Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0020179
Disease: Huntington Disease
Huntington Disease
0.020 GeneticVariation LHGDN Determination of MTHFR polymorphisms and CAG repeats enables screening for subjects with putative early HD onset in order to study neuroprotective compounds in their efficacy to delay HD symptoms. 15354395

2004

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0023470
Disease: Myeloid Leukemia
Myeloid Leukemia
0.020 GeneticVariation LHGDN In this study we describe the genotyping of the MTHFR C677T polymorphism by melting curve analysis with the LightCycler in a case-controlled study of patients with acute lymphocytic leukemia (ALL), myelogenous leukemia (AML), and chronic myelogenous leukemia (CML), and assess the effect of this common polymorphism on the leukemia risk in adult patients in Turkey. 15068389

2003

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0003864
Disease: Arthritis
Arthritis
0.020 GeneticVariation LHGDN The objective of this study was to examine whether there was a correlation between the genotype or haplotype of the MTHFR gene and the efficacy or toxicity of methotrexate (MTX) in the treatment of rheumatoid arthritis. 11927833

2002

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
0.030 GeneticVariation LHGDN Functional polymorphisms in folate metabolism genes influence the risk of meningioma and glioma. 18483342

2008

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.030 GeneticVariation LHGDN The methylenetetrahydrofolate reductase (MTHFR) variant c.677C>T (A222V) influences overall survival of patients with glioblastoma multiforme. 18497326

2008

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.030 GeneticVariation LHGDN Our results are highly suggestive of an important role for MTHFR genotype in susceptibility to retinopathy under hyperglycemia, but not to nephropathy. 18280442

2008

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0032914
Disease: Pre-Eclampsia
Pre-Eclampsia
0.030 GeneticVariation LHGDN Methylenetetrahydrofolate reductase C677T and glutathione S-transferase P1 A313G are associated with a reduced risk of preeclampsia in Maya-Mestizo women. 18712057

2008

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae
0.030 GeneticVariation LHGDN The prevalence of FVL, prothrombin G20210A and MTHFR C677T was related to placental abruption. 17627684

2007

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae
0.030 GeneticVariation LHGDN We examined 2 variants in MTHFR: 677C-->T and 1298A-->C in genomic DNA extracted from maternal blood from the New Jersey-Placental Abruption Study, an ongoing, multicenter case-controlled study. 17904970

2007

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae
0.030 GeneticVariation LHGDN Although the small number of cases of combined inherited thrombophilia, it seems that the presence of FV Leiden/MTHFR T677T double genotype increases the risk for placental abruption. 18225686

2007

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.030 PosttranslationalModification LHGDN Genome-wide hypomethylation in human glioblastomas associated with specific copy number alteration, methylenetetrahydrofolate reductase allele status, and increased proliferation. 16951158

2006

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0085278
Disease: Antiphospholipid Syndrome
Antiphospholipid Syndrome
0.030 GeneticVariation LHGDN Takayasu arteritis with high titre of antiphospholipid antibodies and MTHFR Polymorphism. 16133896

2005

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0032914
Disease: Pre-Eclampsia
Pre-Eclampsia
0.030 GeneticVariation LHGDN Ethnic differences in the association of factor V Leiden mutation and the C677T methylenetetrahydrofolate reductase gene polymorphism with preeclampsia. 14746952

2004

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0032914
Disease: Pre-Eclampsia
Pre-Eclampsia
0.030 GeneticVariation LHGDN We found little evidence of an effect of the child's MTHFR or FVL alleles on the risk of preeclampsia. 15097012

2004

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy
0.030 GeneticVariation LHGDN The MTHFR gene C677T mutation may be a possible risk factor for the development of LVH in the type II diabetic patients. 15469701

2004

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0007282
Disease: Carotid Stenosis
Carotid Stenosis
0.030 GeneticVariation LHGDN Association of methylenetetrahydrofolate reductase gene polymorphism with carotid atherosclerosis depending on smoking status in a Japanese general population. 12775885

2003

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy
0.030 GeneticVariation LHGDN An association study of five genetic loci and left ventricular hypertrophy amongst Gulf Arabs. 11768721

2001

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0004096
Disease: Asthma
Asthma
0.040 GeneticVariation LHGDN Data on MTHFR C677T genotype and allergy were available for 5364 children and on allergy and/or asthma for 7356 mothers. 18070159

2008

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0017605
Disease: Angle Closure Glaucoma
Angle Closure Glaucoma
0.040 GeneticVariation LHGDN C677T polymorphism in the methylenetetrahydrofolate reductase gene is associated with primary closed angle glaucoma. 18385801

2008

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0034885
Disease: Rectal Neoplasms
Rectal Neoplasms
0.040 GeneticVariation LHGDN Dietary intake of folate and co-factors in folate metabolism, MTHFR polymorphisms, and reduced rectal cancer. 17245555

2007

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0034885
Disease: Rectal Neoplasms
Rectal Neoplasms
0.040 GeneticVariation LHGDN A haplotype of the methylenetetrahydrofolate reductase gene predicts poor tumor response in rectal cancer patients receiving preoperative chemoradiation. 17047490

2006

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.040 GeneticVariation LHGDN Hyperhomocysteinemia and the MTHFR C677T polymorphism promote steatosis and fibrosis in chronic hepatitis C patients. 15834927

2005

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0085096
Disease: Peripheral Vascular Diseases
Peripheral Vascular Diseases
0.050 GeneticVariation LHGDN Peripheral arterial disease and methylenetetrahydrofolate reductase (MTHFR) C677T mutations: A case-control study and meta-analysis. 19157768

2009

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma
0.050 GeneticVariation LHGDN MTHFR C677T polymorphism in chronic pancreatitis and pancreatic adenocarcinoma. 18636416

2008

Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.050 GeneticVariation LHGDN The MTHFR C677T polymorphism may play a role in influencing liver fibrosis progression in patients with recurrent hepatitis C, in conjunction with donor age, but not via steatosis promotion. 17900242

2008