| autosomaal recessieve 'common variable immunodeficiency' door mutatie in 'POU class 2 homeobox associating factor 1' (aandoening) | | autosomaal recessieve 'common variable immunodeficiency' door mutatie in POU2AF1 | | autosomaal recessieve CVID door BOB1-deficiëntie
autosomaal recessieve 'common variable'-immunodeficiëntie door POU2AF1-mutatie
autosomaal recessieve gewone variabele immuundeficiëntie door mutatie in POU2AF1
autosomaal recessieve 'common variable immunodeficiency' door mutatie in 'POU class 2 homeobox associating factor 1'
| | Autosomal recessive common variable immunodeficiency due to POU2AF1 mutation | | Autosomal recessive common variable immunodeficiency due to BOB1 deficiency
Autosomal recessive common variable immunodeficiency due to POU class 2 homeobox associating factor 1 mutation
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| | Id | 1354596000 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | D83.8 | | Rule | TRUE | | Advice | ALWAYS D83.8 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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