| Disease Browser
|
Parent Node:
 Campomelic Dysplasia (D055036) |
Parent Node:
Foot Deformities, Congenital (D005532) |
Parent Node:
Hand Deformities, Congenital (D006228) |
Parent Node:
Syndactyly (D013576) |
..Starting node
.. Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome (C565436)
|
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
|
