EC Number   |
Disease |
PubMed ID |
Title of Publication  |
Category |
Confidence Level |
|---|
    1.5.5.1 | acyl-coa dehydrogenase deficiency |
25913573 |
A case of late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency (MADD) with a novel mutation in ETFDH gene. |
causal interaction
unassigned |
4
0 |
| 1.5.5.1 | Multiple Acyl Coenzyme A Dehydrogenase Deficiency |
25913573 |
A case of late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency (MADD) with a novel mutation in ETFDH gene. |
causal interaction
unassigned |
4
0 |
| 1.5.5.1 | Muscle Weakness |
25913573 |
A case of late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency (MADD) with a novel mutation in ETFDH gene. |
causal interaction
unassigned |
4
0 |
| 1.5.5.1 | acyl-coa dehydrogenase deficiency |
23106979 |
A case of late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency with novel mutations in ETFDH gene. |
causal interaction
unassigned |
2
0 |
| 1.5.5.1 | Multiple Acyl Coenzyme A Dehydrogenase Deficiency |
23106979 |
A case of late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency with novel mutations in ETFDH gene. |
causal interaction
unassigned |
2
0 |
| 1.5.5.1 | acyl-coa dehydrogenase deficiency |
33131365 |
A family with riboflavin-reactive lipid deposition myopathy caused by a novel compound heterozygous mutation in the electron transfer flavoprotein dehydrogenase gene. |
causal interaction
unassigned |
4
0 |
| 1.5.5.1 | Multiple Acyl Coenzyme A Dehydrogenase Deficiency |
33131365 |
A family with riboflavin-reactive lipid deposition myopathy caused by a novel compound heterozygous mutation in the electron transfer flavoprotein dehydrogenase gene. |
causal interaction
unassigned |
4
0 |
| 1.5.5.1 | Muscular Diseases |
33131365 |
A family with riboflavin-reactive lipid deposition myopathy caused by a novel compound heterozygous mutation in the electron transfer flavoprotein dehydrogenase gene. |
causal interaction
unassigned |
4
0 |
| 1.5.5.1 | Multiple Acyl Coenzyme A Dehydrogenase Deficiency |
2246866 |
A new variant of glutaric aciduria type II: deficiency of beta-subunit of electron transfer flavoprotein. |
causal interaction
unassigned |
4
0 |
| 1.5.5.1 | acyl-coa dehydrogenase deficiency |
32393189 |
A novel electron transfer flavoprotein dehydrogenase (ETFDH) gene mutation identified in a newborn with glutaric acidemia type II: a case report of a Chinese family. |
causal interaction
ongoing research
unassigned |
4
2
0 |
