Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction   1186734006

SNOMED CT code


SNOMED code1186734006
nameAutosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction
statusactive
date introduced2021-11-30
fully specified name(s)Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (disorder)
synonymsAutosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction
attributes - group1
Pathological processPathological developmental process   308490002
attributes - group4
Clinical courseProgressive   255314001
attributes - group3
Finding siteSpinal cord structure   2748008
Associated morphologyDegenerative abnormality   107669003
attributes - group5
InterpretsIntellectual ability   247573007
Has interpretationImpaired   260379002
attributes - group6
InterpretsAdaptation behavior   406208005
Has interpretationImpaired   260379002
attributes - group7
InterpretsMovement   255324009
attributes - group2
Finding siteRight lower extremity structure   62175007
attributes - group8
Finding siteLeft lower extremity structure   32153003
attributes - group9
Has interpretationAbsent   2667000
InterpretsMovement observable   363847004
parents
  • Intellectual disability   110359009
  • Autosomal recessive hereditary spastic paraplegia   1187279003
  • Chronic metabolic disorder   128289001
  • Complicated hereditary spastic paraplegia   230261006
  • Disorder of lipid metabolism   267431006
  • Developmental hereditary disorder   363070008
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Mental state, behavior and/or psychosocial function finding   384821006
      Behavior finding   844005
        Intellectual disability   110359009
          Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction   1186734006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Autosomal recessive hereditary spastic paraplegia   1187279003
                Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction   1186734006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Chronic disease   27624003
        Chronic metabolic disorder   128289001
          Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction   1186734006

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 recessive complex spastic paraplegia due to Kennedy pathway dysfunction   1186734006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of lipoprotein AND/OR lipid metabolism   48286001
          Disorder of lipid metabolism   267431006
            Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction   1186734006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction   1186734006

ancestors
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