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Up to: Complement deficiency
Classic complement early component deficiency
A genetic deficiency of any early component of the classical pathway (C1q, C1r/s, C2, C4, and C3) that is associated with autoimmune diseases due to the failure of clearance of immune complexes (IC) and apoptotic materials, and the impairment of normal humoral response.
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C1 inhibitor deficiency 5 trials
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Complement component 3 deficiency 2 trials
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Complement component 2 deficiency 0 trials
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Complement component 4a deficiency 0 trials
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Complement component 4b deficiency 0 trials
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Complement component 5 deficiency 0 trials
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Complement component 6 deficiency 0 trials
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Complement component 7 deficiency 0 trials
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Complement component 9 deficiency 0 trials
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Complement component C1s deficiency 0 trials