autosomaal recessieve hereditaire aandoening	dyshormonogene struma	enzymopathie	hereditaire stoornis van schildklierstofwisseling
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defect in jodotyrosinedejodinatie (aandoening)
	defect in jodotyrosinedejodinatie
	jodotyrosinedejodinatiedefect
	Iodotyrosine deiodination defect
	Genetic defect in thyroid hormonogenesis IV Hypothyroidism due to deiodase defect Deiodinase deficiency Hypothyroidism due to iodotyrosine deiodinase defect Iodotyrosine deiodinase deficiency Iodotyrosine dehalogenase deficiency

Id	17885001
Status	Primitive

Associated morphology	vergroting
Finding site	gehele schildklier
Occurrence	congenitaal

SNOMED CT to ICD-10 extended map

Target	E07.1
Rule	TRUE
Advice	ALWAYS E07.1
Correlation	SNOMED CT source code to target map code correlation not specified