All diseases

OMIM ID
158330
OMIM term:
MULLERIAN APLASIA AND HYPERANDROGENISM
Alternative terms:

(∗) Location:
1p36.12  
(†) Associated OMIM genes:
WNT4  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/zd9rsia6