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

Complicated hereditary spastic paraplegia  230261006

Autosomal dominant complex hereditary spastic paraplegia   1259038005

SNOMED CT code


SNOMED code1259038005
nameAutosomal dominant complex hereditary spastic paraplegia
statusactive
date introduced2022-12-31
fully specified name(s)Autosomal dominant complex hereditary spastic paraplegia (disorder)
synonymsAutosomal dominant complex hereditary spastic paraplegia
attributes - group3
Clinical courseProgressive   255314001
attributes - group6
InterpretsMovement   255324009
attributes - group4
Finding siteLeft lower extremity structure   32153003
attributes - group5
Finding siteRight lower extremity structure   62175007
attributes - group2
InterpretsMovement observable   363847004
Has interpretationAbsent   2667000
attributes - group1
Finding siteSpinal cord structure   2748008
Associated morphologyDegenerative abnormality   107669003
parents
  • Complicated hereditary spastic paraplegia   230261006
  • Autosomal dominant hereditary spastic paraplegia   737227004
children
  • Autosomal dominant spastic paraplegia type 17   230263009
  • Autosomal dominant spastic paraplegia type 29   733029008
  • Autosomal dominant spastic paraplegia type 36   723819007
  • Autosomal dominant spastic paraplegia type 38   783622001
  • Autosomal dominant spastic paraplegia type 9A   1187465008
  • Spastic paraplegia with Paget disease of bone syndrome   726622002
  • Spastic paraplegia with precocious puberty syndrome   732958004
  • Spastic paraplegia, intellectual disability, nystagmus, obesity syndrome   1260134001
  • Spastic paraplegia, nephritis, deafness syndrome   733089005
  • Spastic paraplegia, neuropathy, poikiloderma syndrome   763402002
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
        Spastic syndrome   386781001
          Spastic paraplegia   192967009
            Hereditary spastic paraplegia   39912006
              Complicated hereditary spastic paraplegia   230261006
                Autosomal dominant complex hereditary spastic paraplegia   1259038005

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
                Autosomal dominant complex hereditary spastic paraplegia   1259038005

ancestors
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