CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C2919142 Short Stature, CTCAE phenotype Finding 1005
C0027947 Neutropenia disease Hemic and Lymphatic Diseases Disease or Syndrome disease of anatomical entity 118
C1963060 Agitation, CTCAE 3.0 phenotype Finding 87
C4552855 Agitation, CTCAE 5.0 phenotype Finding 87
C0271561 Somatotropin deficiency disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases Disease or Syndrome disease of anatomical entity 75
C1963077 Bone Pain, CTCAE 3.0 phenotype Finding 67
C4554063 Bone Pain, CTCAE 5.0 phenotype Finding 67
C0241144 Petechiae of skin phenotype Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Sign or Symptom 46
C4316812 Fibrinogen Deficiency disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome genetic disease; disease of anatomical entity 34
C0024623 Malignant neoplasm of stomach disease Digestive System Diseases; Neoplasms Neoplastic Process disease of anatomical entity; disease of cellular proliferation 24
C4552938 Productive Cough, CTCAE phenotype Finding 17
C0574002 Edema of foot (finding) phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 14
C0206736 Nevus, Blue disease Neoplasms Neoplastic Process 2
C0262929 Myxoma of the Endocardium disease Neoplasms Neoplastic Process 2
C0002871 Anemia disease Hemic and Lymphatic Diseases Disease or Syndrome disease of anatomical entity Abnormality of blood and blood-forming tissues 299
C0040034 Thrombocytopenia phenotype Hemic and Lymphatic Diseases Disease or Syndrome disease of anatomical entity Abnormality of blood and blood-forming tissues 237
C0030312 Pancytopenia disease Hemic and Lymphatic Diseases Disease or Syndrome disease of anatomical entity Abnormality of blood and blood-forming tissues 77
C0553681 Hypofibrinogenemia disease Disease or Syndrome Abnormality of blood and blood-forming tissues 34
C1860320 Bone marrow hypercellularity phenotype Finding Abnormality of blood and blood-forming tissues 26
C0012739 Disseminated Intravascular Coagulation disease Hemic and Lymphatic Diseases Disease or Syndrome disease of anatomical entity Abnormality of blood and blood-forming tissues 20
C0040038 Thromboembolism phenotype Cardiovascular Diseases Pathologic Function Abnormality of blood and blood-forming tissues 13
C0151945 Thrombosis of cerebral veins disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome Abnormality of blood and blood-forming tissues 9
C0014591 Epistaxis phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Pathologic Function Abnormality of blood and blood-forming tissues; Abnormality of head or neck 81
C0017565 Gingival Hemorrhage phenotype Pathological Conditions, Signs and Symptoms; Stomatognathic Diseases Pathologic Function Abnormality of blood and blood-forming tissues; Abnormality of head or neck 48
C4022608 Oral cavity bleeding phenotype Pathologic Function Abnormality of blood and blood-forming tissues; Abnormality of head or neck 18