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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

• Ocular albinism  (9E1Y)

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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