| autosomaal recessieve 'common variable immunodeficiency' door mutatie in 'phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma' (aandoening) | | autosomaal recessieve 'common variable immunodeficiency' door mutatie in PIK3CG | | autosomaal recessieve 'common variable immunodeficiency' door mutatie in 'phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma'
autosomaal recessieve gewone variabele immuundeficiëntie door mutatie in PIK3CG
autosomaal recessieve CVID door PIK3CG-deficiëntie
autosomaal recessieve 'common variable'-immunodeficiëntie door PIK3CG-mutatie
| | Autosomal recessive combined variable immunodeficiency due to PIK3CG mutation | | Autosomal recessive combined variable immunodeficiency due to phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma mutation
Autosomal recessive CVID (combined variable immunodeficiency) due to PIK3CG deficiency
Autosomal recessive combined variable immunodeficiency due to PIK3CG deficiency
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| | Id | 1354483004 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | D83.8 | | Rule | TRUE | | Advice | ALWAYS D83.8 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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