| dbo:description
|
- Krankheit (de)
- malattia (it)
- medical condition (en)
- медичний стан (uk)
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| dbo:icd10
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| dbo:omim
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| dbo:orpha
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| dbo:wikiPageWikiLink
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| dbp:causes
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- Mutation in the TYR gene on chromosome 11 (en)
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| dbp:frequency
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- Autosomal Recessive Pattern, 1/20,000 people in world (en)
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| dbp:icd
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| dbp:name
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- Oculocutaneous albinism type I (en)
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| dbp:omim
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| dbp:onset
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- Is inherited and phenotypically present beginning at birth (en)
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| dbp:orphanet
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| dbp:symptoms
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- Decreased or absent pigmentation of the hair, skin, and eyes. (en)
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| dbp:synonyms
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| dbp:treatment
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- No currently known treatment (en)
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| dbp:types
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| dbp:wikiPageUsesTemplate
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| dct:subject
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| gold:hypernym
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| rdf:type
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| rdfs:label
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- Oculocutaneous albinism type I (en)
- Okulokutaner Albinismus Typ 1 (de)
- Albinisme oculocutané type I (fr)
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| owl:sameAs
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| prov:wasDerivedFrom
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| foaf:isPrimaryTopicOf
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| foaf:name
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- Oculocutaneous albinism type I (en)
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| is dbo:wikiPageRedirects
of | |
| is dbo:wikiPageWikiLink
of | |
| is foaf:primaryTopic
of | |