Term Name: congenital diarrhea 5 with tufting enteropathy
Synonyms: congenital diarrhoea 5 with tufting enteropathy, congenital familial intractable diarrhea with epithelial or epithelium abnormalities, congenital familial intractable diarrhoea with epithelial or epithelium abnormalities, congenital tufting enteropathy, DIAR5, tufting enteropathy
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.
Ontology: Human Disease [DOID:0060776]   ( DOID:0060776 )

Relationships
is a type of: autosomal recessive disease congenital diarrhea