Disease Browser
Parent Node: Abnormalities, Multiple (D000015) Parent Node: Intellectual Disability (D008607) Parent Node: Syndactyly (D013576) ..Starting node .. Scott Bryant Graham syndrome (C537528) Child Nodes:
Sister Nodes: ..Acrocephalosyndactylia (D000168) 11 ..Aphalangia syndactyly microcephaly (C537787) ..Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly (C566529) ..Aurocephalosyndactyly (C566235) ..Blepharophimosis with ptosis, syndactyly, and short stature (C536235) ..Bonneau Syndrome (C564875) ..Brachydactyly-Syndactyly Syndrome (C565193) ..Ectodermal dysplasia mental retardation syndactyly (C538018) ..ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1 (OMIM:613573) ..ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2 (OMIM:613576) ..Eyebrows duplication of, with stretchable skin and syndactyly (C536383) ..Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome (C565436) ..Filippi syndrome (C538152) ..Frints De Smet Fabry Fryns syndrome (C538062) ..Gollop Coates syndrome (C537283) ..Green Sandford Davison syndrome (C538221) ..Kleiner Holmes syndrome (C536885) ..Kozlowski-Krajewska syndrome (C537615) ..Lacrimoauriculodentodigital syndrome (C538132) ..Landy Donnai syndrome (C537266) ..Martinez Monasterio Pinheiro syndrome (C536027) ..Naguib-Richieri-Costa syndrome (C538332) ..Oculodentodigital Dysplasia (C563160) ..Oculodentodigital Dysplasia, Autosomal Recessive (C567605) ..Oculodentoosseous dysplasia recessive (C537733) ..Orofacial Cleft 7 (C563464) ..Orstavik Lindemann Solberg syndrome (C537137) ..Pavone Fiumara Rizzo syndrome (C536313) ..Pfeiffer Rockelein syndrome (C537890) ..Piepkorn Karp Hickok syndrome (C535774) ..Poland Syndrome (D011045) ..Polydactyly, Postaxial, Type A4 (C563909) ..Polysyndactyly, Crossed (C566773) ..Popliteal Pterygium Syndrome (C562509) ..Popliteal Pterygium Syndrome, Lethal Type (C564874) ..Radio-ulnar synostosis type 1 (C536268) ..Radio-ulnar synostosis type 2 (C536269) ..Rosselli-Gulienetti Syndrome (C563117) ..Sclerosteosis (C537525) ..Scott Bryant Graham syndrome (C537528) ..Short Stature, Facial Dysmorphism, Severe Brachydactyly, and Syndactyly (C567093) ..STAPES ANKYLOSIS WITH BROAD THUMB AND TOES (OMIM:184460) ..Syndactyly Cenani Lenz type (C538150) ..Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction (C563721) ..Syndactyly, type 2 (C538153) ..Syndactyly, type 3 (C538154) ..Syndactyly, Type I (C566096) ..Syndactyly, Type IV (C566092) ..Syndactyly, type v (C538155) ..Syndactyly-Polydactyly-Earlobe Syndrome (C566091) ..Synpolydactyly 1 (C566094) ..Timothy syndrome (C536962) ..Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations (C567475) ..Trueb Burg Bottani syndrome (C536565) ..Winter Shortland Temple syndrome (C536735) ..Zerres Rietschel Majewski syndrome (C536724) ..Zlotogora-Ogur syndrome (C536726) ..Zygodactyly 1 (C565223) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD