CETP, cholesteryl ester transfer protein, 1071

N. diseases: 188; N. variants: 88
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: C0201950
Disease: Cholesterol measurement test
Cholesterol measurement test 		phenotype Laboratory Procedure 1 3 0.100 None 1.000 1 1 2010 2010
CUI: C0342890
Disease: Primary combined hyperlipidemia
Primary combined hyperlipidemia 		disease Disease or Syndrome 1 0.010 None 1.000 1 2009 2009
CUI: C4050214
Disease: Cholesteryl Ester Transfer Protein Measurement
Cholesteryl Ester Transfer Protein Measurement 		phenotype Laboratory Procedure 1 3 0.100 None 1.000 1 2 2018 2018
CUI: C4551591
Disease: Increased HDL cholesterol concentration
Increased HDL cholesterol concentration 		phenotype Nutritional and Metabolic Diseases Finding 3 0.100 None 0
CUI: C4521075
Disease: Childhood Overweight
Childhood Overweight 		phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Finding 4 0.300 None 1.000 1 2014 2014
CUI: C4704955
Disease: Infant Overweight
Infant Overweight 		phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Finding 4 0.300 None 1.000 1 2014 2014
CUI: C4704956
Disease: Adolescent Overweight
Adolescent Overweight 		phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Finding 4 0.300 None 1.000 1 2014 2014
CUI: C3151466
Disease: HEPATIC LIPASE DEFICIENCY (disorder)
HEPATIC LIPASE DEFICIENCY (disorder) 		disease Nutritional and Metabolic Diseases Disease or Syndrome 5 4 0.010 None 1.000 1 2008 2008
CUI: C3875011
Disease: Familial hyperalphalipoproteinemia
Familial hyperalphalipoproteinemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 5 0.010 None 1.000 1 1993 1993
CUI: C4553478
Disease: Infantile Obesity
Infantile Obesity 		phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome 5 0.300 None 1.000 1 2014 2014
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 6 29 0.010 None 1.000 1 2008 2008
CUI: C0856737
Disease: Single vessel disease
Single vessel disease 		disease Cardiovascular Diseases Disease or Syndrome 6 0.010 None 1.000 1 2005 2005
CUI: C2047520
Disease: Mixed hyperlipidemia (disorder)
Mixed hyperlipidemia (disorder) 		disease Nutritional and Metabolic Diseases Disease or Syndrome 6 3 0.010 None 1.000 1 2019 2019
CUI: C0342879
Disease: Primary hypercholesterolemia
Primary hypercholesterolemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 7 2 0.030 None 1.000 3 2002 2017
CUI: C3149462
Disease: HYPERALPHALIPOPROTEINEMIA 1
HYPERALPHALIPOPROTEINEMIA 1 		disease Disease or Syndrome 9 4 0.800 limited 0.933 30 4 1990 2018
CUI: C0542037
Disease: Hypotriglyceridemia
Hypotriglyceridemia 		disease Disease or Syndrome 9 2 0.100 None 0
CUI: C0271738
Disease: Hypocortisolism secondary to another disorder
Hypocortisolism secondary to another disorder 		disease Endocrine System Diseases Disease or Syndrome 13 0.010 None 1.000 1 2017 2017
CUI: C0856738
Disease: Triple vessel disease
Triple vessel disease 		disease Cardiovascular Diseases Disease or Syndrome 13 3 0.010 None 1.000 1 2005 2005
CUI: C0948480
Disease: Coronary Restenosis
Coronary Restenosis 		disease Cardiovascular Diseases Disease or Syndrome 16 2 0.010 None < 0.001 1 2010 2010
CUI: C1299433
Disease: Left main coronary artery disease
Left main coronary artery disease 		disease Cardiovascular Diseases Disease or Syndrome 17 4 0.010 None < 0.001 1 1 2011 2011
CUI: C0263420
Disease: Hyperkeratosis lenticularis perstans
Hyperkeratosis lenticularis perstans 		disease Skin and Connective Tissue Diseases Disease or Syndrome 18 11 0.020 None 1.000 2 1994 2001
CUI: C1704429
Disease: Hypoalphalipoproteinemia, Familial
Hypoalphalipoproteinemia, Familial 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 18 6 0.010 None 1.000 1 2014 2014
CUI: C1706412
Disease: Lipidemias
Lipidemias 		phenotype Nutritional and Metabolic Diseases Finding 18 0.300 None 1.000 1 1999 1999
CUI: C4317171
Disease: Adolescent Obesity
Adolescent Obesity 		phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome 18 9 0.300 None 1.000 1 2014 2014
CUI: C0473527
Disease: Hypoalphalipoproteinemias
Hypoalphalipoproteinemias 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 20 7 0.020 None 0.500 2 1995 2019