Vanishing white matter disease   447351004

SNOMED CT code


SNOMED code447351004
nameVanishing white matter disease
statusactive
date introduced2011-01-31
fully specified name(s)Vanishing white matter disease (disorder)
synonyms
  • Vanishing white matter disease
  • Myelinosis centralis diffusa
  • Childhood ataxia with diffuse central nervous system hypomyelination
  • CACH (childhood ataxia with diffuse central nervous system hypomyelination) syndrome
  • Leucoencephalopathy with vanishing white matter
  • Leukoencephalopathy with vanishing white matter
attributes - group1
Associated morphologyMyelin sheath alteration   125495003
Finding siteMyelinated nerve fiber structure   54115001
attributes - group2
Finding siteCerebral white matter structure   68523003
Associated morphologyDystrophy   4720007
parents
childrenOvarioleukodystrophy   1156768008
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
            Vanishing white matter disease   447351004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Neurological lesion   299735001
      Leukodystrophy   192781003
        Vanishing white matter disease   447351004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of head and neck region   118254002
      Head finding   406122000
        Finding of head region   298364001
          Leukoencephalopathy   22811006
            Vanishing white matter disease   447351004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Degenerative disease of the central nervous system   80690008
          Degenerative brain disorder   52522001
            Cerebral degeneration   418143002
              Vanishing white matter disease   447351004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of coordination   298314008
      Ataxia   20262006
        Hereditary ataxia   763597000
          Vanishing white matter disease   447351004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Vanishing white matter disease   447351004

ancestors
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