Details of Disease | DrugMAP

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.