Achromatopsia

From BugSigDB


Achromatopsia (ACHM) is a rare autosomal recessive retinal disorder characterized by color blindness, nystagmus, photophobia, and severely reduced visual acuity due to the absence or impairment of cone function.
Aliases
  • ACHM
  • achromatopsia
  • Complete or incomplete color blindness
  • complete or incomplete color blindness
  • complete or incomplete colour blindness
  • monochromatism
  • Pingelapese blindness
  • Rod monochromacy
  • Rod monochromatism
  • Total color blindness
  • total color blindness
  • total colour blindness