All diseases

OMIM ID
611584
OMIM term:
WAARDENBURG SYNDROME, TYPE 2E; WS2E
Alternative terms:
WAARDENBURG SYNDROME, TYPE 2E, WITH OR WITHOUT NEUROLOGIC INVOLVEMENT
WS2E, WITH OR WITHOUT NEUROLOGIC INVOLVEMENT
WAARDENBURG SYNDROME, TYPE IIE
(∗) Location:
22q13.1  
(†) Associated OMIM genes:
SOX10  
(‡) Associated MGI genes:

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