achromatopsia (Q432396)

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color blindness that is characterized by a congenital cone color vision disorder, the inability to perceive color and to achieve satisfactory visual acuity at high light levels has material basis in autosomal recessive inheritance
  • ACHM
  • monochromatism
  • monochromacy
  • complete color blindness
  • total color blindness
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Language Label Description Also known as
English
achromatopsia
color blindness that is characterized by a congenital cone color vision disorder, the inability to perceive color and to achieve satisfactory visual acuity at high light levels has material basis in autosomal recessive inheritance
  • ACHM
  • monochromatism
  • monochromacy
  • complete color blindness
  • total color blindness

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