Abnormality of the skeletal system
|
disease |
|
Anatomical Abnormality
|
120
|
5
|
0.110 |
None |
1.000 |
1 |
|
2008 |
2008 |
Congenital amegakaryocytic thrombocytopenia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Congenital Abnormality
|
7
|
4
|
0.090 |
None |
1.000 |
9 |
2
|
2000 |
2018 |
Congenital Abnormality
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
1091
|
73
|
0.020 |
None |
1.000 |
2 |
|
2002 |
2012 |
Myelodysplasia
|
disease |
|
Congenital Abnormality
|
135
|
3
|
0.120 |
None |
1.000 |
2 |
|
1998 |
2012 |
Limb defects
|
group |
|
Congenital Abnormality
|
67
|
2
|
0.020 |
None |
1.000 |
2 |
|
2009 |
2012 |
Congenital defects
|
group |
|
Congenital Abnormality
|
126
|
6
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Thrombocytopenia
|
phenotype |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
376
|
69
|
0.100 |
None |
1.000 |
58 |
1
|
1995 |
2020 |
Thrombocytosis
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
71
|
11
|
0.500 |
None |
0.969 |
29 |
|
1995 |
2020 |
Immune thrombocytopenic purpura
|
disease |
Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
309
|
35
|
0.100 |
None |
1.000 |
25 |
|
1996 |
2019 |
Thrombocythemia, Essential
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
212
|
32
|
0.400 |
None |
0.895 |
19 |
1
|
1995 |
2016 |
Familial thrombocytosis
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
7
|
5
|
0.400 |
None |
0.938 |
16 |
|
1998 |
2015 |
Autoimmune thrombocytopenia
|
disease |
Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
115
|
7
|
0.100 |
None |
1.000 |
10 |
|
2017 |
2019 |
Thrombocytopenia due to platelet alloimmunization
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
111
|
7
|
0.100 |
None |
1.000 |
10 |
|
2017 |
2019 |
Aplastic Anemia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
215
|
16
|
0.090 |
None |
1.000 |
9 |
|
1996 |
2019 |
Hepatitis C
|
disease |
Digestive System Diseases; Infections
|
Disease or Syndrome
|
1736
|
316
|
0.050 |
None |
1.000 |
5 |
|
1998 |
2017 |
Liver Cirrhosis
|
disease |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
|
Disease or Syndrome
|
1099
|
171
|
0.060 |
None |
0.833 |
5 |
|
1997 |
2018 |
Chronic lung disease
|
disease |
Respiratory Tract Diseases
|
Disease or Syndrome
|
112
|
5
|
0.050 |
None |
1.000 |
5 |
|
2018 |
2019 |
Myocardial Infarction
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
1582
|
547
|
0.040 |
None |
1.000 |
4 |
|
2001 |
2019 |
Septicemia
|
disease |
Pathological Conditions, Signs and Symptoms; Infections
|
Disease or Syndrome
|
1279
|
139
|
0.040 |
None |
1.000 |
4 |
|
2010 |
2018 |
Sepsis
|
disease |
Pathological Conditions, Signs and Symptoms; Infections
|
Disease or Syndrome
|
1340
|
139
|
0.040 |
None |
1.000 |
4 |
|
2010 |
2018 |
Cirrhosis
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
815
|
110
|
0.040 |
None |
0.750 |
4 |
|
1997 |
2018 |
Inherited predisposition to essential thrombocythemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
3
|
|
0.040 |
None |
1.000 |
4 |
|
1998 |
2001 |
Pancytopenia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
182
|
6
|
0.030 |
None |
1.000 |
3 |
|
2017 |
2019 |
Thrombocytopenia-Absent Radius Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
9
|
1
|
0.030 |
None |
1.000 |
3 |
|
1998 |
2012 |
Coronary Artery Disease
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1504
|
1022
|
0.030 |
None |
0.667 |
3 |
|
2017 |
2019 |