DO_rare_slim has material basis in disease has basis in autosomal recessive disease congenital diarrhea congenital diarrhea 5 with tufting enteropathy MIM:613217 DOID:0060776 disease_ontology ORDO:92050 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. DIAR5 ICD10CM:P78.3 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 tufting enteropathy autosomal recessive inheritance Abnormality of prenatal development or birth