| autosomaal dominant hyperimmunoglobuline-M-syndroom door deficiëntie van 'activation induced cytidine deaminase' (aandoening) | | autosomaal dominant hyperimmunoglobuline-M-syndroom door deficiëntie van AID | | autosomaal dominant hyperimmunoglobuline-M-syndroom door deficiëntie van 'activation induced cytidine deaminase'
autosomaal dominant hyper-IgM-syndroom type 2
autosomaal dominant hyper-IgM-syndroom door mutatie van AICDA
autosomaal dominant HIGM2
| | Autosomal dominant hyperimmunoglobulin M syndrome due to AID deficiency | | Autosomal dominant hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase deficiency
Autosomal dominant activation-induced cytidine deaminase deficiency
Autosomal dominant hyper-IgM syndrome type 2
Autosomal dominant hyper IgM syndrome due to AICDA
|
| | Id | 1351570003 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | D80.5 | | Rule | TRUE | | Advice | ALWAYS D80.5 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
|
|
