Arthritis, Gouty
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
206
2356
0.110
None
1.000
6
156
2010
2019
Corpuscular Hemoglobin Concentration Mean
phenotype
Laboratory or Test Result
401
4389
0.100
None
1.000
2
97
2010
2012
Ferritin measurement
phenotype
Laboratory Procedure
10
21
0.100
None
1.000
2
1
2011
2011
Finding of Mean Corpuscular Hemoglobin
phenotype
Finding
653
1206
0.100
None
1.000
2
1
2010
2012
×
CUI:
C0018099
Disease:
Gout
Gout
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
205
2354
0.100
None
1.000
5
156
2010
2019
Hyperhomocysteinemia
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Disease or Syndrome
246
45
0.010
None
1.000
1
2015
2015
Hypophosphatemic Rickets, X-Linked Dominant
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases
Disease or Syndrome
54
122
0.010
None
1.000
1
1994
1994
Intelligence
phenotype
Behavior and Behavior Mechanisms
Mental Process
645
2093
0.100
None
1.000
2
4
2018
2019
Iron level result
phenotype
Laboratory or Test Result
12
16
0.100
None
1.000
1
1
2011
2011
Iron measurement
phenotype
Laboratory Procedure
12
16
0.100
None
1.000
1
1
2011
2011
Liver Cirrhosis, Experimental
disease
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
Experimental Model of Disease
870
0.300
None
1.000
2
2006
2014
Malignant Neoplasms
group
Neoplasms
Neoplastic Process
8621
1641
0.010
None
1.000
1
2013
2013
Mean Corpuscular Volume (result)
phenotype
Laboratory or Test Result
269
549
0.100
None
1.000
1
1
2012
2012
Polycystic kidney disease, type 2
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
15
41
0.010
None
1.000
1
8
2012
2012
Primary gout
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
40
5
0.010
None
1.000
1
2014
2014
Primary malignant neoplasm
group
Neoplasms
Neoplastic Process
8221
1374
0.010
None
1.000
1
2013
2013
Red Blood Cell Count measurement
phenotype
Laboratory Procedure
717
1599
0.100
None
1.000
1
6
2009
2009
Rickets, X-Linked Hypophosphatemic
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases
Disease or Syndrome
23
1
0.010
None
1.000
1
1994
1994
Schizophrenia
disease
Mental Disorders
Mental or Behavioral Dysfunction
2872
2897
0.100
None
1.000
1
3
2009
2009
Serum ferritin measurement
phenotype
Laboratory Procedure
10
21
0.100
None
1.000
2
1
2011
2011
Sjogren's Syndrome
disease
Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases
Disease or Syndrome
481
47
0.010
None
1.000
1
1997
1997
Uric acid measurement (procedure)
phenotype
Laboratory Procedure
264
1463
0.100
None
1.000
7
33
2009
2019
Vitamin D-Resistant Rickets, X-Linked
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases
Disease or Syndrome
48
3
0.010
None
1.000
1
1994
1994