Paresis
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
216
49
0.010
None
1.000
1
2019
2019
Pancreatic carcinoma
disease
Digestive System Diseases; Neoplasms; Endocrine System Diseases
Neoplastic Process
2689
322
0.020
None
1.000
2
2019
2019
×
CUI:
C0030193
Disease:
Pain
Pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1554
196
0.010
None
< 0.001
1
2016
2016
Otosclerosis
disease
Otorhinolaryngologic Diseases
Disease or Syndrome
49
11
0.130
None
0.333
3
2004
2019
Other ureteric obstruction
phenotype
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Anatomical Abnormality
52
0.200
None
1.000
1
2010
2010
Osteosarcoma of bone
disease
Neoplasms
Neoplastic Process
2247
151
0.010
None
1.000
1
1998
1998
Osteosarcoma
disease
Neoplasms
Neoplastic Process
2283
178
0.010
None
1.000
1
1998
1998
Osteoporotic Fractures
group
Wounds and Injuries
Disease or Syndrome
108
40
0.020
None
1.000
2
2
2011
2019
Osteoporosis, Senile
disease
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
73
3
0.300
None
0
Osteoporosis, Postmenopausal
disease
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
171
38
0.110
None
1.000
1
4
1991
1991
Osteoporosis, Age-Related
disease
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
89
0.300
None
0
Osteoporosis
disease
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
1098
182
0.670
strong
1.000
7
1
1985
2018
Osteopenia
disease
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
845
61
0.110
None
1.000
2
1
1991
2016
Osteogenesis imperfecta, recessive perinatal lethal
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
Disease or Syndrome; Congenital Abnormality
2
51
0.100
None
1.000
1
16
2016
2016
Osteogenesis imperfecta, dominant perinatal lethal
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
Disease or Syndrome; Congenital Abnormality
8
93
0.660
strong
1.000
21
31
1985
2011
Osteogenesis imperfecta with blue sclerae AND normal teeth
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
Disease or Syndrome
1
0.010
None
1.000
1
1996
1996
Osteogenesis imperfecta type IV (disorder)
disease
Disease or Syndrome; Congenital Abnormality
12
65
0.800
strong
1.000
25
28
1985
2015
Osteogenesis imperfecta type III (disorder)
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
Disease or Syndrome
18
67
0.950
strong
1.000
27
35
1991
2018
Osteogenesis Imperfecta
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
Disease or Syndrome; Congenital Abnormality
90
91
0.700
strong
0.977
172
25
1980
2020
Osteoarthrosis Deformans
disease
Musculoskeletal Diseases
Disease or Syndrome
96
1
0.300
None
1.000
1
2009
2009
Orbital separation excessive
phenotype
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Finding
590
77
0.100
None
0
Oral Submucous Fibrosis
disease
Stomatognathic Diseases
Disease or Syndrome
106
8
0.320
None
1.000
3
1995
2006
Opportunistic Infections
group
Infections
Disease or Syndrome
90
7
0.010
None
< 0.001
1
2013
2013
Nonspecific interstitial pneumonia
disease
Respiratory Tract Diseases
Disease or Syndrome
28
1
0.010
None
1.000
1
2019
2019
Non-Small Cell Lung Carcinoma
disease
Neoplasms; Respiratory Tract Diseases
Neoplastic Process
3926
712
0.010
None
< 0.001
1
2019
2019