Auditory system hereditary disorder	Autosomal dominant hereditary disorder	Cerebellar ataxia	Congenital neurological disorder	Congenital sensorineural hearing loss	Disorder of ear	Disorder of sensory function	Extrapyramidal disease	Hearing loss associated with syndrome	Hereditary ataxia	Myoclonic disorder
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Myoclonus, cerebellar ataxia, deafness syndrome (disorder)
	Myoclonus, cerebellar ataxia, deafness syndrome
	Syndrome with the association of myoclonus, cerebellar ataxia and sensorineural hearing loss. So far, less than 10 cases have been reported in the literature. The hearing loss was generally diagnosed during childhood or early adulthood and the myoclonic jerks began during adolescence. Transmission appears to be autosomal dominant.
	syndroom van myoklonie, cerebellaire ataxie en doofheid
	syndroom van myoclonus, cerebellaire ataxie en gehoorverlies

Id	733065003
Status	Primitive

Interprets

Finding site	Cerebellar structure
Occurrence	Congenital

Finding site	Ear structure
Occurrence	Congenital

Interprets

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	G11.1
Rule	TRUE
Advice	ALWAYS G11.1
Correlation	SNOMED CT source code to target map code correlation not specified

Target	G25.3
Rule	TRUE
Advice	ALWAYS G25.3
Correlation	SNOMED CT source code to target map code correlation not specified

Target	H90.5
Rule	TRUE
Advice	ALWAYS H90.5
Correlation	SNOMED CT source code to target map code correlation not specified