@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:Q1786496 rdfs:label "تسنم الرأس وارتفاق الأصابع"@ar,
        "kraniofaziale Fehlbildung"@de,
        "ακροκεφαλοσυνδακτυλία"@el,
        "acrocephalosyndactylia"@en,
        "acrocefalosindactilia"@es,
        "acrocéphalosyndactylie"@fr,
        "acrocefalosindattilia"@it,
        "acrocefalossindactilia"@pt,
        "akrocefalosindaktilija"@sl,
        "acrocefałosindatilia"@vec,
        "Tật đầu hình tháp dính ngón tay"@vi ;
    schema1:dateModified "2026-07-05T12:31:01+00:00"^^xsd:dateTime ;
    schema1:description "مرض"@ar,
        "Krankheit"@de,
        "group of diseases"@en,
        "craneosinostosis sindrómica causada por mutaciones puntuales genéticas"@es,
        "haigus"@et,
        "famille de maladies"@fr,
        "gruppo di malattie"@it,
        "хвороба"@uk,
        "nhóm bệnh"@vi ;
    schema1:version 2514120782 ;
    wikibase:identifiers 24 ;
    wikibase:sitelinks 7 ;
    wikibase:statements 38 ;
    skos:altLabel "تسنم الرأس وارتفاق الأصابع العنشي"@ar,
        "Apert syndrome"@en,
        "acrocephalopolysyndactyly"@en,
        "acrocephalosyndactyly"@en,
        "acrocefalopilidactilia"@es ;
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    p:P9272 wds:Q1786496-2A53B7CE-84B0-4744-A2D0-17E07CA2F887 ;
    wdtn:P486 <http://id.nlm.nih.gov/mesh/D000168> ;
    wdtn:P5270 <http://purl.obolibrary.org/obo/MONDO_0000078> ;
    wdtn:P6366 <https://makg.org/entity/2779482251> ;
    wdtn:P672 <http://id.nlm.nih.gov/mesh/C05.116.099.370.894.232.015>,
        <http://id.nlm.nih.gov/mesh/C05.116.099.370.894.819.100>,
        <http://id.nlm.nih.gov/mesh/C05.660.207.240.100>,
        <http://id.nlm.nih.gov/mesh/C05.660.585.800.100>,
        <http://id.nlm.nih.gov/mesh/C05.660.906.364.100>,
        <http://id.nlm.nih.gov/mesh/C05.660.906.819.100>,
        <http://id.nlm.nih.gov/mesh/C16.131.621.207.240.100>,
        <http://id.nlm.nih.gov/mesh/C16.131.621.585.800.100>,
        <http://id.nlm.nih.gov/mesh/C16.131.621.906.364.100>,
        <http://id.nlm.nih.gov/mesh/C16.131.621.906.819.100> ;
    wdtn:P699 <http://purl.obolibrary.org/obo/DOID_DOID:12960> ;
    wdt:P11143 "Acrocephalosyndactyly" ;
    wdt:P13082 "Pediatriche/acrocefalosindattilia" ;
    wdt:P13204 "ftw7zusg" ;
    wdt:P1417 "science/acrocephalosyndactyly" ;
    wdt:P1550 "946" ;
    wdt:P1692 "755.55" ;
    wdt:P1748 "C34348" ;
    wdt:P1995 wd:Q1071953 ;
    wdt:P279 wd:Q1360044,
        wd:Q378183 ;
    wdt:P2888 <http://identifiers.org/doid/DOID:12960>,
        <http://purl.obolibrary.org/obo/DOID_12960> ;
    wdt:P2892 "C0001193",
        "C1510455" ;
    wdt:P31 wd:Q112193867 ;
    wdt:P373 "Acrocephalosyndactyly" ;
    wdt:P486 "D000168" ;
    wdt:P492 "101200" ;
    wdt:P494 "Q87.0" ;
    wdt:P5008 wd:Q4099686 ;
    wdt:P5270 "MONDO_0000078" ;
    wdt:P6366 "2779482251" ;
    wdt:P6532 wd:Q1360044,
        wd:Q378183 ;
    wdt:P667 "A90" ;
    wdt:P672 "C05.116.099.370.894.232.015",
        "C05.116.099.370.894.819.100",
        "C05.660.207.240.100",
        "C05.660.585.800.100",
        "C05.660.906.364.100",
        "C05.660.906.819.100",
        "C16.131.621.207.240.100",
        "C16.131.621.585.800.100",
        "C16.131.621.906.364.100",
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    wdt:P699 "DOID:12960" ;
    wdt:P9272 "174" .