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Results 1 - 9 of 9 for C3 deficiency
  1. C3 gene 
    ... the C3 gene have been found to cause C3 deficiency, a rare condition characterized by recurrent bacterial infections beginning in childhood. The genetic changes that cause C3 deficiency lead to an altered version of the C3 ...
    https://medlineplus.gov/genetics/gene/c3 - Genetics
  2. Complement factor I deficiency 
    ... not show signs and symptoms of the condition. C3 inactivator deficiency Complement component 3 inactivator deficiency Hereditary factor I ...
    https://medlineplus.gov/.../condition/complement-factor-i-deficiency - Genetics
  3. C3 glomerulopathy 
    ... Rare Disorders (NORD) ClinicalTrials.gov COMPLEMENT FACTOR H DEFICIENCY; CFHD C3 GLOMERULOPATHY 3; C3G3 PubMed Abrera-Abeleda MA, Nishimura ...
    https://medlineplus.gov/genetics/condition/c3-glomerulopathy - Genetics
  4. CFI gene 
    ... been found in people with glomerulonephritis with isolated C3 deposits. This condition, which may also occur in people with complement factor I deficiency, is characterized by kidney malfunction that can be ...
    https://medlineplus.gov/genetics/gene/cfi - Genetics
  5. C2 gene 
    ... component 2 protein. Without this protein to form C3 convertase, activation of ... leads to increased susceptibility to autoimmune disorders. Researchers ...
    https://medlineplus.gov/genetics/gene/c2 - Genetics
  6. CFH gene 
    ... Most of the CFH gene mutations that cause C3 glomerulopathy change single ... (deficiency) of complement factor H overactivates the complement system, ...
    https://medlineplus.gov/genetics/gene/cfh - Genetics
  7. ITGB2 gene 
    ... and other signs and symptoms of leukocyte adhesion deficiency type 1. More About This Health Condition CD11b/ CD18 CD11c/CD18 CD11d/CD18 CD18 complement receptor C3 beta-subunit complement receptor C3 subunit beta CR3 ...
    https://medlineplus.gov/genetics/gene/itgb2 - Genetics
  8. PHKG2 gene 
    ... testis) phosphorylase kinase, gamma 2 (testis/liver) PSK-C3 serine/threonine-protein kinase PHKG2 ... A, Kishnani PS. Variability of disease spectrum in children with liver phosphorylase kinase deficiency caused by mutations in the PHKG2 gene. Mol ...
    https://medlineplus.gov/genetics/gene/phkg2 - Genetics
  9. C8A gene 
    ... this protein impairs formation of complement component 8. Deficiency of this component prevents ... complement component ...
    https://medlineplus.gov/genetics/gene/c8a - Genetics