Details of Disease

General Information of Disease (ID: DIS2QULB)

Disease Name Atrial fibrillation, familial, 15
Synonyms
ATFB15; NUP155 familial atrial fibrillation; atrial fibrillation, familial, 15; atrial fibrillation 15; atrial fibrillation, familial, type 15; familial atrial fibrillation caused by mutation in NUP155
Definition Any familial atrial fibrillation in which the cause of the disease is a mutation in the NUP155 gene.
Disease Hierarchy
DISL4AGF: Familial atrial fibrillation
DIS2QULB: Atrial fibrillation, familial, 15
Disease Identifiers
MONDO ID
MONDO_0014340
UMLS CUI
C4014269
OMIM ID
615770
MedGen ID
862706

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
NUP155 OTIIAH4E Limited Autosomal recessive [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.