hypertrophic cardiomyopathy 20
hypertrophic cardiomyopathy that hhas material basis in heterozygous mutation in the NEXN gene on chromosome 1p31.1
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hypertrophic cardiomyopathy 20
Summary
hypertrophic cardiomyopathy 20 is a class of disease[1].
Key Facts
- hypertrophic cardiomyopathy 20's instance of is recorded as class of disease[2].
- hypertrophic cardiomyopathy 20's subclass of is recorded as familial hypertrophic cardiomyopathy[3].
- hypertrophic cardiomyopathy 20's OMIM ID is recorded as 613876[4].
- hypertrophic cardiomyopathy 20's Disease Ontology ID is recorded as DOID:0110326[5].
- hypertrophic cardiomyopathy 20's Orphanet ID is recorded as 155[6].
- hypertrophic cardiomyopathy 20's genetic association is recorded as NEXN[7].
- hypertrophic cardiomyopathy 20's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110326[8].
- hypertrophic cardiomyopathy 20's exact match is recorded as http://identifiers.org/doid/DOID:0110326[9].
- hypertrophic cardiomyopathy 20's UMLS CUI is recorded as C3151267[10].
- hypertrophic cardiomyopathy 20's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
- hypertrophic cardiomyopathy 20's Mondo ID is recorded as MONDO_0013477[12].
- hypertrophic cardiomyopathy 20's UniProt disease ID is recorded as DI-03041[13].