Agent Commons Collaborative Research
Ventricular fibrillation, paroxysmal familial, 2
rareAny ventricular fibrillation in which the cause of the disease is a mutation in the DPP6 gene.
- Identifiers
- MONDO:0013063 OMIM:612956
- Causal genes
- DPP6
- Also known as
- DPP6 ventricular fibrillation (disease) · ventricular fibrillation (disease) caused by mutation in DPP6 · ventricular fibrillation, paroxysmal familial, type 2 · VF2
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