Activated Protein C Resistance
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
41
|
30
|
0.100 |
None |
0.947 |
75 |
|
1994 |
2018 |
Factor V Leiden mutation
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
86
|
46
|
0.100 |
None |
0.947 |
57 |
|
1995 |
2019 |
Thrombophilia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
161
|
43
|
0.200 |
None |
1.000 |
55 |
1
|
1994 |
2020 |
Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
1
|
41
|
0.600 |
strong |
1.000 |
45 |
41
|
1987 |
2017 |
Protein C Deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
43
|
14
|
0.800 |
strong |
1.000 |
27 |
8
|
1984 |
2020 |
Sepsis
|
disease |
Pathological Conditions, Signs and Symptoms; Infections
|
Disease or Syndrome
|
1453
|
144
|
0.600 |
None |
1.000 |
23 |
|
2000 |
2019 |
Septicemia
|
disease |
Pathological Conditions, Signs and Symptoms; Infections
|
Disease or Syndrome
|
1285
|
141
|
0.400 |
None |
1.000 |
21 |
|
2000 |
2019 |
Deep Vein Thrombosis
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
230
|
93
|
0.500 |
None |
0.947 |
19 |
8
|
1994 |
2019 |
Severe Sepsis
|
disease |
Pathological Conditions, Signs and Symptoms; Infections
|
Disease or Syndrome
|
181
|
29
|
0.400 |
None |
1.000 |
15 |
1
|
2002 |
2017 |
Ischemic stroke
|
disease |
Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
1159
|
704
|
0.100 |
None |
1.000 |
11 |
|
2009 |
2019 |
Disseminated Intravascular Coagulation
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
117
|
3
|
0.380 |
None |
1.000 |
9 |
1
|
2000 |
2019 |
Hemophilia A
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
143
|
295
|
0.090 |
None |
0.889 |
9 |
|
1988 |
2018 |
Purpura Fulminans
|
disease |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
15
|
1
|
0.370 |
None |
1.000 |
8 |
1
|
1994 |
2018 |
Hemophilia, NOS
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
82
|
8
|
0.080 |
None |
0.875 |
8 |
|
1988 |
2018 |
Pyruvate Carboxylase Deficiency Disease
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
14
|
33
|
0.070 |
None |
1.000 |
7 |
3
|
1993 |
2018 |
Lupus anticoagulant disorder
|
disease |
Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
66
|
14
|
0.070 |
None |
1.000 |
7 |
|
1995 |
2015 |
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
1
|
12
|
0.700 |
strong |
1.000 |
7 |
12
|
1992 |
2015 |
Myocardial Infarction
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
1800
|
680
|
0.050 |
None |
1.000 |
5 |
|
1996 |
2017 |
Protein S Deficiency
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
19
|
14
|
0.050 |
None |
1.000 |
5 |
|
1985 |
2005 |
Antithrombin III Deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
27
|
52
|
0.040 |
None |
1.000 |
4 |
|
1996 |
2018 |
Rheumatoid Arthritis
|
disease |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases
|
Disease or Syndrome
|
2723
|
2387
|
0.030 |
None |
1.000 |
3 |
|
2004 |
2019 |
Coronary heart disease
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1576
|
1178
|
0.030 |
None |
1.000 |
3 |
|
2000 |
2008 |
Neonatal thrombocytopenia (disorder)
|
disease |
Hemic and Lymphatic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
15
|
2
|
0.030 |
None |
1.000 |
3 |
1
|
1994 |
2018 |
Hyperhomocysteinemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
246
|
45
|
0.030 |
None |
0.667 |
3 |
|
1999 |
2002 |
Middle Cerebral Artery Occlusion
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases
|
Acquired Abnormality
|
626
|
|
0.030 |
None |
1.000 |
3 |
|
2009 |
2018 |