EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    2.3.1.16 | 3-hydroxy-2-methylbutyryl-coa dehydrogenase deficiency |
12872843 |
3-Hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency. |
causal interaction
diagnostic usage
unassigned |
4
3
0 |
| 2.3.1.16 | acetyl-coa c-acetyltransferase deficiency |
9435370 |
[Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency in Argentina] |
causal interaction
unassigned |
4
0 |
| 2.3.1.16 | acetyl-coa c-acetyltransferase deficiency |
18753430 |
An unusual cause of interference in a salicylate assay caused by mitochondrial acetoacetyl-CoA thiolase deficiency. |
causal interaction
diagnostic usage
unassigned |
4
3
0 |
| 2.3.1.16 | acetyl-coa c-acyltransferase deficiency |
36452 |
Acetoacetyl CoA thiolase deficiency: a cause of severe ketoacidosis in infancy simulating salicylism. |
causal interaction
unassigned |
4
0 |
| 2.3.1.16 | acetyl-coa c-acyltransferase deficiency |
481963 |
Inhibition of the glycine cleavage system by branched-chain amino acid metabolites. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 2.3.1.16 | acetyl-coa c-acyltransferase deficiency |
500823 |
Inhibition by propionyl-coenzyme A of N-acetylglutamate synthetase in rat liver mitochondria. A possible explanation for hyperammonemia in propionic and methylmalonic acidemia. |
causal interaction
unassigned |
3
0 |
| 2.3.1.16 | acetyl-coa c-acyltransferase deficiency |
758725 |
A variant form of 2-methyl-3-hydroxybutyric and 2-methylacetoacetic aciduria. |
causal interaction
unassigned |
4
0 |
| 2.3.1.16 | acetyl-coa c-acyltransferase deficiency |
890942 |
Calcium levulinate medication. A pitfall in the diagnosis of organic acidurias. |
causal interaction
unassigned |
3
0 |
| 2.3.1.16 | acetyl-coa c-acyltransferase deficiency |
1319041 |
[Beta-ketothiolase deficiency: a case of ketoacidosis with hyperglycinemia] |
causal interaction
unassigned |
4
0 |
| 2.3.1.16 | acetyl-coa c-acyltransferase deficiency |
1346617 |
Identification of three mutant alleles of the gene for mitochondrial acetoacetyl-coenzyme A thiolase. A complete analysis of two generations of a family with 3-ketothiolase deficiency. |
causal interaction
unassigned |
4
0 |
