EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    1.5.1.20 | Abruptio Placentae |
30243226 |
Placenta-mediated pregnancy complications are not associated with fetal or paternal factor V Leiden mutation. |
causal interaction
diagnostic usage
ongoing research
unassigned |
2
2
2
0 |
| 1.5.1.20 | Alzheimer Disease |
11916749 |
High-dose vitamin therapy stimulates variant enzymes with decreased coenzyme binding affinity (increased K(m)): relevance to genetic disease and polymorphisms. |
causal interaction
unassigned |
1
0 |
| 1.5.1.20 | Antiphospholipid Syndrome |
16320685 |
[Mutations of genes associated with thromboses in ischemic stroke in patients with primary antiphospholipid syndrome] |
causal interaction
diagnostic usage
unassigned |
4
4
0 |
| 1.5.1.20 | Arthritis, Rheumatoid |
20863444 |
Associations between the genetic polymorphisms of MTHFR and outcomes of methotrexate treatment in rheumatoid arthritis. |
causal interaction
therapeutic application
unassigned |
3
4
0 |
| 1.5.1.20 | Atherosclerosis |
12163688 |
The effects of diet, genetics and chemicals on toxicity and aberrant DNA methylation: an introduction. |
causal interaction
unassigned |
4
0 |
| 1.5.1.20 | Atherosclerosis |
32675800 |
Expression of the C677T Polymorphism of the 5, 10-Methylenetetrahydrofolate Reductase (MTHFR) Gene in Patients with Carotid Artery Atherosclerosis. |
causal interaction
diagnostic usage
ongoing research
unassigned |
3
1
4
0 |
| 1.5.1.20 | Breast Neoplasms |
19954067 |
[MTHFR polymorphisms, dietary folate intake and risks to breast cancer] |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
2
4
4
1 |
| 1.5.1.20 | Cardiovascular Diseases |
11916749 |
High-dose vitamin therapy stimulates variant enzymes with decreased coenzyme binding affinity (increased K(m)): relevance to genetic disease and polymorphisms. |
causal interaction
unassigned |
1
0 |
| 1.5.1.20 | Cardiovascular Diseases |
12499324 |
Thermolabile methylenetetrahydrofolate reductase, homocysteine, and cardiovascular disease risk: the European Concerted Action Project. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
4
4
0 |
| 1.5.1.20 | Cerebral Infarction |
12901511 |
Association of plasma homocysteine level and N5,N10-methylenetetrahydrofolate reductase gene polymorphism with cerebral infarction. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
4
4
0 |
