dilated cardiomyopathy 1E
dilated cardiomyopathy that has material basis in mutation in the SCN5A gene on chromosome 3p22.2
Press Enter · cited answer in seconds
0 sources
dilated cardiomyopathy 1E
Summary
dilated cardiomyopathy 1E is a rare disease[1].
Key Facts
- dilated cardiomyopathy 1E's instance of is recorded as rare disease[2].
- dilated cardiomyopathy 1E's instance of is recorded as class of disease[3].
- dilated cardiomyopathy 1E's subclass of is recorded as dilated cardiomyopathy[4].
- dilated cardiomyopathy 1E's subclass of is recorded as genetic disease[5].
- dilated cardiomyopathy 1E's subclass of is recorded as autosomal dominant disease[6].
- dilated cardiomyopathy 1E's MeSH descriptor ID is recorded as C563384[7].
- dilated cardiomyopathy 1E's OMIM ID is recorded as 601154[8].
- dilated cardiomyopathy 1E's Disease Ontology ID is recorded as DOID:0110433[9].
- dilated cardiomyopathy 1E's health specialty is recorded as cardiology[10].
- dilated cardiomyopathy 1E's genetic association is recorded as SCN5A[11].
- dilated cardiomyopathy 1E's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110433[12].
- dilated cardiomyopathy 1E's exact match is recorded as http://identifiers.org/doid/DOID:0110433[13].
- dilated cardiomyopathy 1E's UMLS CUI is recorded as C1832680[14].
- dilated cardiomyopathy 1E's ICD-10-CM is recorded as I42.0[15].
- dilated cardiomyopathy 1E's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- dilated cardiomyopathy 1E's Mondo ID is recorded as MONDO_0011003[17].
- dilated cardiomyopathy 1E's UniProt disease ID is recorded as DI-00214[18].