ACE, angiotensin I converting enzyme, 1636

N. diseases: 101; N. variants: 18
Source: CURATED ×
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: C0455503
Disease: H/O: depression
H/O: depression
phenotype Finding 2 0.300 None 1.000 1 2013 2013
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 3 (finding)
disease Finding 1 0.500 None 0
CUI: C0344315
Disease: Depressed mood
Depressed mood
phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 13 0.400 None 1.000 3 1996 2019
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms
phenotype Behavior and Behavior Mechanisms Sign or Symptom 26 0.330 None 1.000 1 1995 2019
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
group Cardiovascular Diseases Disease or Syndrome 36 342 0.400 None 0.956 3 1994 2020
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
group Cardiovascular Diseases Disease or Syndrome 190 233 0.600 None 0.921 3 1986 2020
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
disease Cardiovascular Diseases Disease or Syndrome 65 0.400 None 0.929 1 1992 2020
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
disease Cardiovascular Diseases Disease or Syndrome 24 469 0.400 None 0.920 1 1992 2020
CUI: C0018801
Disease: Heart failure
Heart failure
disease Cardiovascular Diseases Disease or Syndrome 110 82 0.600 None 0.981 1 1992 2020
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
disease Cardiovascular Diseases Disease or Syndrome 110 9 0.600 None 0.984 1 1992 2020
CUI: C0020649
Disease: Hypotension
Hypotension
phenotype Cardiovascular Diseases Finding 53 2 0.400 None 1.000 1 1987 1987
CUI: C0023212
Disease: Left-Sided Heart Failure
Left-Sided Heart Failure
disease Cardiovascular Diseases Disease or Syndrome 110 4 0.300 None 1.000 1 2008 2008
CUI: C0235527
Disease: Heart Failure, Right-Sided
Heart Failure, Right-Sided
disease Cardiovascular Diseases Disease or Syndrome 110 0.310 None 1.000 1 2008 2015
CUI: C0948480
Disease: Coronary Restenosis
Coronary Restenosis
disease Cardiovascular Diseases Disease or Syndrome 5 1 0.360 None 1.000 1 1997 2015
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
disease Cardiovascular Diseases Disease or Syndrome 65 627 0.400 None 0.916 1 1992 2020
CUI: C1959583
Disease: Myocardial Failure
Myocardial Failure
disease Cardiovascular Diseases Disease or Syndrome 110 0.300 None 1.000 1 2008 2008
CUI: C1961112
Disease: Heart Decompensation
Heart Decompensation
phenotype Cardiovascular Diseases Pathologic Function 110 0.300 None 1.000 1 2008 2008
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 268 231 0.320 None 1.000 3 2005 2013
CUI: C0033937
Disease: Psychoses, Drug
Psychoses, Drug
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 21 0.300 None 1.000 1 2007 2007
CUI: C0033941
Disease: Psychoses, Substance-Induced
Psychoses, Substance-Induced
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 17 0.300 None 1.000 1 2007 2007
CUI: C0021295
Disease: Infant, Premature, Diseases
Infant, Premature, Diseases
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 1 0.300 None 1.000 1 2003 2003
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 4 23 0.760 strong 1.000 3 7 2005 2019
CUI: C0017924
Disease: Glycogen Storage Disease Type V
Glycogen Storage Disease Type V
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 2 70 0.340 None 1.000 1 2003 2008
CUI: C0017205
Disease: Gaucher Disease
Gaucher Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 4 41 0.320 None 1.000 1 2003 2018
CUI: C0268250
Disease: Gaucher Disease, Type 2 (disorder)
Gaucher Disease, Type 2 (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 4 34 0.300 None 1.000 1 2003 2003