THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
|
disease |
|
Disease or Syndrome
|
1
|
38
|
0.600 |
strong |
1.000 |
35 |
38
|
1994 |
2016 |
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE
|
disease |
|
Disease or Syndrome
|
1
|
6
|
0.600 |
strong |
1.000 |
5 |
6
|
1995 |
2012 |
Homozygous protein S deficiency
|
disease |
|
Disease or Syndrome
|
1
|
1
|
0.020 |
None |
1.000 |
2 |
1
|
1994 |
2010 |
Acquired purpura fulminans
|
phenotype |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
1993 |
1993 |
Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Recessive
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
1
|
|
0.300 |
None |
|
0 |
|
|
|
Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Dominant
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
1
|
|
0.300 |
None |
|
0 |
|
|
|
PROTEIN S HEERLEN PHENOTYPE
|
phenotype |
|
Finding
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Hereditary protein S deficiency
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
2
|
|
0.080 |
None |
1.000 |
8 |
|
1995 |
2016 |
Superior mesenteric vein thrombosis
|
disease |
Digestive System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Recurrent pulmonary embolism
|
disease |
Respiratory Tract Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Congenital thrombotic disease, due to Protein C deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
2
|
1
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |
Reduced protein S activity
|
phenotype |
|
Finding
|
2
|
3
|
0.100 |
None |
1.000 |
1 |
3
|
2019 |
2019 |
Warfarin-induced skin necrosis
|
phenotype |
|
Finding
|
2
|
|
0.100 |
None |
|
0 |
|
|
|
Congenital thrombophilia
|
disease |
|
Disease or Syndrome
|
3
|
1
|
0.020 |
None |
1.000 |
2 |
|
2005 |
2011 |
Septic Phlebitis, Sagittal Sinus
|
disease |
Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
3
|
|
0.300 |
None |
1.000 |
1 |
|
2008 |
2008 |
Sagittal Sinus Thrombophlebitis
|
disease |
Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
3
|
|
0.300 |
None |
1.000 |
1 |
|
2008 |
2008 |
Hereditary Antithrombin Deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
1994 |
1994 |
Thrombophlebitis
|
disease |
Cardiovascular Diseases
|
Pathologic Function
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Superficial Thrombophlebitis, CTCAE
|
phenotype |
|
Finding
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Acquired Protein S Deficiency
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
4
|
|
0.020 |
None |
0.500 |
2 |
|
2010 |
2013 |
Sagittal Sinus Thrombosis
|
disease |
Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
5
|
1
|
0.300 |
None |
1.000 |
1 |
|
2008 |
2008 |
Superficial Thrombophlebitis
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
5
|
|
0.110 |
None |
1.000 |
1 |
|
1996 |
1996 |
EAR WAX, WET/DRY
|
disease |
|
Disease or Syndrome
|
6
|
1
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Disorder of soft tissue
|
group |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
|
Disease or Syndrome
|
7
|
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Inguinal pain
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
8
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |