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 2   32299009

SNOMED CT code


SNOMED code32299009
nameAnomaly of chromosome pair 2
statusactive
date introduced2002-01-31
fully specified name(s)Anomaly of chromosome pair 2 (disorder)
synonymsAnomaly of chromosome pair 2
attributes - group1
OccurrenceCongenital   255399007
Associated morphologyCellular AND/OR subcellular abnormality   107673000
Finding siteChromosome pair 2   113354003
parentsAnomaly of chromosome pair   362984008
children
  • Deletion of part of chromosome 2   726366008
  • Maternal uniparental disomy of chromosome 2   766237006
  • Mosaic trisomy 2 syndrome   764623009
  • Overgrowth syndrome with 2q37 translocation   1169362009
  • Partial trisomy of chromosome 2   726340005
  • Ring chromosome 2 syndrome   765485000
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 2   32299009

ancestors
sorted most to least specific
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