SERPING1, serpin family G member 1, 710

N. diseases: 207; N. variants: 43
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0013927
Disease: Embolism, Amniotic Fluid
Embolism, Amniotic Fluid 		disease Female Urogenital Diseases and Pregnancy Complications; Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C0085659
Disease: Erythema marginatum
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
CUI: C0376704
Disease: Clinical Capillary Leak Syndrome
Clinical Capillary Leak Syndrome 		disease Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2020 2020
CUI: C0398775
Disease: Hereditary C1 esterase inhibitor deficiency - deficient factor
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
CUI: C0398776
Disease: Hereditary C1 esterase inhibitor deficiency - dysfunctional factor
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
CUI: C0426601
Disease: Swallowing symptoms
Swallowing symptoms 		phenotype Sign or Symptom 1 0.010 None 1.000 1 2017 2017
CUI: C0853619
Disease: Localized swelling
Localized swelling 		phenotype Sign or Symptom 1 0.010 None 1.000 1 1990 1990
CUI: C1852700
Disease: Complement Component 4, Partial Deficiency Of
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
CUI: C0023052
Disease: Laryngeal Edema
Laryngeal Edema 		phenotype Respiratory Tract Diseases; Otorhinolaryngologic Diseases Pathologic Function 1 0.100 None 0
CUI: C0151610
Disease: Edema of the tongue
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
CUI: C4016986
Disease: COMPLEMENT COMPONENT 4, PARTIAL DEFICIENCY OF, DUE TO DYSFUNCTIONAL C1 INHIBITOR
COMPLEMENT COMPONENT 4, PARTIAL DEFICIENCY OF, DUE TO DYSFUNCTIONAL C1 INHIBITOR 		disease Finding 1 1 0.100 None 0 1
CUI: C4476719
Disease: Limbal edema
Limbal edema 		phenotype Pathologic Function 1 0.100 None 0
CUI: C2717906
Disease: Hereditary Angioedema Type I
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
CUI: C3506079
Disease: Acquired C1 inhibitor deficiency
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
CUI: C1862892
Disease: Hereditary Angioedema Type II
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
CUI: C1304177
Disease: Idiopathic angioedema
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
CUI: C2717905
Disease: Hereditary Angioedema Types I and II
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
CUI: C0333240
Disease: Acute edema
Acute edema 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 2 0.020 None 1.000 2 2010 2010
CUI: C0236024
Disease: Edema of pharynx
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
CUI: C1142262
Disease: Intestinal edema
Intestinal edema 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 2 0.100 None 0
CUI: C4025190
Disease: Abnormal epiglottis morphology
Abnormal epiglottis morphology 		phenotype Anatomical Abnormality 2 1 0.100 None 0
CUI: C4025885
Disease: Abnormality of the uvula
Abnormality of the uvula 		phenotype Anatomical Abnormality 2 2 0.100 None 0
CUI: C0236116
Disease: SLE-like symptoms
SLE-like symptoms 		phenotype Skin and Connective Tissue Diseases Sign or Symptom 3 0.010 None 1.000 1 1985 1985
CUI: C0856904
Disease: Allergy to fish
Allergy to fish 		phenotype Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C4021978
Disease: Abnormality of salivation
Abnormality of salivation 		phenotype Finding 3 1 0.100 None 0