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 Bewegungsstörung, seltene paroxysmale Progressive supranukleäre Blickparese - Parkinsonismus Phenylalanin/Tyrosin-Stoffwechselstörung Aminosäure/organische Säuren-Stoffwechselstörung Ataxie, hereditäre Dystonie-Parkinsonismus mit rapidem Beginn Neurodegenerative Krankheit mit Demenz, genetisch bedingte Psychogene Bewegungsstörungen Zerebelläre Ataxie, autosomal-dominante Bewegungsstörung, genetisch bedingte, seltene Dystonie, paroxysmale Neurodegenerative Krankheit mit Demenz Dystonie-Parkinson-Syndrom, X-chromosomales Seltenes genetisches Parkinson-Syndrom Chorea Huntington-ähnliches Syndrom durch C9ORF72-Expansionen Seltenes Parkinson-Syndrom bei neurodegenerativer Störung Psychiatrische Krankheit, seltene Seltene genetisch bedingte Dystonie Ataxie, seltene Multisystematrophie vom Typ Parkinson Episodische Ataxie, hereditäre Paroxysmale kinesiogene Dyskinesie Dopa-responsive Dystonie, autosomal-dominante 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