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Up to: Immunodeficiency disease · Inborn error of immunity

Complement deficiency

A genetic deficiency of any of the component of the complement system (including the classical, alternative, and terminal pathway components), that can either be acquired or inherited.

2 trials tagged with this condition →

  • Atypical hemolytic-uremic syndrome 19 trials Sub-types →
  • Classic complement early component deficiency 0 trials · 7 incl. sub-types Sub-types →
  • Disorder of lectin complement activation pathway 0 trials · 1 incl. sub-types Sub-types →
  • Complement factor I deficiency 0 trials
  • Complement receptor deficiency 0 trials
  • Immunodeficiency due to a classical component pathway complement deficiency 0 trials Sub-types →
  • Immunodeficiency due to a late component of complement deficiency 0 trials Sub-types →
  • Recurrent Neisseria infections due to factor D deficiency 0 trials

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