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 8  48082007

Deletion of part of chromosome 8  726378007

8q partial monosomy syndrome  29379007

8q21.11 microdeletion syndrome   718615003

SNOMED CT code


SNOMED code718615003
name8q21.11 microdeletion syndrome
statusactive
date introduced2017-01-31
fully specified name(s)8q21.11 microdeletion syndrome (disorder)
synonyms
  • 8q21.11 microdeletion syndrome
  • Monosomy 8q21.11
attributes - group2
OccurrenceCongenital   255399007
Finding siteChromosome pair 8   77826001
Associated morphologyDeletion of long arm   64329008
attributes - group3
OccurrenceCongenital   255399007
Finding siteChromosome pair 8   77826001
Associated morphologyPartial monosomy   371169004
parents8q partial monosomy syndrome   29379007
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 8   48082007
              Deletion of part of chromosome 8   726378007
                8q partial monosomy syndrome   29379007
                  8q21.11 microdeletion syndrome   718615003

ancestors
sorted most to least specific
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