SE-ATLAS

Cerebral malformation with epilepsy Familial temporal lobe epilepsy Landau-Kleffner syndrome Paroxysmal hemicrania Fragile X syndrome Rolandic epilepsy Idiopathic acute transverse myelitis Epilepsy with eyelid myoclonia MERRF Neuromyelitis optica spectrum disorder Juvenile myoclonic epilepsy Autosomal dominant epilepsy with auditory features Sturge-Weber syndrome Rett syndrome Wolf-Hirschhorn syndrome Frontotemporal dementia Acute transverse myelitis Isolated optic neuritis Tuberous sclerosis complex Muscular dystrophy Dravet syndrome Autoimmune encephalitis Hemicrania continua SUNCT syndrome Neurocutaneous syndrome with epilepsy Channelopathy with epilepsy Adult-onset myasthenia gravis Angelman syndrome Primary progressive aphasia Familial or sporadic hemiplegic migraine Epilepsy syndrome Motor neuron disease 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 Nächtliche Frontallappenepilepsie, autosomal-dominante Neuromyelitis-optica-Spektrum-Störung ohne anti-MOG- und ohne anti-AQP4-Antikörper Lafora-Krankheit Neurofibromatose Typ 1 Kortikobasales Syndrom Optikusneuritis mit anti-MOG-Antikörper Optikusneuritis, isolierte, ohne anti-MOG-Antikörper Komplexes regionales Schmerzsyndrom