All diseases

OMIM ID
160700
OMIM term:
MYOPIA 2, AUTOSOMAL DOMINANT; MYP2
Alternative terms:

(∗) Location:
18p11.31  
(†) Associated OMIM genes:
(‡) Associated MGI genes:
Adora2a  

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* quick link - http://q.sanger.ac.uk/s6a9cyyj