All diseases

OMIM ID
262300
OMIM term:
ACHROMATOPSIA 3; ACHM3
Alternative terms:
PINGELAPESE BLINDNESS
TOTAL COLORBLINDNESS WITH MYOPIA
ACHROMATOPSIA WITH MYOPIA
ACHM1, FORMERLY
ROD MONOCHROMATISM 1, FORMERLY
ROD MONOCHROMACY 1, FORMERLY; RMCH1, FORMERLY
(∗) Location:
8q21.3  
(†) Associated OMIM genes:
CNGB3  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/iev7pwxn