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References OMIM Gene GeneReviews HGMD HGNC
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)