1p partial monosomy   36369001

SNOMED CT code


SNOMED code36369001
name1p partial monosomy
statusactive
date introduced2002-01-31
fully specified name(s)1p partial monosomy (disorder)
synonyms
  • 1p partial monosomy
  • Partial deletion of the short arm of chromosome 1
attributes - group2
Finding siteShort arm of chromosome   278145009
Associated morphologyPartial monosomy   371169004
OccurrenceCongenital   255399007
attributes - group1
OccurrenceCongenital   255399007
Finding siteChromosome pair 1   46507000
Associated morphologyPartial monosomy   371169004
parentsDeletion of part of chromosome 1   726365007
children
  • 1p21.3 microdeletion syndrome   719600006
  • 1p31p32 microdeletion syndrome   766766005
  • 1p35.2 microdeletion syndrome   1228844002
  • 1p36 deletion syndrome   699306003
  • Distal deletion of short arm of chromosome 1   897524009
  • Medial deletion of short arm of chromosome 1   1003417005
  • Proximal deletion of short arm of chromosome 1   1003914006
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 1   74769007
              Deletion of part of chromosome 1   726365007
                1p partial monosomy   36369001

ancestors
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