hypertrophic cardiomyopathy 6
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the gene encoding the gamma-2 regulatory subunit of AMP-activated protein kinase (PRKAG2)
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hypertrophic cardiomyopathy 6
Summary
hypertrophic cardiomyopathy 6 is a class of disease[1].
Key Facts
- hypertrophic cardiomyopathy 6's instance of is recorded as class of disease[2].
- hypertrophic cardiomyopathy 6's subclass of is recorded as familial hypertrophic cardiomyopathy[3].
- hypertrophic cardiomyopathy 6's MeSH descriptor ID is recorded as C563436[4].
- hypertrophic cardiomyopathy 6's OMIM ID is recorded as 600858[5].
- hypertrophic cardiomyopathy 6's Disease Ontology ID is recorded as DOID:0110312[6].
- hypertrophic cardiomyopathy 6's Orphanet ID is recorded as 155[7].
- hypertrophic cardiomyopathy 6's NCI Thesaurus ID is recorded as C177249[8].
- hypertrophic cardiomyopathy 6's genetic association is recorded as PRKAG2[9].
- hypertrophic cardiomyopathy 6's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110312[10].
- hypertrophic cardiomyopathy 6's exact match is recorded as http://identifiers.org/doid/DOID:0110312[11].
- hypertrophic cardiomyopathy 6's UMLS CUI is recorded as C1833236[12].
- hypertrophic cardiomyopathy 6's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- hypertrophic cardiomyopathy 6's Mondo ID is recorded as MONDO_0010946[14].
- hypertrophic cardiomyopathy 6's UniProt disease ID is recorded as DI-00245[15].