Oculocutaneous albinism type 4 (Q90691): Difference between revisions

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+https://id.who.int/icd/entity/1286886811
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+August 2026Timestamp +2026-08-13T00:00:00Z
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Calendar Gregorian
Precision 1 day
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@@ Property / Collection date: 13 August 2026 / rank @@
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Latest revision as of 17:40, 15 August 2026

OCA4 is characterised by hypopigmentation of the skin and hair plus the characteristics of all other types of OCA. The amount of cutaneous pigmentation in OCA4 ranges from minimal to near normal. Hair colour may darken with time, but does not vary significantly from childhood to adulthood. It is caused by a mutation in SLC45A2 gene.

Language	Label	Description	Also known as
default for all languages	ID_1286886811
English	Oculocutaneous albinism type 4	OCA4 is characterised by hypopigmentation of the skin and hair plus the characteristics of all other types of OCA. The amount of cutaneous pigmentation in OCA4 ranges from minimal to near normal. Hair colour may darken with time, but does not vary significantly from childhood to adulthood. It is caused by a mutation in SLC45A2 gene.