Source: CTD_human

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0740391 Middle Cerebral Artery Occlusion disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Acquired Abnormality 34
C2936380 Neointima disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 6
C0860207 Drug-Induced Liver Disease phenotype Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 404
C1262760 Hepatitis, Drug-Induced disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 404
C3658290 Drug-Induced Acute Liver Injury disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 404
C4277682 Chemical and Drug Induced Liver Injury disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 404
C4279912 Chemically-Induced Liver Toxicity disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 404
C0020538 Hypertensive disease group Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 190
C0028754 Obesity disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome disease of metabolism Growth abnormality 186
C0027051 Myocardial Infarction disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 95
C0034069 Pulmonary Fibrosis disease Respiratory Tract Diseases Disease or Syndrome disease of anatomical entity Abnormality of the respiratory system 83
C4721507 Alveolitis, Fibrosing disease Respiratory Tract Diseases Disease or Syndrome 83
C0004096 Asthma disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the immune system; Abnormality of the respiratory system 80
C0023895 Liver diseases group Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system 71
C0007786 Brain Ischemia disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the nervous system; Abnormality of the cardiovascular system 60
C0009324 Ulcerative Colitis disease Digestive System Diseases Disease or Syndrome genetic disease; disease of anatomical entity Abnormality of the digestive system; Abnormality of the immune system 60
C0263628 Tumoral calcinosis disease Nutritional and Metabolic Diseases Disease or Syndrome 42
C0238281 Middle Cerebral Artery Syndrome phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 34
C0740376 Middle Cerebral Artery Thrombosis disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 34
C0740392 Infarction, Middle Cerebral Artery disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 34
C0751845 Middle Cerebral Artery Embolus phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 34
C0751846 Left Middle Cerebral Artery Infarction phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 34
C0751847 Embolic Infarction, Middle Cerebral Artery phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 34
C0751848 Thrombotic Infarction, Middle Cerebral Artery phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 34
C0751849 Right Middle Cerebral Artery Infarction phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 34