Human genes for Waardenburg syndrome type 2C
Waardenburg syndrome type 2C [DOID:0110951]
A Waardenburg's 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.
Synonyms: Waardenburg syndrome type 2C, DOID:0110951, Waardenburg syndrome type IIC, WS2C, Waardenburg syndrome type IICs