OBO ID: DOID:0110312
Term Name: hypertrophic cardiomyopathy 6 Search Ontology:
Synonyms:
  • cardiomyopathy, familial hypertrophic 6
  • CMH6
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
References:
Ontology: Human Disease   ( DOID:0110312 )
Relationships
is a type of:
OTHER hypertrophic cardiomyopathy 6 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PRKAG2 Cardiomyopathy, hypertrophic 6 600858
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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