Bernard-Soulier Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
46
|
23
|
0.800 |
definitive |
0.981 |
52 |
6
|
1983 |
2019 |
Immune thrombocytopenic purpura
|
disease |
Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
338
|
35
|
0.030 |
None |
1.000 |
3 |
|
1998 |
2020 |
Autoimmune thrombocytopenia
|
disease |
Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
115
|
7
|
0.020 |
None |
1.000 |
2 |
|
1998 |
2020 |
Thrombocytopenia due to platelet alloimmunization
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
111
|
7
|
0.020 |
None |
1.000 |
2 |
|
1998 |
2020 |
Myelolipoma
|
disease |
Neoplasms
|
Neoplastic Process
|
16
|
1
|
0.010 |
None |
1.000 |
1 |
|
2006 |
2006 |
Neonatal thrombocytopenia (disorder)
|
disease |
Hemic and Lymphatic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
15
|
2
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Drug-induced immune thrombocytopenia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Barber Say syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Stomatognathic Diseases
|
Disease or Syndrome
|
21
|
4
|
0.300 |
strong |
1.000 |
1 |
|
2011 |
2011 |
Prehypertension
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
41
|
5
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
SEBASTIAN SYNDROME
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
42
|
13
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Bernard-Soulier Syndrome, Type C
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
1
|
6
|
0.410 |
strong |
1.000 |
1 |
6
|
2019 |
2019 |
Brooke-Spiegler syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
45
|
8
|
0.300 |
strong |
1.000 |
1 |
|
2011 |
2011 |
Childhood Myelodysplastic Syndrome
|
disease |
Hemic and Lymphatic Diseases
|
Neoplastic Process
|
335
|
20
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Macrothrombocytopenia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
34
|
31
|
0.100 |
None |
1.000 |
1 |
3
|
2019 |
2019 |
Neonatal Alloimmune Thrombocytopenia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
29
|
1
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Adult Myelodysplastic Syndrome
|
disease |
Hemic and Lymphatic Diseases
|
Neoplastic Process
|
332
|
20
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Asthma
|
disease |
Respiratory Tract Diseases; Immune System Diseases
|
Disease or Syndrome
|
2096
|
1536
|
0.100 |
None |
|
0 |
|
|
|
Purpura
|
disease |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
68
|
1
|
0.100 |
None |
|
0 |
|
|
|
Spontaneous hematomas
|
disease |
|
Disease or Syndrome
|
33
|
|
0.100 |
None |
|
0 |
|
|
|
Deficiency of Platelet Glycoprotein 1b
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
3
|
|
0.300 |
None |
|
0 |
|
|
|
Abnormal megakaryocyte morphology
|
disease |
|
Finding
|
10
|
|
0.100 |
None |
|
0 |
|
|
|
Thrombocytopenia
|
phenotype |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
592
|
110
|
0.460 |
None |
1.000 |
8 |
2
|
1998 |
2020 |
Carcinogenesis
|
phenotype |
Pathological Conditions, Signs and Symptoms; Neoplasms
|
Neoplastic Process
|
6243
|
355
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
Epistaxis
|
phenotype |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
|
Pathologic Function
|
82
|
4
|
0.100 |
None |
|
0 |
|
|
|
Gastrointestinal Hemorrhage
|
phenotype |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
|
Pathologic Function
|
122
|
24
|
0.100 |
None |
|
0 |
|
|
|