| autosomaal recessieve 'common variable immunodeficiency' door mutatie in 'membrane spanning 4-domains A1' (aandoening) | | autosomaal recessieve 'common variable immunodeficiency' door mutatie in CD20 | | autosomaal recessieve gewone variabele immuundeficiëntie door mutatie in CD20
autosomaal recessieve CVID door CD20-deficiëntie
autosomaal recessieve 'common variable'-immunodeficiëntie door CD20-mutatie
autosomaal recessieve 'common variable immunodeficiency' door mutatie in 'membrane spanning 4-domains A1'
autosomaal recessieve CVID door mutatie in MS4A1
| | Autosomal recessive common variable immunodeficiency due to CD20 mutation | | Autosomal recessive CVID (common variable immunodeficiency) due to CD20 deficiency
Autosomal recessive common variable immunodeficiency due to MS4A1 mutation
Autosomal recessive common variable immunodeficiency due to membrane spanning 4-domains A1 mutation
Autosomal recessive common variable immunodeficiency due to CD20 deficiency
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| | Id | 1351960005 | | 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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