ventricular fibrillation, paroxysmal familial, 2
Findings
No curated finding names ventricular fibrillation, paroxysmal familial, 2 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any ventricular fibrillation in which the cause of the disease is a mutation in the DPP6 gene.
Definition from the Mondo Disease Ontology (MONDO:0013063), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
3 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.
- Sudden cardiac deathHPOHP:0001645
- Occasional (5% to 29% of cases) · Adult onset
- Premature ventricular contractionHPOHP:0006682
- Ventricular fibrillationHPOHP:0001663
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.
- DPP6HGNC:3010
- Limited · Ambry Genetics · Autosomal dominant · 2024
Where it sits
Other names
3 names
Resolves to: ventricular fibrillation, paroxysmal familial, 2
- Also called
- DPP6 ventricular fibrillation (disease)ventricular fibrillation (disease) caused by mutation in DPP6ventricular fibrillation, paroxysmal familial, type 2