All diseases

OMIM ID
608051
OMIM term:
MACULAR DYSTROPHY, RETINAL, 2; MCDR2
Alternative terms:

(∗) Location:
4p15.32  
(†) Associated OMIM genes:
PROM1  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/sv44fxqz