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

SNOMED CT code


SNOMED code722980006
nameDementia due to chromosomal anomaly
statusactive
date introduced2017-01-31
fully specified name(s)Dementia due to chromosomal anomaly (disorder)
synonymsDementia due to chromosomal anomaly
attributes - group1
InterpretsCognitive functions   311465003
Has interpretationImpaired   260379002
attributes - group2
Due toChromosomal disorder   409709004
attributes - group3
Finding siteBrain structure   12738006
parentsDementia associated with another disease   191519005
children
  • Dementia due to fragile X syndrome   1259473000
  • Dementia with Down syndrome   733194007
  • Frontotemporal dementia due to C9orf72 mutation   1260354005
  • Frontotemporal dementia due to FUS mutation   1260355006
  • Frontotemporal dementia due to TARDBP mutation   1260352009
  • Frontotemporal dementia due to VCP mutation   1260353004
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
          Dementia associated with another disease   191519005
            Dementia due to chromosomal anomaly   722980006

ancestors
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Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts.  Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

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