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atrial septal defect 3

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any atrial heart septal defect in which the cause of the disease is a mutation in the MYH6 gene.
Uniprot Description A congenital heart malformation characterized by incomplete closure of the wall between the atria resulting in blood flow from the left to the right atria.
Mondo Term and Equivalent IDs
MONDO:0013567:  atrial septal defect 3
MESH:C563540: 
UMLS:C3279790: