autosomaal recessieve hereditaire aandoening
common variable immunodeficiency
hereditaire aandoening van immuunsysteem
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Autosomal recessive common variable immunodeficiency due to complement C3d receptor 2 mutation (disorder)
Autosomal recessive common variable immunodeficiency due to CD21 mutation
Autosomal recessive common variable immunodeficiency due to CR2 mutation
Autosomal recessive common variable immunodeficiency due to complement C3d receptor 2 mutation
Autosomal recessive CVID (common variable immunodeficiency) due to CD21 deficiency
Autosomal recessive common variable immunodeficiency due to CD21 deficiency
Id1351961009
StatusPrimitive
Finding sitestructuur van immuunsysteem
Pathological processafwijkend immuunproces
SNOMED CT to ICD-10 extended map
TargetD83.8
RuleTRUE
AdviceALWAYS D83.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified