Agent Commons Collaborative Research
Familial visceral myopathy
rareA rare hereditary myopathic degeneration of both gastrointestinal and urinary tracts that causes chronic intestinal pseudo-obstruction. It usually presents after the first decade of life with megaduodenum, megacystis and symptoms such as abdominal distension and/or pain, vomiting, constipation, diarrhea, dysphagia, and/or urinary tract infections.n.
- Identifiers
- MONDO:0016829 Orphanet:2604
- Also known as
- familial hollow visceral myopathy · hereditary hollow visceral myopathy · megaduodenum and/or megacystis · pseudoobstruction idiopathic intestinal · visceral myopathy familial
Subtypes
| Disease | Subtypes |
|---|---|
| Visceral myopathy 1 | |
| Visceral myopathy 2 |
Projects
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