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Familial isolated arrhythmogenic ventricular dysplasia, right dominant form

MedGen UID:
799413
•Concept ID:
CN203147
•
Disease or Syndrome
Synonyms: Familial isolated arrhythmogenic ventricular cardiomyopathy, classic form; familial isolated arrhythmogenic ventricular cardiomyopathy, classic form; familial isolated arrhythmogenic ventricular cardiomyopathy, right dominant form; Familial isolated arrhythmogenic ventricular cardiomyopathy, right dominant form; Familial isolated arrhythmogenic ventricular dysplasia, classic form; familial isolated arrhythmogenic ventricular dysplasia, classic form; familial isolated arrhythmogenic ventricular dysplasia, right dominant form
 
Monarch Initiative: MONDO:0017403
Orphanet: ORPHA293910

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVFamilial isolated arrhythmogenic ventricular dysplasia, right dominant form
Follow this link to review classifications for Familial isolated arrhythmogenic ventricular dysplasia, right dominant form in Orphanet.

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Diagnosis

Genetic factors in dilated cardiomyopathy.
Mestroni L, Milasin J, Vatta M, Pinamonti B, Sinagra G, Rocco C, Matulic M, Falaschi A, Giacca M, Camerini F
Arch Mal Coeur Vaiss 1996 Jul;89 Spec No 2:15-20. PMID: 8881501

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