All diseases

OMIM ID
216900
OMIM term:
ACHROMATOPSIA 2; ACHM2
Alternative terms:
COLORBLINDNESS, TOTAL
ROD MONOCHROMATISM 2
ROD MONOCHROMACY 2; RMCH2
(∗) Location:
2q11.2  
(†) Associated OMIM genes:
CNGA3  
(‡) Associated MGI genes:
Pde6c  

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* quick link - http://q.sanger.ac.uk/wwj412at