hypertrophic cardiomyopathy 8
hypertrophic cardiomyopathy that has material basis in homozygous or heterozygous mutation in the MYL3 gene
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hypertrophic cardiomyopathy 8
Summary
hypertrophic cardiomyopathy 8 is a class of disease[1].
Key Facts
- hypertrophic cardiomyopathy 8's instance of is recorded as class of disease[2].
- hypertrophic cardiomyopathy 8's subclass of is recorded as familial hypertrophic cardiomyopathy[3].
- hypertrophic cardiomyopathy 8's MeSH descriptor ID is recorded as C563866[4].
- hypertrophic cardiomyopathy 8's OMIM ID is recorded as 608751[5].
- hypertrophic cardiomyopathy 8's Disease Ontology ID is recorded as DOID:0110314[6].
- hypertrophic cardiomyopathy 8's Orphanet ID is recorded as 155[7].
- hypertrophic cardiomyopathy 8's genetic association is recorded as MYL3[8].
- hypertrophic cardiomyopathy 8's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110314[9].
- hypertrophic cardiomyopathy 8's exact match is recorded as http://identifiers.org/doid/DOID:0110314[10].
- hypertrophic cardiomyopathy 8's UMLS CUI is recorded as C1837471[11].
- hypertrophic cardiomyopathy 8's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- hypertrophic cardiomyopathy 8's Mondo ID is recorded as MONDO_0012111[13].
- hypertrophic cardiomyopathy 8's UniProt disease ID is recorded as DI-00238[14].