| autosomaal recessieve 'common variable immunodeficiency' door deficiëntie van 'Rac family small GTPase 2' (aandoening) | | autosomaal recessieve 'common variable immunodeficiency' door deficiëntie van RAC2 | | autosomaal recessieve 'common variable immunodeficiency' door deficiëntie van 'Rac family small GTPase 2'
autosomaal recessieve CVID door mutatie in RAC2
| | Autosomal recessive common variable immunodeficiency due to RAC2 deficiency | | Autosomal recessive CVID (common variable immunodeficiency) due to RAC2 mutation
Autosomal recessive common variable immunodeficiency due to Rac family small GTPase 2 deficiency
Autosomal recessive common variable immunodeficiency due to RAC2 mutation
|
| | Id | 1356782005 | | 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 |
|
|
