Travoprost
DrugBank ID: DB00287
Summary
| Metric | Value |
|---|---|
| Total Predictions | 51 |
| KG+DL (Dual Validated) | 0 |
| DL Only | 50 |
| KG Only | 1 |
Predictions
| Indication | Score | Source |
|---|---|---|
| visceral calciphylaxis | 1.0000 | DL |
| arterial thoracic outlet syndrome | 1.0000 | DL |
| venous thoracic outlet syndrome | 1.0000 | DL |
| neurogenic thoracic outlet syndrome | 1.0000 | DL |
| vascular disease | 1.0000 | DL |
| angiodysplasia of stomach | 1.0000 | DL |
| blue toe syndrome | 1.0000 | DL |
| idiopathic spontaneous coronary artery dissection | 1.0000 | DL |
| lymphangiectasis | 1.0000 | DL |
| hemangioendothelioma | 1.0000 | DL |
| hypotrichosis simplex of the scalp | 1.0000 | DL |
| atheroembolism of kidney | 1.0000 | DL |
| arterial dissection-lentiginosis syndrome | 1.0000 | DL |
| congenital hypotrichosis milia | 1.0000 | DL |
| diffuse alopecia areata | 1.0000 | DL |
| alopecia | 1.0000 | DL |
| hypertrichosis (disease) | 1.0000 | DL |
| open-angle glaucoma | 1.0000 | DL |
| primary hereditary glaucoma | 1.0000 | DL |
| malformation syndrome with odontal and/or periodontal component | 1.0000 | DL |
| syndrome with a Dandy-Walker malformation as major feature | 1.0000 | DL |
| isolated genetic hair shaft abnormality | 0.9999 | DL |
| Ambras type hypertrichosis universalis congenita | 0.9999 | DL |
| pulmonary arterial hypertension | 0.9999 | DL |
| pulmonary arteriovenous malformation (disease) | 0.9999 | DL |
| pulmonary arterial hypertension associated with congenital heart disease | 0.9999 | DL |
| pulmonary arterial hypertension associated with HIV infection | 0.9998 | DL |
| pulmonary arterial hypertension associated with chronic hemolytic anemia | 0.9998 | DL |
| pulmonary arterial hypertension associated with connective tissue disease | 0.9998 | DL |
| pulmonary arterial hypertension associated with schistosomiasis | 0.9998 | DL |
| genetic alopecia | 0.9998 | DL |
| persistent fetal circulation syndrome | 0.9995 | DL |
| respiratory failure | 0.9995 | DL |
| subarachnoid hemorrhage (disease) | 0.9993 | DL |
| pseudopelade of Brocq | 0.9992 | DL |
| 16q24.1 microdeletion syndrome | 0.9989 | DL |
| isolated pulmonary capillaritis | 0.9989 | DL |
| primary interstitial lung disease specific to childhood | 0.9989 | DL |
| glaucoma 1, open angle | 0.9988 | DL |
| congenital alveolar capillary dysplasia | 0.9988 | DL |
| open angle glaucoma | 0.9986 | DL |
| congenital pulmonary lymphangiectasia | 0.9985 | DL |
| obsolete patella aplasia, coxa vara, and tarsal synostosis | 0.9982 | DL |
| yellow nail syndrome | 0.9976 | DL |
| pulmonary hypertension, primary, autosomal recessive | 0.9974 | DL |
| familial clubfoot due to 17q23.1q23.2 microduplication | 0.9973 | DL |
| coxopodopatellar syndrome | 0.9972 | DL |
| Wyburn-Mason syndrome | 0.9972 | DL |
| chromosome 17q23.1-q23.2 deletion syndrome | 0.9972 | DL |
| Moyomoya angiopathy | 0.9972 | DL |
Showing top 50 of 51 predictions.
External Links
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.