SE-ATLAS

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