Hereditary angioedema

MONDO:0019623

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.

Also known as: HAE, familial angioneurotic edema, familial angioneurotic oedema, hereditary angioedema, hereditary angioneurotic edema, hereditary angioneurotic oedema, hereditary bradykinine-induced angioedema, hereditary non histamine-induced angioedema

61 clinical trials for this condition and its sub-types, 58 tagged with Hereditary angioedema itself.

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Where it sits in the disease tree

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↑ Hereditary skin disorder (880) ↑ Angioedema (66)

Sub-types of Hereditary angioedema

Hereditary angioedema with C1Inh deficiency 14 trials · 32 incl. sub-types
2 sub-types
- Hereditary angioedema type 1 26 trials
- Hereditary angioedema type 2 26 trials
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

Including sub-types (61) Tagged with Hereditary angioedema (58)

Trials to join now! 19 Not yet recruiting 3 Not yet finished but already full! 16 Completed 20 Terminated 3

Hereditary angioedema

Where it sits in the disease tree

Takhzyro under the microscope: Real-World safety check for rare swelling disease

Can immune fingerprints unlock new treatments for skin disease?

Egyptian HAE patients to be studied for better care insights