hypertrophic cardiomyopathy 2
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the cardiac troponin-T2 gene (TNNT2)
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hypertrophic cardiomyopathy 2
Summary
hypertrophic cardiomyopathy 2 is a class of disease[1].
Key Facts
- hypertrophic cardiomyopathy 2's instance of is recorded as class of disease[2].
- hypertrophic cardiomyopathy 2's subclass of is recorded as familial hypertrophic cardiomyopathy[3].
- hypertrophic cardiomyopathy 2's MeSH descriptor ID is recorded as C566171[4].
- hypertrophic cardiomyopathy 2's OMIM ID is recorded as 115195[5].
- hypertrophic cardiomyopathy 2's Disease Ontology ID is recorded as DOID:0110308[6].
- hypertrophic cardiomyopathy 2's Orphanet ID is recorded as 155[7].
- hypertrophic cardiomyopathy 2's NCI Thesaurus ID is recorded as C142892[8].
- hypertrophic cardiomyopathy 2's genetic association is recorded as TNNT2[9].
- hypertrophic cardiomyopathy 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110308[10].
- hypertrophic cardiomyopathy 2's exact match is recorded as http://identifiers.org/doid/DOID:0110308[11].
- hypertrophic cardiomyopathy 2's UMLS CUI is recorded as C1861864[12].
- hypertrophic cardiomyopathy 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- hypertrophic cardiomyopathy 2's Mondo ID is recorded as MONDO_0007266[14].
- hypertrophic cardiomyopathy 2's UniProt disease ID is recorded as DI-00234[15].