Details of Disease | DrugMAP

General Information of Disease (ID: DISH4OHI)

Disease Name	Long QT syndrome 10
Synonyms	atrial fibrillation, familial, 17; SCN4B long QT syndrome; long QT syndrome type 10; LQT10; long QT syndrome caused by mutation in SCN4B; long QT syndrome 10
Definition	Any long QT syndrome in which the cause of the disease is a mutation in the SCN4B gene.
Disease Hierarchy	DISRNNCY: Familial long QT syndrome DISH4OHI: Long QT syndrome 10
Disease Identifiers	MONDO ID MONDO_0012737 MESH ID C567514 UMLS CUI C2678484 OMIM ID 611819 MedGen ID 394836

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
SCN4B	OT3JSUWO	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.