Details of Disease

General Information of Disease (ID: DISCYA3B)

Disease Name Dilated cardiomyopathy 1W
Synonyms
cardiomyopathy, dilated, 1W; familial isolated dilated cardiomyopathy caused by mutation in VCL; VCL familial isolated dilated cardiomyopathy; CMD1W; cardiomyopathy, dilated, type 1W; dilated cardiomyopathy type 1W
Definition Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the VCL gene.
Disease Hierarchy
DISBHDU9: Familial dilated cardiomyopathy
DISCYA3B: Dilated cardiomyopathy 1W
Disease Identifiers
MONDO ID
MONDO_0012667
MESH ID
C566954
UMLS CUI
C1969639
OMIM ID
611407
MedGen ID
370063

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
VCL OTPQ0JYS Strong Autosomal dominant [1]
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References

1 Metavinculin mutations alter actin interaction in dilated cardiomyopathy. Circulation. 2002 Jan 29;105(4):431-7. doi: 10.1161/hc0402.102930.