SE-ATLAS

Hereditary hyperekplexia Stiff person spectrum disorder Focal stiff limb syndrome Progressive encephalomyelitis with rigidity and myoclonus Rare dystonia Autosomal recessive cerebellar ataxia Fragile X-associated tremor/ataxia syndrome Hereditary spastic paraplegia Gangliocytoma Pineoblastoma Dysembryoplastic neuroepithelial tumor Rosette-forming glioneuronal tumor Malignant peripheral nerve sheath tumor Pituitary adenoma Astrocytoma Multiple system atrophy Congenital myotonia Li-Fraumeni syndrome Proximal myotonic myopathy Medulloblastoma Neurofibromatosis type 1 Full NF2-related schwannomatosis Monogenic disease with epilepsy Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Primary central nervous system lymphoma Limbic encephalitis associated with antibodies to cell membrane antigens Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy Autosomal recessive cerebelloparenchymal disorder type 3 Muscular dystrophy Cowden syndrome Benign schwannoma Dravet syndrome Glioblastoma Superficial siderosis Morvan syndrome Central neurocytoma Epilepsy syndrome Chromosomal anomaly with epilepsy as a major feature Myasthenia gravis Rare epilepsy Atypical teratoid rhabdoid tumor Lethal neonatal spasticity-epileptic encephalopathy syndrome Hyperkalemic periodic paralysis Anaplastic astrocytoma Pleomorphic xanthoastrocytoma 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 Frühinfantile entwicklungsbedingte und epileptische Enzephalopathie KCNQ2-assoziierte entwicklungsbedingte und epileptische Enzephalopathie Neuromyelitis-optica-Spektrum-Störung mit anti-MOG-Antikörper Enzephalopathie, epileptische, ARX-assoziierte Myopathie, nichtdystrophe Fieber-assoziierte Enzephalopathie mit refraktären Anfällen Paragangliom, nicht-funktionelles Prolaktinom Epileptische Enzephalopathie mit globaler zerebraler Demyelinisierung Choroid-Plexuskarzinom Choroidplexuspapillom, atypisches