Trait
Right ventricular cardiomyopathy
Right ventricular dysfunction (global or regional) with functional and morphological right ventricular abnormalities, with or without left ventricular disease.
Summary
- Also called
- Cardiomyopathy, right ventricular
- Body system
- Abnormality of the cardiovascular system
Reference genomeGRCh38hg38
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Get my Genome Test7 genes linked to Right ventricular cardiomyopathy
Changes in these genes cause rare conditions in which Right ventricular cardiomyopathy is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| DSPdesmoplakin | Always | In 1 condition |
| JUPjunction plakoglobin | Always | In 2 conditions |
| PKP2plakophilin 2 | Always | In 1 condition |
| DSC2desmocollin 2 | Not recorded | In 1 condition |
| DSG2desmoglein 2 | Not recorded | In 1 condition |
| TGFB3transforming growth factor beta 3 | Not recorded | In 1 condition |
| TMEM43transmembrane protein 43 | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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