Spontaneous abortion
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications
|
Pathologic Function
|
188
|
|
0.100 |
None |
|
0 |
|
|
|
Joint swelling
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Finding
|
33
|
|
0.100 |
None |
|
0 |
|
|
|
Intermenstrual heavy bleeding
|
phenotype |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications
|
Sign or Symptom
|
10
|
1
|
0.100 |
None |
|
0 |
|
|
|
Gingival Hemorrhage
|
phenotype |
Pathological Conditions, Signs and Symptoms; Stomatognathic Diseases
|
Pathologic Function
|
50
|
2
|
0.100 |
None |
|
0 |
|
|
|
Gastrointestinal Hemorrhage
|
phenotype |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
|
Pathologic Function
|
122
|
24
|
0.100 |
None |
|
0 |
|
|
|
Epistaxis
|
phenotype |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
|
Pathologic Function
|
82
|
4
|
0.100 |
None |
|
0 |
|
|
|
Cerebral Hemorrhage
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases
|
Pathologic Function
|
122
|
78
|
0.100 |
None |
|
0 |
|
|
|
Complement Factor I (C3 inactivator) deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases
|
Disease or Syndrome
|
6
|
12
|
0.100 |
None |
|
0 |
3
|
|
|
FIBRINOGEN MILANO XII, DIGENIC PHENOTYPE
|
disease |
|
Finding
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Peripheral Arterial Diseases
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
319
|
128
|
0.010 |
None |
< 0.001 |
1 |
|
2010 |
2010 |
Arteriosclerosis
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
2006
|
267
|
0.020 |
None |
0.500 |
2 |
|
2007 |
2008 |
Atherosclerosis
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
2044
|
281
|
0.020 |
None |
0.500 |
2 |
|
2007 |
2008 |
Myocardial Infarction
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
1800
|
680
|
0.030 |
None |
0.667 |
3 |
2
|
2008 |
2010 |
Cerebrovascular accident
|
group |
Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
1658
|
591
|
0.040 |
None |
0.750 |
4 |
|
2008 |
2008 |
Hypofibrinogenemia
|
disease |
|
Disease or Syndrome
|
60
|
14
|
0.190 |
None |
1.000 |
10 |
4
|
2005 |
2019 |
Fibrinogen Deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
56
|
4
|
0.700 |
strong |
1.000 |
10 |
1
|
2005 |
2018 |
Congenital hypofibrinogenemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
6
|
10
|
0.740 |
strong |
1.000 |
9 |
3
|
2000 |
2018 |
Venous Thromboembolism
|
phenotype |
Cardiovascular Diseases
|
Disease or Syndrome
|
378
|
408
|
0.160 |
None |
1.000 |
8 |
3
|
2011 |
2019 |
Dysfibrinogenemia, Congenital
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
6
|
8
|
0.610 |
strong |
1.000 |
7 |
5
|
1986 |
2018 |
Dysfibrinogenemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
13
|
6
|
0.060 |
None |
1.000 |
6 |
1
|
2000 |
2017 |
Afibrinogenemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
9
|
|
0.530 |
None |
1.000 |
5 |
|
2000 |
2004 |
Hypodysfibrinogenemia
|
disease |
|
Disease or Syndrome
|
8
|
1
|
0.440 |
strong |
1.000 |
4 |
1
|
2015 |
2019 |
Cardiovascular Diseases
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
1756
|
711
|
0.030 |
None |
1.000 |
3 |
|
2008 |
2012 |
Ischemic stroke
|
disease |
Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
1159
|
704
|
0.020 |
None |
1.000 |
2 |
|
2008 |
2008 |
Deep Vein Thrombosis
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
230
|
93
|
0.020 |
None |
1.000 |
2 |
1
|
2007 |
2010 |