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familial atrial fibrillation

Disease Summary
Associated Targets (51)
Tbio

31

Tclin

12

Tchem

8


Explore Associated Targets
Mondo Description An autosomal dominant heart condition that causes disruptions in the heart's normal rhythm. This condition is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular.
Disease Ontology Description An atrial fibrillation that has_material_basis_in autosomal dominant inheritance of the familial atrial fibrillation (ATFB) genes.
Mondo Term and Equivalent IDs
MONDO:0018054:  familial atrial fibrillation
GARD:0009740: 
OMIMPS:608583: 
Orphanet:334: 
SCTID:715395008: 
UMLS:CN204347: 
GWAS Targets (0)
No GWAS traits found
Disease Hierarchy
Target Novelty (Tin-x)