Tumor Cell Invasion
|
phenotype |
|
Neoplastic Process
|
6626
|
169
|
0.030 |
None |
1.000 |
3 |
|
2010 |
2019 |
Congenital defects
|
group |
|
Congenital Abnormality
|
126
|
6
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Fibrous body
|
disease |
|
Acquired Abnormality
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
Recurrent tumor
|
phenotype |
|
Neoplastic Process
|
735
|
33
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Growth failure
|
phenotype |
|
Disease or Syndrome
|
84
|
7
|
0.010 |
None |
1.000 |
1 |
|
1993 |
1993 |
Hypoplasia of the pituitary gland
|
disease |
|
Disease or Syndrome
|
5
|
1
|
0.010 |
None |
1.000 |
1 |
|
1997 |
1997 |
Hypoplastic pituitary gland
|
disease |
|
Congenital Abnormality
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2006 |
2006 |
Oestrogen receptor positive breast cancer
|
disease |
|
Neoplastic Process
|
510
|
58
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Node-positive breast cancer
|
disease |
|
Neoplastic Process
|
40
|
3
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
Isolated somatotropin deficiency
|
disease |
|
Disease or Syndrome
|
168
|
27
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Gonadotropin deficiency
|
disease |
|
Disease or Syndrome
|
26
|
|
0.010 |
None |
1.000 |
1 |
|
1999 |
1999 |
Aortic valve disorder
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
58
|
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Congenital Abnormality
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
1098
|
73
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Achondroplasia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
46
|
21
|
0.010 |
None |
1.000 |
1 |
|
2006 |
2006 |
Dwarfism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
|
Congenital Abnormality
|
1261
|
77
|
0.050 |
None |
0.800 |
5 |
|
1992 |
2010 |
Congenital Hypothyroidism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
94
|
48
|
0.020 |
None |
1.000 |
2 |
|
1995 |
2001 |
Rubinstein-Taybi Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
31
|
88
|
0.010 |
None |
1.000 |
1 |
|
1996 |
1996 |
Somatotropin deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
154
|
14
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Septo-Optic Dysplasia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
35
|
19
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
Werner Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
130
|
71
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |
ACTH Deficiency, Isolated
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
11
|
11
|
0.010 |
None |
1.000 |
1 |
|
2020 |
2020 |
Severe Combined Immunodeficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases
|
Disease or Syndrome
|
284
|
46
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
Secondary malignant neoplasm of liver
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
951
|
34
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Hypothyroidism
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
613
|
283
|
0.040 |
None |
1.000 |
4 |
|
1995 |
2011 |
Secondary hypothyroidism
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
47
|
2
|
0.040 |
None |
1.000 |
4 |
|
2003 |
2017 |