mosaic variegated aneuploidy
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
Disease or Syndrome
7
0.020
None
1.000
2
1998
2011
Dermatitis, Allergic Contact
disease
Skin and Connective Tissue Diseases; Immune System Diseases
Disease or Syndrome
151
1
0.300
None
1.000
1
2007
2007
Autistic Disorder
disease
Mental Disorders
Mental or Behavioral Dysfunction
1112
395
0.300
None
1.000
1
2008
2008
Aortic Aneurysm, Abdominal
disease
Cardiovascular Diseases
Disease or Syndrome
586
90
0.010
None
1.000
1
2009
2009
Neoplasms
group
Neoplasms
Neoplastic Process
10161
1644
0.030
None
1.000
3
2010
2016
Malignant neoplasm of breast
disease
Neoplasms; Skin and Connective Tissue Diseases
Neoplastic Process
6941
3417
0.100
None
1.000
12
2011
2019
Breast Carcinoma
disease
Neoplasms; Skin and Connective Tissue Diseases
Neoplastic Process
6776
2793
0.100
None
1.000
12
2011
2019
Mosaic variegated aneuploidy syndrome 1
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Disease or Syndrome
10
20
0.020
None
1.000
2
2011
2018
Malignant Childhood Neoplasm
disease
Neoplasms
Neoplastic Process
179
34
0.010
None
1.000
1
2011
2011
Familial dilated cardiomyopathy
disease
Cardiovascular Diseases
Disease or Syndrome
83
47
0.010
None
1.000
1
2013
2013
Hypertrophic Cardiomyopathy
disease
Cardiovascular Diseases
Disease or Syndrome
560
635
0.010
None
1.000
1
2013
2013
Long QT Syndrome
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Disease or Syndrome
105
349
0.010
None
1.000
1
2013
2013
Mammary Neoplasms
group
Neoplasms; Skin and Connective Tissue Diseases
Neoplastic Process
2780
385
0.010
None
1.000
1
2013
2013
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)
disease
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Disease or Syndrome
31
121
0.010
None
1.000
1
2013
2013
Trichohepatoenteric Syndrome
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases
Disease or Syndrome
424
28
0.010
None
1.000
1
2014
2014
×
CUI:
C0030193
Disease:
Pain
Pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1554
196
0.100
None
1.000
20
2016
2019
Peripheral Arterial Diseases
group
Cardiovascular Diseases
Disease or Syndrome
319
128
0.100
None
1.000
1
1
2016
2016
Fatigue
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
760
67
0.050
None
1.000
5
2017
2019
Pain in lower limb
phenotype
Sign or Symptom
31
2
0.040
None
0.750
4
2017
2020
Back Pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
110
10
0.030
None
1.000
3
2017
2019
Depressive Symptoms
phenotype
Behavior and Behavior Mechanisms
Sign or Symptom
421
120
0.020
None
1.000
2
2017
2018
Metabolic Syndrome X
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
1125
591
0.020
None
1.000
2
2017
2018
PREMATURE CHROMATID SEPARATION TRAIT
disease
Disease or Syndrome
19
10
0.020
None
1.000
2
2017
2019
Major Depressive Disorder
disease
Mental Disorders
Mental or Behavioral Dysfunction
1236
1451
0.020
None
1.000
2
2017
2019
Kidney Failure, Chronic
disease
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
827
425
0.010
None
< 0.001
1
2017
2017