| Disease Browser
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Parent Node:
 Abnormalities, Multiple (D000015) |
Parent Node:
Foot Deformities, Congenital (D005532) |
Parent Node:
Hand Deformities, Congenital (D006228) |
Parent Node:
Syndactyly (D013576) |
..Starting node
.. Radio-ulnar synostosis type 1 (C536268)
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Child Nodes:
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Sister Nodes: |
..Acrocephalosyndactylia (D000168)  11
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..Aphalangia syndactyly microcephaly (C537787)
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..Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly (C566529)
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..Aurocephalosyndactyly (C566235)
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..Blepharophimosis with ptosis, syndactyly, and short stature (C536235)
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..Bonneau Syndrome (C564875)
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..Brachydactyly-Syndactyly Syndrome (C565193)
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..Ectodermal dysplasia mental retardation syndactyly (C538018)
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..ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1 (OMIM:613573)
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..ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2 (OMIM:613576)
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..Eyebrows duplication of, with stretchable skin and syndactyly (C536383)
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..Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome (C565436)
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..Filippi syndrome (C538152)
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..Frints De Smet Fabry Fryns syndrome (C538062)
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..Gollop Coates syndrome (C537283)
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..Green Sandford Davison syndrome (C538221)
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..Kleiner Holmes syndrome (C536885)
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..Kozlowski-Krajewska syndrome (C537615)
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..Lacrimoauriculodentodigital syndrome (C538132)
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..Landy Donnai syndrome (C537266)
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..Martinez Monasterio Pinheiro syndrome (C536027)
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..Naguib-Richieri-Costa syndrome (C538332)
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..Oculodentodigital Dysplasia (C563160)
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..Oculodentodigital Dysplasia, Autosomal Recessive (C567605)
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..Oculodentoosseous dysplasia recessive (C537733)
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..Orofacial Cleft 7 (C563464)
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..Orstavik Lindemann Solberg syndrome (C537137)
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..Pavone Fiumara Rizzo syndrome (C536313)
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..Pfeiffer Rockelein syndrome (C537890)
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..Piepkorn Karp Hickok syndrome (C535774)
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..Poland Syndrome (D011045)
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..Polydactyly, Postaxial, Type A4 (C563909)
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..Polysyndactyly, Crossed (C566773)
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..Popliteal Pterygium Syndrome (C562509)
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..Popliteal Pterygium Syndrome, Lethal Type (C564874)
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..Radio-ulnar synostosis type 1 (C536268)
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..Radio-ulnar synostosis type 2 (C536269)
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..Rosselli-Gulienetti Syndrome (C563117)
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..Sclerosteosis (C537525)
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..Scott Bryant Graham syndrome (C537528)
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..Short Stature, Facial Dysmorphism, Severe Brachydactyly, and Syndactyly (C567093)
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..STAPES ANKYLOSIS WITH BROAD THUMB AND TOES (OMIM:184460)
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..Syndactyly Cenani Lenz type (C538150)
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..Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction (C563721)
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..Syndactyly, type 2 (C538153)
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..Syndactyly, type 3 (C538154)
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..Syndactyly, Type I (C566096)
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..Syndactyly, Type IV (C566092)
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..Syndactyly, type v (C538155)
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..Syndactyly-Polydactyly-Earlobe Syndrome (C566091)
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..Synpolydactyly 1 (C566094)
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..Timothy syndrome (C536962)
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..Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations (C567475)
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..Trueb Burg Bottani syndrome (C536565)
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..Winter Shortland Temple syndrome (C536735)
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..Zerres Rietschel Majewski syndrome (C536724)
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..Zlotogora-Ogur syndrome (C536726)
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..Zygodactyly 1 (C565223)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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