ORPHA:300359
PLCG2-associated antibody deficiency and immune dysregulation
Also called FACU, Familial atypical cold urticaria, Familial cold urticaria with common variable immunodeficiency, PLAID
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:300359 is classified under "Immunological diseases" in the Orphanet nomenclature.