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Gene

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GENATLAS PHENOTYPE

last update : 28-01-2009

Symbol	FHCD
Location	6q14.1
Name	familial hypertrophic cardiomyopathy
Corresponding gene	MYO6
Main clinical features	sensorineural deafness and long QT syndrome
Genetic determination	autosomal dominant
Function/system disorder	cardiovascular
	ear
Type	disease

Gene product

Name

myosin VI

Remark(s)