Carbamazepine

Basic Information

Item Value
DrugBank ID DB00564
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 58

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 micturation-induced seizures KG + DL
3 audiogenic seizures KG + DL
4 thinking seizures KG + DL
5 orgasm-induced seizures KG + DL
6 startle epilepsy KG + DL
7 eating seizures KG + DL
8 reading seizures KG + DL
9 beta-ketothiolase deficiency KG + DL
10 Rett syndrome, congenital variant KG + DL
11 14q12 microdeletion syndrome KG + DL
12 status epilepticus KG + DL
13 adolescent/adult onset autosomal dominant epilepsy with auditory features KG + DL
14 facial neuralgia KG + DL
15 guanidinoacetate methyltransferase deficiency KG + DL
16 combined hyperactive dysfunction syndrome of the cranial nerves KG + DL
17 glossopharyngeal nerve neoplasm KG + DL
18 vagus nerve disease KG + DL
19 glossopharyngeal nerve paralysis KG + DL
20 trichotillomania KG + DL
21 myoclonic-atonic epilepsy KG + DL
22 Tourette syndrome KG + DL
23 febrile infection-related epilepsy syndrome KG + DL
24 atypical childhood epilepsy with centrotemporal spikes KG + DL
25 photosensitive occipital lobe epilepsy KG + DL
26 cryptogenic late-onset epileptic spasms KG + DL
27 perioral myoclonia with absences KG + DL
28 restless legs syndrome KG + DL
29 electroclinical syndrome KG + DL
30 nicotine dependence KG + DL
31 methemoglobinemia, alpha type KG + DL
32 idiopathic neonatal atrial flutter KG + DL
33 attention deficit-hyperactivity disorder KG + DL
34 early onset absence epilepsy KG + DL
35 methemoglobin reductase deficiency KG + DL
36 myofascial pain syndrome KG + DL
37 asperger syndrome, susceptibility to KG + DL
38 gaze palsy, familial horizontal, with progressive scoliosis KG + DL
39 multifocal atrial tachycardia (disease) KG + DL
40 childhood onset epileptic encephalopathy KG + DL
41 autism susceptibility 1 KG + DL
42 faciodigitogenital syndrome KG + DL
43 methemoglobinemia KG + DL
44 autism spectrum disorder KG + DL
45 attention deficit hyperactivity disorder, inattentive type KG + DL
46 EAST syndrome KG + DL
47 amelocerebrohypohidrotic syndrome KG + DL
48 early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation KG + DL
49 methemoglobinemia due to deficiency of methemoglobin reductase KG + DL
50 specific developmental disorder KG + DL

(Showing top 50 of 58 predictions)

Disclaimer

These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.


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