Details of Disease

General Information of Disease (ID: DISZBKHJ)

Disease Name Atrial fibrillation, familial, 6
Synonyms ATFB6; atrial fibrillation, familial, type 6; NPPA familial atrial fibrillation; atrial fibrillation, familial, 6; familial atrial fibrillation caused by mutation in NPPA
Definition Any familial atrial fibrillation in which the cause of the disease is a mutation in the NPPA gene.
Disease Hierarchy
DISL4AGF: Familial atrial fibrillation
DISZBKHJ: Atrial fibrillation, familial, 6
Disease Identifiers
MONDO ID
MONDO_0012816
MESH ID
C567400
UMLS CUI
C2677294
OMIM ID
612201
MedGen ID
394252

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
NPPA OTMQNTNX 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.