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 13   17760001

SNOMED CT code


SNOMED code17760001
nameAnomaly of chromosome pair 13
statusactive
date introduced2002-01-31
fully specified name(s)Anomaly of chromosome pair 13 (disorder)
synonymsAnomaly of chromosome pair 13
attributes - group1
OccurrenceCongenital   255399007
Finding siteChromosome pair 13   55401003
Associated morphologyCellular AND/OR subcellular abnormality   107673000
parentsAnomaly of chromosome pair   362984008
children
  • Complete trisomy 13 syndrome   21111006
  • Deletion of part of chromosome 13   726384005
  • Maternal uniparental disomy of chromosome 13   770563005
  • Partial trisomy 13 in Patau's syndrome   254268004
  • Partial trisomy of chromosome 13   726352003
  • Paternal uniparental disomy of chromosome 13   770668007
  • Ring chromosome 13 syndrome   726723004
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 13   17760001

ancestors
sorted most to least specific
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