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 Epilepsie, familiäre partielle Infantile Krampfanfälle - breite Daumen Reflexepilepsie, genetisch-bedingte Jeavons-Syndrom Epilepsie, kryptogenetische, spät beginnende West-Syndrom Epilepsie mit kontinuierlichen Spike-Wave-Entladungen im Schlaf Partialepilepsie, benigne infantile Epilepsie, benigne okzipitale Rolando-Epilepsie-Sprachdyspraxie-Syndrom Epilepsie-Syndrom, neonatales Rolando-Epilepsie - paroxysmal anstrengungsinduzierte Dyskinesie - Schreibkrampf Epilepsie-Syndrom, im Kindesalter beginnend Epilepsie-Syndrom, infantiles Myoklonusepilepsie, progressive Epilepsie-Syndrom, im Erwachsenenalter beginnend Dravet-Syndrom Epileptische Syndrome Lennox-Gastaut-Syndrom Landau-Kleffner-Syndrom Neurokutanes Syndrom mit Epilepsie Monogene Krankheit mit Epilepsie Chromosomenanomalie mit Epilepsie als Hauptmerkmal