dilated cardiomyopathy
Cardiomyopathy which is characterized by dilation and contractile dysfunction of the left and right ventricles. It may be idiopathic, or it may result from a myocardial infarction, myocardial infection, or alcohol abuse. It is a cause of congestive heart failure. [ NCIT:P378 ]
Term info
- Orphanet:217604 (MONDO:equivalentTo)
- NCIT:C84673 (MONDO:equivalentTo)
- MedDRA:10056370 (Orphanet:217604/e)
- MP:0002795 (EFO:0000407)
- ICD9:425.4 (MONDO:relatedTo)
- EFO:0000407 (MONDO:equivalentTo)
- SCTID:195021004 (MONDO:equivalentTo)
- MESH:D002311 (Orphanet:217604/e)
- DOID:12930 (MONDO:equivalentTo)
- ICD10CM:I42.0 (Orphanet:217604/e)
- UMLS:C0007193 (Orphanet:217604/e)
- HP:0001644 (MONDO:otherHierarchy)
disease_grouping, ordo_group_of_disorders
http://identifiers.org/meddra/10056370
Cardiomyopathy which is characterized by dilation and contractile dysfunction of the left and right ventricles. It may be idiopathic, or it may result from a myocardial infarction, myocardial infection, or alcohol abuse. It is a cause of congestive heart failure.
http://identifiers.org/snomedct/195021004, http://identifiers.org/mesh/D002311, http://purl.bioontology.org/ontology/ICD10CM/I42.0, http://linkedlifedata.com/resource/umls/id/C0007193, http://purl.obolibrary.org/obo/DOID_12930, http://purl.obolibrary.org/obo/Orphanet_217604, http://purl.obolibrary.org/obo/NCIT_C84673
dilated cardiomyopathy
congestive cardiomyopathy, familial dilated cardiomyopathy, idiopathic dilation cardiomyopathy, primary dilated cardiomyopathy
MONDO:0005021