SE-ATLAS

CANOMAD syndrome Joubert syndrome with ocular defect X-linked progressive cerebellar ataxia Adult-onset dystonia-parkinsonism Early-onset cerebellar ataxia with retained tendon reflexes Paraneoplastic limbic encephalitis Ataxia-tapetoretinal degeneration syndrome Joubert syndrome with renal defect Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome Ataxia-hypogonadism-choroidal dystrophy syndrome Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia Autosomal recessive spastic ataxia with leukoencephalopathy Autosomal recessive spastic ataxia Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency Joubert syndrome with hepatic defect Spastic ataxia with congenital miosis Autosomal recessive ataxia due to ubiquinone deficiency Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome Sporadic adult-onset ataxia of unknown etiology Variant of Guillain-Barré syndrome Polyneuropathy associated with IgM monoclonal gammopathy with anti-MAG Spinocerebellar ataxia-dysmorphism syndrome X-linked intellectual disability-ataxia-apraxia syndrome Friedreich ataxia Infantile-onset spinocerebellar ataxia Autosomal recessive cerebellar ataxia-movement disorder syndrome Multifocal motor neuropathy Non-hereditary degenerative ataxia Ataxia with vitamin E deficiency Spinocerebellar ataxia type 37 Lethal ataxia with deafness and optic atrophy Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome Subacute inflammatory demyelinating polyneuropathy Ataxia-deafness-intellectual disability syndrome Infantile-onset autosomal recessive nonprogressive cerebellar ataxia Familial paroxysmal ataxia Regional variant of Guillain-Barré syndrome Autosomal recessive spastic ataxia of Charlevoix-Saguenay Autosomal dominant cerebellar ataxia Fragile X-associated tremor/ataxia syndrome Spectrin-associated autosomal recessive cerebellar ataxia Ataxia-telangiectasia Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency Dentatorubral pallidoluysian atrophy Autosomal dominant cerebellar ataxia type II Acquired ataxia Functional variant of Guillain-Barré syndrome TMEM70-related mitochondrial encephalo-cardio-myopathy Spinocerebellar ataxia type 29 Spinocerebellar ataxia with axonal neuropathy type 2 Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome Episodic ataxia type 1 TRIM32-related limb-girdle muscular dystrophy R8 Superficial siderosis Alpha-B crystallin-related late-onset myopathy Paraneoplastic neurologic syndrome Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome Barth syndrome Ataxia-telangiectasia-like disorder Joubert syndrome and related disorders Dystonia 16 Spastic ataxia-corneal dystrophy syndrome Rare ataxia FASTKD2-related infantile mitochondrial encephalomyopathy Fingerprint body myopathy Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency Distal myopathy with posterior leg and anterior hand involvement Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome Glycogen storage disease due to phosphoglycerate mutase deficiency Autosomal recessive ataxia due to PEX10 deficiency Autosomal recessive ataxia, Beauce type Huntington disease Paraparetic variant of Guillain-Barré syndrome Acute and subacute inflammatory demyelinating polyneuropathy Dysequilibrium syndrome Autosomal dominant limb-girdle muscular dystrophy type 1A Carey-Fineman-Ziter syndrome Steroid-responsive encephalopathy associated with autoimmune thyroiditis Acute pure sensory neuropathy Spinocerebellar ataxia type 32 Non-progressive cerebellar ataxia with intellectual disability Myoclonus-cerebellar ataxia-deafness syndrome Distal myopathy with anterior tibial onset Finnish upper limb-onset distal myopathy Joubert syndrome with oculorenal defect CAMOS syndrome Joubert syndrome with Jeune asphyxiating thoracic dystrophy Hereditary spastic paraplegia KLHL9-related early-onset distal myopathy Cataract-ataxia-deafness syndrome Acute pandysautonomia Spinocerebellar ataxia type 35 Multiple system atrophy, cerebellar type Spinocerebellar ataxia type 2 Spinocerebellar ataxia type 1 Spinocerebellar ataxia type 36 Spinocerebellar ataxia type 6 Spinocerebellar ataxia type 31 Spinocerebellar ataxia type 3 Spinocerebellar ataxia type 10 Spinocerebellar ataxia type 8 Marinesco-Sjögren syndrome Cerebellar ataxia, Cayman type Spinocerebellar ataxia type 17 Stiff person spectrum disorder Focal stiff limb syndrome Spinocerebellar ataxia type 14 Progressive encephalomyelitis with rigidity and myoclonus Recessive mitochondrial ataxia syndrome Lewis-Sumner syndrome Neuromyelitis optica spectrum disorder Spinocerebellar ataxia type 12 Hereditary myopathy with lactic acidosis due to ISCU deficiency Spinocerebellar ataxia with axonal neuropathy type 1 Spinocerebellar ataxia type 4 Brody myopathy Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome Ataxie spinocérébelleuse type 27 Ataxie spinocérébelleuse type 11 Ataxie spinocérébelleuse type 5 Ataxie spinocérébelleuse type 30 Syndrome myasthénique de Lambert-Eaton Ataxie spinocérébelleuse type 15/16 Ataxie spinocérébelleuse type 13 Syndrome de cardiomyopathie-hypotonie-acidose lactique Dystonie-parkinsonisme liée à l'X Ataxie spinocérébelleuse type 18 Alpha-cristallinopathie Ataxie spinocérébelleuse type 21 Polyneuropathie dysimmunitaire chronique Desminopathie Syndrome orofaciodigital type 6 Ataxie spinocérébelleuse type 19/22 Ataxie épisodique type 3 Myopathie à inclusion Polyradiculonévrite avec gammopathie monoclonale IgG/IgA/IgM sans activité anticorps connue Ataxie cérébelleuse autosomique récessive d'origine métabolique Maladie de stockage du glycogène avec cardiomyopathie hypertrophique Polyradiculonévrite chronique Ataxie épisodique type 4 Ataxie cérébelleuse congénitale autosomique récessive Ataxie cérébelleuse dégénérative et progressive autosomique récessive Myopathie à casquette Polyradiculonévrite démyélinisante inflammatoire aiguë Ataxie cérébelleuse autosomique récessive due à une anomalie de réparation de l'ADN Rhombencéphalite de Bickerstaff Ataxie cérébelleuse autosomique dominante type I Neuropathie axonale motrice aiguë Syndrome de Christianson Ataxie cérébelleuse autosomique récessive syndromique Neuropathie sensitivo-motrice axonale aiguë Syndrome de Richards-Rundle Syndrome d'ataxie cérébelleuse autosomique récessive-retard psychomoteur Syndrome de Miller Fisher Rétinopathie paranéoplasique Ataxie cérébelleuse autosomique dominante type IV Ataxie cérébelleuse autosomique dominante type III Syndrome de dégénérescence spinocérébelleuse-dystrophie cornéenne Dystonie-parkinsonisme infantile Syndrome POEMS Maladie de Machado-Joseph type 1 Myasthénie auto-immune de l'adulte Ataxie spinocérébelleuse type 28 Ataxie spinocérébelleuse type 23 Myasthénie auto-immune Ataxie spinocérébelleuse type 25 Ataxie spinocérébelleuse type 20 Ataxie spinocérébelleuse type 34 Ataxie spinocérébelleuse liée à l'X type 4 Syndrome d'ataxie cérébelleuse autosomique récessive-épilepsie-déficience intellectuelle par déficit de WWOX Ataxie spinocérébelleuse type 26 Myasthénie auto-immune juvénile Dystonie-parkinsonisme à début rapide Ataxie spastique autosomique dominante type 1 Myopathie congénitale à "central cores" Maladie de Machado-Joseph type 2 X-linked spinocerebellar ataxia type 3 Adult-onset autosomal recessive cerebellar ataxia X-linked non progressive cerebellar ataxia Muscular glycogenosis Severe X-linked mitochondrial encephalomyopathy Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Machado-Joseph disease type 3 Guillain-Barré syndrome Transient neonatal myasthenia gravis Hypertrophic cardiomyopathy due to intensive athletic training Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Fatal infantile cytochrome C oxidase deficiency Hereditary episodic ataxia Rare parkinsonian syndrome due to neurodegenerative disease Episodic ataxia type 7 Hereditary myopathy with early respiratory failure Episodic ataxia type 6 Bethlem muscular dystrophy Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency Joubert syndrome Autosomal recessive cerebellar ataxia with late-onset spasticity Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome Chronic inflammatory demyelinating polyneuropathy Rare parkinsonian syndrome due to intoxication Hereditary ataxia Rare parkinsonian disorder ATTRV122I amyloidosis Episodic ataxia type 5 X-linked sideroblastic anemia and spinocerebellar ataxia Autosomal dominant spastic ataxia EAST syndrome Ataxia-oculomotor apraxia type 1 Duane anomaly-myopathy-scoliosis syndrome Autosomal recessive cerebelloparenchymal disorder type 3 Autosomal recessive cerebellar ataxia X-linked cerebellar ataxia Cerebellar ataxia-hypogonadism syndrome NMDA receptor encephalitis Classic stiff person syndrome Autoimmune encephalopathy with parasomnia and obstructive sleep apnea Neuromyelitis optica spectrum disorder with anti-MOG antibodies Acute transverse myelitis with anti-MOG antibodies Isolated optic neuritis with anti-MOG antibodies Acute sensory ataxic neuropathy Posterior column ataxia-retinitis pigmentosa syndrome Opsoclonus-myoclonus syndrome Spastic ataxia