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
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
C0030567 Parkinson Disease disease Nervous System Diseases Disease or Syndrome genetic disease; disease of anatomical entity 74 224
C0428568 Fasting blood glucose measurement phenotype Laboratory Procedure 73 132
C1261430 Fasting blood sugar result phenotype Laboratory or Test Result 65 113
C0242383 Age related macular degeneration disease Eye Diseases Disease or Syndrome genetic disease; disease of anatomical entity 38 279
C1305855 Body mass index phenotype Clinical Attribute 24 29
C0205682 Waist-Hip Ratio phenotype Organism Attribute 19 33