Source: GWASCAT

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C3828530 Platelet Component Distribution Width Measurement phenotype Laboratory Procedure 134 200
C3548479 response to bronchodilator phenotype Organism Function 131 1106
C0200635 Lymphocyte Count measurement phenotype Laboratory Procedure 130 199
C0518015 Hemoglobin measurement phenotype Laboratory Procedure 129 209
C0013595 Eczema disease Skin and Connective Tissue Diseases Disease or Syndrome disease of anatomical entity Abnormality of the integument; Abnormality of the immune system 129 198
C0018498 Hair Color phenotype Organism Attribute 126 294
C0201976 Creatinine measurement, serum (procedure) phenotype Laboratory Procedure 124 243
C1629609 Age at menopause phenotype Finding 122 190
C0022661 Kidney Failure, Chronic disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome disease of anatomical entity 107 236
C0684249 Carcinoma of lung disease Neoplasms; Respiratory Tract Diseases Neoplastic Process disease of anatomical entity; disease of cellular proliferation 107 198
C1527304 Allergic Reaction phenotype Immune System Diseases Pathologic Function disease of anatomical entity 104 234
C0011854 Diabetes Mellitus, Insulin-Dependent disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome genetic disease; disease of metabolism Abnormality of metabolism/homeostasis; Abnormality of the endocrine system 104 198
C1836230 HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO disease Finding 104 188
C1836231 HIV-1, RESISTANCE TO phenotype Finding 104 188
C1836232 ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO phenotype Finding 104 188
C1836233 AIDS, PROGRESSION TO phenotype Finding 104 188
C0020676 Hypothyroidism disease Endocrine System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the endocrine system 104 185
C0424574 Duration of sleep phenotype Finding 101 200
C0264408 Childhood asthma disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome disease of anatomical entity 101 193
C0201657 C-reactive protein measurement phenotype Laboratory Procedure 100 250
C0857490 Granulocyte count phenotype Laboratory Procedure 100 150
C0525045 Mood Disorders group Mental Disorders Mental or Behavioral Dysfunction disease of mental health 99 218
C0002170 Alopecia disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome disease of anatomical entity Abnormality of the integument; Abnormality of head or neck 98 336
C1861172 Venous Thromboembolism phenotype Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 95 193
C0020538 Hypertensive disease group Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 91 177