SE-ATLAS

Neuroferritinopathie Dystonie-parkinsonisme infantile Tremblement génétique rare Maladie de Machado-Joseph type 1 Ataxie spinocérébelleuse type 28 Syndrome de déficiences motrice et intellectuelle sévères-surdité neurosensorielle-dystonie Ataxie spinocérébelleuse type 23 Géniospasme héréditaire Ataxie spinocérébelleuse type 25 Ataxie spinocérébelleuse type 20 Ataxie spinocérébelleuse type 34 Ataxie spinocérébelleuse liée à l'X type 4 Syndrome de dystonie-aphonie Syndrome d'ataxie cérébelleuse autosomique récessive-épilepsie-déficience intellectuelle par déficit de WWOX Neurodégénérescence par déficit en pantothénate kinase Ataxie spinocérébelleuse type 26 Torticolis paroxystique bénin de l'enfant Atrophie multisystématisée type parkinsonien Dystonie-parkinsonisme à début rapide Maladie de Huntington-like 2 Maladie de Machado-Joseph type 2 Syndrome de paralysie supranucléaire progressive-syndrome corticobasal Ataxie spinocérébelleuse liée à l'X type 3 Ataxie cérébelleuse autosomique récessive de l'adulte Ataxie cérébelleuse liée à l'X non progressive Syndrome de Woodhouse-Sakati Syndrome pseudo-Huntington Maladie de Machado-Joseph type 3 Dystonie primaire type DYT4 Tremblement orthostatique primaire Dystonie primaire type DYT13 Epilepsie myoclonique progressive type 6 Dystonie primaire type DYT6 Dyskinésie paroxystique kinésigénique Syndrome de Dravet Dystonie dopa-sensible autosomique dominante Dyskinésie paroxystique induite par l'effort Ataxie cérébelleuse congénitale autosomique récessive par déficit en MGLUR1 Dyskinésie non kinésigénique paroxystique Chorée bénigne héréditaire Neuroacanthocytose Syndrome de Joubert PANDAS Ataxie cérébelleuse autosomique récessive avec spasticité tardive Syndrome de convulsions infantiles-choréoathétose Dyskinésie paroxystique 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 Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency Paroxysmal dystonia Combined cervical dystonia Joubert syndrome with hepatic defect Primary dystonia, DYT2 type Autosomal recessive ataxia due to ubiquinone deficiency Focal, segmental or multifocal dystonia X-linked intellectual disability-ataxia-apraxia syndrome Huntington disease-like syndrome due to C9ORF72 expansions Infantile-onset spinocerebellar ataxia Friedreich ataxia Autosomal recessive cerebellar ataxia-movement disorder syndrome Lethal ataxia with deafness and optic atrophy Ataxia with vitamin E deficiency Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome Spinocerebellar ataxia type 37 Infantile-onset autosomal recessive nonprogressive cerebellar ataxia Ataxia-deafness-intellectual disability syndrome Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency Autosomal dominant cerebellar ataxia Autosomal dominant cerebellar ataxia type II Spectrin-associated autosomal recessive cerebellar ataxia Fragile X-associated tremor/ataxia syndrome Ataxia-telangiectasia Rare tremor disorder Dentatorubral pallidoluysian atrophy Multiple system atrophy Rare choreic movement disorder Spinocerebellar ataxia with axonal neuropathy type 2 Spinocerebellar ataxia type 29 Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency Posterior column ataxia-retinitis pigmentosa syndrome McLeod neuroacanthocytosis syndrome Ataxia-telangiectasia-like disorder Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome Neurodegenerative disease with chorea Joubert syndrome and related disorders Dystonia 16 Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity Dopa-responsive dystonia Sydenham chorea Early-onset generalized limb-onset dystonia Oromandibular dystonia 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