Minoxidil
DrugBank ID: DB00350
Summary
| Metric | Value |
|---|---|
| Total Predictions | 51 |
| KG+DL (Dual Validated) | 2 |
| DL Only | 48 |
| KG Only | 1 |
Predictions
| Indication | Score | Source |
|---|---|---|
| hypotrichosis simplex of the scalp | 1.0000 | DL |
| congenital hypotrichosis milia | 1.0000 | DL |
| diffuse alopecia areata | 1.0000 | DL |
| alopecia | 1.0000 | KG+DL |
| pseudopelade of Brocq | 0.9992 | DL |
| pulmonary arterial hypertension | 0.9992 | DL |
| pulmonary arteriovenous malformation (disease) | 0.9988 | DL |
| pulmonary arterial hypertension associated with congenital heart disease | 0.9988 | DL |
| primary hereditary glaucoma | 0.9985 | DL |
| pulmonary arterial hypertension associated with HIV infection | 0.9985 | DL |
| pulmonary arterial hypertension associated with chronic hemolytic anemia | 0.9985 | DL |
| pulmonary arterial hypertension associated with connective tissue disease | 0.9985 | DL |
| pulmonary arterial hypertension associated with schistosomiasis | 0.9985 | DL |
| malformation syndrome with odontal and/or periodontal component | 0.9982 | DL |
| Ambras type hypertrichosis universalis congenita | 0.9982 | DL |
| hypertrichosis (disease) | 0.9982 | DL |
| pulmonary hypertension, primary, autosomal recessive | 0.9982 | DL |
| genetic alopecia | 0.9981 | DL |
| pulmonary hypertension | 0.9981 | DL |
| obsolete patella aplasia, coxa vara, and tarsal synostosis | 0.9980 | DL |
| syndrome with a Dandy-Walker malformation as major feature | 0.9979 | DL |
| open-angle glaucoma | 0.9979 | DL |
| isolated genetic hair shaft abnormality | 0.9977 | DL |
| hypertensive disorder | 0.9976 | KG+DL |
| androgenetic alopecia | 0.9974 | DL |
| familial clubfoot due to 17q23.1q23.2 microduplication | 0.9973 | DL |
| chromosome 17q23.1-q23.2 deletion syndrome | 0.9972 | DL |
| hypotrichosis of eyelid | 0.9971 | DL |
| coxopodopatellar syndrome | 0.9968 | DL |
| kyphoscoliotic heart disease | 0.9967 | DL |
| pulmonary hypertension, primary | 0.9963 | DL |
| idiopathic pulmonary arterial hypertension | 0.9962 | DL |
| pulmonary hypertension owing to lung disease and/or hypoxia | 0.9961 | DL |
| pulmonary hypertension with unclear multifactorial mechanism | 0.9961 | DL |
| malignant hypertensive renal disease | 0.9961 | DL |
| malignant renovascular hypertension | 0.9961 | DL |
| idiopathic and/or familial pulmonary arterial hypertension | 0.9959 | DL |
| essential hypertension, genetic | 0.9954 | DL |
| Braddock syndrome | 0.9951 | DL |
| heritable pulmonary arterial hypertension | 0.9947 | DL |
| migraine with brainstem aura | 0.9944 | DL |
| telangiectasia, hereditary hemorrhagic, | 0.9939 | DL |
| migraine disorder | 0.9938 | DL |
| 16q24.1 microdeletion syndrome | 0.9938 | DL |
| Olmsted syndrome | 0.9937 | DL |
| isolated pulmonary capillaritis | 0.9934 | DL |
| primary interstitial lung disease specific to childhood | 0.9934 | DL |
| arterial thoracic outlet syndrome | 0.9915 | DL |
| venous thoracic outlet syndrome | 0.9915 | DL |
| congenital pulmonary lymphangiectasia | 0.9911 | DL |
Showing top 50 of 51 predictions.
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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.