EC Number   |
Disease |
PubMed ID  |
Title of Publication |
Category |
Confidence Level |
|---|
   2.1.1.228 | Intellectual Disability |
33067246 |
tRNA methyltransferase 10 homologue A (TRMT10A) mutation in a Chinese patient with diabetes, insulin resistance, intellectual deficiency and microcephaly. |
causal interaction
ongoing research
unassigned |
4
1
0 |
| 2.1.1.228 | Microcephaly |
33067246 |
tRNA methyltransferase 10 homologue A (TRMT10A) mutation in a Chinese patient with diabetes, insulin resistance, intellectual deficiency and microcephaly. |
causal interaction
ongoing research
unassigned |
4
1
0 |
| 2.1.1.228 | Intellectual Disability |
33448213 |
TRMT10A mutation in a child with diabetes, short stature, microcephaly and hypoplastic kidneys. |
causal interaction
unassigned |
3
0 |
| 2.1.1.228 | Microcephaly |
33448213 |
TRMT10A mutation in a child with diabetes, short stature, microcephaly and hypoplastic kidneys. |
causal interaction
unassigned |
3
0 |
| 2.1.1.228 | Intellectual Disability |
34541035 |
Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases. |
causal interaction
unassigned |
4
0 |
| 2.1.1.228 | Microcephaly |
34541035 |
Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases. |
causal interaction
unassigned |
4
0 |
