Autosomal dominant Charcot-Marie-Tooth disease type 2
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Autosomal dominant Charcot-Marie-Tooth disease type 2DD (disorder)
Autosomal dominant Charcot-Marie-Tooth disease type 2DD
ATP1A1 (ATPase Na+/K+ transporting subunit alpha 1) related autosomal dominant Charcot-Marie-Tooth disease type 2
ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 2
autosomaal dominante motorische en sensorische neuropathie type 2DD
ATP1A1-gerelateerde autosomaal dominante ziekte van Charcot-Marie-Tooth type 2
'ATPase Na+/K+ transporting subunit alpha 1'-gerelateerde ziekte van Charcot-Marie-Tooth type 2
autosomaal dominante HMSN 2DD
autosomaal dominante CMT 2DD
Id1187620007
StatusPrimitive
Finding sitePeripheral nervous system structure
Associated morphologyAtrophy
Finding siteNerve structure
ICD-10 complex map reference set
TargetG60.0
RuleTRUE
AdviceALWAYS G60.0
CorrelationSNOMED CT source code to target map code correlation not specified