EC23.2
Albinism or other specified genetically-determined hypomelanotic disorders
Albinism or other specified genetically-determined hypomelanotic disorders
Classification
ICD-11
Chapter
14: Diseases of the SkinBlock
EC10-EC7YParent Code
EC23Child Codes
2
WHO Foundation
View on WHOChild Codes (2)
Frequently Asked Questions
What is the ICD-11 code for albinism or other specified genetically-determined hypomelanotic disorders?
The ICD-11 code for albinism or other specified genetically-determined hypomelanotic disorders is EC23.2. The full clinical description is "Albinism or other specified genetically-determined hypomelanotic disorders".
What does ICD-11 code EC23.2 mean?
ICD-11 code EC23.2 represents “Albinism or other specified genetically-determined hypomelanotic disorders”. It is classified under Chapter 14: Diseases of the Skin.
What chapter is EC23.2 in?
EC23.2 is in Chapter 14: Diseases of the Skin (codes EA00-EM0Z).
What is the ICD-10 equivalent of ICD-11 code EC23.2?
There is no direct ICD-10 mapping available for EC23.2 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 EC23.2?
EC23.2 has 2 child codes, including: EC23.20 (Oculocutaneous albinism), EC23.2Y (Other specified genetically-determined hypomelanotic disorders).
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