Shprintzen omphalocele syndrome
Other Names for this Disease
- Omphalocele with hypoplasia of pharynx and larynx, learning disability, dysmorphic facies, and scoliosis
- Pharynx and larynx hypoplasia with omphalocele
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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 Shprintzen omphalocele syndrome. Click on the link to view a sample search on this topic.