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Waardenburg syndrome type 4C

Disease Summary
Associated Targets (2)
Tbio

2


Mondo Description A subtype of Waardenburg syndrome type 4 (Waardenburg-Shah syndrome) caused by mutations in SOX10.
Uniprot Description A disorder characterized by the association of Waardenburg features (depigmentation and deafness) with the absence of enteric ganglia in the distal part of the intestine (Hirschsprung disease).
Mondo Term and Equivalent IDs
MONDO:0013202:  Waardenburg syndrome type 4C
MESH:C567679: 
UMLS:C2750452: