Source: CTD_human

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0023893 Liver Cirrhosis, Experimental disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Experimental Model of Disease 774
C0006142 Malignant neoplasm of breast disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process disease of anatomical entity; disease of cellular proliferation 525
C1257931 Mammary Neoplasms, Human disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 525
C4704874 Mammary Carcinoma, Human disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 525
C0027627 Neoplasm Metastasis phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 217
C2585653 Persistent atrial fibrillation phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 156
C3468561 familial atrial fibrillation phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 156
C1959583 Myocardial Failure disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 110
C1961112 Heart Decompensation phenotype Cardiovascular Diseases Pathologic Function 110
C0002152 Alloxan Diabetes disease Nutritional and Metabolic Diseases; Endocrine System Diseases Experimental Model of Disease 108
C0011853 Diabetes Mellitus, Experimental disease Nutritional and Metabolic Diseases; Endocrine System Diseases Experimental Model of Disease 108
C0038433 Streptozotocin Diabetes disease Nutritional and Metabolic Diseases; Endocrine System Diseases Experimental Model of Disease 108
C0019693 HIV Infections group Infections; Immune System Diseases Disease or Syndrome disease by infectious agent 103
C4505456 HIV Coinfection disease Infections; Immune System Diseases Disease or Syndrome 103
C1565662 Acute Kidney Insufficiency disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome disease of anatomical entity 101
C0015695 Fatty Liver disease Digestive System Diseases Disease or Syndrome genetic disease; disease of metabolism 88
C0027055 Myocardial Reperfusion Injury phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 85
C0400966 Non-alcoholic Fatty Liver Disease disease Digestive System Diseases Disease or Syndrome genetic disease; disease of metabolism 70
C3241937 Nonalcoholic Steatohepatitis disease Digestive System Diseases Disease or Syndrome 70
C0920563 Insulin Sensitivity phenotype Nutritional and Metabolic Diseases Pathologic Function 60
C1563937 Atherogenesis phenotype Cardiovascular Diseases Pathologic Function 59
C0032300 Lobar Pneumonia disease Infections; Respiratory Tract Diseases Disease or Syndrome 54
C0887898 Experimental Lung Inflammation disease Infections; Respiratory Tract Diseases Experimental Model of Disease 54
C3714636 Pneumonitis disease Infections; Respiratory Tract Diseases Disease or Syndrome disease of anatomical entity 54
C0016059 Fibrosis phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 50