Congenital omphalocele   18735004

SNOMED CT code


SNOMED code18735004
nameCongenital omphalocele
statusactive
date introduced2002-01-31
fully specified name(s)Congenital omphalocele (disorder)
synonyms
  • Amniocele
  • Congenital omphalocele
  • Omphalocele
attributes - group2
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Associated morphologyHernial opening   414402003
Finding siteUmbilical structure   78220002
attributes - group1
OccurrenceCongenital   255399007
Finding siteIntra-abdominopelvic structure   818986006
Associated morphologyHernia   414403008
parents
children
  • Beckwith-Wiedemann syndrome   81780002
  • Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome   1172589000
  • Familial omphalocele syndrome with facial dysmorphism   770900000
  • Hepatomphalocele   36631002
  • Lethal omphalocele with cleft palate syndrome   719408007
  • Omphalocele - irreducible   196864001
  • Omphalocele with gangrene   196856007
  • Omphalocele with obstruction   1542009
  • Shprintzen Goldberg omphalocele syndrome   716230005
  • Unspecified omphalocele   196872004  removed: 2010-01-31
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    General finding of soft tissue   248402002
      Umbilicus finding   249537008
        Disorder of umbilicus   397320006
          Umbilical hernia   396347007
            Congenital omphalocele   18735004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    General finding of soft tissue   248402002
      Disorder of soft tissue   19660004
        Soft tissue lesion   239953001
          Congenital umbilical hernia   975231000000107
            Congenital omphalocele   18735004

ancestors
sorted most to least specific
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