Source: GWASDB

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C1836230 HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO disease Finding 61 365
C1836231 HIV-1, RESISTANCE TO phenotype Finding 61 365
C1836232 ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO phenotype Finding 61 365
C1836233 AIDS, PROGRESSION TO phenotype Finding 61 365
C0201657 C-reactive protein measurement phenotype Laboratory Procedure 58 436
C2699541 Cytokine Measurement phenotype Laboratory Procedure 57 81
C1527304 Allergic Reaction phenotype Immune System Diseases Pathologic Function disease of anatomical entity 55 819
C0177804 Bone Mineral Density Test phenotype Diagnostic Procedure 54 314
C0032181 Platelet Count measurement phenotype Laboratory Procedure 53 65
C0337438 Glucose measurement phenotype Laboratory Procedure 52 48
C0495706 elevated blood glucose level phenotype Finding 52 48
C0202177 Phospholipid measurement phenotype Laboratory Procedure 51 271
C0021053 Immune System Diseases group Immune System Diseases Disease or Syndrome disease of anatomical entity 49 104
C0019163 Hepatitis B disease Digestive System Diseases; Infections Disease or Syndrome disease by infectious agent 47 265
C0009402 Colorectal Carcinoma disease Digestive System Diseases; Neoplasms Neoplastic Process disease of anatomical entity; disease of cellular proliferation 44 89
C0200665 Platelet mean volume determination (procedure) phenotype Laboratory Procedure 41 77
C0231921 Pulmonary function phenotype Organ or Tissue Function 41 259
C0524587 Mean Corpuscular Volume (result) phenotype Laboratory or Test Result 41 87
C3160731 Pulmonary function (finding) phenotype Finding 41 259
C0036421 Systemic Scleroderma disease Skin and Connective Tissue Diseases Disease or Syndrome disease of anatomical entity 40 78
C0200695 Fetal hemoglobin determination phenotype Laboratory Procedure 40 219
C1168443 Pseudocholinesterase Measurement phenotype Laboratory Procedure 39 568
C0242383 Age related macular degeneration disease Eye Diseases Disease or Syndrome genetic disease; disease of anatomical entity 38 279
C0524957 Corneal Topography phenotype Diagnostic Procedure 38 97
C1861172 Venous Thromboembolism phenotype Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 36 147