| primaire CD59-deficiëntie (aandoening) | | primaire CD59-deficiëntie | | Primary CD59 deficiency | | A rare genetic hematologic and neurologic disease characterized by chronic Coombs-negative hemolysis. The disease is associated with early-onset relapsing immune-mediated inflammatory axonal or demyelinating sensory-motor peripheral polyneuropathy and isolated or recurrent cerebrovascular events (in anterior or posterior circulation). |
| | Id | 778027003 | | 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 | 169464 |
| 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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