Frontotemporal dementia due to VCP mutation   1260353004

SNOMED CT code


SNOMED code1260353004
nameFrontotemporal dementia due to VCP mutation
statusactive
date introduced2023-02-28
fully specified name(s)Frontotemporal dementia due to VCP mutation (disorder)
synonyms
  • Frontotemporal dementia due to valosin containing protein mutation
  • Frontotemporal dementia due to VCP mutation
attributes - group3
Due toAnomaly of chromosome pair 9   5051002
attributes - group1
Finding siteTemporal lobe structure   78277001
Associated morphologyDegenerative abnormality   107669003
attributes - group2
Finding siteFrontal lobe structure   83251001
Associated morphologyDegenerative abnormality   107669003
attributes - group4
InterpretsCognitive functions   311465003
Has interpretationImpaired   260379002
parents
  • Cerebral degeneration associated with another disorder   192794001
  • Frontotemporal dementia   230270009
  • Dementia due to chromosomal anomaly   722980006
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Disorder of the central nervous system   23853001
        Central nervous system complication   87536007
          Cerebral degeneration associated with another disorder   192794001
            Frontotemporal dementia due to VCP mutation   1260353004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of head and neck region   118254002
      Head finding   406122000
        Finding of head region   298364001
          Frontotemporal degeneration   230273006
            Frontotemporal dementia   230270009
              Frontotemporal dementia due to VCP mutation   1260353004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Disorder of the central nervous system   23853001
        Central nervous system complication   87536007
          Dementia associated with another disease   191519005
            Dementia due to chromosomal anomaly   722980006
              Frontotemporal dementia due to VCP mutation   1260353004

ancestors
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