ICD-11 classes
09 Diseases of the visual system
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: