Selenium Sulfide
DrugBank ID: DB00971
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 3 |
| DL Only | 47 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| seborrheic dermatitis | 0.9373 | DL |
| seborrheic keratosis | 0.8977 | KG+DL |
| vulvar inverted follicular keratosis | 0.8952 | DL |
| cutaneous candidiasis | 0.8386 | DL |
| dermatitis | 0.8071 | DL |
| acne keloid | 0.7987 | DL |
| acrodermatitis chronica atrophicans | 0.7963 | DL |
| neonatal dermatomyositis | 0.7870 | DL |
| secondary interstitial lung disease specific to childhood associated with a connective tissue disease | 0.7738 | DL |
| amyopathic dermatomyositis | 0.7710 | DL |
| hydroa vacciniforme, familial | 0.7495 | DL |
| pityriasis simplex | 0.7236 | KG+DL |
| lichen planus, familial | 0.6935 | DL |
| pityriasis versicolor | 0.6767 | KG+DL |
| acne (disease) | 0.6549 | DL |
| nail infection | 0.6478 | DL |
| cholesteatoma (disease) | 0.6274 | DL |
| lichen planus pemphigoides | 0.5961 | DL |
| milia, multiple eruptive | 0.5849 | DL |
| acquired keratosis | 0.5798 | DL |
| isolated congenital adermatoglyphia | 0.5788 | DL |
| annular atrophic lichen planus | 0.5755 | DL |
| hypertrophic lichen planus | 0.5755 | DL |
| lichen planus pigmentosus | 0.5755 | DL |
| hereditary papulotranslucent acrokeratoderma | 0.5744 | DL |
| punctate epithelial keratoconjunctivitis | 0.5671 | DL |
| exanthem (disease) | 0.5656 | DL |
| lichen disease | 0.5617 | DL |
| acute articular rheumatism | 0.5570 | DL |
| spondylolysis (disease) | 0.5550 | DL |
| woolly hair-hypotrichosis-everted lower lip-outstanding ears syndrome | 0.5535 | DL |
| collagenous colitis | 0.5522 | DL |
| laryngostenosis | 0.5491 | DL |
| Beare-Stevenson cutis gyrata syndrome | 0.5486 | DL |
| nephropathy, progressive tubulointerstitial, with cholestatic liver disease | 0.5486 | DL |
| hereditary acrokeratotic poikiloderma, Weary type | 0.5460 | DL |
| keratinization disease | 0.5455 | DL |
| tooth ankylosis | 0.5420 | DL |
| congenital cystic eye multiple ocular and intracranial anomalies | 0.5419 | DL |
| trichodysplasia-xeroderma syndrome | 0.5408 | DL |
| polymorphic light eruption | 0.5398 | DL |
| ring chromosome 4 | 0.5394 | DL |
| CLOVES syndrome | 0.5383 | DL |
| tracheomalacia | 0.5383 | DL |
| endolymphatic sac tumor (disease) | 0.5381 | DL |
| FLOTCH syndrome | 0.5374 | DL |
| cocoon syndrome | 0.5370 | DL |
| Prata-Liberal-Goncalves syndrome | 0.5363 | DL |
| hyperopia | 0.5359 | DL |
| spinal stenosis | 0.5357 | DL |
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Disclaimer
Predictions are for research purposes only and do not constitute medical advice.
Predictions are for research purposes only and do not constitute medical advice.