Spinocerebellar ataxia type 13   719209002

SNOMED CT code


SNOMED code719209002
nameSpinocerebellar ataxia type 13
statusactive
date introduced2017-01-31
fully specified name(s)Spinocerebellar ataxia type 13 (disorder)
synonymsSpinocerebellar ataxia type 13
attributes - group2
Associated morphologyDegenerative abnormality   107669003
Finding siteCerebellar structure   113305005
attributes - group1
Finding siteSpinal cord structure   2748008
Associated morphologyDegenerative abnormality   107669003
parents
  • Autosomal dominant hereditary disorder   11164009
  • Spinocerebellar ataxia   129609000
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
              Spinocerebellar ataxia type 13   719209002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of coordination   298314008
      Ataxia   20262006
        Hereditary ataxia   763597000
          Spinocerebellar ataxia   129609000
            Spinocerebellar ataxia type 13   719209002

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.