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Results 1 - 8 of 8 for Complement component 7 deficiency
  1. Complement component 2 deficiency 
    ... 2 deficiency National Organization for Rare Disorders (NORD) ... damage and autoimmunity in hereditary C2 deficiency. Rheumatology (Oxford). 2007 Jul;46(7):1133-9. doi: 10.1093/rheumatology/kem023. Epub ...
    https://medlineplus.gov/.../complement-component-2-deficiency - Genetics
  2. C8B gene 
    ... J Immunol. 1993 Jun 1;150(11):4943-7. Citation on PubMed Merle NS, Noe ... of complement associated with recurrent meningococcal meningitis--case ...
    https://medlineplus.gov/genetics/gene/c8b - Genetics
  3. Complement component 8 deficiency 
    ... gamma deficiency. J Immunol. 1998 Oct 1;161(7):3762-6. Citation on PubMed ... of complement associated with recurrent meningococcal meningitis--case ...
    https://medlineplus.gov/.../complement-component-8-deficiency - Genetics
  4. C8A gene 
    ... gamma deficiency. J Immunol. 1998 Oct 1;161(7):3762-6. Citation on PubMed ... of complement associated with recurrent meningococcal meningitis--case ...
    https://medlineplus.gov/genetics/gene/c8a - Genetics
  5. Complement factor I deficiency 
    Complement factor I deficiency is a disorder that affects the immune system. People with this condition are prone to recurrent infections, including infections ...
    https://medlineplus.gov/.../condition/complement-factor-i-deficiency - Genetics
  6. CFI gene 
    ... been identified in people with complement factor I deficiency, a disorder characterized by immune system dysfunction. The ... nonfunctional, or absent complement factor I.The lack (deficiency) of functional complement factor I protein allows uncontrolled ...
    https://medlineplus.gov/genetics/gene/cfi - Genetics
  7. SERPING1 gene 
    ... known as hereditary angioedema due to C1-INH deficiency. Hereditary angioedema due to C1-INH deficiency is further divided into two types: type I ... that cause hereditary angioedema due to C1-INH deficiency type I occur throughout the gene and lead ...
    https://medlineplus.gov/genetics/gene/serping1 - Genetics
  8. PIGT gene 
    ... Brodsky RA. Paroxysmal nocturnal hemoglobinuria without GPI-anchor deficiency. J Clin Invest. 2019 Dec 2;129(12): ... novel intellectual disability syndrome caused by GPI anchor deficiency due to homozygous mutations in PIGT. J Med ...
    https://medlineplus.gov/genetics/gene/pigt - Genetics