Source: GWASDB

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C1325327 fibrinogen activity phenotype Molecular Function 26 63
C1561955 Fibrinogen, CTCAE phenotype Finding 26 63
C1272321 Autoantibody measurement phenotype Laboratory Procedure 26 49
C4021107 Non-obstructive azoospermia disease Male Urogenital Diseases Disease or Syndrome Abnormality of the genitourinary system 26 48
C0202239 Uric acid measurement (procedure) phenotype Laboratory Procedure 25 968
C0441683 Hormone measurement group Laboratory Procedure 25 91
C2700366 Adiponectin Measurement phenotype Laboratory Procedure 25 68
C0023980 Longevity phenotype Temporal Concept 25 42
C1306620 Systolic blood pressure measurement phenotype Diagnostic Procedure 25 35
C0546837 Malignant neoplasm of esophagus disease Digestive System Diseases; Neoplasms Neoplastic Process disease of anatomical entity; disease of cellular proliferation 24 44
C0029408 Degenerative polyarthritis disease Musculoskeletal Diseases Disease or Syndrome disease of anatomical entity Abnormality of the skeletal system 24 35
C1278049 Serum gamma-glutamyl transferase measurement phenotype Laboratory Procedure 24 31
C1305855 Body mass index phenotype Clinical Attribute 24 29
C0042487 Venous Thrombosis phenotype Cardiovascular Diseases Pathologic Function disease of anatomical entity Abnormality of blood and blood-forming tissues 23 218
C0429028 QT interval feature (observable entity) phenotype Clinical Attribute 23 99
C0019829 Hodgkin Disease disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process disease of anatomical entity; disease of cellular proliferation Neoplasm; Abnormality of blood and blood-forming tissues 23 52
C0004936 Mental disorders group Mental Disorders Mental or Behavioral Dysfunction disease of mental health 23 49
C0011615 Dermatitis, Atopic disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the integument; Abnormality of the immune system 23 47
C0149931 Migraine Disorders group Nervous System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the nervous system 23 47
C0026764 Multiple Myeloma disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Neoplastic Process disease of anatomical entity; disease of cellular proliferation Neoplasm; Abnormality of blood and blood-forming tissues 22 627
C0005938 Bone Density phenotype Clinical Attribute 22 350
C0026691 Mucocutaneous Lymph Node Syndrome disease Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 22 96
C0035227 Respiratory Function Tests phenotype Diagnostic Procedure 22 34
C0008924 Cleft upper lip disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Congenital Abnormality disease of anatomical entity; syndrome; physical disorder Abnormality of head or neck 21 172
C0233849 Personality Traits group Behavior and Behavior Mechanisms Finding 21 75