hypertrophic cardiomyopathy 18
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the gene encoding phospholamban (PLN) on chromosome 6q22.1
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hypertrophic cardiomyopathy 18
Summary
hypertrophic cardiomyopathy 18 is a class of disease[1].
Key Facts
- hypertrophic cardiomyopathy 18's instance of is recorded as class of disease[2].
- hypertrophic cardiomyopathy 18's subclass of is recorded as familial hypertrophic cardiomyopathy[3].
- hypertrophic cardiomyopathy 18's OMIM ID is recorded as 613874[4].
- hypertrophic cardiomyopathy 18's Disease Ontology ID is recorded as DOID:0110324[5].
- hypertrophic cardiomyopathy 18's Orphanet ID is recorded as 155[6].
- hypertrophic cardiomyopathy 18's genetic association is recorded as PLN[7].
- hypertrophic cardiomyopathy 18's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110324[8].
- hypertrophic cardiomyopathy 18's exact match is recorded as http://identifiers.org/doid/DOID:0110324[9].
- hypertrophic cardiomyopathy 18's UMLS CUI is recorded as C3151265[10].
- hypertrophic cardiomyopathy 18's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
- hypertrophic cardiomyopathy 18's Mondo ID is recorded as MONDO_0013475[12].
- hypertrophic cardiomyopathy 18's UniProt disease ID is recorded as DI-03039[13].