Cerebellar ataxia   85102008

SNOMED CT code


SNOMED code85102008
nameCerebellar ataxia
statusactive
date introduced2002-01-31
fully specified name(s)Cerebellar ataxia (disorder)
synonyms
  • Cerebellar ataxia
  • Cerebellar ataxia (loss of muscle coordination)
attributes - group1
Finding siteCerebellar structure   113305005
parents
children
  • Acute cerebellar ataxia   434311000124104
  • Acute cerebellar ataxia caused by varicella   24059009
  • Ataxia pancytopenia syndrome   768556005
  • Ataxia with deafness and intellectual disability syndrome   720517001
  • Ataxia with tapetoretinal degeneration syndrome   783203003
  • Autosomal dominant cerebellar ataxia type 2   1156796002
  • Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome   722293005
  • Autosomal recessive ataxia due to ubiquinone deficiency   725394006
  • Autosomal recessive cerebellar ataxia Beauce type   725433003
  • Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency   1237625002
  • Autosomal recessive cerebellar ataxia with late-onset spasticity   763348005
  • Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1   715366004
  • Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2   725408001
  • Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome   766814006
  • Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency   773498006
  • Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency   770898002
  • Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome   763312008
  • Autosomal recessive spastic ataxia with leukoencephalopathy   784343003
  • Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome   784347002
  • Boucher Neuhäuser syndrome   715984007
  • Cerebellar ataxia and ectodermal dysplasia   715371006
  • Cerebellar ataxia associated with another disorder   192874000
  • Cerebellar ataxia caused by chemical   1268825008
  • Cerebellar ataxia Cayman type   717332007
  • Cerebellar ataxia due to toxin   230243002  removed: 2023-03-31
  • Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome   1236804009
  • Cerebellar ataxia with oculomotor apraxia type 4   1217230002
  • Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome   763344007
  • Christianson syndrome   702354007
  • CLCN2-related leukoencephalopathy   768663003
  • Congenital cerebellar ataxia due to RNU12 mutation   1177169004
  • Dentatorubropallidoluysian degeneration   68116008
  • Drug-induced cerebellar ataxia   230242007
  • Dyssynergia cerebellaris myoclonica   73495003
  • Early onset cerebellar ataxia   230227009
  • Episodic ataxia type 3   718755009
  • Episodic ataxia type 4   718754008
  • Episodic ataxia type 5   718756005
  • Episodic ataxia type 6   718753002
  • Episodic ataxia type 7   718752007
  • Fragile X associated tremor ataxia syndrome   448045004
  • Friedreich ataxia   10394003
  • Gemignani syndrome   782690007
  • Gillespie syndrome   253176002
  • Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum   724283004
  • Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome   721846006
  • Infantile-onset autosomal recessive non progressive cerebellar ataxia   785300001
  • Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome   1237514002
  • Myoclonus, cerebellar ataxia, deafness syndrome   733065003
  • Non-progressive cerebellar ataxia with intellectual disability   723441001
  • Nothnagel's syndrome   32680009
  • Olivopontocerebellar degeneration   67761004
  • Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome   1237413006
  • Progressive spinocerebellar ataxia with retained tendon reflexes   230238009
  • Saldino-Mainzer dysplasia   254092004
  • Sanger-Brown cerebellar ataxia   37960002
  • Spinocerebellar ataxia   129609000
  • Sporadic adult-onset ataxia of unknown etiology   734023003
  • X-linked non progressive cerebellar ataxia   766818009
  • X-linked progressive cerebellar ataxia   827172005
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of coordination   298314008
      Ataxia   20262006
        Cerebellar ataxia   85102008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Finding of brain   299718000
        Disorder of brain   81308009
          Cerebellar disorder   223176004
            Cerebellar ataxia   85102008

ancestors
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