ICD-11 classes
14 Diseases of the skin
Skin disorders involving specific cutaneous structures
Disorders of the epidermis and epidermal appendages
Disorders of skin colour
EC23 — Genetic disorders of skin pigmentation
EC23.2 — Albinism or other specified genetically-determined...
EC23.20 — Oculocutaneous albinism
ICD-11 EC23.20 — Oculocutaneous albinism
Oculocutaneous albinism is a genetically heterogeneous congenital disorder characterised by decreased or absent pigmentation in the hair, skin, and eyes.
The diagnosis includes nothing.
The diagnosis excludes nothing.
It has no clarifying diagnoses.
The diagnosis is coded elsewhere: