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Features include always present findings: Omphalocele.
Phenotype severity distribution: 1 always present feature.
No clinical trials have been registered for omphalocele, autosomal.
6 publications have been identified in PubMed for omphalocele, autosomal. Kisho has analyzed 4 by research type. Research spans Case Report / Case Series (75%) and Epidemiology / Natural History (25%).
Abdelhady E (2026). [PMID: 41821721](https://pubmed.ncbi.nlm.nih.gov/41821721/). *J Med Cases*. [Case Report / Case Series]
Zhou C (2025). [PMID: 40445021](https://pubmed.ncbi.nlm.nih.gov/40445021/). *Prenat Diagn*. [Case Report / Case Series]
Lausten-Thomsen U (2024). [PMID: 39576336](https://pubmed.ncbi.nlm.nih.gov/39576336/). *Pediatr Surg Int*. [Epidemiology / Natural History]
Zhang W (2024). [PMID: 39091686](https://pubmed.ncbi.nlm.nih.gov/39091686/). *Front Nutr*. [Case Report / Case Series]
Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 1:48 AM UTC
Online Mendelian Inheritance in Man
Genetic and Rare Diseases Info Center
AI-curated news mentioning omphalocele, autosomal
Updated Jun 4, 2026
A case report highlights an unusual omphalocele associated with Cantrell syndrome, contributing to the understanding of this rare condition. This report may provide insights for clinicians dealing with similar cases.