cardiomyopathy
A disease of the heart muscle or myocardium proper. Cardiomyopathies may be classified as either primary or secondary, on the basis of etiology, or on the pathophysiology of the lesion: hypertrophic, dilated, or restrictive. [ NCIT:C34830 ]
Term info
- DOID:0050700 (MONDO:equivalentTo)
- EFO:0000318 (MONDO:equivalentTo)
- MESH:D009202 (Orphanet:167848/e)
- Orphanet:167848 (MONDO:equivalentTo)
- NCIT:C34830 (MONDO:equivalentTo)
- ICD9:425 (EFO:0000318)
- ICD10CM:I42 (MONDO:equivalentTo)
- MedDRA:10007636 (Orphanet:167848/e)
- SCTID:85898001 (MONDO:equivalentTo)
- ICD9:425.4 (MONDO:relatedTo)
- ICD9:425.9 (DOID:0050700)
- GARD:0011958 (MONDO:equivalentTo)
- UMLS:C0878544 (Orphanet:167848/e)
- SCTID:57809008 (MONDO:relatedTo)
disease_grouping, ordo_group_of_disorders
http://identifiers.org/meddra/10007636
A disease of the heart muscle or myocardium proper. Cardiomyopathies may be classified as either primary or secondary, on the basis of etiology, or on the pathophysiology of the lesion: hypertrophic, dilated, or restrictive.
http://purl.bioontology.org/ontology/ICD10CM/I42, http://linkedlifedata.com/resource/umls/id/C0878544, http://purl.obolibrary.org/obo/DOID_0050700, http://purl.obolibrary.org/obo/NCIT_C34830, http://identifiers.org/mesh/D009202, http://identifiers.org/snomedct/85898001, http://purl.obolibrary.org/obo/Orphanet_167848
Cardiomyopathies, cardiomyopathy
MONDO:0004994