ORPHA:528647
Hereditary angioedema with normal C1Inh
Also called HAE with normal C1 inhibitor, HAE with normal C1Inh, Hereditary angioedema with normal C1 inhibitor, Hereditary angioneurotic edema with normal C1 inhibitor, Hereditary angioneurotic edema with normal C1Inh
- Body system
- Immunological diseases
- Inheritance pattern
- Not applicable
- Typical age of onset
- Not documented in Orphadata
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:528647 is classified under "Immunological diseases" in the Orphanet nomenclature.
Common signs
- Angioedema
- Facial edema
- Intestinal edema
- Edema of the upper limbs
- Laryngeal edema
- Abnormal bleeding