Home Page
References OMIM Gene GeneReviews HGMD HGNC
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)