ORPHA:169147
Immunodeficiency due to a classical component pathway complement deficiency
Also called Immunodeficiency due to C1, C4, or C2 component complement deficiency, Immunodeficiency due to an early component of complement 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:169147 is classified under "Immunological diseases" in the Orphanet nomenclature.