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autosomaal dominante 'common variable immunodeficiency' door mutatie in 'nuclear factor kappa B subunit 1' (aandoening)
autosomaal dominante 'common variable immunodeficiency' door mutatie in NFKB1
autosomaal dominante gewone variabele immuundeficiëntie door mutatie in NFKB1
autosomaal dominante 'common variable immunodeficiency' door mutatie in 'nuclear factor kappa B subunit 1'
autosomaal dominante CVID door NFKB1-deficiëntie
autosomaal dominante 'common variable'-immunodeficiëntie door NFKB1-mutatie
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
SNOMED CT to ICD-10 extended map
TargetD83.8
RuleTRUE
AdviceALWAYS D83.8
CorrelationSNOMED CT source code to target map code correlation not specified