ORPHA:100050
Hereditary angioedema type 1
Also called Hereditary angioneurotic edema type 1, HAE 1, HAE-I
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- All ages
- Estimated prevalence
- 1-9 / 100 000 (Italy)
- Rarity class
- 1-9 / 100 000
ORPHA:100050 is classified under "Immunological diseases" in the Orphanet nomenclature.
Common signs
- Facial edema
- Urticaria
- Abnormality of metabolism/homeostasis
- Abdominal pain
- Paresthesia
- Intestinal edema