| hereditair angio-oedeem type III (aandoening) | | hereditair angio-oedeem type III | | Hereditary angioedema with normal C1 esterase inhibitor activity | | Hereditary angioedema - type 3
Hereditary angioneurotic edema with normal C1 esterase inhibitor activity
| | Hereditary angioedema without abnormal C1 inhibitor levels or function. One type has been found mostly in females in which symptoms may be triggered by pregnancy or estrogen-containing oral contraceptives. Mechanisms include mutations of the genes encoding coagulation factor XII, angiopoietin-1, plasminogen and as yet undefined factors. |
| | Id | 427167008 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | D84.1 | | Term | Stoornissen in complementsysteem |
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| SNOMED CT to Orphanet simple map | 528647 |
| SNOMED CT to ICD-10 extended map | | Target | D84.1 | | Rule | TRUE | | Advice | ALWAYS D84.1 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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