Nadroparin
DrugBank ID: DB08813
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 0 |
| DL Only | 50 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| primary release disorder of platelets | 0.9815 | DL |
| Glanzmann thrombasthenia | 0.9814 | DL |
| pseudo-von Willebrand disease | 0.9756 | DL |
| thrombophilia | 0.9728 | DL |
| antithrombin deficiency type 2 | 0.9716 | DL |
| factor 5 excess with spontaneous thrombosis | 0.9703 | DL |
| heparin cofactor 2 deficiency | 0.9699 | DL |
| pulmonary embolism (disease) | 0.9698 | DL |
| amenorrhea (disease) | 0.9654 | DL |
| hemoglobinopathy | 0.9604 | DL |
| migraine with brainstem aura | 0.9517 | DL |
| migraine disorder | 0.9513 | DL |
| partial deletion of the short arm of chromosome 16 | 0.9447 | DL |
| hemolytic anemia due to glucophosphate isomerase deficiency | 0.9402 | DL |
| beta-thalassemia with other manifestations | 0.9402 | DL |
| bleeding diathesis due to a collagen receptor defect | 0.9389 | DL |
| hemorrhagic disorder due to a constitutional thrombocytopenia | 0.9387 | DL |
| fetal and neonatal alloimmune thrombocytopenia | 0.9356 | DL |
| pyropoikilocytosis, hereditary | 0.9354 | DL |
| thromboangiitis obliterans | 0.9354 | DL |
| coronary thrombosis | 0.9338 | DL |
| peripheral vascular disease | 0.9316 | DL |
| migraine with or without aura, susceptibility to | 0.9309 | DL |
| autosomal dominant macrothrombocytopenia | 0.9306 | DL |
| Scott syndrome | 0.9257 | DL |
| headache disorder | 0.9240 | DL |
| pyruvate kinase deficiency of red cells | 0.9219 | DL |
| filariasis | 0.9202 | DL |
| peripheral arterial disease | 0.9192 | DL |
| trigeminal autonomic cephalalgia | 0.9190 | DL |
| myocardial infarction | 0.9107 | DL |
| congenital coronary artery anomaly | 0.9088 | DL |
| priapism | 0.9072 | DL |
| heparin-induced thrombocytopenia (disease) | 0.9025 | DL |
| familial hypodysfibrinogenemia | 0.9010 | DL |
| platelet-type bleeding disorder | 0.8970 | DL |
| intermittent vascular claudication | 0.8968 | DL |
| hereditary thrombophilia due to congenital protein S deficiency | 0.8937 | DL |
| tendinitis | 0.8931 | DL |
| complement factor I deficiency | 0.8916 | DL |
| myocardial infarction (disease) | 0.8888 | DL |
| breast fibrocystic disease | 0.8873 | DL |
| angiodysplasia | 0.8867 | DL |
| idiopathic granulomatous myositis | 0.8854 | DL |
| myositis fibrosa | 0.8854 | DL |
| vascular ectasia | 0.8848 | DL |
| livedo reticularis | 0.8826 | DL |
| ischemic disease | 0.8820 | DL |
| non-inflammatory vasculopathy | 0.8819 | DL |
| thrombotic disease | 0.8812 | 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.