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Disease Ontology Browser
congenital malabsorptive diarrhea 4 (DOID:0060779)
Alliance: disease page
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
Alt IDs: OMIM:610370, ICD10CM:P78.3, ORDO:83620
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
MGI 6.22
The Jackson Laboratory