Tumor Cell Invasion
|
phenotype |
|
Neoplastic Process
|
6626
|
169
|
0.020 |
None |
1.000 |
2 |
|
2007 |
2014 |
Malignant neoplasm of colon and/or rectum
|
disease |
|
Neoplastic Process
|
3669
|
502
|
0.020 |
None |
1.000 |
2 |
|
2019 |
2020 |
diabetes (mellitus) due to autoimmune process
|
disease |
|
Disease or Syndrome
|
2
|
|
0.200 |
None |
1.000 |
1 |
|
1997 |
1997 |
diabetes (mellitus) due to immune mediated pancreatic islet beta-cell destruction
|
disease |
|
Disease or Syndrome
|
2
|
|
0.200 |
None |
1.000 |
1 |
|
1997 |
1997 |
idiopathic diabetes (mellitus)
|
disease |
|
Disease or Syndrome
|
2
|
|
0.200 |
None |
1.000 |
1 |
|
1997 |
1997 |
estrogen receptor-negative breast cancer
|
disease |
|
Neoplastic Process
|
356
|
40
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |
Transient neonatal diabetes mellitus
|
disease |
|
Disease or Syndrome
|
23
|
|
0.100 |
None |
|
0 |
|
|
|
Abnormal oral glucose tolerance
|
phenotype |
|
Finding
|
15
|
|
0.100 |
None |
|
0 |
|
|
|
Retinopathy, CTCAE
|
phenotype |
|
Finding
|
108
|
|
0.100 |
None |
|
0 |
|
|
|
Hypoinsulinaemia (disorder)
|
disease |
|
Disease or Syndrome
|
36
|
|
0.100 |
None |
|
0 |
|
|
|
Elevated hemoglobin A1c
|
phenotype |
|
Finding
|
14
|
|
0.100 |
None |
|
0 |
|
|
|
Abnormal C-peptide level
|
phenotype |
|
Finding
|
14
|
|
0.100 |
None |
|
0 |
|
|
|
Decreased waist to hip ratio
|
phenotype |
|
Finding
|
28
|
|
0.100 |
None |
|
0 |
|
|
|
Coronary heart disease
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1576
|
1178
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Cardiac Arrest
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
411
|
50
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Disease of capillaries
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
61
|
5
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Congenital hypoplasia of pancreas
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
20
|
|
0.100 |
None |
|
0 |
|
|
|
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 |
|
|
|
Autosomal recessive retinitis pigmentosa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Congenital Abnormality
|
82
|
31
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
Saethre-Chotzen Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
30
|
33
|
0.050 |
None |
1.000 |
5 |
|
1997 |
2018 |
Russell-Silver syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
104
|
12
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Multiple Endocrine Neoplasia Type 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
Neoplastic Process
|
145
|
156
|
0.010 |
None |
1.000 |
1 |
|
2009 |
2009 |
Pallister-Hall syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
10
|
39
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
MENTAL RETARDATION, X-LINKED, SNYDER-ROBINSON TYPE
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
32
|
8
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
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 |
|
2018 |
2018 |