Source: RGD

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0011853 Diabetes Mellitus, Experimental disease Nutritional and Metabolic Diseases; Endocrine System Diseases Experimental Model of Disease 472
C0035126 Reperfusion Injury disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Injury or Poisoning 229
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
C0023893 Liver Cirrhosis, Experimental disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Experimental Model of Disease 125
C0011881 Diabetic Nephropathy disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 120
C0376618 Endotoxemia phenotype Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 101
C0014072 Experimental Autoimmune Encephalomyelitis disease Immune System Diseases; Nervous System Diseases Experimental Model of Disease 89
C0242488 Acute Lung Injury disease Respiratory Tract Diseases Injury or Poisoning 74
C0021368 Inflammation phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 68
C0752308 Hypoxia-Ischemia, Brain disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 67
C2316810 Chronic kidney disease stage 5 disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome Abnormality of the genitourinary system 58
C0030193 Pain phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom Constitutional symptom 40
C0267941 Pancreatitis, Acute Necrotizing disease Digestive System Diseases Disease or Syndrome 32
C0242184 Hypoxia phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 26
C0037926 Compression of spinal cord disease Nervous System Diseases; Wounds and Injuries Disease or Syndrome Abnormality of the nervous system 14
C0026766 Multiple Organ Failure phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 11
C0020522 Delayed Hypersensitivity phenotype Immune System Diseases Pathologic Function 6
C0018200 Granuloma, Respiratory Tract phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Pathologic Function 2
C0276653 Invasive Pulmonary Aspergillosis disease Infections; Respiratory Tract Diseases Disease or Syndrome 1
C0341699 Granulomatous interstitial nephritis disease Disease or Syndrome 1
C0243026 Sepsis disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome disease by infectious agent 123
C0007932 Chagas' disease without mention of organ involvement disease Infections Disease or Syndrome disease by infectious agent 5
C0020538 Hypertensive disease group Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 284
C0027051 Myocardial Infarction disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 178