Autosomal recessive hereditary disorder	Congenital cataract	Developmental hereditary disorder	Early onset cerebellar ataxia	Hereditary ataxia	Hereditary disorder of the visual system	Multiple malformation syndrome with unusual brain and/or neuromuscular findings
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Marinesco-Sjögren syndrome (disorder)
	Marinesco-Sjögren syndrome
	Marinesco-Sjogren syndrome Oligophrenic cerebellolenticular degeneration

Id	80734006
Status	Primitive

Finding site

Cerebellar structure

Associated morphology	Opacity
Finding site	Lens clear
Occurrence	Congenital
Pathological process	Pathological developmental process

SNOMED CT to Orphanet simple map

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	G11.1
Term	Vroeg optredende cerebellaire ataxie

Target	Q12.0
Term	Congenitaal cataract

Target	F79.9
Term	Niet gespecificeerde zwakzinnigheid; Zonder vermelding van gedragsstoornissen

Target	R62.8
Term	Overige gespecificeerde achterstand in normale fysiologische ontwikkeling

SNOMED CT to ICD-10 extended map

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