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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
Benign occipital epilepsy of childhood - early onset variant
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.
Id230387008
StatusPrimitive
SNOMED CT to Orphanet simple map98815
SNOMED CT to ICD-10 extended map
TargetG40.0
RuleTRUE
AdviceALWAYS G40.0
CorrelationSNOMED CT source code to target map code correlation not specified
TargetQ07.8
RuleTRUE
AdviceALWAYS Q07.8
CorrelationSNOMED CT source code to target map code correlation not specified