autosomaal recessieve hereditaire aandoening	congenitale afwijking van visueel systeem	hereditaire aandoening van visueel systeem	hereditaire ontwikkelingsstoornis	oculomotorische apraxie
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oculomotorische apraxie Cogan-type (aandoening)
	oculomotorische apraxie Cogan-type
	Ocular motor apraxia Cogan type
	Congenital saccade initiation failure Oculomotor apraxia - Cogan type

Id	405809000
Status	Primitive

Associated morphology	morfologische afwijking
Finding site	structuur van visueel systeem
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

DHD Diagnosis thesaurus reference set

SNOMED CT to Orphanet simple map

1125

SNOMED CT to ICD-10 extended map

Target	H51.8
Rule	TRUE
Advice	ALWAYS H51.8
Correlation	SNOMED CT source code to target map code correlation not specified