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arrhythmogenic right ventricular dysplasia 1

MeSH: C536932ORPHA: 3403

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Clinical Presentation
  4. 4. Classification & Codes

Overview

arrhythmogenic right ventricular dysplasia that has material basis in heterozygous mutation in the TGFB3 gene on chromosome 14q24

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Clinical Presentation

Signs and symptoms associated with arrhythmogenic right ventricular dysplasia 1, sourced from HPO and Orphanet clinical annotations.

Abnormal ventricular myocardium morphologyCongestive heart failureCardiomegalyPericardial effusionRight ventricular failureTricuspid regurgitationRight atrial thrombusRegional right ventricular hypokinesisRight ventricular aneurysmSyncopeTachycardiaHydrops fetalisPleural effusionPulmonary valve atresiaArrhythmia

Classification & Codes

MeSH Code

C536932

Orphanet Code

ORPHA:3403
arrhythmogenic right ventricular dysplasia 1
MeSHC536932
OrphanetORPHA:3403
Treatments0 drug(s)
Symptoms on record15 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO