rdfs: label
ar
bs
de
en
es
fr
it
ja
nn
pl
pt
pt-br
ru
sk
sl
vi
zh
zh-cn
"Hội chứng QT ngắn"@vi
"QT短縮症候群"@ja
"Short-QT-Syndrom"@de
"Sindrom kratkog QT"@bs
"Syndróm krátkeho QT intervalu"@sk
"Síndrome QT curto congênito"@pt
"Síndrome QT curto congênito"@pt-br
"Síndrome de QT corto"@es
"kort QT-tid-syndrom"@nn
"short QT syndrome"@en
"sindrom kratke dobe Q-T"@sl
"sindrome del QT breve"@it
"syndrome du QT court"@fr
"zespół krótkiego QT"@pl
"синдром короткого интервала QT"@ru
"متلازمة كيو تي القصيرة"@ar
"短QT综合征"@zh
"短QT综合征"@zh-cn
skos: altLabel
en
nn
sl
"Familial short QT syndrome"@en
"Ventricular arrhythmia associated with short QT syndrome"@en
"kort QT-syndrom"@nn
"sindrom kratkega intervala Q-T"@sl
schema: description
de
en
fr
it
uk
"Krankheit"@de
"heart conduction disease that is characterized by heart arrhythmia defined as a short QT interval on an EKG (less than 300 ms) that does not significantly change with heart rate, tall and peaked T waves, and a structurally normal heart"@en
"maladie génétique"@fr
"malattia genetica del sistema elettrico del cuore caratterizzata da un intervallo QT breve nell'ECG (≤ 300 ms) che non cambia in maniera significativa con il ritmo cardiaco, alte e appuntite onde T, e un cuore strutturalmente sano."@it
"хвороба"@uk
schema: dateModified
"2026-10-24T00:24:55+00:00"^^xsd:dateTime
schema: version
2560165605
wikibase: identifiers
23
26
wikibase: sitelinks
13
wikibase: statements
62
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p: direct-normalized/P2581
<http://babelnet.org/rdf/s03482714n>
p: direct-normalized/P3201
<http://purl.bioontology.org/ontology/MDRFRE/10007651>
p: direct-normalized/P486
<http://id.nlm.nih.gov/mesh/C580439>
p: direct-normalized/P5270
<http://purl.obolibrary.org/obo/MONDO_0000453>
p: direct-normalized/P6366
<https://makg.org/entity/2779578097>
<https://makg.org/entity/2909049529>
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<http://www.kegg.jp/entry/H00725>
p: direct-normalized/P699
<http://purl.obolibrary.org/obo/DOID_DOID:0050793>
wdt: P10283
"C2779578097"
wdt: P10565
"579658"
wdt: P11143
"Short QT syndrome"
wdt: P14541
"3FEmF6"
wdt: P14914
"D51083"
wdt: P1550
"51083"
wdt: P1692
"426.89"
wdt: P1748
"C71060"
wdt: P1995
cardiology
medical genetics
wdt: P2293
KCNQ1
KCNH2
KCNJ2
CACNA2D1
SLC4A3
wdt: P2581
"03482714n"
wdt: P279
heart conduction disease
QT interval shortened
wdt: P2841
any age
wdt: P2888
<http://identifiers.org/doid/DOID:0050793>
<http://purl.obolibrary.org/obo/DOID_0050793>
<http://www.orpha.net/ORDO/Orphanet_51083>
wdt: P2892
"C2348199"
wdt: P31
type of disease
rare disease
wdt: P3201
"10007651"
wdt: P4229
"I49.8"
wdt: P461
long QT syndrome
wdt: P486
"C580439"
wdt: P492
"609620"
"609621"
"609622"
wdt: P494
"R94.3"
wdt: P5008
WikiProject Medicine
wdt: P5131
QT interval shortened
wdt: P5270
"MONDO_0000453"
wdt: P557
"11105"
wdt: P6366
"2779578097"
"2909049529"
wdt: P646
"/m/02zg91"
wdt: P6532
sudden cardiac death
Ventricular arrhythmia
syncope
bradycardia
atrioventricular block
QT interval shortened
atrial fibrillation
ventricular fibrillation
wdt: P665
"H00725"
wdt: P699
"DOID:0050793"
wdt: P7329
"BC65.2"
wdt: P7464
"short-qt-syndrome"
wdt: P780
palpitation
dyspnea
heart arrhythmia
fatigue
wdt: P7807
"553392015"
wdt: P828
mutation
wdt: P923
electrocardiography
wdt: P924
quinidine
implantable cardioverter-defibrillator