SE-ATLAS

Hyperekplexie, hereditäre Stiff-person-Spektrum-Störung Fokales Stiff-Limb-Syndrom Progressive Enzephalomyelitis mit Rigidität und Myoklonus Dystonie, seltene Zerebelläre Ataxie, autosomal-rezessive Fragiles-X assoziiertes Tremor/Ataxie-Syndrom Hereditäre spastische Paraplegie Gangliozytom Pineoblastom Tumor, dysembryoplastischer neuroepithelialer Tumor, glioneuronaler rosettenbildender Nervenscheidentumor, maligner peripherer Hypophysenadenom Astrozytom Multiple Systematrophie Myotonie, kongenitale Li-Fraumeni-Syndrom Myopathie, myotone proximale Medulloblastom Neurofibromatose Typ 1 Schwannomatose, NF2-assoziierte Monogene Krankheit mit Epilepsie Familiäres Epilepsiesyndrom, idiopathisches oder kryptogenes, mit bekanntem Gen/-ort Primäres Lymphom des Zentralnervensystems Limbische Enzephalitis mit assoziierten Antikörpern gegen Zellwandantigene CADASIL Zerebello-parenchymale Krankheit, autosomal-rezessive, Typ 3 Muskeldystrophie Cowden-Syndrom Schwannom, benignes Dravet-Syndrom Glioblastom Superfizielle Siderose Morvan-Syndrom Neurozytom, zentrales Epileptische Syndrome Chromosomenanomalie mit Epilepsie als Hauptmerkmal Myasthenia gravis Epilepsie, seltene Tumor, atypischer teratoider Letale neonatale Spastik-epileptische Enzephalopathie-Syndrom Paralyse, hyperkaliämische periodische Astrozytom Grad 3 Xanthoastrozytom, pleomorphes Pilocytic astrocytoma Subependymal giant cell astrocytoma Oligodendroglioma Subependymoma Angiocentric glioma Unclassified autosomal dominant spinocerebellar ataxia Amyotrophic lateral sclerosis CLIPPERS CDKL5-deficiency disorder Ganglioglioma Posttransplant acute limbic encephalitis Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy NMDA receptor encephalitis Isaacs syndrome Pyridoxal phosphate-responsive seizures Duchenne and Becker muscular dystrophy Neurofibroma Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome Lambert-Eaton myasthenic syndrome Meningioma Non-specific early-onset epileptic encephalopathy Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation Diffuse intrinsic pontine glioma Neuromyelitis optica spectrum disorder Neurocutaneous syndrome with epilepsy Cerebral malformation with epilepsy Hyperekplexia Metabolic diseases with epilepsy Cerebral diseases of vascular origin with epilepsy Inflammatory and autoimmune disease with epilepsy Infectious disease with epilepsy Multifocal motor neuropathy Acute disseminated encephalomyelitis Progressive supranuclear palsy Primary angiitis of the central nervous system Diffuse astrocytoma Continuous spikes and waves during sleep Pilomyxoid astrocytoma Full schwannomatosis Pituicytoma Ependymoma Chordoid glioma Astroblastoma Sarcoidosis Tuberous sclerosis complex Glial tumor Myotonic dystrophy Classic stiff person syndrome Susac syndrome Hypothalamic hamartomas with gelastic seizures Early infantile epileptic encephalopathy KCNQ2-related epileptic encephalopathy Neuromyelitis optica spectrum disorder with anti-MOG antibodies ARX-related epileptic encephalopathy Non-dystrophic myopathy Febrile infection-related epilepsy syndrome Non-functioning paraganglioma Prolactinoma Epileptic encephalopathy with global cerebral demyelination Choroid plexus carcinoma Atypical papilloma of choroid plexus