SE-ATLAS

Syndrome d'ataxie spastique autosomique récessive-atrophie optique-dysarthrie Ataxie spinocérébelleuse type 32 Ataxie cérébelleuse congénitale autosomique récessive par déficit en MGLUR1 Ataxie cérébelleuse autosomique dominante type IV Syndrome de cataracte-ataxie-surdité Encéphalite limbique avec anticorps anti-nCMAgs Ataxie sporadique tardive d'étiologie indéterminée Syndrome d'ataxie cérébelleuse autosomique récessive-épilepsie-déficience intellectuelle par déficit de WWOX Syndrome d'atrophie musculaire-ataxie-rétinite pigmentaire-diabète Ataxie cérébelleuse autosomique dominante type III Syndrome de Joubert avec atteinte hépatique Encéphalite limbique paranéoplasique classique Syndrome neurologique paranéoplasique Ataxie spinocérébelleuse type 13 Ataxie spinocérébelleuse type 15/16 Syndrome EAST Syndrome d'ataxie-myosis congénital Ataxie épisodique avec troubles de l'élocution Ataxie cérébelleuse non progressive avec déficience intellectuelle Ataxie cérébelleuse autosomique récessive par déficit en ubiquinone Ataxie spinocérébelleuse type 36 Anémie sidéroblastique liée à l'X et ataxie spinocérébelleuse Ataxie spinocérébelleuse type 29 Syndrome de dégénérescence spinocérébelleuse-dystrophie cornéenne Encéphalite limbique paranéoplasique Syndrome d'ataxie du cordon postérieur-rétinite pigmentaire Ataxie spinocérébelleuse type 1 Ataxie spinocérébelleuse type 19/22 Syndrome d'ichtyose-hépatosplénomégalie-dégénérescence cérébelleuse Syndrome d'opsoclonie-myoclonie Ataxie spastique autosomique dominante Ataxie cérébelleuse autosomique récessive type Beauce Ataxie spinocérébelleuse 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 X-linked spinocerebellar ataxia type 4 Autosomal recessive cerebellar ataxia Autosomal recessive spastic ataxia of Charlevoix-Saguenay X-linked non progressive cerebellar ataxia Spinocerebellar ataxia with axonal neuropathy type 1 Autosomal recessive spastic ataxia with leukoencephalopathy Autosomal recessive spastic ataxia Acquired ataxia Autosomal recessive cerebellar ataxia with late-onset spasticity Autosomal recessive congenital cerebellar ataxia Marinesco-Sjögren syndrome Cerebellar ataxia-hypogonadism syndrome Autosomal dominant spastic ataxia type 1 Joubert syndrome and related disorders Autosomal dominant cerebellar ataxia Machado-Joseph disease type 2 Spinocerebellar ataxia type 8 Autosomal recessive degenerative and progressive cerebellar ataxia Spinocerebellar ataxia type 14 Spastic ataxia-corneal dystrophy syndrome Joubert syndrome Hereditary episodic ataxia Myoclonus-cerebellar ataxia-deafness syndrome Spinocerebellar ataxia type 31 Ataxia-telangiectasia Fragile X-associated tremor/ataxia syndrome Christianson syndrome Non-hereditary degenerative ataxia Spinocerebellar ataxia type 12 Autosomal recessive cerebellar ataxia due to a DNA repair defect 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