Sodium Tetradecyl Sulfate
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB00464 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 100 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | esophageal varices without bleeding | KG + DL |
| 2 | esophageal varices with bleeding | KG + DL |
| 3 | Steel syndrome | KG + DL |
| 4 | pseudo-von Willebrand disease | KG + DL |
| 5 | Immunoerythromyeloid hypoplasia | KG + DL |
| 6 | primary release disorder of platelets | KG + DL |
| 7 | reticular dysgenesis | KG + DL |
| 8 | autosomal dominant familial periodic fever | KG + DL |
| 9 | hypophosphatasia | KG + DL |
| 10 | lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome | KG + DL |
| 11 | syndrome with combined immunodeficiency | KG + DL |
| 12 | T-B+ severe combined immunodeficiency due to gamma chain deficiency | KG + DL |
| 13 | hepatic infarction | KG + DL |
| 14 | non-severe combined immunodeficiency | KG + DL |
| 15 | severe combined immunodeficiency due to LCK deficiency | KG + DL |
| 16 | adenosine deaminase deficiency | KG + DL |
| 17 | T-B+ severe combined immunodeficiency due to CD45 deficiency | KG + DL |
| 18 | combined immunodeficiency due to CRAC channel dysfunction | KG + DL |
| 19 | combined immunodeficiency, X-linked | KG + DL |
| 20 | hepatic veno-occlusive disease | KG + DL |
| 21 | absent thumb-short stature-immunodeficiency syndrome | KG + DL |
| 22 | pancytopenia due to IKZF1 mutations | KG + DL |
| 23 | vitamin A deficiency (disease) | KG + DL |
| 24 | facial dysmorphism-immunodeficiency-livedo-short stature syndrome | KG + DL |
| 25 | hepatic veno-occlusive disease-immunodeficiency syndrome | KG + DL |
| 26 | Glanzmann thrombasthenia | KG + DL |
| 27 | peliosis hepatis | KG + DL |
| 28 | familial apolipoprotein C-II deficiency | KG + DL |
| 29 | immuno-osseous dysplasia | KG + DL |
| 30 | autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis | KG + DL |
| 31 | Omenn syndrome | KG + DL |
| 32 | monosomy X | KG + DL |
| 33 | periodic fever-infantile enterocolitis-autoinflammatory syndrome | KG + DL |
| 34 | primary immunodeficiency due to a defect in adaptive immunity | KG + DL |
| 35 | hemolytic uremic syndrome, atypical, susceptibility to, 1 | KG + DL |
| 36 | Charcot-Marie-Tooth disease | KG + DL |
| 37 | late-onset retinal degeneration | KG + DL |
| 38 | severe combined immunodeficiency (disease) | KG + DL |
| 39 | pigmented paravenous retinochoroidal atrophy | KG + DL |
| 40 | macular degeneration, X-linked atrophic | KG + DL |
| 41 | immunodeficiency with factor H anomaly | KG + DL |
| 42 | oligocone trichromacy | KG + DL |
| 43 | purine nucleoside phosphorylase deficiency | KG + DL |
| 44 | retinoschisis of fovea | KG + DL |
| 45 | progressive bifocal chorioretinal atrophy | KG + DL |
| 46 | X-linked retinal dysplasia | KG + DL |
| 47 | cone dystrophy | KG + DL |
| 48 | T-cell immunodeficiency, congenital alopecia, and nail dystrophy | KG + DL |
| 49 | Aland island eye disease | KG + DL |
| 50 | helicoid peripapillary chorioretinal degeneration | KG + DL |
(Showing top 50 of 100 predictions)
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.