Term Name: | Brugada syndrome 3 |
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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 ) |