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Disease association ontology term - MONDO:0015001 - atrial fibrillation, familial, 18

Term summary

ID
MONDO:0015001
Name
atrial fibrillation, familial, 18
Ontology or CV name
Disease association
Definition
Any familial atrial fibrillation in which the cause of the disease is a mutation in the MYL4 gene.

Parents

Annotation

Disease association

MONDO:0015001 - atrial fibrillation, familial, 18

References:

Genes: