Oculocutaneous albinism type 1

rare

Type 1 oculocutaneous albinism (OCA1) describes a group of tyrosine related OCAs that includes OCA1A, OCA1B, type 1 minimal pigment oculocutaneous albinism (OCA1-MP) and type 1 temperature sensitive oculocutaneous albinism (OCA1-TS).

Identifiers: MONDO:0018135 Orphanet:352731
Part of: Disorder of tyrosine metabolism Oculocutaneous albinism
Also known as: ATN · OCA1 · oculocutaneous albinism, tyrosinase negative

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Oculocutaneous albinism type 1A	MONDO:0008745	1	TYR
Minimal pigment oculocutaneous albinism type 1	MONDO:0018136
Temperature-sensitive oculocutaneous albinism type 1	MONDO:0018137

Rare disease

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