Achromatopsia

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.

Also known as: ACHM, Pingelapese blindness, Rod monochromacy, Rod monochromatism, achromatopsia, complete or incomplete color blindness, complete or incomplete colour blindness, total color blindness

34 clinical trials for this condition and its sub-types.