Disease Browser
Parent Node: Coloboma (D003103) Parent Node: Hypogonadism (D007006) Parent Node: Intellectual Disability (D008607) Parent Node: Obesity (D009765) Parent Node: Polydactyly (D017689) ..Starting node .. Biemond syndrome type 2 (C535439) Child Nodes:
Sister Nodes: ..Absence of tibia with polydactyly (C535564) ..Biemond Syndrome II (C565902) ..Biemond syndrome type 2 (C535439) ..Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia (C537100) ..Cortical Blindness, Retardation, and Postaxial Polydactyly (C565674) ..Crossed Polydactyly, Type I (C566783) ..Dandy Walker malformation postaxial polydactyly (C535771) ..Desbuquois syndrome (C535943) ..Ectodermal dysplasia alopecia preaxial polydactyly (C538016) ..Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet (C565067) ..Garret Tripp syndrome (C535646) ..Hirschsprung disease polydactyly heart disease (C538120) ..Hirschsprung Disease with Heart Defects, Laryngeal Anomalies, and Preaxial Polydactyly (C565817) ..Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness (C565518) ..Hirschsprung Disease with Ulnar Polydactyly, Polysyndactyly of Big Toes, and Ventricular Septal Defect (C565517) ..Holoprosencephaly 9 (C563659) ..Hydrolethalus Syndrome 1 (C565504) ..Kozlowski-Krajewska syndrome (C537615) ..Laurence Prosser Rocker syndrome (C537882) ..Liver Fibrocystic Disease and Polydactyly (C565272) ..Maroteaux Fonfria syndrome (C536023) ..McKusick Kaufman syndrome (C538159) ..Meckel Syndrome, Type 4 (C567003) ..Meckel-Like Cerebrorenodigital Syndrome (C567004) ..Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome (C566381) ..Mexican Cardiomelic Dysplasia (C563087) ..Oliver Syndrome (C564931) ..Pallister-Hall Syndrome (D054975) ..Pfeiffer Mayer syndrome (C537888) ..Polydactyly myopia syndrome (C536331) ..Polydactyly preaxial type 1 (C536332) ..Polydactyly, Postaxial (C562429) ..Polydactyly, Postaxial, Type A2 (C566585) ..Polydactyly, Postaxial, Type A3 (C564590) ..Polydactyly, Postaxial, Type A4 (C563909) ..Polydactyly, Postaxial, with Dental and Vertebral Anomalies (C564880) ..Polydactyly, preaxial 4 (C536333) ..POLYDACTYLY, PREAXIAL II (OMIM:174500) ..Polydactyly, Preaxial III (C566784) ..Polysyndactyly, Crossed (C566773) ..Preaxial deficiency, postaxial polydactyly and hypospadias (C538278) ..Preaxial Hallucal Polydactyly (C566632) ..Pseudotrisomy 13 syndrome (C535829) ..Santos Mateus Leal syndrome (C537235) ..Santos Syndrome (C567819) ..Scalp defects postaxial polydactyly (C536622) ..Short Rib-Polydactyly Syndrome (D012779) 3 ..SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY (OMIM:613091) ..Syndactyly, Type IV (C566092) ..Syndactyly-Polydactyly-Earlobe Syndrome (C566091) ..Synpolydactyly 2 (C564278) ..Synpolydactyly 3 (C565216) ..Synpolydactyly With Foot Anomalies (C566095) ..Thai Symphalangism Syndrome (C564303) ..Tibia absent polydactyly arachnoid cyst (C536918) ..Tibia, Absence or Hypoplasia of, with Polydactyly, Retrocerebellar Arachnoid Cyst, and Other Anomalies (C563403) ..Tibia, Hypoplasia of, with Polydactyly (C566046) ..Ulnar Ray Dysgenesis with Postaxial Polydactyly and Renal Cystic Dysplasia (C565783) ..Urioste Martinez-Frias syndrome (C536478) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD