SE-ATLAS

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