The association between NKX2-5 (NK2 Homeobox 5) and Atrial Septal Defect 7 With Or Without Atrioventricular Conduction Defects is well established and manually curated, with its 3 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and causative variation.
Sources3
Clinical variants488
Symptoms18
Compounds0
Trials0
Publications32
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.