Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Hereditary neurological disease · Achromatopsia
Achromatopsia 6
Any achromatopsia caused by a mutation in the PDE6H gene, characterized by incomplete loss of color vision, with a red-green color vision defect and normal or near-normal blue-yellow vision. Reduced visual acuity is also present, but not progressive.
This condition has no sub-types.