200 top medical experts on Hereditary Complement Deficiency Diseases across 14 countries and 9 U.S. states, including 13 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Hereditary Complement Deficiency Diseases: Genetic disorders due to mutations in genes involved in complement system proteins. They are often classified into distinct pathway of complement activation where causative mutations are found (e.g., classical pathway, lectin pathway, alternative pathway, and terminal complement pathway).
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Primary Immunodeficiency Diseases (1,145) and Narrower Categories: Hereditary Angioedemas (737).
  4. Clinical Trials ClinicalTrials.gov : at least 1
  5. Synonyms: Complement Deficiencies,  Inherited Complement Deficiency Diseases


  

        

                    


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