SE-ATLAS

15q13.3 microdeletion syndrome 1p36 deletion syndrome Action myoclonus-renal failure syndrome Acute encephalopathy with inflammation-mediated status epilepticus Adolescent-onset epilepsy syndrome Angelman syndrome Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome Benign adult familial myoclonic epilepsy Benign familial neonatal epilepsy Benign focal seizures of adolescence Benign idiopathic neonatal seizures Benign occipital epilepsy Benign partial infantile seizures CNTNAP2-related developmental and epileptic encephalopathy Central nervous system malformation 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 infantile epileptic encephalopathy Early myoclonic encephalopathy 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 Epilepsy-telangiectasia syndrome Epileptic encephalopathy with global cerebral demyelination Familial acute necrotizing encephalopathy Familial congenital mirror movements Familial infantile myoclonic epilepsy Familial partial epilepsy Febrile infection-related epilepsy syndrome Fragile X syndrome Generalized epilepsy with febrile seizures-plus Hyperekplexia 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 Inflammatory and autoimmune disease with epilepsy Inherited congenital spastic tetraplegia Kleefstra syndrome due to 9q34 microdeletion Landau-Kleffner syndrome Lennox-Gastaut syndrome Malignant migrating focal seizures of infancy Metabolic diseases with epilepsy Miller-Dieker syndrome Miscellaneous movement disorder due to neurodegenerative disease Motor stereotypies Moynahan syndrome Myoclonic epilepsy in non-progressive encephalopathies Myoclonic epilepsy of infancy Myoclonic-astatic epilepsy Neonatal epilepsy syndrome Neurocutaneous syndrome with epilepsy Neuroleptic malignant syndrome Neuromuscular disease New-onset refractory status epilepticus Non-specific early-onset epileptic encephalopathy Oculocerebrocutaneous syndrome PEHO syndrome PEHO-like syndrome Perioral myoclonia with absences Progressive myoclonic epilepsy Progressive myoclonic epilepsy with dystonia Psychogenic movement disorders Rare choreic movement disorder Rare dystonia Rare epilepsy Rare movement disorder Rare myoclonus Rare neuroinflammatory or neuroimmunological disease Rare parkinsonian disorder Rare paroxysmal movement disorder Reflex epilepsy Ring chromosome 14 syndrome Ring chromosome 20 syndrome Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome Rolandic epilepsy-speech dyspraxia syndrome Severe neonatal-onset encephalopathy with microcephaly Tetrasomy 12p W syndrome Wolf-Hirschhorn syndrome