| Preferred Name |
Hereditary Angioedema |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84758 |
| code |
C84758 |
| DEFINITION |
Autosomal dominant inherited disorder characterized by abnormalities of C1 inhibitor. Patients present with swelling of the skin, subcutaneous tissues, and mucosa sites. |
| label |
Hereditary Angioedema |
| Preferred_Name |
Hereditary Angioedema |
| prefixIRI |
C84758 |
| prefLabel |
Hereditary Angioedema |
| Semantic_Type |
Disease or Syndrome |
| UMLS_CUI |
C0019243 |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.obolibrary.org/obo/DOID_14735 | Human Disease Ontology 123 | LOOM | |
| http://purl.bmicc.cn/ontology/ICD11CN/4A00.14 | International Classification of Diseases, 11th Edition, China | LOOM |