Embolism, Amniotic Fluid
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Erythema marginatum
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infections; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Clinical Capillary Leak Syndrome
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2020 |
2020 |
Hereditary C1 esterase inhibitor deficiency - deficient factor
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
|
0.300 |
None |
1.000 |
1 |
|
2014 |
2014 |
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
5
|
0.400 |
None |
1.000 |
1 |
5
|
2014 |
2014 |
Swallowing symptoms
|
phenotype |
|
Sign or Symptom
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Localized swelling
|
phenotype |
|
Sign or Symptom
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
1990 |
1990 |
Complement Component 4, Partial Deficiency Of
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases
|
Disease or Syndrome
|
1
|
|
0.600 |
strong |
1.000 |
1 |
|
1995 |
1995 |
Laryngeal Edema
|
phenotype |
Respiratory Tract Diseases; Otorhinolaryngologic Diseases
|
Pathologic Function
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
Edema of the tongue
|
phenotype |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Skin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases; Stomatognathic Diseases; Cardiovascular Diseases
|
Pathologic Function
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
COMPLEMENT COMPONENT 4, PARTIAL DEFICIENCY OF, DUE TO DYSFUNCTIONAL C1 INHIBITOR
|
disease |
|
Finding
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Limbal edema
|
phenotype |
|
Pathologic Function
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
Hereditary Angioedema Type I
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
2
|
35
|
0.730 |
strong |
0.958 |
24 |
35
|
1988 |
2018 |
Acquired C1 inhibitor deficiency
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
2
|
|
0.080 |
None |
1.000 |
8 |
|
1989 |
2019 |
Hereditary Angioedema Type II
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
2
|
|
0.500 |
None |
1.000 |
4 |
|
1992 |
2014 |
Idiopathic angioedema
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
2
|
|
0.030 |
None |
1.000 |
3 |
|
2009 |
2013 |
Hereditary Angioedema Types I and II
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
2
|
|
0.300 |
None |
1.000 |
3 |
|
1992 |
2009 |
Acute edema
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
2
|
|
0.020 |
None |
1.000 |
2 |
|
2010 |
2010 |
Edema of pharynx
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Immune System Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases; Cardiovascular Diseases
|
Pathologic Function
|
2
|
|
0.100 |
None |
|
0 |
|
|
|
Intestinal edema
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Pathologic Function
|
2
|
|
0.100 |
None |
|
0 |
|
|
|
Abnormal epiglottis morphology
|
phenotype |
|
Anatomical Abnormality
|
2
|
1
|
0.100 |
None |
|
0 |
|
|
|
Abnormality of the uvula
|
phenotype |
|
Anatomical Abnormality
|
2
|
2
|
0.100 |
None |
|
0 |
|
|
|
SLE-like symptoms
|
phenotype |
Skin and Connective Tissue Diseases
|
Sign or Symptom
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
1985 |
1985 |
Allergy to fish
|
phenotype |
|
Disease or Syndrome
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Abnormality of salivation
|
phenotype |
|
Finding
|
3
|
1
|
0.100 |
None |
|
0 |
|
|
|