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hypertrophic cardiomyopathy

Go to external page http://purl.obolibrary.org/obo/MONDO_0005045

A condition in which the myocardium is hypertrophied without an obvious cause. The hypertrophy is generally asymmetric and may be associated with obstruction of the ventricular outflow tract. [ NCIT:C34449 ]

Synonyms: hypertrophic subaortic stenosis hypertrophic cardiomyopathy obstructive hypertrophic cardiomyopathy hypertrophic obstructive cardiomyopathy

This is just here as a test because I lose it

Term information

database cross reference
  • MESH:D002312 (Orphanet:217569/e)
  • DOID:11984 (MONDO:equivalentTo)
  • NANDO:1200286 (https://orcid.org/0000-0003-0011-764X)
  • icd11.foundation:1830681485 (MONDO:equivalentTo)
  • NANDO:2201042 (https://orcid.org/0000-0003-0011-764X)
  • MedDRA:10020871 (Orphanet:217569/e)
  • ICD10CM:I42.1 (MONDO:mondoIsBroaderThanSource)
  • NCIT:C34449 (MONDO:equivalentTo)
  • ICD9:425.1 (https://orcid.org/0000-0002-9584-9618)
  • Orphanet:217569 (MONDO:equivalentTo)
  • NANDO:2100054 (https://orcid.org/0000-0003-0011-764X)
  • ICD9:425.4 (MONDO:relatedTo)
  • ICD9:425.11 (DOID:11984)
  • HP:0001639 (https://orcid.org/0000-0002-9584-9618)
  • MEDGEN:2881 (MONDO:equivalentTo)
  • NANDO:1200288 (https://orcid.org/0000-0003-0011-764X)
  • EFO:0000538 (MONDO:equivalentTo)
  • UMLS:C0007194 (MONDO:equivalentTo)
  • ICD10CM:I42.2 (MONDO:relatedTo)
  • SCTID:233873004 (MONDO:equivalentTo)
  • NANDO:2200229 (https://orcid.org/0000-0003-0011-764X)
Subsets

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

ClinGen label
hypertrophic cardiomyopathy [ NCIT:C34449 DOID:11984 icd11.foundation:1830681485 ]

closeMatch

http://identifiers.org/meddra/10020871

curated content resource

https://search.clinicalgenome.org/kb/conditions/MONDO:0005045

exactMatch

http://linkedlifedata.com/resource/umls/id/C0007194

http://identifiers.org/mesh/D002312

http://identifiers.org/snomedct/233873004

http://purl.obolibrary.org/obo/NCIT_C34449

http://identifiers.org/medgen/2881

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1830681485

http://purl.obolibrary.org/obo/DOID_11984

http://www.orpha.net/ORDO/Orphanet_217569

http://www.ebi.ac.uk/efo/EFO_0000538

has narrow synonym

familial hypertrophic cardiomyopathy

has related synonym

HCM - hypertrophic cardiomyopathy

id

MONDO:0005045

narrowMatch

http://purl.bioontology.org/ontology/ICD10CM/I42.1

relatedMatch

http://purl.bioontology.org/ontology/ICD10CM/I42.2

term tracker item

https://github.com/monarch-initiative/mondo/issues/5962