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Summary Literature (0)
DOID:0060778 - congenital diarrhea 7 with exudative enteropathy

Disease Ontology Definition:A congenital diarrhea characterized by watery diarrhea, protein-losing enteropathy, patchy areas of dystrophic microvilli in the duodenum and patchy areas of villous atrophy that has_material_basis_in homozygous mutation in the DGAT1 gene on chromosome 8q24.3.

Synonyms: 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 diarrhoea 7 with exudative enteropathy,

Xenbase Genes : dgat1, plvap

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014375 - congenital diarrhea 7 with exudative enteropathy


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), congenital diarrhea (is_a)