Diabetes Mellitus, Non-Insulin-Dependent
disease
Nutritional and Metabolic Diseases; Endocrine System Diseases
Disease or Syndrome
3134
2672
0.100
None
0
1
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 12
phenotype
Finding
2
1
0.100
None
0
1
DiGeorge Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases
Disease or Syndrome
111
7
0.200
None
1.000
1
2003
2003
Myelocele
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Congenital Abnormality
5
1
0.300
None
1.000
1
2005
2005
Acquired Meningomyelocele
phenotype
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Acquired Abnormality
4
0.300
None
1.000
1
2005
2005
Meningomyelocele
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Congenital Abnormality
89
27
0.310
None
1.000
1
2005
2005
Prostatic Neoplasms
group
Neoplasms; Male Urogenital Diseases
Neoplastic Process
1722
31
0.310
None
1.000
1
2005
2005
Spina Bifida
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Congenital Abnormality
179
61
0.010
None
< 0.001
1
1
2005
2005
Cardiovascular Diseases
group
Cardiovascular Diseases
Disease or Syndrome
1756
711
0.100
None
1.000
1
1
2008
2008
Tetralogy of Fallot
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Congenital Abnormality
274
83
0.010
None
< 0.001
1
3
2009
2009
Congenital heart disease
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Congenital Abnormality
267
80
0.010
None
1.000
1
2009
2009
Vitamin A Deficiency
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
51
1
0.010
None
1.000
1
2010
2010
Pseudocholinesterase Measurement
phenotype
Laboratory Procedure
39
568
0.100
None
1.000
1
3
2011
2011
Lipids measurement
group
Laboratory Procedure
27
53
0.100
None
1.000
2
2
2009
2012
Phospholipid measurement
phenotype
Laboratory Procedure
58
306
0.100
None
1.000
2
2
2008
2012
Corpuscular Hemoglobin Concentration Mean
phenotype
Laboratory or Test Result
401
4389
0.100
None
1.000
1
2
2012
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
1
1
2012
2012
Calcification of coronary artery
phenotype
Nutritional and Metabolic Diseases; Cardiovascular Diseases
Pathologic Function
51
205
0.100
None
1.000
1
2
2012
2012
Arthritis, Gouty
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
206
2356
0.100
None
1.000
1
1
2012
2012
Serum HDL cholesterol measurement
phenotype
Laboratory Procedure
283
679
0.100
None
1.000
15
35
2008
2013
Serum albumin measurement
phenotype
Laboratory Procedure
433
3282
0.100
None
1.000
3
217
2008
2013
Thyroid Neoplasm
disease
Neoplasms; Endocrine System Diseases
Neoplastic Process
1164
135
0.010
None
1.000
1
2013
2013
Anaplastic carcinoma
disease
Neoplasms
Neoplastic Process
232
3
0.010
None
1.000
1
2013
2013
Arnold-Chiari Malformation, Type I
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Congenital Abnormality
41
1
0.010
None
1.000
1
2013
2013
Gastrointestinal Diseases
group
Digestive System Diseases
Disease or Syndrome
144
14
0.100
None
1.000
1
1
2013
2013