ICD D84.1ORPHA:91378HAE

Hereditary Angioedema

Hereditary angioedema is a rare genetic condition causing recurrent episodes of severe swelling in the skin, abdomen, and airway. It is caused by deficiency or dysfunction of C1 inhibitor. Untreated attacks can be life-threatening. Effective preventive and on-demand treatments are now available on the PBS.

713
Articles
272
Trials (26 AU)
Updated
26 March 2026
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This information is for general awareness only.

For guidance specific to your situation, please speak with your healthcare team.