EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
1.1.1.49 | 5'-nucleotidase deficiency |
2491542 |
[Hemolytic anemias caused by erythrocyte enzyme disorders] |
causal interaction unassigned |
4 0 |
1.1.1.49 | 5'-nucleotidase deficiency |
3352512 |
Enzymatic diagnosis in non-spherocytic hemolytic anemia. |
causal interaction unassigned |
4 0 |
1.1.1.49 | 5'-nucleotidase deficiency |
6289944 |
Hemolytic anemia in hereditary pyrimidine 5'-nucleotidase deficiency: nucleotide inhibition of G6PD and the pentose phosphate shunt. |
causal interaction diagnostic usage ongoing research unassigned |
4 2 4 0 |
1.1.1.49 | 6-phosphogluconolactonase deficiency |
3858849 |
6-Phosphogluconolactonase deficiency, a hereditary erythrocyte enzyme deficiency: possible interaction with glucose-6-phosphate dehydrogenase deficiency. |
causal interaction unassigned |
4 0 |
1.1.1.49 | Abortion, Habitual |
6926920 |
[Glucose-6-phosphate dehydrogenase in couples with habitual abortion] |
unassigned |
0 |
1.1.1.49 | Abortion, Septic |
1715192 |
Pancreatitis in acute hemolysis. |
causal interaction diagnostic usage unassigned |
1 2 0 |
1.1.1.49 | Abortion, Spontaneous |
2774076 |
[Role of disorders of pentosephosphate pathway of glucose oxidation in the pathogenesis of the arrest of fetal development in miscarriage] |
diagnostic usage ongoing research unassigned |
2 1 0 |
1.1.1.49 | Abortion, Spontaneous |
3967893 |
Prenatal selection and fetal development disturbances occurring in carriers of G6PD deficiency. |
causal interaction ongoing research unassigned |
4 1 0 |
1.1.1.49 | Abortion, Spontaneous |
12852494 |
Hofbauer cell activation and its increased glucose-6-phosphate dehydrogenase activity in second trimester-spontaneous abortion: an ultrastructural dual staining enzyme-cytochemical study. |
causal interaction therapeutic application unassigned |
1 1 0 |
1.1.1.49 | Acatalasia |
918959 |
Activities of catalase in leucocytes and glucose-6-phosphate dehydrogenase in erythrocytes of hypocatalasemia and acatalasemia. |
diagnostic usage therapeutic application unassigned |
4 1 0 |