Concept information
Preferred term
Hereditary ataxia (disorder)
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- ARSACS - autosomal recessive spastic ataxia of Charlevoix-Saguenay
- ARSAL - autosomal recessive spastic ataxia with leukoencephalopathy
- Ataxia pancytopenia syndrome
- Ataxia with deafness and intellectual disability syndrome (disorder)
- Ataxia with tapetoretinal degeneration syndrome
- Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome (disorder)
- Autosomal dominant spastic ataxia type 1 (disorder)
- Autosomal recessive ataxia due to ubiquinone deficiency (disorder)
- Autosomal recessive cerebellar ataxia Beauce type (disorder)
- Autosomal recessive cerebellar ataxia due to GBA2 (glucosylceramidase beta 2) deficiency
- Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX (WW domain containing oxidoreductase) deficiency
- Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome (disorder)
- Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 (disorder)
- Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 (disorder)
- Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome
- Autosomal recessive posterior column ataxia and retinitis pigmentosa (disorder)
- Autosomal recessive spastic ataxia type 4
- Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome (disorder)
- Cerebellar ataxia Cayman type (disorder)
- Cerebellar ataxia co-occurrent with ectodermal dysplasia (disorder)
- Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome
- Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder)
- Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome (disorder)
- Childhood-onset spasticity with hyperglycinemia (disorder)
- Congenital cataract with ataxia and deafness syndrome (disorder)
- Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder)
- Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder)
- Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder)
- Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome
- Lethal ataxia-deafness-optic atrophy
- Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome (disorder)
- Leukoencephalopathy with mild cerebellar ataxia and white matter edema
- Myoclonus, cerebellar ataxia, deafness syndrome
- Non-progressive cerebellar ataxia with intellectual disability (disorder)
- Odontoleukodystrophy (disorder)
- Recessive mitochondrial ataxia syndrome (disorder)
- SCAR6 - autosomal recessive spinocerebellar ataxia type 6
- Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome (disorder)
- Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome (disorder)
- Spastic ataxia with congenital miosis
- Spastic paraplegia type 7 (disorder)
- Spectrin-associated autosomal recessive cerebellar ataxia
- Spinocerebellar ataxia
- Spinocerebellar ataxia, amyotrophy, deafness syndrome
- Spinocerebellar ataxia autosomal recessive type 23
- X-linked intellectual disability with ataxia and apraxia syndrome (disorder)
- X-linked neurodegenerative syndrome Bertini type (disorder)
- X-linked non progressive cerebellar ataxia (disorder)
- X-linked progressive cerebellar ataxia
Finding site
Is a
- 363235000
- Ataxia
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/763597000
{{label}}
{{#each values }} {{! loop through ConceptPropertyValue objects }}
{{#if prefLabel }}
{{/if}}
{{/each}}
{{#if notation }}{{ notation }} {{/if}}{{ prefLabel }}
{{#ifDifferentLabelLang lang }} ({{ lang }}){{/ifDifferentLabelLang}}
{{#if vocabName }}
{{ vocabName }}
{{/if}}