Oculocutaneous albinism
MONDO:0018910Oculocutaneous albinism (OCA) describes a group of inherited disorders of melanin biosynthesis characterized by a generalized reduction in pigmentation of hair, skin and eyes and variable ocular findings including nystagmus, reduced visual acuity and photophobia. Variants include OCA1A (the most severe form), OCA1B, OCA1-minimal pigment (OCA1-MP), OCA1-temperature sensitive (OCA1-TS), OCA2, OCA3, OCA4, OCA5, OCA6 and OCA7.
Also known as: OCA, non-syndromic oculocutaneous albinism, nonsyndromic oculocutaneous albinism, albinism, oculocutaneous
4 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Oculocutaneous albinism type 1A
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Autosomal dominant oculocutaneous albinism
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Minimal pigment oculocutaneous albinism type 1
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Oculocutaneous albinism type 1
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Oculocutaneous albinism type 1B
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Oculocutaneous albinism type 2
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Oculocutaneous albinism type 3
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Oculocutaneous albinism type 4
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Oculocutaneous albinism type 5
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Oculocutaneous albinism type 6
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Oculocutaneous albinism type 7
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Oculocutaneous albinism type 8
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Temperature-sensitive oculocutaneous albinism type 1
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