Source: RGD

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0007787 Transient Ischemic Attack disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 170
C0027055 Myocardial Reperfusion Injury phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 161
C0243026 Sepsis disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome disease by infectious agent 123
C0011881 Diabetic Nephropathy disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 120
C0149940 Sciatic Neuropathy disease Nervous System Diseases Disease or Syndrome disease of anatomical entity 109
C0740392 Infarction, Middle Cerebral Artery disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 108
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
C0022661 Kidney Failure, Chronic disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome disease of anatomical entity 85
C0242488 Acute Lung Injury disease Respiratory Tract Diseases Injury or Poisoning 74
C0029866 Other ureteric obstruction phenotype Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Anatomical Abnormality disease of anatomical entity 52
C0015696 Fatty Liver, Alcoholic disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome genetic disease; disease of metabolism 47
C0524620 Metabolic Syndrome X disease Nutritional and Metabolic Diseases Disease or Syndrome genetic disease; syndrome 42
C2936380 Neointima disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 33
C0267941 Pancreatitis, Acute Necrotizing disease Digestive System Diseases Disease or Syndrome 32
C0026846 Muscular Atrophy phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Pathologic Function disease of anatomical entity 28
C1397307 Cardiac fibrosis disease Disease or Syndrome 17
C0007785 Cerebral Infarction disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 12
C0026766 Multiple Organ Failure phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 11
C0019080 Hemorrhage phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 10
C0156181 Peritoneal adhesion disease Digestive System Diseases; Skin and Connective Tissue Diseases Acquired Abnormality 2
C0265010 Ruptured thoracic aortic aneurysm disease Respiratory Tract Diseases; Cardiovascular Diseases; Wounds and Injuries Disease or Syndrome disease of anatomical entity 2
C0265012 Ruptured abdominal aortic aneurysm disease Cardiovascular Diseases; Wounds and Injuries Disease or Syndrome disease of anatomical entity 2
C0375362 Peritoneal adhesions (postoperative) (postinfection) disease Disease or Syndrome 2
C0741160 Aortic Aneurysm, Ruptured disease Cardiovascular Diseases; Wounds and Injuries Disease or Syndrome disease of anatomical entity 2