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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
Benign childhood occipital epilepsy Panayiotopoulos type
Panayiotopoulos syndrome
Early-onset benign childhood occipital epilepsy
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
DHD Diagnosethesaurus-referentieset
referentieset met complexe 'mapping' naar ICD-10
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