EC23
Genetic disorders of skin pigmentation
Genetic disorders of skin pigmentation
Classification
ICD-11
Chapter
14: Diseases of the SkinBlock
EC10-EC7YParent Code
BlockL1-EC1Child Codes
5
WHO Foundation
View on WHOChild Codes (5)
EC23.0Non-syndromic genetically-determined hypermelanosis or lentiginosis
EC23.1Syndromic genetically-determined hypermelanosis or lentiginosis
EC23.2Albinism or other specified genetically-determined hypomelanotic disorders
EC23.YOther specified genetic disorders of skin pigmentation
EC23.ZGenetic disorders of skin pigmentation, unspecified
Frequently Asked Questions
What is the ICD-11 code for genetic disorders of skin pigmentation?
The ICD-11 code for genetic disorders of skin pigmentation is EC23. The full clinical description is "Genetic disorders of skin pigmentation".
What does ICD-11 code EC23 mean?
ICD-11 code EC23 represents “Genetic disorders of skin pigmentation”. It is classified under Chapter 14: Diseases of the Skin.
What chapter is EC23 in?
EC23 is in Chapter 14: Diseases of the Skin (codes EA00-EM0Z).
What is the ICD-10 equivalent of ICD-11 code EC23?
There is no direct ICD-10 mapping available for EC23 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-10. Use the ICD-11 to ICD-10 converter to search for related codes.
What is the difference between ICD-10 and ICD-11?
ICD-11 is the latest revision of the WHO's International Classification of Diseases, succeeding ICD-10. Key differences include: a fully digital-first design, new chapters for sleep-wake disorders, sexual health, and traditional medicine, improved coding for rare diseases, and better integration with electronic health records through extension codes.
What are the subcategories under EC23?
EC23 has 5 child codes, including: EC23.0 (Non-syndromic genetically-determined hypermelanosis or lentiginosis), EC23.1 (Syndromic genetically-determined hypermelanosis or lentiginosis), EC23.2 (Albinism or other specified genetically-determined hypomelanotic disorders), EC23.Y (Other specified genetic disorders of skin pigmentation), and 1 more.
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