autosomaal dominante hereditaire aandoening
common variable immunodeficiency
hereditaire aandoening van immuunsysteem
|||
Autosomal dominant combined variable immunodeficiency due to interferon regulatory factor 2 binding protein 2 mutation (disorder)
Autosomal dominant combined variable immunodeficiency due to IRF2BP2 mutation
Autosomal dominant CVID (combined variable immunodeficiency) due to IRF2BP2 deficiency
Autosomal dominant combined variable immunodeficiency due to IRF2BP2 deficiency
Autosomal dominant combined variable immunodeficiency due to interferon regulatory factor 2 binding protein 2 mutation
Id1354420003
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