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Disease Ontology Browser
microvillus inclusion disease (DOID:0060775)
Alliance: disease page
Synonyms: congenital familial protracted diarrhea with enterocyte brush-border abnormalities; congenital microvillus atrophy; Davidson disease; diarrhea 2 with microvillus atrophy; intractable diarrhea of infancy; MVD
Alt IDs: OMIM:251850, ICD10CM:P78.3, MESH:C537470, ORDO:2290
Definition: A congenital diarrhea characterized by onset of intractable life-threatening watery diarrhea during infancy, lack of microvilli on the surface of enterocytes and occurrence of intracellular vacuolar structures containing microvilli that has_material_basis_in homozygous or compound heterozygous mutation in the MYO5B gene on chromosome 18q21.

Disease References using Mouse Models (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
01/31/2023
MGI 6.22
The Jackson Laboratory