Colorblindness, partial, protan series

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Colorblindness, partial, protan series
MONDO_0010564
OPN1LW Unknown
12051694
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Colorblindness, partial, protan series.
5 View disease cluster →
Red color blindness 1 shared geneOPN1LW Related via 1 shared gene including OPN1LW. Cone monochromatism 1 shared geneOPN1LW Related via 1 shared gene including OPN1LW. X-linked cone dysfunction syndrome with myopia 1 shared geneOPN1LW Related via 1 shared gene including OPN1LW. Blue cone monochromatism 1 shared geneOPN1LW Related via 1 shared gene including OPN1LW. Cone-rod dystrophy 1 shared geneOPN1LW Related via 1 shared gene including OPN1LW.