| autosomaal dominante T-cel-negatieve B-cel-negatieve ernstige gecombineerde immunodeficiëntie door defect van geactiveerd 'Rac family small GTPase 2' (aandoening) | | autosomaal dominante T-cel-negatieve B-cel-negatieve ernstige gecombineerde immunodeficiëntie door defect van geactiveerd RAC2 | | autosomaal dominante T-B-SCID door defect van geactiveerd RAC2
autosomaal dominante T-cel-negatieve B-cel-negatieve 'severe combined immunodeficiency' door defect van geactiveerd RAC2
autosomaal dominante T-cel-negatieve B-cel-negatieve ernstige gecombineerde immunodeficiëntie door defect van geactiveerd 'Rac family small GTPase 2'
| | Autosomal dominant T-cell negative, B-cell negative severe combined immunodeficiency due to activated RAC2 defect | | Autosomal dominant T-cell negative, B-cell negative severe combined immunodeficiency due to activated Rac family small GTPase 2 defect
Autosomal dominant T-B- SCID (severe combined immunodeficiency) due to activated RAC2 defect
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| | Id | 1351235001 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | D81.1 | | Rule | TRUE | | Advice | ALWAYS D81.1 | 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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