Source: CTD_mouse

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0018801 Heart failure disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 3
C0018802 Congestive heart failure disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 3
C0023212 Left-Sided Heart Failure disease Cardiovascular Diseases Disease or Syndrome Abnormality of the cardiovascular system 3
C0235527 Heart Failure, Right-Sided disease Cardiovascular Diseases Disease or Syndrome Abnormality of the cardiovascular system 3
C1959583 Myocardial Failure disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 3
C1961112 Heart Decompensation phenotype Cardiovascular Diseases Pathologic Function 3
C0033141 Cardiomyopathies, Primary group Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 2
C0036529 Myocardial Diseases, Secondary group Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 2
C0878544 Cardiomyopathies group Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 2
C0007193 Cardiomyopathy, Dilated group Cardiovascular Diseases Disease or Syndrome genetic disease; disease of anatomical entity Abnormality of the cardiovascular system 1
C0018799 Heart Diseases group Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 1
C0020538 Hypertensive disease group Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 1
C0151744 Myocardial Ischemia disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 1
C1449563 Cardiomyopathy, Familial Idiopathic disease Cardiovascular Diseases Disease or Syndrome genetic disease; disease of anatomical entity 1
C0013221 Drug toxicity group Chemically-Induced Disorders Injury or Poisoning 3
C0041755 Adverse reaction to drug group Chemically-Induced Disorders Pathologic Function 3
C0376634 Craniofacial Abnormalities group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 1
C0265541 Cranioschisis disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 1
C0497552 Congenital neurologic anomalies group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality Abnormality of the nervous system 1
C0015695 Fatty Liver disease Digestive System Diseases Disease or Syndrome genetic disease; disease of metabolism 3
C2711227 Steatohepatitis disease Digestive System Diseases Disease or Syndrome Abnormality of the digestive system 3
C0008370 Cholestasis disease Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system 2
C0008311 Cholangitis disease Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system; Abnormality of the immune system 1
C0009319 Colitis disease Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system; Abnormality of the immune system 1
C0400966 Non-alcoholic Fatty Liver Disease disease Digestive System Diseases Disease or Syndrome genetic disease; disease of metabolism 1