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Summary Literature (0)
DOID:0060779 - congenital malabsorptive diarrhea 4

Disease Ontology Definition:A congenital diarrhea characterized by chronic unremitting malabsorptive diarrhea and a profound dysgenesis of the enteroendocrine cells that has_material_basis_in mutation in the gene encoding neurogenin-3 (NEUROG3) on chromosome 10q21.3.

Synonyms: congenital malabsorptive diarrhea due to paucity of enteroendocrine cells, congenital malabsorptive diarrhoea 4, congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells, enteric anendocrinosis

Xenbase Genes : neurog3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012479 - congenital malabsorptive diarrhea 4


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)