EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    6.4.1.3 | 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 |
| 6.4.1.3 | acetyl-coa c-acyltransferase deficiency |
7923765 |
Tiglylglycine excreted in urine in disorders of isoleucine metabolism and the respiratory chain measured by stable isotope dilution GC-MS. |
causal interaction
unassigned |
4
0 |
| 6.4.1.3 | Acidosis |
23430497 |
Autism spectrum disorder in a child with propionic acidemia. |
causal interaction
unassigned |
4
0 |
| 6.4.1.3 | Acidosis |
25611862 |
Propionic acidemia in a parturient presenting for induction of labor. |
causal interaction
therapeutic application
unassigned |
3
4
0 |
| 6.4.1.3 | Agammaglobulinemia |
8819559 |
Parathyroid hormone resistance and B cell lymphopenia in propionic acidemia. |
causal interaction
unassigned |
3
0 |
| 6.4.1.3 | carbonic anhydrase deficiency |
24530203 |
Mitochondrial Carbonic Anhydrase VA Deficiency Resulting from CA5A Alterations Presents with Hyperammonemia in Early Childhood. |
causal interaction
unassigned |
4
0 |
| 6.4.1.3 | Cardiomyopathies |
31951825 |
Pathogenic implications of dysregulated miRNAs in propionic acidemia related cardiomyopathy. |
causal interaction
unassigned |
2
0 |
| 6.4.1.3 | Clonorchiasis |
22119288 |
The identification of antigenic proteins: 14-3-3 protein and propionyl-CoA carboxylase in Clonorchis sinensis. |
ongoing research
therapeutic application
unassigned |
2
1
0 |
| 6.4.1.3 | Coma |
31916709 |
Clinical features of 27 Turkish Propionic acidemia patients with 12 novel mutations. |
causal interaction
unassigned |
3
0 |
| 6.4.1.3 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
25611862 |
Propionic acidemia in a parturient presenting for induction of labor. |
causal interaction
therapeutic application
unassigned |
3
4
0 |
