EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    6.1.1.4 | CHARGE Syndrome |
28263850 |
Laser-capture micro dissection combined with next-generation sequencing analysis of cell type-specific deafness gene expression in the mouse cochlea. |
diagnostic usage
unassigned |
2
0 |
| 6.1.1.4 | Coma |
23470551 |
Prognostic value of time-related Glasgow Coma Scale components in severe traumatic brain injury: a prospective evaluation with respect to 1-year survival and functional outcome. |
ongoing research
unassigned |
1
0 |
| 6.1.1.4 | Confusion |
16500825 |
Homosexuality in ancient and modern Korea. |
unassigned |
0 |
| 6.1.1.4 | COVID-19 |
34249208 |
Instagram as a virtual art display for medical students. |
unassigned |
0 |
| 6.1.1.4 | Deafness |
27623246 |
Characterization of a knock-in mouse model of the homozygous p.V37I variant in Gjb2. |
unassigned |
0 |
| 6.1.1.4 | Deafness |
30737337 |
Biallelic variants in LARS2 and KARS cause deafness and (ovario)leukodystrophy. |
causal interaction
diagnostic usage
ongoing research
unassigned |
1
2
2
0 |
| 6.1.1.4 | Deafness |
31767665 |
Biallelic variants in LARS2 and KARS cause deafness and (ovario)leukodystrophy. |
unassigned |
0 |
| 6.1.1.4 | Deafness |
32442335 |
The expanding LARS2 phenotypic spectrum: HLASA, Perrault syndrome with leukodystrophy, and mitochondrial myopathy. |
causal interaction
ongoing research
therapeutic application
unassigned |
3
1
1
0 |
| 6.1.1.4 | Diabetes Mellitus, Type 2 |
15919814 |
Evidence that the mitochondrial leucyl tRNA synthetase (LARS2) gene represents a novel type 2 diabetes susceptibility gene. |
causal interaction
ongoing research
therapeutic application
unassigned |
3
4
1
0 |
| 6.1.1.4 | Diabetes Mellitus, Type 2 |
19847392 |
Genetic association analysis of LARS2 with type 2 diabetes. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
4
4
4
1 |
