SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal dominant hereditary disorder  11164009

Autosomal dominant hereditary spastic paraplegia   737227004

SNOMED CT code


SNOMED code737227004
nameAutosomal dominant hereditary spastic paraplegia
statusactive
date introduced2018-01-31
fully specified name(s)Autosomal dominant hereditary spastic paraplegia (disorder)
synonymsAutosomal dominant hereditary spastic paraplegia
attributes - group2
Clinical courseProgressive   255314001
attributes - group3
Finding siteSpinal cord structure   2748008
Associated morphologyDegenerative abnormality   107669003
attributes - group4
InterpretsMovement   255324009
attributes - group5
Finding siteRight lower extremity structure   62175007
attributes - group6
Finding siteLeft lower extremity structure   32153003
attributes - group1
InterpretsMovement observable   363847004
Has interpretationAbsent   2667000
parents
  • Autosomal dominant hereditary disorder   11164009
  • Hereditary spastic paraplegia   39912006
children
  • Autosomal dominant complex hereditary spastic paraplegia   1259038005
  • Autosomal dominant spastic paraplegia type 10   732948003
  • Autosomal dominant spastic paraplegia type 12   763374004
  • Autosomal dominant spastic paraplegia type 13   783698005
  • Autosomal dominant spastic paraplegia type 19   763375003
  • Autosomal dominant spastic paraplegia type 3   782670003
  • Autosomal dominant spastic paraplegia type 31   763068005
  • Autosomal dominant spastic paraplegia type 37   763369007
  • Autosomal dominant spastic paraplegia type 4   723820001
  • Autosomal dominant spastic paraplegia type 41   763069002
  • Autosomal dominant spastic paraplegia type 42   763070001
  • Autosomal dominant spastic paraplegia type 6   732949006
  • Autosomal dominant spastic paraplegia type 73   1187468005
  • Autosomal dominant spastic paraplegia type 8   785305006
  • Autosomal dominant spastic paraplegia type 9B   1187466009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Autosomal dominant hereditary spastic paraplegia   737227004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Disorder of the central nervous system   23853001
        Spastic syndrome   386781001
          Spastic paraplegia   192967009
            Hereditary spastic paraplegia   39912006
              Autosomal dominant hereditary spastic paraplegia   737227004

ancestors
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cpt crosswalks

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