@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:Q2852249 rdfs:label "شذوذ تطوري"@ar,
        "прыроджаная анамалія"@be-tarask,
        "malformació congènita"@ca,
        "kongenitální abnormalita"@cs,
        "συγγενής ανωμαλία"@el,
        "congenital abnormality"@en,
        "malformación congénita"@es,
        "anomalie du développement"@fr,
        "mínormáltacht ó bhroinn"@ga,
        "malformación conxénita"@gl,
        "születési rendellenesség"@hu,
        "malformazione"@it,
        "先天性異常"@ja,
        "aangeboren defect"@nl,
        "medfødd misdanning"@nn,
        "malformação congénita"@pt,
        "anomalie congenitală"@ro,
        "врожденная аномалия"@ru,
        "prirojena nepravilnost"@sl,
        "konjenital hastalıklar"@tr,
        "先天性异常"@zh ;
    schema1:dateModified "2026-10-13T00:31:33+00:00"^^xsd:dateTime ;
    schema1:description "тып прыроджанага разладу"@be-tarask,
        "condició present al néixer independentment de la causa"@ca,
        "type of congenital disorder"@en,
        "alteración anatómica que ocurre en la etapa intrauterina"@es,
        "tipo de desorde conxénita"@gl,
        "defeito estrutural ou funcional presente desde o nascimento"@pt,
        "tip de tulburare congenitală"@ro,
        "doğumda mevcut olan anormal bir durumdur"@tr ;
    schema1:version 2556398592 ;
    wikibase:identifiers 19 ;
    wikibase:sitelinks 9 ;
    wikibase:statements 52 ;
    skos:altLabel "anomalia congènita"@ca,
        "vrozená vývojová vada"@cs,
        "abnormality"@en,
        "birth defect"@en,
        "congenital abnormalities"@en,
        "malformacion congenita"@es,
        "malformacion congénita"@es,
        "malformacion genetica"@es,
        "malformación congenita"@es,
        "malformación genética"@es,
        "malformation Congénitale"@fr,
        "malformation congenitale"@fr,
        "malformation congénitale"@fr,
        "malformations congénitales"@fr,
        "veleszületett rendellenesség"@hu,
        "malformazione congenita"@it,
        "malformazioni"@it,
        "malformação congênita"@pt,
        "defect congenital"@ro,
        "doğum kusuru"@tr,
        "konjenital bozukluk"@tr ;
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    p:P9341 wds:Q2852249-997f3ecc-47a0-5206-f432-fa01fe217fe4 ;
    wdtn:P2581 <http://babelnet.org/rdf/s00010673n> ;
    wdtn:P4527 <http://data.parliament.uk/terms/90679> ;
    wdtn:P486 <http://id.nlm.nih.gov/mesh/D000013> ;
    wdtn:P508 <http://purl.org/bncf/tid/16348> ;
    wdtn:P672 <http://id.nlm.nih.gov/mesh/C16.131> ;
    wdtn:P8061 <http://aims.fao.org/aos/agrovoc/c_10058> ;
    wdtn:P8408 <http://kbpedia.org/kko/rc/CongenitalCondition> ;
    wdt:P11955 "T019" ;
    wdt:P12385 "malformacio" ;
    wdt:P1296 "0121222" ;
    wdt:P1424 wd:Q20324800 ;
    wdt:P1709 <http://purl.org/biotop/biotop.owl#CongenitalAbnormalStructure> ;
    wdt:P1748 "C2849" ;
    wdt:P18 <http://commons.wikimedia.org/wiki/Special:FilePath/Microcephaly-comparison-500px.jpg>,
        <http://commons.wikimedia.org/wiki/Special:FilePath/NCP14053.jpg>,
        <http://commons.wikimedia.org/wiki/Special:FilePath/Photo%20of%20baby%20with%20FAS.svg>,
        <http://commons.wikimedia.org/wiki/Special:FilePath/Spina-bifida.jpg> ;
    wdt:P1995 wd:Q631521 ;
    wdt:P2579 wd:Q631521 ;
    wdt:P2581 "00010673n" ;
    wdt:P279 wd:Q2057971,
        wd:Q727096 ;
    wdt:P2892 "C0000768",
        "C0266647" ;
    wdt:P3219 "malformations-congenitales" ;
    wdt:P373 "Congenital diseases and disorders" ;
    wdt:P4527 "90679" ;
    wdt:P486 "D000013" ;
    wdt:P493 "740-759.99",
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    wdt:P5008 wd:Q54439832 ;
    wdt:P508 "16348" ;
    wdt:P672 "C16.131" ;
    wdt:P691 "ph612519" ;
    wdt:P7329 "LD9Z" ;
    wdt:P780 wd:Q12133,
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        wd:Q431643,
        wd:Q527065,
        wd:Q773370,
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    wdt:P8408 "CongenitalCondition" ;
    wdt:P9341 "Q000002" .