Details of Disease | DrugMAP

General Information of Disease (ID: DISHUYSG)

Disease Name	Atrial fibrillation, familial, 13
Synonyms	ATFB13; SCN1B familial atrial fibrillation; atrial fibrillation, familial, 13; familial atrial fibrillation caused by mutation in SCN1B; atrial fibrillation, familial, type 13
Definition	Any familial atrial fibrillation in which the cause of the disease is a mutation in the SCN1B gene.
Disease Hierarchy	DISL4AGF: Familial atrial fibrillation DISHUYSG: Atrial fibrillation, familial, 13
Disease Identifiers	MONDO ID MONDO_0014155 UMLS CUI C3809311 OMIM ID 615377 MedGen ID 815641

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
SCN1B	OTGD78J3	Limited	Unknown	[1]
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References

1	Mutations in sodium channel 1- and 2-subunits associated with atrial fibrillation. Circ Arrhythm Electrophysiol. 2009 Jun;2(3):268-75. doi: 10.1161/CIRCEP.108.779181. Epub 2009 Mar 6.