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GENATLAS PHENOTYPE

last update : 23-08-2011

Symbol	CMH14
Location	18p11.3
Name	cardiomyopathy, familial, hypertrophic, 14
Corresponding gene	MYOM1
Main clinical features	hypertrophic cardiomyopathy, with mild to moderate hypertrophy age-related disease penetrance which is quite typical for HCM families
Genetic determination	autosomal dominant
Function/system disorder	cardiovascular
Type	disease

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