| autosomaal recessieve 'common variable immunodeficiency' door mutatie in 'complement C3d receptor 2' (aandoening) | | autosomaal recessieve 'common variable immunodeficiency' door mutatie in CD21 | | autosomaal recessieve CVID door CD21-deficiëntie
autosomaal recessieve CVID door mutatie in CR2
autosomaal recessieve gewone variabele immuundeficiëntie door mutatie in CR2
autosomaal recessieve 'common variable'-immunodeficiëntie door CR2-mutatie
autosomaal recessieve 'common variable immunodeficiency' door mutatie in 'complement C3d receptor 2'
| | Autosomal recessive common variable immunodeficiency due to CD21 mutation | | Autosomal recessive common variable immunodeficiency due to CR2 mutation
Autosomal recessive common variable immunodeficiency due to complement C3d receptor 2 mutation
Autosomal recessive CVID (common variable immunodeficiency) due to CD21 deficiency
Autosomal recessive common variable immunodeficiency due to CD21 deficiency
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| | Id | 1351961009 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | D83.8 | | Rule | TRUE | | Advice | ALWAYS D83.8 | 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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