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 Rare genetic dystonia Rare movement disorder Multiple system atrophy, parkinsonian type Hereditary episodic ataxia Paroxysmale kinesiogene Dyskinesie Dopa-responsive Dystonie, autosomal-dominante Myoklonus, seltener, genetisch bedingter Dystonie, isolierte Dopa-sensitive Dystonie Blepharospasmus-oromandibuläre Dystonie-Syndrom Neuromyelitis-optica-Spektrum-Störung Hereditäre spastische Paraplegie Ataxie, zerebelläre, autosomal-rezessive, degenerative und progressive Enzephalitis, autoimmune Primäre Angiitis des Zentralnervensystems Ataxie, spinozerebelläre, Typ 10 Myasthenia gravis Torticollis, benigner paroxysmaler, des Kindesalters Kortikobasales Syndrom Chronische inflammatorische demyelinisierende Polyneuropathie Tyrosin-Stoffwechselstörung Myoklonus-Dystonie-Syndrom Seltene Form der hyperkinetischen Bewegungsstörung