Waardenburg syndrome type 2C https://www.malacards.org/card/waardenburg_syndrome_type_2c UMLS:C1847722 GARD:0015396 MONDO:0011697 WS2C DOID:0110951 MEDGEN:335755 Waardenburg syndrome, type 2C MESH:C564684 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. OMIM:606662 Waardenburg syndrome type 2