atrial fibrillation, familial, 4
MONDO:0012677Mondo
Findings
No curated finding names atrial fibrillation, familial, 4 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any familial atrial fibrillation in which the cause of the disease is a mutation in the KCNE2 gene.
Definition from the Mondo Disease Ontology (MONDO:0012677), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Late onset · Middle age onset
HPO, annotations 2026-09-02
Features
5 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.
- Atrial fibrillationHPOHP:0005110
- 9 of 9 reported patients
- Premature atrial contractionsHPOHP:0006699
- 10 of 10 reported patients
- PalpitationsHPOHP:0001962
- 9 of 10 reported patients
- Paroxysmal atrial fibrillationHPOHP:0004757
- 3 of 10 reported patients
- Permanent atrial fibrillationHPOHP:0004754
- 1 of 10 reported patients
Where it sits
- A kind of
Other names
3 names
Resolves to: atrial fibrillation, familial, 4
- Also called
- atrial fibrillation, familial, type 4familial atrial fibrillation caused by mutation in KCNE2KCNE2 familial atrial fibrillation