Agent Commons Collaborative Research
Microvillus inclusion disease
rareMicrovillus inclusion disease (MVID) is a very rare, severe, malabsorbative syndrome characterized clinically by protracted or intractable neonatal secretory diarrhea and histologically by inclusion bodies on the intestinal epithelium.
- Identifiers
- MONDO:0009635 OMIM:251850Orphanet:2290
- Causal genes
- MYO5B
- Part of
- Congenital secretory diarrhea
- Also known as
- congenital familial protracted diarrhea · congenital familial protracted diarrhea with enterocyte brush-border abnormalities · congenital familial protracted diarrhoea · congenital familial protracted diarrhoea with enterocyte Brush-border abnormalities · congenital microvillous atrophy
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