About   Help   FAQ
Disease Ontology Browser
congenital diarrhea 5 with tufting enteropathy (DOID:0060776)
Alliance: disease page
Synonyms: congenital familial intractable diarrhea with epithelial or epithelium abnormalities; congenital tufting enteropathy; DIAR5; tufting enteropathy
Alt IDs: OMIM:613217, ICD10CM:P78.3, ORDO:92050
Definition: A congenital diarrhea characterized by intractable diarrhea of infancy with villous atrophy, absence of inflammation, and intestinal epithelial cell dysplasia manifesting as focal epithelial tufts in the duodenum and jejunum that has_material_basis_in homozygous or compound heterozygous mutation in the EPCAM gene on chromosome 2p21.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
11/14/2017
MGI 6.11
The Jackson Laboratory