arrhythmogenic right ventricular cardiomyopathy
http://purl.obolibrary.org/obo/MONDO_0016587
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heart muscle disease that consists in progressive dystrophy of primarily the right ventricular myocardium with fibro-fatty replacement and ventricular dilation, and that is clinically characterized by ventricular arrhythmias and a risk of sudden cardiac death. [ Orphanet:247 ]
Term info
- DOID:0050431 (MONDO:equivalentTo)
- UMLS:C0349788 (Orphanet:247/e)
- NCIT:C84571 (MONDO:equivalentTo)
- GARD:0005847 (MONDO:equivalentTo)
- MedDRA:10058093 (Orphanet:247/e)
- UMLS:CN221565 (MONDO:equivalentTo)
- MESH:D019571 (Orphanet:247/e)
- ICD9:425.4 (MONDO:relatedTo)
- Orphanet:247 (MONDO:equivalentTo)
- UMLS:CN239850 (MONDO:equivalentTo)
- SCTID:281170005 (MONDO:equivalentTo)
gard_rare, disease_grouping, clingen, ordo_group_of_disorders
http://identifiers.org/meddra/10058093
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heart muscle disease that consists in progressive dystrophy of primarily the right ventricular myocardium with fibro-fatty replacement and ventricular dilation, and that is clinically characterized by ventricular arrhythmias and a risk of sudden cardiac death.
http://linkedlifedata.com/resource/umls/id/CN221565, http://linkedlifedata.com/resource/umls/id/C0349788, http://purl.obolibrary.org/obo/NCIT_C84571, http://identifiers.org/snomedct/281170005, http://purl.obolibrary.org/obo/Orphanet_247, http://purl.obolibrary.org/obo/DOID_0050431, http://identifiers.org/mesh/D019571, http://linkedlifedata.com/resource/umls/id/CN239850
ARVC, ARVD, arrhythmogenic RVD, right ventricular dysplasia, arrhythmogenic right ventricular dysplasia/cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy, arrhythmogenic right ventricular dysplasia, ARVC cardiomyopathy
MONDO:0016587