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: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction
phenotype Disease or Syndrome 716 25 0.100 None 1.000 46 2001 2020
CUI: C1397307
Disease: Cardiac fibrosis
Cardiac fibrosis
disease Disease or Syndrome 297 3 0.100 None 1.000 33 2009 2020
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.100 None 1.000 11 2006 2019
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
phenotype Clinical Attribute 507 1037 0.100 None 1.000 5 2 2016 2018
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
phenotype Clinical Attribute 843 1931 0.100 None 1.000 5 4 2016 2019
CUI: C1969372
Disease: Tubulointerstitial fibrosis
Tubulointerstitial fibrosis
phenotype Disease or Syndrome 328 0.050 None 1.000 5 2002 2018
Malignant neoplasm of colon and/or rectum
disease Neoplastic Process 3669 502 0.040 None 1.000 4 1 2009 2020
CUI: C0877008
Disease: Enzyme inhibition disorder
Enzyme inhibition disorder
phenotype Disease or Syndrome 171 1 0.030 None 1.000 3 1996 2007
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
disease Disease or Syndrome 1075 276 0.030 None 1.000 3 1 1988 1999
CUI: C0236734
Disease: Caffeine related disorders
Caffeine related disorders
group Mental or Behavioral Dysfunction 360 56 0.020 None 1.000 2 2019 2019
CUI: C0410158
Disease: Muscle damage
Muscle damage
phenotype Acquired Abnormality 163 4 0.020 None 1.000 2 1 2019 2019
CUI: C0597854
Disease: renin induced hypertension
renin induced hypertension
disease Disease or Syndrome 11 0.020 None 1.000 2 1996 1997
CUI: C0745133
Disease: Isolated systolic hypertension
Isolated systolic hypertension
disease Disease or Syndrome 22 3 0.020 None 1.000 2 1 1996 2002
CUI: C0877009
Disease: Muscle fibrosis
Muscle fibrosis
phenotype Sign or Symptom 34 0.020 None 1.000 2 2017 2019
CUI: C3160844
Disease: PAI-1 polymorphism
PAI-1 polymorphism
disease Disease or Syndrome 10 1 0.020 None 1.000 2 2005 2006
CUI: C3178782
Disease: Aortic Stiffness
Aortic Stiffness
phenotype Disease or Syndrome 61 11 0.020 None 0.500 2 1996 2001
CUI: C4049446
Disease: Neointimal hyperplasia
Neointimal hyperplasia
disease Disease or Syndrome 198 0.020 None 1.000 2 2005 2018
Heart failure with preserved ejection fraction [HFpEF]
disease Disease or Syndrome 89 4 0.020 None 1.000 2 2013 2018
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease
disease Disease or Syndrome 741 81 0.020 None 1.000 2 2018 2019
ST-segment elevation myocardial infarction (STEMI)
disease Disease or Syndrome 51 2 0.020 None 0.500 2 2 2011 2012
CUI: C4728082
Disease: Severe hypoglycaemia
Severe hypoglycaemia
disease Disease or Syndrome 36 2 0.020 None 1.000 2 2001 2009
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
phenotype Organism Function 109 220 0.100 None 1.000 1 8 2011 2011
CUI: C0221505
Disease: Lesion of brain
Lesion of brain
group Disease or Syndrome 188 9 0.010 None 1.000 1 2001 2001
CUI: C0240225
Disease: Liver mass
Liver mass
phenotype Disease or Syndrome 36 0.010 None 1.000 1 2019 2019
CUI: C0282666
Disease: Very Low Birth Weight
Very Low Birth Weight
phenotype Sign or Symptom 42 2 0.010 None 1.000 1 2001 2001