| autosomaal dominante gecombineerde immunodeficiëntie door deficiëntie van 'erbb2 interacting protein' (aandoening) | | autosomaal dominante gecombineerde immunodeficiëntie door deficiëntie van ERBIN | | autosomaal dominante gecombineerde immunodeficiëntie door defect van ERBB2IP
autosomaal dominante gecombineerde immunodeficiëntie door deficiëntie van 'erbb2 interacting protein'
| | Autosomal dominant combined immunodeficiency due to ERBIN deficiency | | Autosomal dominant hyperimmunoglobulin E syndrome due to ERBIN deficiency
Autosomal dominant combined immunodeficiency due to erbb2 interacting protein deficiency
Autosomal dominant hyperimmunoglobulin E syndrome due to ERBB2IP defect
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| | Id | 1351324009 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | D82.4 | | Rule | TRUE | | Advice | ALWAYS D82.4 | 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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