hypertrophic cardiomyopathy 9
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the TTN gene on chromosome 2q31
Press Enter · cited answer in seconds
0 sources
hypertrophic cardiomyopathy 9
Summary
hypertrophic cardiomyopathy 9 is a rare disease[1].
Key Facts
- hypertrophic cardiomyopathy 9's instance of is recorded as rare disease[2].
- hypertrophic cardiomyopathy 9's instance of is recorded as class of disease[3].
- hypertrophic cardiomyopathy 9's subclass of is recorded as familial hypertrophic cardiomyopathy[4].
- hypertrophic cardiomyopathy 9's MeSH descriptor ID is recorded as C566044[5].
- hypertrophic cardiomyopathy 9's OMIM ID is recorded as 613765[6].
- hypertrophic cardiomyopathy 9's Disease Ontology ID is recorded as DOID:0110315[7].
- hypertrophic cardiomyopathy 9's Orphanet ID is recorded as 155[8].
- hypertrophic cardiomyopathy 9's genetic association is recorded as TTN[9].
- hypertrophic cardiomyopathy 9's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110315[10].
- hypertrophic cardiomyopathy 9's exact match is recorded as http://identifiers.org/doid/DOID:0110315[11].
- hypertrophic cardiomyopathy 9's UMLS CUI is recorded as C1861065[12].
- hypertrophic cardiomyopathy 9's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- hypertrophic cardiomyopathy 9's Mondo ID is recorded as MONDO_0013412[14].
- hypertrophic cardiomyopathy 9's UniProt disease ID is recorded as DI-00239[15].