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- NCIT_C177249 IAO_0000115 "An autosomal dominant subtype of familial hypertrophic cardiomyopathy caused by mutation(s) in the PRKAG2 gene, encoding 5'-AMP-activated protein kinase subunit gamma-2." @default.
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- NCIT_C177249 NCIT_P108 "Familial Hypertrophic Cardiomyopathy Type 6" @default.
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- NCIT_C177249 hasExactSynonym "CMH6" @default.
- NCIT_C177249 hasExactSynonym "Familial Hypertrophic Cardiomyopathy Type 6" @default.
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