congenital diarrhea 7 with exudative enteropathy (Monarch Disease Ontology id MONDO_0014375) can be described as follows. Congenital chronic diarrhea with protein-losing enteropathy is a rare, genetic, intestinal disease characterized by early-onset, chronic, non-infectious, non-bloody, watery diarrhea associated with protein-losing enteropathy which results in hypoalbuminemia, hypogammaglobulinemia and elevated stool alpha-1-antitrypsin. Patients typically present severe, intractable diarrhea, failure to thrive, recurrent infections and edema. Also known as: DGAT1 congenital diarrhea, DGAT1 congenital diarrhoea, congenital chronic diarrhea with exudative enteropathy, congenital chronic diarrhea with protein-losing enteropathy, congenital chronic diarrhoea with exudative enteropathy, congenital chronic diarrhoea with protein-losing enteropathy, congenital diarrhea caused by mutation in DGAT1, congenital diarrhoea caused by mutation in DGAT1.