium of ureter,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0012197,intercostal vein,UBERON:0001638,vein
+UBERON:0008813,helicotrema,UBERON:0004121,ectoderm-derived structure
+HP:0010382,Abnormality of the proximal phalanx of the 4th toe,HP:0010184,Abnormality of the proximal phalanges of the toes
+UBERON:0006440,os clitoris,UBERON:0007719,bone of reproductive structure
+HP:0009351,Irregular epiphysis of the proximal phalanx of the 3rd finger,HP:0010273,Irregular epiphyses of the proximal phalanges of the hand
+UBERON:0009116,thymoid,UBERON:0003295,pharyngeal gland
+HP:0008807,Acetabular dysplasia,HP:0003170,Abnormality of the acetabulum
+UBERON:0010908,paraglossale,UBERON:0001474,bone element
+HP:0007263,Spinocerebellar atrophy,HP:0001272,Cerebellar atrophy
+UBERON:0004895,alveolar smooth muscle,UBERON:0004233,lower respiratory tract smooth muscle
+HP:0002699,Abnormality of the foramen magnum,HP:0000929,Abnormality of the skull
+HP:0012240,Increased intramyocellular lipid droplets,HP:0009058,Increased muscle lipid content
+HP:0000944,Abnormality of the metaphyses,HP:0002813,Abnormality of limb bone morphology
+UBERON:2002280,pectoral fin distal radial bone 3,UBERON:2102280,pectoral fin distal radial element 3
+UBERON:0002023,claustrum of brain,UBERON:0002420,basal ganglion
+DOID:6229,childhood mature teratoma of the ovary,DOID:6231,mature teratoma of the ovary
+UBERON:0003351,pharyngeal epithelium,UBERON:0003929,gut epithelium
+UBERON:0001278,epithelium of large intestine,UBERON:0001277,intestinal epithelium
+DOID:5570,malignant acrospiroma,DOID:2095,sweat gland cancer
+UBERON:0009948,clavicular air sac,UBERON:0009060,air sac
+UBERON:4000028,integumentary papilla,UBERON:0001763,odontogenic papilla
+UBERON:3000560,septum semicircularium anterior,UBERON:0004121,ectoderm-derived structure
+UBERON:0002327,trunk of intercostal nerve,UBERON:0001147,trunk of peripheral nerve
+HP:0010415,Bullet-shaped distal phalanx of the 2nd toe,HP:0010356,Abnormality of the distal phalanx of the 2nd toe
+UBERON:0001170,mesentery of small intestine,UBERON:0001206,serosa of small intestine
+UBERON:2000335,crossed tecto-bulbar tract,UBERON:0002164,tectobulbar tract
+HP:0000343,Long philtrum,HP:0000288,Abnormality of the philtrum
+UBERON:0004989,mucosa of appendix,UBERON:0000314,cecum mucosa
+UBERON:0001274,ischium,UBERON:0007830,pelvic girdle bone/zone
+DOID:5043,vulvar granular cell tumor,DOID:0060109,vulvar benign neoplasm
+HP:0010765,Palmar hyperkeratosis,HP:0000962,Hyperkeratosis
+UBERON:0014632,apex of lumbar spinal cord dorsal horn,UBERON:0006983,anatomical point
+UBERON:0006603,presumptive mesoderm,UBERON:0006598,presumptive structure
+HP:0011533,Snowflake retinal degeneration,HP:0007769,Peripheral retinal degeneration
+DOID:11817,urachus cancer,DOID:11054,urinary bladder cancer
+HP:0100420,Partial duplication of the middle phalanx of the 4th toe,HP:0100402,Duplication of the middle phalanx of the 4th toe
+CL:1000285,smooth muscle cell of sigmoid colon,CL:1000280,smooth muscle cell of colon
+UBERON:0011005,endocardium of auricle,UBERON:0002166,endocardium of atrium
+UBERON:2000044,myotome somite 14,UBERON:0003082,myotome
+UBERON:0005631,extraembryonic membrane,UBERON:0000478,extraembryonic structure
+UBERON:0006637,coeliac trunk,UBERON:0000063,organ segment
+NCBITaxon:33993,Neorickettsia,NCBITaxon:942,Anaplasmataceae
+UBERON:0005361,superior glossopharyngeal IX ganglion,UBERON:0001701,glossopharyngeal ganglion
+HP:0001457,Abnormality of the musculature of the upper arm,HP:0001454,Abnormality of the upper arm
+UBERON:0014607,thoracic spinal cord lateral horn,UBERON:0014636,thoracic spinal cord gray matter
+DOID:0060009,MHC class I deficiency,DOID:627,severe combined immunodeficiency
+CL:0002256,supporting cell of carotid body,CL:0000710,neurecto-epithelial cell
+UBERON:3000375,palatine process of the pars facialis of the maxilla,UBERON:0010313,neural crest-derived structure
+UBERON:0009559,metacarpal/tarsal-phalangeal joint,UBERON:0003841,autopod joint
+UBERON:0001609,isthmus of thyroid gland,UBERON:0000064,organ part
+DOID:12271,aniridia,DOID:240,iris disease
+DOID:6034,heart malignant hemangiopericytoma,DOID:5262,heart sarcoma
+HP:0004026,Broad radial metaphysis,HP:0003856,Upper limb metaphyseal widening
+UBERON:0003506,chest blood vessel,UBERON:0003834,thoracic segment blood vessel
+UBERON:0011775,vagus nerve nucleus,UBERON:0000126,cranial nerve nucleus
+UBERON:0005204,larynx submucosa gland,UBERON:0002530,gland
+HP:0005299,Premature peripheral vascular disease,HP:0004950,Peripheral arterial disease
+UBERON:0002596,ventral posterior nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0008987,renal parenchyma,UBERON:0000353,parenchyma
+UBERON:0009599,mesenchyme of interdigital region between digits 4 and 5,UBERON:0009585,interdigital region mesenchyme
+HP:0005281,Hypoplastic nasal bridge,HP:0000422,Abnormality of the nasal bridge
+UBERON:0002254,thyroglossal duct,UBERON:0006590,vestigial embryonic structure
+NCBITaxon:72273,Thiotrichales,NCBITaxon:1236,Gammaproteobacteria
+HP:0012466,Chronic respiratory acidosis,HP:0012468,Chronic acidosis
+DOID:775,intraocular lymphoma,DOID:6903,eye lymphoma
+DOID:7005,gemistocytic astrocytoma,DOID:3069,astrocytoma
+UBERON:0002913,intraparietal sulcus,UBERON:0013118,sulcus of brain
+NCBITaxon:137207,Oligoryzomys longicaudatus,NCBITaxon:29120,Oligoryzomys
+UBERON:0013231,sebaceous gland of eyelid,UBERON:0003484,eye sebaceous gland
+UBERON:2001615,sphenotic spine,UBERON:4100000,skeletal element projection
+UBERON:0003050,olfactory placode,UBERON:0009955,neurogenic placode
+HP:0001118,Juvenile cataract,HP:0000518,Cataract
+UBERON:2000542,medial column,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0003274,Hypoplastic acetabulae,HP:0003170,Abnormality of the acetabulum
+DOID:6021,malignant testicular Leydig cell tumor,DOID:0050616,malignant Leydig cell tumor
+HP:0001686,Loss of voice,HP:0001608,Abnormality of the voice
+UBERON:0001575,extrinsic muscle of tongue,UBERON:0001576,intrinsic muscle of tongue
+HP:0100738,Abnormal eating behavior,HP:0000708,Behavioural/Psychiatric Abnormality
+HP:0005184,Prolonged QTc interval,HP:0001657,Prolonged QT interval
+UBERON:2000313,anal inclinator,UBERON:2005276,inclinator muscle
+HP:0001743,Abnormality of the spleen,HP:0100763,Abnormality of the lymphatic system
+UBERON:0006586,otolymph,UBERON:0007779,transduate
+HP:0009561,Osteolytic defects of the distal phalanx of the 2nd finger,HP:0009839,Osteolytic defects of the distal phalanges of the hand
+UBERON:0013616,primary molar tooth,UBERON:0003655,molar tooth
+HP:0100488,Symphalangism of the proximal phalanx of the hallux with the 1st metatarsal,HP:0100237,Proximal symphalangism (feet)
+UBERON:0006482,Brodmann (1909) area 45,UBERON:0013529,Brodmann area
+UBERON:0006213,carpus cartilage element,UBERON:0010377,mesenchyme from somatopleure
+HP:0010905,Abnormality of histidine metabolism,HP:0010904,Abnormality of histidine family amino acid metabolism
+HP:0005141,Episodes of ventricular tachycardia,HP:0004756,Ventricular tachycardia
+DOID:4307,polyradiculopathy,DOID:4308,polyradiculoneuropathy
+HP:0012612,Abnormal urinary sulfate concentration,HP:0004369,Decreased purine levels
+UBERON:0002808,left temporal lobe,UBERON:0001871,temporal lobe
+DOID:6313,clivus chondroid chordoma,DOID:6312,clivus chordoma
+UBERON:0005956,outflow part of left ventricle,UBERON:0005337,outflow tract of ventricle
+DOID:8223,penile urethral cancer,DOID:736,male urethral cancer
+HP:0004557,Anterior vertebral fusion,HP:0002948,Vertebral fusion
+UBERON:0008344,intestinal villus of ileum,UBERON:0001213,intestinal villus
+UBERON:3000523,pterygoid process of palatoquadrate,UBERON:0004121,ectoderm-derived structure
+DOID:11678,onchocerciasis,DOID:1080,filariasis
+UBERON:3000805,carina proximalis,UBERON:0000064,organ part
+UBERON:0007997,sesamoid bone of manus,UBERON:0005897,manus bone
+HP:0010550,Paraplegia,HP:0010551,Paraplegia/paraparesis
+UBERON:0000128,olivary body,UBERON:0004121,ectoderm-derived structure
+HP:0003963,Lytic defects of the forearm bones,HP:0002973,Abnormality of the forearm
+UBERON:0001633,basilar artery,UBERON:0004573,systemic artery
+DOID:0050928,ovarian melanoma,DOID:2394,ovarian cancer
+CL:1000346,vacuolar absorptive cell of epithelium proper of large intestine,CL:0002071,enterocyte of epithelium of large intestine
+NCBITaxon:943,Ehrlichia,NCBITaxon:942,Anaplasmataceae
+HP:0011558,Double inlet to single ventricle with common atrioventricular orifice,HP:0011557,Double inlet to single ventricle of indeterminate morphology
+HP:0001408,Bile duct proliferation,HP:0012439,Abnormal biliary tract physiology
+HP:0000408,Progressive sensorineural hearing impairment,HP:0000407,Sensorineural hearing impairment
+DOID:4136,myxosarcoma,DOID:201,connective tissue cancer
+DOID:9810,polyarteritis nodosa,DOID:865,vasculitis
+HP:0007451,Ipsilateral lack of facial sweating,HP:0000971,Abnormality of the sweat gland
+HP:0006682,Ventricular extrasystoles,HP:0004308,Ventricular arrhythmia
+UBERON:2005383,dorsal fin proximal radial bone 6,UBERON:2000947,dorsal fin proximal radial bone
+UBERON:0015116,distal tarsal bone 5 pre-cartilage condensation,UBERON:0015114,distal tarsal bone 5 endochondral element
+UBERON:0003442,hindlimb nerve,UBERON:0003440,limb nerve
+CL:1000438,epithelial cell of wall of inferior part of anal canal,CL:0002634,epithelial cell of anal column
+UBERON:0004660,mandible coronoid process,UBERON:4100000,skeletal element projection
+HP:0011401,Delayed peripheral myelination,HP:0003130,Abnormal peripheral myelination
+NCBITaxon:190765,Ochlerotatus <genus>,NCBITaxon:1056966,Aedini
+UBERON:0006773,long bone epiphyseal plate ossification zone,UBERON:0006775,zone of epiphyseal plate
+UBERON:0006938,pinna surface epithelium,UBERON:0015814,outer ear epithelium
+CL:0000648,kidney granular cell,CL:0000192,smooth muscle cell
+UBERON:0002116,ileum,UBERON:0004921,subdivision of digestive tract
+DOID:963,episodic ataxia,DOID:440,neuromuscular disease
+UBERON:0006007,pre-Botzinger complex,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0012473,oral cirrus,UBERON:0000062,organ
+DOID:5341,pineal region yolk sac tumor,DOID:1660,malignant pineal area germ cell neoplasm
+CL:1000296,epithelial cell of urethra,CL:0000066,epithelial cell
+UBERON:0013125,left subcardinal vein,UBERON:0006296,subcardinal vein
+NCBITaxon:58023,Tracheophyta,NCBITaxon:3193,Embryophyta
+HP:0100476,Symphalangism affecting the distal phalanx of the 3rd toe,HP:0100470,Symphalangism affecting the middle phalanx of the 3rd toe
+NCBITaxon:108098,Human adenovirus B,NCBITaxon:10509,Mastadenovirus
+UBERON:3010091,upper lip protuberances,UBERON:3000972,head external integument structure
+HP:0002188,Delayed CNS myelination,HP:0011400,Abnormal CNS myelination
+UBERON:2000936,dorsal fin distal radial bone,UBERON:2100936,dorsal fin distal radial element
+DOID:12935,alcoholic cardiomyopathy,DOID:3978,extrinsic cardiomyopathy
+UBERON:0005062,neural fold,UBERON:0015212,lateral structure
+DOID:0050857,Perrault syndrome,DOID:0050737,autosomal recessive disease
+UBERON:0013711,posterior inferior iliac spine,UBERON:0013713,posterior iliac spine
+DOID:7611,parathyroid oncocytic adenoma,DOID:7608,parathyroid adenoma
+HP:0001397,Hepatic steatosis,HP:0001392,Abnormality of the liver
+HP:0000070,Ureterocele,HP:0000069,Abnormality of the ureter
+UBERON:0001306,cumulus oophorus,UBERON:0014404,female anatomical structure
+DOID:13254,diverticulitis of colon,DOID:5353,colonic disease
+NCBITaxon:27316,Galactomyces,NCBITaxon:34353,Dipodascaceae
+UBERON:0001831,parotid gland,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:7635,gasserian ganglion meningioma,DOID:3565,meningioma
+HP:0100206,Fragmentation of the epiphysis of the distal phalanx of the 5th toe,HP:0100081,Fragmentation of the epiphyses of the 5th toe
+HP:0011304,Broad thumb,HP:0009602,Abnormality of the phalanges of the thumb
+HP:0100144,Stippling of the epiphysis of the distal phalanx of the 3rd toe,HP:0100064,Stippling of the epiphyses of the 3rd toe
+UBERON:0003220,metanephric mesenchyme,UBERON:0003918,kidney mesenchyme
+DOID:3948,adrenocortical carcinoma,DOID:660,adrenal cortex cancer
+HP:0010441,Ectopic accesory finger-like appendage,HP:0001161,Hand polydactyly
+HP:0100164,Pseudoepiphysis of the proximal phalanx of the 3rd toe,HP:0100093,Abnormality of the epiphysis of the proximal phalanx of the 3rd toe
+UBERON:2001522,hypobranchial cartilage,UBERON:2001893,hypobranchial element
+DOID:0050710,3-Methylcrotonyl-CoA carboxylase deficiency,DOID:9252,amino acid metabolic disorder
+CL:1000489,reticular cell of splenic cord,CL:0000432,reticular cell
+DOID:7142,thymus small cell carcinoma,DOID:3284,thymic carcinoma
+UBERON:3000966,angulosplenial,UBERON:0008907,dermal bone
+HP:0002705,"High, narrow palate",HP:0000218,High palate
+HP:0003867,Cortical irregularity (humeral),HP:0010629,Abnormality of the cortex of the humerus
+UBERON:0011938,vibrissa inner root sheath,UBERON:0005941,hair inner root sheath
+HP:0009446,Triangular shaped phalanges of the 3rd finger,HP:0009774,Triangular shaped phalanges of the hand
+CL:0002312,somatotroph,CL:0000638,acidophil cell of pars distalis of adenohypophysis
+CL:1000457,mesothelial cell of visceral peritoneum,CL:1000490,mesothelial cell of peritoneum
+UBERON:0011927,preganglionic sympathetic fiber,UBERON:0011925,preganglionic autonomic fiber
+HP:0010509,Aplasia of the tarsal bones,HP:0008363,Aplasia/Hypoplasia of the tarsal bones
+DOID:2570,malignant histiocytic disease,DOID:3405,histiocytosis
+UBERON:0005022,mucosa of nasopharynx,UBERON:0000355,pharyngeal mucosa
+HP:0010358,Abnormality of the proximal phalanx of the 2nd toe,HP:0010324,Abnormality of phalanx of the 2nd toe
+UBERON:0010418,urethral opening,UBERON:0000161,orifice
+UBERON:0001741,corniculate cartilage,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0008544,splenius cervicis,UBERON:0002252,splenius
+DOID:2451,protein S deficiency,DOID:2452,thrombophilia
+DOID:9722,ophthalmia nodosa,DOID:5614,eye disease
+HP:0009471,Contracture of the proximal interphalangeal joint of the 3rd finger,HP:0009319,Joint contractures of the 3rd finger
+UBERON:0015474,axilla skin,UBERON:0000014,zone of skin
+CL:0000761,type 9 cone bipolar cell (sensu Mus),CL:0000749,ON-bipolar cell
+HP:0011005,Mixed cirrhosis,HP:0001394,Cirrhosis
+UBERON:0015100,distal tarsal cartilage,UBERON:0015064,autopod cartilage
+UBERON:0010379,superior tarsal muscle,UBERON:0003386,smooth muscle of eye
+HP:0007396,Early cutaneous photosensitivity,HP:0000992,Cutaneous photosensitivity
+UBERON:0005405,pararenal fat,UBERON:0001013,adipose tissue
+HP:0010827,Abnormality of the seventh cranial nerve,HP:0001291,Abnormality of the cranial nerves
+NCBITaxon:11619,Junin virus,NCBITaxon:208897,New world arenaviruses
+HP:0009972,Duplication of phalanx of 4th finger,HP:0009997,Duplication of phalanx of hand
+CL:0000108,cholinergic neuron,CL:0000151,secretory cell
+UBERON:0009910,posterior lateral plate mesoderm,UBERON:0000926,mesoderm
+HP:0001475,Male-limited autosomal dominant,HP:0001470,Sex-limited autosomal dominant
+UBERON:3000254,lamella alaris,UBERON:0000064,organ part
+HP:0004195,Osteolytic defects of the phalanges of the 4th finger,HP:0009771,Osteolytic defects of the phalanges of the hand
+UBERON:0013177,dorsal bursa,UBERON:0003566,head connective tissue
+UBERON:0009956,corpuscle of de Quatrefage,UBERON:0000020,sense organ
+DOID:6018,adult central nervous system immature teratoma,DOID:6019,central nervous system immature teratoma
+HP:0002313,Spastic paraparesis,HP:0002061,Lower limb spasticity
+CL:0002117,IgG-negative class switched memory B cell,CL:0000972,class switched memory B cell
+HP:0000757,Lack of insight,HP:0100851,Abnormal emotion/affect behavior
+HP:0011552,Ambiguous atrioventricular connection,HP:0011546,Abnormal atrioventricular connection
+UBERON:0007592,ciliated columnar epithelium,UBERON:0000485,simple columnar epithelium
+UBERON:0010895,sequential hermaphroditic organism,UBERON:0007197,hermaphroditic organism
+UBERON:0003235,epithelium of upper jaw,UBERON:0010371,ecto-epithelium
+UBERON:0003719,Pacinian corpuscle,UBERON:0004120,mesoderm-derived structure
+UBERON:0004797,blood vessel layer,UBERON:0004923,organ component layer
+HP:0010395,Aplasia/Hypoplasia of the proximal phalanx of the 2nd toe,HP:0010325,Aplasia/Hypoplasia of the 2nd toe
+UBERON:0000016,endocrine pancreas,UBERON:0002075,viscus
+HP:0003336,Abnormal enchondral ossification,HP:0011842,Abnormality of skeletal morphology
+UBERON:0001195,inferior pancreaticoduodenal artery,UBERON:0009658,pancreaticoduodenal artery
+HP:0010239,Aplasia of the middle phalanx of the hand,HP:0009802,Aplasia of the phalanges of the hand
+UBERON:0002512,corpus luteum,UBERON:0002368,endocrine gland
+DOID:2668,mesenchymoma,DOID:201,connective tissue cancer
+CL:0002528,mature CD14-positive dermal dendritic cell,CL:0001010,mature dermal dendritic cell
+HP:0007739,Mildly reduced visual acuity,HP:0000505,Visual impairment
+UBERON:0003638,manual digit 4 phalanx,UBERON:0001436,phalanx of manus
+CL:0000406,CNS short range interneuron,CL:0000402,CNS interneuron
+UBERON:2000266,pretecto-mamillary tract,UBERON:0003931,diencephalic white matter
+UBERON:0005496,neural tube lateral wall,UBERON:0004121,ectoderm-derived structure
+NCBITaxon:548681,Herpesvirales,NCBITaxon:35237,"dsDNA viruses, no RNA stage"
+HP:0010071,Osteolytic defects of the 1st metatarsal,HP:0010054,Abnormality of the first metatarsal
+HP:0100427,Broad middle phalanx of the 5th toe,HP:0010384,Broad phalanges of the 5th toe
+HP:0006465,Periosteal thickening of long tubular bones,HP:0011314,Abnormality of long bone morphology
+UBERON:0013279,diaphysis of fibula,UBERON:0004769,diaphysis
+HP:0003278,Square pelvis,HP:0002644,Abnormality of pelvic girdle bone morphology
+UBERON:3010602,granular gland,UBERON:0002530,gland
+UBERON:0007290,presumptive rhombomere 3,UBERON:0006598,presumptive structure
+HP:0009740,Aplasia of the parotid gland,HP:0000197,Abnormality of parotid gland
+HP:0006498,Aplasia/Hypoplasia of the patella,HP:0006493,Aplasia/Hypoplasia involving bones of the lower limbs
+HP:0004589,Dysplasia of second lumbar vertebra,HP:0003468,Abnormality of the vertebrae
+UBERON:0011897,cardiac endomysium,UBERON:0003837,thoracic segment connective tissue
+CL:0002170,keratinized cell of the oral mucosa,CL:0002251,epithelial cell of alimentary canal
+HP:0010091,Symphalangism affecting the proximal phalanx of the hallux,HP:0010064,Symphalangism affecting the phalanges of the hallux
+UBERON:2002085,ural centrum,UBERON:0004376,fin bone
+HP:0006155,Long phalanx of finger,HP:0005918,Abnormality of phalanx of finger
+UBERON:0002195,trabecula of lymph node,UBERON:0000440,trabecula
+HP:0005494,Premature posterior fontanelle closure,HP:0000235,Abnormality of the fontanelles and cranial sutures
+HP:0004558,Cervical platyspondyly,HP:0000926,Platyspondyly
+UBERON:0012471,hepatogastric ligament,UBERON:0003567,abdomen connective tissue
+HP:0011980,Cholesterol gallstones,HP:0001081,Cholelithiasis
+UBERON:0000011,parasympathetic nervous system,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0002101,CD38-positive naive B cell,CL:0000788,naive B cell
+DOID:6762,sternum lymphoma,DOID:5090,sternum cancer
+DOID:397,restrictive cardiomyopathy,DOID:0060036,intrinsic cardiomyopathy
+DOID:5690,atypical lipomatous tumor,DOID:3382,liposarcoma
+HP:0100207,Irregular epiphysis of the distal phalanx of the 5th toe,HP:0100082,Irregular epiphyses of the 5th toe
+HP:0002840,Lymphadenitis,HP:0002733,Abnormality of the lymph nodes
+UBERON:2002063,nuchal plate series,UBERON:0004120,mesoderm-derived structure
+UBERON:2000589,sulcus ypsiloniformis,UBERON:0006846,surface groove
+UBERON:0001052,rectum,UBERON:0004921,subdivision of digestive tract
+UBERON:0000711,splenius capitis,UBERON:0002252,splenius
+UBERON:0006487,hadjikhani et al. (1998) visuotopic area v2d,UBERON:0003022,cerebral cortex lobe
+DOID:7527,acute gonococcal endometritis,DOID:7528,acute endometritis
+HP:0100405,Duplication of the proximal phalanx of the 4th toe,HP:0010211,Duplication of proximal phalanx of toe
+DOID:3199,C-P angle neurinoma,DOID:3192,neurilemmoma
+HP:0100825,Cheilitis,HP:0000159,Abnormality of the lip
+HP:0005942,Desquamative interstitial pneumonitis,HP:0006530,Interstitial pulmonary disease
+HP:0011192,Polymorphic focal epileptiform discharges,HP:0011185,EEG with focal epileptiform discharges
+NCBITaxon:1654,Actinomyces,NCBITaxon:2049,Actinomycetaceae
+HP:0003287,Abnormality of mitochondrial metabolism,HP:0012103,Abnormality of the mitochondrion
+HP:0000372,Abnormality of the auditory canal,HP:0000356,Abnormality of the outer ear
+DOID:0060129,delta chain disease,DOID:0060125,heavy chain disease
+HP:0010023,Small epiphysis of the 1st metacarpal,HP:0009194,Small epiphyses of the metacarpals
+UBERON:0004919,external urethral sphincter,UBERON:0004917,urethral sphincter
+HP:0010294,Palate fistula,HP:0000174,Abnormality of the palate
+HP:0001095,Hypertensive retinopathy,HP:0000479,Abnormality of the retina
+DOID:5538,external ear squamous cell carcinoma,DOID:4288,external ear carcinoma
+UBERON:0004993,mucosa of sigmoid colon,UBERON:0000317,colonic mucosa
+UBERON:0008322,deep artery of clitoris,UBERON:0005156,reproductive structure
+UBERON:2000801,myotome somite 11,UBERON:0003082,myotome
+DOID:14202,adult dermatomyositis,DOID:10223,dermatomyositis
+UBERON:0013476,dermal layer of tongue,UBERON:0004121,ectoderm-derived structure
+HP:0003045,Abnormality of the patella,HP:0002815,Abnormality of the knees
+UBERON:0002761,inferior frontal sulcus,UBERON:0003022,cerebral cortex lobe
+DOID:173,eccrine sweat gland neoplasm,DOID:2664,sweat gland neoplasm
+UBERON:0006930,glandular cuboidal epithelium,UBERON:0000484,simple cuboidal epithelium
+UBERON:0010024,ventral part of pharyngeal pouch 2,UBERON:0000490,unilaminar epithelium
+UBERON:0001643,oculomotor nerve,UBERON:0001785,cranial nerve
+HP:0006290,Discolored lateral incisors,HP:0011063,Abnormality of incisor morphology
+HP:0003130,Abnormal peripheral myelination,HP:0012447,Abnormal myelination
+UBERON:0010854,skin of front of neck,UBERON:0001417,skin of neck
+UBERON:0009961,esophagus smooth muscle longitudinal layer,UBERON:0012369,longitudinal muscle layer
+UBERON:0010580,pedal digit 1 phalanx pre-cartilage condensation,UBERON:0015031,pedal digit 1 phalanx endochondral element
+NCBITaxon:809,Chlamydiaceae,NCBITaxon:51291,Chlamydiales
+DOID:4250,conjunctivochalasis,DOID:4251,conjunctival disease
+UBERON:2001404,preethmoid bone,UBERON:0002513,endochondral bone
+CL:0002249,primitive cardiac myocyte,CL:0002078,meso-epithelial cell
+HP:0004629,Small cervical vertebral bodies,HP:0002773,Small vertebral bodies
+UBERON:0004182,mammary gland cord,UBERON:0003244,epithelium of mammary gland
+HP:0004197,Symphalangism of the 4th finger,HP:0009172,Abnormality of the phalanges of the 4th finger
+HP:0004692,4-5 toe syndactyly,HP:0001770,Toe syndactyly
+HP:0010445,Primum atrial septal defect,HP:0006695,Atrioventricular canal defect
+CL:0002053,"CD22-positive, CD38-low small pre-B cell",CL:0000954,small pre-B-II cell
+HP:0000649,Abnormality of vision evoked potentials,HP:0000504,Abnormality of vision
+HP:0003141,Hyperbetalipoproteinemia,HP:0010980,Hyperlipoproteinemia
+HP:0006243,Phalangeal dislocations,HP:0005918,Abnormality of phalanx of finger
+HP:0010373,Bullet-shaped phalanges of the 4th toe,HP:0010336,Abnormality of the phalanges of the 4th toe
+UBERON:2002159,caudal basal fulcrum,UBERON:2002082,basal fulcrum
+DOID:11282,solar retinopathy,DOID:11086,chorioretinal scar
+UBERON:0011609,ceratohyal element,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0004791,Esophageal ulceration,HP:0002031,Abnormality of the esophagus
+DOID:3689,brachial plexus neuritis,DOID:1803,neuritis
+UBERON:0015142,falciform fat,UBERON:0015143,mesenteric fat pad
+HP:0009094,Cleft lower alveolar ridge,HP:0010289,Alveolar ridge cleft
+CL:1000417,myoepithelial cell of sweat gland,CL:0000185,myoepithelial cell
+HP:0009339,Fragmentation of the epiphysis of the distal phalanx of the 3rd finger,HP:0009332,Abnormality of the epiphysis of the distal phalanx of the 3rd finger
+CL:0002403,mature Vgamma2-positive fetal thymocyte,CL:0002404,fetal thymocyte
+HP:0006262,Aplasia/Hypoplasia of the 5th finger,HP:0004207,Abnormality of the 5th finger
+DOID:9462,cholesteatoma of external ear,DOID:9463,otitis externa
+UBERON:0005432,aortic sac,UBERON:0003498,heart blood vessel
+HP:0004209,Clinodactyly of the 5th finger,HP:0009179,Deviation of the 5th finger
+DOID:525,central nervous system vasculitis,DOID:865,vasculitis
+UBERON:0006300,supracardinal vein,UBERON:0013140,systemic vein
+DOID:1040,chronic lymphocytic leukemia,DOID:1037,lymphoblastic leukemia
+DOID:9087,anal carcinoma in situ,DOID:8719,in situ carcinoma
+UBERON:2001015,myotome somite 17,UBERON:0003082,myotome
+NCBITaxon:1280412,Conoidasida,NCBITaxon:5794,Apicomplexa
+UBERON:0002868,commissural nucleus of vagus nerve,UBERON:0007635,nucleus of medulla oblongata
+UBERON:0004874,somatopleure,UBERON:0005423,developing anatomical structure
+UBERON:2001819,dorsal fin proximal radial bone 2,UBERON:2101819,dorsal fin proximal radial element 2
+CL:0000072,non-branched duct epithelial cell,CL:0000068,duct epithelial cell
+HP:0005403,T lymphocytopenia,HP:0011839,Abnormality of T cell number
+HP:0010571,Elevated levels of phytanic acid,HP:0010965,Abnormality of phytanic acid metabolism
+HP:0002191,Progressive spasticity,HP:0001257,Spasticity
+HP:0009881,Aplasia of the distal phalanges of the hand,HP:0009380,Aplasia of the fingers
+UBERON:0011130,temporomandibular joint primordium,UBERON:0001048,primordium
+HP:0100318,Lafora bodies,HP:0100314,Cerebral inclusion bodies
+UBERON:0002170,upper lobe of right lung,UBERON:0008948,upper lobe of lung
+HP:0200067,Recurrent spontaneous abortion,HP:0005268,Spontaneous abortion
+HP:0001798,Anonychia,HP:0008386,Aplasia/Hypoplasia of the nails
+UBERON:2005409,pars superior ear,UBERON:0000477,anatomical cluster
+CL:0000580,neutrophilic myelocyte,CL:0000776,immature neutrophil
+DOID:9286,priapism,DOID:341,peripheral vascular disease
+HP:0010327,Flexion contracture of the 2nd toe,HP:0010319,Abnormality of the 2nd toe
+UBERON:0009123,otic cup,UBERON:0005423,developing anatomical structure
+UBERON:0011778,motor nucleus of vagal nerve,UBERON:0011775,vagus nerve nucleus
+UBERON:0007632,Barrington's nucleus,UBERON:0002680,regional part of metencephalon
+DOID:7488,posterior urethra cancer,DOID:738,female urethral cancer
+UBERON:0005410,cartilaginous otic capsule,UBERON:0010351,otic capsule cartilage element
+DOID:5711,vulvar liposarcoma,DOID:2096,vulvar sarcoma
+HP:0006575,Intrahepatic cholestasis with episodic jaundice,HP:0001406,Intrahepatic cholestasis
+UBERON:0002273,lateral zone of hypothalamus,UBERON:0000064,organ part
+HP:0008443,Spinal deformities,HP:0000925,Abnormality of the vertebral column
+UBERON:2205374,dorsal fin distal radial cartilage 3,UBERON:2105374,dorsal fin distal radial element 3
+UBERON:0005994,chordae tendineae,UBERON:0005983,heart layer
+UBERON:0006192,mesonephric proximal tubule,UBERON:0005330,mesonephric nephron epithelium
+HP:0100252,Diaphyseal dysplasia,HP:0002652,Skeletal dysplasia
+DOID:5712,cutaneous liposarcoma,DOID:3382,liposarcoma
+HP:0009077,Weakness of long finger extensor muscles,HP:0001421,Abnormality of the musculature of the hand
+HP:0011523,Iris cyst,HP:0000525,Abnormality of the iris
+UBERON:0003677,tooth root,UBERON:0004121,ectoderm-derived structure
+HP:0012286,Abnormal hypothalamus morphology,HP:0002443,Abnormality of the hypothalamus
+HP:0009586,Symphalangism affecting the proximal phalanx of the 2nd finger,HP:0009544,Abnormality of the proximal phalanx of the 2nd finger
+UBERON:0004203,cortical collecting duct,UBERON:0006555,excretory tube
+UBERON:3000651,lamina anterior of maxilla,UBERON:0004120,mesoderm-derived structure
+UBERON:0006081,fundus of gallbladder,UBERON:0000064,organ part
+DOID:0050118,La Crosse encephalitis,DOID:934,viral infectious disease
+HP:0005934,Imperfect vocal cord adduction,HP:0008777,Abnormality of the vocal cords
+HP:0004312,Abnormality of reticulocytes,HP:0001877,Abnormality of erythrocytes
+HP:0006135,Decreased finger mobility,HP:0001155,Abnormality of the hand
+DOID:3098,small cell sarcoma,DOID:201,connective tissue cancer
+UBERON:0005110,metanephric nephron,UBERON:0001285,nephron
+HP:0007626,Mandibular osteomyelitis,HP:0000277,Abnormality of the mandible
+DOID:526,Human immunodeficiency virus infectious disease,DOID:934,viral infectious disease
+UBERON:0001896,medulla oblongata,UBERON:0004121,ectoderm-derived structure
+HP:0005964,Intermittent hypothermia,HP:0002045,Hypothermia
+UBERON:0001550,medial marginal vein,UBERON:0001638,vein
+HP:0006040,Long second metacarpal,HP:0010036,Aplasia/Hypoplasia of the 2nd metacarpal
+HP:0012251,ST segment elevation,HP:0012249,Abnormal ST segment
+UBERON:0002589,lateral corticospinal tract,UBERON:0007702,tract of brain
+HP:0011290,EEG with frontal sharp slow waves,HP:0011195,EEG with focal sharp slow waves
+UBERON:0013587,fused metacarpal bones 3 and 4,UBERON:0013586,fused metapodial bones 3 and 4
+UBERON:2000645,descending octaval nucleus,UBERON:2000401,octaval nerve sensory nucleus
+UBERON:0009556,long pastern bone,UBERON:0014503,proximal phalanx of digit 3
+HP:0011893,Abnormal leukocyte count,HP:0001881,Abnormality of leukocytes
+UBERON:2000178,caudal peduncle,UBERON:0003102,surface structure
+UBERON:0002196,adenohypophysis,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004908,upper digestive tract,UBERON:0004921,subdivision of digestive tract
+HP:0003491,Elevated urine pyrophosphate,HP:0003110,Abnormality of urine homeostasis
+HP:0009184,Contracture of the distal interphalangeal joint of the 5th finger,HP:0009183,Joint contractures of the 5th finger
+UBERON:0013653,velar skeleton,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0100122,Absent epiphysis of the proximal phalanx of the 2nd toe,HP:0100090,Abnormality of the epiphysis of the proximal phalanx of the 2nd toe
+HP:0001473,Metatarsal osteolysis,HP:0001832,Abnormality of the metatarsal bones
+UBERON:0008784,lower limb segment,UBERON:0002529,limb segment
+UBERON:2001578,anterior dorsomedial process of autopalatine,UBERON:0010313,neural crest-derived structure
+CL:0002138,endothelial cell of lymphatic vessel,CL:0002139,endothelial cell of vascular tree
+UBERON:3000653,pars glenoidalis of quadratojugal,UBERON:0004120,mesoderm-derived structure
+UBERON:0010339,1st arch mandibular mesenchyme from head mesenchyme,UBERON:0009584,1st arch mandibular mesenchyme
+HP:0010447,Anal fistula,HP:0100819,Intestinal fistula
+UBERON:0010955,trapezius pre-muscle mass,UBERON:0006904,head mesenchyme from mesoderm
+UBERON:0002307,choroid plexus of lateral ventricle,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2001945,mesethmoid-premaxillary ligament,UBERON:0008846,skeletal ligament
+UBERON:0014712,carapacial ridge ectoderm,UBERON:0005291,embryonic tissue
+UBERON:3000254,lamella alaris,UBERON:0004120,mesoderm-derived structure
+UBERON:0001206,serosa of small intestine,UBERON:0001243,serosa of intestine
+DOID:736,male urethral cancer,DOID:734,urethra cancer
+UBERON:3000041,Bidder's organ,UBERON:0005156,reproductive structure
+DOID:2519,testicular disease,DOID:48,male reproductive system disease
+HP:0011462,Young adult onset,HP:0003581,Adult onset
+CL:0002426,"CD11b-positive, CD27-positive natural killer cell",CL:0002438,NK1.1-positive natural killer cell
+HP:0009433,Osteolytic defects of the middle phalanx of the 3rd finger,HP:0009847,Osteolytic defects of the middle phalanges of the hand
+HP:0003023,Bowing of limbs due to multiple fractures,HP:0002659,Increased susceptibility to fractures
+DOID:7281,uterine corpus adenocarcinofibroma,DOID:4422,malignant adenofibroma
+UBERON:0014667,periventricular nucleus of hypothalamus,UBERON:0006568,hypothalamic nucleus
+HP:0012582,Bilateral renal dysplasia,HP:0000110,Renal dysplasia
+UBERON:0008428,ceratoglossus,UBERON:0002385,muscle tissue
+UBERON:0006210,body-wall mesenchyme,UBERON:0003104,mesenchyme
+UBERON:0013068,palatine torus,UBERON:0004120,mesoderm-derived structure
+HP:0003472,Hypocalcemic tetany,HP:0012638,Abnormality of nervous system physiology
+DOID:3612,retinitis,DOID:5679,retinal disease
+HP:0004049,Decreased carpal angles of wrist,HP:0003019,Abnormality of the wrist
+UBERON:0001872,parietal lobe,UBERON:0003022,cerebral cortex lobe
+HP:0006486,Abnormality of the dental root,HP:0006482,Abnormality of dental morphology
+DOID:2687,skin sarcoma,DOID:4159,skin cancer
+NCBITaxon:34105,Streptobacillus moniliformis,NCBITaxon:34104,Streptobacillus
+DOID:5696,larynx liposarcoma,DOID:2877,larynx sarcoma
+HP:0009264,Enlarged epiphysis of the proximal phalanx of the 4th finger,HP:0009396,Enlarged epiphyses of the 4th finger
+HP:0003917,Pointed humeral metaphysis,HP:0003907,Abnormality of the humeral metaphyses
+HP:0009894,Thickened ears,HP:0000377,Abnormality of the pinna
+UBERON:0008827,forestomach,UBERON:0011954,stomach non-glandular region
+HP:0004800,Duodenal diverticula,HP:0002256,Small bowel diverticula
+HP:0009559,Bullet-shaped distal phalanx of the 2nd finger,HP:0009837,Bullet-shaped distal phalanges of the hand
+HP:0003163,Elevated urinary delta-aminolevulinic acid,HP:0010472,Abnormality of the heme biosynthetic pathway
+HP:0100231,Pseudoepiphysis of the proximal phalanx of the 5th toe,HP:0100084,Pseudoepiphyses of the 5th toe
+DOID:9935,chronic inflammation of lacrimal passage,DOID:1400,lacrimal apparatus disease
+UBERON:0001398,brachial artery,UBERON:0001637,artery
+UBERON:2007032,midbrain neural rod,UBERON:0004121,ectoderm-derived structure
+UBERON:0008917,ampullary organ,UBERON:0010521,electroreceptor organ
+CL:0000834,neutrophil progenitor cell,CL:0002191,granulocytopoietic cell
+UBERON:3010436,blastocoel roof,UBERON:0002050,embryonic structure
+DOID:8167,gallbladder melanoma,DOID:3121,gallbladder cancer
+UBERON:0014380,flexor digitorum brevis muscle,UBERON:0014378,intrinsic muscle of pes
+UBERON:3010346,globe,UBERON:0004121,ectoderm-derived structure
+HP:0003110,Abnormality of urine homeostasis,HP:0001939,Abnormality of metabolism/homeostasis
+HP:0009511,Stippling of the epiphysis of the distal phalanx of the 2nd finger,HP:0009499,Abnormality of the epiphysis of the distal phalanx of the 2nd finger
+UBERON:0006762,suspensory ligament of lens,UBERON:0003566,head connective tissue
+CL:0002606,astrocyte of the spinal cord,CL:0000127,astrocyte
+UBERON:2002257,premaxilla dentigerous process,UBERON:0004120,mesoderm-derived structure
+UBERON:2001560,hypural 1,UBERON:2000364,hypural
+UBERON:0014701,extraembryonic vascular system,UBERON:0007798,vascular system
+DOID:998,eosinophilia-myalgia syndrome,DOID:999,eosinophilia
+HP:0002984,Hypoplasia of the radius,HP:0006501,Aplasia/Hypoplasia of the radius
+UBERON:0002473,intercerebral commissure,UBERON:0005970,brain commissure
+UBERON:3010722,ramus palatinus,UBERON:0001647,facial nerve
+DOID:7040,uveal epithelioid cell melanoma,DOID:6039,uveal melanoma
+DOID:7479,duodenal somatostatinoma,DOID:10021,duodenum cancer
+CL:0000729,tertiary pigment cell,CL:0001658,visual pigment cell (sensu Nematoda and Protostomia)
+HP:0009893,Telangiectasia of the ear,HP:0100585,Teleangiectasia of the skin
+HP:0100924,Sclerosis of the phalanges of the toes,HP:0100925,Sclerosis of bones of the feet
+HP:0100928,Sclerosis of the phalanges of the 4th toe,HP:0100924,Sclerosis of the phalanges of the toes
+HP:0010773,Partial anomalous pulmonary venous return,HP:0010772,Anomalous pulmonary venous return
+HP:0010447,Anal fistula,HP:0004378,Abnormality of the anus
+DOID:3703,prostate colloid adenocarcinoma,DOID:2526,prostate adenocarcinoma
+DOID:13473,central pterygium,DOID:13474,progressive peripheral pterygium
+NCBITaxon:689831,Spinareovirinae,NCBITaxon:10880,Reoviridae
+UBERON:0005431,anterior spinal artery,UBERON:0002458,spinal artery
+HP:0003648,Lacticaciduria,HP:0003355,Aminoaciduria
+UBERON:0004041,spleen primary B follicle,UBERON:0001249,spleen lymphoid follicle
+UBERON:0011575,styloid process of ulna,UBERON:4100000,skeletal element projection
+HP:0001245,Small thenar eminence,HP:0001227,Abnormality of the thenar eminence
+HP:0100945,Sclerosis of the 1st metatarsal,HP:0100930,Sclerosis of the phalanges of the hallux
+DOID:12166,cobblestone retinal degeneration,DOID:12161,peripheral retinal degeneration
+UBERON:0002478,orbitosphenoid,UBERON:0015059,orbitosphenoid endochondral element
+UBERON:2002123,neural arch 5,UBERON:0003861,neural arch
+UBERON:0004206,long descending thin limb bend,UBERON:0006554,urinary system structure
+UBERON:0002678,regional part of medulla oblongata,UBERON:0002616,regional part of brain
+UBERON:0000947,aorta,UBERON:0013768,great vessel of heart
+UBERON:0011900,perimysium,UBERON:0004120,mesoderm-derived structure
+UBERON:0006431,xiphoid process bone,UBERON:0003837,thoracic segment connective tissue
+HP:0009191,Ivory epiphyses of the metacarpals,HP:0005913,Abnormality of metacarpal epiphyses
+UBERON:0009142,entire embryonic mesenchyme,UBERON:0002050,embryonic structure
+UBERON:0002030,nipple,UBERON:0000475,organism subdivision
+HP:0003863,Angulated humerus,HP:0003063,Abnormality of the humerus
+UBERON:0002731,vestibulocochlear nerve root,UBERON:0004121,ectoderm-derived structure
+UBERON:3000561,septum semicircularium laterale,UBERON:0004121,ectoderm-derived structure
+UBERON:0009754,blubber,UBERON:0002190,subcutaneous adipose tissue
+CL:0001040,non-terminally differentiated osteoblast,CL:0001035,bone cell
+HP:0008586,Hypoplasia of the cochlea,HP:0011395,Aplasia/Hypoplasia of the cochlea
+HP:0001226,Acral ulceration and osteomyelitis leading to autoamputation of digits,HP:0200042,Skin ulcer
+UBERON:3000017,anterior process of pars palatina of maxilla,UBERON:0004530,bony projection
+DOID:6787,childhood vagina botryoid rhabdomyosarcoma,DOID:6788,vagina botryoid rhabdomyosarcoma
+HP:0003334,Elevated circulating catecholamine level,HP:0012099,Abnormality of circulating catecholamine level
+UBERON:0010532,primitive nephron,UBERON:0006555,excretory tube
+UBERON:0001275,pubis,UBERON:0007830,pelvic girdle bone/zone
+HP:0002310,Orofacial dyskinesia,HP:0100660,Dyskinesia
+UBERON:0001911,mammary gland,UBERON:0004121,ectoderm-derived structure
+UBERON:0009522,lateral lingual swelling epithelium,UBERON:0010371,ecto-epithelium
+UBERON:0013156,1st arch mandibular endoderm,UBERON:0005911,endo-epithelium
+UBERON:0002364,tympanic membrane,UBERON:0000094,membrane organ
+HP:0007583,Telangiectasia macularis eruptiva perstans,HP:0001009,Telangiectasia
+UBERON:0012467,enclosed anatomical space,UBERON:0000464,anatomical space
+UBERON:0014645,nucleus H,UBERON:0002438,ventral tegmental nucleus
+UBERON:0004059,spinal cord medial motor column,UBERON:0003990,spinal cord motor column
+UBERON:0001789,outer nuclear layer of retina,UBERON:0003902,retinal neural layer
+DOID:7577,pancreatic foamy gland adenocarcinoma,DOID:4074,pancreas adenocarcinoma
+UBERON:2001577,premaxilla ascending process,UBERON:0010313,neural crest-derived structure
+HP:0005316,Peripheral pulmonary vessel aplasia,HP:0004930,Abnormality of the pulmonary vasculature
+HP:0000864,Abnormality of the hypothalamus-pituitary axis,HP:0000818,Abnormality of the endocrine system
+UBERON:0010348,hyoid pre-muscle mass,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0007535,Hypopigmented streaks,HP:0001010,Hypopigmentation of the skin
+UBERON:0000483,epithelium,UBERON:0000119,cell layer
+HP:0001298,Encephalopathy,HP:0002011,Abnormality of the central nervous system
+UBERON:0002247,uterine horn,UBERON:0015212,lateral structure
+HP:0011353,Arterial intimal fibrosis,HP:0011004,Abnormality of the systemic arterial tree
+HP:0009641,Aplasia/Hypoplasia of the distal phalanx of the thumb,HP:0009617,Abnormality of the distal phalanx of the thumb
+UBERON:0000949,endocrine system,UBERON:0000467,anatomical system
+HP:0000125,Pelvic kidney,HP:0000086,Ectopic kidney
+UBERON:0013189,junk chamber,UBERON:0000062,organ
+CL:0002666,type 2 otic fibrocyte,CL:0002665,otic fibrocyte
+UBERON:0001987,placenta,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0006961,Jerky head movements,HP:0002457,Abnormal head movements
+UBERON:0012333,ovarian bursa,UBERON:0000064,organ part
+HP:0011294,EEG with frontal sharp waves,HP:0011196,EEG with focal sharp waves
+HP:0001510,Growth delay,HP:0001507,Growth abnormality
+HP:0009060,Scapular muscle atrophy,HP:0001465,Amyotrophy involving the shoulder musculature
+UBERON:0012427,intestinal brush border,UBERON:0012424,brush border layer
+CL:0002336,buccal mucosa cell,CL:0002261,endothelial cell of viscerocranial mucosa
+UBERON:4200087,iliac peduncle,UBERON:0004530,bony projection
+UBERON:0012294,navicular fossa of spongiose part of urethra,UBERON:0000063,organ segment
+UBERON:0013247,male paramesonephric duct,UBERON:0014403,male anatomical structure
+UBERON:0001871,temporal lobe,UBERON:0000064,organ part
+UBERON:0014889,left hemisphere of cerebellum,UBERON:0002245,cerebellar hemisphere
+UBERON:4300106,ventral limb of posttemporal,UBERON:0004120,mesoderm-derived structure
+UBERON:0008998,cerebrovascular system,UBERON:0000467,anatomical system
+HP:0007024,Pseudobulbar paralysis,HP:0002015,Dysphagia
+DOID:8118,mature gastric teratoma,DOID:5561,gastric teratoma
+UBERON:0009497,epithelium of foregut-midgut junction,UBERON:0000490,unilaminar epithelium
+HP:0009883,Duplication of the distal phalanx of hand,HP:0009997,Duplication of phalanx of hand
+UBERON:0003254,amniotic ectoderm,UBERON:0005292,extraembryonic tissue
+UBERON:0012292,embryonic cloacal fold,UBERON:0002050,embryonic structure
+UBERON:0002778,ventral pallidum,UBERON:0006514,pallidum
+HP:0100306,Muscle fiber hyaline bodies,HP:0100303,Muscle fiber cytoplasmatic inclusion bodies
+UBERON:0012470,wheel papilla,UBERON:0000061,anatomical structure
+NCBITaxon:11020,Barmah Forest virus,NCBITaxon:11019,Alphavirus
+HP:0001212,Prominent fingertip pads,HP:0001211,Abnormality of the fingertips
+CL:0000411,flatworm hypodermal cell,CL:0002371,somatic cell
+DOID:710,splenic manifestation of leukemia,DOID:672,spleen cancer
+CL:0000761,type 9 cone bipolar cell (sensu Mus),CL:0000752,cone retinal bipolar cell
+DOID:0060102,cartilage cancer,DOID:201,connective tissue cancer
+HP:0005411,Chronic intestinal candidiasis,HP:0002728,Chronic mucocutaneous candidiasis
+UBERON:0000408,vertebral ganglion,UBERON:0001806,sympathetic ganglion
+HP:0100310,Epidural hemorrhage,HP:0002170,Intracranial hemorrhage
+NCBITaxon:10519,Human adenovirus 7,NCBITaxon:565302,Human adenovirus B1
+DOID:10997,immature cataract,DOID:9669,senile cataract
+CL:0002027,"CD9-positive, CD41-positive megakaryocyte cell",CL:0000556,megakaryocyte
+HP:0001167,Abnormality of finger,HP:0011297,Abnormality of the digits
+DOID:2346,monoclonal paraproteinemia,DOID:2345,plasma protein metabolism disease
+UBERON:0003582,nasopharynx connective tissue,UBERON:0004119,endoderm-derived structure
+UBERON:0010351,otic capsule cartilage element,UBERON:0003932,cartilage element of chondrocranium
+DOID:13738,infarct of liver,DOID:272,hepatic vascular disease
+UBERON:4200078,clavicular facet,UBERON:0005913,zone of bone organ
+DOID:2683,adenofibroma,DOID:0060084,cell type benign neoplasm
+DOID:12010,anterior ischemic optic neuropathy,DOID:1891,optic nerve disease
+DOID:12276,malignant tumor of undescended testis,DOID:2998,testicular cancer
+CL:1000282,smooth muscle fiber of ascending colon,CL:1000280,smooth muscle cell of colon
+DOID:12003,trachea squamous cell carcinoma,DOID:4876,trachea carcinoma
+CL:0000121,Purkinje cell,CL:0000527,efferent neuron
+UBERON:2001635,pharyngobranchial 1 bone,UBERON:2000527,pharyngobranchial bone
+HP:0000786,Primary amenorrhea,HP:0000141,Amenorrhea
+HP:0009357,Abnormality of the distal phalanx of the 3rd finger,HP:0009316,Abnormality of the phalanges of the 3rd finger
+HP:0009782,Aplasia/Hypoplasia of the biceps,HP:0001468,Aplasia/Hypoplasia involving the musculature of the upper arm
+UBERON:0002597,principal sensory nucleus of trigeminal nerve,UBERON:0009662,hindbrain nucleus
+NCBITaxon:12506,Dobrava-Belgrade virus,NCBITaxon:11598,Hantavirus
+CL:0002425,early T lineage precursor,CL:0000827,pro-T cell
+DOID:117,heart cancer,DOID:176,cardiovascular cancer
+UBERON:2002249,ctenius,UBERON:0004120,mesoderm-derived structure
+UBERON:0014683,parasymphisial tooth whorl,UBERON:0014682,tooth whorl
+DOID:11574,streptococcal meningitis,DOID:9470,bacterial meningitis
+HP:0200005,Abnormal shape of the palpebral fissure,HP:0008050,Abnormality of the palpebral fissures
+DOID:12365,malaria,DOID:2789,parasitic protozoa infectious disease
+HP:0011418,Abnormal insertion of umbilical cord,HP:0010881,Abnormality of the umbilical cord
+HP:0009773,Symphalangism affecting the phalanges of the hand,HP:0005918,Abnormality of phalanx of finger
+UBERON:2000241,midline column,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001343,seminiferous tubule of testis,UBERON:0005904,duct of male reproductive system
+UBERON:0014599,paraventricular nucleus of the hypothalamus magnocellular division - anterior magnocellular part,UBERON:0003048,regional part of hypothalamus
+DOID:0050740,Qazi Markouizos syndrome,DOID:225,syndrome
+HP:0005280,Depressed nasal bridge,HP:0000422,Abnormality of the nasal bridge
+CL:0000895,"naive thymus-derived CD4-positive, alpha-beta T cell",CL:0000898,naive T cell
+HP:0100742,Vascular neoplasm,HP:0002597,Abnormality of the vasculature
+HP:0010410,Symphalangism affecting the middle phalanx of the 2nd toe,HP:0010353,Symphalangism affecting the phalanges of the 2nd toe
+HP:0010414,Broad distal phalanx of the 2nd toe,HP:0010356,Abnormality of the distal phalanx of the 2nd toe
+UBERON:0002912,marginal sulcus,UBERON:0013118,sulcus of brain
+HP:0000284,Abnormality of the ocular region,HP:0000271,Abnormality of the face
+HP:0003108,Hyperglycinuria,HP:0003355,Aminoaciduria
+UBERON:0004505,skeletal muscle tissue of orbicularis oculi,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0000019,Urinary hesitancy,HP:0000009,Functional abnormality of the bladder
+UBERON:0004509,skeletal muscle tissue of trapezius,UBERON:0010313,neural crest-derived structure
+NCBITaxon:523089,Haemaphysalis concinna,NCBITaxon:34622,Haemaphysalis
+DOID:11818,ureteric orifice cancer,DOID:11054,urinary bladder cancer
+DOID:2236,congenital afibrinogenemia,DOID:2214,inherited blood coagulation disease
+UBERON:0010040,stomach non-glandular epithelium,UBERON:0001276,epithelium of stomach
+HP:0009592,Astrocytoma,HP:0100707,Abnormality of the astrocytes
+HP:0007948,Dense posterior cortical cataract,HP:0010924,Posterior cortical cataract
+CL:0002193,myelocyte,CL:0002191,granulocytopoietic cell
+UBERON:0005880,prepollex,UBERON:0005881,limb outgrowth
+HP:0011301,Absent foot,HP:0006494,Aplasia/Hypoplasia involving bones of the feet
+UBERON:0001212,duodenal gland,UBERON:0003408,gland of gut
+UBERON:0002604,ventral nucleus of lateral lemniscus,UBERON:0002680,regional part of metencephalon
+UBERON:2000285,superficial adductor,UBERON:0014794,pectoral appendage muscle
+UBERON:0006004,hair follicle matrix region,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3000374,palatine process of pars palatina of premaxilla,UBERON:0010313,neural crest-derived structure
+HP:0100191,Absent epiphysis of the proximal phalanx of the 4th toe,HP:0100066,Absent epiphyses of the 4th toe
+DOID:4072,duodenal disease,DOID:5295,intestinal disease
+DOID:10652,Alzheimer's disease,DOID:680,tauopathy
+HP:0005832,Dysharmonic delayed bone age,HP:0200000,Dysharmonic bone age
+DOID:4626,hydranencephaly,DOID:2490,congenital nervous system abnormality
+UBERON:0002317,white matter of cerebellum,UBERON:0002316,white matter
+HP:0009320,Abnormality of the epiphyses of the 3rd finger,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+HP:0005234,Neonatal intestinal obstruction,HP:0004796,Gastrointestinal obstruction
+UBERON:2000620,autopalatine,UBERON:0011597,bone of upper jaw
+HP:0009612,Duplication of the distal phalanx of the thumb,HP:0009617,Abnormality of the distal phalanx of the thumb
+DOID:11401,xanthogranulomatous pyelonephritis,DOID:1076,chronic pyelonephritis
+UBERON:0008343,intestinal villus of jejunum,UBERON:0001213,intestinal villus
+HP:0001945,Fever,HP:0004370,Abnormality of temperature regulation
+DOID:6629,nipple carcinoma,DOID:3459,breast carcinoma
+DOID:14418,dracunculiasis,DOID:883,parasitic helminthiasis infectious disease
+UBERON:0003352,epithelium of midgut,UBERON:0003929,gut epithelium
+UBERON:0001765,mammary duct,UBERON:0000058,duct
+HP:0007687,Unilateral ptosis,HP:0000508,Ptosis
+UBERON:0014716,interlobular duct,UBERON:0000058,duct
+UBERON:0004681,vestibular system,UBERON:0001032,sensory system
+HP:0001112,Leber optic atrophy,HP:0000587,Abnormality of the optic nerve
+UBERON:2007001,dorso-rostral cluster,UBERON:0000479,tissue
+HP:0001234,Hitchhiker thumb,HP:0001172,Abnormality of the thumb
+UBERON:0006243,glossopharyngeal IX preganglion,UBERON:0005423,developing anatomical structure
+CL:0000816,immature B cell,CL:0000817,precursor B cell
+UBERON:0004506,skeletal muscle tissue of masseter,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0200003,Splayed epiphyses,HP:0005930,Abnormality of the epiphyses
+UBERON:2001529,epibranchial 3 cartilage,UBERON:2001907,epibranchial 3 element
+HP:0100487,Triangular shaped distal phalanx of the 5th toe,HP:0010390,Triangular shaped phalanges of the 5th toe
+UBERON:3000921,element Y of hind mesopodium,UBERON:0015050,tarsus endochondral element
+NCBITaxon:11102,Hepacivirus,NCBITaxon:11050,Flaviviridae
+UBERON:0006699,foramen cecum of tongue,UBERON:0004121,ectoderm-derived structure
+HP:0002505,Progressive inability to walk,HP:0002540,Inability to walk
+UBERON:0008856,stomach muscularis externa,UBERON:0006660,muscle layer
+DOID:11527,laryngostenosis,DOID:786,laryngeal disease
+HP:0008261,Pancreatic islet cell adenoma,HP:0100568,Neoplasm of the endocrine system
+UBERON:4000097,orthodentine,UBERON:0010365,odontoid tissue
+DOID:9268,glycine encephalopathy,DOID:9252,amino acid metabolic disorder
+CL:0001044,"effector CD4-positive, alpha-beta T cell",CL:0000624,"CD4-positive, alpha-beta T cell"
+HP:0009317,Deviation of the 3rd finger,HP:0004097,Deviation of finger
+UBERON:0007615,prostate gland ventral lobe,UBERON:0001328,lobe of prostate
+HP:0000527,Long eyelashes,HP:0000499,Abnormality of the eyelashes
+UBERON:0002003,peripheral nerve,UBERON:0001021,nerve
+DOID:2762,bone carcinoma,DOID:184,bone cancer
+UBERON:0010962,extensor pre-muscle mass,UBERON:0005865,pre-muscle condensation
+CL:1001588,colon glandular cell,CL:0002658,glandular cell of the large intestine
+HP:0009529,Irregular epiphysis of the proximal phalanx of the 2nd finger,HP:0010273,Irregular epiphyses of the proximal phalanges of the hand
+HP:0010325,Aplasia/Hypoplasia of the 2nd toe,HP:0010760,Absent toe
+UBERON:0012456,Merkel nerve ending,UBERON:0010313,neural crest-derived structure
+HP:0001677,Coronary artery disease,HP:0006704,Abnormality of the coronary arteries
+DOID:9275,tyrosinemia,DOID:9252,amino acid metabolic disorder
+UBERON:0000948,heart,UBERON:0007100,primary circulatory organ
+UBERON:0005117,metanephric distal convoluted tubule,UBERON:0005129,metanephric distal tubule
+UBERON:2000058,polster,UBERON:0002050,embryonic structure
+UBERON:0000161,orifice,UBERON:0004111,anatomical conduit
+HP:0011113,Abnormality of cytokine secretion,HP:0011111,Abnormality of immune serum protein physiology
+UBERON:2000820,presumptive neuron neural tube,UBERON:0004121,ectoderm-derived structure
+HP:0009336,Bracket epiphysis of the distal phalanx of the 3rd finger,HP:0009332,Abnormality of the epiphysis of the distal phalanx of the 3rd finger
+UBERON:2005384,dorsal fin proximal radial bone 7,UBERON:2000947,dorsal fin proximal radial bone
+HP:0012203,Onychomycosis,HP:0002841,Recurrent fungal infections
+HP:0008001,Foveal hyperpigmentation,HP:0000493,Abnormality of the fovea
+HP:0009525,Bracket epiphysis of the proximal phalanx of the 2nd finger,HP:0009489,Bracket epiphyses of the 2nd finger
+UBERON:0001411,basilic vein,UBERON:0003507,arm blood vessel
+UBERON:4000109,mineralized hyaline cartilage tissue,UBERON:0001994,hyaline cartilage tissue
+HP:0010480,Urethral fistula,HP:0000795,Abnormality of the urethra
+DOID:6082,pediatric testicular germ cell tumor,DOID:5557,testicular germ cell cancer
+HP:0011815,Cephalocele,HP:0000929,Abnormality of the skull
+DOID:9714,occlusion of gallbladder,DOID:0000000,gallbladder disease
+UBERON:0002115,jejunum,UBERON:0004921,subdivision of digestive tract
+UBERON:0001772,corneal epithelium,UBERON:0015808,eye epithelium
+HP:0009888,Abnormality of secondary sexual hair,HP:0001595,Abnormality of the hair
+UBERON:0006483,Brodmann (1909) area 46,UBERON:0013529,Brodmann area
+HP:0009561,Osteolytic defects of the distal phalanx of the 2nd finger,HP:0009550,Osteolytic defects of the phalanges of the 2nd finger
+UBERON:0004980,mucosa of ureter,UBERON:0004120,mesoderm-derived structure
+HP:0007351,Upper limb postural tremor,HP:0200085,Limb tremor
+NCBITaxon:4892,Saccharomycetales,NCBITaxon:4891,Saccharomycetes
+HP:0010928,Abnormality of orotic acid metabolism,HP:0004353,Abnormality of pyrimidine metabolism
+HP:0007068,Inferior vermis hypoplasia,HP:0001320,Cerebellar vermis hypoplasia
+UBERON:3010559,retroarticular process of the palatoquadrate,UBERON:4100000,skeletal element projection
+UBERON:0007291,presumptive rhombomere 4,UBERON:0006598,presumptive structure
+CL:0000197,receptor cell,CL:0000003,native cell
+UBERON:0001908,optic tract,UBERON:0011591,tract of diencephalon
+UBERON:3000806,carina medialis,UBERON:0000064,organ part
+HP:0002948,Vertebral fusion,HP:0100240,Synostosis of joints
+HP:0010369,Abnormality of the middle phalanx of the 3rd toe,HP:0010330,Abnormality of the phalanges of the 3rd toe
+HP:0008596,Postlingual sensorineural hearing impairment,HP:0011474,Childhood onset sensorineural hearing impairment
+DOID:7610,mixed cell type adenoma of parathyroid,DOID:7608,parathyroid adenoma
+HP:0010886,Osteochondrosis dissecans,HP:0001367,Abnormal joint morphology
+HP:0001671,Abnormality of the cardiac septa,HP:0002564,Malformation of the heart and great vessels
+HP:0000228,Oral cavity teleangiectasia,HP:0100579,Mucosal telangiectasiae
+UBERON:0011387,constrictor vulvae muscle,UBERON:0011389,bulbospongiosus muscle
+DOID:7634,suprasellar meningioma,DOID:3565,meningioma
+CL:0000209,taste receptor cell,CL:0002076,endo-epithelial cell
+UBERON:0014540,lamina of cerebellum,UBERON:0014530,lamina of neuraxis
+HP:0100189,Stippling of the epiphysis of the middle phalanx of the 4th toe,HP:0100075,Stippling of the epiphyses of the 4th toe
+HP:0011526,Abnormality of lens shape,HP:0000517,Abnormality of the lens
+UBERON:0013207,entepicondylar foramen,UBERON:0005744,bone foramen
+HP:0009468,Deviation of the 2nd finger,HP:0004100,Abnormality of the 2nd finger
+HP:0100165,Small epiphysis of the proximal phalanx of the 3rd toe,HP:0100093,Abnormality of the epiphysis of the proximal phalanx of the 3rd toe
+HP:0100169,Absent epiphysis of the distal phalanx of the 4th toe,HP:0100094,Abnormality of the epiphysis of the distal phalanx of the 4th toe
+DOID:4441,dysgerminoma,DOID:2994,germ cell cancer
+DOID:7503,extrahepatic bile duct papillary adenoma,DOID:5438,extrahepatic bile duct adenoma
+UBERON:0008242,lower back muscle,UBERON:0003833,abdominal segment muscle
+UBERON:1500003,lateral line canal lumen,UBERON:0000464,anatomical space
+HP:0003868,Cortical thickening (humeral),HP:0010629,Abnormality of the cortex of the humerus
+HP:0005366,Recurrent streptococcus pneumoniae infections,HP:0002205,Recurrent respiratory infections
+HP:0002352,Leukoencephalopathy,HP:0002060,Abnormality of the cerebrum
+UBERON:0009855,echinoderm gastric caecum,UBERON:0009854,digestive tract diverticulum
+UBERON:0012078,fovea capitis of femur,UBERON:0005055,zone of long bone
+DOID:9672,noma,DOID:9673,ulcerative stomatitis
+HP:0006999,Basal ganglia gliosis,HP:0002134,Abnormality of the basal ganglia
+UBERON:0015757,heterogeneous tissue,UBERON:0000479,tissue
+HP:0012282,Morbilliform rash,HP:0000988,Skin rash
+HP:0010357,Abnormality of the middle phalanx of the 2nd toe,HP:0010324,Abnormality of phalanx of the 2nd toe
+UBERON:0004834,hepatic duct smooth muscle,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0004291,heart rudiment,UBERON:0012275,meso-epithelium
+UBERON:0007841,furcula,UBERON:0008907,dermal bone
+HP:0100100,Absent epiphysis of the distal phalanx of the 2nd toe,HP:0100044,Absent epiphyses of the 2nd toe
+UBERON:0015863,gastric lymph node,UBERON:0015860,visceral abdominal lymph node
+HP:0009470,Contracture of the metacarpophalangeal joint of the 3rd finger,HP:0009319,Joint contractures of the 3rd finger
+CL:0000214,synovial cell,CL:0002078,meso-epithelial cell
+HP:0009658,Aplasia/Hypoplasia of the phalanges of the thumb,HP:0009767,Aplasia/Hypoplasia of the phalanges of the hand
+UBERON:2000485,central nucleus inferior lobe,UBERON:0006568,hypothalamic nucleus
+UBERON:0010728,sphenoid lesser wing pre-cartilage condensation,UBERON:0009891,facial mesenchyme
+HP:0001561,Polyhydramnios,HP:0001560,Abnormality of the amniotic fluid
+HP:0009850,Triangular shaped middle phalanges of the hand,HP:0009774,Triangular shaped phalanges of the hand
+HP:0000034,Hydrocele testis,HP:0000035,Abnormality of the testis
+NCBITaxon:12939,Anemia,NCBITaxon:693766,Anemiaceae
+HP:0001717,Coronary artery calcification,HP:0003207,Arterial calcification
+UBERON:0005196,spleen germinal center,UBERON:0010754,germinal center
+CL:0002078,meso-epithelial cell,CL:0000066,epithelial cell
+UBERON:0005402,philtrum,UBERON:0004121,ectoderm-derived structure
+DOID:2229,factor XI deficiency,DOID:0050739,autosomal genetic disease
+HP:0012126,Stomach cancer,HP:0006753,Neoplasm of the stomach
+UBERON:2002114,cotylephore,UBERON:0005156,reproductive structure
+HP:0001394,Cirrhosis,HP:0001392,Abnormality of the liver
+UBERON:0009973,ureterovesical junction,UBERON:0003978,valve
+UBERON:0001823,nasal cartilage,UBERON:0003570,respiratory system connective tissue
+UBERON:0003236,epithelium of lower jaw,UBERON:0010371,ecto-epithelium
+UBERON:0002953,lateral lemniscus,UBERON:0003001,lemniscus
+HP:0009519,Ivory epiphysis of the middle phalanx of the 2nd finger,HP:0010263,Ivory epiphyses of the middle phalanges of the hand
+UBERON:0000017,exocrine pancreas,UBERON:0002075,viscus
+DOID:0050185,erythema multiforme,DOID:37,skin disease
+HP:0010252,Ivory epiphyses of the distal phalanges of the hand,HP:0010234,Ivory epiphyses of the phalanges of the hand
+HP:0100205,Enlarged epiphysis of the distal phalanx of the 5th toe,HP:0100080,Enlarged epiphyses of the 5th toe
+UBERON:0003637,manual digit 3 phalanx,UBERON:0001436,phalanx of manus
+CL:0000550,polychromatophilic erythroblast,CL:0000765,erythroblast
+UBERON:0001865,cartilaginous external acoustic tube,UBERON:0004121,ectoderm-derived structure
+UBERON:0005415,zone of polarizing activity of pectoral appendage,UBERON:0005414,zone of polarizing activity
+UBERON:0001951,epithelium of nasopharynx,UBERON:0000485,simple columnar epithelium
+UBERON:3000329,oblique cartilage,UBERON:0003933,cranial cartilage
+HP:0100037,Abnormality of the scalp hair,HP:0001965,Abnormality of the scalp
+HP:0011006,Abnormality of the musculature of the neck,HP:0000464,Abnormality of the neck
+HP:0010070,Curved 1st metatarsal,HP:0010054,Abnormality of the first metatarsal
+HP:0010088,Curved proximal phalanx of the hallux,HP:0010052,Abnormality of the proximal phalanx of the hallux
+HP:0008076,Osteoporotic tarsals,HP:0009132,Abnormal tarsal bone mineral density
+UBERON:0001745,secondary nodular lymphoid tissue,UBERON:0000444,lymphoid follicle
+HP:0000619,Impaired convergence,HP:0000549,Abnormal conjugate eye movement
+UBERON:3010096,vocal sac,UBERON:3000972,head external integument structure
+HP:0000678,Dental crowding,HP:0000692,Misalignment of teeth
+UBERON:0013600,lateral accessory nucleus of optic tract,UBERON:0013598,accessory nucleus of optic tract
+UBERON:2005144,ampullary nerve,UBERON:0004121,ectoderm-derived structure
+CL:0000310,iron accumulating cell,CL:0000308,metal ion accumulating cell
+HP:0009438,Absent middle phalanx of 3rd finger,HP:0010239,Aplasia of the middle phalanx of the hand
+DOID:6112,cerebral meningioma,DOID:368,cerebrum cancer
+HP:0001664,Torsade de pointes,HP:0004308,Ventricular arrhythmia
+UBERON:3000255,lamina anterior of pars facialis,UBERON:0000064,organ part
+UBERON:2000830,sclerotome somite 14,UBERON:0003089,sclerotome
+UBERON:2205376,dorsal fin distal radial cartilage 5,UBERON:2105376,dorsal fin distal radial element 5
+UBERON:2000389,medial funicular nucleus medulla oblongata,UBERON:0007635,nucleus of medulla oblongata
+UBERON:0001135,smooth muscle tissue,UBERON:0002385,muscle tissue
+HP:0008191,Thyroid agenesis,HP:0008188,Thyroid dysgenesis
+DOID:3410,carotid artery thrombosis,DOID:3407,carotid artery disease
+DOID:5077,subependymal giant cell astrocytoma,DOID:4843,subependymal glioma
+HP:0009644,Curved distal phalanx of the thumb,HP:0009653,Curved phalanges of the thumb
+UBERON:0008716,hilum of kidney,UBERON:0004885,hilum
+NCBITaxon:431037,unclassified Roseolovirus,NCBITaxon:40272,Roseolovirus
+UBERON:0009920,optic neural crest,UBERON:0007213,mesenchyme derived from head neural crest
+DOID:3325,hyperglobulinemic purpura,DOID:3326,purpura
+UBERON:0002665,supracallosal gyrus,UBERON:0000200,gyrus
+UBERON:0005445,segment of pes,UBERON:0008784,lower limb segment
+HP:0009518,Irregular epiphysis of the middle phalanx of the 2nd finger,HP:0009493,Irregular epiphyses of the 2nd finger
+UBERON:3010698,m. serratus medius,UBERON:0010891,pectoral complex muscle
+HP:0007840,Long upper eyelashes,HP:0000527,Long eyelashes
+DOID:14534,malignant cardiac peripheral nerve sheath neoplasm,DOID:5940,malignant peripheral nerve sheath tumor
+HP:0004255,Small trapezium,HP:0004252,Abnormality of the trapezium
+UBERON:0007717,sacral subsegment of spinal cord,UBERON:0005844,spinal cord segment
+HP:0005247,Hypoplasia of the abdominal wall musculature,HP:0010318,Aplasia/Hypoplasia of the abdominal wall musculature
+UBERON:0005497,non-neural ectoderm,UBERON:0004121,ectoderm-derived structure
+DOID:3116,kidney benign neoplasm,DOID:731,urinary system benign neoplasm
+DOID:5614,eye disease,DOID:1492,eye and adnexa disease
+HP:0005524,Macrocytic hemolytic disease,HP:0001878,Hemolytic anemia
+UBERON:0004514,skeletal muscle tissue of transversus thoracis,UBERON:0003898,skeletal muscle tissue of trunk
+HP:0012042,Aspirin-induced asthma,HP:0002099,Asthma
+UBERON:0004663,aorta wall,UBERON:0000060,anatomical wall
+HP:0010824,Abnormality of the fifth cranial nerve,HP:0001291,Abnormality of the cranial nerves
+UBERON:0004854,gastrointestinal system mesentery,UBERON:0004782,gastrointestinal system serosa
+UBERON:0008612,muscle of pelvic diaphragm,UBERON:0001325,muscle of pelvis
+UBERON:2001586,pectoral fin radial bone,UBERON:1500006,paired fin radial bone
+CL:1000909,kidney loop of henle epithelial cell,CL:1000494,epithelial cell of renal tubule
+UBERON:0009199,facial suture,UBERON:0009198,craniofacial suture
+UBERON:0008427,transverse foramen of axis,UBERON:0015212,lateral structure
+HP:0100293,Muscle fiber hypertrophy,HP:0004303,Abnormality of muscle fibers
+UBERON:0008323,dorsal artery of clitoris,UBERON:0005156,reproductive structure
+HP:0001660,Truncus arteriosus,HP:0011603,Congenital malformation of the great arteries
+UBERON:0003475,ureteric vein,UBERON:0006554,urinary system structure
+HP:0012738,Agenesis of canine,HP:0011078,Abnormality of canine
+HP:0006420,Asymmetric radial dysplasia,HP:0002818,Abnormality of the radius
+DOID:13341,parasitic conjunctivitis,DOID:2475,chronic conjunctivitis
+UBERON:2000802,myotome somite 15,UBERON:0003082,myotome
+CL:0000598,pyramidal cell,CL:0000117,CNS neuron (sensu Vertebrata)
+HP:0009400,Pseudoepiphyses of the 4th finger,HP:0009174,Abnormality of the epiphyses of the 4th finger
+HP:0012378,Fatigue,HP:0000708,Behavioural/Psychiatric Abnormality
+UBERON:2005259,continuous capillary,UBERON:0004638,blood vessel endothelium
+UBERON:0004675,hypoglossal nerve root,UBERON:0006843,root of cranial nerve
+UBERON:0010025,dorsal part of pharyngeal pouch 3,UBERON:0000490,unilaminar epithelium
+HP:0001999,Abnormal facial shape,HP:0000271,Abnormality of the face
+HP:0012340,Decreased resting energy expenditure,HP:0012338,Abnormal energy expenditure
+UBERON:0002265,olfactory tract,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:12336,male infertility,DOID:48,male reproductive system disease
+UBERON:0003326,mesenchyme of mammary gland,UBERON:0004121,ectoderm-derived structure
+HP:0010728,Aplasia of the retina,HP:0008061,Aplasia/Hypoplasia affecting the retina
+DOID:18,urinary system disease,DOID:7,disease of anatomical entity
+UBERON:0001719,nucleus ambiguus,UBERON:0011775,vagus nerve nucleus
+HP:0009625,Contractures of the metacarpophalangeal joint of the thumb,HP:0009600,Flexion contracture of thumb
+UBERON:0010312,immature eye,UBERON:0005423,developing anatomical structure
+UBERON:0001012,head of radius,UBERON:0005055,zone of long bone
+NCBITaxon:6199,Cestoda,NCBITaxon:6157,Platyhelminthes
+DOID:11036,chronic rapidly progressive glomerulonephritis,DOID:2921,glomerulonephritis
+UBERON:0010409,eye surface,UBERON:0004121,ectoderm-derived structure
+HP:0005899,Metaphyseal dysostosis,HP:0000944,Abnormality of the metaphyses
+HP:0001172,Abnormality of the thumb,HP:0001167,Abnormality of finger
+UBERON:0000084,ureteric bud,UBERON:0007499,epithelial sac
+UBERON:0004327,middle phalanx of pedal digit 5,UBERON:0003863,pedal digit 5 phalanx
+HP:0100542,Abnormal localization of kidney,HP:0012210,Abnormal renal morphology
+CL:0000132,corneal endothelial cell,CL:0000710,neurecto-epithelial cell
+HP:0009302,Bullet-shaped distal phalanx of the 4th finger,HP:0009837,Bullet-shaped distal phalanges of the hand
+HP:0005323,Hemifacial hypertrophy,HP:0000324,Facial asymmetry
+HP:0002217,Slow-growing hair,HP:0011363,Abnormality of hair growth rate
+UBERON:0004012,golgi tendon organ,UBERON:0000020,sense organ
+HP:0009495,Pseudoepiphyses of the 2nd finger,HP:0010235,Pseudoepiphyses of the phalanges of the hand
+UBERON:0004451,trunk or cervical vertebra,UBERON:0002412,vertebra
+UBERON:0003636,manual digit 2 phalanx,UBERON:0001436,phalanx of manus
+HP:0011424,Increased serum zinc,HP:0008277,Abnormality of zinc homeostasis
+HP:0005758,Basilar impression,HP:0000932,Abnormality of the posterior cranial fossa
+UBERON:0014672,distal interphalangeal joint of pedal digit 2,UBERON:0007725,interphalangeal joint of pedal digit 2
+UBERON:2001016,myotome somite 2,UBERON:0003082,myotome
+UBERON:0010297,endochondral scleral ossicle,UBERON:0003462,facial bone
+UBERON:0014684,Helicoprion tooth whorl,UBERON:0014682,tooth whorl
+HP:0004602,Cervical vertebral fusion (C2/C3),HP:0002949,Fused cervical vertebrae
+UBERON:0002867,central gray substance of medulla,UBERON:0007635,nucleus of medulla oblongata
+HP:0003992,Slender ulna,HP:0003100,Slender long bone
+UBERON:0013682,peripheral region of retina,UBERON:0004121,ectoderm-derived structure
+HP:0007728,Congenital miosis,HP:0000616,Miosis
+DOID:6190,rectum Kaposi's sarcoma,DOID:1995,rectum sarcoma
+DOID:4988,alcoholic pancreatitis,DOID:4989,pancreatitis
+NCBITaxon:186817,Bacillaceae,NCBITaxon:1385,Bacillales
+HP:0008222,Female infertility,HP:0000868,Decreased fertility in females
+UBERON:0011371,sternocephalicus muscle,UBERON:0001630,muscle organ
+HP:0002667,Nephroblastoma (Wilms tumor),HP:0002898,Embryonal neoplasm
+HP:0100317,Agyrophilic inclusion bodies,HP:0100314,Cerebral inclusion bodies
+DOID:2181,post-surgical hypoinsulinemia,DOID:1428,endocrine pancreas disease
+UBERON:0005398,female reproductive gland,UBERON:0014404,female anatomical structure
+HP:0010685,Low alkaline phosphatase of renal origin,HP:0012211,Abnormal renal physiology
+UBERON:0012378,muscle layer of urinary bladder,UBERON:0004120,mesoderm-derived structure
+UBERON:0003557,midbrain arachnoid mater,UBERON:0003288,meninx of midbrain
+UBERON:0004659,mandible neck,UBERON:0010313,neural crest-derived structure
+HP:0010148,Triangular epiphysis of the distal phalanx of the hallux,HP:0010124,Abnormality of the epiphysis of the distal phalanx of the hallux
+HP:0009584,Osteolytic defects of the proximal phalanx of the 2nd finger,HP:0009550,Osteolytic defects of the phalanges of the 2nd finger
+UBERON:2000136,otic lateral line neuromast,UBERON:0008904,neuromast
+HP:0003393,Thenar muscle atrophy,HP:0009130,Hand muscle atrophy
+HP:0011442,Abnormality of central motor function,HP:0012638,Abnormality of nervous system physiology
+DOID:13636,Fanconi's anemia,DOID:1342,congenital hypoplastic anemia
+UBERON:0001739,laryngeal cartilage,UBERON:0011004,pharyngeal arch cartilage
+DOID:6993,iris mixed cell melanoma,DOID:6992,intraocular mixed cell type melanoma
+DOID:13461,urethral intrinsic sphincter deficiency,DOID:732,urethral disease
+DOID:5414,lung occult small cell carcinoma,DOID:5409,lung small cell carcinoma
+DOID:0080046,Stickler syndrome,DOID:0050736,autosomal dominant disease
+CL:0000801,gamma-delta intraepithelial T cell,CL:0002496,intraepithelial lymphocyte
+HP:0001771,Achilles tendon contracture,HP:0008366,Contractures involving the joints of the feet
+UBERON:0001646,abducens nerve,UBERON:0001785,cranial nerve
+HP:0010095,Partial duplication of the proximal phalanx of the hallux,HP:0010101,Partial duplication of the phalanges of the hallux
+UBERON:4200008,inter-clavicle joint,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:6992,intraocular mixed cell type melanoma,DOID:1752,ocular melanoma
+UBERON:2001017,myotome somite 22,UBERON:0003082,myotome
+DOID:12400,kleptomania,DOID:10937,impulse control disorder
+HP:0001039,Atheroeruptive xanthoma,HP:0000991,Xanthomatosis
+HP:0011524,Iris melanoma,HP:0000525,Abnormality of the iris
+HP:0012285,Abnormal hypothalamus physiology,HP:0002443,Abnormality of the hypothalamus
+HP:0009587,Triangular shaped proximal phalanx of the 2nd finger,HP:0009544,Abnormality of the proximal phalanx of the 2nd finger
+UBERON:0015131,subepithelial connective tissue of prostatic gland,UBERON:0015130,connective tissue of prostate
+DOID:3751,plantar verrucous skin carcinoma,DOID:3151,skin squamous cell carcinoma
+DOID:3635,congenital myasthenic syndrome,DOID:439,neuromuscular junction disease
+UBERON:0006082,fundus of urinary bladder,UBERON:0000064,organ part
+CL:0005007,Kolmer-Agduhr neuron,CL:0005000,spinal cord interneuron
+HP:0006999,Basal ganglia gliosis,HP:0002171,Gliosis
+UBERON:0016423,compact bone of diaphysis,UBERON:0005808,bone tissue of long bone
+HP:0001311,Abnormal nervous system electrophysiology,HP:0012638,Abnormality of nervous system physiology
+UBERON:2001419,dorsal fin pterygiophore,UBERON:0000477,anatomical cluster
+UBERON:0014711,carapacial ridge mesenchyme,UBERON:0005291,embryonic tissue
+CL:0000584,enterocyte,CL:0000239,brush border epithelial cell
+HP:0001864,Fifth toe clinodactyly,HP:0001863,Toe clinodactyly
+HP:0001799,Short nail,HP:0008386,Aplasia/Hypoplasia of the nails
+HP:0010278,Triangular epiphyses of the proximal phalanges of the hand,HP:0010245,Abnormality of the epiphyses of the proximal phalanges of the hand
+UBERON:0006096,posterior transverse termporal area 42,UBERON:0003022,cerebral cortex lobe
+DOID:3326,purpura,DOID:2213,hemorrhagic disease
+HP:0012250,ST segment depression,HP:0012249,Abnormal ST segment
+HP:0004059,Radial club hand,HP:0009486,Radial deviation of the hand
+HP:0010328,Polydactyly affecting the 2nd toe,HP:0010319,Abnormality of the 2nd toe
+UBERON:0000219,vertebral foramen of atlas,UBERON:0001131,vertebral foramen
+DOID:11847,coronary thrombosis,DOID:3393,coronary artery disease
+HP:0004911,Episodic metabolic acidosis,HP:0001942,Metabolic acidosis
+UBERON:0007366,ruminant stomach,UBERON:0000945,stomach
+HP:0100138,Enlarged epiphysis of the distal phalanx of the 3rd toe,HP:0100058,Enlarged epiphyses of the 3rd toe
+HP:0008948,Proximal upper limb amyotrophy,HP:0007126,Proximal amyotrophy
+UBERON:2000925,hypaxial region somite 10,UBERON:0003895,hypaxial myotome region
+UBERON:0003516,hindlimb blood vessel,UBERON:0003514,limb blood vessel
+UBERON:0007021,juvenile organism,UBERON:0000468,multi-cellular organism
+UBERON:0009588,mesenchyme of interdigital region between manual digits 3 and 4,UBERON:0009598,mesenchyme of interdigital region between digits 3 and 4
+UBERON:0006301,telencephalic part of interventricular foramen,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:169,neuroendocrine tumor,DOID:170,endocrine gland cancer
+HP:0100081,Fragmentation of the epiphyses of the 5th toe,HP:0010166,Fragmentation of the epiphyses of the toes
+HP:0009265,Fragmentation of the epiphysis of the proximal phalanx of the 4th finger,HP:0009397,Fragmentation of the epiphyses of the 4th finger
+UBERON:3000949,posterior ramus of cleithrum,UBERON:0004121,ectoderm-derived structure
+HP:0000061,"Ambiguous genitalia, female",HP:0000055,Abnormality of female external genitalia
+HP:0011525,Iris nevus,HP:0000525,Abnormality of the iris
+DOID:3964,trabecular follicular adenocarcinoma,DOID:3962,follicular thyroid carcinoma
+UBERON:3000654,pars jugalis,UBERON:0004120,mesoderm-derived structure
+UBERON:0001699,sensory root of facial nerve,UBERON:0004674,facial nerve root
+HP:0007414,Neonatal wrinkled skin of hands and feet,HP:0100678,Premature skin wrinkling
+HP:0011734,Central adrenal insufficiency,HP:0000846,Adrenal insufficiency
+UBERON:0003357,epithelium of tongue,UBERON:0003929,gut epithelium
+HP:0011714,Libman-Sacks lesions,HP:0100584,Endocarditis
+HP:0003081,Increased urinary potassium,HP:0012598,Abnormal urine potassium concentration
+HP:0200028,Pretibial myxedema,HP:0011356,Regional abnormality of skin
+HP:0009679,Fragmentation of the epiphysis of the distal phalanx of the thumb,HP:0009690,Fragmentation of the epiphyses of the thumb
+UBERON:0012643,plume,UBERON:0000062,organ
+UBERON:0010341,1st arch mesenchyme from head mesenchyme,UBERON:0006904,head mesenchyme from mesoderm
+UBERON:0001840,semicircular canal,UBERON:0000025,tube
+HP:0011291,EEG with central sharp slow waves,HP:0011195,EEG with focal sharp slow waves
+HP:0004664,Facial midline hemangioma,HP:0000329,Facial hemangioma
+DOID:4411,hepatitis E,DOID:37,skin disease
+UBERON:2002078,hypural plate,UBERON:0002513,endochondral bone
+UBERON:0009478,associated mesenchyme of midgut,UBERON:0004120,mesoderm-derived structure
+UBERON:4000053,vacuolated notochordal tissue,UBERON:0002384,connective tissue
+HP:0100822,Rectocele,HP:0002035,Rectal prolapse
+DOID:14228,oligospermia,DOID:12336,male infertility
+UBERON:0006670,central tendon of diaphragm,UBERON:0003570,respiratory system connective tissue
+UBERON:0005161,pelvic spur,UBERON:0005160,vestigial structure
+HP:0011985,Acholic stools,HP:0001396,Cholestasis
+UBERON:2002056,hypural 6,UBERON:2000364,hypural
+HP:0004048,Narrow joint spaces of wrist,HP:0003019,Abnormality of the wrist
+CL:0000088,female germ line stem cell (sensu Nematoda and Protostomia),CL:0000022,female germ line stem cell
+HP:0006172,"Flattened, squared-off epiphyses of tubular bones",HP:0003053,Epiphyseal deformities of tubular bones
+HP:0005156,Hypoplastic left atrium,HP:0005120,Abnormality of cardiac atrium
+DOID:13081,hemangioma of subcutaneous tissue,DOID:37,skin disease
+HP:0100125,Enlarged epiphysis of the proximal phalanx of the 2nd toe,HP:0100090,Abnormality of the epiphysis of the proximal phalanx of the 2nd toe
+UBERON:0015021,forelimb endochondral element,UBERON:0015061,limb endochondral element
+UBERON:0011096,lacrimal nerve,UBERON:0002003,peripheral nerve
+UBERON:0007118,umbilicus,UBERON:0000479,tissue
+UBERON:0002337,endometrial stroma,UBERON:0003891,stroma
+HP:0003918,Sclerotic humeral metaphysis,HP:0003907,Abnormality of the humeral metaphyses
+HP:0010194,Aplasia/Hypoplasia of the middle phalanges of the toes,HP:0010173,Aplasia/Hypoplasia of the phalanges of the toes
+HP:0007379,Neoplasm of the genitourinary tract,HP:0000119,Abnormality of the genitourinary system
+CL:0000079,stratified epithelial cell,CL:0000066,epithelial cell
+HP:0005365,Severe B lymphocytopenia,HP:0010976,B lymphocytopenia
+DOID:10581,metachromatic leukodystrophy,DOID:1927,sphingolipidosis
+UBERON:3010584,mandibular arch neural crest,UBERON:0004529,anatomical projection
+UBERON:3010437,post-anal gut,UBERON:0002050,embryonic structure
+UBERON:3000170,fenestra precerebralis,UBERON:3000316,nasal opening
+UBERON:0002234,proximal phalanx of manus,UBERON:0001436,phalanx of manus
+CL:0000629,storage cell,CL:0000325,stuff accumulating cell
+UBERON:3000255,lamina anterior of pars facialis,UBERON:0004120,mesoderm-derived structure
+DOID:9279,hyperhomocysteinemia,DOID:9252,amino acid metabolic disorder
+UBERON:0009539,mesenchyme of submandibular gland primordium,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0005220,Multiple intestinal neurofibromatosis,HP:0002242,Abnormality of the intestine
+DOID:10688,hypertrophy of breast,DOID:3463,breast disease
+UBERON:0012289,fused tarsals 2 and 3,UBERON:0010721,distal tarsal bone
+UBERON:0001255,urinary bladder,UBERON:0006554,urinary system structure
+DOID:2394,ovarian cancer,DOID:120,female reproductive organ cancer
+UBERON:0003462,facial bone,UBERON:0010313,neural crest-derived structure
+HP:0100659,Abnormality of the cerebral vasculature,HP:0002597,Abnormality of the vasculature
+HP:0100929,Sclerosis of the phalanges of the 5th toe,HP:0100924,Sclerosis of the phalanges of the toes
+UBERON:0001939,medial mammillary nucleus,UBERON:0002789,regional part of posterior hypothalamic region
+DOID:5427,urinary bladder villous adenoma,DOID:11054,urinary bladder cancer
+UBERON:0002438,ventral tegmental nucleus,UBERON:0007414,nucleus of midbrain tegmentum
+HP:0100031,Neoplasm of the thyroid gland,HP:0100568,Neoplasm of the endocrine system
+UBERON:0013069,popliteal area,UBERON:0004120,mesoderm-derived structure
+UBERON:0002670,anterior ascending limb of lateral sulcus,UBERON:0008334,subarachnoid sulcus
+HP:0010389,Symphalangism affecting the phalanges of the 5th toe,HP:0100235,Synostosis involving bones of the toes
+HP:0002986,Radial bowing,HP:0003956,Bowed forearm bones
+UBERON:2000235,magnocellular superficial pretectal nucleus,UBERON:0014450,pretectal nucleus
+CL:0002310,mammosomatotroph,CL:0000439,prolactin secreting cell
+HP:0100944,Sclerosis of the distal phalanx of the hallux,HP:0100930,Sclerosis of the phalanges of the hallux
+UBERON:0012268,equine forelimb splint bone,UBERON:0003607,forelimb long bone
+HP:0010482,Acromelia of the upper limbs,HP:0010884,Acromelia
+UBERON:0003821,metapodium bone,UBERON:0003606,limb long bone
+DOID:5644,tricuspid valve prolapse,DOID:0050826,tricuspid valve disease
+DOID:12167,secondary vitreoretinal degeneration,DOID:12161,peripheral retinal degeneration
+UBERON:3010455,blastopore lip,UBERON:0002050,embryonic structure
+UBERON:0001713,lower eyelid,UBERON:0001711,eyelid
+HP:0009253,Enlarged epiphysis of the distal phalanx of the 4th finger,HP:0010249,Enlarged epiphyses of the distal phalanges of the hand
+UBERON:0005161,pelvic spur,UBERON:0000026,appendage
+UBERON:3000915,spatium intertarsale,UBERON:0000464,anatomical space
+UBERON:0011511,iliococcygeus muscle,UBERON:0001325,muscle of pelvis
+DOID:2053,reactive cutaneous fibrous lesion,DOID:37,skin disease
+HP:0003864,Bifid humerus,HP:0003063,Abnormality of the humerus
+UBERON:0001125,serratus ventralis,UBERON:0004120,mesoderm-derived structure
+HP:0009381,Short finger,HP:0006265,Aplasia/Hypoplasia of fingers
+UBERON:3000562,septum semircularium posterior,UBERON:0004121,ectoderm-derived structure
+HP:0003111,Abnormality of ion homeostasis,HP:0001939,Abnormality of metabolism/homeostasis
+DOID:9843,monofixation syndrome,DOID:540,strabismus
+DOID:4587,benign meningioma,DOID:0060090,central nervous system organ benign neoplasm
+HP:0010657,Patchy reduction of bone mineral density,HP:0002797,Osteolysis
+UBERON:3000018,anterior ramus of pterygoid,UBERON:0004530,bony projection
+HP:0009318,Aplasia/Hypoplasia of the 3rd finger,HP:0006265,Aplasia/Hypoplasia of fingers
+HP:0007229,Intracerebral periventricular calcifications,HP:0002514,Cerebral calcification
+HP:0007370,Aplasia/Hypoplasia of the corpus callosum,HP:0001273,Abnormality of the corpus callosum
+UBERON:0002276,lamina of spiral limbus,UBERON:0004121,ectoderm-derived structure
+HP:0010087,Bullet-shaped proximal phalanx of the hallux,HP:0010205,Bullet-shaped proximal phalanges of the toes
+HP:0010036,Aplasia/Hypoplasia of the 2nd metacarpal,HP:0005914,Aplasia/Hypoplasia involving the metacarpal bones
+CL:0000216,Sertoli cell,CL:0000630,supportive cell
+HP:0002063,Rigidity,HP:0011442,Abnormality of central motor function
+DOID:1618,breast fibroadenoma,DOID:0060082,breast benign neoplasm
+UBERON:0003995,subarcuate fossa,UBERON:0004704,bone fossa
+HP:0009244,Distal/middle symphalangism of 5th finger,HP:0009178,Symphalangism of middle phalanx of 5th finger
+HP:0000262,Turricephaly,HP:0002648,Abnormality of calvarial morphology
+UBERON:3010060,centrale (fore),UBERON:0012131,centrale
+UBERON:0004207,prebend segment,UBERON:0006554,urinary system structure
+DOID:582,hemoglobinuria,DOID:576,proteinuria
+UBERON:0012369,longitudinal muscle layer,UBERON:0004923,organ component layer
+UBERON:0006010,hyaloid canal,UBERON:0004111,anatomical conduit
+UBERON:0008967,centrum semiovale,UBERON:0002791,regional part of telencephalon
+UBERON:0001327,coccygeus muscle,UBERON:0001325,muscle of pelvis
+HP:0008720,Primary testicular failure,HP:0000035,Abnormality of the testis
+HP:0006532,Recurrent pneumonia,HP:0002090,Pneumonia
+HP:0009751,Aplasia of the pectoralis major muscle,HP:0005258,Pectoral muscle hypoplasia/aplasia
+HP:0007392,Excessive wrinkled skin,HP:0100678,Premature skin wrinkling
+HP:0006169,Decreased mobility 3rd-5th fingers,HP:0006135,Decreased finger mobility
+HP:0005844,Rounded middle phalanx of finger,HP:0009833,Abnormality of the middle phalanges of the hand
+HP:0100041,Broad 3rd toe,HP:0001837,Broad toe
+UBERON:2001944,lateral ethmoid-autopalatine ligament,UBERON:0008846,skeletal ligament
+HP:0009512,Triangular epiphysis of the distal phalanx of the 2nd finger,HP:0009498,Triangular epiphyses of the 2nd finger
+DOID:2075,minor vestibular glands adenoma,DOID:0060088,vestibular gland benign neoplasm
+UBERON:0013515,subdivision of uterine tube,UBERON:0013522,subdivision of tube
+UBERON:0015105,distal tarsal bone 2 endochondral element,UBERON:0015050,tarsus endochondral element
+DOID:1328,Rift Valley fever,DOID:934,viral infectious disease
+HP:0011169,Generalized clonic seizures,HP:0002197,Generalized seizures
+CL:0011003,magnocellular neurosecretory cell,CL:0000381,neurosecretory neuron
+UBERON:0010981,internal intercostal pre-muscle mass,UBERON:0010970,intercostal pre-muscle mass
+HP:0006516,Hypersensitivity pneumonitis,HP:0002088,Abnormality of the lung
+HP:0001022,Albinism,HP:0005599,Hypopigmentation of hair
+UBERON:0013744,wall of crypt of lieberkuhn of small intestine,UBERON:0001902,epithelium of small intestine
+UBERON:0001912,lobule of lactiferous gland,UBERON:0004121,ectoderm-derived structure
+UBERON:4200088,iliac peduncle of the pubis,UBERON:0004530,bony projection
+CL:1001066,kidney arteriole smooth muscle cell,CL:1000891,kidney arterial blood vessel cell
+UBERON:2001604,lateral ethmoid palatine process,UBERON:0004530,bony projection
+DOID:2153,ovarian Wilms' cancer,DOID:2394,ovarian cancer
+UBERON:0002269,pupillary membrane,UBERON:0000158,membranous layer
+HP:0009335,Absent epiphysis of the distal phalanx of the 3rd finger,HP:0009410,Absent epiphyses of the 3rd finger
+DOID:0050846,hemidystonia,DOID:0050837,multifocal dystonia
+DOID:1595,endogenous depression,DOID:1596,mental depression
+HP:0005220,Multiple intestinal neurofibromatosis,HP:0007378,Neoplasm of the gastrointestinal tract
+HP:0009236,Rhomboid or triangular shaped 5th finger proximal phalanx,HP:0009233,Triangular shaped proximal phalanx of the 5th finger
+UBERON:0000979,tibia,UBERON:0003608,hindlimb long bone
+UBERON:2001482,middle lateral line nerve,UBERON:0008906,lateral line nerve
+UBERON:0004116,nerve of tympanic cavity,UBERON:0011779,nerve of head region
+UBERON:0014646,nucleus K,UBERON:0002438,ventral tegmental nucleus
+UBERON:0003570,respiratory system connective tissue,UBERON:0002384,connective tissue
+DOID:9181,amebiasis,DOID:2789,parasitic protozoa infectious disease
+UBERON:0000311,extensor muscle,UBERON:0004120,mesoderm-derived structure
+UBERON:0006848,posterior pretectal nucleus,UBERON:0006569,diencephalic nucleus
+HP:0001060,Axillary pterygia,HP:0001059,Pterygium
+DOID:8340,endocervical type cervical mucinous adenocarcinoma,DOID:3701,cervical mucinous adenocarcinoma
+UBERON:0009889,secondary heart field,UBERON:0005291,embryonic tissue
+CL:0000760,type 8 cone bipolar cell (sensu Mus),CL:0000752,cone retinal bipolar cell
+CL:0000321,seminal fluid secreting cell,CL:0000151,secretory cell
+HP:0002339,Abnormality of the caudate nucleus,HP:0010994,Abnormality of the striatum
+DOID:6052,central nervous system childhood germ cell tumor,DOID:4439,central nervous system germ cell tumor
+UBERON:0002217,synovial joint,UBERON:0000982,skeletal joint
+HP:0002134,Abnormality of the basal ganglia,HP:0010993,Abnormality of the cerebral subcortex
+HP:0010609,Skin tags,HP:0011355,Localized skin lesion
+DOID:11132,prostatic hypertrophy,DOID:47,prostate disease
+DOID:13739,nutmeg liver,DOID:272,hepatic vascular disease
+UBERON:0011088,ligament of knee joint,UBERON:0003577,knee connective tissue
+HP:0011295,EEG with parietal sharp waves,HP:0011196,EEG with focal sharp waves
+DOID:0060104,cerebellar medulloblastoma,DOID:4205,cerebellum cancer
+HP:0000014,Abnormality of the bladder,HP:0010936,Abnormality of the lower urinary tract
+UBERON:0000207,compound eye corneal lens,UBERON:0005389,transparent eye structure
+UBERON:0006220,diencephalic part of interventricular foramen,UBERON:0004111,anatomical conduit
+UBERON:0007269,pectoral appendage musculature,UBERON:0007271,appendage musculature
+CL:1000283,smooth muscle fiber of transverse colon,CL:1000280,smooth muscle cell of colon
+UBERON:0003445,pes nerve,UBERON:0003442,hindlimb nerve
+UBERON:2001636,pharyngobranchial 4 bone,UBERON:2000527,pharyngobranchial bone
+UBERON:0012295,Guérin's valve,UBERON:0000063,organ segment
+CL:0000160,goblet cell,CL:0000319,mucus secreting cell
+DOID:13447,corneal argyrosis,DOID:10124,corneal disease
+UBERON:0014523,oculomotor division of oculomotor nuclear complex,UBERON:0003528,brain grey matter
+CL:0000118,basket cell,CL:0000117,CNS neuron (sensu Vertebrata)
+DOID:2729,dyskeratosis congenita,DOID:37,skin disease
+UBERON:0001943,midbrain tegmentum,UBERON:0002950,regional part of midbrain
+UBERON:0002086,sinoatrial valve,UBERON:0000946,cardial valve
+HP:0200047,Chondritis of pinna,HP:0000377,Abnormality of the pinna
+UBERON:3000651,lamina anterior of maxilla,UBERON:0000064,organ part
+UBERON:0014598,paraventricular nucleus of the hypothalamus descending division - forniceal part,UBERON:0003048,regional part of hypothalamus
+UBERON:0001454,distal tarsal bone 3,UBERON:0010721,distal tarsal bone
+HP:0005297,Premature occlusive vascular disease,HP:0004950,Peripheral arterial disease
+UBERON:0002549,ventral trigeminal tract,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:4868,prostate adenoid cystic carcinoma,DOID:10286,prostate carcinoma
+UBERON:0001381,semimembranosus muscle,UBERON:0003663,hindlimb muscle
+HP:0009854,Curved proximal phalanges of the hand,HP:0009834,Abnormality of the proximal phalanges of the hand
+HP:0002085,Occipital encephalocele,HP:0002084,Encephalocele
+CL:0002077,ecto-epithelial cell,CL:0000066,epithelial cell
+HP:0010192,Triangular shaped distal phalanges of the toes,HP:0010180,Triangular shaped phalanges of the toes
+UBERON:0001169,wall of large intestine,UBERON:0001262,wall of intestine
+UBERON:0001189,left testicular artery,UBERON:0003468,ureteric segment of renal artery
+DOID:0050161,lower respiratory tract disease,DOID:1579,respiratory system disease
+HP:0100106,Ivory epiphysis of the distal phalanx of the 2nd toe,HP:0100050,Ivory epiphyses of the 2nd toe
+DOID:1876,sexual dysfunction,DOID:0060043,sexual disorder
+UBERON:0006661,epicranial aponeurosis,UBERON:0006614,aponeurosis
+UBERON:0009584,1st arch mandibular mesenchyme,UBERON:0010042,1st arch mesenchyme
+CL:0000097,mast cell,CL:0002274,histamine secreting cell
+HP:0004743,Chronic tubulointerstitial nephritis,HP:0001970,Tubulointerstitial nephritis
+HP:0001075,Atrophic scars,HP:0004334,Dermal atrophy
+UBERON:0011687,levator hyomandibulae muscle,UBERON:0005493,hyoid muscle
+UBERON:0004508,skeletal muscle tissue of levator palpebrae superioris,UBERON:0010313,neural crest-derived structure
+UBERON:0005102,late distal convoluted tubule,UBERON:0008408,distal tubular epithelium
+CL:1001009,kidney efferent arteriole cell,CL:1000891,kidney arterial blood vessel cell
+UBERON:0001681,nasal bone,UBERON:0015212,lateral structure
+UBERON:0000458,endocervix,UBERON:0000064,organ part
+DOID:615,leukopenia,DOID:9500,leukocyte disease
+UBERON:0003089,sclerotome,UBERON:0005856,developing mesenchymal condensation
+UBERON:0010083,future dermis,UBERON:0004120,mesoderm-derived structure
+HP:0001187,Hyperextensibility of the finger joints,HP:0001167,Abnormality of finger
+DOID:3451,skin carcinoma,DOID:4159,skin cancer
+DOID:11405,diphtheria,DOID:0050338,primary bacterial infectious disease
+NCBITaxon:39054,Human enterovirus 71,NCBITaxon:138948,Human enterovirus A
+DOID:707,B-cell lymphoma,DOID:0060060,non-Hodgkin lymphoma
+HP:0011833,Overhanging nasal tip,HP:0000436,Abnormality of the nasal tip
+UBERON:0004423,proximal epiphysis of second metacarpal bone,UBERON:0004392,epiphysis of second metacarpal bone
+HP:0002970,Genu varum,HP:0002979,Bowing of the legs
+UBERON:0001914,colostrum,UBERON:0006539,mammary gland fluid/secretion
+DOID:14525,Reye syndrome,DOID:225,syndrome
+UBERON:0001708,jaw skeleton,UBERON:0010912,subdivision of skeleton
+HP:0009844,Broad middle phalanx of finger,HP:0009768,Broad phalanges of the hand
+HP:0006439,Radioulnar dislocation,HP:0003059,Abnormality of the radioulnar joints
+DOID:7380,squamous cell papilloma of skin,DOID:3178,skin papilloma
+UBERON:0004507,skeletal muscle tissue of temporalis,UBERON:0001134,skeletal muscle tissue
+UBERON:0006339,third ventricle choroid plexus stroma,UBERON:0005206,choroid plexus stroma
+UBERON:0001113,lobe of liver,UBERON:0000064,organ part
+CL:0002522,renal filtration cell,CL:0000424,excretory cell
+HP:0002833,Cystic angiomatosis of bone,HP:0012062,Bone cyst
+UBERON:0005425,presumptive neural retina,UBERON:0010312,immature eye
+HP:0003961,Fractured forearm bones,HP:0002973,Abnormality of the forearm
+UBERON:0001513,skin of pes,UBERON:0015790,autopod skin
+UBERON:2002059,posttemporal-parietal joint,UBERON:0000982,skeletal joint
+CL:0002560,inner root sheath cell,CL:0002559,hair follicle cell
+HP:0009209,Ivory epiphysis of the middle phalanx of the 5th finger,HP:0009388,Ivory epiphyses of the 5th finger
+UBERON:0004507,skeletal muscle tissue of temporalis,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:5265,lung leiomyosarcoma,DOID:2784,lung sarcoma
+UBERON:0008842,suspensory ligament of testis,UBERON:0005291,embryonic tissue
+HP:0001699,Sudden death,HP:0011420,Death
+UBERON:0012113,bolus of food,UBERON:0012112,ingested food
+CL:0000081,blood cell,CL:0000988,hematopoietic cell
+HP:0100817,Renovascular hypertension,HP:0000822,Hypertension
+UBERON:3000177,flange of quadratojugal,UBERON:0004120,mesoderm-derived structure
+DOID:8275,intratubular embryonal carcinoma,DOID:5680,embryonal testis carcinoma
+UBERON:2000695,labial cavities,UBERON:0000464,anatomical space
+UBERON:0006041,interdigital region between pedal digits 2 and 3,UBERON:0006019,interdigital region between digits 2 and 3
+UBERON:0003515,forelimb blood vessel,UBERON:0003514,limb blood vessel
+HP:0009267,Ivory epiphysis of the proximal phalanx of the 4th finger,HP:0010274,Ivory epiphyses of the proximal phalanges of the hand
+HP:0000674,Anodontia,HP:0009804,Reduced number of teeth
+UBERON:3000068,cartilago ectochoanalis,UBERON:0010313,neural crest-derived structure
+DOID:4300,superficial basal cell carcinoma,DOID:2513,basal cell carcinoma
+UBERON:0006005,hair follicle isthmus,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0002021,occipital lobe,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:1166,palindromic rheumatism,DOID:225,syndrome
+DOID:3437,laryngitis,DOID:786,laryngeal disease
+UBERON:2000426,rostral parvocellular preoptic nucleus,UBERON:0007251,preoptic nucleus
+UBERON:0000118,lung bud,UBERON:0005911,endo-epithelium
+NCBITaxon:147538,Pezizomycotina,NCBITaxon:716545,saccharomyceta
+HP:0100621,Dysgerminoma,HP:0100615,Ovarian neoplasm
+UBERON:2000294,torus lateralis,UBERON:0006569,diencephalic nucleus
+DOID:3716,mucinous stomach adenocarcinoma,DOID:6217,gastric diffuse adenocarcinoma
+NCBITaxon:7148,Nematocera,NCBITaxon:7147,Diptera
+HP:0009250,Absent epiphysis of the distal phalanx of the 4th finger,HP:0010246,Absent epiphyses of the distal phalanges of the hand
+UBERON:0003820,prostate bud,UBERON:0005291,embryonic tissue
+UBERON:0001395,thoraco-acromial artery,UBERON:0001637,artery
+HP:0000972,Palmoplantar hyperkeratosis,HP:0007556,Plantar hyperkeratosis
+HP:0100693,Iridodonesis,HP:0000525,Abnormality of the iris
+UBERON:0001827,lacrimal gland secretion,UBERON:0000456,bodily secretion
+UBERON:0002944,spinothalamic tract of medulla,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:4200063,ectocondylar tubercle,UBERON:4100000,skeletal element projection
+UBERON:2005100,intervessel commissure,UBERON:0007304,appendage vasculature
+UBERON:0000056,ureter,UBERON:0004120,mesoderm-derived structure
+UBERON:0005097,renal connecting tubule,UBERON:0007685,region of nephron tubule
+UBERON:0010711,pelvic fin skeleton,UBERON:0010713,paired fin skeleton
+UBERON:2001396,parapophysis + rib of vertebra 4,UBERON:0002513,endochondral bone
+CL:0002026,"CD34-negative, CD41-positive, CD42-positive megakaryocyte cell",CL:0000556,megakaryocyte
+UBERON:0004831,esophagus skeletal muscle,UBERON:0003898,skeletal muscle tissue of trunk
+DOID:1672,spontaneous tension pneumothorax,DOID:1673,pneumothorax
+UBERON:0002163,inferior cerebellar peduncle,UBERON:0007416,cerebellar peduncle
+UBERON:0002425,visceral serous pericardium,UBERON:0002357,serous pericardium
+HP:0011112,Abnormality of serum cytokine level,HP:0011111,Abnormality of immune serum protein physiology
+HP:0007338,Hypermetric saccades,HP:0000570,Abnormality of saccadic eye movements
+UBERON:2007005,hemal prezygapophysis,UBERON:0004247,bone of dorsum
+HP:0011129,Bilateral fetal pyelectasis,HP:0010945,Fetal pyelectasis
+UBERON:2005224,yolk larval melanophore stripe,UBERON:2005220,larval melanophore stripe
+UBERON:4000108,non-mineralized hyaline cartilage tissue,UBERON:0001994,hyaline cartilage tissue
+CL:0002351,progenitor cell of endocrine pancreas,CL:0000048,multi fate stem cell
+UBERON:0001400,iliocostalis thoracis muscle,UBERON:0002251,iliocostalis muscle
+HP:0001404,Hepatocellular necrosis,HP:0002605,Hepatic necrosis
+CL:0000577,type EC enteroendocrine cell,CL:0000164,enteroendocrine cell
+HP:0009597,Short proximal phalanx of the 2nd finger,HP:0009536,Short 2nd finger
+HP:0012446,Low CSF 5-methyltetrahydrofolate,HP:0002921,Abnormality of the cerebrospinal fluid
+UBERON:3000519,pseudodentary tooth,UBERON:0003268,tooth of lower jaw
+UBERON:0013618,secondary molar tooth,UBERON:0003655,molar tooth
+HP:0100162,Irregular epiphysis of the proximal phalanx of the 3rd toe,HP:0100093,Abnormality of the epiphysis of the proximal phalanx of the 3rd toe
+HP:0009887,Abnormality of hair pigmentation,HP:0001595,Abnormality of the hair
+DOID:2598,laryngeal benign neoplasm,DOID:0050621,respiratory system benign neoplasm
+HP:0003292,Decreased serum leptin,HP:0004361,Abnormality of circulating leptin level
+UBERON:0005459,left umbilical vein,UBERON:0015212,lateral structure
+UBERON:0000935,anterior commissure,UBERON:0002473,intercerebral commissure
+DOID:12252,Cushing's syndrome,DOID:3947,adrenal gland hyperfunction
+UBERON:0007292,presumptive rhombomere 5,UBERON:0006598,presumptive structure
+DOID:0060174,GABA aminotransferase deficiency,DOID:0060176,gamma-amino butyric acid metabolism disorder
+HP:0001673,Tachycardia (with pheochromocytoma),HP:0001675,Rhythm disturbances associated with pheochromocytoma
+CL:0000711,cumulus cell,CL:0002174,follicular cell of ovary
+CL:0000147,pigment cell,CL:0000325,stuff accumulating cell
+UBERON:3000807,carina distalis,UBERON:0000064,organ part
+UBERON:0006946,efferent duct,UBERON:0005904,duct of male reproductive system
+UBERON:0003332,submucosa of duodenum,UBERON:0001205,submucosa of small intestine
+HP:0000532,Chorioretinal abnormality,HP:0000479,Abnormality of the retina
+DOID:9201,lichen planus,DOID:8574,lichen disease
+UBERON:0004263,upper arm skin,UBERON:0002427,arm skin
+UBERON:0010558,pedal digit 2 metatarsal cartilage element,UBERON:0010681,pedal digit 2 phalanx cartilage element
+HP:0009337,Cone-shaped epiphysis of the distal phalanx of the 3rd finger,HP:0009332,Abnormality of the epiphysis of the distal phalanx of the 3rd finger
+UBERON:2000516,periventricular grey zone,UBERON:0002554,regional part of superior colliculus
+HP:0012262,Abnormal ciliary motility,HP:0012261,Abnormal respiratory motile cilium physiology
+UBERON:3010683,distal-most prepollical element,UBERON:4200140,prepollical element
+HP:0006649,Costochondral pain,HP:0000919,Abnormality of the costochondral junction
+UBERON:0003292,meninx of spinal cord,UBERON:0005174,dorsal region organ
+UBERON:0002370,thymus,UBERON:0004177,hemopoietic organ
+DOID:4440,seminoma,DOID:2994,germ cell cancer
+HP:0011832,Narrow nasal tip,HP:0000436,Abnormality of the nasal tip
+HP:0002679,Abnormality of the sella turcica,HP:0000929,Abnormality of the skull
+UBERON:0002721,lateral sulcus,UBERON:0008334,subarachnoid sulcus
+UBERON:0004142,outflow tract septum,UBERON:0002099,cardiac septum
+HP:0010806,U-Shaped upper lip vermilion,HP:0011339,Abnormality of upper lip vermillion
+UBERON:0010390,lumen of urethra,UBERON:0000464,anatomical space
+HP:0010825,Abnormality of the eleventh cranial nerve,HP:0001291,Abnormality of the cranial nerves
+HP:0001085,Papilledema,HP:0000587,Abnormality of the optic nerve
+UBERON:0005589,rhombomere 8 lateral wall,UBERON:0005501,rhombomere lateral wall
+UBERON:0011844,duct of areolar gland,UBERON:0011845,duct of sebaceous gland
+UBERON:0010843,clavicle cartilage element,UBERON:0005863,cartilaginous condensation
+UBERON:0008230,tibialis,UBERON:0004256,hindlimb zeugopod muscle
+HP:0011061,Abnormality of dental structure,HP:0000164,Abnormality of the teeth
+HP:0100316,Hirano bodies,HP:0100314,Cerebral inclusion bodies
+DOID:8649,tongue cancer,DOID:8618,oral cavity cancer
+UBERON:2005379,dorsal fin distal radial bone 8,UBERON:2000936,dorsal fin distal radial bone
+UBERON:0010377,mesenchyme from somatopleure,UBERON:0005291,embryonic tissue
+CL:0000626,olfactory granule cell,CL:0000120,granule cell
+HP:0008221,Adrenal hyperplasia,HP:0011732,Abnormality of adrenal morphology
+UBERON:0003104,mesenchyme,UBERON:0000479,tissue
+UBERON:3010739,M. flexor antibrachii medialis,UBERON:0010891,pectoral complex muscle
+DOID:2368,gangliosidosis,DOID:1927,sphingolipidosis
+UBERON:0004290,dermomyotome,UBERON:0012275,meso-epithelium
+DOID:3843,diencephalic neoplasm,DOID:1659,supratentorial cancer
+DOID:0050448,hereditary mucosal leukokeratosis,DOID:37,skin disease
+DOID:3909,bronchogenic lung adenocarcinoma,DOID:3910,lung adenocarcinoma
+UBERON:3000590,supraorbital flange,UBERON:4100000,skeletal element projection
+DOID:2801,nonspecific interstitial pneumonia,DOID:2797,idiopathic interstitial pneumonia
+UBERON:0003652,metatarsal bone of digit 3,UBERON:0013583,metapodium bone 3
+HP:0011036,Abnormality of renal excretion,HP:0012211,Abnormal renal physiology
+UBERON:0006480,Brodmann (1909) area 39,UBERON:0013529,Brodmann area
+DOID:0050587,trichotillomania,DOID:10937,impulse control disorder
+DOID:238,pupil disease,DOID:5614,eye disease
+HP:0100935,Sclerosis of the middle phalanx of the 2nd toe,HP:0100947,Sclerosis of the middle phalanges of the toes
+UBERON:0005820,pontine flexure,UBERON:0002050,embryonic structure
+HP:0004606,Unossified vertebral bodies,HP:0004599,Absent or minimally ossified vertebral bodies
+HP:0009201,Stippling of the epiphysis of the proximal phalanx of the 5th finger,HP:0010277,Stippling of the epiphyses of the proximal phalanges of the hand
+UBERON:0011472,ventral lateral sacrocaudal muscle,UBERON:0003665,tail muscle
+DOID:13399,color blindness,DOID:1432,blindness
+HP:0006731,Follicular thyroid carcinoma,HP:0002890,Thyroid carcinoma
+DOID:4000,ovary transitional cell carcinoma,DOID:2152,ovary epithelial cancer
+HP:0012044,Seesaw nystagmus,HP:0012043,Pendular nystagmus
+HP:0100183,Enlarged epiphysis of the middle phalanx of the 4th toe,HP:0100069,Enlarged epiphyses of the 4th toe
+HP:0001204,Distal symphalangism (hands),HP:0009700,Synostosis involving bones of the fingers
+HP:0007183,Focal T2 hyperintense basal ganglia lesion,HP:0012751,Abnormal basal ganglia MRI signal intensity
+DOID:6723,malignant type AB thymoma,DOID:3280,mixed type thymoma
+UBERON:0001326,levator ani muscle,UBERON:0001325,muscle of pelvis
+UBERON:0013121,proximal epiphysis of phalanx of pes,UBERON:0011973,epiphysis of phalanx of pes
+NCBITaxon:451867,Dothideomycetidae,NCBITaxon:147541,Dothideomycetes
+HP:0009563,Distal/middle symphalangism of 2nd finger,HP:0001204,Distal symphalangism (hands)
+HP:0005289,Abnormality of the nasolabial region,HP:0000366,Abnormality of the nose
+CL:0002054,Fraction E immature B cell,CL:0000816,immature B cell
+UBERON:0009621,tail somite,UBERON:0002329,somite
+UBERON:2000740,epaxial region somite 5,UBERON:0003900,epaxial myotome region
+UBERON:0007321,lateral saphenous vein,UBERON:0013145,accessory saphenous vein
+HP:0007881,Central corneal dystrophy,HP:0011493,Central opacification of the cornea
+UBERON:0003517,kidney blood vessel,UBERON:0003497,abdomen blood vessel
+UBERON:2005381,dorsal fin proximal radial bone 4,UBERON:2000947,dorsal fin proximal radial bone
+UBERON:4200079,dorsal iliac process,UBERON:4100000,skeletal element projection
+DOID:2555,granulomatous angiitis,DOID:865,vasculitis
+DOID:7398,cerebral primitive neuroectodermal tumor,DOID:368,cerebrum cancer
+UBERON:0005164,ascending limb of loop of Henle,UBERON:0004135,distal tubule
+HP:0003347,Impaired lymphocyte transformation with phytohemagglutinin,HP:0004332,Abnormality of lymphocytes
+HP:0100767,Abnormality of the placenta,HP:0001194,Abnormalities of placenta and umbilical cord
+UBERON:0004876,urogenital ridge,UBERON:0005423,developing anatomical structure
+DOID:13117,paronychia,DOID:4123,nail disease
+HP:0009424,Osteolytic defects of the distal phalanx of the 3rd finger,HP:0009839,Osteolytic defects of the distal phalanges of the hand
+HP:0001663,Ventricular fibrillation,HP:0004308,Ventricular arrhythmia
+HP:0004429,Recurrent viral infections,HP:0002719,Recurrent infections
+CL:1001111,kidney loop of henle thin descending limb epithelial cell,CL:1000616,kidney outer medulla cell
+UBERON:2000831,sclerotome somite 17,UBERON:0003089,sclerotome
+DOID:6525,choroid mixed cell melanoma,DOID:6522,mixed cell uveal melanoma
+HP:0008785,Delayed ossification of pubic rami,HP:0009105,Abnormal ossification of the pubic bone
+HP:0001395,Hepatic fibrosis,HP:0001392,Abnormality of the liver
+UBERON:0003043,posterior part of anterior commissure,UBERON:0005970,brain commissure
+HP:0100685,Abnormality of Sharpey fibers,HP:0003549,Abnormality of connective tissue
+UBERON:0013206,nasal tentacle,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0007350,Hyperreflexia in upper limbs,HP:0001347,Hyperreflexia
+HP:0100454,Osteolytic defects of the middle phalanx of the 5th toe,HP:0010387,Osteolytic defects of the phalanges of the 5th toe
+UBERON:0012281,perianal gland,UBERON:0002365,exocrine gland
+CL:0002239,ooblast,CL:0000670,primordial germ cell
+DOID:5758,malignant mesenchymoma,DOID:2668,mesenchymoma
+DOID:9745,perianal hematoma,DOID:9746,hemorrhoid
+DOID:8781,rubella,DOID:934,viral infectious disease
+DOID:2782,rectosigmoid junction cancer,DOID:12192,sigmoid colon cancer
+DOID:4556,lung large cell carcinoma,DOID:3908,non-small cell lung carcinoma
+HP:0010464,Streak ovary,HP:0008724,Hypoplasia of the ovary
+HP:0010348,Broad phalanges of the 2nd toe,HP:0010174,Broad phalanx of the toes
+UBERON:0006931,stomach glandular region mucosa,UBERON:0001199,mucosa of stomach
+UBERON:4300026,anterior ventrolateral plate,UBERON:0008907,dermal bone
+HP:0010089,Osteolytic defects of the proximal phalanx of the hallux,HP:0010052,Abnormality of the proximal phalanx of the hallux
+UBERON:0012121,respiratory velum,UBERON:0000171,respiration organ
+UBERON:0003359,epithelium of submandibular gland,UBERON:0003236,epithelium of lower jaw
+HP:0008316,Abnormal mitochondria in muscle tissue,HP:0003287,Abnormality of mitochondrial metabolism
+HP:0005525,Spontaneous hemolytic crises,HP:0001878,Hemolytic anemia
+UBERON:2001930,accessory vomerine tooth plate,UBERON:0011164,neurocranium bone
+UBERON:2007043,hindbrain neural tube,UBERON:0005291,embryonic tissue
+UBERON:0004513,skeletal muscle tissue of internal intercostal muscle,UBERON:0003898,skeletal muscle tissue of trunk
+UBERON:0013218,rete mirabile,UBERON:0002049,vasculature
+UBERON:0013677,serrated projection of ctenactinium,UBERON:4100000,skeletal element projection
+HP:0000729,Autism spectrum disorder,HP:0100851,Abnormal emotion/affect behavior
+DOID:6197,conventional malignant hemangiopericytoma,DOID:264,hemangiopericytoma
+UBERON:0002229,interparietal bone,UBERON:0011164,neurocranium bone
+DOID:13366,Stiff-Person syndrome,DOID:480,movement disease
+UBERON:0004148,cardiac vein,UBERON:0013140,systemic vein
+HP:0010379,Duplication of phalanx of the 4th toe,HP:0010336,Abnormality of the phalanges of the 4th toe
+HP:0009327,Ivory epiphysis of the middle phalanx of the 3rd finger,HP:0010263,Ivory epiphyses of the middle phalanges of the hand
+HP:0007117,Corticospinal tract atrophy,HP:0007372,Atrophy/Degeneration involving the corticospinal tracts
+UBERON:0015876,pelvic lymph node,UBERON:0000029,lymph node
+UBERON:0000993,oviduct,UBERON:0005156,reproductive structure
+CL:0002401,mature dendritic epithelial T cell precursor,CL:0002404,fetal thymocyte
+HP:0007879,Allergic conjunctivitis,HP:0000509,Conjunctivitis
+HP:0009995,Partial duplication of the middle phalanx of the 5th finger,HP:0010005,Partial duplication of the middle phalanges of the hand
+UBERON:0014668,distal interphalangeal joint of manual digit 2,UBERON:0007729,interphalangeal joint of manual digit 2
+UBERON:0001144,testicular vein,UBERON:0001638,vein
+UBERON:2001701,basibranchial 5 bone,UBERON:2001919,basibranchial 5 element
+CL:0002304,non-pigmented ciliary epithelial cell,CL:0005012,multi-ciliated epithelial cell
+UBERON:0001354,inferior epigastric artery,UBERON:0003520,pelvis blood vessel
+HP:0007843,Attenuation of retinal blood vessels,HP:0008046,Abnormality of the retinal vasculature
+UBERON:2002065,ural centrum 1,UBERON:0004120,mesoderm-derived structure
+DOID:7409,vulvar non-keratinizing squamous cell carcinoma,DOID:2101,vulva squamous cell carcinoma
+DOID:13222,submucous uterine fibroid,DOID:13223,uterine fibroid
+UBERON:0003829,urethra muscle,UBERON:0004120,mesoderm-derived structure
+UBERON:0004674,facial nerve root,UBERON:0006843,root of cranial nerve
+UBERON:0011197,parathyroid epithelium,UBERON:0000486,multilaminar epithelium
+CL:0000179,progesterone secreting cell,CL:0000174,steroid hormone secreting cell
+HP:0100943,Sclerosis of the proximal phalanx of the hallux,HP:0100930,Sclerosis of the phalanges of the hallux
+UBERON:0006006,metoptic pilar,UBERON:0010313,neural crest-derived structure
+DOID:12335,male genital organ vascular disease,DOID:48,male reproductive system disease
+HP:0010783,Erythema,HP:0011276,Vascular skin abnormality
+HP:0005586,Hyperpigmentation in sun-exposed areas,HP:0000953,Hyperpigmentation of the skin
+UBERON:0001829,major salivary gland,UBERON:0015212,lateral structure
+UBERON:0011385,parotidoauricular muscle,UBERON:0001583,extrinsic auricular muscle
+DOID:17,musculoskeletal system disease,DOID:7,disease of anatomical entity
+UBERON:2000194,dorsal accessory optic nucleus,UBERON:0014450,pretectal nucleus
+HP:0009626,Contractures of the interphalangeal joint of the thumb,HP:0009600,Flexion contracture of thumb
+UBERON:0010212,laryngeal apparatus,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009232,Symphalangism affecting the proximal phalanx of the 5th finger,HP:0004218,Symphalangism of the 5th finger
+CL:0001023,"Kit-positive, CD34-positive common myeloid progenitor",CL:0001030,CD117-positive common myeloid progenitor OR CD217-positive common lymphoid progenitor
+UBERON:0009078,pessulus,UBERON:0004119,endoderm-derived structure
+UBERON:0011693,extraembryonic portion of umbilical artery,UBERON:0000478,extraembryonic structure
+HP:0100440,Bullet-shaped distal phalanx of the 3rd toe,HP:0010361,Bullet-shaped phalanges of the 3rd toe
+HP:0010021,Ivory epiphysis of the 1st metacarpal,HP:0009191,Ivory epiphyses of the metacarpals
+HP:0009765,Low hanging columella,HP:0009929,Abnormality of the columella
+HP:0002138,Subarachnoid hemorrhage,HP:0002170,Intracranial hemorrhage
+DOID:0060098,osteoblastoma,DOID:0060094,bone benign neoplasm
+DOID:12959,lagophthalmos,DOID:530,eyelid disease
+DOID:11714,gestational diabetes,DOID:9351,diabetes mellitus
+HP:0009419,Stippling of the epiphyses of the 3rd finger,HP:0010237,Epiphyseal stippling of finger phalanges
+HP:0010147,Stippling of the epiphysis of the distal phalanx of the hallux,HP:0010124,Abnormality of the epiphysis of the distal phalanx of the hallux
+UBERON:0004300,distal phalanx,UBERON:0003221,phalanx
+UBERON:0005673,left lung endothelium,UBERON:0003365,epithelium of left lung
+HP:0002326,Transient ischemic attack,HP:0002637,Cerebral ischemia
+HP:0003982,Absent ulna,HP:0006495,Aplasia/Hypoplasia of the ulna
+HP:0001504,Metacarpal osteolysis,HP:0001163,Abnormality of the metacarpal bones
+UBERON:0000107,cleavage stage,UBERON:0000067,embryo stage part
+HP:0010334,Polydactyly affecting the 3rd toe,HP:0010320,Abnormality of the 3rd toe
+NCBITaxon:5042,Eurotiales,NCBITaxon:451871,Eurotiomycetidae
+DOID:9786,bulbar polio,DOID:0050515,paralytic poliomyelitis
+UBERON:0010026,ventral part of pharyngeal pouch 3,UBERON:0000490,unilaminar epithelium
+UBERON:0001645,trigeminal nerve,UBERON:0001785,cranial nerve
+UBERON:2000271,radial bone,UBERON:0002513,endochondral bone
+UBERON:0010298,intramembranous scleral ossicle,UBERON:0003462,facial bone
+HP:0009584,Osteolytic defects of the proximal phalanx of the 2nd finger,HP:0009544,Abnormality of the proximal phalanx of the 2nd finger
+HP:0006992,Anterior basal encephalocele,HP:0002084,Encephalocele
+UBERON:0012086,lumen of parabronchus,UBERON:0012085,lumen of tertiary bronchus
+CL:0000234,phagocyte,CL:0000219,motile cell
+DOID:13943,acute gonococcal prostatitis,DOID:14654,prostatitis
+UBERON:2001406,kinethmoid bone,UBERON:0002513,endochondral bone
+UBERON:0015216,nasal meatus,UBERON:0002553,anatomical cavity
+UBERON:0002651,anterior horn of lateral ventricle,UBERON:0002285,telencephalic ventricle
+UBERON:0004927,submucosa of cecum,UBERON:0003331,submucosa of colon
+UBERON:0011024,extrinsic extensor muscle of manus,UBERON:0000311,extensor muscle
+UBERON:0006142,common plantar digital vein,UBERON:0006139,plantar digital vein
+UBERON:4200038,subscapular fossa,UBERON:0004704,bone fossa
+HP:0010277,Stippling of the epiphyses of the proximal phalanges of the hand,HP:0010245,Abnormality of the epiphyses of the proximal phalanges of the hand
+UBERON:0011649,levator operculi,UBERON:0005493,hyoid muscle
+UBERON:0004658,mandible head,UBERON:0010313,neural crest-derived structure
+UBERON:0012615,umbilical smooth muscle,UBERON:0001135,smooth muscle tissue
+CL:0000353,blastoderm cell,CL:0000007,early embryonic cell
+UBERON:0003590,main bronchus connective tissue,UBERON:0003592,bronchus connective tissue
+UBERON:0001512,skin of ankle,UBERON:0001513,skin of pes
+HP:0002836,Bladder exstrophy,HP:0000014,Abnormality of the bladder
+HP:0012353,Decreased fucosylation of N-linked protein glycosylation,HP:0012352,Abnormal fucosylation of protein N-linked glycosylation
+UBERON:0005140,metanephric short nephron,UBERON:0004195,short nephron
+HP:0009540,Contracture of the proximal interphalangeal joint of the 2nd finger,HP:0009537,Flexion contracture of the 2nd finger
+UBERON:0011575,styloid process of ulna,UBERON:0004120,mesoderm-derived structure
+HP:0000612,Iris coloboma,HP:0000589,Coloboma
+DOID:5392,acidophil adenoma,DOID:3829,pituitary adenoma
+UBERON:3000796,imbricate neural arch,UBERON:0003861,neural arch
+HP:0009239,Aplasia/Hypoplasia of the distal phalanx of the 5th finger,HP:0009376,Aplasia/Hypoplasia of the phalanges of the 5th finger
+HP:0005759,Small flat posterior fossa,HP:0000932,Abnormality of the posterior cranial fossa
+HP:0003713,Muscle fiber necrosis,HP:0004303,Abnormality of muscle fibers
+UBERON:2001018,myotome somite 25,UBERON:0003082,myotome
+UBERON:0005257,manual digit mesenchyme,UBERON:0003859,forelimb mesenchyme
+UBERON:0007775,secondary tooth,UBERON:0001091,calcareous tooth
+UBERON:0009841,upper rhombic lip,UBERON:0002050,embryonic structure
+DOID:8564,lip cancer,DOID:8618,oral cavity cancer
+DOID:10719,toxic diffuse goiter,DOID:7998,hyperthyroidism
+UBERON:0003903,bursa of Fabricius,UBERON:0004177,hemopoietic organ
+HP:0002157,Azotemia,HP:0004364,Abnormality of nitrogen compound homeostasis
+UBERON:0002304,layer of dentate gyrus,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009428,Curved distal phalanx of the 3rd finger,HP:0009838,Curved distal phalanges of the hand
+HP:0000105,Enlarged kidneys,HP:0012210,Abnormal renal morphology
+UBERON:4000109,mineralized hyaline cartilage tissue,UBERON:4000013,mineralized tissue
+UBERON:3000916,apophysis proximalis,UBERON:0000064,organ part
+UBERON:0003687,foramen magnum,UBERON:0005744,bone foramen
+UBERON:0008960,melon organ,UBERON:0010053,echolocation organ
+HP:0005117,Elevated diastolic blood pressure,HP:0000822,Hypertension
+HP:0009491,Enlarged epiphyses of the 2nd finger,HP:0010231,Enlarged epiphyses of the phalanges of the hand
+HP:0002595,Ileus,HP:0005214,Intestinal obstruction
+UBERON:0006493,seventh cervical spinal cord segment,UBERON:0007714,cervical subsegment of spinal cord
+UBERON:2000439,superficial pelvic abductor,UBERON:0014795,pelvic appendage muscle
+UBERON:3010650,cephalodorsosubpharyngeus,UBERON:3000224,hyobranchial muscle
+DOID:5829,uterine ligament endometrioid adenocarcinoma,DOID:3700,uterine ligament adenocarcinoma
+DOID:3377,small cell osteogenic sarcoma,DOID:3378,conventional central osteosarcoma
+CL:0000474,pericardial nephrocyte,CL:0002520,nephrocyte
+UBERON:0001888,lateral olfactory tract,UBERON:0002265,olfactory tract
+DOID:4284,anal margin carcinoma,DOID:4908,anal carcinoma
+DOID:9563,bronchiectasis,DOID:1176,bronchial disease
+UBERON:4200063,ectocondylar tubercle,UBERON:0004120,mesoderm-derived structure
+DOID:2536,chronic inflammatory demyelinating polyneuritis,DOID:2537,inflammatory and toxic neuropathy
+HP:0000215,Thick upper lip vermilion,HP:0012471,Thick vermilion border
+CL:0002243,smooth muscle cell of sphincter of pupil,CL:0000358,sphincter associated smooth muscle cell
+UBERON:0004205,inner medullary collecting duct,UBERON:0006555,excretory tube
+UBERON:0002809,right temporal lobe,UBERON:0001871,temporal lobe
+UBERON:0006597,quadrate bone,UBERON:0011597,bone of upper jaw
+HP:0000144,Decreased fertility,HP:0000080,Abnormality of genital physiology
+HP:0009636,Triangular shaped proximal phalanx of the thumb,HP:0009858,Triangular shaped proximal phalanges of the hand
+UBERON:0001396,lateral thoracic artery,UBERON:0001637,artery
+HP:0003722,Neck flexor weakness,HP:0000467,Neck muscle weakness
+NCBITaxon:1769,Mycobacterium leprae,NCBITaxon:1763,Mycobacterium
+DOID:4968,Nelson syndrome,DOID:3952,adrenal cortex disease
+UBERON:0002854,eleventh thoracic dorsal root ganglion,UBERON:0002835,thoracic dorsal root ganglion
+DOID:11181,serous glue ear,DOID:11180,non-suppurative otitis media
+HP:0003572,Low plasma citrulline,HP:0011965,Abnormality of citrulline metabolism
+HP:0100254,Stenosis of the medullary cavity of the long bones,HP:0100253,Abnormality of the medullary cavity of the long bones
+HP:0004321,Bladder fistula,HP:0100589,Urogenital fistula
+UBERON:0013739,base of crypt of lieberkuhn,UBERON:0011184,epithelium of crypt of lieberkuhn
+UBERON:0003706,laryngeal vocal fold,UBERON:0004119,endoderm-derived structure
+HP:0011707,Mobitz I atrioventricular block,HP:0011706,Second degree atrioventricular block
+UBERON:0003397,mesentery of duodenum,UBERON:0001170,mesentery of small intestine
+DOID:12016,frontal lobe neoplasm,DOID:368,cerebrum cancer
+UBERON:0015020,otic capsule endochondral element,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0009712,endocardium of right ventricle,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:8304,lymph node palisaded myofibroblastoma,DOID:10619,lymph node cancer
+DOID:698,dentin sensitivity,DOID:214,teeth hard tissue disease
+HP:0100421,Partial duplication of the middle phalanx of the 5th toe,HP:0100403,Duplication of the middle phalanx of the 5th toe
+HP:0006019,Reduced proximal interphalangeal joint space,HP:0006261,Abnormality of phalangeal joints of the hand
+DOID:0050061,erysipeloid,DOID:0050338,primary bacterial infectious disease
+CL:0000355,skeletal muscle stem cell,CL:0000188,skeletal muscle cell
+HP:0008112,Plantar flexion contractures,HP:0008366,Contractures involving the joints of the feet
+HP:0005484,Postnatal microcephaly,HP:0000252,Microcephaly
+DOID:14227,azoospermia,DOID:12336,male infertility
+UBERON:0013241,embryonic urethral groove,UBERON:0014403,male anatomical structure
+HP:0100551,Neoplasm of the trachea,HP:0002778,Abnormality of the trachea
+UBERON:0008992,chorion frondosum,UBERON:0004120,mesoderm-derived structure
+HP:0012740,Papilloma,HP:0008069,Neoplasm of the skin
+DOID:0060089,endocrine organ benign neoplasm,DOID:0060085,organ system benign neoplasm
+HP:0009186,Contracture of the metacarpophalangeal joint of the 5th finger,HP:0009183,Joint contractures of the 5th finger
+UBERON:0015022,hindlimb endochondral element,UBERON:0015061,limb endochondral element
+HP:0100124,Cone-shaped epiphysis of the proximal phalanx of the 2nd toe,HP:0100090,Abnormality of the epiphysis of the proximal phalanx of the 2nd toe
+UBERON:0001141,right renal vein,UBERON:0001140,renal vein
+NCBITaxon:5094,Talaromyces,NCBITaxon:28568,Trichocomaceae
+UBERON:0003403,skin of forearm,UBERON:0002427,arm skin
+UBERON:0006026,interdigital region between manual digits 1 and 2,UBERON:0006016,interdigital region between digits 1 and 2
+UBERON:2000239,mesocoracoid bone,UBERON:4300092,mesocoracoid element
+UBERON:2001025,occipital lateral line neuromast,UBERON:0008904,neuromast
+UBERON:0010262,operculum of brain,UBERON:0000477,anatomical cluster
+HP:0002354,Memory impairment,HP:0011446,Abnormality of higher mental function
+HP:0005585,Spotty hyperpigmentation,HP:0007400,Irregular hyperpigmentation
+NCBITaxon:35325,dsRNA viruses,NCBITaxon:10239,Viruses
+UBERON:0000076,external ectoderm,UBERON:0000490,unilaminar epithelium
+UBERON:3000655,processus dorsalis of lamella alaris,UBERON:0004120,mesoderm-derived structure
+UBERON:0010251,anterior meningeal artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:5082,liver cirrhosis,DOID:409,liver disease
+UBERON:0003279,endothelium of trachea,UBERON:0001901,epithelium of trachea
+UBERON:3000171,fenestra prechoanalis,UBERON:3000316,nasal opening
+HP:0001067,Neurofibromas,HP:0008069,Neoplasm of the skin
+HP:0011663,Right ventricular cardiomyopathy,HP:0001638,Cardiomyopathy
+UBERON:0001049,neural tube,UBERON:0005291,embryonic tissue
+UBERON:0011660,hypoplastron,UBERON:0011657,dermal element of plastron
+UBERON:0012644,trophosome,UBERON:0000062,organ
+UBERON:0001256,wall of urinary bladder,UBERON:0006554,urinary system structure
+HP:0100396,Short proximal phalanx of the 4th toe,HP:0100376,Aplasia/Hypoplasia of the proximal phalanx of the 4th toe
+HP:0002747,Respiratory insufficiency due to muscle weakness,HP:0002093,Respiratory insufficiency
+UBERON:2001857,hyoidean artery,UBERON:0003469,respiratory system artery
+DOID:11820,bladder dome cancer,DOID:11054,urinary bladder cancer
+UBERON:0003936,postoptic commissure,UBERON:0011590,commissure of diencephalon
+UBERON:0010169,moustache,UBERON:0010165,collection of hair on face
+UBERON:0001938,lateral mammillary nucleus,UBERON:0002789,regional part of posterior hypothalamic region
+HP:0011816,Parietal encephalocele,HP:0002084,Encephalocele
+CL:0002092,bone marrow cell,CL:0001035,bone cell
+UBERON:0011078,endolymphatic space,UBERON:0002553,anatomical cavity
+UBERON:0012276,endometrium glandular epithelium,UBERON:0004811,endometrium epithelium
+HP:0010519,Increased fetal movement,HP:0001557,Prenatal movement abnormality
+UBERON:0006609,corpus cavernosum,UBERON:0008324,erectile tissue
+UBERON:2000627,posterior ceratohyal,UBERON:0002513,endochondral bone
+UBERON:0002652,posterior median eminence,UBERON:0002784,regional part of diencephalon
+UBERON:0001712,upper eyelid,UBERON:0001711,eyelid
+DOID:9719,proliferative vitreoretinopathy,DOID:9720,vitreous disease
+UBERON:0005777,glomerular basement membrane,UBERON:0005769,basement membrane of epithelium
+CL:0000285,stalk cell,CL:0000263,vegetative cell (sensu Mycetozoa)
+HP:0003869,Cortical thinning (humeral),HP:0010629,Abnormality of the cortex of the humerus
+UBERON:0008895,splanchnocranium,UBERON:0011159,primary subdivision of cranial skeletal system
+UBERON:3000653,pars glenoidalis of quadratojugal,UBERON:0000064,organ part
+CL:0002466,small intestine serosal dendritic cell,CL:0002465,CD11b-positive dendritic cell
+HP:0002398,Degeneration of anterior horn cells,HP:0007373,Atrophy/Degeneration involving motor neurons
+UBERON:4200007,transverse pelvic ridge,UBERON:0004120,mesoderm-derived structure
+UBERON:0012368,circular muscle layer,UBERON:0004923,organ component layer
+DOID:14457,Brucella abortus brucellosis,DOID:11077,brucellosis
+HP:0003072,Hypercalcemia,HP:0004363,Abnormality of calcium homeostasis
+UBERON:0004779,respiratory system lamina propria,UBERON:0000030,lamina propria
+DOID:9153,variola minor,DOID:8736,smallpox
+UBERON:0001073,ileocecal junction,UBERON:0007651,anatomical junction
+UBERON:0002102,forelimb,UBERON:0002101,limb
+HP:0100212,Triangular epiphysis of the distal phalanx of the 5th toe,HP:0100087,Triangular epiphyses of the 5th toe
+HP:0003070,Elbow ankylosis,HP:0009811,Abnormality of the elbow
+DOID:4610,intestinal benign neoplasm,DOID:0050624,gastrointestinal system benign neoplasm
+UBERON:2001562,hypural 3,UBERON:2000364,hypural
+UBERON:3000759,omosternum,UBERON:0005181,thoracic segment organ
+HP:0011292,EEG with occipital sharp waves,HP:0011196,EEG with focal sharp waves
+UBERON:0005207,tonsil capsule,UBERON:0004119,endoderm-derived structure
+HP:0100164,Pseudoepiphysis of the proximal phalanx of the 3rd toe,HP:0100062,Pseudoepiphyses of the 3rd toe
+UBERON:3000381,paranasal commissure,UBERON:0003933,cranial cartilage
+DOID:13080,Jaccoud's syndrome,DOID:417,hypersensitivity reaction type II disease
+NCBITaxon:6032,Apansporoblastina,NCBITaxon:6029,Microsporidia
+HP:0006977,Grammar-specific speech disorder,HP:0002167,Neurological speech impairment
+UBERON:1000003,dewlap,UBERON:1000021,skin of face
+HP:0000915,Pectus excavatum of inferior sternum,HP:0000767,Pectus excavatum
+HP:0005324,Disturbance of facial expression,HP:0005346,Abnormal facial expression
+HP:0002181,Cerebral edema,HP:0000969,Edema
+CL:0002311,mammotroph,CL:0000439,prolactin secreting cell
+UBERON:0002269,pupillary membrane,UBERON:0010312,immature eye
+HP:0001817,Absent fingernail,HP:0001798,Anonychia
+DOID:4054,prostate sarcoma,DOID:10283,prostate cancer
+UBERON:0006638,remnant of urachus,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0004343,Abnormality of glycosphingolipid metabolism,HP:0010969,Abnormality of glycolipid metabolism
+HP:0005115,Supraventricular arrhythmia,HP:0011675,Arrhythmia
+UBERON:0002549,ventral trigeminal tract,UBERON:0007702,tract of brain
+DOID:4193,intracranial thrombosis,DOID:6713,cerebrovascular disease
+HP:0009530,Ivory epiphysis of the proximal phalanx of the 2nd finger,HP:0009501,Abnormality of the epiphysis of the proximal phalanx of the 2nd finger
+UBERON:0003052,midbrain-hindbrain boundary,UBERON:0004121,ectoderm-derived structure
+UBERON:0003298,roof plate of neural tube,UBERON:0005291,embryonic tissue
+HP:0004923,Hyperphenylalaninemia,HP:0010893,Abnormality of phenylalanine metabolism
+UBERON:0003099,cranial neural crest,UBERON:0004121,ectoderm-derived structure
+HP:0012227,Urethral stricture,HP:0008661,Urethral stenosis
+DOID:5534,renal pelvis squamous cell carcinoma,DOID:4919,renal pelvis carcinoma
+DOID:8456,choline deficiency disease,DOID:5113,nutritional deficiency disease
+UBERON:0001680,lacrimal bone,UBERON:0003462,facial bone
+HP:0100042,Broad 4th toe,HP:0001837,Broad toe
+DOID:9463,otitis externa,DOID:379,external ear disease
+CL:1000494,epithelial cell of renal tubule,CL:1000507,kidney tubule cell
+HP:0011551,Right sided atrium to left ventricle and absent left sided atrioventricular connection,HP:0011547,Absent left sided atrioventricular connection
+DOID:2344,polyclonal hypergammaglobulinemia,DOID:2345,plasma protein metabolism disease
+UBERON:2001991,lateral bone,UBERON:0007842,membrane bone
+HP:0009891,Underdeveloped supraorbital ridges,HP:0100538,Abnormality of the supraorbital ridges
+HP:0006517,Congenital alveolar proteinosis,HP:0002088,Abnormality of the lung
+DOID:12783,migraine without aura,DOID:6364,migraine
+UBERON:0002741,diagonal band of Broca,UBERON:0002316,white matter
+UBERON:2001991,lateral bone,UBERON:0004120,mesoderm-derived structure
+DOID:3493,signet ring cell adenocarcinoma,DOID:299,adenocarcinoma
+UBERON:0013118,sulcus of brain,UBERON:0000093,sulcus
+UBERON:0005613,left dorsal aorta,UBERON:0000947,aorta
+HP:0008398,Hypoplastic fifth fingernail,HP:0001804,Hypoplastic fingernail
+HP:0004296,Abnormality of gastrointestinal vasculature,HP:0012718,Morphological abnormality of the gastrointestinal tract
+CL:0002388,multinucleate arthroconidium,CL:0002386,multinucleate macroconidium
+UBERON:2001623,type 1 odontode,UBERON:0004121,ectoderm-derived structure
+UBERON:3001003,cloacal fold,UBERON:0004120,mesoderm-derived structure
+DOID:12206,dengue hemorrhagic fever,DOID:12205,dengue disease
+HP:0000545,Myopia,HP:0000539,Abnormality of refraction
+CL:0011006,lugaro cell,CL:0000402,CNS interneuron
+UBERON:0011013,spinalis muscle,UBERON:0003897,axial muscle
+HP:0009853,Bullet-shaped proximal phalanges of the hand,HP:0009834,Abnormality of the proximal phalanges of the hand
+HP:0008053,Aplasia/Hypoplasia of the iris,HP:0008055,Aplasia/Hypoplasia affecting the uvea
+UBERON:0002773,anterior transverse temporal gyrus,UBERON:0003939,transverse gyrus of Heschl
+HP:0012664,Reduced ejection fraction,HP:0003116,Abnormal echocardiogram
+UBERON:0003854,spinal cord neural plate,UBERON:0003075,neural plate
+UBERON:2002117,ovipositor,UBERON:0005156,reproductive structure
+HP:0006163,Enlarged metacarpophalangeal joints,HP:0006261,Abnormality of phalangeal joints of the hand
+UBERON:0000309,body wall,UBERON:0009569,subdivision of trunk
+CL:0002259,neuroepithelial stem cell,CL:0000723,somatic stem cell
+UBERON:0004214,upper leg nerve,UBERON:0003431,leg nerve
+DOID:0050211,swine influenza,DOID:8469,influenza
+UBERON:0009101,ammocoete,UBERON:0002548,larva
+UBERON:3010750,descending branch of the vagus nerve,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0004573,Anterior wedging of  T11,HP:0008422,Vertebral wedging
+HP:0003791,Deposits immunoreactive to beta-amyloid protein,HP:0004303,Abnormality of muscle fibers
+HP:0008789,Cone-shaped capital femoral epiphysis,HP:0010574,Abnormality of the epiphysis of the femoral head
+DOID:9739,eustachian tube disease,DOID:11180,non-suppurative otitis media
+HP:0001894,Thrombocytosis,HP:0011873,Abnormal platelet count
+UBERON:0012296,urethral crest,UBERON:0000063,organ segment
+HP:0008318,Elevated leukocyte alkaline phosphatase,HP:0003155,Elevated alkaline phosphatase
+UBERON:0002618,trochlear nerve fibers,UBERON:0006843,root of cranial nerve
+HP:0009846,Curved middle phalanges of the hand,HP:0009770,Curved phalanges of the hand
+HP:0003928,Cortical thickening of humeral diaphysis,HP:0003859,Cortical diaphyseal thickening of the upper limbs
+UBERON:0005360,inferior glossopharyngeal IX ganglion,UBERON:0001701,glossopharyngeal ganglion
+DOID:9724,purulent endophthalmitis,DOID:4692,endophthalmitis
+DOID:0050843,oromandibular dystonia,DOID:0050836,focal dystonia
+UBERON:0013746,basibranchial element,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:3663,cutaneous mastocytosis,DOID:350,mastocytosis
+HP:0004972,Elevated mean arterial pressure,HP:0000822,Hypertension
+DOID:946,dientamoebiasis,DOID:2789,parasitic protozoa infectious disease
+DOID:1920,hyperuricemia,DOID:0060158,acquired metabolic disease
+UBERON:0003555,spinal cord pia mater,UBERON:0003292,meninx of spinal cord
+CL:0002198,oncocyte,CL:0002076,endo-epithelial cell
+UBERON:0012355,manual acropodium region,UBERON:0012354,acropodium region
+UBERON:0010550,pedal digit 4 metatarsal pre-cartilage condensation,UBERON:0010583,pedal digit 4 phalanx pre-cartilage condensation
+UBERON:0014436,lesser sciatic notch,UBERON:0014430,sciatic notch
+HP:0005296,Occlusive vascular disease,HP:0004950,Peripheral arterial disease
+UBERON:0009053,dorsal nucleus of trapezoid body,UBERON:0007633,nucleus of trapezoid body
+UBERON:0014790,lingual septum,UBERON:0003037,septum
+DOID:11668,hypopigmentation of eyelid,DOID:10123,pigmentation disease
+HP:0010307,Stridor,HP:0002795,Functional respiratory abnormality
+HP:0006755,Cutaneous leiomyosarcoma,HP:0100243,Leiomyosarcoma
+HP:0100443,Curved middle phalanx of the 3rd toe,HP:0010362,Curved phalanges of the 3rd toe
+DOID:0050125,dengue shock syndrome,DOID:37,skin disease
+HP:0005106,Abnormality of the vertebral endplates,HP:0003312,Abnormal form of the vertebral bodies
+HP:0008821,Hypoplastic inferior ilia,HP:0000946,Hypoplastic ilia
+UBERON:0006840,nucleus of lateral lemniscus,UBERON:0002308,nucleus of brain
+HP:0009819,Lower limb phocomelia,HP:0009829,Phocomelia
+HP:0001182,Tapered finger,HP:0100807,Long fingers
+UBERON:0013133,superior phrenic artery,UBERON:0002057,phrenic artery
+UBERON:3010751,ramus muscularis of vagus nerve,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005101,early distal convoluted tubule,UBERON:0008408,distal tubular epithelium
+UBERON:0001680,lacrimal bone,UBERON:0015212,lateral structure
+HP:0001419,X-linked recessive inheritance,HP:0001417,X-linked inheritance
+DOID:0050471,Carney complex,DOID:0050736,autosomal dominant disease
+UBERON:0011140,superficial part of masseter muscle,UBERON:0000064,organ part
+UBERON:0004153,ventricular septum intermedium,UBERON:0002094,interventricular septum
+CL:0000119,Golgi cell,CL:0000117,CNS neuron (sensu Vertebrata)
+UBERON:2001752,pre-narial cartilage,UBERON:0003932,cartilage element of chondrocranium
+HP:0009171,Triangular epiphyses of the metacarpals,HP:0005913,Abnormality of metacarpal epiphyses
+DOID:6033,heart fibrosarcoma,DOID:5262,heart sarcoma
+HP:0000869,Secondary amenorrhea,HP:0000141,Amenorrhea
+HP:0006011,Cuboidal metacarpal,HP:0010049,Short metacarpal
+UBERON:0001455,cuboid bone,UBERON:0010721,distal tarsal bone
+HP:0007190,Neuronal loss in the cerebral cortex,HP:0002538,Abnormality of the cerebral cortex
+UBERON:0002412,vertebra,UBERON:0010913,vertebral element
+HP:0000555,Leukocoria,HP:0000615,Abnormality of the pupil
+UBERON:0004506,skeletal muscle tissue of masseter,UBERON:0001134,skeletal muscle tissue
+HP:0004609,Patchy distortion of vertebrae,HP:0003312,Abnormal form of the vertebral bodies
+UBERON:0000923,germ layer,UBERON:0010316,germ layer / neural crest
+DOID:5297,rectum leiomyosarcoma,DOID:1995,rectum sarcoma
+UBERON:0013707,iliac spine,UBERON:4100000,skeletal element projection
+DOID:4223,pyoderma,DOID:2723,dermatitis
+DOID:14174,central neurocytoma,DOID:3541,cerebral ventricle cancer
+UBERON:0008281,tooth bud,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005424,presumptive retinal pigmented epithelium,UBERON:0010312,immature eye
+HP:0003960,Exostoses of the forearm bones,HP:0002973,Abnormality of the forearm
+UBERON:0006564,superficial palmar arch,UBERON:0004563,forelimb digital vein
+UBERON:2007026,forebrain neural keel,UBERON:0000479,tissue
+UBERON:2000287,superior dorsal flexor,UBERON:0000366,flexor muscle
+HP:0011407,Proportionate tall stature,HP:0000098,Tall stature
+CL:0002561,outer root sheath cell,CL:0002559,hair follicle cell
+CL:0002075,brush cell of trachebronchial tree,CL:0002204,brush cell
+DOID:6603,Kummell's disease,DOID:1123,spondyloarthropathy
+HP:0010022,Pseudoepiphysis of the 1st metacarpal,HP:0010275,Pseudoepiphyses of the proximal phalanges of the hand
+UBERON:0005270,renal cortex interstitium,UBERON:0005215,kidney interstitium
+UBERON:0001324,common fibular nerve,UBERON:0003431,leg nerve
+UBERON:0015865,pancreaticosplenic lymph node,UBERON:0015860,visceral abdominal lymph node
+HP:0011830,Abnormality of oral mucosa,HP:0000163,Abnormality of the oral cavity
+CL:0002678,memory regulatory T cell,CL:0000813,memory T cell
+UBERON:0007106,chorionic villus,UBERON:0002050,embryonic structure
+HP:0007879,Allergic conjunctivitis,HP:0012393,Allergy
+UBERON:0015103,distal tarsal bone 1 cartilage,UBERON:0015064,autopod cartilage
+HP:0011082,Conical primary incisor,HP:0011065,Conical incisor
+UBERON:0006481,Brodmann (1909) area 44,UBERON:0013529,Brodmann area
+UBERON:0009689,anterior inferior cerebellar artery,UBERON:0003496,head blood vessel
+UBERON:0011619,stylohyoid bone,UBERON:0002513,endochondral bone
+UBERON:0006146,dorsal digital artery of manus,UBERON:0004553,forelimb digital artery
+DOID:9857,interstitial keratitis,DOID:65,connective tissue disease
+HP:0008771,Aplasia/Hypoplasia of the ear,HP:0000598,Abnormality of the ear
+UBERON:0003617,trachea elastic tissue,UBERON:0003571,trachea connective tissue
+UBERON:4000102,osteodentine,UBERON:0010365,odontoid tissue
+UBERON:0008963,hoof,UBERON:0009564,distal limb integumentary appendage
+DOID:8078,childhood central nervous system germinoma,DOID:4438,central nervous system germinoma
+HP:0010624,Aplastic/hypoplastic toenail,HP:0008388,Abnormality of the toenail
+UBERON:0000057,urethra,UBERON:0004120,mesoderm-derived structure
+UBERON:0012238,ureteric bud trunk,UBERON:0010137,polarized epithelium
+HP:0006162,Soft tissue swelling of interphalangeal joints,HP:0006261,Abnormality of phalangeal joints of the hand
+HP:0007076,Extrapyramidal muscular rigidity,HP:0002063,Rigidity
+HP:0200105,Absent fifth toenail,HP:0001802,Absent toenail
+DOID:216,dental caries,DOID:214,teeth hard tissue disease
+DOID:3494,bile duct signet ring cell carcinoma,DOID:4897,bile duct carcinoma
+UBERON:0001539,dorsalis pedis artery,UBERON:0001637,artery
+HP:0008244,Congenital adrenal hypoplasia,HP:0000835,Adrenal hypoplasia
+UBERON:2005346,extrapancreatic duct,UBERON:0004119,endoderm-derived structure
+HP:0005349,Hypoplasia of the epiglottis,HP:0010565,Aplasia/Hypoplasia of the Epiglottis
+UBERON:0002219,subfornical organ,UBERON:0002791,regional part of telencephalon
+CL:0002292,type I cell of carotid body,CL:0000710,neurecto-epithelial cell
+UBERON:3010682,proximal-most prepollical element,UBERON:4200140,prepollical element
+HP:0002842,Recurrent Burkholderia cepacia infections,HP:0005420,Recurrent gram-negative bacterial infections
+UBERON:0002644,intermediate orbital gyrus,UBERON:0007193,orbital gyrus
+HP:0100163,Ivory epiphysis of the proximal phalanx of the 3rd toe,HP:0100093,Abnormality of the epiphysis of the proximal phalanx of the 3rd toe
+UBERON:0010042,1st arch mesenchyme,UBERON:0009494,pharyngeal arch mesenchymal region
+UBERON:0001799,vitreous chamber of eyeball,UBERON:0006311,chamber of eyeball
+UBERON:0010579,manual digit 5 phalanx pre-cartilage condensation,UBERON:0015029,manual digit 5 phalanx endochondral element
+HP:0005132,Pericardial constriction,HP:0001697,Abnormality of the pericardium
+DOID:7912,mixed oligodendroglioma-astrocytoma,DOID:5076,mixed glioma
+HP:0008197,Absence of pubertal development,HP:0008373,Puberty and gonadal disorders
+NCBITaxon:46919,Whitewater Arroyo virus,NCBITaxon:208897,New world arenaviruses
+DOID:8527,monocytic leukemia,DOID:8692,myeloid leukemia
+HP:0007110,Central hypoventilation,HP:0002791,Hypoventilation
+DOID:13096,Sneddon syndrome,DOID:0050828,artery disease
+UBERON:0004835,epididymis smooth muscle,UBERON:0001135,smooth muscle tissue
+HP:0010132,Irregular epiphysis of the proximal phalanx of the hallux,HP:0010118,Irregular epiphyses of the hallux
+HP:0006631,Hypoplastic distal segments of scapulae,HP:0000882,Hypoplastic scapulae
+UBERON:0000303,adductor longus,UBERON:0011144,adductor muscle of hip
+DOID:512,epididymal neoplasm,DOID:2998,testicular cancer
+HP:0006492,Aplasia/Hypoplasia of the fibula,HP:0006493,Aplasia/Hypoplasia involving bones of the lower limbs
+NCBITaxon:63418,Trichophyton equinum,NCBITaxon:5550,Trichophyton
+CL:0000997,immature CD8_alpha-negative CD11b-positive dendritic cell,CL:0000999,CD4-positive CD11b-positive dendritic cell
+UBERON:3010738,M. palmaris profundis,UBERON:0010891,pectoral complex muscle
+HP:0003327,Axial muscle weakness,HP:0001324,Muscle weakness
+DOID:14291,LEOPARD syndrome,DOID:0050736,autosomal dominant disease
+UBERON:0004740,basibranchial bone,UBERON:0001474,bone element
+DOID:7708,perianal skin Paget's disease,DOID:4284,anal margin carcinoma
+UBERON:2005336,presumptive swim bladder,UBERON:0006598,presumptive structure
+HP:0011831,Deviated nasal tip,HP:0000436,Abnormality of the nasal tip
+DOID:0050434,Andersen-Tawil syndrome,DOID:2843,long QT syndrome
+CL:1001601,adrenal gland glandular cell,CL:0000150,glandular epithelial cell
+HP:0010504,Increased length of the tibia,HP:0002992,Abnormality of the tibia
+HP:0009856,Patchy sclerosis of the proximal phalanges of the hand,HP:0009772,Patchy sclerosis of the phalanges of the hand
+HP:0000608,Macular degeneration,HP:0001103,Abnormality of the macula
+UBERON:4300089,propterygium bone,UBERON:4300083,propterygium element
+HP:0011880,Acute disseminated intravascular coagulation,HP:0005521,Disseminated intravascular coagulation
+UBERON:0007293,presumptive rhombomere 6,UBERON:0006598,presumptive structure
+UBERON:0010842,calcaneum cartilage element,UBERON:0005863,cartilaginous condensation
+HP:0007409,"Absence of subcutaneous fat over entire body except buttocks, hips, and thighs",HP:0003758,Reduced subcutaneous adipose tissue
+UBERON:0002489,coronal suture,UBERON:0004120,mesoderm-derived structure
+UBERON:0006964,pars distalis of adenohypophysis,UBERON:0010371,ecto-epithelium
+CL:0002379,meningothelial cell,CL:0000710,neurecto-epithelial cell
+UBERON:0009755,spermaceti,UBERON:0000463,portion of organism substance
+HP:0100315,Lewy bodies,HP:0100314,Cerebral inclusion bodies
+DOID:0060190,ileocolitis,DOID:8778,Crohn's disease
+UBERON:0003398,mesentery of jejunum,UBERON:0001170,mesentery of small intestine
+HP:0004632,cervical segmentation defects,HP:0003422,Vertebral segmentation defect
+HP:0000821,Hypothyroidism,HP:0002926,Abnormality of thyroid physiology
+HP:0010969,Abnormality of glycolipid metabolism,HP:0010968,Abnormality of liposaccharide metabolism
+HP:0007450,Increased groin pigmentation with raindrop depigmentation,HP:0009123,Mixed hypo- and hyperpigmentation of the skin
+HP:0010401,Symphalangism affecting the proximal phalanx of the 2nd toe,HP:0010358,Abnormality of the proximal phalanx of the 2nd toe
+HP:0009402,Stippling of the epiphyses of the 4th finger,HP:0009174,Abnormality of the epiphyses of the 4th finger
+DOID:2800,acute interstitial pneumonia,DOID:2797,idiopathic interstitial pneumonia
+HP:0000021,Megacystis,HP:0010955,Dilatation of the bladder
+UBERON:0010060,pharyngeal opening of pharyngotympanic tube,UBERON:0000464,anatomical space
+UBERON:4300035,supraneural element,UBERON:0010363,endochondral element
+HP:0003607,4-Hydroxyphenylacetic aciduria,HP:0010996,Abnormality of monocarboxylic acid metabolism
+HP:0000802,Impotence,HP:0000080,Abnormality of genital physiology
+UBERON:0014855,posterior leaflet of mitral valve,UBERON:0007151,mitral valve leaflet
+HP:0100936,Sclerosis of the middle phalanx of the 3rd toe,HP:0100947,Sclerosis of the middle phalanges of the toes
+UBERON:2000193,diffuse nuclei,UBERON:0006568,hypothalamic nucleus
+UBERON:0005974,posterior cerebellomedullary cistern,UBERON:0004049,cerebellomedullary cistern
+UBERON:0001640,celiac artery,UBERON:0001193,hepatic artery
+HP:0003239,Phosphoethanolaminuria,HP:0003110,Abnormality of urine homeostasis
+NCBITaxon:1485,Clostridium,NCBITaxon:31979,Clostridiaceae
+HP:0001410,Decreased liver function,HP:0001392,Abnormality of the liver
+HP:0005905,Abnormal cervical curvature,HP:0003319,Abnormality of the cervical spine
+UBERON:0010170,region of neural crest,UBERON:0004121,ectoderm-derived structure
+HP:0002150,Hypercalciuria,HP:0004363,Abnormality of calcium homeostasis
+UBERON:0001921,reuniens nucleus,UBERON:0015233,nucleus of dorsal thalamus
+HP:0009527,Enlarged epiphysis of the proximal phalanx of the 2nd finger,HP:0010271,Enlarged epiphyses of the proximal phalanges of the hand
+HP:0011278,Intrapulmonary sequestration,HP:0100632,Pulmonary sequestration
+HP:0010205,Bullet-shaped proximal phalanges of the toes,HP:0010175,Bullet-shaped phalanges of the toes
+DOID:540,strabismus,DOID:9834,hyperopia
+UBERON:0005469,right thymus lobe,UBERON:0005483,thymus lobe
+DOID:7878,uterine corpus atypical polypoid adenomyoma,DOID:4993,atypical polypoid adenomyoma
+HP:0007156,Asymmetric limb muscle stiffness,HP:0003552,Muscle stiffness
+UBERON:2002079,leptocephalous larva,UBERON:0002548,larva
+DOID:0050579,glycogen storage disease XV,DOID:2747,glycogen storage disease
+UBERON:0004009,cerebellum posterior vermis,UBERON:0004720,cerebellar vermis
+DOID:4409,folliculitis,DOID:421,hair disease
+UBERON:0005193,ethmoidal artery,UBERON:0004573,systemic artery
+HP:0100079,Cone-shaped epiphyses of the 5th toe,HP:0010164,Cone-shaped epiphyses of the toes
+UBERON:0007356,crop,UBERON:0005181,thoracic segment organ
+CL:0002055,CD38-negative immature B cell,CL:0000816,immature B cell
+UBERON:0009038,sulcus ampullaris,UBERON:0006800,anatomical line
+CL:0002205,brush cell of lobular bronchiole,CL:0002208,brush cell of bronchus
+HP:0010111,Short phalanx of hallux,HP:0010058,Aplasia/Hypoplasia of the phalanges of the hallux
+UBERON:0015847,upper left incisor tooth,UBERON:0015212,lateral structure
+UBERON:2005382,dorsal fin proximal radial bone 5,UBERON:2000947,dorsal fin proximal radial bone
+UBERON:0001835,lower lip,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009262,Bracket epiphysis of the proximal phalanx of the 4th finger,HP:0009248,Abnormality of the epiphysis of the proximal phalanx of the 4th finger
+HP:0004253,Absent trapezium/absent ossification of the trapezium,HP:0004252,Abnormality of the trapezium
+HP:0009611,Bifid distal phalanx of the thumb,HP:0010004,Partial duplication of the distal phalanges of the hand
+HP:0001034,Hypermelanotic macule,HP:0012733,Macule
+DOID:2734,keratosis follicularis,DOID:161,keratosis
+DOID:9821,choroideremia,DOID:8466,retinal degeneration
+UBERON:0006009,cusp of cardiac valve,UBERON:0010313,neural crest-derived structure
+DOID:6118,renal pelvis inverted papilloma,DOID:6119,renal pelvis urothelial papilloma
+UBERON:0000476,acellular anatomical structure,UBERON:0000061,anatomical structure
+HP:0000483,Astigmatism,HP:0100691,Abnormality of the curvature of the cornea
+UBERON:0011346,palatine raphe,UBERON:0004121,ectoderm-derived structure
+UBERON:0005406,perirenal fat,UBERON:0001013,adipose tissue
+CL:0000796,"CD8-alpha-beta-positive, alpha-beta intraepithelial T cell",CL:0000797,alpha-beta intraepithelial T cell
+UBERON:0009680,set of upper jaw teeth,UBERON:0009678,tooth row
+HP:0008160,3-hydroxydicarboxylic aciduria,HP:0003215,Dicarboxylic aciduria
+UBERON:0002761,inferior frontal sulcus,UBERON:0013118,sulcus of brain
+HP:0009593,Peripheral Schwannoma,HP:0008069,Neoplasm of the skin
+UBERON:0005653,upper jaw molar epithelium,UBERON:0003235,epithelium of upper jaw
+UBERON:0001252,adventitia of ureter,UBERON:0004120,mesoderm-derived structure
+HP:0001622,Premature birth,HP:0001197,Abnormality of prenatal development or birth
+CL:0000887,lymph node subcapsular sinus macrophage,CL:0000868,lymph node macrophage
+UBERON:2001798,epicentral bone,UBERON:2000526,intermuscular bone
+CL:0002088,interstitial cell of Cajal,CL:0000710,neurecto-epithelial cell
+UBERON:0011300,gray matter of telencephalon,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:600,animal phobia,DOID:599,specific phobia
+HP:0010378,Triangular shaped phalanges of the 4th toe,HP:0010336,Abnormality of the phalanges of the 4th toe
+DOID:9697,gonococcal keratitis,DOID:4677,keratitis
+HP:0012527,Abnormal alpha granule content,HP:0012483,Abnormal alpha granules
+UBERON:0006106,cochlear canal,UBERON:0004120,mesoderm-derived structure
+UBERON:2000692,symplectic,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0010847,ulna pre-cartilage condensation,UBERON:0010882,limb bone pre-cartilage condensation
+DOID:9993,hypoglycemia,DOID:1428,endocrine pancreas disease
+UBERON:0006764,anterior communicating artery,UBERON:0006347,communicating artery
+UBERON:0003666,upper jaw molar,UBERON:0011593,maxillary tooth
+UBERON:0002221,fontanelle,UBERON:0004120,mesoderm-derived structure
+DOID:1979,focal chorioretinitis,DOID:8886,chorioretinitis
+HP:0004619,Lumbar kyphoscoliosis,HP:0008454,Lumbar kyphosis
+DOID:11149,aqueous misdirection,DOID:1686,glaucoma
+DOID:7408,vulvar keratoacanthoma-like carcinoma,DOID:2101,vulva squamous cell carcinoma
+NCBITaxon:723,Actinobacillus ureae,NCBITaxon:713,Actinobacillus
+CL:0000112,columnar neuron,CL:0000540,neuron
+HP:0000893,Bulging of the costochondral junction,HP:0000919,Abnormality of the costochondral junction
+DOID:2706,synovium cancer,DOID:201,connective tissue cancer
+CL:0002325,mammary alveolar cell,CL:0002159,general ecto-epithelial cell
+UBERON:0002837,sacral dorsal root ganglion,UBERON:0000044,dorsal root ganglion
+UBERON:0004180,mammary gland fat,UBERON:0003584,mammary gland connective tissue
+HP:0010845,EEG with generalized slow activity,HP:0011203,EEG with abnormally slow frequencies
+HP:0001129,Large central visual field defect,HP:0001123,Visual field defect
+UBERON:0008888,vesical venous plexus,UBERON:0001593,venous plexus
+UBERON:2007042,spinal cord neural tube,UBERON:0005291,embryonic tissue
+HP:0005386,Recurrent protozoan infections,HP:0002719,Recurrent infections
+HP:0011304,Broad thumb,HP:0001172,Abnormality of the thumb
+DOID:16,integumentary system disease,DOID:7,disease of anatomical entity
+HP:0003463,Increased extraneuronal autofluorescent lipopigment,HP:0011813,Increased cerebral lipofuscin
+CL:0000557,granulocyte monocyte progenitor cell,CL:1001610,bone marrow hematopoietic cell
+DOID:0060039,autoimmune disease of skin and connective tissue,DOID:417,hypersensitivity reaction type II disease
+UBERON:0002884,intercalated amygdaloid nuclei,UBERON:0009663,telencephalic nucleus
+HP:0009152,Abnormality of the epiphyses of the 5th finger,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+HP:0009613,Duplication of the proximal phalanx of the thumb,HP:0009618,Abnormality of the proximal phalanx of the thumb
+DOID:2235,prothrombin deficiency,DOID:0050737,autosomal recessive disease
+HP:0009224,Triangular epiphysis of the middle phalanx of the 4th finger,HP:0009403,Triangular epiphyses of the 4th finger
+UBERON:2000832,sclerotome somite 2,UBERON:0003089,sclerotome
+HP:0003811,Neonatal death,HP:0011420,Death
+HP:0007633,Bilateral microphthalmos,HP:0000568,Microphthalmos
+UBERON:0001496,ascending aorta,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0011535,chondroglossus muscle,UBERON:0004121,ectoderm-derived structure
+HP:0009709,Increased CSF interferon alpha,HP:0002921,Abnormality of the cerebrospinal fluid
+UBERON:0001335,prostatic urethra,UBERON:0005156,reproductive structure
+UBERON:0005041,mucosa of respiratory bronchiole,UBERON:0005039,mucosa of bronchiole
+UBERON:0000994,spermathecum,UBERON:0005156,reproductive structure
+DOID:4479,pseudohypoaldosteronism,DOID:447,renal tubular transport disease
+UBERON:0015250,inferior olivary commissure,UBERON:0014649,white matter of medulla oblongata
+UBERON:0001429,pisiform,UBERON:0001480,proximal carpal bone
+HP:0006772,Renal angiomyolipoma,HP:0009726,Renal neoplasm
+DOID:3389,Papillon-Lefevre disease,DOID:3390,palmoplantar keratosis
+UBERON:0011532,female pubococcygeus muscle,UBERON:0014404,female anatomical structure
+UBERON:0008331,clitoral smooth muscle,UBERON:0014404,female anatomical structure
+HP:0006134,Enlarged metacarpal epiphyses,HP:0010580,Enlarged epiphyses
+DOID:3140,scleredema adultorum,DOID:3141,mucinoses
+HP:0009583,Curved proximal phalanx of the 2nd finger,HP:0009544,Abnormality of the proximal phalanx of the 2nd finger
+DOID:2689,lymphangiosarcoma,DOID:0060073,lymphatic system cancer
+HP:0001273,Abnormality of the corpus callosum,HP:0002500,Abnormality of the cerebral white matter
+DOID:9562,primary ciliary dyskinesia,DOID:0050737,autosomal recessive disease
+CL:0000553,megakaryocyte progenitor cell,CL:0000839,myeloid lineage restricted progenitor cell
+HP:0004732,Impaired renal uric acid clearance,HP:0011036,Abnormality of renal excretion
+HP:0008090,Ankylosis of feet small joints,HP:0001760,Abnormality of the foot
+UBERON:0010743,meningeal cluster,UBERON:0000477,anatomical cluster
+UBERON:0015785,acinus of olfactory gland,UBERON:0011858,acinus of exocrine gland
+UBERON:0001920,paraventricular nucleus of thalamus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0010367,conjunctival vein,UBERON:0003496,head blood vessel
+HP:0009340,Irregular epiphysis of the distal phalanx of the 3rd finger,HP:0010251,Irregular epiphyses of the distal phalanges of the hand
+DOID:0060047,writing disorder,DOID:8927,learning disability
+DOID:12958,paralytic lagophthalmos,DOID:12959,lagophthalmos
+UBERON:0006233,female genital tubercle,UBERON:0011757,differentiated genital tubercle
+DOID:0060165,Kleine-Levin syndrome,DOID:8619,recurrent hypersomnia
+HP:0001450,Y-linked inheritance,HP:0010985,Gonosomal inheritance
+UBERON:3011120,early proximal tubule,UBERON:0004120,mesoderm-derived structure
+UBERON:0002577,pericentral nucleus of inferior colliculus,UBERON:0003528,brain grey matter
+UBERON:0004301,middle phalanx,UBERON:0003221,phalanx
+UBERON:0011957,middle hepatic vein,UBERON:0001143,hepatic vein
+HP:0010020,Irregular epiphysis of the 1st metacarpal,HP:0010273,Irregular epiphyses of the proximal phalanges of the hand
+HP:0011627,Aorto-ventricular tunnel,HP:0001679,Abnormality of the aorta
+UBERON:0000106,zygote stage,UBERON:0000067,embryo stage part
+HP:0009249,Abnormality of the epiphysis of the distal phalanx of the 4th finger,HP:0009282,Abnormality of the distal phalanx of the 4th finger
+DOID:9408,acute myocardial infarction,DOID:5844,myocardial infarction
+HP:0010333,Flexion contracture of 3rd toe,HP:0010320,Abnormality of the 3rd toe
+HP:0012393,Allergy,HP:0100326,Immunologic hypersensitivity
+UBERON:0004695,arterial system smooth muscle,UBERON:0001135,smooth muscle tissue
+UBERON:0001644,trochlear nerve,UBERON:0001785,cranial nerve
+UBERON:0010011,collection of basal ganglia,UBERON:0010009,aggregate regional part of brain
+UBERON:0003358,epithelium of soft palate,UBERON:0003235,epithelium of upper jaw
+DOID:13133,HELLP syndrome,DOID:13129,severe pre-eclampsia
+DOID:3196,cellular schwannoma,DOID:3192,neurilemmoma
+UBERON:2001820,posterior nuchal plate,UBERON:0004247,bone of dorsum
+HP:0009585,Patchy sclerosis of the proximal phalanx of the 2nd finger,HP:0009544,Abnormality of the proximal phalanx of the 2nd finger
+HP:0001426,Multifactorial inheritance,HP:0000005,Mode of inheritance
+UBERON:4200173,dorsal ridge,UBERON:4100000,skeletal element projection
+HP:0000100,Nephrotic syndrome,HP:0012211,Abnormal renal physiology
+DOID:12837,thyroid crisis,DOID:50,thyroid gland disease
+HP:0005483,Abnormality of the epiglottis,HP:0001600,Abnormality of the larynx
+DOID:5595,papillary thymic adenocarcinoma,DOID:4923,thymus adenocarcinoma
+HP:0007894,Hypopigmentation of the fundus,HP:0008051,Abnormality of the retinal pigment epithelium
+DOID:84,osteochondritis dissecans,DOID:0080008,ischemic bone disease
+HP:0010276,Small epiphyses of the proximal phalanges of the hand,HP:0010245,Abnormality of the epiphyses of the proximal phalanges of the hand
+UBERON:0001257,trigone of urinary bladder,UBERON:0006554,urinary system structure
+UBERON:0002067,dermis,UBERON:0004120,mesoderm-derived structure
+CL:0011004,lens fiber cell,CL:0002222,vertebrate lens cell
+UBERON:0003591,lobar bronchus connective tissue,UBERON:0003592,bronchus connective tissue
+HP:0011118,Abnormality of tumor necrosis factor secretion,HP:0011113,Abnormality of cytokine secretion
+DOID:854,collagen disease,DOID:65,connective tissue disease
+UBERON:0012483,serosa of cloaca,UBERON:0000042,serous membrane
+HP:0012354,Increased fucosylation of N-linked protein glycosylation,HP:0012352,Abnormal fucosylation of protein N-linked glycosylation
+UBERON:3010379,inner fin tissue,UBERON:0000479,tissue
+HP:0000611,Choroid coloboma,HP:0000589,Coloboma
+HP:0012530,Abnormal number of dense granules,HP:0012484,Abnormal dense granules
+HP:0010054,Abnormality of the first metatarsal,HP:0010057,Abnormality of the phalanges of the hallux
+HP:0100919,Sclerosis of the phalanges of the 3rd finger,HP:0009316,Abnormality of the phalanges of the 3rd finger
+HP:0010301,Spinal dysraphism,HP:0000925,Abnormality of the vertebral column
+HP:0012215,Testicular microlithiasis,HP:0000035,Abnormality of the testis
+HP:0009494,Ivory epiphyses of the 2nd finger,HP:0100918,Sclerosis of the phalanges of the 2nd finger
+DOID:10283,prostate cancer,DOID:3856,male reproductive organ cancer
+HP:0005752,Flattened moderately deformed vertebrae,HP:0000926,Platyspondyly
+HP:0009340,Irregular epiphysis of the distal phalanx of the 3rd finger,HP:0009415,Irregular epiphyses of the 3rd finger
+CL:0000176,ecdysteroid secreting cell,CL:0000174,steroid hormone secreting cell
+HP:0001239,Wrist flexion contracture,HP:0100360,Contractures of the joints of the upper limbs
+UBERON:0016464,dorsum of nose,UBERON:0004121,ectoderm-derived structure
+UBERON:0002294,biliary system,UBERON:0000467,anatomical system
+UBERON:3000787,collum antibrachii,UBERON:0000064,organ part
+UBERON:0003244,epithelium of mammary gland,UBERON:0012275,meso-epithelium
+DOID:13135,exophthalmic ophthalmoplegia,DOID:12359,endocrine exophthalmos
+DOID:7334,nephrogenic adenoma,DOID:3116,kidney benign neoplasm
+UBERON:0004204,outer medullary collecting duct,UBERON:0006555,excretory tube
+UBERON:0005330,mesonephric nephron epithelium,UBERON:0004211,nephron epithelium
+CL:0002115,B220-positive CD38-positive unswitched memory B cell,CL:0002114,CD38-positive unswitched memory B cell
+UBERON:2001604,lateral ethmoid palatine process,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0002464,Spastic dysarthria,HP:0001260,Dysarthria
+UBERON:0010732,alisphenoid pre-cartilage condensation,UBERON:0009891,facial mesenchyme
+CL:0000741,spinal accessory motor neuron,CL:0000100,motor neuron
+UBERON:2000557,preural 1 vertebra,UBERON:2000734,preural vertebra
+HP:0005853,Congenital foot contraction deformities,HP:0002803,Congenital contracture
+HP:0004320,Vaginal fistula,HP:0100589,Urogenital fistula
+HP:0200049,Upper limb hypertonia,HP:0002509,Limb hypertonia
+UBERON:0006669,alveolar canal,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004986,mucosa of deferent duct,UBERON:0014403,male anatomical structure
+UBERON:0006492,sixth cervical spinal cord segment,UBERON:0007714,cervical subsegment of spinal cord
+UBERON:0012136,prehallux,UBERON:0005881,limb outgrowth
+HP:0012265,Ciliary dyskinesia,HP:0012262,Abnormal ciliary motility
+HP:0007797,Retinal vascular malformation,HP:0008046,Abnormality of the retinal vasculature
+UBERON:0014694,posterior auricular artery,UBERON:0004573,systemic artery
+UBERON:0010723,os vesalianum pedis,UBERON:0010721,distal tarsal bone
+UBERON:0001703,neurocranium,UBERON:0004120,mesoderm-derived structure
+DOID:1398,parasitic infectious disease,DOID:0050117,disease by infectious agent
+DOID:11162,respiratory failure,DOID:850,lung disease
+UBERON:3010651,levator bulbi,UBERON:3000224,hyobranchial muscle
+HP:0000558,Rieger anomaly,HP:0007676,Hypoplasia of the iris
+HP:0006589,Flaring of lower rib cage,HP:0000904,Flaring of rib cage
+UBERON:2205373,dorsal fin distal radial cartilage 2,UBERON:2105373,dorsal fin distal radial element 2
+HP:0009185,Contracture of the proximal interphalangeal joint of the 5th finger,HP:0009183,Joint contractures of the 5th finger
+UBERON:0012269,equine hindlimb splint bone,UBERON:0003608,hindlimb long bone
+UBERON:0010990,transversospinales muscle,UBERON:0003897,axial muscle
+DOID:13861,scleroperikeratitis,DOID:13452,scleritis
+UBERON:0005669,peritoneal cavity mesothelium,UBERON:0001136,mesothelium
+HP:0007717,Chronic irritative conjunctivitis,HP:0000509,Conjunctivitis
+UBERON:0007776,unerupted tooth,UBERON:0001091,calcareous tooth
+HP:0003944,Narrow joint spaces of the elbow,HP:0003943,Abnormality of the joint spaces of the elbow
+UBERON:0003053,ventricular zone,UBERON:0004121,ectoderm-derived structure
+UBERON:0000446,septum of telencephalon,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0015245,septal olfactory organ,UBERON:0000062,organ
+UBERON:0015077,centrale cartilage,UBERON:0015064,autopod cartilage
+CL:0000720,anterior cone cell (sensu Endopterygota),CL:0000718,cone cell (sensu Endopterygota)
+HP:0012750,T2 hypointense brainstem,HP:0012747,Abnormal brainstem MRI signal intensity
+HP:0007343,Limbic malformations,HP:0002060,Abnormality of the cerebrum
+UBERON:0002855,twelfth thoracic dorsal root ganglion,UBERON:0002835,thoracic dorsal root ganglion
+NCBITaxon:44537,Pyretophorus,NCBITaxon:44534,Cellia <subgenus>
+UBERON:0002615,ventral tegmental decussation,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0011627,orbital part of frontal bone,UBERON:0015212,lateral structure
+UBERON:2001946,mesethmoid-maxillary ligament,UBERON:0008846,skeletal ligament
+HP:0011708,Mobitz II atrioventricular block,HP:0011706,Second degree atrioventricular block
+CL:0002603,astrocyte of the cerebellum,CL:0000127,astrocyte
+UBERON:0000391,leptomeninx,UBERON:0002360,meninx
+UBERON:0015230,dorsal vessel heart,UBERON:0007100,primary circulatory organ
+HP:0012577,Thin glomerular basement membrane,HP:0000095,Abnormality of the glomerulus
+HP:0009585,Patchy sclerosis of the proximal phalanx of the 2nd finger,HP:0009551,Patchy sclerosis of the phalanges of the 2nd finger
+UBERON:0003384,skeletal muscle tissue of pharynx,UBERON:0004830,respiratory system skeletal muscle
+UBERON:0010899,synchronous hermaphroditic organism,UBERON:0007197,hermaphroditic organism
+UBERON:0000209,tetrapod frontal bone,UBERON:0008907,dermal bone
+CL:1000719,kidney inner medulla collecting duct intercalated cell,CL:1001432,kidney collecting duct intercalated cell
+UBERON:0010168,collection of eyelashes,UBERON:0010165,collection of hair on face
+UBERON:0011509,sphincter colli profundus muscle,UBERON:0002377,muscle of neck
+DOID:5395,functioning pituitary adenoma,DOID:3829,pituitary adenoma
+HP:0008691,Solitary bladder diverticulum,HP:0000015,Bladder diverticulum
+UBERON:0007023,adult organism,UBERON:0000468,multi-cellular organism
+UBERON:0009986,lateral epicondyle of femur,UBERON:0004120,mesoderm-derived structure
+HP:0009646,Patchy sclerosis of the distal phalanx of the thumb,HP:0100912,Sclerosis of the distal phalanx of the thumb
+UBERON:0012303,ureteral orifice,UBERON:0010418,urethral opening
+UBERON:0010408,ocular angle artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005871,palatine process of maxilla,UBERON:0010313,neural crest-derived structure
+UBERON:4300028,posterior ventrolateral plate,UBERON:0008907,dermal bone
+HP:0010788,Testicular neoplasm,HP:0010785,Gonadal neoplasm
+UBERON:0001142,left renal vein,UBERON:0001140,renal vein
+NCBITaxon:446,Legionella pneumophila,NCBITaxon:445,Legionella
+HP:0100576,Amaurosis fugax,HP:0000505,Visual impairment
+HP:0007109,Periventricular cysts,HP:0010576,Intracranial cystic lesion
+UBERON:0005869,maxillary process of inferior nasal concha,UBERON:4100000,skeletal element projection
+UBERON:3000656,processus posterodorsalis of lamella alaris,UBERON:0004120,mesoderm-derived structure
+NCBITaxon:59142,funestus group,NCBITaxon:59140,Myzomyia
+CL:1000465,chromaffin cell of ovary,CL:0000166,chromaffin cell
+UBERON:0010056,future tongue,UBERON:0003103,compound organ
+HP:0004875,Neonatal inspiratory stridor,HP:0005348,Inspiratory stridor
+DOID:6459,lipoma of the rectum,DOID:6460,large intestine lipoma
+HP:0005435,Impaired T cell function,HP:0011840,Abnormality of T cell physiology
+HP:0010542,Vestibular nystagmus,HP:0009591,Abnormality of the vestibulocochlear nerve
+DOID:3158,hand dermatosis,DOID:37,skin disease
+UBERON:0008918,ampulla of Lorenzini,UBERON:0010521,electroreceptor organ
+HP:0006415,Cortically dense long tubular bones,HP:0000935,Thickened cortex of long bones
+UBERON:0015015,supraoccipital endochondral element,UBERON:0004120,mesoderm-derived structure
+HP:0000794,IgA deposition in the glomerulus,HP:0000095,Abnormality of the glomerulus
+UBERON:3010613,laryngo-tracheal chamber,UBERON:0000464,anatomical space
+HP:0012452,Restless legs,HP:0002360,Sleep disturbance
+UBERON:0007590,cuboidal oviduct epithelium,UBERON:0004804,oviduct epithelium
+UBERON:2000628,caudal fin musculature,UBERON:0007271,appendage musculature
+UBERON:0010189,right atrium venous valve,UBERON:0005208,right atrium valve
+UBERON:2002162,ural vertebra,UBERON:0001095,caudal vertebra
+HP:0002151,Increased serum lactate,HP:0001941,Acidosis
+UBERON:0004354,male inguinal canal,UBERON:0014403,male anatomical structure
+UBERON:3000112,crista dentalis of premaxilla,UBERON:4100000,skeletal element projection
+UBERON:0013140,systemic vein,UBERON:0001638,vein
+HP:0001046,Intermittent jaundice,HP:0000952,Jaundice
+DOID:1616,benign eccrine breast spiradenoma,DOID:0060082,breast benign neoplasm
+UBERON:0004042,spleen secondary B follicle,UBERON:0001249,spleen lymphoid follicle
+HP:0010086,Broad proximal phalanx of the hallux,HP:0010052,Abnormality of the proximal phalanx of the hallux
+UBERON:0010375,pancreas dorsal primordium,UBERON:0004119,endoderm-derived structure
+DOID:445,Bartter disease,DOID:447,renal tubular transport disease
+HP:0009027,Foot dorsiflexor weakness,HP:0001436,Abnormality of the foot musculature
+UBERON:0008989,submocosal esophageal gland,UBERON:0003408,gland of gut
+UBERON:0002374,metacarpal bone,UBERON:0003607,forelimb long bone
+HP:0004004,Irregular radial epiphyses,HP:0010582,Irregular epiphyses
+HP:0011918,Fourth toe clinodactyly,HP:0001863,Toe clinodactyly
+UBERON:0005317,pulmonary artery endothelium,UBERON:0001917,endothelium of artery
+HP:0004922,Atypical hyperphenylalaninemia,HP:0010893,Abnormality of phenylalanine metabolism
+UBERON:0006636,lumbar artery,UBERON:0012254,abdominal aorta artery
+DOID:8937,Waldeyer's ring cancer,DOID:8557,oropharynx cancer
+UBERON:2000504,dorsal retractor,UBERON:0000933,pharyngeal muscle
+HP:0005340,Spastic/hyperactive bladder,HP:0000009,Functional abnormality of the bladder
+UBERON:0003133,reproductive organ,UBERON:0000062,organ
+HP:0011976,Elevated urinary catecholamines,HP:0011281,Abnormality of urine catecholamine concentration
+DOID:6678,tooth and nail syndrome,DOID:225,syndrome
+UBERON:2001561,hypural 2,UBERON:2000364,hypural
+HP:0004299,Hernia of the abdominal wall,HP:0100790,Hernia
+CL:0002633,respiratory basal cell,CL:0000646,basal cell
+UBERON:3010541,median pars intermedia,UBERON:0000064,organ part
+UBERON:0012243,nuptial pad,UBERON:0004121,ectoderm-derived structure
+DOID:7787,breast osteosarcoma,DOID:3357,extraosseous osteosarcoma
+UBERON:0011939,vibrissa outer root sheath,UBERON:0011937,vibrissa root sheath
+HP:0012361,Increased fucosylation of O-linked protein glycosylation,HP:0012359,Abnormal fucosylation of O-linked protein glycosylation
+UBERON:0004048,pontine cistern,UBERON:0004050,subarachnoid cistern
+HP:0012479,Temporomandibular joint crepitus,HP:0010754,Abnormality of the temporomandibular joint
+HP:0000858,Menstrual irregularities,HP:0000140,Abnormality of the menstrual cycle
+DOID:14250,Down syndrome,DOID:0080014,chromosomal disease
+HP:0001809,Split nail,HP:0002164,Nail dysplasia
+HP:0011817,Basal encephalocele,HP:0002084,Encephalocele
+UBERON:0007780,exudate,UBERON:0000463,portion of organism substance
+DOID:10976,membranous glomerulonephritis,DOID:2921,glomerulonephritis
+UBERON:2001480,dorsal anterior lateral line nerve,UBERON:0008906,lateral line nerve
+HP:0003991,Osteosclerosis of the ulna,HP:0002997,Abnormality of the ulna
+HP:0007541,Frontal cutaneous lipoma,HP:0012032,Lipoma
+HP:0000188,Short upper lip,HP:0000177,Abnormality of upper lip
+UBERON:0002461,anterior abdominal wall muscle,UBERON:0002378,muscle of abdomen
+HP:0009857,Symphalangism affecting the proximal phalanges of the hand,HP:0009773,Symphalangism affecting the phalanges of the hand
+CL:0000556,megakaryocyte,CL:1001610,bone marrow hematopoietic cell
+HP:0012258,Abnormal axonemal organization of motile cilia,HP:0005938,Abnormal respiratory motile cilium morphology
+UBERON:4200016,postbranchial lamina,UBERON:0004121,ectoderm-derived structure
+NCBITaxon:27458,Chrysops,NCBITaxon:59848,Chrysopsini
+UBERON:0001681,nasal bone,UBERON:0003462,facial bone
+CL:0002515,interrenal norepinephrine type cell,CL:0002516,interrenal chromaffin cell
+HP:0002663,Delayed epiphyseal ossification,HP:0010656,Abnormal epiphyseal ossification
+HP:0010411,Triangular shaped middle phalanx of the 2nd toe,HP:0010354,Triangular shaped phalanges of the 2nd toe
+HP:0010419,Symphalangism affecting the distal phalanx of the 2nd toe,HP:0010356,Abnormality of the distal phalanx of the 2nd toe
+UBERON:0010005,placental labyrinth villous,UBERON:0014404,female anatomical structure
+HP:0001114,Xanthelasma,HP:0000991,Xanthomatosis
+UBERON:0004330,proximal phalanx of manual digit 4,UBERON:0014504,proximal phalanx of digit 4
+HP:0009957,Complete duplication of the phalanges of the 2nd finger,HP:0009945,Duplication of phalanx of 2nd finger
+HP:0008972,Decreased activity of mitochondrial respiratory chain,HP:0011922,Abnormal activity of mitochondrial respiratory chain
+HP:0011293,EEG with central sharp waves,HP:0011196,EEG with focal sharp waves
+UBERON:0001105,clavicle,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0011790,Activating thyroid-stimulating hormone receptor (TSHR) defect,HP:0011789,Thyroid-stimulating hormone receptor (TSHR) defect
+DOID:4451,renal carcinoma,DOID:263,kidney cancer
+UBERON:0000387,meniscus,UBERON:0000061,anatomical structure
+UBERON:0002478,orbitosphenoid,UBERON:0015212,lateral structure
+CL:1000281,smooth muscle cell of cecum,CL:1000280,smooth muscle cell of colon
+HP:0008048,Abnormality of the line of Schwalbe,HP:0000481,Abnormality of the cornea
+UBERON:0012054,myocoele,UBERON:0002553,anatomical cavity
+UBERON:0001636,posterior cerebral artery,UBERON:0004449,cerebral artery
+DOID:13492,active cochlear Meniere's disease,DOID:9849,Meniere's disease
+DOID:11549,Adie syndrome,DOID:225,syndrome
+UBERON:0001574,palatoglossus muscle,UBERON:0000378,tongue muscle
+UBERON:0015204,glandular system,UBERON:0015203,non-connected functional system
+HP:0100603,Toxemia of pregnancy,HP:0002686,Prenatal maternal abnormality
+HP:0011452,Functional abnormality of the middle ear,HP:0000370,Abnormality of the middle ear
+UBERON:0008334,subarachnoid sulcus,UBERON:0013118,sulcus of brain
+DOID:13329,toxic optic neuropathy,DOID:1210,optic neuritis
+CL:0002472,MHC-II-low non-classical monocyte,CL:0002058,Gr1-low non-classical monocyte
+UBERON:0005319,mesonephric collecting duct,UBERON:0004120,mesoderm-derived structure
+HP:0002299,Brittle hair,HP:0010719,Abnormality of hair texture
+DOID:8408,Meckel's diverticulitis,DOID:7475,diverticulitis
+DOID:0050894,ameloblastoma,DOID:0060084,cell type benign neoplasm
+UBERON:0010533,metanephros cortex,UBERON:0001225,cortex of kidney
+HP:0001493,Falciform retinal fold,HP:0008052,Abnormal retinal folds
+HP:0004019,Irregular radial metaphysis,HP:0003850,Irregular metaphyses of the upper limbs
+HP:0009531,Pseudoepiphysis of the proximal phalanx of the 2nd finger,HP:0009501,Abnormality of the epiphysis of the proximal phalanx of the 2nd finger
+HP:0200070,Peripheral retinal atrophy,HP:0001105,Retinal atrophy
+UBERON:0001452,distal tarsal bone 1,UBERON:0010721,distal tarsal bone
+UBERON:0010910,opisthotic,UBERON:0004120,mesoderm-derived structure
+HP:0008610,Infantile sensorineural hearing impairment,HP:0011474,Childhood onset sensorineural hearing impairment
+HP:0008946,Pelvic girdle amyotrophy,HP:0003797,Limb-girdle muscle atrophy
+DOID:14499,Fabry disease,DOID:1927,sphingolipidosis
+DOID:12583,velocardiofacial syndrome,DOID:0080014,chromosomal disease
+UBERON:0001211,Peyer's patch,UBERON:0001962,gut-associated lymphoid tissue
+HP:0009852,Broad proximal phalanges of the hand,HP:0009834,Abnormality of the proximal phalanges of the hand
+DOID:9811,partial circumpapillary choroid dystrophy,DOID:9794,hereditary choroidal atrophy
+CL:0010004,mononuclear cell of bone marrow,CL:0000842,mononuclear cell
+DOID:8457,pellagra,DOID:5113,nutritional deficiency disease
+UBERON:0002774,posterior transverse temporal gyrus,UBERON:0003939,transverse gyrus of Heschl
+UBERON:0001129,subscapularis muscle,UBERON:0004120,mesoderm-derived structure
+HP:0100043,Broad 5th toe,HP:0001837,Broad toe
+UBERON:0003308,floor plate of telencephalon,UBERON:0002791,regional part of telencephalon
+HP:0002374,Diminished movement,HP:0100022,Abnormality of movement
+DOID:863,nervous system disease,DOID:7,disease of anatomical entity
+UBERON:2202027,pectoral fin proximal radial cartilage 2,UBERON:2102027,pectoral fin proximal radial element 2
+HP:0011431,Fetal fifth finger clinodactyly,HP:0011425,Fetal ultrasound soft marker
+DOID:5636,cervical adenosquamous carcinoma,DOID:3702,cervical adenocarcinoma
+HP:0008282,Unconjugated hyperbilirubinemia,HP:0002904,Hyperbilirubinemia
+DOID:3478,iris cancer,DOID:240,iris disease
+UBERON:0013684,right dorsal thalamus,UBERON:0015212,lateral structure
+CL:0002173,extraglomerular mesangial cell,CL:1000618,juxtaglomerular complex cell
+DOID:4407,phototoxic dermatitis,DOID:2772,irritant dermatitis
+HP:0004893,progressive respiratory failure,HP:0002093,Respiratory insufficiency
+HP:0012425,Stercoral ulcer,HP:0002250,Abnormality of the large intestine
+HP:0000216,Broad secondary alveolar ridge,HP:0000187,Broad alveolar ridges
+DOID:277,chorioangioma,DOID:254,hemangioma of intra-abdominal structure
+DOID:8512,puerperal pulmonary embolism,DOID:9477,pulmonary embolism
+HP:0009220,Ivory epiphysis of the middle phalanx of the 4th finger,HP:0010263,Ivory epiphyses of the middle phalanges of the hand
+DOID:0050844,spasmodic dystonia,DOID:0050836,focal dystonia
+UBERON:0001796,aqueous humor of eyeball,UBERON:0006312,ocular refractive media
+DOID:0060180,colitis,DOID:0050589,inflammatory bowel disease
+UBERON:0008863,stomach smooth muscle outer longitudinal layer,UBERON:0009034,stomach region
+HP:0011372,Aplasia of the inner ear,HP:0008774,Aplasia/Hypoplasia of the inner ear
+NCBITaxon:570,Klebsiella,NCBITaxon:543,Enterobacteriaceae
+HP:0004605,Absent vertebral body mineralization,HP:0004599,Absent or minimally ossified vertebral bodies
+HP:0009665,Bracket epiphysis of the proximal phalanx of the thumb,HP:0010258,Bracket epiphyses of the middle phalanges of the hand
+UBERON:0005619,secondary palatal shelf,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:10584,retinitis pigmentosa,DOID:8466,retinal degeneration
+UBERON:0002048,lung,UBERON:0004119,endoderm-derived structure
+UBERON:2001998,posttemporal-supracleithrum,UBERON:0007829,pectoral girdle bone
+UBERON:0002941,capsule of red nucleus,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0011597,Right aortic arch with left descending aorta and left ductus arteriosus,HP:0012020,Right aortic arch
+DOID:11390,cerebral arteritis,DOID:6713,cerebrovascular disease
+DOID:4648,familial retinoblastoma,DOID:768,retinoblastoma
+NCBITaxon:1280,Staphylococcus aureus,NCBITaxon:1279,Staphylococcus
+UBERON:0011121,cricothyroid joint,UBERON:0011120,laryngeal joint
+UBERON:0002496,stapes base,UBERON:0004119,endoderm-derived structure
+UBERON:0002232,olfactory gland,UBERON:0012278,gland of nasal mucosa
+HP:0003967,Sclerotic forearm bones,HP:0002973,Abnormality of the forearm
+UBERON:0003583,larynx connective tissue,UBERON:0004119,endoderm-derived structure
+CL:0002270,type EC2 enteroendocrine cell,CL:0002272,motilin secreting cell
+UBERON:0006262,malleus pre-cartilage condensation,UBERON:0015018,malleus endochondral element
+HP:0000350,Small forehead,HP:0000290,Abnormality of the forehead
+UBERON:0010514,strand of duvet hair,UBERON:0001037,strand of hair
+UBERON:0005807,rostral ventrolateral medulla,UBERON:0002678,regional part of medulla oblongata
+HP:0007490,Linear arrays of macular hyperkeratoses in flexural areas,HP:0000962,Hyperkeratosis
+UBERON:0005381,dentate gyrus granule cell layer,UBERON:0002304,layer of dentate gyrus
+UBERON:0011388,male bulbospongiosus muscle,UBERON:0011389,bulbospongiosus muscle
+CL:0002144,capillary endothelial cell,CL:0000071,blood vessel endothelial cell
+UBERON:0004140,primary heart field,UBERON:0004120,mesoderm-derived structure
+UBERON:0004273,cartilaginous joint suture,UBERON:0003685,cranial suture
+HP:0001935,Microcytic anemia,HP:0010972,Anemia of inadequate production
+HP:0001909,Leukemia,HP:0004377,Hematological neoplasm
+UBERON:0004311,distal phalanx of manual digit 2,UBERON:0003636,manual digit 2 phalanx
+UBERON:0008821,middle mediastinum,UBERON:0002224,thoracic cavity
+UBERON:0001435,carpal bone,UBERON:0005897,manus bone
+HP:0002342,"Intellectual disability, moderate",HP:0001249,Intellectual disability
+UBERON:0009116,thymoid,UBERON:0006925,digestive gland
+UBERON:0000395,cochlear ganglion,UBERON:0001714,cranial ganglion
+CL:0002651,endothelial cell of venous sinus of spleen,CL:0002262,endothelial cell of sinusoid
+UBERON:0003089,sclerotome,UBERON:0007530,migrating mesenchyme population
+HP:0001347,Hyperreflexia,HP:0007256,Abnormality of pyramidal motor function
+UBERON:0016386,paraaortic lymph node,UBERON:0000029,lymph node
+HP:0012070,Chondroitin sulfate excretion in urine,HP:0008155,Mucopolysacchariduria
+HP:0012319,Absent pigmentation of the abdomen,HP:0200098,Absent skin pigmentation
+UBERON:0002318,white matter of spinal cord,UBERON:0002316,white matter
+UBERON:0001383,muscle of leg,UBERON:0003663,hindlimb muscle
+UBERON:0002325,epithelium of urethra,UBERON:0005911,endo-epithelium
+UBERON:3000619,tympanosquamosal,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000218,myelinating Schwann cell,CL:0000217,insulating cell
+HP:0007374,Atrophy/Degeneration involving the caudate nucleus,HP:0012444,Brain atrophy
+DOID:807,carotid artery occlusion,DOID:5976,occlusion precerebral artery
+DOID:8292,atypical follicular adenoma,DOID:6204,follicular adenoma
+UBERON:0002065,posterior cardinal vein,UBERON:0004344,cardinal vein
+DOID:5078,ganglioglioma,DOID:0060084,cell type benign neoplasm
+DOID:14483,chorea gravidarum,DOID:12859,choreatic disease
+HP:0011862,Abnormal bone collagen fibril morphology,HP:0003330,Abnormal bone structure
+HP:0010902,Abnormality of glutamine family amino acid metabolism,HP:0004337,Abnormality of amino acid metabolism
+HP:0001373,Joint dislocation,HP:0001367,Abnormal joint morphology
+UBERON:0009843,prostate epithelial cord,UBERON:0000428,prostate epithelium
+UBERON:0001683,jugal bone,UBERON:0015212,lateral structure
+UBERON:0001323,tibial nerve,UBERON:0003431,leg nerve
+DOID:230,lateral sclerosis,DOID:231,motor neuron disease
+UBERON:0004323,middle phalanx of manual digit 5,UBERON:0003864,middle phalanx of manus
+UBERON:0015866,pyloric lymph node,UBERON:0015860,visceral abdominal lymph node
+DOID:0050472,monilethrix,DOID:0050736,autosomal dominant disease
+HP:0100583,Corneal perforation,HP:0000481,Abnormality of the cornea
+HP:0011083,Conical maxillary incisor,HP:0011065,Conical incisor
+HP:0000613,Photophobia,HP:0000504,Abnormality of vision
+UBERON:0002672,anterior subcentral sulcus,UBERON:0008334,subarachnoid sulcus
+UBERON:0001089,sweat,UBERON:0000456,bodily secretion
+CL:0000402,CNS interneuron,CL:0000117,CNS neuron (sensu Vertebrata)
+CL:1001111,kidney loop of henle thin descending limb epithelial cell,CL:1000453,epithelial cell of intermediate tubule
+UBERON:0005467,platysma,UBERON:0002377,muscle of neck
+HP:0008362,Aplasia/Hypoplasia of the hallux,HP:0001844,Abnormality of the hallux
+HP:0100221,Small epiphysis of the middle phalanx of the 5th toe,HP:0100098,Abnormality of the epiphysis of the middle phalanx of the 5th toe
+DOID:0050861,colorectal adenocarcinoma,DOID:9256,colorectal cancer
+HP:0003353,Propionyl-CoA carboxylase deficiency,HP:0004337,Abnormality of amino acid metabolism
+DOID:2033,communication disorder,DOID:0060038,specific developmental disorder
+UBERON:0002151,pontine nuclear group,UBERON:0002680,regional part of metencephalon
+HP:0010187,Bullet-shaped distal phalanges of the toes,HP:0010175,Bullet-shaped phalanges of the toes
+HP:0100937,Sclerosis of the middle phalanx of the 4th toe,HP:0100947,Sclerosis of the middle phalanges of the toes
+HP:0012056,Cutaneous melanoma,HP:0008069,Neoplasm of the skin
+UBERON:0005319,mesonephric collecting duct,UBERON:0001232,collecting duct of renal tubule
+UBERON:0011618,basihyal bone,UBERON:0002513,endochondral bone
+DOID:4959,epidermolysis bullosa dystrophica,DOID:2730,epidermolysis bullosa
+UBERON:0010956,pterygopharyngeal part of superior pharyngeal constrictor,UBERON:0000064,organ part
+UBERON:0007521,smooth muscle sphincter,UBERON:0004590,sphincter muscle
+HP:0007047,Atrophy of the dentate nucleus,HP:0100321,Abnormality of the dentate nucleus
+UBERON:0004509,skeletal muscle tissue of trapezius,UBERON:0001134,skeletal muscle tissue
+UBERON:0014376,thenar muscle,UBERON:0014375,intrinsic muscle of manus
+NCBITaxon:153136,Deltaretrovirus,NCBITaxon:327045,Orthoretrovirinae
+UBERON:0005427,corneal primordium,UBERON:0000479,tissue
+NCBITaxon:715340,Pleosporineae,NCBITaxon:92860,Pleosporales
+HP:0006679,Granulomatous coronary arteritis,HP:0012089,Arteritis
+UBERON:3000451,posterior ramus of pterygoid,UBERON:0004120,mesoderm-derived structure
+UBERON:0005427,corneal primordium,UBERON:0010312,immature eye
+UBERON:2000743,epaxial region somite 2,UBERON:0003900,epaxial myotome region
+UBERON:2007029,hindbrain neural keel,UBERON:0000479,tissue
+UBERON:0011900,perimysium,UBERON:0011822,dense irregular connective tissue
+UBERON:0001225,cortex of kidney,UBERON:0001851,cortex
+DOID:5511,dysgerminoma of ovary,DOID:5351,ovarian primitive germ cell tumor
+HP:0009335,Absent epiphysis of the distal phalanx of the 3rd finger,HP:0009332,Abnormality of the epiphysis of the distal phalanx of the 3rd finger
+DOID:959,esophagus squamous cell papilloma,DOID:0050624,gastrointestinal system benign neoplasm
+CL:1000371,transitional myocyte of right branch of atrioventricular bundle,CL:1000481,transitional myocyte of atrioventricular bundle
+UBERON:0005720,hindbrain venous system,UBERON:0004121,ectoderm-derived structure
+DOID:6518,Bartholin's gland adenomyoma,DOID:2068,Bartholin's gland neoplasm
+HP:0006723,Intestinal carcinoid,HP:0007378,Neoplasm of the gastrointestinal tract
+DOID:2556,relapsing polychondritis,DOID:2557,chondromalacia
+DOID:2560,morphine dependence,DOID:2559,opiate dependence
+CL:0000546,T-helper 2 cell,CL:0000492,CD4-positive helper T cell
+HP:0006479,Abnormality of the dental pulp,HP:0011061,Abnormality of dental structure
+DOID:3368,bone Ewing's sarcoma,DOID:3369,peripheral primitive neuroectodermal tumor
+UBERON:0008915,pore,UBERON:0000464,anatomical space
+NCBITaxon:29930,Ixodes pacificus,NCBITaxon:6944,Ixodes
+DOID:1391,Norum disease,DOID:1387,hypolipoproteinemia
+UBERON:0003975,internal female genitalia,UBERON:0003134,female reproductive organ
+HP:0004022,Sclerotic radial metaphysis with longitudinal striations,HP:0003854,Sclerosis of metaphyses of the upper limbs
+UBERON:0001873,caudate nucleus,UBERON:0009663,telencephalic nucleus
+CL:0002621,gingival epithelial cell,CL:0002251,epithelial cell of alimentary canal
+UBERON:0004834,hepatic duct smooth muscle,UBERON:0001135,smooth muscle tissue
+HP:0011364,White hair,HP:0011358,Generalized hypopigmentation of hair
+HP:0005285,Absent nasal bridge,HP:0000422,Abnormality of the nasal bridge
+DOID:2225,megakaryocytic tumor,DOID:0070004,myeloma
+UBERON:2005377,dorsal fin distal radial bone 6,UBERON:2000936,dorsal fin distal radial bone
+CL:0000619,support cell (sensu Nematoda),CL:0000378,support cell (sensu Nematoda and Protostomia)
+UBERON:0005024,mucosa of soft palate,UBERON:0005019,mucosa of palate
+UBERON:2001200,corpuscles of Stannius,UBERON:0004120,mesoderm-derived structure
+DOID:2708,mushroom workers' lung,DOID:841,extrinsic allergic alveolitis
+UBERON:0012066,lobar bronchus of left lung lower lobe,UBERON:0003405,lobar bronchus of left lung
+HP:0011300,Broad fingertip,HP:0001211,Abnormality of the fingertips
+UBERON:0009026,iliac circumflex artery,UBERON:0001637,artery
+HP:0006766,Papillary renal cell carcinoma,HP:0005584,Renal cell carcinoma
+HP:0007374,Atrophy/Degeneration involving the caudate nucleus,HP:0002339,Abnormality of the caudate nucleus
+UBERON:0001655,submental vein,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010400,Patchy sclerosis of the proximal phalanx of the 2nd toe,HP:0010358,Abnormality of the proximal phalanx of the 2nd toe
+UBERON:0006318,orbitalis muscle,UBERON:0006660,muscle layer
+UBERON:0001486,hip joint,UBERON:0011107,synovial joint of pelvic girdle
+UBERON:0009092,inner medulla vasa recta ascending limb,UBERON:0000064,organ part
+UBERON:0009747,tail fold of embryonic disc,UBERON:0005291,embryonic tissue
+UBERON:0006691,tentorium cerebelli,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:1436,corneal ectasia,DOID:10124,corneal disease
+DOID:9858,deep keratitis,DOID:4677,keratitis
+UBERON:0001414,median cubital vein,UBERON:0003507,arm blood vessel
+DOID:1458,postsurgical hypothyroidism,DOID:1459,hypothyroidism
+HP:0008069,Neoplasm of the skin,HP:0011793,Neoplasm by anatomical site
+UBERON:0003956,aqueous drainage system,UBERON:0000467,anatomical system
+UBERON:0011878,muscle layer of esophagus,UBERON:0006660,muscle layer
+UBERON:0001470,glenohumeral joint,UBERON:0008114,joint of girdle
+UBERON:0000378,tongue muscle,UBERON:0004120,mesoderm-derived structure
+DOID:2075,minor vestibular glands adenoma,DOID:2076,vulvar glandular tumor
+UBERON:0002459,inferior palpebral vein,UBERON:0014769,palpebral vein
+UBERON:0014854,anterior leaflet of mitral valve,UBERON:0007151,mitral valve leaflet
+UBERON:0013599,dorsal accessory nucleus of optic tract,UBERON:0013598,accessory nucleus of optic tract
+UBERON:0005933,hair root sheath,UBERON:0004121,ectoderm-derived structure
+UBERON:0004243,prostate gland smooth muscle,UBERON:0001135,smooth muscle tissue
+UBERON:0002885,accessory basal amygdaloid nucleus,UBERON:0009663,telencephalic nucleus
+CL:0002680,PP cell of intestine,CL:0000696,PP cell
+HP:0006894,Hypoplastic olfactory lobes,HP:0001341,Olfactory lobe agenesis
+UBERON:3000692,pedicel,UBERON:0000064,organ part
+UBERON:3000801,caput glenoidale,UBERON:0000064,organ part
+HP:0006494,Aplasia/Hypoplasia involving bones of the feet,HP:0006493,Aplasia/Hypoplasia involving bones of the lower limbs
+HP:0008625,Severe sensorineural hearing impairment,HP:0000407,Sensorineural hearing impairment
+DOID:12298,intrahepatic gall duct cancer,DOID:3121,gallbladder cancer
+UBERON:0006250,infundibular recess of 3rd ventricle,UBERON:0010371,ecto-epithelium
+UBERON:2001938,maxillary barbel,UBERON:2000622,barbel
+HP:0010110,Aplasia of the phalanges of the hallux,HP:0010058,Aplasia/Hypoplasia of the phalanges of the hallux
+DOID:1441,spinocerebellar ataxia,DOID:2478,spinocerebellar degeneration
+HP:0010093,Duplication of the proximal phalanx of the hallux,HP:0010202,Duplication of middle phalanx of toe
+CL:0002070,type I vestibular sensory cell,CL:0000609,vestibular hair cell
+UBERON:0016411,intergluteal cleft,UBERON:0006800,anatomical line
+UBERON:0011143,upper urinary tract,UBERON:0000477,anatomical cluster
+HP:0009401,Small epiphyses of the 4th finger,HP:0009174,Abnormality of the epiphyses of the 4th finger
+UBERON:0011862,pulmonary collagen fibril,UBERON:0004119,endoderm-derived structure
+UBERON:0001408,semispinalis cervicis,UBERON:0011017,semispinalis muscle
+DOID:1187,tibial neuropathy,DOID:1188,mononeuropathy
+HP:0007556,Plantar hyperkeratosis,HP:0000962,Hyperkeratosis
+HP:0011854,Hemoperitoneum,HP:0002585,Abnormality of the peritoneum
+HP:0011016,Abnormality of urine glucose concentration,HP:0003110,Abnormality of urine homeostasis
+HP:0011931,Abnormality of the cerebellar peduncle,HP:0002438,Cerebellar malformation
+DOID:14224,tracheal calcification,DOID:3225,tracheal disease
+DOID:11260,rabies,DOID:934,viral infectious disease
+CL:0002243,smooth muscle cell of sphincter of pupil,CL:0000359,vascular associated smooth muscle cell
+CL:1001099,kidney efferent arteriole endothelial cell,CL:1000412,endothelial cell of arteriole
+HP:0002179,Opisthotonus,HP:0001257,Spasticity
+HP:0009249,Abnormality of the epiphysis of the distal phalanx of the 4th finger,HP:0010243,Abnormality of the epiphyses of the distal phalanx of finger
+CL:0000001,primary cultured cell,CL:0000010,cultured cell
+UBERON:0012487,vaginal sphincter,UBERON:0005156,reproductive structure
+HP:0002841,Recurrent fungal infections,HP:0002719,Recurrent infections
+DOID:13097,intracranial arteriosclerosis,DOID:2349,arteriosclerosis
+DOID:6523,ciliary body mixed cell melanoma,DOID:6522,mixed cell uveal melanoma
+HP:0100070,Fragmentation of the epiphyses of the 4th toe,HP:0010166,Fragmentation of the epiphyses of the toes
+UBERON:2001230,pharyngeal arch 6 skeleton,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0001870,Acroosteolysis of distal phalanges (feet),HP:0001842,Acroosteolysis (feet)
+UBERON:0011754,genital swelling,UBERON:0005156,reproductive structure
+NCBITaxon:197563,Mandibulata,NCBITaxon:6656,Arthropoda
+UBERON:0013768,great vessel of heart,UBERON:0001981,blood vessel
+HP:0006539,Bronchial cartilage hypoplasia,HP:0002109,Abnormality of the bronchi
+UBERON:0004544,epididymis epithelium,UBERON:0014403,male anatomical structure
+UBERON:0007281,presumptive midbrain hindbrain boundary,UBERON:0009774,embryonic midbrain hindbrain boundary
+CL:0002079,pancreatic ductal cell,CL:1000488,cholangiocyte
+CL:0002585,retinal blood vessel endothelial cell,CL:0009004,retinal cell
+UBERON:0015844,molar dental papilla,UBERON:0011641,odontogenic mesenchyme of molar
+UBERON:3010675,bony nodule,UBERON:0004248,pedal digit bone
+HP:0011693,Supraventricular tachycardia with a concealed accessory pathway on the septum,HP:0011689,Supraventricular tachycardia with a concealed accessory connection
+HP:0004254,Delayed ossification of the trapezium,HP:0004252,Abnormality of the trapezium
+HP:0009614,Bifid proximal phalanx of the thumb,HP:0010005,Partial duplication of the middle phalanges of the hand
+CL:0002129,regular atrial cardiac myocyte,CL:0002098,regular cardiac myocyte
+UBERON:0007714,cervical subsegment of spinal cord,UBERON:0005844,spinal cord segment
+DOID:0050675,Birk-Barel syndrome,DOID:0050736,autosomal dominant disease
+HP:0010844,EEG with multifocal slow activity,HP:0011203,EEG with abnormally slow frequencies
+CL:0000042,neutrophilic myeloblast,CL:0000834,neutrophil progenitor cell
+HP:0100160,Enlarged epiphysis of the proximal phalanx of the 3rd toe,HP:0100093,Abnormality of the epiphysis of the proximal phalanx of the 3rd toe
+HP:0010327,Flexion contracture of the 2nd toe,HP:0005830,Flexion contracture of toe
+UBERON:0008001,irregular bone,UBERON:0001474,bone element
+HP:0010087,Bullet-shaped proximal phalanx of the hallux,HP:0010052,Abnormality of the proximal phalanx of the hallux
+HP:0100735,Hypertensive crisis,HP:0000822,Hypertension
+DOID:14330,Parkinson's disease,DOID:0050890,synucleinopathy
+UBERON:0010132,gastroduodenal artery,UBERON:0004573,systemic artery
+UBERON:0014630,ventral gray commissure of spinal cord,UBERON:0002315,gray matter of spinal cord
+HP:0009127,Abnormality of the musculature of the limbs,HP:0003011,Abnormality of the musculature
+HP:0003812,Phenotypic variability,HP:0000004,Onset and clinical course
+HP:0001872,Abnormality of thrombocytes,HP:0001871,Abnormality of  blood and blood-forming tissues
+DOID:11669,hypertrichosis of eyelid,DOID:10120,eyelid degenerative disease
+HP:0009138,Synostosis involving bones of the lower limbs,HP:0100240,Synostosis of joints
+UBERON:0005499,rhombomere 1,UBERON:0001892,rhombomere
+CL:0002219,anchoring trophoblasts,CL:0000351,trophoblast cell
+UBERON:0004673,trigeminal nerve root,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000888,lymph node tingible body macrophage,CL:0000868,lymph node macrophage
+UBERON:0004929,submucosa of ascending colon,UBERON:0003331,submucosa of colon
+UBERON:0008286,feather calamus,UBERON:0000064,organ part
+DOID:6229,childhood mature teratoma of the ovary,DOID:6230,childhood teratoma of the ovary
+CL:0000158,Clara cell,CL:0002328,bronchial epithelial cell
+HP:0001869,Deep plantar creases,HP:0100872,Abnormality of the plantar skin of foot
+HP:0010377,Symphalangism affecting the phalanges of the 4th toe,HP:0010336,Abnormality of the phalanges of the 4th toe
+NCBITaxon:63417,Trichophyton verrucosum,NCBITaxon:5550,Trichophyton
+HP:0010053,Abnormality of the distal phalanx of the hallux,HP:0010182,Abnormality of the distal phalanges of the toes
+UBERON:0002076,cuticle of hair,UBERON:0004121,ectoderm-derived structure
+DOID:4313,epidermolysis bullosa acquisita,DOID:2730,epidermolysis bullosa
+UBERON:0010846,radius pre-cartilage condensation,UBERON:0010882,limb bone pre-cartilage condensation
+HP:0005160,Total anomalous pulmonary venous return,HP:0010772,Anomalous pulmonary venous return
+DOID:2636,ovarian Brenner tumor,DOID:0060112,ovarian benign neoplasm
+HP:0009263,Cone-shaped epiphysis of the proximal phalanx of the 4th finger,HP:0009248,Abnormality of the epiphysis of the proximal phalanx of the 4th finger
+UBERON:3010699,m. serratus inferior,UBERON:0010891,pectoral complex muscle
+CL:0000111,peripheral neuron,CL:0000540,neuron
+UBERON:0011806,dermis of feather follicle,UBERON:0004121,ectoderm-derived structure
+UBERON:0003987,Hassall's corpuscle,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0000160,Narrow mouth,HP:0011337,Abnormality of mouth size
+CL:0000209,taste receptor cell,CL:0000098,sensory epithelial cell
+UBERON:0002435,striatum,UBERON:0011300,gray matter of telencephalon
+UBERON:0009538,mesenchyme of sublingual gland primordium,UBERON:0004121,ectoderm-derived structure
+CL:0002439,NKGA2-positive natural killer cell,CL:0002438,NK1.1-positive natural killer cell
+DOID:12333,male genital organ stricture,DOID:48,male reproductive system disease
+UBERON:2002120,orbitosphenoid septum,UBERON:0010313,neural crest-derived structure
+HP:0011773,Uninodular goiter,HP:0005994,Nodular goiter
+UBERON:0011817,follicle placode,UBERON:0011814,non-neurogenic ectodermal placode
+UBERON:0011343,medial surface of mandible,UBERON:0011342,surface of mandible
+UBERON:0002168,left lung,UBERON:0002048,lung
+DOID:10548,cardia cancer,DOID:10534,stomach cancer
+UBERON:0001253,lamina propria of ureter,UBERON:0004120,mesoderm-derived structure
+UBERON:0012316,primitive palate,UBERON:0007375,roof of mouth
+CL:1000616,kidney outer medulla cell,CL:1000504,kidney medulla cell
+HP:0011809,Paradoxical myotonia,HP:0002486,Myotonia
+DOID:0050246,granulomatous amebic encephalitis,DOID:2789,parasitic protozoa infectious disease
+HP:0100012,Neoplasm of the eye,HP:0012372,Abnormal eye morphology
+UBERON:0010354,Reichert's cartilage pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+UBERON:2000833,sclerotome somite 22,UBERON:0003089,sclerotome
+HP:0008479,Hypoplastic vertebral bodies,HP:0008417,Vertebral hypoplasia
+HP:0000182,Movement abnormality of the tongue,HP:0000157,Abnormality of the tongue
+UBERON:2205375,dorsal fin distal radial cartilage 4,UBERON:2105375,dorsal fin distal radial element 4
+UBERON:0001359,cerebrospinal fluid,UBERON:0007779,transduate
+UBERON:0004211,nephron epithelium,UBERON:0004819,kidney epithelium
+CL:0000980,plasmablast,CL:0000785,mature B cell
+HP:0010149,Absent epiphysis of the 1st metatarsal,HP:0010125,Abnormality of the epiphysis of the 1st metatarsal
+HP:0012528,Abnormal number of alpha granules,HP:0012483,Abnormal alpha granules
+HP:0010323,Abnormality of the epiphyses of the 2nd toe,HP:0010319,Abnormality of the 2nd toe
+UBERON:2005260,fenestrated capillary,UBERON:0001982,capillary
+HP:0010946,Dilatation of the renal pelvis,HP:0010944,Abnormality of the renal pelvis
+UBERON:0005040,mucosa of terminal bronchiole,UBERON:0005039,mucosa of bronchiole
+UBERON:0006270,optic pit,UBERON:0006846,surface groove
+UBERON:0001011,hemolymph,UBERON:0000463,portion of organism substance
+UBERON:0001675,trigeminal ganglion,UBERON:0001714,cranial ganglion
+DOID:5517,stomach carcinoma,DOID:10534,stomach cancer
+UBERON:0013688,tonsil germinal center,UBERON:0010754,germinal center
+UBERON:0001860,endolymphatic duct,UBERON:0004121,ectoderm-derived structure
+UBERON:0001626,left coronary artery,UBERON:0001621,coronary artery
+HP:0009487,Ulnar deviation of the hand,HP:0001193,Ulnar deviation of the hand or of fingers of the hand
+UBERON:0011310,masseteric fossa,UBERON:0005913,zone of bone organ
+UBERON:0001718,mesencephalic nucleus of trigeminal nerve,UBERON:0007414,nucleus of midbrain tegmentum
+UBERON:0005492,hyaloid vessel,UBERON:0004121,ectoderm-derived structure
+UBERON:0002094,interventricular septum,UBERON:0002099,cardiac septum
+UBERON:0008889,uterine venous plexus,UBERON:0001593,venous plexus
+UBERON:2001689,pterygoquadrate cartilage,UBERON:0004121,ectoderm-derived structure
+UBERON:0011783,feather follicle placode,UBERON:0011817,follicle placode
+UBERON:0010020,tubotympanic recess epithelium,UBERON:0015813,middle ear epithelium
+HP:0011825,Tented philtrum,HP:0000288,Abnormality of the philtrum
+UBERON:2000349,epaxialis,UBERON:0001774,muscle of trunk
+DOID:0060054,autonomic peripheral neuropathy,DOID:0060053,peripheral neuropathy
+UBERON:0007829,pectoral girdle bone,UBERON:0010741,bone of pectoral complex
+UBERON:0002629,triangular part of inferior frontal gyrus,UBERON:0004121,ectoderm-derived structure
+DOID:12895,keratoconjunctivitis sicca,DOID:9368,keratoconjunctivitis
+UBERON:3000384,parasagittal crest,UBERON:0004120,mesoderm-derived structure
+UBERON:0013156,1st arch mandibular endoderm,UBERON:0000490,unilaminar epithelium
+HP:0004722,Thickening of the glomerular basement membrane,HP:0000095,Abnormality of the glomerulus
+HP:0004224,Abnormality of the epiphysis of the middle phalanx of the 5th finger,HP:0004219,Abnormality of the middle phalanx of the 5th finger
+HP:0100836,Malignant neoplasm of the central nervous system,HP:0100006,Neoplasm of the central nervous system
+UBERON:0009119,branchial basket,UBERON:0004119,endoderm-derived structure
+CL:0000768,immature basophil,CL:0000767,basophil
+HP:0006237,Prominent interphalangeal joints,HP:0006261,Abnormality of phalangeal joints of the hand
+UBERON:0003085,ventral aorta,UBERON:0000947,aorta
+DOID:7328,iris spindle cell melanoma,DOID:6994,malignant iris melanoma
+HP:0001983,Reduced lymphocyte surface expression of CD43 (sialophorin),HP:0004332,Abnormality of lymphocytes
+UBERON:2000414,presumptive cephalic mesoderm,UBERON:0002050,embryonic structure
+UBERON:3000639,zygomatic ramus of squamosal,UBERON:4100000,skeletal element projection
+DOID:0050794,multiple synostoses syndrome,DOID:1934,dysostosis
+UBERON:0009718,neurohypophyseal duct,UBERON:0000058,duct
+UBERON:2001412,epiotic,UBERON:0011164,neurocranium bone
+DOID:866,vein disease,DOID:178,vascular disease
+HP:0002571,Achalasia,HP:0002579,Gastrointestinal dysmotility
+DOID:5694,esophagus liposarcoma,DOID:3382,liposarcoma
+HP:0009798,Euthyroid goiter,HP:0000853,Goiter
+DOID:11126,acquired thrombocytopenia,DOID:1588,thrombocytopenia
+HP:0007923,Foveal hyperplasia,HP:0000493,Abnormality of the fovea
+HP:0002372,Normal interictal EEG,HP:0002353,EEG abnormality
+UBERON:2001632,ectopterygoid tooth,UBERON:0001091,calcareous tooth
+UBERON:2000714,accessory pretectal nucleus,UBERON:0006569,diencephalic nucleus
+HP:0003932,Sclerotic foci of humeral diaphysis,HP:0003926,Abnormality of the humeral diaphysis
+HP:0009820,Lower limb peromelia,HP:0006494,Aplasia/Hypoplasia involving bones of the feet
+DOID:0050898,phalanx chondroma,DOID:0060094,bone benign neoplasm
+DOID:0050698,funisitis,DOID:65,connective tissue disease
+HP:0001425,Heterogeneous,HP:0000005,Mode of inheritance
+HP:0003933,Sclerosis of humeral diaphysis,HP:0003860,Diaphyseal sclerosis of the upper limbs
+HP:0000384,Preauricular skin tag,HP:0000383,Abnormality of periauricular region
+UBERON:0003720,anterior cranial fossa,UBERON:0008789,cranial fossa
+HP:0007647,Congenital extraocular muscle anomaly,HP:0008049,Abnormality of the extraocular muscles
+UBERON:0001258,neck of urinary bladder,UBERON:0006554,urinary system structure
+UBERON:3011121,late distal segment,UBERON:0004120,mesoderm-derived structure
+DOID:4896,bile duct adenocarcinoma,DOID:4897,bile duct carcinoma
+UBERON:0004302,proximal phalanx,UBERON:0003221,phalanx
+UBERON:0012309,superficial anterior cervical lymph node,UBERON:0012307,anterior cervical lymph node
+CL:0002643,nonkeratinized cell of stratum corneum of esophageal epithelium,CL:0002654,epithelial cell of stratum corneum of esophageal epithelium
+DOID:4376,milk allergic reaction,DOID:3044,food allergy
+HP:0009011,Hypoplasia of serratus anterior muscle,HP:0009131,Abnormality of the musculature of the thorax
+HP:0001631,Defect in the atrial septum,HP:0011994,Abnormality of the atrial septum
+UBERON:0000109,gastrula stage,UBERON:0000067,embryo stage part
+UBERON:0007227,superior vestibular nucleus,UBERON:0007228,vestibular nucleus
+DOID:11148,hypersecretion glaucoma,DOID:1686,glaucoma
+UBERON:0011374,prepuce,UBERON:0000481,multi-tissue structure
+HP:0100052,Small epiphyses of the 2nd toe,HP:0010323,Abnormality of the epiphyses of the 2nd toe
+UBERON:0002063,sinus venosus,UBERON:0004151,cardiac chamber
+HP:0005165,Shortened PR interval,HP:0003115,Abnormal EKG
+UBERON:0001281,hepatic sinusoid,UBERON:0003909,sinusoid
+HP:0200148,Abnormal liver function tests during pregnancy,HP:0002910,Elevated hepatic transaminases
+HP:0100368,Short phalanx of the 5th toe,HP:0010343,Aplasia/Hypoplasia of the 5th toe
+UBERON:2000770,hypaxial region somite 2,UBERON:0003895,hypaxial myotome region
+HP:0011466,Aplasia/Hypoplasia of the gallbladder,HP:0012437,Abnormal gallbladder morphology
+HP:0007351,Upper limb postural tremor,HP:0002174,Postural tremor
+HP:0008460,Hypoplastic spinal processes,HP:0008518,Aplasia/Hypoplasia involving the vertebral column
+DOID:1910,vaginal yolk sac tumor,DOID:119,vaginal cancer
+CL:0002504,enteric smooth muscle cell,CL:0000192,smooth muscle cell
+CL:0001020,mature CD8_alpha-low Langerhans cell,CL:0000841,mature conventional dendritic cell
+HP:0100373,Aplasia/Hypoplasia of the middle phalanx of the 4th toe,HP:0010337,Aplasia/Hypoplasia of the 4th toe
+UBERON:2001633,entopterygoid tooth,UBERON:0001091,calcareous tooth
+UBERON:0012354,acropodium region,UBERON:0012139,segment of autopod
+CL:0000327,extracellular matrix secreting cell,CL:0000151,secretory cell
+UBERON:4200176,ascending process of clavicle,UBERON:4100000,skeletal element projection
+UBERON:0004706,bulbus cordis,UBERON:0002050,embryonic structure
+UBERON:0006116,vagal nerve fiber bundle,UBERON:0011215,cell part cluster of neuraxis
+UBERON:0002852,ninth thoracic dorsal root ganglion,UBERON:0002835,thoracic dorsal root ganglion
+CL:0000682,M cell of gut,CL:0000627,transporting cell
+UBERON:0010733,alisphenoid cartilage element,UBERON:0009891,facial mesenchyme
+HP:0100556,Hemiatrophy,HP:0009826,Limb undergrowth
+DOID:3781,anovulation,DOID:1100,ovarian disease
+UBERON:0004154,atrial septum primum,UBERON:0002085,interatrial septum
+UBERON:0006144,medial plantar digital vein,UBERON:0006139,plantar digital vein
+UBERON:0010404,lateral ventricle subependymal layer,UBERON:0004121,ectoderm-derived structure
+UBERON:3010061,anterior quadratocranial commissure,UBERON:0011004,pharyngeal arch cartilage
+DOID:8410,childhood kidney angiomyolipoma,DOID:8411,kidney angiomyolipoma
+UBERON:0002081,cardiac atrium,UBERON:0004151,cardiac chamber
+HP:0004484,Craniofacial asymmetry,HP:0000324,Facial asymmetry
+DOID:0050535,exudative vitreoretinopathy,DOID:2462,retinal vascular disease
+UBERON:0003090,supraorbital lateral line,UBERON:0010202,lateral line
+UBERON:2001511,interhyal cartilage,UBERON:0011004,pharyngeal arch cartilage
+CL:0000007,early embryonic cell,CL:0002321,embryonic cell
+UBERON:0001028,diaphysis of radius,UBERON:0004769,diaphysis
+UBERON:0011577,flexural organ,UBERON:0004120,mesoderm-derived structure
+UBERON:0009639,body of sphenoid,UBERON:0011164,neurocranium bone
+HP:0006270,Hypoplastic spleen,HP:0010451,Aplasia/Hypoplasia of the spleen
+UBERON:0001986,endothelium,UBERON:0012275,meso-epithelium
+HP:0009711,Retinal hemangioblastoma,HP:0000479,Abnormality of the retina
+UBERON:0010881,limb cartilage element,UBERON:0015061,limb endochondral element
+UBERON:0011845,duct of sebaceous gland,UBERON:0004121,ectoderm-derived structure
+UBERON:0005910,transitional epithelium,UBERON:0005911,endo-epithelium
+UBERON:0011349,pterygomandibular raphe,UBERON:0004121,ectoderm-derived structure
+HP:0003508,Proportionate short stature,HP:0004322,Short stature
+CL:0000971,IgM memory B cell,CL:0001053,IgD-negative memory B cell
+UBERON:0003054,roof plate,UBERON:0004121,ectoderm-derived structure
+UBERON:0002602,emboliform nucleus,UBERON:0008995,nucleus of cerebellar nuclear complex
+HP:0007928,Abnormal flash visual evoked potentials,HP:0000649,Abnormality of vision evoked potentials
+DOID:0050895,bone ameloblastoma,DOID:0060094,bone benign neoplasm
+CL:0000721,equatorial cone cell (sensu Endopterygota),CL:0000718,cone cell (sensu Endopterygota)
+HP:0011952,Acute aspiration pneumonia,HP:0011951,Aspiration pneumonia
+UBERON:0012361,internal anal region,UBERON:0000477,anatomical cluster
+HP:0002168,Scanning speech,HP:0002167,Neurological speech impairment
+DOID:0050871,fibroma,DOID:0060084,cell type benign neoplasm
+CL:0000942,thymic plasmacytoid dendritic cell,CL:0000784,plasmacytoid dendritic cell
+UBERON:0001350,coccyx,UBERON:0004247,bone of dorsum
+HP:0005451,Decreased cranial base ossification,HP:0004331,Decreased skull ossification
+CL:1000320,axial mesoderm cell,CL:0000160,goblet cell
+UBERON:0001432,distal carpal bone 3,UBERON:0001481,distal carpal bone
+UBERON:0004425,proximal epiphysis of fourth metacarpal bone,UBERON:0004416,proximal epiphysis of metacarpal bone
+UBERON:0003367,epithelium of vomeronasal organ,UBERON:0005911,endo-epithelium
+UBERON:0015751,inferior tarsal muscle,UBERON:0003386,smooth muscle of eye
+HP:0000835,Adrenal hypoplasia,HP:0011732,Abnormality of adrenal morphology
+CL:1001217,interlobulary artery smooth muscle cell,CL:1001138,interlobular artery cell
+HP:0100840,Aplasia/Hypoplasia of the eyebrow,HP:0000534,Abnormality of the eyebrow
+HP:0009401,Small epiphyses of the 4th finger,HP:0010236,Small epiphyses of the phalanges of the hand
+UBERON:0014402,sex-specific anatomical structure,UBERON:0000061,anatomical structure
+HP:0006685,Endocardial fibrosis,HP:0004306,Abnormality of the endocardium
+UBERON:0010176,nutrient foramen artery,UBERON:0004573,systemic artery
+DOID:0050629,Aicardi-Goutieres syndrome,DOID:0050737,autosomal recessive disease
+CL:0011000,dorsal horn interneuron,CL:0005000,spinal cord interneuron
+DOID:11746,parametrium malignant neoplasm,DOID:11747,uterine adnexa cancer
+UBERON:0006695,mammillary axonal complex,UBERON:0004121,ectoderm-derived structure
+DOID:3371,chondrosarcoma,DOID:201,connective tissue cancer
+UBERON:0006971,antler,UBERON:0006969,cranial appendage
+HP:0010347,Aplasia/Hypoplasia of the phalanges of the 2nd toe,HP:0010173,Aplasia/Hypoplasia of the phalanges of the toes
+UBERON:0010568,manual digit 4 metacarpus pre-cartilage condensation,UBERON:0010578,manual digit 4 phalanx pre-cartilage condensation
+UBERON:0002360,meninx,UBERON:0000094,membrane organ
+DOID:0050811,congenital adrenal hyperplasia,DOID:1701,steroid inherited metabolic disorder
+HP:0009586,Symphalangism affecting the proximal phalanx of the 2nd finger,HP:0009545,Symphalangism of the 2nd finger
+HP:0006970,Periventricular leukomalacia,HP:0002518,Abnormality of the periventricular white matter
+UBERON:0011299,white matter of telencephalon,UBERON:0003544,brain white matter
+HP:0000941,Short diaphyses,HP:0000940,Abnormal diaphysis morphology
+HP:0001098,Abnormality of the fundus,HP:0004329,Abnormality of the posterior segment of the eye
+UBERON:3010785,m. transversus,UBERON:0008777,hypaxial musclulature
+HP:0005603,Numerous congenital melanocytic nevi,HP:0000995,Melanocytic nevus
+UBERON:2001615,sphenotic spine,UBERON:0004120,mesoderm-derived structure
+UBERON:0000463,portion of organism substance,UBERON:0000465,material anatomical entity
+UBERON:0009620,tail bud paraxial mesoderm,UBERON:0004120,mesoderm-derived structure
+HP:0009429,Aplasia of the distal phalanx of the 3rd finger,HP:0009881,Aplasia of the distal phalanges of the hand
+HP:0010208,Patchy sclerosis of the proximal phalanges of the toes,HP:0010178,Patchy sclerosis of the phalanges of the toes
+HP:0100121,Triangular epiphysis of the middle phalanx of the 2nd toe,HP:0100054,Triangular epiphyses of the 2nd toe
+HP:0001655,Patent foramen ovale,HP:0001631,Defect in the atrial septum
+UBERON:0009538,mesenchyme of sublingual gland primordium,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:5894,adult malignant mesenchymoma,DOID:5758,malignant mesenchymoma
+DOID:469,deep angioma,DOID:255,hemangioma
+DOID:9149,hard palate cancer,DOID:8618,oral cavity cancer
+HP:0002360,Sleep disturbance,HP:0012638,Abnormality of nervous system physiology
+HP:0011117,Abnormality of interleukin secretion,HP:0011113,Abnormality of cytokine secretion
+HP:0010610,Palmar pits,HP:0005922,Abnormal hand morphology
+DOID:0050260,dioctophymiasis,DOID:883,parasitic helminthiasis infectious disease
+HP:0009524,Absent epiphysis of the proximal phalanx of the 2nd finger,HP:0009488,Absent epiphyses of the 2nd finger
+HP:0011762,Pituitary thyrotropic cell adenoma,HP:0002893,Pituitary adenoma
+HP:0009848,Patchy sclerosis of the middle phalanges of the hand,HP:0009772,Patchy sclerosis of the phalanges of the hand
+UBERON:0004071,cerebellum emboliform nucleus,UBERON:0009662,hindbrain nucleus
+UBERON:0009987,medial epicondyle of femur,UBERON:0004120,mesoderm-derived structure
+HP:0100402,Duplication of the middle phalanx of the 4th toe,HP:0010381,Abnormality of the middle phalanx of the 4th toe
+CL:0002563,intestinal epithelial cell,CL:0002251,epithelial cell of alimentary canal
+HP:0011848,Abdominal colic,HP:0002027,Abdominal pain
+HP:0010721,Abnormal hair whorl,HP:0011361,Congenital abnormal hair pattern
+UBERON:0006972,nephridium,UBERON:0006555,excretory tube
+DOID:4773,congenital mesoblastic nephroma,DOID:4772,mesoblastic nephroma
+HP:0003990,Pointed ulna,HP:0002997,Abnormality of the ulna
+DOID:4059,ovary rhabdomyosarcoma,DOID:2146,ovary sarcoma
+HP:0012117,Hyperalbuminemia,HP:0012116,Abnormal albumin level
+UBERON:3000657,dentigerous process,UBERON:0004120,mesoderm-derived structure
+HP:0002663,Delayed epiphyseal ossification,HP:0005930,Abnormality of the epiphyses
+HP:0006140,Premature fusion of phalangeal epiphyses,HP:0005920,Abnormality of the epiphyses of the phalanges of the hand
+HP:0000119,Abnormality of the genitourinary system,HP:0000118,Phenotypic abnormality
+DOID:3329,benign epilepsy with centrotemporal spikes,DOID:0050704,childhood electroclinical syndrome
+DOID:1788,peritoneal mesothelioma,DOID:1790,malignant mesothelioma
+DOID:8454,ariboflavinosis,DOID:5113,nutritional deficiency disease
+HP:0011598,Right aortic arch with retroesophageal left subclavian artery,HP:0012020,Right aortic arch
+NCBITaxon:10368,Human herpesvirus 6,NCBITaxon:431037,unclassified Roseolovirus
+HP:0009380,Aplasia of the fingers,HP:0006265,Aplasia/Hypoplasia of fingers
+UBERON:0009757,ambergris,UBERON:0000463,portion of organism substance
+HP:0003244,Penile hypospadias,HP:0000047,Hypospadias
+UBERON:0004985,mucosa of ejaculatory duct,UBERON:0014403,male anatomical structure
+DOID:6677,diffuse infiltrative lymphocytosis syndrome,DOID:225,syndrome
+HP:0010459,True hermaphroditism,HP:0000062,Ambiguous genitalia
+HP:0003273,Hip contracture,HP:0008800,Limited hip movement
+HP:0009956,Partial duplication of the phalanges of the 2nd finger,HP:0009945,Duplication of phalanx of 2nd finger
+UBERON:0012274,columnar epithelium,UBERON:0000483,epithelium
+CL:0002287,type IV taste receptor cell,CL:0000209,taste receptor cell
+UBERON:0013743,base of crypt of lieberkuhn of small intestine,UBERON:0001902,epithelium of small intestine
+HP:0012478,Temporomandibular joint ankylosis,HP:0010754,Abnormality of the temporomandibular joint
+DOID:3498,pancreatic ductal adenocarcinoma,DOID:4074,pancreas adenocarcinoma
+UBERON:0010081,future common hepatic duct,UBERON:0003703,extrahepatic bile duct
+HP:0011334,Facial shape deformation,HP:0001999,Abnormal facial shape
+HP:0002408,Cerebral arteriovenous malformation,HP:0002060,Abnormality of the cerebrum
+UBERON:3000115,crista lateralis of premaxilla,UBERON:4100000,skeletal element projection
+UBERON:2000779,lateral forebrain bundle telencephalon,UBERON:2000597,telencephalic tracts
+HP:0002145,Frontotemporal dementia,HP:0000726,Dementia
+DOID:0050052,Rocky Mountain spotted fever,DOID:11104,spotted fever
+UBERON:2001481,ventral anterior lateral line nerve,UBERON:0008906,lateral line nerve
+CL:0002471,MHC-II-negative non-classical monocyte,CL:0002058,Gr1-low non-classical monocyte
+HP:0009970,Partial duplication of the proximal phalanx of the 3rd finger,HP:0009964,Duplication of the proximal phalanx of the 3rd finger
+UBERON:3010144,odontoids,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:2739,Gilbert syndrome,DOID:2741,bilirubin metabolic disorder
+NCBITaxon:38323,Bartonella henselae,NCBITaxon:773,Bartonella
+DOID:876,pyomyositis,DOID:633,myositis
+HP:0004582,Irregularity of vertebral bodies,HP:0003312,Abnormal form of the vertebral bodies
+DOID:1523,colon lymphoma,DOID:219,colon cancer
+UBERON:2001148,tooth 1D,UBERON:2000694,ceratobranchial 5 tooth
+UBERON:0015202,lymph heart,UBERON:0015229,accessory circulatory organ
+HP:0009851,Aplasia/Hypoplasia of the proximal phalanges of the hand,HP:0009834,Abnormality of the proximal phalanges of the hand
+HP:0012099,Abnormality of circulating catecholamine level,HP:0003117,Abnormality of circulating hormone level
+UBERON:0001128,sternocleidomastoid,UBERON:0004120,mesoderm-derived structure
+UBERON:0013122,distal epiphysis of phalanx of pes,UBERON:0011973,epiphysis of phalanx of pes
+HP:0003899,Round humeral epiphyses,HP:0003843,Round epiphyses of the upper limbs
+HP:0001859,Distal symphalangism (feet),HP:0100263,Distal symphalangism
+HP:0000244,Brachyturricephaly,HP:0000262,Turricephaly
+HP:0000679,Taurodontia,HP:0011071,Abnormality of permanent molar morphology
+UBERON:0012079,metapterygial axis,UBERON:0006800,anatomical line
+UBERON:2001564,hypural 5,UBERON:2000364,hypural
+HP:0011430,Hypoplasia of fetal nasal bone,HP:0011425,Fetal ultrasound soft marker
+UBERON:0015787,upper respiratory conduit,UBERON:0004111,anatomical conduit
+UBERON:0012244,stratum intermedium of epidermis,UBERON:0004121,ectoderm-derived structure
+HP:0011791,Inactivating thyroid-stimulating hormone receptor (TSHR) defect,HP:0011789,Thyroid-stimulating hormone receptor (TSHR) defect
+UBERON:0014589,anterior nucleus of hypothalamus anterior part,UBERON:0002784,regional part of diencephalon
+UBERON:0014783,cloacal muscle,UBERON:0004120,mesoderm-derived structure
+UBERON:0004049,cerebellomedullary cistern,UBERON:0004050,subarachnoid cistern
+UBERON:0011189,lamina propria of large intestine,UBERON:0004780,gastrointestinal system lamina propria
+UBERON:0000475,organism subdivision,UBERON:0010000,multicellular anatomical structure
+UBERON:0003829,urethra muscle,UBERON:0001630,muscle organ
+DOID:2152,ovary epithelial cancer,DOID:2394,ovarian cancer
+HP:0100003,Peritoneal mesothelioma,HP:0002585,Abnormality of the peritoneum
+DOID:13491,active vestibular Meniere's disease,DOID:9849,Meniere's disease
+HP:0009727,Achromatic retinal patches,HP:0007894,Hypopigmentation of the fundus
+UBERON:0001979,venule,UBERON:0003920,venous blood vessel
+HP:0011894,Impaired thromboxane A2 agonist-induced platelet aggregation,HP:0003540,Impaired platelet aggregation
+HP:0100275,Diffuse cerebellar atrophy,HP:0001272,Cerebellar atrophy
+DOID:2747,glycogen storage disease,DOID:0050728,glycogen metabolism disorder
+DOID:1827,idiopathic generalized epilepsy,DOID:1826,epilepsy syndrome
+HP:0002435,Meningocele,HP:0002414,Spina bifida
+HP:0006335,Persistence of primary teeth,HP:0006292,Abnormality of dental eruption
+HP:0009647,Proximal/distal symphalangism of thumb,HP:0001204,Distal symphalangism (hands)
+UBERON:0002791,regional part of telencephalon,UBERON:0002780,regional part of forebrain
+HP:0001994,Renal Fanconi syndrome,HP:0011038,Abnormality of renal resorption
+HP:0011303,Convex contour of sole,HP:0100872,Abnormality of the plantar skin of foot
+HP:0003892,Absent ossification/Absence of the humeral epiphyses,HP:0011849,Abnormal bone ossification
+UBERON:0006875,handplate,UBERON:0010130,autopod plate
+DOID:9735,acute allergic mucoid otitis media,DOID:9736,blue drum syndrome
+UBERON:4200154,metapodium bone 6,UBERON:0003821,metapodium bone
+UBERON:0001182,superior mesenteric artery,UBERON:0005616,mesenteric artery
+DOID:12087,deep corneal vascularisation,DOID:11382,corneal neovascularization
+UBERON:0010732,alisphenoid pre-cartilage condensation,UBERON:0015058,alisphenoid endochondral element
+HP:0100763,Abnormality of the lymphatic system,HP:0002715,Abnormality of the immune system
+CL:0000428,yolk cell,CL:0000325,stuff accumulating cell
+DOID:0060081,triple-receptor negative breast cancer,DOID:1612,breast cancer
+UBERON:0010878,humeral patagium,UBERON:0010855,skin of forelimb wing
+UBERON:0004464,musculature of thorax,UBERON:0004479,musculature of trunk
+DOID:0050166,tuberculous salpingitis,DOID:2149,urogenital tuberculosis
+UBERON:0013683,left dorsal thalamus,UBERON:0015212,lateral structure
+UBERON:0001051,hypopharynx,UBERON:0000477,anatomical cluster
+CL:1000372,transitional myocyte of atrial part of atrioventricular bundle,CL:1000481,transitional myocyte of atrioventricular bundle
+UBERON:2001607,basipterygoid process of parasphenoid,UBERON:0004530,bony projection
+UBERON:0006326,base of arytenoid,UBERON:0003583,larynx connective tissue
+UBERON:2001920,pseudotympanum,UBERON:0000481,multi-tissue structure
+DOID:14694,Johanson-Blizzard syndrome,DOID:0050737,autosomal recessive disease
+UBERON:0011915,cerebellar glomerulus,UBERON:0001047,neural glomerulus
+DOID:574,peripheral nervous system disease,DOID:863,nervous system disease
+UBERON:0001797,vitreous humor,UBERON:0006312,ocular refractive media
+UBERON:0001075,vertebral centrum,UBERON:0004120,mesoderm-derived structure
+UBERON:0007172,angle of scapula,UBERON:0006800,anatomical line
+UBERON:2000599,torus semicircularis,UBERON:0002966,regional part of midbrain tectum
+UBERON:0001453,distal tarsal bone 2,UBERON:0010721,distal tarsal bone
+HP:0009251,Bracket epiphysis of the distal phalanx of the 4th finger,HP:0010247,Bracket epiphyses of the distal phalanges of the hand
+UBERON:2000639,commissure of the secondary gustatory nuclei,UBERON:0002317,white matter of cerebellum
+UBERON:0009596,mesenchyme of interdigital region between digits 1 and 2,UBERON:0009585,interdigital region mesenchyme
+DOID:2226,chronic myeloproliferative disease,DOID:0070004,myeloma
+DOID:10480,diaphragmatic eventration,DOID:10481,diaphragm disease
+UBERON:0000083,mesonephric tubule,UBERON:0006555,excretory tube
+HP:0003966,Sclerotic foci in forearm bones,HP:0002973,Abnormality of the forearm
+UBERON:0015108,distal tarsal bone 3 endochondral element,UBERON:0015050,tarsus endochondral element
+UBERON:0002064,common cardinal vein,UBERON:0004344,cardinal vein
+DOID:318,progressive muscular atrophy,DOID:319,spinal cord disease
+HP:0012502,Abnormality of the internal capsule,HP:0002500,Abnormality of the cerebral white matter
+DOID:0060049,autoimmune disease of urogenital tract,DOID:417,hypersensitivity reaction type II disease
+HP:0001360,Holoprosencephaly,HP:0007319,Morphological abnormality of the central nervous system
+UBERON:0015829,forebrain ventricular layer,UBERON:0004121,ectoderm-derived structure
+HP:0004594,hump-shaped mound of bone in central and posterior portions of vertebral endplate,HP:0003301,Irregular vertebral endplates
+HP:0011935,Decreased urinary urate,HP:0012610,Abnormality of urinary uric acid concentration
+HP:0005229,Jejunoileal ulceration,HP:0005265,Abnormality of the jejunum
+HP:0009901,Crumpled ear,HP:0000377,Abnormality of the pinna
+UBERON:0006250,infundibular recess of 3rd ventricle,UBERON:0007499,epithelial sac
+CL:0000577,type EC enteroendocrine cell,CL:0000506,enkephalin secreting cell
+DOID:0050845,cranio-facial dystonia,DOID:0050836,focal dystonia
+HP:0100477,Symphalangism affecting the distal phalanx of the 4th toe,HP:0001859,Distal symphalangism (feet)
+UBERON:2000620,autopalatine,UBERON:0002513,endochondral bone
+UBERON:2000611,visceromotor column,UBERON:0000477,anatomical cluster
+HP:0005938,Abnormal respiratory motile cilium morphology,HP:0012253,Abnormal respiratory epithelium morphology
+UBERON:0011370,transverse process of atlas,UBERON:0015212,lateral structure
+DOID:14482,herpes gestationis,DOID:2731,vesiculobullous skin disease
+HP:0001014,Angiokeratoma,HP:0011276,Vascular skin abnormality
+HP:0100382,Aplasia of the middle phalanx of the 4th toe,HP:0100373,Aplasia/Hypoplasia of the middle phalanx of the 4th toe
+DOID:0050937,retroperitoneal neuroblastoma,DOID:5875,retroperitoneal cancer
+CL:0000313,serous secreting cell,CL:0000159,seromucus secreting cell
+UBERON:0006182,mesonephric glomerular mesangium,UBERON:0002320,glomerular mesangium
+HP:0007267,Chronic axonal neuropathy,HP:0003477,Peripheral axonal neuropathy
+UBERON:0005268,renal cortex artery,UBERON:0003644,kidney arterial blood vessel
+UBERON:0008772,proximal epiphysis of tibia,UBERON:0004380,proximal epiphysis
+NCBITaxon:482,Neisseria,NCBITaxon:481,Neisseriaceae
+DOID:14155,acute retrobulbar neuritis,DOID:1210,optic neuritis
+HP:0001000,Abnormality of skin pigmentation,HP:0011121,Abnormality of skin morphology
+UBERON:0007778,umbilical artery endothelium,UBERON:0001917,endothelium of artery
+HP:0010702,Hypergammaglobulinemia,HP:0010701,Abnormal immunoglobulin level
+UBERON:0005817,neuraxis flexure,UBERON:0004121,ectoderm-derived structure
+UBERON:0005599,common dorsal aorta,UBERON:0000947,aorta
+UBERON:0003977,utricle duct,UBERON:0004121,ectoderm-derived structure
+CL:0000244,transitional epithelial cell,CL:0002371,somatic cell
+UBERON:0000997,mammalian vulva,UBERON:0005156,reproductive structure
+UBERON:0004806,vas deferens epithelium,UBERON:0012275,meso-epithelium
+CL:1000721,kidney papillary duct principal cell,CL:1000550,kidney papillary duct principal epithelial cell
+HP:0010889,Morbus Kienboeck,HP:0004248,Abnormality of the lunate bone
+UBERON:0001682,palatine bone,UBERON:0015212,lateral structure
+NCBITaxon:11266,Filoviridae,NCBITaxon:11157,Mononegavirales
+UBERON:0004084,genital labium,UBERON:0014404,female anatomical structure
+HP:0005686,Patchy osteosclerosis,HP:0010658,Patchy changes of bone mineral density
+UBERON:0002235,tubercle of rib,UBERON:0005813,tubercle
+UBERON:0010540,tarsus pre-cartilage condensation,UBERON:0010882,limb bone pre-cartilage condensation
+HP:0006436,Shortening of the tibia,HP:0005736,Short tibia
+HP:0011375,Cochlear aplasia,HP:0011395,Aplasia/Hypoplasia of the cochlea
+DOID:0050174,Kunjin encephalitis,DOID:2365,West Nile encephalitis
+UBERON:0014479,elephant trunk,UBERON:0000026,appendage
+UBERON:0014475,endostylar duct,UBERON:0000025,tube
+UBERON:3000069,cartilago infranarina,UBERON:0010313,neural crest-derived structure
+HP:0012333,Abnormal sudomotor regulation,HP:0012332,Abnormal autonomic nervous system physiology
+HP:0100222,Stippling of the epiphysis of the middle phalanx of the 5th toe,HP:0100098,Abnormality of the epiphysis of the middle phalanx of the 5th toe
+UBERON:0002240,spinal cord,UBERON:0004121,ectoderm-derived structure
+HP:0012273,Increased carotid artery intimal medial thickness,HP:0005344,Abnormality of the carotid arteries
+CL:0000799,immature gamma-delta T cell,CL:0000798,gamma-delta T cell
+DOID:1390,hypobetalipoproteinemia,DOID:1387,hypolipoproteinemia
+DOID:0050634,alopecia universalis,DOID:987,alopecia
+HP:0100934,Sclerosis of the proximal phalanx of the 5th toe,HP:0100946,Sclerosis of the proximal phalanges of the toes
+HP:0100938,Sclerosis of the middle phalanx of the 5th toe,HP:0100947,Sclerosis of the middle phalanges of the toes
+CL:0000867,secondary lymphoid organ macrophage,CL:0000864,tissue-resident macrophage
+DOID:3520,pediatric fibrosarcoma,DOID:3355,fibrosarcoma
+HP:0100326,Immunologic hypersensitivity,HP:0010978,Abnormality of immune system physiology
+UBERON:0005008,mucosa of minor calyx,UBERON:0005006,mucosa of renal pelvis
+HP:0008947,Infantile muscular hypotonia,HP:0001252,Muscular hypotonia
+UBERON:0000311,extensor muscle,UBERON:0001630,muscle organ
+UBERON:0007522,striated muscle sphincter,UBERON:0004590,sphincter muscle
+DOID:720,normocytic anemia,DOID:2355,anemia
+HP:0008945,Loss of ability to walk in early childhood,HP:0006915,Inability to walk by childhood/adolescence
+CL:0000077,mesothelial cell,CL:0000213,lining cell
+UBERON:0014377,hypothenar muscle,UBERON:0014375,intrinsic muscle of manus
+DOID:9282,ocular hypertension,DOID:9283,borderline glaucoma
+HP:0008131,Tarsal stippling,HP:0010766,Ectopic calcification
+UBERON:0005426,lens vesicle,UBERON:0000479,tissue
+DOID:0050924,striated muscle rhabdoid tumor,DOID:4045,muscle cancer
+HP:0005121,Posterior scalloping of vertebral bodies,HP:0004586,Biconcave vertebral bodies
+HP:0001126,Cryptophthalmos,HP:0100887,Abnormality of globe size
+UBERON:0010710,pectoral fin skeleton,UBERON:0010713,paired fin skeleton
+HP:0005109,Abnormality of the Achilles tendon,HP:0001760,Abnormality of the foot
+DOID:7008,protoplasmic astrocytoma,DOID:3069,astrocytoma
+UBERON:0010949,sternooccipital muscle,UBERON:0002377,muscle of neck
+UBERON:0001081,endocardium of ventricle,UBERON:0000487,simple squamous epithelium
+UBERON:2000742,epaxial region somite 17,UBERON:0003900,epaxial myotome region
+UBERON:2007028,spinal cord neural keel,UBERON:0000479,tissue
+HP:0100629,Midline facial cleft,HP:0002006,Facial cleft
+NCBITaxon:13203,Phlebotomus <genus>,NCBITaxon:7198,Phlebotominae
+HP:0003325,Limb-girdle muscle weakness,HP:0001324,Muscle weakness
+HP:0007930,Prominent epicanthal folds,HP:0000286,Epicanthus
+UBERON:0002320,glomerular mesangium,UBERON:0003567,abdomen connective tissue
+UBERON:0003084,heart primordium,UBERON:0001048,primordium
+HP:0005640,Abnormal vertebral segmentation and fusion,HP:0003422,Vertebral segmentation defect
+UBERON:0015115,distal tarsal bone 5 cartilage,UBERON:0015114,distal tarsal bone 5 endochondral element
+UBERON:0001863,scala vestibuli,UBERON:0000477,anatomical cluster
+HP:0011577,Partial atrioventricular canal defect,HP:0006695,Atrioventricular canal defect
+UBERON:0003416,mesenchyme of tongue,UBERON:0004121,ectoderm-derived structure
+UBERON:0010566,manual digit 2 metacarpus pre-cartilage condensation,UBERON:0015044,manual digit 2 metacarpus endochondral element
+DOID:14087,epicondylitis,DOID:3342,bone inflammation disease
+HP:0004050,Absent hand,HP:0005927,Aplasia/Hypoplasia involving bones of the hand
+UBERON:0010850,tibia pre-cartilage condensation,UBERON:0005259,lower leg mesenchyme
+HP:0005824,Second toe clinodactyly,HP:0001863,Toe clinodactyly
+UBERON:0003651,metatarsal bone of digit 2,UBERON:0013582,metapodium bone 2
+HP:0003533,Delayed oxidation of acetaldehyde,HP:0001939,Abnormality of metabolism/homeostasis
+HP:0010343,Aplasia/Hypoplasia of the 5th toe,HP:0010760,Absent toe
+HP:0012687,Agenesis of pineal gland,HP:0012681,Abnormality of pineal morphology
+UBERON:4000104,ganoine,UBERON:0010365,odontoid tissue
+UBERON:0001874,putamen,UBERON:0009663,telencephalic nucleus
+HP:0000805,Enuresis,HP:0000009,Functional abnormality of the bladder
+DOID:11153,miliaria rubra,DOID:1382,miliaria
+UBERON:0001804,capsule of lens,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000411,flatworm hypodermal cell,CL:0000228,multinucleate cell
+HP:0007360,Aplasia/Hypoplasia of the cerebellum,HP:0001317,Abnormality of the cerebellum
+CL:1000302,fibroblast of papillary layer of dermis,CL:0002551,fibroblast of dermis
+HP:0200016,Acrokeratosis,HP:0200036,Skin nodule
+CL:0000990,conventional dendritic cell,CL:0000451,dendritic cell
+DOID:12842,Guillain-Barre syndrome,DOID:5214,demyelinating polyneuropathy
+UBERON:0011495,rectus thoracis muscle,UBERON:0003830,thoracic segment muscle
+UBERON:3010065,M. gracilis major,UBERON:0010890,pelvic complex muscle
+UBERON:0003333,submucosa of jejunum,UBERON:0001205,submucosa of small intestine
+UBERON:0007224,medial entorhinal cortex,UBERON:0000064,organ part
+UBERON:0010935,tensor tympani pre-muscle condensation,UBERON:0005865,pre-muscle condensation
+DOID:8946,severe nonproliferative diabetic retinopathy,DOID:8947,diabetic retinopathy
+UBERON:0009027,vesical artery,UBERON:0001637,artery
+UBERON:0007181,serosa of infundibulum of uterine tube,UBERON:0005156,reproductive structure
+DOID:3267,mucinous ovarian cystadenoma,DOID:3269,ovarian cystadenoma
+UBERON:0014696,anterior choroidal artery,UBERON:0004573,systemic artery
+UBERON:0002713,circular sulcus of insula,UBERON:0002912,marginal sulcus
+UBERON:0005563,trigeminal neural crest,UBERON:0007530,migrating mesenchyme population
+HP:0003949,Abnormality of the elbow metaphyses,HP:0009809,Abnormality of upper limb metaphysis
+HP:0009210,Pseudoepiphysis of the middle phalanx of the 5th finger,HP:0009389,Pseudoepiphyses of the 5th finger
+CL:0000059,ameloblast,CL:0000146,simple columnar epithelial cell
+UBERON:0008820,anterior mediastinum,UBERON:0002224,thoracic cavity
+HP:0011993,Impaired neutrophil bactericidal activity,HP:0011990,Abnormality of neutrophil physiology
+UBERON:0007165,proximal radio-ulnar joint,UBERON:0001528,radio-ulnar joint
+DOID:0050899,brain stem medulloblastoma,DOID:4203,brain stem cancer
+HP:0005878,Enlarged sagittal diameter of the cervical canal,HP:0003319,Abnormality of the cervical spine
+HP:0011532,Subretinal exudate,HP:0001147,Retinal exudate
+HP:0100080,Enlarged epiphyses of the 5th toe,HP:0010165,Enlarged epiphyses of the toes
+UBERON:3000389,paries nasi,UBERON:0003933,cranial cartilage
+UBERON:0014853,commissural leaflet of mitral valve,UBERON:0007151,mitral valve leaflet
+UBERON:0000432,endopeduncular nucleus,UBERON:0009663,telencephalic nucleus
+HP:0009845,Bullet-shaped middle phalanges of the hand,HP:0009769,Bullet-shaped phalanges of the hand
+HP:0000584,Punctate corneal epithelial erosions,HP:0200020,Corneal erosions
+UBERON:0006671,orbital fat pad,UBERON:0003566,head connective tissue
+UBERON:0009010,periurethral tissue,UBERON:0006554,urinary system structure
+UBERON:0002886,lateral amygdaloid nucleus,UBERON:0009663,telencephalic nucleus
+UBERON:0004833,lip skeletal muscle,UBERON:0001134,skeletal muscle tissue
+HP:0200151,Cutaneous mastocytosis,HP:0100495,Mastocytosis
+HP:0010022,Pseudoepiphysis of the 1st metacarpal,HP:0009193,Pseudoepiphyses of the metacarpals
+HP:0010628,Facial palsy,HP:0010827,Abnormality of the seventh cranial nerve
+UBERON:2000834,sclerotome somite 25,UBERON:0003089,sclerotome
+NCBITaxon:5552,Trichosporon <Trichosporonales>,NCBITaxon:34476,mitosporic Tremellales
+CL:0000595,enucleate erythrocyte,CL:0000232,erythrocyte
+UBERON:0012642,vestimentum muscle,UBERON:0001630,muscle organ
+UBERON:0008866,enamel knot,UBERON:0004121,ectoderm-derived structure
+UBERON:2005378,dorsal fin distal radial bone 7,UBERON:2000936,dorsal fin distal radial bone
+UBERON:1700006,paired fin radial cartilage,UBERON:1600006,paired fin radial element
+DOID:9565,dextrocardia,DOID:1682,congenital heart disease
+UBERON:4200181,astragalus head,UBERON:0005913,zone of bone organ
+UBERON:0009093,outer medulla vasa recta ascending limb,UBERON:0000064,organ part
+HP:0011977,Elevated urinary homovanillic acid,HP:0004354,Abnormality of carboxylic acid metabolism
+DOID:12043,kernicterus due to isoimmunization,DOID:11244,neonatal anemia
+HP:0003953,Absent ossification/absent forearm bones,HP:0011849,Abnormal bone ossification
+DOID:8030,periocular meningioma,DOID:3565,meningioma
+DOID:8970,subacute sclerosing panencephalitis,DOID:934,viral infectious disease
+HP:0003738,Exercise-induced myalgia,HP:0003326,Myalgia
+DOID:468,intramuscular hemangioma,DOID:469,deep angioma
+DOID:7756,neonatal leukemia,DOID:7757,childhood leukemia
+NCBITaxon:1743,Propionibacterium,NCBITaxon:31957,Propionibacteriaceae
+HP:0001675,Rhythm disturbances associated with pheochromocytoma,HP:0011675,Arrhythmia
+UBERON:3000802,fossa glenoidalis,UBERON:0000064,organ part
+DOID:0050543,Charcot-Marie-Tooth disease intermediate type,DOID:10595,Charcot-Marie-Tooth disease
+DOID:8140,adrenal gland ganglioneuroblastoma,DOID:3953,adrenal gland cancer
+CL:0002610,raphe nuclei neuron,CL:0000117,CNS neuron (sensu Vertebrata)
+CL:0002215,type IIb muscle cell,CL:0002213,white muscle cell
+HP:0000175,Cleft palate,HP:0100737,Abnormality of the hard palate
+UBERON:0009851,border of sublaminar layers S4 and S5,UBERON:0009740,border between sublaminar layers
+UBERON:3010520,oviducal vein,UBERON:0001638,vein
+UBERON:0003528,brain grey matter,UBERON:0002020,gray matter of neuraxis
+UBERON:2000741,epaxial region somite 14,UBERON:0003900,epaxial myotome region
+CL:0000684,littoral cell of liver,CL:0000077,mesothelial cell
+UBERON:3000792,anterior ramus of cleithrum,UBERON:0004120,mesoderm-derived structure
+HP:0010272,Fragmentation of the epiphyses of the proximal phalanges of the hand,HP:0010232,Fragmentation of the epiphyses of the phalanges of the hand
+UBERON:0011643,puboischiofemoralis internus muscle,UBERON:0003897,axial muscle
+HP:0012145,Abnormality of multiple cell lineages in the bone marrow,HP:0005561,Abnormality of bone marrow cell morphology
+DOID:11971,synostosis,DOID:1934,dysostosis
+HP:0007510,Focal dermal aplasia/hypoplasia,HP:0008065,Aplasia/Hypoplasia of the skin
+DOID:4952,postpoliomyelitis syndrome,DOID:4953,poliomyelitis
+DOID:0060061,cutaneous T cell lymphoma,DOID:0050749,peripheral T-cell lymphoma
+HP:0100185,Irregular epiphysis of the middle phalanx of the 4th toe,HP:0100071,Irregular epiphyses of the 4th toe
+HP:0000618,Blindness,HP:0000505,Visual impairment
+CL:0000110,peptidergic neuron,CL:0000540,neuron
+HP:0009200,Pseudoepiphysis of the proximal phalanx of the 5th finger,HP:0009153,Abnormality of the epiphysis of the proximal phalanx of the 5th finger
+HP:0010843,EEG with focal slow activity,HP:0011203,EEG with abnormally slow frequencies
+HP:0100161,Fragmentation of the epiphysis of the proximal phalanx of the 3rd toe,HP:0100093,Abnormality of the epiphysis of the proximal phalanx of the 3rd toe
+DOID:12332,hematocele of tunica vaginalis testis,DOID:48,male reproductive system disease
+UBERON:0007158,lumen of anal canal,UBERON:0000464,anatomical space
+UBERON:0012101,perinatal stage,UBERON:0000105,life cycle stage
+HP:0000002,Abnormality of body height,HP:0001507,Growth abnormality
+UBERON:0004117,pharyngeal pouch,UBERON:0000490,unilaminar epithelium
+HP:0010805,Upturned corners of mouth,HP:0011338,Abnormality of mouth shape
+UBERON:0002167,right lung,UBERON:0002048,lung
+DOID:11125,qualitative platelet defect,DOID:2218,blood platelet disease
+UBERON:2001818,dorsal fin proximal radial bone 1,UBERON:2101818,dorsal fin proximal radial element 1
+DOID:686,liver carcinoma,DOID:3571,liver cancer
+UBERON:0014595,"paraventricular nucleus of the hypothalamus descending division - medial parvicellular part, ventral zone",UBERON:0003048,regional part of hypothalamus
+HP:0004344,Abnormality of cerebrosidase metabolism,HP:0004343,Abnormality of glycosphingolipid metabolism
+UBERON:0007828,girdle bone/zone,UBERON:0010740,bone of appendage girdle complex
+CL:0000876,splenic white pulp macrophage,CL:0000871,splenic macrophage
+UBERON:0006197,auricular vein,UBERON:0003502,neck blood vessel
+NCBITaxon:451868,Pleosporomycetidae,NCBITaxon:147541,Dothideomycetes
+UBERON:0005985,coronary vessel,UBERON:0000055,vessel
+UBERON:0003077,paraxial mesoderm,UBERON:0007524,dense mesenchyme tissue
+CL:1000442,urothelial cell of trigone of urinary bladder,CL:1001319,bladder cell
+UBERON:0010411,retroperitoneal fat pad,UBERON:0004120,mesoderm-derived structure
+HP:0007610,Blotching pigmentation of the skin,HP:0001000,Abnormality of skin pigmentation
+HP:0002788,Recurrent upper respiratory tract infections,HP:0002205,Recurrent respiratory infections
+DOID:4067,anus sarcoma,DOID:14110,anus cancer
+UBERON:2001231,pharyngeal arch 4 skeleton,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0001773,Short foot,HP:0006494,Aplasia/Hypoplasia involving bones of the feet
+UBERON:2000502,dorsal motor nucleus trigeminal nerve,UBERON:0002633,motor nucleus of trigeminal nerve
+UBERON:0012065,lobar bronchus of left lung upper lobe,UBERON:0003405,lobar bronchus of left lung
+UBERON:0002077,cortex of hair,UBERON:0004121,ectoderm-derived structure
+UBERON:0003979,utricle valve,UBERON:0004121,ectoderm-derived structure
+HP:0000103,Polyuria,HP:0012590,Abnormal urine output
+UBERON:4200022,extracleithrum,UBERON:0007829,pectoral girdle bone
+UBERON:0006087,internal arcuate fiber bundle,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:4561,granulomatous endometritis,DOID:1002,endometritis
+UBERON:0001711,eyelid,UBERON:0004121,ectoderm-derived structure
+HP:0009921,Duane anomaly,HP:0000496,Abnormality of eye movement
+CL:1001006,kidney afferent arteriole cell,CL:1000891,kidney arterial blood vessel cell
+UBERON:0005290,myelencephalon,UBERON:0004733,segmental subdivision of hindbrain
+UBERON:0007330,rhamphotheca,UBERON:0003102,surface structure
+HP:0002691,Platybasia,HP:0002648,Abnormality of calvarial morphology
+UBERON:0001625,right coronary artery,UBERON:0001621,coronary artery
+DOID:0050097,ectothrix infectious disease,DOID:4337,tinea capitis
+DOID:1639,skeletal tuberculosis,DOID:0050598,extrapulmonary tuberculosis
+HP:0001234,Hitchhiker thumb,HP:0009466,Radial deviation of finger
+UBERON:0005248,bulbus cordis myocardium,UBERON:0002050,embryonic structure
+DOID:11379,gnathomiasis,DOID:883,parasitic helminthiasis infectious disease
+HP:0002256,Small bowel diverticula,HP:0002244,Abnormality of the small intestine
+UBERON:0000478,extraembryonic structure,UBERON:0000061,anatomical structure
+DOID:1919,Lesch-Nyhan syndrome,DOID:653,purine-pyrimidine metabolic disorder
+DOID:12526,tarsal tunnel syndrome,DOID:1187,tibial neuropathy
+UBERON:0009539,mesenchyme of submandibular gland primordium,UBERON:0004121,ectoderm-derived structure
+HP:0100385,Aplasia of the proximal phalanx of the 4th toe,HP:0100376,Aplasia/Hypoplasia of the proximal phalanx of the 4th toe
+UBERON:0001532,internal carotid artery,UBERON:0005396,carotid artery segment
+UBERON:0006341,outer renal medulla peritubular capillary,UBERON:0005272,peritubular capillary
+NCBITaxon:39030,Apodemus agrarius,NCBITaxon:10128,Apodemus
+DOID:6639,pediatric CNS choriocarcinoma,DOID:6052,central nervous system childhood germ cell tumor
+HP:0009581,Broad proximal phalanx of the 2nd finger,HP:0009544,Abnormality of the proximal phalanx of the 2nd finger
+DOID:10627,primary optic atrophy,DOID:5723,optic atrophy
+UBERON:2001603,maxilla ascending process,UBERON:0010313,neural crest-derived structure
+UBERON:0010698,manual digit metacarpus pre-cartilage condensation,UBERON:0010586,manual digit phalanx pre-cartilage condensation
+HP:0009724,Subungual fibromas,HP:0010614,Fibroma
+UBERON:2005101,interray vessel,UBERON:0007304,appendage vasculature
+DOID:11726,Emery-Dreifuss muscular dystrophy,DOID:9884,muscular dystrophy
+HP:0100835,Benign neoplasm of the central nervous system,HP:0100006,Neoplasm of the central nervous system
+NCBITaxon:43738,Schizophora,NCBITaxon:480117,Cyclorrhapha
+UBERON:0006610,tunica albuginea,UBERON:0000158,membranous layer
+HP:0000756,Agoraphobia,HP:0100852,Abnormal fear/anxiety-related behavior
+CL:0000192,smooth muscle cell,CL:0008000,non-striated muscle cell
+HP:0005961,Hypoargininemia,HP:0010909,Abnormality of arginine metabolism
+UBERON:0007115,deciduous tooth,UBERON:0001091,calcareous tooth
+UBERON:0007601,ciliated epithelium,UBERON:0000483,epithelium
+DOID:4894,rete ovarii adenocarcinoma,DOID:3713,ovary adenocarcinoma
+UBERON:2000265,presumptive dorsal mesoderm,UBERON:0005423,developing anatomical structure
+UBERON:0001747,parenchyma of thyroid gland,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:865,vasculitis,DOID:178,vascular disease
+UBERON:0002738,isthmus of cingulate gyrus,UBERON:0000064,organ part
+UBERON:0008261,pedicellaria,UBERON:0000026,appendage
+UBERON:0001407,semispinalis thoracis,UBERON:0011017,semispinalis muscle
+UBERON:0007830,pelvic girdle bone/zone,UBERON:0004120,mesoderm-derived structure
+UBERON:0001861,ductus reuniens,UBERON:0004121,ectoderm-derived structure
+UBERON:0002746,intermediate periventricular nucleus,UBERON:0006568,hypothalamic nucleus
+DOID:14324,Plasmodium malariae malaria,DOID:12365,malaria
+HP:0009341,Ivory epiphysis of the distal phalanx of the 3rd finger,HP:0009416,Ivory epiphyses of the 3rd finger
+HP:0010682,Elevated placental alkaline phosphatase,HP:0003155,Elevated alkaline phosphatase
+CL:1000298,mesothelial cell of dura mater,CL:0002319,neural cell
+HP:0005678,Anterior atlanto-occipital dislocation,HP:0003414,Atlantoaxial dislocation
+HP:0003398,Abnormality of the neuromuscular junction,HP:0000759,Abnormality of the peripheral nervous system
+CL:0000842,mononuclear cell,CL:0000226,single nucleate cell
+HP:0008455,Dysplastic sacrum,HP:0005107,Abnormality of the sacrum
+UBERON:0005973,blood-inner ear barrier,UBERON:0004121,ectoderm-derived structure
+UBERON:0006696,mammillothalamic axonal tract,UBERON:0011591,tract of diencephalon
+UBERON:4000077,non-mineralized chondroid tissue,UBERON:0004755,skeletal tissue
+CL:1000617,kidney inner medulla cell,CL:1000504,kidney medulla cell
+UBERON:0001433,distal carpal bone 4,UBERON:0001481,distal carpal bone
+HP:0011800,Midface retrusion,HP:0000309,Abnormality of the midface
+UBERON:0001204,mucosa of small intestine,UBERON:0001242,intestinal mucosa
+UBERON:0004411,proximal epiphysis of humerus,UBERON:0004380,proximal epiphysis
+DOID:3292,monkeypox,DOID:934,viral infectious disease
+HP:0010324,Abnormality of phalanx of the 2nd toe,HP:0010319,Abnormality of the 2nd toe
+UBERON:0011844,duct of areolar gland,UBERON:0001765,mammary duct
+UBERON:3000226,hyolaryngeal complex,UBERON:0000477,anatomical cluster
+UBERON:0001337,spongiose part of urethra,UBERON:0005156,reproductive structure
+HP:0005133,Right ventricular dilatation,HP:0001707,Abnormality of the right ventricle
+DOID:1680,chronic cystitis,DOID:1679,cystitis
+UBERON:0011251,levator claviculae muscle,UBERON:0004518,muscle of vertebral column
+DOID:13271,cutaneous porphyria,DOID:13268,porphyria
+DOID:5695,pediatric liposarcoma,DOID:3382,liposarcoma
+HP:0100208,Ivory epiphysis of the distal phalanx of the 5th toe,HP:0100083,Ivory epiphyses of the 5th toe
+HP:0001807,Ridged nail,HP:0002164,Nail dysplasia
+HP:0011692,Supraventricular tachycardia with a concealed accessory pathway on the right free wall,HP:0011689,Supraventricular tachycardia with a concealed accessory connection
+UBERON:0011665,carapace bone,UBERON:0004247,bone of dorsum
+UBERON:3000827,margo anterior of cleithrum,UBERON:0004120,mesoderm-derived structure
+UBERON:0005446,foramen rotundum,UBERON:0004120,mesoderm-derived structure
+HP:0011491,Reduced number of corneal endothelial cells,HP:0011488,Abnormality of corneal endothelium
+DOID:11520,benign hypertensive renal disease,DOID:1073,renal hypertension
+UBERON:2001581,ural centrum 2,UBERON:0004120,mesoderm-derived structure
+UBERON:0004510,skeletal muscle tissue of pectoralis major,UBERON:0003898,skeletal muscle tissue of trunk
+NCBITaxon:31979,Clostridiaceae,NCBITaxon:186802,Clostridiales
+UBERON:0003281,mesentery of stomach,UBERON:0009034,stomach region
+HP:0011416,Placental infarction,HP:0100767,Abnormality of the placenta
+UBERON:3000016,anterior nasal wall,UBERON:0010363,endochondral element
+UBERON:0010520,head electric organ,UBERON:0006869,electric organ
+UBERON:0005170,ovary stratum granulosum,UBERON:0005156,reproductive structure
+DOID:2163,nasal cavity disease,DOID:2825,nose disease
+UBERON:0003444,pelvis nerve,UBERON:0003825,nerve of abdominal segment
+HP:0010616,Lung fibroma,HP:0010614,Fibroma
+HP:0100668,Intestinal duplication,HP:0002242,Abnormality of the intestine
+UBERON:0003238,epithelium of superior semicircular canal,UBERON:0006937,inner ear epithelium
+UBERON:0000958,medulla of organ,UBERON:0000471,compound organ component
+DOID:7400,Nijmegen breakage syndrome,DOID:0050737,autosomal recessive disease
+UBERON:0006143,proper plantar digital vein,UBERON:0006139,plantar digital vein
+DOID:9868,intestinal disaccharidase deficiency,DOID:2978,carbohydrate metabolic disorder
+UBERON:0003581,eyelid connective tissue,UBERON:0003566,head connective tissue
+HP:0009955,Partial duplication of the proximal phalanx of the 2nd finger,HP:0009947,Duplication of the proximal phalanx of the 2nd finger
+UBERON:2000725,somite 11,UBERON:0002329,somite
+HP:0006590,Premature sternal synostosis,HP:0006714,Aplasia/Hypoplasia of the sternum
+UBERON:0010725,accessory navicular bone,UBERON:0010722,accessory bone
+UBERON:0010881,limb cartilage element,UBERON:0005863,cartilaginous condensation
+HP:0000599,Abnormality of the frontal hairline,HP:0009553,Abnormality of the hairline
+UBERON:0000108,blastula stage,UBERON:0000067,embryo stage part
+HP:0004478,Ethmoidal encephalocele,HP:0011817,Basal encephalocele
+HP:0007976,Cerulean cataract,HP:0007648,Punctate cataract
+HP:0004470,Atretic occipital cephalocele,HP:0011815,Cephalocele
+HP:0012424,Chorioretinitis,HP:0000532,Chorioretinal abnormality
+HP:0011519,Anomalous trichromacy,HP:0007641,Dyschromatopsia
+UBERON:0000156,theca externa,UBERON:0000158,membranous layer
+DOID:8642,Hodgkin's paragranuloma,DOID:8567,Hodgkin's lymphoma
+HP:0012503,Abnormality of the pituitary gland,HP:0000864,Abnormality of the hypothalamus-pituitary axis
+UBERON:0015214,arcuate ligament,UBERON:0003837,thoracic segment connective tissue
+UBERON:3010106,tympanic papilla,UBERON:3000972,head external integument structure
+HP:0005736,Short tibia,HP:0005772,Aplasia/Hypoplasia of the tibia
+UBERON:3000797,non-imbricate neural arch,UBERON:0003861,neural arch
+HP:0006937,Impaired distal tactile sensation,HP:0002936,Distal sensory impairment
+UBERON:0006916,non-keratinized epithelium of tongue,UBERON:0006919,tongue squamous epithelium
+HP:0200053,Hemihypotrophy of lower limb,HP:0100556,Hemiatrophy
+UBERON:0004473,musculature of face,UBERON:0004461,musculature of head
+HP:0003933,Sclerosis of humeral diaphysis,HP:0003926,Abnormality of the humeral diaphysis
+UBERON:0006115,posterior column of fornix,UBERON:0011215,cell part cluster of neuraxis
+UBERON:0002853,tenth thoracic dorsal root ganglion,UBERON:0002835,thoracic dorsal root ganglion
+HP:0010130,Enlarged epiphysis of the proximal phalanx of the hallux,HP:0010116,Enlarged epiphyses of the hallux
+UBERON:0002940,anterior column of fornix,UBERON:0011299,white matter of telencephalon
+DOID:4467,renal clear cell carcinoma,DOID:4450,renal cell carcinoma
+HP:0011688,Supraventricular tachycardia with an accessory connection mediated pathway,HP:0004755,Supraventricular tachycardia
+UBERON:0004424,proximal epiphysis of third metacarpal bone,UBERON:0004416,proximal epiphysis of metacarpal bone
+HP:0100516,Neoplasm of the ureter,HP:0000069,Abnormality of the ureter
+DOID:12282,femoral vein thrombophlebitis,DOID:3875,thrombophlebitis
+UBERON:0001259,mucosa of urinary bladder,UBERON:0006554,urinary system structure
+UBERON:0009201,nephric duct,UBERON:0004819,kidney epithelium
+UBERON:0005880,prepollex,UBERON:0008785,upper limb segment
+UBERON:0002082,cardiac ventricle,UBERON:0004151,cardiac chamber
+DOID:13956,uterine corpus myxoid leiomyoma,DOID:13223,uterine fibroid
+UBERON:2000636,cerebellar crest,UBERON:0004121,ectoderm-derived structure
+DOID:8499,night blindness,DOID:5679,retinal disease
+CL:1000717,kidney outer medulla collecting duct intercalated cell,CL:1001432,kidney collecting duct intercalated cell
+HP:0010951,Abnormality of the third ventricle,HP:0002118,Abnormality of the cerebral ventricles
+HP:0004870,Chronic hemolytic anemia,HP:0001878,Hemolytic anemia
+HP:0100689,Decreased corneal thickness,HP:0011486,Abnormality of corneal thickness
+UBERON:0005897,manus bone,UBERON:0008962,forelimb bone
+UBERON:0001803,epithelium of lens,UBERON:0000484,simple cuboidal epithelium
+UBERON:0002866,caudal part of spinal trigeminal nucleus,UBERON:0003528,brain grey matter
+DOID:0050470,Donohue Syndrome,DOID:0050737,autosomal recessive disease
+CL:0005010,renal intercalated cell,CL:0000075,columnar/cuboidal epithelial cell
+UBERON:0004312,distal phalanx of manual digit 3,UBERON:0003637,manual digit 3 phalanx
+DOID:0050676,Birt-Hogg-Dube syndrome,DOID:0050736,autosomal dominant disease
+UBERON:0011846,acinus of sebaceous gland,UBERON:0004121,ectoderm-derived structure
+HP:0200011,Abnormal length of corpus callosum,HP:0001273,Abnormality of the corpus callosum
+UBERON:2001428,olfactory rosette,UBERON:0004807,respiratory system epithelium
+HP:0008872,Feeding difficulties in infancy,HP:0011968,Feeding difficulties
+HP:0010365,Symphalangism affecting the phalanges of the 3rd toe,HP:0010179,Symphalangism affecting the phalanges of the toes
+UBERON:0012418,respiratory system venous smooth muscle,UBERON:0004696,venous system smooth muscle
+DOID:14755,argininosuccinic aciduria,DOID:9252,amino acid metabolic disorder
+HP:0100494,Abnormality of mast cells,HP:0010987,Abnormality of cellular immune system
+HP:0100511,Abnormality of vitamin D metabolism,HP:0100508,Abnormality of vitamin metabolism
+UBERON:3010783,m. oblique externus,UBERON:0008777,hypaxial musclulature
+DOID:3156,incontinentia pigmenti achromians,DOID:37,skin disease
+HP:0009720,Adenoma sebaceum,HP:0010615,Angiofibromas
+UBERON:0004155,atrial septum secundum,UBERON:0002085,interatrial septum
+UBERON:0009102,supraneural body,UBERON:0004177,hemopoietic organ
+HP:0000913,Posterior rib fusion,HP:0000902,Rib fusion
+HP:0007236,Recurrent subcortical infarcts,HP:0001317,Abnormality of the cerebellum
+CL:1001216,interlobulary artery endothelial cell,CL:1001138,interlobular artery cell
+UBERON:2002009,medial cartilage of palatine,UBERON:0011004,pharyngeal arch cartilage
+CL:0000244,transitional epithelial cell,CL:0000066,epithelial cell
+HP:0100397,Short proximal phalanx of the 5th toe,HP:0100377,Aplasia/Hypoplasia of the proximal phalanx of the 5th toe
+UBERON:2001660,basibranchial tooth,UBERON:0004756,dermal skeletal element
+HP:0006274,Reduced pancreatic beta cells,HP:0006476,Abnormality of the pancreatic islet cells
+UBERON:0008255,right clavicle,UBERON:0001105,clavicle
+UBERON:3010693,ramus posterior profundus of V3,UBERON:0004732,segmental subdivision of nervous system
+UBERON:0003580,lower respiratory tract connective tissue,UBERON:0003570,respiratory system connective tissue
+HP:0000476,Cystic hygroma,HP:0000464,Abnormality of the neck
+DOID:6997,intermediate cell type ciliary body melanoma,DOID:6992,intraocular mixed cell type melanoma
+UBERON:3010692,m. cucullaris,UBERON:0010891,pectoral complex muscle
+DOID:10697,chronic endophthalmitis,DOID:9724,purulent endophthalmitis
+HP:0002007,Frontal bossing,HP:0011218,Abnormal shape of the frontal region
+UBERON:0010333,extraembryonic membrane mesenchyme,UBERON:0004120,mesoderm-derived structure
+UBERON:0002197,median eminence of neurohypophysis,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001576,intrinsic muscle of tongue,UBERON:0000378,tongue muscle
+UBERON:0011807,epidermis of feather follicle,UBERON:0004121,ectoderm-derived structure
+HP:0001302,Pachygyria,HP:0002536,Abnormal cortical gyration
+UBERON:0010882,limb bone pre-cartilage condensation,UBERON:0015061,limb endochondral element
+DOID:10120,eyelid degenerative disease,DOID:530,eyelid disease
+HP:0000675,Macrodontia of permanent maxillary central incisor,HP:0011081,Incisor macrodontia
+UBERON:0002218,tympanic ring,UBERON:0002514,intramembranous bone
+UBERON:3010784,m. oblique internus,UBERON:0008777,hypaxial musclulature
+DOID:3535,Unverricht-Lundborg syndrome,DOID:891,progressive myoclonus epilepsy
+UBERON:2001616,lateral ethmoid wing,UBERON:0004120,mesoderm-derived structure
+HP:0005640,Abnormal vertebral segmentation and fusion,HP:0002948,Vertebral fusion
+HP:0005136,Premature calcification of mitral annulus,HP:0004382,Mitral valve calcification
+HP:0010231,Enlarged epiphyses of the phalanges of the hand,HP:0010580,Enlarged epiphyses
+HP:0007380,Facial telangiectasia,HP:0100585,Teleangiectasia of the skin
+DOID:8881,rosacea,DOID:37,skin disease
+DOID:12132,Wegener's granulomatosis,DOID:865,vasculitis
+HP:0100249,Calcification of muscles,HP:0010766,Ectopic calcification
+UBERON:0001209,serosa of large intestine,UBERON:0001243,serosa of intestine
+HP:0100870,Plantar telangiectasia,HP:0100872,Abnormality of the plantar skin of foot
+DOID:5139,cellular leiomyoma,DOID:127,leiomyoma
+UBERON:0015121,left outer canthus,UBERON:0006726,outer canthus
+HP:0011116,Abnormality of interferon secretion,HP:0011113,Abnormality of cytokine secretion
+DOID:12683,vestibular neuronitis,DOID:12657,vestibulocochlear nerve disease
+DOID:4492,avian influenza,DOID:8469,influenza
+UBERON:0002071,stratum lucidum of epidermis,UBERON:0013754,integumentary system layer
+UBERON:0010286,midbrain neural tube,UBERON:0004121,ectoderm-derived structure
+DOID:4972,myelodysplastic myeloproliferative cancer,DOID:4960,bone marrow cancer
+HP:0100051,Pseudoepiphyses of the 2nd toe,HP:0010323,Abnormality of the epiphyses of the 2nd toe
+HP:0001743,Abnormality of the spleen,HP:0002012,Abnormality of the abdominal organs
+UBERON:0016479,fibrous capsule of liver,UBERON:0004119,endoderm-derived structure
+DOID:11748,round ligament malignant neoplasm,DOID:11747,uterine adnexa cancer
+HP:0011761,Pituitary null cell adenoma,HP:0002893,Pituitary adenoma
+HP:0011081,Incisor macrodontia,HP:0011063,Abnormality of incisor morphology
+UBERON:0009988,condyle of humerus,UBERON:0004120,mesoderm-derived structure
+DOID:0050655,Bamforth-Lazarus syndrome,DOID:1459,hypothyroidism
+CL:1000391,melanocyte of eyelid,CL:0000148,melanocyte
+HP:0009883,Duplication of the distal phalanx of hand,HP:0009832,Abnormality of the distal phalanx of finger
+HP:0000378,Cupped ear,HP:0000377,Abnormality of the pinna
+UBERON:2001026,supraorbital lateral line neuromast,UBERON:0008904,neuromast
+UBERON:0012117,lumen of nutrient foramen,UBERON:0000464,anatomical space
+HP:0011764,Pituitary spindle cell oncocytoma,HP:0011750,Neoplasm of the anterior pituitary
+UBERON:3000658,prechoanal process,UBERON:0004120,mesoderm-derived structure
+HP:0003234,Decreased plasma carnitine,HP:0003287,Abnormality of mitochondrial metabolism
+HP:0100668,Intestinal duplication,HP:0011140,Gastrointestinal duplication
+DOID:0050336,hypophosphatemia,DOID:2485,phosphorus metabolism disease
+UBERON:0004178,aorta smooth muscle tissue,UBERON:0004695,arterial system smooth muscle
+DOID:14456,Brucella melitensis brucellosis,DOID:11077,brucellosis
+UBERON:0007098,mandibular neural crest,UBERON:0003099,cranial neural crest
+NCBITaxon:1647,Erysipelothrix,NCBITaxon:128827,Erysipelotrichaceae
+HP:0010030,Osteolytic defects of the 1st metacarpal,HP:0001504,Metacarpal osteolysis
+UBERON:0009622,pronephric proximal straight tubule,UBERON:0001290,proximal straight tubule
+HP:0006821,"Polymicrogyria, anterior to posterior gradient",HP:0002126,Polymicrogyria
+UBERON:0006656,deep dorsal vein of penis,UBERON:0001638,vein
+UBERON:0002103,hindlimb,UBERON:0002101,limb
+HP:0008752,Laryngeal cartilage malformation,HP:0001600,Abnormality of the larynx
+DOID:7752,extrahepatic biliary papillomatosis,DOID:5468,biliary papillomatosis
+CL:0002288,type V taste receptor cell,CL:0000209,taste receptor cell
+HP:0006424,Elongated radius,HP:0002818,Abnormality of the radius
+UBERON:0004294,glomerular capillary endothelium,UBERON:0004189,glomerular endothelium
+DOID:4553,thymus large cell carcinoma,DOID:3284,thymic carcinoma
+UBERON:0004248,pedal digit bone,UBERON:0012359,pedal digitopodium bone
+UBERON:0004827,thyroid gland medulla,UBERON:0004119,endoderm-derived structure
+DOID:13490,active cochleovestibular Meniere's disease,DOID:9849,Meniere's disease
+CL:0000637,chromophil cell of anterior pituitary gland,CL:0000150,glandular epithelial cell
+DOID:8224,central breast papilloma,DOID:1626,breast duct papilloma
+UBERON:0000328,gut wall,UBERON:0000060,anatomical wall
+DOID:11355,bladder calculus,DOID:9590,lower urinary tract calculus
+HP:0100478,Symphalangism affecting the distal phalanx of the 5th toe,HP:0001859,Distal symphalangism (feet)
+UBERON:0016458,esophageal hiatus,UBERON:0004120,mesoderm-derived structure
+UBERON:0004250,upper arm bone,UBERON:0003460,arm bone
+DOID:8118,mature gastric teratoma,DOID:5566,mature teratoma
+UBERON:0007181,serosa of infundibulum of uterine tube,UBERON:0000042,serous membrane
+CL:0002486,strial intermediate cell,CL:0002491,auditory epithelial cell
+UBERON:0005018,mucosa of nasal septum,UBERON:0001826,nasal cavity mucosa
+UBERON:2001545,sublingual ventral cartilage,UBERON:2001544,sublingual cartilage
+UBERON:0015872,mandibular lymph node,UBERON:0015871,facial lymph node
+HP:0009457,Aplasia/Hypoplasia of the proximal phalanx of the 3rd finger,HP:0009358,Abnormality of the proximal phalanx of the 3rd finger
+HP:0001413,Micronodular cirrhosis,HP:0001394,Cirrhosis
+UBERON:2001147,tooth 2MD,UBERON:2000694,ceratobranchial 5 tooth
+HP:0007759,Opacification of the corneal stroma,HP:0007957,Corneal opacity
+UBERON:4300104,ectocoracoid bone,UBERON:0007829,pectoral girdle bone
+DOID:3627,aortic aneurysm,DOID:520,aortic disease
+UBERON:0001567,cheek,UBERON:0015212,lateral structure
+DOID:8455,pyridoxine deficiency anemia,DOID:5113,nutritional deficiency disease
+UBERON:0001640,celiac artery,UBERON:0005616,mesenteric artery
+DOID:10632,Wolfram syndrome,DOID:630,genetic disease
+HP:0012512,Diffuse optic disc pallor,HP:0000543,Optic disc pallor
+UBERON:0003823,hindlimb zeugopod,UBERON:0008784,lower limb segment
+HP:0011151,Obtundation status,HP:0002133,Status epilepticus
+UBERON:2001563,hypural 4,UBERON:2000364,hypural
+UBERON:0006087,internal arcuate fiber bundle,UBERON:0011215,cell part cluster of neuraxis
+UBERON:0008247,tube foot,UBERON:0000026,appendage
+HP:0008589,Hypoplastic helices,HP:0011039,Abnormality of the helix
+UBERON:0011969,mesotarsal joint,UBERON:0001488,ankle joint
+UBERON:2002019,pterotic-posttemporal-supracleithrum,UBERON:0007829,pectoral girdle bone
+UBERON:0008284,columnella muscle,UBERON:0001630,muscle organ
+DOID:1140,spinal canal and spinal cord meningioma,DOID:5612,spinal cancer
+UBERON:3000862,pubo-ischium,UBERON:0010363,endochondral element
+UBERON:0009870,zone of stomach,UBERON:0009034,stomach region
+DOID:14671,multiple intestinal atresia,DOID:0050737,autosomal recessive disease
+UBERON:0007171,border of scapula,UBERON:0006800,anatomical line
+HP:0000905,Progressive clavicular acroosteolysis,HP:0000889,Abnormality of the clavicles
+UBERON:0001695,squamous part of temporal bone,UBERON:0008907,dermal bone
+HP:0004345,Abnormality of ganglioside metabolism,HP:0004343,Abnormality of glycosphingolipid metabolism
+HP:0003535,3-Methylglutaconic aciduria,HP:0003287,Abnormality of mitochondrial metabolism
+UBERON:0009913,renal lobe,UBERON:0006554,urinary system structure
+HP:0005072,Hyperextensibility at wrists,HP:0001382,Joint hypermobility
+HP:0011033,Impairment of fructose metabolism,HP:0011013,Abnormality of carbohydrate metabolism/homeostasis
+CL:0002517,interrenal epinephrin secreting cell,CL:0002516,interrenal chromaffin cell
+UBERON:0003337,serosa of jejunum,UBERON:0001206,serosa of small intestine
+UBERON:2005029,rostral blood island,UBERON:0000479,tissue
+UBERON:0002907,superior postcentral sulcus,UBERON:0013118,sulcus of brain
+HP:0003965,Pseudarthrosis of the forearm bones,HP:0002973,Abnormality of the forearm
+HP:0004840,Hypochromic microcytic anemia,HP:0001931,Hypochromic anemia
+DOID:0060080,Her2-receptor negative breast cancer,DOID:1612,breast cancer
+UBERON:0006699,foramen cecum of tongue,UBERON:0005160,vestigial structure
+UBERON:2001936,posterior nasal barbel,UBERON:2000622,barbel
+UBERON:0001272,innominate bone,UBERON:0007830,pelvic girdle bone/zone
+HP:0010972,Anemia of inadequate production,HP:0001903,Anemia
+UBERON:0000072,segment of respiratory tract,UBERON:0000063,organ segment
+DOID:10199,breast lipoma,DOID:0060082,breast benign neoplasm
+UBERON:2001578,anterior dorsomedial process of autopalatine,UBERON:4100000,skeletal element projection
+HP:0200111,Absent stapes head,HP:0008628,Abnormality of the stapes
+UBERON:0002599,medial olfactory gyrus,UBERON:0000200,gyrus
+HP:0011440,Alcohol-induced rhabdomyolysis,HP:0003201,Rhabdomyolysis
+HP:0007544,Piebaldism,HP:0001010,Hypopigmentation of the skin
+UBERON:2001516,ceratobranchial cartilage,UBERON:2001898,ceratobranchial element
+UBERON:0015106,distal tarsal bone 2 cartilage,UBERON:0015064,autopod cartilage
+UBERON:0001070,external carotid artery,UBERON:0005396,carotid artery segment
+UBERON:0003355,epithelium of incisor,UBERON:0010371,ecto-epithelium
+HP:0004929,Coronary atherosclerosis,HP:0001677,Coronary artery disease
+CL:0005000,spinal cord interneuron,CL:0000402,CNS interneuron
+DOID:0060002,C1 inhibitor deficiency,DOID:626,complement deficiency
+HP:0003942,Synovial chondromatosis of the elbow,HP:0009811,Abnormality of the elbow
+UBERON:0012109,zygomatic process of frontal bone,UBERON:0005913,zone of bone organ
+UBERON:0010193,renal portal vein,UBERON:0001638,vein
+CL:0000688,perijunctional fibroblast,CL:0000630,supportive cell
+UBERON:0001717,spinal nucleus of trigeminal nerve,UBERON:0007635,nucleus of medulla oblongata
+DOID:7574,pancreatic intraductal papillary-colloid carcinoma,DOID:4074,pancreas adenocarcinoma
+DOID:6161,childhood testicular mixed germ cell tumor,DOID:4743,mixed testicular germ cell tumor
+HP:0002960,Autoimmunity,HP:0010978,Abnormality of immune system physiology
+HP:0012226,Ovarian teratoma,HP:0009792,Teratoma
+UBERON:0008975,shell gland,UBERON:0005398,female reproductive gland
+NCBITaxon:485,Neisseria gonorrhoeae,NCBITaxon:482,Neisseria
+UBERON:0006260,lingual swellings,UBERON:0002050,embryonic structure
+UBERON:3000500,processus posterior of maxilla,UBERON:4100000,skeletal element projection
+UBERON:0015760,mixed stratified cuboidal and columnar epithelium,UBERON:0000486,multilaminar epithelium
+HP:0010063,Patchy sclerosis of the phalanges of the hallux,HP:0010178,Patchy sclerosis of the phalanges of the toes
+UBERON:0005685,midgut dorsal mesentery,UBERON:0002296,dorsal mesentery
+HP:0010995,Abnormality of dicarboxylic acid metabolism,HP:0004354,Abnormality of carboxylic acid metabolism
+DOID:11843,coronary artery anomaly,DOID:3393,coronary artery disease
+HP:0009435,Symphalangism of middle phalanx of 3rd finger,HP:0009849,Symphalangism of middle phalanx of finger
+CL:0000502,type D enteroendocrine cell,CL:0000172,somatostatin secreting cell
+UBERON:0010146,paraurethral duct,UBERON:0000058,duct
+UBERON:0014693,inferior alveolar artery,UBERON:0009654,alveolar artery
+UBERON:0012239,urinary bladder vasculature,UBERON:0006876,vasculature of organ
+DOID:3374,peripheral osteosarcoma,DOID:3376,bone osteosarcoma
+HP:0009804,Reduced number of teeth,HP:0006483,Abnormal number of teeth
+HP:0011441,Abnormality of the medulla oblongata,HP:0002363,Abnormality of the brainstem
+DOID:0050051,Rickettsia parkeri spotted fever,DOID:11104,spotted fever
+HP:0003097,Short femur,HP:0005613,Aplasia/hypoplasia of the femur
+HP:0200015,Symmetric great toe depigmentation,HP:0001000,Abnormality of skin pigmentation
+DOID:962,neurofibroma,DOID:3193,peripheral nerve sheath neoplasm
+UBERON:0011272,embryonic skin basal layer,UBERON:0000490,unilaminar epithelium
+UBERON:0007247,superior olivary nucleus,UBERON:0009662,hindbrain nucleus
+HP:0007447,Diffuse palmoplantar hyperkeratosis,HP:0000972,Palmoplantar hyperkeratosis
+CL:0002389,uninucleate arthroconidium,CL:0002387,arthroconidium
+UBERON:0012356,pedal acropodium region,UBERON:0012354,acropodium region
+CL:0000866,thymic macrophage,CL:0000864,tissue-resident macrophage
+UBERON:0006713,foramen cecum of frontal bone,UBERON:0004121,ectoderm-derived structure
+UBERON:0010365,odontoid tissue,UBERON:0010313,neural crest-derived structure
+HP:0012684,Abnormal pineal volume,HP:0012681,Abnormality of pineal morphology
+UBERON:0004245,oviduct smooth muscle,UBERON:0001135,smooth muscle tissue
+HP:0010730,Double eyebrow,HP:0000534,Abnormality of the eyebrow
+DOID:8573,lichen nitidus,DOID:8574,lichen disease
+HP:0010131,Fragmentation of the epiphysis of the proximal phalanx of the hallux,HP:0010117,Fragmentation of the epiphyses of the hallux
+DOID:3675,childhood kidney neoplasm,DOID:263,kidney cancer
+UBERON:0007681,facial neural crest,UBERON:0010313,neural crest-derived structure
+HP:0100372,Aplasia/Hypoplasia of the middle phalanx of the 3rd toe,HP:0010359,Aplasia/Hypoplasia of the phalanges of the 3rd toe
+UBERON:0001480,proximal carpal bone,UBERON:0015078,proximal carpal endochondral element
+HP:0011960,Substantia nigra gliosis,HP:0002171,Gliosis
+HP:0001062,Atypical nevi (>5mm with irregular edge and pigmentation),HP:0003764,Nevus
+DOID:4287,external ear basal cell carcinoma,DOID:4288,external ear carcinoma
+UBERON:0003065,ciliary marginal zone,UBERON:0000477,anatomical cluster
+HP:0100494,Abnormality of mast cells,HP:0010974,Abnormality of myeloid leukocytes
+UBERON:3010754,ramus recurrens,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0009579,myelencephalon basal plate,UBERON:0004064,neural tube basal plate
+HP:0001227,Abnormality of the thenar eminence,HP:0001421,Abnormality of the musculature of the hand
+UBERON:0002529,limb segment,UBERON:0010538,paired limb/fin segment
+UBERON:0012249,ectocervix,UBERON:0005156,reproductive structure
+UBERON:0001421,pectoral girdle region,UBERON:0007823,appendage girdle region
+UBERON:0002540,lateral line system,UBERON:0001032,sensory system
+HP:0000935,Thickened cortex of long bones,HP:0100039,Thickened cortex of bones
+UBERON:0010344,3rd arch mesenchyme from head mesenchyme,UBERON:0005690,3rd arch mesenchyme
+HP:0005353,Susceptibility to herpesvirus,HP:0004429,Recurrent viral infections
+UBERON:2000202,efferent branchial artery,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0005575,Hemolytic-uremic syndrome,HP:0012211,Abnormal renal physiology
+UBERON:2007055,pillar of the lateral semicircular canal,UBERON:2002223,pillar of the semicircular canal
+UBERON:0010291,layer of sclera,UBERON:0000064,organ part
+HP:0009858,Triangular shaped proximal phalanges of the hand,HP:0009834,Abnormality of the proximal phalanges of the hand
+UBERON:0002768,vestibulospinal tract,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0008489,Spondylolisthesis at L5-S1,HP:0003302,Spondylolisthesis
+HP:0002127,Upper motor neuron abnormality,HP:0002450,Abnormality of the motor neurons
+HP:0200126,Amyolid cardiomyopathy,HP:0001638,Cardiomyopathy
+HP:0001291,Abnormality of the cranial nerves,HP:0002011,Abnormality of the central nervous system
+HP:0001150,Choroidal sclerosis,HP:0000610,Abnormality of the choroid
+HP:0012412,Premature adrenarche,HP:0100000,Early onset of sexual maturation
+UBERON:0004727,cochlear nerve,UBERON:0001785,cranial nerve
+UBERON:0013475,gustatory gland,UBERON:0003409,gland of tongue
+HP:0003324,Generalized muscle weakness,HP:0001324,Muscle weakness
+HP:0011878,Abnormal platelet membrane protein expression,HP:0011869,Abnormal platelet function
+HP:0004959,Dilatation of the descending thoracic aorta,HP:0001724,Aortic dilatation
+UBERON:0011650,epihyoidean,UBERON:0001577,facial nerve muscle
+UBERON:0003314,eye mesenchyme,UBERON:0010312,immature eye
+UBERON:0009953,post-embryonic organism,UBERON:0000468,multi-cellular organism
+NCBITaxon:620,Shigella,NCBITaxon:543,Enterobacteriaceae
+UBERON:0005384,nasal cavity epithelium,UBERON:0003350,epithelium of mucosa
+UBERON:0010349,otic capsule pre-cartilage condensation,UBERON:0015020,otic capsule endochondral element
+DOID:275,gastric hemangioma,DOID:254,hemangioma of intra-abdominal structure
+UBERON:0012471,hepatogastric ligament,UBERON:0004120,mesoderm-derived structure
+UBERON:0002163,inferior cerebellar peduncle,UBERON:0014649,white matter of medulla oblongata
+HP:0008043,Retinal arteriolar constriction,HP:0000630,Abnormality of retinal arteries
+UBERON:0004912,biliary bud,UBERON:0009497,epithelium of foregut-midgut junction
+HP:0010077,Broad distal phalanx of the hallux,HP:0010059,Broad phalanges of the hallux
+UBERON:0016462,periorbital skin,UBERON:1000021,skin of face
+HP:0001003,Multiple lentigines,HP:0001034,Hypermelanotic macule
+HP:0007609,Hypoproteinemic edema,HP:0000969,Edema
+UBERON:2001859,pharyngobranchial 1 tooth plate,UBERON:2002015,pharyngobranchial tooth plate
+UBERON:2001234,hypobranchial 4 bone,UBERON:2001897,hypobranchial 4 element
+UBERON:2205383,dorsal fin proximal radial cartilage 6,UBERON:2105383,dorsal fin proximal radial element 6
+CL:0002574,stromal cell of pancreas,CL:0000499,stromal cell
+CL:0000603,dikaryon,CL:0000227,binucleate cell
+HP:0200097,Oral mucusa blisters,HP:0011830,Abnormality of oral mucosa
+HP:0009526,Cone-shaped epiphysis of the proximal phalanx of the 2nd finger,HP:0010270,Cone-shaped epiphyses of the proximal phalanges of the hand
+DOID:5301,fallopian tube clear cell adenocarcinoma,DOID:3706,fallopian tube adenocarcinoma
+HP:0012585,Renal atrophy,HP:0012210,Abnormal renal morphology
+UBERON:3000453,posterolateral vomerine process,UBERON:0004120,mesoderm-derived structure
+HP:0000855,Insulin resistance,HP:0011014,Abnormal glucose homeostasis
+NCBITaxon:35301,ssRNA negative-strand viruses,NCBITaxon:439488,ssRNA viruses
+NCBITaxon:63419,Trichophyton concentricum,NCBITaxon:5550,Trichophyton
+HP:0008501,Median cleft lip and palate,HP:0009099,Median cleft palate
+HP:0004298,Abnormality of the abdominal wall,HP:0001438,Abnormality of the abdomen
+UBERON:2000745,epaxial region somite 25,UBERON:0003900,epaxial myotome region
+UBERON:0007225,lateral entorhinal cortex,UBERON:0000064,organ part
+UBERON:0007182,muscle layer of infundibulum of uterine tube,UBERON:0005156,reproductive structure
+UBERON:0000477,anatomical cluster,UBERON:0000480,anatomical group
+UBERON:3000433,pineal foramen,UBERON:0004121,ectoderm-derived structure
+UBERON:2005385,dorsal fin proximal radial bone 8,UBERON:2000947,dorsal fin proximal radial bone
+DOID:1591,renovascular hypertension,DOID:1073,renal hypertension
+UBERON:0010865,dactylopatagium medius,UBERON:0010862,dactylopatagium
+UBERON:0015860,visceral abdominal lymph node,UBERON:0002507,abdominal lymph node
+HP:0009315,Triangular shaped proximal phalanx of the 4th finger,HP:0009284,Abnormality of the proximal phalanx of the 4th finger
+HP:0011578,Transitional atrioventricular canal defect,HP:0006695,Atrioventricular canal defect
+UBERON:0011879,mesorchium,UBERON:0000481,multi-tissue structure
+DOID:0050927,duodenum adenoma,DOID:1737,duodenal benign neoplasm
+HP:0005625,Osteoporosis of vertebrae,HP:0000939,Osteoporosis
+HP:0009670,Ivory epiphysis of the proximal phalanx of the thumb,HP:0010263,Ivory epiphyses of the middle phalanges of the hand
+HP:0006352,Failure of eruption of permanent teeth,HP:0000706,Unerupted tooth
+UBERON:0005398,female reproductive gland,UBERON:0003937,sex gland
+CL:0000852,neuromast support cell,CL:0000630,supportive cell
+HP:0005311,Agenesis of pulmonary vessels,HP:0004930,Abnormality of the pulmonary vasculature
+UBERON:4000107,elasmodine,UBERON:0010365,odontoid tissue
+UBERON:0001875,globus pallidus,UBERON:0009663,telencephalic nucleus
+UBERON:0000019,camera-type eye,UBERON:0015212,lateral structure
+UBERON:0012472,hepatoduodenal ligament,UBERON:0005291,embryonic tissue
+UBERON:0004832,anal region skeletal muscle,UBERON:0001134,skeletal muscle tissue
+HP:0004880,Respiratory infections in early life,HP:0002205,Recurrent respiratory infections
+CL:0000499,stromal cell,CL:0002320,connective tissue cell
+UBERON:3000492,processus infrafenestralis,UBERON:0010313,neural crest-derived structure
+HP:0012223,Splenic rupture,HP:0001743,Abnormality of the spleen
+HP:0004313,Hypogammaglobulinemia,HP:0010701,Abnormal immunoglobulin level
+DOID:2960,photosensitive trichothiodystrophy,DOID:0050736,autosomal dominant disease
+UBERON:0006969,cranial appendage,UBERON:0004529,anatomical projection
+UBERON:2001871,Weberian ossicle set,UBERON:0000477,anatomical cluster
+CL:0002222,vertebrate lens cell,CL:0000306,crystallin accumulating cell
+HP:0008053,Aplasia/Hypoplasia of the iris,HP:0008062,Aplasia/Hypoplasia affecting the anterior segment of the eye
+HP:0009473,Joint contracture of the hand,HP:0100360,Contractures of the joints of the upper limbs
+UBERON:2005409,pars superior ear,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:3447,anus adenocarcinoma,DOID:4908,anal carcinoma
+UBERON:0001801,anterior segment of eyeball,UBERON:0004121,ectoderm-derived structure
+HP:0002896,Neoplasm of the liver,HP:0001392,Abnormality of the liver
+UBERON:0015420,ureteral valve,UBERON:0006554,urinary system structure
+UBERON:0003889,fallopian tube,UBERON:0015212,lateral structure
+UBERON:0003667,lower jaw molar,UBERON:0011594,dentary tooth
+HP:0009520,Pseudoepiphysis of the middle phalanx of the 2nd finger,HP:0009495,Pseudoepiphyses of the 2nd finger
+CL:0000938,"CD16-negative, CD56-bright natural killer cell",CL:0000824,mature natural killer cell
+UBERON:0004709,pelvic appendage,UBERON:0004708,paired limb/fin
+UBERON:0001834,upper lip,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0001954,Episodic fever,HP:0001945,Fever
+HP:0003493,Antinuclear antibody positivity,HP:0002960,Autoimmunity
+UBERON:0001862,vestibular labyrinth,UBERON:0004121,ectoderm-derived structure
+HP:0005103,Cartilaginous ossification of pinnae,HP:0000377,Abnormality of the pinna
+CL:0002394,CD141-positive myeloid dendritic cell,CL:0000784,plasmacytoid dendritic cell
+UBERON:0002582,anterior calcarine sulcus,UBERON:0013118,sulcus of brain
+UBERON:0010061,lumen of nasopharynx,UBERON:0000464,anatomical space
+HP:0004690,Thickened Achilles tendon,HP:0005109,Abnormality of the Achilles tendon
+DOID:9952,acute lymphocytic leukemia,DOID:1037,lymphoblastic leukemia
+HP:0002860,Squamous cell carcinoma,HP:0008069,Neoplasm of the skin
+UBERON:2001697,transverse radial,UBERON:0004120,mesoderm-derived structure
+DOID:7537,breast cystic hypersecretory carcinoma,DOID:4922,breast secretory carcinoma
+UBERON:0002068,urachus,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0012151,Hemothorax,HP:0002103,Abnormality of the pleura
+UBERON:0002067,dermis,UBERON:0004923,organ component layer
+UBERON:0002673,vestibular nuclear complex,UBERON:0007635,nucleus of medulla oblongata
+HP:0012688,Abnormality of pineal physiology,HP:0012680,Abnormality of the pineal gland
+UBERON:0002887,basal amygdaloid nucleus,UBERON:0009663,telencephalic nucleus
+HP:0010193,Duplication of distal phalanx of toe,HP:0010182,Abnormality of the distal phalanges of the toes
+UBERON:0005814,arch of atlas,UBERON:0010358,arch of centrum of vertebra
+UBERON:0002598,paracentral sulcus,UBERON:0003022,cerebral cortex lobe
+DOID:11603,infant gynecomastia,DOID:3463,breast disease
+UBERON:3000803,sulcus articularis lateralis,UBERON:0000064,organ part
+DOID:0050542,Charcot-Marie-Tooth disease type X,DOID:10595,Charcot-Marie-Tooth disease
+HP:0008024,Congenital nuclear cataract,HP:0100018,Nuclear cataract
+HP:0000888,Horizontal ribs,HP:0000772,Abnormality of the ribs
+CL:0002611,neuron of the dorsal spinal cord,CL:0000117,CNS neuron (sensu Vertebrata)
+HP:0010364,Patchy sclerosis of the phalanges of the 3rd toe,HP:0010330,Abnormality of the phalanges of the 3rd toe
+HP:0010416,Curved distal phalanx of the 2nd toe,HP:0010350,Curved phalanges of the 2nd toe
+UBERON:0009125,petrosal placode,UBERON:0003078,epibranchial placode
+UBERON:0001448,metatarsal bone,UBERON:0012359,pedal digitopodium bone
+UBERON:0010745,sacral vertebra cartilage element,UBERON:0011094,vertebra cartilage element
+UBERON:0006591,transformed artery,UBERON:0004120,mesoderm-derived structure
+HP:0001096,Keratoconjunctivitis,HP:0000509,Conjunctivitis
+HP:0004371,Abnormality of glycosaminoglycan metabolism,HP:0011012,Abnormality of polysaccharide metabolism
+UBERON:0012140,digitopodium region,UBERON:0012139,segment of autopod
+UBERON:0009192,basisphenoid pre-cartilage condensation,UBERON:0007213,mesenchyme derived from head neural crest
+CL:0000352,epiblast cell,CL:0000052,totipotent stem cell
+HP:0001321,Cerebellar hypoplasia,HP:0007360,Aplasia/Hypoplasia of the cerebellum
+HP:0006596,Restricted chest movement,HP:0001376,Limitation of joint mobility
+UBERON:2001518,ceratobranchial 3 cartilage,UBERON:2001901,ceratobranchial 3 element
+HP:0009261,Absent epiphysis of the proximal phalanx of the 4th finger,HP:0009248,Abnormality of the epiphysis of the proximal phalanx of the 4th finger
+UBERON:0001358,perineal artery,UBERON:0003520,pelvis blood vessel
+HP:0009403,Triangular epiphyses of the 4th finger,HP:0009174,Abnormality of the epiphyses of the 4th finger
+HP:0012199,Cluster headache,HP:0002315,Headache
+UBERON:0005459,left umbilical vein,UBERON:0002066,umbilical vein
+UBERON:0005750,glomerular parietal epithelium,UBERON:0000487,simple squamous epithelium
+HP:0011978,Elevated urinary vanillylmandelic acid,HP:0004354,Abnormality of carboxylic acid metabolism
+UBERON:0002834,cervical dorsal root ganglion,UBERON:0000044,dorsal root ganglion
+HP:0003201,Rhabdomyolysis,HP:0011805,Abnormality of muscle morphology
+DOID:13561,optic disk drusen,DOID:1891,optic nerve disease
+UBERON:0001818,tarsal gland,UBERON:0015251,modified sebaceous gland
+CL:0002577,placental epithelial cell,CL:0000349,extraembryonic cell
+DOID:2170,vaginitis,DOID:121,vaginal disease
+DOID:3197,schwannoma of twelfth cranial nerve,DOID:3192,neurilemmoma
+UBERON:0013628,pollical pad,UBERON:0012349,digital pad
+DOID:687,hepatoblastoma,DOID:3571,liver cancer
+HP:0009016,Upper limb muscle hypoplasia,HP:0001467,Aplasia/Hypoplasia involving the musculature of the upper limbs
+CL:0002551,fibroblast of dermis,CL:0002620,skin fibroblast
+UBERON:0013703,integumentary projection,UBERON:0006003,integumentary adnexa
+UBERON:0003722,middle cranial fossa,UBERON:0008789,cranial fossa
+HP:0000676,Abnormality of the incisor,HP:0000164,Abnormality of the teeth
+DOID:6231,mature teratoma of the ovary,DOID:6232,ovarian biphasic or triphasic teratoma
+UBERON:3010745,M. coccygeosacralis,UBERON:0010890,pelvic complex muscle
+UBERON:0005856,developing mesenchymal condensation,UBERON:0007524,dense mesenchyme tissue
+HP:0000180,Lobulated tongue,HP:0000157,Abnormality of the tongue
+UBERON:0004983,mucosa of vagina,UBERON:0014404,female anatomical structure
+UBERON:2005375,dorsal fin distal radial bone 4,UBERON:2000936,dorsal fin distal radial bone
+UBERON:0005416,zone of polarizing activity of pelvic appendage,UBERON:0003412,pelvic appendage bud mesenchyme
+HP:0001792,Small nail,HP:0008386,Aplasia/Hypoplasia of the nails
+HP:0002055,Curved linear dimple below the lower lip,HP:0000178,Abnormality of lower lip
+UBERON:0008441,webbed manus,UBERON:0002398,manus
+UBERON:0002280,otolith,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003194,imaginal disc-derived wing vein,UBERON:0000476,acellular anatomical structure
+UBERON:0001471,skin of prepuce of penis,UBERON:0001331,skin of penis
+UBERON:0002675,diagonal sulcus,UBERON:0003022,cerebral cortex lobe
+UBERON:0008260,spine appendage,UBERON:0000026,appendage
+DOID:1638,central nervous system tuberculosis,DOID:0050598,extrapulmonary tuberculosis
+DOID:7390,superior vena cava leiomyosarcoma,DOID:175,vascular cancer
+DOID:5990,internal auditory canal meningioma,DOID:833,auditory system cancer
+HP:0012181,Entrapment neuropathy,HP:0009830,Peripheral neuropathy
+HP:0005294,Arterial dissection,HP:0011004,Abnormality of the systemic arterial tree
+UBERON:0014567,layer of hippocampal field,UBERON:0004923,organ component layer
+UBERON:0010197,trunk of common carotid artery,UBERON:0005396,carotid artery segment
+DOID:13775,plantar wart,DOID:934,viral infectious disease
+UBERON:0002209,fibrous joint,UBERON:0011134,nonsynovial joint
+HP:0012655,Elevated CSF dopamine level,HP:0012654,Abnormal CSF dopamine level
+HP:0009951,Partial duplication of the distal phalanx of the 2nd finger,HP:0010004,Partial duplication of the distal phalanges of the hand
+UBERON:4200170,process 3,UBERON:4100000,skeletal element projection
+UBERON:0000127,facial nucleus,UBERON:0009662,hindbrain nucleus
+HP:0010206,Curved proximal phalanges of the toes,HP:0010176,Curved phalanges of the toes
+CL:1001430,urethra urothelial cell,CL:1000296,epithelial cell of urethra
+UBERON:0011639,frontoparietal bone,UBERON:0008907,dermal bone
+UBERON:0004934,submucosa of body of stomach,UBERON:0001200,submucosa of stomach
+DOID:5050,ehrlich tumor carcinoma,DOID:3459,breast carcinoma
+HP:0100321,Abnormality of the dentate nucleus,HP:0001317,Abnormality of the cerebellum
+HP:0011531,Vitreitis,HP:0004327,Abnormality of the vitreous humor
+UBERON:0003414,mesenchyme of mandible,UBERON:0009891,facial mesenchyme
+UBERON:0009192,basisphenoid pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+DOID:1522,cecum lymphoma,DOID:1521,cecum cancer
+HP:0009824,Upper limb undergrowth,HP:0009826,Limb undergrowth
+HP:0007432,Intermittent generalized erythematous papular rash,HP:0200034,Papule
+HP:0004948,Vascular tortuosity,HP:0002597,Abnormality of the vasculature
+DOID:5692,cellular myxoid liposarcoma,DOID:3382,liposarcoma
+UBERON:0005359,spinal cord ependyma,UBERON:0010371,ecto-epithelium
+HP:0010059,Broad phalanges of the hallux,HP:0010057,Abnormality of the phalanges of the hallux
+HP:0012299,Long distal phalanx of finger,HP:0009832,Abnormality of the distal phalanx of finger
+UBERON:0008843,gubernaculum testis,UBERON:0014403,male anatomical structure
+HP:0001274,Agenesis of corpus callosum,HP:0006989,Dysplastic corpus callosum
+UBERON:0011800,dermal pulp of feather shaft,UBERON:0004121,ectoderm-derived structure
+UBERON:0011301,manubrium sternum pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+DOID:14325,mixed malaria,DOID:12365,malaria
+HP:0011490,Abnormality of Descemet's membrane,HP:0011488,Abnormality of corneal endothelium
+DOID:4933,apocrine adenocarcinoma,DOID:4934,apocrine sweat gland cancer
+HP:0003448,Decreased sensory nerve conduction velocity,HP:0000762,Decreased nerve conduction velocity
+HP:0100489,Proximal/middle symphalangism of 2nd toe,HP:0010410,Symphalangism affecting the middle phalanx of the 2nd toe
+UBERON:0011847,acinus of parotid gland,UBERON:0004121,ectoderm-derived structure
+HP:0011735,Adrenocorticotropin (ACTH) deficient adrenal insufficiency,HP:0011734,Central adrenal insufficiency
+UBERON:0000204,ventral part of telencephalon,UBERON:0002791,regional part of telencephalon
+HP:0009582,Bullet-shaped proximal phalanx of the 2nd finger,HP:0009544,Abnormality of the proximal phalanx of the 2nd finger
+HP:0009127,Abnormality of the musculature of the limbs,HP:0002813,Abnormality of limb bone morphology
+HP:0008150,Elevated serum transaminases during infections,HP:0002910,Elevated hepatic transaminases
+UBERON:0011777,nucleus of spinal cord,UBERON:0000125,neural nucleus
+UBERON:2105226,median fin proximal radial element,UBERON:2105225,median fin radial element
+DOID:1248,ocular hyperemia,DOID:4251,conjunctival disease
+UBERON:0010949,sternooccipital muscle,UBERON:0003897,axial muscle
+UBERON:0001255,urinary bladder,UBERON:0004120,mesoderm-derived structure
+UBERON:0006697,mammillotectal axonal tract,UBERON:0011591,tract of diencephalon
+UBERON:0000351,nuchal ligament,UBERON:0008846,skeletal ligament
+DOID:11727,facioscapulohumeral muscular dystrophy,DOID:9884,muscular dystrophy
+UBERON:0011899,epimysium,UBERON:0011822,dense irregular connective tissue
+UBERON:0007306,pronephric glomerular capillary,UBERON:0004212,glomerular capillary
+UBERON:0004105,subungual region,UBERON:0000477,anatomical cluster
+UBERON:0002633,motor nucleus of trigeminal nerve,UBERON:0000126,cranial nerve nucleus
+DOID:4757,sex cord-stromal neoplasm,DOID:0050622,reproductive organ benign neoplasm
+UBERON:2001663,basibranchial 4 tooth,UBERON:0004756,dermal skeletal element
+UBERON:0006125,subdivision of diagonal band,UBERON:0002791,regional part of telencephalon
+HP:0008204,Precocious puberty with Sertoli cell tumor,HP:0000826,Precocious puberty
+HP:0012362,Abnormal sialylation of O-linked protein glycosylation,HP:0012358,Abnormal protein O-linked glycosylation
+UBERON:0005170,ovary stratum granulosum,UBERON:0000158,membranous layer
+UBERON:0001579,olfactory nerve,UBERON:0004121,ectoderm-derived structure
+DOID:4148,gastrointestinal neuroendocrine benign tumor,DOID:0050624,gastrointestinal system benign neoplasm
+HP:0011339,Abnormality of upper lip vermillion,HP:0000177,Abnormality of upper lip
+UBERON:0012469,external anal region,UBERON:0000477,anatomical cluster
+UBERON:2205372,dorsal fin distal radial cartilage 1,UBERON:2105372,dorsal fin distal radial element 1
+UBERON:0013154,1st arch maxillary endoderm,UBERON:0005911,endo-epithelium
+UBERON:0006345,stapedial artery,UBERON:0003496,head blood vessel
+DOID:1926,Gaucher's disease,DOID:1927,sphingolipidosis
+HP:0009896,Abnormality of the antitragus,HP:0000377,Abnormality of the pinna
+HP:0011415,Calcified placenta,HP:0100767,Abnormality of the placenta
+HP:0004676,prominent supraorbital arches in adult,HP:0000336,Prominent supraorbital ridges
+HP:0010617,Cardiac fibroma,HP:0010614,Fibroma
+HP:0010734,Fibrous dysplasia of the bones,HP:0003330,Abnormal bone structure
+UBERON:2000594,supracleithrum,UBERON:0007829,pectoral girdle bone
+CL:0000780,multinuclear odontoclast,CL:0000779,multinuclear osteoclast
+UBERON:2000701,ventral arrector,UBERON:0014794,pectoral appendage muscle
+DOID:12679,nephrocalcinosis,DOID:182,calcinosis
+HP:0005506,Chronic myelogenous leukemia,HP:0005558,Chronic leukemia
+DOID:9212,pityriasis rubra pilaris,DOID:8893,psoriasis
+HP:0005099,Severe hydrops fetalis,HP:0001789,Hydrops fetalis
+UBERON:0003350,epithelium of mucosa,UBERON:0000483,epithelium
+DOID:5688,Werner syndrome,DOID:0050737,autosomal recessive disease
+HP:0000108,Renal corticomedullary cysts,HP:0100957,Abnormality of the renal medulla
+HP:0001886,"Osteomyelitis or necrosis, distal, due to sensory neuropathy (feet)",HP:0001760,Abnormality of the foot
+CL:0002607,migratory enteric neural crest cell,CL:0000333,migratory neural crest cell
+UBERON:0009883,medullary ray,UBERON:0006554,urinary system structure
+UBERON:0013211,cerumen gland,UBERON:0000382,apocrine sweat gland
+UBERON:0010726,os vesalianum manus,UBERON:0010722,accessory bone
+HP:0002216,Premature graying of hair,HP:0007495,Prematurely aged appearance
+UBERON:2000618,ansulate commissure,UBERON:2000318,brainstem and spinal white matter
+HP:0010950,Abnormality of the fourth ventricle,HP:0002118,Abnormality of the cerebral ventricles
+DOID:4560,non specific chronic endometritis,DOID:1002,endometritis
+DOID:3774,chordoid glioma,DOID:3070,malignant glioma
+HP:0003973,Wide radioulnar joints,HP:0003059,Abnormality of the radioulnar joints
+HP:0001955,Unexplained fevers,HP:0001945,Fever
+UBERON:0001774,muscle of trunk,UBERON:0005177,trunk organ
+UBERON:0003993,interventricular foramen of CNS,UBERON:0004111,anatomical conduit
+DOID:138,vaginal squamous tumor,DOID:119,vaginal cancer
+UBERON:2002069,distal cartilage of posterior process of basipterygium,UBERON:0004120,mesoderm-derived structure
+UBERON:3000828,margo posterior of cleithrum,UBERON:0004120,mesoderm-derived structure
+UBERON:0015093,distal carpal bone 4 endochondral element,UBERON:0015049,carpus endochondral element
+HP:0011807,Type 1 muscle fiber atrophy,HP:0100295,Muscle fiber atrophy
+UBERON:0010567,manual digit 3 metacarpus pre-cartilage condensation,UBERON:0010577,manual digit 3 phalanx pre-cartilage condensation
+UBERON:0000990,reproductive system,UBERON:0004120,mesoderm-derived structure
+UBERON:0015793,induseum griseum,UBERON:0013199,stria of neuraxis
+CL:0000981,double negative memory B cell,CL:0001053,IgD-negative memory B cell
+HP:0003934,Slender humeral diaphysis,HP:0003926,Abnormality of the humeral diaphysis
+HP:0002555,Absent pubic hair,HP:0100133,Abnormality of the pubic hair
+UBERON:0002341,epithelium of segmental bronchus,UBERON:0000115,lung epithelium
+DOID:8097,bladder hepatoid adenocarcinoma,DOID:3711,bladder adenocarcinoma
+UBERON:0002073,hair follicle,UBERON:0000025,tube
+HP:0010918,Abnormality of cysteine metabolism,HP:0004339,Abnormality of sulfur amino acid metabolism
+DOID:10371,yaws,DOID:0050338,primary bacterial infectious disease
+UBERON:0000959,optic chiasma,UBERON:0002464,nerve trunk
+UBERON:0003239,epithelium of posterior semicircular canal,UBERON:0006937,inner ear epithelium
+UBERON:0011786,ramus of feather barbule,UBERON:0013703,integumentary projection
+HP:0009789,Perianal abscess,HP:0100838,Recurrent cutaneous abscess formation
+UBERON:0001909,habenular commissure,UBERON:0011590,commissure of diencephalon
+DOID:11503,diabetic autonomic neuropathy,DOID:9743,diabetic neuropathy
+DOID:8463,corneal ulcer,DOID:4677,keratitis
+CL:0000333,migratory neural crest cell,CL:0000219,motile cell
+UBERON:0003831,respiratory system muscle,UBERON:0001630,muscle organ
+DOID:9869,hereditary fructose intolerance syndrome,DOID:2978,carbohydrate metabolic disorder
+CL:0002329,basal epithelial cell of tracheobronchial tree,CL:0002202,epithelial cell of tracheobronchial tree
+DOID:13957,uterine corpus lipoleiomyoma,DOID:13223,uterine fibroid
+HP:0002981,Abnormality of the calf,HP:0002814,Abnormality of the lower limb
+HP:0000131,Uterine leiomyoma,HP:0010784,Uterine neoplasm
+HP:0006784,Paranasal sinus hypoplasia,HP:0005453,Absent/hypoplastic paranasal sinuses
+CL:1000349,basal cell of epithelium of bronchus,CL:0002633,respiratory basal cell
+DOID:0050116,tinea imbricata,DOID:12179,tinea corporis
+HP:0012576,C3 nephropathy,HP:0000095,Abnormality of the glomerulus
+DOID:4044,skeletal muscle neoplasm,DOID:461,muscle benign neoplasm
+HP:0000016,Urinary retention,HP:0000009,Functional abnormality of the bladder
+HP:0000005,Mode of inheritance,HP:0000001,All
+UBERON:0010850,tibia pre-cartilage condensation,UBERON:0010886,hindlimb bone pre-cartilage condensation
+HP:0006279,Beta-cell dysfunction,HP:0006476,Abnormality of the pancreatic islet cells
+DOID:76,stomach disease,DOID:77,gastrointestinal system disease
+UBERON:0013112,viper venom,UBERON:0013076,snake venom
+UBERON:2002077,lateropterygium,UBERON:0002513,endochondral bone
+UBERON:2000807,myotome somite 26,UBERON:0003082,myotome
+UBERON:0008842,suspensory ligament of testis,UBERON:0008841,suspensory ligament
+HP:0100572,Fibrous cardiac diverticulum,HP:0006698,Ventricular aneurysm
+HP:0000089,Renal hypoplasia,HP:0008678,Renal hypoplasia/aplasia
+DOID:4028,angioma serpiginosum,DOID:1272,telangiectasis
+DOID:14498,lipoid proteinosis,DOID:3146,lipid metabolism disorder
+DOID:10156,ileal neoplasm,DOID:7505,small intestine neoplasm
+HP:0009494,Ivory epiphyses of the 2nd finger,HP:0010234,Ivory epiphyses of the phalanges of the hand
+UBERON:2000772,hypaxial region somite 25,UBERON:0003895,hypaxial myotome region
+UBERON:0010856,patagium,UBERON:0000094,membrane organ
+DOID:0080055,achondrogenesis type IB,DOID:0080043,achondrogenesis
+DOID:0050906,conjunctival nevus,DOID:0060096,sensory organ benign neoplasm
+HP:0001830,Postaxial foot polydactyly,HP:0100259,Postaxial polydactyly
+UBERON:0002368,endocrine gland,UBERON:0002530,gland
+DOID:9487,Meckel's diverticulum,DOID:0080015,physical disorder
+UBERON:2000623,basipterygium bone,UBERON:0002513,endochondral bone
+CL:0002538,intrahepatic bile duct epithelial cell,CL:0000182,hepatocyte
+HP:0002711,Exaggerated median tongue furrow,HP:0000221,Furrowed tongue
+UBERON:0002467,filiform papilla,UBERON:0001726,papilla of tongue
+DOID:12118,brown induration,DOID:850,lung disease
+HP:0000567,Chorioretinal coloboma,HP:0000480,Retinal coloboma
+UBERON:2001607,basipterygoid process of parasphenoid,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004850,lymph node endothelium,UBERON:0001986,endothelium
+CL:0000901,Tr1 cell,CL:0000815,regulatory T cell
+UBERON:0003220,metanephric mesenchyme,UBERON:0005291,embryonic tissue
+UBERON:3000260,lamina nariochoanalis,UBERON:0004121,ectoderm-derived structure
+HP:0001241,Capitate-hamate fusion,HP:0009702,Carpal synostosis
+DOID:0060083,immune system cancer,DOID:0050686,organ system cancer
+UBERON:0005203,trachea gland,UBERON:0004119,endoderm-derived structure
+HP:0007131,Acute demyelinating polyneuropathy,HP:0007108,Demyelinating peripheral neuropathy
+HP:0011115,Abnormality of chemokine secretion,HP:0011113,Abnormality of cytokine secretion
+CL:0002244,squamous cell of ectocervix,CL:0002149,epithelial cell of uterus
+UBERON:2002094,dorsal fin pterygiophore 1,UBERON:2001419,dorsal fin pterygiophore
+UBERON:0001706,nasal septum,UBERON:0004120,mesoderm-derived structure
+UBERON:0007832,pelvic girdle skeleton,UBERON:0010719,girdle skeleton
+HP:0000582,Upslanted palpebral fissure,HP:0200006,Slanting of the palpebral fissure
+DOID:7459,acantholytic variant squamous cell breast carcinoma,DOID:5514,breast squamous cell carcinoma
+DOID:6543,acne,DOID:9098,sebaceous gland disease
+HP:0000475,Broad neck,HP:0000464,Abnormality of the neck
+HP:0100209,Pseudoepiphysis of the distal phalanx of the 5th toe,HP:0100084,Pseudoepiphyses of the 5th toe
+HP:0000149,Ovarian gonadoblastoma,HP:0100615,Ovarian neoplasm
+CL:0001034,cell in vitro,CL:0000000,cell
+UBERON:0007318,saphenous vein,UBERON:0004261,lower leg blood vessel
+UBERON:3010827,anterior prenasal cartilage,UBERON:0003406,cartilage of respiratory system
+DOID:3120,gallbladder papillomatosis,DOID:0050625,biliary tract neoplasm
+UBERON:0002198,neurohypophysis,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001788,outer limiting layer of retina,UBERON:0007619,limiting membrane of retina
+UBERON:0002567,basal part of pons,UBERON:0004121,ectoderm-derived structure
+UBERON:0002310,hippocampus fimbria,UBERON:0000064,organ part
+HP:0011414,Hydropic placenta,HP:0100767,Abnormality of the placenta
+HP:0009534,Triangular epiphysis of the proximal phalanx of the 2nd finger,HP:0009501,Abnormality of the epiphysis of the proximal phalanx of the 2nd finger
+UBERON:0007244,inferior olivary nucleus,UBERON:0007635,nucleus of medulla oblongata
+CL:1000325,jejunal goblet cell,CL:1000317,intestinal villus goblet cell
+UBERON:0001433,distal carpal bone 4,UBERON:0015093,distal carpal bone 4 endochondral element
+UBERON:0012152,skeleton of pedal digitopodium,UBERON:0012150,skeleton of digitopodium
+HP:0006217,Limited mobility of proximal interphalangeal joint,HP:0006261,Abnormality of phalangeal joints of the hand
+DOID:3572,intracranial sinus thrombosis,DOID:4193,intracranial thrombosis
+HP:0002143,Abnormality of the spinal cord,HP:0007319,Morphological abnormality of the central nervous system
+UBERON:0009914,renal lobule,UBERON:0006554,urinary system structure
+HP:0000927,Abnormality of skeletal maturation,HP:0011843,Abnormality of skeletal physiology
+HP:0100272,Branchial sinus,HP:0009794,Branchial anomaly
+UBERON:4200156,metapodium bone 8,UBERON:0003821,metapodium bone
+UBERON:2205377,dorsal fin distal radial cartilage 6,UBERON:2105377,dorsal fin distal radial element 6
+UBERON:0010752,exoccipital cartilage element,UBERON:0015051,exoccipital endochondral element
+UBERON:0011117,superior tibiofibular joint,UBERON:0011112,tibiofibular joint
+NCBITaxon:34385,mitosporic Arthrodermataceae,NCBITaxon:34384,Arthrodermataceae
+HP:0009954,Complete duplication of the proximal phalanx of the 2nd finger,HP:0009947,Duplication of the proximal phalanx of the 2nd finger
+HP:0000961,Cyanosis,HP:0001005,Dermatological manifestations of systemic disorders
+UBERON:4200097,intermediate spine,UBERON:0004529,anatomical projection
+DOID:0050642,hypochromic microcytic anemia,DOID:11252,microcytic anemia
+UBERON:0016446,hair of head,UBERON:0001037,strand of hair
+UBERON:0015120,right outer canthus,UBERON:0006726,outer canthus
+HP:0010820,Dacrystic seizures,HP:0011153,Focal motor seizures
+UBERON:0000178,blood,UBERON:0000179,haemolymphatic fluid
+HP:0100050,Ivory epiphyses of the 2nd toe,HP:0010323,Abnormality of the epiphyses of the 2nd toe
+UBERON:3010695,m. serratus superior,UBERON:0010891,pectoral complex muscle
+HP:0004308,Ventricular arrhythmia,HP:0011675,Arrhythmia
+HP:0100200,Stippling of the epiphysis of the proximal phalanx of the 4th toe,HP:0100075,Stippling of the epiphyses of the 4th toe
+HP:0003191,Cleft ala nasi,HP:0000429,Abnormality of the nasal alae
+DOID:10122,hyperpigmentation of eyelid,DOID:10123,pigmentation disease
+UBERON:0011917,thalamic glomerulus,UBERON:0001047,neural glomerulus
+UBERON:3000840,capitulum of radius,UBERON:0005055,zone of long bone
+HP:0009884,Tapered distal phalanges of finger,HP:0009832,Abnormality of the distal phalanx of finger
+UBERON:0009481,cavity of pericardio-peritoneal canal,UBERON:0005082,tube lumen
+DOID:9155,mucocutaneous leishmaniasis,DOID:9065,leishmaniasis
+UBERON:0010090,future falx cerebri,UBERON:0007524,dense mesenchyme tissue
+UBERON:0004183,labyrinthine layer blood vessel,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:9903,meibomian cyst,DOID:9423,blepharitis
+HP:0011763,Pituitary carcinoma,HP:0011750,Neoplasm of the anterior pituitary
+HP:0003913,Irregular humeral metaphyses,HP:0003850,Irregular metaphyses of the upper limbs
+DOID:11389,subdural empyema,DOID:331,central nervous system disease
+HP:0008572,External ear malformation,HP:0000356,Abnormality of the outer ear
+UBERON:0002850,seventh thoracic dorsal root ganglion,UBERON:0002835,thoracic dorsal root ganglion
+HP:0009582,Bullet-shaped proximal phalanx of the 2nd finger,HP:0009548,Bullet-shaped phalanges of the 2nd finger
+DOID:4464,collecting duct carcinoma,DOID:4450,renal cell carcinoma
+UBERON:0012237,superior phrenic vein,UBERON:0012193,phrenic vein
+DOID:2846,bruxism,DOID:535,sleep disorder
+UBERON:0000007,pituitary gland,UBERON:0010133,neuroendocrine gland
+CL:0000770,band form basophil,CL:0000768,immature basophil
+UBERON:4000172,lepidotrichium,UBERON:0008907,dermal bone
+UBERON:0005313,mammary duct terminal end bud,UBERON:0014404,female anatomical structure
+UBERON:3000434,planum antorbitale,UBERON:0010313,neural crest-derived structure
+HP:0000410,Mixed hearing impairment,HP:0000405,Conductive hearing impairment
+HP:0009516,Enlarged epiphysis of the middle phalanx of the 2nd finger,HP:0010260,Enlarged epiphyses of the middle phalanges of the hand
+UBERON:0010164,collection of hairs,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0000494,Downslanted palpebral fissures,HP:0200006,Slanting of the palpebral fissure
+UBERON:0005160,vestigial structure,UBERON:0000061,anatomical structure
+HP:0000972,Palmoplantar hyperkeratosis,HP:0100871,Abnormality of the palm
+UBERON:0001933,retrochiasmatic area,UBERON:0004121,ectoderm-derived structure
+UBERON:0013720,dartos muscle of labia majora,UBERON:0014404,female anatomical structure
+UBERON:0011919,yolk sac blood island,UBERON:0003061,blood island
+UBERON:0004313,distal phalanx of manual digit 4,UBERON:0003638,manual digit 4 phalanx
+UBERON:0009989,condyle of tibia,UBERON:0004120,mesoderm-derived structure
+DOID:8225,microscopic breast papilloma,DOID:1626,breast duct papilloma
+UBERON:0001823,nasal cartilage,UBERON:0003566,head connective tissue
+HP:0005453,Absent/hypoplastic paranasal sinuses,HP:0009120,Aplasia/Hypoplasia involving the sinuses
+UBERON:0010376,pancreas ventral primordium,UBERON:0004119,endoderm-derived structure
+HP:0011222,Depressed glabella,HP:0002056,Abnormality of the glabella
+UBERON:0004030,aqueous vein,UBERON:0009141,craniocervical region vein
+HP:0005905,Abnormal cervical curvature,HP:0010674,Abnormality of the curvature of the vertebral column
+HP:0009666,Cone-shaped epiphysis of the proximal phalanx of the thumb,HP:0010259,Cone-shaped epiphyses of the middle phalanges of the hand
+UBERON:3000659,postchoanal process,UBERON:0004120,mesoderm-derived structure
+UBERON:0007099,hyoid neural crest,UBERON:0003099,cranial neural crest
+UBERON:0010257,6th arch mesenchyme from neural crest,UBERON:0010031,6th arch mesenchyme
+UBERON:0014456,extraperitoneal space,UBERON:0000464,anatomical space
+HP:0012511,Temporal optic disc pallor,HP:0000543,Optic disc pallor
+DOID:3389,Papillon-Lefevre disease,DOID:3388,periodontal disease
+UBERON:2001943,metapterygoid-autopalatine ligament,UBERON:0008846,skeletal ligament
+CL:0002083,type I cell of adrenal medulla,CL:0000336,adrenal medulla chromaffin cell
+HP:0007747,Monocular horizontal nystagmus,HP:0000666,Horizontal nystagmus
+UBERON:2000177,caudal oblique,UBERON:0000933,pharyngeal muscle
+HP:0012347,Abnormal protein N-linked glycosylation,HP:0012346,Abnormal protein glycosylation
+HP:0012399,Pressure ulcer,HP:0200042,Skin ulcer
+CL:0002289,type I taste bud cell,CL:0000209,taste receptor cell
+UBERON:2001577,premaxilla ascending process,UBERON:4100000,skeletal element projection
+DOID:3604,ovarian mucinous cystadenocarcinoma,DOID:3605,ovarian cystadenocarcinoma
+HP:0002542,Olivopontocerebellar atrophy,HP:0001317,Abnormality of the cerebellum
+UBERON:0012300,limb paddle,UBERON:0005423,developing anatomical structure
+UBERON:0005476,spinal nerve trunk,UBERON:0002464,nerve trunk
+DOID:0050781,Ogden syndrome,DOID:0050735,X-linked disease
+DOID:2952,inner ear disease,DOID:2742,auditory system disease
+UBERON:0001690,ear,UBERON:0000020,sense organ
+DOID:10193,classic type lipoma,DOID:3315,lipoma
+UBERON:0001532,internal carotid artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3010449,dorsal marginal zone,UBERON:0004879,marginal zone of embryo
+HP:0001816,Thin nail,HP:0001597,Abnormality of the nail
+DOID:1894,noninfectious dermatoses of eyelid,DOID:9423,blepharitis
+UBERON:0000031,lamina propria of trachea,UBERON:0004779,respiratory system lamina propria
+DOID:14723,beta-ketothiolase deficiency,DOID:0050737,autosomal recessive disease
+HP:0001018,Abnormal palmar dermatoglyphics,HP:0007477,Abnormal dermatoglyphics
+HP:0004272,Cortical thinning of hand bones,HP:0002753,Thin bony cortex
+DOID:2848,melancholia,DOID:1596,mental depression
+UBERON:0001188,right testicular artery,UBERON:0003468,ureteric segment of renal artery
+DOID:9773,female breast upper-outer quadrant cancer,DOID:0050671,female breast cancer
+UBERON:0007224,medial entorhinal cortex,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:0050200,Korean hemorrhagic fever,DOID:11266,hemorrhagic fever with renal syndrome
+DOID:10612,allergic urticaria,DOID:1555,urticaria
+HP:0003964,Osteoporotic forearm bones,HP:0002973,Abnormality of the forearm
+UBERON:2001937,anterior nasal barbel,UBERON:2000622,barbel
+HP:0100645,Cystocele,HP:0000014,Abnormality of the bladder
+UBERON:3000433,pineal foramen,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0003084,Fractures of the long bones,HP:0002757,Recurrent fractures
+UBERON:0001671,temporal vein,UBERON:0003496,head blood vessel
+UBERON:0011675,perichordal ring,UBERON:0002384,connective tissue
+UBERON:0006359,mesoduodenum,UBERON:0001170,mesentery of small intestine
+HP:0007626,Mandibular osteomyelitis,HP:0002754,Osteomyelitis
+HP:0010829,Impaired temperature sensation,HP:0003474,Sensory impairment
+HP:0000813,Bicornuate uterus,HP:0000130,Abnormality of the uterus
+HP:0200094,Frontal open bite,HP:0010807,Open bite
+CL:0000950,IgE plasmablast,CL:0000980,plasmablast
+UBERON:0003092,ultimobranchial body,UBERON:0010314,structure with developmental contribution from neural crest
+CL:1000500,kidney interstitial cell,CL:0002320,connective tissue cell
+DOID:14566,disease of cellular proliferation,DOID:4,disease
+HP:0100826,Neoplasm of the nail,HP:0001597,Abnormality of the nail
+HP:0003943,Abnormality of the joint spaces of the elbow,HP:0009811,Abnormality of the elbow
+HP:0000267,Cranial asymmetry,HP:0002648,Abnormality of calvarial morphology
+UBERON:0001913,milk,UBERON:0006539,mammary gland fluid/secretion
+HP:0002307,Drooling,HP:0000708,Behavioural/Psychiatric Abnormality
+HP:0009231,Patchy sclerosis of the proximal phalanx of the 5th finger,HP:0009150,Abnormality of the proximal phalanx of the 5th finger
+UBERON:0002531,paired fin bud,UBERON:0004357,paired limb/fin bud
+DOID:0050915,rectum adenoma,DOID:1984,rectal neoplasm
+UBERON:0010913,vertebral element,UBERON:0004120,mesoderm-derived structure
+UBERON:0002577,pericentral nucleus of inferior colliculus,UBERON:0002917,regional part of inferior colliculus
+HP:0000220,Velopharyngeal insufficiency,HP:0100736,Abnormality of the soft palate
+UBERON:0001783,optic disc,UBERON:0004121,ectoderm-derived structure
+UBERON:0006338,lateral ventricle choroid plexus stroma,UBERON:0005206,choroid plexus stroma
+NCBITaxon:56211,Calomys laucha,NCBITaxon:29105,Calomys
+UBERON:0004935,submucosa of cardia of stomach,UBERON:0001200,submucosa of stomach
+HP:0000269,Prominent occiput,HP:0011217,Abnormal shape of the occiput
+HP:0008751,Laryngeal cleft,HP:0001600,Abnormality of the larynx
+UBERON:2000648,dorsal fin musculature,UBERON:0007271,appendage musculature
+HP:0006744,Adrenocortical carcinoma,HP:0100641,Neoplasm of the adrenal cortex
+UBERON:0001684,mandible,UBERON:0004742,dentary
+HP:0010996,Abnormality of monocarboxylic acid metabolism,HP:0004354,Abnormality of carboxylic acid metabolism
+UBERON:0001273,ilium,UBERON:0007830,pelvic girdle bone/zone
+UBERON:0009065,anterior thoracic air sac,UBERON:0015212,lateral structure
+HP:0100589,Urogenital fistula,HP:0000119,Abnormality of the genitourinary system
+HP:0007559,Localized epidermolytic hyperkeratosis,HP:0008064,Ichthyosis
+UBERON:0007185,pericardio-peritoneal canal mesothelium,UBERON:0001136,mesothelium
+HP:0010548,Percussion myotonia,HP:0002486,Myotonia
+UBERON:0004320,middle phalanx of manual digit 2,UBERON:0003864,middle phalanx of manus
+DOID:6837,rete ovarii adenoma,DOID:4895,rete ovarii neoplasm
+HP:0005999,Ureteral atresia,HP:0000069,Abnormality of the ureter
+CL:0002549,fibroblast of choroid plexus,CL:0000057,fibroblast
+UBERON:0003374,chorionic ectoderm,UBERON:0000478,extraembryonic structure
+UBERON:0008822,posterior mediastinum,UBERON:0002224,thoracic cavity
+DOID:11963,esophagitis,DOID:6050,esophageal disease
+DOID:0050050,Japanese spotted fever,DOID:11104,spotted fever
+UBERON:0003356,epithelium of nasal septum,UBERON:0010371,ecto-epithelium
+UBERON:0003464,hindlimb bone,UBERON:0002428,limb bone
+HP:0003687,Centrally nucleated skeletal muscle fibers,HP:0004303,Abnormality of muscle fibers
+NCBITaxon:10255,Variola virus,NCBITaxon:10242,Orthopoxvirus
+HP:0009350,Fragmentation of the epiphysis of the proximal phalanx of the 3rd finger,HP:0010272,Fragmentation of the epiphyses of the proximal phalanges of the hand
+CL:0002388,multinucleate arthroconidium,CL:0002387,arthroconidium
+UBERON:0001022,cell body,UBERON:0004121,ectoderm-derived structure
+HP:0100525,Urachus fistula,HP:0010478,Abnormality of the urachus
+HP:0008478,Scheuermann-like vertebral changes,HP:0010891,Morbus Scheuermann
+UBERON:0004224,vas deferens smooth muscle,UBERON:0014403,male anatomical structure
+DOID:1911,endodermal sinus tumor,DOID:2994,germ cell cancer
+DOID:4131,erythrasma,DOID:4223,pyoderma
+UBERON:0015173,helicine branch of uterine artery,UBERON:0015177,helicine artery
+HP:0000586,Shallow orbits,HP:0000520,Proptosis
+HP:0011097,Epileptic spasms,HP:0001250,Seizures
+UBERON:2007054,pillar of the anterior semicircular canal,UBERON:2002223,pillar of the semicircular canal
+CL:0000377,tracheoblast,CL:0000069,branched duct epithelial cell
+HP:0009738,Abnormality of the antihelix,HP:0000377,Abnormality of the pinna
+HP:0009857,Symphalangism affecting the proximal phalanges of the hand,HP:0009834,Abnormality of the proximal phalanges of the hand
+HP:0010942,Echogenic intracardiac focus,HP:0011425,Fetal ultrasound soft marker
+UBERON:0006698,mammillotegmental axonal tract,UBERON:0011591,tract of diencephalon
+UBERON:0002132,dentate nucleus,UBERON:0008995,nucleus of cerebellar nuclear complex
+DOID:2228,thrombocytosis,DOID:0070004,myeloma
+HP:0010374,Curved phalanges of the 4th toe,HP:0010176,Curved phalanges of the toes
+HP:0010102,Aplasia of the distal phalanx of the hallux,HP:0010645,Aplasia of the distal phalanges of the toes
+UBERON:0011122,cricoarytenoid joint,UBERON:0011120,laryngeal joint
+HP:0011102,Ileal atresia,HP:0001549,Abnormality of the ileum
+HP:0100811,Aplasia/Hypoplasia of the colon,HP:0002250,Abnormality of the large intestine
+DOID:2601,juxtacortical chondroma,DOID:2602,chondroma
+HP:0000741,Apathy,HP:0000745,Diminished motivation
+HP:0007220,Demyelinating motor neuropathy,HP:0007108,Demyelinating peripheral neuropathy
+UBERON:0004218,lower leg nerve,UBERON:0003431,leg nerve
+HP:0003323,Progressive muscle weakness,HP:0001324,Muscle weakness
+HP:0012342,Macroprolactinoma,HP:0006767,Pituitary prolactin cell adenoma
+UBERON:0010687,pedal digit metatarsal pre-cartilage condensation,UBERON:0010585,pedal digit phalanx pre-cartilage condensation
+CL:0000939,"CD16-positive, CD56-dim natural killer cell",CL:0000824,mature natural killer cell
+DOID:11103,rickettsialpox,DOID:11104,spotted fever
+UBERON:0009095,tip of renal papilla,UBERON:0000064,organ part
+HP:0002882,Sudden episodic apnea,HP:0002104,Apnea
+UBERON:0012297,male urethral crest,UBERON:0014403,male anatomical structure
+HP:0008583,Underfolded superior helices,HP:0008577,Underfolded helix
+UBERON:0009129,right atrium endocardium,UBERON:0002166,endocardium of atrium
+UBERON:0005063,left ventricular compact myocardium,UBERON:0004127,compact layer of ventricle
+UBERON:0011187,greater tubercle of humerus,UBERON:4100000,skeletal element projection
+CL:0002258,thyroid follicular cell,CL:0002257,epithelial cell of thyroid gland
+CL:0002059,CD8alpha-positive thymic conventional dendritic cell,CL:0000941,thymic conventional dendritic cell
+HP:0007822,Central retinal exudate,HP:0001147,Retinal exudate
+HP:0010082,Symphalangism affecting the distal phalanx of the hallux,HP:0001859,Distal symphalangism (feet)
+HP:0011187,Focal EEG discharges with propagation to ipsilateral hemisphere,HP:0011185,EEG with focal epileptiform discharges
+HP:0006778,Benign genitourinary tract neoplasm,HP:0007379,Neoplasm of the genitourinary tract
+HP:0011797,Papillary renal cell carcinoma type 1,HP:0006766,Papillary renal cell carcinoma
+DOID:7718,osteoclast-like giant cell neoplasm of the pancreas,DOID:3498,pancreatic ductal adenocarcinoma
+UBERON:0005127,metanephric thick ascending limb,UBERON:0005129,metanephric distal tubule
+NCBITaxon:10239,Viruses,NCBITaxon:1,root
+UBERON:2001614,anal fin middle radial bone,UBERON:2101614,anal fin middle radial element
+HP:0007504,Diffuse slow skin atrophy,HP:0007488,Diffuse skin atrophy
+UBERON:0013745,zona intermedia of adrenal gland,UBERON:0009753,adrenal gland cortex zone
+UBERON:0009025,gastroepiploic artery,UBERON:0001637,artery
+UBERON:0009029,pudendal vein,UBERON:0001638,vein
+HP:0008070,Sparse hair,HP:0011357,Abnormality of hair density
+UBERON:0004480,musculature of limb,UBERON:0007271,appendage musculature
+HP:0005731,Cortical irregularity,HP:0003103,Abnormal cortical bone morphology
+NCBITaxon:197912,Influenzavirus B,NCBITaxon:11308,Orthomyxoviridae
+CL:1000370,transitional myocyte of left branch of atrioventricular bundle,CL:1000481,transitional myocyte of atrioventricular bundle
+UBERON:0000454,cerebral subcortex,UBERON:0000064,organ part
+HP:0009314,Symphalangism affecting the proximal phalanx of the 4th finger,HP:0009284,Abnormality of the proximal phalanx of the 4th finger
+HP:0012263,Immotile cilia,HP:0012262,Abnormal ciliary motility
+HP:0009256,Ivory epiphysis of the distal phalanx of the 4th finger,HP:0009399,Ivory epiphyses of the 4th finger
+UBERON:0008196,muscle of pectoral girdle,UBERON:0010891,pectoral complex muscle
+UBERON:0004173,medulla reticulospinal tract,UBERON:0001018,axon tract
+UBERON:0004092,hypothalamus-pituitary axis,UBERON:0000015,anatomical boundary
+HP:0009344,Stippling of the epiphysis of the distal phalanx of the 3rd finger,HP:0009332,Abnormality of the epiphysis of the distal phalanx of the 3rd finger
+UBERON:0012472,hepatoduodenal ligament,UBERON:0004120,mesoderm-derived structure
+HP:0008828,Delayed proximal femoral epiphyseal ossification,HP:0010574,Abnormality of the epiphysis of the femoral head
+HP:0011971,Dermatographic urticaria,HP:0001025,Urticaria
+HP:0003139,Panhypogammaglobulinemia,HP:0004313,Hypogammaglobulinemia
+HP:0003935,Wide humeral diaphysis,HP:0003926,Abnormality of the humeral diaphysis
+UBERON:0015243,lower part of vagina,UBERON:0013515,subdivision of uterine tube
+UBERON:0009891,facial mesenchyme,UBERON:0003104,mesenchyme
+CL:0002628,immature microglial cell,CL:0000129,microglial cell
+UBERON:0007269,pectoral appendage musculature,UBERON:0014793,musculature of pectoral complex
+CL:0000464,epidermoblast,CL:0000055,non-terminally differentiated cell
+DOID:4734,calciphylaxis,DOID:182,calcinosis
+HP:0006541,Chronic obstructive airway disease from birth,HP:0006536,Obstructive lung disease
+UBERON:0005869,maxillary process of inferior nasal concha,UBERON:0004530,bony projection
+HP:0200127,Atrial cardiomyopathy,HP:0001638,Cardiomyopathy
+DOID:9252,amino acid metabolic disorder,DOID:655,inherited metabolic disorder
+UBERON:4200189,pedal toe disc,UBERON:4200151,toe disc
+HP:0009190,Irregular epiphyses of the metacarpals,HP:0003842,Irregular epiphyses of the upper limbs
+UBERON:2005376,dorsal fin distal radial bone 5,UBERON:2000936,dorsal fin distal radial bone
+UBERON:2000744,epaxial region somite 22,UBERON:0003900,epaxial myotome region
+UBERON:0003078,epibranchial placode,UBERON:0010371,ecto-epithelium
+CL:0000158,Clara cell,CL:0000157,surfactant secreting cell
+HP:0006342,Peg-shaped maxillary lateral incisors,HP:0011065,Conical incisor
+UBERON:0011604,carina of sternum,UBERON:0004120,mesoderm-derived structure
+HP:0004188,Abnormality of the 4th finger,HP:0001167,Abnormality of finger
+NCBITaxon:329110,Coquillettidia,NCBITaxon:53550,Culicini
+UBERON:0002560,temporal operculum,UBERON:0003022,cerebral cortex lobe
+UBERON:0002612,transverse orbital sulcus,UBERON:0013118,sulcus of brain
+DOID:6856,pineal region teratoma,DOID:1660,malignant pineal area germ cell neoplasm
+UBERON:0001508,arch of aorta,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0010864,dactylopatagium minus,UBERON:0010862,dactylopatagium
+HP:0002558,Supernumerary nipples,HP:0004404,Abnormality of the nipple
+CL:0002525,metanephric glomerular visceral epithelial cell,CL:0000653,glomerular visceral epithelial cell
+CL:0002142,dark cell of eccrine sweat gland,CL:0000434,eccrine cell
+UBERON:0001413,brachial vein,UBERON:0003507,arm blood vessel
+UBERON:0002419,skin gland,UBERON:0004121,ectoderm-derived structure
+HP:0011694,Supraventricular tachycardia with a manifest accessory pathway,HP:0011688,Supraventricular tachycardia with an accessory connection mediated pathway
+HP:0010617,Cardiac fibroma,HP:0100544,Neoplasm of the heart
+UBERON:0003970,placental labyrinth vasculature,UBERON:0005156,reproductive structure
+HP:0004974,Coarctation of abdominal aorta,HP:0001680,Coarctation of aorta
+DOID:9733,renal tuberculosis,DOID:2149,urogenital tuberculosis
+HP:0012018,EEG with temporal focal spikes,HP:0011193,EEG with focal spikes
+UBERON:2001742,auditory foramen,UBERON:0005744,bone foramen
+HP:0009337,Cone-shaped epiphysis of the distal phalanx of the 3rd finger,HP:0009412,Cone-shaped epiphyses of the 3rd finger
+UBERON:0010221,laryngeal associated mesenchyme,UBERON:0004119,endoderm-derived structure
+DOID:6575,childhood optic tract astrocytoma,DOID:4991,optic nerve astrocytoma
+HP:0007702,Pigmentary retinal deposits,HP:0011512,Hyperpigmentation of the fundus
+DOID:8200,tertiary syphilis,DOID:4166,syphilis
+HP:0010274,Ivory epiphyses of the proximal phalanges of the hand,HP:0100917,Sclerosis of the proximal phalanges of the hand
+HP:0010775,Vascular ring,HP:0011587,Abnormal branching pattern of the aortic arch
+UBERON:0012250,cervix glandular epithelium,UBERON:0004801,cervix epithelium
+UBERON:2000941,nucleus of the medial longitudinal fasciculus synencephalon,UBERON:0006569,diencephalic nucleus
+UBERON:2000638,"commissura rostral, pars dorsalis",UBERON:0002437,cerebral hemisphere white matter
+HP:0011258,Tragal bridge of crus of helix,HP:0009895,Abnormality of the crus of the helix
+UBERON:4000106,vasodentine,UBERON:0010365,odontoid tissue
+HP:0001888,Lymphopenia,HP:0004332,Abnormality of lymphocytes
+UBERON:0012471,hepatogastric ligament,UBERON:0005291,embryonic tissue
+HP:0011457,Loss of eyelashes,HP:0000499,Abnormality of the eyelashes
+HP:0000236,Abnormality of the anterior fontanelle,HP:0011328,Abnormality of fontanelles
+DOID:2754,glycogen storage disease VI,DOID:2747,glycogen storage disease
+UBERON:0012244,stratum intermedium of epidermis,UBERON:0013754,integumentary system layer
+CL:0000890,alternatively activated macrophage,CL:0000861,elicited macrophage
+UBERON:0002949,tectospinal tract,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:0060177,homocarnosinosis,DOID:0060176,gamma-amino butyric acid metabolism disorder
+DOID:0050541,Charcot-Marie-Tooth disease type 4,DOID:10595,Charcot-Marie-Tooth disease
+HP:0009556,Absent tibia,HP:0005772,Aplasia/Hypoplasia of the tibia
+HP:0010363,Osteolytic defects of the phalanges of the 3rd toe,HP:0010330,Abnormality of the phalanges of the 3rd toe
+DOID:2571,Langerhans-cell histiocytosis,DOID:3405,histiocytosis
+HP:0009245,Triangular shaped distal phalanx of the 5th finger,HP:0009875,Triangular shaped distal phalanges of the hand
+CL:0000940,mucosal invariant T cell,CL:0002127,innate effector T cell
+UBERON:0004032,podocyte slit diaphragm,UBERON:0004120,mesoderm-derived structure
+UBERON:0001547,small saphenous vein,UBERON:0007318,saphenous vein
+UBERON:4000160,anocleithrum,UBERON:0007829,pectoral girdle bone
+HP:0006336,Short dental roots,HP:0006486,Abnormality of the dental root
+UBERON:0011938,vibrissa inner root sheath,UBERON:0011937,vibrissa root sheath
+HP:0003697,Scapuloperoneal amyotrophy,HP:0003202,Amyotrophy
+DOID:7684,maxillary sinus adenocarcinoma,DOID:1357,maxillary sinus cancer
+UBERON:0007610,tibial artery,UBERON:0003516,hindlimb blood vessel
+DOID:13095,vertebral artery insufficiency,DOID:224,transient cerebral ischemia
+UBERON:0010541,tarsus cartilage element,UBERON:0010881,limb cartilage element
+CL:0000899,T-helper 17 cell,CL:0000492,CD4-positive helper T cell
+UBERON:0001560,neck of organ,UBERON:0000064,organ part
+UBERON:0006517,kidney calyx,UBERON:0004120,mesoderm-derived structure
+DOID:9867,toxic maculopathy,DOID:2007,degeneration of macula and posterior pole
+UBERON:0011819,lumen of atrioventricular canal,UBERON:0005082,tube lumen
+HP:0010188,Curved distal phalanges of the toes,HP:0010176,Curved phalanges of the toes
+HP:0008193,Primary gonadal insufficiency,HP:0008373,Puberty and gonadal disorders
+DOID:14110,anus cancer,DOID:5672,large intestine cancer
+UBERON:2100947,dorsal fin proximal radial element,UBERON:2101672,dorsal fin radial element
+UBERON:0004359,corpus epididymis,UBERON:0000064,organ part
+UBERON:3010109,anteroventral lateral line nerve (AVLLN),UBERON:0008906,lateral line nerve
+UBERON:0000362,renal medulla,UBERON:0000958,medulla of organ
+HP:0000648,Optic atrophy,HP:0000587,Abnormality of the optic nerve
+HP:0002321,Vertigo,HP:0001751,Vestibular dysfunction
+UBERON:0012255,inferior phrenic artery,UBERON:0012254,abdominal aorta artery
+HP:0007734,Enlarged lacrimal glands,HP:0011482,Abnormality of the lacrimal gland
+HP:0008075,Progressive pes cavus,HP:0001761,Pes cavus
+UBERON:0003682,palatal muscle,UBERON:0010959,craniocervical muscle
+DOID:4920,eccrine adenocarcinoma,DOID:4921,eccrine sweat gland cancer
+CL:0001000,CD8_alpha-positive CD11b-negative dendritic cell,CL:0000990,conventional dendritic cell
+HP:0100921,Sclerosis of the phalanges of the 5th finger,HP:0100899,Sclerosis of the phalanges of the hand
+DOID:2755,Mycobacterium avium complex disease,DOID:0050338,primary bacterial infectious disease
+UBERON:2001502,epiphyseal bar,UBERON:0003932,cartilage element of chondrocranium
+UBERON:0009126,nodosal placode,UBERON:0003078,epibranchial placode
+UBERON:0006592,transformed vein,UBERON:0004120,mesoderm-derived structure
+UBERON:0005745,optic canal,UBERON:0004120,mesoderm-derived structure
+UBERON:0012313,1st arch maxillary ectoderm,UBERON:0005291,embryonic tissue
+HP:0007738,Uncontrolled eye movements,HP:0012547,Abnormal involuntary eye movements
+UBERON:0001802,posterior segment of eyeball,UBERON:0004121,ectoderm-derived structure
+UBERON:0011918,line of Schwalbe,UBERON:0006800,anatomical line
+HP:0006983,Slowly progressive spastic quadriparesis,HP:0002478,Progressive spastic quadriplegia
+UBERON:0007245,nuclear complex of neuraxis,UBERON:0002020,gray matter of neuraxis
+UBERON:0007128,glomeral mesenchyme,UBERON:0005423,developing anatomical structure
+UBERON:0006694,cerebellum vasculature,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0011283,epoophoron,UBERON:0014404,female anatomical structure
+DOID:0060100,musculoskeletal system cancer,DOID:0050686,organ system cancer
+CL:0002045,Fraction A pre-pro B cell,CL:0000826,pro-B cell
+DOID:5515,nasal cavity squamous cell carcinoma,DOID:4931,nasal cavity carcinoma
+DOID:10967,spastic hemiplegia,DOID:0050669,spastic cerebral palsy
+HP:0100729,Large face,HP:0001999,Abnormal facial shape
+HP:0003202,Amyotrophy,HP:0011805,Abnormality of muscle morphology
+CL:0000742,periarticular chondrocyte,CL:1001607,articular chondrocyte
+CL:1001517,stomach enteroendocrine cell,CL:0002659,glandular cell of stomach
+DOID:4594,microcystic meningioma,DOID:3565,meningioma
+HP:0009119,Aplasia/Hypoplasia of the frontal sinuses,HP:0009120,Aplasia/Hypoplasia involving the sinuses
+UBERON:0002338,lamina propria of bronchus,UBERON:0000031,lamina propria of trachea
+UBERON:0005745,optic canal,UBERON:0015212,lateral structure
+DOID:0080038,pycnodysostosis,DOID:2256,osteochondrodysplasia
+DOID:11668,hypopigmentation of eyelid,DOID:10120,eyelid degenerative disease
+UBERON:0004648,esophagus muscularis mucosa,UBERON:0006676,muscularis mucosa
+HP:0002109,Abnormality of the bronchi,HP:0005607,Abnormality of the tracheobronchial system
+HP:0009345,Triangular epiphysis of the distal phalanx of the 3rd finger,HP:0009420,Triangular epiphyses of the 3rd finger
+UBERON:3000628,ventral ramus of squamosal,UBERON:0000064,organ part
+CL:0002612,neuron of the ventral spinal cord,CL:0000117,CNS neuron (sensu Vertebrata)
+HP:0002550,Absent facial hair,HP:0002298,Absent hair
+UBERON:0009191,sphenoid bone pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+CL:0002105,CD38-positive IgG memory B cell,CL:0000979,IgG memory B cell
+CL:0002158,external epithelial cell of tympanic membrane,CL:0002159,general ecto-epithelial cell
+HP:0010142,Fragmentation of the epiphysis of the distal phalanx of the hallux,HP:0010124,Abnormality of the epiphysis of the distal phalanx of the hallux
+UBERON:0010388,proximal segment of rib,UBERON:0005055,zone of long bone
+UBERON:0012279,paraganglion,UBERON:0000480,anatomical group
+DOID:13129,severe pre-eclampsia,DOID:10591,pre-eclampsia
+HP:0002263,Exaggerated cupid's bow,HP:0011339,Abnormality of upper lip vermillion
+HP:0010086,Broad proximal phalanx of the hallux,HP:0010204,Broad proximal phalanges of the toes
+HP:0002307,Drooling,HP:0003781,Excessive salivation
+DOID:10353,fibrosclerosis of breast,DOID:5997,non-proliferative fibrocystic change of the breast
+CL:0000145,professional antigen presenting cell,CL:0000473,defensive cell
+HP:0000219,Thin upper lip vermilion,HP:0000233,Thin vermilion border
+UBERON:0000972,antenna,UBERON:0015212,lateral structure
+UBERON:2000636,cerebellar crest,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0003975,Chevron-shaped/cone-shaped radius,HP:0002818,Abnormality of the radius
+UBERON:0004185,endodermal part of digestive tract,UBERON:0004119,endoderm-derived structure
+UBERON:0015011,tibiotarsus endochondral element,UBERON:0015022,hindlimb endochondral element
+CL:0000410,CNS long range interneuron,CL:0000402,CNS interneuron
+HP:0005928,Synostosis involving the fibula,HP:0009138,Synostosis involving bones of the lower limbs
+DOID:3251,prostate embryonal rhabdomyosarcoma,DOID:3252,prostate rhabdomyosarcoma
+UBERON:0004428,proximal epiphysis of second metatarsal bone,UBERON:0004396,epiphysis of second metatarsal bone
+UBERON:0016404,cervical vertebral arch joint,UBERON:0001067,vertebral arch joint
+UBERON:0001084,skin of head,UBERON:0012180,head or neck skin
+HP:0008738,Partially duplicated kidney,HP:0000075,Renal duplication
+UBERON:0013629,hallical pad,UBERON:0012349,digital pad
+UBERON:0014631,dorsal gray commissure of spinal cord,UBERON:0002315,gray matter of spinal cord
+DOID:7242,uterine corpus cellular leiomyoma,DOID:0060095,uterine benign neoplasm
+DOID:14125,abducens nerve neoplasm,DOID:338,cranial nerve neoplasm
+HP:0006598,Irregular ossification at anterior rib ends,HP:0012306,Abnormal rib ossification
+UBERON:0005972,tunnel of Corti,UBERON:0000464,anatomical space
+HP:0009372,Type A2 brachydactyly,HP:0009370,Type A brachydactyly
+DOID:345,uterine disease,DOID:229,female reproductive system disease
+UBERON:0006107,basolateral amygdaloid nuclear complex,UBERON:0007245,nuclear complex of neuraxis
+UBERON:3000386,cultriform process,UBERON:0004120,mesoderm-derived structure
+UBERON:0003471,artery of lower lip,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0004933,submucosa of fundus of stomach,UBERON:0001200,submucosa of stomach
+HP:0005930,Abnormality of the epiphyses,HP:0011314,Abnormality of long bone morphology
+HP:0006611,Decreased number of sternal ossification centers,HP:0011863,Abnormal sternal ossification
+HP:0000488,Retinopathy,HP:0000479,Abnormality of the retina
+UBERON:0012063,lobar bronchus of right lung middle lobe,UBERON:0003404,lobar bronchus of right lung
+HP:0008491,Premature anterior fontanel closure,HP:0000236,Abnormality of the anterior fontanelle
+DOID:0050862,pyometritis,DOID:345,uterine disease
+CL:0002283,ecto-epithelial cell of viscerocranial mucosa,CL:0002159,general ecto-epithelial cell
+DOID:5693,adult liposarcoma,DOID:3382,liposarcoma
+UBERON:0002281,vestibular membrane of cochlear duct,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0010685,pedal digit phalanx cartilage element,UBERON:0010701,phalanx cartilage element
+HP:0011641,Coronary artery fistula,HP:0006704,Abnormality of the coronary arteries
+DOID:2286,capillary lymphangioma,DOID:1475,lymphangioma
+HP:0010058,Aplasia/Hypoplasia of the phalanges of the hallux,HP:0010057,Abnormality of the phalanges of the hallux
+HP:0200099,Peripheral retinal pigmentation abnormalities,HP:0007703,Abnormal retinal pigmentation
+DOID:10471,patellar tendinitis,DOID:971,tendinitis
+HP:0100201,Triangular epiphysis of the proximal phalanx of the 4th toe,HP:0100076,Triangular epiphyses of the 4th toe
+UBERON:0005488,superior mesenteric plexus,UBERON:0001816,autonomic nerve plexus
+CL:0002067,type A enterocrine cell,CL:0000170,glucagon secreting cell
+DOID:7174,anus basaloid carcinoma,DOID:5525,anal squamous cell carcinoma
+HP:0001741,Phimosis,HP:0100587,Abnormality of the preputium
+DOID:14447,gonadal dysgenesis,DOID:0080014,chromosomal disease
+DOID:10442,hypopyon ulcer,DOID:10443,hypopyon
+HP:0001933,Subcutaneous hemorrhage,HP:0011276,Vascular skin abnormality
+UBERON:0011344,lateral surface of mandible,UBERON:0011342,surface of mandible
+CL:0000525,syncytiotrophoblast cell,CL:0000351,trophoblast cell
+CL:1001096,kidney afferent arteriole endothelial cell,CL:1000412,endothelial cell of arteriole
+HP:0009314,Symphalangism affecting the proximal phalanx of the 4th finger,HP:0004197,Symphalangism of the 4th finger
+DOID:14276,shoulder impingement syndrome,DOID:381,arthropathy
+UBERON:0005749,glomerular tuft,UBERON:0006554,urinary system structure
+UBERON:0001256,wall of urinary bladder,UBERON:0004120,mesoderm-derived structure
+UBERON:0002740,posterior cingulate gyrus,UBERON:0000200,gyrus
+DOID:2529,splenic disease,DOID:75,lymphatic system disease
+DOID:4707,cervicomedullary junction neoplasm,DOID:4706,infratentorial cancer
+UBERON:3000031,ascending process of palatoquadrate,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0005021,mesenchymal lymphangioblast,CL:0005020,lymphangioblast
+UBERON:0007223,osseus cochlea,UBERON:0010313,neural crest-derived structure
+CL:1000721,kidney papillary duct principal cell,CL:1001431,kidney collecting duct principal cell
+UBERON:0003415,mesenchyme of nasal septum,UBERON:0009891,facial mesenchyme
+UBERON:0003529,respiratory system lymphatic vessel endothelium,UBERON:0002042,lymphatic vessel endothelium
+UBERON:0000408,vertebral ganglion,UBERON:0007134,trunk ganglion
+HP:0012143,Abnormality of cells of the megakaryocyte lineage,HP:0005561,Abnormality of bone marrow cell morphology
+DOID:4084,testicular trophoblastic tumor,DOID:4085,trophoblastic neoplasm
+HP:0012154,Anhedonia,HP:0100851,Abnormal emotion/affect behavior
+UBERON:0002731,vestibulocochlear nerve root,UBERON:0000064,organ part
+UBERON:2000106,extension,UBERON:0000475,organism subdivision
+UBERON:0001145,ovarian vein,UBERON:0001638,vein
+HP:0001592,Selective tooth agenesis,HP:0009804,Reduced number of teeth
+UBERON:2005221,dorsal larval melanophore stripe,UBERON:2005220,larval melanophore stripe
+UBERON:0009191,sphenoid bone pre-cartilage condensation,UBERON:0009891,facial mesenchyme
+UBERON:0004886,lung hilus,UBERON:0004885,hilum
+HP:0004213,Abnormality of the phalanges of the 5th finger,HP:0004207,Abnormality of the 5th finger
+UBERON:0007832,pelvic girdle skeleton,UBERON:0004120,mesoderm-derived structure
+UBERON:0001808,parasympathetic ganglion,UBERON:0001805,autonomic ganglion
+HP:0001234,Hitchhiker thumb,HP:0009617,Abnormality of the distal phalanx of the thumb
+DOID:2614,serous surface papilloma,DOID:2615,papilloma
+UBERON:0011801,dermal condensation of feather follicle,UBERON:0004121,ectoderm-derived structure
+DOID:5626,thymus adenosquamous carcinoma,DOID:3284,thymic carcinoma
+CL:0002146,clear cell of eccrine sweat gland,CL:0000318,sweat secreting cell
+HP:0100220,Pseudoepiphysis of the middle phalanx of the 5th toe,HP:0100098,Abnormality of the epiphysis of the middle phalanx of the 5th toe
+UBERON:0011123,stifle joint,UBERON:0001485,knee joint
+HP:0011611,Interrupted aortic arch,HP:0012303,Abnormality of the aortic arch
+UBERON:0007710,intermediate nucleus of lateral lemniscus,UBERON:0006840,nucleus of lateral lemniscus
+CL:0011100,galanergic neuron,CL:0000540,neuron
+DOID:5263,ovary leiomyosarcoma,DOID:2146,ovary sarcoma
+HP:0011820,Membranous choanal atresia,HP:0000453,Choanal atresia
+UBERON:0009201,nephric duct,UBERON:0003914,epithelial tube
+DOID:8096,bladder mixed adenocarcinoma,DOID:3711,bladder adenocarcinoma
+UBERON:0010213,laryngeal pre-cartilage condensation,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005975,hair follicle bulge,UBERON:0004121,ectoderm-derived structure
+HP:0003904,Wide epiphyses of the upper limbs,HP:0010580,Enlarged epiphyses
+UBERON:0002717,rostral interstitial nucleus of medial longitudinal fasciculus,UBERON:0007414,nucleus of midbrain tegmentum
+HP:0007480,Decreased sweating due to autonomic dysfunction,HP:0000966,Hypohidrosis
+CL:0000874,splenic red pulp macrophage,CL:0000871,splenic macrophage
+HP:0012669,Carotid sinus syncope,HP:0001279,Syncope
+UBERON:2002084,pleurostyle,UBERON:2000602,uroneural
+UBERON:0004582,venous system,UBERON:0007798,vascular system
+UBERON:0002967,cingulate gyrus,UBERON:0000200,gyrus
+UBERON:0001553,medial tarsal artery,UBERON:0001637,artery
+HP:0009402,Stippling of the epiphyses of the 4th finger,HP:0010237,Epiphyseal stippling of finger phalanges
+DOID:1513,chronic cervicitis,DOID:2568,cervicitis
+UBERON:0012267,equine splint bone,UBERON:0003821,metapodium bone
+CL:1000348,basal cell of epithelium of trachea,CL:0002633,respiratory basal cell
+UBERON:3010734,M. flexor carpi ulnaris,UBERON:0010891,pectoral complex muscle
+DOID:4692,endophthalmitis,DOID:1242,globe disease
+CL:1000715,kidney cortex collecting duct intercalated cell,CL:1001432,kidney collecting duct intercalated cell
+DOID:987,alopecia,DOID:4535,hypotrichosis
+UBERON:3000002,alary cartilage,UBERON:0003406,cartilage of respiratory system
+HP:0012491,Abnormal dense tubular system,HP:0011875,Abnormal platelet morphology
+UBERON:0001247,falciform ligament,UBERON:0013139,ligament of liver
+UBERON:0002530,gland,UBERON:0000062,organ
+HP:0009516,Enlarged epiphysis of the middle phalanx of the 2nd finger,HP:0009491,Enlarged epiphyses of the 2nd finger
+UBERON:3000829,margo scapularis,UBERON:0004120,mesoderm-derived structure
+DOID:745,epididymis adenomatoid tumor,DOID:0060087,male reproductive organ benign neoplasm
+CL:0000155,peptic cell,CL:0002659,glandular cell of stomach
+UBERON:3010172,subarticular tubercles,UBERON:0005813,tubercle
+DOID:0080054,achondrogenesis type IA,DOID:0080043,achondrogenesis
+CL:0002248,pluripotent stem cell,CL:0000723,somatic stem cell
+HP:0007398,"Asymmetric, linear skin defects",HP:0008065,Aplasia/Hypoplasia of the skin
+DOID:4310,smooth muscle tumor,DOID:461,muscle benign neoplasm
+UBERON:0003576,hip connective tissue,UBERON:0002384,connective tissue
+DOID:10182,diabetic peripheral angiopathy,DOID:9352,type 2 diabetes mellitus
+CL:0000427,GLR cell,CL:0002320,connective tissue cell
+UBERON:0006834,uterus or analog,UBERON:0013522,subdivision of tube
+UBERON:0005043,mucosa of nasolacrimal duct,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010618,Ovarian fibroma,HP:0010614,Fibroma
+DOID:0060161,Kennedy's disease,DOID:12377,spinal muscular atrophy
+HP:0002416,Subependymal cysts,HP:0002118,Abnormality of the cerebral ventricles
+HP:0002977,Aplasia/Hypoplasia involving the central nervous system,HP:0007319,Morphological abnormality of the central nervous system
+UBERON:0001083,myocardium of ventricle,UBERON:0002349,myocardium
+UBERON:0006829,remnant of left anterior vena cava,UBERON:0005194,thoracic vein
+DOID:11724,limb-girdle muscular dystrophy,DOID:9884,muscular dystrophy
+UBERON:0005723,floor plate spinal cord region,UBERON:0001948,regional part of spinal cord
+CL:0002328,bronchial epithelial cell,CL:0002202,epithelial cell of tracheobronchial tree
+HP:0000135,Hypogonadism,HP:0008373,Puberty and gonadal disorders
+HP:0000004,Onset and clinical course,HP:0000001,All
+UBERON:0000019,camera-type eye,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0002549,fibroblast of choroid plexus,CL:0002319,neural cell
+UBERON:2000808,myotome somite 29,UBERON:0003082,myotome
+CL:0002151,late promyelocyte,CL:0000836,promyelocyte
+UBERON:0010863,dactylopatagium brevis,UBERON:0010862,dactylopatagium
+CL:0000919,"CD8-positive, CD25-positive, alpha-beta regulatory T cell",CL:0000795,"CD8-positive, alpha-beta regulatory T cell"
+UBERON:0012180,head or neck skin,UBERON:0000014,zone of skin
+UBERON:0010910,opisthotic,UBERON:0010313,neural crest-derived structure
+UBERON:0001031,neurilemma,UBERON:0003714,neural tissue
+UBERON:0013144,vein of genicular venous plexus,UBERON:0001638,vein
+UBERON:2000771,hypaxial region somite 22,UBERON:0003895,hypaxial myotome region
+UBERON:1000008,left part of face,UBERON:0015212,lateral structure
+HP:0003362,Increased circulating very-low-density lipoprotein cholesterol,HP:0010980,Hyperlipoproteinemia
+HP:0002626,Venous varicosities of celiac and mesenteric vessels,HP:0002619,Varicose veins
+DOID:12117,pulmonary alveolar microlithiasis,DOID:850,lung disease
+HP:0008323,Abnormal rod and cone electroretinograms,HP:0000512,Abnormal electroretinogram
+UBERON:0004068,medial nasal prominence,UBERON:0009292,embryonic nasal process
+UBERON:0005479,superior mesenteric ganglion,UBERON:0003964,prevertebral ganglion
+DOID:2602,chondroma,DOID:0060084,cell type benign neoplasm
+UBERON:0004426,proximal epiphysis of fifth metacarpal bone,UBERON:0004416,proximal epiphysis of metacarpal bone
+CL:1001138,interlobular artery cell,CL:1001045,kidney cortex artery cell
+UBERON:0014593,tuberomammillary nucleus dorsal part,UBERON:0002789,regional part of posterior hypothalamic region
+UBERON:3000437,planum conchale,UBERON:0010313,neural crest-derived structure
+CL:0000253,eurydendroid cell,CL:0000527,efferent neuron
+HP:0000017,Nocturia,HP:0000009,Functional abnormality of the bladder
+HP:0011114,Defective production of NFKB1-dependent cytokines,HP:0011113,Abnormality of cytokine secretion
+HP:0006976,Focal necrotizing encephalopathy,HP:0001298,Encephalopathy
+UBERON:0007831,pectoral girdle skeleton,UBERON:0010719,girdle skeleton
+CL:0000392,crystal cell,CL:0000391,podocyte (sensu Diptera)
+HP:0200136,Oral-pharyngeal dysphagia,HP:0000600,Abnormality of the pharynx
+NCBITaxon:1502,Clostridium perfringens,NCBITaxon:1485,Clostridium
+DOID:0050096,tinea barbae,DOID:8913,dermatophytosis
+CL:0000349,extraembryonic cell,CL:0000548,animal cell
+UBERON:0006677,surface of epithelium,UBERON:0000015,anatomical boundary
+HP:0007585,Skin fragility with non-scarring blistering,HP:0001030,Fragile skin
+UBERON:2001316,anterior lateral line placode,UBERON:0003067,dorsolateral placode
+UBERON:0001871,temporal lobe,UBERON:0003022,cerebral cortex lobe
+DOID:0050558,Ullrich congenital muscular dystrophy,DOID:0050557,congenital muscular dystrophy
+HP:0002825,Caudal appendage,HP:0008519,Abnormality of the coccyx
+HP:0010044,Short 4th metacarpal,HP:0010042,Aplasia/Hypoplasia of the 4th metacarpal
+CL:1000326,ileal goblet cell,CL:1000317,intestinal villus goblet cell
+DOID:14244,epiphora due to excess lacrimation,DOID:13757,excessive tearing
+HP:0009713,Spinal hemangioblastoma,HP:0010302,Spinal cord tumor
+UBERON:4200155,metapodium bone 7,UBERON:0003821,metapodium bone
+HP:0000887,Cupped ribs,HP:0000772,Abnormality of the ribs
+UBERON:0001183,inferior mesenteric artery,UBERON:0005616,mesenteric artery
+HP:0012705,Abnormal metabolic brain imaging by MRS,HP:0012638,Abnormality of nervous system physiology
+UBERON:0002909,posterior subcentral sulcus,UBERON:0013118,sulcus of brain
+UBERON:0007616,layer of synovial tissue,UBERON:0000042,serous membrane
+HP:0011891,Post-partum hemorrhage,HP:0011890,Prolonged bleeding following procedure
+HP:0007321,Deep white matter hypodensities,HP:0007103,Hypointensity of cerebral white matter on MRI
+UBERON:0011679,proximal tarsal bone,UBERON:0001447,tarsal bone
+UBERON:0010723,os vesalianum pedis,UBERON:0010722,accessory bone
+HP:0009303,Osteolytic defects of the distal phalanx of the 4th finger,HP:0009839,Osteolytic defects of the distal phalanges of the hand
+UBERON:0001502,interosseous muscle of manus,UBERON:0006508,interosseous muscle
+UBERON:0001732,pharyngeal tonsil,UBERON:0012330,nasal-associated lymphoid tissue
+CL:1001223,interlobulary vein endothelial cell,CL:0002543,vein endothelial cell
+DOID:11821,bladder lymphoma,DOID:11054,urinary bladder cancer
+HP:0001176,Large hands,HP:0005922,Abnormal hand morphology
+UBERON:0003574,elbow connective tissue,UBERON:0003573,arm connective tissue
+DOID:5763,lung clear cell-sugar-tumor,DOID:3683,lung benign neoplasm
+UBERON:3010694,m. rhomboideus posterior,UBERON:0010891,pectoral complex muscle
+UBERON:2000715,adductor hyohyoid,UBERON:0005493,hyoid muscle
+UBERON:0010335,maxillary process mesenchyme from head mesenchyme,UBERON:0004120,mesoderm-derived structure
+DOID:8849,sublingual gland cancer,DOID:8850,salivary gland cancer
+UBERON:0015189,perineural vascular plexus,UBERON:0013141,capillary bed
+UBERON:0001727,taste bud,UBERON:0000073,regional part of nervous system
+DOID:2723,dermatitis,DOID:37,skin disease
+UBERON:0012173,middle suprarenal artery,UBERON:0012254,abdominal aorta artery
+UBERON:0000965,lens of camera-type eye,UBERON:0005389,transparent eye structure
+UBERON:0012350,carpal pad,UBERON:0001518,skin of wrist
+HP:0003106,Subperiosteal erosions due to secondary hyperparathyroidism,HP:0002813,Abnormality of limb bone morphology
+UBERON:1500007,mesopterygium cartilage,UBERON:4300081,mesopterygium element
+HP:0009232,Symphalangism affecting the proximal phalanx of the 5th finger,HP:0009150,Abnormality of the proximal phalanx of the 5th finger
+UBERON:3010652,ramules nasalis lateralis,UBERON:0001021,nerve
+CL:0000326,glycogen accumulating cell,CL:0000325,stuff accumulating cell
+HP:0006559,Hepatic calcification,HP:0010766,Ectopic calcification
+HP:0100441,Bullet-shaped distal phalanx of the 4th toe,HP:0010373,Bullet-shaped phalanges of the 4th toe
+UBERON:0006173,pronephric proximal tubule,UBERON:0005310,pronephric nephron tubule
+DOID:14261,fragile X syndrome,DOID:0050735,X-linked disease
+HP:0200113,Aphalangy of hands and feet,HP:0010745,Aplasia of the phalanges of the toes
+UBERON:0002851,eighth thoracic dorsal root ganglion,UBERON:0002835,thoracic dorsal root ganglion
+HP:0005856,Ulnar radial head dislocation,HP:0003083,Dislocated radial head
+HP:0000031,Epididymitis,HP:0009714,Abnormality of the epididymis
+DOID:2994,germ cell cancer,DOID:0050687,cell type cancer
+DOID:4465,papillary renal cell carcinoma,DOID:4450,renal cell carcinoma
+DOID:7941,Barrett's adenocarcinoma,DOID:4914,esophagus adenocarcinoma
+UBERON:0010295,substantia propria of sclera,UBERON:0003891,stroma
+HP:0010559,Vertical clivus,HP:0010558,Abnormality of the clivus
+UBERON:0015174,helicine artery of penis,UBERON:0014403,male anatomical structure
+DOID:12306,vitiligo,DOID:417,hypersensitivity reaction type II disease
+HP:0100108,Small epiphysis of the distal phalanx of the 2nd toe,HP:0100052,Small epiphyses of the 2nd toe
+DOID:3250,pleomorphic rhabdomyosarcoma,DOID:3247,rhabdomyosarcoma
+UBERON:0009122,adenohypophyseal placode,UBERON:0002546,cranial placode
+CL:0002082,type II cell of adrenal medulla,CL:0000336,adrenal medulla chromaffin cell
+UBERON:3010752,lobe,UBERON:0000481,multi-tissue structure
+UBERON:3000323,nasopremaxilla,UBERON:0008907,dermal bone
+HP:0005222,Bowel diverticulosis,HP:0002242,Abnormality of the intestine
+UBERON:0011661,xiphiplastron,UBERON:0011657,dermal element of plastron
+HP:0007100,Progressive ventriculomegaly,HP:0002119,Ventriculomegaly
+UBERON:0010063,tympanic cavity epithelium,UBERON:0005911,endo-epithelium
+UBERON:0013608,inferior olive dorsal accessory nucleus,UBERON:0007244,inferior olivary nucleus
+UBERON:0002173,pulmonary alveolar duct,UBERON:0000117,respiratory tube
+DOID:8188,uterine corpus choriocarcinoma,DOID:9460,uterine corpus cancer
+UBERON:0013573,Brodmann (1909) area 40,UBERON:0013529,Brodmann area
+DOID:5973,kidney pelvis papillary carcinoma,DOID:5974,renal pelvis transitional cell carcinoma
+HP:0100578,Lipoatrophy,HP:0009125,Lipodystrophy
+UBERON:0002419,skin gland,UBERON:0006003,integumentary adnexa
+DOID:0050742,nicotine dependence,DOID:9973,substance dependence
+HP:0008981,Calf muscle hypertrophy,HP:0008968,Muscle hypertrophy of the lower extremities
+UBERON:0001212,duodenal gland,UBERON:0011148,submucosal gland
+UBERON:0003236,epithelium of lower jaw,UBERON:0003929,gut epithelium
+DOID:10192,pleomorphic lipoma,DOID:3315,lipoma
+UBERON:0007631,accessory olfactory bulb glomerular layer,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:3000634,vomerine canal,UBERON:0010313,neural crest-derived structure
+DOID:14515,WAGR syndrome,DOID:0080014,chromosomal disease
+HP:0003541,Urinary glycosaminoglycan excretion,HP:0003110,Abnormality of urine homeostasis
+HP:0003927,Cortical irregularity of humeral diaphysis,HP:0003858,Cortical diaphyseal irregularity of the upper limbs
+UBERON:0003965,sympathetic afferent fiber,UBERON:0000061,anatomical structure
+UBERON:0010143,seminal vesicle fluid,UBERON:0006530,seminal fluid
+HP:0001161,Hand polydactyly,HP:0009997,Duplication of phalanx of hand
+HP:0000028,Cryptorchidism,HP:0000032,Abnormality of male external genitalia
+HP:0003233,Hypoalphalipoproteinemia,HP:0010981,Hypolipoproteinemia
+UBERON:0001806,sympathetic ganglion,UBERON:0010313,neural crest-derived structure
+DOID:2609,adenomyoma,DOID:4236,carcinosarcoma
+UBERON:0005871,palatine process of maxilla,UBERON:0004120,mesoderm-derived structure
+UBERON:0007005,cardiac mesoderm,UBERON:0004120,mesoderm-derived structure
+HP:0009245,Triangular shaped distal phalanx of the 5th finger,HP:0004225,Abnormality of the distal phalanx of the 5th finger
+NCBITaxon:1129771,Leptotrichiaceae,NCBITaxon:203491,Fusobacteriales
+DOID:4157,secondary syphilis,DOID:4166,syphilis
+HP:0006690,Myocardial calcification,HP:0001713,Abnormality of cardiac ventricle
+UBERON:0012275,meso-epithelium,UBERON:0000483,epithelium
+HP:0002011,Abnormality of the central nervous system,HP:0012639,Abnormality of nervous system morphology
+HP:0007459,Generalized anhidrosis,HP:0000971,Abnormality of the sweat gland
+UBERON:0011903,gizzard smooth muscle,UBERON:0004222,stomach smooth muscle
+HP:0001831,Short toe,HP:0011927,Short digit
+UBERON:0008436,thoracic vertebral arch,UBERON:0003861,neural arch
+HP:0008639,Gonadal hypoplasia,HP:0000812,Abnormal internal genitalia
+UBERON:0000315,subarachnoid space,UBERON:0000464,anatomical space
+DOID:4683,cutaneous mucoepidermoid carcinoma,DOID:3165,skin benign neoplasm
+UBERON:0010913,vertebral element,UBERON:0004765,skeletal element
+DOID:930,orbital disease,DOID:0050815,adnexa disease
+HP:0012296,Slender distal phalanx of finger,HP:0009832,Abnormality of the distal phalanx of finger
+HP:0011084,Hypocalcification of dental enamel,HP:0006285,Hypomineralization of enamel
+UBERON:0003098,optic stalk,UBERON:0010312,immature eye
+HP:0002630,Fat malabsorption,HP:0002244,Abnormality of the small intestine
+HP:0008962,Calf muscle hypoplasia,HP:0001430,Abnormality of the calf musculature
+UBERON:0010084,future diaphragm,UBERON:0001134,skeletal muscle tissue
+UBERON:0002679,anterodorsal nucleus of thalamus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:0004477,tongue musculature,UBERON:0004461,musculature of head
+HP:0009266,Irregular epiphysis of the proximal phalanx of the 4th finger,HP:0010273,Irregular epiphyses of the proximal phalanges of the hand
+UBERON:0003584,mammary gland connective tissue,UBERON:0014404,female anatomical structure
+HP:0100616,Testicular teratoma,HP:0009792,Teratoma
+UBERON:0006141,palmar digital artery,UBERON:0004553,forelimb digital artery
+UBERON:0006145,dorsal digital artery of pes,UBERON:0004554,hindlimb digital artery
+HP:0011006,Abnormality of the musculature of the neck,HP:0003011,Abnormality of the musculature
+UBERON:0000971,ommatidium,UBERON:0000970,eye
+HP:0009252,Cone-shaped epiphysis of the distal phalanx of the 4th finger,HP:0010248,Cone-shaped epiphyses of the distal phalanges of the hand
+UBERON:0013489,superficial cervical fascia,UBERON:0004923,organ component layer
+UBERON:0004682,corona radiata,UBERON:0002791,regional part of telencephalon
+HP:0001327,Photomyoclonic seizures,HP:0002123,Generalized myoclonic seizures
+UBERON:0015869,retropharyngeal lymph node,UBERON:0012311,deep anterior cervical lymph node
+HP:0009665,Bracket epiphysis of the proximal phalanx of the thumb,HP:0009687,Bracket epiphyses of the thumb
+HP:0007732,Lacrimal gland hypoplasia,HP:0008038,Aplastic/hypoplastic lacrimal glands
+UBERON:0007225,lateral entorhinal cortex,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0002763,Abnormal cartilage morphology,HP:0011842,Abnormality of skeletal morphology
+UBERON:0010733,alisphenoid cartilage element,UBERON:0015058,alisphenoid endochondral element
+UBERON:0001672,anterior cerebral vein,UBERON:0003496,head blood vessel
+HP:0002271,Autonomic dysregulation,HP:0012332,Abnormal autonomic nervous system physiology
+HP:0100706,Abnormality of the oligodendroglia,HP:0100705,Abnormality of the glial cells
+UBERON:0013767,frontal process of maxilla,UBERON:0004529,anatomical projection
+UBERON:0000453,decidua basalis,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0004790,Hypoplasia of the small intestine,HP:0005245,Intestinal hypoplasia
+UBERON:0004327,middle phalanx of pedal digit 5,UBERON:0003866,middle phalanx of pes
+HP:0008988,Pelvic girdle muscle atrophy,HP:0001445,Abnormality of the hip-girdle musculature
+UBERON:0001800,sensory ganglion,UBERON:0000045,ganglion
+UBERON:2002126,caudal-fin ray pump,UBERON:0000477,anatomical cluster
+NCBITaxon:33553,Sciurognathi,NCBITaxon:9989,Rodentia
+UBERON:0010415,barrel cortex,UBERON:0002619,regional part of cerebral cortex
+UBERON:0013224,Ciaccio's gland,UBERON:0013226,accessory lacrimal gland
+UBERON:0004257,upper leg blood vessel,UBERON:0003503,leg blood vessel
+HP:0010612,Plantar pits,HP:0100872,Abnormality of the plantar skin of foot
+UBERON:0015808,eye epithelium,UBERON:0010371,ecto-epithelium
+HP:0004330,Increased skull ossification,HP:0002703,Abnormality of skull ossification
+HP:0009230,Osteolytic defects of the proximal phalanx of the 5th finger,HP:0009150,Abnormality of the proximal phalanx of the 5th finger
+CL:0002629,mature microglial cell,CL:0000129,microglial cell
+UBERON:2005087,pectoral vein,UBERON:0007300,pectoral appendage blood vessel
+DOID:5246,hilar cholangiocellular carcinoma,DOID:4947,cholangiocarcinoma
+NCBITaxon:56210,Calomys callosus,NCBITaxon:29105,Calomys
+DOID:0050852,limb ischemia,DOID:326,ischemia
+DOID:0050640,anauxetic dysplasia,DOID:0080027,spondyloepimetaphyseal dysplasia
+UBERON:0010341,1st arch mesenchyme from head mesenchyme,UBERON:0010042,1st arch mesenchyme
+HP:0008750,Laryngeal atresia,HP:0001600,Abnormality of the larynx
+UBERON:0005427,corneal primordium,UBERON:0010313,neural crest-derived structure
+UBERON:2000747,epaxial region somite 30,UBERON:0003900,epaxial myotome region
+UBERON:0002499,cochlear labyrinth,UBERON:0000064,organ part
+HP:0003321,Biconcave flattened vertebrae,HP:0004586,Biconcave vertebral bodies
+UBERON:0009064,cervical air sac,UBERON:0015212,lateral structure
+DOID:9503,Loeffler syndrome,DOID:5870,eosinophilic pneumonia
+HP:0000978,Bruising susceptibility,HP:0001933,Subcutaneous hemorrhage
+UBERON:3000876,spina pelvis anterior,UBERON:4100000,skeletal element projection
+HP:0100939,Sclerosis of the distal phalanx of the 2nd toe,HP:0100926,Sclerosis of the phalanges of the 2nd toe
+UBERON:0002324,muscle of back,UBERON:0005174,dorsal region organ
+CL:0002548,cardiac fibroblast,CL:0000057,fibroblast
+UBERON:0007146,posterior spinal artery,UBERON:0002458,spinal artery
+UBERON:0004521,vasculature of muscle organ,UBERON:0006876,vasculature of organ
+UBERON:0003357,epithelium of tongue,UBERON:0010371,ecto-epithelium
+UBERON:2000352,external cellular layer,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0000268,Dolichocephaly,HP:0002648,Abnormality of calvarial morphology
+CL:1000550,kidney papillary duct principal epithelial cell,CL:1001225,kidney collecting duct cell
+DOID:13523,loiasis,DOID:37,skin disease
+HP:0007727,Opacification of the corneal epithelium,HP:0007957,Corneal opacity
+UBERON:0015174,helicine artery of penis,UBERON:0015177,helicine artery
+UBERON:0001001,chitin-based cuticle,UBERON:0007491,chitin-based acellular structure
+UBERON:0001719,nucleus ambiguus,UBERON:0007635,nucleus of medulla oblongata
+DOID:10544,pylorus cancer,DOID:10534,stomach cancer
+UBERON:0011742,aortic valve leaflet,UBERON:0011741,cardiac valve leaflet
+HP:0009958,Polydactyly affecting the 3rd finger,HP:0004150,Abnormality of the 3rd finger
+UBERON:0015069,distal carpal cartilage,UBERON:0015068,distal carpal endochondral element
+HP:0009455,Symphalangism affecting the proximal phalanx of the 3rd finger,HP:0009358,Abnormality of the proximal phalanx of the 3rd finger
+UBERON:0013749,metaphysis of humerus,UBERON:0001438,metaphysis
+DOID:3959,adrenal cortical adenocarcinoma,DOID:3948,adrenocortical carcinoma
+UBERON:0011392,internal elastic membrane,UBERON:0000476,acellular anatomical structure
+DOID:8602,gum cancer,DOID:8618,oral cavity cancer
+HP:0000050,Hypoplastic genitalia,HP:0000032,Abnormality of male external genitalia
+NCBITaxon:2,Bacteria,NCBITaxon:131567,cellular organisms
+HP:0003387,Decreased number of large peripheral myelinated nerve fibers,HP:0003380,Decreased number of peripheral myelinated nerve fibers
+HP:0005744,Generalized osteoporosis with pathologic fractures,HP:0000939,Osteoporosis
+UBERON:0000484,simple cuboidal epithelium,UBERON:0000490,unilaminar epithelium
+DOID:6446,ceruminous carcinoma,DOID:4933,apocrine adenocarcinoma
+UBERON:0007846,dense regular connective tissue,UBERON:0007845,regular connective tissue
+HP:0100311,Cerebral ventricular adhesions,HP:0002118,Abnormality of the cerebral ventricles
+HP:0000695,Natal tooth,HP:0006288,Advanced eruption of teeth
+UBERON:0009067,abdominal air sac,UBERON:0015212,lateral structure
+DOID:3388,periodontal disease,DOID:1091,tooth disease
+CL:1000839,kidney proximal straight tubule epithelial cell,CL:1001021,kidney loop of henle descending limb epithelial cell
+UBERON:0007188,mesothelium of serous pericardium,UBERON:0001136,mesothelium
+CL:0000346,hair follicle dermal papilla cell,CL:0000134,mesenchymal cell
+HP:0002938,Lumbar hyperlordosis,HP:0003307,Hyperlordosis
+DOID:6244,familial renal oncocytoma,DOID:6245,renal oncocytoma
+UBERON:2005222,ventral larval melanophore stripe,UBERON:2005220,larval melanophore stripe
+DOID:4447,cystoid macular edema,DOID:4449,macular retinal edema
+CL:0002475,lymphoid MHC-II-negative non-classical monocyte,CL:0002471,MHC-II-negative non-classical monocyte
+DOID:3690,brachial plexus neuropathy,DOID:574,peripheral nervous system disease
+HP:0011315,Unicoronal synostosis,HP:0004440,Coronal craniosynostosis
+HP:0100632,Pulmonary sequestration,HP:0002101,Abnormal lung lobation
+UBERON:0001606,muscle of iris,UBERON:0011222,intra-ocular muscle
+HP:0011038,Abnormality of renal resorption,HP:0012211,Abnormal renal physiology
+UBERON:0000378,tongue muscle,UBERON:0004121,ectoderm-derived structure
+CL:0000035,single fate stem cell,CL:0000723,somatic stem cell
+UBERON:0004540,proper plantar digital artery,UBERON:0006138,plantar digital artery
+DOID:12889,Miller Fisher syndrome,DOID:12842,Guillain-Barre syndrome
+HP:0009498,Triangular epiphyses of the 2nd finger,HP:0010238,Triangular epiphyses of the phalanges of the hand
+HP:0012403,Decreased urine alpha-ketoglutarate concentration,HP:0012401,Abnormal urine alpha-ketoglutarate concentration
+CL:0000573,retinal cone cell,CL:0010009,camera-type eye photoreceptor cell
+UBERON:0005971,amniotic fold,UBERON:0000478,extraembryonic structure
+DOID:285,hairy cell leukemia,DOID:1040,chronic lymphocytic leukemia
+HP:0002588,Duodenal ulcer,HP:0002246,Abnormality of the duodenum
+DOID:5375,hair follicle neoplasm,DOID:3165,skin benign neoplasm
+DOID:14040,autoimmune polyendocrine syndrome,DOID:0060005,autoimmune disease of endocrine system
+HP:0012381,Delayed self-feeding during toddler years,HP:0011968,Feeding difficulties
+UBERON:0000437,arachnoid barrier layer,UBERON:0004121,ectoderm-derived structure
+HP:0011188,Focal EEG discharges with secondary generalization,HP:0011185,EEG with focal epileptiform discharges
+UBERON:0007413,nucleus of pontine reticular formation,UBERON:0009662,hindbrain nucleus
+UBERON:0002856,second lumbar dorsal root ganglion,UBERON:0002836,lumbar dorsal root ganglion
+UBERON:0006565,female urethral meatus,UBERON:0014404,female anatomical structure
+UBERON:0013279,diaphysis of fibula,UBERON:0004120,mesoderm-derived structure
+CL:0000949,IgD plasmablast,CL:0000980,plasmablast
+DOID:684,hepatocellular carcinoma,DOID:686,liver carcinoma
+DOID:7717,colloid carcinoma of the pancreas,DOID:3498,pancreatic ductal adenocarcinoma
+HP:0007836,Mosaic corneal dystrophy,HP:0001131,Corneal dystrophy
+UBERON:0008425,mammary ridge,UBERON:0005423,developing anatomical structure
+HP:0008060,Aplasia/Hypoplasia of the fovea,HP:0008059,Aplasia/Hypoplasia of the macula
+HP:0006203,Decreased movement range in interphalangeal joints,HP:0001376,Limitation of joint mobility
+HP:0004263,Large capitate bone,HP:0004237,Large carpal bones
+UBERON:0002321,extraglomerular mesangium,UBERON:0003567,abdomen connective tissue
+CL:0000622,acinar cell,CL:0000154,protein secreting cell
+NCBITaxon:197911,Influenzavirus A,NCBITaxon:11308,Orthomyxoviridae
+UBERON:0000392,longissimus muscle,UBERON:0004120,mesoderm-derived structure
+UBERON:0007991,proximal sesamoid bone of manus,UBERON:0004249,manual digit bone
+HP:0011576,Intermediate atrioventricular canal defect,HP:0006695,Atrioventricular canal defect
+DOID:9857,interstitial keratitis,DOID:9858,deep keratitis
+HP:0009345,Triangular epiphysis of the distal phalanx of the 3rd finger,HP:0009332,Abnormality of the epiphysis of the distal phalanx of the 3rd finger
+UBERON:0007164,distal radio-ulnar joint,UBERON:0001528,radio-ulnar joint
+HP:0007098,Paroxysmal choreoathetosis,HP:0001266,Choreoathetosis
+HP:0003940,Osteoarthritis of the elbow,HP:0009811,Abnormality of the elbow
+UBERON:0006966,heart capillary,UBERON:0001982,capillary
+UBERON:0015225,atrial foramen intermedium,UBERON:0004111,anatomical conduit
+UBERON:0005147,metanephric renal vesicle,UBERON:0004209,renal vesicle
+UBERON:0013772,left nipple,UBERON:0002030,nipple
+DOID:12185,otosclerosis,DOID:4539,labyrinthine disease
+UBERON:0014544,frontomarginal sulcus,UBERON:0003022,cerebral cortex lobe
+CL:1000492,mesothelial cell of parietal pleura,CL:1000491,mesothelial cell of pleura
+UBERON:0009860,ascidian digestive gland,UBERON:0006925,digestive gland
+UBERON:0011643,puboischiofemoralis internus muscle,UBERON:0004518,muscle of vertebral column
+CL:0000814,mature NK T cell,CL:0002127,innate effector T cell
+UBERON:0001387,fibularis longus,UBERON:0009132,peroneus
+UBERON:0001154,vermiform appendix,UBERON:0013765,digestive system organ
+HP:0007036,Hypoplasia of olfactory tract,HP:0002977,Aplasia/Hypoplasia involving the central nervous system
+UBERON:3010737,M. palmaris longus,UBERON:0010891,pectoral complex muscle
+HP:0010273,Irregular epiphyses of the proximal phalanges of the hand,HP:0010233,Irregular epiphyses of the phalanges of the hand
+UBERON:0011221,ora serrata of retina,UBERON:0007651,anatomical junction
+UBERON:0001187,testicular artery,UBERON:0001637,artery
+DOID:10593,idiopathic progressive polyneuropathy,DOID:1389,polyneuropathy
+UBERON:0000382,apocrine sweat gland,UBERON:0001820,sweat gland
+UBERON:0003656,mesopodium bone,UBERON:0011250,autopod bone
+HP:0012043,Pendular nystagmus,HP:0000639,Nystagmus
+UBERON:2001893,hypobranchial element,UBERON:0010363,endochondral element
+CL:0000130,neuron associated cell (sensu Nematoda and Protostomia),CL:0000095,neuron associated cell
+HP:0012545,Reduced aldolase level,HP:0012400,Abnormal aldolase level
+UBERON:2001741,trigeminofacial foramen,UBERON:0005744,bone foramen
+CL:0000042,neutrophilic myeloblast,CL:0000835,myeloblast
+DOID:0050786,iridogoniodysgenesis syndrome,DOID:0050736,autosomal dominant disease
+DOID:11755,choledocholithiasis,DOID:0000000,gallbladder disease
+CL:0000355,skeletal muscle stem cell,CL:0000048,multi fate stem cell
+HP:0007607,Hypohidrotic ectodermal dysplasia,HP:0000968,Ectodermal dysplasia
+HP:0003232,Mitochondrial malic enzyme reduced,HP:0003287,Abnormality of mitochondrial metabolism
+UBERON:2205385,dorsal fin proximal radial cartilage 8,UBERON:2105385,dorsal fin proximal radial element 8
+NCBITaxon:356,Rhizobiales,NCBITaxon:28211,Alphaproteobacteria
+UBERON:0002511,trabecula carnea,UBERON:0000440,trabecula
+UBERON:0010165,collection of hair on face,UBERON:0014382,collection of hairs on head or neck
+UBERON:0015024,manual digit phalanx endochondral element,UBERON:0015021,forelimb endochondral element
+HP:0010191,Symphalangism affecting the distal phalanges of the toes,HP:0010182,Abnormality of the distal phalanges of the toes
+UBERON:0006108,corticomedial nuclear complex,UBERON:0007245,nuclear complex of neuraxis
+HP:0011539,Atrial situs ambiguous,HP:0011535,Abnormal atrial arrangement
+HP:0003449,Cold-induced muscle cramps,HP:0003394,Muscle cramps
+UBERON:0001328,lobe of prostate,UBERON:0014403,male anatomical structure
+DOID:0050540,Charcot-Marie-Tooth disease type 3,DOID:10595,Charcot-Marie-Tooth disease
+HP:0010362,Curved phalanges of the 3rd toe,HP:0010330,Abnormality of the phalanges of the 3rd toe
+UBERON:0015841,molar dental lamina,UBERON:0015839,molar epithelium
+CL:1000331,serous cell of epithelium of bronchus,CL:0000313,serous secreting cell
+UBERON:0000151,pectoral fin,UBERON:0004710,pectoral appendage
+UBERON:0012439,blastema of regenerating digit tip,UBERON:0005306,blastema
+HP:0008459,Cervical vertebral agenesis,HP:0011041,Aplasia/Hypoplasia of the cervical spine
+UBERON:0004033,podocyte slit junction,UBERON:0004120,mesoderm-derived structure
+UBERON:0015870,lymph node of head,UBERON:0000029,lymph node
+UBERON:2000617,anal erector,UBERON:2005267,erector muscle
+UBERON:0010867,plagiopatagium,UBERON:0010862,dactylopatagium
+HP:0007515,Hypoplastic pilosebaceous units,HP:0008065,Aplasia/Hypoplasia of the skin
+CL:0002074,myocardial endocrine cell,CL:0000163,endocrine cell
+HP:0000571,Hypometric saccades,HP:0000570,Abnormality of saccadic eye movements
+UBERON:4200176,ascending process of clavicle,UBERON:0004530,bony projection
+UBERON:0003415,mesenchyme of nasal septum,UBERON:0004120,mesoderm-derived structure
+HP:0010532,Paroxysmal vertigo,HP:0002321,Vertigo
+UBERON:0010565,manual digit 1 metacarpus pre-cartilage condensation,UBERON:0015043,manual digit 1 metacarpus endochondral element
+UBERON:0001299,glans penis,UBERON:0000064,organ part
+DOID:2705,malignant giant cell tumor,DOID:200,giant cell tumor
+DOID:7175,anal Buschke-Lowenstein tumor,DOID:5525,anal squamous cell carcinoma
+CL:0000553,megakaryocyte progenitor cell,CL:0000763,myeloid cell
+UBERON:0004381,skeleton of limb,UBERON:0011582,paired limb/fin skeleton
+UBERON:0011936,vibrissa hair bulb,UBERON:0005932,bulb of hair follicle
+HP:0002305,Athetosis,HP:0004305,Involuntary movements
+UBERON:0010257,6th arch mesenchyme from neural crest,UBERON:0010359,pharyngeal arch mesenchyme from neural crest
+HP:0011259,Expanded terminal portion of crus of helix,HP:0009895,Abnormality of the crus of the helix
+UBERON:0000993,oviduct,UBERON:0014404,female anatomical structure
+UBERON:2000635,central pretectal nucleus,UBERON:0006569,diencephalic nucleus
+HP:0001220,Interphalangeal joint contractures (hands),HP:0100490,Camptodactyly of finger
+DOID:13800,inclusion conjunctivitis,DOID:0050339,commensal bacterial infectious disease
+UBERON:3010226,postiliac glands,UBERON:3010603,body gland
+UBERON:3000494,processus lingualis of pterygoid,UBERON:0010313,neural crest-derived structure
+HP:0011698,Supraventricular tachycardia with a manifest accessory pathway on the septum,HP:0011694,Supraventricular tachycardia with a manifest accessory pathway
+HP:0010268,Absent epiphyses of the proximal phalanges of the hand,HP:0010228,Absent epiphyses of the phalanges of the hand
+HP:0000347,Micrognathia,HP:0009118,Aplasia/Hypoplasia of the mandible
+UBERON:0010170,region of neural crest,UBERON:0000480,anatomical group
+HP:0008475,Hypoplastic sacral vertebrae,HP:0008417,Vertebral hypoplasia
+HP:0100920,Sclerosis of the phalanges of the 4th finger,HP:0100899,Sclerosis of the phalanges of the hand
+UBERON:2005373,dorsal fin distal radial bone 2,UBERON:2000936,dorsal fin distal radial bone
+HP:0010141,Enlarged epiphysis of the distal phalanx of the hallux,HP:0010124,Abnormality of the epiphysis of the distal phalanx of the hallux
+UBERON:0012312,maxillary process ectoderm,UBERON:0005291,embryonic tissue
+UBERON:0000209,tetrapod frontal bone,UBERON:0010428,flat bone
+CL:1001432,kidney collecting duct intercalated cell,CL:0005010,renal intercalated cell
+DOID:9744,type 1 diabetes mellitus,DOID:9351,diabetes mellitus
+NCBITaxon:61172,Laguna Negra virus,NCBITaxon:11598,Hantavirus
+HP:0012144,Abnormality of cells of the monocyte/macrophage lineage,HP:0005561,Abnormality of bone marrow cell morphology
+UBERON:0009753,adrenal gland cortex zone,UBERON:0000064,organ part
+HP:0000839,Pituitary dwarfism,HP:0000824,Growth hormone deficiency
+HP:0009509,Pseudoepiphysis of the distal phalanx of the 2nd finger,HP:0010253,Pseudoepiphyses of the distal phalanges of the hand
+UBERON:0011856,acinus of lactiferous gland,UBERON:0014404,female anatomical structure
+HP:0004696,Talipes cavus equinovarus,HP:0001762,Talipes equinovarus
+CL:0002046,early pro-B cell,CL:0000826,pro-B cell
+DOID:10486,intestinal atresia,DOID:5295,intestinal disease
+CL:0002194,monopoietic cell,CL:0000839,myeloid lineage restricted progenitor cell
+HP:0003683,Large beaked nose,HP:0000444,Convex nasal ridge
+UBERON:0007159,lumen of colon,UBERON:0000464,anatomical space
+HP:0100386,Aplasia of the proximal phalanx of the 5th toe,HP:0100377,Aplasia/Hypoplasia of the proximal phalanx of the 5th toe
+UBERON:0007650,esophagogastric junction,UBERON:0007651,anatomical junction
+UBERON:0001844,cochlea,UBERON:0004120,mesoderm-derived structure
+HP:0100955,Giant cell granuloma of mandible,HP:0000277,Abnormality of the mandible
+DOID:5974,renal pelvis transitional cell carcinoma,DOID:4919,renal pelvis carcinoma
+UBERON:2001235,hypobranchial 3 bone,UBERON:2001896,hypobranchial 3 element
+UBERON:0012430,tunica fibrosa of eyeball,UBERON:0004923,organ component layer
+HP:0001036,Parakeratosis,HP:0011368,Epidermal thickening
+UBERON:0006682,hypoglossal canal,UBERON:0004111,anatomical conduit
+HP:0009379,Rhomboid or triangular shaped 5th finger distal phalanx,HP:0009245,Triangular shaped distal phalanx of the 5th finger
+DOID:2219,Glanzmann's thrombasthenia,DOID:2218,blood platelet disease
+HP:0010271,Enlarged epiphyses of the proximal phalanges of the hand,HP:0010245,Abnormality of the epiphyses of the proximal phalanges of the hand
+UBERON:0015139,infundibulum of gallbladder,UBERON:0000064,organ part
+HP:0005498,Midline skin dimples over anterior/posterior fontanelles,HP:0000236,Abnormality of the anterior fontanelle
+UBERON:0009194,basisphenoid cartilage condenstion,UBERON:0007213,mesenchyme derived from head neural crest
+NCBITaxon:40119,Parvovirinae,NCBITaxon:10780,Parvoviridae
+HP:0001868,Autoamputation (feet),HP:0001760,Abnormality of the foot
+HP:0002864,Paraganglioma of head and neck,HP:0002668,Paraganglioma
+HP:0009521,Small epiphysis of the middle phalanx of the 2nd finger,HP:0009496,Small epiphyses of the 2nd finger
+HP:0009815,Aplasia/Hypoplasia of the extremities,HP:0002813,Abnormality of limb bone morphology
+HP:0004334,Dermal atrophy,HP:0008065,Aplasia/Hypoplasia of the skin
+HP:0003976,Constricted radius,HP:0002818,Abnormality of the radius
+DOID:7439,polyp of middle ear,DOID:5100,middle ear disease
+UBERON:0000157,theca interna,UBERON:0000158,membranous layer
+HP:0009488,Absent epiphyses of the 2nd finger,HP:0010228,Absent epiphyses of the phalanges of the hand
+HP:0001530,Mild postnatal growth retardation,HP:0008897,Postnatal growth retardation
+CL:0001049,"activated CD8-positive, alpha-beta T cell, human",CL:0000906,"activated CD8-positive, alpha-beta T cell"
+DOID:10968,spastic monoplegia,DOID:0050669,spastic cerebral palsy
+HP:0004013,Medially fused radial epiphyseal plates,HP:0004012,Premature fusion of the radial epiphyseal plates
+UBERON:3000965,basale commune (carpal),UBERON:0001481,distal carpal bone
+HP:0002863,Myelodysplasia,HP:0004377,Hematological neoplasm
+UBERON:0002836,lumbar dorsal root ganglion,UBERON:0000044,dorsal root ganglion
+HP:0005929,Synostosis involving the tibia,HP:0009138,Synostosis involving bones of the lower limbs
+HP:0009945,Duplication of phalanx of 2nd finger,HP:0009541,Abnormality of the phalanges of the 2nd finger
+UBERON:0006296,subcardinal vein,UBERON:0001638,vein
+HP:0200001,Dysharmonic accelerated bone age,HP:0005616,Accelerated skeletal maturation
+DOID:5062,phencyclidine abuse,DOID:302,substance abuse
+UBERON:4300004,scale pocket,UBERON:2001951,skin flap
+UBERON:0005179,pelvic region organ,UBERON:0005173,abdominal segment organ
+HP:0009580,Aplasia/Hypoplasia of the proximal phalanx of the 2nd finger,HP:0009544,Abnormality of the proximal phalanx of the 2nd finger
+UBERON:0011685,preorbitalis muscle,UBERON:0011648,jaw muscle
+HP:0100261,Abnormal tendon morphology,HP:0011842,Abnormality of skeletal morphology
+HP:0005209,Intrahepatic bile duct cysts,HP:0011040,Abnormality of the intrahepatic bile duct
+HP:0009371,Type A1 brachydactyly,HP:0009370,Type A brachydactyly
+HP:0001757,High-frequency sensorineural hearing impairment,HP:0000407,Sensorineural hearing impairment
+UBERON:0002074,hair shaft,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003584,mammary gland connective tissue,UBERON:0005156,reproductive structure
+UBERON:0007135,neural keel,UBERON:0004121,ectoderm-derived structure
+DOID:13724,scurvy,DOID:5113,nutritional deficiency disease
+HP:0002385,Paraparesis,HP:0010551,Paraplegia/paraparesis
+UBERON:2005225,median fin radial bone,UBERON:2105225,median fin radial element
+CL:0002614,neuron of the substantia nigra,CL:0000117,CNS neuron (sensu Vertebrata)
+DOID:4346,variegate porphyria,DOID:3133,acute porphyria
+UBERON:2000853,somite 18,UBERON:0002329,somite
+HP:0009947,Duplication of the proximal phalanx of the 2nd finger,HP:0010006,Duplication of the proximal phalanx of hand
+UBERON:2001505,taenia marginalis anterior,UBERON:0003932,cartilage element of chondrocranium
+HP:0011439,Anesthetic-induced rhabdomylosis,HP:0003201,Rhabdomyolysis
+UBERON:4200001,postpubis,UBERON:0004530,bony projection
+UBERON:0002690,anteroventral periventricular nucleus,UBERON:0002308,nucleus of brain
+UBERON:0003888,extraembryonic coelom,UBERON:0003886,body cavity precursor
+DOID:14177,congenital hypogammaglobulinemia,DOID:2115,B cell deficiency
+UBERON:2000699,entopterygoid vertical strut,UBERON:0010313,neural crest-derived structure
+UBERON:0010185,rete ovarii,UBERON:0005156,reproductive structure
+UBERON:3000840,capitulum of radius,UBERON:0004120,mesoderm-derived structure
+UBERON:0011956,right hepatic vein,UBERON:0001143,hepatic vein
+DOID:2566,corneal dystrophy,DOID:10124,corneal disease
+DOID:4012,papillary transitional carcinoma,DOID:2671,transitional cell carcinoma
+HP:0009515,Cone-shaped epiphysis of the middle phalanx of the 2nd finger,HP:0009490,Cone-shaped epiphyses of the 2nd finger
+HP:0002682,Broad skull,HP:0002648,Abnormality of calvarial morphology
+DOID:4109,tick infestation,DOID:4110,parasitic ectoparasitic infectious disease
+UBERON:0015012,tarsometatarsus endochondral element,UBERON:0015022,hindlimb endochondral element
+DOID:0050930,sublingual gland adenoid cystic carcinoma,DOID:8849,sublingual gland cancer
+HP:0009356,Triangular epiphysis of the proximal phalanx of the 3rd finger,HP:0010278,Triangular epiphyses of the proximal phalanges of the hand
+DOID:7173,cloacogenic carcinoma,DOID:5525,anal squamous cell carcinoma
+HP:0010681,Elevated intestinal alkaline phosphatase,HP:0003155,Elevated alkaline phosphatase
+UBERON:0006953,ejaculatory duct epithelium,UBERON:0014403,male anatomical structure
+UBERON:0006907,slow muscle tissue,UBERON:0001134,skeletal muscle tissue
+DOID:3965,Merkel cell carcinoma,DOID:3451,skin carcinoma
+CL:0010001,stromal cell of bone marrow,CL:0000499,stromal cell
+HP:0006715,Glomus tympanicum paraganglioma,HP:0002864,Paraganglioma of head and neck
+HP:0100025,Overfriendliness,HP:0012433,Abnormal social behavior
+HP:0000723,Restrictive behavior,HP:0100851,Abnormal emotion/affect behavior
+UBERON:0002018,synovial membrane of synovial joint,UBERON:0012275,meso-epithelium
+UBERON:0003282,mesentery of heart,UBERON:0002095,mesentery
+UBERON:0013761,cervical cavity,UBERON:0002553,anatomical cavity
+DOID:10892,hypospadias,DOID:0080015,physical disorder
+UBERON:0004394,epiphysis of fourth metacarpal bone,UBERON:0004390,epiphysis of metacarpal bone
+UBERON:3000395,pars basilaris,UBERON:0004121,ectoderm-derived structure
+UBERON:3000387,subotic alae,UBERON:0004120,mesoderm-derived structure
+NCBITaxon:37162,Mycobacterium avium complex,NCBITaxon:120793,Mycobacterium avium complex (MAC)
+CL:0000873,splenic metallophillic macrophage,CL:0000871,splenic macrophage
+HP:0009288,Curved proximal phalanx of the 4th finger,HP:0009854,Curved proximal phalanges of the hand
+DOID:221,acute perichondritis of pinna,DOID:222,perichondritis of auricle
+UBERON:0008193,pneumatized bone,UBERON:0008001,irregular bone
+UBERON:2005053,nasal ciliary artery,UBERON:0001637,artery
+DOID:8415,carcinoma arising in nasal papillomatosis,DOID:4931,nasal cavity carcinoma
+UBERON:0011803,"feather bud, dermal component",UBERON:0003104,mesenchyme
+HP:0009103,Aplasia/Hypoplasia involving the pelvis,HP:0002644,Abnormality of pelvic girdle bone morphology
+HP:0010952,Mild fetal ventriculomegaly,HP:0002119,Ventriculomegaly
+HP:0012341,Microprolactinoma,HP:0006767,Pituitary prolactin cell adenoma
+UBERON:0007774,secondary dentition,UBERON:0003672,dentition
+UBERON:0006254,ischial cartilage element,UBERON:0015056,ischial endochondral element
+CL:0002195,hepatic stem cell,CL:0000048,multi fate stem cell
+DOID:4810,cerebrotendinous xanthomatosis,DOID:3345,xanthomatosis
+UBERON:2001787,pectoral fin spine,UBERON:4000175,pectoral fin lepidotrichium
+UBERON:0001146,suprarenal vein,UBERON:0001638,vein
+HP:0012280,Hepatic amyloidosis,HP:0001392,Abnormality of the liver
+UBERON:0010686,manual digit phalanx cartilage element,UBERON:0010701,phalanx cartilage element
+CL:0002485,retinal melanocyte,CL:0009004,retinal cell
+UBERON:0005402,philtrum,UBERON:0003102,surface structure
+DOID:6344,melanocytic psammomatous MPNST,DOID:6345,malignant melanocytic neoplasm of the peripheral nerve sheath
+UBERON:0004084,genital labium,UBERON:0015212,lateral structure
+DOID:7533,subareolar duct papillomatosis,DOID:3003,nipple neoplasm
+UBERON:3010022,M. tensor fasciae latae,UBERON:0010890,pelvic complex muscle
+HP:0011737,Corticotropin-releasing hormone (CRH) deficient adrenal insufficiency,HP:0011734,Central adrenal insufficiency
+UBERON:0004938,submucosa of biliary tree,UBERON:0004119,endoderm-derived structure
+UBERON:2201818,dorsal fin proximal radial cartilage 1,UBERON:2101818,dorsal fin proximal radial element 1
+DOID:2277,gonadal disease,DOID:15,reproductive system disease
+UBERON:2000512,facial lobe,UBERON:0007635,nucleus of medulla oblongata
+DOID:4593,pediatric meningioma,DOID:3565,meningioma
+DOID:0050717,methylmalonic aciduria and homocystinuria type cblF,DOID:14749,methylmalonic acidemia
+HP:0003800,Muscle abnormality related to mitochondrial dysfunction,HP:0003011,Abnormality of the musculature
+HP:0001645,Sudden cardiac death,HP:0001695,Cardiac arrest
+UBERON:4200177,supracondyle tubercle,UBERON:0005813,tubercle
+UBERON:2001978,maxillary tooth row,UBERON:0009678,tooth row
+HP:0010777,Bronchomegaly,HP:0002109,Abnormality of the bronchi
+DOID:5638,malignant giant cell tumor of soft parts,DOID:200,giant cell tumor
+HP:0003217,Hyperglutaminemia,HP:0010903,Abnormality of glutamine metabolism
+CL:0000746,cardiac muscle cell,CL:0002494,cardiocyte
+DOID:0060160,survival motor neuron spinal muscular atrophy,DOID:12377,spinal muscular atrophy
+UBERON:0001257,trigone of urinary bladder,UBERON:0004120,mesoderm-derived structure
+UBERON:0000105,life cycle stage,UBERON:0000000,processual entity
+DOID:4058,gallbladder sarcoma,DOID:3121,gallbladder cancer
+DOID:9820,central gyrate choroidal dystrophy,DOID:9821,choroideremia
+UBERON:4000078,chondroid tissue,UBERON:0004755,skeletal tissue
+HP:0004786,Jejunal diverticula,HP:0002256,Small bowel diverticula
+CL:0005022,vascular lymphangioblast,CL:0005020,lymphangioblast
+UBERON:0011803,"feather bud, dermal component",UBERON:0010314,structure with developmental contribution from neural crest
+HP:0004768,Sparse anterior scalp hair,HP:0002209,Sparse scalp hair
+UBERON:0013181,blowhole ligament,UBERON:0003566,head connective tissue
+UBERON:0003254,amniotic ectoderm,UBERON:0010303,extraembryonic epithelium
+DOID:0050767,midface dysplasia,DOID:2256,osteochondrodysplasia
+UBERON:0002802,left parietal lobe,UBERON:0001872,parietal lobe
+DOID:9622,kidney hypertrophy,DOID:557,kidney disease
+HP:0012266,T-wave alternans,HP:0005135,EKG: T-wave abnormalities
+UBERON:0009880,carpal skeleton,UBERON:0009878,mesopodial skeleton
+DOID:13955,uterus interstitial leiomyoma,DOID:13223,uterine fibroid
+UBERON:0002291,central canal of spinal cord,UBERON:0004121,ectoderm-derived structure
+DOID:0050689,brachydactyly-syndactyly syndrome,DOID:0050739,autosomal genetic disease
+UBERON:0005079,eggshell,UBERON:0000476,acellular anatomical structure
+HP:0010821,Gelastic seizures,HP:0011153,Focal motor seizures
+HP:0000122,Unilateral renal agenesis,HP:0000104,Renal agenesis
+HP:0011398,Central hypotonia,HP:0011442,Abnormality of central motor function
+HP:0011518,Dichromacy,HP:0007641,Dyschromatopsia
+HP:0011529,Multiple bilateral congenital hypertrophy of retinal pigment epithelium,HP:0007649,Congenital hypertrophy of retinal pigment epithelium
+UBERON:0007833,osseus semicircular canal,UBERON:0004120,mesoderm-derived structure
+UBERON:0009089,inner medulla vasa recta descending limb,UBERON:0004120,mesoderm-derived structure
+UBERON:0005449,greater sac,UBERON:0004120,mesoderm-derived structure
+HP:0006591,Absent glenoid fossa,HP:0011912,Abnormality of the glenoid fossa
+CL:1000412,endothelial cell of arteriole,CL:1000413,endothelial cell of artery
+CL:0000778,mononuclear osteoclast,CL:0000226,single nucleate cell
+DOID:13159,scrotum squamous cell carcinoma,DOID:3445,scrotal carcinoma
+HP:0100890,Cyst of the ductus choledochus,HP:0100889,Abnormality of the ductus choledochus
+HP:0004954,Descending aortic aneurysm,HP:0004959,Dilatation of the descending thoracic aorta
+DOID:10230,aortic atherosclerosis,DOID:1936,atherosclerosis
+UBERON:0004511,skeletal muscle tissue of rectus abdominis,UBERON:0003898,skeletal muscle tissue of trunk
+DOID:5567,ovarian germ cell teratoma,DOID:3307,teratoma
+HP:0010619,Fibroma of the breast,HP:0010614,Fibroma
+DOID:8252,chronic rhinitis,DOID:4483,rhinitis
+UBERON:0010215,arytenoid swellings,UBERON:0010314,structure with developmental contribution from neural crest
+CL:1000428,stem cell of epidermis,CL:0000723,somatic stem cell
+UBERON:0002451,uterine gland,UBERON:0005398,female reproductive gland
+NCBITaxon:63399,Arthroderma,NCBITaxon:34384,Arthrodermataceae
+UBERON:0003470,artery of upper lip,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+HP:0010075,Duplication of the 1st metatarsal,HP:0010211,Duplication of proximal phalanx of toe
+CL:0002173,extraglomerular mesangial cell,CL:0000650,mesangial cell
+CL:0002181,mucus neck cell of gastric gland,CL:0000651,mucous neck cell
+HP:0001482,Subcutaneous nodule,HP:0200036,Skin nodule
+UBERON:4300114,pelvic sucking disc,UBERON:0000152,pelvic fin
+UBERON:0005597,lung primordium,UBERON:0001048,primordium
+CL:1000275,smooth muscle cell of small intestine,CL:0002504,enteric smooth muscle cell
+UBERON:0003446,ankle nerve,UBERON:0003445,pes nerve
+UBERON:0009610,forebrain neural plate,UBERON:0003075,neural plate
+HP:0100812,Halitosis,HP:0000163,Abnormality of the oral cavity
+UBERON:0002502,round window of inner ear,UBERON:0013685,foramen of skull
+HP:0001058,Poor wound healing,HP:0011354,Generalized abnormality of skin
+HP:0011869,Abnormal platelet function,HP:0001872,Abnormality of thrombocytes
+HP:0002870,Obstructive sleep apnea,HP:0010535,Sleep apnea
+UBERON:0000998,seminal vesicle,UBERON:0006868,seminal fluid secreting gland
+HP:0007766,Optic disc hypoplasia,HP:0008058,Aplasia/Hypoplasia of the optic nerve
+HP:0001876,Pancytopenia,HP:0012145,Abnormality of multiple cell lineages in the bone marrow
+UBERON:0005637,pyloric region epithelium,UBERON:0001276,epithelium of stomach
+UBERON:0007213,mesenchyme derived from head neural crest,UBERON:0005253,head mesenchyme
+DOID:2996,mixed germ cell-sex cord neoplasm,DOID:154,mixed cell type cancer
+HP:0002789,Tachypnea,HP:0002793,Abnormal pattern of respiration
+UBERON:0015020,otic capsule endochondral element,UBERON:0004121,ectoderm-derived structure
+UBERON:0002979,Purkinje cell layer of cerebellar cortex,UBERON:0004130,cerebellar layer
+HP:0100078,Bracket epiphyses of the 5th toe,HP:0010163,Bracket epiphyses of the toes
+HP:0002331,Headache (with pheochromocytoma),HP:0002315,Headache
+UBERON:0005388,photoreceptor array,UBERON:0000479,tissue
+UBERON:0014706,primitive renal collecting duct system,UBERON:0012275,meso-epithelium
+UBERON:0005946,outflow tract of atrium,UBERON:0004145,outflow tract
+UBERON:2000222,isthmic primary nucleus,UBERON:0004132,trigeminal sensory nucleus
+HP:0005616,Accelerated skeletal maturation,HP:0000927,Abnormality of skeletal maturation
+UBERON:0001637,artery,UBERON:0003509,arterial blood vessel
+HP:0005848,Bifid thumb distal phalanx,HP:0009617,Abnormality of the distal phalanx of the thumb
+UBERON:2000809,myotome somite 4,UBERON:0003082,myotome
+UBERON:0011508,sphincter colli superficialis muscle,UBERON:0002377,muscle of neck
+DOID:6996,intermediate cell type choroid melanoma,DOID:6992,intraocular mixed cell type melanoma
+UBERON:0001936,tuberomammillary nucleus,UBERON:0002789,regional part of posterior hypothalamic region
+DOID:0050473,Alstrom syndrome,DOID:0050737,autosomal recessive disease
+HP:0004819,Normocytic hypoplastic anemia,HP:0001908,Hypoplastic anemia
+UBERON:3000111,crista dentalis of maxilla,UBERON:4100000,skeletal element projection
+DOID:1584,acute chest syndrome,DOID:850,lung disease
+HP:0100364,Aplasia of the phalanges of the 5th toe,HP:0010343,Aplasia/Hypoplasia of the 5th toe
+UBERON:2000774,hypaxial region somite 28,UBERON:0003895,hypaxial myotome region
+UBERON:0002107,liver,UBERON:0004119,endoderm-derived structure
+HP:0001142,Lenticonus,HP:0011526,Abnormality of lens shape
+UBERON:0014671,distal interphalangeal joint of manural digit 5,UBERON:0014680,distal interphalangeal joint of digit 5
+HP:0000066,Labial hypoplasia,HP:0000058,Abnormality of the labia
+UBERON:0002696,cuneiform nucleus,UBERON:0007415,nucleus of midbrain reticular formation
+DOID:11387,epidural abscess,DOID:331,central nervous system disease
+HP:0009786,Aplasia/Hypoplasia of the musculature of the thigh,HP:0001437,Abnormality of the musculature of the lower limbs
+UBERON:0001001,chitin-based cuticle,UBERON:0001002,cuticle
+UBERON:0005333,mammary bud,UBERON:0005291,embryonic tissue
+DOID:0050636,familial visceral amyloidosis,DOID:9120,amyloidosis
+HP:0100510,Vitamin C deficiency,HP:0100509,Abnormality of vitamin C metabolism
+CL:1000493,mesothelial cell of visceral pleura,CL:1000491,mesothelial cell of pleura
+HP:0012668,Vasovagal syncope,HP:0001279,Syncope
+DOID:1082,dirofilariasis,DOID:37,skin disease
+UBERON:0004852,cardiovascular system endothelium,UBERON:0001986,endothelium
+UBERON:0002908,subparietal sulcus,UBERON:0013118,sulcus of brain
+UBERON:2005121,middle lateral line placode,UBERON:0003067,dorsolateral placode
+HP:0000508,Ptosis,HP:0012373,Abnormal eye physiology
+HP:0003068,Madelung-like forearm deformities,HP:0002818,Abnormality of the radius
+UBERON:0005043,mucosa of nasolacrimal duct,UBERON:0004121,ectoderm-derived structure
+HP:0008372,Abnormality of vitamin A metabolism,HP:0100508,Abnormality of vitamin metabolism
+UBERON:0005192,deferent duct artery,UBERON:0003513,trunk blood vessel
+HP:0011279,Abnormality of urine bicarbonate concentration,HP:0003110,Abnormality of urine homeostasis
+HP:0000840,Adrenogenital syndrome,HP:0008373,Puberty and gonadal disorders
+UBERON:0008256,left clavicle,UBERON:0001105,clavicle
+HP:0002181,Cerebral edema,HP:0002060,Abnormality of the cerebrum
+HP:0010334,Polydactyly affecting the 3rd toe,HP:0010112,Mesoaxial foot polydactyly
+HP:0009020,Exercise-induced muscle fatigue,HP:0003750,Increased muscle fatiguability
+UBERON:0002735,transverse pontine fibers,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004249,manual digit bone,UBERON:0012358,manual digitopodium bone
+UBERON:3010798,ramulus suprabranchialis anterior,UBERON:3010126,middle lateral line nerve (MLLN)
+DOID:4603,epidermolytic hyperkeratosis,DOID:37,skin disease
+UBERON:0003922,pancreatic bud,UBERON:0005911,endo-epithelium
+UBERON:2001976,interorbital septum,UBERON:0000477,anatomical cluster
+UBERON:0003705,Meckel's diverticulum,UBERON:0006590,vestigial embryonic structure
+HP:0009341,Ivory epiphysis of the distal phalanx of the 3rd finger,HP:0009332,Abnormality of the epiphysis of the distal phalanx of the 3rd finger
+UBERON:0004761,cartilaginous neurocranium,UBERON:0004120,mesoderm-derived structure
+DOID:0050559,Fukuyama congenital muscular dystrophy,DOID:0050557,congenital muscular dystrophy
+UBERON:0003492,bronchus reticular lamina,UBERON:0003490,respiratory system reticular lamina
+UBERON:0003526,respiratory system capillary,UBERON:0003504,respiratory system blood vessel
+HP:0000551,Abnormality of color vision,HP:0000504,Abnormality of vision
+DOID:13649,polyneuropathy in collagen vascular disease,DOID:1389,polyneuropathy
+HP:0001271,Polyneuropathy,HP:0009830,Peripheral neuropathy
+DOID:6307,ectopic thymus,DOID:533,thymus gland disease
+UBERON:0004117,pharyngeal pouch,UBERON:0005911,endo-epithelium
+DOID:13884,sick sinus syndrome,DOID:0050824,sinoatrial node disease
+UBERON:0009916,wall of ureter,UBERON:0006554,urinary system structure
+DOID:13241,Behcet's disease,DOID:865,vasculitis
+UBERON:0009016,ciliary stroma,UBERON:0003566,head connective tissue
+HP:0009244,Distal/middle symphalangism of 5th finger,HP:0004225,Abnormality of the distal phalanx of the 5th finger
+HP:0001629,Ventricular septal defect,HP:0010438,Abnormality of the ventricular septum
+DOID:1495,cystic echinococcosis,DOID:37,skin disease
+NCBITaxon:106179,phagocytophilum group,NCBITaxon:768,Anaplasma
+UBERON:0003304,mesoderm blood island,UBERON:0012275,meso-epithelium
+HP:0009217,Enlarged epiphysis of the middle phalanx of the 4th finger,HP:0009396,Enlarged epiphyses of the 4th finger
+UBERON:3000020,anterolateral process of frontoparietal,UBERON:4100000,skeletal element projection
+UBERON:0008192,tendon of triceps brachii,UBERON:0000043,tendon
+UBERON:0002033,arrector muscle of hair,UBERON:0001135,smooth muscle tissue
+UBERON:0006691,tentorium cerebelli,UBERON:0004121,ectoderm-derived structure
+HP:0009140,Synostosis involving bones of the feet,HP:0001760,Abnormality of the foot
+HP:0008250,Infantile hypercalcemia,HP:0003072,Hypercalcemia
+HP:0010034,Short 1st metacarpal,HP:0010049,Short metacarpal
+UBERON:4200069,sternal keel,UBERON:0004120,mesoderm-derived structure
+UBERON:3000842,capitulum ulnae,UBERON:0005055,zone of long bone
+DOID:206,hereditary multiple exostoses,DOID:203,exostosis
+HP:0003971,Broad forearm bones,HP:0002973,Abnormality of the forearm
+UBERON:0001530,common carotid artery plus branches,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:2282,hidradenitis,DOID:1383,sweat gland disease
+CL:0002593,smooth muscle cell of the internal thoracic artery,CL:0002595,smooth muscle cell of the subclavian artery
+HP:0009456,Triangular shaped proximal phalanx of the 3rd finger,HP:0009358,Abnormality of the proximal phalanx of the 3rd finger
+HP:0006978,Dysmyelinating leukodystrophy,HP:0002415,Leukodystrophy
+DOID:9719,proliferative vitreoretinopathy,DOID:5679,retinal disease
+HP:0009953,Partial duplication of the middle phalanx of the 2nd finger,HP:0010005,Partial duplication of the middle phalanges of the hand
+NCBITaxon:44542,gambiae species complex,NCBITaxon:44537,Pyretophorus
+HP:0008194,Multiple pancreatic beta-cell adenomas,HP:0008261,Pancreatic islet cell adenoma
+UBERON:0002945,ventral posteromedial nucleus of thalamus,UBERON:0003528,brain grey matter
+DOID:13226,oculoglandular tularemia,DOID:2123,tularemia
+UBERON:0011113,inferior tibiofibular joint,UBERON:0011112,tibiofibular joint
+UBERON:2000703,ventral motor nucleus trigeminal nerve,UBERON:0002633,motor nucleus of trigeminal nerve
+UBERON:0013609,inferior olive medial accessory nucleus,UBERON:0007244,inferior olivary nucleus
+HP:0007220,Demyelinating motor neuropathy,HP:0007178,Motor polyneuropathy
+HP:0001776,Bilateral talipes equinovarus,HP:0001762,Talipes equinovarus
+UBERON:0005158,parenchyma of central nervous system,UBERON:0000353,parenchyma
+UBERON:2001686,bony shelf above orbit,UBERON:0000477,anatomical cluster
+DOID:3191,nemaline myopathy,DOID:422,congenital structural myopathy
+HP:0005035,Shortening of all phalanges of the toes,HP:0001831,Short toe
+UBERON:0000199,neck of radius,UBERON:0004120,mesoderm-derived structure
+UBERON:0005105,posterior mesonephric tubule,UBERON:0000083,mesonephric tubule
+UBERON:4200012,ectepicondylar flange,UBERON:4100000,skeletal element projection
+HP:0011085,Hypomature dental enamel,HP:0006285,Hypomineralization of enamel
+UBERON:0007132,head kidney,UBERON:0006554,urinary system structure
+UBERON:0008776,inner cell mass derived hypoblast,UBERON:0000089,hypoblast (generic)
+DOID:5656,cranial nerve disease,DOID:870,neuropathy
+DOID:8227,atypical breast papilloma,DOID:1626,breast duct papilloma
+UBERON:0003932,cartilage element of chondrocranium,UBERON:0003933,cranial cartilage
+UBERON:0005146,metanephric nephron tubule,UBERON:0005134,metanephric nephron epithelium
+HP:0002465,Poor speech,HP:0002167,Neurological speech impairment
+HP:0012678,Iron accumulation in substantia nigra,HP:0012675,Iron accumulation in brain
+HP:0010884,Acromelia,HP:0009815,Aplasia/Hypoplasia of the extremities
+UBERON:0005754,rostral part of nephrogenic cord,UBERON:0005423,developing anatomical structure
+UBERON:0001466,pedal digit,UBERON:0002544,digit
+UBERON:0003534,tail skin,UBERON:0000014,zone of skin
+HP:0010835,Dissociated sensory loss,HP:0003474,Sensory impairment
+CL:0002171,globose cell of olfactory epithelium,CL:0002169,basal cell of olfactory epithelium
+HP:0009532,Small epiphysis of the proximal phalanx of the 2nd finger,HP:0009501,Abnormality of the epiphysis of the proximal phalanx of the 2nd finger
+DOID:3210,Pelizaeus-Merzbacher disease,DOID:10579,leukodystrophy
+HP:0003281,Increased serum ferritin,HP:0011031,Abnormality of iron homeostasis
+UBERON:0012127,feather barbicel,UBERON:0013703,integumentary projection
+UBERON:0000997,mammalian vulva,UBERON:0014404,female anatomical structure
+HP:0000214,Lip telangiectasia,HP:0000159,Abnormality of the lip
+UBERON:0001168,wall of small intestine,UBERON:0001262,wall of intestine
+UBERON:2000459,ventromedial thalamic nucleus,UBERON:0015234,nucleus of ventral thalamus
+UBERON:0003320,mesenchyme of hip,UBERON:0003104,mesenchyme
+DOID:7878,uterine corpus atypical polypoid adenomyoma,DOID:4994,adenomyoma of uterine corpus
+UBERON:0003336,serosa of duodenum,UBERON:0001206,serosa of small intestine
+UBERON:0001905,pineal body,UBERON:0003296,gland of diencephalon
+HP:0010361,Bullet-shaped phalanges of the 3rd toe,HP:0010330,Abnormality of the phalanges of the 3rd toe
+CL:0002281,type S enteroendocrine cell,CL:0000167,peptide hormone secreting cell
+UBERON:0002000,gluteal muscle,UBERON:0004120,mesoderm-derived structure
+DOID:14042,bipolar I disorder,DOID:3312,bipolar disorder
+UBERON:0000303,adductor longus,UBERON:0004252,hindlimb stylopod muscle
+DOID:1159,functional gastric disease,DOID:76,stomach disease
+UBERON:0001422,facial lymphatic vessel,UBERON:0001473,lymphatic vessel
+HP:0100707,Abnormality of the astrocytes,HP:0100705,Abnormality of the glial cells
+UBERON:0012170,core of nucleus accumbens,UBERON:0002791,regional part of telencephalon
+HP:0011724,Uhl's anomaly,HP:0011723,Congenital malformation of the right heart
+UBERON:0011197,parathyroid epithelium,UBERON:0005911,endo-epithelium
+UBERON:0008829,cerebellum external granule cell layer,UBERON:0002956,granular layer of cerebellar cortex
+UBERON:2005117,anterior lateral line primordium,UBERON:2000228,lateral line primordium
+HP:0100096,Abnormality of the epiphysis of the proximal phalanx of the 4th toe,HP:0010335,Abnormality of the epiphyses of the 4th toe
+HP:0001059,Pterygium,HP:0001367,Abnormal joint morphology
+CL:0000790,immature alpha-beta T cell,CL:0000789,alpha-beta T cell
+UBERON:0007365,rumen,UBERON:0011954,stomach non-glandular region
+NCBITaxon:10257,Parapoxvirus,NCBITaxon:10241,Chordopoxvirinae
+HP:0100229,Irregular epiphysis of the proximal phalanx of the 5th toe,HP:0100099,Abnormality of the epiphysis of the proximal phalanx of the 5th toe
+DOID:769,neuroblastoma,DOID:2621,autonomic nervous system neoplasm
+CL:1000479,purkinje myocyte of atrioventricular node,CL:1000410,myocyte of atrioventricular node
+HP:0004331,Decreased skull ossification,HP:0002703,Abnormality of skull ossification
+UBERON:0001710,lower jaw region,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2002023,second preethmoid,UBERON:0011164,neurocranium bone
+UBERON:0014388,kidney collecting duct epithelium,UBERON:0004211,nephron epithelium
+HP:0100444,Curved middle phalanx of the 4th toe,HP:0010374,Curved phalanges of the 4th toe
+HP:0012255,Dynein arm defect of motile cilia,HP:0005938,Abnormal respiratory motile cilium morphology
+HP:0002729,Follicular hyperplasia,HP:0002716,Lymphadenopathy
+HP:0009855,Osteolytic defects of the proximal phalanges of the hand,HP:0009834,Abnormality of the proximal phalanges of the hand
+DOID:6742,synchronous bilateral breast carcinoma,DOID:6741,bilateral breast cancer
+CL:0002356,primitive reticulocyte,CL:0002417,primitive erythroid lineage cell
+UBERON:0014614,cervical spinal cord white matter,UBERON:0002318,white matter of spinal cord
+UBERON:2000870,epaxial region somite 26,UBERON:0003900,epaxial myotome region
+CL:0000783,multinucleated phagocyte,CL:0000518,phagocyte (sensu Vertebrata)
+DOID:4071,duodenogastric reflux,DOID:76,stomach disease
+UBERON:2000746,epaxial region somite 28,UBERON:0003900,epaxial myotome region
+UBERON:2202026,pectoral fin proximal radial cartilage 1,UBERON:2102026,pectoral fin proximal radial element 1
+UBERON:0010423,primary lymphoid nodule of tonsil,UBERON:0010422,primary nodular lymphoid tissue
+HP:0008198,Congenital hypoparathyroidism,HP:0000829,Hypoparathyroidism
+UBERON:2001416,pelvic fin distal radial bone 3,UBERON:1500008,pelvic fin distal radial bone
+UBERON:0003044,uncinate fasciculus,UBERON:0005838,fasciculus of brain
+HP:0000979,Purpura,HP:0001933,Subcutaneous hemorrhage
+HP:0100614,Myositis,HP:0011805,Abnormality of muscle morphology
+UBERON:0012284,animal hemisphere,UBERON:0012286,hemisphere of embryo
+CL:0000345,dental papilla cell,CL:0000134,mesenchymal cell
+UBERON:0012114,cud,UBERON:0012113,bolus of food
+HP:0009596,Aplasia of the proximal phalanx of the 2nd finger,HP:0010242,Aplasia of the proximal phalanges of the hand
+HP:0100936,Sclerosis of the middle phalanx of the 3rd toe,HP:0100927,Sclerosis of the phalanges of the 3rd toe
+UBERON:0011085,palatoquadrate arch,UBERON:0004121,ectoderm-derived structure
+UBERON:0007990,proximal sesamoid bone of pes,UBERON:0004248,pedal digit bone
+UBERON:3000948,articular process,UBERON:4100000,skeletal element projection
+UBERON:4200016,postbranchial lamina,UBERON:4100000,skeletal element projection
+DOID:2156,ovarian germ cell cancer,DOID:2394,ovarian cancer
+UBERON:0003040,central gray substance of midbrain,UBERON:0007414,nucleus of midbrain tegmentum
+HP:0010784,Uterine neoplasm,HP:0000130,Abnormality of the uterus
+UBERON:0000396,vallate papilla,UBERON:0014389,gustatory papilla of tongue
+HP:0010215,Contractures of the metatarsophalangeal joint of the hallux,HP:0010212,Flexion contracture of the hallux
+DOID:14753,isovaleric acidemia,DOID:0060159,organic acidemia
+HP:0012402,Increased urine alpha-ketoglutarate concentration,HP:0012401,Abnormal urine alpha-ketoglutarate concentration
+CL:1001225,kidney collecting duct cell,CL:1000497,kidney cell
+NCBITaxon:11079,Murray Valley encephalitis virus,NCBITaxon:11071,Japanese encephalitis virus group
+HP:0005597,Congenital alopecia totalis,HP:0007418,Alopecia totalis
+UBERON:0000114,lung connective tissue,UBERON:0003837,thoracic segment connective tissue
+HP:0006176,Two carpal ossification centers present at birth,HP:0006257,Abnormality of carpal bone ossification
+HP:0200119,Acute hepatitis,HP:0012115,Hepatitis
+UBERON:0011937,vibrissa root sheath,UBERON:0005933,hair root sheath
+HP:0009042,Marked muscular hypertrophy,HP:0003712,Muscle hypertrophy
+HP:0003131,Cystinuria,HP:0010918,Abnormality of cysteine metabolism
+UBERON:0004937,submucosa of pylorus,UBERON:0001200,submucosa of stomach
+DOID:7716,mixed ductal-endocrine carcinoma,DOID:3498,pancreatic ductal adenocarcinoma
+CL:0000554,gastrin stimulating hormone secreting cell,CL:0000167,peptide hormone secreting cell
+HP:0005332,Recurrent mandibular subluxations,HP:0000277,Abnormality of the mandible
+HP:0100409,Complete duplication of the distal phalanx of the 5th toe,HP:0100400,Duplication of the distal phalanx of the 5th toe
+CL:0000011,migratory trunk neural crest cell,CL:0000333,migratory neural crest cell
+DOID:7558,glossopharyngeal motor neuropathy,DOID:683,motor neuritis
+DOID:9428,intracranial hypertension,DOID:936,brain disease
+DOID:14152,spinal cord sarcoma,DOID:5612,spinal cancer
+UBERON:0009066,posterior thoracic air sac,UBERON:0015212,lateral structure
+CL:1000452,parietal epithelial cell,CL:1000450,epithelial cell of glomerular capsule
+DOID:0050013,carbohydrate metabolism disease,DOID:0060158,acquired metabolic disease
+HP:0002050,"Macroorchidism, postpubertal",HP:0000053,Macroorchidism
+UBERON:0004482,musculature of lower limb,UBERON:0007270,pelvic appendage musculature
+HP:0001765,Hammertoe,HP:0001780,Abnormality of toe
+UBERON:0004322,middle phalanx of manual digit 4,UBERON:0003864,middle phalanx of manus
+DOID:2797,idiopathic interstitial pneumonia,DOID:552,pneumonia
+UBERON:2005223,lateral larval melanophore stripe,UBERON:2005220,larval melanophore stripe
+DOID:5132,leiomyoma cutis,DOID:2438,dermis tumor
+DOID:817,interstitial myocarditis,DOID:819,mediastinitis
+HP:0003890,Prominent deltoid tuberosities,HP:0003889,Abnormality of the deltoid tuberosities
+HP:0010413,Aplasia/Hypoplasia of the distal phalanx of the 2nd toe,HP:0010347,Aplasia/Hypoplasia of the phalanges of the 2nd toe
+HP:0009342,Pseudoepiphysis of the distal phalanx of the 3rd finger,HP:0009332,Abnormality of the epiphysis of the distal phalanx of the 3rd finger
+UBERON:3010684,proximal-most prehallical element,UBERON:4200141,prehallical element
+UBERON:0014775,prosomere,UBERON:0004731,neuromere
+HP:0004792,Rectoperineal fistula,HP:0004871,Perineal fistula
+UBERON:0014916,velar vocal fold,UBERON:0004121,ectoderm-derived structure
+UBERON:0001070,external carotid artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0001443,chest,UBERON:0009569,subdivision of trunk
+DOID:916,liver neoplasm,DOID:3117,hepatobiliary benign neoplasm
+UBERON:2002224,pleuroperitoneal cavity,UBERON:0000464,anatomical space
+DOID:12580,Cri-Du-Chat syndrome,DOID:0080014,chromosomal disease
+DOID:11230,acute orbital inflammation,DOID:930,orbital disease
+HP:0006099,Metacarpophalangeal joint hyperextensibility,HP:0011911,Abnormality of metacarpophalangeal joint
+DOID:5724,seminal vesicle cystadenoma,DOID:3855,seminal vesicle tumor
+HP:0009519,Ivory epiphysis of the middle phalanx of the 2nd finger,HP:0009494,Ivory epiphyses of the 2nd finger
+HP:0009943,Complete duplication of the phalanges of the thumb,HP:0009998,Complete duplication of phalanx of hand
+DOID:9621,non-congenital cyst of kidney,DOID:2975,cystic kidney
+HP:0004275,Duplication of hand bones,HP:0009142,Duplication of bones involving the upper extremities
+DOID:12377,spinal muscular atrophy,DOID:231,motor neuron disease
+UBERON:0009620,tail bud paraxial mesoderm,UBERON:0007524,dense mesenchyme tissue
+UBERON:0000485,simple columnar epithelium,UBERON:0000490,unilaminar epithelium
+HP:0006801,Hyperactive deep tendon reflexes,HP:0001347,Hyperreflexia
+HP:0008058,Aplasia/Hypoplasia of the optic nerve,HP:0008057,Aplasia/Hypoplasia affecting the fundus
+UBERON:0006227,ethmoid bone primordium,UBERON:0001048,primordium
+UBERON:0004848,respiratory system arterial endothelium,UBERON:0004702,respiratory system blood vessel endothelium
+HP:0009007,Hypoplastic biceps,HP:0009016,Upper limb muscle hypoplasia
+UBERON:0001804,capsule of lens,UBERON:0004121,ectoderm-derived structure
+DOID:4970,prosopagnosia,DOID:4090,agnosia
+CL:0000409,scolopidial sheath cell,CL:0000618,sheath cell
+HP:0006943,Diffuse spongiform leukoencephalopathy,HP:0002352,Leukoencephalopathy
+UBERON:0004145,outflow tract,UBERON:0004120,mesoderm-derived structure
+UBERON:0005103,mesonephric epithelium,UBERON:0004819,kidney epithelium
+UBERON:0003307,floor plate of midbrain,UBERON:0003306,floor plate of neural tube
+UBERON:2001999,posterior cleithral process,UBERON:0004120,mesoderm-derived structure
+UBERON:0010532,primitive nephron,UBERON:0001285,nephron
+HP:0010740,Osteopathia striata,HP:0010766,Ectopic calcification
+HP:0005218,Anoperineal fistula,HP:0004871,Perineal fistula
+CL:0002523,mesonephric glomerular visceral epithelial cell,CL:0000653,glomerular visceral epithelial cell
+UBERON:0004353,female inguinal canal,UBERON:0014404,female anatomical structure
+UBERON:2001858,suprapharyngobranchial,UBERON:2000527,pharyngobranchial bone
+UBERON:2001892,interhyal element,UBERON:0010363,endochondral element
+CL:0000889,myeloid suppressor cell,CL:0000766,myeloid leukocyte
+HP:0011497,Iris neovascularization,HP:0007905,Abnormal iris vasculature
+UBERON:0003950,inner ear canal,UBERON:0000464,anatomical space
+CL:0002173,extraglomerular mesangial cell,CL:1000500,kidney interstitial cell
+UBERON:4200023,anterior dorsal fin,UBERON:0003097,dorsal fin
+UBERON:0010075,sacral neural crest,UBERON:0005291,embryonic tissue
+DOID:4986,nonparalytic poliomyelitis,DOID:4953,poliomyelitis
+HP:0009226,Short proximal phalanx of the 5th finger,HP:0010241,Short proximal phalanx of finger
+HP:0003941,Stippled calcification of the elbow,HP:0009811,Abnormality of the elbow
+HP:0000759,Abnormality of the peripheral nervous system,HP:0012639,Abnormality of nervous system morphology
+CL:1001608,foreskin fibroblast,CL:0002620,skin fibroblast
+DOID:11721,glycogen storage disease VII,DOID:2747,glycogen storage disease
+UBERON:2200271,radial cartilage,UBERON:2100271,radial element
+HP:0008186,Adrenocortical cytomegaly,HP:0011732,Abnormality of adrenal morphology
+UBERON:0006307,urogenital membrane,UBERON:0002050,embryonic structure
+UBERON:0005849,cervical spinal cord lateral column,UBERON:0014614,cervical spinal cord white matter
+UBERON:0010848,radius-ulna cartilage element,UBERON:0005863,cartilaginous condensation
+HP:0100431,Broad distal phalanx of the 3rd toe,HP:0010360,Broad phalanges of the 3rd toe
+UBERON:2000089,actinotrichium,UBERON:0004121,ectoderm-derived structure
+DOID:0060175,succinic semialdehyde dehydrogenase deficiency,DOID:0060176,gamma-amino butyric acid metabolism disorder
+HP:0009306,Triangular shaped distal phalanx of the 4th finger,HP:0009875,Triangular shaped distal phalanges of the hand
+UBERON:2000278,secondary gustatory nucleus medulla oblongata,UBERON:0007635,nucleus of medulla oblongata
+UBERON:0005042,inner epithelial layer of tympanic membrane,UBERON:0005911,endo-epithelium
+HP:0100375,Aplasia/Hypoplasia of the proximal phalanx of the 3rd toe,HP:0010359,Aplasia/Hypoplasia of the phalanges of the 3rd toe
+UBERON:0010224,right pupil,UBERON:0001771,pupil
+HP:0004768,Sparse anterior scalp hair,HP:0000599,Abnormality of the frontal hairline
+HP:0007115,Orbital encephalocele,HP:0002084,Encephalocele
+UBERON:0005214,inner renal medulla interstitium,UBERON:0005211,renal medulla interstitium
+DOID:7685,pancreatic non-invasive intraductal papillary-mucinous carcinoma,DOID:7574,pancreatic intraductal papillary-colloid carcinoma
+UBERON:0012438,blastema of regenerating fin/limb,UBERON:0005306,blastema
+HP:0012666,Severely reduced ejection fraction,HP:0012664,Reduced ejection fraction
+HP:0200084,Giant cell hepatitis,HP:0012115,Hepatitis
+HP:0007372,Atrophy/Degeneration involving the corticospinal tracts,HP:0002492,Abnormality of the corticospinal tract
+CL:0002420,immature T cell,CL:0000084,T cell
+DOID:5292,mediastinum leiomyosarcoma,DOID:4050,mediastinum sarcoma
+HP:0100757,Pancreatoblastoma,HP:0002894,Neoplasm of the pancreas
+HP:0011907,Reduced alpha/beta synthesis ratio,HP:0005560,Imbalanced hemoglobin synthesis
+UBERON:0003099,cranial neural crest,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001806,sympathetic ganglion,UBERON:0001805,autonomic ganglion
+DOID:3809,epidural spinal canal meningioma,DOID:1140,spinal canal and spinal cord meningioma
+UBERON:0005605,hepatic duct intrahepatic part,UBERON:0007501,arborizing epithelial duct system
+HP:0012544,Elevated aldolase level,HP:0012400,Abnormal aldolase level
+HP:0007873,Abnormally prominent line of Schwalbe,HP:0008048,Abnormality of the line of Schwalbe
+UBERON:0012308,superficial lateral cervical lymph node,UBERON:0004870,superficial cervical lymph node
+UBERON:0005968,infundibulum of hair follicle,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:0050787,juvenile polyposis syndrome,DOID:0050736,autosomal dominant disease
+UBERON:2000523,inferior reticular formation,UBERON:0002579,regional part of medullary reticular formation
+DOID:10314,endocarditis,DOID:0050825,endocardium disease
+UBERON:0011220,mastoid process of temporal bone,UBERON:0000075,subdivision of skeletal system
+UBERON:0005117,metanephric distal convoluted tubule,UBERON:0001292,distal convoluted tubule
+UBERON:0004798,respiratory system basal lamina,UBERON:0000482,basal lamina of epithelium
+DOID:11506,suppurative otitis media,DOID:10754,otitis media
+UBERON:0011615,basihyal cartilage,UBERON:0011004,pharyngeal arch cartilage
+UBERON:0013773,right nipple,UBERON:0002030,nipple
+HP:0005997,Restricted neck movement due to contractures,HP:0005986,Limitation of neck motion
+HP:0010192,Triangular shaped distal phalanges of the toes,HP:0010182,Abnormality of the distal phalanges of the toes
+UBERON:0004128,optic vesicle,UBERON:0000479,tissue
+HP:0011538,Atrial situs inversus,HP:0011535,Abnormal atrial arrangement
+UBERON:2001636,pharyngobranchial 4 bone,UBERON:2001913,pharyngobranchial 4 element
+HP:0002435,Meningocele,HP:0007319,Morphological abnormality of the central nervous system
+UBERON:0000368,adductor brevis,UBERON:0004252,hindlimb stylopod muscle
+HP:0009970,Partial duplication of the proximal phalanx of the 3rd finger,HP:0010003,Partial duplication of the proximal phalanges of the hand
+CL:1000330,serous cell of epithelium of trachea,CL:0000313,serous secreting cell
+UBERON:3000777,epicoracoid horn,UBERON:0000064,organ part
+DOID:4554,type C thymoma,DOID:3275,thymoma
+DOID:3649,pyruvate decarboxylase deficiency,DOID:2978,carbohydrate metabolic disorder
+UBERON:0000115,lung epithelium,UBERON:0004815,lower respiratory tract epithelium
+HP:0009675,Absent epiphysis of the distal phalanx of the thumb,HP:0009686,Absent epiphyses of the thumb
+UBERON:0010866,dactylopatagium major,UBERON:0010862,dactylopatagium
+DOID:11267,keratomalacia,DOID:1237,corneal degeneration
+HP:0010911,Hyperleucinemia,HP:0004357,Abnormality of leucine metabolism
+UBERON:0003972,placenta junctional zone,UBERON:0005156,reproductive structure
+UBERON:2005055,median palatocerebral vein,UBERON:0003496,head blood vessel
+DOID:11661,blue color blindness,DOID:13399,color blindness
+DOID:0050935,cervical neuroblastoma,DOID:371,extracranial neuroblastoma
+UBERON:2000775,hypaxial region somite 30,UBERON:0003895,hypaxial myotome region
+UBERON:0006835,arthropod oviduct,UBERON:0012275,meso-epithelium
+UBERON:0009572,lumen of central canal of spinal cord,UBERON:0000464,anatomical space
+UBERON:0001054,Malpighian tubule,UBERON:0009773,renal tubule
+HP:0005305,Cerebral venous thrombosis,HP:0004936,Venous thrombosis
+UBERON:0001605,ciliary muscle,UBERON:0011222,intra-ocular muscle
+UBERON:0002028,hindbrain,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:7363,vulvar keratinizing squamous cell carcinoma,DOID:2101,vulva squamous cell carcinoma
+HP:0006507,Aplasia/Hypoplasia of the humerus,HP:0003063,Abnormality of the humerus
+UBERON:0007679,intersomitic vein,UBERON:0014907,intersomitic vessel
+UBERON:2005303,caudal fin lymph vessel,UBERON:0007384,appendage lymph vessel
+UBERON:0010585,pedal digit phalanx pre-cartilage condensation,UBERON:0015030,pedal digit phalanx endochondral element
+UBERON:0003667,lower jaw molar,UBERON:0003655,molar tooth
+DOID:7596,asbestos-related lung carcinoma,DOID:3905,lung carcinoma
+HP:0010518,Thyroglossal cyst,HP:0011772,Abnormality of thyroid morphology
+DOID:2065,syringoma,DOID:2664,sweat gland neoplasm
+UBERON:0004552,digital artery,UBERON:0001637,artery
+UBERON:2001297,vagal placode 1,UBERON:0003078,epibranchial placode
+UBERON:0001612,facial artery,UBERON:0004573,systemic artery
+CL:1001318,renal interstitial pericyte,CL:0000669,pericyte cell
+NCBITaxon:126331,mitosporic Magnaporthaceae,NCBITaxon:81093,Magnaporthaceae
+HP:0011697,Supraventricular tachycardia with a manifest accessory pathway on the right free wall,HP:0011694,Supraventricular tachycardia with a manifest accessory pathway
+UBERON:3000493,processus internus of pseudoangular,UBERON:0010313,neural crest-derived structure
+DOID:0060192,Crohn's colitis,DOID:8778,Crohn's disease
+UBERON:0002284,hyponychium,UBERON:0010371,ecto-epithelium
+HP:0011324,Multiple suture craniosynostosis,HP:0001363,Craniosynostosis
+HP:0010140,Cone-shaped epiphysis of the distal phalanx of the hallux,HP:0010124,Abnormality of the epiphysis of the distal phalanx of the hallux
+DOID:4062,testis sarcoma,DOID:2998,testicular cancer
+UBERON:0010378,mesenchyme from splanchnopleure,UBERON:0005291,embryonic tissue
+UBERON:0010559,pedal digit 3 metatarsal cartilage element,UBERON:0010682,pedal digit 3 phalanx cartilage element
+DOID:709,splenic manifestation of hairy cell leukemia,DOID:285,hairy cell leukemia
+CL:0002382,multinucleate conidium,CL:0000599,conidium
+HP:0008707,Absent scrotum,HP:0000045,Abnormality of the scrotum
+CL:1000217,growth plate cartilage chondrocyte,CL:0000138,chondrocyte
+HP:0009522,Stippling of the epiphysis of the middle phalanx of the 2nd finger,HP:0009497,Stippling of the epiphyses of the 2nd finger
+UBERON:2000072,somite 1,UBERON:0002329,somite
+HP:0012555,Absent nail of hallux,HP:0001802,Absent toenail
+UBERON:0003960,styloid process of temporal bone,UBERON:4100000,skeletal element projection
+UBERON:0011803,"feather bud, dermal component",UBERON:0004121,ectoderm-derived structure
+UBERON:0002835,thoracic dorsal root ganglion,UBERON:0000044,dorsal root ganglion
+UBERON:0011192,superior ophthalmic vein,UBERON:0011191,ophthalmic vein
+UBERON:4100010,post-glenoid process,UBERON:0004530,bony projection
+UBERON:0003368,epithelium of hard palate,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0006794,Loss of ability to walk in first decade,HP:0002505,Progressive inability to walk
+HP:0002832,Calcific stippling,HP:0010766,Ectopic calcification
+UBERON:0008856,stomach muscularis externa,UBERON:0009034,stomach region
+UBERON:0001837,duct of salivary gland,UBERON:0004121,ectoderm-derived structure
+HP:0002508,Brainstem dysplasia,HP:0002363,Abnormality of the brainstem
+UBERON:0005428,vagal neural crest,UBERON:0004121,ectoderm-derived structure
+UBERON:4200178,proximal mesomere,UBERON:4200160,mesomere (fin)
+UBERON:0011745,pulmonary valve leaflets,UBERON:0011741,cardiac valve leaflet
+HP:0009473,Joint contracture of the hand,HP:0009810,Abnormality of the joints of the upper limbs
+HP:0009203,Absent epiphysis of the middle phalanx of the 5th finger,HP:0010257,Absent epiphyses of the middle phalanges of the hand
+UBERON:0007329,pancreatic duct,UBERON:0003928,digestive system duct
+UBERON:0006214,carpus pre-cartilage condensation,UBERON:0015049,carpus endochondral element
+HP:0007549,Desquamation of skin soon after birth,HP:0011354,Generalized abnormality of skin
+UBERON:2005374,dorsal fin distal radial bone 3,UBERON:2000936,dorsal fin distal radial bone
+UBERON:2005050,palatocerebral artery,UBERON:0001637,artery
+UBERON:0003847,thyroid artery,UBERON:0001637,artery
+DOID:13336,congenital toxoplasmosis,DOID:9965,toxoplasmosis
+HP:0008754,Laryngeal calcifications,HP:0010766,Ectopic calcification
+UBERON:2001504,occipital arch cartilage,UBERON:0003932,cartilage element of chondrocranium
+HP:0010270,Cone-shaped epiphyses of the proximal phalanges of the hand,HP:0010245,Abnormality of the epiphyses of the proximal phalanges of the hand
+NCBITaxon:7162,Ochlerotatus triseriatus,NCBITaxon:119225,Protomacleaya
+UBERON:3000332,oculomotor foramen,UBERON:3000051,braincase and otic capsule opening
+HP:0009821,Forearm undergrowth,HP:0009824,Upper limb undergrowth
+HP:0009659,Partial absence of thumb,HP:0009658,Aplasia/Hypoplasia of the phalanges of the thumb
+UBERON:0003662,forelimb muscle,UBERON:0003661,limb muscle
+HP:0005224,Rectal abscess,HP:0002034,Abnormality of the rectum
+HP:0100888,Interdigital loops,HP:0007477,Abnormal dermatoglyphics
+UBERON:0002398,manus,UBERON:0008785,upper limb segment
+CL:0002586,retinal pigment epithelial cell,CL:0009004,retinal cell
+HP:0009302,Bullet-shaped distal phalanx of the 4th finger,HP:0009405,Bullet-shaped phalanges of the 4th finger
+HP:0002314,Degeneration of the lateral corticospinal tracts,HP:0007372,Atrophy/Degeneration involving the corticospinal tracts
+UBERON:0000014,zone of skin,UBERON:0000064,organ part
+UBERON:0001427,scaphoid,UBERON:0001480,proximal carpal bone
+DOID:3816,glossopharyngeal nerve paralysis,DOID:3817,cranial nerve palsy
+CL:0008005,obliquely striated somatic muscle cell,CL:0000228,multinucleate cell
+DOID:10755,petrositis,DOID:1019,osteomyelitis
+UBERON:3010685,distal-most prehallical element,UBERON:4200141,prehallical element
+UBERON:0001184,renal artery,UBERON:0012254,abdominal aorta artery
+UBERON:0011901,hair matrix,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2005272,immature gonad,UBERON:0005156,reproductive structure
+DOID:0050918,vaginal carcinoma,DOID:119,vaginal cancer
+CL:0000438,luteinizing hormone secreting cell,CL:0000163,endocrine cell
+UBERON:0004778,larynx submucosa,UBERON:0004777,respiratory system submucosa
+CL:0000354,blastemal cell,CL:0000048,multi fate stem cell
+DOID:10187,esophageal lipoma,DOID:0050624,gastrointestinal system benign neoplasm
+UBERON:0005826,gracile fasciculus of spinal cord,UBERON:0005837,fasciculus of spinal cord
+UBERON:0000934,ventral nerve cord,UBERON:0005053,nerve cord
+HP:0002527,Falls,HP:0001288,Gait disturbance
+UBERON:0011686,spiracularis muscle,UBERON:0011648,jaw muscle
+HP:0011534,Abnormal spatial orientation of the cardiac segments,HP:0002564,Malformation of the heart and great vessels
+HP:0011522,Protanopia,HP:0000642,Red-green dyschromatopsia
+HP:0011256,Crus of helix connected to antihelix,HP:0009895,Abnormality of the crus of the helix
+UBERON:0003241,epithelium of utricle,UBERON:0006932,vestibular epithelium
+UBERON:0010161,lumen of blood vessel,UBERON:0000464,anatomical space
+HP:0100718,Uterine rupture,HP:0000130,Abnormality of the uterus
+UBERON:0004674,facial nerve root,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:8012,benign pericardial teratoma,DOID:0060091,cardiovascular organ benign neoplasm
+UBERON:0013635,sphincter colli muscle,UBERON:0002377,muscle of neck
+DOID:14253,retinal dystrophy in systemic or cerebroretinal lipidoses,DOID:8501,fundus dystrophy
+UBERON:0011800,dermal pulp of feather shaft,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004345,trophectoderm,UBERON:0000490,unilaminar epithelium
+DOID:8119,anal canal Paget's disease,DOID:3692,anal canal adenocarcinoma
+UBERON:0012448,corpuscles of herbst,UBERON:0012449,mechanoreceptor
+UBERON:0009847,prostate field,UBERON:0004902,urogenital sinus epithelium
+UBERON:0005749,glomerular tuft,UBERON:0004120,mesoderm-derived structure
+HP:0004382,Mitral valve calcification,HP:0005146,Cardiac valve calcification
+HP:0001724,Aortic dilatation,HP:0001679,Abnormality of the aorta
+DOID:3743,cervical verrucous carcinoma,DOID:3744,cervical squamous cell carcinoma
+UBERON:0011955,left hepatic vein,UBERON:0001143,hepatic vein
+HP:0100691,Abnormality of the curvature of the cornea,HP:0000481,Abnormality of the cornea
+DOID:6294,corpus callosum lipoma,DOID:6291,cerebral hemisphere lipoma
+DOID:7725,epilepsy with generalized tonic-clonic seizures,DOID:0050705,adolescence-adult electroclinical syndrome
+UBERON:0009056,two-pass circulatory system,UBERON:0009055,closed circulatory system
+HP:0003977,Deformed radius,HP:0002818,Abnormality of the radius
+UBERON:0010757,rib 8,UBERON:0002228,rib
+UBERON:0015013,fibula endochondral element,UBERON:0015022,hindlimb endochondral element
+UBERON:0005147,metanephric renal vesicle,UBERON:0005134,metanephric nephron epithelium
+DOID:419,scleroderma,DOID:854,collagen disease
+UBERON:4300021,anterolateral plate,UBERON:0008907,dermal bone
+HP:0008464,Absent spinous processes of lower thoracic and lumbar vertebrae,HP:0008516,Abnormality of the vertebral spinous processes
+DOID:0050735,X-linked disease,DOID:0050177,monogenic disease
+UBERON:0006029,interdigital region between manual digits 2 and 3,UBERON:0006013,interdigital region between manual digits
+UBERON:2001140,dorsal tooth row,UBERON:0009678,tooth row
+HP:0100370,Aplasia/Hypoplasia of the distal phalanx of the 4th toe,HP:0010337,Aplasia/Hypoplasia of the 4th toe
+HP:0000451,Triangular nasal tip,HP:0000436,Abnormality of the nasal tip
+UBERON:0003283,mesentery of oesophagus,UBERON:0002095,mesentery
+UBERON:0007126,pharyngeal pouch 5,UBERON:0004117,pharyngeal pouch
+UBERON:4200171,process 4,UBERON:4100000,skeletal element projection
+HP:0009737,Lisch nodules,HP:0010568,Hamartoma of the eye
+UBERON:0004393,epiphysis of third metacarpal bone,UBERON:0004390,epiphysis of metacarpal bone
+UBERON:2201588,pectoral fin distal radial cartilage,UBERON:2101588,pectoral fin distal radial element
+UBERON:4300106,ventral limb of posttemporal,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:4000088,mineralized cartilage tissue,UBERON:0002418,cartilage tissue
+DOID:13725,beriberi,DOID:5113,nutritional deficiency disease
+UBERON:0012420,coprodeum,UBERON:0000064,organ part
+UBERON:0006723,cochlear modiolus,UBERON:0004120,mesoderm-derived structure
+HP:0011445,Athetoid cerebral palsy,HP:0100021,Cerebral palsy
+UBERON:3000295,median symphysis,UBERON:0000064,organ part
+CL:0002211,type I muscle cell,CL:0000189,slow muscle cell
+UBERON:0002402,pleural cavity,UBERON:0002323,coelemic cavity lumen
+HP:0009242,Osteolytic defects of the distal phalanx of the 5th finger,HP:0004225,Abnormality of the distal phalanx of the 5th finger
+UBERON:2000854,somite 21,UBERON:0002329,somite
+UBERON:0010945,jugulohyoideus muscle,UBERON:0002377,muscle of neck
+UBERON:0002073,hair follicle,UBERON:0004121,ectoderm-derived structure
+DOID:401,multidrug-resistant tuberculosis,DOID:399,tuberculosis
+UBERON:3000798,presacral shield,UBERON:0004120,mesoderm-derived structure
+DOID:14150,spinal cord lymphoma,DOID:5612,spinal cancer
+UBERON:0006255,ischial pre-cartilage condensation,UBERON:0015056,ischial endochondral element
+UBERON:0006301,telencephalic part of interventricular foramen,UBERON:0004121,ectoderm-derived structure
+UBERON:0003835,abdominal segment blood vessel,UBERON:0003513,trunk blood vessel
+UBERON:0004054,internal male genitalia,UBERON:0004175,internal genitalia
+CL:0010011,cerebral cortex GABAergic interneuron,CL:0010012,cerebral cortex neuron
+DOID:3481,septicemic plague,DOID:3482,plague
+HP:0011528,Single isolated congenital hypertrophy of retinal pigment epithelium,HP:0007649,Congenital hypertrophy of retinal pigment epithelium
+UBERON:0002048,lung,UBERON:0000171,respiration organ
+HP:0004276,Exostoses of hand bones,HP:0100777,Exostoses
+UBERON:3010538,pars nervosa,UBERON:0004120,mesoderm-derived structure
+UBERON:0015090,distal carpal bone 3 endochondral element,UBERON:0015049,carpus endochondral element
+HP:0005979,Metabolic ketoacidosis,HP:0001942,Metabolic acidosis
+HP:0006228,Valgus hand deformity,HP:0005922,Abnormal hand morphology
+UBERON:0001431,distal carpal bone 2,UBERON:0015087,distal carpal bone 2 endochondral element
+UBERON:2005032,optic vein,UBERON:0009141,craniocervical region vein
+UBERON:0004650,tongue keratinized epithelium,UBERON:0006919,tongue squamous epithelium
+UBERON:3000785,trochlear groove of humerus,UBERON:0000064,organ part
+UBERON:0006647,adventitia of ductus deferens,UBERON:0014403,male anatomical structure
+HP:0003332,Absent primary metaphyseal spongiosa,HP:0005089,Abnormal metaphyseal trabeculation
+UBERON:0001258,neck of urinary bladder,UBERON:0004120,mesoderm-derived structure
+HP:0100678,Premature skin wrinkling,HP:0007495,Prematurely aged appearance
+UBERON:0002113,kidney,UBERON:0015212,lateral structure
+DOID:10188,skin lipoma,DOID:3165,skin benign neoplasm
+HP:0009640,Symphalangism of the proximal phalanx of the thumb with the 1st metatcarpal,HP:0009703,Synostosis involving the 1st metacarpal
+UBERON:0011785,ramus of feather barb,UBERON:0013703,integumentary projection
+HP:0007081,Late-onset muscular dystrophy,HP:0003560,Muscular dystrophy
+HP:0010604,Cyst of the eyelid,HP:0010732,Nodular changes affecting the eyelids
+HP:0000556,Retinal dystrophy,HP:0000479,Abnormality of the retina
+UBERON:4200029,adductor crest,UBERON:0004530,bony projection
+UBERON:0005705,primary palate mesenchyme,UBERON:0010258,mesenchyme from rhombencephalic neural crest
+UBERON:0004339,vault of skull,UBERON:0004120,mesoderm-derived structure
+HP:0000646,Amblyopia,HP:0000505,Visual impairment
+DOID:1825,childhood absence epilepsy,DOID:0050704,childhood electroclinical syndrome
+UBERON:0000218,vertebral arch of axis,UBERON:0003861,neural arch
+DOID:2217,Bernard-Soulier syndrome,DOID:2218,blood platelet disease
+DOID:0050815,adnexa disease,DOID:1492,eye and adnexa disease
+HP:0002896,Neoplasm of the liver,HP:0007378,Neoplasm of the gastrointestinal tract
+DOID:12679,nephrocalcinosis,DOID:557,kidney disease
+UBERON:0009193,sphenoid cartilage element,UBERON:0009891,facial mesenchyme
+HP:0012298,Long middle  phalanx of finger,HP:0009833,Abnormality of the middle phalanges of the hand
+HP:0005580,Duplication of renal pelvis,HP:0010944,Abnormality of the renal pelvis
+UBERON:0003582,nasopharynx connective tissue,UBERON:0003570,respiratory system connective tissue
+UBERON:0002501,oval window,UBERON:0013685,foramen of skull
+DOID:14464,neuroleptic malignant syndrome,DOID:679,basal ganglia disease
+UBERON:0000981,femur,UBERON:0003608,hindlimb long bone
+HP:0006785,Limb-girdle muscular dystrophy,HP:0003797,Limb-girdle muscle atrophy
+HP:0011738,Corticotropin-releasing hormone receptor (CRHR) defect,HP:0011734,Central adrenal insufficiency
+HP:0009594,Retinal hamartoma,HP:0000479,Abnormality of the retina
+HP:0002905,Hyperphosphatemia,HP:0100529,Abnormality of phosphate homeostasis
+UBERON:0003493,trachea reticular lamina,UBERON:0003490,respiratory system reticular lamina
+HP:0008264,Neutrophil inclusion bodies,HP:0011992,Abnormality of neutrophil morphology
+DOID:5566,mature teratoma,DOID:3307,teratoma
+HP:0009663,Abnormality of the epiphysis of the proximal phalanx of the thumb,HP:0009599,Abnormality of the epiphyses of the thumb
+DOID:321,tropical spastic paraparesis,DOID:934,viral infectious disease
+HP:0002269,Abnormality of neuronal migration,HP:0007319,Morphological abnormality of the central nervous system
+HP:0012257,Absent inner dynein arms,HP:0200106,Absent/shortened dynein arms
+UBERON:0010259,1st arch mesenchyme from neural crest,UBERON:0010359,pharyngeal arch mesenchyme from neural crest
+HP:0002389,Cavum septum pellucidum,HP:0007375,Abnormality of the septum pellucidum
+HP:0003262,Smooth muscle antibody positivity,HP:0002960,Autoimmunity
+UBERON:0012447,podotheca,UBERON:0003102,surface structure
+HP:0000239,Large fontanelles,HP:0011328,Abnormality of fontanelles
+UBERON:0015151,Harderian gland duct,UBERON:0000058,duct
+UBERON:0008841,suspensory ligament,UBERON:0008845,nonskeletal ligament
+UBERON:0002230,head of rib,UBERON:0005055,zone of long bone
+UBERON:2000381,lateral line sensory nucleus,UBERON:0007635,nucleus of medulla oblongata
+CL:0001023,"Kit-positive, CD34-positive common myeloid progenitor",CL:0001059,"common myeloid progenitor, CD34-positive"
+HP:0005580,Duplication of renal pelvis,HP:0000075,Renal duplication
+HP:0009680,Irregular epiphysis of the distal phalanx of the thumb,HP:0010251,Irregular epiphyses of the distal phalanges of the hand
+UBERON:0001334,female urethra,UBERON:0000057,urethra
+UBERON:0003374,chorionic ectoderm,UBERON:0004121,ectoderm-derived structure
+CL:1000706,ureter urothelial cell,CL:0000731,urothelial cell
+UBERON:0014404,female anatomical structure,UBERON:0014402,sex-specific anatomical structure
+HP:0100451,Curved distal phalanx of the 5th toe,HP:0010386,Curved phalanges of the 5th toe
+DOID:0050534,congenital stationary night blindness,DOID:8499,night blindness
+HP:0009445,Symphalangism of the 3rd finger,HP:0009700,Synostosis involving bones of the fingers
+UBERON:0002731,vestibulocochlear nerve root,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010072,Patchy sclerosis of the 1st metatarsal,HP:0100945,Sclerosis of the 1st metatarsal
+DOID:12984,vagus nerve neoplasm,DOID:338,cranial nerve neoplasm
+UBERON:4200101,m.scapulotriceps,UBERON:0003662,forelimb muscle
+UBERON:0001912,lobule of lactiferous gland,UBERON:0000064,organ part
+UBERON:0002652,posterior median eminence,UBERON:0004120,mesoderm-derived structure
+CL:1000445,myoepithelial cell of dilator pupillae,CL:0000185,myoepithelial cell
+DOID:4923,thymus adenocarcinoma,DOID:3284,thymic carcinoma
+DOID:7949,stroma-dominant and stroma-poor composite ganglioneuroblastoma,DOID:5193,nodular ganglioneuroblastoma
+HP:0009288,Curved proximal phalanx of the 4th finger,HP:0009284,Abnormality of the proximal phalanx of the 4th finger
+NCBITaxon:506,Alcaligenaceae,NCBITaxon:80840,Burkholderiales
+UBERON:0005565,facio-acoustic neural crest,UBERON:0003099,cranial neural crest
+UBERON:0014460,supratemporal fenestra,UBERON:0014459,temporal fenestra
+HP:0007505,Progressive hyperpigmentation,HP:0000953,Hyperpigmentation of the skin
+DOID:12043,kernicterus due to isoimmunization,DOID:2383,neonatal jaundice
+DOID:724,female stress incontinence,DOID:365,bladder disease
+DOID:2889,retrocochlear disease,DOID:2742,auditory system disease
+UBERON:0002963,caudal pontine reticular nucleus,UBERON:0003528,brain grey matter
+DOID:12055,sarcoid meningitis,DOID:11335,sarcoidosis
+HP:0009854,Curved proximal phalanges of the hand,HP:0009770,Curved phalanges of the hand
+HP:0002188,Delayed CNS myelination,HP:0012448,Delayed myelination
+UBERON:0006478,Brodmann (1909) area 37,UBERON:0013529,Brodmann area
+UBERON:0001808,parasympathetic ganglion,UBERON:0010313,neural crest-derived structure
+UBERON:0004481,musculature of upper limb,UBERON:0007269,pectoral appendage musculature
+HP:0009583,Curved proximal phalanx of the 2nd finger,HP:0009549,Curved phalanges of the 2nd finger
+UBERON:0001261,lamina propria of urinary bladder,UBERON:0000030,lamina propria
+HP:0008714,Ureterovesical stenosis,HP:0000071,Ureteral stenosis
+UBERON:0011908,gastrocnemius lateralis,UBERON:0011906,muscle head
+HP:0000885,Broad ribs,HP:0000772,Abnormality of the ribs
+UBERON:0003396,mesentery of colon,UBERON:0003335,serosa of colon
+UBERON:3010560,anterior process of the palatoquadrate,UBERON:4100000,skeletal element projection
+DOID:14711,FG syndrome,DOID:0050735,X-linked disease
+NCBITaxon:11159,Paramyxovirinae,NCBITaxon:11158,Paramyxoviridae
+UBERON:0002309,medial longitudinal fasciculus,UBERON:0005838,fasciculus of brain
+DOID:1338,congenital dyserythropoietic anemia,DOID:589,congenital hemolytic anemia
+HP:0100528,Pleuropulmonary blastoma,HP:0100527,Neoplasia of the pleura
+HP:0004243,Abnormality of the scaphoid,HP:0001191,Abnormality of the carpal bones
+HP:0005026,mesomelic/rhizomelic limb shortening,HP:0008905,Rhizomelia
+UBERON:0012294,navicular fossa of spongiose part of urethra,UBERON:0014403,male anatomical structure
+UBERON:0012298,female urethral crest,UBERON:0014404,female anatomical structure
+UBERON:3000110,crista contacta,UBERON:4100000,skeletal element projection
+DOID:6084,pediatric ovarian germ cell tumor,DOID:2156,ovarian germ cell cancer
+UBERON:0009611,midbrain neural plate,UBERON:0003075,neural plate
+HP:0100742,Vascular neoplasm,HP:0011793,Neoplasm by anatomical site
+UBERON:0013208,Grueneberg ganglion,UBERON:0015245,septal olfactory organ
+HP:0010803,Everted upper lip vermilion,HP:0012472,Eclabion
+HP:0011780,Thyroid hemiagenesis,HP:0008188,Thyroid dysgenesis
+DOID:0050716,methylmalonic aciduria and homocystinuria type cblD,DOID:14749,methylmalonic acidemia
+UBERON:3000784,ulnar condyle,UBERON:0000064,organ part
+CL:0000871,splenic macrophage,CL:0000867,secondary lymphoid organ macrophage
+UBERON:0006266,nasolacrimal groove,UBERON:0004807,respiratory system epithelium
+UBERON:0011976,epiphysis of distal phalanx of pes,UBERON:0011973,epiphysis of phalanx of pes
+HP:0002913,Myoglobinuria,HP:0003110,Abnormality of urine homeostasis
+HP:0009829,Phocomelia,HP:0009815,Aplasia/Hypoplasia of the extremities
+DOID:11755,choledocholithiasis,DOID:4137,common bile duct disease
+HP:0009533,Stippling of the epiphysis of the proximal phalanx of the 2nd finger,HP:0009501,Abnormality of the epiphysis of the proximal phalanx of the 2nd finger
+HP:0100526,Neoplasm of the lungs,HP:0100606,Neoplasm of the respiratory system
+DOID:12842,Guillain-Barre syndrome,DOID:0060033,autoimmune disease of peripheral nervous system
+DOID:4463,multilocular clear cell renal cell carcinoma,DOID:4450,renal cell carcinoma
+HP:0009978,Complete duplication of the distal phalanx of the 4th finger,HP:0010001,Complete duplication of the distal phalanges of the hand
+NCBITaxon:111527,pseudomallei group,NCBITaxon:32008,Burkholderia
+HP:0006901,Impaired thermal sensitivity,HP:0004370,Abnormality of temperature regulation
+DOID:8251,adult pleomorphic rhabdomyosarcoma,DOID:3250,pleomorphic rhabdomyosarcoma
+UBERON:0009559,metacarpal/tarsal-phalangeal joint,UBERON:0011139,synovial limb joint
+HP:0008410,Subungual hyperkeratotic fragments,HP:0000962,Hyperkeratosis
+UBERON:0016447,hair of trunk,UBERON:0001037,strand of hair
+UBERON:0005204,larynx submucosa gland,UBERON:0004119,endoderm-derived structure
+DOID:12385,shigellosis,DOID:0050338,primary bacterial infectious disease
+HP:0100213,Absent epiphysis of the middle phalanx of the 5th toe,HP:0100077,Absent epiphyses of the 5th toe
+DOID:3457,invasive lobular carcinoma,DOID:0050938,breast lobular carcinoma
+UBERON:0001191,common iliac artery,UBERON:0005609,iliac artery
+DOID:0050474,Netherton syndrome,DOID:0050737,autosomal recessive disease
+HP:0010052,Abnormality of the proximal phalanx of the hallux,HP:0010183,Abnormality of the middle phalanges of the toes
+UBERON:0003623,manual digit 3,UBERON:0002389,manual digit
+CL:0000771,eosinophil,CL:0000094,granulocyte
+HP:0009416,Ivory epiphyses of the 3rd finger,HP:0100919,Sclerosis of the phalanges of the 3rd finger
+CL:0002359,placental hematopoietic stem cell,CL:0000349,extraembryonic cell
+UBERON:0009630,root of thoracic nerve,UBERON:0009623,spinal nerve root
+DOID:14037,aorta atresia,DOID:520,aortic disease
+DOID:8409,microinvasive cervical squamous cell carcinoma,DOID:3744,cervical squamous cell carcinoma
+UBERON:0007652,esophageal sphincter,UBERON:0004590,sphincter muscle
+UBERON:0011511,iliococcygeus muscle,UBERON:0003897,axial muscle
+CL:0002630,actinomycete-type spore,CL:0000520,prokaryotic cell
+HP:0008369,Abnormal tarsal ossification,HP:0010675,Abnormal foot bone ossification
+UBERON:0011210,migration pathway NC-derived mesenchyme,UBERON:0007530,migrating mesenchyme population
+UBERON:2002064,uroneural 1,UBERON:2000602,uroneural
+UBERON:0014388,kidney collecting duct epithelium,UBERON:0000484,simple cuboidal epithelium
+UBERON:3000823,sinus interglenoidalis,UBERON:0000464,anatomical space
+HP:0005606,Hyperpigmented nevi and streak,HP:0000995,Melanocytic nevus
+CL:0002538,intrahepatic bile duct epithelial cell,CL:0000069,branched duct epithelial cell
+DOID:14219,renal tubular acidosis,DOID:447,renal tubular transport disease
+UBERON:0001786,fovea centralis,UBERON:0004121,ectoderm-derived structure
+HP:0008402,Ridged fingernail,HP:0001231,Abnormality of the fingernails
+HP:0005152,Oncocytic cardiomyopathy,HP:0001638,Cardiomyopathy
+DOID:4248,coronary stenosis,DOID:3393,coronary artery disease
+UBERON:0004159,atrial septum intermedium,UBERON:0002085,interatrial septum
+DOID:1988,rectum lymphoma,DOID:1993,rectum cancer
+HP:0009243,Patchy sclerosis of the distal phalanx of the 5th finger,HP:0004225,Abnormality of the distal phalanx of the 5th finger
+UBERON:0007685,region of nephron tubule,UBERON:0001231,nephron tubule
+UBERON:0004984,mucosa of seminal vesicle,UBERON:0014403,male anatomical structure
+DOID:13812,adhesions of uterus,DOID:345,uterine disease
+UBERON:0003830,thoracic segment muscle,UBERON:0001774,muscle of trunk
+HP:0000735,Impaired social interactions,HP:0012433,Abnormal social behavior
+DOID:3687,MELAS syndrome,DOID:890,mitochondrial encephalomyopathy
+HP:0005363,Partial humoral immunodeficiency,HP:0002721,Immunodeficiency
+UBERON:3000562,septum semircularium posterior,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:6483,rete testis adenoma,DOID:5639,rete testis neoplasm
+HP:0003175,Hypoplastic ischia,HP:0003174,Abnormality of the ischium
+UBERON:3010799,ramulus suprabranchialis posterior,UBERON:3010126,middle lateral line nerve (MLLN)
+NCBITaxon:83141,Parasitengona,NCBITaxon:83138,Anystina
+HP:0012677,Iron accumulation in globus pallidus,HP:0012675,Iron accumulation in brain
+UBERON:0002642,cuneate fasciculus of medulla,UBERON:0005838,fasciculus of brain
+UBERON:0005753,caudal part of nephrogenic cord,UBERON:0005423,developing anatomical structure
+CL:0000173,pancreatic D cell,CL:0000083,epithelial cell of pancreas
+UBERON:0009494,pharyngeal arch mesenchymal region,UBERON:0007524,dense mesenchyme tissue
+UBERON:0006175,pronephric distal tubule,UBERON:0005310,pronephric nephron tubule
+UBERON:0004368,Reichert's cartilage,UBERON:0010313,neural crest-derived structure
+UBERON:0010710,pectoral fin skeleton,UBERON:0007272,pectoral appendage skeleton
+UBERON:0004697,Peyer's patch germinal center,UBERON:0010754,germinal center
+HP:0006600,Progressive calcification of costochondral cartilage,HP:0000919,Abnormality of the costochondral junction
+UBERON:0001292,distal convoluted tubule,UBERON:0012275,meso-epithelium
+UBERON:0011645,iliofemoralis muscle,UBERON:0001325,muscle of pelvis
+UBERON:0006580,mantle cavity,UBERON:0000464,anatomical space
+UBERON:2000874,epaxial region somite 7,UBERON:0003900,epaxial myotome region
+UBERON:0015172,endometrial blood vessel,UBERON:0014404,female anatomical structure
+HP:0012315,Histiocytoma,HP:0012316,Fibrous tissue neoplasm
+UBERON:0005085,ectodermal placode,UBERON:0001048,primordium
+CL:0002505,liver CD103-negative dendritic cell,CL:0002454,"Cd4-negative, CD8_alpha-negative, CD11b-positive dendritic cell"
+HP:0011550,Biventricular heart with straddling right sided atrioventricular valve and absent left sided atrioventricular connection,HP:0011547,Absent left sided atrioventricular connection
+CL:0002280,type N enteroendocrine cell,CL:0000167,peptide hormone secreting cell
+DOID:5632,optic nerve sheath meningioma,DOID:3419,optic nerve neoplasm
+HP:0010541,Cutis gyrata of scalp,HP:0001965,Abnormality of the scalp
+HP:0100163,Ivory epiphysis of the proximal phalanx of the 3rd toe,HP:0100061,Ivory epiphyses of the 3rd toe
+HP:0100095,Abnormality of the epiphysis of the middle phalanx of the 4th toe,HP:0010335,Abnormality of the epiphyses of the 4th toe
+UBERON:2001042,sclerotome somite 24,UBERON:0003089,sclerotome
+DOID:11212,hydrophthalmos,DOID:0050593,primary congenital glaucoma
+DOID:3378,conventional central osteosarcoma,DOID:3376,bone osteosarcoma
+UBERON:0001809,enteric ganglion,UBERON:0001808,parasympathetic ganglion
+HP:0001013,Eruptive xanthomas,HP:0000991,Xanthomatosis
+HP:0001341,Olfactory lobe agenesis,HP:0007319,Morphological abnormality of the central nervous system
+NCBITaxon:29105,Calomys,NCBITaxon:40141,Sigmodontinae
+DOID:1375,neonatal urinary tract infectious disease,DOID:18,urinary system disease
+DOID:0050130,osmotic diarrhea,DOID:13250,diarrhea
+HP:0003355,Aminoaciduria,HP:0004337,Abnormality of amino acid metabolism
+DOID:3132,porphyria cutanea tarda,DOID:2723,dermatitis
+DOID:11295,retinal microaneurysm,DOID:2462,retinal vascular disease
+HP:0009497,Stippling of the epiphyses of the 2nd finger,HP:0010237,Epiphyseal stippling of finger phalanges
+HP:0000065,Labial hypertrophy,HP:0000058,Abnormality of the labia
+UBERON:0004141,heart tube,UBERON:0005291,embryonic tissue
+UBERON:0005375,spinal cord ventral column,UBERON:0002318,white matter of spinal cord
+UBERON:2002022,dermethmoid,UBERON:0011164,neurocranium bone
+UBERON:0007425,decussation of diencephalon,UBERON:0003931,diencephalic white matter
+HP:0006362,Varus deformity of humeral neck,HP:0003887,Abnormality of the humeral heads
+CL:0002537,amnion mesenchymal stem cell,CL:0000134,mesenchymal cell
+UBERON:0002315,gray matter of spinal cord,UBERON:0002020,gray matter of neuraxis
+UBERON:0002046,thyroid gland,UBERON:0004119,endoderm-derived structure
+HP:0004419,Recurrent thrombophlebitis,HP:0004418,Thrombophlebitis
+UBERON:0012447,podotheca,UBERON:0004121,ectoderm-derived structure
+UBERON:2205378,dorsal fin distal radial cartilage 7,UBERON:2105378,dorsal fin distal radial element 7
+NCBITaxon:36051,mitosporic Chaetothyriales,NCBITaxon:34395,Chaetothyriales
+HP:0011996,Elevated factor V activity,HP:0010990,Abnormality of the common coagulation pathway
+HP:0009939,Mandibular aplasia,HP:0009118,Aplasia/Hypoplasia of the mandible
+UBERON:2002103,ceratobranchial series,UBERON:0000477,anatomical cluster
+DOID:5194,intermixed schwannian stroma-rich ganglioneuroblastoma,DOID:4163,ganglioneuroblastoma
+HP:0009216,Cone-shaped epiphysis of the middle phalanx of the 4th finger,HP:0009395,Cone-shaped epiphyses of the 4th finger
+HP:0008839,Hypoplastic pelvis,HP:0009103,Aplasia/Hypoplasia involving the pelvis
+UBERON:0012171,shell of nucleus accumbens,UBERON:0002791,regional part of telencephalon
+DOID:9602,necrotizing fasciitis,DOID:9598,fasciitis
+NCBITaxon:197913,Influenzavirus C,NCBITaxon:11308,Orthomyxoviridae
+UBERON:0007958,central carpal bone,UBERON:0012131,centrale
+CL:1000373,transitional myocyte of ventricular part of atrioventricular bundle,CL:1000481,transitional myocyte of atrioventricular bundle
+DOID:4423,sea-blue histiocyte syndrome,DOID:1927,sphingolipidosis
+HP:0009255,Irregular epiphysis of the distal phalanx of the 4th finger,HP:0009398,Irregular epiphyses of the 4th finger
+UBERON:0003016,postcommissural fornix,UBERON:0011591,tract of diencephalon
+HP:0004639,Elevated amniotic fluid alpha-fetoprotein,HP:0006254,Elevated alpha-fetoprotein
+HP:0001667,Right ventricular hypertrophy,HP:0001707,Abnormality of the right ventricle
+HP:0008555,Absent vestibular function,HP:0001756,Vestibular hypofunction
+DOID:2871,endometrial carcinoma,DOID:1380,endometrial cancer
+HP:0011236,Angulated antihelix,HP:0009738,Abnormality of the antihelix
+HP:0001541,Ascites,HP:0002012,Abnormality of the abdominal organs
+CL:1000280,smooth muscle cell of colon,CL:1000279,smooth muscle cell of large intestine
+DOID:0050544,hypermethioninemia,DOID:9252,amino acid metabolic disorder
+UBERON:2002071,distal cartilage of internal anterior process of basipterygium,UBERON:4100000,skeletal element projection
+UBERON:0003469,respiratory system artery,UBERON:0003643,respiratory system arterial blood vessel
+UBERON:0011106,cruciate ligament of atlas,UBERON:0004120,mesoderm-derived structure
+UBERON:0013188,monkey lips dorsal bursa complex,UBERON:0000481,multi-tissue structure
+CL:0000468,neuroglioblast,CL:0000047,neuronal stem cell
+DOID:12236,primary biliary cirrhosis,DOID:0060049,autoimmune disease of urogenital tract
+HP:0009453,Osteolytic defects of the proximal phalanx of the 3rd finger,HP:0009358,Abnormality of the proximal phalanx of the 3rd finger
+HP:0005819,Short middle phalanx of finger,HP:0009803,Short phalanx of finger
+UBERON:0010711,pelvic fin skeleton,UBERON:0007273,pelvic appendage skeleton
+UBERON:0011981,manual digit 6,UBERON:0002389,manual digit
+HP:0011302,Long palm,HP:0100871,Abnormality of the palm
+UBERON:0002475,saphenous nerve,UBERON:0003431,leg nerve
+HP:0100403,Duplication of the middle phalanx of the 5th toe,HP:0010202,Duplication of middle phalanx of toe
+UBERON:2001613,dorsal fin middle radial bone,UBERON:2101613,dorsal fin middle radial element
+DOID:1792,pancreas lymphoma,DOID:1793,pancreatic cancer
+UBERON:2000911,transverse process of neural arch 3,UBERON:0004120,mesoderm-derived structure
+UBERON:0001425,pectoral lymphatic vessel,UBERON:0001473,lymphatic vessel
+UBERON:2001415,pelvic fin distal radial bone 2,UBERON:1500008,pelvic fin distal radial bone
+HP:0001669,Transposition of the great arteries,HP:0011603,Congenital malformation of the great arteries
+UBERON:0003045,dorsal longitudinal fasciculus,UBERON:0005838,fasciculus of brain
+HP:0100708,Abnormality of the microglia,HP:0100705,Abnormality of the glial cells
+UBERON:0000056,ureter,UBERON:0006555,excretory tube
+UBERON:0002172,alveolar atrium,UBERON:0004119,endoderm-derived structure
+HP:0001137,Alternating esotropia,HP:0000565,Esotropia
+UBERON:0003407,cartilage of nasal septum,UBERON:0010313,neural crest-derived structure
+UBERON:0011510,cloacal bursa,UBERON:0004120,mesoderm-derived structure
+UBERON:0004321,middle phalanx of manual digit 3,UBERON:0003864,middle phalanx of manus
+HP:0200095,Anterior open bite,HP:0010807,Open bite
+UBERON:2005118,middle lateral line primordium,UBERON:2000228,lateral line primordium
+UBERON:0005213,outer renal medulla interstitium,UBERON:0005211,renal medulla interstitium
+DOID:8272,anterior urethra cancer,DOID:738,female urethral cancer
+DOID:12798,mucopolysaccharidosis,DOID:3211,lysosomal storage disease
+UBERON:0003462,facial bone,UBERON:0003457,head bone
+HP:0003067,Madelung deformity,HP:0003019,Abnormality of the wrist
+UBERON:0005891,coelomic epithelium,UBERON:0000483,epithelium
+HP:0010037,Aplasia of the 2nd metacarpal,HP:0010048,Aplasia of metacarpal bones
+DOID:1824,status epilepticus,DOID:1826,epilepsy syndrome
+UBERON:0010996,articular cartilage of joint,UBERON:0001994,hyaline cartilage tissue
+HP:0003970,Undermodelled forearm bones,HP:0002973,Abnormality of the forearm
+HP:0010214,Contractures of the interphalangeal joint of the hallux,HP:0010212,Flexion contracture of the hallux
+UBERON:0008814,pharyngeal system,UBERON:0002050,embryonic structure
+UBERON:2000873,epaxial region somite 4,UBERON:0003900,epaxial myotome region
+CL:1000682,kidney medulla interstitial cell,CL:1000500,kidney interstitial cell
+UBERON:0000079,male reproductive system,UBERON:0014403,male anatomical structure
+UBERON:2000749,epaxial region somite 9,UBERON:0003900,epaxial myotome region
+DOID:2870,endometrial adenocarcinoma,DOID:2871,endometrial carcinoma
+UBERON:0014710,carapacial ridge,UBERON:0002050,embryonic structure
+DOID:14151,spinal cord melanoma,DOID:5612,spinal cancer
+UBERON:0001426,jugular lymphatic vessel,UBERON:0001473,lymphatic vessel
+UBERON:0001568,muscle of larynx,UBERON:0003831,respiratory system muscle
+DOID:12522,bagassosis,DOID:841,extrinsic allergic alveolitis
+CL:1000451,epithelial cell of visceral layer of glomerular capsule,CL:1000450,epithelial cell of glomerular capsule
+CL:1001434,olfactory bulb interneuron,CL:0000402,CNS interneuron
+UBERON:3000878,intumescentia bilateralis superior,UBERON:4100000,skeletal element projection
+UBERON:0009567,nail of pedal digit,UBERON:0001705,nail
+UBERON:0002414,lumbar vertebra,UBERON:0002412,vertebra
+HP:0010655,Epiphyseal stippling,HP:0010766,Ectopic calcification
+UBERON:0001839,bony labyrinth,UBERON:0010313,neural crest-derived structure
+HP:0100933,Sclerosis of the proximal phalanx of the 4th toe,HP:0100928,Sclerosis of the phalanges of the 4th toe
+CL:1000245,posterior lateral line ganglion neuron,CL:0000540,neuron
+UBERON:0001022,cell body,UBERON:0000470,cell part
+UBERON:0006070,coccygeal vertebra,UBERON:0001095,caudal vertebra
+HP:0009343,Small epiphysis of the distal phalanx of the 3rd finger,HP:0009332,Abnormality of the epiphysis of the distal phalanx of the 3rd finger
+UBERON:2007059,neurogenic field,UBERON:0004121,ectoderm-derived structure
+UBERON:2001053,primitive internal carotid artery,UBERON:0001637,artery
+HP:0008936,Muscular hypotonia of the trunk,HP:0001252,Muscular hypotonia
+DOID:6041,choroid spindle cell melanoma,DOID:6037,spindle cell intraocular melanoma
+HP:0002173,Hypoglycemic seizures,HP:0011145,Symptomatic seizures
+UBERON:0006680,trachealis,UBERON:0003387,smooth muscle of trachea
+CL:1000351,basal cell of epithelium of respiratory bronchiole,CL:1000352,basal cell of epithelium of lobular bronchiole
+HP:0010014,Abnormality of the epiphysis of the 1st metacarpal,HP:0005913,Abnormality of metacarpal epiphyses
+NCBITaxon:7165,Anopheles gambiae,NCBITaxon:44542,gambiae species complex
+HP:0006906,Congenital intracerebral calcification,HP:0002514,Cerebral calcification
+UBERON:0010223,left pupil,UBERON:0001771,pupil
+HP:0000076,Vesicoureteral reflux,HP:0000069,Abnormality of the ureter
+HP:0007800,Increased axial globe length,HP:0100887,Abnormality of globe size
+HP:0006688,Paroxysmal tachycardia,HP:0001649,Tachycardia
+HP:0010904,Abnormality of histidine family amino acid metabolism,HP:0004337,Abnormality of amino acid metabolism
+DOID:9398,epiglottitis,DOID:974,upper respiratory tract disease
+DOID:5259,colon leiomyosarcoma,DOID:5260,colon sarcoma
+HP:0001772,Talipes equinovalgus,HP:0001883,Talipes
+DOID:1085,Edwards syndrome,DOID:0080014,chromosomal disease
+HP:0005623,Absent ossification of calvaria,HP:0005474,Decreased calvarial ossification
+DOID:3345,xanthomatosis,DOID:9455,lipid storage disease
+HP:0100001,Malignant mesothelioma,HP:0011793,Neoplasm by anatomical site
+CL:0000026,invertebrate nurse cell,CL:0000039,germ line cell
+HP:0009650,Short distal phalanx of the thumb,HP:0009882,Short distal phalanx of finger
+UBERON:4200080,fibular crest,UBERON:0004530,bony projection
+UBERON:0009504,associated mesenchyme of main bronchus,UBERON:0003104,mesenchyme
+HP:0011217,Abnormal shape of the occiput,HP:0002648,Abnormality of calvarial morphology
+HP:0012509,Reduced thyroxin-binding globulin,HP:0010876,Abnormality of circulating protein level
+DOID:0050687,cell type cancer,DOID:162,cancer
+HP:0100223,Triangular epiphysis of the middle phalanx of the 5th toe,HP:0100098,Abnormality of the epiphysis of the middle phalanx of the 5th toe
+HP:0100227,Enlarged epiphysis of the proximal phalanx of the 5th toe,HP:0100099,Abnormality of the epiphysis of the proximal phalanx of the 5th toe
+UBERON:0004035,subplate,UBERON:0014950,layer of developing cerebral cortex
+UBERON:4100011,postacetabular buttress,UBERON:0004530,bony projection
+UBERON:2002218,parallel fiber,UBERON:0004121,ectoderm-derived structure
+HP:0003993,Broad ulna,HP:0002997,Abnormality of the ulna
+CL:1000417,myoepithelial cell of sweat gland,CL:1000448,epithelial cell of sweat gland
+UBERON:0002336,corpus callosum,UBERON:0002473,intercerebral commissure
+HP:0005043,irregular proximal humeral metaphyses,HP:0003913,Irregular humeral metaphyses
+UBERON:2001505,taenia marginalis anterior,UBERON:0004120,mesoderm-derived structure
+UBERON:0014727,intercalated duct of salivary gland,UBERON:0014725,intercalated duct
+UBERON:0001463,manual digit 1,UBERON:0006048,digit 1
+DOID:6258,type 1 papillary adenoma of the kidney,DOID:6257,chromophil adenoma of the kidney
+UBERON:0010008,mammalian cotyledon,UBERON:0000478,extraembryonic structure
+CL:0000169,type B pancreatic cell,CL:0000164,enteroendocrine cell
+UBERON:0011135,intervertebral cartilage,UBERON:0007844,cartilage element
+UBERON:0000074,renal glomerulus,UBERON:0004120,mesoderm-derived structure
+DOID:2664,sweat gland neoplasm,DOID:3165,skin benign neoplasm
+UBERON:0009881,anterior lateral plate mesoderm,UBERON:0005291,embryonic tissue
+HP:0100379,Aplasia of the distal phalanx of the 4th toe,HP:0100370,Aplasia/Hypoplasia of the distal phalanx of the 4th toe
+DOID:4765,pulmonary blastoma,DOID:1324,lung cancer
+HP:0011537,Left atrial isomerism,HP:0011535,Abnormal atrial arrangement
+UBERON:0000439,arachnoid trabecula,UBERON:0004121,ectoderm-derived structure
+HP:0011463,Childhood onset,HP:0011007,Age of onset
+UBERON:0009129,right atrium endocardium,UBERON:0012275,meso-epithelium
+DOID:9861,miliary tuberculosis,DOID:0050598,extrapulmonary tuberculosis
+DOID:5283,vagina leiomyosarcoma,DOID:1901,vagina sarcoma
+CL:0002463,SIRPa-positive adipose dendritic cell,CL:0002462,adipose dendritic cell
+HP:0010368,Abnormality of the distal phalanx of the 3rd toe,HP:0010330,Abnormality of the phalanges of the 3rd toe
+UBERON:0001515,thoracic aorta,UBERON:0005800,segment of aorta
+DOID:0050575,D-2-hydroxyglutaric aciduria,DOID:0050573,2-hydroxyglutaric aciduria
+HP:0011477,Upbeat nystagmus,HP:0010544,Vertical nystagmus
+HP:0012665,Moderately reduced ejection fraction,HP:0012664,Reduced ejection fraction
+CL:0002657,glandular cell of esophagus,CL:0002252,epithelial cell of esophagus
+HP:0004619,Lumbar kyphoscoliosis,HP:0002751,Kyphoscoliosis
+UBERON:2000626,bulbo-spinal tract,UBERON:2000318,brainstem and spinal white matter
+HP:0010892,Abnormality of branched chain family amino acid metabolism,HP:0004337,Abnormality of amino acid metabolism
+UBERON:0003834,thoracic segment blood vessel,UBERON:0003513,trunk blood vessel
+UBERON:0009865,Hatschek's pit,UBERON:0006846,surface groove
+UBERON:0001503,dorsal interosseous of manus,UBERON:0001502,interosseous muscle of manus
+HP:0010459,True hermaphroditism,HP:0000811,Abnormal external genitalia
+HP:0012522,Spider hemangioma,HP:0100585,Teleangiectasia of the skin
+HP:0005807,Absent distal phalanges,HP:0009835,Aplasia/Hypoplasia of the distal phalanges of the hand
+HP:0006704,Abnormality of the coronary arteries,HP:0011004,Abnormality of the systemic arterial tree
+DOID:3230,high pressure neurological syndrome,DOID:331,central nervous system disease
+HP:0100694,Tibial torsion,HP:0002992,Abnormality of the tibia
+UBERON:3000547,rostral process,UBERON:0004120,mesoderm-derived structure
+HP:0010153,Fragmentation of the epiphysis of the 1st metatarsal,HP:0010117,Fragmentation of the epiphyses of the hallux
+HP:0005948,Cystic lung disease,HP:0002088,Abnormality of the lung
+UBERON:3010667,m. intertransversarius capitis inferior,UBERON:0004465,musculature of neck
+UBERON:0002606,neuropil,UBERON:0011215,cell part cluster of neuraxis
+UBERON:0010255,3rd arch mesenchyme from neural crest,UBERON:0010359,pharyngeal arch mesenchyme from neural crest
+HP:0011257,Serpiginous crus of helix,HP:0009895,Abnormality of the crus of the helix
+HP:0010047,Short 5th metacarpal,HP:0010045,Aplasia/Hypoplasia of the 5th metacarpal
+UBERON:0006308,vagal X nerve trunk,UBERON:0002050,embryonic structure
+UBERON:0006947,male genital duct,UBERON:0015212,lateral structure
+HP:0009568,Aplasia/Hypoplasia of the middle phalanx of the 2nd finger,HP:0009543,Abnormality of the middle phalanx of the 2nd finger
+HP:0009564,Triangular shaped distal phalanx of the 2nd finger,HP:0009542,Abnormality of the distal phalanx of the 2nd finger
+HP:0009051,Increased muscle glycogen content,HP:0012269,Abnormal muscle glycogen content
+UBERON:0005883,neural tube lateral wall mantle layer,UBERON:0004061,neural tube mantle layer
+DOID:0060191,gastroduodenal Crohn's disease,DOID:8778,Crohn's disease
+UBERON:2001744,replacement tooth trench,UBERON:0000464,anatomical space
+HP:0003481,Segmental peripheral demyelination/remyelination,HP:0011096,Peripheral demyelination
+HP:0012207,Reduced sperm motility,HP:0012206,Abnormal sperm motility
+UBERON:2000587,sphenotic,UBERON:0002513,endochondral bone
+UBERON:0005810,cervical vertebra 1 anterior tubercle,UBERON:4100000,skeletal element projection
+CL:0002381,uninucleate conidium,CL:0000599,conidium
+HP:0009785,Triceps aplasia,HP:0100854,Aplasia of the musculature
+CL:1000716,kidney outer medulla collecting duct principal cell,CL:1001431,kidney collecting duct principal cell
+CL:1001005,glomerular capillary endothelial cell,CL:1000892,kidney capillary endothelial cell
+HP:0006668,Twelfth rib hypoplasia,HP:0000773,Short ribs
+HP:0009741,Nephrosclerosis,HP:0012210,Abnormal renal morphology
+UBERON:3010820,suboccular arch,UBERON:0000064,organ part
+CL:0000791,mature alpha-beta T cell,CL:0000789,alpha-beta T cell
+DOID:271,hemangioma of liver,DOID:254,hemangioma of intra-abdominal structure
+UBERON:2005056,palatocerebral vein,UBERON:0003496,head blood vessel
+DOID:6917,predominantly cortical thymoma,DOID:3282,dendritic cell thymoma
+DOID:9709,rosacea conjunctivitis,DOID:6195,conjunctivitis
+CL:0000322,pneumocyte,CL:0010003,epithelial cell of alveolus of lung
+UBERON:0012309,superficial anterior cervical lymph node,UBERON:0004870,superficial cervical lymph node
+DOID:384,Wolff-Parkinson-White syndrome,DOID:10273,heart conduction disease
+UBERON:0003087,anterior cardinal vein,UBERON:0004344,cardinal vein
+UBERON:0012419,taenia coli,UBERON:0004220,large intestine smooth muscle
+HP:0001466,Contiguous gene syndrome,HP:0000005,Mode of inheritance
+CL:1000495,small intestine goblet cell,CL:1001598,small intestine glandular cell
+DOID:0050788,proximal symphalangism,DOID:0050736,autosomal dominant disease
+UBERON:0003666,upper jaw molar,UBERON:0003655,molar tooth
+HP:0009542,Abnormality of the distal phalanx of the 2nd finger,HP:0009541,Abnormality of the phalanges of the 2nd finger
+HP:0010700,Total cataract,HP:0000518,Cataract
+DOID:10439,Mooren's ulcer,DOID:8463,corneal ulcer
+UBERON:0011137,axial skeletal system,UBERON:0000075,subdivision of skeletal system
+UBERON:0012251,ectocervical epithelium,UBERON:0004801,cervix epithelium
+DOID:367,olfactory nerve disease,DOID:936,brain disease
+UBERON:0003284,mesentery of midgut,UBERON:0002095,mesentery
+UBERON:2001298,vagal placode 2,UBERON:0003078,epibranchial placode
+HP:0001723,Restrictive cardiomyopathy,HP:0001638,Cardiomyopathy
+HP:0005086,Knee osteoarthritis,HP:0002815,Abnormality of the knees
+HP:0003897,Irregular ossification of the humeral epiphyses,HP:0011849,Abnormal bone ossification
+UBERON:0003388,mesothelium of pericardial cavity,UBERON:0001136,mesothelium
+UBERON:0011644,puboischiofemoralis externus muscle,UBERON:0001325,muscle of pelvis
+HP:0000918,Scapular exostoses,HP:0100777,Exostoses
+HP:0000808,Penoscrotal hypospadias,HP:0003244,Penile hypospadias
+UBERON:0007154,inferior epigastric vein,UBERON:0006356,epigastric vein
+HP:0100277,Periauricular skin pits,HP:0000383,Abnormality of periauricular region
+UBERON:2001340,nucleus of the tract of the postoptic commissure,UBERON:0006569,diencephalic nucleus
+UBERON:0011380,female external urethral sphincter,UBERON:0004919,external urethral sphincter
+UBERON:0011830,duct of lesser vestibular gland,UBERON:0010146,paraurethral duct
+HP:0012538,Gluten intolerance,HP:0001984,Intolerance to protein
+UBERON:0002074,hair shaft,UBERON:0004121,ectoderm-derived structure
+DOID:9415,allergic asthma,DOID:2841,asthma
+UBERON:0003573,arm connective tissue,UBERON:0003588,forelimb connective tissue
+UBERON:0002958,medial lemniscus of pons,UBERON:0003002,medial lemniscus
+DOID:9849,Meniere's disease,DOID:9848,endolymphatic hydrops
+UBERON:2000073,somite 5,UBERON:0002329,somite
+HP:0007421,Telangiectases of the cheeks,HP:0007380,Facial telangiectasia
+DOID:2775,long bone adamantinoma,DOID:2776,adamantinoma
+HP:0000733,Stereotypic behavior,HP:0000708,Behavioural/Psychiatric Abnormality
+DOID:11638,presbyopia,DOID:10034,eye accommodation disease
+HP:0009311,Bullet-shaped proximal phalanx of the 4th finger,HP:0009284,Abnormality of the proximal phalanx of the 4th finger
+HP:0009309,Triangular shaped middle phalanx of the 4th finger,HP:0009407,Triangular shaped phalanges of the 4th finger
+DOID:0050731,vitamin B12 deficiency,DOID:0050718,vitamin metabolic disorder
+DOID:422,congenital structural myopathy,DOID:423,myopathy
+DOID:758,situs inversus,DOID:0050545,visceral heterotaxy
+HP:0008138,Equinus calcaneus,HP:0008364,Abnormality of the calcaneus
+UBERON:0001622,lacrimal artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0003709,circle of Willis,UBERON:0004573,systemic artery
+NCBITaxon:131567,cellular organisms,NCBITaxon:1,root
+HP:0006932,Transient psychotic episodes,HP:0000725,Psychotic episodes
+HP:0004247,Small scaphoid,HP:0004243,Abnormality of the scaphoid
+DOID:8986,narcolepsy,DOID:535,sleep disorder
+UBERON:0008857,stomach smooth muscle circular layer,UBERON:0009034,stomach region
+HP:0009370,Type A brachydactyly,HP:0001156,Brachydactyly syndrome
+DOID:3259,orbit rhabdomyosarcoma,DOID:9987,orbit sarcoma
+UBERON:0010580,pedal digit 1 phalanx pre-cartilage condensation,UBERON:0010562,pedal digit 1 mesenchyme
+UBERON:0010078,optic choroid vascular plexus,UBERON:0005629,vascular plexus
+UBERON:0005197,segmental spinal nerve,UBERON:0001780,spinal nerve
+UBERON:0010160,lumen of lymphatic vessel,UBERON:0000464,anatomical space
+UBERON:0002233,tectorial membrane of cochlea,UBERON:0005764,acellular membrane
+HP:0010185,Aplasia/Hypoplasia of the distal phalanges of the toes,HP:0010182,Abnormality of the distal phalanges of the toes
+UBERON:3000459,prearticular coronoid process,UBERON:0004120,mesoderm-derived structure
+HP:0005736,Short tibia,HP:0003026,Short long bones
+UBERON:2001881,rib of vertebra 4,UBERON:0002228,rib
+UBERON:0008199,chin,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0000777,mesangial phagocyte,CL:0002681,kidney cortical cell
+UBERON:2001232,pharyngeal arch 5 skeleton,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0012323,Sleep myoclonus,HP:0001336,Myoclonus
+UBERON:0005157,epithelial fold,UBERON:0000483,epithelium
+UBERON:0011184,epithelium of crypt of lieberkuhn,UBERON:0001277,intestinal epithelium
+HP:0002715,Abnormality of the immune system,HP:0000118,Phenotypic abnormality
+UBERON:0007811,craniocervical region,UBERON:0000475,organism subdivision
+HP:0006012,Widened metacarpal shaft,HP:0005916,Abnormal metacarpal morphology
+UBERON:0003663,hindlimb muscle,UBERON:0003661,limb muscle
+UBERON:0004912,biliary bud,UBERON:0003914,epithelial tube
+CL:0000934,"CD4-positive, alpha-beta cytotoxic T cell",CL:0000910,cytotoxic T cell
+UBERON:0009090,outer medulla vasa recta descending limb,UBERON:0000064,organ part
+UBERON:0003128,cranium,UBERON:0000075,subdivision of skeletal system
+UBERON:0011193,inferior ophthalmic vein,UBERON:0011191,ophthalmic vein
+DOID:9651,systolic heart failure,DOID:6000,congestive heart failure
+DOID:970,tenosynovitis,DOID:381,arthropathy
+DOID:653,purine-pyrimidine metabolic disorder,DOID:655,inherited metabolic disorder
+UBERON:0005813,tubercle,UBERON:0004529,anatomical projection
+UBERON:0003728,mediastinum,UBERON:0002224,thoracic cavity
+UBERON:0008887,rectal venous plexus,UBERON:0001593,venous plexus
+UBERON:0002480,ventral lateral geniculate nucleus,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:2000500,dorsal erector,UBERON:2005267,erector muscle
+CL:0000523,mononuclear cytotrophoblast cell,CL:0000351,trophoblast cell
+DOID:10242,ehrlichiosis,DOID:0050338,primary bacterial infectious disease
+CL:1000327,appendix goblet cell,CL:1001585,appendix glandular cell
+HP:0011419,Placental abruption,HP:0100767,Abnormality of the placenta
+HP:0011521,Deuteranopia,HP:0000642,Red-green dyschromatopsia
+UBERON:0002299,alveolus of lung,UBERON:0003215,alveolus
+UBERON:0009751,cardiac mesenchyme,UBERON:0004120,mesoderm-derived structure
+HP:0001540,Diastasis recti,HP:0010991,Abnormality of the abdominal musculature
+UBERON:3000681,hyoid apparatus opening,UBERON:0010272,hyoid apparatus
+DOID:11516,hypertensive heart disease,DOID:114,heart disease
+UBERON:0004392,epiphysis of second metacarpal bone,UBERON:0004390,epiphysis of metacarpal bone
+UBERON:0004675,hypoglossal nerve root,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0013154,1st arch maxillary endoderm,UBERON:0000490,unilaminar epithelium
+CL:0002214,type IIa muscle cell,CL:0002212,type II muscle cell
+UBERON:2005051,communicating vessel palatocerebral artery,UBERON:0001637,artery
+HP:0002983,Micromelia,HP:0009826,Limb undergrowth
+HP:0010538,Small sella turcica,HP:0002679,Abnormality of the sella turcica
+HP:0007200,Episodic hypersomnia,HP:0004372,Reduced consciousness/confusion
+UBERON:0004917,urethral sphincter,UBERON:0003829,urethra muscle
+UBERON:0005461,levator scapulae muscle,UBERON:0004120,mesoderm-derived structure
+UBERON:0005412,optic fissure,UBERON:0006846,surface groove
+UBERON:0000101,lobe of lung,UBERON:0000064,organ part
+HP:0003978,Fractured radius,HP:0002818,Abnormality of the radius
+HP:0007777,Chorioretinal scars,HP:0100699,Scarring
+UBERON:0000366,flexor muscle,UBERON:0001630,muscle organ
+UBERON:0001428,lunate,UBERON:0001480,proximal carpal bone
+UBERON:0008935,albumen gland,UBERON:0005398,female reproductive gland
+HP:0000290,Abnormality of the forehead,HP:0000271,Abnormality of the face
+UBERON:0007331,maxillary rhamphotheca,UBERON:0007330,rhamphotheca
+DOID:7024,mucinous intrahepatic cholangiocarcinoma,DOID:4928,intrahepatic cholangiocarcinoma
+DOID:11266,hemorrhagic fever with renal syndrome,DOID:934,viral infectious disease
+UBERON:0005083,nipple sheath,UBERON:0008367,breast epithelium
+DOID:4591,lymphoplasmacyte-rich meningioma,DOID:3565,meningioma
+HP:0100496,Abnormality of the vitamin B3 metabolism,HP:0004340,Abnormality of vitamin B metabolism
+UBERON:0004030,aqueous vein,UBERON:0003496,head blood vessel
+NCBITaxon:34621,Dermacentor variabilis,NCBITaxon:34619,Dermacentor
+HP:0001547,Abnormality of the rib cage,HP:0000765,Abnormality of the thorax
+UBERON:0007125,pharyngeal pouch 4,UBERON:0004117,pharyngeal pouch
+UBERON:0006856,interrenal gland,UBERON:0006554,urinary system structure
+UBERON:0005051,mediastinum testis,UBERON:0005423,developing anatomical structure
+UBERON:0012421,urodeum,UBERON:0000064,organ part
+DOID:3697,acute transudative otitis media,DOID:11180,non-suppurative otitis media
+HP:0010691,Mirror image foot polydactyly,HP:0001829,Foot polydactyly
+HP:0011696,Supraventricular tachycardia with a manifest accessory pathway on the left free wall,HP:0011694,Supraventricular tachycardia with a manifest accessory pathway
+HP:0006361,Irregular femoral epiphyses,HP:0010582,Irregular epiphyses
+UBERON:2005266,pterotic fossa,UBERON:0004704,bone fossa
+HP:0003537,Hypouricemia,HP:0004369,Decreased purine levels
+HP:0009241,Bullet-shaped distal phalanx of the 5th finger,HP:0004225,Abnormality of the distal phalanx of the 5th finger
+HP:0002783,Recurrent lower respiratory tract infections,HP:0002205,Recurrent respiratory infections
+DOID:11396,pulmonary edema,DOID:11162,respiratory failure
+UBERON:0005805,dorsal aorta,UBERON:0003513,trunk blood vessel
+UBERON:0011241,ethmoid region,UBERON:0004120,mesoderm-derived structure
+CL:0001022,CD115-positive monocyte,CL:0000576,monocyte
+CL:0002108,CD38-negative IgG memory B cell,CL:0000979,IgG memory B cell
+HP:0009063,Progressive distal muscle weakness,HP:0002460,Distal muscle weakness
+DOID:5195,peripheral nervous system ganglioneuroblastoma,DOID:4163,ganglioneuroblastoma
+UBERON:0009899,pole of cerebral hemisphere,UBERON:0004121,ectoderm-derived structure
+UBERON:3010731,M. coracobrachialis brevis,UBERON:0010891,pectoral complex muscle
+UBERON:3000842,capitulum ulnae,UBERON:0004120,mesoderm-derived structure
+UBERON:0002973,parahippocampal gyrus,UBERON:0003022,cerebral cortex lobe
+UBERON:0001659,transverse facial vein,UBERON:0003502,neck blood vessel
+UBERON:0009057,one-pass circulatory system,UBERON:0009055,closed circulatory system
+UBERON:0008804,stylopharyngeus muscle,UBERON:0004119,endoderm-derived structure
+NCBITaxon:40411,Chrysosporium,NCBITaxon:34383,mitosporic Onygenales
+HP:0002876,Episodic tachypnea,HP:0002789,Tachypnea
+DOID:13499,jejunal cancer,DOID:10154,small intestine cancer
+CL:1001217,interlobulary artery smooth muscle cell,CL:1001064,kidney artery smooth muscle cell
+CL:0002530,immature CD1a-positive dermal dendritic cell,CL:0002529,CD1a-positive dermal dendritic cell
+HP:0010036,Aplasia/Hypoplasia of the 2nd metacarpal,HP:0010010,Abnormality of the 2nd metacarpal
+UBERON:0016400,infrapatellar fat pad,UBERON:0003577,knee connective tissue
+DOID:8593,chronic monocytic leukemia,DOID:8527,monocytic leukemia
+UBERON:0002130,cerebellar nuclear complex,UBERON:0004121,ectoderm-derived structure
+DOID:4353,ciliary body disease,DOID:240,iris disease
+UBERON:0004427,proximal epiphysis of first metatarsal bone,UBERON:0004395,epiphysis of first metatarsal bone
+CL:0001054,CD14-positive monocyte,CL:0000576,monocyte
+UBERON:3000639,zygomatic ramus of squamosal,UBERON:0010313,neural crest-derived structure
+HP:0100931,Sclerosis of the proximal phalanx of the 2nd toe,HP:0100946,Sclerosis of the proximal phalanges of the toes
+HP:0100939,Sclerosis of the distal phalanx of the 2nd toe,HP:0100948,Sclerosis of the distal phalanges of the toes
+UBERON:2000394,molecular layer corpus cerebelli,UBERON:0000479,tissue
+UBERON:0002658,medial lemniscus of midbrain,UBERON:0002635,regional part of midbrain tegmentum
+DOID:4541,nominal aphasia,DOID:0060046,aphasia
+CL:0000560,band form neutrophil,CL:0000776,immature neutrophil
+UBERON:0006724,osseus spiral lamina,UBERON:0004120,mesoderm-derived structure
+HP:0008767,Self-mutilation of tongue and lips due to involuntary movements,HP:0000742,Self-mutilation
+DOID:971,tendinitis,DOID:633,myositis
+DOID:611,leukocyte-adhesion deficiency syndrome,DOID:3262,phagocyte bactericidal dysfunction
+HP:0002367,Visual hallucinations,HP:0000738,Hallucinations
+UBERON:0014458,female bulbospongiosus muscle,UBERON:0011389,bulbospongiosus muscle
+HP:0008496,Multiple rows of eyelashes,HP:0000499,Abnormality of the eyelashes
+UBERON:0014403,male anatomical structure,UBERON:0014402,sex-specific anatomical structure
+UBERON:2001732,vertebral element 5,UBERON:0010913,vertebral element
+UBERON:0010258,mesenchyme from rhombencephalic neural crest,UBERON:0007213,mesenchyme derived from head neural crest
+UBERON:0002228,rib,UBERON:0004120,mesoderm-derived structure
+HP:0100184,Fragmentation of the epiphysis of the middle phalanx of the 4th toe,HP:0100095,Abnormality of the epiphysis of the middle phalanx of the 4th toe
+DOID:5402,vaginal adenoma,DOID:0060114,vaginal benign neoplasm
+HP:0008822,Hypoplastic ischiopubic rami,HP:0003173,Hypoplastic pubic bones
+DOID:2000,otosalpingitis,DOID:9739,eustachian tube disease
+UBERON:0001807,paravertebral ganglion,UBERON:0001806,sympathetic ganglion
+UBERON:0001660,maxillary vein,UBERON:0009141,craniocervical region vein
+UBERON:0002286,third ventricle,UBERON:0004086,brain ventricle
+UBERON:2001660,basibranchial tooth,UBERON:0001091,calcareous tooth
+UBERON:0006086,stria medullaris,UBERON:0013199,stria of neuraxis
+UBERON:0014523,oculomotor division of oculomotor nuclear complex,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0007503,epithelial vesicle,UBERON:0000483,epithelium
+UBERON:0009631,root of lumbar spinal nerve,UBERON:0009623,spinal nerve root
+DOID:222,perichondritis of auricle,DOID:9463,otitis externa
+HP:0012256,Absent outer dynein arms,HP:0200106,Absent/shortened dynein arms
+UBERON:0011683,adductor mandibulae,UBERON:0011648,jaw muscle
+UBERON:0001259,mucosa of urinary bladder,UBERON:0004120,mesoderm-derived structure
+UBERON:0000474,female reproductive system,UBERON:0000990,reproductive system
+UBERON:0011392,internal elastic membrane,UBERON:0003614,blood vessel elastic tissue
+UBERON:0006059,falx cerebri,UBERON:0004121,ectoderm-derived structure
+UBERON:3000688,prominentia apicalis dorsalis,UBERON:0000072,segment of respiratory tract
+UBERON:0011907,gastrocnemius medialis,UBERON:0011906,muscle head
+UBERON:0010426,oropharyngeal choana,UBERON:0004121,ectoderm-derived structure
+DOID:11723,Duchenne muscular dystrophy,DOID:9884,muscular dystrophy
+UBERON:0002231,body of rib,UBERON:0005055,zone of long bone
+UBERON:0004423,proximal epiphysis of second metacarpal bone,UBERON:0004416,proximal epiphysis of metacarpal bone
+UBERON:2001904,epibranchial element,UBERON:0010363,endochondral element
+DOID:2349,arteriosclerosis,DOID:0050828,artery disease
+CL:0000686,cerebrospinal fluid secreting cell,CL:0000151,secretory cell
+UBERON:2001626,premaxillary tooth,UBERON:0003267,tooth of upper jaw
+CL:1001135,arcuate artery cell,CL:1001045,kidney cortex artery cell
+UBERON:0003121,aortic arch 4,UBERON:0004363,aortic arch
+UBERON:2001875,opercular series,UBERON:0000477,anatomical cluster
+UBERON:0007684,uriniferous tubule,UBERON:0004819,kidney epithelium
+HP:0000403,Recurrent otitis media,HP:0000388,Otitis media
+HP:0003394,Muscle cramps,HP:0011804,Abnormality of muscle physiology
+HP:0009990,Duplication of the proximal phalanx of the 5th finger,HP:0010006,Duplication of the proximal phalanx of hand
+UBERON:0002732,longitudinal pontine fibers,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0012062,Bone cyst,HP:0003330,Abnormal bone structure
+UBERON:0012081,patella pre-cartilage condensation,UBERON:0005291,embryonic tissue
+HP:0009748,Large earlobe,HP:0000363,Abnormality of earlobe
+UBERON:3010691,m. opercularis,UBERON:0010891,pectoral complex muscle
+CL:0001003,mature CD8_alpha-negative CD11b-positive dendritic cell,CL:0000999,CD4-positive CD11b-positive dendritic cell
+UBERON:0009194,basisphenoid cartilage condenstion,UBERON:0009891,facial mesenchyme
+HP:0004924,Abnormal oral glucose tolerance,HP:0001952,Abnormal glucose tolerance
+HP:0009616,Bifid first metacarpal,HP:0010003,Partial duplication of the proximal phalanges of the hand
+UBERON:3010173,supernumerary tubercles,UBERON:0005813,tubercle
+UBERON:0003583,larynx connective tissue,UBERON:0003570,respiratory system connective tissue
+UBERON:0004293,parasympathetic nerve,UBERON:0001021,nerve
+UBERON:0005245,lobar bronchus of right lung caudal lobe,UBERON:0003404,lobar bronchus of right lung
+CL:0000783,multinucleated phagocyte,CL:0000228,multinucleate cell
+CL:0005013,single ciliated epithelial cell,CL:0000064,ciliated cell
+DOID:262,kidney hemangiopericytoma,DOID:263,kidney cancer
+UBERON:2001594,caudal fin lower lobe,UBERON:0003102,surface structure
+HP:0009828,Peromelia,HP:0009815,Aplasia/Hypoplasia of the extremities
+UBERON:2001928,articular fossa of opercle,UBERON:0004704,bone fossa
+HP:0009272,Aplasia/Hypoplasia of the 4th finger,HP:0006265,Aplasia/Hypoplasia of fingers
+UBERON:0006479,Brodmann (1909) area 38,UBERON:0013529,Brodmann area
+DOID:6043,ciliary body spindle cell melanoma,DOID:6037,spindle cell intraocular melanoma
+DOID:12707,myoclonic cerebellar dyssynergia,DOID:2478,spinocerebellar degeneration
+HP:0005490,Postnatal macrocephaly,HP:0000256,Macrocephaly
+HP:0006184,Decreased palmar creases,HP:0010488,Aplasia/Hypoplasia of the palmar creases
+HP:0000391,Thickened helices,HP:0011039,Abnormality of the helix
+DOID:0050883,infantile cerebellar-retinal degeneration,DOID:1289,neurodegenerative disease
+UBERON:0006516,dorsal pallidum,UBERON:0006514,pallidum
+DOID:6468,mucinous cystadenofibroma,DOID:5482,cystadenofibroma
+DOID:0050855,renal fibrosis,DOID:557,kidney disease
+HP:0003402,Decreased miniature endplate potentials,HP:0003398,Abnormality of the neuromuscular junction
+UBERON:0002080,heart right ventricle,UBERON:0002082,cardiac ventricle
+UBERON:3000438,planum internasale,UBERON:0010313,neural crest-derived structure
+DOID:0060050,autoimmune disease of blood,DOID:417,hypersensitivity reaction type II disease
+DOID:8997,polycythemia vera,DOID:8432,polycythemia
+UBERON:0006914,squamous epithelium,UBERON:0000483,epithelium
+HP:0000972,Palmoplantar hyperkeratosis,HP:0100872,Abnormality of the plantar skin of foot
+CL:0002154,early promyelocyte,CL:0000836,promyelocyte
+HP:0011912,Abnormality of the glenoid fossa,HP:0000782,Abnormality of the scapula
+DOID:134,vaginal glandular tumor,DOID:119,vaginal cancer
+HP:0005372,Abnormality of B cell physiology,HP:0002846,Abnormality of B cells
+DOID:10054,skin amelanotic melanoma,DOID:8923,skin melanoma
+UBERON:0000314,cecum mucosa,UBERON:0000317,colonic mucosa
+UBERON:2001518,ceratobranchial 3 cartilage,UBERON:2001516,ceratobranchial cartilage
+HP:0005517,T-cell lymphoma/leukemia,HP:0012190,T-cell lymphoma
+HP:0012375,Chemosis,HP:0000502,Abnormality of the conjunctiva
+HP:0003419,Low back pain,HP:0003418,Back pain
+DOID:0050715,methylmalonic aciduria and homocystinuria type cblC,DOID:14749,methylmalonic acidemia
+UBERON:0006642,muscle layer of oviduct,UBERON:0014404,female anatomical structure
+UBERON:0006646,muscle layer of epididymis,UBERON:0014403,male anatomical structure
+UBERON:0011975,epiphysis of middle phalanx of pes,UBERON:0011973,epiphysis of phalanx of pes
+CL:0000020,spermatogonium,CL:0000015,male germ cell
+UBERON:0011106,cruciate ligament of atlas,UBERON:0003568,neck connective tissue
+DOID:6259,type 2 papillary adenoma of the kidney,DOID:6257,chromophil adenoma of the kidney
+UBERON:0002396,vomer,UBERON:0012071,palate bone
+HP:0100527,Neoplasia of the pleura,HP:0100606,Neoplasm of the respiratory system
+HP:0010043,Aplasia of the 4th metacarpal,HP:0010042,Aplasia/Hypoplasia of the 4th metacarpal
+CL:0002244,squamous cell of ectocervix,CL:0000076,squamous epithelial cell
+UBERON:0003322,mesenchyme of shoulder,UBERON:0003104,mesenchyme
+HP:0012276,Digital flexor tenosynovitis,HP:0100261,Abnormal tendon morphology
+UBERON:3010749,M. iliolumbaris,UBERON:0010890,pelvic complex muscle
+UBERON:0014594,tuberomammillary nucleus ventral part,UBERON:0002789,regional part of posterior hypothalamic region
+UBERON:0008855,placenta metrial gland,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:8057,olfactory groove meningioma,DOID:4436,anterior cranial fossa meningioma
+CL:0000548,animal cell,CL:0000255,eukaryotic cell
+CL:0000483,bombesin stimulating hormone secreting cell,CL:0000167,peptide hormone secreting cell
+NCBITaxon:197562,Pancrustacea,NCBITaxon:197563,Mandibulata
+DOID:5680,embryonal testis carcinoma,DOID:3308,embryonal carcinoma
+DOID:5560,mediastinal mesenchymal tumor,DOID:5559,mediastinal cancer
+UBERON:0011222,intra-ocular muscle,UBERON:0004277,eye muscle
+HP:0006285,Hypomineralization of enamel,HP:0000682,Abnormality of dental enamel
+HP:0100305,Ring fibers,HP:0004303,Abnormality of muscle fibers
+DOID:13953,uterine corpus dissecting leiomyoma,DOID:13223,uterine fibroid
+HP:0002821,Neuropathic arthropathy,HP:0003040,Arthropathy
+UBERON:0011776,spinal cord dorsal commissural nucleus,UBERON:0011777,nucleus of spinal cord
+HP:0002408,Cerebral arteriovenous malformation,HP:0100026,Arteriovenous malformation
+UBERON:0002462,erector spinae muscle group,UBERON:0001015,musculature
+UBERON:0002971,periolivary nucleus,UBERON:0002680,regional part of metencephalon
+UBERON:0011867,extensor carpi radialis muscle,UBERON:0011024,extrinsic extensor muscle of manus
+CL:0002308,epithelial cell of skin gland,CL:0002159,general ecto-epithelial cell
+UBERON:0001841,anterior semicircular canal,UBERON:0001840,semicircular canal
+HP:0009579,Proximal/middle symphalangism of the 2nd finger,HP:0009586,Symphalangism affecting the proximal phalanx of the 2nd finger
+UBERON:0002228,rib,UBERON:0015019,rib endochondral element
+CL:0000157,surfactant secreting cell,CL:0000151,secretory cell
+DOID:0050741,alcohol dependence,DOID:9973,substance dependence
+HP:0012142,Pancreatic squamous cell carcinoma,HP:0002894,Neoplasm of the pancreas
+UBERON:0003622,manual digit 2,UBERON:0002389,manual digit
+HP:0009265,Fragmentation of the epiphysis of the proximal phalanx of the 4th finger,HP:0010272,Fragmentation of the epiphyses of the proximal phalanges of the hand
+HP:0009336,Bracket epiphysis of the distal phalanx of the 3rd finger,HP:0009411,Bracket epiphyses of the 3rd finger
+DOID:0050677,Bjornstad syndrome,DOID:0050737,autosomal recessive disease
+DOID:6315,ovarian solid teratoma,DOID:6231,mature teratoma of the ovary
+DOID:1588,thrombocytopenia,DOID:2218,blood platelet disease
+UBERON:0000201,endothelial blood brain barrier,UBERON:0000483,epithelium
+HP:0009233,Triangular shaped proximal phalanx of the 5th finger,HP:0009150,Abnormality of the proximal phalanx of the 5th finger
+DOID:5565,adult teratoma,DOID:3307,teratoma
+DOID:0050584,gummatous syphilis,DOID:8200,tertiary syphilis
+UBERON:2200646,anal fin distal radial cartilage,UBERON:2100646,anal fin distal radial element
+UBERON:0008962,forelimb bone,UBERON:0010741,bone of pectoral complex
+UBERON:0003611,respiratory system elastic tissue,UBERON:0003570,respiratory system connective tissue
+DOID:4922,breast secretory carcinoma,DOID:3458,breast adenocarcinoma
+UBERON:0004367,Descemet's membrane,UBERON:0010313,neural crest-derived structure
+DOID:4400,dermatosis papulosa nigra,DOID:2723,dermatitis
+CL:1001221,arcuate vein smooth muscle cell,CL:1001142,arcuate vein cell
+UBERON:0001886,choroid plexus,UBERON:0005629,vascular plexus
+UBERON:0012199,posterior intercostal vein,UBERON:0012197,intercostal vein
+HP:0100898,Connective tissue nevi,HP:0003549,Abnormality of connective tissue
+CL:0002358,pyrenocyte,CL:0002417,primitive erythroid lineage cell
+DOID:13046,acute sphenoidal sinusitis,DOID:10794,sphenoid sinusitis
+UBERON:0001968,semen,UBERON:0000463,portion of organism substance
+UBERON:0004890,right lung accessory lobe,UBERON:0006518,right lung lobe
+HP:0009945,Duplication of phalanx of 2nd finger,HP:0009997,Duplication of phalanx of hand
+DOID:13514,venous tributary occlusion of retina,DOID:1729,retinal vascular occlusion
+HP:0007586,Telangiectases producing 'marbled' skin,HP:0100585,Teleangiectasia of the skin
+DOID:13811,chronic subinvolution of uterus,DOID:345,uterine disease
+UBERON:0007303,pharyngeal vasculature,UBERON:0006876,vasculature of organ
+UBERON:0001333,male urethra,UBERON:0000057,urethra
+UBERON:0013778,skin of sole of pes,UBERON:0013776,skin of palmar/plantar part of autopod
+HP:0012643,Foveal hypopigmentation,HP:0008002,Abnormality of macular pigmentation
+HP:0012177,Abnormal natural killer cell physiology,HP:0012176,Abnormality of natural killer cells
+UBERON:0004047,basal cistern,UBERON:0004050,subarachnoid cistern
+HP:0010790,Hyoplasia of the Leydig cells,HP:0010789,Abnormality of the Leydig cells
+CL:0002146,clear cell of eccrine sweat gland,CL:0000434,eccrine cell
+DOID:9362,status asthmaticus,DOID:2841,asthma
+HP:0010739,Osteopoikilosis,HP:0011001,Increased bone mineral density
+UBERON:0003235,epithelium of upper jaw,UBERON:0003929,gut epithelium
+DOID:3641,conus medullaris neoplasm,DOID:5612,spinal cancer
+HP:0002463,Language impairment,HP:0002167,Neurological speech impairment
+DOID:8630,upper lip cancer,DOID:8564,lip cancer
+HP:0007364,Aplasia/Hypoplasia of the cerebrum,HP:0002060,Abnormality of the cerebrum
+UBERON:0004429,proximal epiphysis of third metatarsal bone,UBERON:0004397,epiphysis of third metatarsal bone
+HP:0003992,Slender ulna,HP:0002997,Abnormality of the ulna
+HP:0006565,Increased hepatocellular lipid droplets,HP:0006561,Lipid accumulation in hepatocytes
+HP:0003306,Spinal rigidity,HP:0000925,Abnormality of the vertebral column
+CL:0002222,vertebrate lens cell,CL:0002371,somatic cell
+HP:0011250,Bifid antitragus,HP:0009896,Abnormality of the antitragus
+UBERON:0003024,principal part of ventral posteromedial nucleus,UBERON:0003528,brain grey matter
+HP:0002139,Arrhinencephaly,HP:0002323,Anencephaly
+HP:0004921,Abnormality of magnesium homeostasis,HP:0010927,Abnormality of divalent inorganic cation homeostasis
+UBERON:0006842,lymphatic capillary,UBERON:0010523,microcirculatory vessel
+HP:0100267,Lip pit,HP:0000159,Abnormality of the lip
+UBERON:0015107,distal tarsal bone 2 pre-cartilage condensation,UBERON:0015105,distal tarsal bone 2 endochondral element
+DOID:4156,primary syphilis,DOID:4166,syphilis
+UBERON:0010347,6th arch mesenchyme from head mesenchyme,UBERON:0006904,head mesenchyme from mesoderm
+UBERON:2001450,apical ectodermal ridge pelvic fin,UBERON:0004121,ectoderm-derived structure
+UBERON:0004991,mucosa of transverse colon,UBERON:0000317,colonic mucosa
+HP:0012637,Renal calcium wasting,HP:0011280,Abnormality of urine calcium concentration
+UBERON:3000022,antorbital process,UBERON:4100000,skeletal element projection
+UBERON:2000993,lateral wall neural rod,UBERON:0005291,embryonic tissue
+UBERON:2005038,supraintestinal vein,UBERON:0003513,trunk blood vessel
+UBERON:2001820,posterior nuchal plate,UBERON:2001815,nuchal plate
+CL:1001220,arcuate vein endothelial cell,CL:0002543,vein endothelial cell
+UBERON:0005256,trunk mesenchyme,UBERON:0005291,embryonic tissue
+DOID:13945,cadasil,DOID:10579,leukodystrophy
+DOID:3610,breast mucinous carcinoma,DOID:3458,breast adenocarcinoma
+UBERON:0014934,cerebral cortex mantle layer,UBERON:0014950,layer of developing cerebral cortex
+HP:0100094,Abnormality of the epiphysis of the distal phalanx of the 4th toe,HP:0010335,Abnormality of the epiphyses of the 4th toe
+UBERON:0004723,interlobular artery,UBERON:0003644,kidney arterial blood vessel
+UBERON:2001043,sclerotome somite 27,UBERON:0003089,sclerotome
+UBERON:0013598,accessory nucleus of optic tract,UBERON:0009661,midbrain nucleus
+HP:0003859,Cortical diaphyseal thickening of the upper limbs,HP:0009808,Anomaly of the upper limb diaphyses
+HP:0010934,Xanthinuria,HP:0010933,Abnormality of xanthine metabolism
+UBERON:0010566,manual digit 2 metacarpus pre-cartilage condensation,UBERON:0010576,manual digit 2 phalanx pre-cartilage condensation
+HP:0006291,Marked delay in eruption of permanent teeth,HP:0000696,Delayed eruption of permanent teeth
+CL:0002473,MHC-II-high non-classical monocyte,CL:0002058,Gr1-low non-classical monocyte
+HP:0011028,Abnormality of blood circulation,HP:0011025,Abnormality of cardiovascular system physiology
+UBERON:0012108,postorbital bar,UBERON:0005913,zone of bone organ
+HP:0000153,Abnormality of the mouth,HP:0000271,Abnormality of the face
+UBERON:0002918,medial parabrachial nucleus,UBERON:0007634,parabrachial nucleus
+NCBITaxon:49202,Dermacentor marginatus,NCBITaxon:34619,Dermacentor
+HP:0006088,1-5 finger complete cutaneous syndactyly,HP:0010554,Cutaneous finger syndactyly
+DOID:0060162,dentatorubral-pallidoluysian atrophy,DOID:2478,spinocerebellar degeneration
+UBERON:2000240,metapterygoid,UBERON:0002513,endochondral bone
+HP:0012432,Chronic fatigue,HP:0012378,Fatigue
+UBERON:0006582,statolith,UBERON:0000476,acellular anatomical structure
+DOID:5798,macrotrabecular hepatoblastoma,DOID:687,hepatoblastoma
+UBERON:0001768,uvea,UBERON:0002203,vasculature of eye
+UBERON:0001545,anterior tibial vein,UBERON:0010370,tibial vein
+UBERON:0005146,metanephric nephron tubule,UBERON:0005106,metanephric tubule
+UBERON:0007142,left internal carotid artery,UBERON:0001532,internal carotid artery
+UBERON:0011598,coronoid bone,UBERON:0008907,dermal bone
+UBERON:0013217,zygomatic plate,UBERON:0004120,mesoderm-derived structure
+UBERON:0003833,abdominal segment muscle,UBERON:0001774,muscle of trunk
+DOID:11840,coronary artery vasospasm,DOID:3393,coronary artery disease
+UBERON:2001700,caudal-fin stay,UBERON:0004376,fin bone
+HP:0000796,Urethral obstruction,HP:0000795,Abnormality of the urethra
+DOID:0050812,"spondyloepimetaphyseal dysplasia, Pakistani type",DOID:0080027,spondyloepimetaphyseal dysplasia
+UBERON:0005442,external oblique,UBERON:0002461,anterior abdominal wall muscle
+CL:0000845,marginal zone B cell,CL:0000785,mature B cell
+UBERON:0009671,nasal fin,UBERON:0000481,multi-tissue structure
+UBERON:0011379,male external urethral sphincter,UBERON:0004919,external urethral sphincter
+UBERON:0002295,scala media,UBERON:0011060,perilymphatic channel
+UBERON:4200014,lateral tuber of ulna,UBERON:4100000,skeletal element projection
+UBERON:0001848,auricular cartilage,UBERON:0007844,cartilage element
+HP:0011235,Additional crus of antihelix,HP:0009738,Abnormality of the antihelix
+CL:1000854,kidney blood vessel cell,CL:0002584,renal cortical epithelial cell
+DOID:0050131,motility-related diarrhea,DOID:13250,diarrhea
+UBERON:0003674,cuspid,UBERON:0001091,calcareous tooth
+UBERON:0002473,intercerebral commissure,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2002070,internal anterior process of basipterygium,UBERON:4100000,skeletal element projection
+HP:0010213,Contractures of the tarsometatarsal joint of the hallux,HP:0010212,Flexion contracture of the hallux
+DOID:14116,multiple symmetric lipomatosis,DOID:3153,lipomatosis
+UBERON:2000285,superficial adductor,UBERON:0011145,adductor muscle
+UBERON:0002944,spinothalamic tract of medulla,UBERON:0007702,tract of brain
+HP:0011479,Abnormality of the lacrimal punctum,HP:0000614,Abnormality of the nasolacrimal system
+CL:0000358,sphincter associated smooth muscle cell,CL:0000192,smooth muscle cell
+UBERON:0004267,back connective tissue,UBERON:0002384,connective tissue
+CL:0010004,mononuclear cell of bone marrow,CL:1001610,bone marrow hematopoietic cell
+DOID:6976,micropapillary variant infiltrating bladder urothelial carcinoma,DOID:6477,invasive bladder transitional cell carcinoma
+UBERON:0010585,pedal digit phalanx pre-cartilage condensation,UBERON:0010886,hindlimb bone pre-cartilage condensation
+CL:1000681,kidney cortex interstitial cell,CL:1000500,kidney interstitial cell
+UBERON:0006693,protein-based cuticle,UBERON:0001002,cuticle
+UBERON:0013759,internal cervical os,UBERON:0013758,cervical os
+UBERON:0001945,superior colliculus,UBERON:0002966,regional part of midbrain tectum
+HP:0001953,Diabetic ketoacidosis,HP:0000819,Diabetes mellitus
+HP:0006505,Abnormality involving the epiphyses of the limbs,HP:0005930,Abnormality of the epiphyses
+HP:0003914,Irregular ossification of humeral metaphyses,HP:0011849,Abnormal bone ossification
+UBERON:2002145,anterior swim bladder bud,UBERON:0000479,tissue
+HP:0006926,Metachromatic leukodystrophy variant,HP:0002415,Leukodystrophy
+HP:0008141,Dislocation of toes,HP:0001780,Abnormality of toe
+HP:0006916,Intraaxonal accumulation of curvilinear autofluorescent lipopigment storage material,HP:0003205,Curvilinear intracellular accumulation of autofluorescent lipopigment storage material
+UBERON:0003909,sinusoid,UBERON:2005260,fenestrated capillary
+DOID:7340,pediatric ovarian dysgerminoma,DOID:5511,dysgerminoma of ovary
+DOID:9502,chronic eosinophilic pneumonia,DOID:5870,eosinophilic pneumonia
+UBERON:0012499,serosa of uterine tube,UBERON:0014404,female anatomical structure
+DOID:4194,glucose metabolism disease,DOID:0050013,carbohydrate metabolism disease
+HP:0007807,Optic nerve compression,HP:0001293,Cranial nerve compression
+CL:0000540,neuron,CL:0002319,neural cell
+HP:0006064,Limited interphalangeal movement,HP:0006261,Abnormality of phalangeal joints of the hand
+CL:0000388,tendon cell,CL:0000135,fibrocyte
+UBERON:0015241,parapineal organ,UBERON:0003103,compound organ
+UBERON:0013428,ophryon,UBERON:0006983,anatomical point
+HP:0009319,Joint contractures of the 3rd finger,HP:0100490,Camptodactyly of finger
+UBERON:0012329,keratinized stratified squamous epithelium,UBERON:0006915,stratified squamous epithelium
+HP:0010076,Aplasia/Hypoplasia of the distal phalanx of the hallux,HP:0010058,Aplasia/Hypoplasia of the phalanges of the hallux
+UBERON:0002567,basal part of pons,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2001427,anterior naris,UBERON:0005928,external naris
+UBERON:0010345,4th arch mesenchyme from head mesenchyme,UBERON:0005691,4th arch mesenchyme
+UBERON:0014689,middle temporal sulcus,UBERON:0014687,temporal sulcus
+UBERON:0002447,palatine gland,UBERON:0001830,minor salivary gland
+HP:0008278,Cerebellar cortical atrophy,HP:0001272,Cerebellar atrophy
+HP:0003271,Visceromegaly,HP:0002012,Abnormality of the abdominal organs
+HP:0004970,Ascending aortic dilation,HP:0005111,Dilatation of the ascending aorta
+HP:0006503,Aplasia/Hypoplasia involving forearm bones,HP:0006496,Aplasia/Hypoplasia involving bones of the upper limbs
+HP:0000361,Pulsatile tinnitus (tympanic paraganglioma),HP:0008629,Pulsatile tinnitus
+UBERON:0013748,ulnar metaphysis,UBERON:0001438,metaphysis
+HP:0005901,Chronic recurrent multifocal osteomyelitis,HP:0002754,Osteomyelitis
+HP:0009454,Patchy sclerosis of the proximal phalanx of the 3rd finger,HP:0009358,Abnormality of the proximal phalanx of the 3rd finger
+HP:0011864,Elevated plasma pyrophosphate,HP:0100529,Abnormality of phosphate homeostasis
+UBERON:0011591,tract of diencephalon,UBERON:0007702,tract of brain
+UBERON:0010359,pharyngeal arch mesenchyme from neural crest,UBERON:0005291,embryonic tissue
+HP:0000395,Prominent antihelix,HP:0009738,Abnormality of the antihelix
+HP:0002669,Osteosarcoma,HP:0010622,Neoplasm of the skeletal system
+UBERON:0005460,left vitelline vein,UBERON:0005487,vitelline vein
+DOID:4653,intraocular retinoblastoma,DOID:768,retinoblastoma
+UBERON:2000872,epaxial region somite 29,UBERON:0003900,epaxial myotome region
+HP:0005195,Polyarticular arthropathy,HP:0003040,Arthropathy
+UBERON:0004527,alveolar process of maxilla,UBERON:0004103,alveolar ridge
+DOID:2977,primary hyperoxaluria,DOID:2978,carbohydrate metabolic disorder
+HP:0100541,Femoral hernia,HP:0004299,Hernia of the abdominal wall
+HP:0001773,Short foot,HP:0001772,Talipes equinovalgus
+UBERON:0012646,tubeworm tube,UBERON:0000062,organ
+UBERON:2000748,epaxial region somite 6,UBERON:0003900,epaxial myotome region
+HP:0010062,Osteolytic defects of the phalanges of the hallux,HP:0010177,Osteolytic defects of the phalanges of the toes
+UBERON:0010412,epididymal fat pad,UBERON:0003916,fat pad
+UBERON:0003649,metacarpal bone of digit 5,UBERON:0015047,manual digit 5 metacarpus endochondral element
+UBERON:0005124,metanephric proximal convoluted tubule,UBERON:0005151,metanephric proximal tubule
+DOID:1949,cholecystitis,DOID:0000000,gallbladder disease
+HP:0004260,Large hamate bone,HP:0004237,Large carpal bones
+UBERON:0008288,feather rachis,UBERON:0011784,feather shaft
+DOID:9351,diabetes mellitus,DOID:4194,glucose metabolism disease
+UBERON:0000332,yellow bone marrow,UBERON:0001013,adipose tissue
+UBERON:2000592,superficial pelvic adductor,UBERON:0014795,pelvic appendage muscle
+UBERON:0008582,superior longitudinal muscle of tongue,UBERON:0012369,longitudinal muscle layer
+UBERON:0002130,cerebellar nuclear complex,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0001701,Pericarditis,HP:0001697,Abnormality of the pericardium
+NCBITaxon:42415,Sigmodon hispidus,NCBITaxon:42414,Sigmodon
+UBERON:2007005,hemal prezygapophysis,UBERON:0004120,mesoderm-derived structure
+UBERON:3010182,tibial glands,UBERON:3010606,limb glands
+UBERON:0004200,kidney pyramid,UBERON:0006554,urinary system structure
+UBERON:3010706,lateral line nucleus,UBERON:0000064,organ part
+HP:0000637,Long palpebral fissure,HP:0200007,Abnormal size of the palpebral fissures
+HP:0009619,Accessory phalanx of the thumb,HP:0009602,Abnormality of the phalanges of the thumb
+HP:0005745,Congenital foot contractures,HP:0002803,Congenital contracture
+HP:0012720,Neoplasm of the nose,HP:0000366,Abnormality of the nose
+HP:0004213,Abnormality of the phalanges of the 5th finger,HP:0005918,Abnormality of phalanx of finger
+UBERON:2001299,vagal placode 3,UBERON:0003078,epibranchial placode
+UBERON:0008596,mentalis,UBERON:0001577,facial nerve muscle
+DOID:2750,glycogen storage disease IV,DOID:2747,glycogen storage disease
+CL:0000199,mechanoreceptor cell,CL:0000006,neuronal receptor cell
+DOID:0050591,tooth agenesis,DOID:1091,tooth disease
+UBERON:2001201,ventral lateral mesoderm,UBERON:2000083,ventral mesoderm
+CL:1000350,basal cell of epithelium of terminal bronchiole,CL:1000352,basal cell of epithelium of lobular bronchiole
+UBERON:2000851,somite 12,UBERON:0002329,somite
+UBERON:0011332,extrinsic tongue pre-muscle mass,UBERON:0005865,pre-muscle condensation
+HP:0010367,Duplication of phalanx of the 3rd toe,HP:0010330,Abnormality of the phalanges of the 3rd toe
+HP:0008826,Dislocation of the femoral head,HP:0003368,Abnormality of the femoral head
+UBERON:0006239,future central tendon,UBERON:0004120,mesoderm-derived structure
+HP:0002166,Impaired vibration sensation in the lower limbs,HP:0002495,Impaired vibratory sensation
+DOID:0050574,L-2-hydroxyglutaric aciduria,DOID:0050573,2-hydroxyglutaric aciduria
+HP:0010293,Aplasia/Hypoplasia of the uvula,HP:0000172,Abnormality of the uvula
+UBERON:0002494,papillary muscle of heart,UBERON:0000064,organ part
+UBERON:4300013,paired fin radial skeleton,UBERON:0004120,mesoderm-derived structure
+CL:0001007,interstitial dendritic cell,CL:0002465,CD11b-positive dendritic cell
+UBERON:0011698,midgut loop,UBERON:0004921,subdivision of digestive tract
+UBERON:0003279,endothelium of trachea,UBERON:0001986,endothelium
+HP:0010068,Broad first metatarsal,HP:0001783,Broad metatarsal
+UBERON:0003387,smooth muscle of trachea,UBERON:0004233,lower respiratory tract smooth muscle
+UBERON:0005680,right lung accessory lobe segmental bronchus,UBERON:0002184,segmental bronchus
+DOID:13413,hepatic encephalopathy,DOID:936,brain disease
+DOID:7016,tendon sheath lipoma,DOID:315,synovium neoplasm
+HP:0009201,Stippling of the epiphysis of the proximal phalanx of the 5th finger,HP:0009391,Stippling of the epiphyses of the 5th finger
+HP:0004953,Abdominal aortic aneurysm,HP:0004942,Aortic aneurysm
+UBERON:0003097,dorsal fin,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0009503,associated mesenchyme of hindgut,UBERON:0003104,mesenchyme
+HP:0011218,Abnormal shape of the frontal region,HP:0002648,Abnormality of calvarial morphology
+UBERON:0014777,spinal neuromere,UBERON:0004731,neuromere
+HP:0100228,Fragmentation of the epiphysis of the proximal phalanx of the 5th toe,HP:0100099,Abnormality of the epiphysis of the proximal phalanx of the 5th toe
+UBERON:0012367,muscle layer of intestine,UBERON:0006660,muscle layer
+UBERON:0002786,abducens nerve fibers,UBERON:0010314,structure with developmental contribution from neural crest
+NCBITaxon:45709,Sabia virus,NCBITaxon:208897,New world arenaviruses
+HP:0010970,Blood group antigen abnormality,HP:0001877,Abnormality of erythrocytes
+DOID:4334,splenic manifestation of prolymphocytic leukemia,DOID:1039,prolymphocytic leukemia
+HP:0011360,Acquired abnormal hair pattern,HP:0010720,Abnormal hair pattern
+UBERON:0011974,epiphysis of proximal phalanx of pes,UBERON:0011973,epiphysis of phalanx of pes
+DOID:13252,mesenteric vascular occlusion,DOID:341,peripheral vascular disease
+DOID:5732,pyosalpinx,DOID:5733,salpingitis
+HP:0100011,Scleral schwannoma,HP:0100012,Neoplasm of the eye
+DOID:0050547,familial medullary thyroid carcinoma,DOID:3973,thyroid medullary carcinoma
+DOID:4791,supratentorial primitive neuroectodermal tumor,DOID:1659,supratentorial cancer
+HP:0010046,Aplasia of the 5th metacarpal,HP:0010045,Aplasia/Hypoplasia of the 5th metacarpal
+UBERON:0003082,myotome,UBERON:0012275,meso-epithelium
+UBERON:0000473,testis,UBERON:0000991,gonad
+UBERON:0002859,fifth lumbar dorsal root ganglion,UBERON:0002836,lumbar dorsal root ganglion
+HP:0011536,Right atrial isomerism,HP:0011535,Abnormal atrial arrangement
+UBERON:3010105,anterodorsal lateral line nerve (ADLLN),UBERON:0008906,lateral line nerve
+UBERON:0003234,extensor pollicis longus muscle,UBERON:0011024,extrinsic extensor muscle of manus
+UBERON:0001103,diaphragm,UBERON:0003830,thoracic segment muscle
+HP:0003819,Death in childhood,HP:0011420,Death
+DOID:7665,non-gestational ovarian choriocarcinoma,DOID:5550,choriocarcinoma of ovary
+CL:0002464,SIRPa-negative adipose dendritic cell,CL:0002462,adipose dendritic cell
+HP:0100753,Schizophrenia,HP:0000708,Behavioural/Psychiatric Abnormality
+UBERON:0001514,descending aorta,UBERON:0005800,segment of aorta
+DOID:5556,testicular malignant germ cell cancer,DOID:5557,testicular germ cell cancer
+DOID:13810,familial hypercholesterolemia,DOID:1168,familial hyperlipidemia
+HP:0008180,Mildly elevated creatine phosphokinase,HP:0003236,Elevated serum creatine phosphokinase
+UBERON:0000487,simple squamous epithelium,UBERON:0000490,unilaminar epithelium
+DOID:9120,amyloidosis,DOID:0060158,acquired metabolic disease
+HP:0004330,Increased skull ossification,HP:0011001,Increased bone mineral density
+HP:0007109,Periventricular cysts,HP:0002518,Abnormality of the periventricular white matter
+HP:0001324,Muscle weakness,HP:0011804,Abnormality of muscle physiology
+UBERON:0004147,cardiac Purkinje fiber,UBERON:0004120,mesoderm-derived structure
+UBERON:2001733,mesethmoid ventral diverging lamella,UBERON:4100000,skeletal element projection
+UBERON:0009091,vasa recta ascending limb,UBERON:0000064,organ part
+DOID:3223,complex regional pain syndrome,DOID:11465,autonomic nervous system disease
+UBERON:0009878,mesopodial skeleton,UBERON:0004120,mesoderm-derived structure
+HP:0005224,Rectal abscess,HP:0002722,Recurrent abscess formation
+HP:0000581,Blepharophimosis,HP:0200007,Abnormal size of the palpebral fissures
+CL:0000847,ciliated olfactory receptor neuron,CL:0000064,ciliated cell
+CL:0000047,neuronal stem cell,CL:0000048,multi fate stem cell
+HP:0008723,"Gonadal dysgenesis with female appearance, male",HP:0000133,Gonadal dysgenesis
+DOID:3861,medullomyoblastoma,DOID:0050902,medulloblastoma
+HP:0007274,Recurrent bacterial meningitis,HP:0006946,Recurrent meningitis
+HP:0010661,Absence of the third cerebral ventricle,HP:0010951,Abnormality of the third ventricle
+UBERON:0005399,male reproductive gland,UBERON:0003937,sex gland
+UBERON:0005562,thymus primordium,UBERON:0001048,primordium
+UBERON:0009651,nephron tubule basement membrane,UBERON:0005769,basement membrane of epithelium
+UBERON:0005932,bulb of hair follicle,UBERON:0004121,ectoderm-derived structure
+UBERON:4200040,acrocoracoid process,UBERON:4100000,skeletal element projection
+UBERON:0010256,4th arch mesenchyme from neural crest,UBERON:0010359,pharyngeal arch mesenchyme from neural crest
+DOID:0050441,mucosulfatidosis,DOID:1927,sphingolipidosis
+CL:0002503,adventitial cell,CL:0000630,supportive cell
+DOID:456,ascariasis,DOID:883,parasitic helminthiasis infectious disease
+UBERON:0006309,venous vitelline plexus,UBERON:0002050,embryonic structure
+UBERON:0004519,muscle of anal triangle,UBERON:0002379,perineal muscle
+HP:0009028,Generalized weakness of limb muscles,HP:0009127,Abnormality of the musculature of the limbs
+HP:0009569,Broad middle phalanx of the 2nd finger,HP:0009543,Abnormality of the middle phalanx of the 2nd finger
+UBERON:0001986,endothelium,UBERON:0000487,simple squamous epithelium
+UBERON:0011107,synovial joint of pelvic girdle,UBERON:0008114,joint of girdle
+HP:0008116,Flexion limitation of toes,HP:0001436,Abnormality of the foot musculature
+DOID:9423,blepharitis,DOID:530,eyelid disease
+UBERON:0011655,interclavicle,UBERON:0008907,dermal bone
+DOID:13078,eumycotic mycetoma,DOID:1563,dermatomycosis
+UBERON:0004288,skeleton,UBERON:0000477,anatomical cluster
+HP:0009218,Fragmentation of the epiphysis of the middle phalanx of the 4th finger,HP:0009397,Fragmentation of the epiphyses of the 4th finger
+UBERON:0005194,thoracic vein,UBERON:0003834,thoracic segment blood vessel
+UBERON:0001822,orbital septum,UBERON:0004121,ectoderm-derived structure
+UBERON:0004882,eponychium,UBERON:0004121,ectoderm-derived structure
+UBERON:0009907,sensory root of trigeminal nerve,UBERON:0004673,trigeminal nerve root
+HP:0007798,Foveal dystrophy,HP:0000493,Abnormality of the fovea
+HP:0009310,Broad proximal phalanx of the 4th finger,HP:0009284,Abnormality of the proximal phalanx of the 4th finger
+UBERON:0013469,external occipital protuberance,UBERON:0004120,mesoderm-derived structure
+UBERON:4200135,puboischiadic bar,UBERON:0007844,cartilage element
+UBERON:4200105,nerve foramen,UBERON:0004111,anatomical conduit
+CL:1000715,kidney cortex collecting duct intercalated cell,CL:0002584,renal cortical epithelial cell
+DOID:0050789,tarsal-carpal coalition syndrome,DOID:0050736,autosomal dominant disease
+HP:0009543,Abnormality of the middle phalanx of the 2nd finger,HP:0009541,Abnormality of the phalanges of the 2nd finger
+HP:0100797,Toenail dysplasia,HP:0008388,Abnormality of the toenail
+UBERON:0011138,post-cranial axial skeletal system,UBERON:0000075,subdivision of skeletal system
+HP:0007516,Redundant skin on fingers,HP:0001582,Redundant skin
+HP:0000272,Malar flattening,HP:0012369,Malar anomaly
+UBERON:2205384,dorsal fin proximal radial cartilage 7,UBERON:2105384,dorsal fin proximal radial element 7
+HP:0005093,Absent proximal radial epiphyses,HP:0010596,Abnormality of the proximal radial epiphysis
+HP:0200125,Mitochondrial respiratory chain defects,HP:0003287,Abnormality of mitochondrial metabolism
+HP:0009132,Abnormal tarsal bone mineral density,HP:0004348,Abnormality of bone mineral density
+DOID:7442,monoclonal gammopathy of uncertain significance,DOID:6536,plasma cell neoplasm
+HP:0003906,Broad humeral epiphyseal plate,HP:0003905,Abnormality of the humeral epiphyseal plate
+UBERON:0005410,cartilaginous otic capsule,UBERON:0009891,facial mesenchyme
+NCBITaxon:11320,Influenza A virus,NCBITaxon:197911,Influenzavirus A
+UBERON:0011643,puboischiofemoralis internus muscle,UBERON:0001325,muscle of pelvis
+HP:0001412,Enteroviral hepatitis,HP:0006562,Viral hepatitis
+HP:0009772,Patchy sclerosis of the phalanges of the hand,HP:0005686,Patchy osteosclerosis
+HP:0012064,Unicameral bone cyst,HP:0012062,Bone cyst
+UBERON:0009204,medial nasal process mesenchyme,UBERON:0009501,mesenchyme of fronto-nasal process
+UBERON:0000981,femur,UBERON:0008202,bone of hip region
+HP:0000108,Renal corticomedullary cysts,HP:0011035,Abnormality of the renal cortex
+UBERON:0002252,splenius,UBERON:0004518,muscle of vertebral column
+UBERON:0007155,superior epigastric vein,UBERON:0006356,epigastric vein
+UBERON:2005372,dorsal fin distal radial bone 1,UBERON:2000936,dorsal fin distal radial bone
+UBERON:0014511,somatosensory system,UBERON:0001032,sensory system
+HP:0004755,Supraventricular tachycardia,HP:0005115,Supraventricular arrhythmia
+HP:0006205,Irregular phalanges,HP:0005918,Abnormality of phalanx of finger
+UBERON:0006234,femur pre-cartilage condensation,UBERON:0015052,femur endochondral element
+HP:0009823,Aplasia involving bones of the upper limbs,HP:0009825,Aplasia involving bones of the extremities
+UBERON:0003364,epithelium of right lung,UBERON:0000115,lung epithelium
+DOID:11637,accommodative spasm,DOID:10034,eye accommodation disease
+HP:0001402,Hepatocellular carcinoma,HP:0002896,Neoplasm of the liver
+HP:0009304,Patchy sclerosis of the distal phalanx of the 4th finger,HP:0009406,Patchy sclerosis of the phalanges of the 4th finger
+DOID:10923,sickle cell anemia,DOID:0050737,autosomal recessive disease
+UBERON:2000210,gigantocellular part of magnocellular preoptic nucleus,UBERON:0000479,tissue
+UBERON:0001294,inner medulla of kidney,UBERON:0000064,organ part
+UBERON:0010523,microcirculatory vessel,UBERON:0000055,vessel
+UBERON:2000777,hypaxial region somite 9,UBERON:0003895,hypaxial myotome region
+UBERON:0011183,corpus spongiosum of penis,UBERON:0005156,reproductive structure
+NCBITaxon:713,Actinobacillus,NCBITaxon:712,Pasteurellaceae
+DOID:3517,conventional fibrosarcoma,DOID:3355,fibrosarcoma
+HP:0011520,Deuteranomoly,HP:0000642,Red-green dyschromatopsia
+HP:0008256,Adrenocortical adenoma,HP:0100641,Neoplasm of the adrenal cortex
+UBERON:0004240,gall bladder smooth muscle,UBERON:0001135,smooth muscle tissue
+UBERON:0000329,hair root,UBERON:0004121,ectoderm-derived structure
+UBERON:0002073,hair follicle,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005354,malleus processus brevis,UBERON:0010313,neural crest-derived structure
+UBERON:3000953,ceratobranchials II--IV,UBERON:0000477,anatomical cluster
+UBERON:0004512,skeletal muscle tissue of supraspinatus,UBERON:0001134,skeletal muscle tissue
+HP:0002242,Abnormality of the intestine,HP:0012718,Morphological abnormality of the gastrointestinal tract
+DOID:14251,vitreoretinal dystrophy,DOID:8501,fundus dystrophy
+DOID:4992,optic nerve glioma,DOID:3419,optic nerve neoplasm
+UBERON:0004528,alveolar ridge of mandible,UBERON:0004103,alveolar ridge
+UBERON:2001880,rib of vertebra 3,UBERON:0002228,rib
+UBERON:0002113,kidney,UBERON:0000489,cavitated compound organ
+DOID:2055,post-traumatic stress disorder,DOID:2030,anxiety disorder
+UBERON:0002450,decidua,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:14497,Wolman disease,DOID:9455,lipid storage disease
+DOID:2817,cranial nerve III tumor,DOID:338,cranial nerve neoplasm
+HP:0007678,Lacrimal duct stenosis,HP:0000579,Nasolacrimal duct obstruction
+UBERON:0005110,metanephric nephron,UBERON:0004120,mesoderm-derived structure
+UBERON:0003825,nerve of abdominal segment,UBERON:0003439,nerve of trunk region
+HP:0012247,Specific anosmia,HP:0000458,Anosmia
+UBERON:0014694,posterior auricular artery,UBERON:0009655,auricular artery
+DOID:5767,hilar lung neoplasm,DOID:3683,lung benign neoplasm
+NCBITaxon:1762,Mycobacteriaceae,NCBITaxon:85007,Corynebacterineae
+HP:0009705,Synostosis involving the 2nd metacarpal,HP:0010010,Abnormality of the 2nd metacarpal
+DOID:3907,lung squamous cell carcinoma,DOID:3908,non-small cell lung carcinoma
+CL:0000542,lymphocyte,CL:0002087,nongranular leukocyte
+NCBITaxon:34620,Dermacentor andersoni,NCBITaxon:34619,Dermacentor
+UBERON:0011147,Verson's gland,UBERON:0002365,exocrine gland
+UBERON:2000271,radial bone,UBERON:2100271,radial element
+UBERON:0006574,pectinate line,UBERON:0000015,anatomical boundary
+HP:0005689,Dermatoglyphic ridges abnormal,HP:0001018,Abnormal palmar dermatoglyphics
+UBERON:0004391,epiphysis of first metacarpal bone,UBERON:0004390,epiphysis of metacarpal bone
+HP:0010186,Broad distal phalanx of the toes,HP:0010182,Abnormality of the distal phalanges of the toes
+UBERON:0001311,inferior vesical artery,UBERON:0005192,deferent duct artery
+UBERON:0002612,transverse orbital sulcus,UBERON:0003022,cerebral cortex lobe
+HP:0009240,Broad distal phalanx of the 5th finger,HP:0004225,Abnormality of the distal phalanx of the 5th finger
+UBERON:0001675,trigeminal ganglion,UBERON:0010313,neural crest-derived structure
+UBERON:2000852,somite 15,UBERON:0002329,somite
+UBERON:0001952,epithelium of oropharynx,UBERON:0004808,gastrointestinal system epithelium
+HP:0002592,Gastric ulcer,HP:0004295,Abnormality of the gastric mucosa
+HP:0005830,Flexion contracture of toe,HP:0001780,Abnormality of toe
+DOID:856,biotinidase deficiency,DOID:857,multiple carboxylase deficiency
+HP:0010081,Patchy sclerosis of the distal phalanx of the hallux,HP:0010063,Patchy sclerosis of the phalanges of the hallux
+UBERON:0004866,actinopterygian frontal bone,UBERON:0008907,dermal bone
+HP:0006174,Metacarpal diaphyseal endosteal sclerosis,HP:0011001,Increased bone mineral density
+UBERON:0006089,dorsal external arcuate fiber bundle,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0011593,maxillary tooth,UBERON:0003267,tooth of upper jaw
+DOID:12029,sympathetic ophthalmia,DOID:12030,panuveitis
+UBERON:0005316,endocardial endothelium,UBERON:0004638,blood vessel endothelium
+UBERON:2001958,ceratobranchial 3 bone distal cartilage,UBERON:4000003,permanent cartilage
+UBERON:0003129,skull,UBERON:0000075,subdivision of skeletal system
+DOID:10811,nasal cavity cancer,DOID:0050615,respiratory system cancer
+HP:0010039,Aplasia/Hypoplasia of the 3rd metacarpal,HP:0010011,Abnormality of the 3rd metacarpal
+DOID:0060101,benign glioma,DOID:0060084,cell type benign neoplasm
+HP:0009167,Irregular epiphysis of the distal phalanx of the 5th finger,HP:0009198,Abnormality of the epiphysis of the distal phalanx of the 5th finger
+UBERON:2005030,dorsal ciliary vein,UBERON:0009141,craniocervical region vein
+HP:0002246,Abnormality of the duodenum,HP:0002244,Abnormality of the small intestine
+HP:0010078,Bullet-shaped distal phalanx of the hallux,HP:0010187,Bullet-shaped distal phalanges of the toes
+UBERON:0005810,cervical vertebra 1 anterior tubercle,UBERON:0005813,tubercle
+UBERON:0013135,interdental plate,UBERON:0005913,zone of bone organ
+DOID:9506,acute ethmoiditis,DOID:9507,ethmoid sinusitis
+UBERON:0000461,minor vestibular gland,UBERON:0010145,paraurethral gland
+UBERON:0002994,nucleus of pretectal area,UBERON:0014450,pretectal nucleus
+HP:0010917,Abnormality of tyrosine metabolism,HP:0004338,Abnormality of aromatic amino acid family metabolism
+CL:0002638,bronchioalveolar stem cell,CL:1000350,basal cell of epithelium of terminal bronchiole
+UBERON:0006857,interrenal primordium,UBERON:0006554,urinary system structure
+HP:0008724,Hypoplasia of the ovary,HP:0010462,Aplasia/Hypoplasia of the ovary
+UBERON:0013155,1st arch mandibular ectoderm,UBERON:0000490,unilaminar epithelium
+UBERON:4400007,camptotrichium,UBERON:4300037,bony fin ray
+UBERON:0006799,glandular epithelium,UBERON:0000483,epithelium
+HP:0011684,Non-restrictive ventricular septal defect,HP:0001629,Ventricular septal defect
+UBERON:2000947,dorsal fin proximal radial bone,UBERON:2001672,dorsal fin radial bone
+UBERON:0005967,conotruncal ridge,UBERON:0005256,trunk mesenchyme
+DOID:3068,glioblastoma multiforme,DOID:3069,astrocytoma
+UBERON:0003427,abdominal fat pad,UBERON:0007808,adipose tissue of abdominal region
+UBERON:0011242,ethmoid cartilage,UBERON:0004120,mesoderm-derived structure
+UBERON:0004344,cardinal vein,UBERON:0001638,vein
+HP:0009517,Fragmentation of the epiphysis of the middle phalanx of the 2nd finger,HP:0010261,Fragmentation of the epiphyses of the middle phalanges of the hand
+UBERON:0003500,corneal blood vessel,UBERON:0003496,head blood vessel
+UBERON:0013477,blowhole,UBERON:0005928,external naris
+DOID:1440,Machado-Joseph disease,DOID:1441,spinocerebellar ataxia
+UBERON:0007332,mandibular rhamphotheca,UBERON:0007330,rhamphotheca
+UBERON:0005582,rhombomere 6 floor plate,UBERON:0005500,rhombomere floor plate
+UBERON:0006908,fast muscle tissue,UBERON:0001134,skeletal muscle tissue
+HP:0100932,Sclerosis of the proximal phalanx of the 3rd toe,HP:0100946,Sclerosis of the proximal phalanges of the toes
+HP:0003634,Generalized amyoplasia,HP:0100854,Aplasia of the musculature
+DOID:5039,myoblastoma,DOID:461,muscle benign neoplasm
+UBERON:0004650,tongue keratinized epithelium,UBERON:0012329,keratinized stratified squamous epithelium
+HP:0008273,Transient aminoaciduria,HP:0003355,Aminoaciduria
+NCBITaxon:5796,Coccidia,NCBITaxon:1280412,Conoidasida
+DOID:3753,Hermansky-Pudlak syndrome,DOID:0050737,autosomal recessive disease
+UBERON:0004422,proximal epiphysis of first metacarpal bone,UBERON:0004416,proximal epiphysis of metacarpal bone
+HP:0011863,Abnormal sternal ossification,HP:0000766,Abnormality of the sternum
+UBERON:0005600,crus commune,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0007724,interphalangeal joint of pedal digit 1,UBERON:0007721,interphalangeal joint of pes
+CL:1000415,epithelial cell of gall bladder,CL:0000066,epithelial cell
+HP:0200059,Metastatic angiosarcoma,HP:0200058,Angiosarcoma
+DOID:474,histiocytoid hemangioma,DOID:255,hemangioma
+HP:0010277,Stippling of the epiphyses of the proximal phalanges of the hand,HP:0010237,Epiphyseal stippling of finger phalanges
+HP:0011649,Patent ductus arteriosus after premature birth,HP:0001643,Patent ductus arteriosus
+DOID:6101,signet ring cell variant cervical mucinous adenocarcinoma,DOID:3701,cervical mucinous adenocarcinoma
+UBERON:4200013,flexor surface,UBERON:0006984,anatomical surface
+UBERON:0003467,sesamoid bone of gastrocnemius,UBERON:0001479,sesamoid bone
+UBERON:0002285,telencephalic ventricle,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0000505,Visual impairment,HP:0000504,Abnormality of vision
+HP:0100185,Irregular epiphysis of the middle phalanx of the 4th toe,HP:0100095,Abnormality of the epiphysis of the middle phalanx of the 4th toe
+HP:0000773,Short ribs,HP:0006712,Aplasia/Hypoplasia of the ribs
+HP:0006101,Finger syndactyly,HP:0001159,Syndactyly
+DOID:1247,blood coagulation disease,DOID:74,hematopoietic system disease
+CL:0002531,mature CD1a-positive dermal dendritic cell,CL:0002529,CD1a-positive dermal dendritic cell
+UBERON:0003280,endothelium of main bronchus,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:1492,eye and adnexa disease,DOID:0050155,sensory system disease
+CL:0000515,skeletal muscle myoblast,CL:0000056,myoblast
+UBERON:0005076,hindbrain-spinal cord boundary,UBERON:0000015,anatomical boundary
+UBERON:0009632,root of cervical nerve,UBERON:0009623,spinal nerve root
+UBERON:0001975,serosa of esophagus,UBERON:0000042,serous membrane
+UBERON:2001593,caudal fin upper lobe,UBERON:0003102,surface structure
+DOID:11223,small intestine diverticulitis,DOID:5295,intestinal disease
+UBERON:0011684,levator palatoquadrati,UBERON:0011648,jaw muscle
+UBERON:0000433,posterior paraventricular nucleus of thalamus,UBERON:0001920,paraventricular nucleus of thalamus
+HP:0004406,"Spontaneous, recurrent epistaxis",HP:0000421,Epistaxis
+UBERON:0008780,inner cell mass derived epiblast,UBERON:0002532,epiblast (generic)
+UBERON:3000689,prominentia apicalis ventralis,UBERON:0000072,segment of respiratory tract
+DOID:14019,Brucella canis brucellosis,DOID:11077,brucellosis
+HP:0009911,Abnormality of the temporal bone,HP:0000929,Abnormality of the skull
+CL:0000464,epidermoblast,CL:0000710,neurecto-epithelial cell
+UBERON:0005707,upper jaw incisor odontogenic papilla,UBERON:0010258,mesenchyme from rhombencephalic neural crest
+UBERON:0010427,ciliary processes,UBERON:0004121,ectoderm-derived structure
+UBERON:0011806,dermis of feather follicle,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0002448,Progressive encephalopathy,HP:0001298,Encephalopathy
+HP:0000883,Thin ribs,HP:0000772,Abnormality of the ribs
+UBERON:0000167,oral cavity,UBERON:0002553,anatomical cavity
+UBERON:0000052,fornix of brain,UBERON:0007702,tract of brain
+UBERON:0003122,aortic arch 5,UBERON:0004363,aortic arch
+UBERON:0012376,retromolar triangle,UBERON:0004121,ectoderm-derived structure
+UBERON:0002803,right parietal lobe,UBERON:0001872,parietal lobe
+UBERON:0009129,right atrium endocardium,UBERON:0005291,embryonic tissue
+DOID:12554,hemolytic-uremic syndrome,DOID:583,hemolytic anemia
+CL:0002681,kidney cortical cell,CL:1000497,kidney cell
+HP:0007675,Progressive night blindness,HP:0000662,Night blindness
+CL:0000154,protein secreting cell,CL:0000151,secretory cell
+UBERON:0004913,hepatopancreatic ampulla,UBERON:0004119,endoderm-derived structure
+HP:0000458,Anosmia,HP:0004408,Abnormality of the sense of smell
+UBERON:0004113,muscle of auditory ossicle,UBERON:0002376,cranial muscle
+HP:0100690,Mosaic central corneal dystrophy,HP:0007881,Central corneal dystrophy
+UBERON:0004645,urinary bladder urothelium,UBERON:0000365,urothelium
+UBERON:0003366,epithelium of uterine horn,UBERON:0006955,uterine epithelium
+CL:1000286,smooth muscle cell of rectum,CL:1000279,smooth muscle cell of large intestine
+UBERON:0001648,vestibulocochlear nerve,UBERON:0001785,cranial nerve
+CL:0002142,dark cell of eccrine sweat gland,CL:0000318,sweat secreting cell
+UBERON:0005244,lobar bronchus of right lung cranial lobe,UBERON:0003404,lobar bronchus of right lung
+UBERON:0011566,lumen of esophagus,UBERON:0000464,anatomical space
+CL:1001005,glomerular capillary endothelial cell,CL:0002144,capillary endothelial cell
+HP:0100119,Small epiphysis of the middle phalanx of the 2nd toe,HP:0100089,Abnormality of the epiphysis of the middle phalanx of the 2nd toe
+UBERON:0004688,costo-cervical trunk,UBERON:0001637,artery
+DOID:12697,locked-in syndrome,DOID:863,nervous system disease
+UBERON:2000096,cardinal system,UBERON:0004537,blood vasculature
+HP:0005879,Congenital finger flexion contractures,HP:0002803,Congenital contracture
+UBERON:3010205,postminimus,UBERON:0010885,hindlimb cartilage element
+HP:0009827,Amelia,HP:0009815,Aplasia/Hypoplasia of the extremities
+UBERON:2002262,anal fin spine,UBERON:4000176,anal fin lepidotrichium
+DOID:0050222,selective IgM deficiency disease,DOID:11702,dysgammaglobulinemia
+HP:0007440,Generalized hyperpigmentation,HP:0000953,Hyperpigmentation of the skin
+HP:0009882,Short distal phalanx of finger,HP:0009381,Short finger
+UBERON:0001015,musculature,UBERON:0000480,anatomical group
+UBERON:0005042,inner epithelial layer of tympanic membrane,UBERON:0009647,tympanic membrane epithelium
+DOID:3298,vaccinia,DOID:934,viral infectious disease
+CL:0002114,CD38-positive unswitched memory B cell,CL:0000970,unswitched memory B cell
+UBERON:0005810,cervical vertebra 1 anterior tubercle,UBERON:0004120,mesoderm-derived structure
+HP:0005925,Abnormalities of the diaphyses of the hand,HP:0009808,Anomaly of the upper limb diaphyses
+UBERON:2000676,sagitta,UBERON:0002280,otolith
+NCBITaxon:745,Pasteurella,NCBITaxon:712,Pasteurellaceae
+UBERON:0000076,external ectoderm,UBERON:0005291,embryonic tissue
+UBERON:0010284,lacrimal punctum,UBERON:0004121,ectoderm-derived structure
+UBERON:3011045,gasserian ganglion,UBERON:0000045,ganglion
+HP:0100605,Neoplasm of the larynx,HP:0100606,Neoplasm of the respiratory system
+UBERON:0003010,lateral pes lemniscus,UBERON:0014891,brainstem white matter
+HP:0010054,Abnormality of the first metatarsal,HP:0010184,Abnormality of the proximal phalanges of the toes
+HP:0008765,Auditory hallucinations,HP:0000738,Hallucinations
+UBERON:3000662,processus posterior of parasphenoid,UBERON:4100000,skeletal element projection
+DOID:9335,scotoma,DOID:5614,eye disease
+UBERON:2001519,ceratobranchial 4 cartilage,UBERON:2001516,ceratobranchial cartilage
+UBERON:2201819,dorsal fin proximal radial cartilage 2,UBERON:2101819,dorsal fin proximal radial element 2
+UBERON:0010036,anterior tegmental nucleus,UBERON:0006331,brainstem nucleus
+CL:0002229,light chief cell of parathyroid gland,CL:0000446,chief cell of parathyroid gland
+UBERON:0009680,set of upper jaw teeth,UBERON:0004121,ectoderm-derived structure
+HP:0010237,Epiphyseal stippling of finger phalanges,HP:0010660,Abnormal hand bone ossification
+UBERON:0010008,mammalian cotyledon,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0009480,endoderm of buccopharyngeal membrane,UBERON:0000925,endoderm
+CL:1001220,arcuate vein endothelial cell,CL:1001142,arcuate vein cell
+UBERON:0009590,mesenchyme of interdigital region between pedal digits 1 and 2,UBERON:0009601,mesenchyme of interdigital region of pes
+HP:0008400,Onycholysis of distal fingernails,HP:0001231,Abnormality of the fingernails
+UBERON:0001940,supramammillary nucleus,UBERON:0006568,hypothalamic nucleus
+UBERON:0007629,medial septal complex,UBERON:0002663,septal nuclear complex
+UBERON:3010748,M. coccygeoiliacus,UBERON:0010890,pelvic complex muscle
+DOID:11720,distal muscular dystrophy,DOID:9884,muscular dystrophy
+DOID:11569,neurocirculatory asthenia,DOID:4737,somatoform disorder
+UBERON:0002198,neurohypophysis,UBERON:0003296,gland of diencephalon
+UBERON:0011253,gland of anal sac,UBERON:0003408,gland of gut
+HP:0010535,Sleep apnea,HP:0002104,Apnea
+UBERON:3010262,capitulum of radio-ulna,UBERON:0005913,zone of bone organ
+UBERON:0008488,cremaster muscle,UBERON:0001630,muscle organ
+HP:0005201,Anomalous splenoportal venous system,HP:0006707,Abnormality of the hepatic vasculature
+UBERON:0012645,opisthosome,UBERON:0000062,organ
+DOID:3904,bronchus carcinoma,DOID:1325,bronchus cancer
+UBERON:0001003,skin epidermis,UBERON:0007376,outer epithelium
+UBERON:0002537,hermaphrodite gonad,UBERON:0007198,hermaphrodite anatomical structure
+HP:0000610,Abnormality of the choroid,HP:0000553,Abnormality of the uvea
+DOID:0060051,autoimmune disease of cardiovascular system,DOID:417,hypersensitivity reaction type II disease
+UBERON:0014621,cervical spinal cord ventral horn,UBERON:0002257,ventral horn of spinal cord
+NCBITaxon:1639,Listeria monocytogenes,NCBITaxon:1637,Listeria
+HP:0000834,Abnormality of the adrenal glands,HP:0000818,Abnormality of the endocrine system
+UBERON:0003488,abdominal mammary gland,UBERON:0001911,mammary gland
+CL:0000018,spermatid,CL:0000413,haploid cell
+HP:0003979,Lytic defects of the radius,HP:0002818,Abnormality of the radius
+UBERON:3000560,septum semicircularium anterior,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004835,epididymis smooth muscle,UBERON:0014403,male anatomical structure
+UBERON:0013612,tooth cingulid,UBERON:0010313,neural crest-derived structure
+UBERON:0001953,presubiculum,UBERON:0000064,organ part
+HP:0009340,Irregular epiphysis of the distal phalanx of the 3rd finger,HP:0009332,Abnormality of the epiphysis of the distal phalanx of the 3rd finger
+DOID:0060140,cortical deafness,DOID:4090,agnosia
+UBERON:0007195,stroma of bone marrow,UBERON:0002384,connective tissue
+UBERON:0002575,posterior orbital gyrus,UBERON:0007193,orbital gyrus
+UBERON:0014770,palpebral artery,UBERON:0001637,artery
+HP:0000272,Malar flattening,HP:0001999,Abnormal facial shape
+CL:0002623,acinar cell of salivary gland,CL:0000622,acinar cell
+DOID:11130,secondary hypertension,DOID:10763,hypertension
+HP:0005068,absent styloid processes,HP:0004035,Abnormality of the styloid process
+UBERON:3010181,humeral glands,UBERON:3010606,limb glands
+HP:0004966,Medial calcification of large arteries,HP:0012455,Large artery calcification
+UBERON:0012288,centroquartal bone,UBERON:0001447,tarsal bone
+CL:0000171,pancreatic A cell,CL:0000083,epithelial cell of pancreas
+HP:0000852,Pseudohypoparathyroidism,HP:0011767,Abnormality of the parathyroid physiology
+UBERON:0011303,lamprey sucker,UBERON:0000475,organism subdivision
+UBERON:0000344,mucosa,UBERON:0004923,organ component layer
+UBERON:0010115,future dura mater,UBERON:0002360,meninx
+UBERON:0005932,bulb of hair follicle,UBERON:0000479,tissue
+UBERON:0000355,pharyngeal mucosa,UBERON:0004119,endoderm-derived structure
+CL:0000359,vascular associated smooth muscle cell,CL:0000192,smooth muscle cell
+HP:0007108,Demyelinating peripheral neuropathy,HP:0009830,Peripheral neuropathy
+UBERON:0011983,manual digit 8,UBERON:0002389,manual digit
+UBERON:0004123,myocardial layer,UBERON:0005983,heart layer
+HP:0007985,Retinal arteriolar occlusion,HP:0000630,Abnormality of retinal arteries
+HP:0010366,Triangular shaped phalanges of the 3rd toe,HP:0010180,Triangular shaped phalanges of the toes
+HP:0007817,Horizontal supranuclear gaze palsy,HP:0000605,Supranuclear gaze palsy
+DOID:5681,ovarian embryonal carcinoma,DOID:3308,embryonal carcinoma
+NCBITaxon:5587,Rhinocladiella,NCBITaxon:82104,mitosporic Herpotrichiellaceae
+UBERON:2001417,pelvic fin distal radial bone 1,UBERON:1500008,pelvic fin distal radial bone
+DOID:1729,retinal vascular occlusion,DOID:341,peripheral vascular disease
+CL:1000695,kidney interstitial alternatively activated macrophage,CL:0000890,alternatively activated macrophage
+HP:0100533,Inflammatory abnormality of the eye,HP:0012373,Abnormal eye physiology
+CL:0002207,brush cell of trachea,CL:0000307,tracheal epithelial cell
+DOID:6760,lung lymphoma,DOID:1324,lung cancer
+UBERON:0002738,isthmus of cingulate gyrus,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0008226,Androgen insufficiency,HP:0008373,Puberty and gonadal disorders
+UBERON:0001312,superior vesical artery,UBERON:0006554,urinary system structure
+UBERON:2000202,efferent branchial artery,UBERON:0003469,respiratory system artery
+DOID:13035,louse-borne relapsing fever,DOID:13034,relapsing fever
+DOID:3996,urinary system cancer,DOID:0050686,organ system cancer
+HP:0001882,Leukopenia,HP:0011893,Abnormal leukocyte count
+UBERON:0003625,manual digit 5,UBERON:0002389,manual digit
+DOID:11199,hypoparathyroidism,DOID:11201,parathyroid gland disease
+DOID:0050612,gall bladder carcinoma in situ,DOID:8719,in situ carcinoma
+UBERON:2001244,epibranchial 5 cartilage,UBERON:2001527,epibranchial cartilage
+HP:0000063,Fused labia minora,HP:0000058,Abnormality of the labia
+HP:0008008,Progressive central visual loss,HP:0007663,Decreased central vision
+HP:0007506,Congenital absence of skin of limbs,HP:0007383,Congenital localized absence of skin
+HP:0100780,Conjunctival hamartoma,HP:0000502,Abnormality of the conjunctiva
+HP:0004471,Aplasia cutis congenita over the scalp vertex,HP:0007385,Aplasia cutis congenita of scalp
+CL:0000823,immature natural killer cell,CL:0000623,natural killer cell
+HP:0010575,Dysplasia of the femoral head,HP:0003368,Abnormality of the femoral head
+UBERON:0008826,pulmonary surfactant,UBERON:0006538,respiratory system fluid/secretion
+HP:0010107,Short proximal phalanx of hallux,HP:0010111,Short phalanx of hallux
+UBERON:2205381,dorsal fin proximal radial cartilage 4,UBERON:2105381,dorsal fin proximal radial element 4
+HP:0012316,Fibrous tissue neoplasm,HP:0011792,Neoplasm by histology
+HP:0100381,Absent middle phalanx of the 3rd toe,HP:0100372,Aplasia/Hypoplasia of the middle phalanx of the 3rd toe
+UBERON:0006476,Brodmann (1909) area 33,UBERON:0013529,Brodmann area
+HP:0012431,Episodic fatigue,HP:0012378,Fatigue
+HP:0003042,Elbow dislocation,HP:0009811,Abnormality of the elbow
+DOID:11459,pseudotumor cerebri,DOID:6713,cerebrovascular disease
+UBERON:0013485,crypt of Lieberkuhn of colon,UBERON:0001984,crypt of lieberkuhn of large intestine
+UBERON:0004463,musculature of hindlimb stylopod,UBERON:0004466,musculature of leg
+UBERON:0003267,tooth of upper jaw,UBERON:0001091,calcareous tooth
+HP:0009382,Absent epiphyses of the 5th finger,HP:0010228,Absent epiphyses of the phalanges of the hand
+HP:0008754,Laryngeal calcifications,HP:0001600,Abnormality of the larynx
+HP:0007272,Progressive psychomotor deterioration,HP:0002344,Progressive neurologic deterioration
+HP:0000179,Thick lower lip vermilion,HP:0012471,Thick vermilion border
+HP:0009459,Short proximal phalanx of the 3rd finger,HP:0010241,Short proximal phalanx of finger
+UBERON:0015106,distal tarsal bone 2 cartilage,UBERON:0015105,distal tarsal bone 2 endochondral element
+UBERON:3000972,head external integument structure,UBERON:3000961,external integument structure
+UBERON:0004400,bone tissue of epiphysis,UBERON:0005808,bone tissue of long bone
+UBERON:0004992,mucosa of descending colon,UBERON:0000317,colonic mucosa
+CL:0002482,dermal melanocyte,CL:1000458,melanocyte of skin
+HP:0005567,Renal magnesium wasting,HP:0012607,Abnormal urine magnesium concentration
+DOID:9600,plantar fasciitis,DOID:9598,fasciitis
+HP:0004484,Craniofacial asymmetry,HP:0000267,Cranial asymmetry
+UBERON:0005419,pectoral appendage bud,UBERON:0004357,paired limb/fin bud
+HP:0001319,Neonatal hypotonia,HP:0001252,Muscular hypotonia
+HP:0001543,Gastroschisis,HP:0010866,Abdominal wall defect
+HP:0100935,Sclerosis of the middle phalanx of the 2nd toe,HP:0100926,Sclerosis of the phalanges of the 2nd toe
+HP:0006554,Acute hepatic failure,HP:0001399,Hepatic failure
+DOID:3269,ovarian cystadenoma,DOID:0060112,ovarian benign neoplasm
+UBERON:0008715,muscle tissue of prostate,UBERON:0002385,muscle tissue
+UBERON:0005335,chorioallantoic membrane,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0011268,sublingua,UBERON:0013765,digestive system organ
+HP:0011455,Absent malleus,HP:0011454,Abnormality of the malleus
+UBERON:2005000,basal communicating artery,UBERON:0001637,artery
+HP:0100648,Neoplasm of the tongue,HP:0100649,Neoplasm of the oral cavity
+CL:0007000,preameloblast,CL:0000055,non-terminally differentiated cell
+UBERON:0005193,ethmoidal artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0004201,kidney outer medulla inner stripe,UBERON:0006554,urinary system structure
+DOID:10034,eye accommodation disease,DOID:5614,eye disease
+HP:0011365,Patchy hypopigmentation of hair,HP:0005599,Hypopigmentation of hair
+UBERON:0000373,tapetum of corpus callosum,UBERON:0002437,cerebral hemisphere white matter
+UBERON:0004997,mucosa of pyloric antrum,UBERON:0004998,mucosa of pylorus
+HP:0011251,Underdeveloped antitragus,HP:0009896,Abnormality of the antitragus
+HP:0009440,Broad phalanges of the 3rd finger,HP:0009768,Broad phalanges of the hand
+HP:0003426,First dorsal interossei muscle atrophy,HP:0007181,Interosseus muscle atrophy
+UBERON:0000313,tibial cartilage tissue,UBERON:0004270,lower leg connective tissue
+CL:0000781,mononuclear odontoclast,CL:0000778,mononuclear osteoclast
+UBERON:0014876,distal epiphysis of distal phalanx of pedal digit,UBERON:0014887,distal epiphysis of distal phalanx of digit
+UBERON:0001546,posterior tibial vein,UBERON:0010370,tibial vein
+UBERON:0002776,ventral nuclear group,UBERON:0015233,nucleus of dorsal thalamus
+UBERON:2005029,rostral blood island,UBERON:0004120,mesoderm-derived structure
+DOID:12388,neurohypophyseal diabetes insipidus,DOID:26,pancreas disease
+HP:0010373,Bullet-shaped phalanges of the 4th toe,HP:0010175,Bullet-shaped phalanges of the toes
+HP:0007536,Aplasia cutis congenita of midline scalp vertex,HP:0004471,Aplasia cutis congenita over the scalp vertex
+DOID:2962,Cockayne syndrome,DOID:0050737,autosomal recessive disease
+HP:0100401,Duplication of the middle phalanx of the 3rd toe,HP:0010202,Duplication of middle phalanx of toe
+UBERON:0007753,metatarsophalangeal joint of pedal digit 2,UBERON:0003696,metatarsophalangeal joint
+HP:0012498,Nuchal cord,HP:0001787,Abnormal delivery
+UBERON:0006835,arthropod oviduct,UBERON:0003914,epithelial tube
+HP:0002619,Varicose veins,HP:0005293,Venous insufficiency
+UBERON:0010526,fibularis brevis,UBERON:0009132,peroneus
+HP:0009845,Bullet-shaped middle phalanges of the hand,HP:0009833,Abnormality of the middle phalanges of the hand
+UBERON:2000510,external levatores,UBERON:0000933,pharyngeal muscle
+NCBITaxon:327794,unclassified Phlebovirus,NCBITaxon:11584,Phlebovirus
+UBERON:0012486,muscle layer of cloaca,UBERON:0006660,muscle layer
+CL:0002128,Tc17 cell,CL:0000908,"CD8-positive, alpha-beta cytokine secreting effector T cell"
+DOID:0050813,spondyloepiphyseal dysplasia with congenital joint dislocations,DOID:0080027,spondyloepimetaphyseal dysplasia
+HP:0009752,Cleft in skull base,HP:0002693,Abnormality of the skull base
+DOID:8400,malignant cornea melanoma,DOID:6199,cornea cancer
+HP:0002625,Deep venous thrombosis,HP:0004936,Venous thrombosis
+UBERON:0009672,oronasal membrane,UBERON:0000481,multi-tissue structure
+UBERON:0014695,deep auricular artery,UBERON:0009655,auricular artery
+HP:0004451,Postauricular skin tag,HP:0000383,Abnormality of periauricular region
+UBERON:0006342,left subhepatic recess,UBERON:0005252,omental bursa cavity
+UBERON:0001132,parathyroid gland,UBERON:0002368,endocrine gland
+UBERON:2001044,sclerotome somite 3,UBERON:0003089,sclerotome
+DOID:1498,cholera,DOID:0050338,primary bacterial infectious disease
+DOID:14139,anus lymphoma,DOID:14110,anus cancer
+DOID:3410,carotid artery thrombosis,DOID:4193,intracranial thrombosis
+CL:0000911,effector T cell,CL:0002419,mature T cell
+HP:0100781,Abnormality of the sacroiliac joint,HP:0001367,Abnormal joint morphology
+HP:0006519,Alveolar cell carcinoma,HP:0100552,Neoplasm of the tracheobronchial system
+UBERON:0006844,cusp of tooth,UBERON:0004121,ectoderm-derived structure
+DOID:4490,malignant peritoneal solitary fibrous tumor,DOID:1725,peritoneum cancer
+HP:0008102,Expanded metatarsals with widened medullary cavities,HP:0001832,Abnormality of the metatarsal bones
+UBERON:0006200,caudal humeral circumflex vein,UBERON:0001638,vein
+UBERON:0013463,temporal fossa,UBERON:0004704,bone fossa
+HP:0100898,Connective tissue nevi,HP:0003764,Nevus
+HP:0012410,Pure red cell aplasia,HP:0012131,Abnormal number of erythroid precursors
+HP:0001833,Long foot,HP:0001760,Abnormality of the foot
+UBERON:0002873,interpolar part of spinal trigeminal nucleus,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2001179,epidermal superficial stratum,UBERON:0004121,ectoderm-derived structure
+CL:0000019,sperm,CL:0000064,ciliated cell
+DOID:1702,ichthyosis vulgaris,DOID:0050736,autosomal dominant disease
+DOID:6562,ethmoid sinus inverted papilloma,DOID:1364,ethmoidal sinus neoplasm
+DOID:3310,atopic dermatitis,DOID:2723,dermatitis
+DOID:9741,biliary tract disease,DOID:3118,hepatobiliary disease
+UBERON:0014696,anterior choroidal artery,UBERON:0013151,choroidal artery
+HP:0001566,Widely-spaced maxillary central incisors,HP:0000699,Diastema
+HP:0006175,Proximal phalangeal periosteal thickening,HP:0009834,Abnormality of the proximal phalanges of the hand
+HP:0100181,Bracket epiphysis of the middle phalanx of the 4th toe,HP:0100067,Bracket epiphyses of the 4th toe
+HP:0006350,Obliteration of the pulp chamber,HP:0006479,Abnormality of the dental pulp
+UBERON:0003475,ureteric vein,UBERON:0003520,pelvis blood vessel
+DOID:1404,residual stage angle-closure glaucoma,DOID:1405,primary angle-closure glaucoma
+HP:0011167,Focal tonic seizures,HP:0011153,Focal motor seizures
+UBERON:2101417,pelvic fin distal radial element 1,UBERON:1600008,pelvic fin distal radial element
+HP:0012346,Abnormal protein glycosylation,HP:0012345,Abnormal glycosylation
+HP:0008057,Aplasia/Hypoplasia affecting the fundus,HP:0008056,Aplasia/Hypoplasia affecting the eye
+HP:0011835,Absent scaphoid,HP:0004231,Carpal bone aplasia
+HP:0009013,Congenital absence of gluteal muscles,HP:0001471,Aplasia/Hypoplasia of the musculature of the pelvis
+UBERON:0012285,vegetal hemisphere,UBERON:0012286,hemisphere of embryo
+UBERON:0009565,nail of manual digit,UBERON:0001705,nail
+UBERON:0003199,egg chamber,UBERON:0000464,anatomical space
+HP:0005206,Pancreatic pseudocyst,HP:0012090,Abnormality of pancreas morphology
+UBERON:0011190,lunule of nail,UBERON:0004923,organ component layer
+DOID:12491,Vagus nerve disease,DOID:3418,glossopharyngeal nerve disease
+HP:0000470,Short neck,HP:0000464,Abnormality of the neck
+UBERON:3000563,seydels palatal process,UBERON:0010313,neural crest-derived structure
+HP:0002490,Increased CSF lactate,HP:0002921,Abnormality of the cerebrospinal fluid
+UBERON:0010391,parametrium,UBERON:0002095,mesentery
+DOID:3258,orbit embryonal rhabdomyosarcoma,DOID:3259,orbit rhabdomyosarcoma
+UBERON:0002378,muscle of abdomen,UBERON:0005172,abdomen organ
+HP:0100476,Symphalangism affecting the distal phalanx of the 3rd toe,HP:0001859,Distal symphalangism (feet)
+UBERON:2002073,distal cartilage of middle anterior process of basipterygium,UBERON:4100000,skeletal element projection
+HP:0000081,Duplicated collecting system,HP:0004742,Abnormality of the renal collecting system
+CL:0001026,"CD34-positive, CD38-positive common myeloid progenitor",CL:0000995,"CD34-positive, CD38-positive common myeloid progenitor OR CD34-positive, CD38-positive common lymphoid progenitor"
+HP:0001495,Carpal osteolysis,HP:0002797,Osteolysis
+DOID:6658,pulmonary large cell neuroendocrine carcinoma,DOID:4556,lung large cell carcinoma
+UBERON:0002783,central tegmental tract of pons,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0004245,Comma-shaped scaphoid,HP:0004243,Abnormality of the scaphoid
+NCBITaxon:520,Bordetella pertussis,NCBITaxon:517,Bordetella
+HP:0003179,Protrusio acetabuli,HP:0003170,Abnormality of the acetabulum
+HP:0003153,Cystathioninuria,HP:0003355,Aminoaciduria
+UBERON:0001382,pectineus muscle,UBERON:0004252,hindlimb stylopod muscle
+CL:1001318,renal interstitial pericyte,CL:1000497,kidney cell
+HP:0009292,Broad distal phalanx of the 4th finger,HP:0009836,Broad distal phalanx of finger
+HP:0009731,Cerebral hamartomata,HP:0010566,Hamartoma
+CL:0000198,pain receptor cell,CL:0000006,neuronal receptor cell
+DOID:4901,peritoneal serous adenocarcinoma,DOID:1791,peritoneal carcinoma
+UBERON:0001985,corneal endothelium,UBERON:0001772,corneal epithelium
+NCBITaxon:327045,Orthoretrovirinae,NCBITaxon:11632,Retroviridae
+UBERON:0003976,saccule duct,UBERON:0004121,ectoderm-derived structure
+UBERON:0001612,facial artery,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0005132,metanephric long nephron,UBERON:0005110,metanephric nephron
+DOID:13444,glanders,DOID:0050338,primary bacterial infectious disease
+CL:0000562,nucleate erythrocyte,CL:0000232,erythrocyte
+HP:0009228,Bullet-shaped proximal phalanx of the 5th finger,HP:0009150,Abnormality of the proximal phalanx of the 5th finger
+UBERON:2001246,epibranchial 2 bone,UBERON:2000658,epibranchial bone
+DOID:0050261,thelaziasis,DOID:883,parasitic helminthiasis infectious disease
+HP:0009377,Patchy sclerosis of the phalanges of the 5th finger,HP:0009772,Patchy sclerosis of the phalanges of the hand
+HP:0000348,High forehead,HP:0000290,Abnormality of the forehead
+UBERON:0001033,gustatory system,UBERON:0000467,anatomical system
+HP:0000991,Xanthomatosis,HP:0011355,Localized skin lesion
+UBERON:0004172,pons reticulospinal tract,UBERON:0001018,axon tract
+HP:0010590,Abnormality of the distal femoral epiphysis,HP:0006499,Abnormality of femoral epiphyses
+HP:0000965,Cutis marmorata,HP:0011276,Vascular skin abnormality
+UBERON:0005487,vitelline vein,UBERON:0002050,embryonic structure
+UBERON:3010719,dilated medial process of metacarpal IV,UBERON:0004120,mesoderm-derived structure
+HP:0011023,Abnormality of prostaglandin metabolism,HP:0011022,Abnormality of unsaturated fatty acid metabolism
+UBERON:0008575,oblique arytenoid,UBERON:0010958,arytenoid muscle
+UBERON:0014491,middle phalanx of digit 5,UBERON:0004301,middle phalanx
+UBERON:0002568,amiculum of dentate nucleus,UBERON:0010314,structure with developmental contribution from neural crest
+CL:1000615,kidney cortex tubule cell,CL:1000494,epithelial cell of renal tubule
+CL:0000709,R8 photoreceptor cell,CL:0000488,visible light photoreceptor cell
+HP:0100933,Sclerosis of the proximal phalanx of the 4th toe,HP:0100946,Sclerosis of the proximal phalanges of the toes
+DOID:8502,bullous skin disease,DOID:2723,dermatitis
+DOID:7166,thyroiditis,DOID:50,thyroid gland disease
+DOID:2751,glycogen storage disease VIII,DOID:2747,glycogen storage disease
+UBERON:0008595,levator anguli oris,UBERON:0001577,facial nerve muscle
+UBERON:0010543,acropodial skeleton,UBERON:0004120,mesoderm-derived structure
+CL:0000614,basophilic myelocyte,CL:0002087,nongranular leukocyte
+HP:0000603,Central scotoma,HP:0000575,Scotoma
+NCBITaxon:33392,Endopterygota,NCBITaxon:33340,Neoptera
+UBERON:0004528,alveolar ridge of mandible,UBERON:0010313,neural crest-derived structure
+CL:1000693,kidney interstitial fibrocyte,CL:0000135,fibrocyte
+HP:0000613,Photophobia,HP:0000708,Behavioural/Psychiatric Abnormality
+HP:0010366,Triangular shaped phalanges of the 3rd toe,HP:0010330,Abnormality of the phalanges of the 3rd toe
+HP:0010709,2-4 finger syndactyly,HP:0006101,Finger syndactyly
+HP:0001952,Abnormal glucose tolerance,HP:0011014,Abnormal glucose homeostasis
+HP:0010732,Nodular changes affecting the eyelids,HP:0200036,Skin nodule
+CL:0001006,dermal dendritic cell,CL:0002465,CD11b-positive dendritic cell
+CL:0002655,epithelial cell of stratum spinosum of esophageal epithelium,CL:0002252,epithelial cell of esophagus
+UBERON:0013491,cervical fascia,UBERON:0003568,neck connective tissue
+UBERON:0004325,middle phalanx of pedal digit 3,UBERON:0014489,middle phalanx of digit 3
+CL:0001040,non-terminally differentiated osteoblast,CL:0000062,osteoblast
+DOID:3322,gangliosidosis GM1,DOID:2368,gangliosidosis
+UBERON:0007270,pelvic appendage musculature,UBERON:0007271,appendage musculature
+HP:0010791,Hyperplasia of the Leydig cells,HP:0010789,Abnormality of the Leydig cells
+CL:1000360,microfold cell of epithelium proper of large intestine,CL:0000682,M cell of gut
+HP:0009313,Patchy sclerosis of the proximal phalanx of the 4th finger,HP:0009284,Abnormality of the proximal phalanx of the 4th finger
+HP:0006606,Irregular chondrocostal junctions,HP:0000919,Abnormality of the costochondral junction
+DOID:14283,primary hypertrophic osteoarthropathy,DOID:225,syndrome
+DOID:8892,pityriasis rosea,DOID:8893,psoriasis
+HP:0011234,Absent antihelix,HP:0009738,Abnormality of the antihelix
+UBERON:0014776,mesomere,UBERON:0004731,neuromere
+HP:0009697,Contractures of the distal interphalangeal joints of the fingers,HP:0001220,Interphalangeal joint contractures (hands)
+DOID:1628,intraductal papillary breast neoplasm,DOID:3013,intraductal breast neoplasm
+UBERON:0004148,cardiac vein,UBERON:0003498,heart blood vessel
+DOID:2986,IgA glomerulonephritis,DOID:2921,glomerulonephritis
+DOID:10540,gastric lymphoma,DOID:10534,stomach cancer
+DOID:5731,chronic salpingitis,DOID:5733,salpingitis
+NCBITaxon:452564,mitosporic Davidiellaceae,NCBITaxon:452563,Davidiellaceae
+HP:0009663,Abnormality of the epiphysis of the proximal phalanx of the thumb,HP:0009618,Abnormality of the proximal phalanx of the thumb
+UBERON:2001089,myoseptum,UBERON:0004120,mesoderm-derived structure
+UBERON:3000922,prehallux skeleton,UBERON:0004120,mesoderm-derived structure
+UBERON:0002149,superior salivatory nucleus,UBERON:0004133,salivatory nucleus
+UBERON:0005056,external female genitalia,UBERON:0004176,external genitalia
+HP:0012206,Abnormal sperm motility,HP:0000025,Functional abnormality of male internal genitalia
+UBERON:4300110,lateral ethmoid cartilage,UBERON:0007844,cartilage element
+HP:0007548,Palmoplantar keratosis with erythema and scale,HP:0000972,Palmoplantar hyperkeratosis
+UBERON:0010953,nasalis muscle,UBERON:0008522,nasal muscle
+HP:0100754,Mania,HP:0000708,Behavioural/Psychiatric Abnormality
+HP:0007497,Focal friction-related palmoplantar hyperkeratosis,HP:0000972,Palmoplantar hyperkeratosis
+UBERON:0004849,respiratory system venous endothelium,UBERON:0004702,respiratory system blood vessel endothelium
+HP:0100028,Ectopic thyroid,HP:0008188,Thyroid dysgenesis
+HP:0009783,Biceps aplasia,HP:0100854,Aplasia of the musculature
+CL:1000714,kidney cortex collecting duct principal cell,CL:1001431,kidney collecting duct principal cell
+UBERON:0001993,reticular layer of dermis,UBERON:0004121,ectoderm-derived structure
+UBERON:0011531,male pubococcygeus muscle,UBERON:0011528,pubococcygeus muscle
+NCBITaxon:33208,Metazoa,NCBITaxon:33154,Opisthokonta
+UBERON:2002082,basal fulcrum,UBERON:2002291,fulcrum
+UBERON:0007244,inferior olivary nucleus,UBERON:0002574,regional part of inferior olivary complex
+DOID:14213,hypophosphatasia,DOID:0050736,autosomal dominant disease
+UBERON:0011017,semispinalis muscle,UBERON:0004518,muscle of vertebral column
+HP:0007054,Hyperreflexia proximally,HP:0001347,Hyperreflexia
+HP:0000753,Autism with high cognitive abilities,HP:0000729,Autism spectrum disorder
+DOID:8616,Peyronie's disease,DOID:1529,penile disease
+HP:0001744,Splenomegaly,HP:0003271,Visceromegaly
+HP:0011908,Unilateral radial aplasia,HP:0003974,Absent radius
+UBERON:0001200,submucosa of stomach,UBERON:0009034,stomach region
+HP:0010035,Aplasia of the 1st metacarpal,HP:0010048,Aplasia of metacarpal bones
+DOID:5484,fibrous synovial sarcoma,DOID:5485,synovial sarcoma
+UBERON:2001192,supraneural 3 bone,UBERON:2000442,supraneural bone
+HP:0010164,Cone-shaped epiphyses of the toes,HP:0010579,Cone-shaped epiphysis
+DOID:9369,orbital plasma cell granuloma,DOID:1397,chronic orbital inflammation
+UBERON:0004686,gastro-splenic ligament,UBERON:0004120,mesoderm-derived structure
+UBERON:0015794,left lung lobar bronchus epithelium,UBERON:0003365,epithelium of left lung
+UBERON:0011283,epoophoron,UBERON:0006590,vestigial embryonic structure
+HP:0002555,Absent pubic hair,HP:0002298,Absent hair
+HP:0009829,Phocomelia,HP:0011314,Abnormality of long bone morphology
+UBERON:0001823,nasal cartilage,UBERON:0004121,ectoderm-derived structure
+HP:0100822,Rectocele,HP:0100672,Vaginal hernia
+HP:0100281,Chronic colitis,HP:0002583,Colitis
+UBERON:2001286,caudal vein plexus,UBERON:0010204,tail vasculature
+UBERON:2000776,hypaxial region somite 6,UBERON:0003895,hypaxial myotome region
+UBERON:0001617,mental artery,UBERON:0001637,artery
+HP:0001791,Fetal ascites,HP:0001197,Abnormality of prenatal development or birth
+CL:1000714,kidney cortex collecting duct principal cell,CL:0002584,renal cortical epithelial cell
+HP:0010281,Cleft lower lip,HP:0000202,Oral cleft
+UBERON:0006644,tunica albuginea of ovary,UBERON:0014404,female anatomical structure
+UBERON:3000179,foramen acusticum,UBERON:3000051,braincase and otic capsule opening
+NCBITaxon:42408,Neotoma albigula,NCBITaxon:42407,Neotoma
+DOID:4232,extraosseous Ewing's sarcoma,DOID:3369,peripheral primitive neuroectodermal tumor
+DOID:10685,separation anxiety disorder,DOID:2030,anxiety disorder
+DOID:1724,duodenal ulcer,DOID:750,peptic ulcer disease
+HP:0005174,Membranous subvalvular aortic stenosis,HP:0001682,Subaortic stenosis
+DOID:12157,aseptic meningitis,DOID:10310,viral meningitis
+UBERON:0011108,synovial joint of pectoral girdle,UBERON:0008114,joint of girdle
+HP:0010236,Small epiphyses of the phalanges of the hand,HP:0010585,Small epiphyses
+UBERON:3000450,posterior mental process,UBERON:0010313,neural crest-derived structure
+UBERON:0009205,lateral nasal process mesenchyme,UBERON:0009501,mesenchyme of fronto-nasal process
+UBERON:0004527,alveolar process of maxilla,UBERON:0010313,neural crest-derived structure
+HP:0006880,Cerebellar hemangioblastoma,HP:0010797,Hemangioblastoma
+UBERON:0010937,salpingopharyngeus muscle,UBERON:0000933,pharyngeal muscle
+DOID:2661,myoepithelioma,DOID:2664,sweat gland neoplasm
+UBERON:2000857,somite 4,UBERON:0002329,somite
+CL:0002400,Fraction B/C precursor B cell,CL:0000817,precursor B cell
+UBERON:0005205,vagina stroma,UBERON:0014404,female anatomical structure
+HP:0008994,Proximal muscle weakness in lower limbs,HP:0003701,Proximal muscle weakness
+HP:0003361,Tryptophanuria,HP:0003355,Aminoaciduria
+HP:0100076,Triangular epiphyses of the 4th toe,HP:0010335,Abnormality of the epiphyses of the 4th toe
+UBERON:0004922,postnatal subventricular zone,UBERON:0004923,organ component layer
+NCBITaxon:7198,Phlebotominae,NCBITaxon:7197,Psychodidae
+DOID:10069,subglottis neoplasm,DOID:2598,laryngeal benign neoplasm
+UBERON:0003113,dermatocranium,UBERON:0011159,primary subdivision of cranial skeletal system
+UBERON:0003211,median eye,UBERON:0000970,eye
+UBERON:0003603,lower respiratory tract cartilage,UBERON:0003580,lower respiratory tract connective tissue
+HP:0100140,Irregular epiphysis of the distal phalanx of the 3rd toe,HP:0100060,Irregular epiphyses of the 3rd toe
+HP:0011107,Recurrent aphthous stomatitis,HP:0010280,Stomatitis
+HP:0012671,Abulia,HP:0000745,Diminished motivation
+DOID:8800,lung carcinoma in situ,DOID:8719,in situ carcinoma
+UBERON:0005416,zone of polarizing activity of pelvic appendage,UBERON:0005414,zone of polarizing activity
+HP:0011736,Primary hyperaldosteronism,HP:0000859,Hyperaldosteronism
+HP:0010494,Acromelia of the lower limbs,HP:0006493,Aplasia/Hypoplasia involving bones of the lower limbs
+UBERON:4300024,spinal plate,UBERON:0008907,dermal bone
+DOID:3534,Lafora disease,DOID:1289,neurodegenerative disease
+DOID:4839,sebaceous adenocarcinoma,DOID:4840,sebaceous carcinoma
+HP:0000033,"Ambiguous genitalia, male",HP:0000062,Ambiguous genitalia
+UBERON:2007041,forebrain neural tube,UBERON:0005291,embryonic tissue
+HP:0011606,Transposition of the great arteries with intact ventricular septum,HP:0001669,Transposition of the great arteries
+HP:0000456,Bifid nasal tip,HP:0000436,Abnormality of the nasal tip
+HP:0002205,Recurrent respiratory infections,HP:0011947,Respiratory tract infection
+UBERON:3000384,parasagittal crest,UBERON:0000064,organ part
+UBERON:0007735,metacarpophalangeal joint of manual digit 1,UBERON:0003695,metacarpophalangeal joint
+UBERON:0002711,nucleus of posterior commissure,UBERON:0007414,nucleus of midbrain tegmentum
+HP:0012065,Multiple bony cystic lesions,HP:0012062,Bone cyst
+UBERON:0006937,inner ear epithelium,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001550,medial marginal vein,UBERON:0004261,lower leg blood vessel
+DOID:4664,filamentary keratitis,DOID:4677,keratitis
+DOID:166,melanotic neuroectodermal tumor,DOID:0060094,bone benign neoplasm
+CL:1000374,transitional myocyte of posterior division of left branch of atrioventricular bundle,CL:1000370,transitional myocyte of left branch of atrioventricular bundle
+HP:0012663,Mildly reduced ejection fraction,HP:0012664,Reduced ejection fraction
+CL:0000756,type 4 cone bipolar cell (sensu Mus),CL:0000750,OFF-bipolar cell
+UBERON:0012291,lateral malleolus of fibula,UBERON:0004120,mesoderm-derived structure
+UBERON:0005111,metanephric pyramid,UBERON:0004120,mesoderm-derived structure
+UBERON:0002226,basilar membrane of cochlea,UBERON:0004121,ectoderm-derived structure
+HP:0010017,Cone-shaped epiphysis of the 1st metacarpal,HP:0006059,Cone-shaped metacarpal epiphyses
+CL:0000602,pressoreceptor cell,CL:1000082,stretch receptor cell
+UBERON:0014857,zoea stage,UBERON:0000069,larval stage
+DOID:6492,breast epithelioid hemangioma,DOID:476,breast hemangioma
+HP:0005976,Hyperkalemic metabolic acidosis,HP:0001942,Metabolic acidosis
+HP:0100558,Hemiatrophy of upper limb,HP:0100560,Upper limb asymmetry
+UBERON:0009206,lateral nasal process surface ectoderm,UBERON:0000924,ectoderm
+DOID:10200,chest wall lipoma,DOID:0060097,thoracic benign neoplasm
+DOID:0050939,uterine corpus endometrial carcinoma,DOID:9460,uterine corpus cancer
+UBERON:0013160,epithalamus ventricular layer,UBERON:0004022,embryonic neuroepithelium
+UBERON:0011146,silk gland,UBERON:0002365,exocrine gland
+UBERON:0010995,deep part of masseter muscle,UBERON:0000064,organ part
+HP:0011255,Absent crus of helix,HP:0009895,Abnormality of the crus of the helix
+UBERON:0013601,medial accessory nucleus of optic tract,UBERON:0013598,accessory nucleus of optic tract
+HP:0009980,Complete duplication of the proximal phalanx of the 4th finger,HP:0009973,Complete duplication of the phalanges of the 4th finger
+UBERON:0000329,hair root,UBERON:0000021,cutaneous appendage
+HP:0000512,Abnormal electroretinogram,HP:0000479,Abnormality of the retina
+DOID:14252,dystrophies primarily involving the retinal pigment epithelium,DOID:8501,fundus dystrophy
+DOID:9409,diabetes insipidus,DOID:557,kidney disease
+DOID:11394,adult respiratory distress syndrome,DOID:11162,respiratory failure
+HP:0009703,Synostosis involving the 1st metacarpal,HP:0010009,Abnormality of the 1st metacarpal
+DOID:7103,diaphragma sellae meningioma,DOID:3643,sella turcica neoplasm
+CL:0002177,folliculostellate cell of pars distalis of adenohypophysis,CL:2000004,pituitary gland cell
+HP:0007525,"Yellow subcutaneous tissue covered by thin, scaly skin",HP:0001001,Abnormality of subcutaneous fat tissue
+UBERON:0000950,gracilis,UBERON:0011144,adductor muscle of hip
+HP:0003952,Sclerotic foci of metaphyses of the elbow,HP:0003854,Sclerosis of metaphyses of the upper limbs
+UBERON:0001679,ethmoid bone,UBERON:0002513,endochondral bone
+UBERON:0002282,stria vascularis of cochlear duct,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0006699,foramen cecum of tongue,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2001959,ceratobranchial 4 bone proximal cartilage,UBERON:4000003,permanent cartilage
+HP:0100490,Camptodactyly of finger,HP:0006261,Abnormality of phalangeal joints of the hand
+CL:0000383,nephrogenic mesenchyme stem cell,CL:0000134,mesenchymal cell
+UBERON:2001817,middle nuchal plate,UBERON:0004247,bone of dorsum
+UBERON:0014779,liver reticuloendothelial system,UBERON:0000363,reticuloendothelial system
+UBERON:0007213,mesenchyme derived from head neural crest,UBERON:0014387,mesenchyme derived from neural crest
+UBERON:0001240,muscularis mucosae of intestine,UBERON:0006676,muscularis mucosa
+HP:0009166,Fragmentation of the epiphysis of the distal phalanx of the 5th finger,HP:0009198,Abnormality of the epiphysis of the distal phalanx of the 5th finger
+UBERON:0010527,cavity of bone organ,UBERON:0002558,organ cavity
+HP:0000492,Abnormality of the eyelid,HP:0000284,Abnormality of the ocular region
+UBERON:0009753,adrenal gland cortex zone,UBERON:0004120,mesoderm-derived structure
+HP:0006515,Interstitial pneumonitis,HP:0006530,Interstitial pulmonary disease
+UBERON:0001964,least splanchnic nerve,UBERON:0006554,urinary system structure
+UBERON:0003242,epithelium of saccule,UBERON:0006932,vestibular epithelium
+UBERON:2001701,basibranchial 5 bone,UBERON:0002513,endochondral bone
+HP:0005194,Flattened metatarsal heads,HP:0001832,Abnormality of the metatarsal bones
+UBERON:0010958,arytenoid muscle,UBERON:0006328,laryngeal intrinsic muscle
+HP:0006165,Proportionate shortening of all digits,HP:0006265,Aplasia/Hypoplasia of fingers
+HP:0002506,Diffuse cerebral atrophy,HP:0002059,Cerebral atrophy
+HP:0012413,Notched primary central incisor,HP:0011063,Abnormality of incisor morphology
+HP:0010275,Pseudoepiphyses of the proximal phalanges of the hand,HP:0010245,Abnormality of the epiphyses of the proximal phalanges of the hand
+HP:0004242,Broad carpal bones,HP:0004237,Large carpal bones
+UBERON:0008311,penile bulb artery,UBERON:0004573,systemic artery
+HP:0006846,Acute encephalopathy,HP:0001298,Encephalopathy
+UBERON:0002553,anatomical cavity,UBERON:0000464,anatomical space
+DOID:8433,thyroid malformation,DOID:50,thyroid gland disease
+HP:0009964,Duplication of the proximal phalanx of the 3rd finger,HP:0009358,Abnormality of the proximal phalanx of the 3rd finger
+UBERON:3000500,processus posterior of maxilla,UBERON:0010313,neural crest-derived structure
+DOID:13446,basilar artery occlusion,DOID:5976,occlusion precerebral artery
+UBERON:2001700,caudal-fin stay,UBERON:0008907,dermal bone
+CL:0000535,secondary neuron,CL:0000540,neuron
+CL:0000514,smooth muscle myoblast,CL:0000056,myoblast
+UBERON:0002147,reticulotegmental nucleus,UBERON:0002680,regional part of metencephalon
+DOID:5587,Volkmann contracture,DOID:65,connective tissue disease
+UBERON:0006648,adventitia of seminal vesicle,UBERON:0014403,male anatomical structure
+HP:0100805,Precocious menopause,HP:0000869,Secondary amenorrhea
+HP:0009662,Abnormality of the epiphysis of the distal phalanx of the thumb,HP:0009599,Abnormality of the epiphyses of the thumb
+HP:0003614,Trimethylaminuria,HP:0003110,Abnormality of urine homeostasis
+UBERON:0002557,linear nucleus,UBERON:0007414,nucleus of midbrain tegmentum
+HP:0004362,Abnormality of the enteric ganglia,HP:0012331,Abnormal autonomic nervous system morphology
+UBERON:0007127,pharyngeal pouch 6,UBERON:0004117,pharyngeal pouch
+HP:0005532,Macrocytic dyserythropoietic anemia,HP:0001972,Macrocytic anemia
+UBERON:0011627,orbital part of frontal bone,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0002332,ciliated cell of the bronchus,CL:0002145,ciliated columnar cell of tracheobronchial tree
+UBERON:0011657,dermal element of plastron,UBERON:0008907,dermal bone
+UBERON:0012103,suspensory ligament of breast,UBERON:0000158,membranous layer
+HP:0002894,Neoplasm of the pancreas,HP:0001732,Abnormality of the pancreas
+CL:1000720,kidney papillary duct intercalated cell,CL:1001432,kidney collecting duct intercalated cell
+UBERON:0012462,proctodeum portion of cloaca,UBERON:0000064,organ part
+UBERON:2000300,ventral hypohyal bone,UBERON:0002513,endochondral bone
+UBERON:0002110,gallbladder,UBERON:0013765,digestive system organ
+DOID:1757,facial hemiatrophy,DOID:1756,facial nerve disease
+UBERON:4200176,ascending process of clavicle,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0007319,medial saphenous vein,UBERON:0013145,accessory saphenous vein
+UBERON:0013206,nasal tentacle,UBERON:0000021,cutaneous appendage
+UBERON:0004153,ventricular septum intermedium,UBERON:0010313,neural crest-derived structure
+HP:0011648,Patent ductus arteriosus after birth at term,HP:0001643,Patent ductus arteriosus
+UBERON:0001568,muscle of larynx,UBERON:0004119,endoderm-derived structure
+NCBITaxon:11158,Paramyxoviridae,NCBITaxon:11157,Mononegavirales
+UBERON:3000844,sulcus longitudinalis,UBERON:0004120,mesoderm-derived structure
+HP:0100853,Hypoplastic areola,HP:0000769,Abnormality of the breast
+UBERON:0010163,eyebrow,UBERON:0010165,collection of hair on face
+DOID:1936,atherosclerosis,DOID:2348,arteriosclerotic cardiovascular disease
+UBERON:0004053,external male genitalia,UBERON:0004176,external genitalia
+UBERON:0011531,male pubococcygeus muscle,UBERON:0014403,male anatomical structure
+DOID:1687,neovascular glaucoma,DOID:1686,glaucoma
+DOID:6214,ovarian papillary neoplasm,DOID:2152,ovary epithelial cancer
+HP:0004820,Acute myelomonocytic leukemia,HP:0012324,Myeloid leukemia
+UBERON:0001794,inner limiting layer of retina,UBERON:0007619,limiting membrane of retina
+UBERON:0001647,facial nerve,UBERON:0001785,cranial nerve
+NCBITaxon:169449,Coelopinae,NCBITaxon:169440,Coelopidae
+UBERON:0007228,vestibular nucleus,UBERON:0007635,nucleus of medulla oblongata
+HP:0009998,Complete duplication of phalanx of hand,HP:0009997,Duplication of phalanx of hand
+CL:0000863,inflammatory macrophage,CL:0000861,elicited macrophage
+HP:0006109,Absent phalangeal crease,HP:0006143,Abnormal finger flexion creases
+HP:0010019,Fragmentation of the epiphysis of the 1st metacarpal,HP:0009690,Fragmentation of the epiphyses of the thumb
+NCBITaxon:77643,Mycobacterium tuberculosis complex,NCBITaxon:1763,Mycobacterium
+DOID:8068,intraductal breast myoepitheliosis,DOID:7521,breast myoepitheliosis
+UBERON:0011304,tunicate postabdomen,UBERON:0000475,organism subdivision
+UBERON:2001926,posterior myodome,UBERON:0004704,bone fossa
+DOID:8469,influenza,DOID:934,viral infectious disease
+HP:0000389,Chronic otitis media,HP:0000388,Otitis media
+DOID:11385,expressive language disorder,DOID:93,language disorder
+HP:0000504,Abnormality of vision,HP:0012373,Abnormal eye physiology
+UBERON:0016476,primary incisor tooth,UBERON:0001098,incisor tooth
+UBERON:0010033,posterior part of tongue,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0000818,Abnormality of the endocrine system,HP:0000118,Phenotypic abnormality
+UBERON:2001990,epibranchial arborescent organ,UBERON:0004119,endoderm-derived structure
+HP:0011906,Reduced beta/alpha synthesis ratio,HP:0005560,Imbalanced hemoglobin synthesis
+CL:0002279,type L enteroendocrine cell,CL:0000164,enteroendocrine cell
+HP:0001814,Deep-set nails,HP:0002164,Nail dysplasia
+HP:0004894,Laryngotracheal stenosis,HP:0001602,Laryngeal stenosis
+HP:0002651,Spondyloepimetaphyseal dysplasia,HP:0002652,Skeletal dysplasia
+DOID:4660,indolent systemic mastocytosis,DOID:3664,mast cell neoplasm
+UBERON:0001484,articular capsule,UBERON:0000094,membrane organ
+UBERON:0006263,Meckel's cartilage pre-cartilage condensation,UBERON:0005291,embryonic tissue
+HP:0011406,Infancy onset short-trunk short stature,HP:0003521,Disproportionate short-trunk short stature
+HP:0002194,Delayed gross motor development,HP:0001270,Motor delay
+UBERON:0006717,autopodial skeleton,UBERON:0010712,limb skeleton subdivision
+CL:0007011,enteric neuron,CL:0000029,neuron neural crest derived
+DOID:6576,childhood optic nerve glioma,DOID:4992,optic nerve glioma
+HP:0009165,Stippling of the epiphysis of the distal phalanx of the 5th finger,HP:0009198,Abnormality of the epiphysis of the distal phalanx of the 5th finger
+UBERON:3000661,crista vomeri,UBERON:4100000,skeletal element projection
+DOID:2072,vulvar squamous tumor,DOID:1245,vulva cancer
+UBERON:2001623,type 1 odontode,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0000607,Periorbital wrinkles,HP:0000606,Abnormality of the periorbital region
+CL:0000557,granulocyte monocyte progenitor cell,CL:0000763,myeloid cell
+UBERON:0014461,infratemporal fenestra,UBERON:0014459,temporal fenestra
+UBERON:0009633,root of sacral nerve,UBERON:0009623,spinal nerve root
+HP:0000227,Tongue telangiectasia,HP:0000228,Oral cavity teleangiectasia
+HP:0009450,Broad proximal phalanx of the 3rd finger,HP:0009358,Abnormality of the proximal phalanx of the 3rd finger
+CL:0000713,corona radiata cell,CL:0000711,cumulus cell
+HP:0009375,Bullet-shaped phalanges of the 5th finger,HP:0009769,Bullet-shaped phalanges of the hand
+UBERON:0002118,right ovary,UBERON:0015212,lateral structure
+UBERON:0002872,inferior salivatory nucleus,UBERON:0007635,nucleus of medulla oblongata
+UBERON:0000152,pelvic fin,UBERON:0004709,pelvic appendage
+HP:0010367,Duplication of phalanx of the 3rd toe,HP:0010181,Duplication of phalanx of toe
+HP:0001241,Capitate-hamate fusion,HP:0004259,Abnormality of the hamate bone
+CL:0000599,conidium,CL:0000605,fungal asexual spore
+HP:0100748,Muscular edema,HP:0000969,Edema
+CL:0002112,B220-positive CD38-negative unswitched memory B cell,CL:0002111,CD38-negative unswitched memory B cell
+UBERON:0011807,epidermis of feather follicle,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0000364,Hearing abnormality,HP:0000598,Abnormality of the ear
+UBERON:0007808,adipose tissue of abdominal region,UBERON:0003567,abdomen connective tissue
+UBERON:0011642,oral epithelium from ectoderm,UBERON:0000490,unilaminar epithelium
+DOID:13951,uterine corpus epithelioid leiomyoma,DOID:13223,uterine fibroid
+DOID:254,hemangioma of intra-abdominal structure,DOID:255,hemangioma
+DOID:11819,ureter cancer,DOID:3996,urinary system cancer
+UBERON:0000329,hair root,UBERON:0010314,structure with developmental contribution from neural crest
+CL:0002637,keratinized epithelial cell of the anal canal,CL:0002634,epithelial cell of anal column
+HP:0006713,Aplasia/Hypoplasia of the scapulae,HP:0006711,Aplasia/Hypoplasia involving bones of the thorax
+DOID:5477,clear cell adenofibroma,DOID:2683,adenofibroma
+HP:0002723,Absence of bactericidal oxidative 'respiratory burst' in phagocytes,HP:0010977,Abnormality of phagocytes
+HP:0004432,Agammaglobulinemia,HP:0010701,Abnormal immunoglobulin level
+HP:0001386,Joint swelling,HP:0001367,Abnormal joint morphology
+CL:1001052,kidney cortex vein cell,CL:1000893,kidney venous blood vessel cell
+UBERON:0002424,oral epithelium,UBERON:0003350,epithelium of mucosa
+HP:0008740,Longitudinal vaginal septum,HP:0001153,Septate vagina
+UBERON:0009058,faveolus,UBERON:0004119,endoderm-derived structure
+DOID:5563,malignant teratoma,DOID:3307,teratoma
+UBERON:0012344,holocrine gland,UBERON:0002365,exocrine gland
+HP:0012279,Hyposerinemia,HP:0012278,Abnormality of serine metabolism
+HP:0000215,Thick upper lip vermilion,HP:0011339,Abnormality of upper lip vermillion
+UBERON:0000372,extensor digitorum brevis,UBERON:0000311,extensor muscle
+HP:0008080,Hallux varus,HP:0010051,Deviation/Displacement of the hallux
+UBERON:2001250,pharyngobranchial 2 bone,UBERON:2000527,pharyngobranchial bone
+UBERON:0002119,left ovary,UBERON:0015212,lateral structure
+UBERON:2001609,pharyngobranchial 2 bone uncinate process,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0011027,Abnormality of the fallopian tube,HP:0000008,Abnormality of female internal genitalia
+UBERON:0001332,prepuce of penis,UBERON:0011374,prepuce
+UBERON:0009591,mesenchyme of interdigital region between pedal digits 2 and 3,UBERON:0009601,mesenchyme of interdigital region of pes
+UBERON:4000115,mineralized bone tissue,UBERON:4000013,mineralized tissue
+HP:0009779,3-4 toe syndactyly,HP:0001770,Toe syndactyly
+DOID:8872,penis carcinoma in situ,DOID:8719,in situ carcinoma
+HP:0004881,Episodic hypoventilation,HP:0002791,Hypoventilation
+UBERON:0007628,lateral septal complex,UBERON:0002663,septal nuclear complex
+UBERON:3000237,infrarostral cartilage,UBERON:0007844,cartilage element
+UBERON:4000174,caudal fin lepidotrichium,UBERON:4000172,lepidotrichium
+UBERON:0007413,nucleus of pontine reticular formation,UBERON:0002680,regional part of metencephalon
+UBERON:0007473,lumen of epithelial sac,UBERON:0012467,enclosed anatomical space
+CL:0002618,endothelial cell of umbilical vein,CL:0002543,vein endothelial cell
+HP:0004418,Thrombophlebitis,HP:0004936,Venous thrombosis
+HP:0004403,Proximal esophageal atresia,HP:0002032,Esophageal atresia
+DOID:10329,pneumoconiosis due to talc,DOID:10316,pneumoconiosis
+HP:0100182,Cone-shaped epiphysis of the middle phalanx of the 4th toe,HP:0100095,Abnormality of the epiphysis of the middle phalanx of the 4th toe
+UBERON:0012295,Guérin's valve,UBERON:0014403,male anatomical structure
+DOID:9360,intrinsic asthma,DOID:2841,asthma
+DOID:11265,trachoma,DOID:0050339,commensal bacterial infectious disease
+DOID:3373,juxtacortical osteosarcoma,DOID:3374,peripheral osteosarcoma
+UBERON:0009614,hindbrain neural plate,UBERON:0003075,neural plate
+HP:0012012,EEG with parietal focal spike waves,HP:0011197,EEG with focal spike waves
+DOID:7584,subglottis verrucous carcinoma,DOID:7585,subglottis squamous cell carcinoma
+UBERON:0000085,morula,UBERON:0000922,embryo
+UBERON:0013171,cricothyroid ligament,UBERON:0001743,ligament of larynx
+HP:0010906,Hyperhistidinemia,HP:0010905,Abnormality of histidine metabolism
+DOID:0050611,pharynx carcinoma in situ,DOID:8719,in situ carcinoma
+DOID:1529,penile disease,DOID:48,male reproductive system disease
+UBERON:0005819,cervical flexure,UBERON:0005817,neuraxis flexure
+UBERON:0015851,upper right incisor tusk,UBERON:0003450,upper jaw incisor
+UBERON:0006106,cochlear canal,UBERON:0005913,zone of bone organ
+UBERON:0002427,arm skin,UBERON:0003531,forelimb skin
+DOID:1094,attention deficit hyperactivity disorder,DOID:0060038,specific developmental disorder
+UBERON:3010231,costal folds,UBERON:3000977,body external integument structure
+UBERON:0011982,manual digit 7,UBERON:0002389,manual digit
+UBERON:0003324,mesenchyme of lower jaw,UBERON:0003104,mesenchyme
+UBERON:0001151,tail of pancreas,UBERON:0004119,endoderm-derived structure
+HP:0009666,Cone-shaped epiphysis of the proximal phalanx of the thumb,HP:0009688,Cone-shaped epiphyses of the thumb
+CL:0000269,prestalk cell,CL:0000263,vegetative cell (sensu Mycetozoa)
+DOID:8207,hilar lung carcinoma,DOID:7696,lung hilum cancer
+HP:0003530,Glutaric acidemia,HP:0001941,Acidosis
+UBERON:0004329,proximal phalanx of manual digit 3,UBERON:0014503,proximal phalanx of digit 3
+DOID:13626,photokeratitis,DOID:4677,keratitis
+HP:0004347,Weakness of muscles of respiration,HP:0002795,Functional respiratory abnormality
+DOID:3683,lung benign neoplasm,DOID:0050621,respiratory system benign neoplasm
+UBERON:0001843,lateral semicircular canal,UBERON:0001840,semicircular canal
+UBERON:0015840,incisor dental lamina,UBERON:0003355,epithelium of incisor
+UBERON:0007845,regular connective tissue,UBERON:0002384,connective tissue
+HP:0009058,Increased muscle lipid content,HP:0004303,Abnormality of muscle fibers
+UBERON:0002216,symphysis,UBERON:0002209,fibrous joint
+DOID:13036,tick-borne relapsing fever,DOID:13034,relapsing fever
+UBERON:0005078,lamina terminalis of neural tube,UBERON:0005291,embryonic tissue
+HP:0004015,Abnormality of radial metaphyses,HP:0009809,Abnormality of upper limb metaphysis
+DOID:0050659,biotin-responsive basal ganglia disease,DOID:679,basal ganglia disease
+HP:0002074,Increased neuronal autofluorescent lipopigment,HP:0011813,Increased cerebral lipofuscin
+UBERON:3000561,septum semicircularium laterale,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003624,manual digit 4,UBERON:0002389,manual digit
+DOID:6735,schwannoma of jugular foramen,DOID:956,peripheral nerve schwannoma
+UBERON:0001601,extra-ocular muscle,UBERON:0004277,eye muscle
+HP:0100876,Infra-orbital crease,HP:0000315,Abnormality of the orbital region
+UBERON:0003309,floor plate of diencephalon,UBERON:0002784,regional part of diencephalon
+DOID:9402,epididymitis,DOID:48,male reproductive system disease
+UBERON:0013227,crypt of Henle,UBERON:0013226,accessory lacrimal gland
+UBERON:0014675,distal interphalangeal joint of pedal digit 5,UBERON:0014680,distal interphalangeal joint of digit 5
+HP:0001785,Ankle swelling,HP:0003028,Abnormality of the ankles
+HP:0008458,Progressive congenital scoliosis,HP:0002650,Scoliosis
+HP:0100362,Aplasia of the phalanges of the 3rd toe,HP:0010331,Aplasia/Hypoplasia of the 3rd toe
+CL:1000510,kidney glomerular epithelial cell,CL:1000746,glomerular cell
+CL:0000824,mature natural killer cell,CL:0000623,natural killer cell
+HP:0009826,Limb undergrowth,HP:0009815,Aplasia/Hypoplasia of the extremities
+HP:0010924,Posterior cortical cataract,HP:0100019,Cortical cataract
+HP:0007410,Palmoplantar hyperhidrosis,HP:0000975,Hyperhidrosis
+HP:0010625,Anterior pituitary dysgenesis,HP:0011747,Abnormality of the anterior pituitary
+UBERON:0006477,Brodmann (1909) area 34,UBERON:0013529,Brodmann area
+HP:0000717,Autism,HP:0000729,Autism spectrum disorder
+UBERON:0004936,submucosa of pyloric antrum,UBERON:0004937,submucosa of pylorus
+DOID:7127,radiation cystitis,DOID:1679,cystitis
+HP:0010376,Patchy sclerosis of the phalanges of the 4th toe,HP:0010178,Patchy sclerosis of the phalanges of the toes
+UBERON:0002680,regional part of metencephalon,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0009518,Irregular epiphysis of the middle phalanx of the 2nd finger,HP:0009500,Abnormality of the epiphysis of the middle phalanx of the 2nd finger
+UBERON:0002904,lateral occipital sulcus,UBERON:0013118,sulcus of brain
+HP:0001800,Hypoplastic toenails,HP:0010624,Aplastic/hypoplastic toenail
+HP:0001322,Brain very small,HP:0006872,Cerebral hypoplasia
+HP:0012270,Decreased muscle glycogen content,HP:0012269,Abnormal muscle glycogen content
+UBERON:0010232,placodal ectoderm,UBERON:0000479,tissue
+HP:0010057,Abnormality of the phalanges of the hallux,HP:0010161,Abnormality of the phalanges of the toes
+DOID:4330,non-langerhans-cell histiocytosis,DOID:3405,histiocytosis
+UBERON:0002566,superior precentral sulcus,UBERON:0003022,cerebral cortex lobe
+UBERON:0002203,vasculature of eye,UBERON:0002200,vasculature of head
+HP:0010333,Flexion contracture of 3rd toe,HP:0001836,Camptodactyly (feet)
+DOID:9368,keratoconjunctivitis,DOID:5614,eye disease
+HP:0003173,Hypoplastic pubic bones,HP:0009104,Aplasia/Hypoplasia of the pubic bone
+HP:0002216,Premature graying of hair,HP:0009887,Abnormality of hair pigmentation
+UBERON:0010081,future common hepatic duct,UBERON:0003914,epithelial tube
+UBERON:3000961,external integument structure,UBERON:0000061,anatomical structure
+DOID:3512,neurofibrosarcoma,DOID:962,neurofibroma
+HP:0100880,Nephrogenic rest,HP:0012210,Abnormal renal morphology
+HP:0004423,Cranium bifidum occultum,HP:0002084,Encephalocele
+UBERON:0004202,kidney outer medulla outer stripe,UBERON:0006554,urinary system structure
+DOID:231,motor neuron disease,DOID:1289,neurodegenerative disease
+HP:0001223,Pointed proximal second through fifth metacarpals,HP:0006119,Proximal tapering of metacarpals
+CL:0008008,striated visceral muscle cell,CL:0000737,striated muscle cell
+HP:0003316,Butterfly vertebrae,HP:0008428,Vertebral clefting
+HP:0100909,Sclerosis of the proximal phalanx of the 3rd finger,HP:0100919,Sclerosis of the phalanges of the 3rd finger
+UBERON:0001781,layer of retina,UBERON:0004121,ectoderm-derived structure
+UBERON:0003268,tooth of lower jaw,UBERON:0001091,calcareous tooth
+DOID:6316,Bartholin's gland adenocarcinoma,DOID:3999,Bartholin's gland carcinoma
+DOID:5740,small intestinal vasoactive intestinal peptide producing tumor,DOID:10154,small intestine cancer
+CL:0000481,cholecystokin stimulating hormone secreting cell,CL:0000167,peptide hormone secreting cell
+UBERON:0003123,aortic arch 6,UBERON:0004363,aortic arch
+UBERON:0006250,infundibular recess of 3rd ventricle,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003648,metacarpal bone of digit 4,UBERON:0015046,manual digit 4 metacarpus endochondral element
+HP:0009846,Curved middle phalanges of the hand,HP:0009833,Abnormality of the middle phalanges of the hand
+DOID:9601,ischemic fasciitis,DOID:9598,fasciitis
+UBERON:0002708,posterior periventricular nucleus,UBERON:0002789,regional part of posterior hypothalamic region
+HP:0007589,Aplasia cutis congenita on trunk or limbs,HP:0001057,Aplasia cutis congenita
+UBERON:0014936,cerebral cortex ventricular layer,UBERON:0014950,layer of developing cerebral cortex
+HP:0002848,Specific anti-polysaccharide antibody deficiency,HP:0012475,Specific antibody deficiency
+UBERON:0015064,autopod cartilage,UBERON:0007844,cartilage element
+UBERON:2001045,sclerotome somite 5,UBERON:0003089,sclerotome
+CL:0001001,immature CD8_alpha-negative CD11b-negative dendritic cell,CL:0000998,CD8_alpha-negative CD11b-negative dendritic cell
+UBERON:0001257,trigone of urinary bladder,UBERON:0000064,organ part
+HP:0008780,Congenital bilateral hip dislocation,HP:0001374,Congenital hip dislocation
+HP:0011045,Agenesis of permanent maxillary central incisor,HP:0006293,Agenesis of maxillary central incisor
+HP:0002084,Encephalocele,HP:0007319,Morphological abnormality of the central nervous system
+HP:0004216,Osteolytic defects of the phalanges of the 5th finger,HP:0004213,Abnormality of the phalanges of the 5th finger
+HP:0100030,Accessory ectopic thyroid tissue,HP:0100028,Ectopic thyroid
+DOID:1973,fallopian tube adenosarcoma,DOID:1970,fallopian tube carcinosarcoma
+UBERON:3010027,M. sartorius,UBERON:0010890,pelvic complex muscle
+DOID:9538,multiple myeloma,DOID:0070004,myeloma
+UBERON:0000388,epiglottis,UBERON:0004119,endoderm-derived structure
+HP:0010038,Short 2nd metacarpal,HP:0010049,Short metacarpal
+HP:0009698,Contractures of the proximal interphalangeal joints of the fingers,HP:0001220,Interphalangeal joint contractures (hands)
+HP:0001832,Abnormality of the metatarsal bones,HP:0001760,Abnormality of the foot
+CL:0000071,blood vessel endothelial cell,CL:0002139,endothelial cell of vascular tree
+UBERON:0004292,cardiac skeleton,UBERON:0003837,thoracic segment connective tissue
+CL:0000283,pstO/ALC,CL:0000265,anterior like cell
+HP:0009452,Curved proximal phalanx of the 3rd finger,HP:0009358,Abnormality of the proximal phalanx of the 3rd finger
+HP:0012748,Focal T2 hyperintense brainstem lesion,HP:0012747,Abnormal brainstem MRI signal intensity
+DOID:10211,cholelithiasis,DOID:0000000,gallbladder disease
+HP:0003438,Absent Achilles reflex,HP:0200101,Decreased/absent ankle reflexes
+UBERON:0002512,corpus luteum,UBERON:0005398,female reproductive gland
+DOID:4308,polyradiculoneuropathy,DOID:1389,polyneuropathy
+HP:0100210,Small epiphysis of the distal phalanx of the 5th toe,HP:0100085,Small epiphyses of the 5th toe
+HP:0000960,Sacral dimple,HP:0010781,Skin dimples
+HP:0002612,Congenital hepatic fibrosis,HP:0001395,Hepatic fibrosis
+UBERON:0010410,inguinal fat pad,UBERON:0003916,fat pad
+UBERON:0010974,external intercostal pre-muscle mass,UBERON:0010970,intercostal pre-muscle mass
+DOID:11459,pseudotumor cerebri,DOID:9428,intracranial hypertension
+HP:0012356,Decreased mannosylation of N-linked protein glycosylation,HP:0012355,Abnormal mannosylation of N-linked protein glycosylation
+UBERON:0002270,hyaloid artery,UBERON:0000078,mixed ectoderm/mesoderm/endoderm-derived structure
+UBERON:0011289,pharyngobasilar fascia,UBERON:0006614,aponeurosis
+DOID:2275,pharyngitis,DOID:974,upper respiratory tract disease
+UBERON:2002083,fringing fulcrum,UBERON:2002291,fulcrum
+DOID:10869,fourth cranial nerve palsy,DOID:10863,paralytic squint
+UBERON:0012137,pedal digit 7,UBERON:0001466,pedal digit
+HP:0003674,Onset,HP:0000004,Onset and clinical course
+HP:0001270,Motor delay,HP:0001263,Global developmental delay
+HP:0007420,Spontaneous hematomas,HP:0001933,Subcutaneous hemorrhage
+HP:0009468,Deviation of the 2nd finger,HP:0004097,Deviation of finger
+UBERON:2002072,middle anterior process of basipterygium,UBERON:4100000,skeletal element projection
+UBERON:0003960,styloid process of temporal bone,UBERON:0004530,bony projection
+UBERON:0003459,chest bone,UBERON:0005175,chest organ
+UBERON:0002329,somite,UBERON:0012275,meso-epithelium
+UBERON:0000102,lung vasculature,UBERON:0006876,vasculature of organ
+DOID:8514,acute pulmonary heart disease,DOID:8515,Cor pulmonale
+UBERON:0014697,posterior choroidal artery,UBERON:0013151,choroidal artery
+UBERON:2002261,dorsal fin spine,UBERON:4000177,dorsal fin lepidotrichium
+UBERON:0002446,patella,UBERON:0011141,appendicular ossicle
+HP:0007621,Telangiectasia of extensor surfaces,HP:0100585,Teleangiectasia of the skin
+UBERON:0011191,ophthalmic vein,UBERON:0009141,craniocervical region vein
+UBERON:0010970,intercostal pre-muscle mass,UBERON:0005865,pre-muscle condensation
+HP:0007646,Absent lower eyelashes,HP:0000561,Absent eyelashes
+DOID:3039,cecum adenocarcinoma,DOID:1519,cecum carcinoma
+UBERON:0003715,splanchnic nerve,UBERON:0001021,nerve
+DOID:5475,uterine corpus adenofibroma,DOID:0060095,uterine benign neoplasm
+HP:0000073,Ureteral duplication,HP:0000069,Abnormality of the ureter
+HP:0009227,Broad proximal phalanx of the 5th finger,HP:0009150,Abnormality of the proximal phalanx of the 5th finger
+UBERON:0014623,substantia gelatinosa of cervical spinal cord dorsal horn,UBERON:0002181,substantia gelatinosa
+UBERON:2001247,epibranchial 3 bone,UBERON:2000658,epibranchial bone
+UBERON:0000156,theca externa,UBERON:0014404,female anatomical structure
+HP:0008815,Narrow sacroiliac notches in infancy,HP:0008803,Narrow sacroiliac notch
+UBERON:3000650,processus frontalis of maxilla,UBERON:0010313,neural crest-derived structure
+DOID:3132,porphyria cutanea tarda,DOID:3133,acute porphyria
+UBERON:0004171,trigeminothalamic tract,UBERON:0001018,axon tract
+UBERON:2001933,sensory canal tubule,UBERON:2001612,sensory canal
+DOID:14415,Legg-Calve-Perthes Disease,DOID:8125,osteochondrosis
+HP:0004400,Abnormality of the pylorus,HP:0002577,Abnormality of the stomach
+DOID:7840,pancreatic non-functioning delta cell tumor,DOID:7698,non-functioning pancreatic endocrine tumor
+HP:0003986,Exostoses of the radius,HP:0003960,Exostoses of the forearm bones
+UBERON:0004639,afferent arteriole,UBERON:0001980,arteriole
+UBERON:0002061,truncus arteriosus,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0001715,oculomotor nuclear complex,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0003889,Abnormality of the deltoid tuberosities,HP:0003063,Abnormality of the humerus
+UBERON:0005920,superior nasal concha,UBERON:0003973,nasal concha of ethmoid bone
+DOID:14725,autosomal dominant microcephaly,DOID:0050736,autosomal dominant disease
+UBERON:0010758,subdivision of organism along appendicular axis,UBERON:0000475,organism subdivision
+UBERON:0002857,first lumbar dorsal root ganglion,UBERON:0002836,lumbar dorsal root ganglion
+UBERON:0011308,pars reflexa of masseter,UBERON:0000064,organ part
+UBERON:0007193,orbital gyrus,UBERON:0015593,frontal gyrus
+HP:0000579,Nasolacrimal duct obstruction,HP:0011481,Abnormality of the lacrimal duct
+DOID:6844,kidney pelvis sarcomatoid transitional cell carcinoma,DOID:0050620,infiltrating renal pelvis transitional cell carcinoma
+HP:0004562,Beaking of vertebral bodies T12-L3,HP:0004568,Beaking of vertebral bodies
+DOID:256,hemangioma of spleen,DOID:254,hemangioma of intra-abdominal structure
+HP:0011080,Abnormality of premolar morphology,HP:0006482,Abnormality of dental morphology
+UBERON:2000911,transverse process of neural arch 3,UBERON:4100000,skeletal element projection
+UBERON:0006600,presumptive enteric nervous system,UBERON:0006598,presumptive structure
+UBERON:0000002,uterine cervix,UBERON:0001560,neck of organ
+CL:0002421,nucleated reticulocyte,CL:0000558,reticulocyte
+NCBITaxon:945,Ehrlichia chaffeensis,NCBITaxon:106178,canis group
+UBERON:0003023,pontine tegmentum,UBERON:0000064,organ part
+UBERON:0004889,lobar bronchus vasculature,UBERON:0000102,lung vasculature
+DOID:12168,ulnar nerve lesion,DOID:572,mononeuritis of upper limb and mononeuritis multiplex
+HP:0100377,Aplasia/Hypoplasia of the proximal phalanx of the 5th toe,HP:0010394,Abnormality of the proximal phalanx of the 5th toe
+UBERON:4200008,inter-clavicle joint,UBERON:0008114,joint of girdle
+DOID:6498,seborrheic keratosis,DOID:161,keratosis
+UBERON:0001097,axillary lymph node,UBERON:0003968,peripheral lymph node
+HP:0011233,Antihelical shelf,HP:0009738,Abnormality of the antihelix
+UBERON:2005316,fin fold pectoral fin bud,UBERON:0000481,multi-tissue structure
+CL:1001587,uterine cervix glandular cell,CL:0002535,epithelial cell of cervix
+HP:0009999,Partial duplication of the phalanx of hand,HP:0009997,Duplication of phalanx of hand
+HP:0011640,Single coronary artery origin,HP:0011636,Abnormal origin of the coronary arteries
+HP:0003029,Enlargement of the ankles,HP:0003028,Abnormality of the ankles
+HP:0005390,Recurrent opportunistic infections,HP:0002719,Recurrent infections
+DOID:1283,enterocele,DOID:1285,rectal disease
+DOID:7538,breast ductal adenoma,DOID:1625,breast adenoma
+DOID:4491,persian gulf syndrome,DOID:225,syndrome
+DOID:3828,chromophobe adenoma,DOID:3829,pituitary adenoma
+UBERON:0004468,set of muscles of vertebral column,UBERON:0004120,mesoderm-derived structure
+UBERON:2005022,opercular artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+UBERON:0010546,metapodial skeleton,UBERON:0004120,mesoderm-derived structure
+DOID:2752,glycogen storage disease II,DOID:2747,glycogen storage disease
+DOID:3952,adrenal cortex disease,DOID:9553,adrenal gland disease
+HP:0009148,Small epiphysis of the distal phalanx of the 5th finger,HP:0010254,Small epiphyses of the distal phalanges of the hand
+CL:0000630,supportive cell,CL:0000003,native cell
+UBERON:3000505,processus pterygoideus of maxilla,UBERON:4100000,skeletal element projection
+CL:0000334,vegetative cell (sensu Fungi),CL:0000521,fungal cell
+DOID:7583,glottis verrucous carcinoma,DOID:7031,glottis squamous cell carcinoma
+UBERON:2000508,pelvic fin radial bone,UBERON:0010742,bone of pelvic complex
+CL:0002241,pulmonary interstitial fibroblast,CL:0000057,fibroblast
+HP:0004493,Craniofacial hyperostosis,HP:0000271,Abnormality of the face
+HP:0001362,Skull defect,HP:0002648,Abnormality of calvarial morphology
+DOID:2596,larynx cancer,DOID:0050615,respiratory system cancer
+UBERON:0010077,cuboidal epithelium,UBERON:0000483,epithelium
+HP:0100241,Ectopic respiratory mucosa,HP:0002973,Abnormality of the forearm
+UBERON:2005025,dorsal longitudinal anastomotic vessel,UBERON:0003524,tail blood vessel
+NCBITaxon:6934,Parasitiformes,NCBITaxon:6933,Acari
+HP:0009281,Aplasia of the 4th finger,HP:0009272,Aplasia/Hypoplasia of the 4th finger
+UBERON:0001201,serosa of stomach,UBERON:0009034,stomach region
+DOID:3611,acute retinal necrosis syndrome,DOID:3612,retinitis
+DOID:0050721,serine deficiency,DOID:9252,amino acid metabolic disorder
+UBERON:0016430,palmar branch of median nerve,UBERON:0003433,arm nerve
+UBERON:0001720,cochlear nucleus,UBERON:0007635,nucleus of medulla oblongata
+CL:0000853,olfactory epithelial support cell,CL:0000630,supportive cell
+UBERON:0001672,anterior cerebral vein,UBERON:0001663,cerebral vein
+UBERON:0015106,distal tarsal bone 2 cartilage,UBERON:0010885,hindlimb cartilage element
+UBERON:2001508,trabecula communis,UBERON:0004120,mesoderm-derived structure
+UBERON:0000077,mixed endoderm/mesoderm-derived structure,UBERON:0004120,mesoderm-derived structure
+HP:0000408,Progressive sensorineural hearing impairment,HP:0001730,Progressive hearing impairment
+HP:0008322,Abnormal mitochondrial morphology,HP:0012103,Abnormality of the mitochondrion
+HP:0001022,Albinism,HP:0007513,Generalized hypopigmentation
+HP:0005746,Osteosclerosis of calvaria and base of the skull,HP:0005450,Calvarial osteosclerosis
+HP:0002653,Bone pain,HP:0011843,Abnormality of skeletal physiology
+HP:0009129,Upper limb amyotrophy,HP:0003202,Amyotrophy
+UBERON:2000442,supraneural bone,UBERON:4300035,supraneural element
+HP:0007982,Central tapetoretinal dystrophy,HP:0000556,Retinal dystrophy
+CL:0007020,bottle cell,CL:0000007,early embryonic cell
+HP:0010269,Bracket epiphyses of the proximal phalanges of the hand,HP:0010229,Bracket epiphyses of the phalanges of the hand
+UBERON:0004255,forelimb stylopod muscle,UBERON:0001499,muscle of arm
+DOID:10991,basal ganglia cerebrovascular disease,DOID:6713,cerebrovascular disease
+UBERON:0001516,abdominal aorta,UBERON:0005800,segment of aorta
+UBERON:3010195,lateral appendix,UBERON:0004119,endoderm-derived structure
+UBERON:2000968,hypaxial region somite 21,UBERON:0003895,hypaxial myotome region
+UBERON:0006756,median lingual swelling,UBERON:0005423,developing anatomical structure
+UBERON:0004525,cardiac muscle tissue of trabecula carnea of right ventricle,UBERON:0003381,cardiac muscle of right ventricle
+HP:0004928,Peripheral arterial stenosis,HP:0004950,Peripheral arterial disease
+HP:0100821,Urethrocele,HP:0100672,Vaginal hernia
+HP:0100075,Stippling of the epiphyses of the 4th toe,HP:0010335,Abnormality of the epiphyses of the 4th toe
+HP:0004930,Abnormality of the pulmonary vasculature,HP:0002597,Abnormality of the vasculature
+HP:0100282,Acute colitis,HP:0002583,Colitis
+UBERON:0004925,submucosa of laryngopharynx,UBERON:0004924,submucosa of pharynx
+HP:0009306,Triangular shaped distal phalanx of the 4th finger,HP:0009407,Triangular shaped phalanges of the 4th finger
+NCBITaxon:337677,Cricetidae,NCBITaxon:337687,Muroidea
+CL:0002309,corticotroph,CL:0000467,adrenocorticotropic hormone secreting cell
+UBERON:0010739,distal carpal bone 5,UBERON:0001481,distal carpal bone
+UBERON:0002059,submandibular ganglion,UBERON:0001808,parasympathetic ganglion
+HP:0012271,Episodic upper airway obstruction,HP:0002781,Upper airway obstruction
+UBERON:0005882,neural tube alar plate,UBERON:0005423,developing anatomical structure
+UBERON:2000267,primary olfactory fiber layer,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001618,buccal artery,UBERON:0001637,artery
+HP:0001804,Hypoplastic fingernail,HP:0001792,Small nail
+UBERON:0002734,superior temporal sulcus,UBERON:0014687,temporal sulcus
+UBERON:0014372,fibroelastic membrane of larynx,UBERON:0004119,endoderm-derived structure
+UBERON:0005564,gonad primordium,UBERON:0001048,primordium
+DOID:3516,adult fibrosarcoma,DOID:3355,fibrosarcoma
+UBERON:4200042,brevis shelf,UBERON:4100000,skeletal element projection
+HP:0008462,Cervical instability,HP:0005881,Spinal instability
+HP:0009617,Abnormality of the distal phalanx of the thumb,HP:0009602,Abnormality of the phalanges of the thumb
+UBERON:0002996,nucleus of optic tract,UBERON:0014450,pretectal nucleus
+UBERON:0004687,lieno-renal ligament,UBERON:0004120,mesoderm-derived structure
+UBERON:0007573,migrating epithelium,UBERON:0000483,epithelium
+UBERON:0007307,pronephric glomerular basement membrane,UBERON:0005777,glomerular basement membrane
+HP:0100340,Fibular deviation of the 4th toe,HP:0010338,Deviation/Displacement of the 4th toe
+HP:0001886,"Osteomyelitis or necrosis, distal, due to sensory neuropathy (feet)",HP:0000763,Sensory neuropathy
+DOID:3252,prostate rhabdomyosarcoma,DOID:4054,prostate sarcoma
+DOID:2283,keratopathy,DOID:10124,corneal disease
+DOID:4919,renal pelvis carcinoma,DOID:263,kidney cancer
+HP:0010365,Symphalangism affecting the phalanges of the 3rd toe,HP:0010330,Abnormality of the phalanges of the 3rd toe
+UBERON:3000518,pseudodentary,UBERON:0008907,dermal bone
+HP:0006873,Symmetrical progressive peripheral demyelination,HP:0007262,Symmetric peripheral demyelination
+CL:0002187,basal cell of epidermis,CL:0000646,basal cell
+CL:0002324,myoepithelial cell of mammary gland,CL:1000416,myoepithelial cell of lactiferous gland
+HP:0009503,Bracket epiphysis of the distal phalanx of the 2nd finger,HP:0009489,Bracket epiphyses of the 2nd finger
+HP:0011128,Acute esophageal necrosis,HP:0002031,Abnormality of the esophagus
+DOID:2815,cranial nerve malignant neoplasm,DOID:338,cranial nerve neoplasm
+UBERON:0007364,reticulorumen,UBERON:0009034,stomach region
+DOID:3321,gangliosidosis GM2,DOID:2368,gangliosidosis
+UBERON:0014856,cysticercus stage,UBERON:0000069,larval stage
+DOID:13001,carotid stenosis,DOID:3407,carotid artery disease
+UBERON:2000364,hypural,UBERON:0004376,fin bone
+HP:0009312,Osteolytic defects of the proximal phalanx of the 4th finger,HP:0009284,Abnormality of the proximal phalanx of the 4th finger
+UBERON:0002046,thyroid gland,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0012343,Decreased serum ferritin,HP:0011031,Abnormality of iron homeostasis
+UBERON:0010505,periosteal dura mater,UBERON:0010507,layer of dura mater
+HP:0005895,Radial deviation of thumb terminal phalanx,HP:0009617,Abnormality of the distal phalanx of the thumb
+UBERON:0001240,muscularis mucosae of intestine,UBERON:0004221,intestine smooth muscle
+UBERON:0012478,cloacal gland,UBERON:0004120,mesoderm-derived structure
+UBERON:4300025,posterior dorsolateral plate,UBERON:0008907,dermal bone
+DOID:0050686,organ system cancer,DOID:162,cancer
+UBERON:0002307,choroid plexus of lateral ventricle,UBERON:0001886,choroid plexus
+DOID:6065,urinary tract non-invasive transitional cell neoplasm,DOID:5433,urinary tract papillary transitional cell benign neoplasm
+UBERON:0000950,gracilis,UBERON:0004252,hindlimb stylopod muscle
+UBERON:0002148,locus ceruleus,UBERON:0002680,regional part of metencephalon
+DOID:5709,mixed-type liposarcoma,DOID:3382,liposarcoma
+CL:0000556,megakaryocyte,CL:0000763,myeloid cell
+HP:0004246,Delayed ossification of the scaphoid,HP:0004243,Abnormality of the scaphoid
+UBERON:0011140,superficial part of masseter muscle,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0011607,Transposition of the great arteries with ventricular septal defect,HP:0001669,Transposition of the great arteries
+UBERON:0007122,pharyngeal pouch 1,UBERON:0004117,pharyngeal pouch
+HP:0010102,Aplasia of the distal phalanx of the hallux,HP:0010110,Aplasia of the phalanges of the hallux
+HP:0000455,Broad nasal tip,HP:0000436,Abnormality of the nasal tip
+HP:0005968,Temperature instability,HP:0004370,Abnormality of temperature regulation
+DOID:0060028,Good syndrome,DOID:2583,agammaglobulinemia
+DOID:9903,meibomian cyst,DOID:9098,sebaceous gland disease
+HP:0001993,Ketoacidosis,HP:0001946,Ketosis
+UBERON:0003389,mesothelium of diaphragm,UBERON:0001136,mesothelium
+HP:0007434,Plaque-like facial hemangioma,HP:0000329,Facial hemangioma
+UBERON:2201671,anal fin radial cartilage,UBERON:2205225,median fin radial cartilage
+UBERON:2000103,supramaxilla,UBERON:0008907,dermal bone
+UBERON:0001551,vein of hindlimb zeugopod,UBERON:0004261,lower leg blood vessel
+UBERON:2000858,somite 8,UBERON:0002329,somite
+HP:0012635,Iris hypoperfusion,HP:0007905,Abnormal iris vasculature
+DOID:3707,endometrial mucinous adenocarcinoma,DOID:2870,endometrial adenocarcinoma
+UBERON:4000122,acellular bone tissue,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:3917,pancreatic serous cystadenoma,DOID:3918,pancreatic cystadenoma
+CL:0000755,type 3 cone bipolar cell (sensu Mus),CL:0000750,OFF-bipolar cell
+UBERON:0010528,pneumatic cavity of bone,UBERON:0010527,cavity of bone organ
+UBERON:0003295,pharyngeal gland,UBERON:0004119,endoderm-derived structure
+DOID:552,pneumonia,DOID:850,lung disease
+UBERON:0004718,Brodmann (1909) area 26,UBERON:0013529,Brodmann area
+DOID:6491,breast capillary hemangioma,DOID:476,breast hemangioma
+NCBITaxon:27317,Galactomyces geotrichum,NCBITaxon:27316,Galactomyces
+HP:0012672,Akinetic mutism,HP:0000745,Diminished motivation
+UBERON:0014769,palpebral vein,UBERON:0003502,neck blood vessel
+DOID:5390,clear cell adenoma,DOID:657,adenoma
+UBERON:2001191,supraneural 2 bone,UBERON:2000442,supraneural bone
+UBERON:0010234,palatopharyngeus muscle,UBERON:0003831,respiratory system muscle
+UBERON:3000290,medial inferior prenasal cartilage,UBERON:0010313,neural crest-derived structure
+DOID:11316,histoplasmosis retinitis,DOID:3612,retinitis
+UBERON:0010254,2nd arch mesenchyme from neural crest,UBERON:0010359,pharyngeal arch mesenchyme from neural crest
+UBERON:0007640,hippocampus stratum lacunosum moleculare,UBERON:0002305,layer of hippocampus
+DOID:679,basal ganglia disease,DOID:936,brain disease
+DOID:2388,renal artery disease,DOID:0050828,artery disease
+UBERON:0005316,endocardial endothelium,UBERON:0008307,heart endothelium
+UBERON:0003428,gonadal fat pad,UBERON:0003916,fat pad
+NCBITaxon:1637,Listeria,NCBITaxon:186820,Listeriaceae
+UBERON:0002620,tuber cinereum,UBERON:0004121,ectoderm-derived structure
+HP:0009138,Synostosis involving bones of the lower limbs,HP:0100491,Abnormality of the joints of the lower limbs
+DOID:5162,arteriolosclerosis,DOID:2349,arteriosclerosis
+UBERON:0001476,deltoid,UBERON:0001482,muscle of shoulder
+HP:0001177,Preaxial hand polydactyly,HP:0001161,Hand polydactyly
+HP:0100798,Fingernail dysplasia,HP:0002164,Nail dysplasia
+UBERON:0001855,cochlear duct of membranous labyrinth,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0003125,vitelline membrane,UBERON:0005764,acellular membrane
+UBERON:3000260,lamina nariochoanalis,UBERON:4100000,skeletal element projection
+UBERON:0002227,spiral organ of cochlea,UBERON:0004121,ectoderm-derived structure
+HP:0009508,Ivory epiphysis of the distal phalanx of the 2nd finger,HP:0010252,Ivory epiphyses of the distal phalanges of the hand
+UBERON:2000139,immature otolith,UBERON:0002050,embryonic structure
+HP:0100488,Symphalangism of the proximal phalanx of the hallux with the 1st metatarsal,HP:0010073,Synostosis involving the 1st metatarsal
+UBERON:0010074,chromaffin system,UBERON:0000480,anatomical group
+UBERON:0004888,right lung hilus,UBERON:0004886,lung hilus
+UBERON:2000120,lateral line ganglion,UBERON:0003338,ganglion of peripheral nervous system
+UBERON:0002289,midbrain cerebral aqueduct,UBERON:0004086,brain ventricle
+UBERON:0010380,enteric nerve,UBERON:0010313,neural crest-derived structure
+DOID:4438,central nervous system germinoma,DOID:4439,central nervous system germ cell tumor
+DOID:6848,adult vagina botryoid rhabdomyosarcoma,DOID:6788,vagina botryoid rhabdomyosarcoma
+CL:0000798,gamma-delta T cell,CL:0000084,T cell
+UBERON:0015144,autopod hair,UBERON:0001037,strand of hair
+DOID:6086,malignant leptomeningeal tumor,DOID:3565,meningioma
+HP:0001430,Abnormality of the calf musculature,HP:0001437,Abnormality of the musculature of the lower limbs
+CL:0001013,mature interstitial dendritic cell,CL:0001007,interstitial dendritic cell
+HP:0000907,Anterior rib cupping,HP:0000887,Cupped ribs
+HP:0010178,Patchy sclerosis of the phalanges of the toes,HP:0100924,Sclerosis of the phalanges of the toes
+CL:1000500,kidney interstitial cell,CL:1000497,kidney cell
+DOID:12236,primary biliary cirrhosis,DOID:5082,liver cirrhosis
+HP:0003691,Scapular winging,HP:0000782,Abnormality of the scapula
+CL:1001287,outer medulla vasa recta descending limb cell,CL:1001285,vasa recta descending limb cell
+UBERON:0007738,metacarpophalangeal joint of manual digit 2,UBERON:0003695,metacarpophalangeal joint
+CL:1000706,ureter urothelial cell,CL:1000601,ureteral cell
+DOID:1884,viral hepatitis,DOID:2237,hepatitis
+DOID:0050900,sacrum chordoma,DOID:4153,spinal chordoma
+UBERON:0013074,cornual sinus,UBERON:0002553,anatomical cavity
+CL:0002532,CD16-positive myeloid dendritic cell,CL:0000782,myeloid dendritic cell
+UBERON:0006640,crus of clitoris,UBERON:0005156,reproductive structure
+DOID:13348,laryngeal cartilage cancer,DOID:2596,larynx cancer
+HP:0008850,Severe postnatal growth retardation,HP:0008897,Postnatal growth retardation
+UBERON:2001508,trabecula communis,UBERON:0003932,cartilage element of chondrocranium
+UBERON:0011582,paired limb/fin skeleton,UBERON:0010912,subdivision of skeleton
+HP:0010274,Ivory epiphyses of the proximal phalanges of the hand,HP:0010245,Abnormality of the epiphyses of the proximal phalanges of the hand
+UBERON:0009124,geniculate placode,UBERON:0003078,epibranchial placode
+UBERON:4300019,dorsal fin basal cartilage,UBERON:0005174,dorsal region organ
+HP:0008494,Inferior lens subluxation,HP:0001132,Lens subluxation
+DOID:472,subglottic angioma,DOID:255,hemangioma
+UBERON:0005014,mucosa of female urethra,UBERON:0014404,female anatomical structure
+DOID:4697,perineurioma,DOID:3193,peripheral nerve sheath neoplasm
+UBERON:0014635,dorsal nerve root of cervical spinal cord,UBERON:0002261,dorsal root of spinal cord
+UBERON:0011741,cardiac valve leaflet,UBERON:0010313,neural crest-derived structure
+HP:0000802,Impotence,HP:0100639,Erectile abnormalities
+CL:0002182,surface mucosal cell of stomach,CL:0000319,mucus secreting cell
+DOID:11776,blind hypertensive eye,DOID:9799,eye degenerative disease
+UBERON:2000579,rostral mesencephalo-cerebellar tract,UBERON:0002316,white matter
+DOID:5502,lice infestation,DOID:4110,parasitic ectoparasitic infectious disease
+UBERON:0001032,sensory system,UBERON:0000467,anatomical system
+UBERON:0014685,pterygoid plexus,UBERON:0001593,venous plexus
+HP:0001842,Acroosteolysis (feet),HP:0009134,Osteolysis involving bones of the feet
+HP:0003744,Genetic anticipation with paternal anticipation bias,HP:0003743,Genetic anticipation
+DOID:5046,mediastinal granular cell myoblastoma,DOID:4691,malignant mediastinal neurogenic neoplasm
+UBERON:0001628,posterior communicating artery,UBERON:0000077,mixed endoderm/mesoderm-derived structure
+DOID:9854,lingual-facial-buccal dyskinesia,DOID:480,movement disease
+HP:0002308,Arnold-Chiari malformation,HP:0002438,Cerebellar malformation
+HP:0200066,Ribbonlike corneal degeneration,HP:0007705,Corneal degeneration
+UBERON:0005568,rhombomere 1 roof plate,UBERON:0005502,rhombomere roof plate
+HP:0012508,Metamorphopsia,HP:0000504,Abnormality of vision
+UBERON:0000114,lung connective tissue,UBERON:0003580,lower respiratory tract connective tissue
+UBERON:2005149,distal epidermal cap of regenerating fin/limb,UBERON:0007567,regenerating anatomical structure
+CL:0000862,suppressor macrophage,CL:0000861,elicited macrophage
+UBERON:0002468,foliate papilla,UBERON:0014389,gustatory papilla of tongue
+UBERON:0006257,laryngotracheal groove,UBERON:0004119,endoderm-derived structure
+DOID:6160,childhood choriocarcinoma of the testis,DOID:5551,choriocarcinoma of the testis
+UBERON:0010285,midbrain basal plate,UBERON:0003528,brain grey matter
+UBERON:2005248,trans-choroid plexus branch,UBERON:0003499,brain blood vessel
+CL:0001658,visual pigment cell (sensu Nematoda and Protostomia),CL:0000149,visual pigment cell
+UBERON:0011804,"feather bud, epidermal component",UBERON:0010314,structure with developmental contribution from neural crest
+DOID:12969,central nervous system leukemia,DOID:3620,central nervous system cancer
+UBERON:2001347,stratum fibrosum et griseum superficiale,UBERON:0004121,ectoderm-derived structure
+UBERON:0009197,basioccipital pre-cartilage condensation,UBERON:0005866,pre-cartilage condensation
+UBERON:0011244,perpendicular plate of ethmoid,UBERON:0004120,mesoderm-derived structure
+HP:0001212,Prominent fingertip pads,HP:0011298,Prominent digit pad
+CL:0000809,"double-positive, alpha-beta thymocyte",CL:0000893,thymocyte
+DOID:859,holocarboxylase synthetase deficiency,DOID:857,multiple carboxylase deficiency
+HP:0005135,EKG: T-wave abnormalities,HP:0003115,Abnormal EKG
+HP:0009462,Radial deviation of the 3rd finger,HP:0009317,Deviation of the 3rd finger
+HP:0009489,Bracket epiphyses of the 2nd finger,HP:0010229,Bracket epiphyses of the phalanges of the hand
+DOID:2187,amelogenesis imperfecta,DOID:693,dental enamel hypoplasia
+NCBITaxon:41283,Chrysosporium parvum,NCBITaxon:40411,Chrysosporium
+DOID:3530,chronic wasting disease,DOID:649,prion disease
+DOID:4706,infratentorial cancer,DOID:1319,brain cancer
+DOID:2656,breast intracanalicular fibroadenoma,DOID:1618,breast fibroadenoma
+DOID:0050739,autosomal genetic disease,DOID:0050177,monogenic disease
+HP:0100118,Pseudoepiphysis of the middle phalanx of the 2nd toe,HP:0100089,Abnormality of the epiphysis of the middle phalanx of the 2nd toe
+UBERON:0008946,lung parenchyma,UBERON:0004119,endoderm-derived structure
+HP:0008055,Aplasia/Hypoplasia affecting the uvea,HP:0000553,Abnormality of the uvea
+CL:0002309,corticotroph,CL:0000639,basophil cell of pars distalis of adenohypophysis
+UBERON:0000397,colonic epithelium,UBERON:0001278,epithelium of large intestine
+UBERON:0007136,rectouterine fold,UBERON:0004120,mesoderm-derived structure
+UBERON:0001102,cartilage of main bronchus,UBERON:0001956,cartilage of bronchus
+UBERON:0008367,breast epithelium,UBERON:0000483,epithelium
+UBERON:0007726,interphalangeal joint of pedal digit 3,UBERON:0007721,interphalangeal joint of pes
+HP:0010014,Abnormality of the epiphysis of the 1st metacarpal,HP:0010009,Abnormality of the 1st metacarpal
+DOID:10619,lymph node cancer,DOID:0060073,lymphatic system cancer
+DOID:13174,dissociated nystagmus,DOID:9650,pathologic nystagmus
+UBERON:0010034,copula linguae,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:2001412,epiotic,UBERON:0010313,neural crest-derived structure
+UBERON:0004900,right lung middle lobe lobar bronchus mesenchyme,UBERON:0004901,right lung lobar bronchus mesenchyme
+HP:0001884,Talipes calcaneovalgus,HP:0001883,Talipes
+HP:0009106,Abnormal pelvis bone ossification,HP:0002644,Abnormality of pelvic girdle bone morphology
+HP:0004771,Premature graying of body hair,HP:0002216,Premature graying of hair
+UBERON:0008800,parietal endoderm,UBERON:0000478,extraembryonic structure
+CL:0002278,GIP cell,CL:0000164,enteroendocrine cell
+HP:0009463,Ulnar deviation of the 3rd finger,HP:0009317,Deviation of the 3rd finger
+UBERON:2002026,pectoral fin proximal radial bone 1,UBERON:2102026,pectoral fin proximal radial element 1
+HP:0012643,Foveal hypopigmentation,HP:0000493,Abnormality of the fovea
+UBERON:0009962,excretory gland,UBERON:0002530,gland
+DOID:11518,abnormal pupillary function,DOID:238,pupil disease
+UBERON:2001663,basibranchial 4 tooth,UBERON:0001091,calcareous tooth
+HP:0003919,Sclerotic humeral metaphysis with longitudinal striations,HP:0003918,Sclerotic humeral metaphysis
+DOID:0080056,achondrogenesis type II,DOID:0080043,achondrogenesis
+UBERON:2001517,ceratobranchial 2 cartilage,UBERON:2001516,ceratobranchial cartilage
+HP:0006888,Meningoencephalocele,HP:0002084,Encephalocele
+HP:0011513,Retinal cavernous angioma,HP:0007797,Retinal vascular malformation
+HP:0000987,Atypical scarring of skin,HP:0100699,Scarring
+CL:0000185,myoepithelial cell,CL:0000183,contractile cell
+HP:0002000,Short columella,HP:0009929,Abnormality of the columella
+DOID:10203,external auditory meatus lipoma,DOID:0060096,sensory organ benign neoplasm
+UBERON:0006516,dorsal pallidum,UBERON:0005401,cerebral hemisphere grey matter
+UBERON:0006877,vasculature of liver,UBERON:0002201,vasculature of trunk
+UBERON:0006643,tunica albuginea of testis,UBERON:0014403,male anatomical structure
+HP:0005474,Decreased calvarial ossification,HP:0004331,Decreased skull ossification
+UBERON:0001879,nucleus of diagonal band,UBERON:0001877,medial septal nucleus
+DOID:11823,hepatorenal syndrome,DOID:409,liver disease
+HP:0009843,Aplasia/Hypoplasia of the middle phalanges of the hand,HP:0009767,Aplasia/Hypoplasia of the phalanges of the hand
+UBERON:2001927,anterior myodome,UBERON:0004704,bone fossa
+HP:0009451,Bullet-shaped proximal phalanx of the 3rd finger,HP:0009358,Abnormality of the proximal phalanx of the 3rd finger
+HP:0010919,Abnormality of homocysteine metabolism,HP:0004339,Abnormality of sulfur amino acid metabolism
+UBERON:0002513,endochondral bone,UBERON:0010363,endochondral element
+UBERON:3000735,mid-dorsal keel,UBERON:0000064,organ part
+UBERON:0012151,skeleton of manual digitopodium,UBERON:0012150,skeleton of digitopodium
+UBERON:0003414,mesenchyme of mandible,UBERON:0003324,mesenchyme of lower jaw
+UBERON:4000087,cosmine,UBERON:0010365,odontoid tissue
+UBERON:0002087,atrioventricular canal,UBERON:0004120,mesoderm-derived structure
+DOID:5845,anterolateral myocardial infarction,DOID:5844,myocardial infarction
+UBERON:0002493,uterine artery,UBERON:0015212,lateral structure
+CL:0002076,endo-epithelial cell,CL:0002371,somatic cell
+DOID:14548,steroid-induced glaucoma - borderline,DOID:9283,borderline glaucoma
+UBERON:0009100,nephric fold,UBERON:0005423,developing anatomical structure
+UBERON:2000104,suprapreopercle,UBERON:0008907,dermal bone
+HP:0005255,Absence of pectoralis minor muscle,HP:0011957,Abnormality of the  pectoral muscle
+DOID:5284,retroperitoneal leiomyosarcoma,DOID:12341,retroperitoneal sarcoma
+CL:0002534,mature CD16-positive myeloid dendritic cell,CL:0000841,mature conventional dendritic cell
+UBERON:0002110,gallbladder,UBERON:0005172,abdomen organ
+UBERON:0006298,submandibular gland primordium,UBERON:0001048,primordium
+UBERON:0005357,brain ependyma,UBERON:0004670,ependyma
+UBERON:0011587,pre-dentine,UBERON:0010365,odontoid tissue
+HP:0000807,Glandular hypospadias,HP:0000047,Hypospadias
+HP:0000287,Increased facial adipose tissue,HP:0000291,Abnormality of facial adipose tissue
+CL:0000524,spheroplast,CL:0000371,protoplast
+HP:0006712,Aplasia/Hypoplasia of the ribs,HP:0006711,Aplasia/Hypoplasia involving bones of the thorax
+HP:0002396,Cogwheel rigidity,HP:0002063,Rigidity
+UBERON:0010568,manual digit 4 metacarpus pre-cartilage condensation,UBERON:0015046,manual digit 4 metacarpus endochondral element
+HP:0006596,Restricted chest movement,HP:0001547,Abnormality of the rib cage
+CL:0002140,acinar cell of sebaceous gland,CL:0000317,sebum secreting cell
+HP:0005991,Limited neck flexion,HP:0005986,Limitation of neck motion
+DOID:14791,Leber congenital amaurosis,DOID:5679,retinal disease
+UBERON:0001399,deep brachial artery,UBERON:0001637,artery
+HP:0011130,Abnormality of renal calyx morphology,HP:0012210,Abnormal renal morphology
+HP:0100781,Abnormality of the sacroiliac joint,HP:0002867,Abnormality of the ilium
+UBERON:0002875,medial pericuneate nucleus,UBERON:0007635,nucleus of medulla oblongata
+HP:0011917,Short 5th toe,HP:0001831,Short toe
+UBERON:0007144,tail of embryo,UBERON:0002050,embryonic structure
+UBERON:0002710,cingulate sulcus,UBERON:0008334,subarachnoid sulcus
+UBERON:0003252,thoracic rib cage,UBERON:0004120,mesoderm-derived structure
+HP:0010074,Triangular shaped 1st metatarsal,HP:0010210,Triangular shaped proximal phalanges of the toes
+DOID:6554,ovarian clear cell malignant adenofibroma,DOID:2394,ovarian cancer
+UBERON:2202029,pectoral fin proximal radial cartilage 4,UBERON:2102029,pectoral fin proximal radial element 4
+UBERON:0011892,anterior uvea,UBERON:0004121,ectoderm-derived structure
+UBERON:4200049,cartilago sesamoides,UBERON:0001479,sesamoid bone
+CL:0002625,seminiferous tubule epithelial cell,CL:0000068,duct epithelial cell
+HP:0005162,Impaired left ventricular function,HP:0001711,Abnormality of the left ventricle
+CL:0000124,glial cell (sensu Nematoda and Protostomia),CL:0000125,glial cell
+UBERON:2007012,lateral forebrain bundle,UBERON:0002316,white matter
+UBERON:0003676,patellar ligament,UBERON:0011088,ligament of knee joint
+HP:0009206,Enlarged epiphysis of the middle phalanx of the 5th finger,HP:0010260,Enlarged epiphyses of the middle phalanges of the hand
+DOID:118,pericardial effusion,DOID:0050829,pericardium disease
+DOID:10328,siderosis,DOID:10316,pneumoconiosis
+CL:1001209,inner medulla vasa recta ascending limb cell,CL:1001131,vasa recta ascending limb cell
+HP:0005428,Severe recurrent varicella,HP:0004429,Recurrent viral infections
+HP:0100183,Enlarged epiphysis of the middle phalanx of the 4th toe,HP:0100095,Abnormality of the epiphysis of the middle phalanx of the 4th toe
+UBERON:2001046,sclerotome somite 8,UBERON:0003089,sclerotome
+HP:0012013,EEG with temporal focal spike waves,HP:0011197,EEG with focal spike waves
+HP:0002436,Occipital meningocele,HP:0002435,Meningocele
+UBERON:0002924,terminal nerve,UBERON:0001785,cranial nerve
+UBERON:3000811,glenoid end of clavicle,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:6314,ovarian fetiform teratoma,DOID:6231,mature teratoma of the ovary
+HP:0009288,Curved proximal phalanx of the 4th finger,HP:0009285,Curved phalanges of the 4th finger
+UBERON:0012141,manual digitopodium region,UBERON:0012140,digitopodium region
+DOID:0050610,oral cavity carcinoma in situ,DOID:8719,in situ carcinoma
+UBERON:0009078,pessulus,UBERON:0003406,cartilage of respiratory system
+UBERON:0008250,cardiac stomach,UBERON:0004921,subdivision of digestive tract
+HP:0002060,Abnormality of the cerebrum,HP:0100547,Abnormality of the forebrain
+HP:0100397,Short proximal phalanx of the 5th toe,HP:0100368,Short phalanx of the 5th toe
+DOID:4271,microsporidiosis,DOID:2473,opportunistic mycosis
+UBERON:0013517,coccygeal vertebra cartilage element,UBERON:0013503,caudal vertebra cartilage element
+UBERON:4200018,calcaneal tuber,UBERON:0005913,zone of bone organ
+DOID:3008,invasive ductal carcinoma,DOID:3007,breast ductal carcinoma
+UBERON:0001102,cartilage of main bronchus,UBERON:0003590,main bronchus connective tissue
+UBERON:0003054,roof plate,UBERON:0000119,cell layer
+UBERON:0006474,Brodmann (1909) area 30,UBERON:0013529,Brodmann area
+HP:0009025,Increased connective tissue,HP:0003549,Abnormality of connective tissue
+UBERON:0005440,ductus arteriosus,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0000304,tendon sheath,UBERON:0004923,organ component layer
+UBERON:0009592,mesenchyme of interdigital region between pedal digits 3 and 4,UBERON:0009601,mesenchyme of interdigital region of pes
+HP:0002020,Gastroesophageal reflux,HP:0002577,Abnormality of the stomach
+CL:0002492,strial marginal cell,CL:0002491,auditory epithelial cell
+DOID:11824,multicentric reticulohistiocytosis,DOID:225,syndrome
+NCBITaxon:117568,mitosporic Pleosporaceae,NCBITaxon:28556,Pleosporaceae
+UBERON:0004990,mucosa of ascending colon,UBERON:0000317,colonic mucosa
+DOID:0050440,familial partial lipodystrophy,DOID:811,lipodystrophy
+DOID:6496,extraskeletal myxoid chondrosarcoma,DOID:5861,myxoid chondrosarcoma
+HP:0011100,Intestinal atresia,HP:0002589,Gastrointestinal atresia
+DOID:0080014,chromosomal disease,DOID:630,genetic disease
+UBERON:0001842,posterior semicircular canal,UBERON:0001840,semicircular canal
+HP:0100832,Mouches volantes,HP:0000504,Abnormality of vision
+HP:0003836,Stippled calcification of the shoulder,HP:0003043,Abnormality of the shoulder
+HP:0010626,Anterior pituitary agenesis,HP:0010625,Anterior pituitary dysgenesis
+CL:0002166,epithelial cell of Malassez,CL:0002159,general ecto-epithelial cell
+UBERON:0002424,oral epithelium,UBERON:0003929,gut epithelium
+DOID:0060142,form agnosia,DOID:4090,agnosia
+UBERON:0000370,adductor magnus,UBERON:0011144,adductor muscle of hip
+UBERON:2000280,medial division,UBERON:0002946,regional part of cerebellum
+DOID:5154,borna disease,DOID:934,viral infectious disease
+UBERON:0003482,vein of trabecular bone,UBERON:0005744,bone foramen
+HP:0009825,Aplasia involving bones of the extremities,HP:0009815,Aplasia/Hypoplasia of the extremities
+UBERON:0002949,tectospinal tract,UBERON:0007702,tract of brain
+UBERON:0015852,narwhal tusk,UBERON:0003450,upper jaw incisor
+HP:0009120,Aplasia/Hypoplasia involving the sinuses,HP:0009116,Aplasia/Hypoplasia involving bones of the skull
+UBERON:2001589,propterygium cartilage,UBERON:2201587,pectoral fin proximal radial cartilage
+HP:0100633,Esophagitis,HP:0002031,Abnormality of the esophagus
+HP:0002345,Action tremor,HP:0001337,Tremor
+HP:0010305,Absence of the sacrum,HP:0008517,Aplasia/Hypoplasia of the sacrum
+HP:0002781,Upper airway obstruction,HP:0002087,Abnormality of the upper respiratory tract
+UBERON:0009848,zona limitans intrathalamica,UBERON:0006800,anatomical line
+CL:0000162,parietal cell,CL:0002659,glandular cell of stomach
+HP:0010570,Low maternal serum alpha-fetoprotein,HP:0011436,Abnormal maternal serum screening
+DOID:5161,Monckeberg arteriosclerosis,DOID:2349,arteriosclerosis
+UBERON:0003514,limb blood vessel,UBERON:0007301,appendage blood vessel
+DOID:9191,diabetic macular edema,DOID:8947,diabetic retinopathy
+HP:0007803,Monochromacy,HP:0000551,Abnormality of color vision
+UBERON:0011300,gray matter of telencephalon,UBERON:0003528,brain grey matter
+HP:0012458,Medial calcification of small arteries,HP:0012456,Medial arterial calcification
+HP:0100588,Paraphimosis,HP:0100587,Abnormality of the preputium
+DOID:9541,osteosclerotic myeloma,DOID:9538,multiple myeloma
+UBERON:2001517,ceratobranchial 2 cartilage,UBERON:2001900,ceratobranchial 2 element
+UBERON:0003365,epithelium of left lung,UBERON:0000115,lung epithelium
+UBERON:0014935,cerebral cortex marginal layer,UBERON:0014950,layer of developing cerebral cortex
+HP:0005013,Dysplastic distal radial epiphyses,HP:0010597,Abnormality of the distal radial epiphysis
+UBERON:0015088,distal carpal bone 2 cartilage,UBERON:0010883,forelimb cartilage element
+DOID:3173,fallopian tube serous papilloma,DOID:0060111,fallopian tube benign neoplasm
+UBERON:0014393,sweat of axilla,UBERON:0001089,sweat
+CL:0000775,neutrophil,CL:0000094,granulocyte
+UBERON:2001832,parasphenoid-basioccipital joint,UBERON:0000982,skeletal joint
+UBERON:0010569,manual digit 5 metacarpus pre-cartilage condensation,UBERON:0010579,manual digit 5 phalanx pre-cartilage condensation
+UBERON:0014734,allocortex,UBERON:0002619,regional part of cerebral cortex
+HP:0012116,Abnormal albumin level,HP:0010876,Abnormality of circulating protein level
+DOID:12351,alcoholic hepatitis,DOID:2237,hepatitis
+UBERON:2002116,epibranchial organ,UBERON:0004119,endoderm-derived structure
+UBERON:0011901,hair matrix,UBERON:0004121,ectoderm-derived structure
+DOID:0060158,acquired metabolic disease,DOID:0014667,disease of metabolism
+CL:1000324,duodenal goblet cell,CL:1000317,intestinal villus goblet cell
+UBERON:3000057,canalis semicircularis anterior,UBERON:0001840,semicircular canal
+HP:0100839,Hepatic agenesis,HP:0001392,Abnormality of the liver
+CL:0000747,cyanophore,CL:0000147,pigment cell
+NCBITaxon:33090,Viridiplantae,NCBITaxon:2759,Eukaryota
+HP:0009519,Ivory epiphysis of the middle phalanx of the 2nd finger,HP:0009500,Abnormality of the epiphysis of the middle phalanx of the 2nd finger
+UBERON:0010046,entire pharyngeal arch associated mesenchyme,UBERON:0005291,embryonic tissue
+UBERON:0004328,proximal phalanx of manual digit 2,UBERON:0014502,proximal phalanx of digit 2
+HP:0010156,Pseudoepiphysis of the 1st metatarsal,HP:0010120,Pseudoepiphyses of the hallux
+HP:0008055,Aplasia/Hypoplasia affecting the uvea,HP:0008056,Aplasia/Hypoplasia affecting the eye
+UBERON:0002240,spinal cord,UBERON:0000489,cavitated compound organ
+HP:0011444,Decorticate rigidity,HP:0002063,Rigidity
+DOID:10327,anthracosis,DOID:10316,pneumoconiosis
+HP:0003489,Acute episodes of neuropathic symptoms,HP:0009830,Peripheral neuropathy
+HP:0001437,Abnormality of the musculature of the lower limbs,HP:0009127,Abnormality of the musculature of the limbs
+DOID:12678,hypercalcemia,DOID:10575,calcium metabolism disease
+HP:0100376,Aplasia/Hypoplasia of the proximal phalanx of the 4th toe,HP:0010371,Aplasia/Hypoplasia of the phalanges of the 4th toe
+HP:0009426,Distal/middle symphalangism of 3rd finger,HP:0009435,Symphalangism of middle phalanx of 3rd finger
+UBERON:0003118,aortic arch 1,UBERON:0004363,aortic arch
+HP:0009358,Abnormality of the proximal phalanx of the 3rd finger,HP:0009316,Abnormality of the phalanges of the 3rd finger
+UBERON:0006639,crus penis,UBERON:0000064,organ part
+UBERON:0010977,flexor pre-muscle mass,UBERON:0004120,mesoderm-derived structure
+UBERON:2001925,spiracular canal,UBERON:0005744,bone foramen
+DOID:867,maxillary sinus cholesteatoma,DOID:869,cholesteatoma
+HP:0010085,Aplasia/Hypoplasia of the proximal phalanx of the hallux,HP:0010058,Aplasia/Hypoplasia of the phalanges of the hallux
+UBERON:2000426,rostral parvocellular preoptic nucleus,UBERON:2002219,parvocellular preoptic nucleus
+HP:0003861,Broad diaphyses of the upper limbs,HP:0009808,Anomaly of the upper limb diaphyses
+UBERON:0009193,sphenoid cartilage element,UBERON:0003932,cartilage element of chondrocranium
+NCBITaxon:6933,Acari,NCBITaxon:6854,Arachnida
+DOID:2590,familial nephrotic syndrome,DOID:1184,nephrotic syndrome
+HP:0004010,Small radial epiphyses,HP:0010585,Small epiphyses
+UBERON:2000078,ventral actinotrichium,UBERON:2000089,actinotrichium
+UBERON:0007377,stratum compactum,UBERON:0004121,ectoderm-derived structure
+CL:0000648,kidney granular cell,CL:1000618,juxtaglomerular complex cell
+HP:0100739,Bulimia,HP:0100738,Abnormal eating behavior
+DOID:5147,dartoic leiomyoma,DOID:0050622,reproductive organ benign neoplasm
+HP:0005202,Helicobacter pylori infection,HP:0004798,Recurrent infection of the gastrointestinal tract
+UBERON:0007143,right internal carotid artery,UBERON:0001532,internal carotid artery
+UBERON:0006918,parakeratinized epithelium of tongue,UBERON:0013193,parakeratinized epithelium
+DOID:14484,sporotrichosis,DOID:0050292,primary systemic mycosis
+HP:0009949,Duplication of the middle phalanx of the 2nd finger,HP:0010008,Duplication of the middle phalanx of hand
+DOID:0050201,nephropathia epidemica,DOID:11266,hemorrhagic fever with renal syndrome
+UBERON:0002181,substantia gelatinosa,UBERON:0004121,ectoderm-derived structure
+UBERON:0004133,salivatory nucleus,UBERON:0006331,brainstem nucleus
+CL:1001097,kidney afferent arteriole smooth muscle cell,CL:1001066,kidney arteriole smooth muscle cell
+CL:0002669,type 3 otic fibrocyte,CL:0002665,otic fibrocyte
+UBERON:0009954,vomeronasal system,UBERON:0001032,sensory system
+UBERON:0003091,thyroid primordium,UBERON:0001048,primordium
+UBERON:0010166,coat of hair,UBERON:0010164,collection of hairs
+DOID:11729,Lyme disease,DOID:0050338,primary bacterial infectious disease
+NCBITaxon:33218,Enoplia,NCBITaxon:119088,Enoplea
+UBERON:0003625,manual digit 5,UBERON:0006052,digit 5
+UBERON:0004100,renal collecting system,UBERON:0006554,urinary system structure
+HP:0011932,Abnormality of the superior cerebellar peduncle,HP:0011931,Abnormality of the cerebellar peduncle
+CL:0001002,mature CD8_alpha-negative CD11b-negative dendritic cell,CL:0000998,CD8_alpha-negative CD11b-negative dendritic cell
+CL:0002010,pre-conventional dendritic cell,CL:0002031,hematopoietic lineage restricted progenitor cell
+UBERON:0010886,hindlimb bone pre-cartilage condensation,UBERON:0003860,hindlimb mesenchyme
+UBERON:2001251,pharyngobranchial 4 cartilage,UBERON:2001913,pharyngobranchial 4 element
+HP:0001489,Vitreous detachment,HP:0004327,Abnormality of the vitreous humor
+HP:0010476,Aplasia/Hypoplasia of the bladder,HP:0000014,Abnormality of the bladder
+DOID:4930,nasal cavity adenocarcinoma,DOID:4931,nasal cavity carcinoma
+UBERON:4100016,posterior process of ilium,UBERON:0004530,bony projection
+UBERON:0015097,distal carpal bone 5 cartilage,UBERON:0015064,autopod cartilage
+DOID:9673,ulcerative stomatitis,DOID:9637,stomatitis
+UBERON:2001426,posterior naris,UBERON:0005928,external naris
+HP:0002067,Bradykinesia,HP:0002071,Abnormality of extrapyramidal motor function
+HP:0003985,Exostoses of the ulna,HP:0003960,Exostoses of the forearm bones
+UBERON:0013752,diaphysis of metacarpal bone,UBERON:0004769,diaphysis
+HP:0002416,Subependymal cysts,HP:0010576,Intracranial cystic lesion
+HP:0009855,Osteolytic defects of the proximal phalanges of the hand,HP:0009771,Osteolytic defects of the phalanges of the hand
+HP:0100730,Bronchogenic cyst,HP:0002088,Abnormality of the lung
+DOID:0060001,withdrawal disorder,DOID:303,substance-related disorder
+CL:0000612,eosinophilic myelocyte,CL:0002087,nongranular leukocyte
+HP:0011884,Abnormal umbilical stump bleeding,HP:0001892,Abnormal bleeding
+UBERON:0000376,hindlimb stylopod,UBERON:0008784,lower limb segment
+UBERON:4000118,cellular bone tissue,UBERON:4000115,mineralized bone tissue
+UBERON:0013235,ventrum,UBERON:0000475,organism subdivision
+UBERON:0005643,foregut duodenum epithelium,UBERON:0008346,duodenal epithelium
+HP:0001145,Chorioretinopathy,HP:0000532,Chorioretinal abnormality
+HP:0100480,Proximal/middle symphalangism of 3rd toe,HP:0010378,Triangular shaped phalanges of the 4th toe
+UBERON:0002825,superior part of vestibular ganglion,UBERON:0000064,organ part
+DOID:3772,intraventricular meningioma,DOID:3565,meningioma
+HP:0002193,Pseudobulbar behavioral symptoms,HP:0100851,Abnormal emotion/affect behavior
+UBERON:4200092,flexor tubercle of ungual,UBERON:0013703,integumentary projection
+UBERON:3011040,first pancreatic bud,UBERON:0002050,embryonic structure
+UBERON:0014852,chorda tendinea of right ventricle,UBERON:0005994,chordae tendineae
+UBERON:0000155,theca cell layer,UBERON:0014404,female anatomical structure
+UBERON:0004518,muscle of vertebral column,UBERON:0001630,muscle organ
+UBERON:0004368,Reichert's cartilage,UBERON:0003566,head connective tissue
+UBERON:0005250,stomatodeum gland,UBERON:0002530,gland
+DOID:0050508,variola major,DOID:8736,smallpox
+NCBITaxon:34064,Francisellaceae,NCBITaxon:72273,Thiotrichales
+UBERON:0010911,ossicle,UBERON:0004765,skeletal element
+HP:0009404,Broad phalanges of the 4th finger,HP:0009172,Abnormality of the phalanges of the 4th finger
+HP:0004887,Respiratory failure requiring assisted ventilation,HP:0002093,Respiratory insufficiency
+DOID:3705,fallopian tube mucinous tumor,DOID:0060111,fallopian tube benign neoplasm
+UBERON:0015249,digit skin,UBERON:0015790,autopod skin
+HP:0008167,Very long chain fatty acid accumulation,HP:0010964,Abnormality of long-chain fatty-acid metabolism
+CL:0000117,CNS neuron (sensu Vertebrata),CL:0000540,neuron
+UBERON:0006198,dorsal intercostal artery,UBERON:0005612,intercostal artery
+CL:0002028,basophil mast progenitor cell,CL:0000763,myeloid cell
+DOID:11829,degenerative myopia,DOID:11830,myopia
+DOID:5821,methotrexate-associated lymphoproliferation,DOID:0060058,lymphoma
+HP:0009109,Denervation of the diaphragm,HP:0000775,Abnormality of the diaphragm
+UBERON:2002270,pelvic fin spine,UBERON:4200075,fin spine
+HP:0001868,Autoamputation (feet),HP:0001218,Autoamputation
+UBERON:0014800,spinotrapezius muscle,UBERON:0002380,trapezius muscle
+DOID:5364,pulmonary coin lesion,DOID:3683,lung benign neoplasm
+CL:0010009,camera-type eye photoreceptor cell,CL:0009004,retinal cell
+HP:0010079,Curved distal phalanx of the hallux,HP:0010188,Curved distal phalanges of the toes
+HP:0007359,Focal seizures,HP:0001250,Seizures
+DOID:640,encephalomyelitis,DOID:331,central nervous system disease
+UBERON:0002387,pes,UBERON:0002470,autopod region
+HP:0009618,Abnormality of the proximal phalanx of the thumb,HP:0009602,Abnormality of the phalanges of the thumb
+UBERON:0003826,upper leg bone,UBERON:0005893,leg bone
+CL:0000040,monoblast,CL:0000763,myeloid cell
+CL:0002601,uterine smooth muscle cell,CL:0000192,smooth muscle cell
+HP:0009332,Abnormality of the epiphysis of the distal phalanx of the 3rd finger,HP:0009357,Abnormality of the distal phalanx of the 3rd finger
+DOID:5118,ovarian cystic teratoma,DOID:6231,mature teratoma of the ovary
+UBERON:0002412,vertebra,UBERON:0002513,endochondral bone
+HP:0100581,Megacalicosis,HP:0011130,Abnormality of renal calyx morphology
+HP:0009437,Aplasia/Hypoplasia of the middle phalanx of the 3rd finger,HP:0004172,Abnormality of the middle phalanx of the 3rd finger
+HP:0100211,Stippling of the epiphysis of the distal phalanx of the 5th toe,HP:0100086,Stippling of the epiphyses of the 5th toe
+UBERON:0006581,mantle muscle,UBERON:0001630,muscle organ
+UBERON:0005487,vitelline vein,UBERON:0013140,systemic vein
+DOID:9274,hyperlysinemia,DOID:9252,amino acid metabolic disorder
+UBERON:0002162,area postrema,UBERON:0002678,regional part of medulla oblongata
+UBERON:0000033,head,UBERON:0011676,subdivision of organism along main body axis
+DOID:348,blepharochalasis,DOID:530,eyelid disease
+HP:0000433,Abnormality of the nasal mucosa,HP:0000366,Abnormality of the nose
+UBERON:2001681,cornu mesial process,UBERON:4100000,skeletal element projection
+HP:0009843,Aplasia/Hypoplasia of the middle phalanges of the hand,HP:0009833,Abnormality of the middle phalanges of the hand
+UBERON:0005013,mucosa of male urethra,UBERON:0014403,male anatomical structure
+CL:0002240,marrow fibroblast,CL:0000057,fibroblast
+HP:0006459,Dorsal subluxation of ulna,HP:0002997,Abnormality of the ulna
+CL:0002635,nonkeratinized epithelial cell of anal column,CL:0002634,epithelial cell of anal column
+CL:0002422,enucleated reticulocyte,CL:0000558,reticulocyte
+UBERON:0008337,inguinal part of abdomen,UBERON:0000475,organism subdivision
+UBERON:2005311,pronephric glomerular capsule epithelium,UBERON:0004211,nephron epithelium
+HP:0005945,Laryngeal obstruction,HP:0001600,Abnormality of the larynx
+DOID:6935,ureter inverted papilloma,DOID:6936,ureter urothelial papilloma
+HP:0011674,Cardiac teratoma,HP:0100544,Neoplasm of the heart
+UBERON:2005317,pectoral fin fold,UBERON:0000481,multi-tissue structure
+HP:0009280,Short 4th finger,HP:0009272,Aplasia/Hypoplasia of the 4th finger
+UBERON:0010245,retinal tapetum lucidum,UBERON:0004868,tapetum lucidum of camera-type eye
+NCBITaxon:6268,Anisakis,NCBITaxon:6267,Anisakidae
+HP:0009546,Triangular shaped phalanges of the 2nd finger,HP:0009541,Abnormality of the phalanges of the 2nd finger
+UBERON:2001583,preural centrum 1+ ural centrum 1,UBERON:0003106,urostyle
+UBERON:0006443,prinicipal vein of limb,UBERON:0003514,limb blood vessel
+UBERON:3010082,M. pulmonum proprius,UBERON:0010890,pelvic complex muscle
+UBERON:0009671,nasal fin,UBERON:0004119,endoderm-derived structure
+HP:0009952,Complete duplication of the middle phalanx of the 2nd finger,HP:0010002,Complete duplication of the middle phalanges of the hand
+UBERON:0002858,third lumbar dorsal root ganglion,UBERON:0002836,lumbar dorsal root ganglion
+HP:0005004,Flattened proximal radial epiphyses,HP:0010597,Abnormality of the distal radial epiphysis
+UBERON:0005500,rhombomere floor plate,UBERON:0002050,embryonic structure
+HP:0012710,Ingrown nail,HP:0001597,Abnormality of the nail
+HP:0002087,Abnormality of the upper respiratory tract,HP:0012252,Abnormal respiratory system morphology
+HP:0000223,Abnormality of taste sensation,HP:0000157,Abnormality of the tongue
+HP:0001802,Absent toenail,HP:0010624,Aplastic/hypoplastic toenail
+UBERON:3000774,ilial shaft,UBERON:0000064,organ part
+CL:0002073,transitional myocyte,CL:0002086,specialized cardiac myocyte
+DOID:3978,extrinsic cardiomyopathy,DOID:0050700,cardiomyopathy
+DOID:11129,dislocation of ear ossicle,DOID:2742,auditory system disease
+CL:0010003,epithelial cell of alveolus of lung,CL:0000082,epithelial cell of lung
+DOID:1439,pyuria,DOID:18,urinary system disease
+UBERON:0006601,presumptive ectoderm,UBERON:0006598,presumptive structure
+DOID:3323,Sandhoff disease,DOID:3321,gangliosidosis GM2
+HP:0001363,Craniosynostosis,HP:0002648,Abnormality of calvarial morphology
+HP:0006496,Aplasia/Hypoplasia involving bones of the upper limbs,HP:0002817,Abnormality of the upper limb
+UBERON:4200018,calcaneal tuber,UBERON:0004530,bony projection
+UBERON:2001363,neural complex,UBERON:0004120,mesoderm-derived structure
+HP:0006849,Hypodysplasia of the corpus callosum,HP:0002079,Hypoplasia of the corpus callosum
+CL:0000987,IgA plasma cell,CL:0000974,long lived plasma cell
+UBERON:0014908,cerebellopontine angle,UBERON:0000477,anatomical cluster
+HP:0001880,Eosinophilia,HP:0001974,Leukocytosis
+HP:0100476,Symphalangism affecting the distal phalanx of the 3rd toe,HP:0010365,Symphalangism affecting the phalanges of the 3rd toe
+HP:0008978,Necrotizing myopathy,HP:0003198,Myopathy
+UBERON:0001615,transverse facial artery,UBERON:0001637,artery
+CL:0000509,gastrin secreting cell,CL:0000167,peptide hormone secreting cell
+UBERON:0014736,periallocortex,UBERON:0002619,regional part of cerebral cortex
+DOID:0050720,ornithine translocase deficiency,DOID:9252,amino acid metabolic disorder
+UBERON:0009039,lymph node germinal center,UBERON:0010754,germinal center
+HP:0005033,Distal ulnar hypoplasia,HP:0003022,Hypoplasia of the ulna
+DOID:7539,pregnancy adenoma,DOID:1625,breast adenoma
+DOID:0050791,persistent mullerian duct syndrome,DOID:3765,pseudohermaphroditism
+UBERON:3000942,firmisternal girdle,UBERON:0007831,pectoral girdle skeleton
+HP:0003337,Reduced prothrombin consumption,HP:0012200,Abnormality of prothrombin
+UBERON:0002659,superior medullary velum,UBERON:0003035,regional part of cerebellar white matter
+HP:0009667,Enlarged epiphysis of the proximal phalanx of the thumb,HP:0009689,Enlarged epiphyses of the thumb
+UBERON:2001154,anal fin musculature,UBERON:0007271,appendage musculature
+UBERON:0011309,body of mandible,UBERON:0010313,neural crest-derived structure
+UBERON:0002251,iliocostalis muscle,UBERON:0004518,muscle of vertebral column
+UBERON:0004254,forelimb zeugopod muscle,UBERON:0001499,muscle of arm
+UBERON:3010045,centrale 1,UBERON:0012131,centrale
+HP:0000072,Hydroureter,HP:0000069,Abnormality of the ureter
+HP:0010080,Osteolytic defects of the distal phalanx of the hallux,HP:0010062,Osteolytic defects of the phalanges of the hallux
+HP:0100074,Small epiphyses of the 4th toe,HP:0010335,Abnormality of the epiphyses of the 4th toe
+NCBITaxon:43219,Herpotrichiellaceae,NCBITaxon:34395,Chaetothyriales
+UBERON:0003912,chitinous tooth,UBERON:0003913,tooth-like structure
+UBERON:0003926,photoreceptor outer segment layer,UBERON:0004121,ectoderm-derived structure
+HP:0003696,Absent epiphysis of the distal phalanx of the 5th finger,HP:0010246,Absent epiphyses of the distal phalanges of the hand
+UBERON:0002058,ciliary ganglion,UBERON:0001808,parasympathetic ganglion
+DOID:6886,ureter small cell carcinoma,DOID:4939,ureter carcinoma
+UBERON:0003371,pelvic appendage bud ectoderm,UBERON:0010371,ecto-epithelium
+UBERON:0012303,ureteral orifice,UBERON:0004120,mesoderm-derived structure
+CL:0000723,somatic stem cell,CL:0000034,stem cell
+CL:0000766,myeloid leukocyte,CL:0000763,myeloid cell
+UBERON:0007524,dense mesenchyme tissue,UBERON:0003104,mesenchyme
+UBERON:0001755,distal part of styloid process of temporal bone,UBERON:0005913,zone of bone organ
+DOID:5196,fallopian tube adenomatoid tumor,DOID:0060111,fallopian tube benign neoplasm
+HP:0004339,Abnormality of sulfur amino acid metabolism,HP:0004337,Abnormality of amino acid metabolism
+UBERON:0002839,second cervical dorsal root ganglion,UBERON:0002834,cervical dorsal root ganglion
+HP:0010980,Hyperlipoproteinemia,HP:0010979,Abnormality of the level of lipoprotein cholesterol
+UBERON:0001497,muscle of pelvic girdle,UBERON:0010890,pelvic complex muscle
+HP:0011141,Age-related cataract,HP:0000518,Cataract
+UBERON:0002032,areola,UBERON:0014404,female anatomical structure
+HP:0008716,Urethrovaginal fistula,HP:0010480,Urethral fistula
+UBERON:0001322,sciatic nerve,UBERON:0002003,peripheral nerve
+HP:0100341,Tibial deviation of the 4th toe,HP:0010338,Deviation/Displacement of the 4th toe
+CL:0000600,heterokaryon,CL:0000521,fungal cell
+DOID:223,basilar artery insufficiency,DOID:224,transient cerebral ischemia
+UBERON:0006844,cusp of tooth,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0012063,Aneurysmal bone cyst,HP:0012062,Bone cyst
+NCBITaxon:56212,Calomys musculinus,NCBITaxon:29105,Calomys
+HP:0010615,Angiofibromas,HP:0010614,Fibroma
+UBERON:0007589,ciliated columnar oviduct epithelium,UBERON:0004804,oviduct epithelium
+UBERON:4000090,integumentary skeleton,UBERON:0010912,subdivision of skeleton
+CL:1000377,dense-core granulated cell of epithelium of trachea,CL:0002066,Feyrter cell
+HP:0000777,Abnormality of the thymus,HP:0100763,Abnormality of the lymphatic system
+UBERON:0013591,postsylvian sulcus,UBERON:0008334,subarachnoid sulcus
+UBERON:0000457,cavernous artery,UBERON:0000063,organ segment
+UBERON:0000398,cartilage tissue of sternum,UBERON:0004120,mesoderm-derived structure
+UBERON:0011858,acinus of exocrine gland,UBERON:0009842,acinus
+DOID:11262,ornithosis,DOID:0050338,primary bacterial infectious disease
+HP:0003127,Hypocalciuria,HP:0004363,Abnormality of calcium homeostasis
+UBERON:0010506,meningeal dura mater,UBERON:0010507,layer of dura mater
+UBERON:2002266,epineural 4,UBERON:2000507,epineural
+UBERON:2001281,branchiostegal ray 2,UBERON:2000476,branchiostegal ray
+HP:0100954,Open operculum,HP:0006872,Cerebral hypoplasia
+HP:0009706,Synostosis involving the 3rd metacarpal,HP:0010011,Abnormality of the 3rd metacarpal
+UBERON:0013224,Ciaccio's gland,UBERON:0013229,eyelid gland
+UBERON:0011608,hyomandibular element,UBERON:0010363,endochondral element
+HP:0012493,Middle cerebral artery stenosis,HP:0012492,Cerebral artery stenosis
+UBERON:0011611,ceratohyal bone,UBERON:0002513,endochondral bone
+DOID:4543,retrograde amnesia,DOID:10914,amnestic disorder
+HP:0012441,Sphincter of Oddi dyskinesia,HP:0012396,Biliary dyskinesia
+UBERON:0003427,abdominal fat pad,UBERON:0003916,fat pad
+UBERON:0005355,malleus neck,UBERON:0010313,neural crest-derived structure
+UBERON:0012249,ectocervix,UBERON:0000064,organ part
+UBERON:0007350,arcopallium,UBERON:0002791,regional part of telencephalon
+HP:0009394,Bracket epiphyses of the 4th finger,HP:0009174,Abnormality of the epiphyses of the 4th finger
+HP:0005181,Premature coronary artery disease,HP:0001677,Coronary artery disease
+UBERON:0001902,epithelium of small intestine,UBERON:0006799,glandular epithelium
+HP:0009692,Ivory epiphyses of the thumb,HP:0010234,Ivory epiphyses of the phalanges of the hand
+UBERON:0006293,spleen primordium,UBERON:0005291,embryonic tissue
+DOID:11888,Schwannoma of ureter,DOID:956,peripheral nerve schwannoma
+HP:0001646,Abnormality of the aortic valve,HP:0001654,Abnormality of the heart valves
+HP:0005406,Recurrent bacterial skin infections,HP:0001581,Recurrent skin infections
+UBERON:3000450,posterior mental process,UBERON:0004529,anatomical projection
+UBERON:0009973,ureterovesical junction,UBERON:0007651,anatomical junction
+UBERON:0009471,dorsum of tongue,UBERON:0004121,ectoderm-derived structure
+DOID:150,disease of mental health,DOID:4,disease
+HP:0010732,Nodular changes affecting the eyelids,HP:0000492,Abnormality of the eyelid
+CL:0005011,renal alpha-intercalated cell,CL:0005010,renal intercalated cell
+HP:0002357,Dysphasia,HP:0002167,Neurological speech impairment
+UBERON:0001239,muscularis mucosae of large intestine,UBERON:0001240,muscularis mucosae of intestine
+DOID:2458,papillary conjunctivitis,DOID:6195,conjunctivitis
+DOID:3711,bladder adenocarcinoma,DOID:4007,bladder carcinoma
+UBERON:0006855,ureter muscle layer,UBERON:0006660,muscle layer
+DOID:0050073,invasive aspergillosis,DOID:13564,aspergillosis
+UBERON:0006449,third lumbar spinal cord segment,UBERON:0007716,lumbar subsegment of spinal cord
+HP:0000884,Prominent sternum,HP:0000766,Abnormality of the sternum
+UBERON:4200136,triphycercal tail,UBERON:4000164,caudal fin
+HP:0010065,Triangular shaped phalanges of the hallux,HP:0010057,Abnormality of the phalanges of the hallux
+UBERON:0001194,splenic artery,UBERON:0004573,systemic artery
+HP:0006774,Ovarian papillary adenocarcinoma,HP:0100615,Ovarian neoplasm
+DOID:2456,blepharoconjunctivitis,DOID:6195,conjunctivitis
+DOID:0002116,pterygium,DOID:10124,corneal disease
+HP:0002987,Elbow flexion contracture,HP:0100360,Contractures of the joints of the upper limbs
+UBERON:0000075,subdivision of skeletal system,UBERON:0011216,organ system subdivision
+HP:0012397,Aortic atherosclerosis,HP:0002621,Atherosclerosis
+CL:1001286,inner medulla vasa recta descending limb cell,CL:1001285,vasa recta descending limb cell
+HP:0002805,Accelerated bone age after puberty,HP:0005616,Accelerated skeletal maturation
+UBERON:3000393,pars amphibiorum,UBERON:0004121,ectoderm-derived structure
+HP:0011380,Morphological abnormality of the semicircular canal,HP:0011390,Morphological abnormality of the inner ear
+HP:0000934,Chondrocalcinosis,HP:0010766,Ectopic calcification
+UBERON:2001475,sublingual dorsal ossification,UBERON:2001275,sublingual
+HP:0010273,Irregular epiphyses of the proximal phalanges of the hand,HP:0010245,Abnormality of the epiphyses of the proximal phalanges of the hand
+UBERON:0001856,semicircular duct,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:2710,sick building syndrome,DOID:841,extrinsic allergic alveolitis
+UBERON:0004865,actinopterygian parietal bone,UBERON:0008907,dermal bone
+HP:0001370,Rheumatoid arthritis,HP:0001369,Arthritis
+DOID:5679,retinal disease,DOID:5614,eye disease
+HP:0100214,Bracket epiphysis of the middle phalanx of the 5th toe,HP:0100078,Bracket epiphyses of the 5th toe
+UBERON:0005113,metanephric cortex mesenchyme,UBERON:0004120,mesoderm-derived structure
+UBERON:0007657,anular ligament of radius,UBERON:0004268,lower arm connective tissue
+DOID:1521,cecum cancer,DOID:5672,large intestine cancer
+HP:0012174,Glioblastoma multiforme,HP:0009733,Glioma
+UBERON:2005017,primordial midbrain channel,UBERON:0009141,craniocervical region vein
+UBERON:0002936,magnocellular part of red nucleus,UBERON:0003528,brain grey matter
+HP:0007018,Attention deficit hyperactivity disorder,HP:0000736,Short attention span
+DOID:4552,large cell carcinoma,DOID:305,carcinoma
+HP:0005225,Intestinal edema,HP:0000969,Edema
+HP:0003358,Elevated intracellular cystine,HP:0004339,Abnormality of sulfur amino acid metabolism
+UBERON:0011694,embryo portion of umbilical artery,UBERON:0001637,artery
+UBERON:0013747,basibranchial cartilage,UBERON:0013746,basibranchial element
+HP:0009223,Stippling of the epiphysis of the middle phalanx of the 4th finger,HP:0010266,Stippling of the epiphyses of the middle phalanges of the hand
+HP:0008518,Aplasia/Hypoplasia involving the vertebral column,HP:0000925,Abnormality of the vertebral column
+DOID:4304,signet ring basal cell carcinoma,DOID:2513,basal cell carcinoma
+UBERON:0013427,occipital bun,UBERON:0004120,mesoderm-derived structure
+HP:0005539,T-cell chronic lymphocytic lymphoma/leukemia,HP:0005526,Lymphoid leukemia
+UBERON:2000488,ceratobranchial bone,UBERON:2001898,ceratobranchial element
+DOID:2600,laryngeal carcinoma,DOID:2596,larynx cancer
+HP:0007765,Deep anterior chamber,HP:0000593,Abnormality of the anterior chamber
+UBERON:0011376,iliothoracic muscle,UBERON:0008242,lower back muscle
+UBERON:0000103,life cycle stage boundary,UBERON:0000000,processual entity
+UBERON:0002076,cuticle of hair,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0010189,Osteolytic defects of the distal phalanges of the toes,HP:0010182,Abnormality of the distal phalanges of the toes
+UBERON:0004358,caput epididymis,UBERON:0000064,organ part
+HP:0010287,Abnormality of the submandibular glands,HP:0010286,Abnormality of the salivary glands
+HP:0010203,Aplasia/Hypoplasia of the proximal phalanges of the toes,HP:0010173,Aplasia/Hypoplasia of the phalanges of the toes
+DOID:1412,bacteriuria,DOID:18,urinary system disease
+HP:0009293,Broad middle phalanx of the 4th finger,HP:0009844,Broad middle phalanx of finger
+DOID:1287,cardiovascular system disease,DOID:7,disease of anatomical entity
+UBERON:2000855,somite 24,UBERON:0002329,somite
+UBERON:0001477,infraspinatus muscle,UBERON:0001482,muscle of shoulder
+CL:0000765,erythroblast,CL:0000764,erythroid lineage cell
+UBERON:0010307,conjunctival fornix,UBERON:0010305,region of conjunctiva
+DOID:12731,pars planitis,DOID:12732,intermediate uveitis
+UBERON:0001361,femoral vein,UBERON:0001638,vein
+DOID:5907,penis non-invasive verrucous carcinoma,DOID:5908,penis verrucous carcinoma
+HP:0000369,Low-set ears,HP:0000357,Abnormal location of ears
+UBERON:3000869,ilial protuberance,UBERON:0004530,bony projection
+UBERON:2005034,parachordal vessel,UBERON:0003513,trunk blood vessel
+DOID:2926,Klippel-Trenaunay syndrome,DOID:225,syndrome
+DOID:4014,sarcomatoid transitional cell carcinoma,DOID:2671,transitional cell carcinoma
+HP:0011691,Supraventricular tachycardia with a concealed accessory pathway on the left free wall,HP:0011689,Supraventricular tachycardia with a concealed accessory connection
+DOID:1415,gyrate atrophy,DOID:1417,choroid disease
+DOID:6082,pediatric testicular germ cell tumor,DOID:5554,childhood neoplasm of the testis
+DOID:6212,ovarian endometrial cancer,DOID:2152,ovary epithelial cancer
+HP:0000680,Delayed eruption of primary teeth,HP:0006481,Abnormality of primary teeth
+UBERON:0003396,mesentery of colon,UBERON:0004854,gastrointestinal system mesentery
+HP:0000710,Hyperorality,HP:0000708,Behavioural/Psychiatric Abnormality
+UBERON:2000913,molecular layer valvula cerebelli,UBERON:0000479,tissue
+UBERON:4300022,anteroventral plate,UBERON:0008907,dermal bone
+HP:0003609,Foam cells with lamellar inclusion bodies,HP:0003651,Foam cells
+DOID:0050738,Y-linked disease,DOID:0050177,monogenic disease
+HP:0001501,6 metacarpals,HP:0005917,Supernumerary metacarpal bones
+HP:0011138,Abnormality of skin adnexa,HP:0001574,Abnormality of the integument
+CL:0000503,theca cell,CL:0000499,stromal cell
+HP:0008148,Impaired epinephrine-induced platelet aggregation,HP:0003540,Impaired platelet aggregation
+HP:0009657,Triangular shaped phalanges of the thumb,HP:0009602,Abnormality of the phalanges of the thumb
+UBERON:0008799,transverse palatine fold,UBERON:0004121,ectoderm-derived structure
+UBERON:0006810,olecranon,UBERON:0005055,zone of long bone
+HP:0011687,AV nodal tachycardia,HP:0004755,Supraventricular tachycardia
+UBERON:0006641,appendix epididymis,UBERON:0005156,reproductive structure
+UBERON:4000176,anal fin lepidotrichium,UBERON:4000172,lepidotrichium
+UBERON:0003848,gonadal vein,UBERON:0001638,vein
+UBERON:2001348,stratum marginale,UBERON:0004121,ectoderm-derived structure
+HP:0006837,Congenital Horner syndrome,HP:0002277,Horner syndrome
+DOID:4873,anterior horn cell disease,DOID:12377,spinal muscular atrophy
+HP:0002787,Tracheal calcification,HP:0010766,Ectopic calcification
+UBERON:0009748,cephalic neural fold,UBERON:0005062,neural fold
+CL:0000754,type 2 cone bipolar cell (sensu Mus),CL:0000750,OFF-bipolar cell
+CL:0002277,type I enteroendocrine cell,CL:0000164,enteroendocrine cell
+UBERON:0008994,equine glandular stomach,UBERON:0000945,stomach
+UBERON:0000122,neuron projection bundle,UBERON:0005162,multi cell component structure
+UBERON:0004115,blood vessel of tympanic cavity,UBERON:0003496,head blood vessel
+DOID:4743,mixed testicular germ cell tumor,DOID:3306,mixed germ cell cancer
+UBERON:0013747,basibranchial cartilage,UBERON:0011004,pharyngeal arch cartilage
+HP:0002604,Gastrointestinal telangiectasia,HP:0100579,Mucosal telangiectasiae
+HP:0007994,Peripheral visual field loss,HP:0001123,Visual field defect
+UBERON:0013558,Brodmann (1909) area 27,UBERON:0013529,Brodmann area
+UBERON:0005080,metanephric ureteric bud,UBERON:0000084,ureteric bud
+CL:1001131,vasa recta ascending limb cell,CL:1001036,vasa recta cell
+HP:0100117,Ivory epiphysis of the middle phalanx of the 2nd toe,HP:0100089,Abnormality of the epiphysis of the middle phalanx of the 2nd toe
+NCBITaxon:58262,Culicoidini,NCBITaxon:43801,Ceratopogoninae
+HP:0001528,Hemihypertrophy,HP:0100555,Asymmetric growth
+HP:0005469,Flat occiput,HP:0011217,Abnormal shape of the occiput
+HP:0007657,Diffuse nuclear cataract,HP:0100018,Nuclear cataract
+DOID:2639,breast pericanalicular fibroadenoma,DOID:1618,breast fibroadenoma
+DOID:14305,tuberculous empyema,DOID:3798,pleural empyema
+HP:0009982,Partial duplication of the middle phalanx of the 4th finger,HP:0009974,Partial duplication of the phalanges of the 4th finger
+NCBITaxon:5498,Cladosporium,NCBITaxon:452564,mitosporic Davidiellaceae
+UBERON:2201587,pectoral fin proximal radial cartilage,UBERON:2101587,pectoral fin proximal radial element
+UBERON:0008781,blastodisc derived epiblast,UBERON:0002532,epiblast (generic)
+HP:0007377,Abnormality of somatosensory evoked potentials,HP:0001311,Abnormal nervous system electrophysiology
+HP:0002890,Thyroid carcinoma,HP:0100031,Neoplasm of the thyroid gland
+DOID:3385,bacterial vaginosis,DOID:2170,vaginitis
+UBERON:0003326,mesenchyme of mammary gland,UBERON:0003104,mesenchyme
+UBERON:0005708,lower jaw incisor odontogenic papilla,UBERON:0010258,mesenchyme from rhombencephalic neural crest
+HP:0004197,Symphalangism of the 4th finger,HP:0009773,Symphalangism affecting the phalanges of the hand
+NCBITaxon:45659,Human adenovirus 3,NCBITaxon:565302,Human adenovirus B1
+UBERON:2000597,telencephalic tracts,UBERON:0011299,white matter of telencephalon
+UBERON:0011308,pars reflexa of masseter,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0007725,interphalangeal joint of pedal digit 2,UBERON:0007721,interphalangeal joint of pes
+HP:0100620,Germinoma,HP:0100728,Germ cell neoplasia
+UBERON:0002568,amiculum of dentate nucleus,UBERON:0003544,brain white matter
+DOID:3905,lung carcinoma,DOID:1324,lung cancer
+UBERON:0015061,limb endochondral element,UBERON:0004120,mesoderm-derived structure
+HP:0100041,Broad 3rd toe,HP:0010320,Abnormality of the 3rd toe
+HP:0000039,Epispadias,HP:0100627,Displacement of the external urethral meatus
+UBERON:3000846,element Y of fore mesopodium,UBERON:0004120,mesoderm-derived structure
+DOID:77,gastrointestinal system disease,DOID:7,disease of anatomical entity
+UBERON:0001724,sphenoidal sinus,UBERON:0001825,paranasal sinus
+DOID:929,myopathy of extraocular muscle,DOID:423,myopathy
+DOID:6566,posterior uveal melanoma,DOID:6039,uveal melanoma
+UBERON:3010240,Nobelian rod,UBERON:0007844,cartilage element
+UBERON:0001649,glossopharyngeal nerve,UBERON:0001785,cranial nerve
+UBERON:2002160,ural centrum 3,UBERON:2002085,ural centrum
+UBERON:0004821,pulmonary alveolus epithelium,UBERON:0000115,lung epithelium
+HP:0000128,Renal potassium wasting,HP:0012598,Abnormal urine potassium concentration
+HP:0100723,Gastrointestinal stroma tumor,HP:0007378,Neoplasm of the gastrointestinal tract
+UBERON:0005840,sacral spinal cord dorsal column,UBERON:0006079,subdivision of spinal cord dorsal column
+CL:0010021,cardiac myoblast,CL:0000056,myoblast
+HP:0000879,Short sternum,HP:0006714,Aplasia/Hypoplasia of the sternum
+HP:0009955,Partial duplication of the proximal phalanx of the 2nd finger,HP:0010003,Partial duplication of the proximal phalanges of the hand
+UBERON:0000434,anterior paraventricular nucleus of thalamus,UBERON:0001920,paraventricular nucleus of thalamus
+HP:0010198,Osteolytic defects of the middle phalanges of the toes,HP:0010177,Osteolytic defects of the phalanges of the toes
+HP:0100548,Exstrophy,HP:0004298,Abnormality of the abdominal wall
+UBERON:0002750,medial longitudinal fasciculus of medulla,UBERON:0010314,structure with developmental contribution from neural crest
+UBERON:0001290,proximal straight tubule,UBERON:0006853,renal cortex tubule
+DOID:3009,breast neuroendocrine neoplasm,DOID:0060082,breast benign neoplasm
+HP:0006747,Ganglioneuroblastoma,HP:0003006,Neuroblastoma
+HP:0002113,Pulmonary infiltrates,HP:0002088,Abnormality of the lung
+UBERON:0011360,ampulla caudalis,UBERON:0000464,anatomical space
+DOID:6564,neurilemmoma of the pleura,DOID:956,peripheral nerve schwannoma
+DOID:13365,reading disorder,DOID:8927,learning disability
+HP:0009523,Triangular epiphysis of the middle phalanx of the 2nd finger,HP:0009498,Triangular epiphyses of the 2nd finger
+DOID:14450,46 XX gonadal dysgenesis,DOID:14447,gonadal dysgenesis
+UBERON:0003885,mesometrium,UBERON:0001297,serosa of uterus
+HP:0009207,Fragmentation of the epiphysis of the middle phalanx of the 5th finger,HP:0010261,Fragmentation of the epiphyses of the middle phalanges of the hand
+UBERON:0010701,phalanx cartilage element,UBERON:0010702,digit mesenchyme
+HP:0100180,Absent epiphysis of the middle phalanx of the 4th toe,HP:0100095,Abnormality of the epiphysis of the middle phalanx of the 4th toe
+UBERON:0004645,urinary bladder urothelium,UBERON:0012275,meso-epithelium
+UBERON:0002412,vertebra,UBERON:0008001,irregular bone
+UBERON:0008712,stylohyoid muscle,UBERON:0001577,facial nerve muscle
+HP:0012295,Slender middle phalanx of finger,HP:0009833,Abnormality of the middle phalanges of the hand
+HP:0007541,Frontal cutaneous lipoma,HP:0008069,Neoplasm of the skin
+HP:0005028,Widened proximal tibial metaphyses,HP:0003016,Metaphyseal widening
+HP:0001056,Milia,HP:0011355,Localized skin lesion
+CL:0000637,chromophil cell of anterior pituitary gland,CL:0000166,chromaffin cell
+NCBITaxon:1655,Actinomyces naeslundii,NCBITaxon:1654,Actinomyces
+HP:0012053,Low serum calcifediol (25-hydroxycholecalciferol),HP:0100511,Abnormality of vitamin D metabolism
+CL:0000730,leading edge cell,CL:0002371,somatic cell
+HP:0012029,Abnormality of urine hormone level,HP:0000818,Abnormality of the endocrine system
+UBERON:0006377,remnant of Rathke's pouch,UBERON:0004121,ectoderm-derived structure
+DOID:12096,sodoku disease,DOID:0050338,primary bacterial infectious disease
+UBERON:0010059,hypoglossal cord,UBERON:0002036,striated muscle tissue
+UBERON:0006059,falx cerebri,UBERON:0004120,mesoderm-derived structure
+UBERON:0008592,levator labii superioris alaeque nasi,UBERON:0001577,facial nerve muscle
+HP:0011198,EEG with generalized epileptiform discharges,HP:0011182,Epileptiform EEG discharges
+UBERON:0002874,lateral pericuneate nucleus,UBERON:0007635,nucleus of medulla oblongata
+NCBITaxon:203692,Spirochaetia,NCBITaxon:203691,Spirochaetes
+UBERON:3010069,intermedium (fore),UBERON:0004120,mesoderm-derived structure
+UBERON:0010284,lacrimal punctum,UBERON:0000161,orifice
+HP:0007048,Large basal ganglia,HP:0002134,Abnormality of the basal ganglia
+CL:0000267,prespore cell,CL:0000263,vegetative cell (sensu Mycetozoa)
+UBERON:3000882,interilial region,UBERON:0005913,zone of bone organ
+UBERON:0004645,urinary bladder urothelium,UBERON:0003350,epithelium of mucosa
+HP:0005256,Unilateral absence of pectoralis major muscle,HP:0011957,Abnormality of the  pectoral muscle
+UBERON:0003334,serosa of rectum,UBERON:0001209,serosa of large intestine
+UBERON:0001716,secondary palate,UBERON:0004121,ectoderm-derived structure
+HP:0007010,Poor fine motor coordination,HP:0002275,Poor motor coordination
+UBERON:0002031,epithelium of bronchus,UBERON:0004815,lower respiratory tract epithelium
+HP:0004746,Dense deposit disease,HP:0000099,Glomerulonephritis
+UBERON:0001825,paranasal sinus,UBERON:0002553,anatomical cavity
+CL:0000155,peptic cell,CL:0000154,protein secreting cell
+UBERON:0000412,dermal papilla,UBERON:0004120,mesoderm-derived structure
+HP:0007153,Progressive extrapyramidal movement disorder,HP:0002071,Abnormality of extrapyramidal motor function
+UBERON:0002658,medial lemniscus of midbrain,UBERON:0014891,brainstem white matter
+DOID:479,angiokeratoma,DOID:255,hemangioma
+CL:0008003,somatic muscle myotube,CL:0002372,myotube
+HP:0005495,Metopic suture patent to nasal root,HP:0005556,Abnormality of the metopic suture
+CL:0000182,hepatocyte,CL:0000417,endopolyploid cell
+DOID:0060082,breast benign neoplasm,DOID:0060097,thoracic benign neoplasm
+HP:0003038,Fibular hypoplasia,HP:0003026,Short long bones
+HP:0100186,Ivory epiphysis of the middle phalanx of the 4th toe,HP:0100072,Ivory epiphyses of the 4th toe
+UBERON:0011620,basihyal lingual process,UBERON:4100000,skeletal element projection
+UBERON:0003890,Mullerian duct,UBERON:0015212,lateral structure
+HP:0004325,Decreased body weight,HP:0004323,Abnormality of body weight
+UBERON:0002413,cervical vertebra,UBERON:0004451,trunk or cervical vertebra
+UBERON:0007026,primitive gut,UBERON:0002050,embryonic structure
+HP:0009287,Curved middle phalanx of the 4th finger,HP:0009285,Curved phalanges of the 4th finger
+HP:0002224,Woolly hair,HP:0010719,Abnormality of hair texture
+UBERON:0012142,pedal digitopodium region,UBERON:0012140,digitopodium region
+HP:0009496,Small epiphyses of the 2nd finger,HP:0010236,Small epiphyses of the phalanges of the hand
+HP:0009142,Duplication of bones involving the upper extremities,HP:0002817,Abnormality of the upper limb
+UBERON:0002635,regional part of midbrain tegmentum,UBERON:0010314,structure with developmental contribution from neural crest
+HP:0003003,Colon cancer,HP:0100273,Neoplasm of the colon
+UBERON:0005933,hair root sheath,UBERON:0000479,tissue
+HP:0004002,Flattened radial epiphyses,HP:0003999,Abnormality of radial epiphyses
+UBERON:0006213,carpus cartilage element,UBERON:0015049,carpus endochondral element
+UBERON:0006475,Brodmann (1909) area 31,UBERON:0013529,Brodmann area
+UBERON:3010787,pars transversalis,UBERON:0008777,hypaxial musclulature
+HP:0001449,Duplication of metatarsal bones,HP:0001832,Abnormality of the metatarsal bones
+UBERON:0009593,mesenchyme of interdigital region between pedal digits 4 and 5,UBERON:0009601,mesenchyme of interdigital region of pes
+HP:0004634,Cuboid-shaped vertebral bodies,HP:0003312,Abnormal form of the vertebral bodies
+DOID:3890,acute intermittent porphyria,DOID:3133,acute porphyria
+DOID:4796,space motion sickness,DOID:2951,motion sickness
+HP:0009516,Enlarged epiphysis of the middle phalanx of the 2nd finger,HP:0009500,Abnormality of the epiphysis of the middle phalanx of the 2nd finger
+CL:0000893,thymocyte,CL:0002420,immature T cell
+UBERON:0003253,neck of rib,UBERON:0004120,mesoderm-derived structure
+UBERON:3000516,pseudobasal process,UBERON:0004121,ectoderm-derived structure
+UBERON:3000512,processus zygomatico-maxillaris,UBERON:0004120,mesoderm-derived structure
+HP:0007975,Hypometric horizontal saccades,HP:0000571,Hypometric saccades
+HP:0012457,Medial calcification of medium-sized arteries,HP:0012456,Medial arterial calcification
+UBERON:0008593,zygomaticus major muscle,UBERON:0010437,zygomaticus muscle
+CL:1000298,mesothelial cell of dura mater,CL:0000077,mesothelial cell
+UBERON:0003464,hindlimb bone,UBERON:0010742,bone of pelvic complex
+UBERON:3000565,skeletal support for eminentia olfactoria,UBERON:0010313,neural crest-derived structure
+UBERON:4200010,ventral humeral ridge,UBERON:4100000,skeletal element projection
+HP:0009919,Retinoblastoma,HP:0100012,Neoplasm of the eye
+DOID:0060141,finger agnosia,DOID:4090,agnosia
+HP:0007588,Reticular hyperpigmentation,HP:0007400,Irregular hyperpigmentation
+DOID:10209,extrahepatic bile duct lipoma,DOID:0050625,biliary tract neoplasm
+HP:0005830,Flexion contracture of toe,HP:0100490,Camptodactyly of finger
+UBERON:0002745,ventral amygdalofugal projection,UBERON:0011299,white matter of telencephalon
+HP:0009399,Ivory epiphyses of the 4th finger,HP:0010234,Ivory epiphyses of the phalanges of the hand
+UBERON:0012428,proximal convoluted tubule brush border,UBERON:0006554,urinary system structure
+UBERON:0000956,cerebral cortex,UBERON:0002791,regional part of telencephalon
+HP:0012559,Increased T3/T4 ratio,HP:0012558,Abnormal T3/T4 ratio
+UBERON:0001941,lateral habenular nucleus,UBERON:0007692,nucleus of thalamus
+HP:0100107,Pseudoepiphysis of the distal phalanx of the 2nd toe,HP:0100051,Pseudoepiphyses of the 2nd toe
+DOID:1005,endometrial disease,DOID:345,uterine disease
+DOID:5160,arteriosclerosis obliterans,DOID:2349,arteriosclerosis
+UBERON:0007262,intervertebral disk of fifth cervical vertebra,UBERON:0007252,intervertebral disk of cervical vertebra
+UBERON:0007750,metatarsophalangeal joint of pedal digit 1,UBERON:0003696,metatarsophalangeal joint
+UBERON:0005815,anterior tubercle of transverse process of cervical vertebra,UBERON:0004120,mesoderm-derived structure
+UBERON:0001252,adventitia of ureter,UBERON:0006554,urinary system structure
+UBERON:0002408,parietal serous pericardium,UBERON:0000042,serous membrane
+HP:0011787,Central hypothyroidism,HP:0000821,Hypothyroidism
+HP:0006381,Rudimentary fibula,HP:0004986,Rudimentary to absent fibulae
+UBERON:0008922,sublaminar layer S1,UBERON:0009733,sublaminar layers S1 or S2 or S3
+UBERON:0008926,sublaminar layer S5,UBERON:0009732,sublaminar layers S1 or S2 or S5
+HP:0009229,Curved proximal phalanx of the 5th finger,HP:0009150,Abnormality of the proximal phalanx of the 5th finger
+UBERON:0009960,esophagus smooth muscle circular layer,UBERON:0004120,mesoderm-derived structure
+DOID:0050882,spinocerebellar ataxia type 5,DOID:1441,spinocerebellar ataxia
+HP:0004248,Abnormality of the lunate bone,HP:0001191,Abnormality of the carpal bones
+DOID:13033,balanitis,DOID:1529,penile disease
+HP:0010627,Anterior pituitary hypoplasia,HP:0010625,Anterior pituitary dysgenesis
+HP:0004214,Curved phalanges of the 5th finger,HP:0004213,Abnormality of the phalanges of the 5th finger
+UBERON:0010936,thyropharyngeus muscle,UBERON:0001630,muscle organ
+UBERON:0013067,colorectal mucosa,UBERON:0001207,mucosa of large intestine
+DOID:8675,lymphosarcoma,DOID:0060073,lymphatic system cancer
+UBERON:0014392,sweat of palm,UBERON:0001089,sweat
+UBERON:2001831,pterosphenoid-orbitosphenoid joint,UBERON:0000982,skeletal joint
+UBERON:2001252,pharyngobranchial 3 bone,UBERON:2001912,pharyngobranchial 3 element
+UBERON:2001924,occipital artery foramen,UBERON:0005744,bone foramen
+HP:0006370,Distal ulnar epiphyseal stippling,HP:0010600,Abnormality of the distal ulnar epiphysis
+UBERON:0005197,segmental spinal nerve,UBERON:0010313,neural crest-derived structure
+HP:0005312,Pulmonary aterial intimal fibrosis,HP:0004414,Abnormality of the pulmonary artery
+NCBITaxon:4890,Ascomycota,NCBITaxon:451864,Dikarya
+NCBITaxon:91061,Bacilli,NCBITaxon:1239,Firmicutes
+CL:0000281,pstAB/ALC,CL:0000265,anterior like cell
+DOID:5539,ureter squamous cell carcinoma,DOID:4939,ureter carcinoma
+DOID:8930,retromolar area cancer,DOID:8618,oral cavity cancer
+UBERON:0012110,frontal process of zygomatic bone,UBERON:0004120,mesoderm-derived structure
+UBERON:3000069,cartilago infranarina,UBERON:0003406,cartilage of respiratory system
+UBERON:3000540,recessus vaginiformis,UBERON:0000464,anatomical space
+UBERON:0013682,peripheral region of retina,UBERON:0000481,multi-tissue structure
+HP:0100159,Cone-shaped epiphysis of the proximal phalanx of the 3rd toe,HP:0100057,Cone-shaped epiphyses of the 3rd toe
+DOID:4301,vulva basal cell carcinoma,DOID:1294,vulva carcinoma
+HP:0011166,Focal myoclonic seizures,HP:0011153,Focal motor seizures
+UBERON:0004251,hindlimb zeugopod bone,UBERON:0005893,leg bone
+HP:0000174,Abnormality of the palate,HP:0000163,Abnormality of the oral cavity
+HP:0012526,Absence of alpha granules,HP:0012528,Abnormal number of alpha granules
+CL:0002668,type 4 otic fibrocyte,CL:0002665,otic fibrocyte
+UBERON:0007634,parabrachial nucleus,UBERON:0009662,hindbrain nucleus
+UBERON:0002693,occipitotemporal sulcus,UBERON:0008334,subarachnoid sulcus
+UBERON:0001727,taste bud,UBERON:0004119,endoderm-derived structure
+DOID:10326,Caplan's syndrome,DOID:10316,pneumoconiosis
+UBERON:0004980,mucosa of ureter,UBERON:0006554,urinary system structure
+UBERON:0004431,proximal epiphysis of fifth metatarsal bone,UBERON:0004399,epiphysis of fifth metatarsal bone
+UBERON:0003119,aortic arch 2,UBERON:0004363,aortic arch
+UBERON:3000653,pars glenoidalis of quadratojugal,UBERON:0010313,neural crest-derived structure
+UBERON:0014524,electromotor division of oculomotor nuclear complex,UBERON:0003528,brain grey matter
+HP:0003521,Disproportionate short-trunk short stature,HP:0003498,Disproportionate short stature
+UBERON:0006526,right lung alveolar system,UBERON:0004119,endoderm-derived structure
+HP:0012010,EEG with frontal focal spike waves,HP:0011197,EEG with focal spike waves
+CL:0000501,granulosa cell,CL:0002174,follicular cell of ovary
+UBERON:0002932,trapezoid body,UBERON:0002316,white matter
+UBERON:2002210,mossy fiber,UBERON:0010314,structure with developmental contribution from neural crest
+DOID:0050819,Matthew-Wood syndrome,DOID:0050739,autosomal genetic disease
+UBERON:4200029,adductor crest,UBERON:0004120,mesoderm-derived structure
+DOID:0050552,Sugio-Kajii syndrome,DOID:0050736,autosomal dominant disease
+UBERON:0001449,phalanx of pes,UBERON:0004248,pedal digit bone
+UBERON:4200185,entepicondyle fossa,UBERON:0004704,bone fossa
+HP:0004734,Renal cortical microcysts,HP:0000803,Renal cortical cysts
+HP:0000704,Periodontitis,HP:0000164,Abnormality of the teeth
+HP:0100439,Bullet-shaped proximal phalanx of the 5th toe,HP:0010385,Bullet-shaped phalanges of the 5th toe
+CL:0002074,myocardial endocrine cell,CL:0002086,specialized cardiac myocyte
+HP:0006748,Adrenal pheochromocytoma,HP:0100642,Neoplasm of the adrenal medulla
+HP:0004704,Short fifth metatarsal,HP:0010743,Short metatarsal
+UBERON:0010018,spiral valve of conus arteriosus,UBERON:0003978,valve
+CL:0000421,coelomocyte,CL:0000519,phagocyte (sensu Nematoda and Protostomia)
+UBERON:2001245,epibranchial 4 bone,UBERON:2000658,epibranchial bone
+UBERON:2001870,supraneural 3 cartilage,UBERON:4300036,supraneural cartilage
+UBERON:0001552,kidney arcuate artery,UBERON:0003644,kidney arterial blood vessel
+HP:0006210,Postaxial oligodactyly,HP:0001180,Oligodactyly (hands)
+UBERON:0010395,lymph node primary follicle,UBERON:0010748,lymph node follicle
+HP:0005102,Cochlear degeneration,HP:0000375,Abnormality of cochlea
+UBERON:0005712,midgut duodenum mesentery,UBERON:0003284,mesentery of midgut
+DOID:10031,compensatory emphysema,DOID:9675,pulmonary emphysema
+UBERON:0008574,transverse arytenoid,UBERON:0010958,arytenoid muscle
+UBERON:0012175,acoustico-facial VII-VIII ganglion complex,UBERON:0001714,cranial ganglion
diff --git a/src/ontology/reports/omim-subClassesExt.csv b/src/ontology/reports/omim-subClassesExt.csv
new file mode 100644
index 0000000..aebc7d8
--- /dev/null
+++ b/src/ontology/reports/omim-subClassesExt.csv
@@ -0,0 +1,1213 @@
+baseClass,baseLabel,superClass,superLabel
+OMIM:146450,"Hypospadias 3, Autosomal",DOID:10892,hypospadias
+OMIM:605376,"Heterotaxy, Visceral, 2, Autosomal",DOID:0050545,visceral heterotaxy
+OMIM:163800,"Sick Sinus Syndrome 2, Autosomal Dominant",DOID:13884,sick sinus syndrome
+OMIM:608967,Moved To 609192,DOID:0050466,Loeys-Dietz syndrome
+OMIM:613235,"Factor Xiii, B Subunit, Deficiency Of",DOID:2211,factor XIII deficiency
+OMIM:614464,Joubert Syndrome 15,DOID:0050777,Joubert syndrome
+OMIM:611022,"Deafness, Autosomal Recessive 24",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:613501,"Agammaglobulinemia 3, Autosomal Recessive",DOID:2583,agammaglobulinemia
+OMIM:608244,Otosclerosis 3,DOID:12185,otosclerosis
+OMIM:609054,"Fanconi Anemia, Complementation Group J",DOID:13636,Fanconi's anemia
+OMIM:601992,Friedreich Ataxia 2,DOID:12705,Friedreich ataxia
+OMIM:300049,"Heterotopia, Periventricular, X-Linked Dominant",DOID:0050454,periventricular nodular heterotopia
+OMIM:605192,"Deafness, Autosomal Dominant 23",DOID:0050564,autosomal dominant nonsyndromic deafness
+DOID:1520,colon carcinoma,OMIM:114500,Colorectal Cancer
+OMIM:300215,"Lissencephaly, X-Linked, 2",DOID:0050453,lissencephaly
+OMIM:200170,Acanthosis Nigricans With Muscle Cramps And Acral Enlargement,DOID:3138,acanthosis nigricans
+OMIM:607625,"Niemann-Pick Disease, Type C2",DOID:14504,Niemann-Pick disease
+OMIM:612964,Premature Ovarian Failure 7,DOID:5426,premature ovarian failure
+OMIM:148300,Keratoconus 1,DOID:10126,keratoconus
+OMIM:130900,"Amelogenesis Imperfecta, Type Iii",DOID:2187,amelogenesis imperfecta
+OMIM:611560,Joubert Syndrome 7,DOID:0050777,Joubert syndrome
+OMIM:188000,Thrombocytopenia 2,DOID:1588,thrombocytopenia
+OMIM:615490,"Charcot-Marie-Tooth Disease, Axonal, Type 2r",DOID:0050539,Charcot-Marie-Tooth disease type 2
+OMIM:158300,"Arthrogryposis, Distal, Type 7",DOID:0050646,distal arthrogryposis
+OMIM:254900,"Epilepsy, Progressive Myoclonic 4, With Or Without Renal Failure",DOID:891,progressive myoclonus epilepsy
+OMIM:614845,Nephronophthisis 15,DOID:12712,nephronophthisis
+OMIM:611363,Atrial Septal Defect 4,DOID:1882,atrial heart septal defect
+OMIM:601780,"Ceroid Lipofuscinosis, Neuronal, 6",DOID:14503,neuronal ceroid lipofuscinosis
+OMIM:252930,"Mucopolysaccharidosis, Type Iiic",DOID:12801,mucopolysaccharidosis III
+OMIM:104510,"Amelogenesis Imperfecta, Type Iv",DOID:2187,amelogenesis imperfecta
+OMIM:613224,Noonan Syndrome 6,DOID:3490,Noonan syndrome
+OMIM:609006,"Deafness, Autosomal Recessive 36, With Or Without Vestibular Involvement",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:614228,"Charcot-Marie-Tooth Disease, Axonal, Type 2o",DOID:0050539,Charcot-Marie-Tooth disease type 2
+OMIM:187370,"Arthrogryposis, Distal, Type 10",DOID:0050646,distal arthrogryposis
+OMIM:112700,"Brachydactyly, Type A3",DOID:0050581,brachydactyly
+OMIM:614465,Joubert Syndrome 16,DOID:0050777,Joubert syndrome
+OMIM:141500,"Migraine, Familial Hemiplegic, 1",DOID:0060178,familial hemiplegic migraine
+OMIM:613502,"Agammaglobulinemia 4, Autosomal Recessive",DOID:2583,agammaglobulinemia
+OMIM:614629,Keratoconus 7,DOID:10126,keratoconus
+OMIM:109730,Aortic Valve Disease 1,DOID:1712,aortic valve stenosis
+OMIM:605909,"Parkinson Disease 6, Autosomal Recessive Early-Onset",DOID:14330,Parkinson's disease
+OMIM:604804,"Microcephaly 3, Primary, Autosomal Recessive",DOID:10907,microcephaly
+OMIM:610852,"Ciliary Dyskinesia, Primary, 6",DOID:9562,primary ciliary dyskinesia
+OMIM:177700,"Glaucoma 1, Open Angle, P",DOID:1067,open-angle glaucoma
+OMIM:151400,"Leukemia, Chronic Lymphocytic",DOID:1040,chronic lymphocytic leukemia
+OMIM:614196,"Nephrotic Syndrome, Type 6",DOID:1184,nephrotic syndrome
+OMIM:175100,Familial Adenomatous Polyposis 1,DOID:0050424,familial adenomatous polyposis
+OMIM:612529,"Amelogenesis Imperfecta, Hypomaturation Type, Iia2",DOID:2187,amelogenesis imperfecta
+OMIM:305390,"Exudative Vitreoretinopathy 2, X-Linked",DOID:0050535,exudative vitreoretinopathy
+OMIM:608751,"Cardiomyopathy, Familial Hypertrophic, 8",DOID:11984,hypertrophic cardiomyopathy
+OMIM:614844,Nephronophthisis 14,DOID:12712,nephronophthisis
+OMIM:259440,"Osteogenesis Imperfecta, Type Ix",DOID:12347,osteogenesis imperfecta
+OMIM:220290,"Deafness, Autosomal Recessive 1a",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:224120,"Anemia, Congenital Dyserythropoietic, Type Ia",DOID:1338,congenital dyserythropoietic anemia
+OMIM:614628,Keratoconus 8,DOID:10126,keratoconus
+OMIM:608591,"Charcot-Marie-Tooth Disease, Axonal, Type 2g",DOID:0050539,Charcot-Marie-Tooth disease type 2
+OMIM:600316,"Deafness, Autosomal Recessive 3",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:610738,"Neutropenia, Severe Congenital, 3, Autosomal Recessive",DOID:0050590,severe congenital neutropenia
+OMIM:604841,"Stickler Syndrome, Type Ii",DOID:0080046,Stickler syndrome
+OMIM:613839,Megaloblastic Anemia Due To Dihydrofolate Reductase Deficiency,DOID:13382,megaloblastic anemia
+OMIM:615300,Perrault Syndrome 4,DOID:0050857,Perrault syndrome
+OMIM:277970,Wiskott-Aldrich Syndrome,DOID:9169,Wiskott-Aldrich syndrome
+OMIM:600901,"Fanconi Anemia, Complementation Group E",DOID:13636,Fanconi's anemia
+OMIM:611571,Otosclerosis 4,DOID:12185,otosclerosis
+OMIM:270970,"Spherocytosis, Type 3",DOID:12971,hereditary spherocytosis
+OMIM:240200,"Hypoadrenocorticism, Familial",DOID:13774,Addison's disease
+OMIM:121201,"Seizures, Benign Familial Neonatal, 2",DOID:14264,benign neonatal seizures
+OMIM:276950,Vacterl Association With Hydrocephalus,DOID:14679,VACTERL association
+OMIM:137750,"Glaucoma 1, Open Angle, A",DOID:1067,open-angle glaucoma
+OMIM:145000,Hyperparathyroidism 1,DOID:13543,hyperparathyroidism
+OMIM:613500,"Agammaglobulinemia 2, Autosomal Recessive",DOID:2583,agammaglobulinemia
+OMIM:130600,Elliptocytosis 2,DOID:2373,hereditary elliptocytosis
+OMIM:608840,"Muscular Dystrophy-Dystroglycanopathy (Congenital With Mental Retardation), Type B, 6",DOID:0050557,congenital muscular dystrophy
+OMIM:301050,"Alport Syndrome, X-Linked",DOID:10983,Alport syndrome
+OMIM:609456,"Muscular Dystrophy, Congenital, Merosin-Positive",DOID:0050557,congenital muscular dystrophy
+OMIM:300558,"Mental Retardation, X-Linked 30",DOID:0050776,non-specific X-linked mental retardation
+OMIM:613097,"Tooth Agenesis, Selective, 6",DOID:0050591,tooth agenesis
+OMIM:613286,"Cardiomyopathy, Dilated, 1ff",DOID:12930,dilated cardiomyopathy
+OMIM:278700,"Xeroderma Pigmentosum, Complementation Group A",DOID:0050427,xeroderma pigmentosum
+OMIM:613678,Brachyolmia Type 2,DOID:0050690,brachyolmia
+OMIM:605594,"Deafness, Autosomal Dominant 39, With Dentinogenesis Imperfecta 1",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:603233,"Pseudohypoparathyroidism, Type Ib",DOID:4184,pseudohypoparathyroidism
+OMIM:610629,Diamond-Blackfan Anemia 3,DOID:1339,Diamond-Blackfan anemia
+DOID:4647,trilateral retinoblastoma,OMIM:180200,Retinoblastoma
+OMIM:109543,"Leukemia, Chronic Lymphocytic, Susceptibility To, 2",DOID:1040,chronic lymphocytic leukemia
+OMIM:612644,"Deafness, Autosomal Dominant 2b",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:300537,"Heterotopia, Periventricular, Ehlers-Danlos Variant",DOID:0050454,periventricular nodular heterotopia
+OMIM:607516,"Migraine With Or Without Aura, Susceptibility To, 6",DOID:0060178,familial hemiplegic migraine
+OMIM:611572,Otosclerosis 7,DOID:12185,otosclerosis
+OMIM:112500,"Brachydactyly, Type A1",DOID:0050581,brachydactyly
+OMIM:133701,"Exostoses, Multiple, Type Ii",DOID:206,hereditary multiple exostoses
+OMIM:607682,"Epilepsy, Idiopathic Generalized, Susceptibility To, 9",DOID:1827,idiopathic generalized epilepsy
+OMIM:603965,Focal Segmental Glomerulosclerosis 2,DOID:1312,focal segmental glomerulosclerosis
+OMIM:601847,"Cholestasis, Progressive Familial Intrahepatic, 2",DOID:1852,intrahepatic cholestasis
+OMIM:104000,Alopecia Areata 1,DOID:986,alopecia areata
+OMIM:118100,"Klippel-Feil Syndrome 1, Autosomal Dominant",DOID:10426,Klippel-Feil syndrome
+OMIM:615636,Joubert Syndrome 21,DOID:0050777,Joubert syndrome
+OMIM:606324,"Parkinson Disease 7, Autosomal Recessive Early-Onset",DOID:14330,Parkinson's disease
+OMIM:608898,"Hemophagocytic Lymphohistiocytosis, Familial, 3",DOID:0050120,hemophagocytic lymphohistiocytosis
+OMIM:502500,"Alzheimer Disease, Susceptibility To, Mitochondrial",DOID:10652,Alzheimer's disease
+OMIM:267200,Renal Tubular Acidosis Iii,DOID:14219,renal tubular acidosis
+OMIM:236670,"Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 1",DOID:0050560,Walker-Warburg syndrome
+OMIM:613763,"Cataract 16, Multiple Types",DOID:0050537,posterior polar cataract
+OMIM:615605,Fanconi Renotubular Syndrome 3,DOID:1062,Fanconi syndrome
+OMIM:610188,Joubert Syndrome 5,DOID:0050777,Joubert syndrome
+OMIM:250100,Metachromatic Leukodystrophy,DOID:10581,metachromatic leukodystrophy
+OMIM:610759,Cornelia De Lange Syndrome 3,DOID:11725,Cornelia de Lange syndrome
+OMIM:256300,"Nephrotic Syndrome, Type 1",DOID:1184,nephrotic syndrome
+OMIM:257320,Lissencephaly 2,DOID:0050453,lissencephaly
+OMIM:612643,"Deafness, Autosomal Dominant 3b",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:151660,"Lipodystrophy, Familial Partial, Type 2",DOID:0050440,familial partial lipodystrophy
+OMIM:133700,"Exostoses, Multiple, Type I",DOID:206,hereditary multiple exostoses
+OMIM:613027,Glycogen Storage Disease Ixc,DOID:0050594,glycogen storage disease IX
+OMIM:613252,"Cardiomyopathy, Dilated, 1ee",DOID:12930,dilated cardiomyopathy
+OMIM:612900,"Cerebral Palsy, Spastic Quadriplegic, 2",DOID:10970,spastic quadriplegia
+OMIM:608340,"Charcot-Marie-Tooth Disease, Recessive Intermediate A",DOID:0050543,Charcot-Marie-Tooth disease intermediate type
+OMIM:613376,"Neuronopathy, Distal Hereditary Motor, Type Iic",DOID:0050582,distal hereditary motor neuropathy
+OMIM:134600,Fanconi Renotubular Syndrome 1,DOID:1062,Fanconi syndrome
+OMIM:610832,"Fanconi Anemia, Complementation Group N",DOID:13636,Fanconi's anemia
+OMIM:614135,"Epiphyseal Dysplasia, Multiple, 6",DOID:12721,multiple epiphyseal dysplasia
+OMIM:226000,Endocardial Fibroelastosis,DOID:12929,endocardial fibroelastosis
+OMIM:306955,"Heterotaxy, Visceral, 1, X-Linked",DOID:0050545,visceral heterotaxy
+OMIM:147421,Inclusion Body Myositis,DOID:3429,inclusion body myositis
+OMIM:309583,"Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type",DOID:0050888,syndromic intellectual disability
+OMIM:601154,"Cardiomyopathy, Dilated, 1e",DOID:12930,dilated cardiomyopathy
+OMIM:257220,"Niemann-Pick Disease, Type C1",DOID:14504,Niemann-Pick disease
+OMIM:614653,"Neuropathy, Hereditary Sensory And Autonomic, Type Vi",DOID:0050548,hereditary sensory neuropathy
+OMIM:608716,"Microcephaly 5, Primary, Autosomal Recessive",DOID:10907,microcephaly
+OMIM:602522,"Bartter Syndrome, Type 4a",DOID:445,Bartter disease
+OMIM:612527,Diamond-Blackfan Anemia 4,DOID:1339,Diamond-Blackfan anemia
+OMIM:256050,"Atelosteogenesis, Type Ii",DOID:0050648,atelosteogenesis
+OMIM:612528,Diamond-Blackfan Anemia 5,DOID:1339,Diamond-Blackfan anemia
+OMIM:601518,"Prostate Cancer, Hereditary, 1",DOID:10283,prostate cancer
+OMIM:608644,"Ciliary Dyskinesia, Primary, 3",DOID:9562,primary ciliary dyskinesia
+OMIM:612645,"Deafness, Autosomal Recessive 1b",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:613823,Seckel Syndrome 5,DOID:0050569,Seckel syndrome
+OMIM:609823,"Deafness, Autosomal Recessive 28",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:614623,Keratoconus 6,DOID:10126,keratoconus
+OMIM:607631,"Epilepsy, Juvenile Absence, Susceptibility To, 1",DOID:4890,juvenile myoclonic epilepsy
+OMIM:104200,"Alport Syndrome, Autosomal Dominant",DOID:10983,Alport syndrome
+OMIM:142945,Holoprosencephaly 3,DOID:4621,holoprosencephaly
+OMIM:123100,Craniosynostosis 1,DOID:2340,craniosynostosis
+OMIM:211980,Lung Cancer,DOID:1324,lung cancer
+OMIM:615397,"Meckel Syndrome, Type 11",DOID:0050778,Meckel syndrome
+OMIM:608908,Myopia 6,DOID:11830,myopia
+OMIM:101000,"Neurofibromatosis, Type Ii",DOID:8712,neurofibromatosis
+OMIM:613642,"Cardiomyopathy, Dilated, 1gg",DOID:12930,dilated cardiomyopathy
+OMIM:115200,"Cardiomyopathy, Dilated, 1a",DOID:12930,dilated cardiomyopathy
+OMIM:614820,Alternating Hemiplegia Of Childhood 2,DOID:0050635,alternating hemiplegia of childhood
+OMIM:613702,"Klippel-Feil Syndrome 3, Autosomal Dominant",DOID:10426,Klippel-Feil syndrome
+OMIM:254100,"Muscular Dystrophy, Congenital, With Rapid Progression",DOID:0050557,congenital muscular dystrophy
+OMIM:202110,"Adrenal Hyperplasia, Congenital, Due To 17-Alpha-Hydroxylase Deficiency",DOID:0050811,congenital adrenal hyperplasia
+OMIM:146520,Hypotrichosis 2,DOID:4535,hypotrichosis
+OMIM:300770,"Surfactant Metabolism Dysfunction, Pulmonary, 4",DOID:12120,pulmonary alveolar proteinosis
+OMIM:106600,"Tooth Agenesis, Selective, 1",DOID:0050591,tooth agenesis
+OMIM:166220,"Osteogenesis Imperfecta, Type Iv",DOID:12347,osteogenesis imperfecta
+OMIM:609800,"Generalized Epilepsy With Febrile Seizures Plus, Type 4",DOID:0060170,generalized epilepsy with febrile seizures plus
+OMIM:613985,Beta-Thalassemia,DOID:12241,beta thalassemia
+DOID:1455,geographic tongue,OMIM:137400,Geographic Tongue And Fissured Tongue
+OMIM:614622,Keratoconus 5,DOID:10126,keratoconus
+OMIM:601472,"Charcot-Marie-Tooth Disease, Axonal, Type 2d",DOID:0050539,Charcot-Marie-Tooth disease type 2
+OMIM:614475,Atrial Septal Defect 9,DOID:1882,atrial heart septal defect
+OMIM:607831,"Charcot-Marie-Tooth Disease, Axonal, Type 2k",DOID:0050539,Charcot-Marie-Tooth disease type 2
+OMIM:612965,"46,Xy Sex Reversal 3",DOID:14448,46 XY gonadal dysgenesis
+OMIM:615010,Aicardi-Goutieres Syndrome 6,DOID:0050629,Aicardi-Goutieres syndrome
+OMIM:610189,Senior-Loken Syndrome 6,DOID:0050576,Senior-Loken syndrome
+OMIM:613159,Nephronophthisis-Like Nephropathy 1,DOID:12712,nephronophthisis
+OMIM:615219,"Hydrocephalus, Nonsyndromic, Autosomal Recessive 2",DOID:10908,hydrocephalus
+OMIM:607855,"Muscular Dystrophy, Congenital Merosin-Deficient, 1a",DOID:0050557,congenital muscular dystrophy
+OMIM:115196,"Cardiomyopathy, Familial Hypertrophic, 3",DOID:11984,hypertrophic cardiomyopathy
+OMIM:259720,"Osteopetrosis, Autosomal Recessive 5",DOID:13533,osteopetrosis
+OMIM:310300,"Emery-Dreifuss Muscular Dystrophy 1, X-Linked",DOID:11726,Emery-Dreifuss muscular dystrophy
+OMIM:608762,"Epilepsy, Idiopathic Generalized, Susceptibility To, 3",DOID:1827,idiopathic generalized epilepsy
+OMIM:610333,Aicardi-Goutieres Syndrome 4,DOID:0050629,Aicardi-Goutieres syndrome
+OMIM:604145,"Cardiomyopathy, Dilated, 1g",DOID:12930,dilated cardiomyopathy
+OMIM:144400,Moved To 143890,DOID:13810,familial hypercholesterolemia
+OMIM:609583,Joubert Syndrome 4,DOID:0050777,Joubert syndrome
+OMIM:114300,"Arthrogryposis, Distal, Type 3",DOID:0050646,distal arthrogryposis
+OMIM:115195,"Cardiomyopathy, Familial Hypertrophic, 2",DOID:11984,hypertrophic cardiomyopathy
+OMIM:188700,"Blount Disease, Infantile",DOID:14798,Blount's disease
+OMIM:609053,"Fanconi Anemia, Complementation Group I",DOID:13636,Fanconi's anemia
+OMIM:608895,"Macular Degeneration, Age-Related, 3",DOID:10871,age related macular degeneration
+OMIM:168000,Paragangliomas 1,DOID:0050773,paraganglioma
+OMIM:610698,"Macular Degeneration, Age-Related, 4",DOID:10871,age related macular degeneration
+OMIM:600757,Orofacial Cleft 3,DOID:0050567,orofacial cleft
+OMIM:613345,"Hypokalemic Periodic Paralysis, Type 2",DOID:14452,hypokalemic periodic paralysis
+OMIM:304900,"Diabetes Insipidus, Neurohypophyseal Type",DOID:12388,neurohypophyseal diabetes insipidus
+OMIM:215100,"Rhizomelic Chondrodysplasia Punctata, Type 1",DOID:2580,rhizomelic chondrodysplasia punctata
+OMIM:259200,"Blount Disease, Adolescent",DOID:14798,Blount's disease
+OMIM:615220,"Osteogenesis Imperfecta, Type Xv",DOID:12347,osteogenesis imperfecta
+OMIM:607791,"Charcot-Marie-Tooth Disease, Dominant Intermediate D",DOID:0050543,Charcot-Marie-Tooth disease intermediate type
+OMIM:611777,Brugada Syndrome 2,DOID:0050451,Brugada syndrome
+OMIM:100050,"Aarskog Syndrome, Autosomal Dominant",DOID:6683,Aarskog-Scott syndrome
+OMIM:614436,"Charcot-Marie-Tooth Disease, Axonal, Type 2p",DOID:0050539,Charcot-Marie-Tooth disease type 2
+OMIM:614279,"46,Xy Sex Reversal 8",DOID:14448,46 XY gonadal dysgenesis
+OMIM:187300,"Telangiectasia, Hereditary Hemorrhagic, Of Rendu, Osler, And Weber",DOID:1270,hereditary hemorrhagic telangiectasia
+OMIM:600858,"Cardiomyopathy, Familial Hypertrophic, 6",DOID:11984,hypertrophic cardiomyopathy
+OMIM:615185,"Charcot-Marie-Tooth Disease, Dominant Intermediate F",DOID:0050543,Charcot-Marie-Tooth disease intermediate type
+OMIM:105250,"Amyloidosis, Primary Localized Cutaneous, 1",DOID:0050639,primary cutaneous amyloidosis
+OMIM:125500,"Dentinogenesis Imperfecta, Shields Type Iii",DOID:4154,dentinogenesis imperfecta
+OMIM:608837,Carney Complex Variant,DOID:0050471,Carney complex
+OMIM:607641,"Neuronopathy, Distal Hereditary Motor, Type Viib",DOID:0050582,distal hereditary motor neuropathy
+OMIM:119530,Orofacial Cleft 1,DOID:0050567,orofacial cleft
+OMIM:118200,"Charcot-Marie-Tooth Disease, Demyelinating, Type 1b",DOID:0050538,Charcot-Marie-Tooth disease type 1
+OMIM:162350,"Ceroid Lipofuscinosis, Neuronal, 4b, Autosomal Dominant",DOID:14503,neuronal ceroid lipofuscinosis
+OMIM:609265,Li-Fraumeni Syndrome 2,DOID:3012,Li-Fraumeni syndrome
+OMIM:246300,"Leprosy, Susceptibility To, 3",DOID:1024,leprosy
+OMIM:613881,"Cardiomyopathy, Dilated, 1hh",DOID:12930,dilated cardiomyopathy
+OMIM:300905,"Charcot-Marie-Tooth Disease, X-Linked Dominant, 6",DOID:0050542,Charcot-Marie-Tooth disease type X
+OMIM:613091,Short-Rib Thoracic Dysplasia 3 With Or Without Polydactyly,DOID:0050592,asphyxiating thoracic dystrophy
+OMIM:601067,"Usher Syndrome, Type Id",DOID:0050439,Usher syndrome
+OMIM:613388,Fanconi Renotubular Syndrome 2,DOID:1062,Fanconi syndrome
+OMIM:609260,"Charcot-Marie-Tooth Disease, Axonal, Type 2a2",DOID:0050539,Charcot-Marie-Tooth disease type 2
+OMIM:604625,"Tooth Agenesis, Selective, 3",DOID:0050591,tooth agenesis
+OMIM:612518,"Ciliary Dyskinesia, Primary, 10",DOID:9562,primary ciliary dyskinesia
+OMIM:614120,Hydrolethalus Syndrome 2,DOID:0050779,hydrolethalus syndrome
+OMIM:612650,"Ciliary Dyskinesia, Primary, 12",DOID:9562,primary ciliary dyskinesia
+OMIM:612794,Atrial Septal Defect 5,DOID:1882,atrial heart septal defect
+OMIM:277580,"Waardenburg Syndrome, Type 4a",DOID:9258,Waardenburg's syndrome
+OMIM:614370,"Surfactant Metabolism Dysfunction, Pulmonary, 5",DOID:12120,pulmonary alveolar proteinosis
+OMIM:207410,Antley-Bixler Syndrome Without Genital Anomalies Or Disordered Steroidogenesis,DOID:0050462,Antley-Bixler syndrome
+OMIM:193510,"Waardenburg Syndrome, Type 2a",DOID:9258,Waardenburg's syndrome
+OMIM:500003,"Striatonigral Degeneration, Infantile, Mitochondrial",DOID:4751,striatonigral degeneration
+OMIM:613310,Exudative Vitreoretinopathy 5,DOID:0050535,exudative vitreoretinopathy
+OMIM:252900,"Mucopolysaccharidosis, Type Iiia",DOID:12801,mucopolysaccharidosis III
+OMIM:186200,"Syndactyly, Type Iv",DOID:11193,syndactyly
+OMIM:611548,Premature Ovarian Failure 5,DOID:5426,premature ovarian failure
+OMIM:614202,"Mental Retardation, Autosomal Recessive 15",DOID:0050889,non-syndromic intellectual disability
+OMIM:265120,"Surfactant Metabolism Dysfunction, Pulmonary, 1",DOID:12120,pulmonary alveolar proteinosis
+OMIM:614116,"Neuropathy, Hereditary Sensory, Type Ie",DOID:0050548,hereditary sensory neuropathy
+OMIM:201300,"Neuropathy, Hereditary Sensory And Autonomic, Type Iia",DOID:0050548,hereditary sensory neuropathy
+OMIM:609909,"Cardiomyopathy, Dilated, 1p",DOID:12930,dilated cardiomyopathy
+OMIM:192600,"Cardiomyopathy, Familial Hypertrophic, 1",DOID:11984,hypertrophic cardiomyopathy
+OMIM:300000,"Opitz Gbbb Syndrome, X-Linked",DOID:0050780,Opitz-GBBB syndrome
+OMIM:615436,"Aortic Aneurysm, Familial Thoracic 8",DOID:14004,thoracic aortic aneurysm
+OMIM:614706,"Ceroid Lipofuscinosis, Neuronal, 11",DOID:14503,neuronal ceroid lipofuscinosis
+OMIM:613885,"Meckel Syndrome, Type 8",DOID:0050778,Meckel syndrome
+OMIM:203780,"Alport Syndrome, Autosomal Recessive",DOID:10983,Alport syndrome
+OMIM:612555,"Breast-Ovarian Cancer, Familial, Susceptibility To, 2",DOID:5683,hereditary breast ovarian cancer
+OMIM:142946,Holoprosencephaly 4,DOID:4621,holoprosencephaly
+OMIM:600143,"Ceroid Lipofuscinosis, Neuronal, 8",DOID:14503,neuronal ceroid lipofuscinosis
+OMIM:615523,"Corneal Dystrophy, Fuchs Endothelial, 8",DOID:11555,Fuchs' endothelial dystrophy
+OMIM:314550,"Vesicoureteral Reflux, X-Linked",DOID:9620,vesicoureteral reflux
+OMIM:191100,Tuberous Sclerosis 1,DOID:13515,tuberous sclerosis
+OMIM:612526,"Lipodystrophy, Congenital Generalized, Type 3",DOID:0050585,congenital generalized lipodystrophy
+OMIM:100600,Acanthosis Nigricans,DOID:3138,acanthosis nigricans
+OMIM:614019,Lissencephaly 4,DOID:0050453,lissencephaly
+OMIM:610618,"Angioedema, Hereditary, Type Iii",DOID:14735,hereditary angioedema
+OMIM:269650,Secretory Component Deficiency,DOID:0060025,immunoglobulin alpha deficiency
+OMIM:307700,"Hypoparathyroidism, X-Linked",DOID:11199,hypoparathyroidism
+OMIM:300511,Premature Ovarian Failure 2a,DOID:5426,premature ovarian failure
+OMIM:609529,Immunoglobulin A Deficiency 2,DOID:0060025,immunoglobulin alpha deficiency
+OMIM:607499,"Bulimia Nervosa, Susceptibility To, 1",DOID:12129,bulimia nervosa
+OMIM:300299,"Neutropenia, Severe Congenital, X-Linked",DOID:0050590,severe congenital neutropenia
+OMIM:613119,Brugada Syndrome 6,DOID:0050451,Brugada syndrome
+OMIM:613172,"Cardiomyopathy, Dilated, 1dd",DOID:12930,dilated cardiomyopathy
+OMIM:614430,Atrioventricular Septal Defect 4,DOID:0050651,atrioventricular septal defect
+OMIM:607731,"Charcot-Marie-Tooth Disease, Axonal, Type 2h",DOID:0050539,Charcot-Marie-Tooth disease type 2
+OMIM:602485,"Hyperinsulinemic Hypoglycemia, Familial, 3",DOID:13317,hyperinsulinemic hypoglycemia
+OMIM:613673,"Anemia, Congenital Dyserythropoietic, Type Iv",DOID:1338,congenital dyserythropoietic anemia
+OMIM:614592,Bent Bone Dysplasia Syndrome,DOID:10591,pre-eclampsia
+OMIM:615665,Joubert Syndrome 22,DOID:0050777,Joubert syndrome
+OMIM:614700,"Immunodeficiency, Common Variable, 8, With Autoimmunity",DOID:12177,common variable immunodeficiency
+OMIM:192350,Vater Association,DOID:14679,VACTERL association
+OMIM:606943,"Usher Syndrome, Type Ig",DOID:0050439,Usher syndrome
+OMIM:300510,Ovarian Dysgenesis 2,DOID:5426,premature ovarian failure
+OMIM:611497,"Osteopetrosis, Autosomal Recessive 6",DOID:13533,osteopetrosis
+OMIM:611726,"Epilepsy, Progressive Myoclonic 3, With Or Without Intracellular Inclusions",DOID:891,progressive myoclonus epilepsy
+OMIM:606889,Alzheimer Disease 4,DOID:10652,Alzheimer's disease
+OMIM:112800,"Brachydactyly, Type A4",DOID:0050581,brachydactyly
+OMIM:615632,"Neuropathy, Hereditary Sensory, Type If",DOID:0050548,hereditary sensory neuropathy
+OMIM:151100,Leopard Syndrome 1,DOID:14291,LEOPARD syndrome
+OMIM:602347,"Cholestasis, Progressive Familial Intrahepatic, 3",DOID:1852,intrahepatic cholestasis
+OMIM:615235,"Cardiomyopathy, Dilated, 1jj",DOID:12930,dilated cardiomyopathy
+OMIM:600116,"Parkinson Disease 2, Autosomal Recessive Juvenile",DOID:14330,Parkinson's disease
+OMIM:611879,"Cardiomyopathy, Dilated, 1z",DOID:12930,dilated cardiomyopathy
+OMIM:193007,"Vertigo, Benign Recurrent",DOID:13941,benign paroxysmal positional nystagmus
+OMIM:257200,"Niemann-Pick Disease, Type A",DOID:14504,Niemann-Pick disease
+OMIM:612285,Joubert Syndrome 9,DOID:0050777,Joubert syndrome
+OMIM:614819,Weill-Marchesani Syndrome 3,DOID:0050475,Weill-Marchesani syndrome
+OMIM:246400,Letterer-Siwe Disease,DOID:2571,Langerhans-cell histiocytosis
+DOID:5557,testicular germ cell cancer,OMIM:273300,Testicular Germ Cell Tumor
+OMIM:615382,Nephronophthisis 16,DOID:12712,nephronophthisis
+OMIM:241500,"Hypophosphatasia, Infantile",DOID:14213,hypophosphatasia
+OMIM:266120,"Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due To",DOID:583,hemolytic anemia
+OMIM:162400,"Neuropathy, Hereditary Sensory And Autonomic, Type Ia",DOID:0050548,hereditary sensory neuropathy
+OMIM:613820,Nephronophthisis 12,DOID:12712,nephronophthisis
+OMIM:613108,"Candidiasis, Familial, 4",DOID:2058,chronic mucocutaneous candidiasis
+OMIM:603467,"Fanconi Anemia, Complementation Group F",DOID:13636,Fanconi's anemia
+OMIM:614753,Sotos Syndrome 2,DOID:14748,Sotos syndrome
+OMIM:305700,"Spermatogenic Failure, X-Linked, 1",DOID:0050457,Sertoli cell-only syndrome
+OMIM:611878,"Cardiomyopathy, Dilated, 1y",DOID:12930,dilated cardiomyopathy
+OMIM:193900,White Sponge Nevus 1,DOID:0050448,hereditary mucosal leukokeratosis
+OMIM:604827,"Epilepsy, Idiopathic Generalized, Susceptibility To, 7",DOID:1827,idiopathic generalized epilepsy
+OMIM:608890,"Waardenburg Syndrome, Type 2d",DOID:9258,Waardenburg's syndrome
+OMIM:601494,"Cardiomyopathy, Dilated, 1d",DOID:12930,dilated cardiomyopathy
+OMIM:269720,"Seizures, Benign Familial Neonatal, Autosomal Recessive",DOID:14264,benign neonatal seizures
+OMIM:604233,"Generalized Epilepsy With Febrile Seizures Plus, Type 1",DOID:0060170,generalized epilepsy with febrile seizures plus
+OMIM:610725,"Nephrotic Syndrome, Type 3",DOID:1184,nephrotic syndrome
+OMIM:608583,"Atrial Fibrillation, Familial, 1",DOID:0050650,familial atrial fibrillation
+OMIM:613426,"Cardiomyopathy, Dilated, 1s",DOID:12930,dilated cardiomyopathy
+OMIM:614429,Ventricular Septal Defect 1,DOID:1657,ventricular septal defect
+OMIM:609887,"Glaucoma 1, Open Angle, G",DOID:1067,open-angle glaucoma
+OMIM:225250,"Hypothyroidism, Congenital, Nongoitrous, 5",DOID:0050328,congenital hypothyroidism
+OMIM:614165,Paragangliomas 5,DOID:0050773,paraganglioma
+OMIM:112450,"Brachydactyly, Preaxial, With Hallux Varus And Thumb Abduction",DOID:0050581,brachydactyly
+OMIM:606217,"Atrioventricular Septal Defect, Susceptibility To, 2",DOID:0050651,atrioventricular septal defect
+OMIM:300436,"Mental Retardation, X-Linked 46",DOID:0050776,non-specific X-linked mental retardation
+OMIM:600721,D-2-Hydroxyglutaric Aciduria 1,DOID:0050575,D-2-hydroxyglutaric aciduria
+OMIM:260000,"Hyperoxaluria, Primary, Type Ii",DOID:2977,primary hyperoxaluria
+OMIM:608049,"Autism, Susceptibility To, 3",DOID:12849,autistic disorder
+OMIM:601493,"Cardiomyopathy, Dilated, 1c",DOID:12930,dilated cardiomyopathy
+OMIM:615573,"Nephrotic Syndrome, Type 9",DOID:1184,nephrotic syndrome
+OMIM:610913,"Surfactant Metabolism Dysfunction, Pulmonary, 2",DOID:12120,pulmonary alveolar proteinosis
+OMIM:147480,"Cholestasis, Intrahepatic, Of Pregnancy, 1",DOID:1852,intrahepatic cholestasis
+OMIM:602096,Alzheimer Disease 5,DOID:10652,Alzheimer's disease
+OMIM:611584,"Waardenburg Syndrome, Type 2e",DOID:9258,Waardenburg's syndrome
+OMIM:602482,"Axenfeld-Rieger Syndrome, Type 3",DOID:14686,Axenfeld-Rieger syndrome
+OMIM:610017,Multiple Synostoses Syndrome 2,DOID:0050794,multiple synostoses syndrome
+OMIM:606346,"Deafness, Autosomal Dominant 22",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:601317,"Deafness, Autosomal Dominant 11",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:160150,"Myopathy, Centronuclear, 1",DOID:14717,centronuclear myopathy
+OMIM:606693,Kufor-Rakeb Syndrome,DOID:14330,Parkinson's disease
+OMIM:613980,"Atrial Fibrillation, Familial, 9",DOID:0050650,familial atrial fibrillation
+OMIM:138800,"Goiter, Multinodular 1, With Or Without Sertoli-Leydig Cell Tumors",DOID:0050489,multinodular goiter
+OMIM:146300,"Hypophosphatasia, Adult",DOID:14213,hypophosphatasia
+OMIM:610127,"Ceroid Lipofuscinosis, Neuronal, 10",DOID:14503,neuronal ceroid lipofuscinosis
+OMIM:601678,"Bartter Syndrome, Antenatal, Type 1",DOID:445,Bartter disease
+OMIM:204300,"Ceroid Lipofuscinosis, Neuronal, 4a, Autosomal Recessive",DOID:14503,neuronal ceroid lipofuscinosis
+OMIM:230900,"Gaucher Disease, Type Ii",DOID:1926,Gaucher's disease
+OMIM:612551,"Focal Segmental Glomerulosclerosis 4, Susceptibility To",DOID:1312,focal segmental glomerulosclerosis
+OMIM:607736,"Charcot-Marie-Tooth Disease, Axonal, Type 2j",DOID:0050539,Charcot-Marie-Tooth disease type 2
+OMIM:157170,Holoprosencephaly 2,DOID:4621,holoprosencephaly
+OMIM:300143,"Mental Retardation, X-Linked 21",DOID:0050776,non-specific X-linked mental retardation
+OMIM:301200,"Amelogenesis Imperfecta, Type Ie",DOID:2187,amelogenesis imperfecta
+OMIM:601098,"Charcot-Marie-Tooth Disease, Demyelinating, Type 1c",DOID:0050538,Charcot-Marie-Tooth disease type 1
+OMIM:609464,"Sarcoidosis, Early-Onset",DOID:11335,sarcoidosis
+OMIM:259420,"Osteogenesis Imperfecta, Type Iii",DOID:12347,osteogenesis imperfecta
+OMIM:214300,"Klippel-Feil Syndrome 2, Autosomal Recessive",DOID:10426,Klippel-Feil syndrome
+OMIM:188570,"Thyroid Hormone Resistance, Generalized, Autosomal Dominant",DOID:11633,thyroid hormone resistance syndrome
+OMIM:224100,"Anemia, Congenital Dyserythropoietic, Type Ii",DOID:1338,congenital dyserythropoietic anemia
+OMIM:278850,"46,Xx Sex Reversal 2",DOID:14450,46 XX gonadal dysgenesis
+OMIM:612098,"Cardiomyopathy, Familial Hypertrophic, 11",DOID:11984,hypertrophic cardiomyopathy
+OMIM:613877,"Lipodystrophy, Familial Partial, Type 4",DOID:0050440,familial partial lipodystrophy
+OMIM:601316,"Deafness, Autosomal Dominant 10",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:613424,"Cardiomyopathy, Dilated, 1r",DOID:12930,dilated cardiomyopathy
+OMIM:301000,Wiskott-Aldrich Syndrome,DOID:9169,Wiskott-Aldrich syndrome
+OMIM:608456,"Familial Adenomatous Polyposis, 2",DOID:0050424,familial adenomatous polyposis
+OMIM:600669,"Epilepsy, Idiopathic Generalized",DOID:1827,idiopathic generalized epilepsy
+OMIM:300494,"Asperger Syndrome, X-Linked, Susceptibility To, 1",DOID:0050432,Asperger syndrome
+OMIM:608569,"Cardiomyopathy, Dilated, 1o",DOID:12930,dilated cardiomyopathy
+OMIM:613480,"Lymphedema, Hereditary, Ic",DOID:0050580,hereditary lymphedema
+OMIM:241510,"Hypophosphatasia, Childhood",DOID:14213,hypophosphatasia
+OMIM:614199,"Nephrotic Syndrome, Type 5, With Or Without Ocular Abnormalities",DOID:1184,nephrotic syndrome
+OMIM:613192,"Mental Retardation, Autosomal Recessive 13",DOID:0050889,non-syndromic intellectual disability
+OMIM:233700,"Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I",DOID:3265,chronic granulomatous disease
+OMIM:216330,"Cleidocranial Dysplasia, Recessive Form",DOID:13994,cleidocranial dysplasia
+OMIM:615224,"Advanced Sleep Phase Syndrome, Familial, 2",DOID:0050628,advanced sleep phase syndrome
+OMIM:612877,"Cardiomyopathy, Dilated, 1bb",DOID:12930,dilated cardiomyopathy
+OMIM:278750,"Xeroderma Pigmentosum, Variant Type",DOID:0050427,xeroderma pigmentosum
+OMIM:615530,"Parkinson Disease 20, Early-Onset",DOID:14330,Parkinson's disease
+OMIM:302802,"Charcot-Marie-Tooth Disease, X-Linked Recessive, 3",DOID:0050542,Charcot-Marie-Tooth disease type X
+OMIM:603221,"Myopia 3, Autosomal Dominant",DOID:11830,myopia
+OMIM:604369,Salla Disease,DOID:3659,sialuria
+OMIM:611561,"Meckel Syndrome, Type 5",DOID:0050778,Meckel syndrome
+OMIM:615577,"Immunodeficiency, Common Variable, 10",DOID:12177,common variable immunodeficiency
+OMIM:307000,Hydrocephalus Due To Congenital Stenosis Of Aqueduct Of Sylvius,DOID:10908,hydrocephalus
+OMIM:607734,"Charcot-Marie-Tooth Disease, Demyelinating, Type 1f",DOID:0050538,Charcot-Marie-Tooth disease type 1
+OMIM:170400,"Hypokalemic Periodic Paralysis, Type 1",DOID:14452,hypokalemic periodic paralysis
+OMIM:600994,"Deafness, Autosomal Dominant 5",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:601859,Autoimmune Lymphoproliferative Syndrome,DOID:6688,autoimmune lymphoproliferative syndrome
+OMIM:612124,"Cardiomyopathy, Familial Hypertrophic, 12",DOID:11984,hypertrophic cardiomyopathy
+OMIM:614302,"Emery-Dreifuss Muscular Dystrophy 7, Autosomal Dominant",DOID:11726,Emery-Dreifuss muscular dystrophy
+OMIM:608567,"Sick Sinus Syndrome 1, Autosomal Recessive",DOID:13884,sick sinus syndrome
+OMIM:145600,"Malignant Hyperthermia, Susceptibility To, 1",DOID:8545,malignant hyperthermia
+OMIM:607688,"Parkinson Disease 11, Autosomal Dominant",DOID:14330,Parkinson's disease
+OMIM:613795,Loeys-Dietz Syndrome 3,DOID:0050466,Loeys-Dietz syndrome
+OMIM:302801,"Charcot-Marie-Tooth Disease, X-Linked Recessive, 2",DOID:0050542,Charcot-Marie-Tooth disease type X
+OMIM:120435,Lynch Syndrome I,DOID:3883,Lynch syndrome
+OMIM:300845,"Moyamoya Disease 4 With Short Stature, Hypergonadotropic Hypogonadism, And Facial Dysmorphism",DOID:13099,Moyamoya disease
+OMIM:273900,Thrombocytopenia 3,DOID:1588,thrombocytopenia
+OMIM:227650,"Fanconi Anemia, Complementation Group A",DOID:13636,Fanconi's anemia
+OMIM:613270,"Corneal Dystrophy, Fuchs Endothelial, 6",DOID:11555,Fuchs' endothelial dystrophy
+OMIM:610220,"Deafness, Autosomal Recessive 59",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:241520,"Hypophosphatemic Rickets, Autosomal Recessive, 1",DOID:0050445,X-linked hypophosphatemia
+OMIM:613717,Treacher Collins Syndrome 2,DOID:2908,Treacher Collins syndrome
+OMIM:302800,"Charcot-Marie-Tooth Disease, X-Linked Dominant, 1",DOID:0050542,Charcot-Marie-Tooth disease type X
+OMIM:613697,"Cardiomyopathy, Dilated, 1v",DOID:12930,dilated cardiomyopathy
+OMIM:613193,"Ciliary Dyskinesia, Primary, 13",DOID:9562,primary ciliary dyskinesia
+OMIM:613123,Brugada Syndrome 8,DOID:0050451,Brugada syndrome
+OMIM:608874,Orofacial Cleft 5,DOID:0050567,orofacial cleft
+OMIM:612096,Otosclerosis 8,DOID:12185,otosclerosis
+OMIM:604387,Nephronophthisis 3,DOID:12712,nephronophthisis
+OMIM:253000,"Mucopolysaccharidosis, Type Iva",DOID:12804,mucopolysaccharidosis IV
+OMIM:115197,"Cardiomyopathy, Familial Hypertrophic, 4",DOID:11984,hypertrophic cardiomyopathy
+OMIM:608629,Joubert Syndrome 3,DOID:0050777,Joubert syndrome
+OMIM:232220,Glycogen Storage Disease Ib,DOID:2749,glycogen storage disease I
+OMIM:604757,Craniosynostosis 2,DOID:2340,craniosynostosis
+OMIM:613195,Weill-Marchesani-Like Syndrome,DOID:0050475,Weill-Marchesani syndrome
+OMIM:610682,"Osteogenesis Imperfecta, Type Vii",DOID:12347,osteogenesis imperfecta
+OMIM:248390,Treacher Collins Syndrome 3,DOID:2908,Treacher Collins syndrome
+OMIM:613404,"Arthrogryposis, Renal Dysfunction, And Cholestasis 2",DOID:0050763,ARC syndrome
+OMIM:166600,"Osteopetrosis, Autosomal Dominant 2",DOID:13533,osteopetrosis
+OMIM:108720,"Atelosteogenesis, Type I",DOID:0050648,atelosteogenesis
+OMIM:607628,"Epilepsy, Idiopathic Generalized, Susceptibility To, 11",DOID:1827,idiopathic generalized epilepsy
+OMIM:612301,"Osteopetrosis, Autosomal Recessive 7",DOID:13533,osteopetrosis
+OMIM:600737,"Inclusion Body Myopathy 2, Autosomal Recessive",DOID:3429,inclusion body myositis
+OMIM:213300,Joubert Syndrome 1,DOID:0050777,Joubert syndrome
+OMIM:610297,"Parkinson Disease 13, Autosomal Dominant, Susceptibility To",DOID:14330,Parkinson's disease
+OMIM:607569,"Myopathy, Distal, With Early Respiratory Failure, Autosomal Dominant",DOID:11720,distal muscular dystrophy
+OMIM:255200,"Myopathy, Centronuclear, 2",DOID:14717,centronuclear myopathy
+OMIM:610193,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 10",DOID:0050431,arrhythmogenic right ventricular cardiomyopathy
+OMIM:103230,"Adrenocortical Hypofunction, Chronic Primary Congenital",DOID:13774,Addison's disease
+OMIM:609620,Short Qt Syndrome 1,DOID:0050793,short QT syndrome
+OMIM:108721,"Atelosteogenesis, Type Iii",DOID:0050648,atelosteogenesis
+OMIM:604367,"Lipodystrophy, Familial Partial, Type 3",DOID:0050440,familial partial lipodystrophy
+OMIM:608864,"Orofacial Cleft 6, Susceptibility To",DOID:0050567,orofacial cleft
+OMIM:614083,"Fanconi Anemia, Complementation Group L",DOID:13636,Fanconi's anemia
+OMIM:116600,"Cataract 6, Multiple Types",DOID:0050537,posterior polar cataract
+OMIM:301940,"Brachydactyly, Mononen Type",DOID:0050581,brachydactyly
+OMIM:613752,Hypermethioninemia With S-Adenosylhomocysteine Hydrolase Deficiency,DOID:0050544,hypermethioninemia
+OMIM:263200,"Polycystic Kidney Disease, Autosomal Recessive",DOID:898,polycystic kidney disease
+OMIM:605543,"Parkinson Disease 4, Autosomal Dominant",DOID:14330,Parkinson's disease
+OMIM:607200,Thyroid Dyshormonogenesis 6,DOID:0050328,congenital hypothyroidism
+OMIM:112600,"Brachydactyly, Type A2",DOID:0050581,brachydactyly
+OMIM:613243,"Cardiomyopathy, Familial Hypertrophic, 13",DOID:11984,hypertrophic cardiomyopathy
+OMIM:608393,"Microcephaly 6, Primary, Autosomal Recessive",DOID:10907,microcephaly
+OMIM:300486,"Mental Retardation, X-Linked, With Cerebellar Hypoplasia And Distinctive Facial Appearance",DOID:0050888,syndromic intellectual disability
+OMIM:300497,"Asperger Syndrome, X-Linked, Susceptibility To, 2",DOID:0050432,Asperger syndrome
+OMIM:612999,"Emery-Dreifuss Muscular Dystrophy 5, Autosomal Dominant",DOID:11726,Emery-Dreifuss muscular dystrophy
+OMIM:602771,Rigid Spine Muscular Dystrophy 1,DOID:0050557,congenital muscular dystrophy
+OMIM:612656,"Episodic Ataxia, Type 6",DOID:963,episodic ataxia
+OMIM:612201,"Atrial Fibrillation, Familial, 6",DOID:0050650,familial atrial fibrillation
+OMIM:300844,"Mental Retardation, X-Linked 19",DOID:0050776,non-specific X-linked mental retardation
+OMIM:614082,"Fanconi Anemia, Complementation Group G",DOID:13636,Fanconi's anemia
+OMIM:145001,Hyperparathyroidism 2,DOID:13543,hyperparathyroidism
+OMIM:300425,"Autism, Susceptibility To, X-Linked 1",DOID:12849,autistic disorder
+OMIM:173900,Polycystic Kidney Disease 1,DOID:898,polycystic kidney disease
+OMIM:125851,"Maturity-Onset Diabetes Of The Young, Type 2",DOID:0050524,maturity-onset diabetes of the young
+OMIM:607450,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 8",DOID:0050431,arrhythmogenic right ventricular cardiomyopathy
+OMIM:613120,Brugada Syndrome 7,DOID:0050451,Brugada syndrome
+OMIM:129490,"Ectodermal Dysplasia 10a, Hypohidrotic/Hair/Nail Type, Autosomal Dominant",DOID:14793,hypohidrotic ectodermal dysplasia
+OMIM:604370,"Breast-Ovarian Cancer, Familial, Susceptibility To, 1",DOID:5683,hereditary breast ovarian cancer
+OMIM:256450,"Hyperinsulinemic Hypoglycemia, Familial, 1",DOID:13317,hyperinsulinemic hypoglycemia
+OMIM:310470,"Neuropathy, Hereditary Sensory, X-Linked",DOID:0050548,hereditary sensory neuropathy
+OMIM:307800,"Hypophosphatemic Rickets, X-Linked Dominant",DOID:0050445,X-linked hypophosphatemia
+OMIM:271930,"Striatonigral Degeneration, Infantile",DOID:4751,striatonigral degeneration
+OMIM:615528,"Parkinson Disease 19, Juvenile-Onset",DOID:14330,Parkinson's disease
+OMIM:202700,"Neutropenia, Severe Congenital, 1, Autosomal Dominant",DOID:0050590,severe congenital neutropenia
+OMIM:158590,"Neuronopathy, Distal Hereditary Motor, Type Iia",DOID:0050582,distal hereditary motor neuropathy
+OMIM:613307,"Deafness, Autosomal Recessive 79",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:211600,"Cholestasis, Progressive Familial Intrahepatic, 1",DOID:1852,intrahepatic cholestasis
+OMIM:612437,"Epilepsy, Progressive Myoclonic 1b",DOID:891,progressive myoclonus epilepsy
+OMIM:602087,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 4",DOID:0050431,arrhythmogenic right ventricular cardiomyopathy
+OMIM:611913,"Chromosome 16p11.2 Deletion Syndrome, 593-Kb",DOID:12849,autistic disorder
+OMIM:600156,"Hirschsprung Disease, Susceptibility To, 5",DOID:10426,Klippel-Feil syndrome
+OMIM:113000,"Brachydactyly, Type B1",DOID:0050581,brachydactyly
+OMIM:193100,"Hypophosphatemic Rickets, Autosomal Dominant",DOID:0050445,X-linked hypophosphatemia
+OMIM:241200,"Bartter Syndrome, Antenatal, Type 2",DOID:445,Bartter disease
+OMIM:613000,"Palmoplantar Keratoderma, Nonepidermolytic, Focal",DOID:0050428,nonepidermolytic palmoplantar keratoderma
+OMIM:142623,"Hirschsprung Disease, Susceptibility To, 1",DOID:10487,Hirschsprung's disease
+OMIM:614432,Ventricular Septal Defect 3,DOID:1657,ventricular septal defect
+OMIM:220400,Jervell And Lange-Nielsen Syndrome 1,DOID:2842,Jervell-Lange Nielsen syndrome
+OMIM:232240,Glycogen Storage Disease Ic,DOID:2749,glycogen storage disease I
+OMIM:105650,Diamond-Blackfan Anemia 1,DOID:1339,Diamond-Blackfan anemia
+OMIM:614099,Cranioectodermal Dysplasia 3,DOID:0080033,craniometaphyseal dysplasia
+OMIM:606966,Nephronophthisis 4,DOID:12712,nephronophthisis
+OMIM:210210,3-Methylcrotonyl-Coa Carboxylase 2 Deficiency,DOID:0050710,3-Methylcrotonyl-CoA carboxylase deficiency
+OMIM:611880,"Cardiomyopathy, Dilated, 2a",DOID:12930,dilated cardiomyopathy
+OMIM:266900,Senior-Loken Syndrome 1,DOID:0050576,Senior-Loken syndrome
+OMIM:163500,"Night Blindness, Congenital Stationary, Autosomal Dominant 2",DOID:0050534,congenital stationary night blindness
+OMIM:231000,"Gaucher Disease, Type Iii",DOID:1926,Gaucher's disease
+OMIM:608474,"Myopia 5, Autosomal Dominant",DOID:11830,myopia
+OMIM:212750,Celiac Disease,DOID:10608,celiac disease
+OMIM:300125,"Migraine, Familial Typical, Susceptibility To, 2",DOID:0060178,familial hemiplegic migraine
+OMIM:218700,"Hypothyroidism, Congenital, Nongoitrous, 2",DOID:0050328,congenital hypothyroidism
+OMIM:193000,Vesicoureteral Reflux 1,DOID:9620,vesicoureteral reflux
+OMIM:613751,"Heterotaxy, Visceral, 4, Autosomal",DOID:0050545,visceral heterotaxy
+OMIM:615506,"Telangiectasia, Hereditary Hemorrhagic, Type 5",DOID:1270,hereditary hemorrhagic telangiectasia
+OMIM:602086,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 3",DOID:0050431,arrhythmogenic right ventricular cardiomyopathy
+OMIM:614431,Ventricular Septal Defect 2,DOID:1657,ventricular septal defect
+OMIM:600101,"Deafness, Autosomal Dominant 2a",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:276900,"Usher Syndrome, Type I",DOID:0050439,Usher syndrome
+OMIM:216400,Cockayne Syndrome A,DOID:2962,Cockayne syndrome
+OMIM:612702,Hypogonadotropic Hypogonadism 6 With Or Without Anosmia,DOID:3614,Kallmann syndrome
+OMIM:610247,"Esophagitis, Eosinophilic, 1",DOID:13922,eosinophilic esophagitis
+OMIM:153670,"Bernard-Soulier Syndrome, Type A2, Autosomal Dominant",DOID:2217,Bernard-Soulier syndrome
+OMIM:155720,"Melanoma, Uveal",DOID:6039,uveal melanoma
+OMIM:151623,Li-Fraumeni Syndrome 1,DOID:3012,Li-Fraumeni syndrome
+OMIM:614167,"Myopia 21, Autosomal Dominant",DOID:11830,myopia
+OMIM:610651,"Xeroderma Pigmentosum, Complementation Group B",DOID:0050427,xeroderma pigmentosum
+OMIM:613863,"Generalized Epilepsy With Febrile Seizures Plus, Type 7",DOID:0060170,generalized epilepsy with febrile seizures plus
+OMIM:276901,"Usher Syndrome, Type Iia",DOID:0050439,Usher syndrome
+OMIM:604348,"Advanced Sleep Phase Syndrome, Familial, 1",DOID:0050628,advanced sleep phase syndrome
+OMIM:218300,Craniodiaphyseal Dysplasia,DOID:0080033,craniometaphyseal dysplasia
+OMIM:613550,Nephronophthisis 11,DOID:12712,nephronophthisis
+OMIM:300067,"Lissencephaly, X-Linked, 1",DOID:0050453,lissencephaly
+OMIM:607841,"Deafness, Autosomal Dominant 48",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:187550,"Thalassemia, Beta+, Silent Allele",DOID:12241,beta thalassemia
+OMIM:218400,"Craniometaphyseal Dysplasia, Autosomal Recessive",DOID:0080033,craniometaphyseal dysplasia
+OMIM:614087,"Fanconi Anemia, Complementation Group M",DOID:13636,Fanconi's anemia
+OMIM:615112,Urofacial Syndrome 2,DOID:0050816,urofacial syndrome
+OMIM:105600,"Anemia, Congenital Dyserythropoietic, Type Iii",DOID:1338,congenital dyserythropoietic anemia
+OMIM:610628,Hypogonadotropic Hypogonadism 4 With Or Without Anosmia,DOID:3614,Kallmann syndrome
+OMIM:230650,"Gm1-Gangliosidosis, Type Iii",DOID:3322,gangliosidosis GM1
+OMIM:603902,"Beta-Thalassemia, Dominant Inclusion Body Type",DOID:12241,beta thalassemia
+OMIM:179010,"Pyloric Stenosis, Infantile Hypertrophic, 1",DOID:12638,hypertrophic pyloric stenosis
+OMIM:276902,"Usher Syndrome, Type Iiia",DOID:0050439,Usher syndrome
+OMIM:607903,Hypotrichosis 6,DOID:4535,hypotrichosis
+OMIM:614209,"Meckel Syndrome, Type 9",DOID:0050778,Meckel syndrome
+OMIM:602097,"Usher Syndrome, Type Ie",DOID:0050439,Usher syndrome
+OMIM:610951,"Ceroid Lipofuscinosis, Neuronal, 7",DOID:14503,neuronal ceroid lipofuscinosis
+OMIM:179830,"Renal Tubular Acidosis, Proximal",DOID:14219,renal tubular acidosis
+OMIM:253900,"Muscular Dystrophy, Congenital, Producing Arthrogryposis",DOID:0050557,congenital muscular dystrophy
+OMIM:166800,Otosclerosis 1,DOID:12185,otosclerosis
+OMIM:256731,"Ceroid Lipofuscinosis, Neuronal, 5",DOID:14503,neuronal ceroid lipofuscinosis
+OMIM:300752,"Protoporphyria, Erythropoietic, X-Linked",DOID:13270,erythropoietic protoporphyria
+OMIM:300696,"Myopathy, X-Linked, With Postural Muscle Atrophy",DOID:11726,Emery-Dreifuss muscular dystrophy
+OMIM:162200,"Neurofibromatosis, Type I",DOID:8712,neurofibromatosis
+OMIM:300849,"Mental Retardation, X-Linked 41",DOID:0050776,non-specific X-linked mental retardation
+OMIM:614851,Seckel Syndrome 7,DOID:0050569,Seckel syndrome
+OMIM:609622,Short Qt Syndrome 3,DOID:0050793,short QT syndrome
+OMIM:252920,"Mucopolysaccharidosis, Type Iiib",DOID:12801,mucopolysaccharidosis III
+OMIM:104500,"Amelogenesis Imperfecta, Type Ib",DOID:2187,amelogenesis imperfecta
+OMIM:613849,"Osteogenesis Imperfecta, Type Xii",DOID:12347,osteogenesis imperfecta
+OMIM:125700,"Diabetes Insipidus, Neurohypophyseal",DOID:12388,neurohypophyseal diabetes insipidus
+OMIM:278730,"Xeroderma Pigmentosum, Complementation Group D",DOID:0050427,xeroderma pigmentosum
+OMIM:300100,Adrenoleukodystrophy,DOID:10588,adrenoleukodystrophy
+OMIM:607487,"Cardiomyopathy, Dilated, 1n",DOID:12930,dilated cardiomyopathy
+OMIM:615544,Periventricular Nodular Heterotopia 6,DOID:0050454,periventricular nodular heterotopia
+OMIM:600376,"Telangiectasia, Hereditary Hemorrhagic, Type 2",DOID:1270,hereditary hemorrhagic telangiectasia
+OMIM:256730,"Ceroid Lipofuscinosis, Neuronal, 1",DOID:14503,neuronal ceroid lipofuscinosis
+OMIM:605751,"Seizures, Benign Familial Infantile, 2",DOID:0060169,benign familial infantile epilepsy
+OMIM:126200,"Multiple Sclerosis, Susceptibility To",DOID:2377,multiple sclerosis
+OMIM:122470,Cornelia De Lange Syndrome 1,DOID:11725,Cornelia de Lange syndrome
+OMIM:115210,"Cardiomyopathy, Familial Restrictive, 1",DOID:397,restrictive cardiomyopathy
+OMIM:609621,Short Qt Syndrome 2,DOID:0050793,short QT syndrome
+OMIM:603909,"Autoimmune Lymphoproliferative Syndrome, Type Iia",DOID:6688,autoimmune lymphoproliferative syndrome
+OMIM:600962,"Palmoplantar Keratoderma, Nonepidermolytic",DOID:0050428,nonepidermolytic palmoplantar keratoderma
+OMIM:615285,"Neutropenia, Severe Congenital, 5, Autosomal Recessive",DOID:0050590,severe congenital neutropenia
+OMIM:613848,"Osteogenesis Imperfecta, Type X",DOID:12347,osteogenesis imperfecta
+OMIM:113300,"Brachydactyly, Type E1",DOID:0050581,brachydactyly
+OMIM:605479,"Cholestasis, Benign Recurrent Intrahepatic, 2",DOID:1852,intrahepatic cholestasis
+OMIM:605389,Hypotrichosis 1,DOID:4535,hypotrichosis
+OMIM:276904,"Usher Syndrome, Type Ic",DOID:0050439,Usher syndrome
+OMIM:310490,Cowchock Syndrome,DOID:0050542,Charcot-Marie-Tooth disease type X
+OMIM:612225,"Maturity-Onset Diabetes Of The Young, Type 9",DOID:0050524,maturity-onset diabetes of the young
+OMIM:610329,Aicardi-Goutieres Syndrome 3,DOID:0050629,Aicardi-Goutieres syndrome
+OMIM:222300,Wolfram Syndrome 1,DOID:10632,Wolfram syndrome
+OMIM:609634,"Migraine, Familial Hemiplegic, 3",DOID:0060178,familial hemiplegic migraine
+OMIM:614227,"Hyperuricemic Nephropathy, Familial Juvenile, 3",DOID:0060062,familial juvenile hyperuricemic nephropathy
+OMIM:607745,"Seizures, Benign Familial Infantile, 3",DOID:0060169,benign familial infantile epilepsy
+OMIM:201810,"3-Beta-Hydroxysteroid Dehydrogenase, Type Ii, Deficiency Of",DOID:0050811,congenital adrenal hyperplasia
+OMIM:601553,"Hypotrichosis, Congenital, With Juvenile Macular Dystrophy",DOID:4535,hypotrichosis
+OMIM:609813,"Spondylocostal Dysostosis 3, Autosomal Recessive",DOID:0050568,spondylocostal dysostosis
+OMIM:607594,"Immunodeficiency, Common Variable, 1",DOID:12177,common variable immunodeficiency
+OMIM:610168,Loeys-Dietz Syndrome 2,DOID:0050466,Loeys-Dietz syndrome
+OMIM:607822,Alzheimer Disease 3,DOID:10652,Alzheimer's disease
+OMIM:600794,"Neuronopathy, Distal Hereditary Motor, Type Va",DOID:0050582,distal hereditary motor neuropathy
+OMIM:125850,"Maturity-Onset Diabetes Of The Young, Type 1",DOID:0050524,maturity-onset diabetes of the young
+OMIM:305450,Opitz-Kaveggia Syndrome,DOID:14711,FG syndrome
+OMIM:613707,Leopard Syndrome 3,DOID:14291,LEOPARD syndrome
+OMIM:605588,"Charcot-Marie-Tooth Disease, Axonal, Type 2b1",DOID:0050539,Charcot-Marie-Tooth disease type 2
+OMIM:113200,"Brachydactyly, Type D",DOID:0050581,brachydactyly
+OMIM:613981,Hypotrichosis 3,DOID:4535,hypotrichosis
+OMIM:258100,Oguchi Disease 1,DOID:8498,hereditary night blindness
+OMIM:256370,"Nephrotic Syndrome, Type 4",DOID:1184,nephrotic syndrome
+OMIM:232200,Glycogen Storage Disease Ia,DOID:2749,glycogen storage disease I
+OMIM:613873,"Cardiomyopathy, Familial Hypertrophic, 17",DOID:11984,hypertrophic cardiomyopathy
+OMIM:614335,"Arthrogryposis, Distal, Type 1b",DOID:0050646,distal arthrogryposis
+OMIM:608367,"Myopia 17, Autosomal Dominant",DOID:11830,myopia
+OMIM:605589,"Charcot-Marie-Tooth Disease, Axonal, Type 2b2",DOID:0050539,Charcot-Marie-Tooth disease type 2
+OMIM:613412,"Esophagitis, Eosinophilic, 2",DOID:13922,eosinophilic esophagitis
+OMIM:109720,"Biliary Cirrhosis, Primary, 1",DOID:12236,primary biliary cirrhosis
+OMIM:253280,"Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 3",DOID:0050560,Walker-Warburg syndrome
+OMIM:607482,"Cardiomyopathy, Dilated, 1m",DOID:12930,dilated cardiomyopathy
+OMIM:610099,"Myopathy, Distal, 3",DOID:11720,distal muscular dystrophy
+OMIM:612653,"Spherocytosis, Type 4",DOID:12971,hereditary spherocytosis
+OMIM:600625,Orofacial Cleft 11,DOID:0050567,orofacial cleft
+OMIM:252940,"Mucopolysaccharidosis, Type Iiid",DOID:12801,mucopolysaccharidosis III
+OMIM:204650,"Amelogenesis Imperfecta, Type Ic",DOID:2187,amelogenesis imperfecta
+OMIM:180849,Rubinstein-Taybi Syndrome 1,DOID:1933,Rubinstein-Taybi syndrome
+OMIM:160300,"Myopathy, Distal, With Onset In Infancy",DOID:11720,distal muscular dystrophy
+OMIM:614455,"Charcot-Marie-Tooth Disease, Dominant Intermediate E",DOID:0050543,Charcot-Marie-Tooth disease intermediate type
+OMIM:606394,"Maturity-Onset Diabetes Of The Young, Type 6",DOID:0050524,maturity-onset diabetes of the young
+OMIM:608654,"Neuropathy, Hereditary Sensory And Autonomic, Type V",DOID:0050548,hereditary sensory neuropathy
+DOID:12309,urticaria pigmentosa,OMIM:154800,Mast Cell Disease
+OMIM:613060,"Epilepsy, Idiopathic Generalized, Susceptibility To, 10",DOID:1827,idiopathic generalized epilepsy
+OMIM:145410,"Opitz Gbbb Syndrome, Autosomal Dominant",DOID:0050780,Opitz-GBBB syndrome
+OMIM:612690,"Spherocytosis, Type 5",DOID:12971,hereditary spherocytosis
+OMIM:300590,Cornelia De Lange Syndrome 2,DOID:11725,Cornelia de Lange syndrome
+OMIM:606744,Seckel Syndrome 2,DOID:0050569,Seckel syndrome
+OMIM:216820,"Coloboma, Ocular",DOID:12270,coloboma
+OMIM:614089,Atrial Septal Defect 3,DOID:1882,atrial heart septal defect
+OMIM:614424,Joubert Syndrome 14,DOID:0050777,Joubert syndrome
+OMIM:614699,"Immunodeficiency, Common Variable, 7",DOID:12177,common variable immunodeficiency
+OMIM:609975,"Hyperinsulinemic Hypoglycemia, Familial, 4",DOID:13317,hyperinsulinemic hypoglycemia
+OMIM:607060,"Parkinson Disease 8, Autosomal Dominant",DOID:14330,Parkinson's disease
+OMIM:613615,Senior-Loken Syndrome 7,DOID:0050576,Senior-Loken syndrome
+OMIM:300554,"Hypophosphatemic Rickets, X-Linked Recessive",DOID:0050445,X-linked hypophosphatemia
+OMIM:613453,"Deafness, Autosomal Recessive 91",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:244400,"Ciliary Dyskinesia, Primary, 1",DOID:9562,primary ciliary dyskinesia
+DOID:6126,anal canal carcinoma,OMIM:105580,Anal Canal Carcinoma
+OMIM:300387,"Mental Retardation, X-Linked 63",DOID:0050776,non-specific X-linked mental retardation
+OMIM:605373,Paragangliomas 3,DOID:0050773,paraganglioma
+OMIM:229300,Friedreich Ataxia 1,DOID:12705,Friedreich ataxia
+OMIM:613762,"46,Xy Sex Reversal 6",DOID:14448,46 XY gonadal dysgenesis
+OMIM:612004,Thrombocytopenia 4,DOID:1588,thrombocytopenia
+OMIM:313900,Thrombocytopenia 1,DOID:1588,thrombocytopenia
+OMIM:614450,"Hypothyroidism, Congenital, Nongoitrous, 6",DOID:0050328,congenital hypothyroidism
+OMIM:601820,"Hyperinsulinemic Hypoglycemia, Familial, 2",DOID:13317,hyperinsulinemic hypoglycemia
+DOID:768,retinoblastoma,OMIM:180200,Retinoblastoma
+OMIM:107970,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 1",DOID:0050431,arrhythmogenic right ventricular cardiomyopathy
+OMIM:235555,"Bile Acid Synthesis Defect, Congenital, 2",DOID:0050674,congenital bile acid synthesis defect
+OMIM:613657,D-2-Hydroxyglutaric Aciduria 2,DOID:0050575,D-2-hydroxyglutaric aciduria
+OMIM:148820,"Waardenburg Syndrome, Type 3",DOID:9258,Waardenburg's syndrome
+OMIM:608681,"Spondylocostal Dysostosis 2, Autosomal Recessive",DOID:0050568,spondylocostal dysostosis
+OMIM:201910,"Adrenal Hyperplasia, Congenital, Due To 21-Hydroxylase Deficiency",DOID:0050811,congenital adrenal hyperplasia
+OMIM:613319,Miyoshi Muscular Dystrophy 3,DOID:11720,distal muscular dystrophy
+OMIM:614251,Parkinson Disease 18,DOID:14330,Parkinson's disease
+OMIM:118210,"Charcot-Marie-Tooth Disease, Axonal, Type 2a1",DOID:0050539,Charcot-Marie-Tooth disease type 2
+OMIM:608638,"Asperger Syndrome, Susceptibility To, 1",DOID:0050432,Asperger syndrome
+OMIM:614203,Parkinson Disease 17,DOID:14330,Parkinson's disease
+OMIM:601369,"Deafness, Autosomal Dominant 9",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:275200,"Hypothyroidism, Congenital, Nongoitrous, 1",DOID:0050328,congenital hypothyroidism
+OMIM:611493,"Atrial Fibrillation, Familial, 4",DOID:0050650,familial atrial fibrillation
+OMIM:615631,"Anemia, Congenital Dyserythropoietic, Type Ib",DOID:1338,congenital dyserythropoietic anemia
+OMIM:613107,"Neutropenia, Severe Congenital, 2, Autosomal Dominant",DOID:0050590,severe congenital neutropenia
+OMIM:614672,"Cardiomyopathy, Dilated, 2b",DOID:12930,dilated cardiomyopathy
+OMIM:613641,"Charcot-Marie-Tooth Disease, Recessive Intermediate B",DOID:0050543,Charcot-Marie-Tooth disease intermediate type
+OMIM:174200,"Polydactyly, Postaxial, Type A1",DOID:1148,polydactyly
+OMIM:613951,"Fanconi Anemia, Complementation Group P",DOID:13636,Fanconi's anemia
+OMIM:607684,"Charcot-Marie-Tooth Disease, Axonal, Type 2e",DOID:0050539,Charcot-Marie-Tooth disease type 2
+OMIM:600204,"Epiphyseal Dysplasia, Multiple, 2",DOID:12721,multiple epiphyseal dysplasia
+OMIM:610921,"Surfactant Metabolism Dysfunction, Pulmonary, 3",DOID:12120,pulmonary alveolar proteinosis
+OMIM:147950,Hypogonadotropic Hypogonadism 2 With Or Without Anosmia,DOID:3614,Kallmann syndrome
+OMIM:137600,"Iridogoniodysgenesis, Type 2",DOID:0050786,iridogoniodysgenesis syndrome
+OMIM:153700,"Macular Dystrophy, Vitelliform",DOID:0050661,vitelliform macular dystrophy
+OMIM:300291,"Ectodermal Dysplasia, Hypohidrotic, With Immune Deficiency",DOID:14793,hypohidrotic ectodermal dysplasia
+OMIM:613610,Cranioectodermal Dysplasia 2,DOID:0050577,Sensenbrenner syndrome
+OMIM:613382,"Brachydactyly, Type E2",DOID:0050581,brachydactyly
+OMIM:613690,"Cardiomyopathy, Familial Hypertrophic, 7",DOID:11984,hypertrophic cardiomyopathy
+OMIM:120200,"Coloboma, Ocular",DOID:12270,coloboma
+OMIM:170650,"Periodontitis, Aggressive, 1",DOID:1474,aggressive periodontitis
+OMIM:186300,"Syndactyly, Type V",DOID:11193,syndactyly
+OMIM:612703,"Microcephaly 7, Primary, Autosomal Recessive",DOID:10907,microcephaly
+OMIM:160120,"Episodic Ataxia, Type 1",DOID:963,episodic ataxia
+OMIM:254130,Miyoshi Muscular Dystrophy 1,DOID:11720,distal muscular dystrophy
+OMIM:162270,"Neurofibromatosis, Type Iv, Of Riccardi",DOID:8712,neurofibromatosis
+OMIM:613391,"Deafness, Autosomal Recessive 84a",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:610535,"Glaucoma 1, Open Angle, M",DOID:1067,open-angle glaucoma
+OMIM:233420,"46,Xy Sex Reversal 7",DOID:14448,46 XY gonadal dysgenesis
+OMIM:310400,"Myopathy, Centronuclear, X-Linked",DOID:14717,centronuclear myopathy
+OMIM:606069,"Hemochromatosis, Type 4",DOID:2352,hemochromatosis
+OMIM:112440,"Brachydactyly, Combined B And E Types",DOID:0050581,brachydactyly
+OMIM:202550,"Aganglionosis, Total Intestinal",DOID:10487,Hirschsprung's disease
+OMIM:302045,"Cardiomyopathy, Dilated, 3b",DOID:12930,dilated cardiomyopathy
+OMIM:610623,"Cataract 11, Multiple Types",DOID:0050537,posterior polar cataract
+OMIM:615735,"Palmoplantar Keratoderma, Nonepidermolytic, Focal Or Diffuse",DOID:0050428,nonepidermolytic palmoplantar keratoderma
+OMIM:278780,"Xeroderma Pigmentosum, Complementation Group G",DOID:0050427,xeroderma pigmentosum
+OMIM:613266,"Waardenburg Syndrome, Type 4c",DOID:9258,Waardenburg's syndrome
+OMIM:613819,Short-Rib Thoracic Dysplasia 4 With Or Without Polydactyly,DOID:0050592,asphyxiating thoracic dystrophy
+OMIM:252350,Moyamoya Disease 1,DOID:13099,Moyamoya disease
+OMIM:305400,Aarskog-Scott Syndrome,DOID:6683,Aarskog-Scott syndrome
+OMIM:610915,"Osteogenesis Imperfecta, Type Viii",DOID:12347,osteogenesis imperfecta
+OMIM:606392,"Maturity-Onset Diabetes Of The Young, Type 4",DOID:0050524,maturity-onset diabetes of the young
+OMIM:614869,"Usher Syndrome, Type Ij",DOID:0050439,Usher syndrome
+OMIM:108145,"Arthrogryposis, Distal, Type 5",DOID:0050646,distal arthrogryposis
+OMIM:607101,"Deafness, Autosomal Recessive 30",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:615589,Otosclerosis 10,DOID:12185,otosclerosis
+OMIM:613857,Orofacial Cleft 13,DOID:0050567,orofacial cleft
+OMIM:153100,"Lymphedema, Hereditary, Ia",DOID:0050580,hereditary lymphedema
+OMIM:267010,"Meckel Syndrome, Type 7",DOID:0050778,Meckel syndrome
+OMIM:607765,"Bile Acid Synthesis Defect, Congenital, 1",DOID:0050674,congenital bile acid synthesis defect
+OMIM:604401,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 6",DOID:0050431,arrhythmogenic right ventricular cardiomyopathy
+OMIM:612158,"Cardiomyopathy, Dilated, 1aa",DOID:12930,dilated cardiomyopathy
+OMIM:607373,"Autism, Susceptibility To, 8",DOID:12849,autistic disorder
+OMIM:300882,Cornelia De Lange Syndrome 5,DOID:11725,Cornelia de Lange syndrome
+OMIM:611944,"Lymphedema, Hereditary, Ib",DOID:0050580,hereditary lymphedema
+OMIM:612347,Jervell And Lange-Nielsen Syndrome 2,DOID:2842,Jervell-Lange Nielsen syndrome
+OMIM:601682,"Glaucoma 1, Primary Open Angle, C",DOID:1067,open-angle glaucoma
+OMIM:193500,"Waardenburg Syndrome, Type 1",DOID:9258,Waardenburg's syndrome
+OMIM:603629,"Deafness, Autosomal Recessive 21",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:606996,Senior-Loken Syndrome 4,DOID:0050576,Senior-Loken syndrome
+OMIM:235400,"Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 1",DOID:12554,hemolytic-uremic syndrome
+OMIM:609637,Holoprosencephaly 5,DOID:4621,holoprosencephaly
+OMIM:602481,"Migraine, Familial Hemiplegic, 2",DOID:0060178,familial hemiplegic migraine
+OMIM:612291,Joubert Syndrome 8,DOID:0050777,Joubert syndrome
+OMIM:601495,"Agammaglobulinemia 1, Autosomal Recessive",DOID:2583,agammaglobulinemia
+OMIM:259730,"Osteopetrosis, Autosomal Recessive 3",DOID:13533,osteopetrosis
+OMIM:615272,"Fanconi Anemia, Complementation Group Q",DOID:13636,Fanconi's anemia
+OMIM:604400,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 5",DOID:0050431,arrhythmogenic right ventricular cardiomyopathy
+OMIM:613708,"Neuropathy, Hereditary Sensory, Type Id",DOID:0050548,hereditary sensory neuropathy
+OMIM:613616,"Hyperoxaluria, Primary, Type Iii",DOID:2977,primary hyperoxaluria
+OMIM:310370,"Myoclonic Epilepsy, Progressive",DOID:891,progressive myoclonus epilepsy
+OMIM:230500,"Gm1-Gangliosidosis, Type I",DOID:3322,gangliosidosis GM1
+OMIM:606071,"Hereditary Motor And Sensory Neuropathy, Type Iic",DOID:0050539,Charcot-Marie-Tooth disease type 2
+OMIM:604403,"Generalized Epilepsy With Febrile Seizures Plus, Type 2",DOID:0060170,generalized epilepsy with febrile seizures plus
+OMIM:108200,"Arthrogryposis, Distal, Type 6",DOID:0050646,distal arthrogryposis
+OMIM:606995,Senior-Loken Syndrome 3,DOID:0050576,Senior-Loken syndrome
+OMIM:613313,"Hemochromatosis, Type 2b",DOID:2352,hemochromatosis
+OMIM:600652,"Deafness, Autosomal Dominant 4a",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:610829,Holoprosencephaly 9,DOID:4621,holoprosencephaly
+OMIM:133540,Cockayne Syndrome B,DOID:2962,Cockayne syndrome
+OMIM:613676,Seckel Syndrome 4,DOID:0050569,Seckel syndrome
+OMIM:118300,Charcot-Marie-Tooth Disease And Deafness,DOID:0050538,Charcot-Marie-Tooth disease type 1
+OMIM:613265,"Waardenburg Syndrome, Type 4b",DOID:9258,Waardenburg's syndrome
+OMIM:613694,"Cardiomyopathy, Dilated, 1u",DOID:12930,dilated cardiomyopathy
+OMIM:607616,"Niemann-Pick Disease, Type B",DOID:14504,Niemann-Pick disease
+OMIM:277440,"Vitamin D-Dependent Rickets, Type 2a",DOID:10609,rickets
+OMIM:300633,"Hypospadias 1, X-Linked",DOID:10892,hypospadias
+OMIM:236600,"Hydrocephalus, Nonsyndromic, Autosomal Recessive 1",DOID:10908,hydrocephalus
+OMIM:214950,"Bile Acid Synthesis Defect, Congenital, 4",DOID:0050674,congenital bile acid synthesis defect
+OMIM:614377,Nephronophthisis 13,DOID:12712,nephronophthisis
+OMIM:167200,Pachyonychia Congenita 1,DOID:0050449,pachyonychia congenita
+OMIM:119600,Cleidocranial Dysplasia,DOID:13994,cleidocranial dysplasia
+OMIM:603278,Focal Segmental Glomerulosclerosis 1,DOID:1312,focal segmental glomerulosclerosis
+OMIM:611528,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 12",DOID:0050431,arrhythmogenic right ventricular cardiomyopathy
+OMIM:613659,Gastric Cancer,DOID:10534,stomach cancer
+OMIM:218330,Cranioectodermal Dysplasia 1,DOID:0050577,Sensenbrenner syndrome
+OMIM:605724,"Fanconi Anemia, Complementation Group D1",DOID:13636,Fanconi's anemia
+OMIM:150400,"Tooth Agenesis, Selective, 4",DOID:0050591,tooth agenesis
+OMIM:610828,Holoprosencephaly 7,DOID:4621,holoprosencephaly
+OMIM:604377,"Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 1",DOID:0050713,fatal infantile encephalocardiomyopathy
+OMIM:603622,"Deafness, Autosomal Dominant 17",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:611451,"Deafness, Autosomal Recessive 63",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:301800,"Anus, Imperforate",DOID:10488,imperforate anus
+OMIM:613244,"Colorectal Cancer, Hereditary Nonpolyposis, Type 8",DOID:3883,Lynch syndrome
+OMIM:602092,"Deafness, Autosomal Recessive 18a",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:614050,"Atrial Fibrillation, Familial, 12",DOID:0050650,familial atrial fibrillation
+OMIM:114480,Breast Cancer,DOID:1612,breast cancer
+OMIM:608600,"Lipodystrophy, Familial Partial, Type 1",DOID:0050440,familial partial lipodystrophy
+OMIM:613824,Nephronophthisis 9,DOID:12712,nephronophthisis
+OMIM:137920,Renal Cysts And Diabetes Syndrome,DOID:0050524,maturity-onset diabetes of the young
+OMIM:608631,"Asperger Syndrome, Susceptibility To, 2",DOID:0050432,Asperger syndrome
+OMIM:607039,"Deafness, Autosomal Recessive 22",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:602722,"Renal Tubular Acidosis, Distal, Autosomal Recessive",DOID:14219,renal tubular acidosis
+OMIM:300422,Fg Syndrome 4,DOID:14711,FG syndrome
+OMIM:613411,Oguchi Disease 2,DOID:8498,hereditary night blindness
+OMIM:611407,"Cardiomyopathy, Dilated, 1w",DOID:12930,dilated cardiomyopathy
+OMIM:310500,"Night Blindness, Congenital Stationary, Type 1a",DOID:0050534,congenital stationary night blindness
+OMIM:261100,Megaloblastic Anemia 1,DOID:13382,megaloblastic anemia
+OMIM:122860,"Craniodiaphyseal Dysplasia, Autosomal Dominant",DOID:0080033,craniometaphyseal dysplasia
+OMIM:600060,"Deafness, Autosomal Recessive 2",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:311070,"Charcot-Marie-Tooth Disease, X-Linked Recessive, 5",DOID:0050542,Charcot-Marie-Tooth disease type X
+OMIM:274300,"Thyroid Hormone Resistance, Generalized, Autosomal Recessive",DOID:11633,thyroid hormone resistance syndrome
+OMIM:613740,"Cardiomyopathy, Dilated, 1t",DOID:12930,dilated cardiomyopathy
+OMIM:610444,"Night Blindness, Congenital Stationary, Autosomal Dominant 3",DOID:0050534,congenital stationary night blindness
+OMIM:602390,"Hemochromatosis, Type 2a",DOID:2352,hemochromatosis
+OMIM:612563,Diamond-Blackfan Anemia 8,DOID:1339,Diamond-Blackfan anemia
+OMIM:177000,"Protoporphyria, Erythropoietic",DOID:13270,erythropoietic protoporphyria
+OMIM:607361,"Meckel Syndrome, Type 3",DOID:0050778,Meckel syndrome
+OMIM:606762,"Hyperinsulinemic Hypoglycemia, Familial, 6",DOID:13317,hyperinsulinemic hypoglycemia
+OMIM:108300,"Stickler Syndrome, Type I",DOID:0080046,Stickler syndrome
+OMIM:313500,"Tooth Agenesis, Selective, X-Linked, 1",DOID:0050591,tooth agenesis
+OMIM:613876,"Cardiomyopathy, Familial Hypertrophic, 20",DOID:11984,hypertrophic cardiomyopathy
+OMIM:612717,"Myopia 15, Autosomal Dominant",DOID:11830,myopia
+OMIM:251100,"Methylmalonic Aciduria, Cbla Type",DOID:14749,methylmalonic acidemia
+OMIM:193700,"Arthrogryposis, Distal, Type 2a",DOID:0050646,distal arthrogryposis
+OMIM:608484,"Congenital Corneal Opacities, Cornea Guttata, And Corectopia",DOID:12185,otosclerosis
+OMIM:137215,"Gastric Cancer, Hereditary Diffuse",DOID:10534,stomach cancer
+OMIM:613765,"Cardiomyopathy, Familial Hypertrophic, 9",DOID:11984,hypertrophic cardiomyopathy
+OMIM:610445,"Night Blindness, Congenital Stationary, Autosomal Dominant 1",DOID:0050534,congenital stationary night blindness
+OMIM:613706,Noonan Syndrome 7,DOID:3490,Noonan syndrome
+OMIM:153800,"Macular Degeneration, Age-Related, 2",DOID:10871,age related macular degeneration
+OMIM:163950,Noonan Syndrome 1,DOID:3490,Noonan syndrome
+OMIM:275100,"Hypothyroidism, Congenital, Nongoitrous, 4",DOID:0050328,congenital hypothyroidism
+OMIM:153600,"Macroglobulinemia, Waldenstrom, Susceptibility To, 1",DOID:0050747,lymphoplasmacytic lymphoma
+OMIM:209850,Autism,DOID:12849,autistic disorder
+OMIM:614474,Atrioventricular Septal Defect 5,DOID:0050651,atrioventricular septal defect
+OMIM:154230,"46,Xy Sex Reversal 4",DOID:14448,46 XY gonadal dysgenesis
+OMIM:186100,"Syndactyly, Type Iii",DOID:11193,syndactyly
+OMIM:613347,"Pancreatic Cancer, Susceptibility To, 2",DOID:1793,pancreatic cancer
+OMIM:614615,Joubert Syndrome 17,DOID:0050777,Joubert syndrome
+OMIM:230400,Galactosemia,DOID:9870,galactosemia
+OMIM:613875,"Cardiomyopathy, Familial Hypertrophic, 19",DOID:11984,hypertrophic cardiomyopathy
+DOID:2998,testicular cancer,OMIM:273300,Testicular Germ Cell Tumor
+OMIM:607832,"Focal Segmental Glomerulosclerosis 3, Susceptibility To",DOID:1312,focal segmental glomerulosclerosis
+OMIM:611953,"Macular Degeneration, Age-Related, 11",DOID:10871,age related macular degeneration
+OMIM:609254,Senior-Loken Syndrome 5,DOID:0050576,Senior-Loken syndrome
+OMIM:255500,"Myopia 18, Autosomal Recessive",DOID:11830,myopia
+OMIM:259700,"Osteopetrosis, Autosomal Recessive 1",DOID:13533,osteopetrosis
+OMIM:233690,"Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative",DOID:3265,chronic granulomatous disease
+OMIM:614701,Cornelia De Lange Syndrome 4,DOID:11725,Cornelia de Lange syndrome
+OMIM:614728,Seckel Syndrome 6,DOID:0050569,Seckel syndrome
+DOID:350,mastocytosis,OMIM:154800,Mast Cell Disease
+OMIM:615085,"Osteopetrosis, Autosomal Recessive 8",DOID:13533,osteopetrosis
+OMIM:300018,"46,Xy Sex Reversal 2",DOID:14448,46 XY gonadal dysgenesis
+OMIM:247440,"Lymphedema, Congenital Recessive",DOID:0050580,hereditary lymphedema
+OMIM:612998,"Emery-Dreifuss Muscular Dystrophy 4, Autosomal Dominant",DOID:11726,Emery-Dreifuss muscular dystrophy
+OMIM:613086,"Glaucoma 3, Primary Congenital, D",DOID:0050593,primary congenital glaucoma
+OMIM:608594,"Lipodystrophy, Congenital Generalized, Type 1",DOID:0050585,congenital generalized lipodystrophy
+OMIM:609706,"Deafness, Autosomal Recessive 53",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:614674,"Periodic Fever, Menstrual Cycle-Dependent",DOID:9620,vesicoureteral reflux
+OMIM:613874,"Cardiomyopathy, Familial Hypertrophic, 18",DOID:11984,hypertrophic cardiomyopathy
+OMIM:611134,"Meckel Syndrome, Type 4",DOID:0050778,Meckel syndrome
+OMIM:613838,"Cardiomyopathy, Familial Hypertrophic, 16",DOID:11984,hypertrophic cardiomyopathy
+OMIM:204700,"Amelogenesis Imperfecta, Hypomaturation Type, Iia1",DOID:2187,amelogenesis imperfecta
+OMIM:615559,"Immunodeficiency, Common Variable, 9",DOID:12177,common variable immunodeficiency
+OMIM:125490,Dentinogenesis Imperfecta 1,DOID:4154,dentinogenesis imperfecta
+OMIM:601072,"Deafness, Autosomal Recessive 8",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:146200,"Hypoparathyroidism, Familial Isolated",DOID:11199,hypoparathyroidism
+OMIM:225750,Aicardi-Goutieres Syndrome 1,DOID:0050629,Aicardi-Goutieres syndrome
+OMIM:604928,Wolfram Syndrome 2,DOID:10632,Wolfram syndrome
+OMIM:609040,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 9",DOID:0050431,arrhythmogenic right ventricular cardiomyopathy
+OMIM:600974,"Deafness, Autosomal Recessive 7",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:601071,"Deafness, Autosomal Recessive 9",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:264700,"Vitamin D Hydroxylation-Deficient Rickets, Type 1a",DOID:10609,rickets
+OMIM:613684,Rubinstein-Taybi Syndrome 2,DOID:1933,Rubinstein-Taybi syndrome
+OMIM:613211,"Amelogenesis Imperfecta, Hypomaturation Type, Iia3",DOID:2187,amelogenesis imperfecta
+OMIM:615362,"Ceroid Lipofuscinosis, Neuronal, 13",DOID:14503,neuronal ceroid lipofuscinosis
+OMIM:608161,"Macular Dystrophy, Vitelliform, Adult-Onset",DOID:0050661,vitelliform macular dystrophy
+OMIM:273680,"Thanatophoric Dysplasia, Glasgow Variant",DOID:13481,thanatophoric dysplasia
+OMIM:615376,"Charcot-Marie-Tooth Disease, Recessive Intermediate C",DOID:0050543,Charcot-Marie-Tooth disease intermediate type
+OMIM:189800,Preeclampsia/Eclampsia 1,DOID:10591,pre-eclampsia
+OMIM:265400,"Pulmonary Hypertension, Primary, Autosomal Recessive",DOID:14557,primary pulmonary hypertension
+OMIM:601626,"Leukemia, Acute Myeloid",DOID:9119,acute myeloid leukemia
+OMIM:610380,Moved To 610168,DOID:0050466,Loeys-Dietz syndrome
+OMIM:126800,Duane Retraction Syndrome 1,DOID:12557,Duane retraction syndrome
+OMIM:600882,"Charcot-Marie-Tooth Disease, Axonal, Type 2b",DOID:0050539,Charcot-Marie-Tooth disease type 2
+OMIM:305100,"Ectodermal Dysplasia 1, Hypohidrotic, X-Linked",DOID:14793,hypohidrotic ectodermal dysplasia
+OMIM:610153,"Deafness, Autosomal Recessive 49",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:271530,"Brachyolmia Type 1, Hobaek Type",DOID:0050690,brachyolmia
+OMIM:603194,"Meckel Syndrome, Type 2",DOID:0050778,Meckel syndrome
+OMIM:601868,"Deafness, Autosomal Dominant 13",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:201710,Lipoid Congenital Adrenal Hyperplasia,DOID:0050811,congenital adrenal hyperplasia
+OMIM:603553,"Hemophagocytic Lymphohistiocytosis, Familial, 2",DOID:0050120,hemophagocytic lymphohistiocytosis
+OMIM:605637,"Inclusion Body Myopathy 3, Autosomal Dominant",DOID:3429,inclusion body myositis
+OMIM:278760,"Xeroderma Pigmentosum, Complementation Group F",DOID:0050427,xeroderma pigmentosum
+OMIM:600996,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 2",DOID:0050431,arrhythmogenic right ventricular cardiomyopathy
+OMIM:608323,"Charcot-Marie-Tooth Disease, Dominant Intermediate C",DOID:0050543,Charcot-Marie-Tooth disease intermediate type
+OMIM:609192,Loeys-Dietz Syndrome 1,DOID:0050466,Loeys-Dietz syndrome
+OMIM:208500,Short-Rib Thoracic Dysplasia 1 With Or Without Polydactyly,DOID:0050592,asphyxiating thoracic dystrophy
+OMIM:614613,Acrodysostosis 2 With Or Without Hormone Resistance,DOID:14669,acrodysostosis
+OMIM:607271,Caspase 8 Deficiency,DOID:6688,autoimmune lymphoproliferative syndrome
+OMIM:612631,"Adenylate Kinase Deficiency, Hemolytic Anemia Due To",DOID:583,hemolytic anemia
+OMIM:608641,"Deafness, Autosomal Dominant 28",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:249000,"Meckel Syndrome, Type 1",DOID:0050778,Meckel syndrome
+OMIM:607004,"Brachydactyly, Type A1, B",DOID:0050581,brachydactyly
+OMIM:193400,"Von Willebrand Disease, Type 1",DOID:12531,von Willebrand's disease
+OMIM:187601,"Thanatophoric Dysplasia, Type Ii",DOID:13481,thanatophoric dysplasia
+OMIM:603552,"Hemophagocytic Lymphohistiocytosis, Familial, 4",DOID:0050120,hemophagocytic lymphohistiocytosis
+OMIM:614433,Atrial Septal Defect 8,DOID:1882,atrial heart septal defect
+OMIM:614321,"Myopathy, Distal, Tateyama Type",DOID:11720,distal muscular dystrophy
+OMIM:613225,"Factor Xiii, A Subunit, Deficiency Of",DOID:2211,factor XIII deficiency
+OMIM:601680,"Arthrogryposis, Distal, Type 2b",DOID:0050646,distal arthrogryposis
+OMIM:142690,"Acne Inversa, Familial, 1",DOID:2280,hidradenitis suppurativa
+OMIM:613327,"Lipodystrophy, Congenital Generalized, Type 4",DOID:0050585,congenital generalized lipodystrophy
+OMIM:615244,"Nephrotic Syndrome, Type 8",DOID:1184,nephrotic syndrome
+OMIM:612953,"Parkinson Disease 14, Autosomal Recessive",DOID:14330,Parkinson's disease
+OMIM:612561,Diamond-Blackfan Anemia 6,DOID:1339,Diamond-Blackfan anemia
+OMIM:168601,"Parkinson Disease 1, Autosomal Dominant",DOID:14330,Parkinson's disease
+OMIM:606768,"Myopathy, Distal, With Anterior Tibial Onset",DOID:11720,distal muscular dystrophy
+OMIM:611603,Lissencephaly 3,DOID:0050453,lissencephaly
+OMIM:160700,"Myopia 2, Autosomal Dominant",DOID:11830,myopia
+OMIM:300860,"Mental Retardation, X-Linked, Syndromic, Nascimento Type",DOID:0050888,syndromic intellectual disability
+OMIM:615119,"Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 2",DOID:0050713,fatal infantile encephalocardiomyopathy
+OMIM:615184,"Cardiomyopathy, Dilated, 1ii",DOID:12930,dilated cardiomyopathy
+DOID:4440,seminoma,OMIM:273300,Testicular Germ Cell Tumor
+OMIM:113650,Branchiootorenal Syndrome 1,DOID:14702,branchiootorenal syndrome
+OMIM:311360,Premature Ovarian Failure 1,DOID:5426,premature ovarian failure
+OMIM:600110,Stargardt Disease 3,DOID:0050817,Stargardt disease
+OMIM:162000,"Hyperuricemic Nephropathy, Familial Juvenile, 1",DOID:0060062,familial juvenile hyperuricemic nephropathy
+OMIM:606705,"Deafness, Autosomal Dominant 36",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:612562,Diamond-Blackfan Anemia 7,DOID:1339,Diamond-Blackfan anemia
+OMIM:612926,"Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 6",DOID:12554,hemolytic-uremic syndrome
+OMIM:210200,3-Methylcrotonyl-Coa Carboxylase 1 Deficiency,DOID:0050710,3-Methylcrotonyl-CoA carboxylase deficiency
+OMIM:611884,"Ciliary Dyskinesia, Primary, 7",DOID:9562,primary ciliary dyskinesia
+OMIM:253010,Mucopolysaccharidosis Type Ivb,DOID:12804,mucopolysaccharidosis IV
+OMIM:614022,"Atrial Fibrillation, Familial, 10",DOID:0050650,familial atrial fibrillation
+OMIM:600309,Atrioventricular Septal Defect 3,DOID:0050651,atrioventricular septal defect
+OMIM:178600,"Pulmonary Hypertension, Primary, 1",DOID:14557,primary pulmonary hypertension
+OMIM:613309,Diamond-Blackfan Anemia 10,DOID:1339,Diamond-Blackfan anemia
+OMIM:206100,"Anemia, Hypochromic Microcytic, With Iron Overload 1",DOID:0050642,hypochromic microcytic anemia
+OMIM:615420,"Myopia 22, Autosomal Dominant",DOID:11830,myopia
+OMIM:121070,"Arthrogryposis, Distal, Type 2e",DOID:0050646,distal arthrogryposis
+OMIM:602459,"Deafness, Autosomal Dominant 15",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:613268,"Corneal Dystrophy, Fuchs Endothelial, 4",DOID:11555,Fuchs' endothelial dystrophy
+OMIM:614376,Short-Rib Thoracic Dysplasia 5 With Or Without Polydactyly,DOID:0050592,asphyxiating thoracic dystrophy
+OMIM:300071,"Night Blindness, Congenital Stationary, Type 2a",DOID:0050534,congenital stationary night blindness
+OMIM:610003,"Ceroid Lipofuscinosis, Neuronal, 8, Northern Epilepsy Variant",DOID:14503,neuronal ceroid lipofuscinosis
+OMIM:612925,"Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 5",DOID:12554,hemolytic-uremic syndrome
+OMIM:614408,"Myopathy, Centronuclear, 3",DOID:14717,centronuclear myopathy
+OMIM:613757,"Macular Degeneration, Age-Related, 6",DOID:10871,age related macular degeneration
+OMIM:615550,Diamond-Blackfan Anemia 12,DOID:1339,Diamond-Blackfan anemia
+OMIM:182212,Shprintzen-Goldberg Craniosynostosis Syndrome,DOID:2340,craniosynostosis
+OMIM:106100,"Angioedema, Hereditary, Type I",DOID:14735,hereditary angioedema
+OMIM:608565,"Deafness, Autosomal Recessive 35",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:108500,"Episodic Ataxia, Type 2",DOID:963,episodic ataxia
+OMIM:108120,"Arthrogryposis, Distal, Type 1a",DOID:0050646,distal arthrogryposis
+OMIM:187600,"Thanatophoric Dysplasia, Type I",DOID:13481,thanatophoric dysplasia
+OMIM:132400,"Epiphyseal Dysplasia, Multiple, 1",DOID:12721,multiple epiphyseal dysplasia
+OMIM:300495,"Autism, Susceptibility To, X-Linked 2",DOID:12849,autistic disorder
+OMIM:613100,"Glaucoma 1, Open Angle, O",DOID:1067,open-angle glaucoma
+OMIM:607634,"Osteopetrosis, Autosomal Dominant 1",DOID:13533,osteopetrosis
+OMIM:236680,Hydrolethalus Syndrome 1,DOID:0050779,hydrolethalus syndrome
+OMIM:612924,"Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 4",DOID:12554,hemolytic-uremic syndrome
+OMIM:613087,Atrial Septal Defect 6,DOID:1882,atrial heart septal defect
+OMIM:174500,"Polydactyly, Preaxial Ii",DOID:1148,polydactyly
+OMIM:611377,"Brachydactyly, Type B2",DOID:0050581,brachydactyly
+OMIM:300496,"Autism, Susceptibility To, X-Linked 3",DOID:12849,autistic disorder
+OMIM:607084,"Deafness, Autosomal Recessive 31",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:610476,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 11",DOID:0050431,arrhythmogenic right ventricular cardiomyopathy
+OMIM:204500,"Ceroid Lipofuscinosis, Neuronal, 2",DOID:14503,neuronal ceroid lipofuscinosis
+OMIM:222765,"Rhizomelic Chondrodysplasia Punctata, Type 2",DOID:2580,rhizomelic chondrodysplasia punctata
+OMIM:300855,Ogden Syndrome,DOID:0050781,Ogden syndrome
+OMIM:609968,"Hyperinsulinemic Hypoglycemia, Familial, 5",DOID:13317,hyperinsulinemic hypoglycemia
+OMIM:613287,"Charcot-Marie-Tooth Disease, Axonal, Type 2n",DOID:0050539,Charcot-Marie-Tooth disease type 2
+OMIM:121050,"Arthrogryposis, Distal, Type 9",DOID:0050646,distal arthrogryposis
+OMIM:143465,Attention Deficit-Hyperactivity Disorder,DOID:1094,attention deficit hyperactivity disorder
+OMIM:612541,"Neutropenia, Severe Congenital, 4, Autosomal Recessive",DOID:0050590,severe congenital neutropenia
+OMIM:605820,Nonaka Myopathy,DOID:3429,inclusion body myositis
+OMIM:607821,"Deafness, Autosomal Recessive 37",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:608673,"Charcot-Marie-Tooth Disease, Axonal, Type 2l",DOID:0050539,Charcot-Marie-Tooth disease type 2
+OMIM:608758,"Cardiomyopathy, Familial Hypertrophic, 10",DOID:11984,hypertrophic cardiomyopathy
+OMIM:306400,"Granulomatous Disease, Chronic, X-Linked",DOID:3265,chronic granulomatous disease
+OMIM:160980,"Carney Complex, Type 1",DOID:0050471,Carney complex
+OMIM:612923,"Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 3",DOID:12554,hemolytic-uremic syndrome
+OMIM:613216,"Night Blindness, Congenital Stationary, Type 1c",DOID:0050534,congenital stationary night blindness
+OMIM:614129,Perrault Syndrome 3,DOID:0050857,Perrault syndrome
+OMIM:186500,Multiple Synostoses Syndrome 1,DOID:0050794,multiple synostoses syndrome
+OMIM:227646,"Fanconi Anemia, Complementation Group D2",DOID:13636,Fanconi's anemia
+OMIM:614816,Loeys-Dietz Syndrome 4,DOID:0050466,Loeys-Dietz syndrome
+OMIM:615065,"Arthrogryposis, Distal, Type 5d",DOID:0050646,distal arthrogryposis
+OMIM:614018,"Epilepsy, Progressive Myoclonic 6",DOID:891,progressive myoclonus epilepsy
+OMIM:610508,"Maturity-Onset Diabetes Of The Young, Type 7",DOID:0050524,maturity-onset diabetes of the young
+OMIM:230350,Galactose Epimerase Deficiency,DOID:9870,galactosemia
+OMIM:610021,"Hyperinsulinemic Hypoglycemia, Familial, 7",DOID:13317,hyperinsulinemic hypoglycemia
+OMIM:184840,"Stickler Syndrome, Type Iii",DOID:0080046,Stickler syndrome
+OMIM:181350,"Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant",DOID:11726,Emery-Dreifuss muscular dystrophy
+OMIM:608088,"Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux",DOID:0050548,hereditary sensory neuropathy
+OMIM:607677,"Charcot-Marie-Tooth Disease, Axonal, Type 2i",DOID:0050539,Charcot-Marie-Tooth disease type 2
+OMIM:612922,"Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 2",DOID:12554,hemolytic-uremic syndrome
+OMIM:104310,Alzheimer Disease 2,DOID:10652,Alzheimer's disease
+OMIM:227645,"Fanconi Anemia, Complementation Group C",DOID:13636,Fanconi's anemia
+OMIM:604250,"Hemochromatosis, Type 3",DOID:2352,hemochromatosis
+OMIM:611498,Nephronophthisis 7,DOID:12712,nephronophthisis
+OMIM:605472,"Usher Syndrome, Type Iic",DOID:0050439,Usher syndrome
+OMIM:108800,Atrial Septal Defect 1,DOID:1882,atrial heart septal defect
+OMIM:271630,"Brachyolmia Type 1, Toledo Type",DOID:0050690,brachyolmia
+OMIM:614900,Diamond-Blackfan Anemia 11,DOID:1339,Diamond-Blackfan anemia
+OMIM:609404,Preeclampsia/Eclampsia 4,DOID:10591,pre-eclampsia
+OMIM:615191,Lissencephaly 5,DOID:0050453,lissencephaly
+OMIM:104300,Alzheimer Disease,DOID:10652,Alzheimer's disease
+OMIM:608996,Premature Ovarian Failure 3,DOID:5426,premature ovarian failure
+OMIM:231200,Bernard-Soulier Syndrome,DOID:2217,Bernard-Soulier syndrome
+OMIM:614504,"Usher Syndrome, Type Iiib",DOID:0050439,Usher syndrome
+OMIM:312780,"Russell-Silver Syndrome, X-Linked",DOID:14744,Partington syndrome
+OMIM:608328,Weill-Marchesani Syndrome 2,DOID:0050475,Weill-Marchesani syndrome
+OMIM:610878,Vesicoureteral Reflux 2,DOID:9620,vesicoureteral reflux
+OMIM:613982,"Osteogenesis Imperfecta, Type Vi",DOID:12347,osteogenesis imperfecta
+OMIM:203300,Hermansky-Pudlak Syndrome 1,DOID:3753,Hermansky-Pudlak syndrome
+OMIM:613832,"Epilepsy, Progressive Myoclonic 5",DOID:891,progressive myoclonus epilepsy
+OMIM:607554,"Atrial Fibrillation, Familial, 3",DOID:0050650,familial atrial fibrillation
+OMIM:166210,"Osteogenesis Imperfecta, Type Ii",DOID:12347,osteogenesis imperfecta
+OMIM:614990,"Usher Syndrome, Type Ik",DOID:0050439,Usher syndrome
+OMIM:261750,Glycogen Storage Disease Ixb,DOID:0050594,glycogen storage disease IX
+OMIM:614131,Focal Segmental Glomerulosclerosis 6,DOID:1312,focal segmental glomerulosclerosis
+OMIM:613251,"Cardiomyopathy, Familial Hypertrophic, 14",DOID:11984,hypertrophic cardiomyopathy
+OMIM:210600,Seckel Syndrome 1,DOID:0050569,Seckel syndrome
+OMIM:146550,Hypotrichosis 4,DOID:4535,hypotrichosis
+OMIM:613554,"Von Willebrand Disease, Type 2",DOID:12531,von Willebrand's disease
+DOID:7173,cloacogenic carcinoma,OMIM:105580,Anal Canal Carcinoma
+OMIM:122600,"Spondylocostal Dysostosis 5, Autosomal Dominant",DOID:0050568,spondylocostal dysostosis
+OMIM:601631,"Iridogoniodysgenesis, Type 1",DOID:0050786,iridogoniodysgenesis syndrome
+OMIM:300210,"Mental Retardation, X-Linked 58",DOID:0050776,non-specific X-linked mental retardation
+OMIM:300367,"Thrombocytopenia, X-Linked, With Or Without Dyserythropoietic Anemia",DOID:1588,thrombocytopenia
+OMIM:600971,"Deafness, Autosomal Recessive 6",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:254770,"Epilepsy, Myoclonic Juvenile",DOID:4890,juvenile myoclonic epilepsy
+OMIM:613737,"Acne Inversa, Familial, 3",DOID:2280,hidradenitis suppurativa
+OMIM:133780,Exudative Vitreoretinopathy 1,DOID:0050535,exudative vitreoretinopathy
+OMIM:259710,"Osteopetrosis, Autosomal Recessive 2",DOID:13533,osteopetrosis
+OMIM:614847,"Epilepsy, Idiopathic Generalized, Susceptibility To, 12",DOID:1827,idiopathic generalized epilepsy
+OMIM:613285,"Deafness, Autosomal Recessive 25",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:600121,"Rhizomelic Chondrodysplasia Punctata, Type 3",DOID:2580,rhizomelic chondrodysplasia punctata
+OMIM:613312,"Hypophosphatemic Rickets, Autosomal Recessive, 2",DOID:0050445,X-linked hypophosphatemia
+OMIM:278740,"Xeroderma Pigmentosum, Complementation Group E",DOID:0050427,xeroderma pigmentosum
+OMIM:224900,"Ectodermal Dysplasia 10b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive",DOID:14793,hypohidrotic ectodermal dysplasia
+OMIM:104290,Alternating Hemiplegia Of Childhood 1,DOID:0050635,alternating hemiplegia of childhood
+OMIM:610733,Noonan Syndrome 4,DOID:3490,Noonan syndrome
+OMIM:613065,"Leukemia, Acute Lymphoblastic",DOID:9952,acute lymphocytic leukemia
+OMIM:300273,"Goiter, Multinodular 2",DOID:0050489,multinodular goiter
+OMIM:600884,"Cardiomyopathy, Dilated, 1b",DOID:12930,dilated cardiomyopathy
+OMIM:251200,"Microcephaly 1, Primary, Autosomal Recessive",DOID:10907,microcephaly
+OMIM:613308,Diamond-Blackfan Anemia 9,DOID:1339,Diamond-Blackfan anemia
+OMIM:610265,"Deafness, Autosomal Recessive 67",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:613812,"Bile Acid Synthesis Defect, Congenital, 3",DOID:0050674,congenital bile acid synthesis defect
+OMIM:607432,Lissencephaly 1,DOID:0050453,lissencephaly
+OMIM:609533,"Deafness, Autosomal Recessive 23",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:101800,Acrodysostosis 1 With Or Without Hormone Resistance,DOID:14669,acrodysostosis
+OMIM:612462,"Pseudohypoparathyroidism, Type Ic",DOID:4184,pseudohypoparathyroidism
+OMIM:604801,"Muscular Dystrophy, Congenital, 1b",DOID:0050557,congenital muscular dystrophy
+OMIM:613493,"Immunodeficiency, Common Variable, 3",DOID:12177,common variable immunodeficiency
+OMIM:601144,Brugada Syndrome 1,DOID:0050451,Brugada syndrome
+OMIM:607678,"Charcot-Marie-Tooth Disease, Demyelinating, Type 1d",DOID:0050538,Charcot-Marie-Tooth disease type 1
+OMIM:614856,"Osteogenesis Imperfecta, Type Xiii",DOID:12347,osteogenesis imperfecta
+OMIM:613558,"Deafness, Autosomal Dominant 51",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:249900,Metachromatic Leukodystrophy Due To Saposin B Deficiency,DOID:10581,metachromatic leukodystrophy
+OMIM:605583,"Deafness, Autosomal Dominant 25",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:606595,"Charcot-Marie-Tooth Disease, Axonal, Type 2f",DOID:0050539,Charcot-Marie-Tooth disease type 2
+OMIM:123155,"Hydrocephalus, Autosomal Dominant",DOID:10908,hydrocephalus
+OMIM:612240,"Atrial Fibrillation, Familial, 7",DOID:0050650,familial atrial fibrillation
+OMIM:243300,"Cholestasis, Benign Recurrent Intrahepatic, 1",DOID:1852,intrahepatic cholestasis
+OMIM:201750,Antley-Bixler Syndrome With Genital Anomalies And Disordered Steroidogenesis,DOID:0050462,Antley-Bixler syndrome
+OMIM:306000,Glycogen Storage Disease Ixa1,DOID:0050594,glycogen storage disease IX
+DOID:11514,fissured tongue,OMIM:137400,Geographic Tongue And Fissured Tongue
+OMIM:614065,"Myopathy, Distal, 4",DOID:11720,distal muscular dystrophy
+OMIM:608265,"Deafness, Autosomal Recessive 39",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:118220,"Charcot-Marie-Tooth Disease, Demyelinating, Type 1a",DOID:0050538,Charcot-Marie-Tooth disease type 1
+OMIM:601386,"Deafness, Autosomal Recessive 12",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:613375,"Maturity-Onset Diabetes Of The Young, Type 11",DOID:0050524,maturity-onset diabetes of the young
+OMIM:614823,Aortic Valve Disease 2,DOID:1712,aortic valve stenosis
+OMIM:613780,"Aortic Aneurysm, Familial Thoracic 7",DOID:14004,thoracic aortic aneurysm
+OMIM:613080,"46,Xy Sex Reversal 5",DOID:14448,46 XY gonadal dysgenesis
+OMIM:613736,"Acne Inversa, Familial, 2",DOID:2280,hidradenitis suppurativa
+OMIM:153200,"Lymphedema, Hereditary, Ii",DOID:0050580,hereditary lymphedema
+OMIM:400044,"46,Xy Sex Reversal 1",DOID:14448,46 XY gonadal dysgenesis
+OMIM:600155,"Hirschsprung Disease, Susceptibility To, 2",DOID:10487,Hirschsprung's disease
+OMIM:610205,Alagille Syndrome 2,DOID:9245,Alagille syndrome
+OMIM:601764,"Seizures, Benign Familial Infantile, 1",DOID:0060169,benign familial infantile epilepsy
+OMIM:611263,Short-Rib Thoracic Dysplasia 2 With Or Without Polydactyly,DOID:0050592,asphyxiating thoracic dystrophy
+OMIM:611383,"Usher Syndrome, Type Iid",DOID:0050439,Usher syndrome
+OMIM:603720,"Deafness, Autosomal Recessive 16",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:612692,"Agammaglobulinemia 6, Autosomal Recessive",DOID:2583,agammaglobulinemia
+OMIM:614815,Joubert Syndrome 18,DOID:0050777,Joubert syndrome
+OMIM:600995,"Nephrotic Syndrome, Type 2",DOID:1184,nephrotic syndrome
+OMIM:603786,Stargardt Disease 4,DOID:0050817,Stargardt disease
+OMIM:614807,"Myopathy, Centronuclear, 4",DOID:14717,centronuclear myopathy
+OMIM:256100,Nephronophthisis 1,DOID:12712,nephronophthisis
+OMIM:608636,Chromosome 15q11-Q13 Duplication Syndrome,DOID:12849,autistic disorder
+OMIM:108900,Atrial Septal Defect 7 With Or Without Atrioventricular Conduction Defects,DOID:1882,atrial heart septal defect
+OMIM:300758,"Hypospadias 2, X-Linked",DOID:10892,hypospadias
+OMIM:601650,Paragangliomas 2,DOID:0050773,paraganglioma
+OMIM:613496,"Immunodeficiency, Common Variable, 6",DOID:12177,common variable immunodeficiency
+OMIM:604321,"Microcephaly 4, Primary, Autosomal Recessive",DOID:10907,microcephaly
+OMIM:120300,Coloboma Of Macula,DOID:12270,coloboma
+OMIM:174700,"Polydactyly, Preaxial Iv",DOID:1148,polydactyly
+OMIM:267700,"Hemophagocytic Lymphohistiocytosis, Familial, 1",DOID:0050120,hemophagocytic lymphohistiocytosis
+OMIM:613204,"Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency",DOID:0050557,congenital muscular dystrophy
+OMIM:614049,"Atrial Fibrillation, Familial, 11",DOID:0050650,familial atrial fibrillation
+OMIM:118450,Alagille Syndrome 1,DOID:9245,Alagille syndrome
+OMIM:300321,Fg Syndrome 2,DOID:14711,FG syndrome
+OMIM:613370,"Maturity-Onset Diabetes Of The Young, Type 10",DOID:0050524,maturity-onset diabetes of the young
+OMIM:609812,"Maturity-Onset Diabetes Of The Young, Type 8, With Exocrine Dysfunction",DOID:0050524,maturity-onset diabetes of the young
+OMIM:233710,"Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type Ii",DOID:3265,chronic granulomatous disease
+OMIM:300804,Joubert Syndrome 10,DOID:0050777,Joubert syndrome
+OMIM:610427,"Night Blindness, Congenital Stationary, Type 2b",DOID:0050534,congenital stationary night blindness
+OMIM:132900,"Aortic Aneurysm, Familial Thoracic 4",DOID:14004,thoracic aortic aneurysm
+OMIM:609636,Alzheimer Disease 10,DOID:10652,Alzheimer's disease
+OMIM:612444,"Ciliary Dyskinesia, Primary, 9",DOID:9562,primary ciliary dyskinesia
+OMIM:153840,"Macular Dystrophy, Atypical Vitelliform",DOID:0050661,vitelliform macular dystrophy
+OMIM:608091,Joubert Syndrome 2,DOID:0050777,Joubert syndrome
+OMIM:613205,"Muscular Dystrophy, Congenital, Lmna-Related",DOID:0050557,congenital muscular dystrophy
+OMIM:609310,"Colorectal Cancer, Hereditary Nonpolyposis, Type 2",DOID:3883,Lynch syndrome
+OMIM:613092,"Hyperuricemic Nephropathy, Familial Juvenile, 2",DOID:0060062,familial juvenile hyperuricemic nephropathy
+OMIM:614779,"Heterotaxy, Visceral, 6, Autosomal",DOID:0050545,visceral heterotaxy
+OMIM:609942,Noonan Syndrome 3,DOID:3490,Noonan syndrome
+OMIM:137100,Immunoglobulin A Deficiency 1,DOID:0060025,immunoglobulin alpha deficiency
+OMIM:613494,"Immunodeficiency, Common Variable, 4",DOID:12177,common variable immunodeficiency
+OMIM:611277,"Generalized Epilepsy With Febrile Seizures Plus, Type 3",DOID:0060170,generalized epilepsy with febrile seizures plus
+DOID:9256,colorectal cancer,OMIM:114500,Colorectal Cancer
+OMIM:117550,Sotos Syndrome 1,DOID:14748,Sotos syndrome
+OMIM:615008,"Nephrotic Syndrome, Type 7",DOID:1184,nephrotic syndrome
+OMIM:611876,Brugada Syndrome 4,DOID:0050451,Brugada syndrome
+OMIM:615234,"Anemia, Hypochromic Microcytic, With Iron Overload 2",DOID:0050642,hypochromic microcytic anemia
+OMIM:102300,"Restless Legs Syndrome, Susceptibility To, 1",DOID:0050425,restless legs syndrome
+OMIM:603513,"Cerebral Palsy, Spastic Quadriplegic, 1",DOID:10970,spastic quadriplegia
+OMIM:613495,"Immunodeficiency, Common Variable, 5",DOID:12177,common variable immunodeficiency
+OMIM:615548,"Neuropathy, Hereditary Sensory And Autonomic, Type Vii",DOID:0050548,hereditary sensory neuropathy
+OMIM:277600,Weill-Marchesani Syndrome 1,DOID:0050475,Weill-Marchesani syndrome
+OMIM:166200,"Osteogenesis Imperfecta, Type I",DOID:12347,osteogenesis imperfecta
+OMIM:113500,Brachyolmia Type 3,DOID:0050690,brachyolmia
+OMIM:300833,"46,Xx Sex Reversal 3",DOID:14450,46 XX gonadal dysgenesis
+OMIM:230800,"Gaucher Disease, Type I",DOID:1926,Gaucher's disease
+OMIM:604379,Hypotrichosis 7,DOID:4535,hypotrichosis
+OMIM:615512,Triosephosphate Isomerase Deficiency,DOID:0050884,triosephosphate isomerase deficiency
+OMIM:611875,Brugada Syndrome 3,DOID:0050451,Brugada syndrome
+OMIM:100070,"Aortic Aneurysm, Familial Abdominal, 1",DOID:7693,abdominal aortic aneurysm
+OMIM:612649,"Ciliary Dyskinesia, Primary, 11",DOID:9562,primary ciliary dyskinesia
+OMIM:202370,Peroxisome Biogenesis Disorder 2b,DOID:10588,adrenoleukodystrophy
+OMIM:607078,"Epiphyseal Dysplasia, Multiple, 5",DOID:12721,multiple epiphyseal dysplasia
+OMIM:608097,"Periventricular Heterotopia With Microcephaly, Autosomal Recessive",DOID:0050454,periventricular nodular heterotopia
+OMIM:612310,Premature Ovarian Failure 6,DOID:5426,premature ovarian failure
+OMIM:611465,Gallbladder Disease 4,DOID:0000000,gallbladder disease
+OMIM:614300,Hypermethioninemia Due To Adenosine Kinase Deficiency,DOID:0050544,hypermethioninemia
+OMIM:613254,Tuberous Sclerosis 2,DOID:13515,tuberous sclerosis
+OMIM:613955,"Amyloidosis, Primary Localized Cutaneous, 2",DOID:0050639,primary cutaneous amyloidosis
+OMIM:606483,"Charcot-Marie-Tooth Disease, Dominant Intermediate A",DOID:0050543,Charcot-Marie-Tooth disease intermediate type
+OMIM:256800,"Insensitivity To Pain, Congenital, With Anhidrosis",DOID:0050548,hereditary sensory neuropathy
+OMIM:309510,Partington X-Linked Mental Retardation Syndrome,DOID:14744,Partington syndrome
+OMIM:176807,Prostate Cancer,DOID:10283,prostate cancer
+OMIM:236730,Urofacial Syndrome 1,DOID:0050816,urofacial syndrome
+OMIM:260300,"Parkinson Disease 15, Autosomal Recessive Early-Onset",DOID:14330,Parkinson's disease
+OMIM:613101,"Hemophagocytic Lymphohistiocytosis, Familial, 5",DOID:0050120,hemophagocytic lymphohistiocytosis
+OMIM:615238,"Lipodystrophy, Familial Partial, Type 5",DOID:0050440,familial partial lipodystrophy
+OMIM:300872,Epsilon-Trimethyllysine Hydroxylase Deficiency,DOID:12849,autistic disorder
+OMIM:612422,"Cardiomyopathy, Familial Restrictive, 3",DOID:397,restrictive cardiomyopathy
+OMIM:300716,"Mental Retardation, X-Linked 95",DOID:0050776,non-specific X-linked mental retardation
+OMIM:613095,Polycystic Kidney Disease 2,DOID:898,polycystic kidney disease
+OMIM:614926,Perrault Syndrome 2,DOID:0050857,Perrault syndrome
+OMIM:157300,"Migraine With Or Without Aura, Susceptibility To, 1",DOID:6364,migraine
+OMIM:611788,"Aortic Aneurysm, Familial Thoracic 6",DOID:14004,thoracic aortic aneurysm
+OMIM:612838,Brugada Syndrome 5,DOID:0050451,Brugada syndrome
+OMIM:181000,"Sarcoidosis, Susceptibility To, 1",DOID:11335,sarcoidosis
+OMIM:607364,"Bartter Syndrome, Type 3",DOID:445,Bartter disease
+OMIM:612961,Multiple Synostoses Syndrome 3,DOID:0050794,multiple synostoses syndrome
+OMIM:606482,"Charcot-Marie-Tooth Disease, Dominant Intermediate B",DOID:0050543,Charcot-Marie-Tooth disease intermediate type
+OMIM:614175,"Meckel Syndrome, Type 10",DOID:0050778,Meckel syndrome
+OMIM:607453,"Deafness, Autosomal Dominant 44",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:112910,"Brachydactyly, Type A6",DOID:0050581,brachydactyly
+OMIM:312750,Rett Syndrome,DOID:1206,Rett syndrome
+OMIM:136800,"Corneal Dystrophy, Fuchs Endothelial, 1",DOID:11555,Fuchs' endothelial dystrophy
+OMIM:251110,"Methylmalonic Aciduria, Cblb Type",DOID:14749,methylmalonic acidemia
+OMIM:611490,"Osteopetrosis,  Autosomal Recessive 4",DOID:13533,osteopetrosis
+OMIM:610968,"Osteogenesis Imperfecta, Type Xi",DOID:12347,osteogenesis imperfecta
+OMIM:180500,"Axenfeld-Rieger Syndrome, Type 1",DOID:14686,Axenfeld-Rieger syndrome
+OMIM:277480,"Von Willebrand Disease, Type 3",DOID:12531,von Willebrand's disease
+OMIM:278720,"Xeroderma Pigmentosum, Complementation Group C",DOID:0050427,xeroderma pigmentosum
+OMIM:278150,Hypotrichosis 8,DOID:4535,hypotrichosis
+OMIM:610181,Aicardi-Goutieres Syndrome 2,DOID:0050629,Aicardi-Goutieres syndrome
+OMIM:400045,"46,Xx Sex Reversal 1",DOID:14450,46 XX gonadal dysgenesis
+OMIM:614213,"Neuropathy, Hereditary Sensory, Type Iic",DOID:0050548,hereditary sensory neuropathy
+OMIM:613090,"Bartter Syndrome, Type 4b",DOID:445,Bartter disease
+OMIM:612370,Hypogonadotropic Hypogonadism 5 With Or Without Anosmia,DOID:3614,Kallmann syndrome
+OMIM:168600,"Parkinson Disease, Late-Onset",DOID:14330,Parkinson's disease
+OMIM:600785,"Vitamin D-Dependent Rickets, Type 2b, With Normal Vitamin D Receptor",DOID:10609,rickets
+OMIM:613255,"Cardiomyopathy, Familial Hypertrophic, 15",DOID:11984,hypertrophic cardiomyopathy
+OMIM:230600,"Gm1-Gangliosidosis, Type Ii",DOID:3322,gangliosidosis GM1
+OMIM:207500,"Anus, Imperforate",DOID:10488,imperforate anus
+OMIM:610967,"Osteogenesis Imperfecta, Type V",DOID:12347,osteogenesis imperfecta
+OMIM:300514,"Fanconi Anemia, Complementation Group B",DOID:13636,Fanconi's anemia
+OMIM:610688,Joubert Syndrome 6,DOID:0050777,Joubert syndrome
+OMIM:124900,"Deafness, Autosomal Dominant 1",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:204200,"Ceroid Lipofuscinosis, Neuronal, 3",DOID:14503,neuronal ceroid lipofuscinosis
+OMIM:605362,"Cardiomyopathy, Dilated, 1j",DOID:12930,dilated cardiomyopathy
+OMIM:613640,"Neuropathy, Hereditary Sensory And Autonomic, Type Ic",DOID:0050548,hereditary sensory neuropathy
+OMIM:233400,Perrault Syndrome 1,DOID:0050857,Perrault syndrome
+OMIM:613122,"Cardiomyopathy, Dilated, 1cc",DOID:12930,dilated cardiomyopathy
+OMIM:613454,"Rett Syndrome, Congenital Variant",DOID:1206,Rett syndrome
+OMIM:614378,Cranioectodermal Dysplasia 4,DOID:0080033,craniometaphyseal dysplasia
+OMIM:614173,Joubert Syndrome 13,DOID:0050777,Joubert syndrome
+OMIM:160500,"Myopathy, Distal, 1",DOID:11720,distal muscular dystrophy
+OMIM:613079,"Deafness, Autosomal Recessive 77",DOID:0050565,autosomal recessive nonsyndromic deafness
+OMIM:609161,"Striatal Degeneration, Autosomal Dominant",DOID:4751,striatonigral degeneration
+OMIM:607941,Atrial Septal Defect 2,DOID:1882,atrial heart septal defect
+OMIM:609055,"Ceroid Lipofuscinosis, Neuronal, 9",DOID:14503,neuronal ceroid lipofuscinosis
+OMIM:613390,"Fanconi Anemia, Complementation Group O",DOID:13636,Fanconi's anemia
+OMIM:606612,"Muscular Dystrophy-Dystroglycanopathy (Congenital With Or Without Mental Retardation), Type B, 5",DOID:0050557,congenital muscular dystrophy
+OMIM:235200,"Hemochromatosis, Type 1",DOID:2352,hemochromatosis
+OMIM:614972,"Cholestasis, Intrahepatic, Of Pregnancy 3",DOID:1852,intrahepatic cholestasis
+OMIM:202010,"Adrenal Hyperplasia, Congenital, Due To Steroid 11-Beta-Hydroxylase Deficiency",DOID:0050811,congenital adrenal hyperplasia
+OMIM:248200,Stargardt Disease 1,DOID:0050817,Stargardt disease
+OMIM:208085,"Arthrogryposis, Renal Dysfunction, And Cholestasis 1",DOID:0050763,ARC syndrome
+OMIM:613705,Orofacial Cleft 10,DOID:0050567,orofacial cleft
+OMIM:236100,Holoprosencephaly,DOID:4621,holoprosencephaly
+OMIM:257270,"Night Blindness, Congenital Stationary, Type 1b",DOID:0050534,congenital stationary night blindness
+OMIM:613074,"Deafness, Autosomal Dominant 50",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:612284,"Meckel Syndrome, Type 6",DOID:0050778,Meckel syndrome
+OMIM:274900,Thyroid Dyshormonogenesis 5,DOID:0050328,congenital hypothyroidism
+OMIM:608233,Hermansky-Pudlak Syndrome 2,DOID:3753,Hermansky-Pudlak syndrome
+OMIM:310460,"Myopia 1, X-Linked",DOID:11830,myopia
+OMIM:606685,"Cardiomyopathy, Dilated, 1l",DOID:12930,dilated cardiomyopathy
+OMIM:167210,Pachyonychia Congenita 2,DOID:0050449,pachyonychia congenita
+OMIM:600496,"Maturity-Onset Diabetes Of The Young, Type 3",DOID:0050524,maturity-onset diabetes of the young
+OMIM:605387,"Cataract 31, Multiple Types",DOID:0050537,posterior polar cataract
+OMIM:613237,Focal Segmental Glomerulosclerosis 5,DOID:1312,focal segmental glomerulosclerosis
+OMIM:608634,"Neuronopathy, Distal Hereditary Motor, Type Iib",DOID:0050582,distal hereditary motor neuropathy
+OMIM:601544,"Deafness, Autosomal Dominant 3a",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:256860,"Neuropathy, Hereditary Sensory, Atypical",DOID:0050548,hereditary sensory neuropathy
+OMIM:244200,Hypogonadotropic Hypogonadism 3 With Or Without Anosmia,DOID:3614,Kallmann syndrome
+OMIM:612952,Aicardi-Goutieres Syndrome 5,DOID:0050629,Aicardi-Goutieres syndrome
+OMIM:601813,Exudative Vitreoretinopathy 4,DOID:0050535,exudative vitreoretinopathy
+OMIM:274500,Thyroid Dyshormonogenesis 2a,DOID:0050328,congenital hypothyroidism
+OMIM:269700,"Lipodystrophy, Congenital Generalized, Type 2",DOID:0050585,congenital generalized lipodystrophy
+OMIM:615072,"Brachydactyly, Type A1, C",DOID:0050581,brachydactyly
+OMIM:610896,Branchiootorenal Syndrome 2,DOID:14702,branchiootorenal syndrome
+OMIM:300147,"Prostate Cancer, Hereditary, X-Linked 1",DOID:10283,prostate cancer
+OMIM:601543,"Deafness, Autosomal Dominant 12",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:602541,"Muscular Dystrophy, Congenital, Megaconial Type",DOID:0050557,congenital muscular dystrophy
+OMIM:613506,"Agammaglobulinemia 5, Autosomal Dominant",DOID:2583,agammaglobulinemia
+OMIM:613115,"Neuropathy, Hereditary Sensory And Autonomic, Type Iib",DOID:0050548,hereditary sensory neuropathy
+OMIM:602088,Nephronophthisis 2,DOID:12712,nephronophthisis
+OMIM:274400,Thyroid Dyshormonogenesis 1,DOID:0050328,congenital hypothyroidism
+OMIM:182900,"Spherocytosis, Type 1",DOID:12971,hereditary spherocytosis
+OMIM:611553,Noonan Syndrome 5,DOID:3490,Noonan syndrome
+OMIM:269921,Sialuria,DOID:3659,sialuria
+OMIM:602083,"Usher Syndrome, Type If",DOID:0050439,Usher syndrome
+OMIM:121200,"Seizures, Benign Familial Neonatal, 1",DOID:14264,benign neonatal seizures
+OMIM:240500,"Immunodeficiency, Common Variable, 2",DOID:12177,common variable immunodeficiency
+OMIM:611554,Leopard Syndrome 2,DOID:14291,LEOPARD syndrome
+OMIM:212050,"Candidiasis, Familial, 2",DOID:2058,chronic mucocutaneous candidiasis
+OMIM:604356,Duane Retraction Syndrome 2,DOID:12557,Duane retraction syndrome
+OMIM:614970,Joubert Syndrome 20,DOID:0050777,Joubert syndrome
+OMIM:610158,"Corneal Dystrophy, Fuchs Endothelial, 2",DOID:11555,Fuchs' endothelial dystrophy
+OMIM:178110,"Arthrogryposis, Distal, Type 8",DOID:0050646,distal arthrogryposis
+OMIM:615214,"Agammaglobulinemia 7, Autosomal Recessive",DOID:2583,agammaglobulinemia
+OMIM:604765,"Cardiomyopathy, Dilated, 1i",DOID:12930,dilated cardiomyopathy
+OMIM:611804,Elliptocytosis 1,DOID:2373,hereditary elliptocytosis
+OMIM:123000,"Craniometaphyseal Dysplasia, Autosomal Dominant",DOID:0080033,craniometaphyseal dysplasia
+OMIM:615616,"Arrhythmogenic Right Ventricular Dysplasia, Familial, 13",DOID:0050431,arrhythmogenic right ventricular cardiomyopathy
+OMIM:113100,"Brachydactyly, Type C",DOID:0050581,brachydactyly
+OMIM:154500,Treacher Collins Syndrome 1,DOID:2908,Treacher Collins syndrome
+OMIM:611615,"Cardiomyopathy, Dilated, 1x",DOID:12930,dilated cardiomyopathy
+OMIM:600081,"Vitamin D Hydroxylation-Deficient Rickets, Type 1b",DOID:10609,rickets
+OMIM:185900,Chromosome 2q35 Duplication Syndrome,DOID:11193,syndactyly
+OMIM:167320,Inclusion Body Myopathy With Early-Onset Paget Disease With Or Without Frontotemporal Dementia 1,DOID:0050881,inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+OMIM:186000,Synpolydactyly 1,DOID:11193,syndactyly
+OMIM:604717,"Deafness, Autosomal Dominant 20",DOID:0050564,autosomal dominant nonsyndromic deafness
+OMIM:226900,"Epiphyseal Dysplasia, Multiple, 4",DOID:12721,multiple epiphyseal dysplasia
+OMIM:277300,"Spondylocostal Dysostosis 1, Autosomal Recessive",DOID:0050568,spondylocostal dysostosis
+OMIM:613686,"Spondylocostal Dysostosis 4, Autosomal Recessive",DOID:0050568,spondylocostal dysostosis
+OMIM:614042,Moyamoya Disease 5,DOID:13099,Moyamoya disease
diff --git a/src/ontology/sparql/subClasses.sparql b/src/ontology/sparql/subClasses.sparql
new file mode 100644
index 0000000..1ec0ba8
--- /dev/null
+++ b/src/ontology/sparql/subClasses.sparql
@@ -0,0 +1,14 @@
+prefix oio: <http://www.geneontology.org/formats/oboInOwl#>
+prefix owl: <http://www.w3.org/2002/07/owl#>
+prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#>
+
+SELECT ?baseClass ?baseLabel ?superClass ?superLabel WHERE 
+{
+  ?baseClass rdfs:subClassOf ?superClass .
+  ?baseClass rdfs:label ?baseLabel .
+  ?superClass rdfs:label ?superLabel .
+
+  FILTER (!isBlank(?baseClass)) 
+  FILTER (!isBlank(?superClass))
+
+}
diff --git a/src/ontology/sparql/subClassesExt.sparql b/src/ontology/sparql/subClassesExt.sparql
new file mode 100644
index 0000000..c9350d5
--- /dev/null
+++ b/src/ontology/sparql/subClassesExt.sparql
@@ -0,0 +1,22 @@
+prefix oio: <http://www.geneontology.org/formats/oboInOwl#>
+prefix owl: <http://www.w3.org/2002/07/owl#>
+prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#>
+prefix DOID: <http://purl.obolibrary.org/obo/DOID_>
+
+SELECT ?baseClass ?baseLabel ?superClass ?superLabel WHERE 
+{
+  ?baseClass rdfs:subClassOf ?superClass .
+  ?baseClass rdfs:label ?baseLabel .
+  ?superClass rdfs:label ?superLabel .
+
+  FILTER (!isBlank(?baseClass)) 
+  FILTER (!isBlank(?superClass))
+
+   BIND(REPLACE(str(?baseClass), '_.*$', "") AS ?basePrefix)
+   BIND(REPLACE(str(?superClass), '_.*$', "") AS ?superPrefix)
+
+  FILTER(?basePrefix != ?superPrefix)
+
+  FILTER(?superClass != DOID:630)
+
+}
diff --git a/src/ontology/util/curiefy-purls.pl b/src/ontology/util/curiefy-purls.pl
new file mode 100755
index 0000000..750cf1a
--- /dev/null
+++ b/src/ontology/util/curiefy-purls.pl
@@ -0,0 +1,4 @@
+#!/usr/bin/perl -pn
+if (m@http://purl.obolibrary.org/obo/([A-Za-z]+)_@) {
+    s@http://purl.obolibrary.org/obo/([A-Za-z]+)_@$1:@g;
+}