SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Chromosomal disorder  409709004

Congenital chromosomal disease  74345006

Anomaly of chromosome pair  362984008

Anomaly of chromosome pair 6   44710007

SNOMED CT code


SNOMED code44710007
nameAnomaly of chromosome pair 6
statusactive
date introduced2002-01-31
fully specified name(s)Anomaly of chromosome pair 6 (disorder)
synonymsAnomaly of chromosome pair 6
attributes - group1
OccurrenceCongenital   255399007
Associated morphologyCellular AND/OR subcellular abnormality   107673000
Finding siteChromosome pair 6   45202000
parentsAnomaly of chromosome pair   362984008
children
  • Deletion of part of chromosome 6   726374009
  • Maternal uniparental disomy of chromosome 6   766239009
  • Partial trisomy of chromosome 6   726345000
  • Paternal uniparental disomy of chromosome 6   770670003
  • Ring chromosome 6 syndrome   765488003
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Chromosomal disorder   409709004
        Congenital chromosomal disease   74345006
          Anomaly of chromosome pair   362984008
            Anomaly of chromosome pair 6   44710007

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.