Benign occipital lobe epilepsy	Childhood epilepsy with occipital paroxysms	Childhood seizure
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Benign occipital epilepsy of childhood - late onset variant (disorder)
	Benign occipital epilepsy of childhood - late onset variant
	Benign childhood occipital epilepsy, Gastaut type Late-onset benign childhood occipital epilepsy
	A rare genetic neurological disorder with characteristics of childhood to mid-adolescence onset of frequent, brief, diurnal simple partial seizures which usually begin with visual hallucinations (e.g. phosphenes) and/or ictal blindness and may associate non visual seizures (such as deviation of the eyes, oculo clonic seizures), forced eyelid closure and blinking and sensory hallucinations. Post-ictal headache is common while impairment of consciousness is rare.
	benigne occipitale epilepsie Gastaut-type
	Gastaut type ideopathic childhood occipital epilepsy G-ICOE

Id	230388003
Status	Primitive

Finding site	Occipital lobe structure
Occurrence	Childhood

ICD-10 complex map reference set

Target	G40.0
Rule	TRUE
Advice	ALWAYS G40.0
Correlation	SNOMED CT source code to target map code correlation not specified