Statements (27)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:arrhythmia
genetic disorder |
| gptkbp:affects |
heart
|
| gptkbp:cause |
gptkb:atrial_fibrillation
gptkb:ventricular_fibrillation abnormally short QT interval increased risk of sudden cardiac death |
| gptkbp:diagnosedBy |
genetic testing
electrocardiogram |
| gptkbp:firstDescribed |
2000
|
| gptkbp:gene |
gptkb:KCNJ2
gptkb:KCNQ1 gptkb:KCNH2 |
| https://www.w3.org/2000/01/rdf-schema#label |
Short QT syndrome
|
| gptkbp:ICD-10_code |
I45.81
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:OMIM |
609620
|
| gptkbp:prevalence |
rare
|
| gptkbp:riskFactor |
family history of sudden cardiac death
sudden infant death |
| gptkbp:symptom |
sudden cardiac arrest
palpitations syncope |
| gptkbp:treatment |
gptkb:implantable_cardioverter-defibrillator
antiarrhythmic drugs |
| gptkbp:bfsParent |
gptkb:Short_QT_syndrome_3
|
| gptkbp:bfsLayer |
7
|