| syndroom van rolandische epilepsie, paroxismale inspanningsgeïnduceerde dystonie en schrijverskramp (aandoening) | | syndroom van rolandische epilepsie, paroxismale inspanningsgeïnduceerde dystonie en schrijverskramp | | syndroom van rolandische epilepsie, paroxismale dystonie door inspanning en schrijverskramp
| | Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome | | A rare genetic epilepsy syndrome characterized by infantile or childhood onset of focal motor seizures remitting with age, as well as childhood onset of exercise-induced dystonia which often persists into adulthood. Additional reported features include nystagmus and postural tremor of the hands. |
| | Id | 1231737000 | | Status | Primitive |
| SNOMED CT to Orphanet simple map | 163727 |
| SNOMED CT to ICD-10 extended map | | Target | G40.4 | | Rule | TRUE | | Advice | ALWAYS G40.4 | 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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