| Disease Browser
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Parent Node:
 Abnormalities, Multiple (D000015) |
Parent Node:
Foot Deformities, Congenital (D005532) |
..Starting node
.. Fried Goldberg Mundel syndrome (C535640)
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Child Nodes:
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Sister Nodes: |
..Acheiropodia (C536014)
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..Acrootoocular Syndrome (C564866)
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..Anonychia-onychodystrophy with hypoplasia or absence of distal phalanges (C537766)
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..Aphalangia, Partial, with Syndactyly and Duplication of Metatarsal IV (C563942)
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..BRACHYDACTYLY, TYPE E1 (OMIM:113300)
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..BRACHYDACTYLY, TYPE E2 (OMIM:613382)
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..Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia (C537100)
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..Camptosynpolydactyly, Complex (C564383)
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..CAPOS syndrome (C535351)
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..Charcot-Marie-Tooth Disease, Foot Deformity of (C564179)
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..Cleft Palate, Deafness, and Oligodontia (C565844)
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..Clubfoot (D003025)  9
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..Craniosynostosis, Adelaide Type (C563471)
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..Daneman Davy Mancer syndrome (C535986)
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..Deafness, congenital onychodystrophy, recessive form (C538204)
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..Digitotalar Dysmorphism (C565097)
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..Ectrodactyly and Ectodermal Dysplasia without Cleft Lip/Palate (C565065)
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..Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 (C565799)
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..Eiken Skeletal Dysplasia (C564010)
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..Fairbank disease (C536393)
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..Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome (C565436)
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..Frias syndrome (C535639)
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..Fried Goldberg Mundel syndrome (C535640)
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..Frints De Smet Fabry Fryns syndrome (C538062)
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..Fuhrmann syndrome (C538189)
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..Game Friedman Paradice syndrome (C535406)
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..Growth Retardation, Small and Puffy Hands and Feet, and Eczema (C565528)
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..Hairy palms and soles (C535620)
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..Hand foot uterus syndrome (C535627)
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..Jackson-Weiss syndrome (C537559)
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..Johnson Munson syndrome (C535881)
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..Laurin-Sandrow syndrome (C535689)
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..Macrodactyly of the foot (C537719)
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..MAMMARY-DIGITAL-NAIL SYNDROME (OMIM:613689)
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..Metatarsus Varus, Type I (C563585)
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..Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism (C537686)
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..Mononen Karnes Senac syndrome (C535914)
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..Monophalangy of Great Toe (C563570)
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..Nicolaides Baraitser syndrome (C536116)
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..NOG-Related-Symphalangism Spectrum Disorder (C536943)
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..Oculodentodigital Dysplasia (C563160)
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..Odontotrichoungual-Digital-Palmar Syndrome (C566598)
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..Oslam syndrome (C537138)
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..Pfeiffer Tietze Welte syndrome (C537891)
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..Polydactyly, Postaxial, with Dental and Vertebral Anomalies (C564880)
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..Radial defect Robin sequence (C536261)
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..Radio-ulnar synostosis type 1 (C536268)
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..Radio-ulnar synostosis type 2 (C536269)
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..Ray Peterson Scott syndrome (C535292)
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..Richieri Costa Guion-Almeida syndrome (C535676)
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..Sandhaus Ben-Ami syndrome (C537233)
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..Second Metatarsal-Metacarpal Syndrome (C564824)
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..Split hand split foot nystagmus (C537319)
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..Split-Hand/Foot Malformation With Sensorineural Hearing Loss (C565647)
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..Stoll Alembik Dott syndrome (C537497)
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..Symphalangism with Multiple Anomalies of Hands and Feet (C566098)
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..Symphalangism, Distal (C566099) 1
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..Synpolydactyly 2 (C564278)
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..Synpolydactyly With Foot Anomalies (C566095)
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..Talonavicular coalition (C536895)
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..Teebi syndrome (C536951)
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..TERMINAL OSSEOUS DYSPLASIA (OMIM:300244)
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..Trichorhinophalangeal Syndrome, Type III (C566033)
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..Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet (C564759)
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..Ulnar hypoplasia lobster claw deformity of feet (C536936)
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..Van Maldergem Wetzburger Verloes syndrome (C536530)
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..Vertical talus, congenital (C536345)
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..Zechi-Ceide Syndrome (C567865)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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