Lamotrigine
DrugBank ID: DB00555
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 2 |
| DL Only | 48 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| trigeminal nerve neoplasm | 0.9997 | DL |
| trigeminal neuralgia | 0.9989 | DL |
| visual epilepsy | 0.9954 | DL |
| audiogenic seizures | 0.9938 | DL |
| eating seizures | 0.9938 | DL |
| micturation-induced seizures | 0.9938 | DL |
| orgasm-induced seizures | 0.9938 | DL |
| startle epilepsy | 0.9938 | DL |
| thinking seizures | 0.9938 | DL |
| reading seizures | 0.9930 | DL |
| restless legs syndrome | 0.9890 | DL |
| beta-ketothiolase deficiency | 0.9879 | DL |
| status epilepticus | 0.9861 | DL |
| Rett syndrome, congenital variant | 0.9851 | DL |
| 14q12 microdeletion syndrome | 0.9841 | DL |
| partial epilepsy | 0.9797 | DL |
| adolescent/adult onset autosomal dominant epilepsy with auditory features | 0.9762 | DL |
| epilepsy with generalized tonic-clonic seizures | 0.9757 | DL |
| Lennox-Gastaut syndrome | 0.9744 | KG+DL |
| guanidinoacetate methyltransferase deficiency | 0.9725 | DL |
| atypical childhood epilepsy with centrotemporal spikes | 0.9671 | DL |
| cryptogenic late-onset epileptic spasms | 0.9671 | DL |
| photosensitive occipital lobe epilepsy | 0.9671 | DL |
| febrile infection-related epilepsy syndrome | 0.9670 | DL |
| perioral myoclonia with absences | 0.9636 | DL |
| partial motor epilepsy | 0.9609 | DL |
| cutis verticis gyrata | 0.9457 | KG+DL |
| epilepsy | 0.9333 | DL |
| facial neuralgia | 0.9151 | DL |
| combined hyperactive dysfunction syndrome of the cranial nerves | 0.9088 | DL |
| childhood onset epileptic encephalopathy | 0.9045 | DL |
| early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation | 0.8917 | DL |
| benign occipital epilepsy | 0.8890 | DL |
| myoclonic-atonic epilepsy | 0.8775 | DL |
| electroclinical syndrome | 0.8359 | DL |
| familial hemiplegic migraine | 0.8291 | DL |
| polymicrogyria with optic nerve hypoplasia | 0.8249 | DL |
| glossopharyngeal motor neuropathy | 0.8228 | DL |
| intellectual disability-hypotonia-spasticity-sleep disorder syndrome | 0.8104 | DL |
| PSAT deficiency | 0.8046 | DL |
| early onset absence epilepsy | 0.8032 | DL |
| SATB2 associated disorder | 0.7947 | DL |
| serine biosynthesis pathway deficiency, infantile/juvenile form | 0.7923 | DL |
| acne (disease) | 0.7897 | DL |
| Cantu sanchez-corona fragoso syndrome | 0.7891 | DL |
| Cartwright Nelson Fryns syndrome | 0.7891 | DL |
| Davis Lafer syndrome | 0.7891 | DL |
| intellectual disability-hypotonia-skin hyperpigmentation syndrome | 0.7891 | DL |
| intellectual disability-microcephaly-phalangeal-facial abnormalities syndrome | 0.7891 | DL |
| shoulder and girdle defects-familial intellectual disability syndrome | 0.7891 | DL |
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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.