| vatbaarheid voor luchtweginfectie door mutatie in CD8-alfaketen (aandoening) | | vatbaarheid voor luchtweginfectie door mutatie in CD8-alfaketen | | familiaire CD8-deficiëntie
gevoeligheid voor luchtweginfectie door mutatie in CD8-alfaketen
familiale CD8-deficiëntie
| | Susceptibility to respiratory infection associated with CD8alpha chain mutation | | Familial CD8 deficiency
| | A rare primary immunodeficiency due to a defect in adaptive immunity characterized by the absence of CD8+ T cells with normal immunoglobulin and specific antibody titers in blood and susceptibility to recurrent respiratory bacterial and viral infections. Symptom severity range from fatal respiratory insufficiency to mild or asymptomatic phenotypes. |
| | Id | 766983005 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | D84.8 | | Term | Overige gespecificeerde immunodeficiënties |
| Target | Q99.9 | | Term | Chromosoomafwijking, niet gespecificeerd |
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| SNOMED CT to Orphanet simple map | 169085 |
| SNOMED CT to ICD-10 extended map | | Target | D84.8 | | Rule | TRUE | | Advice | ALWAYS D84.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
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