| 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. |
| | Id | 765093009 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | G40.0 | | Term | Lokalisatiegebonden (focale)(partiële) idiopathische epilepsie en epileptische syndromen met aanvallen van lokale oorsprong |
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| SNOMED CT to Orphanet simple map | 163721 |
| SNOMED CT to ICD-10 extended map | | Target | G40.0 | | Rule | TRUE | | Advice | ALWAYS G40.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
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