Oculocutaneous albinism type 6

MONDO:0018264

A form of oculocutaneous albinism characterized by light hair at birth that darkens with age, white skin, transparent irides, photophobia, nystagmus, foveal hypoplasia and reduced visual acuity.

Also known as: OCA6, albinism, oculocutaneous, type VI, skin/hair/eye pigmentation 4, fair/dark skin

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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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