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: C1840375
Disease: Elevated diastolic blood pressure
Elevated diastolic blood pressure 		phenotype Cardiovascular Diseases Finding 14 1 0.100 None 0
CUI: C0021308
Disease: Infarction
Infarction 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 15 0.020 None 1.000 2 2006 2007
CUI: C0233612
Disease: Waxy flexibility
Waxy flexibility 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 15 0.300 None 1.000 1 1977 1977
CUI: C2076596
Disease: Influenza A (H5N1)
Influenza A (H5N1) 		disease Disease or Syndrome 15 0.010 None 1.000 1 2014 2014
CUI: C3495427
Disease: Fanconi-Bickel Syndrome
Fanconi-Bickel Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 15 17 0.010 None 1.000 1 2017 2017
CUI: C3713420
Disease: Familial Hyperaldosteronism
Familial Hyperaldosteronism 		disease Endocrine System Diseases Disease or Syndrome 15 0.010 None 1.000 1 1997 1997
CUI: C0020501
Disease: Primary Hyperoxaluria
Primary Hyperoxaluria 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 16 11 0.020 None 1.000 2 1991 2014
CUI: C0333291
Disease: Bleeding ulcer
Bleeding ulcer 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 16 1 0.020 None 1.000 2 2011 2012
CUI: C3888198
Disease: BESTROPHINOPATHY, AUTOSOMAL RECESSIVE
BESTROPHINOPATHY, AUTOSOMAL RECESSIVE 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 17 32 0.030 None 1.000 3 2013 2018
CUI: C0344911
Disease: Left ventricular dilatation
Left ventricular dilatation 		disease Congenital Abnormality 17 3 0.010 None < 0.001 1 1 1996 1996
CUI: C1303258
Disease: Acute ST segment elevation myocardial infarction (disorder)
Acute ST segment elevation myocardial infarction (disorder) 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 17 0.010 None 1.000 1 2017 2017
CUI: C1849300
Disease: Widely patent fontanelles and sutures
Widely patent fontanelles and sutures 		phenotype Finding 17 0.100 None 0
CUI: C0020564
Disease: Hypertrophy
Hypertrophy 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 18 0.300 None 1.000 6 2002 2015
CUI: C0597048
Disease: Neurogenic hypertension
Neurogenic hypertension 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 18 0.050 None 1.000 5 2007 2020
CUI: C0003460
Disease: Anuria
Anuria 		phenotype Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 18 0.400 None 1.000 1 1995 1995
CUI: C1536221
Disease: Non ST segment elevation myocardial infarction
Non ST segment elevation myocardial infarction 		disease Disease or Syndrome 18 0.010 None 1.000 1 2018 2018
CUI: C4700045
Disease: Non-ST-segment elevation myocardial infarction (NSTEMI)
Non-ST-segment elevation myocardial infarction (NSTEMI) 		disease Disease or Syndrome 18 1 0.010 None 1.000 1 2018 2018
CUI: C0221043
Disease: Liddle Syndrome
Liddle Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 19 6 0.010 None 1.000 1 1995 1995
CUI: C1850889
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 19 150 0.010 None 1.000 1 2019 2019
CUI: C2720436
Disease: Fibrosis of pleura
Fibrosis of pleura 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 19 0.010 None 1.000 1 2018 2018
CUI: C0553980
Disease: Endomyocardial Fibrosis
Endomyocardial Fibrosis 		phenotype Cardiovascular Diseases Pathologic Function 20 0.300 None 1.000 5 2010 2019
CUI: C0086025
Disease: Codependency
Codependency 		disease Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 20 2 0.010 None 1.000 1 2017 2017
CUI: C2697932
Disease: Loeys-Dietz Syndrome
Loeys-Dietz Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 20 35 0.010 None 1.000 1 2014 2014
CUI: C2242703
Disease: Cardio-Renal Syndrome
Cardio-Renal Syndrome 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases Disease or Syndrome 21 0.020 None 1.000 2 2018 2019
CUI: C0235222
Disease: Diastolic hypertension
Diastolic hypertension 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 21 1 0.010 None 1.000 1 1996 1996