EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    2.8.3.5 | 3-oxoacid coa-transferase deficiency |
4258782 |
Succinyl-CoA: 3-ketoacid CoA-transferase deficiency. A cause for ketoacidosis in infancy. |
causal interaction
unassigned |
4
0 |
| 2.8.3.5 | 3-oxoacid coa-transferase deficiency |
7474899 |
A new Japanese case of succinyl-CoA: 3-ketoacid CoA-transferase deficiency. |
causal interaction
unassigned |
4
0 |
| 2.8.3.5 | 3-oxoacid coa-transferase deficiency |
9590068 |
[Succinyl-CoA: 3-ketoacid CoA transferase deficiency] |
causal interaction
unassigned |
3
0 |
| 2.8.3.5 | 3-oxoacid coa-transferase deficiency |
11528975 |
[Succinyl-CoA: 3-ketoacid CoA transferase deficiency] |
causal interaction
unassigned |
3
0 |
| 2.8.3.5 | 3-oxoacid coa-transferase deficiency |
11757586 |
Neonatal hypoglycaemia in severe succinyl-CoA: 3-oxoacid CoA-transferase deficiency. |
causal interaction
unassigned |
4
0 |
| 2.8.3.5 | 3-oxoacid coa-transferase deficiency |
19450972 |
Management and communication problems in a patient with succinyl-CoA transferase deficiency in pregnancy and labour. |
causal interaction
unassigned |
4
0 |
| 2.8.3.5 | 3-oxoacid coa-transferase deficiency |
23233542 |
Successful adaptation to ketosis by mice with tissue-specific deficiency of ketone body oxidation. |
causal interaction
unassigned |
3
0 |
| 2.8.3.5 | 3-oxoacid coa-transferase deficiency |
28695376 |
Heterozygous carriers of succinyl-CoA:3-oxoacid CoA transferase deficiency can develop severe ketoacidosis. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 2.8.3.5 | 3-oxoacid coa-transferase deficiency |
30799594 |
A Rare Cause of Life-Threatening Ketoacidosis: Novel Compound Heterozygous OXCT1 Mutations Causing Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. |
causal interaction
unassigned |
4
0 |
| 2.8.3.5 | 3-oxoacid coa-transferase deficiency |
31073471 |
A Case of Succinyl-CoA:3-Oxoacid CoA Transferase Deficiency Presenting with Severe Acidosis in a 14-Month-Old Female: Evidence for Pathogenicity of a Point Mutation in the OXCT1 Gene. |
causal interaction
unassigned |
4
0 |
