C3, complement C3, 718

N. diseases: 343; N. variants: 49
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: C0033687
Disease: Proteinuria
Proteinuria
phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Finding 239 20 0.100 None 0
CUI: C0003460
Disease: Anuria
Anuria
phenotype Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 18 0.100 None 0
MACULAR DEGENERATION, AGE-RELATED, 9, SUSCEPTIBILITY TO
phenotype Finding 1 1 0.100 None 0 1
CUI: C1837512
Disease: Decreased serum complement C3
Decreased serum complement C3
phenotype Finding 12 0.100 None 0
CUI: C0700225
Disease: Serum creatinine raised
Serum creatinine raised
phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Finding 27 2 0.100 None 0
CUI: C0151539
Disease: Blood urea increased
Blood urea increased
phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Finding 12 0.100 None 0
CUI: C0221021
Disease: Microangiopathic hemolytic anemia
Microangiopathic hemolytic anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 31 0.100 None 0
CUI: C1844383
Disease: Recurrent bacterial infection
Recurrent bacterial infection
phenotype Infections Finding 69 0.100 None 0
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia
phenotype Hemic and Lymphatic Diseases Disease or Syndrome 592 110 0.100 None 0
CUI: C1332655
Disease: Complement component 3 deficiency
Complement component 3 deficiency
disease Disease or Syndrome 6 1 0.630 strong 1.000 15 1 1972 2013
COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases Disease or Syndrome 1 2 0.700 strong 1.000 5 2 1972 2016
CUI: C0272242
Disease: Complement deficiency disease
Complement deficiency disease
group Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 42 0.300 strong 1.000 1 1972 1972
CUI: C0027121
Disease: Myositis
Myositis
disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 254 43 0.010 None 1.000 1 1975 1975
CUI: C0024790
Disease: Paroxysmal nocturnal hemoglobinuria
Paroxysmal nocturnal hemoglobinuria
disease Hemic and Lymphatic Diseases Disease or Syndrome 132 12 0.030 None 0.667 3 1976 2017
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases Disease or Syndrome 852 704 0.010 None 1.000 1 1976 1976
CUI: C0030809
Disease: Pemphigus Vulgaris
Pemphigus Vulgaris
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 115 39 0.320 None 1.000 3 1977 2019
CUI: C0030807
Disease: Pemphigus
Pemphigus
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 67 3 0.310 None 1.000 2 1977 2019
CUI: C0263313
Disease: Pemphigus Foliaceus
Pemphigus Foliaceus
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 51 16 0.300 None 1.000 1 1977 1977
CUI: C0853888
Disease: Hypocomplementaemia
Hypocomplementaemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 14 1 0.020 None 1.000 2 1980 2018
CUI: C0262988
Disease: Vasculitis of the skin
Vasculitis of the skin
disease Skin and Connective Tissue Diseases; Cardiovascular Diseases Disease or Syndrome 21 1 0.020 None 1.000 2 1980 2017
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 1883 1172 0.200 None 0.897 29 3 1981 2020
CUI: C0024131
Disease: Lupus Vulgaris
Lupus Vulgaris
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 526 44 0.040 None 1.000 4 1982 2019
CUI: C0024138
Disease: Lupus Erythematosus, Discoid
Lupus Erythematosus, Discoid
disease Skin and Connective Tissue Diseases Disease or Syndrome 552 46 0.040 None 1.000 4 1982 2019
CUI: C0409974
Disease: Lupus Erythematosus
Lupus Erythematosus
disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 558 44 0.040 None 1.000 4 1982 2019
CUI: C0878521
Disease: Beta thalassemia trait
Beta thalassemia trait
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 34 5 0.010 None 1.000 1 1984 1984