hypertrophic cardiomyopathy 26
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the FLNC gene on chromosome 7q32
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hypertrophic cardiomyopathy 26
Summary
hypertrophic cardiomyopathy 26 is a rare disease[1].
Key Facts
- hypertrophic cardiomyopathy 26's instance of is recorded as rare disease[2].
- hypertrophic cardiomyopathy 26's instance of is recorded as class of disease[3].
- hypertrophic cardiomyopathy 26's subclass of is recorded as hypertrophic cardiomyopathy[4].
- hypertrophic cardiomyopathy 26's subclass of is recorded as familial hypertrophic cardiomyopathy[5].
- hypertrophic cardiomyopathy 26's OMIM ID is recorded as 617047[6].
- hypertrophic cardiomyopathy 26's Disease Ontology ID is recorded as DOID:0110327[7].
- hypertrophic cardiomyopathy 26's NCI Thesaurus ID is recorded as C179295[8].
- hypertrophic cardiomyopathy 26's genetic association is recorded as FLNC[9].
- hypertrophic cardiomyopathy 26's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110327[10].
- hypertrophic cardiomyopathy 26's exact match is recorded as http://identifiers.org/doid/DOID:0110327[11].
- hypertrophic cardiomyopathy 26's UMLS CUI is recorded as C4310749[12].
- hypertrophic cardiomyopathy 26's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- hypertrophic cardiomyopathy 26's Mondo ID is recorded as MONDO_0014883[14].
- hypertrophic cardiomyopathy 26's UniProt disease ID is recorded as DI-04771[15].