SE-ATLAS

Action myoclonus-renal failure syndrome Acute encephalopathy with inflammation-mediated status epilepticus Adolescent-onset epilepsy syndrome Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome Benign occipital epilepsy Benign partial infantile seizures CNTNAP2-related developmental and epileptic encephalopathy Cerebral diseases of vascular origin with epilepsy Cerebral malformation with epilepsy Childhood-onset epilepsy syndrome Chromosomal anomaly with epilepsy as a major feature Continuous spikes and waves during sleep Cryptogenic late-onset epileptic spasms DEND syndrome Dravet syndrome Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation Early-onset progressive encephalopathy with migrant continuous myoclonus Epilepsy syndrome Epilepsy with eyelid myoclonia Epilepsy with myoclonic absences Familial infantile myoclonic epilepsy Familial partial epilepsy Febrile infection-related epilepsy syndrome Generalized epilepsy with febrile seizures-plus Idiopathic hemiconvulsion-hemiplegia syndrome Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Infantile epilepsy syndrome Infantile spasms syndrome Infantile spasms-broad thumbs syndrome Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression Infectious disease with epilepsy Inflammatory and autoimmune disease with epilepsy Landau-Kleffner syndrome Lennox-Gastaut syndrome Metabolic diseases with epilepsy Monogenic disease with epilepsy Moynahan syndrome Myoclonic epilepsy in non-progressive encephalopathies Myoclonic epilepsy of infancy Myoclonic-astatic epilepsy Neonatal epilepsy syndrome Neurocutaneous syndrome with epilepsy Oculocerebrocutaneous syndrome PEHO syndrome PEHO-like syndrome Perioral myoclonia with absences Progressive myoclonic epilepsy Progressive myoclonic epilepsy with dystonia Rare epilepsy Reflex epilepsy Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome Rolandic epilepsy-speech dyspraxia syndrome W syndrome