SE-ATLAS

3-methylglutaconic aciduria type 3 Adult-onset autosomal recessive cerebellar ataxia Adult-onset dystonia-parkinsonism Ataxia with vitamin E deficiency Ataxia-deafness-intellectual disability syndrome Ataxia-oculomotor apraxia type 1 Ataxia-telangiectasia Ataxia-telangiectasia variant Ataxia-telangiectasia-like disorder 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 dominant dopa-responsive dystonia Autosomal dominant focal dystonia, DYT25 type Autosomal recessive ataxia due to PEX10 deficiency Autosomal recessive ataxia due to ubiquinone deficiency Autosomal recessive ataxia, Beauce type Autosomal recessive cerebellar ataxia Autosomal recessive cerebellar ataxia due to a DNA repair defect Autosomal recessive cerebellar ataxia with late-onset spasticity Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome 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-epilepsy-intellectual disability syndrome due to WWOX 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 cerebelloparenchymal disorder type 3 Autosomal recessive congenital cerebellar ataxia Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency Autosomal recessive congenital cerebellar ataxia due to MGLUR1 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 Benign adult familial myoclonic epilepsy Benign hereditary chorea Benign paroxysmal torticollis of infancy Blepharospasm-oromandibular dystonia syndrome Brain dopamine-serotonin vesicular transport disease Brain-lung-thyroid syndrome CAMOS syndrome Cerebellar ataxia, Cayman type Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Cerebellar ataxia-ectodermal dysplasia syndrome Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia Choreoacanthocytosis 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 dystonia Dopa-responsive dystonia due to sepiapterin reductase deficiency Dravet syndrome Dysequilibrium syndrome Dystonia 16 Dystonia-aphonia syndrome 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 Hemidystonia-hemiatrophy syndrome Hereditary geniospasm Huntington disease Huntington disease-like 1 Huntington disease-like 2 Huntington disease-like 3 Huntington disease-like syndrome Huntington disease-like syndrome due to C9ORF72 expansions Infantile convulsions and choreoathetosis Infantile dystonia-parkinsonism 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 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 Juvenile Huntington disease Juvenile myoclonic epilepsy Lethal ataxia with deafness and optic atrophy Machado-Joseph disease type 1 Machado-Joseph disease type 2 Machado-Joseph disease type 3 Marinesco-Sjögren syndrome McLeod neuroacanthocytosis syndrome Mohr-Tranebjaerg syndrome Multiple system atrophy Multiple system atrophy, cerebellar type Multiple system atrophy, parkinsonian type Myoclonus-dystonia syndrome Neuroacanthocytosis Neurodegenerative disease with chorea Neuroferritinopathy Non-progressive cerebellar ataxia with intellectual disability Orofaciodigital syndrome type 6 Oromandibular dystonia PANDAS Pantothenate kinase-associated neurodegeneration Paroxysmal dyskinesia Paroxysmal dystonia Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity Paroxysmal exertion-induced dyskinesia Paroxysmal kinesigenic dyskinesia Paroxysmal non-kinesigenic dyskinesia Persistent combined dystonia Posterior column ataxia-retinitis pigmentosa syndrome Postinfectious autoimmune disease with chorea Primary dystonia, DYT13 type Primary dystonia, DYT17 type Primary dystonia, DYT2 type Primary dystonia, DYT21 type Primary dystonia, DYT4 type Primary dystonia, DYT6 type Primary orthostatic tremor Progressive myoclonic epilepsy type 3 Progressive myoclonic epilepsy type 5 Progressive myoclonic epilepsy type 6 Progressive supranuclear palsy-corticobasal syndrome Rapid-onset dystonia-parkinsonism Rare choreic movement disorder Rare disorder with dystonia and other neurologic or systemic manifestation Rare dystonia Rare genetic dystonia Rare genetic tremor disorder Rare tremor disorder Recessive mitochondrial ataxia syndrome Sensorineural hearing loss-early graying-essential tremor syndrome Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome 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 20 Spinocerebellar ataxia type 21 Spinocerebellar ataxia type 23 Spinocerebellar ataxia type 25 Spinocerebellar ataxia type 26 Spinocerebellar ataxia type 27 Spinocerebellar ataxia type 28 Spinocerebellar ataxia type 29 Spinocerebellar ataxia type 3 Spinocerebellar ataxia type 30 Spinocerebellar ataxia type 31 Spinocerebellar ataxia type 32 Spinocerebellar ataxia type 34 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 Sydenham chorea Tremor-nystagmus-duodenal ulcer syndrome Wilson disease Woodhouse-Sakati syndrome X-linked cerebellar ataxia X-linked dystonia-parkinsonism X-linked intellectual disability-ataxia-apraxia syndrome X-linked non progressive cerebellar ataxia X-linked progressive cerebellar ataxia X-linked sideroblastic anemia and spinocerebellar ataxia X-linked spinocerebellar ataxia type 3 X-linked spinocerebellar ataxia type 4