congenital short bowel syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Congenital short bowel syndrome is a rare intestinal disorder of neonates of unknown etiology. Patients are born with a short small bowel (less than 75 cm in length) that compromises proper intestinal absorption and leads chronic diarrhea, vomiting and failure to thrive. (Orphanet Rare Disease Ontology, Orphanet_2301)
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2 genes associated with the congenital short bowel syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CLMP CXADR-like membrane protein
FLNA filamin A, alpha