deafness, autosomal dominant 22, with hypertrophic cardiomyopathy Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/606346
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Genes

1 genes associated with the deafness, autosomal dominant 22, with hypertrophic cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
MYO6 myosin VI