cardiomyopathy, familial hypertrophic, 8 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/608751
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Genes

1 genes associated with the cardiomyopathy, familial hypertrophic, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
MYL3 myosin, light chain 3, alkali; ventricular, skeletal, slow