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SNOMED CT Concept 64572001 and Descendents

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This value set includes content from SNOMED CT, which is copyright © 2002+ International Health Terminology Standards Development Organisation (IHTSDO), and distributed by agreement between IHTSDO and HL7. Implementer use of SNOMED CT is not covered by this agreement

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Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUBCN deficiency

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Acute cerebellar ataxia caused by varicella

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Ataxia co-occurrent and due to abetalipoproteinaemia

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Ataxia with tapetoretinal degeneration syndrome

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Ataxia, photosensitivity, short stature syndrome

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Cerebellar ataxia and ectodermal dysplasia

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Cerebral paralysis with homolateral ataxia

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Cerebral paresis with homolateral ataxia

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Myoclonic epilepsy myopathy sensory ataxia

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Myoclonus, cerebellar ataxia, deafness syndrome

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Progressive cerebellar ataxia with hypogonadism

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Progressive myoclonus epilepsy with ataxia

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Acquired ataxia due to vitamin deficiency

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Amyotrophic lateral sclerosis with spinocerebellar ataxia

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Ataxia as sequela of cerebrovascular accident

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Ataxia as sequela of cerebrovascular disease

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Autosomal dominant cerebellar ataxia type 2

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Autosomal dominant spastic ataxia type 1

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Autosomal recessive cerebellar ataxia Beauce type

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Autosomal recessive spastic ataxia with leucoencephalopathy

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Cerebellar ataxia associated with another disorder

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Chorea due to ataxia telangiectasia syndrome

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Dilated cardiomyopathy due to Friedreich's ataxia

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Dystonia due to ataxia telangiectasia syndrome

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Early onset cerebellar ataxia with hypogonadism

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Early onset cerebellar ataxia with myoclonus

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Fragile X associated tremor ataxia syndrome

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Hypertrophic cardiomyopathy due to Friedreich ataxia

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Neuropathy in association with hereditary ataxia

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Progressive cerebellar ataxia with palatal myoclonus

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X-linked non progressive cerebellar ataxia

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Ataxia co-occurrent and due to phytanic acid storage disease

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Ataxia as sequela of embolic cerebrovascular accident

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Ataxia as sequela of haemorrhagic cerebrovascular accident

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Ataxia due to disorder of immune function

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Ataxia with deafness and intellectual disability syndrome

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Autosomal recessive ataxia due to ubiquinone deficiency

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Autosomal recessive cerebellar ataxia, psychomotor delay syndrome

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Autosomal recessive spastic ataxia of Charlevoix-Saguenay

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Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome

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Cerebellar ataxia with oculomotor apraxia type 4

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Congenital cataract with ataxia and deafness syndrome

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Congenital cerebellar ataxia due to RNU12 mutation

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Early onset cerebellar ataxia with essential tremor

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Intellectual disability, hyperkinetic movement, truncal ataxia syndrome

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Progressive spinocerebellar ataxia with decreased tendon reflexes

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Progressive spinocerebellar ataxia with retained tendon reflexes

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Spastic ataxia, dysarthria due to glutaminase deficiency

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Spinocerebellar ataxia due to vitamin E deficiency

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Spinocerebellar ataxia with axonal neuropathy type 1

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Sporadic adult-onset ataxia of unknown aetiology

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X-linked sideroblastic anaemia with spinocerebellar ataxia

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Ataxia due to and following ischaemic cerebrovascular accident

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Ataxia due to multiple system atrophy, cerebellar variant

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Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome

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Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency

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Autosomal recessive cerebellar ataxia due to STUB1 deficiency

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Autosomal recessive cerebellar ataxia with late-onset spasticity

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Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome

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Autosomal recessive posterior column ataxia and retinitis pigmentosa

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Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome

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Benign paroxysmal tonic upgaze of childhood with ataxia

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Early onset cerebellar ataxia with retained tendon reflexes

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Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome

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Infantile-onset autosomal recessive non progressive cerebellar ataxia

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Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus

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Paroxysmal dystonic choreoathetosis with episodic ataxia and spasticity

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Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome

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Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1

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Ataxia due to chronic infection of central nervous system

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Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2

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Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

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Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome

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Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome

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Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome

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Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome

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X-linked intellectual disability with ataxia and apraxia syndrome

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Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome

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Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency

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Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency

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Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome

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Autosomal recessive cerebelloparenchymal disorder type 3

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Autosomal recessive spastic paraplegia type 58

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Early onset cerebellar ataxia with retinitis pigmentosa and optic atrophy

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Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome

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Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome

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Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome

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Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome

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Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goitre, and primary gonadal insufficiency

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Joubert syndrome with congenital hepatic fibrosis

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Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome