SE-ATLAS

Early-onset generalized limb-onset dystonia Miscellaneous movement disorder due to neurodegenerative disease Spinocerebellar ataxia with oculomotor anomaly Rare inborn errors of metabolism Frontotemporal neurodegeneration with movement disorder Generalized isolated dystonia Rare genetic hyperkinetic movement disorder Disorder of tyrosine metabolism Paroxysmal dyskinesia Persistent combined dystonia Combined dystonia Autosomal recessive dopa-responsive dystonia Neurometabolic disease Myoclonus-dystonia syndrome Atypical progressive supranuclear palsy syndrome Rare dystonia Huntington disease Primary dystonia, DYT21 type Rare genetic neurological disorder Rare neurodegenerative disease Huntington disease-like syndrome Rare disorder with dystonia and other neurologic or systemic manifestation Autosomal dominant cerebellar ataxia type I Combined cervical dystonia Spinocerebellar ataxia type 8 Focal, segmental or multifocal dystonia Genetic neurodegenerative disease Rare dementia Rare paroxysmal movement disorder Progressive supranuclear palsy-parkinsonism syndrome Disorder of phenylalanin or tyrosine metabolism Disorder of amino acid and other organic acid metabolism Hereditary ataxia Rapid-onset dystonia-parkinsonism Genetic neurodegenerative disease with dementia Psychogenic movement disorders Autosomal dominant cerebellar ataxia Rare genetic movement disorder Paroxysmal dystonia Neurodegenerative disease with dementia X-linked dystonia-parkinsonism Rare genetic parkinsonian disorder Huntington disease-like syndrome due to C9ORF72 expansions Rare parkinsonian syndrome due to genetic neurodegenerative disease Rare neurologic disease with psychiatric involvement Rare genetic dystonia Rare ataxia Multiple system atrophy, parkinsonian type Hereditary episodic ataxia Paroxysmal kinesigenic dyskinesia Autosomal dominant dopa-responsive dystonia Rare genetic myoclonus Isolated dystonia Rare hyperkinetic movement disorder Dopa-responsive dystonia Progressive supranuclear palsy Rare parkinsonian disorder Primary myoclonus Multiple system atrophy Rare movement disorder Blepharospasm-oromandibular dystonia syndrome Neuromyelitis optica spectrum disorder Hereditary spastic paraplegia Autosomal recessive degenerative and progressive cerebellar ataxia Autoimmune encephalitis Primary angiitis of the central nervous system Spinocerebellar ataxia type 10 Myasthenia gravis Benign paroxysmal torticollis of infancy Corticobasal syndrome Chronic inflammatory demyelinating polyneuropathy