EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    2.7.1.6 | 3-hydroxyacyl-coa dehydrogenase deficiency |
9061562 |
Inherited metabolic diseases affecting the carrier. |
causal interaction
therapeutic application
unassigned |
4
3
0 |
| 2.7.1.6 | Adrenoleukodystrophy |
9061562 |
Inherited metabolic diseases affecting the carrier. |
causal interaction
therapeutic application
unassigned |
4
3
0 |
| 2.7.1.6 | alpha 1-Antitrypsin Deficiency |
9061562 |
Inherited metabolic diseases affecting the carrier. |
causal interaction
therapeutic application
unassigned |
4
3
0 |
| 2.7.1.6 | Bacterial Infections |
6695877 |
Recurrent sepsis with deficiencies of C2 and galactokinase. |
causal interaction
diagnostic usage
unassigned |
2
1
0 |
| 2.7.1.6 | Biliary Atresia |
19951499 |
[Citrin deficiency is an important etiology for cholestatic liver disease in children] |
causal interaction
diagnostic usage
unassigned |
3
1
0 |
| 2.7.1.6 | Blindness |
21264483 |
The effect of a Pro(28)Thr point mutation on the local structure and stability of human galactokinase enzyme-a theoretical study. |
causal interaction
unassigned |
3
0 |
| 2.7.1.6 | Brain Diseases |
32807972 |
Galactokinase deficiency: lessons from the GalNet registry. |
causal interaction
unassigned |
4
0 |
| 2.7.1.6 | Burkitt Lymphoma |
2137369 |
Coregulation of the human O6-methylguanine-DNA methyltransferase with two unrelated genes that are closely linked. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
1
1
0 |
| 2.7.1.6 | Capsule Opacification |
7352874 |
Presenile cataract formation and decreased activity of galactosemic enzymes. |
causal interaction
diagnostic usage
unassigned |
1
3
0 |
| 2.7.1.6 | Carcinoma, Hepatocellular |
27919945 |
The Leloir Pathway of Galactose Metabolism - A Novel Therapeutic Target for Hepatocellular Carcinoma. |
causal interaction
ongoing research
therapeutic application
unassigned |
1
4
1
0 |
