EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    5.3.1.8 | 6-phosphofructokinase deficiency |
139680 |
[Exercise-induced muscular weakness, myalgia and contractures. I. A clinical review] |
causal interaction
unassigned |
3
0 |
| 5.3.1.8 | 6-phosphofructokinase deficiency |
847445 |
[Exercise-induced muscular weakness, myalgia and contractures. II. Casuistic contribution] |
causal interaction
unassigned |
4
0 |
| 5.3.1.8 | Adenocarcinoma |
34511962 |
Phosphomannose Isomerase High Expression Associated with Better Prognosis in Pancreatic Ductal Adenocarcinoma. |
causal interaction
diagnostic usage
unassigned |
4
4
0 |
| 5.3.1.8 | Alcohol Withdrawal Delirium |
5573906 |
Activity of aldolase, aminotransferases, phosphohexoisomerase and ceruloplasmin in the course of delirium tremens. |
unassigned |
0 |
| 5.3.1.8 | Alcohol Withdrawal Delirium |
5805104 |
[Activity of aldolase, aminotransferases, phosphohexoisomerase and ceruloplasmin in the course of delirium tremens] |
unassigned |
0 |
| 5.3.1.8 | Anemia |
13605990 |
[Erythrocyte enzymes; activity of glycolytic enzymes of erythrocytes in anemia: phosphoglucomutase, phosphohexoisomerase, diphosphofructaldolase, lactic acid dehydrogenase.] |
ongoing research
unassigned |
1
0 |
| 5.3.1.8 | Biliary Tract Diseases |
5941685 |
[Serum iron and copper levels and serum activity of phosphohexoisomerase and glutamic-pyruvic transaminase in patients with liver and biliary tract disease] |
diagnostic usage
ongoing research
unassigned |
4
3
0 |
| 5.3.1.8 | Blindness |
24421398 |
Mannose supplements induce embryonic lethality and blindness in phosphomannose isomerase hypomorphic mice. |
causal interaction
ongoing research
unassigned |
3
1
0 |
| 5.3.1.8 | Congenital Disorders of Glycosylation |
9525984 |
Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 5.3.1.8 | Congenital Disorders of Glycosylation |
9585601 |
Phosphomannose isomerase deficiency: a carbohydrate-deficient glycoprotein syndrome with hepatic-intestinal presentation. |
causal interaction
unassigned |
3
0 |
