Disease: Atrial Fibrillation ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.110 GeneticVariation disease LHGDN Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy. 11748095 2001
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.110 GeneticVariation disease BEFREE We identified a novel mutation (Arg531Gly) in the gamma-2 regulatory subunit (PRKAG2) of AMP-activated protein kinase (AMPK) to be responsible for a syndrome associated with ventricular preexcitation and early onset of atrial fibrillation and conduction disease. 11748095 2001
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.110 Biomarker disease HPO