SE-ATLAS

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