Details of Disease

General Information of Disease (ID: DIS21MGL)

Disease Name Brugada syndrome 2
Synonyms Brugada syndrome type 2; BRGDA2; Brugada syndrome caused by mutation in GPD1L; Brugada syndrome 2; GPD1L Brugada syndrome
Definition Any Brugada syndrome in which the cause of the disease is a mutation in the GPD1L gene.
Disease Hierarchy
DISSGN0E: Brugada syndrome
DIS21MGL: Brugada syndrome 2
Disease Identifiers
MONDO ID
MONDO_0012728
MESH ID
C567087
UMLS CUI
C2673193
OMIM ID
611777
MedGen ID
382031

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
GPD1L OTVLWW9T Limited Unknown [1]
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References

1 The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources. Genet Med. 2022 Aug;24(8):1732-1742. doi: 10.1016/j.gim.2022.04.017. Epub 2022 May 4.