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OMIM

Gene

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GENATLAS PHENOTYPE

last update : 06-01-2014

Symbol	CMD1W
Location	10q22.2
Name	cardiomyopathy, dilated 1W
Corresponding gene	VCL
Other symbol(s)	CMD1L, CMD15, CMD1N
Main clinical features	adult-onset, in any cases associated with juvenile-onset neurosensory hearing loss
Genetic determination	autosomal dominant
Function/system disorder	cardiovascular
Type	disease

Gene product

Name

vinculin

Remark(s)