PRKAG2 cardiac syndrome

GPTKB entity

Statements (24)
Predicate Object
gptkbp:instanceOf genetic disorder
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
https://www.w3.org/2000/01/rdf-schema#label PRKAG2 cardiac syndrome
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