Bleeding Disorder Due To P2RY12 Defect
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
2
|
4
|
0.800 |
None |
1.000 |
5 |
4
|
2001 |
2015 |
Thrombosis
|
phenotype |
Cardiovascular Diseases
|
Pathologic Function
|
98
|
|
0.500 |
None |
1.000 |
2 |
|
2007 |
2009 |
Myocardial Infarction
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
1800
|
680
|
0.400 |
None |
0.895 |
19 |
3
|
2008 |
2020 |
Lupus Erythematosus, Systemic
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases
|
Disease or Syndrome
|
1883
|
1172
|
0.310 |
None |
1.000 |
1 |
|
2004 |
2004 |
Hemorrhage
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Pathologic Function
|
47
|
|
0.300 |
None |
1.000 |
1 |
|
2001 |
2001 |
Libman-Sacks Disease
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases
|
Disease or Syndrome
|
59
|
|
0.300 |
None |
1.000 |
1 |
|
2004 |
2004 |
Thrombus
|
phenotype |
Cardiovascular Diseases
|
Pathologic Function
|
46
|
|
0.300 |
None |
1.000 |
1 |
|
2007 |
2007 |
Neuralgia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
767
|
16
|
0.240 |
None |
1.000 |
5 |
|
2010 |
2019 |
Hereditary vascular fragility
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
|
0.200 |
None |
1.000 |
2 |
|
2001 |
2003 |
Other specified hemorrhagic conditions
|
phenotype |
Hemic and Lymphatic Diseases
|
Pathologic Function
|
1
|
|
0.200 |
None |
1.000 |
2 |
|
2001 |
2003 |
von Willebrand Disease
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
62
|
78
|
0.200 |
None |
1.000 |
2 |
|
2001 |
2003 |
Aortic Aneurysm, Abdominal
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
586
|
90
|
0.200 |
None |
1.000 |
1 |
|
2009 |
2009 |
Acute Lung Injury
|
disease |
Respiratory Tract Diseases
|
Injury or Poisoning
|
93
|
3
|
0.200 |
None |
1.000 |
1 |
|
2011 |
2011 |
Hyperalgesia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
451
|
4
|
0.200 |
None |
1.000 |
1 |
|
2010 |
2010 |
Acute Coronary Syndrome
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
440
|
139
|
0.100 |
None |
0.970 |
66 |
|
2012 |
2020 |
Acute Chest Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
405
|
135
|
0.100 |
None |
1.000 |
49 |
1
|
2012 |
2020 |
Coronary Artery Disease
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1708
|
1577
|
0.100 |
None |
1.000 |
26 |
|
2005 |
2020 |
Coronary heart disease
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1576
|
1178
|
0.100 |
None |
1.000 |
24 |
3
|
2005 |
2020 |
ST segment elevation myocardial infarction
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
264
|
16
|
0.100 |
None |
0.909 |
22 |
|
2017 |
2019 |
Coronary Arteriosclerosis
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1282
|
440
|
0.100 |
None |
1.000 |
21 |
|
2005 |
2020 |
Acute myocardial infarction
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
766
|
118
|
0.100 |
None |
1.000 |
13 |
|
2010 |
2020 |
Impaired ADP-induced platelet aggregation
|
phenotype |
|
Finding
|
3
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Epistaxis
|
phenotype |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
|
Pathologic Function
|
82
|
4
|
0.100 |
None |
|
0 |
|
|
|
Ecchymosis
|
phenotype |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases
|
Pathologic Function
|
41
|
2
|
0.100 |
None |
|
0 |
|
|
|
Persistent bleeding after trauma
|
phenotype |
|
Finding
|
9
|
|
0.100 |
None |
|
0 |
|
|
|