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hereditaire motorische en sensorische neuropathie type 2 (aandoening)
hereditaire motorische en sensorische neuropathie type 2
HMSN 2
CMT 2
ziekte van Charcot-Marie-Tooth type 2
Charcot-Marie-Tooth disease, type II
Inherited neuronal peroneal muscular atrophy
Hereditary motor and sensory neuropathy type II
Charcot Marie Tooth disease, type 2
Peroneal muscular atrophy of neuronal type
Id398187000
StatusPrimitive
Associated morphologyatrophia
Finding sitestructuur van zenuw
referentieset met zeldzame neuromusculaire aandoeningen
DHD Diagnosethesaurus-referentieset
referentieset met complexe 'mapping' naar ICD-10
TargetG60.0
RuleTRUE
AdviceALWAYS G60.0
CorrelationSNOMED CT source code to target map code correlation not specified
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