EC Number   |
Disease |
PubMed ID  |
Title of Publication |
Category |
Confidence Level |
|---|
    1.1.1.35 | Neoplasms |
356174 |
Glucose tolerance in relation to skeletal muscle enzyme activities in cancer patients. |
diagnostic usage
unassigned |
4
0 |
| 1.1.1.35 | 3-hydroxyacyl-coa dehydrogenase deficiency |
1835339 |
Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathy. |
causal interaction
therapeutic application
unassigned |
4
3
0 |
| 1.1.1.35 | Brain Diseases |
1835339 |
Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathy. |
causal interaction
therapeutic application
unassigned |
4
3
0 |
| 1.1.1.35 | Myoglobinuria |
1835339 |
Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathy. |
causal interaction
therapeutic application
unassigned |
4
3
0 |
| 1.1.1.35 | 3-hydroxyacyl-coa dehydrogenase deficiency |
2019931 |
Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. |
causal interaction
unassigned |
4
0 |
| 1.1.1.35 | Myoglobinuria |
2019931 |
Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. |
causal interaction
unassigned |
4
0 |
| 1.1.1.35 | 3-hydroxyacyl-coa dehydrogenase deficiency |
2044590 |
3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment. |
causal interaction
unassigned |
4
0 |
| 1.1.1.35 | Perinatal Death |
2044590 |
3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment. |
causal interaction
unassigned |
4
0 |
| 1.1.1.35 | 3-hydroxyacyl-coa dehydrogenase deficiency |
2326309 |
The L-3-hydroxyacyl-CoA dehydrogenase deficiency. |
causal interaction
unassigned |
4
0 |
| 1.1.1.35 | Glycogen Storage Disease Type V |
2388659 |
Increased muscular beta-hydroxyacyl CoA dehydrogenase with McArdle's disease. |
causal interaction
unassigned |
3
0 |
