EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   2.4.99.9 | Adenocarcinoma |
17711504 |
GM3 synthase gene is a novel biomarker for histological classification and drug sensitivity against epidermal growth factor receptor tyrosine kinase inhibitors in non-small cell lung cancer. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
4
4
3
4 |
| 2.4.99.9 | Arthritis, Experimental |
22768242 |
Ganglioside GM3 has an essential role in the pathogenesis and progression of rheumatoid arthritis. |
causal interaction
ongoing research
unassigned |
3
4
0 |
| 2.4.99.9 | Blindness |
17050284 |
Etiology of vision loss in ganglioside GM3 synthase deficiency. |
causal interaction
unassigned |
4
0 |
| 2.4.99.9 | Blindness, Cortical |
23436467 |
Cutaneous dyspigmentation in patients with ganglioside GM3 synthase deficiency. |
causal interaction
unassigned |
4
0 |
| 2.4.99.9 | Carcinoma |
12515997 |
Clinicopathologic evaluation of CDw75 antigen expression in colorectal adenocarcinomas. |
causal interaction
unassigned |
4
0 |
| 2.4.99.9 | Carcinoma |
17711504 |
GM3 synthase gene is a novel biomarker for histological classification and drug sensitivity against epidermal growth factor receptor tyrosine kinase inhibitors in non-small cell lung cancer. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
4
4
3
4 |
| 2.4.99.9 | Carcinoma, Non-Small-Cell Lung |
17711504 |
GM3 synthase gene is a novel biomarker for histological classification and drug sensitivity against epidermal growth factor receptor tyrosine kinase inhibitors in non-small cell lung cancer. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
4
4
3
4 |
| 2.4.99.9 | Congenital Abnormalities |
19470479 |
Mice lacking ganglioside GM3 synthase exhibit complete hearing loss due to selective degeneration of the organ of Corti. |
causal interaction
ongoing research
therapeutic application
unassigned |
1
2
1
0 |
| 2.4.99.9 | Deafness |
19470479 |
Mice lacking ganglioside GM3 synthase exhibit complete hearing loss due to selective degeneration of the organ of Corti. |
causal interaction
ongoing research
therapeutic application
unassigned |
1
2
1
0 |
| 2.4.99.9 | Epilepsy |
22814679 |
Disorders of phospholipids, sphingolipids and fatty acids biosynthesis: toward a new category of inherited metabolic diseases. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
