autosomaal recessieve hereditaire aandoening	depletie van mitochondriaal DNA	hereditaire cerebellaire degeneratie	hereditaire stoornis van metabolisme van zenuwstelsel	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

Occurrence

Associated morphology	degeneratieve afwijking
Finding site	structuur van medulla spinalis

Associated morphology	degeneratieve afwijking
Finding site	structuur van cerebellum

DHD Diagnosis thesaurus reference set

SNOMED CT to Orphanet simple map

254881

SNOMED CT to ICD-10 extended map

Target	E88.8
Rule	TRUE
Advice	ALWAYS E88.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
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