Autosomal dominant Charcot-Marie-Tooth disease type 2
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Autosomal dominant Charcot-Marie-Tooth disease type 2N (disorder)
Autosomal dominant Charcot-Marie-Tooth disease type 2N
A mild form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, with characteristics of distal legs sensory loss and weakness that can be asymmetric. Tendon reflexes are reduced in the knees and absent in ankles. Progression is slow.
autosomaal dominante hereditaire motorische en sensorische neuropathie type 2N
autosomaal dominante HMSN 2N
autosomaal dominante ziekte van Charcot-Marie-Tooth type 2N
autosomaal dominante CMT 2N
Id719515001
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