Carbamazepine
DrugBank ID: DB00564
Summary
| Metric | Value |
|---|---|
| Total Predictions | 52 |
| KG+DL (Dual Validated) | 4 |
| DL Only | 46 |
| KG Only | 2 |
Predictions
| Indication | Score | Source |
|---|---|---|
| trigeminal nerve neoplasm | 1.0000 | DL |
| trigeminal neuralgia | 0.9999 | KG+DL |
| visual epilepsy | 0.9999 | DL |
| audiogenic seizures | 0.9997 | DL |
| eating seizures | 0.9997 | DL |
| micturation-induced seizures | 0.9997 | DL |
| orgasm-induced seizures | 0.9997 | DL |
| startle epilepsy | 0.9997 | DL |
| thinking seizures | 0.9997 | DL |
| reading seizures | 0.9997 | DL |
| beta-ketothiolase deficiency | 0.9989 | DL |
| Rett syndrome, congenital variant | 0.9987 | DL |
| 14q12 microdeletion syndrome | 0.9987 | DL |
| status epilepticus | 0.9984 | DL |
| partial epilepsy | 0.9975 | DL |
| partial motor epilepsy | 0.9965 | DL |
| epilepsy with generalized tonic-clonic seizures | 0.9960 | DL |
| glossopharyngeal motor neuropathy | 0.9953 | KG+DL |
| adolescent/adult onset autosomal dominant epilepsy with auditory features | 0.9950 | DL |
| facial neuralgia | 0.9948 | DL |
| guanidinoacetate methyltransferase deficiency | 0.9947 | DL |
| combined hyperactive dysfunction syndrome of the cranial nerves | 0.9944 | DL |
| epilepsy | 0.9943 | DL |
| glossopharyngeal nerve neoplasm | 0.9908 | DL |
| vagus nerve disease | 0.9908 | DL |
| glossopharyngeal nerve paralysis | 0.9908 | DL |
| Lennox-Gastaut syndrome | 0.9898 | KG+DL |
| trichotillomania | 0.9891 | DL |
| cutis verticis gyrata | 0.9883 | KG+DL |
| myoclonic-atonic epilepsy | 0.9870 | DL |
| Tourette syndrome | 0.9867 | DL |
| febrile infection-related epilepsy syndrome | 0.9853 | DL |
| atypical childhood epilepsy with centrotemporal spikes | 0.9841 | DL |
| cryptogenic late-onset epileptic spasms | 0.9841 | DL |
| photosensitive occipital lobe epilepsy | 0.9841 | DL |
| perioral myoclonia with absences | 0.9835 | DL |
| restless legs syndrome | 0.9816 | DL |
| electroclinical syndrome | 0.9737 | DL |
| nicotine dependence | 0.9730 | DL |
| methemoglobinemia, alpha type | 0.9719 | DL |
| idiopathic neonatal atrial flutter | 0.9688 | DL |
| attention deficit-hyperactivity disorder | 0.9676 | DL |
| early onset absence epilepsy | 0.9629 | DL |
| methemoglobin reductase deficiency | 0.9613 | DL |
| myofascial pain syndrome | 0.9551 | DL |
| asperger syndrome, susceptibility to | 0.9544 | DL |
| gaze palsy, familial horizontal, with progressive scoliosis | 0.9530 | DL |
| multifocal atrial tachycardia (disease) | 0.9528 | DL |
| childhood onset epileptic encephalopathy | 0.9523 | DL |
| autism susceptibility 1 | 0.9494 | DL |
Showing top 50 of 52 predictions.
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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.