NKX2-5, NK2 homeobox 5, 1482

N. diseases: 165; N. variants: 55
Disease: ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1843687
Disease: ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)
ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder) 		0.300 GermlineCausalMutation disease ORPHANET A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation. 23525379 2013
CUI: C1843687
Disease: ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)
ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder) 		0.300 GermlineCausalMutation disease ORPHANET Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation. 22818067 2012