EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   1.5.7.1 | Abortion, Habitual |
15952099 |
Prevalence of hyperhomocysteinemia in adult gluten-sensitive enteropathy at diagnosis: role of B12, folate, and genetics. |
causal interaction
unassigned |
1
0 |
| 1.5.7.1 | Acquired Immunodeficiency Syndrome |
12633043 |
[Superior mesenteric venous thrombosis. Report of 2 cases and review of the literature] |
causal interaction
therapeutic application
unassigned |
4
2
0 |
| 1.5.7.1 | Arteriosclerosis |
26756640 |
Homocysteine Metabolism, Atherosclerosis, and Diseases of Aging. |
unassigned |
0 |
| 1.5.7.1 | Asthma |
26333700 |
Is Folate Status a Risk Factor for Asthma or Other Allergic Diseases? |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
4
4
0 |
| 1.5.7.1 | Cardiovascular Diseases |
11406421 |
Polymorphic methyl group metabolism genes in patients with transitional cell carcinoma of the urinary bladder. |
diagnostic usage
ongoing research
unassigned |
3
1
0 |
| 1.5.7.1 | Colorectal Neoplasms |
23125859 |
Folate Intake, MTHFR Polymorphisms, and the Risk of Colorectal Cancer: A Systematic Review and Meta-Analysis. |
diagnostic usage
ongoing research
therapeutic application
unassigned |
4
3
1
0 |
| 1.5.7.1 | Coronary Artery Disease |
17264399 |
Relationship of the 1793G-A and 677C-T polymorphisms of the 5,10-methylenetetrahydrofolate reductase gene to coronary artery disease. |
causal interaction
diagnostic usage
ongoing research
unassigned |
2
1
1
0 |
| 1.5.7.1 | Coronary Artery Disease |
32572074 |
Association of the methylene-tetrahydrofolate reductase gene rs1801133 C677T variant with serum homocysteine levels, and the severity of coronary artery disease. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
3
3
2
1 |
| 1.5.7.1 | cystathionine beta-synthase deficiency |
9211199 |
Disorders of homocysteine metabolism. |
causal interaction
unassigned |
4
0 |
| 1.5.7.1 | Diabetes Mellitus |
24452036 |
Association of ACE and MTHFR genetic polymorphisms with type 2 diabetes mellitus: Susceptibility and complications. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
4
1
1
0 |
