All diseases

OMIM ID
193500
OMIM term:
WAARDENBURG SYNDROME, TYPE 1; WS1
Alternative terms:

(∗) Location:
2q36.1  
(†) Associated OMIM genes:
PAX3  
(‡) Associated MGI genes:
Mitf   Pax3  

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* quick link - http://q.sanger.ac.uk/ink2u6a6