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familial isolated arrhythmogenic right ventricular dysplasia

Go to external page http://purl.obolibrary.org/obo/MONDO_0016342

Familial isolated arrhythmogenic right ventricular dysplasia (ARVC) is the familial autosomal dominant form of ARVC, a heart muscle disease characterized by life-threatening ventricular arrhythmias with left bundle branch block configuration that may manifest with palpitations, ventricular tachycardia, syncope and sudden fatal attacks, and that is due to dystrophy and fibro-fatty replacement of the right ventricular myocardium that may lead to right ventricular aneurysms. [ Orphanet:217656 ]

Synonyms: familial isolated arrhythmogenic right ventricular cardiomyopathy familial isolated ARVC familial isolated arrhythmogenic ventricular dysplasia familial isolated ARVD familial isolated arrhythmogenic right ventricular dysplasia familial isolated arrhythmogenic ventricular cardiomyopathy

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:217656 (MONDO:equivalentTo)
  • UMLS:C4274968 (MONDO:equivalentTo)
  • SCTID:715865008 (MONDO:equivalentTo)
  • GARD:17129 (Orphanet:217656)
  • OMIMPS:107970 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease, rare, nord_rare, orphanet_rare, clingen

exactMatch

http://linkedlifedata.com/resource/umls/id/C4274968

http://identifiers.org/snomedct/715865008

http://www.orpha.net/ORDO/Orphanet_217656

https://omim.org/phenotypicSeries/PS107970

id

MONDO:0016342

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0016342