Source: LHGDN

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0021368 Inflammation phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 360
C1956346 Coronary Artery Disease disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 161
C0040053 Thrombosis phenotype Cardiovascular Diseases Pathologic Function disease of anatomical entity 66
C0398623 Thrombophilia disease Hemic and Lymphatic Diseases Disease or Syndrome genetic disease; disease of anatomical entity Abnormality of blood and blood-forming tissues 9
C0008533 Hemophilia B disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome genetic disease; disease of anatomical entity 2
C0015523 Hereditary Factor XI Deficiency disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome genetic disease Abnormality of blood and blood-forming tissues 2