A genetic resource for genes and mutations related to epilepsy
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Browse by epileptic phenotype
Epileptic encephalopathy (EE)
Ohtahara syndrome
West syndrome
Dravet syndrome (SMEI)
Lennox-Gastaut syndrome (LGS)
Landau-Kleffner syndrome (LKS)
X-linked infantile spasms (ISSX)
Encephalopathy with early epilepsy
Early-onset epileptic encephalopathy (EOEE)
Early infantile epileptic encephalopathy (EIEE)
Malignant migrating partial seizures of infancy (MMPSI)
Electrical status epilepticus of slow-wave sleep (ESES)
Continuous spike and waves during slow sleep (CSWS)
Benign epilepsy
Benign epilepsy with centrotemporal spikes (BECTS, rolandic epilepsy)
Benign familial infantile epilepsy (BFIE)
Benign familial neonatal convulsions (BFNC)
Benign familial neonatal-infantile seizures (BFNIS)
Benign infantile epilepsy (BIE)
Benign neonatal epilepsy (BNE)
Benign neonatal-infantile seizures (BNIS)
Progressive myoclonic epilepsy (PME)
Progressive myoclonic epilepsy of Unverricht-Lundborg type (EPM1)
Progressive myoclonic epilepsy of Lafora type (EPM2, Lafora disease)
Progressive myoclonic epilepsy(PME)
Autosomal dominant epilepsy
Autosomal dominant lateral temporal epilepsy (ADLTE)
Autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE)
Autosomal dominant partial epilepsy with auditory features (ADPEAF)
Autosomal dominant cortical myoclonic and epilepsy (ADCME)
Borderline epilepsy
Borderline GEFS+
Borderline SMEI (SMEB)
SMEI-borderland-spike wave (SMEB-SW)
SMEI-borderland more than one feature (SMEB-O)
SMEI-borderland-myoclonic seizures (SMEB-M)
Generalized epilepsy
Generalized epilepsy with febrile seizures plus (GEFS+)
Generalized epilepsy with febrile seizures plus 2 (GEFS2+)
Generalized tonic-clonic seizures (GTCS)
Idiopathic generalized epilepsy (IGE)
Childhood absence epilepsy (CAE)
Juvenile absence epilepsy (JAE)
Juvenile myoclonic epilepsy(JME)
Partial epilepsy
Familial focal epilepsy with variable foci (FFEVF)
Partial epilepsy with febrile seizures plus (PEFS+)
Complex partial epilepsy (CPE)
Atypical benign partial epilepsy (ABPE)
Cryptogenic focal epilepsy (CFE)
Focal epilepsy (FE)
Myoclonic epilepsy with ragged-red fibers (MERRF)
Myoclonic epilepsy with ragged-red fibers (MERRF)
Myoclonic epilepsy with ragged-red fibers/Mitochondrial Encephalomyopathy overlap syndrome (MERRF/MELAS overlap syndrome)
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Data content
Chromosome
Mutation type
CNV
Gender
Age of onset
Inheritance
Copyright© 2014, EpilepsyGene Team | All rights researved
Last updated: Jul 6, 2014
Browse by epileptic phenotype