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Achromatopsia

MONDO:0018852

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

33 clinical trials for this condition and its sub-types, 4 tagged with Achromatopsia itself.

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Sub-types of Achromatopsia

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