autosomaal recessieve hereditaire aandoening
gecombineerde immunodeficiëntie
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Autosomal recessive combined immunodeficiency due to REL proto-oncogene NF-kappa-B subunit mutation (disorder)
Autosomal recessive combined immunodeficiency due to REL mutation
Autosomal recessive combined immunodeficiency due to c-Rel deficiency
Autosomal recessive combined immunodeficiency due to REL proto-oncogene NF-kappa-B subunit mutation
Id1351780001
StatusPrimitive
Pathological processafwijkend immuunproces
SNOMED CT to ICD-10 extended map
TargetD81.8
RuleTRUE
AdviceALWAYS D81.8
CorrelationSNOMED CT source code to target map code correlation not specified