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

Anomaly of chromosome X  111312006

Turner syndrome  38804009

Turner's phenotype, other variant karyotypes   268298003

SNOMED CT code


SNOMED code268298003
nameTurner's phenotype, other variant karyotypes
statusremoved
date introduced2002-01-31
date removed2010-01-31
fully specified name(s)Turner's phenotype, other variant karyotypes (disorder)
synonymsTurner's phenotype, other variant karyotypes
parentsTurner syndrome   38804009
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
              Anomaly of chromosome X   111312006
                Turner syndrome   38804009
                  Turner's phenotype, other variant karyotypes   268298003  removed: 2010-01-31

ancestors
sorted most to least specific
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