Term info
- HP:0001639 (https://orcid.org/0000-0002-9584-9618)
- MedDRA:10020871 (Orphanet:217569/e)
- EFO:0000538 (MONDO:equivalentTo)
- SCTID:233873004 (MONDO:equivalentTo)
- UMLS:C0007194 (Orphanet:217569/e)
- ICD9:425.1 (https://orcid.org/0000-0002-9584-9618)
- ICD9:425.4 (MONDO:relatedTo)
- MESH:D002312 (Orphanet:217569/e)
- ICD10CM:I42.1 (MONDO:equivalentTo)
- DOID:11984 (MONDO:equivalentTo)
- NCIT:C34449 (MONDO:equivalentTo)
- ICD9:425.11 (DOID:11984)
- Orphanet:217569 (MONDO:equivalentTo)
disease_grouping, clingen, ordo_group_of_disorders
https://github.com/monarch-initiative/mondo/issues/5962
http://identifiers.org/meddra/10020871
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.
http://linkedlifedata.com/resource/umls/id/C0007194, http://identifiers.org/mesh/D002312, http://identifiers.org/snomedct/233873004, http://purl.bioontology.org/ontology/ICD10CM/I42.1, http://purl.obolibrary.org/obo/NCIT_C34449, http://purl.obolibrary.org/obo/DOID_11984, http://purl.obolibrary.org/obo/Orphanet_217569
hypertrophic subaortic stenosis, hypertrophic cardiomyopathy, obstructive hypertrophic cardiomyopathy, hypertrophic obstructive cardiomyopathy
familial hypertrophic cardiomyopathy
HCM - hypertrophic cardiomyopathy
MONDO:0005045