Other Names for this Disease
- Type - Epigastric - defect in the cephalic fold
- Type - Hypogastric - defect in the caudal fold
On this page
- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Paraomphalocele. Click on the link to view a sample search on this topic.