|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
2 genes associated with the congenital short bowel syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.