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Results 1 - 10 of 16 for Complement component 7 deficiency
  1. ... 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 ...
  2. Travelers' Health: Meningococcal Disease (Centers for Disease Control and Prevention)  
    Meningitis/Related Issues ... Meningitis ... Meningococcal Disease/Related Issues ... Meningococcal Disease ... Centers for Disease Control and Prevention ... Information about ...
  3. ... J Immunol. 1993 Jun 1;150(11):4943-7. Citation on PubMed Merle NS, Noe ... of complement associated with recurrent meningococcal meningitis--case ...
  4. ... gamma deficiency. J Immunol. 1998 Oct 1;161(7):3762-6. Citation on PubMed ... of complement associated with recurrent meningococcal meningitis--case ...
  5. ... gamma deficiency. J Immunol. 1998 Oct 1;161(7):3762-6. Citation on PubMed ... of complement associated with recurrent meningococcal meningitis--case ...
  6. Complement factor I deficiency is a disorder that affects the immune system. People with this condition are prone to recurrent infections, including infections ...
  7. Travelers' Health: Immunocompromised Travelers (Centers for Disease Control and Prevention)  
    Traveler's Health/Related Issues ... Traveler's Health ... Immune System and Disorders/Related Issues ... Immune System and Disorders ... Centers for Disease Control and ...
  8. ... 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 ...
  9. ... 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 ...
  10. ... 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 ...
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