|OBO ID: DOID:0060775|
|Term Name:||microvillus inclusion disease||Search Ontology:|
|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. https://www.ncbi.nlm.nih.gov/pubmed/18724368|
|Ontology:||Human Disease (DOID:0060775)|
|is a type of:||
OTHER microvillus inclusion disease PAGES
PHENOTYPE No data available
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