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autosomaal dominant overervende ziekte van Parkinson met late debuutleeftijd (aandoening)
autosomaal dominant overervende ziekte van Parkinson met late debuutleeftijd
autosomaal dominant overervende laat beginnende ziekte van Parkinson
Autosomal dominant late onset Parkinson disease
Hereditary late onset Parkinson disease
A form of Parkinson disease with age of onset of more than 50 years, tremor at rest, gait complaints and falls, bradykinesia, rigidity and painful cramps. Patients usually present a low risk of developing non-motor symptoms, dystonia, dyskinesia and levodopa-induced dyskinesia. The exact etiology is still unknown but mutations in the genes SNCA (4q21.3-q22), LRRK2 (12q12), and VPS35 (16q12) have been implicated in its pathogenesis. Transmission is autosomal dominant.
Id716662004
StatusPrimitive
referentieset met complexe 'mapping' naar ICD-10
TargetG20
RuleTRUE
AdviceALWAYS G20
CorrelationSNOMED CT source code to target map code correlation not specified