C0002170 |
Alopecia
|
disease |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the integument; Abnormality of head or neck
|
98 |
336 |
C4049090 |
Alopecia, Androgenetic, 1
|
disease |
|
Disease or Syndrome
|
disease of anatomical entity
|
|
39 |
104 |
C2678038 |
Alopecia, Androgenetic, 2
|
disease |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
39 |
104 |
C2676272 |
Alopecia, Androgenetic, 3
|
disease |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
39 |
104 |
C4083212 |
Alopecia, Male Pattern
|
disease |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the integument
|
39 |
104 |
C0162311 |
Androgenetic Alopecia
|
disease |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
39 |
104 |
C0038013 |
Ankylosing spondylitis
|
disease |
Musculoskeletal Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
160 |
345 |
C0200641 |
Blood basophil count (lab test)
|
phenotype |
|
Laboratory Procedure
|
|
|
272 |
452 |
C0005890 |
Body Height
|
phenotype |
|
Organism Attribute
|
|
|
1903 |
3972 |
C0007222 |
Cardiovascular Diseases
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the cardiovascular system
|
225 |
326 |
C0008313 |
Cholangitis, Sclerosing
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the digestive system; Abnormality of the immune system
|
149 |
276 |
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
|
45 |
98 |
C1956346 |
Coronary Artery Disease
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the cardiovascular system
|
252 |
551 |
C0201976 |
Creatinine measurement, serum (procedure)
|
phenotype |
|
Laboratory Procedure
|
|
|
124 |
243 |
C0010346 |
Crohn Disease
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
Abnormality of the digestive system; Abnormality of the immune system
|
239 |
616 |
C0201983 |
Dehydroepiandrosterone sulfate measurement (procedure)
|
phenotype |
|
Laboratory Procedure
|
|
|
18 |
27 |
C0011860 |
Diabetes Mellitus, Non-Insulin-Dependent
|
disease |
Nutritional and Metabolic Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
disease of metabolism
|
Abnormality of metabolism/homeostasis; Abnormality of the endocrine system
|
353 |
844 |
C0200638 |
Eosinophil count procedure
|
phenotype |
|
Laboratory Procedure
|
|
|
607 |
1133 |
C1261502 |
Finding of Mean Corpuscular Hemoglobin
|
phenotype |
|
Finding
|
|
|
633 |
1159 |
C0017654 |
Glomerular Filtration Rate
|
phenotype |
|
Diagnostic Procedure
|
|
|
399 |
1031 |
C0857490 |
Granulocyte count
|
phenotype |
|
Laboratory Procedure
|
|
|
100 |
150 |
C0021390 |
Inflammatory Bowel Diseases
|
group |
Digestive System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the digestive system; Abnormality of the immune system
|
178 |
354 |
C0524587 |
Mean Corpuscular Volume (result)
|
phenotype |
|
Laboratory or Test Result
|
|
|
250 |
495 |
C0200633 |
Neutrophil count (procedure)
|
phenotype |
|
Laboratory Procedure
|
|
|
145 |
234 |
C0029489 |
Other alopecia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
|
|
39 |
104 |