Topiramate

DrugBank ID: DB00273

Summary

Metric	Value
Total Predictions	50
KG+DL (Dual Validated)	2
DL Only	48
KG Only	0

Predictions

Indication	Score	Source
trigeminal nerve neoplasm	0.9970	DL
visual epilepsy	0.9928	DL
audiogenic seizures	0.9921	DL
eating seizures	0.9921	DL
micturation-induced seizures	0.9921	DL
orgasm-induced seizures	0.9921	DL
startle epilepsy	0.9921	DL
thinking seizures	0.9921	DL
reading seizures	0.9909	DL
trigeminal neuralgia	0.9892	DL
beta-ketothiolase deficiency	0.9751	DL
status epilepticus	0.9715	DL
Rett syndrome, congenital variant	0.9703	DL
14q12 microdeletion syndrome	0.9687	DL
restless legs syndrome	0.9522	DL
Lennox-Gastaut syndrome	0.9412	KG+DL
partial motor epilepsy	0.9356	DL
adolescent/adult onset autosomal dominant epilepsy with auditory features	0.9327	DL
partial epilepsy	0.9317	DL
febrile infection-related epilepsy syndrome	0.9305	DL
atypical childhood epilepsy with centrotemporal spikes	0.9297	DL
cryptogenic late-onset epileptic spasms	0.9297	DL
photosensitive occipital lobe epilepsy	0.9297	DL
perioral myoclonia with absences	0.9243	DL
guanidinoacetate methyltransferase deficiency	0.9194	DL
epilepsy with generalized tonic-clonic seizures	0.9190	DL
cutis verticis gyrata	0.9125	KG+DL
epilepsy	0.8986	DL
early onset absence epilepsy	0.8060	DL
childhood onset epileptic encephalopathy	0.7847	DL
familial hemiplegic migraine	0.7752	DL
myoclonic-atonic epilepsy	0.7627	DL
benign occipital epilepsy	0.7232	DL
early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation	0.7140	DL
nicotine dependence	0.6836	DL
acute encephalopathy with biphasic seizures and late reduced diffusion	0.6735	DL
electroclinical syndrome	0.6364	DL
macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome	0.6166	DL
obsolete hypertension, diastolic, resistance to	0.5959	DL
myopathy due to calsequestrin and SERCA1 protein overload	0.5852	DL
epidural abscess	0.5780	DL
TBCK-related intellectual disability syndrome	0.5732	DL
3-methylcrotonyl-CoA carboxylase 2 deficiency	0.5683	DL
Birk-Barel syndrome	0.5621	DL
hypermobility syndrome	0.5544	DL
childhood encephalopathy due to thiamine pyrophosphokinase deficiency	0.5534	DL
lissencephaly 6 with microcephaly	0.5521	DL
cerebral palsy spastic monoplegic	0.5504	DL
congenital cystic eye multiple ocular and intracranial anomalies	0.5498	DL
myotonia permanens	0.5495	DL

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Disclaimer
Predictions are for research purposes only and do not constitute medical advice.