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Rare disease search prototype built on Orphanet data

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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