dilated cardiomyopathy 1AA
dilated cardiomyopathy that has material basis in mutation in the ACTN2 gene on chromosome 1q43
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dilated cardiomyopathy 1AA
Summary
dilated cardiomyopathy 1AA is a rare disease[1].
Key Facts
- dilated cardiomyopathy 1AA's instance of is recorded as rare disease[2].
- dilated cardiomyopathy 1AA's instance of is recorded as class of disease[3].
- dilated cardiomyopathy 1AA's subclass of is recorded as dilated cardiomyopathy[4].
- dilated cardiomyopathy 1AA's subclass of is recorded as genetic disease[5].
- dilated cardiomyopathy 1AA's subclass of is recorded as autosomal dominant disease[6].
- dilated cardiomyopathy 1AA's MeSH descriptor ID is recorded as C567407[7].
- dilated cardiomyopathy 1AA's OMIM ID is recorded as 612158[8].
- dilated cardiomyopathy 1AA's Disease Ontology ID is recorded as DOID:0110428[9].
- dilated cardiomyopathy 1AA's health specialty is recorded as cardiology[10].
- dilated cardiomyopathy 1AA's genetic association is recorded as ACTN2[11].
- dilated cardiomyopathy 1AA's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110428[12].
- dilated cardiomyopathy 1AA's exact match is recorded as http://identifiers.org/doid/DOID:0110428[13].
- dilated cardiomyopathy 1AA's UMLS CUI is recorded as C2677338[14].
- dilated cardiomyopathy 1AA's ICD-10-CM is recorded as I42.0[15].
- dilated cardiomyopathy 1AA's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- dilated cardiomyopathy 1AA's Mondo ID is recorded as MONDO_0012808[17].
- dilated cardiomyopathy 1AA's UniProt disease ID is recorded as DI-00211[18].