hypertrophic cardiomyopathy 13
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the TNNC1 gene on chromosome 3p21
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hypertrophic cardiomyopathy 13
Summary
hypertrophic cardiomyopathy 13 is a class of disease[1].
Key Facts
- hypertrophic cardiomyopathy 13's instance of is recorded as class of disease[2].
- hypertrophic cardiomyopathy 13's subclass of is recorded as familial hypertrophic cardiomyopathy[3].
- hypertrophic cardiomyopathy 13's MeSH descriptor ID is recorded as C567686[4].
- hypertrophic cardiomyopathy 13's OMIM ID is recorded as 613243[5].
- hypertrophic cardiomyopathy 13's Disease Ontology ID is recorded as DOID:0110319[6].
- hypertrophic cardiomyopathy 13's Orphanet ID is recorded as 155[7].
- hypertrophic cardiomyopathy 13's genetic association is recorded as TNNC1[8].
- hypertrophic cardiomyopathy 13's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110319[9].
- hypertrophic cardiomyopathy 13's exact match is recorded as http://identifiers.org/doid/DOID:0110319[10].
- hypertrophic cardiomyopathy 13's UMLS CUI is recorded as C2750472[11].
- hypertrophic cardiomyopathy 13's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- hypertrophic cardiomyopathy 13's Mondo ID is recorded as MONDO_0013195[13].
- hypertrophic cardiomyopathy 13's UniProt disease ID is recorded as DI-02553[14].