SE-ATLAS

Action myoclonus-renal failure syndrome Acute encephalopathy with biphasic seizures and late reduced diffusion Acute encephalopathy with inflammation-mediated status epilepticus Adolescent-onset epilepsy syndrome Adult neuronal ceroid lipofuscinosis Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome Audiogenic seizures Autosomal dominant epilepsy with auditory features Autosomal dominant nocturnal frontal lobe epilepsy Benign familial infantile epilepsy Benign familial mesial temporal lobe epilepsy Benign familial neonatal epilepsy Benign familial neonatal-infantile seizures CLN1 disease CLN10 disease CLN11 disease CLN13 disease CLN2 disease CLN4A disease CLN4B disease CLN5 disease CLN6 disease CLN7 disease CLN8 disease CLN9 disease CNTNAP2-related developmental and epileptic encephalopathy Cerebral diseases of vascular origin with epilepsy Childhood absence epilepsy Childhood-onset epilepsy syndrome Congenital neuronal ceroid lipofuscinosis DEND syndrome Dravet syndrome Early infantile epileptic encephalopathy Early-onset Lafora body disease Eating reflex epilepsy Epilepsy syndrome Familial encephalopathy with neuroserpin inclusion bodies Familial focal epilepsy with variable foci Familial infantile myoclonic epilepsy Familial mesial temporal lobe epilepsy with febrile seizures Familial partial epilepsy Familial temporal lobe epilepsy Febrile infection-related epilepsy syndrome Focal epilepsy-intellectual disability-cerebro-cerebellar malformation Generalized epilepsy with febrile seizures-plus Generalized epilepsy-paroxysmal dyskinesia syndrome Hot water reflex epilepsy Idiopathic hemiconvulsion-hemiplegia syndrome Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Infantile epilepsy syndrome Infantile neuronal ceroid lipofuscinosis Infantile spasms syndrome Infantile spasms-broad thumbs syndrome Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression Juvenile absence epilepsy Juvenile myoclonic epilepsy Juvenile neuronal ceroid lipofuscinosis Lafora disease Late infantile neuronal ceroid lipofuscinosis Limbic encephalitis with LGI1 antibodies MERRF Malignant migrating focal seizures of infancy Mesial temporal lobe epilepsy with hippocampal sclerosis Micturation-induced seizures Moynahan syndrome NMDA receptor encephalitis Neonatal epilepsy syndrome Neurocutaneous syndrome with epilepsy New-onset refractory status epilepticus OBSOLETE: CLN3 disease Oculocerebrocutaneous syndrome Orgasm-induced seizures PEHO syndrome PEHO-like syndrome Photosensitive epilepsy Progressive epilepsy-intellectual disability syndrome, Finnish type Progressive myoclonic epilepsy Progressive myoclonic epilepsy type 1 Progressive myoclonic epilepsy type 3 Progressive myoclonic epilepsy type 5 Progressive myoclonic epilepsy type 6 Progressive myoclonic epilepsy with dystonia Rare epilepsy Reading seizures Reflex epilepsy Rolandic epilepsy Severe neonatal-onset encephalopathy with microcephaly Startle epilepsy Sturge-Weber syndrome Thinking seizures W syndrome