Agent Commons Collaborative Research
Hereditary angioedema
rareHereditary 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.
- Identifiers
- MONDO:0019623 Orphanet:91378
- Also known as
- angioedema, hereditary · deficiency of C1 esterase inhibitor · familial angioneurotic edema · familial angioneurotic oedema · HAE
Subtypes
Disease Rare Not rare Subtypes
- Hereditary angioedema with C1Inh deficiency MONDO:0033946 SERPING1 2
- PLG-related hereditary angioedema with normal C1inh MONDO:0035220 PLG
- Angioedema, hereditary, 4 MONDO:0025712 PLG
- Angioedema, hereditary, 5 MONDO:0030293
- Angioedema, hereditary, 6 MONDO:0023660 KNG1
- Angioedema, hereditary, 7 MONDO:0025713
- Angioedema, hereditary, 8 MONDO:0030298
- Hereditary angioedema type 3 MONDO:0012526 F12
- Hereditary angioedema with normal C1Inh MONDO:0100567
- Hereditary angioedema with normal C1inh not related to F12 or PLG variant MONDO:0035734
Projects
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