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