Details of Disease

General Information of Disease (ID: DISQPZCZ)

Disease Name Visceral myopathy 2
Disease Hierarchy
DISGJL4K: Familial visceral myopathy
DISQPZCZ: Visceral myopathy 2
Disease Identifiers
MONDO ID
MONDO_0859157
UMLS CUI
C5543466
OMIM ID
619350
MedGen ID
1783630

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
MYH11 OTVNVWY3 Limited Autosomal dominant [1]
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References

1 Identification of a dominant MYH11 causal variant in chronic intestinal pseudo-obstruction: Results of whole-exome sequencing. Clin Genet. 2019 Nov;96(5):473-477. doi: 10.1111/cge.13617. Epub 2019 Aug 13.