Oculocutaneous albinism in eye skin is a series of hereditary disease related to melanin biosynthesis, which is mainly short of melanin of eye, skin, hair and brings various hazard to patients.

眼皮肤白化病是一组与黑色素生物合成有关的遗传性疾病，表现为眼、皮肤、毛发黑色素缺乏等。

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Oculocutaneous albinism type 1 is caused by a mutation in a gene on chromosome 11.

CNN: Albinism

Oculocutaneous albinism type 2 is caused by a mutation in a gene on chromosome 15.

CNN: Albinism

Oculocutaneous albinism is caused by a mutation in one of four genes.

CNN: Albinism