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Familial isolated arrhythmogenic ventricular dysplasia, left dominant form

MedGen UID:: 798298
•Concept ID:: CN203145
•: Disease or Syndrome

Synonyms:	Familial isolated arrhythmogenic ventricular cardiomyopathy, left dominant form; familial isolated arrhythmogenic ventricular cardiomyopathy, left dominant form; familial isolated arrhythmogenic ventricular dysplasia, left dominant form

Monarch Initiative:	MONDO:0017401
Orphanet:	ORPHA293888

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GTR
MeSH
Orphanet

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVFamilial isolated arrhythmogenic ventricular dysplasia, left dominant form

Disorder by Site
- Disorder of cardiovascular system
  - Abnormality of the cardiovascular system
    - Abnormal heart morphology
      - Arrhythmogenic right ventricular cardiomyopathy
        Familial isolated arrhythmogenic right ventricular dysplasia
        Familial isolated arrhythmogenic ventricular dysplasia, left dominant form

Follow this link to review classifications for Familial isolated arrhythmogenic ventricular dysplasia, left dominant form in Orphanet.

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Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form

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