Familial omphalocele syndrome with facial dysmorphism
MONDO:0017235Familial 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.
0 clinical trials for this condition and its sub-types, 0 tagged with Familial omphalocele syndrome with facial dysmorphism itself.
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