Pulmonary Embolism
|
disease |
Respiratory Tract Diseases; Cardiovascular Diseases
|
Pathologic Function
|
93
|
16
|
0.100 |
None |
|
0 |
|
|
|
Recurrent thrombophlebitis
|
phenotype |
Cardiovascular Diseases
|
Finding
|
5
|
|
0.100 |
None |
|
0 |
|
|
|
Recurrent spontaneous abortion
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications
|
Finding
|
7
|
|
0.100 |
None |
|
0 |
|
|
|
Arterial thrombosis
|
phenotype |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Pathologic Function
|
33
|
1
|
0.100 |
None |
|
0 |
|
|
|
Recurrent thromboembolism
|
phenotype |
Cardiovascular Diseases
|
Finding
|
2
|
|
0.100 |
None |
|
0 |
|
|
|
Mesenteric Venous Thrombosis
|
phenotype |
Digestive System Diseases; Cardiovascular Diseases
|
Pathologic Function
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Occlusion of artery (disorder)
|
phenotype |
|
Pathologic Function
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Retinal Vein Occlusion
|
disease |
Eye Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
76
|
15
|
0.100 |
None |
|
0 |
|
|
|
Superficial Thrombophlebitis, CTCAE
|
phenotype |
|
Finding
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Portal Vein Thrombosis, CTCAE
|
phenotype |
|
Finding
|
7
|
|
0.100 |
None |
|
0 |
|
|
|
Superficial Thrombophlebitis
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
5
|
|
0.100 |
None |
|
0 |
|
|
|
Reduced antithrombin antigen
|
phenotype |
|
Finding
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
Recurrent cerebral infarction
|
disease |
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
< 0.001 |
1 |
|
1993 |
1993 |
Legg-Calve-Perthes Disease
|
disease |
Musculoskeletal Diseases
|
Disease or Syndrome
|
36
|
9
|
0.010 |
None |
< 0.001 |
1 |
|
2002 |
2002 |
Sudden sensorineural hearing loss
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
72
|
38
|
0.010 |
None |
< 0.001 |
1 |
|
2006 |
2006 |
Homocystinuria
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases
|
Disease or Syndrome
|
39
|
27
|
0.020 |
None |
0.500 |
2 |
|
1986 |
1994 |
Hypoplasminogenemia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
9
|
3
|
0.020 |
None |
0.500 |
2 |
|
1995 |
1996 |
Factor V Leiden mutation
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
86
|
46
|
0.090 |
None |
0.889 |
9 |
|
1997 |
2016 |
Antithrombin III Deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
27
|
52
|
1.000 |
strong |
0.987 |
75 |
44
|
1984 |
2019 |
Deep Vein Thrombosis
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
230
|
93
|
0.500 |
None |
1.000 |
15 |
4
|
1976 |
2019 |
Venous Thromboembolism
|
phenotype |
Cardiovascular Diseases
|
Disease or Syndrome
|
378
|
408
|
0.400 |
None |
1.000 |
13 |
1
|
1979 |
2019 |
Thrombophilia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
161
|
43
|
0.100 |
None |
1.000 |
13 |
|
1992 |
2017 |
Activated Protein C Resistance
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
41
|
30
|
0.100 |
None |
1.000 |
12 |
|
1996 |
2015 |
Lupus anticoagulant disorder
|
disease |
Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
66
|
14
|
0.090 |
None |
1.000 |
9 |
|
1994 |
2012 |
Protein S Deficiency
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
19
|
14
|
0.070 |
None |
1.000 |
7 |
|
1988 |
2012 |