Auditory system hereditary disorder	Autosomal dominant hereditary disorder	Congenital anomaly of the kidney	Congenital hearing disorder	Congenital hearing loss	Developmental hereditary disorder	Developmental malformation of branchial arch	Hearing loss	Hereditary nephropathy	Multiple malformation syndrome with facial defects as major feature
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Melnick-Fraser syndrome (disorder)
	Melnick-Fraser syndrome
	Branchio-oto-renal syndrome BOR syndrome
	branchio-otorenaal syndroom
	syndroom van Melnick-Fraser Melnick-Fraser-syndroom
	branchio-otorenaal syndroom
	BOR syndroom; erfelijke aandoening van de nek (branchio), de oren (oto) en de nieren (renaal), waarbij milde tot ernstige afwijkingen aan de nieren zijn en de nek en oren niet goed zijn ontwikkeld.

Id	290006
Status	Primitive

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

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

Associated morphology	Morphologically abnormal structure
Finding site	Structure of auditory system
Occurrence	Congenital
Pathological process	Pathological developmental process

Interprets

Associated morphology	Morphologically abnormal structure
Finding site	Branchial arch structure
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q87.0
Rule	TRUE
Advice	ALWAYS Q87.0
Correlation	SNOMED CT source code to target map code correlation not specified