Hereditary Factor XIII Deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
10
|
4
|
0.980 |
strong |
1.000 |
14 |
4
|
1992 |
2019 |
Factor Xiii, A Subunit, Deficiency Of
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Finding
|
1
|
28
|
0.700 |
strong |
1.000 |
11 |
28
|
1992 |
2017 |
Deep Vein Thrombosis
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
230
|
93
|
0.410 |
None |
1.000 |
2 |
1
|
1999 |
2002 |
Myocardial Infarction
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
1800
|
680
|
0.380 |
None |
1.000 |
9 |
3
|
2002 |
2019 |
Venous Thrombosis
|
phenotype |
Cardiovascular Diseases
|
Pathologic Function
|
117
|
218
|
0.320 |
None |
1.000 |
3 |
|
1999 |
2008 |
Thrombophilia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
161
|
43
|
0.310 |
None |
1.000 |
1 |
1
|
2019 |
2019 |
Dermatitis, Allergic Contact
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases
|
Disease or Syndrome
|
151
|
1
|
0.300 |
None |
1.000 |
1 |
|
2007 |
2007 |
THROMBOPHILIA DUE TO THROMBIN DEFECT
|
phenotype |
|
Finding
|
4
|
2
|
0.300 |
None |
|
0 |
|
|
|
MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO
|
phenotype |
|
Finding
|
9
|
3
|
0.300 |
None |
|
0 |
|
|
|
Gastric ulcer
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
136
|
7
|
0.200 |
None |
1.000 |
1 |
|
2001 |
2001 |
Alzheimer's Disease
|
disease |
Nervous System Diseases; Mental Disorders
|
Disease or Syndrome
|
3397
|
1843
|
0.140 |
None |
1.000 |
6 |
2
|
1998 |
2019 |
Pulmonary Embolism
|
disease |
Respiratory Tract Diseases; Cardiovascular Diseases
|
Pathologic Function
|
93
|
16
|
0.120 |
None |
1.000 |
2 |
|
2003 |
2003 |
Malignant neoplasm of prostate
|
disease |
Neoplasms; Male Urogenital Diseases
|
Neoplastic Process
|
4502
|
1082
|
0.120 |
None |
1.000 |
2 |
1
|
1996 |
2013 |
Coagulation factor measurement
|
phenotype |
|
Laboratory Procedure
|
14
|
26
|
0.100 |
None |
1.000 |
1 |
2
|
2013 |
2013 |
von Willebrand's factor (lab test)
|
phenotype |
|
Laboratory Procedure
|
55
|
427
|
0.100 |
None |
1.000 |
1 |
34
|
2013 |
2013 |
Antibody measurement (procedure)
|
group |
|
Laboratory Procedure
|
5
|
8
|
0.100 |
None |
1.000 |
1 |
1
|
2013 |
2013 |
Hematoma of cord
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Injury or Poisoning
|
2
|
|
0.100 |
None |
|
0 |
|
|
|
Inflammation of large intestine
|
phenotype |
Digestive System Diseases
|
Disease or Syndrome
|
12
|
1
|
0.100 |
None |
|
0 |
|
|
|
Increased tendency to bruise
|
phenotype |
Wounds and Injuries
|
Finding
|
133
|
14
|
0.100 |
None |
|
0 |
|
|
|
Thromboembolism
|
phenotype |
Cardiovascular Diseases
|
Pathologic Function
|
25
|
3
|
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 |
|
|
|
Prolonged bleeding after dental extraction
|
phenotype |
|
Pathologic Function
|
8
|
|
0.100 |
None |
|
0 |
|
|
|
Liver Failure
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
293
|
20
|
0.100 |
None |
|
0 |
|
|
|
Intracranial Hemorrhage
|
group |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases
|
Pathologic Function
|
40
|
2
|
0.100 |
None |
|
0 |
|
|
|
Thrombosis of cerebral veins
|
disease |
Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
35
|
11
|
0.100 |
None |
|
0 |
|
|
|