| Metadata | |
|---|---|
| ID | DOID:0110221 |
| Name | Brugada syndrome 4 |
| Definition | A Brugada syndrome that has_material_basis_in heterozygous mutation in the gene encoding the beta-2 subunit of the voltage-dependent L-type calcium channel (CACNB2) on chromosome 10p12. https://www.ncbi.nlm.nih.gov/pubmed/17224476 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
BRGDA4 [EXACT] |
| Parent Relationships |
is_a Brugada syndrome |