Oculocutaneous albinism type 3

MONDO:0008747

Type 3 oculocutaneous albinism (OCA3) is a form of oculocutaneous albinism (OCA) characterized by rufous or brown albinism and occurring mainly in the African population.

Also known as: OCA3, Red oculocutaneous albinism, TYRP1 oculocutaneous albinism, oculocutaneous albinism caused by mutation in TYRP1, oculocutaneous albinism type 3, rufous oculocutaneous albinism, xanthous oculocutaneous albinism, ROCA

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Broader categories

Disease (680) Metabolic disease (233) Hereditary disease (176) Skin disorder (132) Inborn errors of metabolism (45) Human disease (14) Skin pigmentation disorder (11) Hereditary skin disorder (6) Oculocutaneous albinism (4) Disease of genetic or genomic mechanism (2)

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