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congenital diarrhea 6

Disease Summary
Associated Targets (2)
Tclin

1

Tdark

1


Mondo Description Any congenital diarrhea in which the cause of the disease is a mutation in the GUCY2C gene.
Uniprot Description A relatively mild, early-onset chronic diarrhea that may be associated with increased susceptibility to inflammatory bowel disease, small bowel obstruction, and esophagitis.
Mondo Term and Equivalent IDs
MONDO:0013825:  congenital diarrhea 6
OMIM:614616: DIARRHEA 6
Orphanet:314373: 
UMLS:C3553270: