arrhythmogenic right ventricular dysplasia, familial, 14
MONDO:0030062Mondo
Findings
No curated finding names arrhythmogenic right ventricular dysplasia, familial, 14 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Middle age onset · Juvenile onset · Young adult onset
HPO, annotations 2026-09-02
Features
7 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- PalpitationsHPOHP:0001962
- 7 of 7 reported patients
- Chest painHPOHP:0100749
- 4 of 7 reported patients
- Left bundle branch blockHPOHP:0011713
- 4 of 7 reported patients
- Premature ventricular contractionHPOHP:0006682
- 2 of 7 reported patients
- PresyncopeHPOHP:0031972
- 2 of 7 reported patients
- Ventricular tachycardiaHPOHP:0004756
- 2 of 7 reported patients
- Right ventricular dilatationHPOHP:0005133
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- CDH2HGNC:1759
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2020
- Moderate · Ambry Genetics · Autosomal dominant · 2018
- Limited · Ambry Genetics · Autosomal dominant · 2025
Where it sits
Other names
2 names
Resolves to: arrhythmogenic right ventricular dysplasia, familial, 14
- Also called
- Arrhythmogenic Right Ventricular Cardiomyopathy 14ARVD14