Membranous conjunctivitis
|
disease |
Infections; Eye Diseases
|
Disease or Syndrome
|
1
|
|
0.020 |
None |
1.000 |
2 |
|
2002 |
2019 |
Axillary vein thrombosis
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
1988 |
1988 |
Streptococcal infection of skin
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Decreased level of plasminogen
|
phenotype |
|
Finding
|
1
|
|
0.400 |
strong |
|
0 |
|
|
|
Ligneous conjunctivitis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
2
|
1
|
0.600 |
None |
1.000 |
16 |
1
|
1997 |
2019 |
Leukocyte Disorders
|
group |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
2
|
|
0.300 |
None |
1.000 |
1 |
|
2018 |
2018 |
Streptococcal impetigo
|
disease |
Infections
|
Disease or Syndrome
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Fibrinolytic disorder
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
1984 |
1984 |
Invasive Group A beta-hemolytic streptococcal disease
|
disease |
Infections
|
Disease or Syndrome
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Chronic irritative conjunctivitis
|
disease |
Eye Diseases
|
Disease or Syndrome
|
2
|
|
0.100 |
None |
|
0 |
|
|
|
Plasminogen Deficiency, Type I
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
3
|
13
|
0.800 |
definitive |
1.000 |
28 |
12
|
1982 |
2019 |
Dirofilariasis
|
disease |
Infections; Animal Diseases
|
Disease or Syndrome
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Placentitis (disorder)
|
phenotype |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Infections
|
Disease or Syndrome
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Stroke of undetermined etiology
|
disease |
|
Disease or Syndrome
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Abnormality of fontanelles
|
disease |
|
Anatomical Abnormality
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Fibrin thrombus
|
disease |
Cardiovascular Diseases
|
Acquired Abnormality
|
4
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Hereditary angioedema with normal C1 inhibitor
|
disease |
|
Disease or Syndrome
|
4
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Pleural effusion associated with pulmonary infection
|
disease |
Respiratory Tract Diseases
|
Disease or Syndrome
|
5
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Abnormality of the middle ear
|
phenotype |
|
Finding
|
5
|
|
0.100 |
None |
|
0 |
|
|
|
PAI-1 4G/5G polymorphism
|
disease |
|
Disease or Syndrome
|
6
|
3
|
0.020 |
None |
1.000 |
2 |
|
2011 |
2016 |
Tick-borne relapsing fever
|
disease |
Infections
|
Disease or Syndrome
|
6
|
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |
Livedo Reticularis
|
disease |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
6
|
|
0.010 |
None |
1.000 |
1 |
|
1983 |
1983 |
Dysfibrinogenemia, Congenital
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
6
|
8
|
0.010 |
None |
1.000 |
1 |
|
1988 |
1988 |
Secondary antiphospholipid syndrome
|
disease |
Immune System Diseases
|
Disease or Syndrome
|
6
|
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Temporal Arteritis
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
6
|
6
|
0.100 |
None |
1.000 |
1 |
1
|
2017 |
2017 |