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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 characterized by 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.
Id778003000
StatusPrimitive
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetG60.0
TermHereditaire motorische en sensorische neuropathie
SNOMED CT to Orphanet simple map324585
SNOMED CT to ICD-10 extended map
TargetG60.0
RuleTRUE
AdviceALWAYS G60.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified