| hereditair angio-oedeem type III (aandoening) | | hereditair angio-oedeem type III |  | Dit betekent dat je huid of slijmvliezen opzwellen. Dat komt omdat je lichaam te veel heeft van een stof die ervoor zorgt dat er vocht uit je bloedvaten naar je huid en slijmvliezen lekt. Je bent met dit probleem geboren. | | 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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