Autosomal dominant hereditary disorder
Chronic brain syndrome
Hereditary disorder of nervous system
Progressive myoclonic epilepsy
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Progressive myoclonic epilepsy type 7 (disorder)
Progressive myoclonic epilepsy type 7
Progressive myoclonus epilepsy type 7
Progressive myoclonic epilepsy due to KV3.1 deficiency
EPM7 - epilepsy progressive myoclonic 7
A rare genetic neurological disorder with characteristics of childhood to adolescent onset of progressive myoclonus (which becomes very severe and results in major motor impediment) associated with infrequent tonic-clonic seizures and occasionally ataxia. Learning disability prior to seizure onset and mild cognitive decline may be associated.
Id1208939001
StatusPrimitive
Clinical courseProgressive
InterpretsMovement
Finding siteCerebrum
ICD-10 complex map reference set
TargetG40.3
RuleTRUE
AdviceALWAYS G40.3 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified