SE-ATLAS

Progressive encephalomyelitis with rigidity and myoclonus Focal stiff limb syndrome Hereditary hyperekplexia Stiff person spectrum disorder Rare dystonia Autosomal recessive cerebellar ataxia Fragile X-associated tremor/ataxia syndrome Classic stiff person syndrome Hereditary spastic paraplegia Primary central nervous system lymphoma Primary angiitis of the central nervous system Anaplastic astrocytoma Diffuse astrocytoma Cowden syndrome Multifocal motor neuropathy Autosomal recessive cerebelloparenchymal disorder type 3 Muscular dystrophy Diffuse intrinsic pontine glioma Pleomorphic xanthoastrocytoma Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy Pilomyxoid astrocytoma Atypical teratoid rhabdoid tumor Gangliocytoma Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy Central neurocytoma Hyperkalemic periodic paralysis Progressive supranuclear palsy Ganglioglioma Subependymal giant cell astrocytoma Oligodendroglioma Glioblastoma Subependymoma Ependymoma Choroid plexus carcinoma CLIPPERS Angiocentric glioma Prolactinoma Chordoid glioma Astroblastoma Amyotrophic lateral sclerosis Glial tumor Myotonic dystrophy Pilocytic astrocytoma Lambert-Eaton myasthenic syndrome Full schwannomatosis Atypical papilloma of choroid plexus Duchenne and Becker muscular dystrophy Superficial siderosis Pituicytoma Susac syndrome Non-functioning paraganglioma Benign schwannoma Dysembryoplastic neuroepithelial tumor Craniopharyngioma Rosette-forming glioneuronal tumor Pineoblastoma Malignant peripheral nerve sheath tumor Pituitary adenoma Proximal myotonic myopathy Multiple system atrophy Neurofibromatosis type 1 Full NF2-related schwannomatosis Congenital myotonia Li-Fraumeni syndrome Astrocytoma Medulloblastoma Monogenic disease with epilepsy Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Non-dystrophic myopathy Neuromyelitis optica spectrum disorder Hyperekplexia Metabolic diseases with epilepsy Cerebral diseases of vascular origin with epilepsy Neurofibroma Unclassified autosomal dominant spinocerebellar ataxia Sarcoidosis Meningioma Neuromyelitis optica spectrum disorder with anti-MOG antibodies Morvan syndrome Tuberous sclerosis complex Dravet syndrome CDKL5-deficiency disorder Limbic encephalitis associated with antibodies to cell membrane antigens Epilepsy syndrome ARX-related epileptic encephalopathy Neurocutaneous syndrome with epilepsy Chromosomal anomaly with epilepsy as a major feature Cerebral malformation with epilepsy Myasthenia gravis Posttransplant acute limbic encephalitis Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome Inflammatory and autoimmune disease with epilepsy Infectious disease with epilepsy Rare epilepsy Febrile infection-related epilepsy syndrome Hypothalamic hamartomas with gelastic seizures Lethal neonatal spasticity-epileptic encephalopathy syndrome Acute disseminated encephalomyelitis Early infantile epileptic encephalopathy NMDA receptor encephalitis Isaacs syndrome KCNQ2-related epileptic encephalopathy Epileptic encephalopathy with global cerebral demyelination Non-specific early-onset epileptic encephalopathy Continuous spikes and waves during sleep Frühinfantile epileptische Enzephalopathie und Intelligenzminderung durch GRIN2A-Genmutation Pyridoxalphosphat-abhängige Epilepsie