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Dictionary » Dyschromatopsia


Introduction: Dyschromatopsia

Description of Dyschromatopsia

Dyschromatopsia: 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, HUMAN) that code the photopigments for red, green and blue.
Source: Diseases Database

Dyschromatopsia: Related Topics

These medical condition or symptom topics may be relevant to medical information for Dyschromatopsia:

Terms associated with Dyschromatopsia:

Terms Similar to Dyschromatopsia:

Source: Diseases Database

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