All diseases

OMIM ID
303900
OMIM term:
COLORBLINDNESS, PARTIAL, PROTAN SERIES; CBP
Alternative terms:
PROTANOPIA
RED COLORBLINDNESS PROTANOMALY, INCLUDED
(∗) Location:
Xq28  
(†) Associated OMIM genes:
OPN1LW  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/a577pj2s