EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
1.1.1.49 | Acatalasia |
6008761 |
[Glucose-6-phosphate dehydrogenase activity in the red blood cell in hypo-catalasemia and acatalasemia] |
ongoing research unassigned |
3 0 |
1.1.1.49 | Acatalasia |
14075877 |
A DUAL HEREDITARY RED BLOOD CELL DEFECT IN ONE FAMILY: HYPOCATALASEMIA AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY. |
ongoing research therapeutic application unassigned |
1 1 0 |
1.1.1.49 | acetylcholinesterase deficiency |
324358 |
Paroxysmal nocturnal hemoglobinuria (PNH) as a clonal disorder. |
causal interaction unassigned |
1 0 |
1.1.1.49 | Acidosis |
931243 |
[Generalized saturnine paralysis. Discovery of a double congenital disease: glucose-6-phosphate dehydrogenase deficiency (new variant) and distal tubular acidosis] |
unassigned |
0 |
1.1.1.49 | Acidosis |
2783145 |
Stimulation of rat-kidney hexose monophosphate shunt dehydrogenase activity by chronic metabolic acidosis. |
ongoing research unassigned |
4 0 |
1.1.1.49 | Acidosis |
6500036 |
[Effect of sodium oxybutyrate on metabolic indices in ischemic hypoxia of muscle tissue] |
unassigned |
0 |
1.1.1.49 | Acidosis |
7075753 |
[Biochemical markers of strophanthin arrhythmia] |
causal interaction unassigned |
1 0 |
1.1.1.49 | Acidosis |
8449345 |
Alterations of rat kidney, liver and erythrocytes glucose 6-phosphate dehydrogenase activity by chronic acidosis. |
ongoing research unassigned |
4 0 |
1.1.1.49 | Acidosis |
9679548 |
Patients with genetic defects in the gamma-glutamyl cycle. |
causal interaction therapeutic application unassigned |
4 4 0 |
1.1.1.49 | Acidosis |
20554515 |
Predictors of Acute Bilirubin Encephalopathy Among Nigerian Term Babies with Moderate-to-severe Hyperbilirubinaemia. |
causal interaction unassigned |
2 0 |