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: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.960 Biomarker disease CTD_human
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.960 Biomarker disease HPO
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.960 Biomarker disease GENOMICS_ENGLAND
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.960 Biomarker disease GENOMICS_ENGLAND
CUI: C0152101
Disease: Hypoplastic Left Heart Syndrome
Hypoplastic Left Heart Syndrome 		0.810 Biomarker disease CTD_human
CUI: C0152101
Disease: Hypoplastic Left Heart Syndrome
Hypoplastic Left Heart Syndrome 		0.810 Biomarker disease HPO
CUI: C3276096
Disease: ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS
ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS 		0.800 Biomarker disease CTD_human
CUI: C3276096
Disease: ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS
ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C3276096
Disease: ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS
ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C3502353
Disease: Atrial Septal Defect with Atrioventricular Conduction Defects
Atrial Septal Defect with Atrioventricular Conduction Defects 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C1857586
Disease: CONOTRUNCAL HEART MALFORMATIONS (disorder)
CONOTRUNCAL HEART MALFORMATIONS (disorder) 		0.600 Biomarker disease CTD_human
CUI: C1857586
Disease: CONOTRUNCAL HEART MALFORMATIONS (disorder)
CONOTRUNCAL HEART MALFORMATIONS (disorder) 		0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C2673630
Disease: HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5 (disorder)
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5 (disorder) 		0.600 Biomarker disease CTD_human
CUI: C2673630
Disease: HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5 (disorder)
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5 (disorder) 		0.600 Biomarker disease GENOMICS_ENGLAND
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
CUI: C3280795
Disease: HYPOPLASTIC LEFT HEART SYNDROME 2
HYPOPLASTIC LEFT HEART SYNDROME 2 		0.500 Biomarker disease GENOMICS_ENGLAND
CUI: C3280795
Disease: HYPOPLASTIC LEFT HEART SYNDROME 2
HYPOPLASTIC LEFT HEART SYNDROME 2 		0.500 Biomarker disease GENOMICS_ENGLAND
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.490 Biomarker group CTD_human
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.490 Biomarker group HPO
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.460 Biomarker disease HPO
CUI: C0344724
Disease: Ostium secundum atrial septal defect
Ostium secundum atrial septal defect 		0.430 Biomarker disease HPO
CUI: C0018816
Disease: Heart Septal Defects
Heart Septal Defects 		0.420 Biomarker group HPO
CUI: C0018816
Disease: Heart Septal Defects
Heart Septal Defects 		0.420 Biomarker group GENOMICS_ENGLAND
CUI: C0149630
Disease: Bicuspid aortic valve
Bicuspid aortic valve 		0.420 Biomarker disease HPO