Human Phenotype Ontology 
Grandparent Node:
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Positional foot deformity (HP:0005656)help
Parent Node:
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Talipes (HP:0001883)help
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Talipes equinovarus (HP:0001762)help
Term ID: 1762
Name: Talipes equinovarus
Synonym: Club feet; Club foot; Clubfeet; Clubfoot; Equinovarus; Foot, talipes equinovarus; Pes equinovarus; Pes equinus; Talipes varus
Definition: Talipes equinovarus (also called clubfoot) typically has four main components: inversion and adduction of the forefoot; inversion of the heel and hindfoot; equinus (limitation of extension) of the ankle and subtalar joint; and internal rotation of the leg.
Comments:
Reference: HP:0001762
Genes and Diseases:
 
       Child Nodes:
........expandBilateral talipes equinovarus (HP:0001776) help
........expandTalipes cavus equinovarus (HP:0004696) help

 Sister Nodes: 
..expandTalipes calcaneovalgus (HP:0001884) help
..expandTalipes calcaneovarus (HP:0008124) help
..expandTalipes equinovalgus (HP:0001772) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0001762HP:0001762Talipes equinovarus0ADGRG6 CL E G H57211616503Lethal congenital contracture syndrome 9616503C4225303OMIM165213841612243
HP:0001762HP:0001762Talipes equinovarus0ALDH18A1 CL E G H5832219150Cutis laxa-corneal clouding-oligophrenia syndrome219150C0268354OMIM1332529722138250
HP:0001762HP:0001762Talipes equinovarus0ALG12 CL E G H79087607143ALG12-congenital disorder of glycosylation607143C2931001OMIM11626319358607144
HP:0001762HP:0001762Talipes equinovarus0ALG3 CL E G H10195601110Congenital disorder of glycosylation type 1D601110C1832736OMIM11912323056608750
HP:0001762HP:0001762Talipes equinovarus0AMER1 CL E G H139285300373Osteopathia striata with cranial sclerosis300373C0432268OMIM14121926837300647
HP:0001762HP:0001762Talipes equinovarus0AP4E1 CL E G H23431613744Spastic paraplegia 51, autosomal recessive613744C3151056OMIM118178573607244
HP:0001762HP:0001762Talipes equinovarus0AP4M1 CL E G H9179612936Spastic paraplegia 50, autosomal recessive612936C2752008OMIM115150574602296
HP:0001762HP:0001762Talipes equinovarus0AP4S1 CL E G H11154614067Spastic paraplegia 52, autosomal recessive614067C3279743OMIM1859575607243
HP:0001762HP:0001762Talipes equinovarus0ARHGAP31 CL E G H57514100300Adams-Oliver syndrome 1100300CN028867OMIM1710329216610911
HP:0001762HP:0001762Talipes equinovarus0ARSI CL E G H340075401815ORPHA127032521610009
HP:0001762HP:0001762Talipes equinovarus0ATP6V0A2 CL E G H23545278250Wrinkly skin syndrome278250C0406587OMIM15630918481611716
HP:0001762HP:0001762Talipes equinovarus0ATP6V1E1 CL E G H529617402CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC617402C4479387OMIM1278857108746
HP:0001762HP:0001762Talipes equinovarus0ATRX CL E G H546847ORPHA1170663886300032
HP:0001762HP:0001762Talipes equinovarus0ATRX CL E G H546301040ATR-X syndrome301040C1845055OMIM1170663886300032
HP:0001762HP:0001762Talipes equinovarus0ATRX CL E G H546309580Mental retardation-hypotonic facies syndrome X-linked, 1309580C0796003OMIM1170663886300032
HP:0001762HP:0001762Talipes equinovarus0B3GALT6 CL E G H12679293359ORPHA14023217978615291
HP:0001762HP:0001762Talipes equinovarus0B3GALT6 CL E G H126792615349Ehlers-Danlos syndrome, progeroid type, 2615349C3809210OMIM14023217978615291
HP:0001762HP:0001762Talipes equinovarus0B3GALT6 CL E G H126792271640Spondyloepimetaphyseal dysplasia with joint laxity271640C0432243OMIM14023217978615291
HP:0001762HP:0001762Talipes equinovarus0B3GAT3 CL E G H26229245600Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects245600C3278404OMIM11343923606374
HP:0001762HP:0001762Talipes equinovarus0B9D1 CL E G H27077614209Meckel syndrome, type 9614209C3280155OMIM11015824123614144
HP:0001762HP:0001762Talipes equinovarus0BICD2 CL E G H23299618291618291618291OMIM13532317208609797
HP:0001762HP:0001762Talipes equinovarus0BICD2 CL E G H23299615290Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant615290C3809049OMIM13532317208609797
HP:0001762HP:0001762Talipes equinovarus0BMPER CL E G H168667608022Diaphanospondylodysostosis608022C1842691OMIM11914824154608699
HP:0001762HP:0001762Talipes equinovarus0BMPR1B CL E G H658609441Acromesomelic dysplasia, Demirhan type609441C4225404OMIM1241951077603248
HP:0001762HP:0001762Talipes equinovarus0BRPF1 CL E G H7862617333Intellectual developmental disorder with dysmorphic facies and ptosis617333C4310617OMIM11811514255602410
HP:0001762HP:0001762Talipes equinovarus0C12orf57 CL E G H113246218340Temtamy syndrome218340C1857512OMIM1812529521615140
HP:0001762HP:0001762Talipes equinovarus0C12orf65 CL E G H91574320375ORPHA11111426784613541
HP:0001762HP:0001762Talipes equinovarus0C12orf65 CL E G H91574615035Spastic paraplegia 55, autosomal recessive615035C3539506OMIM11111426784613541
HP:0001762HP:0001762Talipes equinovarus0CANT1 CL E G H124583251450Desbuquois dysplasia 1251450C4012146OMIM12816619721613165
HP:0001762HP:0001762Talipes equinovarus0CC2D2A CL E G H57545612284Meckel syndrome type 6612284C2676790OMIM19658429253612013
HP:0001762HP:0001762Talipes equinovarus0CCBE1 CL E G H147372235510Hennekam lymphangiectasia-lymphedema syndrome235510C0340834OMIM11330529426612753
HP:0001762HP:0001762Talipes equinovarus0CCDC47 CL E G H57003618268618268618268OMIM1520248560
HP:0001762HP:0001762Talipes equinovarus0CEP55 CL E G H55165236500Hydranencephaly with renal aplasia-dysplasia236500C1856053OMIM12341161610000
HP:0001762HP:0001762Talipes equinovarus0CHMP1A CL E G H5119614961Pontocerebellar hypoplasia type 8614961C3554209OMIM131068740164010
HP:0001762HP:0001762Talipes equinovarus0CHRM3 CL E G H1131100100Prune belly syndrome100100C0033770OMIM18891952118494
HP:0001762HP:0001762Talipes equinovarus0CHRNG CL E G H1146265000Multiple pterygium syndrome Escobar type265000C0265261OMIM1351601967100730
HP:0001762HP:0001762Talipes equinovarus0CHST14 CL E G H113189601776Ehlers-Danlos syndrome, musculocontractural type601776C1866294OMIM1229624464608429
HP:0001762HP:0001762Talipes equinovarus0CHST3 CL E G H9469245600Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects245600C3278404OMIM1392651971603799
HP:0001762HP:0001762Talipes equinovarus0CHST3 CL E G H9469143095Spondyloepiphyseal dysplasia with congenital joint dislocations143095C1840471OMIM1392651971603799
HP:0001762HP:0001762Talipes equinovarus0COG1 CL E G H9382611209COG1 congenital disorder of glycosylation611209C1970016OMIM131346545606973
HP:0001762HP:0001762Talipes equinovarus0COG4 CL E G H2583985172ORPHA1614118620606976
HP:0001762HP:0001762Talipes equinovarus0COG4 CL E G H25839618150SAUL-WILSON SYNDROME618150OMIM1614118620606976
HP:0001762HP:0001762Talipes equinovarus0COL2A1 CL E G H128094068ORPHA15707312200120140
HP:0001762HP:0001762Talipes equinovarus0COL2A1 CL E G H1280183900Spondyloepiphyseal dysplasia183900C0038015OMIM15707312200120140
HP:0001762HP:0001762Talipes equinovarus0COL3A1 CL E G H1281130050Ehlers-Danlos syndrome, type 4130050C0268338OMIM164516472201120180
HP:0001762HP:0001762Talipes equinovarus0COL3A1 CL E G H1281286Imaizumi Kuroki syndromeORPHA164516472201120180
HP:0001762HP:0001762Talipes equinovarus0COL5A1 CL E G H1289286Imaizumi Kuroki syndromeORPHA115916302209120215
HP:0001762HP:0001762Talipes equinovarus0COL6A1 CL E G H1291254090Ullrich congenital muscular dystrophy 1254090CN033863OMIM113710072211120220
HP:0001762HP:0001762Talipes equinovarus0COL6A2 CL E G H1292254090Ullrich congenital muscular dystrophy 1254090CN033863OMIM119111482212120240
HP:0001762HP:0001762Talipes equinovarus0COL6A3 CL E G H1293254090Ullrich congenital muscular dystrophy 1254090CN033863OMIM114316342213120250
HP:0001762HP:0001762Talipes equinovarus0CPLX1 CL E G H108151941904p partial monosomy syndrome194190C1956097OMIM131432309605032
HP:0001762HP:0001762Talipes equinovarus0CRIPT CL E G H9419615789Short stature with microcephaly and distinctive facies615789C4014339OMIM142714312604594
HP:0001762HP:0001762Talipes equinovarus0CRLF1 CL E G H9244272430Cold-induced sweating syndrome 1272430C1848947OMIM137562364604237
HP:0001762HP:0001762Talipes equinovarus0CTBP1 CL E G H14871941904p partial monosomy syndrome194190C1956097OMIM111642494602618
HP:0001762HP:0001762Talipes equinovarus0CTDP1 CL E G H9150604168Congenital Cataracts, Facial Dysmorphism, and Neuropathy604168C1858726OMIM112472498604927
HP:0001762HP:0001762Talipes equinovarus0DCHS1 CL E G H8642601390601390601390OMIM12418013681603057
HP:0001762HP:0001762Talipes equinovarus0DES CL E G H1674181400Scapuloperoneal syndrome, neurogenic, Kaeser type181400C1867005OMIM11264942770125660
HP:0001762HP:0001762Talipes equinovarus0DOK7 CL E G H285489208150Pena-Shokeir syndrome type I208150C1276035OMIM17545826594610285
HP:0001762HP:0001762Talipes equinovarus0DONSON CL E G H29980251230Microcephaly-micromelia syndrome251230C1855079OMIM121762993611428
HP:0001762HP:0001762Talipes equinovarus0DPYS CL E G H1807222748Dihydropyrimidinase deficiency222748C0342803OMIM1301083013613326
HP:0001762HP:0001762Talipes equinovarus0DSE CL E G H29940615539Ehlers-Danlos syndrome, musculocontractural type 2615539C3809845OMIM1311521144605942
HP:0001762HP:0001762Talipes equinovarus0DST CL E G H667614653Neuropathy, hereditary sensory and autonomic, type VI614653C3539003OMIM1910171090113810
HP:0001762HP:0001762Talipes equinovarus0EIF2S3 CL E G H196885282ORPHA151783267300161
HP:0001762HP:0001762Talipes equinovarus0EIF4A3 CL E G H9775268305Richieri Costa Pereira syndrome268305C1849348OMIM123418683608546
HP:0001762HP:0001762Talipes equinovarus0ERCC5 CL E G H2073616570Cerebrooculofacioskeletal syndrome 3616570C1851443OMIM1592633437133530
HP:0001762HP:0001762Talipes equinovarus0EVC CL E G H2121225500Chondroectodermal dysplasia225500C0013903OMIM1846523497604831
HP:0001762HP:0001762Talipes equinovarus0EVC2 CL E G H132884225500Chondroectodermal dysplasia225500C0013903OMIM17656719747607261
HP:0001762HP:0001762Talipes equinovarus0EZH2 CL E G H2146277590Weaver syndrome277590C0265210OMIM1422353527601573
HP:0001762HP:0001762Talipes equinovarus0FAT4 CL E G H79633615546Van Maldergem syndrome 2615546C3809875OMIM13731723109612411
HP:0001762HP:0001762Talipes equinovarus0FBXO7 CL E G H25793171695ORPHA11710913586605648
HP:0001762HP:0001762Talipes equinovarus0FBXO7 CL E G H25793260300Parkinson disease 15260300C1850100OMIM11710913586605648
HP:0001762HP:0001762Talipes equinovarus0FGD4 CL E G H121512609311Charcot-Marie-Tooth disease, type 4H609311C1836336OMIM13041519125611104
HP:0001762HP:0001762Talipes equinovarus0FGFRL1 CL E G H538341941904p partial monosomy syndrome194190C1956097OMIM171993693605830
HP:0001762HP:0001762Talipes equinovarus0FKBP10 CL E G H60681259450Bruck syndrome 1259450C1850168OMIM14416118169607063
HP:0001762HP:0001762Talipes equinovarus0FKBP10 CL E G H606812771Hydrocephalus costovertebral dysplasia Sprengel anomalyORPHA14416118169607063
HP:0001762HP:0001762Talipes equinovarus0FLNA CL E G H2316309350Melnick-Needles syndrome309350C0025237OMIM127114723754300017
HP:0001762HP:0001762Talipes equinovarus0FLNB CL E G H231756305ORPHA11225203755603381
HP:0001762HP:0001762Talipes equinovarus0FLNB CL E G H2317108720Atelosteogenesis type 1108720C0265283OMIM11225203755603381
HP:0001762HP:0001762Talipes equinovarus0FLNB CL E G H2317108721Atelosteogenesis type 3108721C3668942OMIM11225203755603381
HP:0001762HP:0001762Talipes equinovarus0FLNB CL E G H2317150250Larsen syndrome, dominant type150250C1835564OMIM11225203755603381
HP:0001762HP:0001762Talipes equinovarus0FLNB CL E G H2317272460Spondylocarpotarsal synostosis syndrome272460C1848934OMIM11225203755603381
HP:0001762HP:0001762Talipes equinovarus0FOXG1 CL E G H2290613454Rett syndrome, congenital variant613454C3150705OMIM11693573811164874
HP:0001762HP:0001762Talipes equinovarus0FUZ CL E G H801993027Iris dysplasia hypertelorism deafnessORPHA153526219610622
HP:0001762HP:0001762Talipes equinovarus0GAN CL E G H8139643ORPHA1804354137605379
HP:0001762HP:0001762Talipes equinovarus0GAN CL E G H8139256850Giant axonal neuropathy256850C1850386OMIM1804354137605379
HP:0001762HP:0001762Talipes equinovarus0GCH1 CL E G H264398808ORPHA12522084193600225
HP:0001762HP:0001762Talipes equinovarus0GCH1 CL E G H2643128230Dystonia 5, Dopa-responsive type128230C1851920OMIM12522084193600225
HP:0001762HP:0001762Talipes equinovarus0GDAP1 CL E G H54332607831Charcot-Marie-Tooth disease type 2K607831C1842983OMIM110335115968606598
HP:0001762HP:0001762Talipes equinovarus0GDAP1 CL E G H54332608340Charcot-Marie-Tooth disease, recessive intermediate A608340C1842197OMIM110335115968606598
HP:0001762HP:0001762Talipes equinovarus0GNPTAB CL E G H79158252500I cell disease252500C2673377OMIM118846229670607840
HP:0001762HP:0001762Talipes equinovarus0GPC3 CL E G H2719312870Simpson-Golabi-Behmel syndrome312870C0796154OMIM1985264451300037
HP:0001762HP:0001762Talipes equinovarus0GPC4 CL E G H2239312870Simpson-Golabi-Behmel syndrome312870C0796154OMIM151964452300168
HP:0001762HP:0001762Talipes equinovarus0GPX4 CL E G H2879250220Spondylometaphyseal dysplasia Sedaghatian type250220C1855229OMIM14564556138322
HP:0001762HP:0001762Talipes equinovarus0GSC CL E G H145258602471Short stature, auditory canal atresia, mandibular hypoplasia, and skeletal abnormalities602471C1865361OMIM17364612138890
HP:0001762HP:0001762Talipes equinovarus0GTPBP2 CL E G H54676617988JABERI-ELAHI SYNDROME617988CN244943OMIM15214670607434
HP:0001762HP:0001762Talipes equinovarus0GUSB CL E G H2990253220Mucopolysaccharidosis type VII253220C0085132OMIM1661574696611499
HP:0001762HP:0001762Talipes equinovarus0HBA1 CL E G H303998791ORPHA12173464823141800
HP:0001762HP:0001762Talipes equinovarus0HBA2 CL E G H304098791ORPHA12962744824141850
HP:0001762HP:0001762Talipes equinovarus0HIST1H1E CL E G H3008617537RAHMAN SYNDROME617537C4479637OMIM154718142220
HP:0001762HP:0001762Talipes equinovarus0HRAS CL E G H3265218040Costello syndrome218040C0587248OMIM1342955173190020
HP:0001762HP:0001762Talipes equinovarus0HSD17B4 CL E G H3295261515Bifunctional peroxisomal enzyme deficiency261515C0342870OMIM11013055213601860
HP:0001762HP:0001762Talipes equinovarus0HSD17B4 CL E G H3295233400Perrault syndrome 1233400OMIM11013055213601860
HP:0001762HP:0001762Talipes equinovarus0HSPB1 CL E G H331599940ORPHA1482265246602195
HP:0001762HP:0001762Talipes equinovarus0HSPG2 CL E G H3339224410Lethal Kniest-like syndrome224410C0432208OMIM1678625273142461
HP:0001762HP:0001762Talipes equinovarus0HSPG2 CL E G H3339255800Schwartz Jampel syndrome type 1255800C0036391OMIM1678625273142461
HP:0001762HP:0001762Talipes equinovarus0IFIH1 CL E G H64135182250Singleton-Merten syndrome 1182250C4225427OMIM12828618873606951
HP:0001762HP:0001762Talipes equinovarus0IGHMBP2 CL E G H3508604320Spinal muscular atrophy, distal, autosomal recessive, 1604320C1858517OMIM11436835542600502
HP:0001762HP:0001762Talipes equinovarus0IRF6 CL E G H3664119500Popliteal pterygium syndrome119500C0265259OMIM13422046121607199
HP:0001762HP:0001762Talipes equinovarus0ITGA8 CL E G H8516191830Renal adysplasia191830C1619700OMIM18566144604063
HP:0001762HP:0001762Talipes equinovarus0JPH1 CL E G H56704607831Charcot-Marie-Tooth disease type 2K607831C1842983OMIM113514201605266
HP:0001762HP:0001762Talipes equinovarus0KAT6B CL E G H2352285201ORPHA17622817582605880
HP:0001762HP:0001762Talipes equinovarus0KAT6B CL E G H23522606170Genitopatellar syndrome606170C1853566OMIM17622817582605880
HP:0001762HP:0001762Talipes equinovarus0KDM5C CL E G H8242300534Mental retardation, syndromic, Claes-Jensen type, X-linked300534C1845243OMIM15632711114314690
HP:0001762HP:0001762Talipes equinovarus0KIAA1109 CL E G H84162617822ALKURAYA-KUCINSKAS SYNDROME617822CN737163OMIM1167126953611565
HP:0001762HP:0001762Talipes equinovarus0KY CL E G H339855496689ORPHA133926576605739
HP:0001762HP:0001762Talipes equinovarus0KY CL E G H339855617114Myopathy, myofibrillar, 7617114C4310711OMIM133926576605739
HP:0001762HP:0001762Talipes equinovarus0L1CAM CL E G H3897303350Spastic paraplegia 1303350C0795953OMIM12935196470308840
HP:0001762HP:0001762Talipes equinovarus0LETM1 CL E G H39541941904p partial monosomy syndrome194190C1956097OMIM141756556604407
HP:0001762HP:0001762Talipes equinovarus0LETM1 CL E G H3954280Halal Setton Wang syndromeORPHA141756556604407
HP:0001762HP:0001762Talipes equinovarus0LGI4 CL E G H163175617468Arthrogryposis multiplex congenita, neurogenic, with myelin defect617468C4479539OMIM194818712608303
HP:0001762HP:0001762Talipes equinovarus0LIFR CL E G H39773206ORPHA1323466597151443
HP:0001762HP:0001762Talipes equinovarus0LIMS2 CL E G H55679616827Muscular dystrophy, limb-girdle, type 2W616827C4225192OMIM1410916084607908
HP:0001762HP:0001762Talipes equinovarus0LMX1B CL E G H4010161200Nail-patella syndrome161200C0027341OMIM11953046654602575
HP:0001762HP:0001762Talipes equinovarus0MAP3K7 CL E G H6885617137Frontometaphyseal dysplasia 2617137C4310697OMIM113646859602614
HP:0001762HP:0001762Talipes equinovarus0MCTP2 CL E G H557841596ORPHA1910125636616297
HP:0001762HP:0001762Talipes equinovarus0MEGF10 CL E G H84466614399Myopathy, areflexia, respiratory distress, and dysphagia, early-onset614399C3280679OMIM11949529634612453
HP:0001762HP:0001762Talipes equinovarus0MEGF8 CL E G H1954614976Carpenter syndrome 2614976C3554247OMIM1192253233604267
HP:0001762HP:0001762Talipes equinovarus0MFSD2A CL E G H84879616486Primary autosomal recessive microcephaly 15616486C4225310OMIM163325897614397
HP:0001762HP:0001762Talipes equinovarus0MTMR2 CL E G H8898601382Charcot-Marie-Tooth disease, type 4B1601382C1832399OMIM1242907450603557
HP:0001762HP:0001762Talipes equinovarus0MUSK CL E G H4593208150Pena-Shokeir syndrome type I208150C1276035OMIM1222777525601296
HP:0001762HP:0001762Talipes equinovarus0MYH3 CL E G H4621601680Distal arthrogryposis type 2B601680C1834523OMIM1453157573160720
HP:0001762HP:0001762Talipes equinovarus0MYH3 CL E G H46212053Ectodermal dysplasia neurosensory deafnessORPHA1453157573160720
HP:0001762HP:0001762Talipes equinovarus0MYH3 CL E G H4621193700Freeman-Sheldon syndrome193700C0265224OMIM1453157573160720
HP:0001762HP:0001762Talipes equinovarus0MYH8 CL E G H4626158300Hecht syndrome158300C0265226OMIM132257578160741
HP:0001762HP:0001762Talipes equinovarus0MYMK CL E G H3898271358ORPHA175733778615345
HP:0001762HP:0001762Talipes equinovarus0MYMK CL E G H389827254940Congenital nonprogressive myopathy with Moebius and Robin sequences254940C1850746OMIM175733778615345
HP:0001762HP:0001762Talipes equinovarus0NALCN CL E G H2592322053Ectodermal dysplasia neurosensory deafnessORPHA16524719082611549
HP:0001762HP:0001762Talipes equinovarus0NDE1 CL E G H54820605013Microhydranencephaly605013C1857977OMIM120116117619609449
HP:0001762HP:0001762Talipes equinovarus0NEK8 CL E G H284086615415Renal-hepatic-pancreatic dysplasia 2615415C3809434OMIM11813913387609799
HP:0001762HP:0001762Talipes equinovarus0NEK9 CL E G H91754617022Lethal congenital contracture syndrome 10617022C4310760OMIM134518591609798
HP:0001762HP:0001762Talipes equinovarus0NELFA CL E G H7469280Halal Setton Wang syndromeORPHA1416712768606026
HP:0001762HP:0001762Talipes equinovarus0NSD2 CL E G H74681941904p partial monosomy syndrome194190C1956097OMIM11422012766602952
HP:0001762HP:0001762Talipes equinovarus0NSD2 CL E G H7468280Halal Setton Wang syndromeORPHA11422012766602952
HP:0001762HP:0001762Talipes equinovarus0OFD1 CL E G H8481300209Simpson-Golabi-Behmel syndrome, type 2300209C1846175OMIM11625102567300170
HP:0001762HP:0001762Talipes equinovarus0ORC1 CL E G H4998224690Meier-Gorlin syndrome 1224690CN030358OMIM1121038487601902
HP:0001762HP:0001762Talipes equinovarus0ORC6 CL E G H23594613803Meier-Gorlin syndrome 3613803C3151113OMIM169017151607213
HP:0001762HP:0001762Talipes equinovarus0OTUD6B CL E G H51633505237ORPHA164724281612021
HP:0001762HP:0001762Talipes equinovarus0OTUD6B CL E G H51633617452Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies617452C4479520OMIM164724281612021
HP:0001762HP:0001762Talipes equinovarus0PEX1 CL E G H5189214100Zellweger syndrome214100C0043459OMIM11404898850602136
HP:0001762HP:0001762Talipes equinovarus0PEX2 CL E G H5828614866Peroxisome biogenesis disorder 5a (zellweger)614866C3553940OMIM1182089717170993
HP:0001762HP:0001762Talipes equinovarus0PEX26 CL E G H55670614872Peroxisome biogenesis disorder 7A614872C3539168OMIM12727722965608666
HP:0001762HP:0001762Talipes equinovarus0PEX5 CL E G H5830214110Peroxisome biogenesis disorder 2a (zellweger)214110C1859228OMIM1142809719600414
HP:0001762HP:0001762Talipes equinovarus0PEX5 CL E G H5830616716Rhizomelic chondrodysplasia punctata type 5616716C4225237OMIM1142809719600414
HP:0001762HP:0001762Talipes equinovarus0PI4KA CL E G H5297616531Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis616531C4225295OMIM144398983600286
HP:0001762HP:0001762Talipes equinovarus0PIEZO2 CL E G H63895617146Arthrogryposis, distal, with impaired proprioception and touch617146C4310692OMIM13232926270613629
HP:0001762HP:0001762Talipes equinovarus0PIEZO2 CL E G H63895114300Gordon's syndrome114300C0220666OMIM13232926270613629
HP:0001762HP:0001762Talipes equinovarus0PIEZO2 CL E G H63895248700Marden-Walker syndrome248700C0796033OMIM13232926270613629
HP:0001762HP:0001762Talipes equinovarus0PITX1 CL E G H5307119800Talipes equinovarus119800C0009081OMIM118349004602149
HP:0001762HP:0001762Talipes equinovarus0PLEKHG5 CL E G H57449611067Distal spinal muscular atrophy, autosomal recessive 4611067C1970211OMIM11256329105611101
HP:0001762HP:0001762Talipes equinovarus0PLOD1 CL E G H5351225400Ehlers-Danlos syndrome, hydroxylysine-deficient225400C0268342OMIM1424409081153454
HP:0001762HP:0001762Talipes equinovarus0PLOD2 CL E G H5352609220Bruck syndrome 2609220C1836602OMIM1231459082601865
HP:0001762HP:0001762Talipes equinovarus0PLOD2 CL E G H53522771Hydrocephalus costovertebral dysplasia Sprengel anomalyORPHA1231459082601865
HP:0001762HP:0001762Talipes equinovarus0PLOD3 CL E G H8985612394Bone fragility with contractures, arterial rupture, and deafness612394C2676285OMIM13919083603066
HP:0001762HP:0001762Talipes equinovarus0PLXND1 CL E G H23129570ORPHA181049107604282
HP:0001762HP:0001762Talipes equinovarus0PTRH2 CL E G H51651616263Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset616263C4015728OMIM123424265608625
HP:0001762HP:0001762Talipes equinovarus0RAB11B CL E G H9230617807NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER617807C4540498OMIM12149761604198
HP:0001762HP:0001762Talipes equinovarus0RAB3GAP2 CL E G H25782212720Martsolf syndrome212720C0796037OMIM11629417168609275
HP:0001762HP:0001762Talipes equinovarus0RAPSN CL E G H5913208150Pena-Shokeir syndrome type I208150C1276035OMIM1602119863601592
HP:0001762HP:0001762Talipes equinovarus0RBM10 CL E G H8241311900TARP syndrome311900C1839463OMIM1101979896300080
HP:0001762HP:0001762Talipes equinovarus0RECQL4 CL E G H9401268400Rothmund-Thomson syndrome268400C0032339OMIM112220289949603780
HP:0001762HP:0001762Talipes equinovarus0REV3L CL E G H5980570ORPHA191249968602776
HP:0001762HP:0001762Talipes equinovarus0RUSC2 CL E G H9853617773MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61617773C4540424OMIM148223625611053
HP:0001762HP:0001762Talipes equinovarus0RYR1 CL E G H6261597ORPHA1688309410483180901
HP:0001762HP:0001762Talipes equinovarus0RYR1 CL E G H6261178145ORPHA1688309410483180901
HP:0001762HP:0001762Talipes equinovarus0SAMD9 CL E G H54809617053Mirage syndrome617053C4284088OMIM127881348610456
HP:0001762HP:0001762Talipes equinovarus0SATB2 CL E G H23314612313Chromosome 2q32-q33 deletion syndrome612313C2676739OMIM110627421637608148
HP:0001762HP:0001762Talipes equinovarus0SBF2 CL E G H81846604563Charcot-Marie-Tooth disease, type 4B2604563C1858278OMIM1297172135607697
HP:0001762HP:0001762Talipes equinovarus0SCARF2 CL E G H91179600920Marden Walker like syndrome600920C1833136OMIM11335419869613619
HP:0001762HP:0001762Talipes equinovarus0SETBP1 CL E G H26040269150Schinzel-Giedion syndrome269150C0265227OMIM14721215573611060
HP:0001762HP:0001762Talipes equinovarus0SF3B4 CL E G H10262154400Nager syndrome154400C0265245OMIM1385810771605593
HP:0001762HP:0001762Talipes equinovarus0SH3PXD2B CL E G H285590249420Frank Ter Haar syndrome249420C1855305OMIM12026629242613293
HP:0001762HP:0001762Talipes equinovarus0SHROOM4 CL E G H57477300434Stocco dos Santos syndrome300434C1845530OMIM1922829215300579
HP:0001762HP:0001762Talipes equinovarus0SLC25A19 CL E G H60386613710Striatal necrosis, bilateral, and progressive polyneuropathy613710C3150973OMIM189314409606521
HP:0001762HP:0001762Talipes equinovarus0SLC26A2 CL E G H183693307ORPHA15531810994606718
HP:0001762HP:0001762Talipes equinovarus0SLC26A2 CL E G H183693298ORPHA15531810994606718
HP:0001762HP:0001762Talipes equinovarus0SLC26A2 CL E G H1836256050Atelosteogenesis type 2256050C1850554OMIM15531810994606718
HP:0001762HP:0001762Talipes equinovarus0SLC26A2 CL E G H1836222600Diastrophic dysplasia222600C0220726OMIM15531810994606718
HP:0001762HP:0001762Talipes equinovarus0SLC26A2 CL E G H1836226900Multiple epiphyseal dysplasia 4226900C1847593OMIM15531810994606718
HP:0001762HP:0001762Talipes equinovarus0SLC6A9 CL E G H6536617301Glycine encephalopathy with normal serum glycine617301C4310943OMIM135411056601019
HP:0001762HP:0001762Talipes equinovarus0SMOC1 CL E G H64093206920Anophthalmos with limb anomalies206920C0599973OMIM1155420318608488
HP:0001762HP:0001762Talipes equinovarus0SMS CL E G H6611309583Snyder Robinson syndrome309583C0796160OMIM11520611123300105
HP:0001762HP:0001762Talipes equinovarus0SNCA CL E G H6622171695ORPHA13713011138163890
HP:0001762HP:0001762Talipes equinovarus0SNX14 CL E G H57231616354Spinocerebellar ataxia, autosomal recessive 20616354C4225355OMIM1196114977616105
HP:0001762HP:0001762Talipes equinovarus0SOX9 CL E G H6662140Atresia of small intestineORPHA114915511204608160
HP:0001762HP:0001762Talipes equinovarus0SOX9 CL E G H6662114290Camptomelic dysplasia114290C1861922OMIM114915511204608160
HP:0001762HP:0001762Talipes equinovarus0TBX15 CL E G H6913260660Cousin syndrome260660C1850040OMIM153811594604127
HP:0001762HP:0001762Talipes equinovarus0TBX4 CL E G H9496238578ORPHA15913511603601719
HP:0001762HP:0001762Talipes equinovarus0TCTN2 CL E G H79867613885Meckel syndrome type 8613885C3836857OMIM11520325774613846
HP:0001762HP:0001762Talipes equinovarus0TGDS CL E G H23483616145Catel Manzke syndrome616145C1844887OMIM178120324616146
HP:0001762HP:0001762Talipes equinovarus0TGFBR1 CL E G H7046609192Loeys-Dietz syndrome 1609192C2697933OMIM17954111772190181
HP:0001762HP:0001762Talipes equinovarus0TGFBR2 CL E G H7048610168Loeys-Dietz syndrome 2610168C2674876OMIM114857211773190182
HP:0001762HP:0001762Talipes equinovarus0TH CL E G H7054101150ORPHA17734511782191290
HP:0001762HP:0001762Talipes equinovarus0TNNI2 CL E G H7136601680Distal arthrogryposis type 2B601680C1834523OMIM1118711946191043
HP:0001762HP:0001762Talipes equinovarus0TNNT3 CL E G H7140601680Distal arthrogryposis type 2B601680C1834523OMIM149111950600692
HP:0001762HP:0001762Talipes equinovarus0TPM2 CL E G H7169108120Distal arthrogryposis type 1A108120C0220662OMIM14019912011190990
HP:0001762HP:0001762Talipes equinovarus0TPM2 CL E G H7169601680Distal arthrogryposis type 2B601680C1834523OMIM14019912011190990
HP:0001762HP:0001762Talipes equinovarus0TRAIP CL E G H10293616777Seckel syndrome 9616777C4225212OMIM122730764605958
HP:0001762HP:0001762Talipes equinovarus0TRIM2 CL E G H23321615490Charcot-Marie-Tooth disease, axonal, type 2R615490C3809655OMIM1816915974614141
HP:0001762HP:0001762Talipes equinovarus0TRPV4 CL E G H59341600175Distal spinal muscular atrophy, congenital nonprogressive600175C1838492OMIM18253918083605427
HP:0001762HP:0001762Talipes equinovarus0TRPV4 CL E G H59341181405Scapuloperoneal spinal muscular atrophy181405C0751335OMIM18253918083605427
HP:0001762HP:0001762Talipes equinovarus0USP8 CL E G H9101401795ORPHA118512631603158
HP:0001762HP:0001762Talipes equinovarus0VANGL1 CL E G H818393027Iris dysplasia hypertelorism deafnessORPHA12024015512610132
HP:0001762HP:0001762Talipes equinovarus0WDR73 CL E G H84942251300Galloway-Mowat syndrome 1251300CN031715OMIM1129525928616144
HP:0001762HP:0001762Talipes equinovarus0WHCR CL E G H74671941904p partial monosomy syndrome194190C1956097OMIM1127640
HP:0001762HP:0001762Talipes equinovarus0WNT7A CL E G H7476228930Fuhrmann syndrome228930C1856728OMIM1115012786601570
HP:0001762HP:0001762Talipes equinovarus0ZC4H2 CL E G H55906314580Wieacker Wolff syndrome314580C0796200OMIM11719424931300897
HP:0001762HP:0001762Talipes equinovarus0ZFYVE27 CL E G H118813610244Spastic paraplegia 33, autosomal dominant610244C1853251OMIM1411326559610243
HP:0001762HP:0001762Talipes equinovarus0ZNF148 CL E G H7707617260Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies617260C4310644OMIM144212933601897
HP:0001762HP:0001762Talipes equinovarus0ZSWIM6 CL E G H57688603671Acromelic frontonasal dysostosis603671C1863616OMIM126229316615951
HP:0001762HP:0001762Talipes equinovarus0ZSWIM6 CL E G H576881827DextrocardiaC0011813ORPHA126229316615951
HP:0001762HP:0001762Talipes equinovarus1ADGRG6 CL E G H57211616503Lethal congenital contracture syndrome 9616503C4225303OMIM165213841612243
HP:0001762HP:0001762Talipes equinovarus1ALDH18A1 CL E G H5832219150Cutis laxa-corneal clouding-oligophrenia syndrome219150C0268354OMIM1332529722138250
HP:0001762HP:0001762Talipes equinovarus1ALG12 CL E G H79087607143ALG12-congenital disorder of glycosylation607143C2931001OMIM11626319358607144
HP:0001762HP:0001762Talipes equinovarus1ALG3 CL E G H10195601110Congenital disorder of glycosylation type 1D601110C1832736OMIM11912323056608750
HP:0001762HP:0001762Talipes equinovarus1AMER1 CL E G H139285300373Osteopathia striata with cranial sclerosis300373C0432268OMIM14121926837300647
HP:0001762HP:0001762Talipes equinovarus1AP4E1 CL E G H23431613744Spastic paraplegia 51, autosomal recessive613744C3151056OMIM118178573607244
HP:0001762HP:0001762Talipes equinovarus1AP4M1 CL E G H9179612936Spastic paraplegia 50, autosomal recessive612936C2752008OMIM115150574602296
HP:0001762HP:0001762Talipes equinovarus1AP4S1 CL E G H11154614067Spastic paraplegia 52, autosomal recessive614067C3279743OMIM1859575607243
HP:0001762HP:0001762Talipes equinovarus1ARHGAP31 CL E G H57514100300Adams-Oliver syndrome 1100300CN028867OMIM1710329216610911
HP:0001762HP:0001762Talipes equinovarus1ARSI CL E G H340075401815ORPHA127032521610009
HP:0001762HP:0001762Talipes equinovarus1ATP6V0A2 CL E G H23545278250Wrinkly skin syndrome278250C0406587OMIM15630918481611716
HP:0001762HP:0001762Talipes equinovarus1ATP6V1E1 CL E G H529617402CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC617402C4479387OMIM1278857108746
HP:0001762HP:0001762Talipes equinovarus1ATRX CL E G H546847ORPHA1170663886300032
HP:0001762HP:0001762Talipes equinovarus1ATRX CL E G H546301040ATR-X syndrome301040C1845055OMIM1170663886300032
HP:0001762HP:0001762Talipes equinovarus1ATRX CL E G H546309580Mental retardation-hypotonic facies syndrome X-linked, 1309580C0796003OMIM1170663886300032
HP:0001762HP:0001762Talipes equinovarus1B3GALT6 CL E G H12679293359ORPHA14023217978615291
HP:0001762HP:0001762Talipes equinovarus1B3GALT6 CL E G H126792615349Ehlers-Danlos syndrome, progeroid type, 2615349C3809210OMIM14023217978615291
HP:0001762HP:0001762Talipes equinovarus1B3GALT6 CL E G H126792271640Spondyloepimetaphyseal dysplasia with joint laxity271640C0432243OMIM14023217978615291
HP:0001762HP:0001762Talipes equinovarus1B3GAT3 CL E G H26229245600Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects245600C3278404OMIM11343923606374
HP:0001762HP:0001762Talipes equinovarus1B9D1 CL E G H27077614209Meckel syndrome, type 9614209C3280155OMIM11015824123614144
HP:0001762HP:0001762Talipes equinovarus1BICD2 CL E G H23299618291618291618291OMIM13532317208609797
HP:0001762HP:0001762Talipes equinovarus1BICD2 CL E G H23299615290Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant615290C3809049OMIM13532317208609797
HP:0001762HP:0001762Talipes equinovarus1BMPER CL E G H168667608022Diaphanospondylodysostosis608022C1842691OMIM11914824154608699
HP:0001762HP:0001762Talipes equinovarus1BMPR1B CL E G H658609441Acromesomelic dysplasia, Demirhan type609441C4225404OMIM1241951077603248
HP:0001762HP:0001762Talipes equinovarus1BRPF1 CL E G H7862617333Intellectual developmental disorder with dysmorphic facies and ptosis617333C4310617OMIM11811514255602410
HP:0001762HP:0001762Talipes equinovarus1C12orf57 CL E G H113246218340Temtamy syndrome218340C1857512OMIM1812529521615140
HP:0001762HP:0001762Talipes equinovarus1C12orf65 CL E G H91574320375ORPHA11111426784613541
HP:0001762HP:0001762Talipes equinovarus1C12orf65 CL E G H91574615035Spastic paraplegia 55, autosomal recessive615035C3539506OMIM11111426784613541
HP:0001762HP:0001762Talipes equinovarus1CANT1 CL E G H124583251450Desbuquois dysplasia 1251450C4012146OMIM12816619721613165
HP:0001762HP:0001762Talipes equinovarus1CC2D2A CL E G H57545612284Meckel syndrome type 6612284C2676790OMIM19658429253612013
HP:0001762HP:0001762Talipes equinovarus1CCBE1 CL E G H147372235510Hennekam lymphangiectasia-lymphedema syndrome235510C0340834OMIM11330529426612753
HP:0001762HP:0001762Talipes equinovarus1CCDC47 CL E G H57003618268618268618268OMIM1520248560
HP:0001762HP:0001762Talipes equinovarus1CEP55 CL E G H55165236500Hydranencephaly with renal aplasia-dysplasia236500C1856053OMIM12341161610000
HP:0001762HP:0001762Talipes equinovarus1CHMP1A CL E G H5119614961Pontocerebellar hypoplasia type 8614961C3554209OMIM131068740164010
HP:0001762HP:0001762Talipes equinovarus1CHRM3 CL E G H1131100100Prune belly syndrome100100C0033770OMIM18891952118494
HP:0001762HP:0001762Talipes equinovarus1CHRNG CL E G H1146265000Multiple pterygium syndrome Escobar type265000C0265261OMIM1351601967100730
HP:0001762HP:0001762Talipes equinovarus1CHST14 CL E G H113189601776Ehlers-Danlos syndrome, musculocontractural type601776C1866294OMIM1229624464608429
HP:0001762HP:0001762Talipes equinovarus1CHST3 CL E G H9469245600Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects245600C3278404OMIM1392651971603799
HP:0001762HP:0001762Talipes equinovarus1CHST3 CL E G H9469143095Spondyloepiphyseal dysplasia with congenital joint dislocations143095C1840471OMIM1392651971603799
HP:0001762HP:0001762Talipes equinovarus1COG1 CL E G H9382611209COG1 congenital disorder of glycosylation611209C1970016OMIM131346545606973
HP:0001762HP:0001762Talipes equinovarus1COG4 CL E G H2583985172ORPHA1614118620606976
HP:0001762HP:0001762Talipes equinovarus1COG4 CL E G H25839618150SAUL-WILSON SYNDROME618150OMIM1614118620606976
HP:0001762HP:0001762Talipes equinovarus1COL2A1 CL E G H128094068ORPHA15707312200120140
HP:0001762HP:0001762Talipes equinovarus1COL2A1 CL E G H1280183900Spondyloepiphyseal dysplasia183900C0038015OMIM15707312200120140
HP:0001762HP:0001762Talipes equinovarus1COL3A1 CL E G H1281130050Ehlers-Danlos syndrome, type 4130050C0268338OMIM164516472201120180
HP:0001762HP:0001762Talipes equinovarus1COL3A1 CL E G H1281286Imaizumi Kuroki syndromeORPHA164516472201120180
HP:0001762HP:0001762Talipes equinovarus1COL5A1 CL E G H1289286Imaizumi Kuroki syndromeORPHA115916302209120215
HP:0001762HP:0001762Talipes equinovarus1COL6A1 CL E G H1291254090Ullrich congenital muscular dystrophy 1254090CN033863OMIM113710072211120220
HP:0001762HP:0001762Talipes equinovarus1COL6A2 CL E G H1292254090Ullrich congenital muscular dystrophy 1254090CN033863OMIM119111482212120240
HP:0001762HP:0001762Talipes equinovarus1COL6A3 CL E G H1293254090Ullrich congenital muscular dystrophy 1254090CN033863OMIM114316342213120250
HP:0001762HP:0001762Talipes equinovarus1CPLX1 CL E G H108151941904p partial monosomy syndrome194190C1956097OMIM131432309605032
HP:0001762HP:0001762Talipes equinovarus1CRIPT CL E G H9419615789Short stature with microcephaly and distinctive facies615789C4014339OMIM142714312604594
HP:0001762HP:0001762Talipes equinovarus1CRLF1 CL E G H9244272430Cold-induced sweating syndrome 1272430C1848947OMIM137562364604237
HP:0001762HP:0001762Talipes equinovarus1CTBP1 CL E G H14871941904p partial monosomy syndrome194190C1956097OMIM111642494602618
HP:0001762HP:0001762Talipes equinovarus1CTDP1 CL E G H9150604168Congenital Cataracts, Facial Dysmorphism, and Neuropathy604168C1858726OMIM112472498604927
HP:0001762HP:0001762Talipes equinovarus1DCHS1 CL E G H8642601390601390601390OMIM12418013681603057
HP:0001762HP:0001762Talipes equinovarus1DES CL E G H1674181400Scapuloperoneal syndrome, neurogenic, Kaeser type181400C1867005OMIM11264942770125660
HP:0001762HP:0001762Talipes equinovarus1DOK7 CL E G H285489208150Pena-Shokeir syndrome type I208150C1276035OMIM17545826594610285
HP:0001762HP:0001762Talipes equinovarus1DONSON CL E G H29980251230Microcephaly-micromelia syndrome251230C1855079OMIM121762993611428
HP:0001762HP:0001762Talipes equinovarus1DPYS CL E G H1807222748Dihydropyrimidinase deficiency222748C0342803OMIM1301083013613326
HP:0001762HP:0001762Talipes equinovarus1DSE CL E G H29940615539Ehlers-Danlos syndrome, musculocontractural type 2615539C3809845OMIM1311521144605942
HP:0001762HP:0001762Talipes equinovarus1DST CL E G H667614653Neuropathy, hereditary sensory and autonomic, type VI614653C3539003OMIM1910171090113810
HP:0001762HP:0001762Talipes equinovarus1EIF2S3 CL E G H196885282ORPHA151783267300161
HP:0001762HP:0001762Talipes equinovarus1EIF4A3 CL E G H9775268305Richieri Costa Pereira syndrome268305C1849348OMIM123418683608546
HP:0001762HP:0001762Talipes equinovarus1ERCC5 CL E G H2073616570Cerebrooculofacioskeletal syndrome 3616570C1851443OMIM1592633437133530
HP:0001762HP:0001762Talipes equinovarus1EVC CL E G H2121225500Chondroectodermal dysplasia225500C0013903OMIM1846523497604831
HP:0001762HP:0001762Talipes equinovarus1EVC2 CL E G H132884225500Chondroectodermal dysplasia225500C0013903OMIM17656719747607261
HP:0001762HP:0001762Talipes equinovarus1EZH2 CL E G H2146277590Weaver syndrome277590C0265210OMIM1422353527601573
HP:0001762HP:0001762Talipes equinovarus1FAT4 CL E G H79633615546Van Maldergem syndrome 2615546C3809875OMIM13731723109612411
HP:0001762HP:0001762Talipes equinovarus1FBXO7 CL E G H25793171695ORPHA11710913586605648
HP:0001762HP:0001762Talipes equinovarus1FBXO7 CL E G H25793260300Parkinson disease 15260300C1850100OMIM11710913586605648
HP:0001762HP:0001762Talipes equinovarus1FGD4 CL E G H121512609311Charcot-Marie-Tooth disease, type 4H609311C1836336OMIM13041519125611104
HP:0001762HP:0001762Talipes equinovarus1FGFRL1 CL E G H538341941904p partial monosomy syndrome194190C1956097OMIM171993693605830
HP:0001762HP:0001762Talipes equinovarus1FKBP10 CL E G H60681259450Bruck syndrome 1259450C1850168OMIM14416118169607063
HP:0001762HP:0001762Talipes equinovarus1FKBP10 CL E G H606812771Hydrocephalus costovertebral dysplasia Sprengel anomalyORPHA14416118169607063
HP:0001762HP:0001762Talipes equinovarus1FLNA CL E G H2316309350Melnick-Needles syndrome309350C0025237OMIM127114723754300017
HP:0001762HP:0001762Talipes equinovarus1FLNB CL E G H231756305ORPHA11225203755603381
HP:0001762HP:0001762Talipes equinovarus1FLNB CL E G H2317108720Atelosteogenesis type 1108720C0265283OMIM11225203755603381
HP:0001762HP:0001762Talipes equinovarus1FLNB CL E G H2317108721Atelosteogenesis type 3108721C3668942OMIM11225203755603381
HP:0001762HP:0001762Talipes equinovarus1FLNB CL E G H2317150250Larsen syndrome, dominant type150250C1835564OMIM11225203755603381
HP:0001762HP:0001762Talipes equinovarus1FLNB CL E G H2317272460Spondylocarpotarsal synostosis syndrome272460C1848934OMIM11225203755603381
HP:0001762HP:0001762Talipes equinovarus1FOXG1 CL E G H2290613454Rett syndrome, congenital variant613454C3150705OMIM11693573811164874
HP:0001762HP:0001762Talipes equinovarus1FUZ CL E G H801993027Iris dysplasia hypertelorism deafnessORPHA153526219610622
HP:0001762HP:0001762Talipes equinovarus1GAN CL E G H8139643ORPHA1804354137605379
HP:0001762HP:0001762Talipes equinovarus1GAN CL E G H8139256850Giant axonal neuropathy256850C1850386OMIM1804354137605379
HP:0001762HP:0001762Talipes equinovarus1GCH1 CL E G H264398808ORPHA12522084193600225
HP:0001762HP:0001762Talipes equinovarus1GCH1 CL E G H2643128230Dystonia 5, Dopa-responsive type128230C1851920OMIM12522084193600225
HP:0001762HP:0001762Talipes equinovarus1GDAP1 CL E G H54332607831Charcot-Marie-Tooth disease type 2K607831C1842983OMIM110335115968606598
HP:0001762HP:0001762Talipes equinovarus1GDAP1 CL E G H54332608340Charcot-Marie-Tooth disease, recessive intermediate A608340C1842197OMIM110335115968606598
HP:0001762HP:0001762Talipes equinovarus1GNPTAB CL E G H79158252500I cell disease252500C2673377OMIM118846229670607840
HP:0001762HP:0001762Talipes equinovarus1GPC3 CL E G H2719312870Simpson-Golabi-Behmel syndrome312870C0796154OMIM1985264451300037
HP:0001762HP:0001762Talipes equinovarus1GPC4 CL E G H2239312870Simpson-Golabi-Behmel syndrome312870C0796154OMIM151964452300168
HP:0001762HP:0001762Talipes equinovarus1GPX4 CL E G H2879250220Spondylometaphyseal dysplasia Sedaghatian type250220C1855229OMIM14564556138322
HP:0001762HP:0001762Talipes equinovarus1GSC CL E G H145258602471Short stature, auditory canal atresia, mandibular hypoplasia, and skeletal abnormalities602471C1865361OMIM17364612138890
HP:0001762HP:0001762Talipes equinovarus1GTPBP2 CL E G H54676617988JABERI-ELAHI SYNDROME617988CN244943OMIM15214670607434
HP:0001762HP:0001762Talipes equinovarus1GUSB CL E G H2990253220Mucopolysaccharidosis type VII253220C0085132OMIM1661574696611499
HP:0001762HP:0001762Talipes equinovarus1HBA1 CL E G H303998791ORPHA12173464823141800
HP:0001762HP:0001762Talipes equinovarus1HBA2 CL E G H304098791ORPHA12962744824141850
HP:0001762HP:0001762Talipes equinovarus1HIST1H1E CL E G H3008617537RAHMAN SYNDROME617537C4479637OMIM154718142220
HP:0001762HP:0001762Talipes equinovarus1HRAS CL E G H3265218040Costello syndrome218040C0587248OMIM1342955173190020
HP:0001762HP:0001762Talipes equinovarus1HSD17B4 CL E G H3295261515Bifunctional peroxisomal enzyme deficiency261515C0342870OMIM11013055213601860
HP:0001762HP:0001762Talipes equinovarus1HSD17B4 CL E G H3295233400Perrault syndrome 1233400OMIM11013055213601860
HP:0001762HP:0001762Talipes equinovarus1HSPB1 CL E G H331599940ORPHA1482265246602195
HP:0001762HP:0001762Talipes equinovarus1HSPG2 CL E G H3339224410Lethal Kniest-like syndrome224410C0432208OMIM1678625273142461
HP:0001762HP:0001762Talipes equinovarus1HSPG2 CL E G H3339255800Schwartz Jampel syndrome type 1255800C0036391OMIM1678625273142461
HP:0001762HP:0001762Talipes equinovarus1IFIH1 CL E G H64135182250Singleton-Merten syndrome 1182250C4225427OMIM12828618873606951
HP:0001762HP:0001762Talipes equinovarus1IGHMBP2 CL E G H3508604320Spinal muscular atrophy, distal, autosomal recessive, 1604320C1858517OMIM11436835542600502
HP:0001762HP:0001762Talipes equinovarus1IRF6 CL E G H3664119500Popliteal pterygium syndrome119500C0265259OMIM13422046121607199
HP:0001762HP:0001762Talipes equinovarus1ITGA8 CL E G H8516191830Renal adysplasia191830C1619700OMIM18566144604063
HP:0001762HP:0001762Talipes equinovarus1JPH1 CL E G H56704607831Charcot-Marie-Tooth disease type 2K607831C1842983OMIM113514201605266
HP:0001762HP:0001762Talipes equinovarus1KAT6B CL E G H2352285201ORPHA17622817582605880
HP:0001762HP:0001762Talipes equinovarus1KAT6B CL E G H23522606170Genitopatellar syndrome606170C1853566OMIM17622817582605880
HP:0001762HP:0001762Talipes equinovarus1KDM5C CL E G H8242300534Mental retardation, syndromic, Claes-Jensen type, X-linked300534C1845243OMIM15632711114314690
HP:0001762HP:0001762Talipes equinovarus1KIAA1109 CL E G H84162617822ALKURAYA-KUCINSKAS SYNDROME617822CN737163OMIM1167126953611565
HP:0001762HP:0001762Talipes equinovarus1KY CL E G H339855496689ORPHA133926576605739
HP:0001762HP:0001762Talipes equinovarus1KY CL E G H339855617114Myopathy, myofibrillar, 7617114C4310711OMIM133926576605739
HP:0001762HP:0001762Talipes equinovarus1L1CAM CL E G H3897303350Spastic paraplegia 1303350C0795953OMIM12935196470308840
HP:0001762HP:0001762Talipes equinovarus1LETM1 CL E G H39541941904p partial monosomy syndrome194190C1956097OMIM141756556604407
HP:0001762HP:0001762Talipes equinovarus1LETM1 CL E G H3954280Halal Setton Wang syndromeORPHA141756556604407
HP:0001762HP:0001762Talipes equinovarus1LGI4 CL E G H163175617468Arthrogryposis multiplex congenita, neurogenic, with myelin defect617468C4479539OMIM194818712608303
HP:0001762HP:0001762Talipes equinovarus1LIFR CL E G H39773206ORPHA1323466597151443
HP:0001762HP:0001762Talipes equinovarus1LIMS2 CL E G H55679616827Muscular dystrophy, limb-girdle, type 2W616827C4225192OMIM1410916084607908
HP:0001762HP:0001762Talipes equinovarus1LMX1B CL E G H4010161200Nail-patella syndrome161200C0027341OMIM11953046654602575
HP:0001762HP:0001762Talipes equinovarus1MAP3K7 CL E G H6885617137Frontometaphyseal dysplasia 2617137C4310697OMIM113646859602614
HP:0001762HP:0001762Talipes equinovarus1MCTP2 CL E G H557841596ORPHA1910125636616297
HP:0001762HP:0001762Talipes equinovarus1MEGF10 CL E G H84466614399Myopathy, areflexia, respiratory distress, and dysphagia, early-onset614399C3280679OMIM11949529634612453
HP:0001762HP:0001762Talipes equinovarus1MEGF8 CL E G H1954614976Carpenter syndrome 2614976C3554247OMIM1192253233604267
HP:0001762HP:0001762Talipes equinovarus1MFSD2A CL E G H84879616486Primary autosomal recessive microcephaly 15616486C4225310OMIM163325897614397
HP:0001762HP:0001762Talipes equinovarus1MTMR2 CL E G H8898601382Charcot-Marie-Tooth disease, type 4B1601382C1832399OMIM1242907450603557
HP:0001762HP:0001762Talipes equinovarus1MUSK CL E G H4593208150Pena-Shokeir syndrome type I208150C1276035OMIM1222777525601296
HP:0001762HP:0001762Talipes equinovarus1MYH3 CL E G H4621601680Distal arthrogryposis type 2B601680C1834523OMIM1453157573160720
HP:0001762HP:0001762Talipes equinovarus1MYH3 CL E G H46212053Ectodermal dysplasia neurosensory deafnessORPHA1453157573160720
HP:0001762HP:0001762Talipes equinovarus1MYH3 CL E G H4621193700Freeman-Sheldon syndrome193700C0265224OMIM1453157573160720
HP:0001762HP:0001762Talipes equinovarus1MYH8 CL E G H4626158300Hecht syndrome158300C0265226OMIM132257578160741
HP:0001762HP:0001762Talipes equinovarus1MYMK CL E G H3898271358ORPHA175733778615345
HP:0001762HP:0001762Talipes equinovarus1MYMK CL E G H389827254940Congenital nonprogressive myopathy with Moebius and Robin sequences254940C1850746OMIM175733778615345
HP:0001762HP:0001762Talipes equinovarus1NALCN CL E G H2592322053Ectodermal dysplasia neurosensory deafnessORPHA16524719082611549
HP:0001762HP:0001762Talipes equinovarus1NDE1 CL E G H54820605013Microhydranencephaly605013C1857977OMIM120116117619609449
HP:0001762HP:0001762Talipes equinovarus1NEK8 CL E G H284086615415Renal-hepatic-pancreatic dysplasia 2615415C3809434OMIM11813913387609799
HP:0001762HP:0001762Talipes equinovarus1NEK9 CL E G H91754617022Lethal congenital contracture syndrome 10617022C4310760OMIM134518591609798
HP:0001762HP:0001762Talipes equinovarus1NELFA CL E G H7469280Halal Setton Wang syndromeORPHA1416712768606026
HP:0001762HP:0001762Talipes equinovarus1NSD2 CL E G H74681941904p partial monosomy syndrome194190C1956097OMIM11422012766602952
HP:0001762HP:0001762Talipes equinovarus1NSD2 CL E G H7468280Halal Setton Wang syndromeORPHA11422012766602952
HP:0001762HP:0001762Talipes equinovarus1OFD1 CL E G H8481300209Simpson-Golabi-Behmel syndrome, type 2300209C1846175OMIM11625102567300170
HP:0001762HP:0001762Talipes equinovarus1ORC1 CL E G H4998224690Meier-Gorlin syndrome 1224690CN030358OMIM1121038487601902
HP:0001762HP:0001762Talipes equinovarus1ORC6 CL E G H23594613803Meier-Gorlin syndrome 3613803C3151113OMIM169017151607213
HP:0001762HP:0001762Talipes equinovarus1OTUD6B CL E G H51633505237ORPHA164724281612021
HP:0001762HP:0001762Talipes equinovarus1OTUD6B CL E G H51633617452Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies617452C4479520OMIM164724281612021
HP:0001762HP:0001762Talipes equinovarus1PEX1 CL E G H5189214100Zellweger syndrome214100C0043459OMIM11404898850602136
HP:0001762HP:0001762Talipes equinovarus1PEX2 CL E G H5828614866Peroxisome biogenesis disorder 5a (zellweger)614866C3553940OMIM1182089717170993
HP:0001762HP:0001762Talipes equinovarus1PEX26 CL E G H55670614872Peroxisome biogenesis disorder 7A614872C3539168OMIM12727722965608666
HP:0001762HP:0001762Talipes equinovarus1PEX5 CL E G H5830214110Peroxisome biogenesis disorder 2a (zellweger)214110C1859228OMIM1142809719600414
HP:0001762HP:0001762Talipes equinovarus1PEX5 CL E G H5830616716Rhizomelic chondrodysplasia punctata type 5616716C4225237OMIM1142809719600414
HP:0001762HP:0001762Talipes equinovarus1PI4KA CL E G H5297616531Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis616531C4225295OMIM144398983600286
HP:0001762HP:0001762Talipes equinovarus1PIEZO2 CL E G H63895617146Arthrogryposis, distal, with impaired proprioception and touch617146C4310692OMIM13232926270613629
HP:0001762HP:0001762Talipes equinovarus1PIEZO2 CL E G H63895114300Gordon's syndrome114300C0220666OMIM13232926270613629
HP:0001762HP:0001762Talipes equinovarus1PIEZO2 CL E G H63895248700Marden-Walker syndrome248700C0796033OMIM13232926270613629
HP:0001762HP:0001762Talipes equinovarus1PITX1 CL E G H5307119800Talipes equinovarus119800C0009081OMIM118349004602149
HP:0001762HP:0001762Talipes equinovarus1PLEKHG5 CL E G H57449611067Distal spinal muscular atrophy, autosomal recessive 4611067C1970211OMIM11256329105611101
HP:0001762HP:0001762Talipes equinovarus1PLOD1 CL E G H5351225400Ehlers-Danlos syndrome, hydroxylysine-deficient225400C0268342OMIM1424409081153454
HP:0001762HP:0001762Talipes equinovarus1PLOD2 CL E G H5352609220Bruck syndrome 2609220C1836602OMIM1231459082601865
HP:0001762HP:0001762Talipes equinovarus1PLOD2 CL E G H53522771Hydrocephalus costovertebral dysplasia Sprengel anomalyORPHA1231459082601865
HP:0001762HP:0001762Talipes equinovarus1PLOD3 CL E G H8985612394Bone fragility with contractures, arterial rupture, and deafness612394C2676285OMIM13919083603066
HP:0001762HP:0001762Talipes equinovarus1PLXND1 CL E G H23129570ORPHA181049107604282
HP:0001762HP:0001762Talipes equinovarus1PTRH2 CL E G H51651616263Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset616263C4015728OMIM123424265608625
HP:0001762HP:0001762Talipes equinovarus1RAB11B CL E G H9230617807NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER617807C4540498OMIM12149761604198
HP:0001762HP:0001762Talipes equinovarus1RAB3GAP2 CL E G H25782212720Martsolf syndrome212720C0796037OMIM11629417168609275
HP:0001762HP:0001762Talipes equinovarus1RAPSN CL E G H5913208150Pena-Shokeir syndrome type I208150C1276035OMIM1602119863601592
HP:0001762HP:0001762Talipes equinovarus1RBM10 CL E G H8241311900TARP syndrome311900C1839463OMIM1101979896300080
HP:0001762HP:0001762Talipes equinovarus1RECQL4 CL E G H9401268400Rothmund-Thomson syndrome268400C0032339OMIM112220289949603780
HP:0001762HP:0001762Talipes equinovarus1REV3L CL E G H5980570ORPHA191249968602776
HP:0001762HP:0001762Talipes equinovarus1RUSC2 CL E G H9853617773MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61617773C4540424OMIM148223625611053
HP:0001762HP:0001762Talipes equinovarus1RYR1 CL E G H6261178145ORPHA1688309410483180901
HP:0001762HP:0001762Talipes equinovarus1RYR1 CL E G H6261597ORPHA1688309410483180901
HP:0001762HP:0001762Talipes equinovarus1SAMD9 CL E G H54809617053Mirage syndrome617053C4284088OMIM127881348610456
HP:0001762HP:0001762Talipes equinovarus1SATB2 CL E G H23314612313Chromosome 2q32-q33 deletion syndrome612313C2676739OMIM110627421637608148
HP:0001762HP:0001762Talipes equinovarus1SBF2 CL E G H81846604563Charcot-Marie-Tooth disease, type 4B2604563C1858278OMIM1297172135607697
HP:0001762HP:0001762Talipes equinovarus1SCARF2 CL E G H91179600920Marden Walker like syndrome600920C1833136OMIM11335419869613619
HP:0001762HP:0001762Talipes equinovarus1SETBP1 CL E G H26040269150Schinzel-Giedion syndrome269150C0265227OMIM14721215573611060
HP:0001762HP:0001762Talipes equinovarus1SF3B4 CL E G H10262154400Nager syndrome154400C0265245OMIM1385810771605593
HP:0001762HP:0001762Talipes equinovarus1SH3PXD2B CL E G H285590249420Frank Ter Haar syndrome249420C1855305OMIM12026629242613293
HP:0001762HP:0001762Talipes equinovarus1SHROOM4 CL E G H57477300434Stocco dos Santos syndrome300434C1845530OMIM1922829215300579
HP:0001762HP:0001762Talipes equinovarus1SLC25A19 CL E G H60386613710Striatal necrosis, bilateral, and progressive polyneuropathy613710C3150973OMIM189314409606521
HP:0001762HP:0001762Talipes equinovarus1SLC26A2 CL E G H183693298ORPHA15531810994606718
HP:0001762HP:0001762Talipes equinovarus1SLC26A2 CL E G H183693307ORPHA15531810994606718
HP:0001762HP:0001762Talipes equinovarus1SLC26A2 CL E G H1836256050Atelosteogenesis type 2256050C1850554OMIM15531810994606718
HP:0001762HP:0001762Talipes equinovarus1SLC26A2 CL E G H1836222600Diastrophic dysplasia222600C0220726OMIM15531810994606718
HP:0001762HP:0001762Talipes equinovarus1SLC26A2 CL E G H1836226900Multiple epiphyseal dysplasia 4226900C1847593OMIM15531810994606718
HP:0001762HP:0001762Talipes equinovarus1SLC6A9 CL E G H6536617301Glycine encephalopathy with normal serum glycine617301C4310943OMIM135411056601019
HP:0001762HP:0001762Talipes equinovarus1SMOC1 CL E G H64093206920Anophthalmos with limb anomalies206920C0599973OMIM1155420318608488
HP:0001762HP:0001762Talipes equinovarus1SMS CL E G H6611309583Snyder Robinson syndrome309583C0796160OMIM11520611123300105
HP:0001762HP:0001762Talipes equinovarus1SNCA CL E G H6622171695ORPHA13713011138163890
HP:0001762HP:0001762Talipes equinovarus1SNX14 CL E G H57231616354Spinocerebellar ataxia, autosomal recessive 20616354C4225355OMIM1196114977616105
HP:0001762HP:0001762Talipes equinovarus1SOX9 CL E G H6662140Atresia of small intestineORPHA114915511204608160
HP:0001762HP:0001762Talipes equinovarus1SOX9 CL E G H6662114290Camptomelic dysplasia114290C1861922OMIM114915511204608160
HP:0001762HP:0001762Talipes equinovarus1TBX15 CL E G H6913260660Cousin syndrome260660C1850040OMIM153811594604127
HP:0001762HP:0001762Talipes equinovarus1TBX4 CL E G H9496238578ORPHA15913511603601719
HP:0001762HP:0001762Talipes equinovarus1TCTN2 CL E G H79867613885Meckel syndrome type 8613885C3836857OMIM11520325774613846
HP:0001762HP:0001762Talipes equinovarus1TGDS CL E G H23483616145Catel Manzke syndrome616145C1844887OMIM178120324616146
HP:0001762HP:0001762Talipes equinovarus1TGFBR1 CL E G H7046609192Loeys-Dietz syndrome 1609192C2697933OMIM17954111772190181
HP:0001762HP:0001762Talipes equinovarus1TGFBR2 CL E G H7048610168Loeys-Dietz syndrome 2610168C2674876OMIM114857211773190182
HP:0001762HP:0001762Talipes equinovarus1TH CL E G H7054101150ORPHA17734511782191290
HP:0001762HP:0001762Talipes equinovarus1TNNI2 CL E G H7136601680Distal arthrogryposis type 2B601680C1834523OMIM1118711946191043
HP:0001762HP:0001762Talipes equinovarus1TNNT3 CL E G H7140601680Distal arthrogryposis type 2B601680C1834523OMIM149111950600692
HP:0001762HP:0001762Talipes equinovarus1TPM2 CL E G H7169108120Distal arthrogryposis type 1A108120C0220662OMIM14019912011190990
HP:0001762HP:0001762Talipes equinovarus1TPM2 CL E G H7169601680Distal arthrogryposis type 2B601680C1834523OMIM14019912011190990
HP:0001762HP:0001762Talipes equinovarus1TRAIP CL E G H10293616777Seckel syndrome 9616777C4225212OMIM122730764605958
HP:0001762HP:0001762Talipes equinovarus1TRIM2 CL E G H23321615490Charcot-Marie-Tooth disease, axonal, type 2R615490C3809655OMIM1816915974614141
HP:0001762HP:0001762Talipes equinovarus1TRPV4 CL E G H59341600175Distal spinal muscular atrophy, congenital nonprogressive600175C1838492OMIM18253918083605427
HP:0001762HP:0001762Talipes equinovarus1TRPV4 CL E G H59341181405Scapuloperoneal spinal muscular atrophy181405C0751335OMIM18253918083605427
HP:0001762HP:0001762Talipes equinovarus1USP8 CL E G H9101401795ORPHA118512631603158
HP:0001762HP:0001762Talipes equinovarus1VANGL1 CL E G H818393027Iris dysplasia hypertelorism deafnessORPHA12024015512610132
HP:0001762HP:0001762Talipes equinovarus1WDR73 CL E G H84942251300Galloway-Mowat syndrome 1251300CN031715OMIM1129525928616144
HP:0001762HP:0001762Talipes equinovarus1WHCR CL E G H74671941904p partial monosomy syndrome194190C1956097OMIM1127640
HP:0001762HP:0001762Talipes equinovarus1WNT7A CL E G H7476228930Fuhrmann syndrome228930C1856728OMIM1115012786601570
HP:0001762HP:0001762Talipes equinovarus1ZC4H2 CL E G H55906314580Wieacker Wolff syndrome314580C0796200OMIM11719424931300897
HP:0001762HP:0001762Talipes equinovarus1ZFYVE27 CL E G H118813610244Spastic paraplegia 33, autosomal dominant610244C1853251OMIM1411326559610243
HP:0001762HP:0001762Talipes equinovarus1ZNF148 CL E G H7707617260Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies617260C4310644OMIM144212933601897
HP:0001762HP:0001762Talipes equinovarus1ZSWIM6 CL E G H57688603671Acromelic frontonasal dysostosis603671C1863616OMIM126229316615951
HP:0001762HP:0001762Talipes equinovarus1ZSWIM6 CL E G H576881827DextrocardiaC0011813ORPHA126229316615951
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0001762HP:0001762Talipes equinovarus0ACTA1 CL E G H582020ORPHA0217272129102610
HP:0001762HP:0001762Talipes equinovarus0ALDH18A1 CL E G H5832616603Cutis laxa, autosomal dominant 3616603C4225268OMIM0332529722138250
HP:0001762HP:0001762Talipes equinovarus0ANK1 CL E G H286251066ORPHA0111388492612641
HP:0001762HP:0001762Talipes equinovarus0AP4B1 CL E G H10717614066Spastic paraplegia 47, autosomal recessive614066C3279738OMIM021140572607245
HP:0001762HP:0001762Talipes equinovarus0ARVCF CL E G H421567ORPHA02477728602269
HP:0001762HP:0001762Talipes equinovarus0B4GALT7 CL E G H11285130070Ehlers-Danlos syndrome progeroid type130070C1869122OMIM09138930604327
HP:0001762HP:0001762Talipes equinovarus0BCOR CL E G H54880300166Oculofaciocardiodental syndrome300166C1846265OMIM05541520893300485
HP:0001762HP:0001762Talipes equinovarus0BIN1 CL E G H274169186ORPHA0173151052601248
HP:0001762HP:0001762Talipes equinovarus0BIN1 CL E G H274255200Autosomal recessive centronuclear myopathy255200C0410204OMIM0173151052601248
HP:0001762HP:0001762Talipes equinovarus0BMPR1B CL E G H65893388ORPHA0241951077603248
HP:0001762HP:0001762Talipes equinovarus0CHN1 CL E G H1123233D ercole syndromeORPHA0111111943118423
HP:0001762HP:0001762Talipes equinovarus0CHRM3 CL E G H11312970Idiopathic diffuse interstitial fibrosisORPHA08891952118494
HP:0001762HP:0001762Talipes equinovarus0COL1A2 CL E G H1278617821EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2617821CN706304OMIM05237942198120160
HP:0001762HP:0001762Talipes equinovarus0COL25A1 CL E G H84570233D ercole syndromeORPHA044118603610004
HP:0001762HP:0001762Talipes equinovarus0COL2A1 CL E G H128093346ORPHA05707312200120140
HP:0001762HP:0001762Talipes equinovarus0COLQ CL E G H829298915ORPHA0702622226603033
HP:0001762HP:0001762Talipes equinovarus0COMT CL E G H1312567ORPHA0155552228116790
HP:0001762HP:0001762Talipes equinovarus0DYM CL E G H54808223800Dyggve-Melchior-Clausen syndrome223800C0265286OMIM03712421317607461
HP:0001762HP:0001762Talipes equinovarus0DYNC2H1 CL E G H79659613091Short-rib thoracic dysplasia 3 with or without polydactyly613091C2751311OMIM02078892962603297
HP:0001762HP:0001762Talipes equinovarus0EBP CL E G H1068235173ORPHA0912373133300205
HP:0001762HP:0001762Talipes equinovarus0ECEL1 CL E G H9427615065Distal arthrogryposis type 5D615065C3554415OMIM0331063147605896
HP:0001762HP:0001762Talipes equinovarus0EED CL E G H87263447ORPHA09493188605984
HP:0001762HP:0001762Talipes equinovarus0EHMT1 CL E G H79813610253Chromosome 9q deletion syndrome610253C0795833OMIM09474624650607001
HP:0001762HP:0001762Talipes equinovarus0ENTPD1 CL E G H953615683Spastic paraplegia 64, autosomal recessive615683C3810289OMIM06533363601752
HP:0001762HP:0001762Talipes equinovarus0EZH2 CL E G H21463447ORPHA0422353527601573
HP:0001762HP:0001762Talipes equinovarus0FBN2 CL E G H2201121050Congenital contractural arachnodactyly121050C0220668OMIM011314023604612570
HP:0001762HP:0001762Talipes equinovarus0FKBP14 CL E G H55033614557Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss614557C3281160OMIM068618625614505
HP:0001762HP:0001762Talipes equinovarus0FKTN CL E G H2218611588Limb-girdle muscular dystrophy-dystroglycanopathy, type C4611588C1969040OMIM0594503622607440
HP:0001762HP:0001762Talipes equinovarus0GDF5 CL E G H820093388ORPHA059984220601146
HP:0001762HP:0001762Talipes equinovarus0GDF5 CL E G H8200610017Multiple synostoses syndrome 2610017C1832708OMIM059984220601146
HP:0001762HP:0001762Talipes equinovarus0GDF5 CL E G H8200113100Type C brachydactyly113100C1862103OMIM059984220601146
HP:0001762HP:0001762Talipes equinovarus0GP1BB CL E G H2812567ORPHA0534044440138720
HP:0001762HP:0001762Talipes equinovarus0GPC3 CL E G H2719373Quinquaud's decalvans folliculitisORPHA0985264451300037
HP:0001762HP:0001762Talipes equinovarus0GPC4 CL E G H2239373Quinquaud's decalvans folliculitisORPHA051964452300168
HP:0001762HP:0001762Talipes equinovarus0HACD1 CL E G H92002020ORPHA01339639610467
HP:0001762HP:0001762Talipes equinovarus0HACE1 CL E G H57531616756Spastic paraplegia and psychomotor retardation with or without seizures616756C4225215OMIM0136321033610876
HP:0001762HP:0001762Talipes equinovarus0HIRA CL E G H7290567ORPHA053994916600237
HP:0001762HP:0001762Talipes equinovarus0HSPG2 CL E G H3339800ORPHA0678625273142461
HP:0001762HP:0001762Talipes equinovarus0HYLS1 CL E G H219844236680Hydrolethalus syndrome 1236680C1856016OMIM0212226558610693
HP:0001762HP:0001762Talipes equinovarus0IGHMBP2 CL E G H3508616155Charcot-Marie-Tooth disease, axonal, type 2S616155C4015349OMIM01436835542600502
HP:0001762HP:0001762Talipes equinovarus0IHH CL E G H354993388ORPHA0331155956600726
HP:0001762HP:0001762Talipes equinovarus0ITGA7 CL E G H36792020ORPHA0103706143600536
HP:0001762HP:0001762Talipes equinovarus0JMJD1C CL E G H221037567ORPHA02950912313604503
HP:0001762HP:0001762Talipes equinovarus0KDM5C CL E G H824285279ORPHA05632711114314690
HP:0001762HP:0001762Talipes equinovarus0KIF1A CL E G H547614255Mental retardation, autosomal dominant 9614255C3280283OMIM0431059888601255
HP:0001762HP:0001762Talipes equinovarus0LAMB2 CL E G H391398915ORPHA01273686487150325
HP:0001762HP:0001762Talipes equinovarus0MAFB CL E G H9935233D ercole syndromeORPHA0251056408608968
HP:0001762HP:0001762Talipes equinovarus0MAP3K20 CL E G H517762020ORPHA073617797609479
HP:0001762HP:0001762Talipes equinovarus0MED13L CL E G H23389616789Mental retardation and distinctive facial features with or without cardiac defects616789C4225208OMIM08135022962608771
HP:0001762HP:0001762Talipes equinovarus0MEGF8 CL E G H195465759ORPHA0192253233604267
HP:0001762HP:0001762Talipes equinovarus0MYBPC1 CL E G H4604614335Distal arthrogryposis type 1B614335C3280526OMIM081157549160794
HP:0001762HP:0001762Talipes equinovarus0MYL2 CL E G H46332020ORPHA0672827583160781
HP:0001762HP:0001762Talipes equinovarus0MYPN CL E G H84665617336Nemaline myopathy 11, autosomal recessive617336C4479186OMIM04666423246608517
HP:0001762HP:0001762Talipes equinovarus0NSD1 CL E G H643243447ORPHA052589614234606681
HP:0001762HP:0001762Talipes equinovarus0NT5C2 CL E G H22978613162Spastic paraplegia 45, autosomal recessive613162C3888209OMIM081008022600417
HP:0001762HP:0001762Talipes equinovarus0PLOD1 CL E G H53511900ORPHA0424409081153454
HP:0001762HP:0001762Talipes equinovarus0RAB23 CL E G H5171565759ORPHA01510514263606144
HP:0001762HP:0001762Talipes equinovarus0RBM8A CL E G H9939274000Radial aplasia-thrombocytopenia syndrome274000C0175703OMIM0142059905605313
HP:0001762HP:0001762Talipes equinovarus0RREB1 CL E G H6239567ORPHA01217110449602209
HP:0001762HP:0001762Talipes equinovarus0RYR1 CL E G H6261169186ORPHA0688309410483180901
HP:0001762HP:0001762Talipes equinovarus0SATB2 CL E G H23314251019ORPHA010627421637608148
HP:0001762HP:0001762Talipes equinovarus0SC5D CL E G H6309607330Lathosterolosis607330C1846421OMIM0618210547602286
HP:0001762HP:0001762Talipes equinovarus0SCYL1 CL E G H57410466794ORPHA0115714372607982
HP:0001762HP:0001762Talipes equinovarus0SCYL1 CL E G H57410616719Spinocerebellar ataxia, autosomal recessive 21616719C4225236OMIM0115714372607982
HP:0001762HP:0001762Talipes equinovarus0SEC24C CL E G H9632567ORPHA02410705607185
HP:0001762HP:0001762Talipes equinovarus0SELENON CL E G H571902020ORPHA06335415999606210
HP:0001762HP:0001762Talipes equinovarus0SF3B4 CL E G H102621788ORPHA0385810771605593
HP:0001762HP:0001762Talipes equinovarus0SKI CL E G H6497182212Shprintzen-Goldberg syndrome182212C1321551OMIM02450210896164780
HP:0001762HP:0001762Talipes equinovarus0SMAD3 CL E G H4088613795Loeys-Dietz syndrome 3613795C3151087OMIM0955926769603109
HP:0001762HP:0001762Talipes equinovarus0SMOC1 CL E G H640931106ORPHA0155420318608488
HP:0001762HP:0001762Talipes equinovarus0SPEG CL E G H10290169186ORPHA01319816901615950
HP:0001762HP:0001762Talipes equinovarus0SUZ12 CL E G H235123447ORPHA037217101606245
HP:0001762HP:0001762Talipes equinovarus0TAZ CL E G H69013020603-Methylglutaconic aciduria type 2302060C0574083OMIM015840011577300394
HP:0001762HP:0001762Talipes equinovarus0TBX1 CL E G H6899567ORPHA08255311592602054
HP:0001762HP:0001762Talipes equinovarus0TCTN2 CL E G H79867616654Joubert syndrome 24616654C4084841OMIM01520325774613846
HP:0001762HP:0001762Talipes equinovarus0TGFB2 CL E G H7042614816Loeys-Dietz syndrome 4614816C3553762OMIM04334111768190220
HP:0001762HP:0001762Talipes equinovarus0TGFB3 CL E G H7043615582Loeys-Dietz syndrome 5615582C3810012OMIM03425311769190230
HP:0001762HP:0001762Talipes equinovarus0TMCO1 CL E G H54499213980Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome213980C1859252OMIM053318188614123
HP:0001762HP:0001762Talipes equinovarus0TMTC3 CL E G H160418617255Lissencephaly 8617255C4310646OMIM0104426899617218
HP:0001762HP:0001762Talipes equinovarus0TPM2 CL E G H71692020ORPHA04019912011190990
HP:0001762HP:0001762Talipes equinovarus0TPM3 CL E G H71702020ORPHA02822512012191030
HP:0001762HP:0001762Talipes equinovarus0TTN CL E G H7273169186ORPHA03461438512403188840
HP:0001762HP:0001762Talipes equinovarus0TWIST2 CL E G H117581200110Ablepharon macrostomia syndrome200110C1860224OMIM098820670607556
HP:0001762HP:0001762Talipes equinovarus0UFD1 CL E G H7353567ORPHA0436812520601754
HP:0001762HP:0001762Talipes equinovarus1ACTA1 CL E G H582020ORPHA0217272129102610
HP:0001762HP:0001762Talipes equinovarus1ALDH18A1 CL E G H5832616603Cutis laxa, autosomal dominant 3616603C4225268OMIM0332529722138250
HP:0001762HP:0001762Talipes equinovarus1ANK1 CL E G H286251066ORPHA0111388492612641
HP:0001762HP:0001762Talipes equinovarus1AP4B1 CL E G H10717614066Spastic paraplegia 47, autosomal recessive614066C3279738OMIM021140572607245
HP:0001762HP:0001762Talipes equinovarus1ARVCF CL E G H421567ORPHA02477728602269
HP:0001762HP:0001762Talipes equinovarus1B4GALT7 CL E G H11285130070Ehlers-Danlos syndrome progeroid type130070C1869122OMIM09138930604327
HP:0001762HP:0001762Talipes equinovarus1BCOR CL E G H54880300166Oculofaciocardiodental syndrome300166C1846265OMIM05541520893300485
HP:0001762HP:0001762Talipes equinovarus1BIN1 CL E G H274169186ORPHA0173151052601248
HP:0001762HP:0001762Talipes equinovarus1BIN1 CL E G H274255200Autosomal recessive centronuclear myopathy255200C0410204OMIM0173151052601248
HP:0001762HP:0001762Talipes equinovarus1BMPR1B CL E G H65893388ORPHA0241951077603248
HP:0001762HP:0001762Talipes equinovarus1CHN1 CL E G H1123233D ercole syndromeORPHA0111111943118423
HP:0001762HP:0001762Talipes equinovarus1CHRM3 CL E G H11312970Idiopathic diffuse interstitial fibrosisORPHA08891952118494
HP:0001762HP:0001762Talipes equinovarus1COL1A2 CL E G H1278617821EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2617821CN706304OMIM05237942198120160
HP:0001762HP:0001762Talipes equinovarus1COL25A1 CL E G H84570233D ercole syndromeORPHA044118603610004
HP:0001762HP:0001762Talipes equinovarus1COL2A1 CL E G H128093346ORPHA05707312200120140
HP:0001762HP:0001762Talipes equinovarus1COLQ CL E G H829298915ORPHA0702622226603033
HP:0001762HP:0001762Talipes equinovarus1COMT CL E G H1312567ORPHA0155552228116790
HP:0001762HP:0001762Talipes equinovarus1DYM CL E G H54808223800Dyggve-Melchior-Clausen syndrome223800C0265286OMIM03712421317607461
HP:0001762HP:0001762Talipes equinovarus1DYNC2H1 CL E G H79659613091Short-rib thoracic dysplasia 3 with or without polydactyly613091C2751311OMIM02078892962603297
HP:0001762HP:0001762Talipes equinovarus1EBP CL E G H1068235173ORPHA0912373133300205
HP:0001762HP:0001762Talipes equinovarus1ECEL1 CL E G H9427615065Distal arthrogryposis type 5D615065C3554415OMIM0331063147605896
HP:0001762HP:0001762Talipes equinovarus1EED CL E G H87263447ORPHA09493188605984
HP:0001762HP:0001762Talipes equinovarus1EHMT1 CL E G H79813610253Chromosome 9q deletion syndrome610253C0795833OMIM09474624650607001
HP:0001762HP:0001762Talipes equinovarus1ENTPD1 CL E G H953615683Spastic paraplegia 64, autosomal recessive615683C3810289OMIM06533363601752
HP:0001762HP:0001762Talipes equinovarus1EZH2 CL E G H21463447ORPHA0422353527601573
HP:0001762HP:0001762Talipes equinovarus1FBN2 CL E G H2201121050Congenital contractural arachnodactyly121050C0220668OMIM011314023604612570
HP:0001762HP:0001762Talipes equinovarus1FKBP14 CL E G H55033614557Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss614557C3281160OMIM068618625614505
HP:0001762HP:0001762Talipes equinovarus1FKTN CL E G H2218611588Limb-girdle muscular dystrophy-dystroglycanopathy, type C4611588C1969040OMIM0594503622607440
HP:0001762HP:0001762Talipes equinovarus1GDF5 CL E G H820093388ORPHA059984220601146
HP:0001762HP:0001762Talipes equinovarus1GDF5 CL E G H8200610017Multiple synostoses syndrome 2610017C1832708OMIM059984220601146
HP:0001762HP:0001762Talipes equinovarus1GDF5 CL E G H8200113100Type C brachydactyly113100C1862103OMIM059984220601146
HP:0001762HP:0001762Talipes equinovarus1GP1BB CL E G H2812567ORPHA0534044440138720
HP:0001762HP:0001762Talipes equinovarus1GPC3 CL E G H2719373Quinquaud's decalvans folliculitisORPHA0985264451300037
HP:0001762HP:0001762Talipes equinovarus1GPC4 CL E G H2239373Quinquaud's decalvans folliculitisORPHA051964452300168
HP:0001762HP:0001762Talipes equinovarus1HACD1 CL E G H92002020ORPHA01339639610467
HP:0001762HP:0001762Talipes equinovarus1HACE1 CL E G H57531616756Spastic paraplegia and psychomotor retardation with or without seizures616756C4225215OMIM0136321033610876
HP:0001762HP:0001762Talipes equinovarus1HIRA CL E G H7290567ORPHA053994916600237
HP:0001762HP:0001762Talipes equinovarus1HSPG2 CL E G H3339800ORPHA0678625273142461
HP:0001762HP:0001762Talipes equinovarus1HYLS1 CL E G H219844236680Hydrolethalus syndrome 1236680C1856016OMIM0212226558610693
HP:0001762HP:0001762Talipes equinovarus1IGHMBP2 CL E G H3508616155Charcot-Marie-Tooth disease, axonal, type 2S616155C4015349OMIM01436835542600502
HP:0001762HP:0001762Talipes equinovarus1IHH CL E G H354993388ORPHA0331155956600726
HP:0001762HP:0001762Talipes equinovarus1ITGA7 CL E G H36792020ORPHA0103706143600536
HP:0001762HP:0001762Talipes equinovarus1JMJD1C CL E G H221037567ORPHA02950912313604503
HP:0001762HP:0001762Talipes equinovarus1KDM5C CL E G H824285279ORPHA05632711114314690
HP:0001762HP:0001762Talipes equinovarus1KIF1A CL E G H547614255Mental retardation, autosomal dominant 9614255C3280283OMIM0431059888601255
HP:0001762HP:0001762Talipes equinovarus1LAMB2 CL E G H391398915ORPHA01273686487150325
HP:0001762HP:0001762Talipes equinovarus1MAFB CL E G H9935233D ercole syndromeORPHA0251056408608968
HP:0001762HP:0001762Talipes equinovarus1MAP3K20 CL E G H517762020ORPHA073617797609479
HP:0001762HP:0001762Talipes equinovarus1MED13L CL E G H23389616789Mental retardation and distinctive facial features with or without cardiac defects616789C4225208OMIM08135022962608771
HP:0001762HP:0001762Talipes equinovarus1MEGF8 CL E G H195465759ORPHA0192253233604267
HP:0001762HP:0001762Talipes equinovarus1MYBPC1 CL E G H4604614335Distal arthrogryposis type 1B614335C3280526OMIM081157549160794
HP:0001762HP:0001762Talipes equinovarus1MYL2 CL E G H46332020ORPHA0672827583160781
HP:0001762HP:0001762Talipes equinovarus1MYPN CL E G H84665617336Nemaline myopathy 11, autosomal recessive617336C4479186OMIM04666423246608517
HP:0001762HP:0001762Talipes equinovarus1NSD1 CL E G H643243447ORPHA052589614234606681
HP:0001762HP:0001762Talipes equinovarus1NT5C2 CL E G H22978613162Spastic paraplegia 45, autosomal recessive613162C3888209OMIM081008022600417
HP:0001762HP:0001762Talipes equinovarus1PLOD1 CL E G H53511900ORPHA0424409081153454
HP:0001762HP:0001762Talipes equinovarus1RAB23 CL E G H5171565759ORPHA01510514263606144
HP:0001762HP:0001762Talipes equinovarus1RBM8A CL E G H9939274000Radial aplasia-thrombocytopenia syndrome274000C0175703OMIM0142059905605313
HP:0001762HP:0001762Talipes equinovarus1RREB1 CL E G H6239567ORPHA01217110449602209
HP:0001762HP:0001762Talipes equinovarus1RYR1 CL E G H6261169186ORPHA0688309410483180901
HP:0001762HP:0001762Talipes equinovarus1SATB2 CL E G H23314251019ORPHA010627421637608148
HP:0001762HP:0001762Talipes equinovarus1SC5D CL E G H6309607330Lathosterolosis607330C1846421OMIM0618210547602286
HP:0001762HP:0001762Talipes equinovarus1SCYL1 CL E G H57410466794ORPHA0115714372607982
HP:0001762HP:0001762Talipes equinovarus1SCYL1 CL E G H57410616719Spinocerebellar ataxia, autosomal recessive 21616719C4225236OMIM0115714372607982
HP:0001762HP:0001762Talipes equinovarus1SEC24C CL E G H9632567ORPHA02410705607185
HP:0001762HP:0001762Talipes equinovarus1SELENON CL E G H571902020ORPHA06335415999606210
HP:0001762HP:0001762Talipes equinovarus1SF3B4 CL E G H102621788ORPHA0385810771605593
HP:0001762HP:0001762Talipes equinovarus1SKI CL E G H6497182212Shprintzen-Goldberg syndrome182212C1321551OMIM02450210896164780
HP:0001762HP:0001762Talipes equinovarus1SMAD3 CL E G H4088613795Loeys-Dietz syndrome 3613795C3151087OMIM0955926769603109
HP:0001762HP:0001762Talipes equinovarus1SMOC1 CL E G H640931106ORPHA0155420318608488
HP:0001762HP:0001762Talipes equinovarus1SPEG CL E G H10290169186ORPHA01319816901615950
HP:0001762HP:0001762Talipes equinovarus1SUZ12 CL E G H235123447ORPHA037217101606245
HP:0001762HP:0001762Talipes equinovarus1TAZ CL E G H69013020603-Methylglutaconic aciduria type 2302060C0574083OMIM015840011577300394
HP:0001762HP:0001762Talipes equinovarus1TBX1 CL E G H6899567ORPHA08255311592602054
HP:0001762HP:0001762Talipes equinovarus1TCTN2 CL E G H79867616654Joubert syndrome 24616654C4084841OMIM01520325774613846
HP:0001762HP:0001762Talipes equinovarus1TGFB2 CL E G H7042614816Loeys-Dietz syndrome 4614816C3553762OMIM04334111768190220
HP:0001762HP:0001762Talipes equinovarus1TGFB3 CL E G H7043615582Loeys-Dietz syndrome 5615582C3810012OMIM03425311769190230
HP:0001762HP:0001762Talipes equinovarus1TMCO1 CL E G H54499213980Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome213980C1859252OMIM053318188614123
HP:0001762HP:0001762Talipes equinovarus1TMTC3 CL E G H160418617255Lissencephaly 8617255C4310646OMIM0104426899617218
HP:0001762HP:0001762Talipes equinovarus1TPM2 CL E G H71692020ORPHA04019912011190990
HP:0001762HP:0001762Talipes equinovarus1TPM3 CL E G H71702020ORPHA02822512012191030
HP:0001762HP:0001762Talipes equinovarus1TTN CL E G H7273169186ORPHA03461438512403188840
HP:0001762HP:0001762Talipes equinovarus1TWIST2 CL E G H117581200110Ablepharon macrostomia syndrome200110C1860224OMIM098820670607556
HP:0001762HP:0001762Talipes equinovarus1UFD1 CL E G H7353567ORPHA0436812520601754


Genes (249) :ACTA1 ADGRG6 ALDH18A1 ALG12 ALG3 AMER1 ANK1 AP4B1 AP4E1 AP4M1 AP4S1 ARHGAP31 ARSI ARVCF ATP6V0A2 ATP6V1E1 ATRX B3GALT6 B3GAT3 B4GALT7 B9D1 BCOR BICD2 BIN1 BMPER BMPR1B BRPF1 C12ORF57 C12ORF65 C12orf57 C12orf65 CANT1 CC2D2A CCBE1 CCDC47 CEP55 CHMP1A CHN1 CHRM3 CHRNG CHST14 CHST3 COG1 COG4 COL1A2 COL25A1 COL2A1 COL3A1 COL5A1 COL6A1 COL6A2 COL6A3 COLQ COMT COQ8A CPLX1 CRIPT CRLF1 CTBP1 CTDP1 CTU2 DCHS1 DES DHCR24 DOK7 DONSON DPYS DSE DST DYM DYNC2H1 EBP ECEL1 EED EHMT1 EIF2S3 EIF4A3 ENTPD1 ERCC5 EVC EVC2 EZH2 FAT4 FBN2 FBXO7 FGD4 FGFRL1 FKBP10 FKBP14 FKTN FLNA FLNB FOXG1 FUZ GAN GCH1 GDAP1 GDF5 GNPTAB GP1BB GPC3 GPC4 GPX4 GSC GTPBP2 GUSB HACD1 HACE1 HBA1 HBA2 HIRA HIST1H1E HRAS HSD17B4 HSPB1 HSPG2 HYLS1 IFIH1 IGHMBP2 IHH IRF6 ITGA7 ITGA8 JMJD1C JPH1 KAT6B KDM5C KIAA1109 KIF1A KY L1CAM LAMB2 LETM1 LGI4 LIFR LIMS2 LMX1B MAFB MAP3K20 MAP3K7 MCTP2 MED13L MEGF10 MEGF8 MFSD2A MTMR2 MUSK MYBPC1 MYH3 MYH7 MYH8 MYL2 MYMK MYPN NALCN NDE1 NDRG1 NEK8 NEK9 NELFA NSD1 NSD2 NT5C2 OFD1 ORC1 ORC6 OTUD6B PEX1 PEX2 PEX26 PEX5 PI4KA PIEZO2 PITX1 PLEKHG5 PLOD1 PLOD2 PLOD3 PLXND1 PTRH2 RAB11B RAB23 RAB3GAP2 RAPSN RBM10 RBM8A RECQL4 REV3L RREB1 RSPO2 RUSC2 RYR1 SAMD9 SATB2 SBF2 SC5D SCARF2 SCYL1 SEC24C SELENON SETBP1 SF3B4 SH3PXD2B SHROOM4 SKI SLC25A19 SLC26A2 SLC6A9 SMAD3 SMOC1 SMS SNCA SNX14 SOX9 SPEG SUZ12 TAF1 TAZ TBX1 TBX15 TBX4 TCTN2 TGDS TGFB2 TGFB3 TGFBR1 TGFBR2 TH TMCO1 TMTC3 TNNI2 TNNT3 TPM2 TPM3 TRAIP TRIM2 TRPV4 TTN TWIST2 UFD1 USP8 VANGL1 WDR73 WHCR WNT7A ZC4H2 ZFYVE27 ZNF148 ZSWIM6

Diseases (263) :2020 616503 616603 219150 607143 601110 300373 251066 614066 613744 612936 614067 100300 401815 567 278250 617402 847 301040 309580 93359 615349 271640 245600 130070 614209 300166 618291 615290 169186 255200 608022 93388 609441 617333 218340 320375 615035 251450 612284 235510 618268 236500 614961 233 2970 100100 265000 601776 143095 611209 85172 618150 617821 93346 94068 183900 130050 286 254090 98915 194190 615789 272430 604168 601390 181400 208150 251230 222748 615539 614653 223800 613091 35173 615065 3447 610253 85282 268305 615683 616570 225500 277590 615546 121050 171695 260300 609311 259450 2771 614557 611588 309350 56305 108720 108721 150250 272460 613454 3027 643 256850 98808 128230 607831 608340 610017 113100 252500 373 312870 250220 602471 617988 253220 616756 98791 617537 218040 261515 233400 99940 800 224410 255800 236680 182250 616155 604320 119500 191830 85201 606170 85279 300534 617822 614255 496689 617114 303350 280 617468 3206 616827 161200 617137 1596 616789 614399 65759 614976 616486 601382 614335 601680 2053 193700 158300 1358 254940 617336 605013 615415 617022 613162 300209 224690 613803 505237 617452 214100 614866 614872 214110 616716 616531 617146 114300 248700 119800 611067 1900 225400 609220 612394 570 616263 617807 212720 311900 274000 268400 617773 178145 597 617053 251019 612313 604563 607330 600920 466794 616719 269150 1788 154400 249420 300434 182212 613710 93298 93307 256050 222600 226900 617301 613795 1106 206920 309583 616354 140 114290 302060 260660 238578 616654 613885 616145 614816 615582 609192 610168 101150 213980 617255 108120 616777 615490 600175 181405 200110 401795 251300 228930 314580 610244 617260 603671 1827 139485 618142 602398 302960 615072 59135 601455 1154 108145 618022 56304 300966
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.