Source: ANIMAL_MODELS

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 476
C0035126 Reperfusion Injury disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Injury or Poisoning 231
C0007787 Transient Ischemic Attack disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 170
C0376618 Endotoxemia phenotype Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 101
C0024668 Mammary Neoplasms, Experimental phenotype Neoplasms Neoplastic Process; Experimental Model of Disease 81
C0038454 Cerebrovascular accident group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the nervous system; Abnormality of the cardiovascular system 64
C0017658 Glomerulonephritis disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome disease of anatomical entity Abnormality of the genitourinary system; Abnormality of the immune system 46
C0004626 Pneumonia, Bacterial group Infections; Respiratory Tract Diseases Disease or Syndrome disease of anatomical entity 14
C0003838 Arterial Occlusive Diseases group Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 3
C0477317 Other primary thrombocytopenia group Hemic and Lymphatic Diseases Disease or Syndrome genetic disease; disease of anatomical entity 3
C4304021 Autosomal dominant macrothrombocytopenia disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome genetic disease; disease of anatomical entity 2
C1861195 Glanzmann Thrombasthenia, Autosomal Dominant disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome genetic disease; disease of anatomical entity 2
C0040015 Thrombasthenia disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome genetic disease; disease of anatomical entity Abnormality of blood and blood-forming tissues 1