benigne rolandische epilepsie
Congenital neurological disorder
hereditaire aandoening van zenuwstelsel
spraakdyspraxie en taaldyspraxie
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syndroom van rolandische epilepsie en spraakdyspraxie (aandoening)
syndroom van rolandische epilepsie en spraakdyspraxie
syndroom van rolandische epilepsie en verbale dyspraxie
Rolandic epilepsy, speech dyspraxia syndrome
Rare genetic epilepsy characterized by speech disorder (including a range of symptoms from dysarthria, speech dyspraxia, receptive and expressive language delay/regression and acquired aphasia to subtle impairments of conversational speech) and epilepsy (mostly focal and secondary generalized childhood-onset seizures, sometimes with aura). Mild to severe intellectual disability may also be observed.
Id765093009
StatusPrimitive
Has interpretationafwijkend
InterpretsAbility to perform functions related to communication
Pathological processproces van pathologische ontwikkeling
Finding sitestructuur van cerebrum
Occurrencecongenitaal
referentieset met complexe 'mapping' naar ICD-10
TargetG40.0
RuleTRUE
AdviceALWAYS G40.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified