| familiaire congenitale spiegelbewegingen (aandoening) | | familiaire congenitale spiegelbewegingen | | familiaire congenitale contralaterale synkinesie
| | Familial congenital mirror movements | | Familial congenital controlateral synkinesia
Hereditary congenital mirror movements
Hereditary congenital controlateral synkinesia
Isolated congenital controlateral synkinesia
Isolated congenital mirror movements
| | A rare genetic movement disorder with characteristics of involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities. |
| | Id | 784348007 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | G25.8 | | Term | Overige gespecificeerde extrapiramidale aandoeningen en aandoeningen met abnormale bewegingen |
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| SNOMED CT to Orphanet simple map | 238722 |
| SNOMED CT to ICD-10 extended map | | Target | G25.8 | | Rule | TRUE | | Advice | ALWAYS G25.8 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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