hypertrophic cardiomyopathy 10
hypertrophic cardiomyopathy that has material basis in mutation in the MYL2 gene
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hypertrophic cardiomyopathy 10
Summary
hypertrophic cardiomyopathy 10 is a class of disease[1].
Key Facts
- hypertrophic cardiomyopathy 10's instance of is recorded as class of disease[2].
- hypertrophic cardiomyopathy 10's subclass of is recorded as familial hypertrophic cardiomyopathy[3].
- hypertrophic cardiomyopathy 10's MeSH descriptor ID is recorded as C563865[4].
- hypertrophic cardiomyopathy 10's OMIM ID is recorded as 608758[5].
- hypertrophic cardiomyopathy 10's Disease Ontology ID is recorded as DOID:0110316[6].
- hypertrophic cardiomyopathy 10's Orphanet ID is recorded as 155[7].
- hypertrophic cardiomyopathy 10's genetic association is recorded as MYL2[8].
- hypertrophic cardiomyopathy 10's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110316[9].
- hypertrophic cardiomyopathy 10's exact match is recorded as http://identifiers.org/doid/DOID:0110316[10].
- hypertrophic cardiomyopathy 10's UMLS CUI is recorded as C1834460[11].
- hypertrophic cardiomyopathy 10's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- hypertrophic cardiomyopathy 10's Mondo ID is recorded as MONDO_0012112[13].
- hypertrophic cardiomyopathy 10's UniProt disease ID is recorded as DI-00240[14].