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 1   74769007

SNOMED CT code


SNOMED code74769007
nameAnomaly of chromosome pair 1
statusactive
date introduced2002-01-31
fully specified name(s)Anomaly of chromosome pair 1 (disorder)
synonymsAnomaly of chromosome pair 1
attributes - group1
OccurrenceCongenital   255399007
Associated morphologyCellular AND/OR subcellular abnormality   107673000
Finding siteChromosome pair 1   46507000
parentsAnomaly of chromosome pair   362984008
children
  • Deletion of part of chromosome 1   726365007
  • Maternal uniparental disomy of chromosome 1   770562000
  • Mosaic trisomy 1 syndrome   829974003
  • Partial trisomy of chromosome 1   726338000
  • Paternal uniparental disomy of chromosome 1   766719006
  • Ring chromosome 1 syndrome   47017007
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 1   74769007

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.