Disease: ATRIAL FIBRILLATION, FAMILIAL, 9 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3151431
Disease: ATRIAL FIBRILLATION, FAMILIAL, 9
ATRIAL FIBRILLATION, FAMILIAL, 9 		0.700 Biomarker disease GENOMICS_ENGLAND Current topics in catecholaminergic polymorphic ventricular tachycardia. 27761157 2016
CUI: C3151431
Disease: ATRIAL FIBRILLATION, FAMILIAL, 9
ATRIAL FIBRILLATION, FAMILIAL, 9 		0.700 Biomarker disease GENOMICS_ENGLAND Ion channelopathies in human induced pluripotent stem cell derived cardiomyocytes: a dynamic clamp study with virtual IK1. 25691870 2015
CUI: C3151431
Disease: ATRIAL FIBRILLATION, FAMILIAL, 9
ATRIAL FIBRILLATION, FAMILIAL, 9 		0.700 GeneticVariation disease UNIPROT A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation. 15922306 2005
CUI: C3151431
Disease: ATRIAL FIBRILLATION, FAMILIAL, 9
ATRIAL FIBRILLATION, FAMILIAL, 9 		0.700 Biomarker disease GENOMICS_ENGLAND Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome). 12163457 2002
CUI: C3151431
Disease: ATRIAL FIBRILLATION, FAMILIAL, 9
ATRIAL FIBRILLATION, FAMILIAL, 9 		0.700 CausalMutation disease CLINVAR
CUI: C3151431
Disease: ATRIAL FIBRILLATION, FAMILIAL, 9
ATRIAL FIBRILLATION, FAMILIAL, 9 		0.700 Biomarker disease CTD_human