Hereditary spastic paraplegia   39912006

SNOMED CT code


SNOMED code39912006
nameHereditary spastic paraplegia
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary spastic paraplegia (disorder)
synonyms
  • HSP - Hereditary spastic paraplegia
  • Spastic congenital paraplegia
  • Hereditary spastic paraplegia
  • Strumpell-Lorrain disease
  • Familial spastic paraplegia syndrome
attributes - group2
Clinical courseProgressive   255314001
attributes - group3
Finding siteSpinal cord structure   2748008
Associated morphologyDegenerative abnormality   107669003
attributes - group6
InterpretsMovement   255324009
attributes - group4
Finding siteRight lower extremity structure   62175007
attributes - group5
Finding siteLeft lower extremity structure   32153003
attributes - group1
InterpretsMovement observable   363847004
Has interpretationAbsent   2667000
parents
children
  • Autosomal dominant hereditary spastic paraplegia   737227004
  • Autosomal recessive hereditary spastic paraplegia   1187279003
  • Autosomal spastic paraplegia type 30   763377006
  • Complicated hereditary spastic paraplegia   230261006
  • Hereditary sensory-motor neuropathy, type V   76043009  removed: 2020-01-31
  • Pure hereditary spastic paraplegia   230260007
  • X-linked hereditary spastic paraplegia   724775006
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Degenerative disease of the central nervous system   80690008
          Hereditary degenerative disease of central nervous system   106018006
            Hereditary spastic paraplegia   39912006

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

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Chronic disease   27624003
        Chronic nervous system disorder   128283000
          Chronic myelopathy   434371000124108
            Hereditary spastic paraplegia   39912006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Chronic disease   27624003
        Chronic nervous system disorder   128283000
          Chronic paraplegia   698292000
            Hereditary spastic paraplegia   39912006

ancestors
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cpt crosswalks

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