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- C2775849878 created "2018-01-05" @default.
- C2775849878 modified "2023-10-19" @default.
- C2775849878 type Concept @default.
- C2775849878 seeAlso "https://en.wikipedia.org/wiki/Oculocutaneous%20albinism" @default.
- C2775849878 sameAs Q2017741 @default.
- C2775849878 sameAs 2775849878 @default.
- C2775849878 broader C104317684 @default.
- C2775849878 broader C127313418 @default.
- C2775849878 broader C151730666 @default.
- C2775849878 broader C185592680 @default.
- C2775849878 broader C2775902910 @default.
- C2775849878 broader C54355233 @default.
- C2775849878 broader C55493867 @default.
- C2775849878 broader C86803240 @default.
- C2775849878 inScheme concepts @default.
- C2775849878 note "autosomal recessive disease characterized by abnormal pigmentation of the skin, hair and eyes" @default.
- C2775849878 prefLabel "Oculocutaneous albinism" @default.
- C2775849878 related C107538193 @default.
- C2775849878 related C151913843 @default.
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- C2775849878 related C94435474 @default.
- C2775849878 citedByCount "25288" @default.
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- C2775849878 level "3" @default.
- C2775849878 magId "2775849878" @default.
- C2775849878 umlsCui "C0078918" @default.
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