Hypouricemia, Renal, 2
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
2
8
0.720
None
1.000
5
7
2008
2019
Renal hypouricemia
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
4
18
0.600
None
1.000
19
3
2008
2019
Hyperuricemia
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
196
76
0.500
None
0.958
24
3
2008
2020
×
CUI:
C0018099
Disease:
Gout
Gout
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
205
2354
0.400
None
1.000
13
352
2007
2019
Hypouricemia
phenotype
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
14
8
0.180
None
1.000
8
3
2011
2020
Arthritis, Gouty
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
206
2356
0.120
None
1.000
15
351
2007
2019
Uric acid measurement (procedure)
phenotype
Laboratory Procedure
264
1463
0.100
None
1.000
33
314
2007
2019
Kidney Failure, Chronic
disease
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
827
425
0.100
None
1.000
2
3
2018
2018
Body Height
phenotype
Organism Attribute
1903
3972
0.100
None
1.000
1
1
2019
2019
Glomerular Filtration Rate
phenotype
Diagnostic Procedure
399
1033
0.100
None
1.000
1
1
2018
2018
Red Blood Cell Count measurement
phenotype
Laboratory Procedure
717
1599
0.100
None
1.000
1
1
2019
2019
Creatinine measurement, serum (procedure)
phenotype
Laboratory Procedure
124
243
0.100
None
1.000
1
1
2018
2018
Pseudocholinesterase Measurement
phenotype
Laboratory Procedure
39
568
0.100
None
1.000
1
8
2011
2011
Vital capacity
phenotype
Clinical Attribute
430
746
0.100
None
1.000
1
1
2019
2019
elevated blood glucose level
phenotype
Finding
89
111
0.100
None
1.000
1
1
2011
2011
Glucose measurement
phenotype
Laboratory Procedure
89
111
0.100
None
1.000
1
1
2011
2011
Mean Corpuscular Volume (result)
phenotype
Laboratory or Test Result
269
549
0.100
None
1.000
1
1
2016
2016
Malignant neoplasm of esophagus
disease
Digestive System Diseases; Neoplasms
Neoplastic Process
1286
214
0.100
None
1.000
1
1
2011
2011
URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 2
phenotype
Finding
1
3
0.100
None
0
3
Kidney Failure, Acute
disease
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
826
32
0.070
None
1.000
7
2
2005
2015
Pre-renal acute kidney injury
disease
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
67
4
0.050
None
1.000
5
2005
2015
Parkinson Disease
disease
Nervous System Diseases
Disease or Syndrome
2078
990
0.040
None
0.750
4
2
2011
2018
Diabetes Mellitus, Non-Insulin-Dependent
disease
Nutritional and Metabolic Diseases; Endocrine System Diseases
Disease or Syndrome
3134
2672
0.040
None
1.000
4
1
2015
2018
Kidney Calculi
disease
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
190
71
0.040
None
1.000
4
4
2010
2018
Nephrolithiasis
disease
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
242
99
0.040
None
1.000
4
4
2010
2018