Statements (24)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:genetic_disorder
gptkb:cardiac_syndrome |
| gptkbp:affectsOrgan |
heart
|
| gptkbp:associatedWith |
gptkb:arrhythmia
gptkb:Wolff-Parkinson-White_syndrome |
| gptkbp:characterizedBy |
ventricular pre-excitation
cardiac hypertrophy conduction system disease |
| gptkbp:diagnosedBy |
genetic testing
electrocardiogram |
| gptkbp:firstDescribed |
2001
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:mutationAssociatedWith |
PRKAG2 gene
|
| gptkbp:OMIM |
602743
|
| gptkbp:prevalence |
rare
|
| gptkbp:symptom |
palpitations
sudden cardiac death syncope |
| gptkbp:treatment |
gptkb:implantable_cardioverter-defibrillator
catheter ablation antiarrhythmic drugs |
| gptkbp:bfsParent |
gptkb:PRKAG2
|
| gptkbp:bfsLayer |
7
|
| https://www.w3.org/2000/01/rdf-schema#label |
PRKAG2 cardiac syndrome
|