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GENATLAS PHENOTYPE

last update : 13/07/2006

Symbol	CMH8
Location	3p21.3
Name	cardiomyopathy, familial, hypertrophic, 8
Corresponding gene	MYL3
Main clinical features	hypertrophy of the cardiac papillary muscles causing mid cavity obstruction
Genetic determination	autosomal recessive
Function/system disorder	cardiovascular
Type	disease

Gene product

Name	myosin, light polypeptide 3, essential (MYL3)