Rare Non-Neoplastic Disorder
Achromatopsia
Achromatopsia
Achromatopsia
An autosomal recessive genetic disorder affecting the cone cells of the eye. It may be complete, in which the individual can only perceive black, white, or shades or gray, or incomplete, in which the individual has a residual amount of color vision.
C0152200
C84528
Disease or Syndrome