Source: RGD

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0017661 IGA Glomerulonephritis disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the genitourinary system 3
C0008311 Cholangitis disease Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system; Abnormality of the immune system 2
C0751895 Vasospasm, Intracranial disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 2
C0018202 Granulomatous Angiitis disease Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 1
C0019061 Hemolytic-Uremic Syndrome disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Hemic and Lymphatic Diseases Disease or Syndrome disease of anatomical entity Abnormality of the genitourinary system 1
C0276653 Invasive Pulmonary Aspergillosis disease Infections; Respiratory Tract Diseases Disease or Syndrome 1
C0341699 Granulomatous interstitial nephritis disease Disease or Syndrome 1
C0027055 Myocardial Reperfusion Injury phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 161
C0020429 Hyperalgesia phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom Abnormality of the nervous system 127
C0020542 Pulmonary Hypertension phenotype Respiratory Tract Diseases Pathologic Function disease of anatomical entity 104
C0376618 Endotoxemia phenotype Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 101
C0021368 Inflammation phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 68
C2750441 LIVER DISEASE, ALCOHOLIC, SUSCEPTIBILITY TO, 1 phenotype Finding genetic disease; disease of metabolism 57
C3150651 FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 2 phenotype Finding genetic disease; disease of metabolism 57
C0030193 Pain phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom Constitutional symptom 40
C0242184 Hypoxia phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 26
C0042487 Venous Thrombosis phenotype Cardiovascular Diseases Pathologic Function disease of anatomical entity Abnormality of blood and blood-forming tissues 15
C0026766 Multiple Organ Failure phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 11
C0034063 Pulmonary Edema phenotype Respiratory Tract Diseases Pathologic Function disease of anatomical entity Abnormality of metabolism/homeostasis; Abnormality of the respiratory system 8
C0020522 Delayed Hypersensitivity phenotype Immune System Diseases Pathologic Function 6
C0029191 Orchitis phenotype Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the genitourinary system 6
C0553980 Endomyocardial Fibrosis phenotype Cardiovascular Diseases Pathologic Function disease of anatomical entity Abnormality of the cardiovascular system 5
C0018200 Granuloma, Respiratory Tract phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Pathologic Function 2
C0020538 Hypertensive disease group Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 284
C0038454 Cerebrovascular accident group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the nervous system; Abnormality of the cardiovascular system 64