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Familial isolated arrhythmogenic ventricular dysplasia, biventricular form

MedGen UID:: 1843254
•Concept ID:: C5679932
•: Disease or Syndrome

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

Monarch Initiative:	MONDO:0017402
Orphanet:	ORPHA293899

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GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVFamilial isolated arrhythmogenic ventricular dysplasia, biventricular 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, biventricular form

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Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form

MedGen
PHATRDRAFT_50885 [Phaeodactylum tricornutum CCAP 1055/1]
PHATRDRAFT_50885 [Phaeodactylum tricornutum CCAP 1055/1]
Gene ID:7200500

Gene
SSDH [Phaeodactylum tricornutum CCAP 1055/1]
SSDH [Phaeodactylum tricornutum CCAP 1055/1]
Gene ID:7195958

Gene
Protanomaly
Protanomaly

MedGen
Congenital myasthenic syndrome 20
Congenital myasthenic syndrome 20

MedGen

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