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| Term | microvillus inclusion disease | ID (Ontology) | DOID:0060775 (Human Disease) |
| 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. | ||
| Also Known As | "congenital familial protracted diarrhea with enterocyte brush-border abnormalities" ; "congenital microvillus atrophy" ; "Davidson disease" (for all, see Synonyms field below) | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal recessive disease__ physical disorder | |__congenital diarrhea__________| diarrhea | |__congenital diarrhea__________| microvillus inclusion disease 2 rec. |
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| Is a |
autosomal recessive disease congenital diarrhea |
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External Crossreferences & Linkouts
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GARD:7039 ICD10CM:P78.3 MESH:C537470 MIM:251850 ORDO:2290 |
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