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

SNOMED CT code


SNOMED code37650008
nameHereditary cerebellar degeneration
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary cerebellar degeneration (disorder)
synonymsHereditary cerebellar degeneration
attributes - group1
Associated morphologyDegenerative abnormality   107669003
Finding siteCerebellar structure   113305005
parents
  • Hereditary degenerative disease of central nervous system   106018006
  • Cerebellar degeneration   95646004
children
  • Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome   722293005
  • Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency   770898002
  • Friedreich ataxia   10394003
  • Hereditary cerebellar atrophy   431641000124107
  • Infantile cerebellar and retinal degeneration   782822006
  • Myoclonic epilepsy myopathy sensory ataxia   699328003
  • Spinocerebellar ataxia   129609000
  • Spinocerebellar ataxia type 5   138191000119100  removed: 2017-03-01
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

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Finding of brain   299718000
        Disorder of brain   81308009
          Cerebellar disorder   223176004
            Cerebellar degeneration   95646004
              Hereditary cerebellar degeneration   37650008

ancestors
sorted most to least specific
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