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. [ Orphanet:91378 ]
Synonyms: HANE hereditary angioedema familial angioneurotic oedema hereditary non histamine-induced angioedema hereditary angioneurotic edema hereditary bradykinine-induced angioedema HAE familial angioneurotic edema hereditary angioneurotic oedema
Term information
- OMIMPS:106100 (MONDO:equivalentTo)
- MedDRA:10019860 (Orphanet:91378/e)
- GARD:5979 (MONDO:GARD)
- NCIT:C84758 (MONDO:equivalentTo)
- UMLS:C0019243 (MONDO:equivalentTo)
- MESH:D054179 (MONDO:equivalentTo)
- icd11.foundation:795969334 (Orphanet:91378)
- SCTID:82966003 (MONDO:equivalentTo)
- NANDO:2200795 (https://orcid.org/0000-0003-0011-764X)
- MEDGEN:9229 (MONDO:equivalentTo)
- DOID:14735 (MONDO:equivalentTo)
- Orphanet:91378 (MONDO:equivalentTo)
- NANDO:1200365 (https://orcid.org/0000-0003-0011-764X)
gard_rare, otar, rare, ordo_group_of_disorders
http://www.orpha.net/ORDO/Orphanet_91378
https://omim.org/phenotypicSeries/PS106100
http://identifiers.org/snomedct/82966003
http://purl.obolibrary.org/obo/NCIT_C84758
http://linkedlifedata.com/resource/umls/id/C0019243
http://purl.obolibrary.org/obo/DOID_14735
http://identifiers.org/mesh/D054179
http://identifiers.org/medgen/9229