Autosomal recessive hereditary disorder	Congenital anomaly of visual system	Developmental hereditary disorder	Hereditary disorder of the visual system	Oculomotor apraxia
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Ocular motor apraxia Cogan type (disorder)
	Ocular motor apraxia Cogan type
	Congenital saccade initiation failure Oculomotor apraxia - Cogan type
	oculomotorische apraxie Cogan-type

Id	405809000
Status	Primitive

Associated morphology	Morphologically abnormal structure
Finding site	Structure of visual system
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

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