WormBase Tree Display for DO_term: DOID:0060775
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| DOID:0060775 | Name | microvillus inclusion disease | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| 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. | ||||
| Synonym | Exact | Davidson disease | |||
| MVD | |||||
| congenital familial protracted diarrhea with enterocyte brush-border abnormalities | |||||
| congenital microvillus atrophy | |||||
| diarrhea 2 with microvillus atrophy | |||||
| intractable diarrhea of infancy | |||||
| Parent | Is_a | DOID:0050737 | |||
| DOID:0060774 | |||||
| DB_info | Database | OMIM | disease | 251850 | |
| Attribute_of | Gene_by_orthology | WBGene00002036 |
