Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE
0.430 GeneticVariation disease BEFREE We recently reported 2 linked polymorphisms within regulatory regions of the gene for the atrial gap junction protein connexin40 (Cx40) at nucleotides -44 (G-->A) and +71 (A-->G), which were associated with familial atrial standstill. 15297374 2004
CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE
0.430 GeneticVariation disease BEFREE In this study, familial AS was associated with the concurrence of a cardiac sodium channel mutation and rare polymorphisms in the atrial-specific Cx40 gene. 12522116 2003
CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE
0.430 Biomarker disease HPO
CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE
0.430 Biomarker disease CTD_human
CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE
0.430 Biomarker disease BEFREE Incomplete penetrance observed in atrial standstill has been attributed in part to the digenic inheritance of polymorphisms in the atrial-specific gap junction connexin 40 (Cx40) in conjunction with an SCN5A mutation. 16188595 2005