Isosorbide dinitrate
DrugBank ID: DB00883
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 0 |
| DL Only | 50 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| alopecia | 0.9999 | DL |
| congenital hypotrichosis milia | 0.9999 | DL |
| hypotrichosis simplex of the scalp | 0.9999 | DL |
| pulmonary hypertension | 0.9998 | DL |
| diffuse alopecia areata | 0.9998 | DL |
| vascular disease | 0.9997 | DL |
| hypertrichosis (disease) | 0.9997 | DL |
| kyphoscoliotic heart disease | 0.9996 | DL |
| visceral calciphylaxis | 0.9996 | DL |
| arterial thoracic outlet syndrome | 0.9995 | DL |
| venous thoracic outlet syndrome | 0.9995 | DL |
| malformation syndrome with odontal and/or periodontal component | 0.9995 | DL |
| Ambras type hypertrichosis universalis congenita | 0.9995 | DL |
| neurogenic thoracic outlet syndrome | 0.9995 | DL |
| syndrome with a Dandy-Walker malformation as major feature | 0.9995 | DL |
| blue toe syndrome | 0.9995 | DL |
| angiodysplasia of stomach | 0.9994 | DL |
| pulmonary arterial hypertension | 0.9994 | DL |
| hemangioendothelioma | 0.9994 | DL |
| isolated genetic hair shaft abnormality | 0.9994 | DL |
| lymphangiectasis | 0.9994 | DL |
| pulmonary hypertension, primary, autosomal recessive | 0.9994 | DL |
| idiopathic spontaneous coronary artery dissection | 0.9994 | DL |
| atheroembolism of kidney | 0.9993 | DL |
| arterial dissection-lentiginosis syndrome | 0.9993 | DL |
| obsolete patella aplasia, coxa vara, and tarsal synostosis | 0.9992 | DL |
| headache disorder | 0.9992 | DL |
| benign prostatic hyperplasia (disease) | 0.9991 | DL |
| familial clubfoot due to 17q23.1q23.2 microduplication | 0.9990 | DL |
| chromosome 17q23.1-q23.2 deletion syndrome | 0.9989 | DL |
| coxopodopatellar syndrome | 0.9989 | DL |
| idiopathic pulmonary arterial hypertension | 0.9989 | DL |
| pulmonary hypertension, primary | 0.9988 | DL |
| pulmonary arterial hypertension associated with congenital heart disease | 0.9988 | DL |
| trigeminal autonomic cephalalgia | 0.9987 | DL |
| subarachnoid hemorrhage (disease) | 0.9987 | DL |
| pulmonary arterial hypertension associated with HIV infection | 0.9986 | DL |
| pulmonary arterial hypertension associated with chronic hemolytic anemia | 0.9986 | DL |
| pulmonary arterial hypertension associated with connective tissue disease | 0.9986 | DL |
| pulmonary arterial hypertension associated with schistosomiasis | 0.9986 | DL |
| pulmonary arteriovenous malformation (disease) | 0.9986 | DL |
| idiopathic and/or familial pulmonary arterial hypertension | 0.9986 | DL |
| genetic alopecia | 0.9985 | DL |
| pseudopelade of Brocq | 0.9985 | DL |
| open-angle glaucoma | 0.9984 | DL |
| primary hereditary glaucoma | 0.9984 | DL |
| heritable pulmonary arterial hypertension | 0.9982 | DL |
| migraine disorder | 0.9982 | DL |
| gastrointestinal hamartoma | 0.9979 | DL |
| Moyomoya angiopathy | 0.9978 | 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.