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atrial fibrillation, familial, 12
Disease Summary
Associated Targets (1)
Tclin
1
Mondo Description Any familial atrial fibrillation in which the cause of the disease is a mutation in the ABCC9 gene.
Uniprot Description A familial form of atrial fibrillation, a common sustained cardiac rhythm disturbance. Atrial fibrillation is characterized by disorganized atrial electrical activity and ineffective atrial contraction promoting blood stasis in the atria and reduces ventricular filling. It can result in palpitations, syncope, thromboembolic stroke, and congestive heart failure.
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
OMIM:614050
UMLS:C3279695
MONDO:0013545
High level summary of knowledge for a disease, including descriptions and datasource references.