GDF1, growth differentiation factor 1, 2657

N. diseases: 136; N. variants: 14
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 		0.710 Biomarker disease GENOMICS_ENGLAND
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.710 CausalMutation disease CLINVAR
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.710 Biomarker disease HPO
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.710 SusceptibilityMutation disease ORPHANET
CUI: C3151221
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C3151221
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6 		0.700 CausalMutation disease CLINVAR
CUI: C3151221
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6 		0.700 Biomarker disease CTD_human
CUI: C3151221
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C3178806
Disease: Right Atrial Isomerism
Right Atrial Isomerism 		0.620 Biomarker disease HPO
CUI: C3178806
Disease: Right Atrial Isomerism
Right Atrial Isomerism 		0.620 Biomarker disease CTD_human
CUI: C0175707
Disease: Asplenia Syndrome
Asplenia Syndrome 		0.600 CausalMutation disease CLINVAR
CUI: C0175707
Disease: Asplenia Syndrome
Asplenia Syndrome 		0.600 Biomarker disease CTD_human
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects 		0.430 GeneticVariation group CLINVAR
CUI: C0040761
Disease: Transposition of Great Vessels
Transposition of Great Vessels 		0.410 CausalMutation disease CLINVAR
CUI: C0040761
Disease: Transposition of Great Vessels
Transposition of Great Vessels 		0.410 Biomarker disease HPO
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle 		0.400 CausalMutation disease CLINVAR
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle 		0.400 Biomarker disease HPO
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		0.400 Biomarker disease CTD_human
CUI: C0265357
Disease: Polysplenia Syndrome
Polysplenia Syndrome 		0.300 Biomarker disease CTD_human
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus 		0.300 Biomarker disease CTD_human
CUI: C3178807
Disease: Left Atrial Isomerism
Left Atrial Isomerism 		0.300 Biomarker disease CTD_human
CUI: C4277690
Disease: Ciliopathies
Ciliopathies 		0.300 Biomarker disease GENOMICS_ENGLAND
CUI: C0265908
Disease: Congenital atresia of pulmonary artery
Congenital atresia of pulmonary artery 		0.110 Biomarker disease HPO
CUI: C1389018
Disease: Atrioventricular Septal Defect
Atrioventricular Septal Defect 		0.110 Biomarker disease HPO
CUI: C0003492
Disease: Aortic coarctation
Aortic coarctation 		0.100 Biomarker disease HPO