SE-ATLAS

Neuroferritinopathy Infantile dystonia-parkinsonism Rare genetic tremor disorder Machado-Joseph disease type 1 Spinocerebellar ataxia type 28 Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome Spinocerebellar ataxia type 23 Hereditary geniospasm Spinocerebellar ataxia type 25 Spinocerebellar ataxia type 20 Spinocerebellar ataxia type 34 X-linked spinocerebellar ataxia type 4 Dystonia-aphonia syndrome Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency Pantothenate kinase-associated neurodegeneration Spinocerebellar ataxia type 26 Benign paroxysmal torticollis of infancy Multiple system atrophy, parkinsonian type Rapid-onset dystonia-parkinsonism Huntington disease-like 2 Machado-Joseph disease type 2 Progressive supranuclear palsy-corticobasal syndrome X-linked spinocerebellar ataxia type 3 Adult-onset autosomal recessive cerebellar ataxia X-linked non progressive cerebellar ataxia Woodhouse-Sakati syndrome Huntington disease-like syndrome Machado-Joseph disease type 3 Primary dystonia, DYT4 type Primary orthostatic tremor Primary dystonia, DYT13 type Progressive myoclonic epilepsy type 6 Primary dystonia, DYT6 type Paroxysmal kinesigenic dyskinesia Dravet syndrome Autosomal dominant dopa-responsive dystonia Paroxysmal exertion-induced dyskinesia Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency Paroxysmal non-kinesigenic dyskinesia Benign hereditary chorea Neuroacanthocytosis Joubert syndrome PANDAS Autosomal recessive cerebellar ataxia with late-onset spasticity Infantile convulsions and choreoathetosis Paroxysmal dyskinesia Choreoacanthocytosis Benign adult familial myoclonic epilepsy Myoclonus-dystonia syndrome Ataxia-telangiectasia variant X-linked sideroblastic anemia and spinocerebellar ataxia Brain dopamine-serotonin vesicular transport disease Sensorineural hearing loss-early graying-essential tremor syndrome Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome Tremor-nystagmus-duodenal ulcer syndrome Ataxia-oculomotor apraxia type 1 Autosomal dominant focal dystonia, DYT25 type 3-methylglutaconic aciduria type 3 Autosomal recessive cerebelloparenchymal disorder type 3 Primary dystonia, DYT17 type Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Rare disorder with dystonia and other neurologic or systemic manifestation Autosomal recessive cerebellar ataxia Dopa-responsive dystonia due to sepiapterin reductase deficiency X-linked cerebellar ataxia Cerebellar ataxia-ectodermal dysplasia syndrome X-linked progressive cerebellar ataxia Joubert syndrome with ocular defect Intellectual disability-hyperkinetic movement-truncal ataxia syndrome Adult-onset dystonia-parkinsonism Autosomal recessive dopa-responsive dystonia Early-onset cerebellar ataxia with retained tendon reflexes Wilson disease Rare genetic dystonia Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome Joubert syndrome with renal defect Autosomal-rezessive spinozerebelläre Ataxie mit Beginn in der Kindheit, langsam fortschreitend Zerebelläre Ataxie durch GRID2-Mangel, autosomal-rezessive kongenitale Dystonie, paroxysmale Zervikale Dystonie, kombinierte Joubert-Syndrom mit hepatischem Defekt Dystonie, primäre, Typ DYT2 Ataxie, autosomal-rezessive, durch Ubiquinon-Mangel Fokale, segmentale oder multifokale Dystonie X-chromosomale Intelligenzminderung-Ataxie-Apraxie-Syndrom Chorea Huntington-ähnliches Syndrom durch C9ORF72-Expansionen Ataxie, infantile spinozerebelläre Friedreich-Ataxie Autosomal-rezessive zerebelläre Ataxie-Bewegungsstörungen-Syndrom Letale Ataxie mit Schwerhörigkeit und Optikusatrophie Ataxie mit Vitamin E-Mangel Autosomal-rezessive spinozerebelläre Ataxie-Blindheit-Schwerhörigkeit-Syndrom Ataxie, spinozerebelläre, Typ 37 Autosomal-rezessive zerebelläre Ataxie, infantile, nicht-progressive Ataxie-Schwerhörigkeit-Intelligenzminderung-Syndrom Autosomal-rezessive zerebelläre Ataxie-Epilepsie-Intelligenzminderung-Syndrom durch TUD-Mangel Zerebelläre Ataxie, autosomal-dominante Ataxie, zerebelläre, autosomal-dominante, Typ II Zerebelläre Ataxie, autosomal-rezessive, Spectrin-assoziierte Fragiles-X assoziiertes Tremor/Ataxie-Syndrom Ataxia-Teleangiectasia Tremorkrankheit, seltene Atrophie, dentatorubrale-pallidolysiale Multiple Systematrophie Seltene Bewegungsstörung mit Chorea Spinozerebelläre Ataxie mit axonaler Neuropathie Typ 2 Ataxie, spinozerebelläre, Typ 29 Autosomal-rezessive zerebelläre Ataxie-Epilepsie-Intelligenzminderung-Syndrom durch RUBCN-Mangel Hinterstrangataxie - Retinitis pigmentosa McLeod Neuro-Akanthozytose-Syndrom Ataxia-Teleangiectasia-ähnliche Krankheit Zirrhose-Dystonie-Polyzythämie-Hypermanganämie-Syndrom Neurodegenerative Krankheit mit Chorea Joubert-Syndrom und verwandte Krankheiten Dystonie 16 Paroxysmale dystonische Choreoathetose mit episodischer Ataxie und Spastik Dopa-sensitive Dystonie Sydenham-Chorea Früh beginnende generalisierte Dystonie der Extremitäten Dystonie, oromandibuläre Postinfectious autoimmune disease with chorea Autosomal recessive ataxia due to PEX10 deficiency Non-progressive cerebellar ataxia with intellectual disability Isolated dystonia Autosomal recessive ataxia, Beauce type Huntington disease Blepharospasm-oromandibular dystonia syndrome Persistent combined dystonia Dysequilibrium syndrome Primary dystonia, DYT21 type Mohr-Tranebjaerg syndrome Spinocerebellar ataxia type 32 Brain-lung-thyroid syndrome Huntington disease-like 1 Developmental malformations-deafness-dystonia syndrome CAMOS syndrome Joubert syndrome with oculorenal defect Hemidystonia-hemiatrophy syndrome Joubert syndrome with Jeune asphyxiating thoracic dystrophy Combined dystonia Huntington disease-like 3 Classic pantothenate kinase-associated neurodegeneration Progressive myoclonic epilepsy type 5 Spinocerebellar ataxia type 35 Generalized isolated dystonia Progressive myoclonic epilepsy type 3 Spinocerebellar ataxia type 2 Frontotemporal dementia Spinocerebellar ataxia type 1 Spinocerebellar ataxia type 6 Spinocerebellar ataxia type 36 Spinocerebellar ataxia type 31 Spinocerebellar ataxia type 3 Spinocerebellar ataxia type 8 Atypical pantothenate kinase-associated neurodegeneration Spinocerebellar ataxia type 17 Multiple system atrophy, cerebellar type Marinesco-Sjögren syndrome Cerebellar ataxia, Cayman type Recessive mitochondrial ataxia syndrome Spinocerebellar ataxia type 12 Spinocerebellar ataxia with axonal neuropathy type 1 Spinocerebellar ataxia type 10 Juvenile Huntington disease Spinocerebellar ataxia type 4 Spinocerebellar ataxia type 14 Spinocerebellar ataxia type 27 Spinocerebellar ataxia type 11 Spinocerebellar ataxia type 5 Spinocerebellar ataxia type 30 Spinocerebellar ataxia type 15/16 X-linked dystonia-parkinsonism Spinocerebellar ataxia type 13 Spinocerebellar ataxia type 18 Spinocerebellar ataxia type 21 Spinocerebellar ataxia type 19/22 Orofaciodigital syndrome type 6 Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome Autosomal recessive congenital cerebellar ataxia Autosomal recessive degenerative and progressive cerebellar ataxia Rare dystonia Autosomal recessive metabolic cerebellar ataxia Autosomal recessive cerebellar ataxia due to a DNA repair defect Juvenile myoclonic epilepsy Autosomal recessive syndromic cerebellar ataxia Christianson syndrome Autosomal recessive cerebellar ataxia-psychomotor delay syndrome Autosomal dominant cerebellar ataxia type I Autosomal dominant cerebellar ataxia type IV Infantile epileptic-dyskinetic encephalopathy Spinocerebellar ataxia type 7 Autosomal dominant cerebellar ataxia type III