Minimal pigment oculocutaneous albinism type 1

MONDO:0018136

Type 1 minimal pigment oculocutaneous albinism (OCA1-MP) is an extremely rare form of OCA1 with minimal pigment present, characterized by blond hair, variable iris transillumination, visual acuity ranging from 20/80-20/200 and white skin, with or without skin nevi.

Also known as: MP OCA type 1, OCA1-MP

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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) Inborn disorder of amino acid metabolism (4) Oculocutaneous albinism (4)

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