EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    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 | 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 | 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 | 3-hydroxyacyl-coa dehydrogenase deficiency |
2326309 |
The L-3-hydroxyacyl-CoA dehydrogenase deficiency. |
causal interaction
unassigned |
4
0 |
| 1.1.1.35 | 3-hydroxyacyl-coa dehydrogenase deficiency |
7494405 |
Disorders of mitochondrial long-chain fatty acid oxidation. |
causal interaction
unassigned |
4
0 |
| 1.1.1.35 | 3-hydroxyacyl-coa dehydrogenase deficiency |
7562284 |
Heterozygosity for long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency and deterioration in liver function in a newborn infant infected with human immunodeficiency virus. |
causal interaction
unassigned |
1
0 |
| 1.1.1.35 | 3-hydroxyacyl-coa dehydrogenase deficiency |
7748366 |
Clinical and neurophysiologic response of myopathy and neuropathy in long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency to oral prednisone. |
causal interaction
ongoing research
unassigned |
4
4
0 |
| 1.1.1.35 | 3-hydroxyacyl-coa dehydrogenase deficiency |
7813533 |
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: a severe fatty acid oxidation disorder. |
causal interaction
unassigned |
4
0 |
| 1.1.1.35 | 3-hydroxyacyl-coa dehydrogenase deficiency |
7967472 |
Long-chain 3-hydroxyacyl-CoA dehydrogenase in chorionic villi, fetal liver and fibroblasts and prenatal diagnosis of 3-hydroxyacyl-CoA dehydrogenase deficiency. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
4
1
0 |
| 1.1.1.35 | 3-hydroxyacyl-coa dehydrogenase deficiency |
8294091 |
Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. |
causal interaction
unassigned |
4
0 |
