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split hand-foot malformation 6
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any split hand-foot malformation in which the cause of the disease is a mutation in the WNT10B gene.
Uniprot Description A limb malformation involving the central rays of the autopod and presenting with syndactyly, median clefts of the hands and feet, and aplasia and/or hypoplasia of the phalanges, metacarpals, and metatarsals. Some patients have been found to have mental retardation, ectodermal and craniofacial findings, and orofacial clefting.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0090026
MESH:C567616
OMIM:225300
UMLS:C2749665
MONDO:0009157
High level summary of knowledge for a disease, including descriptions and datasource references.