All diseases

OMIM ID
613265
OMIM term:
WAARDENBURG SYNDROME, TYPE 4B; WS4B
Alternative terms:
WAARDENBURG SYNDROME, TYPE 4B, WITH HIRSCHSPRUNG DISEASE
WAARDENBURG SYNDROME, TYPE IVB
(∗) Location:
20q13.32  
(†) Associated OMIM genes:
EDN3  
(‡) Associated MGI genes:
Edn3  

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