Spastic paraplegia, nephritis, deafness syndrome   733089005

SNOMED CT code


SNOMED code733089005
nameSpastic paraplegia, nephritis, deafness syndrome
statusactive
date introduced2017-07-31
fully specified name(s)Spastic paraplegia, nephritis, deafness syndrome (disorder)
synonyms
  • Spastic paraplegia, nephritis, deafness syndrome
  • Fitzsimmons Watson Mellor syndrome
attributes - group5
Associated morphologyDegenerative abnormality   107669003
Finding siteSpinal cord structure   2748008
OccurrenceCongenital   255399007
attributes - group4
InterpretsHearing   47078008
attributes - group7
OccurrenceCongenital   255399007
Finding siteKidney structure   64033007
attributes - group9
OccurrenceCongenital   255399007
Finding siteLower limb structure   61685007
attributes - group6
OccurrenceCongenital   255399007
Finding siteEar structure   117590005
parents
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
              Spastic paraplegia, nephritis, deafness syndrome   733089005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital paraplegia   192949002
          Hereditary spastic paraplegia   39912006
            Complicated hereditary spastic paraplegia   230261006
              Spastic paraplegia, nephritis, deafness syndrome   733089005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Clinical history and observation findings   250171008
      Functional finding   118228005
        Hearing finding   118230007
          Hearing disorder   128540005
            Hearing loss   15188001
              Hearing loss associated with syndrome   232333009
                Spastic paraplegia, nephritis, deafness syndrome   733089005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Disorder by body site   123946008
        Disorder of head   118934005
          Disorder of ear   25906001
            Spastic paraplegia, nephritis, deafness syndrome   733089005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Ear and auditory finding   118236001
        Disorder of auditory system   362966006
          Auditory system hereditary disorder   362991006
            Spastic paraplegia, nephritis, deafness syndrome   733089005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Hereditary disorder by system   363137000
            Hereditary disorder of the urinary system   363338001
              Hereditary nephropathy   367591000119105
                Spastic paraplegia, nephritis, deafness syndrome   733089005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital hearing disorder   95827002
          Congenital sensorineural hearing loss   700453005
            Spastic paraplegia, nephritis, deafness syndrome   733089005

ancestors
sorted most to least specific
cpt crosswalks

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.

Access to this feature is available in the following products:
  • CPT® to SNOMED Crosswalks

demo
request yours today
subscribe
start today
newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.