H53.51
Achromatopsia
Approximate Synonyms
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Achromatopsia eye condition)
Clinical Information
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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.
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Severely deficient color perception, typically with monochromacy and reduced visual acuity. The atypical form can include normal visual acuity with pseudomonochromacy.
Details
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H53.51 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
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The 2023 edition of ICD-10-CM H53.51 became effective on October 1, 2022.
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This is the American ICD-10-CM version of H53.51 – other international versions of ICD-10 H53.51 may differ.