Sildenafil
DrugBank ID: DB00203
Summary
| Metric | Value |
|---|---|
| Total Predictions | 53 |
| KG+DL (Dual Validated) | 1 |
| DL Only | 49 |
| KG Only | 3 |
Predictions
| Indication | Score | Source |
|---|---|---|
| Ambras type hypertrichosis universalis congenita | 0.9841 | DL |
| malformation syndrome with odontal and/or periodontal component | 0.9823 | DL |
| syndrome with a Dandy-Walker malformation as major feature | 0.9803 | DL |
| isolated genetic hair shaft abnormality | 0.9786 | DL |
| hypertrichosis (disease) | 0.9783 | DL |
| homozygous familial hypercholesterolemia | 0.9377 | DL |
| hypoalphalipoproteinemia | 0.9011 | DL |
| familial isolated trichomegaly | 0.7978 | DL |
| genetic alopecia | 0.7503 | DL |
| obsolete patella aplasia, coxa vara, and tarsal synostosis | 0.7000 | DL |
| hypotrichosis simplex of the scalp | 0.6988 | DL |
| pulmonary hypertension, primary, autosomal recessive | 0.6919 | DL |
| familial clubfoot due to 17q23.1q23.2 microduplication | 0.6883 | DL |
| kyphoscoliotic heart disease | 0.6849 | DL |
| pulmonary hypertension | 0.6806 | DL |
| migraine with brainstem aura | 0.6769 | DL |
| chromosome 17q23.1-q23.2 deletion syndrome | 0.6676 | DL |
| pulmonary arterial hypertension associated with congenital heart disease | 0.6660 | DL |
| congenital hypotrichosis milia | 0.6608 | DL |
| coxopodopatellar syndrome | 0.6568 | DL |
| pulmonary arteriovenous malformation (disease) | 0.6554 | DL |
| syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy | 0.6527 | DL |
| pulmonary arterial hypertension | 0.6437 | KG+DL |
| pulmonary arterial hypertension associated with HIV infection | 0.6381 | DL |
| pulmonary arterial hypertension associated with chronic hemolytic anemia | 0.6381 | DL |
| pulmonary arterial hypertension associated with connective tissue disease | 0.6381 | DL |
| pulmonary arterial hypertension associated with schistosomiasis | 0.6381 | DL |
| obsolete familial combined hyperlipidemia | 0.6369 | DL |
| migraine disorder | 0.6188 | DL |
| diffuse alopecia areata | 0.6090 | DL |
| pulmonary hypertension, primary | 0.5961 | DL |
| idiopathic pulmonary arterial hypertension | 0.5912 | DL |
| mitral valve prolapse, myxomatous | 0.5891 | DL |
| oculoauricular syndrome | 0.5823 | DL |
| blepharoptosis-myopia-ectopia lentis syndrome | 0.5804 | DL |
| sclerocornea, autosomal dominant | 0.5785 | DL |
| obsolete susceptibility to ischemic stroke | 0.5782 | DL |
| melanoma, malignant familial intraocular | 0.5773 | DL |
| dysosteosclerosis | 0.5730 | DL |
| Torg-Winchester syndrome | 0.5712 | DL |
| craniofacial dystonia | 0.5711 | DL |
| hypercarotenemia and vitamin A deficiency, autosomal recessive | 0.5709 | DL |
| melorheostosis | 0.5689 | DL |
| ovarian fibroma (disease) | 0.5678 | DL |
| autosomal dominant vitreoretinochoroidopathy | 0.5676 | DL |
| algoneurodystrophy | 0.5664 | DL |
| congenital cystic eye multiple ocular and intracranial anomalies | 0.5636 | DL |
| fibrosis of extraocular muscles, congenital, with synergistic divergence | 0.5624 | DL |
| sudden arrhythmia death syndrome | 0.5620 | DL |
| Carney complex, | 0.5615 | 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.