Selenium Sulfide
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB00971 |
| 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 | seborrheic dermatitis | DL |
| 2 | vulvar inverted follicular keratosis | KG + DL |
| 3 | cutaneous candidiasis | KG + DL |
| 4 | acne keloid | KG + DL |
| 5 | acrodermatitis chronica atrophicans | KG + DL |
| 6 | neonatal dermatomyositis | KG + DL |
| 7 | secondary interstitial lung disease specific to childhood associated with a connective tissue disease | KG + DL |
| 8 | amyopathic dermatomyositis | KG + DL |
| 9 | hydroa vacciniforme, familial | KG + DL |
| 10 | lichen planus, familial | KG + DL |
| 11 | acne (disease) | KG + DL |
| 12 | nail infection | KG + DL |
| 13 | cholesteatoma (disease) | KG + DL |
| 14 | lichen planus pemphigoides | KG + DL |
| 15 | milia, multiple eruptive | KG + DL |
| 16 | acquired keratosis | KG + DL |
| 17 | isolated congenital adermatoglyphia | KG + DL |
| 18 | hypertrophic lichen planus | KG + DL |
| 19 | lichen planus pigmentosus | KG + DL |
| 20 | annular atrophic lichen planus | KG + DL |
| 21 | hereditary papulotranslucent acrokeratoderma | KG + DL |
| 22 | punctate epithelial keratoconjunctivitis | KG + DL |
| 23 | exanthem (disease) | KG + DL |
| 24 | lichen disease | KG + DL |
| 25 | acute articular rheumatism | KG + DL |
| 26 | spondylolysis (disease) | KG + DL |
| 27 | woolly hair-hypotrichosis-everted lower lip-outstanding ears syndrome | KG + DL |
| 28 | collagenous colitis | KG + DL |
| 29 | laryngostenosis | KG + DL |
| 30 | Beare-Stevenson cutis gyrata syndrome | KG + DL |
| 31 | nephropathy, progressive tubulointerstitial, with cholestatic liver disease | KG + DL |
| 32 | hereditary acrokeratotic poikiloderma, Weary type | KG + DL |
| 33 | keratinization disease | KG + DL |
| 34 | tooth ankylosis | KG + DL |
| 35 | congenital cystic eye multiple ocular and intracranial anomalies | KG + DL |
| 36 | trichodysplasia-xeroderma syndrome | KG + DL |
| 37 | polymorphic light eruption | KG + DL |
| 38 | ring chromosome 4 | KG + DL |
| 39 | CLOVES syndrome | KG + DL |
| 40 | tracheomalacia | KG + DL |
| 41 | endolymphatic sac tumor (disease) | KG + DL |
| 42 | FLOTCH syndrome | KG + DL |
| 43 | cocoon syndrome | KG + DL |
| 44 | Prata-Liberal-Goncalves syndrome | KG + DL |
| 45 | hyperopia | KG + DL |
| 46 | spinal stenosis | KG + DL |
| 47 | pili bifurcati | KG + DL |
| 48 | benign vaginal mixed epithelial and mesenchymal neoplasm | KG + DL |
| 49 | taurodontism (disease) | KG + DL |
| 50 | twin reversal arterial perfusion syndrome | 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.