All diseases

OMIM ID
613105
OMIM term:
CHOROIDAL DYSTROPHY, CENTRAL AREOLAR 2; CACD2
Alternative terms:

(∗) Location:
6p21.1  
(†) Associated OMIM genes:
PRPH2  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/7q52lf2k