familial omphalocele syndrome with facial dysmorphism https://www.malacards.org/card/familial_omphalocele_syndrome_with_facial_dysmorphism MEDGEN:1655514 UMLS:C4749579 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. GARD:0021086 MONDO:0017235 Orphanet:280403 disorder of development or morphogenesis