congenitale hypothyreoïdie	passagère hypothyreoïdie
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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.

Id	770631009
Status	Primitive

Finding site	structuur van schildklier
Occurrence	congenitaal

Clinical course

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	P72.2
Term	Overige voorbijgaande neonatale stoornissen van schildklierfunctie, niet elders geclassificeerd

SNOMED CT to Orphanet simple map

226316

SNOMED CT to ICD-10 extended map

Target	P72.2
Rule	TRUE
Advice	ALWAYS P72.2
Correlation	SNOMED CT source code to target map code correlation not specified