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genetische passagère congenitale hypothyreoïdie (aandoening)
genetische passagère congenitale hypothyreoïdie
genetische voorbijgaande congenitale hypothyroïdie
Genetic transient congenital hypothyroidism
A rare thyroid disease with characteristics of a gene mutation induced, temporary deficiency of thyroid hormones at birth, which later reverts to normal with or without replacement therapy in the first few months or years of life.
Id770631009
StatusPrimitive
Clinical coursetransitoir
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetP72.2
TermOverige voorbijgaande neonatale stoornissen van schildklierfunctie, niet elders geclassificeerd
SNOMED CT to Orphanet simple map226316
SNOMED CT to ICD-10 extended map
TargetP72.2
RuleTRUE
AdviceALWAYS P72.2
CorrelationSNOMED CT source code to target map code correlation not specified