Brugada syndrome 7
MONDO:0013146Mondo
Findings
No curated finding names Brugada syndrome 7 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any Brugada syndrome in which the cause of the disease is a mutation in the SCN3B gene.
Definition from the Mondo Disease Ontology (MONDO:0013146), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Middle age onset · Late young adult onset
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.
- Permanent atrial fibrillationHPOHP:0004754
- 2 of 3 reported patients
- Paroxysmal atrial fibrillationHPOHP:0004757
- 1 of 3 reported patients
- Prolonged P waveHPOHP:0034308
- 1 of 3 reported patients
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.
- SCN3BHGNC:20665
- Limited · Genomics England PanelApp · Autosomal dominant · 2021
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2019
- Limited · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2019
Where it sits
- A kind of
Other names
4 names
Resolves to: Brugada syndrome 7
- Also called
- BRGDA7Brugada syndrome caused by mutation in SCN3BBrugada syndrome type 7SCN3B Brugada syndrome