Albinism or other specified genetically-determined hypomelanotic disorders
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
A large group of heritable disorders in which cutaneous melanin production is reduced or absent, mainly as the result of defects in enzymes required for normal melanin biosynthesis.
code elsewhere
sections/codes in this section (EC23.2-EC23.2)
- Oculocutaneous albinism (EC23.20)
- Other specified genetically-determined hypomelanotic disorders (EC23.2Y)
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