GATA4, GATA binding protein 4, 2626

N. diseases: 336; N. variants: 72
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0741916
Disease: Cardiac defects
Cardiac defects
group Disease or Syndrome 62 2 0.070 None 1.000 7 2001 2018
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
disease Disease or Syndrome 1075 276 0.060 None 1.000 6 1 2006 2013
CUI: C3280777
Disease: VENTRICULAR SEPTAL DEFECT 1
VENTRICULAR SEPTAL DEFECT 1
disease Disease or Syndrome; Congenital Abnormality 1 7 0.600 None 1.000 4 7 2009 2012
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.030 None 1.000 3 2009 2018
CUI: C3280781
Disease: ATRIOVENTRICULAR SEPTAL DEFECT 4
ATRIOVENTRICULAR SEPTAL DEFECT 4
disease Disease or Syndrome; Congenital Abnormality 1 3 0.600 None 1.000 3 3 2003 2007
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
phenotype Laboratory Procedure 563 1418 0.100 None 1.000 2 2 2012 2019
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
phenotype Clinical Attribute 843 1931 0.100 None 1.000 2 3 2018 2019
CUI: C0000846
Disease: Agenesis
Agenesis
disease Congenital Abnormality 161 44 0.010 None 1.000 1 2010 2010
CUI: C0028259
Disease: Nodule
Nodule
phenotype Acquired Abnormality 278 19 0.010 None 1.000 1 2017 2017
CUI: C0220810
Disease: Congenital defects
Congenital defects
group Congenital Abnormality 126 6 0.010 None 1.000 1 2009 2009
CUI: C0243066
Disease: Atresia
Atresia
disease Congenital Abnormality 44 1 0.010 None 1.000 1 1997 1997
CUI: C0344622
Disease: Double inlet left ventricle
Double inlet left ventricle
disease Congenital Abnormality 4 1 0.010 None 1.000 1 2007 2007
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
disease Mental or Behavioral Dysfunction 1825 553 0.110 None 1.000 1 2016 2016
CUI: C0687132
Disease: heavy drinking
heavy drinking
disease Mental or Behavioral Dysfunction 57 7 0.010 None 1.000 1 1 2016 2016
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia
disease Neoplastic Process 860 154 0.010 None 1.000 1 2017 2017
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction
phenotype Disease or Syndrome 716 25 0.010 None 1.000 1 2018 2018
CUI: C0857175
Disease: Postinfarction
Postinfarction
disease Disease or Syndrome 49 1 0.010 None 1.000 1 2010 2010
Low Grade Gastric Intraepithelial Neoplasia
disease Neoplastic Process 2 0.010 None 1.000 1 2010 2010
CUI: C1409792
Disease: Coronary sinus defect
Coronary sinus defect
disease Congenital Abnormality 5 0.200 None 1.000 1 2012 2012
CUI: C1853238
Disease: Conotruncal defect
Conotruncal defect
disease Congenital Abnormality 51 45 0.010 None 1.000 1 2007 2007
CUI: C2013199
Disease: Oppositional Behavior
Oppositional Behavior
phenotype Sign or Symptom 4 0.010 None 1.000 1 2018 2018
Patent or persistent ostium secundum defect (type II)
disease Disease or Syndrome 4 0.200 None 1.000 1 2012 2012
Patent or persistent sinus venosus defect
disease Disease or Syndrome 4 0.200 None 1.000 1 2012 2012
TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE
disease Disease or Syndrome 1 1 0.700 None 1.000 1 1 2011 2011
Human immunodeficiency virus (HIV) II infection category B1
disease Disease or Syndrome 985 56 0.010 None 1.000 1 1993 1993