ORPHA:169150
Immunodeficiency due to a late component of complement deficiency
Also called Immunodeficiency due to C5 to C9 component complement deficiency, Terminal complement pathway deficiency
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Not documented in Orphadata
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:169150 is classified under "Immunological diseases" in the Orphanet nomenclature.