@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:Q2092064 rdfs:label "هيموفيليا أ"@ar,
        "Hemofiliya A"@az,
        "হিমোফিলিয়া এ"@bn,
        "hemofília A"@ca,
        "hemophilia A"@en,
        "hemofilio A"@eo,
        "hemofilia A"@es,
        "هموفیلی ای"@fa,
        "A-verenvuototauti"@fi,
        "hémophilie A"@fr,
        "માતૃપક્ષી રુધિરસ્રાવિતા"@gu,
        "Հեմոֆիլիա A"@hy,
        "emofilia A"@it,
        "血友病A"@ja,
        "A형혈우병"@ko,
        "haemophilia A"@la,
        "Hemofilia A"@ms,
        "ହେମୋଫିଲିଆ ଏ"@or,
        "hemofilia A"@pt,
        "hemofilie A"@ro,
        "гемофилия A"@ru,
        "hemofilija A"@sl,
        "Hemofili A"@tr,
        "гемофілія А"@uk,
        "血友病A型"@zh ;
    schema1:dateModified "2026-10-24T00:51:44+00:00"^^xsd:dateTime ;
    schema1:description "Krankheit"@de,
        "X-linked disease that has material basis in Factor VIII deficiency, which results in the formation of fibrin deficient clots which makes coagulation much more prolonged"@en,
        "trastorno genético asociado con hemorragia grave"@es,
        "بیماری خونی ژنتیکی"@fa,
        "hematologinen sairaus"@fi,
        "maladie"@fr,
        "રોગ"@gu,
        "forma più comune di emofilia, caratterizzata da emorragie spontanee o prolungate"@it,
        "ଏହ ଏକ ରକ୍ତସ୍ରାବ ଜନିତ ରୋଗ ଯାହା ଜେନେଟିକ ପରିବର୍ତ୍ତନ ହେତୁ ଘଟିଥାଏ ।"@or,
        "boală legată de cromozomul X care are o bază materială în deficitul de factor VIII, care duce la formarea de cheaguri deficitare de fibrină, ceea ce prelungește mult coagularea"@ro,
        "наиболее частая форма гемофилии, вызванная дефицитом фактора свёртывания крови VIII"@ru,
        "X-vezana bolezen, ki nastane zaradi pomanjkanja faktorja VIII, kar povzroči nastajanje strdkov s pomanjkanjem fibrina, zaradi česar se koagulacija močno podaljša"@sl,
        "найбільш часта форма гемофілії, викликана дефіцитом фактора згортання крові VIII"@uk ;
    schema1:version 2560169538 ;
    wikibase:identifiers 31,
        34 ;
    wikibase:sitelinks 16 ;
    wikibase:statements 65 ;
    skos:altLabel "Congenital factor VIII disorder"@en,
        "Hemophilia A"@en,
        "Hemophilia A (disorder)"@en,
        "Subhemophilia"@en,
        "factor VIII deficiency"@en,
        "haemophilia A"@en,
        "هموفیلی A"@fa,
        "هموفیلی آ"@fa,
        "A-hemofilia"@fi,
        "hemofilia A"@fi,
        "verenvuototauti A"@fi,
        "hémophilie classique"@fr,
        "હિમોફિલિયા એ"@gu,
        "第VIII因子欠乏症"@ja,
        "第VIII因子欠損症"@ja,
        "혈우병 A"@ko,
        "甲型血友病"@zh ;
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