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 9   5051002

SNOMED CT code


SNOMED code5051002
nameAnomaly of chromosome pair 9
statusactive
date introduced2002-01-31
fully specified name(s)Anomaly of chromosome pair 9 (disorder)
synonymsAnomaly of chromosome pair 9
attributes - group1
OccurrenceCongenital   255399007
Finding siteChromosome pair 9   13526007
Associated morphologyCellular AND/OR subcellular abnormality   107673000
parentsAnomaly of chromosome pair   362984008
children
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 9   5051002

ancestors
sorted most to least specific
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