C1325327 |
fibrinogen activity
|
phenotype |
|
Molecular Function
|
|
|
26 |
63 |
C1561955 |
Fibrinogen, CTCAE
|
phenotype |
|
Finding
|
|
|
26 |
63 |
C1272321 |
Autoantibody measurement
|
phenotype |
|
Laboratory Procedure
|
|
|
26 |
49 |
C4021107 |
Non-obstructive azoospermia
|
disease |
Male Urogenital Diseases
|
Disease or Syndrome
|
|
Abnormality of the genitourinary system
|
26 |
48 |
C0202239 |
Uric acid measurement (procedure)
|
phenotype |
|
Laboratory Procedure
|
|
|
25 |
968 |
C0441683 |
Hormone measurement
|
group |
|
Laboratory Procedure
|
|
|
25 |
91 |
C2700366 |
Adiponectin Measurement
|
phenotype |
|
Laboratory Procedure
|
|
|
25 |
68 |
C0023980 |
Longevity
|
phenotype |
|
Temporal Concept
|
|
|
25 |
42 |
C1306620 |
Systolic blood pressure measurement
|
phenotype |
|
Diagnostic Procedure
|
|
|
25 |
35 |
C0546837 |
Malignant neoplasm of esophagus
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
|
24 |
44 |
C0029408 |
Degenerative polyarthritis
|
disease |
Musculoskeletal Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the skeletal system
|
24 |
35 |
C1278049 |
Serum gamma-glutamyl transferase measurement
|
phenotype |
|
Laboratory Procedure
|
|
|
24 |
31 |
C1305855 |
Body mass index
|
phenotype |
|
Clinical Attribute
|
|
|
24 |
29 |
C0042487 |
Venous Thrombosis
|
phenotype |
Cardiovascular Diseases
|
Pathologic Function
|
disease of anatomical entity
|
Abnormality of blood and blood-forming tissues
|
23 |
218 |
C0429028 |
QT interval feature (observable entity)
|
phenotype |
|
Clinical Attribute
|
|
|
23 |
99 |
C0019829 |
Hodgkin Disease
|
disease |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
Neoplasm; Abnormality of blood and blood-forming tissues
|
23 |
52 |
C0004936 |
Mental disorders
|
group |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
disease of mental health
|
|
23 |
49 |
C0011615 |
Dermatitis, Atopic
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the integument; Abnormality of the immune system
|
23 |
47 |
C0149931 |
Migraine Disorders
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the nervous system
|
23 |
47 |
C0026764 |
Multiple Myeloma
|
disease |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
Neoplasm; Abnormality of blood and blood-forming tissues
|
22 |
627 |
C0005938 |
Bone Density
|
phenotype |
|
Clinical Attribute
|
|
|
22 |
350 |
C0026691 |
Mucocutaneous Lymph Node Syndrome
|
disease |
Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
22 |
96 |
C0035227 |
Respiratory Function Tests
|
phenotype |
|
Diagnostic Procedure
|
|
|
22 |
34 |
C0008924 |
Cleft upper lip
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
|
Congenital Abnormality
|
disease of anatomical entity; syndrome; physical disorder
|
Abnormality of head or neck
|
21 |
172 |
C0233849 |
Personality Traits
|
group |
Behavior and Behavior Mechanisms
|
Finding
|
|
|
21 |
75 |