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Autosomal dominant slowed nerve conduction velocity (disorder)
Autosomal dominant slowed nerve conduction velocity
A hereditary demyelinating motor and sensory neuropathy with characteristics of slowed nerve conduction velocities in the absence of clinically apparent neurological deficits, gait abnormalities or muscular atrophy, associated with a germline mutation in the ARGHEF10 gene.
autosomaal dominante vertraagde zenuwgeleiding
Id764854006
StatusPrimitive
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