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Brugada syndrome 7
Summary
- Synonym
-
- BRGDA7
- Definition
- A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN3B gene on chromosome 11q24.
- Super Class
- Brugada syndrome autosomal dominant disease
External Links
- Disease Ontology
- DOID:0110224
- Mondo Disease Ontology
- MeSH
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9NY72 | Sodium channel regulatory subunit beta-3 |
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q8BHK2 | Sodium channel regulatory subunit beta-3 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001663 | Ventricular fibrillation |
| HP:0004755 | Supraventricular tachycardia |
