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 genetic disease   1259476008

SNOMED CT code


SNOMED code1259476008
nameDementia due to genetic disease
statusactive
date introduced2023-01-31
fully specified name(s)Dementia due to genetic disease (disorder)
synonymsDementia due to genetic disease
attributes - group2
Finding siteBrain structure   12738006
attributes - group1
InterpretsCognitive functions   311465003
Has interpretationImpaired   260379002
attributes - group3
Due toGenetic disease   782964007
parentsDementia associated with another disease   191519005
children
  • Dementia due to atypical pantothenate kinase associated neurodegeneration   1259679007
  • Dementia due to classical pantothenate kinase associated neurodegeneration   1259990004
  • Dementia due to familial Creutzfeldt-Jakob disease   1259478009
  • Dementia due to fatal familial insomnia   1259480003
  • Dementia due to fragile X syndrome   1259473000
  • Dementia due to Gerstmann Straussler Scheinker syndrome   1259469003
  • Dementia due to Huntington chorea   442344002
  • Dementia due to Rett syndrome   130121000119104
  • Dementia due to Wilson disease   1259511006
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 genetic disease   1259476008

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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