autosomaal recessieve hereditaire aandoening	Congenital neurological disorder	depletie van mitochondriaal DNA	hereditaire cerebellaire degeneratie	spinocerebellaire aandoening
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myoclonic epilepsy myopathy sensory ataxia (aandoening)
	myoclonic epilepsy myopathy sensory ataxia
	MEMSA
	Myoclonic epilepsy myopathy sensory ataxia
	Spinocerebellar ataxia with epilepsy MEMSA - myoclonic epilepsy myopathy sensory ataxia

Id	699328003
Status	Primitive

Associated morphology	degeneratieve afwijking
Finding site	structuur van cerebellum

Associated morphology	degeneratieve afwijking
Finding site	structuur van medulla spinalis

Occurrence

DHD Diagnosethesaurus-referentieset

referentieset met complexe 'mapping' naar ICD-10

Target	G11.9
Rule	TRUE
Advice	ALWAYS G11.9
Correlation	SNOMED CT source code to target map code correlation not specified

Target	G40.3
Rule	TRUE
Advice	ALWAYS G40.3
Correlation	SNOMED CT source code to target map code correlation not specified