Auditory system hereditary disorder	Autosomal recessive hereditary disorder	Congenital anomaly of ear with impairment of hearing	Congenital anomaly of vestibule of inner ear	Congenital sensorineural hearing loss	Developmental hereditary disorder	Goiter	Inherited disorder of thyroid metabolism
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Pendred's syndrome (disorder)
	Pendred's syndrome
	Genetic defect in thyroid hormonogenesis II B GDTH IIB Thyroid hormone organification defect II B Hypothyroidism with sensorineural deafness Goiter-deafness syndrome Pendred syndrome
	Pendred-syndroom
	syndroom van Pendred
	Aangeboren struma, overmatige schildklierwerking gepaard gaand met doofheid.

Id	70348004
Status	Primitive

Associated morphology	Enlargement
Finding site	Entire thyroid gland

Associated morphology	Morphologically abnormal structure
Finding site	Vestibular apparatus
Occurrence	Congenital
Pathological process	Pathological developmental process

Interprets

Finding site	Thyroid structure
Occurrence	Congenital

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

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