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