SE-ATLAS

Rare inborn errors of metabolism Frontotemporal neurodegeneration with movement disorder Early-onset generalized limb-onset dystonia Miscellaneous movement disorder due to neurodegenerative disease Spinocerebellar ataxia with oculomotor anomaly Rare dystonia Huntington disease Generalized isolated dystonia Rare genetic hyperkinetic movement disorder Paroxysmal dyskinesia Persistent combined dystonia Combined dystonia Autosomal recessive dopa-responsive dystonia Neurometabolic disease Atypical progressive supranuclear palsy syndrome Primary dystonia, DYT21 type Rare genetic neurological disorder Rare neurodegenerative disease Rare disorder with dystonia and other neurologic or systemic manifestation Neurodegenerative disease with dementia Rare ataxia Progressive supranuclear palsy Rare parkinsonian disorder Huntington disease-like syndrome Primary myoclonus 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 Autosomal dominant cerebellar ataxia Rare genetic movement disorder Paroxysmal dystonia Multiple system atrophy 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 Dystonie génétique rare Anomalie rare du mouvement Atrophie multisystématisée type parkinsonien Ataxie épisodique héréditaire Dyskinésie paroxystique kinésigénique Dystonie dopa-sensible autosomique dominante Myoclonie génétique rare Dystonie isolée Dystonie dopa-sensible Syndrome de Meige Neuromyélite optique Paraplégie spastique héréditaire Ataxie cérébelleuse dégénérative et progressive autosomique récessive Encéphalite auto-immune Angéite primaire du système nerveux central Ataxie spinocérébelleuse type 10 Myasthénie auto-immune Torticolis paroxystique bénin de l'enfant Syndrome corticobasal Polyradiculonévrite inflammatoire démyélinisante chronique Trouble du métabolisme de la tyrosine Dystonie myoclonique héréditaire Trouble du mouvement hyperkinétique rare