EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   2.1.1.61 | Liver Failure |
25407320 |
Reversible infantile mitochondrial diseases. |
causal interaction
unassigned |
4
0 |
| 2.1.1.61 | Liver Failure |
25665837 |
Hepatic Copper Accumulation: A Novel Feature in Transient Infantile Liver Failure Due to TRMU Mutations? |
causal interaction
ongoing research
unassigned |
3
1
0 |
| 2.1.1.61 | Liver Failure, Acute |
25665837 |
Hepatic Copper Accumulation: A Novel Feature in Transient Infantile Liver Failure Due to TRMU Mutations? |
causal interaction
ongoing research
unassigned |
3
1
0 |
| 2.1.1.61 | Liver Failure, Acute |
33365252 |
Leigh syndrome associated with TRMU gene mutations. |
causal interaction
unassigned |
4
0 |
| 2.1.1.61 | Mitochondrial Diseases |
23814040 |
Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiency. |
causal interaction
unassigned |
2
0 |
| 2.1.1.61 | Mitochondrial Diseases |
25407320 |
Reversible infantile mitochondrial diseases. |
causal interaction
unassigned |
4
0 |
| 2.1.1.61 | Mitochondrial Myopathies |
25407320 |
Reversible infantile mitochondrial diseases. |
causal interaction
unassigned |
4
0 |
