secundum atrial septal defect Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A kind of atrial septum defect arising from an enlarged foramen ovale, inadequate growth of the septum secundum, or excessive absorption of the septum primum. (Human Phenotype Ontology, HP_0001684)
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5 genes associated with the secundum atrial septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GATA6 GATA binding protein 6
MYH6 myosin, heavy chain 6, cardiac muscle, alpha
NF1 neurofibromin 1
NKX2-5 NK2 homeobox 5
PTF1A pancreas specific transcription factor, 1a