EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
1.5.5.1 | Acidosis |
8617498 |
Assignment of Etfdh, Etfb, and Etfa to chromosomes 3, 7, and 13: the mouse homologs of genes responsible for glutaric acidemia type II in human. |
causal interaction ongoing research therapeutic application unassigned |
4 1 1 0 |
1.5.5.1 | Acidosis |
17912479 |
Cardiomyopathy in multiple Acyl-CoA dehydrogenase deficiency: a clinico-pathological correlation and review of literature. |
causal interaction therapeutic application unassigned |
2 1 0 |
1.5.5.1 | Acidosis |
17977044 |
Risk of sudden death and acute life-threatening events in patients with glutaric acidemia type II. |
unassigned |
0 |
1.5.5.1 | acyl-coa dehydrogenase deficiency |
7360517 |
Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoprotein. |
causal interaction unassigned |
3 0 |
1.5.5.1 | acyl-coa dehydrogenase deficiency |
9889013 |
Isolated isobutyryl-CoA dehydrogenase deficiency: an unrecognized defect in human valine metabolism. |
causal interaction diagnostic usage unassigned |
1 3 0 |
1.5.5.1 | acyl-coa dehydrogenase deficiency |
16165386 |
Identification of the human mitochondrial FAD transporter and its potential role in multiple acyl-CoA dehydrogenase deficiency. |
causal interaction ongoing research unassigned |
2 2 0 |
1.5.5.1 | acyl-coa dehydrogenase deficiency |
16510302 |
Electron transfer flavoprotein deficiency: functional and molecular aspects. |
causal interaction diagnostic usage therapeutic application unassigned |
4 2 1 0 |
1.5.5.1 | acyl-coa dehydrogenase deficiency |
17050691 |
Structure of electron transfer flavoprotein-ubiquinone oxidoreductase and electron transfer to the mitochondrial ubiquinone pool. |
causal interaction ongoing research unassigned |
1 2 0 |
1.5.5.1 | acyl-coa dehydrogenase deficiency |
17912479 |
Cardiomyopathy in multiple Acyl-CoA dehydrogenase deficiency: a clinico-pathological correlation and review of literature. |
causal interaction therapeutic application unassigned |
2 1 0 |
1.5.5.1 | acyl-coa dehydrogenase deficiency |
19249206 |
ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. |
causal interaction diagnostic usage unassigned |
2 2 0 |