Brugada syndrome 3

Term ID

DOID:0110220

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. https://www.ncbi.nlm.nih.gov/pubmed/17224476

References

• GARD:10361
• ICD10CM:I49.8
• MESH:C567509
• OMIM:611875

Ontology

Human Disease   ( DOID:0110220 )