SE-ATLAS

Acute disseminated encephalomyelitis Amyotrophic lateral sclerosis Anoctamin-5-related limb-girdle muscular dystrophy R12 Autosomal dominant cerebellar ataxia Autosomal dominant progressive external ophthalmoplegia Autosomal recessive axonal neuropathy with neuromyotonia Autosomal recessive limb-girdle muscular dystrophy Autosomal recessive progressive external ophthalmoplegia Becker muscular dystrophy Behçet disease Blepharospasm-oromandibular dystonia syndrome CLIPPERS Calpain-3-related limb-girdle muscular dystrophy R1 Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy Cerebral sinovenous thrombosis Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy Chronic inflammatory demyelinating polyneuropathy Classic stiff person syndrome Corticobasal syndrome Dermatomyositis Distal myopathy Dopa-responsive dystonia Duchenne muscular dystrophy FKRP-related limb-girdle muscular dystrophy R9 Fabry disease Facioscapulohumeral dystrophy Familial Mediterranean fever Focal stiff limb syndrome Fragile X-associated tremor/ataxia syndrome Giant cell arteritis Glial tumor Glioblastoma Glycogen storage disease due to acid maltase deficiency Guillain-Barré syndrome Hereditary ATTR amyloidosis Hereditary hyperekplexia Hereditary neuropathy with liability to pressure palsies Hereditary spastic paraplegia Herpes simplex virus encephalitis Huntington disease Hyperkalemic periodic paralysis Hypokalemic periodic paralysis Idiopathic intracranial hypertension Immune-mediated necrotizing myopathy Inclusion body myositis Isolated dystonia Kennedy disease Lambert-Eaton myasthenic syndrome Late-onset distal myopathy, Markesbery-Griggs type Leber hereditary optic neuropathy Leukodystrophy Limb-girdle muscular dystrophy Limbic encephalitis Limbic encephalitis with LGI1 antibodies Limbic encephalitis with caspr2 antibodies Lyme disease MELAS Malignant hyperthermia of anesthesia Marfan syndrome Meningioma Meningococcal meningitis Mitochondrial DNA-related progressive external ophthalmoplegia Moyamoya disease Multifocal motor neuropathy Multiple system atrophy, cerebellar type Multiple system atrophy, parkinsonian type Muscular dystrophy Myasthenia gravis Myofibrillar myopathy NMDA receptor encephalitis Neuralgic amyotrophy Neuromyelitis optica spectrum disorder Paramyotonia congenita of Von Eulenburg Persistent idiopathic facial pain Primary angiitis of the central nervous system Primary lateral sclerosis Progressive encephalomyelitis with rigidity and myoclonus Progressive muscular atrophy Progressive supranuclear palsy Proximal myotonic myopathy Proximal spinal muscular atrophy type 2 Proximal spinal muscular atrophy type 3 Rare dystonia Reversible cerebral vasoconstriction syndrome SUNCT syndrome Sporadic Creutzfeldt-Jakob disease Steinert myotonic dystrophy Stiff person spectrum disorder Susac syndrome Thomsen and Becker disease Trigeminal neuralgia Tuberculous meningitis Wilson disease