Autosomal dominant hereditary disorder	Chronic brain syndrome	Hereditary disorder of nervous system	Progressive myoclonic epilepsy
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Progressive myoclonic epilepsy type 5 (disorder)
	Progressive myoclonic epilepsy type 5
	Progressive myoclonus epilepsy type 5 PME type 5 - progressive myoclonic epilepsy type 5
	A rare genetic neurological disorder characterized by early-onset progressive ataxia associated with myoclonic seizures, generalized tonic-clonic seizures (which are often sleep-related) and normal to mild intellectual disability. Dysarthria, upward gaze palsy, sensory neuropathy, developmental delay and autistic disorder have also been associated.
	progressieve myoklonische epilepsie type 5
	progressieve myoclonusepilepsie type 5 PME type 5

Id	783055005
Status	Primitive

Clinical course

Finding site

Interprets

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	G40.3
Rule	TRUE
Advice	ALWAYS G40.3 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified