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:

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