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GENATLAS PHENOTYPE

last update : 19/06/2006

Symbol	CMH6
Location	14q11.2
Name	hypertrophic cardiomyopathy, familial, 6
Corresponding gene	MYH6
Main clinical features	frequent sudden death
Genetic determination
Function/system disorder	cardiovascular
Type	disease

Gene product

Name	cardiac myosin heavy chain-alpha

Remark(s)