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autosomaal recessieve 'common variable immunodeficiency' door mutatie in 'complement C3d receptor 2' (aandoening)
autosomaal recessieve 'common variable immunodeficiency' door mutatie in CD21
autosomaal recessieve CVID door CD21-deficiëntie
autosomaal recessieve CVID door mutatie in CR2
autosomaal recessieve gewone variabele immuundeficiëntie door mutatie in CR2
autosomaal recessieve 'common variable'-immunodeficiëntie door CR2-mutatie
autosomaal recessieve 'common variable immunodeficiency' door mutatie in 'complement C3d receptor 2'
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
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