| Disease Browser
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Parent Node:
 Foot Deformities (D005530) |
Parent Node:
Limb Deformities, Congenital (D017880) |
Parent Node:
Lower Extremity Deformities, Congenital (D038061) |
..Starting node
.. Foot Deformities, Congenital (D005532)
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Child Nodes:
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| ........Acheiropodia (C536014) |
| ........Acrootoocular Syndrome (C564866) |
| ........Anonychia-onychodystrophy with hypoplasia or absence of distal phalanges (C537766) |
| ........Aphalangia, Partial, with Syndactyly and Duplication of Metatarsal IV (C563942) |
| ........BRACHYDACTYLY, TYPE E1 (OMIM:113300) |
| ........BRACHYDACTYLY, TYPE E2 (OMIM:613382) |
| ........Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia (C537100) |
| ........Camptosynpolydactyly, Complex (C564383) |
| ........CAPOS syndrome (C535351) |
| ........Charcot-Marie-Tooth Disease, Foot Deformity of (C564179) |
| ........Cleft Palate, Deafness, and Oligodontia (C565844) |
........Clubfoot (D003025)  9 |
| ........Craniosynostosis, Adelaide Type (C563471) |
| ........Daneman Davy Mancer syndrome (C535986) |
| ........Deafness, congenital onychodystrophy, recessive form (C538204) |
| ........Digitotalar Dysmorphism (C565097) |
| ........Ectrodactyly and Ectodermal Dysplasia without Cleft Lip/Palate (C565065) |
| ........Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 (C565799) |
| ........Eiken Skeletal Dysplasia (C564010) |
| ........Fairbank disease (C536393) |
| ........Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome (C565436) |
| ........Frias syndrome (C535639) |
| ........Fried Goldberg Mundel syndrome (C535640) |
| ........Frints De Smet Fabry Fryns syndrome (C538062) |
| ........Fuhrmann syndrome (C538189) |
| ........Game Friedman Paradice syndrome (C535406) |
| ........Growth Retardation, Small and Puffy Hands and Feet, and Eczema (C565528) |
| ........Hairy palms and soles (C535620) |
| ........Hand foot uterus syndrome (C535627) |
| ........Jackson-Weiss syndrome (C537559) |
| ........Johnson Munson syndrome (C535881) |
| ........Laurin-Sandrow syndrome (C535689) |
| ........Macrodactyly of the foot (C537719) |
| ........MAMMARY-DIGITAL-NAIL SYNDROME (OMIM:613689) |
| ........Metatarsus Varus, Type I (C563585) |
| ........Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism (C537686) |
| ........Mononen Karnes Senac syndrome (C535914) |
| ........Monophalangy of Great Toe (C563570) |
| ........Nicolaides Baraitser syndrome (C536116) |
| ........NOG-Related-Symphalangism Spectrum Disorder (C536943) |
| ........Oculodentodigital Dysplasia (C563160) |
| ........Odontotrichoungual-Digital-Palmar Syndrome (C566598) |
| ........Oslam syndrome (C537138) |
| ........Pfeiffer Tietze Welte syndrome (C537891) |
| ........Polydactyly, Postaxial, with Dental and Vertebral Anomalies (C564880) |
| ........Radial defect Robin sequence (C536261) |
| ........Radio-ulnar synostosis type 1 (C536268) |
| ........Radio-ulnar synostosis type 2 (C536269) |
| ........Ray Peterson Scott syndrome (C535292) |
| ........Richieri Costa Guion-Almeida syndrome (C535676) |
| ........Sandhaus Ben-Ami syndrome (C537233) |
| ........Second Metatarsal-Metacarpal Syndrome (C564824) |
| ........Split hand split foot nystagmus (C537319) |
| ........Split-Hand/Foot Malformation With Sensorineural Hearing Loss (C565647) |
| ........Stoll Alembik Dott syndrome (C537497) |
| ........Symphalangism with Multiple Anomalies of Hands and Feet (C566098) |
| ........Symphalangism, Distal (C566099) 1 |
| ........Synpolydactyly 2 (C564278) |
| ........Synpolydactyly With Foot Anomalies (C566095) |
| ........Talonavicular coalition (C536895) |
| ........Teebi syndrome (C536951) |
| ........TERMINAL OSSEOUS DYSPLASIA (OMIM:300244) |
| ........Trichorhinophalangeal Syndrome, Type III (C566033) |
| ........Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet (C564759) |
| ........Ulnar hypoplasia lobster claw deformity of feet (C536936) |
| ........Van Maldergem Wetzburger Verloes syndrome (C536530) |
| ........Vertical talus, congenital (C536345) |
| ........Zechi-Ceide Syndrome (C567865) |
Sister Nodes: |
..Corneodermatoosseous syndrome (C536444)
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..Ectrodactyly cardiopathy dysmorphism (C536187)
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..Ectrodactyly of Lower Limbs, Congenital Heart Defect, and Micrognathia (C563344)
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..Familial streblodactyly (C536852)
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..Foot Deformities, Congenital (D005532) 78
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..Holt-Oram syndrome (C535326)
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..Merlob Grunebaum Reisner syndrome (C537461)
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..Mermaid syndrome (C538595)
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..Nasodigitoacoustic syndrome (C538337)
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..Popliteal Pterygium Syndrome (C562509)
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..Tibia, Bowing of, with Pseudarthrosis and Pectus Excavatum (C563787)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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