Browse

Explore conditions, clinical trials, and the organisations running them.

Up to: Hereditary skin disorder · Angioedema

Hereditary angioedema

Hereditary angioedema (HAE) is a genetic disease characterized by the occurrence of transitory and recurrent subcutaneous and/or submucosal edemas resulting in swelling and/or abdominal pain.

58 trials tagged with this condition →

Hereditary angioedema with C1Inh deficiency 14 trials · 32 incl. sub-types Sub-types →
Hereditary angioedema type 3 2 trials
Hereditary angioedema with normal C1Inh 2 trials
PLG-related hereditary angioedema with normal C1inh 0 trials
Angioedema, hereditary, 4 0 trials
Angioedema, hereditary, 5 0 trials
Angioedema, hereditary, 6 0 trials
Angioedema, hereditary, 7 0 trials
Angioedema, hereditary, 8 0 trials
Hereditary angioedema with normal C1inh not related to F12 or PLG variant 0 trials