hypertrophic cardiomyopathy 16
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the MYOZ2 gene on chromosome 4q26
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hypertrophic cardiomyopathy 16
Summary
hypertrophic cardiomyopathy 16 is a class of disease[1].
Key Facts
- hypertrophic cardiomyopathy 16's instance of is recorded as class of disease[2].
- hypertrophic cardiomyopathy 16's subclass of is recorded as familial hypertrophic cardiomyopathy[3].
- hypertrophic cardiomyopathy 16's OMIM ID is recorded as 613838[4].
- hypertrophic cardiomyopathy 16's Disease Ontology ID is recorded as DOID:0110322[5].
- hypertrophic cardiomyopathy 16's Orphanet ID is recorded as 155[6].
- hypertrophic cardiomyopathy 16's genetic association is recorded as MYOZ2[7].
- hypertrophic cardiomyopathy 16's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110322[8].
- hypertrophic cardiomyopathy 16's exact match is recorded as http://identifiers.org/doid/DOID:0110322[9].
- hypertrophic cardiomyopathy 16's UMLS CUI is recorded as C3151204[10].
- hypertrophic cardiomyopathy 16's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
- hypertrophic cardiomyopathy 16's Mondo ID is recorded as MONDO_0013455[12].
- hypertrophic cardiomyopathy 16's UniProt disease ID is recorded as DI-03037[13].