SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Chromosomal disorder  409709004

Congenital chromosomal disease  74345006

Anomaly of chromosome pair  362984008

Anomaly of sex chromosome  95462004

Sex chromosome abnormality - female phenotype   254277006

SNOMED CT code


SNOMED code254277006
nameSex chromosome abnormality - female phenotype
statusactive
date introduced2002-01-31
fully specified name(s)Sex chromosome abnormality - female phenotype (disorder)
synonymsSex chromosome abnormality - female phenotype
attributes - group1
OccurrenceCongenital   255399007
Associated morphologyCellular AND/OR subcellular abnormality   107673000
Finding siteSex chromosome   32247007
parentsAnomaly of sex chromosome   95462004
children
  • [X]Other specified sex chromosome abnormalities, female phenotype   205994000  removed: 2009-01-31
  • Female with more than three X chromosomes   254282004
  • Mosaicism - lines with various numbers of X chromosomes   254283009
  • Trisomy X syndrome   35111009
  • Turner syndrome   38804009
  • XY females   8234004
  • XY, female phenotype   205693008
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 sex chromosome   95462004
              Sex chromosome abnormality - female phenotype   254277006

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.