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 |