ORPHA:537072
PLG-related hereditary angioedema with normal C1Inh
Also called PLG-related HAE with normal C1 inhibitor
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Adolescent, Adult, Childhood, Elderly
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:537072 is classified under "Immunological diseases" in the Orphanet nomenclature.