hypertrophic cardiomyopathy 17
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the junctophilin gene (JPH2) on chromosome 20q12
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hypertrophic cardiomyopathy 17
Summary
hypertrophic cardiomyopathy 17 is a class of disease[1].
Key Facts
- hypertrophic cardiomyopathy 17's instance of is recorded as class of disease[2].
- hypertrophic cardiomyopathy 17's subclass of is recorded as familial hypertrophic cardiomyopathy[3].
- hypertrophic cardiomyopathy 17's OMIM ID is recorded as 613873[4].
- hypertrophic cardiomyopathy 17's Disease Ontology ID is recorded as DOID:0110323[5].
- hypertrophic cardiomyopathy 17's Orphanet ID is recorded as 155[6].
- hypertrophic cardiomyopathy 17's NCI Thesaurus ID is recorded as C172093[7].
- hypertrophic cardiomyopathy 17's genetic association is recorded as JPH2[8].
- hypertrophic cardiomyopathy 17's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110323[9].
- hypertrophic cardiomyopathy 17's exact match is recorded as http://identifiers.org/doid/DOID:0110323[10].
- hypertrophic cardiomyopathy 17's UMLS CUI is recorded as C3151264[11].
- hypertrophic cardiomyopathy 17's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- hypertrophic cardiomyopathy 17's Mondo ID is recorded as MONDO_0013474[13].
- hypertrophic cardiomyopathy 17's UniProt disease ID is recorded as DI-03038[14].