hereditaire stoornis van schildklierstofwisseling
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proteolysedefect van thyreoglobuline (aandoening)
proteolysedefect van thyreoglobuline
thyroglobulineproteolysedefect
proteolysedefect van Tg
Thyroglobulin proteolysis defect
Id43449002
StatusPrimitive
Finding sitestructuur van schildklier
Occurrencecongenitaal
DHD Diagnosis thesaurus reference set
SNOMED CT to ICD-10 extended map
TargetE07.8
RuleTRUE
AdviceALWAYS E07.8
CorrelationSNOMED CT source code to target map code correlation not specified