dilated cardiomyopathy 1J
dilated cardiomyopathy that has material basis in mutation in the EYA4 gene on chromosome 6q23.2
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dilated cardiomyopathy 1J
Summary
dilated cardiomyopathy 1J is a rare disease[1].
Key Facts
- dilated cardiomyopathy 1J's instance of is recorded as rare disease[2].
- dilated cardiomyopathy 1J's instance of is recorded as class of disease[3].
- dilated cardiomyopathy 1J's subclass of is recorded as dilated cardiomyopathy[4].
- dilated cardiomyopathy 1J's subclass of is recorded as syndrome associated with dilated cardiomyopathy[5].
- dilated cardiomyopathy 1J's subclass of is recorded as genetic disease[6].
- dilated cardiomyopathy 1J's subclass of is recorded as monogenic disease[7].
- dilated cardiomyopathy 1J's MeSH descriptor ID is recorded as C565337[8].
- dilated cardiomyopathy 1J's OMIM ID is recorded as 605362[9].
- dilated cardiomyopathy 1J's Disease Ontology ID is recorded as DOID:0110440[10].
- dilated cardiomyopathy 1J's Orphanet ID is recorded as 217622[11].
- dilated cardiomyopathy 1J's genetic association is recorded as EYA4[12].
- dilated cardiomyopathy 1J's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110440[13].
- dilated cardiomyopathy 1J's exact match is recorded as http://identifiers.org/doid/DOID:0110440[14].
- dilated cardiomyopathy 1J's UMLS CUI is recorded as C1854368[15].
- dilated cardiomyopathy 1J's UMLS CUI is recorded as C5679819[16].
- dilated cardiomyopathy 1J's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
- dilated cardiomyopathy 1J's Mondo ID is recorded as MONDO_0011541[18].
- dilated cardiomyopathy 1J's UniProt disease ID is recorded as DI-00217[19].