| autosomaal dominante intermediaire hereditaire motorische en sensorische neuropathie met neuropathische pijn (aandoening) | | autosomaal dominante intermediaire hereditaire motorische en sensorische neuropathie met neuropathische pijn | | autosomaal dominante intermediaire ziekte van Charcot-Marie-Tooth met neuropathische pijn
| | Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain | | A rare subtype of autosomal dominant intermediate Charcot-Marie-Tooth disease with characteristics of debilitating neuropathic pain associated with mild distal symmetrical lower limb sensory loss and mild or absent motor dysfunction. Patients typically manifest with burning, aching, shooting or throbbing pain and intermittent paresthesia in toes, heels and ankles. |
| | Id | 778003000 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | G60.0 | | Term | Hereditaire motorische en sensorische neuropathie |
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| SNOMED CT to Orphanet simple map | 324585 |
| SNOMED CT to ICD-10 extended map | | Target | G60.0 | | Rule | TRUE | | Advice | ALWAYS G60.0 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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