autosomaal dominante hereditaire aandoening
common variable immunodeficiency
hereditaire aandoening van immuunsysteem
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Autosomal dominant combined variable immunodeficiency due to tumor necrosis factor-like weak inducer of apoptosis mutation (disorder)
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
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