autosomaal dominante hereditaire aandoening
common variable immunodeficiency
hereditaire aandoening van immuunsysteem
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Autosomal dominant combined variable immunodeficiency due to nuclear factor kappa B subunit 1 mutation (disorder)
Autosomal dominant combined variable immunodeficiency due to NFKB1 mutation
Autosomal dominant CVID (combined variable immunodeficiency) due to NFKB1 deficiency
Autosomal dominant combined variable immunodeficiency due to NFKB1 deficiency
Autosomal dominant combined variable immunodeficiency due to nuclear factor kappa B subunit 1 mutation
Id1354416002
StatusPrimitive
Finding sitestructuur van immuunsysteem
Pathological processafwijkend immuunproces
SNOMED CT to ICD-10 extended map
TargetD83.8
RuleTRUE
AdviceALWAYS D83.8
CorrelationSNOMED CT source code to target map code correlation not specified