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 20   9839007

SNOMED CT code


SNOMED code9839007
nameAnomaly of chromosome pair 20
statusactive
date introduced2002-01-31
fully specified name(s)Anomaly of chromosome pair 20 (disorder)
synonymsAnomaly of chromosome pair 20
attributes - group1
OccurrenceCongenital   255399007
Finding siteChromosome pair 20   25610001
Associated morphologyCellular AND/OR subcellular abnormality   107673000
parentsAnomaly of chromosome pair   362984008
children
  • Complete trisomy 20 syndrome   53346000
  • Congenital hereditary endothelial dystrophy   417651000
  • Deletion of part of chromosome 20   726395004
  • Maternal uniparental disomy of chromosome 20   715735007
  • Mosaic trisomy 20 syndrome   764624003
  • Partial trisomy of chromosome 20   726360002
  • Paternal uniparental disomy of chromosome 20   715736008
  • Ring chromosome 20 syndrome   23686004
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 20   9839007

ancestors
sorted most to least specific
cpt crosswalks

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