| autosomaal recessief hyperimmunoglobuline-M-syndroom door deficiëntie van 'activation induced cytidine deaminase' (aandoening) | | autosomaal recessief hyperimmunoglobuline-M-syndroom door deficiëntie van AID | | autosomaal recessief hyperimmunoglobuline-M-syndroom door deficiëntie van 'activation induced cytidine deaminase'
autosomaal recessief hyper-IgM-syndroom door mutatie van AICDA
autosomaal recessief hyper-IgM-syndroom type 2
autosomaal recessief HIGM2
| | Autosomal recessive hyperimmunoglobulin M syndrome due to AID deficiency | | Autosomal recessive hyper-IgM syndrome type 2
Autosomal recessive activation-induced cytidine deaminase deficiency
Autosomal recessive hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase deficiency
Autosomal recessive hyper IgM syndrome due to AICDA
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| | Id | 1351572006 | | 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 |
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