Dopamine
DrugBank ID: DB00988
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 0 |
| DL Only | 50 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| hypotensive disorder | 0.9714 | DL |
| postural orthostatic tachycardia syndrome | 0.8800 | DL |
| variably protease-sensitive prionopathy | 0.8687 | DL |
| multiple system atrophy | 0.8479 | DL |
| hypotrichosis simplex of the scalp | 0.8341 | DL |
| gastroduodenitis | 0.8175 | DL |
| congenital hypotrichosis milia | 0.8091 | DL |
| common cold | 0.8036 | DL |
| diffuse alopecia areata | 0.7695 | DL |
| peptic ulcer disease | 0.7504 | DL |
| rhinitis | 0.7213 | DL |
| obsolete neurogenic bladder (disease) | 0.6900 | DL |
| osteoarthritis susceptibility | 0.6863 | DL |
| alopecia | 0.6777 | DL |
| acromesomelic dysplasia, Hunter-Thompson type | 0.6479 | DL |
| trigeminal autonomic cephalalgia | 0.6259 | DL |
| headache disorder | 0.6170 | DL |
| mitral valve prolapse, myxomatous | 0.6018 | DL |
| sclerocornea, autosomal dominant | 0.5921 | DL |
| fibrosis of extraocular muscles, congenital, with synergistic divergence | 0.5863 | DL |
| idiopathic bronchiectasis | 0.5849 | DL |
| faciodigitogenital syndrome | 0.5820 | DL |
| hyperparathyroidism, primary, caused by water clear cell hyperplasia | 0.5804 | DL |
| osteoarthritis | 0.5787 | DL |
| brachyolmia | 0.5774 | DL |
| brachyolmia-amelogenesis imperfecta syndrome | 0.5772 | DL |
| trichotillomania | 0.5743 | DL |
| hypospadias 3, autosomal | 0.5716 | DL |
| sella turcica, bridged | 0.5716 | DL |
| triphalangeal thumb, Nonopposable | 0.5716 | DL |
| hypercarotenemia and vitamin A deficiency, autosomal recessive | 0.5613 | DL |
| cholangiocarcinoma, susceptibility to | 0.5607 | DL |
| atrial flutter (disease) | 0.5596 | DL |
| retinal aplasia | 0.5580 | DL |
| thiopurine immunosuppressant-induced pancreatitis | 0.5572 | DL |
| myosclerosis | 0.5567 | DL |
| ACys amyloidosis | 0.5563 | DL |
| myoglobinuria, recurrent | 0.5561 | DL |
| melanoma, malignant familial intraocular | 0.5555 | DL |
| pseudoachondroplasia | 0.5534 | DL |
| lattice degeneration of retina leading to retinal detachment | 0.5529 | DL |
| cervical hypertrichosis with underlying kyphoscoliosis | 0.5517 | DL |
| sudden arrhythmia death syndrome | 0.5517 | DL |
| susceptibility to mononeuropathy of the median nerve, mild | 0.5503 | DL |
| FADD-related immunodeficiency | 0.5491 | DL |
| celiac artery stenosis from compression by median arcuate ligament of diaphragm | 0.5483 | DL |
| scleral staphyloma (disease) | 0.5469 | DL |
| hernia, anterior diaphragmatic | 0.5466 | DL |
| pancreas, dorsal, agenesis of | 0.5457 | DL |
| tarsal coalition | 0.5445 | 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.