Waardenburg syndrome type 2B (DOID:0110947)
Alliance: disease page
Synonyms: Waardenburg syndrome type IIB; WS2B
Alt IDs: OMIM:600193, MESH:C536465
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 1p21-p13.3.