@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:Q3508705 rdfs:label "متلازمة تيموثي"@ar,
        "Timothyjev sindrom"@bs,
        "síndrome de Timothy"@ca,
        "Timothy-Syndrom"@de,
        "Timothy syndrome"@en,
        "síndrome de Timothy"@es,
        "syndrome de Timothy"@fr,
        "टीमोठी सिंड्रोम"@hi,
        "Timothyjev sindrom"@hr,
        "ティモシー症候群"@ja,
        "티모시 증후군"@ko,
        "síndrome de Timothy"@pt,
        "Ugonjwa wa Timothy"@sw,
        "sìndrome de Timothy"@vec ;
    schema1:dateModified "2026-10-24T00:29:26+00:00"^^xsd:dateTime ;
    schema1:description "مرض من الأمراض"@ar,
        "Krankheit"@de,
        "autosomal dominant disease that is characterized by cardiac, hand/foot, facial, and neurodevelopmental features; the two forms are type 1 (classic) and type 2, a rare form that has material basis in mutations in a transcript variant of CACNA1C"@en,
        "QT延長症候群や合指症などを起こす常染色体顕性遺伝の先天性疾患"@ja,
        "Ni ugonjwa wa kinasaba unaosababsihwa na mabadiliko katika jeni CACNA1C na huathiri mfumo wa moyo,mfumo wa neva na viungo vingine kama miguu.Kuna aina mbili za ugonjwa huu.Aina 1 na aina 2"@sw,
        "хвороба"@uk ;
    schema1:version 2560166256 ;
    wikibase:identifiers 17,
        19 ;
    wikibase:sitelinks 11 ;
    wikibase:statements 46 ;
    skos:altLabel "LQT8"@en,
        "Long QT syndrome type 8"@en,
        "Long QT syndrome-syndactyly syndrome"@en,
        "Long Qt Syndrome With Syndactyly"@en,
        "TIMOTHY SYNDROME"@en,
        "TIMOTHY SYNDROME; TS"@en,
        "TS"@en,
        "long QT syndrome 8"@en,
        "obsolete Timothy syndrome"@en,
        "Sindrome de Timothy"@es,
        "Syndrome de timothy"@fr,
        "LTQ AINA 8"@sw,
        "Ugonjwa unaohusiana na CACNA 1"@sw ;
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    p:P11430 wds:Q3508705-5c0397e6-4c1c-6374-1451-a95a19dc1183 ;
    p:P1193 wds:Q3508705-979DCED5-4B8A-4128-9790-2C93BB188AD5 ;
    p:P138 wds:Q3508705-c1661c0b-40e5-c7e3-8834-52e47cc910e5 ;
    p:P14914 wds:Q3508705-390BBE86-9348-4EF6-BB4E-B73E4ECC5A90 ;
    p:P1550 wds:Q3508705-EDB88F36-B57F-4ED3-9E75-7AB9910F50D3,
        wds:Q3508705-F4692D84-C4AC-48DC-9973-DAA1B9751D45 ;
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    p:P1995 wds:Q3508705-2E1DADE7-5B85-4D1E-A8E4-857D6973FF02 ;
    p:P2293 wds:Q3508705-1A434243-DC55-4DAA-AFE5-BE50353B130B ;
    p:P279 wds:Q3508705-778957cc-4dcf-7047-f942-07aeafe513a9,
        wds:Q3508705-A58F72E7-3F38-4D5A-9837-3047015798A7,
        wds:Q3508705-B7F4CD70-26A1-4C14-B011-59FD78B0B64E ;
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        wds:Q3508705-7BB18263-2BA3-42E4-8669-5E50358A6AF8 ;
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        wds:Q3508705-7226101E-BCCB-4305-938A-A64E6E0D35E8,
        wds:Q3508705-90E7BDEE-1D11-4EBC-B9AF-346146B40AB6,
        wds:Q3508705-955544C1-5E14-479C-BE37-928842DDB063,
        wds:Q3508705-CDDD69C0-796C-4B7E-959B-1E7C9264EBFD,
        wds:Q3508705-FEABC285-CF4F-40D7-9443-9ACD5B309C97 ;
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        wds:Q3508705-B5FEF1AF-C955-44F9-9605-65741D420F41 ;
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    p:P4229 wds:Q3508705-3A1A0CD7-DE6B-43BE-AFB3-41E7FB5C44B2,
        wds:Q3508705-CF91B6BC-D0F0-4249-B814-09ACCF70D607 ;
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    p:P492 wds:Q3508705-9D691605-78A1-41F5-9076-B706B27716D0 ;
    p:P5008 wds:Q3508705-DA926E70-A461-4826-A0DE-61C538502AC8 ;
    p:P5270 wds:Q3508705-689AEFC9-672D-4EA2-A4FC-549D4659FE65 ;
    p:P557 wds:Q3508705-BAB66B6E-A529-4512-8423-D9D9B7B051EE ;
    p:P6366 wds:Q3508705-8A6A7E19-9B46-4A1C-9B17-4A2E7728F36D ;
    p:P646 wds:Q3508705-25BAC56D-A58F-4280-88F3-5F00C7AFD48B ;
    p:P6532 wds:Q3508705-E24B704B-ACC4-4D4A-B47B-DDDCE5B26E7C,
        wds:Q3508705-EDFCC1DF-46AB-4A4A-902D-A4545476E09C ;
    p:P699 wds:Q3508705-7F347C12-ED3B-44B6-A8F3-97D4F254A137,
        wds:Q3508705-D47BA98D-68C3-44CD-9C56-B5F8E5CD848B ;
    p:P7464 wds:Q3508705-5DFEA770-9B4B-4BBC-AFC0-68C65ACC346C ;
    p:P780 wds:Q3508705-1bf16c4b-4bfb-e1fc-149e-9e975a6980f3,
        wds:Q3508705-737b49cc-4ed5-9ef6-6e9e-b5cb1f1169a2,
        wds:Q3508705-8a3ba5cf-4fbe-4751-34c9-5a90fdf344bf,
        wds:Q3508705-e8fa485c-476c-6def-33ef-9f9a91f985c9,
        wds:Q3508705-f3bda678-49a6-f75c-40ff-1214387bf739,
        wds:Q3508705-f7810dbc-423f-2522-b623-4dc39ebe15ac ;
    wdtn:P486 <http://id.nlm.nih.gov/mesh/C536962> ;
    wdtn:P5270 <http://purl.obolibrary.org/obo/MONDO_0010979> ;
    wdtn:P6366 <https://makg.org/entity/2778802284> ;
    wdt:P11143 "Timothy syndrome" ;
    wdt:P11430 "DI-02370" ;
    wdt:P1193 0.000001 ;
    wdt:P138 wd:Q63380872 ;
    wdt:P14914 "D65283" ;
    wdt:P1550 "65283",
        "768" ;
    wdt:P1748 "C142894" ;
    wdt:P1995 wd:Q83042 ;
    wdt:P2293 wd:Q14905744 ;
    wdt:P279 wd:Q179630,
        wd:Q18553439,
        wd:Q653924 ;
    wdt:P2841 wd:Q21953121,
        wd:Q21953125 ;
    wdt:P2888 <http://identifiers.org/doid/DOID:0060173>,
        <http://purl.obolibrary.org/obo/DOID_0060173>,
        <http://www.orpha.net/ORDO/Orphanet_65283>,
        <http://www.orpha.net/ORDO/Orphanet_768> ;
    wdt:P2892 "C1832916" ;
    wdt:P31 wd:Q112193867,
        wd:Q929833 ;
    wdt:P373 "Timothy syndrome" ;
    wdt:P4229 "G72.3",
        "I45.8" ;
    wdt:P4317 "9294" ;
    wdt:P486 "C536962" ;
    wdt:P492 "601005" ;
    wdt:P5008 wd:Q4099686 ;
    wdt:P5270 "MONDO_0010979" ;
    wdt:P557 "34006" ;
    wdt:P6366 "2778802284" ;
    wdt:P646 "/m/045b9s" ;
    wdt:P6532 wd:Q12192,
        wd:Q173022 ;
    wdt:P7464 "timothy-syndrome" ;
    wdt:P780 wd:Q1361515,
        wd:Q180007,
        wd:Q209583,
        wd:Q217111,
        wd:Q848662,
        wd:Q939364 .