Human genes for blue color blindness
Blue color blindness [DOID:11661]
A color blindness that is characterised by a selective deficiency of blue vision, has_material_basis_in autosomal dominant inheritance of a mutation in the OPN1SW gene and is associated with a deficiency or absence of blue-sensitive cone photoreceptor function.
Synonyms: blue color blindness, blue color blindnesses, DOID:11661, Tritan defect, Tritanopia ...
Linkouts: OMIM