All diseases

OMIM ID
303700
OMIM term:
BLUE CONE MONOCHROMACY; BCM
Alternative terms:
BLUE CONE MONOCHROMATISM
COLORBLINDNESS, BLUE-MONO-CONE-MONOCHROMATIC TYPE; CBBM CONE DYSTROPHY 5, X-LINKED, INCLUDED; COD5, INCLUDED
(∗) Location:
Xq28  
(†) Associated OMIM genes:
OPN1LW   OPN1MW  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/yzepx2b3