EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    2.1.1.2 | arginase deficiency |
34471603 |
Creatine metabolism in patients with urea cycle disorders. |
causal interaction
diagnostic usage
unassigned |
4
2
0 |
| 2.1.1.2 | aromatic-l-amino-acid decarboxylase deficiency |
31930732 |
Targeted cerebrospinal fluid analysis for inborn errors of metabolism on an LC-MS/MS analysis platform. |
causal interaction
diagnostic usage
unassigned |
4
2
0 |
| 2.1.1.2 | Brain Diseases |
17171576 |
Guanidinoacetate methyltransferase deficiency masquerading as a mitochondrial encephalopathy. |
causal interaction
unassigned |
4
0 |
| 2.1.1.2 | Carcinoma |
19021765 |
Enzymes of creatine biosynthesis, arginine and methionine metabolism in normal and malignant cells. |
causal interaction
diagnostic usage
ongoing research
unassigned |
1
3
3
0 |
| 2.1.1.2 | Carcinoma |
21769499 |
A short review on creatine-creatine kinase system in relation to cancer and some experimental results on creatine as adjuvant in cancer therapy. |
causal interaction
diagnostic usage
unassigned |
4
3
0 |
| 2.1.1.2 | Carcinoma, Hepatocellular |
3970526 |
Guanidinoacetate methyltransferase activity in tissues and cultured cells. |
causal interaction
ongoing research
unassigned |
1
1
0 |
| 2.1.1.2 | cathepsin d deficiency |
19760908 |
Metabolic epilepsies: approaches to a diagnostic challenge. |
causal interaction
unassigned |
4
0 |
| 2.1.1.2 | Diffuse Cerebral Sclerosis of Schilder |
19760908 |
Metabolic epilepsies: approaches to a diagnostic challenge. |
causal interaction
unassigned |
4
0 |
| 2.1.1.2 | Epilepsy |
11087795 |
Brain creatine depletion: guanidinoacetate methyltransferase deficiency (improving with creatine supplementation). |
causal interaction
therapeutic application
unassigned |
3
1
0 |
| 2.1.1.2 | Epilepsy |
12597058 |
Inborn errors of creatine metabolism and epilepsy: clinical features, diagnosis, and treatment. |
causal interaction
therapeutic application
unassigned |
4
4
0 |
