@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:Q5160437 rdfs:label "فرط الأنسولينية الخلقي"@ar,
        "Kongenitaler Hyperinsulinismus"@de,
        "congenital hyperinsulinism"@en,
        "denaska hiperinsulinismo"@eo,
        "Synnynnäinen hyperinsulinismi"@fi,
        "hyperinsulinisme congénital"@fr,
        "הפרשת יתר מולדת של אינסולין"@he,
        "Բնածին հիպերինսուլինիզմ"@hy,
        "先天性高インスリン血症"@ja,
        "wrodzony hiperinsulinizm"@pl,
        "Hiperinsulinismo isolado congênito"@pt,
        "Hiperinsulinismo isolado congênito"@pt-br,
        "kongenitalni hiperinsulinizem"@sl,
        "Конгенитални хиперинсулинизам"@sr,
        "konjenital hiperinsülinizm"@tr,
        "Вроджений гіперінсулінізм"@uk ;
    schema1:dateModified "2026-10-24T00:29:38+00:00"^^xsd:dateTime ;
    schema1:description "Angeborene Erkrankung der Bauchspeicheldrüse"@de,
        "genetic disease"@en,
        "maladie génétique se manifestant par une hypoglycémie"@fr,
        "הפרעה מולדת"@he,
        "choroba uwarunkowana genetycznie"@pl ;
    schema1:version 2560166288 ;
    wikibase:identifiers 19,
        22 ;
    wikibase:sitelinks 11 ;
    wikibase:statements 43 ;
    skos:altLabel "CHI"@en,
        "PHHI"@en,
        "Persistent hyperinsulinemic hypoglycemia of infancy"@en,
        "PHHI"@he ;
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    wdtn:P4527 <http://data.parliament.uk/terms/512659> ;
    wdtn:P486 <http://id.nlm.nih.gov/mesh/D044903> ;
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    wdtn:P6366 <https://makg.org/entity/2777643638> ;
    wdtn:P672 <http://id.nlm.nih.gov/mesh/C06.689.150>,
        <http://id.nlm.nih.gov/mesh/C16.614.200>,
        <http://id.nlm.nih.gov/mesh/C18.452.394.968.250>,
        <http://id.nlm.nih.gov/mesh/C18.452.394.984.200> ;
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        "C131425" ;
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        wd:Q123028,
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        "C1257959",
        "C3888018" ;
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        "C16.614.200",
        "C18.452.394.968.250",
        "C18.452.394.984.200" ;
    wdt:P7464 "congenital-hyperinsulinism" ;
    wdt:P9272 "38055" .

