| benigne occipitale epilepsie Gastaut-type (aandoening) | | benigne occipitale epilepsie Gastaut-type | | Gastaut type ideopathic childhood occipital epilepsy
G-ICOE
| | Childhood occipital visual epilepsy | | Benign childhood occipital epilepsy, Gastaut type
Late onset occipital epilepsy of childhood
Occipital epilepsy of childhood, Gastaut type
COVE - childhood occipital visual 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. |
| | Id | 230388003 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | G40.0 | | Rule | TRUE | | Advice | ALWAYS G40.0 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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