complement deficiency
MONDO:0003832Mondo
Findings
No curated finding names complement deficiency yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
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.
Definition from the Mondo Disease Ontology (MONDO:0003832), read 2026-09-29. CC BY 4.0.
Where it sits
- Narrower terms (8)
- atypical hemolytic-uremic syndrome
- classic complement early component deficiency
- complement factor I deficiency
- complement receptor deficiency
- disorder of lectin complement activation pathway
- immunodeficiency due to a classical component pathway complement deficiency
- immunodeficiency due to a late component of complement deficiency
- recurrent Neisseria infections due to factor D deficiency
Other names
3 names
Resolves to: complement deficiency
- Also called
- complement activation diseasedisorder of complement activationimmunodeficiency due to a complement cascade component deficiency