C5, complement C5, 727

N. diseases: 129; N. variants: 20
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: C0086438
Disease: Hypogammaglobulinemia
Hypogammaglobulinemia
disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 76 2 0.010 None 1.000 1 1977 1977
CUI: C2347126
Disease: Microscopic Polyarteritis
Microscopic Polyarteritis
disease Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 77 7 0.010 None 1.000 1 2019 2019
CUI: C2745963
Disease: Kashin-Beck Disease
Kashin-Beck Disease
disease Musculoskeletal Diseases Disease or Syndrome 77 43 0.010 None 1.000 1 2015 2015
CUI: C3887638
Disease: Failure to thrive in infant
Failure to thrive in infant
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 81 4 0.010 None 1.000 1 1977 1977
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization
disease Disease or Syndrome 85 26 0.010 None 1.000 1 2007 2007
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis
disease Immune System Diseases; Cardiovascular Diseases Disease or Syndrome 86 3 0.030 None 1.000 3 2015 2018
CUI: C0025295
Disease: Meningitis, Pneumococcal
Meningitis, Pneumococcal
disease Infections; Nervous System Diseases Disease or Syndrome 88 13 0.010 None 1.000 1 2011 2011
CUI: C0701807
Disease: Acute anterior uveitis
Acute anterior uveitis
disease Eye Diseases Disease or Syndrome 90 30 0.010 None 1.000 1 1 2015 2015
CUI: C3887898
Disease: Infantile Spasm
Infantile Spasm
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 93 39 0.010 None 1.000 1 2018 2018
CUI: C0035439
Disease: Rheumatic Heart Disease
Rheumatic Heart Disease
disease Infections; Cardiovascular Diseases Disease or Syndrome 102 33 0.010 None < 0.001 1 2009 2009
CUI: C3495801
Disease: Granulomatosis with polyangiitis
Granulomatosis with polyangiitis
disease Respiratory Tract Diseases; Immune System Diseases; Cardiovascular Diseases Disease or Syndrome 126 18 0.010 None 1.000 1 2019 2019
CUI: C4554344
Disease: IgE-mediated food allergy
IgE-mediated food allergy
disease Immune System Diseases Disease or Syndrome 126 16 0.010 None 1.000 1 2019 2019
CUI: C0239998
Disease: Recurrent infections
Recurrent infections
phenotype Pathological Conditions, Signs and Symptoms; Infections; Musculoskeletal Diseases Finding 127 14 0.100 None 0
CUI: C0021359
Disease: Infertility
Infertility
phenotype Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Pathologic Function 130 5 0.010 None 1.000 1 2007 2007
CUI: C0024790
Disease: Paroxysmal nocturnal hemoglobinuria
Paroxysmal nocturnal hemoglobinuria
disease Hemic and Lymphatic Diseases Disease or Syndrome 132 12 0.010 None 1.000 1 2019 2019
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 133 82 0.020 None 1.000 2 1 2010 2012
CUI: C0017205
Disease: Gaucher Disease
Gaucher Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 143 82 0.020 None 1.000 2 2017 2018
CUI: C0037769
Disease: West Syndrome
West Syndrome
disease Nervous System Diseases Disease or Syndrome 149 28 0.010 None 1.000 1 2018 2018
CUI: C0085409
Disease: Polyendocrinopathies, Autoimmune
Polyendocrinopathies, Autoimmune
group Immune System Diseases; Endocrine System Diseases Disease or Syndrome 166 21 0.010 None 1.000 1 2017 2017
CUI: C2315100
Disease: Pediatric failure to thrive
Pediatric failure to thrive
disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Mental Disorders Disease or Syndrome 166 122 0.010 None 1.000 1 1977 1977
CUI: C0154830
Disease: Proliferative diabetic retinopathy
Proliferative diabetic retinopathy
disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases Disease or Syndrome 180 45 0.010 None 1.000 1 2016 2016
Malformations of Cortical Development, Group II
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 180 101 0.010 None 1.000 1 2017 2017
CUI: C0016059
Disease: Fibrosis
Fibrosis
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 184 0.010 None 1.000 1 2008 2008
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome 206 2356 0.010 None 1.000 1 2017 2017
CUI: C0027055
Disease: Myocardial Reperfusion Injury
Myocardial Reperfusion Injury
phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 226 0.200 None 1.000 2 1998 2012