Autosomal recessive hereditary disorder
Combined immunodeficiency disease
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Susceptibility to respiratory infection associated with CD8alpha chain mutation (disorder)
Susceptibility to respiratory infection associated with CD8alpha chain mutation
Familial CD8 deficiency
A rare primary immunodeficiency due to a defect in adaptive immunity characterized by the absence of CD8+ T cells with normal immunoglobulin and specific antibody titers in blood and susceptibility to recurrent respiratory bacterial and viral infections. Symptom severity range from fatal respiratory insufficiency to mild or asymptomatic phenotypes.
Id766983005
StatusPrimitive
Pathological processAbnormal immune process
SNOMED CT to Orphanet simple map
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetD84.8
TermOverige gespecificeerde immunodeficiënties
TargetQ99.9
TermChromosoomafwijking, niet gespecificeerd
SNOMED CT to ICD-10 extended map
TargetD84.8
RuleTRUE
AdviceALWAYS D84.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified