OBO ID: DOID:0060775 |
Term Name: | microvillus inclusion disease | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0060775 ) |
OTHER microvillus inclusion disease PAGES
ZEBRAFISH MODELS
Fish | Conditions | Citations |
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myo5bt30834/t30834 | standard conditions | Sidhaye et al., 2016 |
PHENOTYPE
No data available
CITATIONS (2)
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