NKX2-5, NK2 homeobox 5, 1482

N. diseases: 165; N. variants: 55
Disease: VENTRICULAR SEPTAL DEFECT 3 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3280785
Disease: VENTRICULAR SEPTAL DEFECT 3
VENTRICULAR SEPTAL DEFECT 3 		0.500 GeneticVariation disease UNIPROT A novel NKX2-5 mutation in familial ventricular septal defect. 21165553 2011
CUI: C3280785
Disease: VENTRICULAR SEPTAL DEFECT 3
VENTRICULAR SEPTAL DEFECT 3 		0.500 GeneticVariation disease UNIPROT Mutations of the GATA4 and NKX2.5 genes in Chinese pediatric patients with non-familial congenital heart disease. 21110066 2010
CUI: C3280785
Disease: VENTRICULAR SEPTAL DEFECT 3
VENTRICULAR SEPTAL DEFECT 3 		0.500 Biomarker disease GENOMICS_ENGLAND
CUI: C3280785
Disease: VENTRICULAR SEPTAL DEFECT 3
VENTRICULAR SEPTAL DEFECT 3 		0.500 Biomarker disease GENOMICS_ENGLAND