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16
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Complement component 7 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 ...
- 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 ...
- ... J Immunol. 1993 Jun 1;150(11):4943-7. Citation on PubMed Merle NS, Noe ... of complement associated with recurrent meningococcal meningitis--case ...
- ... gamma deficiency. J Immunol. 1998 Oct 1;161(7):3762-6. Citation on PubMed ... of complement associated with recurrent meningococcal meningitis--case ...
- ... gamma deficiency. J Immunol. 1998 Oct 1;161(7):3762-6. Citation on PubMed ... of complement associated with recurrent meningococcal meningitis--case ...
- Complement factor I deficiency is a disorder that affects the immune system. People with this condition are prone to recurrent infections, including infections ...
- 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 ...
- ... 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 ...
- ... 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 ...
- ... 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 ...