| Term Name: | Brugada syndrome 3 | 
|---|---|
| Synonyms: | BRGDA3 | 
| Definition: | A Brugada syndrome that has_material_basis_in heterozygous mutation in the gene encoding the alpha-1C subunit of the L-type voltage-dependent calcium channel (CACNA1C) on chromosome 12p13. | 
| Ontology: | Human Disease [DOID:0110220] ( DOID:0110220 ) |