@prefix p: <http://www.wikidata.org/prop/> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix schema1: <http://schema.org/> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
@prefix wd: <http://www.wikidata.org/entity/> .
@prefix wds: <http://www.wikidata.org/entity/statement/> .
@prefix wdt: <http://www.wikidata.org/prop/direct/> .
@prefix wdtn: <http://www.wikidata.org/prop/direct-normalized/> .
@prefix wikibase: <http://wikiba.se/ontology#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

wd:Q3144934 rdfs:label "داء الاصطباغ الدموي الوراثي"@ar,
        "İrsi hemoxromatoz"@az,
        "hemocromatosi hereditària"@ca,
        "hemocromatedd"@cy,
        "Hæmokromatose"@da,
        "Hämochromatose klassische"@de,
        "hereditary haemochromatosis"@en,
        "Hemokromatozo"@eo,
        "hemocromatosis hereditaria"@es,
        "hemokromatoosi"@fi,
        "hémochromatose classique"@fr,
        "Haemacrómatóis cineál 1"@ga,
        "Hemocromatose"@gl,
        "hemochromatosis (primer)"@hu,
        "emocromatosi ereditaria"@it,
        "ヘモクロマトーシス"@ja,
        "hemokromatose"@nb,
        "Hemochromatose"@nl,
        "HFE-hemokromatose"@nn,
        "Hemochromatoza pierwotna"@pl,
        "гемохроматоз"@ru,
        "dedna hemokromatoza"@sl,
        "hemokromatos"@sv,
        "HFE遺傳性血色病"@zh,
        "HFE遺傳性血色病"@zh-hant ;
    schema1:dateModified "2026-08-03T01:46:58+00:00"^^xsd:dateTime ;
    schema1:description "مرض وراثي"@ar,
        "Krankheit"@de,
        "metal metabolism disorder characterized by the accumulation of iron in various organs of the body"@en,
        "enfermedad sanguínea del metabolismo del hierro"@es,
        "forme la plus commune d'hémochromatose héréditaire"@fr,
        "öröklött anyagcsere-betegség"@hu,
        "malattia"@it,
        "genetyczna choroba metabolizmu żelaza"@pl,
        "ärftlig sjukdom"@sv,
        "хвороба"@uk ;
    schema1:version 2526566052 ;
    wikibase:identifiers 30 ;
    wikibase:sitelinks 17 ;
    wikibase:statements 49 ;
    skos:altLabel "داء الاصطباغ الدموي الوراثى"@ar,
        "داء الهيموكروماتوزيز الوراثي"@ar,
        "داء ترسب الأصبغة الدموية الوراثي"@ar,
        "hemocromatosi clàssica"@ca,
        "Celtic curse"@en,
        "HFE hereditary hemochromatosis"@en,
        "Haemochromatosis"@en,
        "Hemochromatosis, Hereditary"@en,
        "diabetes bronze"@en,
        "hemochromatosis"@en,
        "iron storage disorder"@en,
        "hemocromatosis clásica"@es,
        "Hémochromatose idiopathique"@fr,
        "hémochromatose type 1"@fr,
        "HFE"@hu,
        "idiopatiás hemochromatosis"@hu,
        "idiopátiás hemokromatózis"@hu,
        "diabete bronzino"@it,
        "遺伝性ヘモクロマトーシス"@ja,
        "遺伝性血色素症"@ja,
        "血色沉著症"@zh,
        "血鐵沉積症"@zh ;
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    wdtn:P5270 <http://purl.obolibrary.org/obo/MONDO_0006507> ;
    wdtn:P6366 <https://makg.org/entity/2777895808>,
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    wdtn:P665 <http://www.kegg.jp/entry/H00211> ;
    wdtn:P672 <http://id.nlm.nih.gov/mesh/C16.320.565.618.337>,
        <http://id.nlm.nih.gov/mesh/C18.452.565.500.480>,
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    wdt:P1299 wd:Q131676056 ;
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        "E83.110",
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        "235200" ;
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