SE-ATLAS

Cerebral malformation with epilepsy Familial temporal lobe epilepsy Landau-Kleffner syndrome Paroxysmal hemicrania Fragile X syndrome Idiopathic acute transverse myelitis Epilepsy with eyelid myoclonia MERRF Juvenile myoclonic epilepsy Autosomal dominant epilepsy with auditory features Rolandic epilepsy Neuromyelitis optica spectrum disorder Sturge-Weber syndrome Wolf-Hirschhorn syndrome Acute transverse myelitis Rett syndrome Frontotemporal dementia Isolated optic neuritis Dravet syndrome Hemicrania continua SUNCT syndrome Neurocutaneous syndrome with epilepsy Channelopathy with epilepsy Primary progressive aphasia Tuberous sclerosis complex Autoimmune encephalitis Angelman syndrome Familial or sporadic hemiplegic migraine Epilepsy syndrome Chromosomal anomaly with epilepsy as a major feature Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Monogenic disease with epilepsy Lennox-Gastaut syndrome Metabolic diseases with epilepsy Cerebral diseases of vascular origin with epilepsy Infectious disease with epilepsy Acute transverse myelitis with anti-MOG antibodies Neuromyelitis optica spectrum disorder with anti-MOG antibodies Progressive myoclonic epilepsy Inflammatory and autoimmune disease with epilepsy Neuromyelitis optica spectrum disorder with anti-AQP4 antibodies Autosomal dominant nocturnal frontal lobe epilepsy Neuromyelitis optica spectrum disorder without anti-MOG and without anti-AQP4 antibodies Lafora disease Neurofibromatosis type 1 Corticobasal syndrome Isolated optic neuritis with anti-MOG antibodies Isolated optic neuritis without anti-MOG antibodies Complex regional pain syndrome