Details of Disease

General Information of Disease (ID: DISON7YO)

Disease Name Atrial fibrillation, familial, 18
Synonyms
atrial fibrillation, familial, 18; ATFB18; atrial fibrillation, familial, 18; MYL4 familial atrial fibrillation; atrial fibrillation, familial, type 18; familial atrial fibrillation caused by mutation in MYL4; ATFB18
Definition Any familial atrial fibrillation in which the cause of the disease is a mutation in the MYL4 gene.
Disease Hierarchy
DISL4AGF: Familial atrial fibrillation
DISON7YO: Atrial fibrillation, familial, 18
Disease Identifiers
MONDO ID
MONDO_0015001
UMLS CUI
C4310636
OMIM ID
617280
MedGen ID
934603

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
MYL4 OTURFCSE Strong Autosomal dominant [1]
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References

1 A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation. Nat Commun. 2016 Apr 12;7:11303. doi: 10.1038/ncomms11303.