THYROID CARCINOMA, SPORADIC MEDULLARY
|
disease |
|
Neoplastic Process
|
22
|
11
|
0.030 |
None |
1.000 |
3 |
|
2014 |
2020 |
Adult Acute Lymphocytic Leukemia
|
disease |
|
Neoplastic Process
|
860
|
154
|
0.020 |
None |
1.000 |
2 |
|
1996 |
2018 |
Morphologically abnormal structure (morphologic abnormality)
|
group |
|
Anatomical Abnormality
|
20
|
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
Tonic clonic movements
|
disease |
|
Disease or Syndrome
|
22
|
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
HIV-1 infection
|
disease |
|
Disease or Syndrome
|
695
|
94
|
0.010 |
None |
< 0.001 |
1 |
|
2007 |
2007 |
Luminal A Breast Carcinoma
|
disease |
|
Neoplastic Process
|
153
|
11
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Human immunodeficiency virus (HIV) II infection category B1
|
disease |
|
Disease or Syndrome
|
985
|
56
|
0.010 |
None |
1.000 |
1 |
|
1992 |
1992 |
Elevated circulating parathyroid hormone level
|
phenotype |
|
Finding
|
18
|
1
|
0.100 |
None |
|
0 |
|
|
|
Increased glucagon level
|
phenotype |
|
Finding
|
6
|
|
0.100 |
None |
|
0 |
|
|
|
Confetti-like hypopigmented macules
|
phenotype |
|
Finding
|
8
|
|
0.100 |
None |
|
0 |
|
|
|
Increased circulating cortisol level
|
phenotype |
|
Finding
|
11
|
|
0.100 |
None |
|
0 |
|
|
|
Mental Depression
|
disease |
Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
1478
|
271
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Depressed mood
|
phenotype |
Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
1461
|
269
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Drug usage
|
phenotype |
Chemically-Induced Disorders; Mental Disorders
|
Mental or Behavioral Dysfunction
|
170
|
21
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Congenital chromosomal disease
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
757
|
47
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Congenital Hyperinsulinism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
62
|
27
|
0.100 |
None |
|
0 |
|
|
|
Retinopathy of Prematurity
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
202
|
16
|
0.020 |
None |
1.000 |
2 |
|
2001 |
2016 |
Congenital dyserythropoietic anemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
24
|
13
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Multiple Endocrine Neoplasia Type 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
Neoplastic Process
|
145
|
156
|
0.320 |
None |
1.000 |
3 |
|
2009 |
2011 |
Multiple Endocrine Neoplasia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
Neoplastic Process
|
65
|
11
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
Familial medullary thyroid carcinoma
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
Neoplastic Process
|
56
|
45
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |
Angelman Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
94
|
135
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
ARTERIAL TORTUOSITY SYNDROME
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
37
|
23
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Cholestasis, Extrahepatic
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
87
|
|
0.100 |
None |
|
0 |
|
|
|
Esophagitis
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
105
|
7
|
0.100 |
None |
|
0 |
|
|
|