Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.100 GeneticVariation group BEFREE Two Common MTHFR Gene Polymorphisms (C677T and A1298C) and Fetal Congenital Heart Disease Risk: An Updated Meta-Analysis with Trial Sequential Analysis. 29554656 2018
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.100 Biomarker group BEFREE Risk factors and methylenetetrahydrofolate reductase gene in congenital heart disease. 29600076 2018
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.100 GeneticVariation group BEFREE <b>Background:</b> We performed the present study to better elucidate the correlations of methylenetetrahydrofolate reductase (<i>MTHFR</i>) and methionine synthase reductase (<i>MTRR</i>) gene polymorphisms with the risk of congenital heart diseases (CHD).<b>Methods:</b> Eligible articles were searched in PubMed, Medline, Embase and CNKI. 30333252 2018
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.100 GeneticVariation group BEFREE Genetic polymorphism of methylenetetrahydrofolate reductase as a potential risk factor for congenital heart disease: A meta-analysis in Chinese pediatric population. 28591039 2017
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.100 GeneticVariation group BEFREE The methylenetetrahydrofolate reductase (MTHFR) gene encoding a critical enzyme, potentially affects susceptibility to some congenital defects like congenital heart disease (CHD). 26990189 2016
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.100 GeneticVariation group BEFREE The association of the MTHFR c.1625A>C genetic variant with the risk of congenital heart diseases in the Chinese. 25494855 2015
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.100 Biomarker group BEFREE Study on Environmental Causes and SNPs of MTHFR, MS and CBS Genes Related to Congenital Heart Disease. 26035828 2015
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.100 GeneticVariation group BEFREE The association between c.1333C > T genetic polymorphism of MTHFR gene and the risk of congenital heart diseases. 24387084 2014
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.100 GeneticVariation group BEFREE Association analysis between MTHFR genetic polymorphisms and the risk of congenital heart diseases in Chinese Han population. 24720776 2014
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.100 GeneticVariation group BEFREE Association between MTHFR polymorphisms and congenital heart disease: a meta-analysis based on 9,329 cases and 15,076 controls. 25472587 2014
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.100 GeneticVariation group BEFREE MTHFR C677T and A1298C gene polymorphisms and their relation to homocysteine level in Egyptian children with congenital heart diseases. 23933414 2013
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.100 GeneticVariation group BEFREE Association between the C677T polymorphism of the methylene tetrahydrofolate reductase (MTHFR) gene and congenital heart disease (CHD) is contentious. 23876493 2013
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.100 GeneticVariation group BEFREE Methylenetetrahydrofolate reductase gene 677CT polymorphism and isolated congenital heart disease in a Mexican population. 22197386 2012
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.100 GeneticVariation group BEFREE Data on the association between the MTHFR C677T polymorphism and congenital heart disease (CHD) are conflicting. 21793799 2011
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.100 GeneticVariation group BEFREE Our results suggest that MTHFR polymorphism can be considered a susceptibility gene for this congenital heart disease. 19894660 2009
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.100 GeneticVariation group BEFREE The aim of this retrospective case control study was to investigate whether the occurrence of the MTHFR polymorphism is increased in mothers and fathers of children with a congenital heart disease (CHD) in our population. 17510921 2007
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.100 GeneticVariation group BEFREE The aim of this study is to investigate whether MTHFR C677T functional genetic variant is associated with an increased risk of congenital heart disease (CHD) development using a family-based case-control design and the Transmission Disequilibrium Test (TDT) approach. 16207540 2005
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.100 GeneticVariation group BEFREE Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases. 16305696 2005
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.100 GeneticVariation group BEFREE However, no data are available so far with respect to the MTHFR 677TT genotype in children with underlying structural congenital heart disease (CHD). 11470464 2001