NKX2-5, NK2 homeobox 5, 1482

N. diseases: 165; N. variants: 55
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia
0.110 GeneticVariation phenotype BEFREE A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias. 25503402 2015
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia
0.110 Biomarker phenotype HPO