All diseases

OMIM ID
613266
OMIM term:
WAARDENBURG SYNDROME, TYPE 4C; WS4C
Alternative terms:
WAARDENBURG SYNDROME WITH HIRSCHSPRUNG DISEASE, TYPE 4C
WAARDENBURG SYNDROME, TYPE IVC
(∗) Location:
22q13.1  
(†) Associated OMIM genes:
SOX10  
(‡) Associated MGI genes:

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