SE-ATLAS

Atypical progressive supranuclear palsy syndrome Autosomal dominant cerebellar ataxia Autosomal dominant cerebellar ataxia type I Autosomal dominant dopa-responsive dystonia Autosomal recessive dopa-responsive dystonia Combined cervical dystonia Combined dystonia Disorder of amino acid and other organic acid metabolism Disorder of phenylalanin or tyrosine metabolism Disorder of tyrosine metabolism Dopa-responsive dystonia Early-onset generalized limb-onset dystonia Focal, segmental or multifocal dystonia Frontotemporal neurodegeneration with movement disorder Generalized isolated dystonia Genetic neurodegenerative disease Genetic neurodegenerative disease with dementia Hereditary ataxia Hereditary episodic ataxia Huntington disease Huntington disease-like syndrome Huntington disease-like syndrome due to C9ORF72 expansions Isolated dystonia Miscellaneous movement disorder due to neurodegenerative disease Multiple system atrophy Multiple system atrophy, parkinsonian type Myoclonus-dystonia syndrome Neurodegenerative disease with dementia Neurometabolic disease Paroxysmal dyskinesia Paroxysmal dystonia Paroxysmal kinesigenic dyskinesia Persistent combined dystonia Primary dystonia, DYT21 type Primary myoclonus Progressive supranuclear palsy Progressive supranuclear palsy-parkinsonism syndrome Psychogenic movement disorders Rapid-onset dystonia-parkinsonism Rare ataxia Rare dementia Rare disorder with dystonia and other neurologic or systemic manifestation Rare dystonia Rare genetic dystonia Rare genetic hyperkinetic movement disorder Rare genetic movement disorder Rare genetic myoclonus Rare genetic neurological disorder Rare genetic parkinsonian disorder Rare hyperkinetic movement disorder Rare inborn errors of metabolism Rare movement disorder Rare neurodegenerative disease Rare neurologic disease with psychiatric involvement Rare parkinsonian disorder Rare parkinsonian syndrome due to genetic neurodegenerative disease Rare paroxysmal movement disorder Spinocerebellar ataxia type 8 Spinocerebellar ataxia with oculomotor anomaly X-linked dystonia-parkinsonism