MLXIPL, MLX interacting protein like, 51085

N. diseases: 9; N. variants: 23
Source: GWASDB ×
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: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
disease Nutritional and Metabolic Diseases Disease or Syndrome 27 48 0.120 None 1.000 1 1 2010 2017
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
phenotype Laboratory Procedure 317 744 0.100 None 1.000 3 4 2008 2019
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome 113 2272 0.100 None 1.000 1 5 2013 2013
CUI: C0018099
Disease: Gout
Gout
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome 114 2275 0.100 None 1.000 1 5 2013 2013
High density lipoprotein measurement
phenotype Laboratory Procedure 284 681 0.100 None 1.000 1 2 2012 2019
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
phenotype Laboratory Procedure 283 679 0.100 None 1.000 1 2 2012 2012
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
phenotype Laboratory Procedure 426 3265 0.100 None 1.000 1 22 2012 2012
CUI: C0523744
Disease: Lipids measurement
Lipids measurement
group Laboratory Procedure 15 18 0.100 None 1.000 1 1 2012 2012
Serum gamma-glutamyl transferase measurement
phenotype Laboratory Procedure 24 31 0.100 None 1.000 1 1 2011 2011