Details of Disease

General Information of Disease (ID: DISTWTOD)

Disease Name Brugada syndrome 7
Synonyms atrial fibrillation, familial, 16; Brugada syndrome caused by mutation in SCN3B; BRGDA7; SCN3B Brugada syndrome; Brugada syndrome 7; Brugada syndrome type 7
Definition Any Brugada syndrome in which the cause of the disease is a mutation in the SCN3B gene.
Disease Hierarchy
DISSGN0E: Brugada syndrome
DISTWTOD: Brugada syndrome 7
Disease Identifiers
MONDO ID
MONDO_0013146
MESH ID
C567734
UMLS CUI
C2751088
OMIM ID
613120
MedGen ID
413472

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
SCN3B OTNTQT9O Limited Autosomal dominant [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.