atrial fibrillation, familial, 10
MONDO:0013530Mondo
Findings
No curated finding names atrial fibrillation, familial, 10 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 SCN5A gene.
Definition from the Mondo Disease Ontology (MONDO:0013530), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Middle age onset
HPO, annotations 2026-09-02
Features
9 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.
- Tricuspid regurgitationHPOHP:0005180
- 2 of 2 reported patients
- BradycardiaHPOHP:0001662
- 5 of 6 reported patients
- Left atrial enlargementHPOHP:0031295
- 1 of 2 reported patients
- Paroxysmal atrial fibrillationHPOHP:0004757
- 1 of 2 reported patients
- Permanent atrial fibrillationHPOHP:0004754
- 1 of 2 reported patients
- Right ventricular dilatationHPOHP:0005133
- 3 of 6 reported patients
- StrokeHPOHP:0001297
Where it sits
Other names
3 names
Resolves to: atrial fibrillation, familial, 10
- Also called
- atrial fibrillation, familial, type 10familial atrial fibrillation caused by mutation in SCN5ASCN5A familial atrial fibrillation