autosomaal recessieve hereditaire aandoening	congenitale neuropathie	depletie van mitochondriaal DNA	hereditaire ataxie	hereditaire stoornis van metabolisme van zenuwstelsel	vroeg optredende cerebellaire ataxie
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mitochondriaal recessief ataxiesyndroom (aandoening)
	mitochondriaal recessief ataxiesyndroom
	Recessive mitochondrial ataxia syndrome
	MIRAS - mitochondrial recessive ataxia syndrome
	A rare, mitochondrial DNA maintenance syndrome characterized by early-onset cerebellar ataxia, and variable combination of epilepsy, headache, dysarthria, ophthalmoplegia, peripheral neuropathy, intellectual disability, psychiatric symptoms and movement disorders.

Id	782696001
Status	Primitive

Finding site	structuur van cerebellum
Occurrence	congenitaal

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	G11.8
Term	Overige gespecificeerde vormen van hereditaire ataxie

SNOMED CT to Orphanet simple map

94125

SNOMED CT to ICD-10 extended map

Target	G11.8
Rule	TRUE
Advice	ALWAYS G11.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified