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Autosomal dominant agammaglobulinemia due to PU.1 deficiency (disorder)
Autosomal dominant agammaglobulinemia due to PU.1 deficiency
Agammaglobulinemia due to SPI1 defect
Id1351647002
StatusPrimitive
Occurrencecongenitaal
Pathological processafwijkend immuunproces
SNOMED CT to ICD-10 extended map
TargetD80.0
RuleTRUE
AdviceALWAYS D80.0
CorrelationSNOMED CT source code to target map code correlation not specified