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 ]

Synonyms: Cardiomyopathies cardiomyopathy

This is just here as a test because I lose it

Term information

database cross reference
  • ICD9:425 (EFO:0000318)
  • MedDRA:10007636 (Orphanet:167848/e)
  • icd11.foundation:282225286 (MONDO:equivalentTo)
  • SCTID:57809008 (MONDO:relatedTo)
  • SCTID:85898001 (MONDO:equivalentTo)
  • EFO:0000318 (MONDO:equivalentTo)
  • MEDGEN:209232 (MONDO:equivalentTo)
  • ICD10CM:I42 (MONDO:equivalentTo)
  • Orphanet:167848 (MONDO:equivalentTo)
  • ICD9:425.4 (MONDO:relatedTo)
  • NCIT:C34830 (MONDO:equivalentTo)
  • UMLS:C0878544 (MONDO:equivalentTo)
  • MESH:D009202 (Orphanet:167848/e)
  • ICD9:425.9 (DOID:0050700)
  • DOID:0050700 (MONDO:equivalentTo)
Subsets

matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, matrix_llm__tag_qualy_lost_other, disease_grouping, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, mondo_top_grouping_member, matrix_txgnn_grouping_cardiovascular_disorder, mondo_top_grouping_musculoskeletal_system_disorder, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, matrix_txgnn_grouping_member, harrisons_view_cardiovascular_disorder, mondo_top_grouping_cardiovascular_disorder, harrisons_view_member, harrisons_view_musculoskeletal_system_disorder, ordo_group_of_disorders

closeMatch

http://identifiers.org/meddra/10007636

exactMatch

http://www.orpha.net/ORDO/Orphanet_167848

http://purl.bioontology.org/ontology/ICD10CM/I42

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/282225286

http://linkedlifedata.com/resource/umls/id/C0878544

http://purl.obolibrary.org/obo/NCIT_C34830

http://purl.obolibrary.org/obo/DOID_0050700

http://identifiers.org/mesh/D009202

http://identifiers.org/snomedct/85898001

http://identifiers.org/medgen/209232

http://www.ebi.ac.uk/efo/EFO_0000318

id

MONDO:0004994