Autosomal dominant Charcot-Marie-Tooth disease type 2
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Autosomal dominant Charcot-Marie-Tooth disease type 2G (disorder)
Autosomal dominant Charcot-Marie-Tooth disease type 2G
A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy with onset associated with development of foot deformity and walking difficulties between the first and the eighth decades. Weakness and sensory loss involve primarily the legs and ankles, tendon reflexes are reduced. The disease has a slowly progressive course.
autosomaal dominante hereditaire motorische en sensorische neuropathie type 2G
autosomaal dominante CMT 2G
autosomaal dominante HMSN 2G
autosomaal dominante ziekte van Charcot-Marie-Tooth type 2G
Id719511005
StatusPrimitive
Finding sitePeripheral nervous system structure
Associated morphologyAtrophy
Finding siteNerve structure
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetG60.0
RuleTRUE
AdviceALWAYS G60.0
CorrelationSNOMED CT source code to target map code correlation not specified