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<< < Results 31 - 36 of 36
EC Number
Disease
PubMed ID
Title of Publication
Category
Confidence Level
Nervous System Diseases
tRNA Methyltransferase Defects and Intellectual Disability.
diagnostic usage
ongoing research
therapeutic application
unassigned
2
1
1
0
Microcephaly
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
Diabetes Mellitus
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
Epilepsy
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
Intellectual Disability
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
Microcephaly
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
<< < Results 31 - 36 of 36