You are using an outdated browser. Please upgrade your browser to improve your experience.

familial visceral myopathy

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description A 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.
Mondo Term and Equivalent IDs
MONDO:0016829:  familial visceral myopathy
GARD:0003443: 
Orphanet:2604: 
SCTID:63684002: 
UMLS:C0266833: 
UMLS:C1835084: 
UMLS:CN202146: