All diseases

OMIM ID
115660
OMIM term:
CATARACT, CONGENITAL, CERULEAN TYPE, 1; CCA1
Alternative terms:

(∗) Location:
17q24  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/b8gzc3h0