Hyperprolinemia type 2   717181004

SNOMED CT code


SNOMED code717181004
nameHyperprolinemia type 2
statusactive
date introduced2016-07-31
fully specified name(s)Hyperprolinemia type 2 (disorder)
synonyms
  • Hyperprolinemia type 2
  • Hyperprolinaemia type 2
  • Hyperprolinemia type II
  • Hyperprolinaemia type II
attributes - group1
Due toDeficiency of pyrroline-5-carboxylate reductase   124177001
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of acid-base balance   26436007
          Acidemia   70731005
            Aminoacidemia   46556004
              Hyperprolinemia   59655002
                Hyperprolinemia type 2   717181004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Hyperprolinemia type 2   717181004

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.