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Disease association ontology term - MONDO:0013567 - atrial septal defect 3

Term summary

ID
MONDO:0013567
Name
atrial septal defect 3
Ontology or CV name
Disease association
Definition
Any atrial heart septal defect in which the cause of the disease is a mutation in the MYH6 gene.

Parents

Annotation

Disease association

MONDO:0013567 - atrial septal defect 3

References:

Genes: