The association between OPN1MW (Opsin 1, Medium Wave Sensitive) and Blue Cone Monochromacy is well established and manually curated, with its 5 contributing sources — 4 of them expert-curated — recording a known molecular basis, pathogenic variants, and a causative germline mutation.
Sources5
Clinical variants2
Symptoms19
Compounds0
Trials0
Publications7
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.