Human Phenotype Ontology 
Grandparent Node:
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Abnormal digit morphology (HP:0011297)help
Parent Node:
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Abnormality of toe (HP:0001780)help
Parent Node:
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Syndactyly (HP:0001159)help
..Starting node
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Toe syndactyly (HP:0001770)help
Term ID: 1770
Name: Toe syndactyly
Synonym: Foot syndactyly; Fused toes; Syndactyly of feet; Syndactyly of toes; Webbed toes
Definition: Webbing or fusion of the toes, involving soft parts only or including bone structure. Bony fusions are referred to as "bony" Syndactyly if the fusion occurs in a radio-ulnar axis. Fusions of bones of the toes in a proximo-distal axis are referred to as "Symphalangism".
Comments:
Reference: HP:0001770
Genes and Diseases:
 
       Child Nodes:
........expand1-3 toe syndactyly (HP:0001459) help
........expand2-3 toe syndactyly (HP:0004691) help
........expand4-5 toe syndactyly (HP:0004692) help
........expand3-4 toe syndactyly (HP:0009779) help
........expandCutaneous syndactyly of toes (HP:0010621) help
................... HP:0005709 2-3 toe cutaneous syndactyly
................... HP:0005767 1-2 toe complete cutaneous syndactyly
................... HP:0005768 2-4 toe cutaneous syndactyly
........expand1-2 toe syndactyly (HP:0010711) help
........expand1-4 toe syndactyly (HP:0010712) help
........expand1-5 toe syndactyly (HP:0010713) help
........expand2-4 toe syndactyly (HP:0010714) help
........expand2-5 toe syndactyly (HP:0010715) help
........expand3-5 toe syndactyly (HP:0010716) help
........expandOsseous syndactyly of toes (HP:0010717) help

 Sister Nodes: 
..expandCutaneous syndactyly (HP:0012725) help
..expandFinger syndactyly (HP:0006101) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0001770HP:0001770Toe syndactyly0APC CL E G H3243258Lindstrom syndromeORPHA119517734583611731
HP:0001770HP:0001770Toe syndactyly0ARHGAP31 CL E G H57514100300Adams-Oliver syndrome 1100300CN028867OMIM1710329216610911
HP:0001770HP:0001770Toe syndactyly0ATP6V1B2 CL E G H526124480Deafness, congenital, with onychodystrophy, autosomal dominant124480C2675730OMIM1493854606939
HP:0001770HP:0001770Toe syndactyly0B3GLCT CL E G H145173709ORPHA11518120207610308
HP:0001770HP:0001770Toe syndactyly0BMP4 CL E G H652607932Microphthalmia syndromic 6607932C1864689OMIM148891071112262
HP:0001770HP:0001770Toe syndactyly0CCNQ CL E G H92002140952ORPHA11122828434300708
HP:0001770HP:0001770Toe syndactyly0CCNQ CL E G H92002300707STAR syndrome300707C2678045OMIM11122828434300708
HP:0001770HP:0001770Toe syndactyly0CD96 CL E G H10225211750C syndrome211750C0796095OMIM134716892606037
HP:0001770HP:0001770Toe syndactyly0CPLANE1 CL E G H65250277170Orofaciodigital syndrome 6277170C2745997OMIM111859425801614571
HP:0001770HP:0001770Toe syndactyly0DEAF1 CL E G H10522819ORPHA11712914677602635
HP:0001770HP:0001770Toe syndactyly0EFNB1 CL E G H1947304110Craniofrontonasal dysplasia304110C0220767OMIM11181813226300035
HP:0001770HP:0001770Toe syndactyly0FBLN1 CL E G H2192608180Synpolydactyly 2608180C1842422OMIM151003600135820
HP:0001770HP:0001770Toe syndactyly0FGFR1 CL E G H226093258ORPHA12653883688136350
HP:0001770HP:0001770Toe syndactyly0FGFR2 CL E G H226393259ORPHA11593363689176943
HP:0001770HP:0001770Toe syndactyly0FGFR2 CL E G H226393260ORPHA11593363689176943
HP:0001770HP:0001770Toe syndactyly0FGFR2 CL E G H226393258ORPHA11593363689176943
HP:0001770HP:0001770Toe syndactyly0FGFR2 CL E G H226387ORPHA11593363689176943
HP:0001770HP:0001770Toe syndactyly0FGFR2 CL E G H2263101400Saethre-Chotzen syndrome101400C0175699OMIM11593363689176943
HP:0001770HP:0001770Toe syndactyly0FIG4 CL E G H9896216340Yunis Varon syndrome216340C1857663OMIM17142516873609390
HP:0001770HP:0001770Toe syndactyly0FLI1 CL E G H23132308Fetal minoxidil syndromeORPHA171253749193067
HP:0001770HP:0001770Toe syndactyly0FLII CL E G H2314819ORPHA121533750600362
HP:0001770HP:0001770Toe syndactyly0FLNA CL E G H2316311300Oto-palato-digital syndrome, type I311300C0265251OMIM127114723754300017
HP:0001770HP:0001770Toe syndactyly0FLNA CL E G H2316304120Oto-palato-digital syndrome, type II304120C1844696OMIM127114723754300017
HP:0001770HP:0001770Toe syndactyly0FRAS1 CL E G H801442052ORPHA16167519185607830
HP:0001770HP:0001770Toe syndactyly0FREM2 CL E G H3416402052ORPHA12551025396608945
HP:0001770HP:0001770Toe syndactyly0GJA1 CL E G H26972710Hm syndromeORPHA11091414274121014
HP:0001770HP:0001770Toe syndactyly0GLI3 CL E G H2737380ORPHA12445374319165240
HP:0001770HP:0001770Toe syndactyly0GLI3 CL E G H2737672Angiofollicular ganglionic hyperplasiaORPHA12445374319165240
HP:0001770HP:0001770Toe syndactyly0GPC3 CL E G H2719373Quinquaud's decalvans folliculitisORPHA1985264451300037
HP:0001770HP:0001770Toe syndactyly0GPC4 CL E G H2239373Quinquaud's decalvans folliculitisORPHA151964452300168
HP:0001770HP:0001770Toe syndactyly0GRIP1 CL E G H234262052ORPHA11815918708604597
HP:0001770HP:0001770Toe syndactyly0HDAC4 CL E G H97591001Branchial arch defectsORPHA11622314063605314
HP:0001770HP:0001770Toe syndactyly0HDAC8 CL E G H55869199Cardiac hydatid cysts with intracavitary expansionORPHA15622713315300269
HP:0001770HP:0001770Toe syndactyly0HDAC8 CL E G H55869300882Cornelia de Lange syndrome 5300882C3550903OMIM15622713315300269
HP:0001770HP:0001770Toe syndactyly0HOXD13 CL E G H323993409ORPHA142715136142989
HP:0001770HP:0001770Toe syndactyly0IQSEC2 CL E G H23096819ORPHA15753929059300522
HP:0001770HP:0001770Toe syndactyly0IQSEC2 CL E G H23096217377ORPHA15753929059300522
HP:0001770HP:0001770Toe syndactyly0IRF6 CL E G H36641300ORPHA13422046121607199
HP:0001770HP:0001770Toe syndactyly0KCNJ2 CL E G H3759170390Andersen Tawil syndrome170390C1563715OMIM1943436263600681
HP:0001770HP:0001770Toe syndactyly0KIF7 CL E G H374654200990Acrocallosal syndrome, Schinzel type200990C0796147OMIM14538630497611254
HP:0001770HP:0001770Toe syndactyly0KMT2A CL E G H4297199Cardiac hydatid cysts with intracavitary expansionORPHA11273797132159555
HP:0001770HP:0001770Toe syndactyly0LMBR1 CL E G H643272378ORPHA11124013243605522
HP:0001770HP:0001770Toe syndactyly0LMBR1 CL E G H6432793405ORPHA11124013243605522
HP:0001770HP:0001770Toe syndactyly0LRP4 CL E G H40383258Lindstrom syndromeORPHA1343756696604270
HP:0001770HP:0001770Toe syndactyly0MEGF8 CL E G H195465759ORPHA1192253233604267
HP:0001770HP:0001770Toe syndactyly0NECTIN1 CL E G H58183253Limb dystoniaORPHA1151959706600644
HP:0001770HP:0001770Toe syndactyly0NIPBL CL E G H25836199Cardiac hydatid cysts with intracavitary expansionORPHA143780928862608667
HP:0001770HP:0001770Toe syndactyly0NOG CL E G H9241184460Stapes ankylosis with broad thumb and toes184460C1866656OMIM164477866602991
HP:0001770HP:0001770Toe syndactyly0PHGDH CL E G H26227256520Neu-Laxova syndrome 1256520CN032230OMIM1231458923606879
HP:0001770HP:0001770Toe syndactyly0PIK3CA CL E G H529060040ORPHA1573798975171834
HP:0001770HP:0001770Toe syndactyly0PORCN CL E G H648402092EhrlichiosisORPHA112121017652300651
HP:0001770HP:0001770Toe syndactyly0PORCN CL E G H64840305600Focal dermal hypoplasia305600C0016395OMIM112121017652300651
HP:0001770HP:0001770Toe syndactyly0RAB23 CL E G H5171565759ORPHA11510514263606144
HP:0001770HP:0001770Toe syndactyly0RAB23 CL E G H51715201000Carpenter syndrome 1201000C1275078OMIM11510514263606144
HP:0001770HP:0001770Toe syndactyly0RAD21 CL E G H5885199Cardiac hydatid cysts with intracavitary expansionORPHA1131499811606462
HP:0001770HP:0001770Toe syndactyly0RAI1 CL E G H10743819ORPHA11164049834607642
HP:0001770HP:0001770Toe syndactyly0RIPK4 CL E G H541011234Chang Davidson Carlson syndromeORPHA116222496605706
HP:0001770HP:0001770Toe syndactyly0SC5D CL E G H630946059ORPHA1618210547602286
HP:0001770HP:0001770Toe syndactyly0SETD5 CL E G H55209199Cardiac hydatid cysts with intracavitary expansionORPHA13823625566615743
HP:0001770HP:0001770Toe syndactyly0SF3B4 CL E G H10262154400Nager syndrome154400C0265245OMIM1385810771605593
HP:0001770HP:0001770Toe syndactyly0SHH CL E G H646993405ORPHA122121010848600725
HP:0001770HP:0001770Toe syndactyly0SIN3A CL E G H25942613406Witteveen-kolk syndrome613406C3150674OMIM11611619353607776
HP:0001770HP:0001770Toe syndactyly0SMC1A CL E G H8243199Cardiac hydatid cysts with intracavitary expansionORPHA110048411111300040
HP:0001770HP:0001770Toe syndactyly0SMC3 CL E G H9126199Cardiac hydatid cysts with intracavitary expansionORPHA1282132468606062
HP:0001770HP:0001770Toe syndactyly0SMO CL E G H66081553ORPHA177111119601500
HP:0001770HP:0001770Toe syndactyly0SMOC1 CL E G H640931106ORPHA1155420318608488
HP:0001770HP:0001770Toe syndactyly0SMOC1 CL E G H64093206920Anophthalmos with limb anomalies206920C0599973OMIM1155420318608488
HP:0001770HP:0001770Toe syndactyly0TBR1 CL E G H107161617ORPHA1187811590604616
HP:0001770HP:0001770Toe syndactyly0TBX15 CL E G H6913260660Cousin syndrome260660C1850040OMIM153811594604127
HP:0001770HP:0001770Toe syndactyly0TCTN3 CL E G H26123258860Orofacial-digital syndrome IV258860C0406727OMIM1129524519613847
HP:0001770HP:0001770Toe syndactyly0TP63 CL E G H8626978ORPHA112828215979603273
HP:0001770HP:0001770Toe syndactyly0TP63 CL E G H8626103285ADULT syndrome103285C1863204OMIM112828215979603273
HP:0001770HP:0001770Toe syndactyly0TP63 CL E G H8626604292Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3604292C1858562OMIM112828215979603273
HP:0001770HP:0001770Toe syndactyly0TWIST1 CL E G H7291101400Saethre-Chotzen syndrome101400C0175699OMIM120911512428601622
HP:0001770HP:0001770Toe syndactyly0WNT10B CL E G H7480225300Split-hand/foot malformation 6225300C2749665OMIM1203712775601906
HP:0001770HP:0001770Toe syndactyly0WNT7A CL E G H7476228930Fuhrmann syndrome228930C1856728OMIM1115012786601570
HP:0001770HP:0001770Toe syndactyly1APC CL E G H3243258Lindstrom syndromeORPHA119517734583611731
HP:0001770HP:0001770Toe syndactyly1ARHGAP31 CL E G H57514100300Adams-Oliver syndrome 1100300CN028867OMIM1710329216610911
HP:0001770HP:0001770Toe syndactyly1ATP6V1B2 CL E G H526124480Deafness, congenital, with onychodystrophy, autosomal dominant124480C2675730OMIM1493854606939
HP:0001770HP:0001770Toe syndactyly1B3GLCT CL E G H145173709ORPHA11518120207610308
HP:0001770HP:0001770Toe syndactyly1BMP4 CL E G H652607932Microphthalmia syndromic 6607932C1864689OMIM148891071112262
HP:0001770HP:0001770Toe syndactyly1CCNQ CL E G H92002140952ORPHA11122828434300708
HP:0001770HP:0001770Toe syndactyly1CCNQ CL E G H92002300707STAR syndrome300707C2678045OMIM11122828434300708
HP:0001770HP:0001770Toe syndactyly1CD96 CL E G H10225211750C syndrome211750C0796095OMIM134716892606037
HP:0001770HP:0001770Toe syndactyly1CPLANE1 CL E G H65250277170Orofaciodigital syndrome 6277170C2745997OMIM111859425801614571
HP:0001770HP:0001770Toe syndactyly1DEAF1 CL E G H10522819ORPHA11712914677602635
HP:0001770HP:0001770Toe syndactyly1EFNB1 CL E G H1947304110Craniofrontonasal dysplasia304110C0220767OMIM11181813226300035
HP:0001770HP:0001770Toe syndactyly1FBLN1 CL E G H2192608180Synpolydactyly 2608180C1842422OMIM151003600135820
HP:0001770HP:0001770Toe syndactyly1FGFR1 CL E G H226093258ORPHA12653883688136350
HP:0001770HP:0001770Toe syndactyly1FGFR2 CL E G H226393260ORPHA11593363689176943
HP:0001770HP:0001770Toe syndactyly1FGFR2 CL E G H226393258ORPHA11593363689176943
HP:0001770HP:0001770Toe syndactyly1FGFR2 CL E G H226387ORPHA11593363689176943
HP:0001770HP:0001770Toe syndactyly1FGFR2 CL E G H226393259ORPHA11593363689176943
HP:0001770HP:0001770Toe syndactyly1FGFR2 CL E G H2263101400Saethre-Chotzen syndrome101400C0175699OMIM11593363689176943
HP:0001770HP:0001770Toe syndactyly1FIG4 CL E G H9896216340Yunis Varon syndrome216340C1857663OMIM17142516873609390
HP:0001770HP:0001770Toe syndactyly1FLI1 CL E G H23132308Fetal minoxidil syndromeORPHA171253749193067
HP:0001770HP:0001770Toe syndactyly1FLII CL E G H2314819ORPHA121533750600362
HP:0001770HP:0001770Toe syndactyly1FLNA CL E G H2316311300Oto-palato-digital syndrome, type I311300C0265251OMIM127114723754300017
HP:0001770HP:0001770Toe syndactyly1FLNA CL E G H2316304120Oto-palato-digital syndrome, type II304120C1844696OMIM127114723754300017
HP:0001770HP:0001770Toe syndactyly1FRAS1 CL E G H801442052ORPHA16167519185607830
HP:0001770HP:0001770Toe syndactyly1FREM2 CL E G H3416402052ORPHA12551025396608945
HP:0001770HP:0001770Toe syndactyly1GJA1 CL E G H26972710Hm syndromeORPHA11091414274121014
HP:0001770HP:0001770Toe syndactyly1GLI3 CL E G H2737380ORPHA12445374319165240
HP:0001770HP:0001770Toe syndactyly1GLI3 CL E G H2737672Angiofollicular ganglionic hyperplasiaORPHA12445374319165240
HP:0001770HP:0001770Toe syndactyly1GPC3 CL E G H2719373Quinquaud's decalvans folliculitisORPHA1985264451300037
HP:0001770HP:0001770Toe syndactyly1GPC4 CL E G H2239373Quinquaud's decalvans folliculitisORPHA151964452300168
HP:0001770HP:0001770Toe syndactyly1GRIP1 CL E G H234262052ORPHA11815918708604597
HP:0001770HP:0001770Toe syndactyly1HDAC4 CL E G H97591001Branchial arch defectsORPHA11622314063605314
HP:0001770HP:0001770Toe syndactyly1HDAC8 CL E G H55869199Cardiac hydatid cysts with intracavitary expansionORPHA15622713315300269
HP:0001770HP:0001770Toe syndactyly1HDAC8 CL E G H55869300882Cornelia de Lange syndrome 5300882C3550903OMIM15622713315300269
HP:0001770HP:0001770Toe syndactyly1HOXD13 CL E G H323993409ORPHA142715136142989
HP:0001770HP:0001770Toe syndactyly1IQSEC2 CL E G H23096819ORPHA15753929059300522
HP:0001770HP:0001770Toe syndactyly1IQSEC2 CL E G H23096217377ORPHA15753929059300522
HP:0001770HP:0001770Toe syndactyly1IRF6 CL E G H36641300ORPHA13422046121607199
HP:0001770HP:0001770Toe syndactyly1KCNJ2 CL E G H3759170390Andersen Tawil syndrome170390C1563715OMIM1943436263600681
HP:0001770HP:0001770Toe syndactyly1KIF7 CL E G H374654200990Acrocallosal syndrome, Schinzel type200990C0796147OMIM14538630497611254
HP:0001770HP:0001770Toe syndactyly1KMT2A CL E G H4297199Cardiac hydatid cysts with intracavitary expansionORPHA11273797132159555
HP:0001770HP:0001770Toe syndactyly1LMBR1 CL E G H643272378ORPHA11124013243605522
HP:0001770HP:0001770Toe syndactyly1LMBR1 CL E G H6432793405ORPHA11124013243605522
HP:0001770HP:0001770Toe syndactyly1LRP4 CL E G H40383258Lindstrom syndromeORPHA1343756696604270
HP:0001770HP:0001770Toe syndactyly1MEGF8 CL E G H195465759ORPHA1192253233604267
HP:0001770HP:0001770Toe syndactyly1NECTIN1 CL E G H58183253Limb dystoniaORPHA1151959706600644
HP:0001770HP:0001770Toe syndactyly1NIPBL CL E G H25836199Cardiac hydatid cysts with intracavitary expansionORPHA143780928862608667
HP:0001770HP:0001770Toe syndactyly1NOG CL E G H9241184460Stapes ankylosis with broad thumb and toes184460C1866656OMIM164477866602991
HP:0001770HP:0001770Toe syndactyly1PHGDH CL E G H26227256520Neu-Laxova syndrome 1256520CN032230OMIM1231458923606879
HP:0001770HP:0001770Toe syndactyly1PIK3CA CL E G H529060040ORPHA1573798975171834
HP:0001770HP:0001770Toe syndactyly1PORCN CL E G H648402092EhrlichiosisORPHA112121017652300651
HP:0001770HP:0001770Toe syndactyly1PORCN CL E G H64840305600Focal dermal hypoplasia305600C0016395OMIM112121017652300651
HP:0001770HP:0001770Toe syndactyly1RAB23 CL E G H5171565759ORPHA11510514263606144
HP:0001770HP:0001770Toe syndactyly1RAB23 CL E G H51715201000Carpenter syndrome 1201000C1275078OMIM11510514263606144
HP:0001770HP:0001770Toe syndactyly1RAD21 CL E G H5885199Cardiac hydatid cysts with intracavitary expansionORPHA1131499811606462
HP:0001770HP:0001770Toe syndactyly1RAI1 CL E G H10743819ORPHA11164049834607642
HP:0001770HP:0001770Toe syndactyly1RIPK4 CL E G H541011234Chang Davidson Carlson syndromeORPHA116222496605706
HP:0001770HP:0001770Toe syndactyly1SC5D CL E G H630946059ORPHA1618210547602286
HP:0001770HP:0001770Toe syndactyly1SETD5 CL E G H55209199Cardiac hydatid cysts with intracavitary expansionORPHA13823625566615743
HP:0001770HP:0001770Toe syndactyly1SF3B4 CL E G H10262154400Nager syndrome154400C0265245OMIM1385810771605593
HP:0001770HP:0001770Toe syndactyly1SHH CL E G H646993405ORPHA122121010848600725
HP:0001770HP:0001770Toe syndactyly1SIN3A CL E G H25942613406Witteveen-kolk syndrome613406C3150674OMIM11611619353607776
HP:0001770HP:0001770Toe syndactyly1SMC1A CL E G H8243199Cardiac hydatid cysts with intracavitary expansionORPHA110048411111300040
HP:0001770HP:0001770Toe syndactyly1SMC3 CL E G H9126199Cardiac hydatid cysts with intracavitary expansionORPHA1282132468606062
HP:0001770HP:0001770Toe syndactyly1SMO CL E G H66081553ORPHA177111119601500
HP:0001770HP:0001770Toe syndactyly1SMOC1 CL E G H640931106ORPHA1155420318608488
HP:0001770HP:0001770Toe syndactyly1SMOC1 CL E G H64093206920Anophthalmos with limb anomalies206920C0599973OMIM1155420318608488
HP:0001770HP:0001770Toe syndactyly1TBR1 CL E G H107161617ORPHA1187811590604616
HP:0001770HP:0001770Toe syndactyly1TBX15 CL E G H6913260660Cousin syndrome260660C1850040OMIM153811594604127
HP:0001770HP:0001770Toe syndactyly1TCTN3 CL E G H26123258860Orofacial-digital syndrome IV258860C0406727OMIM1129524519613847
HP:0001770HP:0001770Toe syndactyly1TP63 CL E G H8626978ORPHA112828215979603273
HP:0001770HP:0001770Toe syndactyly1TP63 CL E G H8626103285ADULT syndrome103285C1863204OMIM112828215979603273
HP:0001770HP:0001770Toe syndactyly1TP63 CL E G H8626604292Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3604292C1858562OMIM112828215979603273
HP:0001770HP:0001770Toe syndactyly1TWIST1 CL E G H7291101400Saethre-Chotzen syndrome101400C0175699OMIM120911512428601622
HP:0001770HP:0001770Toe syndactyly1WNT10B CL E G H7480225300Split-hand/foot malformation 6225300C2749665OMIM1203712775601906
HP:0001770HP:0001770Toe syndactyly1WNT7A CL E G H7476228930Fuhrmann syndrome228930C1856728OMIM1115012786601570
HP:0001770HP:0001770Toe syndactyly2APC CL E G H3243258Lindstrom syndromeORPHA119517734583611731
HP:0001770HP:0001770Toe syndactyly2ARHGAP31 CL E G H57514100300Adams-Oliver syndrome 1100300CN028867OMIM1710329216610911
HP:0001770HP:0001770Toe syndactyly2ATP6V1B2 CL E G H526124480Deafness, congenital, with onychodystrophy, autosomal dominant124480C2675730OMIM1493854606939
HP:0001770HP:0001770Toe syndactyly2B3GLCT CL E G H145173709ORPHA11518120207610308
HP:0001770HP:0001770Toe syndactyly2BMP4 CL E G H652607932Microphthalmia syndromic 6607932C1864689OMIM148891071112262
HP:0001770HP:0001770Toe syndactyly2CCNQ CL E G H92002140952ORPHA11122828434300708
HP:0001770HP:0001770Toe syndactyly2CCNQ CL E G H92002300707STAR syndrome300707C2678045OMIM11122828434300708
HP:0001770HP:0001770Toe syndactyly2CD96 CL E G H10225211750C syndrome211750C0796095OMIM134716892606037
HP:0001770HP:0001770Toe syndactyly2CPLANE1 CL E G H65250277170Orofaciodigital syndrome 6277170C2745997OMIM111859425801614571
HP:0001770HP:0001770Toe syndactyly2DEAF1 CL E G H10522819ORPHA11712914677602635
HP:0001770HP:0001770Toe syndactyly2EFNB1 CL E G H1947304110Craniofrontonasal dysplasia304110C0220767OMIM11181813226300035
HP:0001770HP:0001770Toe syndactyly2FBLN1 CL E G H2192608180Synpolydactyly 2608180C1842422OMIM151003600135820
HP:0001770HP:0001770Toe syndactyly2FGFR1 CL E G H226093258ORPHA12653883688136350
HP:0001770HP:0001770Toe syndactyly2FGFR2 CL E G H226393258ORPHA11593363689176943
HP:0001770HP:0001770Toe syndactyly2FGFR2 CL E G H226387ORPHA11593363689176943
HP:0001770HP:0001770Toe syndactyly2FGFR2 CL E G H226393259ORPHA11593363689176943
HP:0001770HP:0001770Toe syndactyly2FGFR2 CL E G H226393260ORPHA11593363689176943
HP:0001770HP:0001770Toe syndactyly2FGFR2 CL E G H2263101400Saethre-Chotzen syndrome101400C0175699OMIM11593363689176943
HP:0001770HP:0001770Toe syndactyly2FIG4 CL E G H9896216340Yunis Varon syndrome216340C1857663OMIM17142516873609390
HP:0001770HP:0001770Toe syndactyly2FLI1 CL E G H23132308Fetal minoxidil syndromeORPHA171253749193067
HP:0001770HP:0001770Toe syndactyly2FLII CL E G H2314819ORPHA121533750600362
HP:0001770HP:0001770Toe syndactyly2FLNA CL E G H2316311300Oto-palato-digital syndrome, type I311300C0265251OMIM127114723754300017
HP:0001770HP:0001770Toe syndactyly2FLNA CL E G H2316304120Oto-palato-digital syndrome, type II304120C1844696OMIM127114723754300017
HP:0001770HP:0001770Toe syndactyly2FRAS1 CL E G H801442052ORPHA16167519185607830
HP:0001770HP:0001770Toe syndactyly2FREM2 CL E G H3416402052ORPHA12551025396608945
HP:0001770HP:0001770Toe syndactyly2GJA1 CL E G H26972710Hm syndromeORPHA11091414274121014
HP:0001770HP:0001770Toe syndactyly2GLI3 CL E G H2737380ORPHA12445374319165240
HP:0001770HP:0001770Toe syndactyly2GLI3 CL E G H2737672Angiofollicular ganglionic hyperplasiaORPHA12445374319165240
HP:0001770HP:0001770Toe syndactyly2GPC3 CL E G H2719373Quinquaud's decalvans folliculitisORPHA1985264451300037
HP:0001770HP:0001770Toe syndactyly2GPC4 CL E G H2239373Quinquaud's decalvans folliculitisORPHA151964452300168
HP:0001770HP:0001770Toe syndactyly2GRIP1 CL E G H234262052ORPHA11815918708604597
HP:0001770HP:0001770Toe syndactyly2HDAC4 CL E G H97591001Branchial arch defectsORPHA11622314063605314
HP:0001770HP:0001770Toe syndactyly2HDAC8 CL E G H55869199Cardiac hydatid cysts with intracavitary expansionORPHA15622713315300269
HP:0001770HP:0001770Toe syndactyly2HDAC8 CL E G H55869300882Cornelia de Lange syndrome 5300882C3550903OMIM15622713315300269
HP:0001770HP:0001770Toe syndactyly2HOXD13 CL E G H323993409ORPHA142715136142989
HP:0001770HP:0001770Toe syndactyly2IQSEC2 CL E G H23096819ORPHA15753929059300522
HP:0001770HP:0001770Toe syndactyly2IQSEC2 CL E G H23096217377ORPHA15753929059300522
HP:0001770HP:0001770Toe syndactyly2IRF6 CL E G H36641300ORPHA13422046121607199
HP:0001770HP:0001770Toe syndactyly2KCNJ2 CL E G H3759170390Andersen Tawil syndrome170390C1563715OMIM1943436263600681
HP:0001770HP:0001770Toe syndactyly2KIF7 CL E G H374654200990Acrocallosal syndrome, Schinzel type200990C0796147OMIM14538630497611254
HP:0001770HP:0001770Toe syndactyly2KMT2A CL E G H4297199Cardiac hydatid cysts with intracavitary expansionORPHA11273797132159555
HP:0001770HP:0001770Toe syndactyly2LMBR1 CL E G H6432793405ORPHA11124013243605522
HP:0001770HP:0001770Toe syndactyly2LMBR1 CL E G H643272378ORPHA11124013243605522
HP:0001770HP:0001770Toe syndactyly2LRP4 CL E G H40383258Lindstrom syndromeORPHA1343756696604270
HP:0001770HP:0001770Toe syndactyly2MEGF8 CL E G H195465759ORPHA1192253233604267
HP:0001770HP:0001770Toe syndactyly2NECTIN1 CL E G H58183253Limb dystoniaORPHA1151959706600644
HP:0001770HP:0001770Toe syndactyly2NIPBL CL E G H25836199Cardiac hydatid cysts with intracavitary expansionORPHA143780928862608667
HP:0001770HP:0001770Toe syndactyly2NOG CL E G H9241184460Stapes ankylosis with broad thumb and toes184460C1866656OMIM164477866602991
HP:0001770HP:0001770Toe syndactyly2PHGDH CL E G H26227256520Neu-Laxova syndrome 1256520CN032230OMIM1231458923606879
HP:0001770HP:0001770Toe syndactyly2PIK3CA CL E G H529060040ORPHA1573798975171834
HP:0001770HP:0001770Toe syndactyly2PORCN CL E G H648402092EhrlichiosisORPHA112121017652300651
HP:0001770HP:0001770Toe syndactyly2PORCN CL E G H64840305600Focal dermal hypoplasia305600C0016395OMIM112121017652300651
HP:0001770HP:0001770Toe syndactyly2RAB23 CL E G H5171565759ORPHA11510514263606144
HP:0001770HP:0001770Toe syndactyly2RAB23 CL E G H51715201000Carpenter syndrome 1201000C1275078OMIM11510514263606144
HP:0001770HP:0001770Toe syndactyly2RAD21 CL E G H5885199Cardiac hydatid cysts with intracavitary expansionORPHA1131499811606462
HP:0001770HP:0001770Toe syndactyly2RAI1 CL E G H10743819ORPHA11164049834607642
HP:0001770HP:0001770Toe syndactyly2RIPK4 CL E G H541011234Chang Davidson Carlson syndromeORPHA116222496605706
HP:0001770HP:0001770Toe syndactyly2SC5D CL E G H630946059ORPHA1618210547602286
HP:0001770HP:0001770Toe syndactyly2SETD5 CL E G H55209199Cardiac hydatid cysts with intracavitary expansionORPHA13823625566615743
HP:0001770HP:0001770Toe syndactyly2SF3B4 CL E G H10262154400Nager syndrome154400C0265245OMIM1385810771605593
HP:0001770HP:0001770Toe syndactyly2SHH CL E G H646993405ORPHA122121010848600725
HP:0001770HP:0001770Toe syndactyly2SIN3A CL E G H25942613406Witteveen-kolk syndrome613406C3150674OMIM11611619353607776
HP:0001770HP:0001770Toe syndactyly2SMC1A CL E G H8243199Cardiac hydatid cysts with intracavitary expansionORPHA110048411111300040
HP:0001770HP:0001770Toe syndactyly2SMC3 CL E G H9126199Cardiac hydatid cysts with intracavitary expansionORPHA1282132468606062
HP:0001770HP:0001770Toe syndactyly2SMO CL E G H66081553ORPHA177111119601500
HP:0001770HP:0001770Toe syndactyly2SMOC1 CL E G H640931106ORPHA1155420318608488
HP:0001770HP:0001770Toe syndactyly2SMOC1 CL E G H64093206920Anophthalmos with limb anomalies206920C0599973OMIM1155420318608488
HP:0001770HP:0001770Toe syndactyly2TBR1 CL E G H107161617ORPHA1187811590604616
HP:0001770HP:0001770Toe syndactyly2TBX15 CL E G H6913260660Cousin syndrome260660C1850040OMIM153811594604127
HP:0001770HP:0001770Toe syndactyly2TCTN3 CL E G H26123258860Orofacial-digital syndrome IV258860C0406727OMIM1129524519613847
HP:0001770HP:0001770Toe syndactyly2TP63 CL E G H8626978ORPHA112828215979603273
HP:0001770HP:0001770Toe syndactyly2TP63 CL E G H8626103285ADULT syndrome103285C1863204OMIM112828215979603273
HP:0001770HP:0001770Toe syndactyly2TP63 CL E G H8626604292Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3604292C1858562OMIM112828215979603273
HP:0001770HP:0001770Toe syndactyly2TWIST1 CL E G H7291101400Saethre-Chotzen syndrome101400C0175699OMIM120911512428601622
HP:0001770HP:0001770Toe syndactyly2WNT10B CL E G H7480225300Split-hand/foot malformation 6225300C2749665OMIM1203712775601906
HP:0001770HP:0001770Toe syndactyly2WNT7A CL E G H7476228930Fuhrmann syndrome228930C1856728OMIM1115012786601570
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0001770HP:0001770Toe syndactyly0ARL6IP6 CL E G H1511881556ORPHA031924048616495
HP:0001770HP:0001770Toe syndactyly0BCR CL E G H613261330ORPHA022111014151410
HP:0001770HP:0001770Toe syndactyly0BRCA1 CL E G H67284ORPHA02824114981100113705
HP:0001770HP:0001770Toe syndactyly0BRCA2 CL E G H67584ORPHA03025127061101600185
HP:0001770HP:0001770Toe syndactyly0BRIP1 CL E G H8399084ORPHA0202305020473605882
HP:0001770HP:0001770Toe syndactyly0CD96 CL E G H102251308Chorioretinopathy dominant form microcephalyORPHA034716892606037
HP:0001770HP:0001770Toe syndactyly0CEP120 CL E G H153241474ORPHA098726690613446
HP:0001770HP:0001770Toe syndactyly0CRKL CL E G H1399261330ORPHA0163762363602007
HP:0001770HP:0001770Toe syndactyly0CUL4B CL E G H845085293ORPHA0402472555300304
HP:0001770HP:0001770Toe syndactyly0DACT1 CL E G H51339857Benign familial infantile epilepsyORPHA085017748607861
HP:0001770HP:0001770Toe syndactyly0DYNC2H1 CL E G H79659474ORPHA02078892962603297
HP:0001770HP:0001770Toe syndactyly0DYNC2LI1 CL E G H51626474ORPHA01417324595617083
HP:0001770HP:0001770Toe syndactyly0ERCC4 CL E G H207284ORPHA0723483436133520
HP:0001770HP:0001770Toe syndactyly0FANCA CL E G H217584ORPHA068917063582607139
HP:0001770HP:0001770Toe syndactyly0FANCB CL E G H218784ORPHA0213523583300515
HP:0001770HP:0001770Toe syndactyly0FANCC CL E G H217684ORPHA0658823584613899
HP:0001770HP:0001770Toe syndactyly0FANCD2 CL E G H217784ORPHA0644293585613984
HP:0001770HP:0001770Toe syndactyly0FANCE CL E G H217884ORPHA0172013586613976
HP:0001770HP:0001770Toe syndactyly0FANCF CL E G H218884ORPHA0162023587613897
HP:0001770HP:0001770Toe syndactyly0FANCG CL E G H218984ORPHA0923253588602956
HP:0001770HP:0001770Toe syndactyly0FANCI CL E G H5521584ORPHA04552125568611360
HP:0001770HP:0001770Toe syndactyly0FANCL CL E G H5512084ORPHA02417620748608111
HP:0001770HP:0001770Toe syndactyly0FANCM CL E G H5769784ORPHA05369723168609644
HP:0001770HP:0001770Toe syndactyly0FGFR2 CL E G H2263168624ORPHA01593363689176943
HP:0001770HP:0001770Toe syndactyly0GLI3 CL E G H2737146510Pallister-Hall syndrome146510C0265220OMIM02445374319165240
HP:0001770HP:0001770Toe syndactyly0IFT140 CL E G H9742474ORPHA07253029077614620
HP:0001770HP:0001770Toe syndactyly0IFT172 CL E G H26160474ORPHA02726930391607386
HP:0001770HP:0001770Toe syndactyly0IFT80 CL E G H57560474ORPHA01321129262611177
HP:0001770HP:0001770Toe syndactyly0LIG4 CL E G H3981235ORPHA0403176601601837
HP:0001770HP:0001770Toe syndactyly0MAD2L2 CL E G H1045984ORPHA01546764604094
HP:0001770HP:0001770Toe syndactyly0MAPK1 CL E G H5594261330ORPHA031126871176948
HP:0001770HP:0001770Toe syndactyly0MEF2C CL E G H4208228384ORPHA0892456996600662
HP:0001770HP:0001770Toe syndactyly0NEK9 CL E G H9175464754ORPHA034518591609798
HP:0001770HP:0001770Toe syndactyly0NSUN2 CL E G H54888235ORPHA0726025994610916
HP:0001770HP:0001770Toe syndactyly0NXN CL E G H643591507Congenital unilateral pulmonary hypoplasiaORPHA0513018008612895
HP:0001770HP:0001770Toe syndactyly0OTUD6B CL E G H51633505237ORPHA064724281612021
HP:0001770HP:0001770Toe syndactyly0PALB2 CL E G H7972884ORPHA0417350326144610355
HP:0001770HP:0001770Toe syndactyly0RAD51 CL E G H588884ORPHA016369817179617
HP:0001770HP:0001770Toe syndactyly0RAD51C CL E G H588984ORPHA013111309820602774
HP:0001770HP:0001770Toe syndactyly0RFWD3 CL E G H5515984ORPHA024925539614151
HP:0001770HP:0001770Toe syndactyly0ROR2 CL E G H49201507Congenital unilateral pulmonary hypoplasiaORPHA04025810257602337
HP:0001770HP:0001770Toe syndactyly0SALL1 CL E G H6299857Benign familial infantile epilepsyORPHA08818210524602218
HP:0001770HP:0001770Toe syndactyly0SALL4 CL E G H57167959ORPHA05714815924607343
HP:0001770HP:0001770Toe syndactyly0SC5D CL E G H6309607330Lathosterolosis607330C1846421OMIM0618210547602286
HP:0001770HP:0001770Toe syndactyly0SIN3A CL E G H2594294065ORPHA01611619353607776
HP:0001770HP:0001770Toe syndactyly0SLX4 CL E G H8446484ORPHA07281823845613278
HP:0001770HP:0001770Toe syndactyly0SMC3 CL E G H9126610759Cornelia de Lange syndrome 3610759C1853099OMIM0282132468606062
HP:0001770HP:0001770Toe syndactyly0TBX22 CL E G H50945921Bone dysplasia corpus callosum agenesisORPHA03018811600300307
HP:0001770HP:0001770Toe syndactyly0TFAP2B CL E G H702146627ORPHA0155711743601601
HP:0001770HP:0001770Toe syndactyly0TP63 CL E G H862669085ORPHA012828215979603273
HP:0001770HP:0001770Toe syndactyly0TP63 CL E G H86261896Dominant cleft palateORPHA012828215979603273
HP:0001770HP:0001770Toe syndactyly0TTC21B CL E G H79809474ORPHA06333425660612014
HP:0001770HP:0001770Toe syndactyly0TWIST2 CL E G H117581200110Ablepharon macrostomia syndrome200110C1860224OMIM098820670607556
HP:0001770HP:0001770Toe syndactyly0TWIST2 CL E G H117581920Bone dysplasia Azouz typeORPHA098820670607556
HP:0001770HP:0001770Toe syndactyly0UBE2T CL E G H2908984ORPHA071825009610538
HP:0001770HP:0001770Toe syndactyly0WDR19 CL E G H57728474ORPHA04529418340608151
HP:0001770HP:0001770Toe syndactyly0WDR34 CL E G H89891474ORPHA02128296613363
HP:0001770HP:0001770Toe syndactyly0WDR60 CL E G H55112474ORPHA01321862615462
HP:0001770HP:0001770Toe syndactyly0XRCC2 CL E G H751684ORPHA02335812829600375
HP:0001770HP:0001770Toe syndactyly1ARL6IP6 CL E G H1511881556ORPHA031924048616495
HP:0001770HP:0001770Toe syndactyly1BCR CL E G H613261330ORPHA022111014151410
HP:0001770HP:0001770Toe syndactyly1BRCA1 CL E G H67284ORPHA02824114981100113705
HP:0001770HP:0001770Toe syndactyly1BRCA2 CL E G H67584ORPHA03025127061101600185
HP:0001770HP:0001770Toe syndactyly1BRIP1 CL E G H8399084ORPHA0202305020473605882
HP:0001770HP:0001770Toe syndactyly1CD96 CL E G H102251308Chorioretinopathy dominant form microcephalyORPHA034716892606037
HP:0001770HP:0001770Toe syndactyly1CEP120 CL E G H153241474ORPHA098726690613446
HP:0001770HP:0001770Toe syndactyly1CRKL CL E G H1399261330ORPHA0163762363602007
HP:0001770HP:0001770Toe syndactyly1CUL4B CL E G H845085293ORPHA0402472555300304
HP:0001770HP:0001770Toe syndactyly1DACT1 CL E G H51339857Benign familial infantile epilepsyORPHA085017748607861
HP:0001770HP:0001770Toe syndactyly1DYNC2H1 CL E G H79659474ORPHA02078892962603297
HP:0001770HP:0001770Toe syndactyly1DYNC2LI1 CL E G H51626474ORPHA01417324595617083
HP:0001770HP:0001770Toe syndactyly1ERCC4 CL E G H207284ORPHA0723483436133520
HP:0001770HP:0001770Toe syndactyly1FANCA CL E G H217584ORPHA068917063582607139
HP:0001770HP:0001770Toe syndactyly1FANCB CL E G H218784ORPHA0213523583300515
HP:0001770HP:0001770Toe syndactyly1FANCC CL E G H217684ORPHA0658823584613899
HP:0001770HP:0001770Toe syndactyly1FANCD2 CL E G H217784ORPHA0644293585613984
HP:0001770HP:0001770Toe syndactyly1FANCE CL E G H217884ORPHA0172013586613976
HP:0001770HP:0001770Toe syndactyly1FANCF CL E G H218884ORPHA0162023587613897
HP:0001770HP:0001770Toe syndactyly1FANCG CL E G H218984ORPHA0923253588602956
HP:0001770HP:0001770Toe syndactyly1FANCI CL E G H5521584ORPHA04552125568611360
HP:0001770HP:0001770Toe syndactyly1FANCL CL E G H5512084ORPHA02417620748608111
HP:0001770HP:0001770Toe syndactyly1FANCM CL E G H5769784ORPHA05369723168609644
HP:0001770HP:0001770Toe syndactyly1FGFR2 CL E G H2263168624ORPHA01593363689176943
HP:0001770HP:0001770Toe syndactyly1GLI3 CL E G H2737146510Pallister-Hall syndrome146510C0265220OMIM02445374319165240
HP:0001770HP:0001770Toe syndactyly1IFT140 CL E G H9742474ORPHA07253029077614620
HP:0001770HP:0001770Toe syndactyly1IFT172 CL E G H26160474ORPHA02726930391607386
HP:0001770HP:0001770Toe syndactyly1IFT80 CL E G H57560474ORPHA01321129262611177
HP:0001770HP:0001770Toe syndactyly1LIG4 CL E G H3981235ORPHA0403176601601837
HP:0001770HP:0001770Toe syndactyly1MAD2L2 CL E G H1045984ORPHA01546764604094
HP:0001770HP:0001770Toe syndactyly1MAPK1 CL E G H5594261330ORPHA031126871176948
HP:0001770HP:0001770Toe syndactyly1MEF2C CL E G H4208228384ORPHA0892456996600662
HP:0001770HP:0001770Toe syndactyly1NEK9 CL E G H9175464754ORPHA034518591609798
HP:0001770HP:0001770Toe syndactyly1NSUN2 CL E G H54888235ORPHA0726025994610916
HP:0001770HP:0001770Toe syndactyly1NXN CL E G H643591507Congenital unilateral pulmonary hypoplasiaORPHA0513018008612895
HP:0001770HP:0001770Toe syndactyly1OTUD6B CL E G H51633505237ORPHA064724281612021
HP:0001770HP:0001770Toe syndactyly1PALB2 CL E G H7972884ORPHA0417350326144610355
HP:0001770HP:0001770Toe syndactyly1RAD51 CL E G H588884ORPHA016369817179617
HP:0001770HP:0001770Toe syndactyly1RAD51C CL E G H588984ORPHA013111309820602774
HP:0001770HP:0001770Toe syndactyly1RFWD3 CL E G H5515984ORPHA024925539614151
HP:0001770HP:0001770Toe syndactyly1ROR2 CL E G H49201507Congenital unilateral pulmonary hypoplasiaORPHA04025810257602337
HP:0001770HP:0001770Toe syndactyly1SALL1 CL E G H6299857Benign familial infantile epilepsyORPHA08818210524602218
HP:0001770HP:0001770Toe syndactyly1SALL4 CL E G H57167959ORPHA05714815924607343
HP:0001770HP:0001770Toe syndactyly1SC5D CL E G H6309607330Lathosterolosis607330C1846421OMIM0618210547602286
HP:0001770HP:0001770Toe syndactyly1SIN3A CL E G H2594294065ORPHA01611619353607776
HP:0001770HP:0001770Toe syndactyly1SLX4 CL E G H8446484ORPHA07281823845613278
HP:0001770HP:0001770Toe syndactyly1SMC3 CL E G H9126610759Cornelia de Lange syndrome 3610759C1853099OMIM0282132468606062
HP:0001770HP:0001770Toe syndactyly1TBX22 CL E G H50945921Bone dysplasia corpus callosum agenesisORPHA03018811600300307
HP:0001770HP:0001770Toe syndactyly1TFAP2B CL E G H702146627ORPHA0155711743601601
HP:0001770HP:0001770Toe syndactyly1TP63 CL E G H862669085ORPHA012828215979603273
HP:0001770HP:0001770Toe syndactyly1TP63 CL E G H86261896Dominant cleft palateORPHA012828215979603273
HP:0001770HP:0001770Toe syndactyly1TTC21B CL E G H79809474ORPHA06333425660612014
HP:0001770HP:0001770Toe syndactyly1TWIST2 CL E G H117581200110Ablepharon macrostomia syndrome200110C1860224OMIM098820670607556
HP:0001770HP:0001770Toe syndactyly1TWIST2 CL E G H117581920Bone dysplasia Azouz typeORPHA098820670607556
HP:0001770HP:0001770Toe syndactyly1UBE2T CL E G H2908984ORPHA071825009610538
HP:0001770HP:0001770Toe syndactyly1WDR19 CL E G H57728474ORPHA04529418340608151
HP:0001770HP:0001770Toe syndactyly1WDR34 CL E G H89891474ORPHA02128296613363
HP:0001770HP:0001770Toe syndactyly1WDR60 CL E G H55112474ORPHA01321862615462
HP:0001770HP:0001770Toe syndactyly1XRCC2 CL E G H751684ORPHA02335812829600375
HP:0001770HP:0001770Toe syndactyly2ARL6IP6 CL E G H1511881556ORPHA031924048616495
HP:0001770HP:0001770Toe syndactyly2BCR CL E G H613261330ORPHA022111014151410
HP:0001770HP:0001770Toe syndactyly2BRCA1 CL E G H67284ORPHA02824114981100113705
HP:0001770HP:0001770Toe syndactyly2BRCA2 CL E G H67584ORPHA03025127061101600185
HP:0001770HP:0001770Toe syndactyly2BRIP1 CL E G H8399084ORPHA0202305020473605882
HP:0001770HP:0001770Toe syndactyly2CD96 CL E G H102251308Chorioretinopathy dominant form microcephalyORPHA034716892606037
HP:0001770HP:0001770Toe syndactyly2CEP120 CL E G H153241474ORPHA098726690613446
HP:0001770HP:0001770Toe syndactyly2CRKL CL E G H1399261330ORPHA0163762363602007
HP:0001770HP:0001770Toe syndactyly2CUL4B CL E G H845085293ORPHA0402472555300304
HP:0001770HP:0001770Toe syndactyly2DACT1 CL E G H51339857Benign familial infantile epilepsyORPHA085017748607861
HP:0001770HP:0001770Toe syndactyly2DYNC2H1 CL E G H79659474ORPHA02078892962603297
HP:0001770HP:0001770Toe syndactyly2DYNC2LI1 CL E G H51626474ORPHA01417324595617083
HP:0001770HP:0001770Toe syndactyly2ERCC4 CL E G H207284ORPHA0723483436133520
HP:0001770HP:0001770Toe syndactyly2FANCA CL E G H217584ORPHA068917063582607139
HP:0001770HP:0001770Toe syndactyly2FANCB CL E G H218784ORPHA0213523583300515
HP:0001770HP:0001770Toe syndactyly2FANCC CL E G H217684ORPHA0658823584613899
HP:0001770HP:0001770Toe syndactyly2FANCD2 CL E G H217784ORPHA0644293585613984
HP:0001770HP:0001770Toe syndactyly2FANCE CL E G H217884ORPHA0172013586613976
HP:0001770HP:0001770Toe syndactyly2FANCF CL E G H218884ORPHA0162023587613897
HP:0001770HP:0001770Toe syndactyly2FANCG CL E G H218984ORPHA0923253588602956
HP:0001770HP:0001770Toe syndactyly2FANCI CL E G H5521584ORPHA04552125568611360
HP:0001770HP:0001770Toe syndactyly2FANCL CL E G H5512084ORPHA02417620748608111
HP:0001770HP:0001770Toe syndactyly2FANCM CL E G H5769784ORPHA05369723168609644
HP:0001770HP:0001770Toe syndactyly2FGFR2 CL E G H2263168624ORPHA01593363689176943
HP:0001770HP:0001770Toe syndactyly2GLI3 CL E G H2737146510Pallister-Hall syndrome146510C0265220OMIM02445374319165240
HP:0001770HP:0001770Toe syndactyly2IFT140 CL E G H9742474ORPHA07253029077614620
HP:0001770HP:0001770Toe syndactyly2IFT172 CL E G H26160474ORPHA02726930391607386
HP:0001770HP:0001770Toe syndactyly2IFT80 CL E G H57560474ORPHA01321129262611177
HP:0001770HP:0001770Toe syndactyly2LIG4 CL E G H3981235ORPHA0403176601601837
HP:0001770HP:0001770Toe syndactyly2MAD2L2 CL E G H1045984ORPHA01546764604094
HP:0001770HP:0001770Toe syndactyly2MAPK1 CL E G H5594261330ORPHA031126871176948
HP:0001770HP:0001770Toe syndactyly2MEF2C CL E G H4208228384ORPHA0892456996600662
HP:0001770HP:0001770Toe syndactyly2NEK9 CL E G H9175464754ORPHA034518591609798
HP:0001770HP:0001770Toe syndactyly2NSUN2 CL E G H54888235ORPHA0726025994610916
HP:0001770HP:0001770Toe syndactyly2NXN CL E G H643591507Congenital unilateral pulmonary hypoplasiaORPHA0513018008612895
HP:0001770HP:0001770Toe syndactyly2OTUD6B CL E G H51633505237ORPHA064724281612021
HP:0001770HP:0001770Toe syndactyly2PALB2 CL E G H7972884ORPHA0417350326144610355
HP:0001770HP:0001770Toe syndactyly2RAD51 CL E G H588884ORPHA016369817179617
HP:0001770HP:0001770Toe syndactyly2RAD51C CL E G H588984ORPHA013111309820602774
HP:0001770HP:0001770Toe syndactyly2RFWD3 CL E G H5515984ORPHA024925539614151
HP:0001770HP:0001770Toe syndactyly2ROR2 CL E G H49201507Congenital unilateral pulmonary hypoplasiaORPHA04025810257602337
HP:0001770HP:0001770Toe syndactyly2SALL1 CL E G H6299857Benign familial infantile epilepsyORPHA08818210524602218
HP:0001770HP:0001770Toe syndactyly2SALL4 CL E G H57167959ORPHA05714815924607343
HP:0001770HP:0001770Toe syndactyly2SC5D CL E G H6309607330Lathosterolosis607330C1846421OMIM0618210547602286
HP:0001770HP:0001770Toe syndactyly2SIN3A CL E G H2594294065ORPHA01611619353607776
HP:0001770HP:0001770Toe syndactyly2SLX4 CL E G H8446484ORPHA07281823845613278
HP:0001770HP:0001770Toe syndactyly2SMC3 CL E G H9126610759Cornelia de Lange syndrome 3610759C1853099OMIM0282132468606062
HP:0001770HP:0001770Toe syndactyly2TBX22 CL E G H50945921Bone dysplasia corpus callosum agenesisORPHA03018811600300307
HP:0001770HP:0001770Toe syndactyly2TFAP2B CL E G H702146627ORPHA0155711743601601
HP:0001770HP:0001770Toe syndactyly2TP63 CL E G H862669085ORPHA012828215979603273
HP:0001770HP:0001770Toe syndactyly2TP63 CL E G H86261896Dominant cleft palateORPHA012828215979603273
HP:0001770HP:0001770Toe syndactyly2TTC21B CL E G H79809474ORPHA06333425660612014
HP:0001770HP:0001770Toe syndactyly2TWIST2 CL E G H117581200110Ablepharon macrostomia syndrome200110C1860224OMIM098820670607556
HP:0001770HP:0001770Toe syndactyly2TWIST2 CL E G H117581920Bone dysplasia Azouz typeORPHA098820670607556
HP:0001770HP:0001770Toe syndactyly2UBE2T CL E G H2908984ORPHA071825009610538
HP:0001770HP:0001770Toe syndactyly2WDR19 CL E G H57728474ORPHA04529418340608151
HP:0001770HP:0001770Toe syndactyly2WDR34 CL E G H89891474ORPHA02128296613363
HP:0001770HP:0001770Toe syndactyly2WDR60 CL E G H55112474ORPHA01321862615462
HP:0001770HP:0001770Toe syndactyly2XRCC2 CL E G H751684ORPHA02335812829600375


Genes (146) :APC ARCN1 ARHGAP31 ARL6IP6 ATP6V1B2 B3GLCT BCOR BCR BHLHA9 BMP2 BMP4 BMPR1B BRCA1 BRCA2 BRIP1 CCNQ CD96 CDC45 CEP120 CEP55 CKAP2L CLCF1 COL4A3BP CPLANE1 CRKL CUL4B DACT1 DDX11 DEAF1 DHCR7 DYNC2H1 DYNC2LI1 EBP EFNB1 ERCC4 FANCA FANCB FANCC FANCD2 FANCE FANCF FANCG FANCI FANCL FANCM FBLN1 FGF9 FGFR1 FGFR2 FIG4 FLI1 FLII FLNA FRAS1 FREM2 GDF5 GJA1 GLI3 GNE GPC3 GPC4 GRIP1 HDAC4 HDAC8 HOXD13 IFT140 IFT172 IFT80 IL11RA IQSEC2 IRF6 KCNJ2 KCTD1 KIF7 KMT2A LIG4 LMBR1 LRP4 MAD2L2 MAPK1 MCTP2 MEF2C MEGF8 MEIS2 MYCN MYH8 NECTIN1 NECTIN4 NEDD4L NEK9 NIPBL NOG NSUN2 NXN OTUD6B PALB2 PHGDH PIGY PIK3CA PORCN RAB23 RAD21 RAD51 RAD51C RAI1 RBBP8 RBPJ RFWD3 RIPK4 ROR2 SALL1 SALL4 SC5D SETD5 SF3B4 SHANK3 SHH SIK3 SIN3A SLC12A6 SLX4 SMAD4 SMARCAD1 SMC1A SMC3 SMO SMOC1 SOX5 TBR1 TBX15 TBX22 TCTN3 TFAP2B TP63 TRIO TTC21B TWIST1 TWIST2 TXNL4A UBE2T WDR19 WDR34 WDR60 WNT10B WNT7A XRCC2

Diseases (137) :3258 100300 1556 124480 709 261330 607932 84 140952 300707 211750 1308 474 277170 85293 857 819 304110 608180 93258 168624 87 93259 93260 101400 216340 2308 311300 304120 2052 2710 380 672 146510 373 1001 199 300882 93409 217377 1300 170390 200990 235 93405 2378 228384 65759 3253 64754 184460 1507 505237 256520 60040 2092 305600 201000 1234 959 46059 607330 154400 94065 613406 610759 1553 1106 206920 1617 260660 921 258860 46627 978 69085 103285 1896 604292 200110 920 225300 228930 617164 2712 300166 157801 112600 617063 236500 272440 610313 616351 613398 818 270400 300960 612961 123150 1540 164200 175700 174700 3166 269921 93406 186300 186000 614188 181270 186200 600987 164280 158300 225060 617201 122470 611377 186500 616809 276280 251255 614814 107480 606232 618162 218000 139210 129200 601707 313892 106260 617061 608572 257850 1596 613573
 

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