dyshormonogene struma	hereditaire stoornis van schildklierstofwisseling
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defect in jodotyrosylkoppeling (aandoening)
	defect in jodotyrosylkoppeling
	jodotyrosylkoppelingsdefect
	Iodotyrosyl coupling defect
	GDTH III - genetic defect in thyroid hormonogenesis III Congenital thyroid hormone coupling defect Thyroid hormone coupling defect Genetic defect in thyroid hormonogenesis III Hypothyroidism due to coupling defect

Id	23536000
Status	Primitive

Associated morphology	vergroting
Finding site	gehele schildklier
Occurrence	congenitaal

SNOMED CT to ICD-10 extended map

Target	E03.0
Rule	TRUE
Advice	ALWAYS E03.0
Correlation	SNOMED CT source code to target map code correlation not specified