hypertrophic cardiomyopathy 3
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22
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hypertrophic cardiomyopathy 3
Summary
hypertrophic cardiomyopathy 3 is a class of disease[1].
Key Facts
- hypertrophic cardiomyopathy 3's instance of is recorded as class of disease[2].
- hypertrophic cardiomyopathy 3's subclass of is recorded as familial hypertrophic cardiomyopathy[3].
- hypertrophic cardiomyopathy 3's MeSH descriptor ID is recorded as C566170[4].
- hypertrophic cardiomyopathy 3's OMIM ID is recorded as 115196[5].
- hypertrophic cardiomyopathy 3's Disease Ontology ID is recorded as DOID:0110309[6].
- hypertrophic cardiomyopathy 3's Orphanet ID is recorded as 155[7].
- hypertrophic cardiomyopathy 3's NCI Thesaurus ID is recorded as C182076[8].
- hypertrophic cardiomyopathy 3's genetic association is recorded as TPM1[9].
- hypertrophic cardiomyopathy 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110309[10].
- hypertrophic cardiomyopathy 3's exact match is recorded as http://identifiers.org/doid/DOID:0110309[11].
- hypertrophic cardiomyopathy 3's UMLS CUI is recorded as C1861863[12].
- hypertrophic cardiomyopathy 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- hypertrophic cardiomyopathy 3's Mondo ID is recorded as MONDO_0007267[14].
- hypertrophic cardiomyopathy 3's UniProt disease ID is recorded as DI-00235[15].