Spinocerebellar ataxia   129609000

SNOMED CT code


SNOMED code129609000
nameSpinocerebellar ataxia
statusactive
date introduced2002-01-31
fully specified name(s)Spinocerebellar ataxia (disorder)
synonymsSpinocerebellar ataxia
attributes - group2
Associated morphologyDegenerative abnormality   107669003
Finding siteSpinal cord structure   2748008
attributes - group1
Associated morphologyDegenerative abnormality   107669003
Finding siteCerebellar structure   113305005
parents
children
  • Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome   1187643003
  • Adult-onset autosomal recessive cerebellar ataxia   785302009
  • Amyotrophic lateral sclerosis with spinocerebellar ataxia   1259129005
  • ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis   789657008
  • Autosomal recessive cerebellar ataxia due to STUB1 deficiency   782719004
  • Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUBCN deficiency   782721009
  • Autosomal recessive cerebellar ataxia, psychomotor delay syndrome   783060009
  • Autosomal recessive cerebelloparenchymal disorder type 3   715369006
  • Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome   1204415006
  • Azorean disease   91952008
  • Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia   785301002
  • Corneal cerebellar syndrome   720750004
  • Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome   771469002
  • Infantile onset spinocerebellar ataxia   724227000
  • PUM1-associated developmental disability, ataxia, seizure syndrome   1260097007
  • Richards-Rundle syndrome   715415005
  • Spinocerebellar ataxia due to vitamin E deficiency   1186850007
  • Spinocerebellar ataxia dysmorphism syndrome   733033001
  • Spinocerebellar ataxia type 1   715748006
  • Spinocerebellar ataxia type 10   715754007
  • Spinocerebellar ataxia type 11   719207000
  • Spinocerebellar ataxia type 12   719208005
  • Spinocerebellar ataxia type 13   719209002
  • Spinocerebellar ataxia type 14   719210007
  • Spinocerebellar ataxia type 15/16   716724006
  • Spinocerebellar ataxia type 17   719249005
  • Spinocerebellar ataxia type 18   719250005
  • Spinocerebellar ataxia type 19   719251009
  • Spinocerebellar ataxia type 2   715751004
  • Spinocerebellar ataxia type 20   718771009
  • Spinocerebellar ataxia type 21   718774001
  • Spinocerebellar ataxia type 23   718772002
  • Spinocerebellar ataxia type 25   718770005
  • Spinocerebellar ataxia type 26   718769009
  • Spinocerebellar ataxia type 27   719252002
  • Spinocerebellar ataxia type 28   715824008
  • Spinocerebellar ataxia type 29   715825009
  • Spinocerebellar ataxia type 30   719253007
  • Spinocerebellar ataxia type 31   715826005
  • Spinocerebellar ataxia type 32   719254001
  • Spinocerebellar ataxia type 34   719255000
  • Spinocerebellar ataxia type 35   719300001
  • Spinocerebellar ataxia type 36   711158005
  • Spinocerebellar ataxia type 37   719301002
  • Spinocerebellar ataxia type 38   734021001
  • Spinocerebellar ataxia type 4   715755008
  • Spinocerebellar ataxia type 40   734020000
  • Spinocerebellar ataxia type 41   1208512000
  • Spinocerebellar ataxia type 42   1208513005
  • Spinocerebellar ataxia type 43   1208516002
  • Spinocerebellar ataxia type 45   1279840000
  • Spinocerebellar ataxia type 46   1279839002
  • Spinocerebellar ataxia type 5   719302009
  • Spinocerebellar ataxia type 6   715752006
  • Spinocerebellar ataxia type 7   715726000
  • Spinocerebellar ataxia type 8   715753001
  • Spinocerebellar ataxia with axonal neuropathy type 1   765091006
  • X-linked sideroblastic anemia with spinocerebellar ataxia   719816006
  • X-linked spinocerebellar ataxia type 3   719817002
  • X-linked spinocerebellar ataxia type 4   719818007
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Degenerative disease of the central nervous system   80690008
          Hereditary degenerative disease of central nervous system   106018006
            Hereditary cerebellar degeneration   37650008
              Spinocerebellar ataxia   129609000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of coordination   298314008
      Ataxia   20262006
        Hereditary ataxia   763597000
          Spinocerebellar ataxia   129609000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of coordination   298314008
      Ataxia   20262006
        Cerebellar ataxia   85102008
          Spinocerebellar ataxia   129609000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Finding of brain   299718000
        Disorder of brain   81308009
          Cerebellar disorder   223176004
            Spinocerebellar disease   91502009
              Spinocerebellar ataxia   129609000

ancestors
sorted most to least specific
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