Clonazepam
DrugBank ID: DB01068
Summary
| Metric | Value |
|---|---|
| Total Predictions | 51 |
| KG+DL (Dual Validated) | 2 |
| DL Only | 48 |
| KG Only | 1 |
Predictions
| Indication | Score | Source |
|---|---|---|
| restless legs syndrome | 0.9965 | DL |
| insomnia (disease) | 0.9932 | DL |
| trigeminal nerve neoplasm | 0.9930 | DL |
| sleep disorder, initiating and maintaining sleep | 0.9875 | DL |
| acute encephalopathy with biphasic seizures and late reduced diffusion | 0.9860 | DL |
| visual epilepsy | 0.9785 | DL |
| trigeminal neuralgia | 0.9766 | DL |
| status epilepticus | 0.9697 | DL |
| adolescent/adult onset autosomal dominant epilepsy with auditory features | 0.9682 | DL |
| reading seizures | 0.9657 | DL |
| epilepsy with generalized tonic-clonic seizures | 0.9653 | DL |
| audiogenic seizures | 0.9653 | DL |
| eating seizures | 0.9653 | DL |
| micturation-induced seizures | 0.9653 | DL |
| orgasm-induced seizures | 0.9653 | DL |
| startle epilepsy | 0.9653 | DL |
| thinking seizures | 0.9653 | DL |
| beta-ketothiolase deficiency | 0.9568 | DL |
| Lennox-Gastaut syndrome | 0.9565 | KG+DL |
| Rett syndrome, congenital variant | 0.9560 | DL |
| 14q12 microdeletion syndrome | 0.9548 | DL |
| partial epilepsy | 0.9527 | DL |
| febrile infection-related epilepsy syndrome | 0.9482 | DL |
| guanidinoacetate methyltransferase deficiency | 0.9462 | DL |
| perioral myoclonia with absences | 0.9452 | DL |
| atypical childhood epilepsy with centrotemporal spikes | 0.9434 | DL |
| cryptogenic late-onset epileptic spasms | 0.9434 | DL |
| photosensitive occipital lobe epilepsy | 0.9434 | DL |
| myoclonic-atonic epilepsy | 0.9414 | DL |
| electroclinical syndrome | 0.9357 | DL |
| epilepsy, childhood absence, susceptibility to | 0.9293 | DL |
| attention deficit-hyperactivity disorder | 0.9208 | DL |
| faciodigitogenital syndrome | 0.9156 | DL |
| partial motor epilepsy | 0.9125 | DL |
| Wernicke-Korsakoff syndrome | 0.9114 | DL |
| cutis verticis gyrata | 0.9095 | KG+DL |
| benign occipital epilepsy | 0.9075 | DL |
| childhood onset epileptic encephalopathy | 0.9059 | DL |
| trichotillomania | 0.9018 | DL |
| neonatal epilepsy syndrome | 0.8998 | DL |
| myofascial pain syndrome | 0.8991 | DL |
| early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation | 0.8893 | DL |
| inborn disorder of pyrimidine metabolism | 0.8885 | DL |
| familial hemiplegic migraine | 0.8876 | DL |
| non-neonatal early infantile epileptic encephalopathy | 0.8876 | DL |
| rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome | 0.8863 | DL |
| neonatal/infantile epilepsy syndrome | 0.8834 | DL |
| inborn disorder of purine metabolism | 0.8793 | DL |
| early onset absence epilepsy | 0.8778 | DL |
| developmental and epileptic encephalopathy, 85, with or without midline brain defects | 0.8768 | DL |
Showing top 50 of 51 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.