×

CPT Changes

Current book and archives back to 2000
Easy-to-read online book format
Linked to and from code details

learn more

close

EC23 Genetic disorders of skin pigmentation

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Genetic disorders of the skin characterised by disordered pigmentation, including albinism and inherited forms of lentiginosis.

sections/codes in this section (EC23-EC23)

• Non-syndromic genetically-determined hypermelanosis or lentiginosis  (EC23.0)
• Syndromic genetically-determined hypermelanosis or lentiginosis  (EC23.1)
• Albinism or other specified genetically-determined hypomelanotic disorders  (EC23.2)
• Other specified genetic disorders of skin pigmentation  (EC23.Y)
• Genetic disorders of skin pigmentation, unspecified  (EC23.Z)

Thank you for choosing Find-A-Code, please Sign In to remove ads.