Cystic fibrosis due to heterozygous deltaF508 mutation   1296527009

SNOMED CT code


SNOMED code1296527009
nameCystic fibrosis due to heterozygous deltaF508 mutation
statusactive
date introduced2023-12-01
fully specified name(s)Cystic fibrosis due to heterozygous deltaF508 mutation (disorder)
synonyms
  • Cystic fibrosis due to heterozygous deltaF508 mutation
  • DeltaF508 heterozygous mucoviscidosis
  • DeltaF508 heterozygous cystic fibrosis
attributes - group2
Finding siteRespiratory tract structure   321667001
attributes - group1
InterpretsMucociliary clearance   63533009
Has interpretationImpaired   260379002
parentsCystic fibrosis   190905008
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Functional finding   118228005
      Mucociliary clearance defect   233660001
        Inherited mucociliary clearance defect   233661002
          Cystic fibrosis   190905008
            Cystic fibrosis due to heterozygous deltaF508 mutation   1296527009

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.