Source: GWASDB

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C0005823 Blood Pressure phenotype Organism Function 85 190
C0006142 Malignant neoplasm of breast disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process disease of anatomical entity; disease of cellular proliferation 82 223
C0005893 Body mass index procedure phenotype Diagnostic Procedure 78 231
C0578022 Finding of body mass index phenotype Finding 78 231
C0027051 Myocardial Infarction disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 76 94
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
C0008312 Primary biliary cirrhosis disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system 72 561
C0376358 Malignant neoplasm of prostate disease Neoplasms; Male Urogenital Diseases Neoplastic Process disease of anatomical entity; disease of cellular proliferation Abnormality of the genitourinary system 72 177
C0021390 Inflammatory Bowel Diseases group Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system; Abnormality of the immune system 72 122
C0023508 White Blood Cell Count procedure phenotype Laboratory Procedure 71 339
C0242379 Malignant neoplasm of lung disease Neoplasms; Respiratory Tract Diseases Neoplastic Process disease of anatomical entity; disease of cellular proliferation Neoplasm; Abnormality of the respiratory system 66 166
C1261430 Fasting blood sugar result phenotype Laboratory or Test Result 65 113
C0919677 Protein C measurement phenotype Laboratory Procedure 62 517
C1168438 Protein C antigen measurement phenotype Laboratory Procedure 62 517
C0014772 Red Blood Cell Count measurement phenotype Laboratory Procedure 61 480
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
C0042900 Vitiligo disease Skin and Connective Tissue Diseases Disease or Syndrome disease of anatomical entity Abnormality of the integument 61 121
C0201657 C-reactive protein measurement phenotype Laboratory Procedure 58 436
C0028754 Obesity disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome disease of metabolism Growth abnormality 58 186
C0009324 Ulcerative Colitis disease Digestive System Diseases Disease or Syndrome genetic disease; disease of anatomical entity Abnormality of the digestive system; Abnormality of the immune system 57 112
C2699541 Cytokine Measurement phenotype Laboratory Procedure 57 81