Aminophylline
DrugBank ID: DB01223
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 0 |
| DL Only | 50 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| migraine disorder | 0.9988 | DL |
| migraine with brainstem aura | 0.9984 | DL |
| migraine with or without aura, susceptibility to | 0.9982 | DL |
| atrophoderma vermiculata | 0.9960 | DL |
| ulerythema ophryogenesis | 0.9950 | DL |
| Prinzmetal angina | 0.9933 | DL |
| pulmonary hypertension | 0.9923 | DL |
| sciatic neuropathy | 0.9907 | DL |
| hyperthyroidism | 0.9906 | DL |
| kyphoscoliotic heart disease | 0.9901 | DL |
| peripheral arterial disease | 0.9893 | DL |
| tendinitis | 0.9886 | DL |
| fibromyalgia | 0.9885 | DL |
| resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta | 0.9884 | DL |
| peripheral vascular disease | 0.9884 | DL |
| idiopathic granulomatous myositis | 0.9873 | DL |
| myositis fibrosa | 0.9873 | DL |
| female breast carcinoma | 0.9872 | DL |
| amenorrhea (disease) | 0.9845 | DL |
| ischemic disease | 0.9828 | DL |
| rheumatoid arthritis | 0.9827 | DL |
| inclusion body myositis | 0.9824 | DL |
| non-inflammatory vasculopathy | 0.9822 | DL |
| keratosis pilaris | 0.9820 | DL |
| angiodysplasia | 0.9820 | DL |
| thrombotic disease | 0.9810 | DL |
| vascular ectasia | 0.9809 | DL |
| headache disorder | 0.9807 | DL |
| fibrocartilaginous embolism | 0.9805 | DL |
| venous thromboembolism | 0.9805 | DL |
| intermittent vascular claudication | 0.9790 | DL |
| hyperthyroxinemia | 0.9777 | DL |
| congenital renal artery stenosis | 0.9768 | DL |
| vein disease | 0.9753 | DL |
| brachydactyly-syndactyly syndrome | 0.9753 | DL |
| trigeminal autonomic cephalalgia | 0.9747 | DL |
| intracranial arteriosclerosis | 0.9735 | DL |
| Raynaud disease | 0.9712 | DL |
| nephrogenic syndrome of inappropriate antidiuresis | 0.9706 | DL |
| leprosy | 0.9703 | DL |
| colobomatous microphthalmia-rhizomelic dysplasia syndrome | 0.9692 | DL |
| Graves disease | 0.9690 | DL |
| vascular insufficiency disorder | 0.9686 | DL |
| Monckeberg arteriosclerosis | 0.9659 | DL |
| pulmonary hypertension, primary, autosomal recessive | 0.9651 | DL |
| cytomegalovirus infection | 0.9633 | DL |
| genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability | 0.9632 | DL |
| infectious bovine rhinotracheitis | 0.9622 | DL |
| malignant catarrh | 0.9622 | DL |
| arterial calcification of infancy | 0.9597 | 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.