Ataxia
Hereditary disorder of nervous system
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Hereditary ataxia (disorder)
Hereditary ataxia
hereditaire ataxie
erfelijke coördinatiestoornis
Id763597000
StatusDefined
Finding siteStructure of nervous system
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetG11.9
RuleTRUE
AdviceALWAYS G11.9
CorrelationSNOMED CT source code to target map code correlation not specified
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Arts syndrome
Ataxia co-occurrent and due to abetalipoproteinemia
Ataxia co-occurrent and due to phytanic acid storage disease
Ataxia pancytopenia syndrome
Ataxia with deafness and intellectual disability syndrome
Ataxia with tapetoretinal degeneration syndrome
Autosomal dominant cerebellar ataxia type 2
Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome
Autosomal dominant spastic ataxia type 1
Autosomal recessive ataxia due to ubiquinone deficiency
Autosomal recessive cerebellar ataxia Beauce type
Autosomal recessive cerebellar ataxia with late-onset spasticity
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2
Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency
Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome
Autosomal recessive posterior column ataxia and retinitis pigmentosa
Autosomal recessive spastic ataxia of Charlevoix-Saguenay
Autosomal recessive spastic ataxia with leukoencephalopathy
Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome
Boucher Neuhäuser syndrome
CAMOS syndrome
Cerebellar ataxia and ectodermal dysplasia
Cerebellar ataxia Cayman type
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome
Cerebellar ataxia with oculomotor apraxia type 4
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome
Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome
Childhood-onset spasticity with hyperglycinemia
Christianson syndrome
CLCN2-related leukoencephalopathy
Congenital cataract with ataxia and deafness syndrome
Congenital cerebellar ataxia due to RNU12 mutation
Dentatorubropallidoluysian degeneration1
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome
Episodic ataxia9
Fragile X associated tremor ataxia syndrome
Gemignani syndrome
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome
Infantile-onset autosomal recessive non progressive cerebellar ataxia
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome
Intellectual disability, hyperkinetic movement, truncal ataxia syndrome
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome
Marinesco-Sjögren syndrome
Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus
Myoclonus, cerebellar ataxia, deafness syndrome
Neuhauser Eichner Opitz syndrome
Neuropathy in association with hereditary ataxia
NKX6-2-related autosomal recessive hypomyelinating leukodystrophy
Non-progressive cerebellar ataxia with intellectual disability
Odontoleukodystrophy
Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome
Progressive cerebellar ataxia with hypogonadism
Recessive mitochondrial ataxia syndrome
Saldino-Mainzer dysplasia
Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome
Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome
Spastic ataxia with congenital miosis
Spastic paraplegia type 7
Spectrin-associated autosomal recessive cerebellar ataxia
Spinocerebellar ataxia57
Vanishing white matter disease1
X-linked intellectual disability with ataxia and apraxia syndrome
X-linked neurodegenerative syndrome Bertini type
X-linked non progressive cerebellar ataxia
X-linked progressive cerebellar ataxia