All diseases

OMIM ID
600881
OMIM term:
CATARACT, CONGENITAL ZONULAR, WITH SUTURAL OPACITIES; CCZS
Alternative terms:

(∗) Location:
17q11.2  
(†) Associated OMIM genes:
CRYBA1  
(‡) Associated MGI genes:
Cryba1  

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* quick link - http://q.sanger.ac.uk/w83h03g3