Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4205
Gene Symbol: MEF2A
MEF2A
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.100 GeneticVariation LHGDN [Study on novel mutations of MEF2A gene in Chinese patients with coronary artery disease]. 16767660

2006
Entrez Id: 4205
Gene Symbol: MEF2A
MEF2A
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.100 GeneticVariation LHGDN These studies support that MEF2A mutations are not a common cause of CAD in white people and argue strongly against a role for the MEF2A 21-bp deletion in autosomal dominant CAD. 15841183

2005
Entrez Id: 4205
Gene Symbol: MEF2A
MEF2A
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.100 GeneticVariation LHGDN Positional cloning based on genome-wide linkage analysis with large families identified the first non - lipid-related disease-causing gene, MEF2A (encoding a transcriptional factor), for coronary artery disease and myocardiaI infarction. 15861005

2005
Entrez Id: 4205
Gene Symbol: MEF2A
MEF2A
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.100 GeneticVariation LHGDN Here, we describe an autosomal dominant form of CAD/MI (adCAD1) that is caused by the deletion of seven amino acids in transcription factor MEF2A. 14645853

2003