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Disease association ontology term - MONDO:0018054 - familial atrial fibrillation

Term summary

ID
MONDO:0018054
Name
familial atrial fibrillation
Ontology or CV name
Disease association
Definition
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.

Parents

Annotation

Disease association

MONDO:0014340 - atrial fibrillation, familial, 15

References:

Genes:

MONDO:0015001 - atrial fibrillation, familial, 18

References:

Genes: