Specific code 2015 ICD-9-CM Diagnosis Code 368.54
  • 2015
  • Billable Code
  • ICD-9-CM 368.54 will be replaced by an equivalent ICD-10-CM code (or codes) when the United States transitions from ICD-9-CM to ICD-10-CM on October 1, 2015.
  • ICD-9-CM 368.54 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
Clinical Information
  • 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
  • Severely deficient color perception, typically with monochromacy and reduced visual acuity. The atypical form can include normal visual acuity with pseudomonochromacy
Applies To
  • Monochromatism (cone) (rod)
Convert to ICD-10-CM: 368.54 converts directly to:
  • 2015 ICD-10-CM H53.51 Achromatopsia
ICD-9-CM Volume 2 Index entries containing back-references to 368.54:
  • Achromate (congenital) 368.54
  • Achromatopia 368.54
  • Achromatopsia (congenital) 368.54
  • Blindness (acquired) (congenital) (both eyes) 369.00
  • Monochromatism (cone) (rod) 368.54
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 368.54 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2015 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.