SE-ATLAS

3-Methylglutaconazidurie Typ 3 Adult-onset dystonia-parkinsonism Ataxia with vitamin E deficiency Ataxia-Teleangiectasia Variante Ataxia-deafness-intellectual disability syndrome Ataxia-telangiectasia Ataxia-telangiectasia-like disorder Ataxie mit okulomotorischer Apraxie Typ 1 Ataxie, spinozerebelläre X-chromosomale, Typ 3 Ataxie, spinozerebelläre X-chromosomale, Typ 4 Ataxie, spinozerebelläre, Typ 20 Ataxie, spinozerebelläre, Typ 23 Ataxie, spinozerebelläre, Typ 25 Ataxie, spinozerebelläre, Typ 26 Ataxie, spinozerebelläre, Typ 28 Ataxie, spinozerebelläre, Typ 34 Ataxie, zerebelläre, nicht-progressive, X-chromosomale Atypical pantothenate kinase-associated neurodegeneration Autosomal dominant cerebellar ataxia Autosomal dominant cerebellar ataxia type I Autosomal dominant cerebellar ataxia type II Autosomal dominant cerebellar ataxia type III Autosomal dominant cerebellar ataxia type IV Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome Autosomal recessive ataxia due to PEX10 deficiency Autosomal recessive ataxia due to ubiquinone deficiency Autosomal recessive ataxia, Beauce type Autosomal recessive cerebellar ataxia due to a DNA repair defect Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency Autosomal recessive cerebellar ataxia-movement disorder syndrome Autosomal recessive cerebellar ataxia-psychomotor delay syndrome Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome Autosomal recessive congenital cerebellar ataxia Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency Autosomal recessive degenerative and progressive cerebellar ataxia Autosomal recessive dopa-responsive dystonia Autosomal recessive metabolic cerebellar ataxia Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome Autosomal recessive syndromic cerebellar ataxia Autosomal-rezessive kongenitale zerebelläre Ataxie durch MGLUR1-Mangel Autosomal-rezessive zerebelläre Ataxie - Epilepsie - Intelligenzminderung Autosomal-rezessive zerebelläre Ataxie mit Beginn im Erwachsenenalter Autosomal-rezessive zerebelläre Ataxie-Epilepsie-Intelligenzminderung-Syndrom Blepharospasm-oromandibular dystonia syndrome Brain-lung-thyroid syndrome CAMOS syndrome Cerebellar ataxia, Cayman type Cerebellar ataxia-ectodermal dysplasia syndrome Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia Chorea Huntington-ähnliche Krankheit 2 Chorea Huntington-ähnliches Syndrom Chorea, benigne hereditäre Choreoakanthozytose Christianson syndrome Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome Classic pantothenate kinase-associated neurodegeneration Combined cervical dystonia Combined dystonia Dentatorubral pallidoluysian atrophy Developmental malformations-deafness-dystonia syndrome Dopa-responsive Dystonie durch Sepiapterin-Reduktase-Mangel Dopa-responsive Dystonie, autosomal-dominante Dopa-responsive dystonia Dravet-Syndrom Dysequilibrium syndrome Dyskinesie, paroxysmale Dystonia 16 Dystonia-Aphonie-Syndrom Dystonie, fokale, autosomal-dominante, Typ DYT25 Dystonie, primäre, Typ DYT13 Dystonie, primäre, Typ DYT17 Dystonie, primäre, Typ DYT4 Dystonie, primäre, Typ DYT6 Dystonie-Parkinsonismus mit rapidem Beginn Early-onset cerebellar ataxia with retained tendon reflexes Early-onset generalized limb-onset dystonia Focal, segmental or multifocal dystonia Fragile X-associated tremor/ataxia syndrome Friedreich ataxia Frontotemporal dementia Generalized isolated dystonia Geniospasmus, hereditärer Hemidystonia-hemiatrophy syndrome Huntington disease Huntington disease-like 1 Huntington disease-like 3 Huntington disease-like syndrome due to C9ORF72 expansions Infantile Dystonie-Parkinsonismus Infantile Konvulsionen und Choreoathetose Infantile epileptic-dyskinetic encephalopathy Infantile-onset autosomal recessive nonprogressive cerebellar ataxia Infantile-onset spinocerebellar ataxia Intellectual disability-hyperkinetic movement-truncal ataxia syndrome Isolated dystonia Joubert syndrome and related disorders Joubert syndrome with Jeune asphyxiating thoracic dystrophy Joubert syndrome with hepatic defect Joubert syndrome with ocular defect Joubert syndrome with oculorenal defect Joubert syndrome with renal defect Joubert-Syndrom Juvenile Huntington disease Juvenile myoclonic epilepsy Lethal ataxia with deafness and optic atrophy Machado-Joseph-Krankheit Typ 1 Machado-Joseph-Krankheit Typ 2 Machado-Joseph-Krankheit Typ 3 Marinesco-Sjögren syndrome McLeod neuroacanthocytosis syndrome Mohr-Tranebjaerg syndrome Multiple system atrophy Multiple system atrophy, cerebellar type Multisystematrophie vom Typ Parkinson Myoklonus-Dystonie-Syndrom Myoklonusepilepsie, adulte benigne familiäre Myoklonusepilepsie, progressive, Typ 6 Neuroakanthozytose Neurodegenerative disease with chorea Neuroferritinopathie Non-progressive cerebellar ataxia with intellectual disability Orofaciodigital syndrome type 6 Oromandibular dystonia PANDAS Pantothenat-Kinase-assoziierte Neurodegeneration Paroxysmal dystonia Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity Paroxysmale anstrengungsinduzierte Dyskinesie Paroxysmale kinesiogene Dyskinesie Paroxysmale nicht-kinesiogene Dyskinesie Persistent combined dystonia Posterior column ataxia-retinitis pigmentosa syndrome Postinfectious autoimmune disease with chorea Primary dystonia, DYT2 type Primary dystonia, DYT21 type Progressive myoclonic epilepsy type 3 Progressive myoclonic epilepsy type 5 Progressive supranukleäre Blickparese - kortikobasales Syndrom Rare choreic movement disorder Rare dystonia Rare genetic dystonia Rare tremor disorder Recessive mitochondrial ataxia syndrome Schwere motorische und intellektuelle Beeinträchtigung-sensorinsorineurale Schwerhörigkeit-Dystonie-Syndrom Seltene Störung mit Dystonie und weiteren neurologischen oder systemischen Manifestationen Sensorineurale Schwerhörigkeit - frühes Ergrauen - essentieller Tremor Spectrin-associated autosomal recessive cerebellar ataxia Spinocerebellar ataxia type 1 Spinocerebellar ataxia type 10 Spinocerebellar ataxia type 11 Spinocerebellar ataxia type 12 Spinocerebellar ataxia type 13 Spinocerebellar ataxia type 14 Spinocerebellar ataxia type 15/16 Spinocerebellar ataxia type 17 Spinocerebellar ataxia type 18 Spinocerebellar ataxia type 19/22 Spinocerebellar ataxia type 2 Spinocerebellar ataxia type 21 Spinocerebellar ataxia type 27 Spinocerebellar ataxia type 29 Spinocerebellar ataxia type 3 Spinocerebellar ataxia type 30 Spinocerebellar ataxia type 31 Spinocerebellar ataxia type 32 Spinocerebellar ataxia type 35 Spinocerebellar ataxia type 36 Spinocerebellar ataxia type 37 Spinocerebellar ataxia type 4 Spinocerebellar ataxia type 5 Spinocerebellar ataxia type 6 Spinocerebellar ataxia type 7 Spinocerebellar ataxia type 8 Spinocerebellar ataxia with axonal neuropathy type 1 Spinocerebellar ataxia with axonal neuropathy type 2 Störung des zerebralen vesikulären Dopamin-Serotonin-Transportes Sydenham chorea Torticollis, benigner paroxysmaler, des Kindesalters Tremor - Nystagmus - Ulkus Tremor, orthostatischer primärer Tremorkrankheit, seltene, genetisch bedingte Wilson disease Woodhouse-Sakati-Syndrom X-chromosomale sideroblastische Anämie und spinozerebelläre Ataxie X-linked cerebellar ataxia X-linked dystonia-parkinsonism X-linked intellectual disability-ataxia-apraxia syndrome X-linked progressive cerebellar ataxia Zerebello-parenchymale Krankheit, autosomal-rezessive, Typ 3 Zerebelläre Ataxie - Areflexie - Pes cavus - Optikusatrophie - sensorineurale Schwerhörigkeit Zerebelläre Ataxie, autosomal-rezessive Zerebelläre Ataxie, autosomal-rezessive, mit spät-einsetzender Spastik