Spironolactone
DrugBank ID: DB00421
Summary
| Metric | Value |
|---|---|
| Total Predictions | 53 |
| KG+DL (Dual Validated) | 2 |
| DL Only | 48 |
| KG Only | 3 |
Predictions
| Indication | Score | Source |
|---|---|---|
| hypotrichosis simplex of the scalp | 0.9926 | DL |
| congenital hypotrichosis milia | 0.9904 | DL |
| diffuse alopecia areata | 0.9841 | DL |
| alopecia | 0.9783 | DL |
| hypertensive disorder | 0.9775 | KG+DL |
| malignant hypertensive renal disease | 0.9754 | DL |
| malignant renovascular hypertension | 0.9754 | DL |
| pulmonary hypertension owing to lung disease and/or hypoxia | 0.9733 | DL |
| pulmonary hypertension with unclear multifactorial mechanism | 0.9733 | DL |
| Braddock syndrome | 0.9664 | DL |
| chronic pulmonary heart disease | 0.9555 | DL |
| Waterhouse-Friderichsen syndrome | 0.8558 | KG+DL |
| primary hereditary glaucoma | 0.8405 | DL |
| acute pulmonary heart disease | 0.8118 | DL |
| pregnancy associated osteoporosis | 0.7856 | DL |
| Worth syndrome | 0.7584 | DL |
| autosomal dominant neovascular inflammatory vitreoretinopathy | 0.7568 | DL |
| open-angle glaucoma | 0.7440 | DL |
| congestive heart failure | 0.7404 | DL |
| postmenopausal osteoporosis | 0.7328 | DL |
| familial hyperreninemic hypoaldosteronism | 0.7271 | DL |
| gastroenteritis, transmissible, of swine | 0.7198 | DL |
| succinyl-CoA:3-ketoacid CoA transferase deficiency | 0.6994 | DL |
| familial hypoaldosteronism | 0.6617 | DL |
| aldosterone-producing adrenal cortex adenoma | 0.6409 | DL |
| corticosterone methyloxidase type 1 deficiency | 0.6371 | DL |
| primary unilateral adrenal hyperplasia | 0.6340 | DL |
| familial hyperaldosteronism | 0.6298 | DL |
| potassium deficiency disease | 0.6234 | DL |
| glucocorticoid-remediable aldosteronism | 0.6070 | DL |
| thiopurine immunosuppressant-induced pancreatitis | 0.6038 | DL |
| sudden arrhythmia death syndrome | 0.5907 | DL |
| obsolete hypertension, diastolic, resistance to | 0.5815 | DL |
| spinal chordoma | 0.5770 | DL |
| ABetaA21G amyloidosis | 0.5737 | DL |
| Wilms tumor, aniridia, genitourinary anomalies, intellectual disability, and obesity syndrome | 0.5727 | DL |
| Peters anomaly-cataract syndrome | 0.5727 | DL |
| Aloi Tomasini Isaia syndrome | 0.5718 | DL |
| alcoholic ketoacidosis | 0.5706 | DL |
| metabolic acidosis | 0.5706 | DL |
| radial defect robin sequence | 0.5702 | DL |
| drug-related renal tubular dysgenesis | 0.5696 | DL |
| renal tubular dysgenesis due to twin-twin transfusion | 0.5696 | DL |
| recurrent infections-inflammatory syndrome due to zinc metabolism disorder syndrome | 0.5693 | DL |
| inherited Fanconi renotubular syndrome | 0.5673 | DL |
| 46,XY disorder of sex development due to a defect in testosterone metabolism by peripheral tissue | 0.5641 | DL |
| Kozlowski Warren Fisher syndrome | 0.5639 | DL |
| non-syndromic diaphragmatic or abdominal wall malformation | 0.5632 | DL |
| aldosterone-producing adenoma with seizures and neurological abnormalities | 0.5619 | DL |
| mitral valve prolapse, myxomatous | 0.5604 | DL |
Showing top 50 of 53 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.