SE-ATLAS

Spinocerebellar degeneration-corneal dystrophy syndrome Oromandibular dystonia Machado-Joseph disease type 2 Autosomal recessive spastic paraplegia type 61 Autosomal recessive spastic paraplegia type 66 Autosomal recessive spastic paraplegia type 70 Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency Adult-onset cervical dystonia, DYT23 type Early-onset cerebellar ataxia with retained tendon reflexes Autosomal dominant spastic ataxia Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome Autosomal recessive spastic paraplegia type 71 Spinocerebellar ataxia type 31 Ataxia-telangiectasia variant Sporadic adult-onset ataxia of unknown etiology Progressive encephalomyelitis with rigidity and myoclonus Spinocerebellar ataxia type 13 Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency Persistent combined dystonia Autosomal spastic paraplegia type 18 X-linked dystonia-parkinsonism Dystonia 16 Adult-onset dystonia-parkinsonism Early-onset generalized limb-onset dystonia Autosomal recessive dopa-responsive dystonia Generalized isolated dystonia Primary dystonia, DYT17 type Primary dystonia, DYT6 type Isolated dystonia Myoclonus-cerebellar ataxia-deafness syndrome Myoclonus-dystonia syndrome Spinocerebellar ataxia type 41 Primary dystonia, DYT21 type Marinesco-Sjögren syndrome Posterior column ataxia-retinitis pigmentosa syndrome Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome Primary dystonia, DYT27 type Dystonia-aphonia syndrome Autosomal recessive ataxia, Beauce type X-linked complex spastic paraplegia Spinocerebellar ataxia type 30 X-linked spastic paraplegia type 34 Autosomal dominant spastic paraplegia type 37 Friedreich ataxia Ataxia with vitamin E deficiency Autosomal recessive spastic ataxia of Charlevoix-Saguenay Autosomal dominant spastic paraplegia type 38 Ataxia-telangiectasia Autosomal recessive spastic paraplegia type 32 Sandifer syndrome Autosomal recessive spastic paraplegia type 35 Autosomal dominant complex spastic paraplegia Autosomal recessive complex spastic paraplegia Autosomal dominant pure spastic paraplegia Autosomal recessive pure spastic paraplegia Autosomal dominant spastic paraplegia type 4 Autosomal dominant spastic paraplegia type 3 Autosomal recessive spastic paraplegia type 5A Autosomal dominant spastic paraplegia type 8 Autosomal spastic paraplegia type 58 Complex hereditary spastic paraplegia Pure hereditary spastic paraplegia Autosomal dominant spastic paraplegia type 10 Autosomal dominant spastic paraplegia type 9 Autosomal dominant spastic paraplegia type 12 Autosomal recessive spastic paraplegia type 14 Cranio-cervical dystonia with laryngeal and upper-limb involvement Autosomal dominant spastic paraplegia type 13 X-linked spastic paraplegia type 16 Adult-onset autosomal recessive cerebellar ataxia Autosomal recessive spastic paraplegia type 15 Autosomal dominant spastic paraplegia type 19 Autosomal dominant spastic paraplegia type 17 Autosomal recessive spastic paraplegia type 20 Autosomal recessive spastic paraplegia type 23 Autosomal recessive spastic paraplegia type 25 Autosomal recessive spastic paraplegia type 24 Autosomal recessive spastic paraplegia type 27 Autosomal recessive spastic paraplegia type 26 Ataxia-oculomotor apraxia type 1 Autosomal dominant spastic paraplegia type 29 Autosomal recessive spastic paraplegia type 28 Autosomal dominant spastic paraplegia type 31 Autosomal spastic paraplegia type 30 Spectrin-associated autosomal recessive cerebellar ataxia X-linked progressive cerebellar ataxia Spastic ataxia with congenital miosis Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia Infantile-onset spinocerebellar ataxia Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency Ataxia-deafness-intellectual disability syndrome Hereditary spastic paraplegia Spastic paraplegia type 7 Autosomal dominant spastic paraplegia type 73 Spastic paraplegia type 2 Autosomal recessive cerebellar ataxia-movement disorder syndrome Spastic paraplegia-Paget disease of bone syndrome Autosomal recessive spastic paraplegia type 11 Blepharospasm-oromandibular dystonia syndrome Autosomal recessive spastic paraplegia type 77 X-linked spinocerebellar ataxia type 4 X-linked spinocerebellar ataxia type 3 Autosomal recessive cerebellar ataxia due to a DNA repair defect Autosomal recessive spastic paraplegia type 75 Spastic ataxia Primary dystonia, DYT2 type Focal, segmental or multifocal dystonia Pure or complex hereditary spastic paraplegia Autosomal recessive spastic paraplegia type 48 Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity Pure or complex autosomal dominant spastic paraplegia X-linked intellectual disability-spastic paraplegia with iron deposits syndrome Autosomal dominant spastic paraplegia type 42 Cataract-ataxia-deafness syndrome Pure or complex X-linked spastic paraplegia Rapid-onset dystonia-parkinsonism Pure or complex autosomal recessive spastic paraplegia Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome Autosomal dominant spastic paraplegia type 41 Autosomal dominant spastic paraplegia type 36 MT-ATP6-related mitochondrial spastic paraplegia PCNA-related progressive neurodegenerative photosensitivity syndrome Autosomal recessive spastic paraplegia type 55 Autosomal recessive spastic paraplegia type 43 Autosomal recessive spastic paraplegia type 54 Aromatic L-amino acid decarboxylase deficiency Autosomal recessive spastic paraplegia type 62 Autosomal recessive spastic paraplegia type 46 Hereditary sensory and autonomic neuropathy due to TECPR2 mutation Autosomal recessive spastic paraplegia type 59 Autosomal recessive spastic paraplegia type 45 Autosomal recessive spastic paraplegia type 63 Autosomal recessive spastic paraplegia type 60 Autosomal dominant spastic ataxia type 1 Spastic paraplegia-optic atrophy-neuropathy syndrome Autosomal recessive spastic paraplegia type 64 Autosomal recessive spastic paraplegia type 44 Paroxysmal dyskinesia Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency Autosomal recessive spastic paraplegia type 67 Autosomal recessive cerebellar ataxia due to STUB1 deficiency Autosomal recessive spastic paraplegia type 56 Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome Autosomal recessive spastic paraplegia type 69 MASA syndrome Spinocerebellar ataxia type 34 Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency Spastic ataxia-corneal dystrophy syndrome Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Episodic ataxia with slurred speech Episodic ataxia type 6 Episodic ataxia type 7 Spinocerebellar ataxia type 42 Hyperekplexia Sporadic hyperekplexia Familial paroxysmal ataxia Autosomal dominant cerebellar ataxia Dentatorubral pallidoluysian atrophy X-linked spasticity-intellectual disability-epilepsy syndrome Hereditary episodic ataxia Hereditary geniospasm Hereditary hyperekplexia Stiff person spectrum disorder Hyperekplexia-epilepsy syndrome Cerebellar ataxia-hypogonadism syndrome Ataxia-hypogonadism-choroidal dystrophy syndrome Opsoclonus-myoclonus syndrome Spinocerebellar ataxia-dysmorphism syndrome Intellectual disability-hyperkinetic movement-truncal ataxia syndrome Spinocerebellar ataxia type 37 Familial cortical myoclonus Spinocerebellar ataxia type 32 Autosomal recessive spastic paraplegia type 53 Inherited congenital spastic tetraplegia Autosomal recessive ataxia due to ubiquinone deficiency Spinocerebellar ataxia type 36 Spinocerebellar ataxia type 35 Dysequilibrium syndrome Autosomal recessive spastic paraplegia type 57 Episodic ataxia type 1 Autosomal recessive spastic ataxia with leukoencephalopathy Spinocerebellar ataxia type 28 Spinocerebellar ataxia type 23 Spinocerebellar ataxia type 25 Spinocerebellar ataxia type 26 Progressive autosomal recessive ataxia-deafness syndrome Dopa-responsive dystonia Spastic paraparesis-deafness syndrome Machado-Joseph disease type 1 Machado-Joseph disease type 3 Episodic ataxia type 3 Episodic ataxia type 4 HSD10 disease, atypical type Classic stiff person syndrome Autosomal recessive spastic ataxia Autosomal recessive cerebellar ataxia with late-onset spasticity Spinocerebellar ataxia type 38 Worster-Drought syndrome Brain dopamine-serotonin vesicular transport disease Benign hereditary chorea Focal stiff limb syndrome Recessive mitochondrial ataxia syndrome Autosomal dominant cerebellar ataxia type I Spinocerebellar ataxia type 1 Spinocerebellar ataxia type 7 Spinocerebellar ataxia type 3 Autosomal dominant cerebellar ataxia type III Spinocerebellar ataxia type 17 Spinocerebellar ataxia type 4 Spinocerebellar ataxia type 27 Spinocerebellar ataxia type 11 Spinocerebellar ataxia type 5 Spinocerebellar ataxia type 15/16 Ataxia-telangiectasia-like disorder Spinocerebellar ataxia type 18 Spinocerebellar ataxia type 21 Spinocerebellar ataxia type 19/22 Paroxysmal kinesigenic dyskinesia Paroxysmal exertion-induced dyskinesia Paroxysmal non-kinesigenic dyskinesia Severe intellectual disability-progressive spastic diplegia syndrome Autosomal recessive ataxia due to PEX10 deficiency Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome Primary orthostatic tremor CAMOS syndrome Fragile X-associated tremor/ataxia syndrome Autosomal recessive cerebellar ataxia-psychomotor delay syndrome Episodic ataxia type 5 Autosomal dominant spastic paraplegia type 6 Autosomal recessive spastic paraplegia type 21 Cerebellar ataxia-ectodermal dysplasia syndrome Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome Autosomal recessive spastic paraplegia type 39 Spinocerebellar ataxia type 20 X-linked pure spastic paraplegia Benign paroxysmal torticollis of infancy Spinocerebellar ataxia type 40 Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome Combined dystonia Autosomal spastic paraplegia type 72 Dopa-responsive dystonia due to sepiapterin reductase deficiency Autosomal dominant cerebellar ataxia type IV Spinocerebellar ataxia type 2 Spinocerebellar ataxia type 6 Spinocerebellar ataxia type 10 Spinocerebellar ataxia type 8 Spinocerebellar ataxia type 14 Spinocerebellar ataxia type 12 X-linked cerebellar ataxia Primary dystonia, DYT4 type Primary dystonia, DYT13 type Autosomal dominant dopa-responsive dystonia