Details of Disease

General Information of Disease (ID: DISAODPR)

Disease Name Atrial fibrillation, familial, 14
Synonyms ATFB14; atrial fibrillation, familial, 14; atrial fibrillation, familial, type 14; familial atrial fibrillation caused by mutation in SCN2B; SCN2B familial atrial fibrillation
Definition Any familial atrial fibrillation in which the cause of the disease is a mutation in the SCN2B gene.
Disease Hierarchy
DISL4AGF: Familial atrial fibrillation
DISAODPR: Atrial fibrillation, familial, 14
Disease Identifiers
MONDO ID
MONDO_0014156
UMLS CUI
C3809312
OMIM ID
615378
MedGen ID
815642

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
SCN2B OTFAHJ38 Moderate Autosomal dominant [1]
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References

1 Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and Reclassifications. Hum Mutat. 2017 May;38(5):600-608. doi: 10.1002/humu.23183. Epub 2017 Feb 13.