FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Brugada syndrome 4 ID (Ontology) DOID:0110221 (Human Disease)
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.
Also Known As "BRGDA4"
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 Genes
 Brugada syndrome 4       1
 for disease ribbon | Brugada syndrome 4       1
 model of | Brugada syndrome 4       1
Spanning Tree (Parents/Children)
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monogenic disease_________
heart conduction disease__|
                          Brugada syndrome
                           |__Brugada syndrome 4  1 rec.
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Synonyms
  • "BRGDA4" EXACT OMO:0003012
Secondary IDs
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GARD:10362
ICD10CM:I49.8
MESH:C567508
MIM:611876