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Disease association ontology term - MONDO:0016829 - familial visceral myopathy

Term summary

ID
MONDO:0016829
Name
familial visceral myopathy
Ontology or CV name
Disease association
Definition
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.

Parents

Annotation

Disease association

MONDO:0020754 - visceral myopathy 1

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Genes:

MONDO:0859157 - visceral myopathy 2

References:

Genes: