Disease: Atrial Fibrillation, Familial, 4 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1862394
Disease: Atrial Fibrillation, Familial, 4
Atrial Fibrillation, Familial, 4 		0.700 Biomarker disease GENOMICS_ENGLAND Short QT syndrome. 16301704 2005
CUI: C1862394
Disease: Atrial Fibrillation, Familial, 4
Atrial Fibrillation, Familial, 4 		0.700 GeneticVariation disease UNIPROT Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation. 15368194 2004
CUI: C1862394
Disease: Atrial Fibrillation, Familial, 4
Atrial Fibrillation, Familial, 4 		0.700 GeneticVariation disease CLINVAR Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation. 15368194 2004
CUI: C1862394
Disease: Atrial Fibrillation, Familial, 4
Atrial Fibrillation, Familial, 4 		0.700 Biomarker disease GENOMICS_ENGLAND Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome. 11468227 2001
CUI: C1862394
Disease: Atrial Fibrillation, Familial, 4
Atrial Fibrillation, Familial, 4 		0.700 CausalMutation disease CLINVAR
CUI: C1862394
Disease: Atrial Fibrillation, Familial, 4
Atrial Fibrillation, Familial, 4 		0.700 Biomarker disease CTD_human