oculocutaneous albinism (Q2017741)

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autosomal recessive disease characterized by abnormal pigmentation of the skin, hair and eyes
  • Albinism, Oculocutaneous
  • OCA
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Language Label Description Also known as
English
oculocutaneous albinism
autosomal recessive disease characterized by abnormal pigmentation of the skin, hair and eyes
  • Albinism, Oculocutaneous
  • OCA

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Identifiers

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EC23.20
Oculocutaneous albinism
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