Complement deficiency
MONDO:0003832A 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.
Also known as: complement activation disease, complement deficiency, disorder of complement activation, immunodeficiency due to a complement cascade component deficiency
77 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Atypical hemolytic-uremic syndrome
(18)
C1 inhibitor deficiency
(3)
Complement component 3 deficiency
(1)
Mannose-binding lectin deficiency
(1)
Atypical hemolytic-uremic syndrome with anti-factor H antibodies
(0)
Atypical hemolytic-uremic syndrome with B factor anomaly
(0)
Atypical hemolytic-uremic syndrome with C3 anomaly
(0)
Atypical hemolytic uremic syndrome with complement gene abnormality
(0)
Atypical hemolytic-uremic syndrome with DGKE deficiency
(0)
Atypical hemolytic-uremic syndrome with H factor anomaly
(0)
Atypical hemolytic-uremic syndrome with I factor anomaly
(0)
Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly
(0)
Atypical hemolytic-uremic syndrome with thrombomodulin anomaly
(0)
C1Q deficiency
(0)
C1Q deficiency 1
(0)
C1Q deficiency 2
(0)
C1Q deficiency 3
(0)
Classic complement early component deficiency
(0)
Complement component 2 deficiency
(0)
Complement component 4a deficiency
(0)