Inborn errors of metabolism marker   259357003

SNOMED CT code


SNOMED code259357003
nameInborn errors of metabolism marker
statusactive
date introduced2002-01-31
fully specified name(s)Inborn errors of metabolism marker (substance)
synonymsInborn errors of metabolism marker
parentsBody substance   91720002
children
  • Amino acid metabolism disorder marker   259358008
  • Carbohydrate metabolism disorder marker   259381005
  • Glycoprotein and mucolipid storage disease marker   259398005
  • Glycosaminoglycanoses marker   259449002
  • Lactic acidemia and mitochondrial disorder marker   259413003
  • Lipoprotein and neutral lipid disorder marker   259417002
  • Long-chain-alcohol dehydrogenase   88689003
  • Lysosomal storage disease marker   259428003
  • Mitochondrial adenosine triphosphate synthase subunit c   259538006
  • Organic acid metabolism disorder marker   259456008
  • Peroxisomal disorder marker   259485002
  • Phosphoethanolamine pyrophosphate   259540001
  • Porphyrin and heme metabolism disorder marker   259495009
  • Propionate and methylmalonate metabolism disorder marker   259508000
  • Purine and pyrimidine metabolism disorder marker   259515008
  • Steroid metabolism disorder marker   259532007
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Substance   105590001
    Body substance   91720002
      Inborn errors of metabolism marker   259357003

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.