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 21  70156005

Complete monosomy 21   78740005

SNOMED CT code


SNOMED code78740005
nameComplete monosomy 21
statusactive
date introduced2002-01-31
fully specified name(s)Complete monosomy 21 (disorder)
synonymsComplete monosomy 21
attributes - group1
OccurrenceCongenital   255399007
Finding siteChromosome pair 21   43009003
Associated morphologyMonosomy   86277003
parents
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 21   70156005
              Complete monosomy 21   78740005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Chromosomal disorder   409709004
        Congenital chromosomal disease   74345006
          Anomaly of chromosome pair   362984008
            Monosomy and deletion from autosome   205627002
              Complete monosomy of autosome   726364006
                Complete monosomy 21   78740005

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.