Source: GWASDB

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C0523465 Serum albumin measurement phenotype Laboratory Procedure 426 3265
C0202236 Triglycerides measurement phenotype Laboratory Procedure 317 744
C0018099 Gout disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome disease of anatomical entity Abnormality of the skeletal system 114 2275
C0003868 Arthritis, Gouty disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome disease of anatomical entity Abnormality of the skeletal system 113 2272
C1168438 Protein C antigen measurement phenotype Laboratory Procedure 62 517
C0919677 Protein C measurement phenotype Laboratory Procedure 62 517