autosomaal dominante motorische en sensorische neuropathie type 2
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autosomaal dominante hereditaire motorische en sensorische neuropathie type 2A1 (aandoening)
autosomaal dominante hereditaire motorische en sensorische neuropathie type 2A1
autosomaal dominante CMT 2A1
autosomaal dominante HMSN 2A1
autosomaal dominante ziekte van Charcot-Marie-Tooth type 2A1
Autosomal dominant Charcot-Marie-Tooth disease type 2A1
A form of axonal Charcot-Marie-Tooth disease a peripheral sensorimotor neuropathy. Presents with a more prominent muscle weakness in lower than upper limbs and frequent postural tremor.
Id717016001
StatusPrimitive
Finding sitestructuur van perifeer zenuwstelsel
Associated morphologyatrophia
Finding sitestructuur van zenuw
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 map99946
SNOMED CT to ICD-10 extended map
TargetG60.0
RuleTRUE
AdviceALWAYS G60.0
CorrelationSNOMED CT source code to target map code correlation not specified