1.(MeSH)Defects of color vision are mainly hereditary traits but can be secondary to acquired or developmental abnormalities in the CONES (RETINA). Severity of hereditary defects of color vision depends on the degree of mutation of the OPSIN genes (on X CHROMOSOME and CHROMOSOME 3) that code the photopigments for red, green and blue.;Severely deficient color perception, typically with monochromacy and reduced visual acuity. The atypical form can include normal visual acuity with pseudomonochromacy.
C10.597.751.941.256, C11.966.256, C23.888.592.763.941.256, Achromatopsia (MeSH), Color Blindness (MeSH), color-blindness (MeSH), Color Blindness, Acquired (MeSH), Color Blindness, Blue (MeSH), Color Blindness, Green (MeSH), Color Blindness, Inherited (MeSH), Color Blindness, Red (MeSH), Color Blindness, Red-Green (MeSH), Color Vision Defects (MeSH), Deutan Defect (MeSH), Monochromatopsia (MeSH), Protan Defect (MeSH)
Color Perception, Color Vision[Analogie]
Tritan Defect (n.) [MeSH]
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