autosomaal hereditaire aandoening	congenitale neuropathie	familiaire aandoening	hereditaire aandoening van zenuwstelsel	spiegelbewegingen
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familiaire congenitale spiegelbewegingen (aandoening)
	familiaire congenitale spiegelbewegingen
	familiaire congenitale contralaterale synkinesie
	Familial congenital mirror movements
	Familial congenital controlateral synkinesia Hereditary congenital mirror movements Hereditary congenital controlateral synkinesia Isolated congenital controlateral synkinesia Isolated congenital mirror movements
	A rare, genetic, movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities.

Id	784348007
Status	Primitive

Finding site	structuur van systema nervosum
Occurrence	congenitaal

Interprets

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	G25.8
Term	Overige gespecificeerde extrapiramidale aandoeningen en aandoeningen met abnormale bewegingen

SNOMED CT to Orphanet simple map

238722

SNOMED CT to ICD-10 extended map

Target	G25.8
Rule	TRUE
Advice	ALWAYS G25.8
Correlation	SNOMED CT source code to target map code correlation not specified