Waardenburg syndrome type 4C (DOID:0110955)
Alliance: disease page
Synonyms: Waardenburg syndrome type IVC; Waardenburg syndrome with Hirschsprung disease type 4C; WS4C
Alt IDs: OMIM:613266
Definition: A Waardenburg syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and Hirschsprung disease that has_material_basis_in heterozygous mutation in the SOX10 gene on chromosome 22q13.