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.
Low density lipoprotein cholesterol measurement
phenotype Laboratory Procedure 483 1142 0.100 None 1.000 4 1 2012 2019
High density lipoprotein measurement
phenotype Laboratory Procedure 545 1440 0.100 None 1.000 4 4 2012 2019
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
phenotype Laboratory Procedure 486 1243 0.100 None 1.000 2 1 2012 2018
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
phenotype Laboratory Procedure 269 555 0.100 None 1.000 2 1 2012 2012
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
phenotype Laboratory Procedure 1156 2575 0.100 None 1.000 1 3 2018 2018
Granulocyte Colony Stimulating Factor Measurement
phenotype Laboratory Procedure 4 7 0.100 None 1.000 1 1 2017 2017
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
disease Nervous System Diseases; Mental Disorders Disease or Syndrome 3397 1843 0.100 None 1.000 1 2 2018 2018
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement
phenotype Laboratory Procedure 27 52 0.100 None 1.000 1 1 2009 2009
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
phenotype Laboratory Procedure 39 568 0.100 None 1.000 1 1 2011 2011
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
phenotype Laboratory Procedure 283 679 0.100 None 1.000 1 4 2012 2012
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
phenotype Laboratory Procedure 563 1418 0.100 None 1.000 1 1 2018 2018
apolipoprotein C-II (Wakayama) phenotype
phenotype Finding 2 1 0.100 None 0 1
CUI: C4017137
Disease: APOLIPOPROTEIN C-II (SAN FRANCISCO)
APOLIPOPROTEIN C-II (SAN FRANCISCO)
phenotype Finding 2 1 0.100 None 0 1
APOLIPOPROTEIN C-II VARIANT PHENOTYPE
phenotype Finding 2 1 0.100 None 0 1
APOLIPOPROTEIN C-II (BARI) PHENOTYPE
phenotype Finding 2 1 0.100 None 0 1
APOLIPOPROTEIN C-II (PARIS) PHENOTYPE
phenotype Finding 2 1 0.100 None 0 1
APOLIPOPROTEIN C-II (PADOVA) PHENOTYPE
phenotype Finding 2 1 0.100 None 0 1
Apolipoprotein C-II Deficiency (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 3 5 0.100 None 0 5
APOLIPOPROTEIN C-II (AUCKLAND) PHENOTYPE
phenotype Finding 2 1 0.100 None 0 1
CUI: C0015695
Disease: Fatty Liver
Fatty Liver
disease Digestive System Diseases Disease or Syndrome 875 35 0.010 None 1.000 1 2008 2008
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
disease Digestive System Diseases; Infections Disease or Syndrome 1768 347 0.010 None 1.000 1 2008 2008
CUI: C2711227
Disease: Steatohepatitis
Steatohepatitis
disease Digestive System Diseases Disease or Syndrome 1143 75 0.010 None 1.000 1 2008 2008
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 1800 680 0.010 None 1.000 1 2019 2019