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 Classic stiff person syndrome Unclassified autosomal dominant spinocerebellar ataxia Gangliocytoma Diffuse intrinsic pontine glioma Central neurocytoma Ganglioglioma Primary central nervous system lymphoma Atypical teratoid rhabdoid tumor Multifocal motor neuropathy Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy Autosomal recessive cerebelloparenchymal disorder type 3 Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy Muscular dystrophy Hyperkalemic periodic paralysis Progressive supranuclear palsy Primary angiitis of the central nervous system Anaplastic astrocytoma Diffuse astrocytoma Cowden syndrome Pleomorphic xanthoastrocytoma Pilomyxoid astrocytoma Pilocytic astrocytoma Full schwannomatosis Subependymal giant cell astrocytoma Pituicytoma Oligodendroglioma Subependymoma Ependymoma Duchenne and Becker muscular dystrophy Benign schwannoma Angiocentric glioma Neurofibroma Chordoid glioma Astroblastoma Amyotrophic lateral sclerosis CLIPPERS Glial tumor Myotonic dystrophy Susac syndrome Glioblastoma Non-functioning paraganglioma Lambert-Eaton myasthenic syndrome Prolactinoma Meningioma Superficial siderosis Choroid plexus carcinoma Atypical papilloma of choroid plexus Pineoblastoma Li-Fraumeni syndrome Dysembryoplastic neuroepithelial tumor Rosette-forming glioneuronal tumor Malignant peripheral nerve sheath tumor Pituitary adenoma Proximal myotonic myopathy Astrocytoma Multiple system atrophy Medulloblastoma Neurofibromatosis type 1 Full NF2-related schwannomatosis Congenital myotonia Craniopharyngioma