Phenobarbital
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB01174 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 80 |
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 | startle epilepsy | KG + DL |
| 3 | orgasm-induced seizures | KG + DL |
| 4 | eating seizures | KG + DL |
| 5 | audiogenic seizures | KG + DL |
| 6 | micturation-induced seizures | KG + DL |
| 7 | thinking seizures | KG + DL |
| 8 | reading seizures | KG + DL |
| 9 | trigeminal neuralgia | KG + DL |
| 10 | beta-ketothiolase deficiency | KG + DL |
| 11 | idiopathic neonatal atrial flutter | KG + DL |
| 12 | 14q12 microdeletion syndrome | KG + DL |
| 13 | Rett syndrome, congenital variant | KG + DL |
| 14 | status epilepticus | KG + DL |
| 15 | multifocal atrial tachycardia (disease) | KG + DL |
| 16 | facial neuralgia | KG + DL |
| 17 | restless legs syndrome | KG + DL |
| 18 | combined hyperactive dysfunction syndrome of the cranial nerves | KG + DL |
| 19 | cauda equina syndrome | KG + DL |
| 20 | adolescent/adult onset autosomal dominant epilepsy with auditory features | KG + DL |
| 21 | partial motor epilepsy | KG + DL |
| 22 | His bundle tachycardia | KG + DL |
| 23 | myofascial pain syndrome | KG + DL |
| 24 | guanidinoacetate methyltransferase deficiency | KG + DL |
| 25 | trichotillomania | KG + DL |
| 26 | Tourette syndrome | KG + DL |
| 27 | obsolete neurogenic bladder (disease) | KG + DL |
| 28 | myoclonic-atonic epilepsy | KG + DL |
| 29 | acne (disease) | KG + DL |
| 30 | neuralgia | KG + DL |
| 31 | glossopharyngeal motor neuropathy | KG + DL |
| 32 | methemoglobinemia, alpha type | KG + DL |
| 33 | familial sick sinus syndrome | KG + DL |
| 34 | migraine with brainstem aura | KG + DL |
| 35 | electroclinical syndrome | KG + DL |
| 36 | methemoglobinemia | KG + DL |
| 37 | methemoglobin reductase deficiency | KG + DL |
| 38 | methemoglobinemia due to deficiency of methemoglobin reductase | KG + DL |
| 39 | sinoatrial node dysfunction and deafness | KG + DL |
| 40 | glossopharyngeal nerve paralysis | KG + DL |
| 41 | sick sinus syndrome | KG + DL |
| 42 | vagus nerve disease | KG + DL |
| 43 | glossopharyngeal nerve neoplasm | KG + DL |
| 44 | acquired peripheral neuropathy | KG + DL |
| 45 | Johanson-Blizzard syndrome | KG + DL |
| 46 | dysgammaglobulinemia (disease) | KG + DL |
| 47 | sciatic neuropathy | KG + DL |
| 48 | pyruvate dehydrogenase E3 deficiency | KG + DL |
| 49 | obsolete heart block | KG + DL |
| 50 | atrioventricular block (disease) | KG + DL |
(Showing top 50 of 80 predictions)
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.