Source: GWASCAT

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C0373595 Creatinine clearance measurement phenotype Laboratory Procedure 0 51
C0030305 Pancreatitis disease Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system; Abnormality of the immune system 0 6
C0030809 Pemphigus Vulgaris disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome disease of anatomical entity 0 6
C0523708 5-Hydroxyindoleacetic acid measurement phenotype Laboratory Procedure 0 5
C0021364 Male infertility phenotype Male Urogenital Diseases Disease or Syndrome disease of anatomical entity Abnormality of the genitourinary system 0 4
C0751908 Vestibular Neuronitis disease Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome disease of anatomical entity 0 4
C1720994 Eye Movement Measurements phenotype Diagnostic Procedure 0 4
C0024419 Waldenstrom Macroglobulinemia disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Neoplastic Process genetic disease; disease of metabolism; disease of anatomical entity; disease of cellular proliferation Abnormality of metabolism/homeostasis; Abnormality of the immune system; Neoplasm; Abnormal cellular phenotype; Abnormality of blood and blood-forming tissues 0 3
C0085215 Ovarian Failure, Premature disease Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Disease or Syndrome disease of anatomical entity 0 3
C0020450 Hyperemesis Gravidarum phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Sign or Symptom Abnormality of prenatal development or birth 0 2
C0025874 Metrorrhagia phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Pathologic Function Abnormality of the genitourinary system; Abnormality of the endocrine system 0 2
C0030807 Pemphigus disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome disease of anatomical entity 0 2
C0227791 Vaginal Discharge phenotype Female Urogenital Diseases and Pregnancy Complications Finding disease of anatomical entity 0 2
C0263313 Pemphigus Foliaceus disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 0 2
C0373785 Thrombomodulin Assay phenotype Laboratory Procedure 0 2
C0456103 Sepsis of the newborn disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infections Disease or Syndrome Abnormality of the immune system 0 2
C0523807 Oxygen saturation measurement phenotype Laboratory Procedure 0 2
C0557163 Household income phenotype Finding 0 2
C1168401 Squamous cell carcinoma of the head and neck disease Neoplasms Neoplastic Process disease of cellular proliferation 0 2
C1332201 Adult Diffuse Large B-Cell Lymphoma disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process disease of anatomical entity; disease of cellular proliferation 0 2
C1838604 EPILEPSY, CHILDHOOD ABSENCE, 1 disease Disease or Syndrome 0 2
C2609414 Acute kidney injury disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Injury or Poisoning disease of anatomical entity Abnormality of the genitourinary system 0 2
C3827961 Spontaneous Preterm Birth phenotype Female Urogenital Diseases and Pregnancy Complications Finding 0 2
C0003615 Appendicitis disease Digestive System Diseases; Infections Disease or Syndrome disease of anatomical entity 0 1
C0010073 Coronary Artery Vasospasm disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 0 1