| syndroom van Morvan (aandoening) | | syndroom van Morvan | | Morvan-syndroom
syndroom van limbische encefalitis, neuromyotonie, hyperhidrose, polyneuropathie
| | Morvan syndrome | | Limbic encephalitis, neuromyotonia, hyperhidrosis, polyneuropathy syndrome
Morvan fibrillary chorea
| | A rare life threatening acquired neurologic disease with characteristics of neuromyotonia, dysautonomia and encephalopathy with severe insomnia. Signs involving central (e.g. hallucinations, confusion, amnesia, myoclonus), autonomic (e.g. variations in blood pressure, hyperhidrosis) and peripheral (e.g. painful cramps, myokymia) hyperactivity, as well as systemic manifestations (such as weight loss, pruritus, fever), are reported. Thymoma is present in some cases. |
| | Id | 763803004 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | G60.8 | | Term | Overige gespecificeerde hereditaire en idiopathische neuropathieën |
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| SNOMED CT to Orphanet simple map | 83467 |
| SNOMED CT to ICD-10 extended map | | Target | G60.8 | | Rule | TRUE | | Advice | ALWAYS G60.8 | 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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