@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:Q182005 rdfs:label "متلازمة هولت-أورام"@ar,
        "Holt-Orama sindromu"@az,
        "Holt-Oram-Syndrom"@de,
        "ހިތާއި އަތުގެ ބަލި"@dv,
        "Holt-Oram syndrome"@en,
        "Síndrome de Holt Oram"@es,
        "Holt–Oramin oireyhtymä"@fi,
        "syndrome de Holt-Oram"@fr,
        "sindrome di Holt-Oram"@it,
        "Холт-Орам синдромы"@kk,
        "Zespół Holt-Orama"@pl,
        "Síndrome Holt-Oram"@pt,
        "Síndrome Holt-Oram"@pt-br,
        "Синдром Холта — Орама"@ru,
        "Holt-Oramov sindrom"@sl,
        "Holt-Oram症候群"@zh ;
    schema1:dateModified "2026-10-24T00:14:23+00:00"^^xsd:dateTime ;
    schema1:description "أمراض العظام"@ar,
        "Krankheit"@de,
        "autosomal dominant disease characterized by congenital anomalies located_in heart and located_in upper limb."@en,
        "association de malformations cardiaques de gravité variable avec des anomalies des membres supérieurs"@fr,
        "patologia autosomica dominante con vari difetti strutturali del cuore e degli arti superiori"@it,
        "хвороба"@uk,
        "常染色體顯性疾病，其特徵為先天性異常位於心臟並位於上肢。"@zh ;
    schema1:version 2560163811 ;
    wikibase:identifiers 20,
        23 ;
    wikibase:sitelinks 13 ;
    wikibase:statements 47 ;
    skos:altLabel "HOLT-ORAM SYNDROME"@en,
        "HOLT-ORAM SYNDROME; HOS"@en,
        "HOS"@en,
        "Heart-hand syndrome type 1"@en,
        "Holt–Oram syndrome"@en,
        "Hos1"@en,
        "atrio-digital syndrome"@en,
        "atrio-digital syndrome type 1"@en,
        "atriodigital dysplasia"@en,
        "atriodigital dysplasia type 1"@en,
        "heart-hand syndrome"@en,
        "Sindrome de Holt Oram"@es,
        "dysplasie atrio-digitale type 1"@fr,
        "atriodigitalna displazija tipa 1"@sl,
        "kardiomelični sindrom"@sl,
        "sindrom srca in roke"@sl ;
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    p:P13772 wds:Q182005-FFE8F5F8-FAFF-4D01-AFDB-A6424E8695C8 ;
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    p:P1995 wds:Q182005-584FACE7-7D28-4E06-8605-D6C2B6011E48 ;
    p:P2293 wds:Q182005-CCED21AC-793D-40EB-AEC1-82334E085977 ;
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    p:P699 wds:Q182005-BCEC8634-E249-4228-851F-18942E92BB2A ;
    wdtn:P486 <http://id.nlm.nih.gov/mesh/C535326> ;
    wdtn:P5270 <http://purl.obolibrary.org/obo/MONDO_0007732> ;
    wdtn:P5806 <http://snomed.info/id/205814003> ;
    wdtn:P6366 <https://makg.org/entity/2778830980>,
        <https://makg.org/entity/2908925816> ;
    wdtn:P665 <http://www.kegg.jp/entry/H00433> ;
    wdtn:P699 <http://purl.obolibrary.org/obo/DOID_DOID:0060468> ;
    wdt:P11143 "Holt–Oram syndrome" ;
    wdt:P11430 "DI-01752" ;
    wdt:P13772 "holt-oram-syndrome" ;
    wdt:P138 wd:Q112515385,
        wd:Q6779785 ;
    wdt:P14914 "D00392" ;
    wdt:P1550 "392" ;
    wdt:P1692 "759.89" ;
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    wdt:P1995 wd:Q1071953 ;
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    wdt:P2841 wd:Q21953121,
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    wdt:P2888 <http://identifiers.org/doid/DOID:0060468>,
        <http://purl.obolibrary.org/obo/DOID_0060468>,
        <http://www.orpha.net/ORDO/Orphanet_392> ;
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    wdt:P31 wd:Q112193867,
        wd:Q929833 ;
    wdt:P4229 "Q87.2" ;
    wdt:P4233 "holtoram-syndrome" ;
    wdt:P4317 "6666" ;
    wdt:P486 "C535326" ;
    wdt:P492 "142900" ;
    wdt:P5008 wd:Q4099686 ;
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    wdt:P699 "DOID:0060468" .