autosomaal recessief hyperimmunoglobuline M-syndroom
constitutionele 'mismatch repair'-deficiëntiesyndroom
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autosomaal recessief hyperimmunoglobuline-M-syndroom door deficiëntie van 'mutator S homolog 6' (aandoening)
autosomaal recessief hyperimmunoglobuline-M-syndroom door deficiëntie van MSH6
autosomaal recessief hyperimmunoglobuline-M-syndroom door deficiëntie van 'mutator S homolog 6'
autosomaal recessief hyper-IgM-syndroom door MSH6-deficiëntie
Autosomal recessive hyperimmunoglobulin M syndrome due to MSH6 deficiency
Autosomal recessive hyperimmunoglobulin M syndrome due to mutator S homolog 6 deficiency
Hyper IgM syndrome due to MSH6
Autosomal recessive hyperimmunoglobulin M syndrome due to mutS homolog 6 deficiency
Id1351576009
StatusPrimitive
Pathological processafwijkend immuunproces
SNOMED CT to ICD-10 extended map
TargetD80.5
RuleTRUE
AdviceALWAYS D80.5 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified