| autosomaal recessieve gecombineerde immunodeficiëntie door mutatie van 'RELB proto-oncogene, NF-kB subunit' (aandoening) | | autosomaal recessieve gecombineerde immunodeficiëntie door mutatie van RELB | | autosomaal recessieve gecombineerde immunodeficiëntie door mutatie van 'RELB proto-oncogene, NF-kB subunit'
autosomaal recessieve gecombineerde immunodeficiëntie door deficiëntie van RelB
| | Autosomal recessive combined immunodeficiency due to RELB mutation | | Autosomal recessive combined immunodeficiency due to RELB deficiency
Autosomal recessive combined immunodeficiency due to RelB mutation
Autosomal recessive combined immunodeficiency due to RELB proto-oncogene, NF-kB subunit mutation
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| | Id | 1351650004 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | D81.8 | | Rule | TRUE | | Advice | ALWAYS D81.8 | 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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