| Metadata | |
|---|---|
| ID | DOID:0110220 |
| Name | Brugada syndrome 3 |
| 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. https://www.ncbi.nlm.nih.gov/pubmed/17224476 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
BRGDA3 [EXACT] |
| Parent Relationships |
is_a Brugada syndrome |