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  2. Color blindness - Wikipedia

    en.wikipedia.org/wiki/Color_blindness

    An 'affected' gene is either missing (as in Protanopia and Deuteranopia - Dichromacy) or is a chimeric gene (as in Protanomaly and Deuteranomaly). Since the OPN1LW and OPN1MW genes are on the X chromosome, they are sex-linked , and therefore affect males and females disproportionately.

  3. Congenital red–green color blindness - Wikipedia

    en.wikipedia.org/wiki/Congenital_red–green...

    This gene deletion leads to protanopia or deuteranopia (congenital red–green dichromacy). [citation needed] Unequal homologous combination that creates chimeric genes and therefore underlies protanomaly and deuteranomaly. The third gene array shows a dichromatic genotype; the fourth shows a deuteranomalous genotype.

  4. Cone cell - Wikipedia

    en.wikipedia.org/wiki/Cone_cell

    Congenital red–green color blindness – partial color blindness where either one cone class is absent (dichromacy, including protanopia, deuteranopia & tritanopia) or the spectral sensitivity of one cone class is shifted (anomalous trichromacy, including protanomaly, deuteranomaly)

  5. EnChroma - Wikipedia

    en.wikipedia.org/wiki/EnChroma

    Common colors of confusion include blue vs. purple, yellow vs. neon green, grey vs. cyan vs. pink, red vs. orange vs. green vs. brown. [7] Neither dichromatic (protanopia or deuteranopia) users nor tritan users are targeted by EnChroma. [8] As of December 2023, EnChroma markets SuperX lenses to non-colorblind users. [9]

  6. Dichromacy - Wikipedia

    en.wikipedia.org/wiki/Dichromacy

    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 100,000, but is not sex-linked, so affects females and males at similar rates.

  7. OPN1MW2 - Wikipedia

    en.wikipedia.org/wiki/OPN1MW2

    Unequal homologous combination that leads to gene deletion and therefore underlies congenital dichromacy (protanopia and deuteranopia). The third gene array shows a deuteranopia genotype; the fourth shows a normal color vision genotype. OPN1MW2 is a duplication of the OPN1MW gene arising from unequal homologous recombination. During this ...

  8. Evolution of color vision - Wikipedia

    en.wikipedia.org/wiki/Evolution_of_color_vision

    Today, most mammals possess dichromatic vision, corresponding to protanopia red–green colour blindness. They can thus see violet, blue, green and yellow light, but cannot see ultraviolet or deep red light. [5] [6] This was probably a feature of the first mammalian ancestors, which were likely small, nocturnal, and burrowing.

  9. Protanomaly - Wikipedia

    en.wikipedia.org/?title=Protanomaly&redirect=no

    From Wikipedia, the free encyclopedia. Redirect page