FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
7
|
|
0.400 |
None |
1.000 |
15 |
|
1998 |
2019 |
Familial Multiple Coagulation Factor Deficiency I
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
2
|
6
|
0.700 |
definitive |
1.000 |
9 |
5
|
1998 |
2011 |
Blood Coagulation Disorders
|
group |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
267
|
31
|
0.080 |
None |
1.000 |
8 |
|
1999 |
2013 |
Familial multiple factor deficiency syndrome, type I
|
disease |
|
Disease or Syndrome
|
4
|
|
0.040 |
None |
1.000 |
4 |
|
2004 |
2011 |
Hemophilia A
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
143
|
295
|
0.030 |
None |
1.000 |
3 |
|
1999 |
2008 |
Factor VIII Deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
9
|
1
|
0.030 |
None |
1.000 |
3 |
|
1999 |
2008 |
Coagulation factor deficiency syndrome
|
group |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
13
|
2
|
0.020 |
None |
1.000 |
2 |
|
2004 |
2012 |
Deficiency of factor V [labile]
|
disease |
|
Disease or Syndrome
|
3
|
|
0.020 |
None |
0.500 |
2 |
|
2005 |
2011 |
Coronary Arteriosclerosis
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1282
|
440
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Coronary heart disease
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1576
|
1178
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
IGA Glomerulonephritis
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases
|
Disease or Syndrome
|
456
|
130
|
0.010 |
None |
1.000 |
1 |
|
1997 |
1997 |
Hematological Disease
|
group |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
255
|
16
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Malaria
|
disease |
Infections
|
Disease or Syndrome
|
685
|
148
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Vitamin K Deficiency
|
disease |
Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
19
|
2
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Thanatophoric dysplasia, type 2
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
11
|
17
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |
Congenital dyserythropoietic anemia, type II
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
21
|
14
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
6
|
4
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Coronary Artery Disease
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1708
|
1577
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Factor V deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
6
|
1
|
0.100 |
None |
|
0 |
|
|
|
Reduced factor VIII activity
|
phenotype |
|
Finding
|
4
|
1
|
0.100 |
None |
|
0 |
|
|
|
Cardiac troponin I measurement
|
phenotype |
|
Laboratory Procedure
|
11
|
14
|
0.100 |
None |
1.000 |
1 |
1
|
2019 |
2019 |
Adenoma
|
group |
Neoplasms
|
Neoplastic Process
|
1183
|
103
|
0.010 |
None |
1.000 |
1 |
|
2009 |
2009 |
Carcinoma
|
group |
Neoplasms
|
Neoplastic Process
|
2462
|
103
|
0.010 |
None |
1.000 |
1 |
|
2009 |
2009 |
Colorectal Neoplasms
|
group |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
1296
|
609
|
0.010 |
None |
1.000 |
1 |
|
2009 |
2009 |
Neoplasms
|
group |
Neoplasms
|
Neoplastic Process
|
10161
|
1644
|
0.010 |
None |
1.000 |
1 |
|
2009 |
2009 |