Brugada syndrome 1 (Q27677682)
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Brugada syndrome that has material basis in heterozygous mutation in the SCN5A gene on chromosome 3p22
- BRGDA1
- Right Bundle Branch Block, St Segment Elevation, and Sudden Death Syndrome
- Brugada Syndrome type 1
- Cardiac Conduction Defect, Nonspecific
- Sudden Unexplained Nocturnal Death Syndrome
- BRUGADA SYNDROME 1; BRGDA1
- BRUGADA SYNDROME 1
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Brugada syndrome 1 |
Brugada syndrome that has material basis in heterozygous mutation in the SCN5A gene on chromosome 3p22 |
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