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Color blindness or color vision deficiency ( CVD) is the decreased ability to see color or differences in color. [ 2] The severity of color blindness ranges from mostly unnoticeable to full absence of color perception. Color blindness is usually an inherited problem or variation in the functionality of one or more of the three classes of cone ...
The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child. There are over 6,000 known genetic disorders in humans.
Monochromacy (from Greek mono, meaning "one" and chromo, meaning "color") is the ability of organisms to perceive only light intensity without respect to spectral composition. Organisms with monochromacy lack color vision and can only see in shades of grey ranging from black to white. Organisms with monochromacy are called monochromats.
Achromatopsia. Achromatopsia, also known as rod monochromacy, is a medical syndrome that exhibits symptoms relating to five conditions, most notably monochromacy. Historically, the name referred to monochromacy in general, but now typically refers only to an autosomal recessive congenital color vision condition.
Cerebral achromatopsia. Cerebral achromatopsia is a type of color blindness caused by damage to the cerebral cortex of the brain, rather than abnormalities in the cells of the eye's retina. It is often confused with congenital achromatopsia but underlying physiological deficits of the disorders are completely distinct.
Color Blindness is a more contemporary form of ahistorical racism that is epitomized by the phrase, "I do not see color." In essence the term refers to one who places racism squarely in the past. Whiteness is a vague racial-socio-economic category that has shifted definition over time.
Deuteranopia is a severe form of red-green color blindness, in which the M-cone is absent. It is sex-linked and affects about 1% of males. Color vision is very similar to protanopia. [2] Tritanopia is a severe form of blue-yellow color blindness, in which the S-cone is absent. It is much rarer than the other types, occurring in about 1 in ...
Heterochromia iridum. Heterochromia is a variation in coloration most often used to describe color differences of the iris, but can also be applied to color variation of hair [ 1] or skin. Heterochromia is determined by the production, delivery, and concentration of melanin (a pigment ). It may be inherited, or caused by genetic mosaicism ...