| benigne occipitale epilepsie Panayiotopoulos-type (aandoening) | | benigne occipitale epilepsie Panayiotopoulos-type | | benigne nachtelijke occipitale epilepsie op kinderleeftijd
Panayiotopoulos-syndroom
benign nocturnal childhood occipital epilepsy syndrome
syndroom van Panayiotopoulos
| | Self-limited epilepsy with autonomic seizures | | SeLEAS - self-limited epilepsy with autonomic seizures
Panayiotopoulos syndrome
Early-onset benign childhood occipital epilepsy
Benign childhood occipital epilepsy Panayiotopoulos type
| | A rare genetic neurological disorder characterized by late infancy to early-adolescence onset of prolonged, nocturnal seizures which begin with autonomic features (e.g. vomiting, pallor, sweating) and associate tonic eye deviation, impairment of consciousness and may evolve to a hemi-clonic or generalized convulsion. Autonomic status epilepticus may be the only clinical event in some cases. |
| | Id | 230387008 | | Status | Primitive |
| SNOMED CT to Orphanet simple map | 98815 |
| 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 |
| Target | Q07.8 | | Rule | TRUE | | Advice | ALWAYS Q07.8 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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