Keloid
disease
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
Acquired Abnormality
165
15
0.010
None
1.000
1
2018
2018
Cicatrix, Hypertrophic
disease
Pathological Conditions, Signs and Symptoms
Acquired Abnormality
185
3
0.010
None
1.000
1
2018
2018
Keratosis pilaris
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Acquired Abnormality
30
4
0.010
None
1.000
1
2018
2018
Abnormality of the periventricular white matter
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Anatomical Abnormality
45
7
0.100
None
0
Congenital chromosomal disease
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormality
757
47
0.010
None
1.000
1
1987
1987
Malformations of Cortical Development, Group II
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Congenital Abnormality
180
101
0.010
None
1.000
1
2016
2016
Movement Disorders
group
Nervous System Diseases
Disease or Syndrome
362
247
0.100
None
1.000
14
1
1981
2016
Chronic Obstructive Airway Disease
disease
Respiratory Tract Diseases
Disease or Syndrome
1428
852
0.100
None
1.000
12
2017
2020
Asthma
disease
Respiratory Tract Diseases; Immune System Diseases
Disease or Syndrome
2096
1536
0.040
None
1.000
4
2017
2019
Diabetes Mellitus, Non-Insulin-Dependent
disease
Nutritional and Metabolic Diseases; Endocrine System Diseases
Disease or Syndrome
3134
2672
0.120
None
1.000
3
2
2012
2018
Alzheimer's Disease
disease
Nervous System Diseases; Mental Disorders
Disease or Syndrome
3397
1843
0.110
None
1.000
2
1
2002
2016
Pneumonia
disease
Infections; Respiratory Tract Diseases
Disease or Syndrome
1032
33
0.020
None
1.000
2
2018
2019
Retinal Dystrophies
group
Eye Diseases
Disease or Syndrome
219
227
0.120
None
0.500
2
2014
2016
Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms; Cardiovascular Diseases
Disease or Syndrome
1
12
0.610
strong
1.000
2
12
2011
2014
×
CUI:
C0010709
Disease:
Cyst
Cyst
disease
Pathological Conditions, Signs and Symptoms; Neoplasms
Disease or Syndrome
221
6
0.010
None
< 0.001
1
2014
2014
Fetal Growth Retardation
phenotype
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
Disease or Syndrome
1037
21
0.010
None
1.000
1
2016
2016
Hyperlipidemia
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
472
83
0.010
None
1.000
1
2019
2019
Male infertility
phenotype
Male Urogenital Diseases
Disease or Syndrome
516
146
0.010
None
1.000
1
2005
2005
Lupus Erythematosus, Systemic
disease
Skin and Connective Tissue Diseases; Immune System Diseases
Disease or Syndrome
1883
1172
0.010
None
1.000
1
1
2013
2013
Myopathy
group
Musculoskeletal Diseases; Nervous System Diseases
Disease or Syndrome
634
166
0.010
None
1.000
1
2017
2017
Muscular Dystrophy
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
Disease or Syndrome
280
67
0.010
None
1.000
1
2018
2018
Myopia
disease
Eye Diseases
Disease or Syndrome
490
167
0.110
None
1.000
1
1
2016
2016
Peripheral Neuropathy
group
Nervous System Diseases
Disease or Syndrome
351
81
0.010
None
1.000
1
2018
2018
Prune Belly Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Disease or Syndrome
83
2
0.010
None
1.000
1
2016
2016
Pulmonary Fibrosis
disease
Respiratory Tract Diseases
Disease or Syndrome
924
25
0.010
None
1.000
1
2018
2018