Deletion of part of short arm of chromosome 16   726388008

SNOMED CT code


SNOMED code726388008
nameDeletion of part of short arm of chromosome 16
statusactive
date introduced2017-07-31
fully specified name(s)Deletion of part of short arm of chromosome 16 (disorder)
synonymsDeletion of part of short arm of chromosome 16
attributes - group1
OccurrenceCongenital   255399007
Finding siteShort arm of chromosome   278145009
Associated morphologyPartial monosomy   371169004
attributes - group2
Associated morphologyPartial monosomy   371169004
OccurrenceCongenital   255399007
Finding siteChromosome pair 16   39220001
parentsDeletion of part of chromosome 16   726387003
children
  • 16p11.2p12.2 microdeletion syndrome   719576009
  • 16p12.2 microdeletion syndrome   768471006
  • 16p13.11 microdeletion syndrome   719577000
  • 16p13.2 microdeletion syndrome   1228890005
  • Alpha-thalassemia intellectual disability syndrome linked to chromosome 16   734349003
  • Chromosome 16p11.2 deletion syndrome   699307007
  • Distal 16p11.2 microdeletion syndrome   733521003
  • Proximal 16p11.2 microdeletion syndrome   718227006
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 16   53392002
              Deletion of part of chromosome 16   726387003
                Deletion of part of short arm of chromosome 16   726388008

ancestors
sorted most to least specific
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