Wikidata

(Q2017741)

English

oculocutaneous albinism

autosomal recessive disease characterized by abnormal pigmentation of the skin, hair and eyes

  • Albinism, Oculocutaneous
  • OCA
In more languages

Statements

health specialty
ophthalmology
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dermatology
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Identifiers

KEGG ID
H00168
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ICD-11 ID (MMS)
EC23.20
subject named as
Oculocutaneous albinism
0 references
Mondo ID
MONDO_0018910
0 references
 
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