AGT, angiotensinogen, 183

N. diseases: 765; N. variants: 43
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: C0403528
Disease: Henoch-Schönlein nephritis
Henoch-Schönlein nephritis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 5 0.010 None 1.000 1 2006 2006
CUI: C2732413
Disease: Postexertional fatigue
Postexertional fatigue 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 0.010 None 1.000 1 2018 2018
CUI: C3695318
Disease: Chronic kidney disease due to hypertension
Chronic kidney disease due to hypertension 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases Disease or Syndrome 5 0.010 None 1.000 1 2015 2015
CUI: C4277533
Disease: Dissection, Blood Vessel
Dissection, Blood Vessel 		phenotype Cardiovascular Diseases Pathologic Function 5 0.300 None 1.000 1 2007 2007
CUI: C2936381
Disease: Neointima Formation
Neointima Formation 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 6 0.300 None 1.000 2 2009 2018
CUI: C0340557
Disease: Atherosclerotic renal artery stenosis
Atherosclerotic renal artery stenosis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases Disease or Syndrome 6 4 0.010 None 1.000 1 3 2006 2006
CUI: C0406670
Disease: Vulvodynia
Vulvodynia 		disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 6 1 0.010 None 1.000 1 2017 2017
CUI: C1135361
Disease: Persistent pulmonary hypertension
Persistent pulmonary hypertension 		disease Disease or Syndrome 6 0.010 None 1.000 1 2004 2004
CUI: C3838731
Disease: Familial hyperaldosteronism type 1
Familial hyperaldosteronism type 1 		disease Endocrine System Diseases Disease or Syndrome 6 0.010 None 1.000 1 1995 1995
CUI: C4551893
Disease: Toxemia of pregnancy
Toxemia of pregnancy 		disease Female Urogenital Diseases and Pregnancy Complications; Cardiovascular Diseases Disease or Syndrome 6 0.010 None 1.000 1 1995 1995
CUI: C0238015
Disease: Autonomic Dysreflexia
Autonomic Dysreflexia 		disease Nervous System Diseases Disease or Syndrome 7 0.010 None 1.000 1 2017 2017
CUI: C0302465
Disease: Dissecting Abdominal Aortic Aneurysm
Dissecting Abdominal Aortic Aneurysm 		disease Cardiovascular Diseases Disease or Syndrome 7 0.010 None 1.000 1 2016 2016
CUI: C0333205
Disease: Mural thrombus
Mural thrombus 		disease Cardiovascular Diseases Disease or Syndrome 7 1 0.010 None 1.000 1 2017 2017
CUI: C0345049
Disease: Ascending aorta dilatation
Ascending aorta dilatation 		disease Anatomical Abnormality 7 0.010 None 1.000 1 2010 2010
CUI: C1260883
Disease: Mural thrombus of heart
Mural thrombus of heart 		disease Cardiovascular Diseases Disease or Syndrome 7 1 0.010 None 1.000 1 2017 2017
CUI: C0266313
Disease: Allanson Pantzar McLeod syndrome
Allanson Pantzar McLeod syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 8 23 0.710 None 1.000 5 3 2005 2015
CUI: C0021313
Disease: Infection of kidney
Infection of kidney 		group Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 8 0.010 None 1.000 1 2019 2019
CUI: C0332886
Disease: Coarctation
Coarctation 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Anatomical Abnormality 8 0.010 None 1.000 1 2012 2012
CUI: C2062593
Disease: Mesial temporal sclerosis
Mesial temporal sclerosis 		disease Disease or Syndrome 8 0.010 None 1.000 1 2008 2008
CUI: C0023195
Disease: Lecithin Acyltransferase Deficiency
Lecithin Acyltransferase Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 9 22 0.010 None 1.000 1 2008 2008
CUI: C1333324
Disease: Barretts esophagus with dysplasia
Barretts esophagus with dysplasia 		disease Digestive System Diseases; Neoplasms Disease or Syndrome 9 0.010 None 1.000 1 2019 2019
CUI: C1866956
Disease: Aortic root dilation
Aortic root dilation 		disease Disease or Syndrome 9 0.010 None < 0.001 1 2018 2018
CUI: C4509223
Disease: Heart failure with reduced ejection fraction [HFrEF]
Heart failure with reduced ejection fraction [HFrEF] 		disease Disease or Syndrome 9 0.010 None 1.000 1 2020 2020
CUI: C4721438
Disease: Mitral valve dysplasia
Mitral valve dysplasia 		disease Cardiovascular Diseases Disease or Syndrome 9 1 0.010 None 1.000 1 2015 2015
CUI: C0266619
Disease: Potter's facies
Potter's facies 		disease Congenital Abnormality 9 0.100 None 0