EC Number   |
Disease |
PubMed ID |
Title of Publication  |
Category |
Confidence Level |
|---|
   2.1.1.228 | Nervous System Diseases |
30415557 |
tRNA Methyltransferase Defects and Intellectual Disability. |
diagnostic usage
ongoing research
therapeutic application
unassigned |
2
1
1
0 |
| 2.1.1.228 | Microcephaly |
24204302 |
tRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in humans. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
1
1
0 |
| 2.1.1.228 | Diabetes Mellitus |
26526202 |
tRNA methyltransferase homologue gene TRMT10A mutation in young adult-onset diabetes with intellectual disability, microcephaly and epilepsy. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
1
3
0 |
| 2.1.1.228 | Epilepsy |
26526202 |
tRNA methyltransferase homologue gene TRMT10A mutation in young adult-onset diabetes with intellectual disability, microcephaly and epilepsy. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
1
3
0 |
| 2.1.1.228 | Intellectual Disability |
26526202 |
tRNA methyltransferase homologue gene TRMT10A mutation in young adult-onset diabetes with intellectual disability, microcephaly and epilepsy. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
1
3
0 |
| 2.1.1.228 | Microcephaly |
26526202 |
tRNA methyltransferase homologue gene TRMT10A mutation in young adult-onset diabetes with intellectual disability, microcephaly and epilepsy. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
1
3
0 |
