FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Brugada syndrome 2 ID (Ontology) DOID:0110219 (Human Disease)
Definition A Brugada syndrome that has_material_basis_in heterozygous mutation in the GPD1L gene on chromosome 3p22.
Also Known As "BRGDA2"
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 Genes
 Brugada syndrome 2       3
 for disease ribbon | Brugada syndrome 2       3
 model of | Brugada syndrome 2       3
Spanning Tree (Parents/Children)
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monogenic disease_________
heart conduction disease__|
                          Brugada syndrome
                           |__Brugada syndrome 2  3 rec.
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Is a Brugada syndrome
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Synonyms
  • "BRGDA2" EXACT OMO:0003012
Secondary IDs
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ICD10CM:I49.8
MESH:C567087
MIM:611777