Adapalene
DrugBank ID: DB00210
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 1 |
| DL Only | 49 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| acne (disease) | 0.9999 | KG+DL |
| zinc, elevated plasma | 0.9951 | DL |
| isolated congenital adermatoglyphia | 0.9880 | DL |
| Beare-Stevenson cutis gyrata syndrome | 0.9878 | DL |
| demodicidosis of sebaceous gland | 0.9545 | DL |
| pyogenic arthritis-pyoderma gangrenosum-acne syndrome | 0.9530 | DL |
| prolidase deficiency | 0.8933 | DL |
| drug-induced osteoporosis | 0.8721 | DL |
| seborrheic dermatitis | 0.8628 | DL |
| sebaceous gland anomaly | 0.8516 | DL |
| inherited skin tumor | 0.8292 | DL |
| familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome | 0.7983 | DL |
| Ehlers-Danlos syndrome | 0.7882 | DL |
| seborrheic keratosis | 0.7223 | DL |
| vulvar inverted follicular keratosis | 0.7207 | DL |
| malignant atrophic papulosis | 0.7073 | DL |
| hyperkeratosis-hyperpigmentation syndrome | 0.6936 | DL |
| familial pityriasis rubra pilaris | 0.6826 | DL |
| Legius syndrome | 0.6725 | DL |
| familial acanthosis nigricans | 0.6463 | DL |
| familial chilblain lupus | 0.6342 | DL |
| urticaria, familial localized heat | 0.6310 | DL |
| cocoon syndrome | 0.6266 | DL |
| Wiskott-Aldrich syndrome 2 | 0.6156 | DL |
| alkaptonuria | 0.6135 | DL |
| Ramon syndrome | 0.6106 | DL |
| familial primary localized cutaneous amyloidosis | 0.6102 | DL |
| mitral valve prolapse, myxomatous | 0.6101 | DL |
| esophageal varices with bleeding | 0.6094 | DL |
| esophageal varices without bleeding | 0.6094 | DL |
| woolly hair, autosomal recessive 3 | 0.6041 | DL |
| band keratopathy | 0.6019 | DL |
| oculootodental syndrome | 0.5946 | DL |
| micromelic bone dysplasia with cloverleaf skull | 0.5910 | DL |
| omphalocele (disease) | 0.5898 | DL |
| cornea plana 1, autosomal dominant | 0.5895 | DL |
| musk, inability to smell | 0.5895 | DL |
| polyhydramnios, chronic idiopathic | 0.5895 | DL |
| melorheostosis | 0.5894 | DL |
| dysosteosclerosis | 0.5892 | DL |
| inherited cutis laxa | 0.5883 | DL |
| lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmune hemolytic anemia, and glomerulonephritis | 0.5862 | DL |
| blepharocheilodontic syndrome | 0.5862 | DL |
| hemolytic anemia due to adenylate kinase deficiency | 0.5844 | DL |
| taurodontia-absent teeth-sparse hair syndrome | 0.5825 | DL |
| cholangiocarcinoma, susceptibility to | 0.5819 | DL |
| X-linked keloid scarring-reduced joint mobility-increased optic cup-to-disc ratio syndrome | 0.5812 | DL |
| milia, multiple eruptive | 0.5812 | DL |
| hantavirus hemorrhagic fever with renal syndrome | 0.5808 | DL |
| sclerocornea, autosomal dominant | 0.5771 | 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.