ataxia
Basic Information
- Description
- A neurological and physiological symptom that is characterized by an inability to coordinate voluntary muscular movements that is symptomatic of some nervous disorders.
- Identifier
- SYMP_0000005
- Notation
- SYMP:0000005
- Category
- symptoms
- Synonyms
-
- uncoordination
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- GRID2-related spinocerebellar ataxia
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- Gordon Holmes syndrome
- Hartnup disease
- Joubert syndrome 1
- Joubert syndrome 10
- Joubert syndrome 14
- Joubert syndrome 16
- Joubert syndrome 18
- Joubert syndrome 20
- Joubert syndrome 21
- Joubert syndrome 22
- Joubert syndrome 23
- Joubert syndrome 24
- Joubert syndrome 25
- Joubert syndrome 26
- Joubert syndrome 27
- Joubert syndrome 29
- Joubert syndrome 3
- Joubert syndrome 30
- Joubert syndrome 31
- Joubert syndrome 32
- Joubert syndrome 33
- Joubert syndrome 5
- Joubert syndrome 6
- Joubert syndrome 7
- Kohlschutter-Tonz syndrome
- Laurence-Moon syndrome
- MERRF syndrome
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- NARP syndrome
- PHARC syndrome
- Peroxisome biogenesis disorder 6B
- RELA fusion-positive ependymoma
- Revesz syndrome
- Sandhoff disease
- Troyer syndrome
- Wernicke encephalopathy
- X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance
- X-linked sideroblastic anemia with ataxia
- X-linked spinocerebellar ataxia 4
- X-linked spinocerebellar ataxia 5
- abetalipoproteinemia
- aceruloplasminemia
- adult brainstem gliosarcoma
- agenesis of corpus callosum, cardiac, ocular, and genital syndrome
- alpha-mannosidosis
- ataxia-oculomotor apraxia type 4
- autosomal dominant intellectual developmental disorder 11
- autosomal dominant progressive external ophthalmoplegia 1
- autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5
- autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6
- autosomal recessive cerebellar ataxia
- autosomal recessive intellectual developmental disorder 73
- autosomal recessive intellectual developmental disorder 76
- autosomal recessive progressive external ophthalmoplegia 1
- autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3
- autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4
- autosomal recessive spinocerebellar ataxia 12
- autosomal recessive spinocerebellar ataxia 15
- autosomal recessive spinocerebellar ataxia 19
- autosomal recessive spinocerebellar ataxia 20
- autosomal recessive spinocerebellar ataxia 30
- autosomal recessive spinocerebellar ataxia 31
- autosomal recessive spinocerebellar ataxia 32
- autosomal recessive spinocerebellar ataxia 7
- basal ganglia calcification
- baylisascariasis
- biotin-responsive basal ganglia disease
- cerebellar ataxia type 47
- cerebellar ataxia type 48
- cerebellar disease
- cerebellar hyplasia/atrophy, epilepsy, and global developmental delay
- cerebellopontine angle primitive neuroectodermal tumor
- childhood supratentorial embryonal tumor with multilayered rosettes, C19MC-altered
- choreatic disease
- classic dopamine transporter deficiency syndrome
- coenzyme Q10 deficiency disease
- combined oxidative phosphorylation deficiency 15
- combined oxidative phosphorylation deficiency 17
- combined oxidative phosphorylation deficiency 28
- combined oxidative phosphorylation deficiency 31
- combined oxidative phosphorylation deficiency 53
- congenital disorder of glycosylation Ih
- congenital disorder of glycosylation Iu
- congenital muscular dystrophy-dystroglycanopathy A14
- copper deficiency myelopathy
- dicarboxylic aminoaciduria
- dominant optic atrophy plus syndrome
- dysgammaglobulinemia
- eosinophilic meningitis
- episodic ataxia type 2
- episodic ataxia type 3
- episodic ataxia type 7
- familial hemiplegic migraine 3
- familial isolated deficiency of vitamin E
- gangliosidosis
- glutamate-cysteine ligase deficiency
- hemosiderosis
- hereditary spastic paraplegia
- hereditary spastic paraplegia 10
- hereditary spastic paraplegia 18
- hereditary spastic paraplegia 23
- hereditary spastic paraplegia 29
- hereditary spastic paraplegia 39
- hereditary spastic paraplegia 43
- hereditary spastic paraplegia 48
- hereditary spastic paraplegia 79B
- hypomyelinating leukodystrophy 10
- hypomyelinating leukodystrophy 11
- large cell medulloblastoma
- leukoencephalopathy with vanishing white matter
- louping ill
- medulloblastoma non-WNT/non-SHH
- megalencephalic leukoencephalopathy with subcortical cysts
- megalencephalic leukoencephalopathy with subcortical cysts 2A
- mevalonic aciduria
- mitochondrial DNA depletion syndrome 12a
- mitochondrial DNA depletion syndrome 7
- mitochondrial DNA depletion syndrome 8a
- mitochondrial complex III deficiency nuclear type 1
- mitochondrial complex III deficiency nuclear type 4
- mitochondrial complex IV deficiency nuclear type 11
- mitochondrial complex IV deficiency nuclear type 13
- mitochondrial complex IV deficiency nuclear type 14
- mitochondrial complex IV deficiency nuclear type 18
- mitochondrial complex IV deficiency nuclear type 21
- mitochondrial complex IV deficiency nuclear type 3
- mitochondrial complex IV deficiency nuclear type 7
- mitochondrial complex IV deficiency nuclear type 8
- mitochondrial complex V (ATP synthase) deficiency mitochondrial type 1
- mitochondrial complex V (ATP synthase) deficiency nuclear type 1
- mitochondrial complex V (ATP synthase) deficiency nuclear type 6
- mitochondrial type mitochondrial complex I deficiency 1
- muscular dystrophy-dystroglycanopathy type C8
- myopathy with extrapyramidal signs
- neuroacanthocytosis
- neurodegeneration with brain iron accumulation 2b
- neurodegeneration with brain iron accumulation 3
- neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities
- neurodevelopmental disorder with cerebellar atrophy and motor dysfunction
- neurodevelopmental disorder with eye movement abnormalities and ataxia
- neurodevelopmental disorder with midbrain and hindbrain malformations
- neurodevelopmental disorder with spastic paraplegia and microcephaly
- neuronal ceroid lipofuscinosis 1
- neuronal ceroid lipofuscinosis 2
- neuronal ceroid lipofuscinosis 7
- neuronal intranuclear inclusion disease
- nuclear type mitochondrial complex I deficiency
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- nuclear type mitochondrial complex I deficiency 14
- nuclear type mitochondrial complex I deficiency 16
- nuclear type mitochondrial complex I deficiency 28
- nuclear type mitochondrial complex I deficiency 5
- obsolete Arteriviridae infectious disease
- obsolete Bornaviridae infectious disease
- obsolete Koolen-De Vries syndrome
- obsolete bovine trypanosomiasis
- obsolete canine distemper
- obsolete childhood supratentorial neoplasm
- obsolete congenital disorder of glycosylation type 2m
- obsolete demyelinating encephalopathy
- obsolete infantile onset spinocerebellar ataxia
- obsolete lentiginosis profusa
- obsolete mannosidase deficiency disease
- obsolete mitochondrial disease
- obsolete pediatric central nervous system tumor
- obsolete peripheral dysostosis
- obsolete primitive neuroectodermal tumor with Leptomeningeal Spread
- obsolete sideroblastic anemia with spinocerebellar ataxia
- obsolete spondylosis and allied disorder
- obsolete swine erysipelas
- oculodentodigital dysplasia
- olivopontocerebellar atrophy
- organophosphate-induced delayed polyneuropathy
- pernicious anemia
- peroxisome biogenesis disorder 7A
- posterior fossa group A ependymoma
- posterior fossa group B ependymoma
- primary autosomal recessive microcephaly 15
- primary coenzyme Q10 deficiency 1
- primary coenzyme Q10 deficiency 2
- primary coenzyme Q10 deficiency 3
- primary coenzyme Q10 deficiency 4
- primary coenzyme Q10 deficiency 8
- progressive myoclonus epilepsy 1A
- progressive myoclonus epilepsy 4
- progressive myoclonus epilepsy 9
- purulent labyrinthitis
- pyruvate carboxylase deficiency disease
- sleeping sickness
- spastic ataxia 7
- spinocerebellar ataxia 45
- spinocerebellar ataxia type 14
- spinocerebellar ataxia type 17
- spinocerebellar ataxia type 27
- spinocerebellar ataxia type 30
- spinocerebellar ataxia type 38
- spinocerebellar ataxia type 4
- spinocerebellar ataxia type 7
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