Metadata | |
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ID | DOID:0110312 |
Name | hypertrophic cardiomyopathy 6 |
Definition | A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the gene encoding the gamma-2 regulatory subunit of AMP-activated protein kinase (PRKAG2). https://www.ncbi.nlm.nih.gov/pubmed/11586962 |
Xrefs | |
Synonyms |
cardiomyopathy, familial hypertrophic 6 [EXACT] CMH6 [EXACT] |
Parent Relationships |