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 |