All diseases

OMIM ID
601286
OMIM term:
CATARACT, NONNUCLEAR POLYMORPHIC CONGENITAL, AUTOSOMAL DOMINANT
Alternative terms:
CCP; PCC
CATARACT, POLYMORPHIC CONGENITAL
(∗) Location:
2q33.3  
(†) Associated OMIM genes:
CRYGD  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/sucp8eho