Waardenburg syndrome type 2C (DOID:0110951)
Alliance: disease page
Synonyms: Waardenburg syndrome type IIC; WS2C
Alt IDs: OMIM:606662
Definition: A Waardenburg syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and absence of lateral displacement of the inner canthus of each eye that has_material_basis_in variation in the chromosome region 8p23.