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Familial isolated arrhythmogenic ventricular dysplasia, left dominant form

MedGen UID:: 1842559
•Concept ID:: C5679933
•: 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

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVFamilial isolated arrhythmogenic ventricular dysplasia, left dominant form

Abnormal cardiovascular system morphology
- Abnormal heart morphology
  - Abnormal myocardium morphology
    - Cardiomyopathy
      - Arrhythmogenic right ventricular cardiomyopathy
        Familial isolated arrhythmogenic right ventricular dysplasia
        Familial isolated arrhythmogenic ventricular dysplasia, left dominant form

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

MedGen
Mageh1 MAGE family member H1 [Mus musculus]
Mageh1 MAGE family member H1 [Mus musculus]
Gene ID:75625

Gene
sapM [Mycobacterium tuberculosis H37Rv]
sapM [Mycobacterium tuberculosis H37Rv]
Gene ID:887988

Gene
MIR496 microRNA 496 [Homo sapiens]
MIR496 microRNA 496 [Homo sapiens]
Gene ID:574454

Gene
CTA1 [Saccharomyces cerevisiae S288C]
CTA1 [Saccharomyces cerevisiae S288C]
Gene ID:851843

Gene

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