ICD10 code of Omphalocele and ICD9 code

The ICD-10-CM code for Omphalocele is Q79.2 (Exomphalos), while the legacy ICD-9-CM code is 756.72. These codes are used universally by healthcare providers and insurance systems to classify this specific congenital abdominal wall defect for diagnostic and billing purposes.

What is an Omphalocele?

An Omphalocele is a rare congenital birth defect where an infant's intestines, liver, or other organs protrude outside of the abdomen through the navel. These organs are contained within a thin, transparent sac. Omphalocele occurs in approximately 1 in 4,000 to 1 in 7,000 live births, and it is often associated with other genetic syndromes or chromosomal abnormalities.

How is an Omphalocele diagnosed?

Omphalocele is frequently identified during routine prenatal ultrasound screenings, often as early as the first or second trimester. Following a prenatal diagnosis, a multidisciplinary team—including pediatric surgeons, neonatologists, and geneticists—will monitor the pregnancy closely. At DiseaseMaps.org, we have 4 community members who have navigated the diagnosis and management of Omphalocele, providing a space for shared experience.

Are there different types of Omphalocele?

Clinical classification of Omphalocele generally depends on the size of the defect and the organs involved:

• Small Omphalocele: Contains only a small portion of the bowel.


• Giant Omphalocele: Contains the liver and other major organs, often requiring a staged surgical repair.


• Syndromic vs. Non-syndromic: Whether the Omphalocele occurs in isolation or as part of a syndrome like Beckwith-Wiedemann syndrome.

Next steps

• Consult with a pediatric surgeon or a maternal-fetal medicine specialist to discuss surgical repair options.


• Request a referral to a clinical geneticist to screen for underlying chromosomal associations.


• Connect with the community at DiseaseMaps.org to find support from families who have managed an Omphalocele diagnosis.

Medical disclaimer: This information is for educational purposes only and does not replace professional medical advice, diagnosis, or treatment; always seek the advice of your physician regarding a medical condition.

References

• NIH Genetic and Rare Diseases Information Center (GARD): Omphalocele.


• Orphanet: Exomphalos (ORPHA:68356).


• ICD-10-CM Browser: Q79.2 (Exomphalos).


• National Organization for Rare Disorders (NORD): Rare Disease Database.