SE-ATLAS

Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome Spinocerebellar ataxia type 32 Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency Autosomal dominant cerebellar ataxia type IV Cataract-ataxia-deafness syndrome Limbic encephalitis with nCMAgs antibodies Sporadic adult-onset ataxia of unknown etiology Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome Autosomal dominant cerebellar ataxia type III Joubert syndrome with hepatic defect Classic paraneoplastic limbic encephalitis Paraneoplastic neurologic syndrome Spinocerebellar ataxia type 13 Spinocerebellar ataxia type 15/16 EAST syndrome Spastic ataxia with congenital miosis Episodic ataxia with slurred speech Non-progressive cerebellar ataxia with intellectual disability Autosomal recessive ataxia due to ubiquinone deficiency Spinocerebellar ataxia type 36 X-linked sideroblastic anemia and spinocerebellar ataxia Spinocerebellar ataxia type 29 Spinocerebellar degeneration-corneal dystrophy syndrome Paraneoplastic limbic encephalitis Posterior column ataxia-retinitis pigmentosa syndrome Spinocerebellar ataxia type 1 Spinocerebellar ataxia type 19/22 Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome Opsoclonus-myoclonus syndrome Autosomal dominant spastic ataxia Autosomal recessive ataxia, Beauce type Spinocerebellar ataxia type 18 Ataxia-telangiectasia-like disorder Spinocerebellar ataxia type 28 Machado-Joseph disease type 1 Spinocerebellar ataxia type 20 Ataxia-oculomotor apraxia type 1 Spinocerebellar ataxia-dysmorphism syndrome Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome Spinocerebellar ataxia type 3 Spinocerebellar ataxia type 37 X-linked intellectual disability-ataxia-apraxia syndrome Orofaciodigital syndrome type 6 Spinocerebellar ataxia type 23 Infantile-onset spinocerebellar ataxia X-linked cerebellar ataxia Friedreich ataxia Spinocerebellar ataxia type 2 Spinocerebellar ataxia type 21 Limbic encephalitis associated with antibodies to cell membrane antigens Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome Dysequilibrium syndrome Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency Multiple system atrophy, cerebellar type Autosomal recessive cerebellar ataxia-movement disorder syndrome Cerebellar ataxia, Cayman type Autosomal recessive cerebelloparenchymal disorder type 3 Lethal ataxia with deafness and optic atrophy Spinocerebellar ataxia type 26 Ataxia with vitamin E deficiency Autosomal recessive ataxia due to PEX10 deficiency Episodic ataxia type 6 Episodic ataxia type 4 Spinocerebellar ataxia type 17 Steroid-responsive encephalopathy associated with autoimmune thyroiditis Spinocerebellar ataxia type 34 Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Ataxia-deafness-intellectual disability syndrome Infantile-onset autosomal recessive nonprogressive cerebellar ataxia Spinocerebellar ataxia type 25 Childhood-onset spasticity with hyperglycinemia Familial paroxysmal ataxia Episodic ataxia type 3 Spinocerebellar ataxia type 6 Autosomal recessive metabolic cerebellar ataxia Spinocerebellar ataxia type 10 Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency NMDA receptor encephalitis Ataxie spinocérébelleuse liée à l'X type 4 Ataxie cérébelleuse autosomique récessive Ataxie spastique autosomique récessive de Charlevoix-Saguenay Ataxie cérébelleuse liée à l'X non progressive Syndrome d'ataxie spinocérébelleuse-neuropathie axonale type 1 Ataxie spastique autosomique récessive avec leucoencéphalopathie Ataxie spastique autosomique récessive Ataxie acquise Ataxie cérébelleuse autosomique récessive avec spasticité tardive Ataxie cérébelleuse congénitale autosomique récessive Syndrome de Marinesco-Sjögren Syndrome d'ataxie cérébelleuse-hypogonadisme Ataxie spastique autosomique dominante type 1 Syndrome de Joubert et maladies associées Ataxie cérébelleuse autosomique dominante Maladie de Machado-Joseph type 2 Ataxie spinocérébelleuse type 8 Ataxie cérébelleuse dégénérative et progressive autosomique récessive Ataxie spinocérébelleuse type 14 Syndrome d'ataxie spinocérébelleuse-dystrophie cornéenne Syndrome de Joubert Ataxie épisodique héréditaire Syndrome de myoclonie-ataxie cérébelleuse-surdité Ataxie spinocérébelleuse type 31 Ataxie-télangiectasie Syndrome tremblement-ataxie lié à une prémutation de l'X fragile Syndrome de Christianson Ataxie dégénérative non héréditaire Ataxie spinocérébelleuse type 12 Ataxie cérébelleuse autosomique récessive due à une anomalie de réparation de l'ADN X-linked progressive cerebellar ataxia Dentatorubral pallidoluysian atrophy Episodic ataxia type 7 Rare ataxia Spectrin-associated autosomal recessive cerebellar ataxia Spastic ataxia Recessive mitochondrial ataxia syndrome Joubert syndrome with oculorenal defect Spinocerebellar ataxia type 30 Autosomal dominant cerebellar ataxia type I CAMOS syndrome Spinocerebellar ataxia type 4 X-linked spinocerebellar ataxia type 3 Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency Joubert syndrome with renal defect Episodic ataxia type 5 Early-onset cerebellar ataxia with retained tendon reflexes Spinocerebellar ataxia with axonal neuropathy type 2 Spinocerebellar ataxia type 27 Hereditary ataxia Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome Autosomal recessive syndromic cerebellar ataxia Richards-Rundle syndrome Superficial siderosis Episodic ataxia type 1 Limbic encephalitis with LGI1 antibodies Ataxia-tapetoretinal degeneration syndrome Spinocerebellar ataxia type 7 Autosomal recessive cerebellar ataxia-psychomotor delay syndrome Spinocerebellar ataxia type 11 Spinocerebellar ataxia type 35 Machado-Joseph disease type 3 Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome Adult-onset autosomal recessive cerebellar ataxia Joubert syndrome with ocular defect Lambert-Eaton myasthenic syndrome Cancer-associated retinopathy Spinocerebellar ataxia type 5 Autosomal dominant cerebellar ataxia type II Joubert syndrome with Jeune asphyxiating thoracic dystrophy Ataxia-hypogonadism-choroidal dystrophy syndrome