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autosomaal recessieve 'common variable immunodeficiency' door mutatie in 'B cell-activating factor receptor' (aandoening)
autosomaal recessieve 'common variable immunodeficiency' door mutatie in BAFF-R
autosomaal recessieve 'common variable immunodeficiency' door mutatie in 'B cell-activating factor receptor'
autosomaal recessieve 'common variable'-immunodeficiƫntie door BAFF-R-mutatie
autosomaal recessieve 'common variable immunodeficiency' door TNFRSF13C-mutatie
autosomaal recessieve CVID door BAFF-R-deficiƫntie
Autosomal recessive combined variable immunodeficiency due to BAFF receptor deficiency
Autosomal recessive CVID (combined variable immunodeficiency) due to TNFRSF13C mutation
Autosomal recessive combined variable immunodeficiency due to B cell-activating factor receptor mutation
Autosomal recessive combined variable immunodeficiency due to BAFF-R deficiency
Autosomal recessive combined variable immunodeficiency due to BAFF-R mutation
Id1352023006
StatusPrimitive
SNOMED CT to ICD-10 extended map
TargetD83.0
RuleTRUE
AdviceALWAYS D83.0
CorrelationSNOMED CT source code to target map code correlation not specified