All diseases

OMIM ID
148820
OMIM term:
WAARDENBURG SYNDROME, TYPE 3; WS3
Alternative terms:
WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES
WAARDENBURG SYNDROME, TYPE III
KLEIN-WAARDENBURG SYNDROME
(∗) Location:
2q36.1  
(†) Associated OMIM genes:
PAX3  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/csiq6ne2