familial omphalocele syndrome with facial dysmorphism
MONDO:0017235Mondo
Findings
No curated finding names familial omphalocele syndrome with facial dysmorphism yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Familial omphalocele syndrome with facial dysmorphism is a rare genetic developmental defect during embryogenesis characterized by omphalocele associated with facial dysmorphism including flat face, short, upturned nose, long and wide philtrum and flattened maxillary arch and abnormalities of hands.
Definition from the Mondo Disease Ontology (MONDO:0017235), read 2026-09-29. CC BY 4.0.