GATA4, GATA binding protein 4, 2626

N. diseases: 336; N. variants: 72
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		0.900 GeneticVariation disease CLINVAR
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		0.900 Biomarker disease GENOMICS_ENGLAND
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		0.900 CausalMutation disease CLINVAR
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		0.900 Biomarker disease CTD_human
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.800 CausalMutation disease CLINVAR
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.800 Biomarker disease HPO
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.800 Biomarker disease CTD_human
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C3809858
Disease: TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE
TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE 		0.700 CausalMutation disease CLINVAR
CUI: C3809858
Disease: TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE
TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C3809858
Disease: TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE
TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C3809858
Disease: TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE
TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE 		0.700 Biomarker disease CTD_human
CUI: C3280777
Disease: VENTRICULAR SEPTAL DEFECT 1
VENTRICULAR SEPTAL DEFECT 1 		0.600 CausalMutation disease CLINVAR
CUI: C3280777
Disease: VENTRICULAR SEPTAL DEFECT 1
VENTRICULAR SEPTAL DEFECT 1 		0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C3280777
Disease: VENTRICULAR SEPTAL DEFECT 1
VENTRICULAR SEPTAL DEFECT 1 		0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C3280781
Disease: ATRIOVENTRICULAR SEPTAL DEFECT 4
ATRIOVENTRICULAR SEPTAL DEFECT 4 		0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C3280781
Disease: ATRIOVENTRICULAR SEPTAL DEFECT 4
ATRIOVENTRICULAR SEPTAL DEFECT 4 		0.600 CausalMutation disease CLINVAR
CUI: C3280781
Disease: ATRIOVENTRICULAR SEPTAL DEFECT 4
ATRIOVENTRICULAR SEPTAL DEFECT 4 		0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.500 Biomarker group HPO
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.500 Biomarker group CTD_human
CUI: C0235833
Disease: Congenital diaphragmatic hernia
Congenital diaphragmatic hernia 		0.460 Biomarker disease HPO
CUI: C1389016
Disease: ATRIOVENTRICULAR CANAL DEFECT
ATRIOVENTRICULAR CANAL DEFECT 		0.450 Biomarker disease HPO
CUI: C1389016
Disease: ATRIOVENTRICULAR CANAL DEFECT
ATRIOVENTRICULAR CANAL DEFECT 		0.450 Biomarker disease CTD_human
CUI: C0344724
Disease: Ostium secundum atrial septal defect
Ostium secundum atrial septal defect 		0.410 GeneticVariation disease CLINVAR