Related Conditions
Omphalocele with obstruction(child)
Beckwith-Wiedemann syndrome(child)
Hepatomphalocele(child)
Omphalocele with gangrene(child)
Omphalocele - irreducible(child)
Shprintzen Goldberg omphalocele syndrome(child)
Lethal omphalocele with cleft palate syndrome(child)
Familial omphalocele syndrome with facial dysmorphism(child)
Gershoni Baruch syndrome(child)
Umbilical hernia(parent)
Congenital umbilical hernia(parent)
Quick Facts
- SNOMED CT
- 18735004
- UMLS CUI
- C0795690
- Fully Specified Name
- Congenital omphalocele (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.