red color blindness
Findings
No curated finding names red color blindness yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Protanopia is a severe type of color vision deficiency caused by the complete absence of red retinal photoreceptors. Protans have difficulties distinguishing between blue and green colors and also between red and green colors. It is a form of dichromatism in which the subject can only perceive light wavelengths from 400 to 650 nm, instead of the usual 700 nm. Pure reds cannot be seen, instead appearing black; purple colors cannot be distinguished from blues; more orange-tinted reds may appear as very dim yellows, and all orange-yellow-green shades of too long a wavelength to stimulate the blue receptors appear as a similar yellow hue. It is hereditary, sex-linked, and present in 1% of males.
Definition from the Mondo Disease Ontology (MONDO:0010565), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- OPN1LWHGNC:9936
- Definitive · ClinGen · X-linked · 2025
- Strong · Labcorp Genetics (formerly Invitae) · X-linked · 2021
Where it sits
Other names
4 names
Resolves to: red color blindness
- Also called
- colorblindness, protanpartial achromatopsia, protan typeprotan defectprotanopia