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: C1142262
Disease: Intestinal edema
Intestinal edema 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 2 0.100 None 0
CUI: C0019243
Disease: Angioedemas, Hereditary
Angioedemas, Hereditary 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases Disease or Syndrome 54 7 0.600 strong 0.991 335 2 1971 2020
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 1883 1172 0.120 None 1.000 2 1985 2019
CUI: C0024143
Disease: Lupus Nephritis
Lupus Nephritis 		disease Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 503 64 0.300 None 1.000 1 1985 1985
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: C0018378
Disease: Guillain-Barre Syndrome
Guillain-Barre Syndrome 		disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 163 13 0.010 None 1.000 1 1985 1985
CUI: C0015230
Disease: Exanthema
Exanthema 		phenotype Skin and Connective Tissue Diseases Sign or Symptom 251 14 0.010 None 1.000 1 1986 1986
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: C2931758
Disease: Acquired angioedema
Acquired angioedema 		disease Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases Disease or Syndrome 4 0.400 None 1.000 16 1989 2019
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: C0272242
Disease: Complement deficiency disease
Complement deficiency disease 		group Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 42 0.320 strong 1.000 3 1989 2018
CUI: C0017658
Disease: Glomerulonephritis
Glomerulonephritis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 391 7 0.010 None 1.000 1 1989 1989
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		disease Digestive System Diseases; Neoplasms Neoplastic Process 5725 942 0.030 None 1.000 3 1990 2006
CUI: C0023903
Disease: Liver neoplasms
Liver neoplasms 		group Digestive System Diseases; Neoplasms Neoplastic Process 1424 7 0.020 None 1.000 2 1990 1994
CUI: C0853619
Disease: Localized swelling
Localized swelling 		phenotype Sign or Symptom 1 0.010 None 1.000 1 1990 1990
CUI: C0751753
Disease: Carbamoyl-Phosphate Synthase I Deficiency Disease
Carbamoyl-Phosphate Synthase I Deficiency Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 18 0.020 None 1.000 2 1991 2020
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: 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: C0017638
Disease: Glioma
Glioma 		disease Neoplasms Neoplastic Process 3097 353 0.010 None 1.000 1 1993 1993
CUI: C0041834
Disease: Erythema
Erythema 		phenotype Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 227 8 0.110 None 1.000 1 1993 1993
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 302 18 0.150 None 1.000 5 1 1995 2015
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		group Infections Disease or Syndrome 1471 42 0.020 None 0.500 2 1995 2010
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		disease Digestive System Diseases; Infections Disease or Syndrome 1768 347 0.010 None 1.000 1 1995 1995
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: C0042109
Disease: Urticaria
Urticaria 		disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 168 11 0.050 None 1.000 5 1996 2019