Oculocutaneous albinism type I
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|Oculocutaneous albinism type I|
|Other names||OCA1A or OCAIA|
Oculocutaneous albinism type I or type 1A  is an autosomal recessive skin disease. This subtype of oculocutaneous albinism is caused when the gene for tyrosinase (symbol TYR or OCA1) does not function properly.
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