REN, renin, 5972

N. diseases: 721; N. variants: 25
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: C0155761
Disease: Hyperplasia of renal artery
Hyperplasia of renal artery
disease Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C0156245
Disease: Unilateral small kidney
Unilateral small kidney
disease Congenital Abnormality 1 0.010 None 1.000 1 2019 2019
CUI: C0264639
Disease: High-renin essential hypertension
High-renin essential hypertension
disease Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2001 2001
CUI: C0264693
Disease: Acute coronary insufficiency
Acute coronary insufficiency
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2014 2014
CUI: C0521623
Disease: Kidney crystallization
Kidney crystallization
disease Nutritional and Metabolic Diseases Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C0877138
Disease: Osteopenia periarticular
Osteopenia periarticular
disease Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C1301626
Disease: Hypertension with albuminuria
Hypertension with albuminuria
disease Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C2063386
Disease: Left atrial appendage thrombosis
Left atrial appendage thrombosis
disease Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C2902961
Disease: Page kidney
Page kidney
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C4016362
Disease: HYPERPRORENINEMIA, FAMILIAL
HYPERPRORENINEMIA, FAMILIAL
disease Finding 1 1 0.100 None 0 1
CUI: C0039235
Disease: Tachycardia, Ectopic Junctional
Tachycardia, Ectopic Junctional
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 2 0.010 None 1.000 1 2011 2011
Metabolic acidosis, NAG, acidifying salts
disease Nutritional and Metabolic Diseases Disease or Syndrome 2 0.010 None 1.000 1 2000 2000
Pre-eclampsia added to pre-existing hypertension
disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C0403519
Disease: Proteinuric diabetic nephropathy
Proteinuric diabetic nephropathy
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 2 0.010 None 1.000 1 2017 2017
CUI: C1504568
Disease: Stenosis of middle cerebral artery
Stenosis of middle cerebral artery
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 2 0.010 None 1.000 1 2003 2003
Hyperuricemic Nephropathy, Familial Juvenile 2
disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 2 1 0.710 None 1.000 1 1 2009 2009
CUI: C3665771
Disease: Hypocalvaria
Hypocalvaria
disease Congenital Abnormality 2 0.010 None 1.000 1 2019 2019
CUI: C3665927
Disease: Renal hypoperfusion
Renal hypoperfusion
disease Disease or Syndrome 2 0.010 None 1.000 1 2000 2000
Hypertensive cerebrovascular disease
disease Disease or Syndrome 2 0.010 None 1.000 1 1995 1995
CUI: C0264638
Disease: Low-renin essential hypertension
Low-renin essential hypertension
disease Cardiovascular Diseases Disease or Syndrome 3 0.020 None 1.000 2 2001 2012
CUI: C1504533
Disease: Post transplant erythrocytosis
Post transplant erythrocytosis
disease Disease or Syndrome 3 0.020 None 1.000 2 2003 2018
CUI: C0340908
Disease: Arteriovenous fistula stenosis
Arteriovenous fistula stenosis
disease Cardiovascular Diseases Disease or Syndrome 3 0.010 None 1.000 1 2004 2004
CUI: C0597853
Disease: high renin hypertension
high renin hypertension
disease Disease or Syndrome 3 0.010 None 1.000 1 2000 2000
CUI: C1096285
Disease: Arterial fibrosis
Arterial fibrosis
disease Disease or Syndrome 3 0.010 None 1.000 1 2018 2018
CUI: C1862170
Disease: Brachydactyly with hypertension
Brachydactyly with hypertension
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 3 5 0.010 None 1.000 1 2002 2002