GDF1, growth differentiation factor 1, 2657

N. diseases: 136; N. variants: 14
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: C4531036
Disease: Abdominal situs ambiguus
Abdominal situs ambiguus 		phenotype Anatomical Abnormality 1 0.100 None 0
CUI: C3151221
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 2 2 0.700 None 1.000 2 2 2007 2017
CUI: C4015619
Disease: EPILEPSY, PROGRESSIVE MYOCLONIC, 8
EPILEPSY, PROGRESSIVE MYOCLONIC, 8 		disease Disease or Syndrome 2 2 0.100 None 0 2
CUI: C1956410
Disease: Double Outlet Right Ventricle, Noncommitted VSD
Double Outlet Right Ventricle, Noncommitted VSD 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 3 0.300 None 1.000 1 2007 2007
CUI: C1956411
Disease: Double Outlet Right Ventricle, Subaortic VSD
Double Outlet Right Ventricle, Subaortic VSD 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome; Congenital Abnormality 3 0.300 None 1.000 1 2007 2007
CUI: C1956412
Disease: Double Outlet Right Ventricle, Subpulmonary VSD
Double Outlet Right Ventricle, Subpulmonary VSD 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 3 0.300 None 1.000 1 2007 2007
CUI: C1970501
Disease: Hypoplastic pulmonary veins
Hypoplastic pulmonary veins 		phenotype Finding 3 0.100 None 0
CUI: C1956413
Disease: Taussig-Bing Anomaly
Taussig-Bing Anomaly 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 4 0.300 None 1.000 1 2007 2007
CUI: C0035615
Disease: Right aortic arch (disorder)
Right aortic arch (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 4 1 0.100 None 0
CUI: C0694453
Disease: Neurotic, stress-related and somatoform disorders
Neurotic, stress-related and somatoform disorders 		group Mental Disorders Mental or Behavioral Dysfunction 5 0.010 None 1.000 1 2019 2019
CUI: C1282979
Disease: Transient hypoparathyroidism
Transient hypoparathyroidism 		disease Pathological Conditions, Signs and Symptoms; Endocrine System Diseases Disease or Syndrome 5 0.010 None < 0.001 1 2017 2017
CUI: C3178807
Disease: Left Atrial Isomerism
Left Atrial Isomerism 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases Congenital Abnormality 6 0.300 None 0
CUI: C0265357
Disease: Polysplenia Syndrome
Polysplenia Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases Congenital Abnormality 7 0.300 None 0
CUI: C4684942
Disease: Refractory Thyroid Gland Carcinoma
Refractory Thyroid Gland Carcinoma 		disease Neoplasms; Endocrine System Diseases Neoplastic Process 10 2 0.010 None 1.000 1 2018 2018
CUI: C0242855
Disease: Congenital atresia of pulmonary valve
Congenital atresia of pulmonary valve 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 11 3 0.010 None 1.000 1 2011 2011
CUI: C0392482
Disease: Common atrium
Common atrium 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 11 1 0.100 None 0
CUI: C0022738
Disease: Klippel-Feil Syndrome
Klippel-Feil Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 12 5 0.010 None 1.000 1 2012 2012
CUI: C1857586
Disease: CONOTRUNCAL HEART MALFORMATIONS (disorder)
CONOTRUNCAL HEART MALFORMATIONS (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 13 22 0.500 None 1.000 3 1 2006 2017
CUI: C0175707
Disease: Asplenia Syndrome
Asplenia Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 13 5 0.600 None 1.000 1 3 2010 2010
CUI: C0344917
Disease: Left ventricular outflow tract obstruction
Left ventricular outflow tract obstruction 		disease Congenital Abnormality 13 2 0.100 None 0 1
CUI: C3178806
Disease: Right Atrial Isomerism
Right Atrial Isomerism 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases Congenital Abnormality 14 0.620 strong 1.000 3 2010 2018
CUI: C1856659
Disease: Polysplenia
Polysplenia 		disease Congenital Abnormality 15 0.100 None 0
CUI: C4551903
Disease: Total anomalous pulmonary venous return
Total anomalous pulmonary venous return 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome 16 0.100 None 0
CUI: C0149955
Disease: Annular pancreas
Annular pancreas 		disease Digestive System Diseases Congenital Abnormality 19 1 0.200 None 1.000 1 2000 2000
CUI: C0265908
Disease: Congenital atresia of pulmonary artery
Congenital atresia of pulmonary artery 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases Congenital Abnormality 19 5 0.110 None 1.000 1 2011 2011