Primidone
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB00794 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 35 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | trigeminal nerve neoplasm | KG + DL |
| 2 | orgasm-induced seizures | KG + DL |
| 3 | micturation-induced seizures | KG + DL |
| 4 | eating seizures | KG + DL |
| 5 | audiogenic seizures | KG + DL |
| 6 | thinking seizures | KG + DL |
| 7 | startle epilepsy | KG + DL |
| 8 | reading seizures | KG + DL |
| 9 | trigeminal neuralgia | KG + DL |
| 10 | beta-ketothiolase deficiency | KG + DL |
| 11 | Rett syndrome, congenital variant | KG + DL |
| 12 | status epilepticus | KG + DL |
| 13 | 14q12 microdeletion syndrome | KG + DL |
| 14 | guanidinoacetate methyltransferase deficiency | KG + DL |
| 15 | adolescent/adult onset autosomal dominant epilepsy with auditory features | KG + DL |
| 16 | restless legs syndrome | KG + DL |
| 17 | myoclonic-atonic epilepsy | KG + DL |
| 18 | facial neuralgia | KG + DL |
| 19 | combined hyperactive dysfunction syndrome of the cranial nerves | KG + DL |
| 20 | atypical childhood epilepsy with centrotemporal spikes | KG + DL |
| 21 | cryptogenic late-onset epileptic spasms | KG + DL |
| 22 | photosensitive occipital lobe epilepsy | KG + DL |
| 23 | febrile infection-related epilepsy syndrome | KG + DL |
| 24 | perioral myoclonia with absences | KG + DL |
| 25 | electroclinical syndrome | KG + DL |
| 26 | glossopharyngeal motor neuropathy | KG + DL |
| 27 | childhood onset epileptic encephalopathy | KG + DL |
| 28 | early onset absence epilepsy | KG + DL |
| 29 | vagus nerve disease | KG + DL |
| 30 | glossopharyngeal nerve paralysis | KG + DL |
| 31 | glossopharyngeal nerve neoplasm | KG + DL |
| 32 | epilepsy, nocturnal frontal lobe | KG + DL |
| 33 | early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation | KG + DL |
| 34 | benign occipital epilepsy | KG + DL |
| 35 | myofascial pain syndrome | KG + DL |
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.