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autosomaal dominante 'common variable immunodeficiency' door mutatie in 'tumor necrosis factor-like weak inducer of apoptosis' (aandoening)
autosomaal dominante 'common variable immunodeficiency' door mutatie in TWEAK
autosomaal dominante 'common variable immunodeficiency' door mutatie in 'tumor necrosis factor-like weak inducer of apoptosis'
autosomaal dominante CVID door TWEAK-deficiëntie
autosomaal dominante CVID door mutatie in TNFSF12
autosomaal dominante 'common variable'-immunodeficiëntie door TWEAK-mutatie
autosomaal dominante gewone variabele immuundeficiëntie door mutatie in TWEAK
Autosomal dominant combined variable immunodeficiency due to TWEAK mutation
Autosomal dominant combined variable immunodeficiency due to tumor necrosis factor-like weak inducer of apoptosis mutation
Autosomal dominant combined variable immunodeficiency due to TWEAK deficiency
Autosomal dominant CVID (combined variable immunodeficiency) due to TNFSF12 mutation
Id1352026003
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