Myoclonus, myoclonic, myoclonia (familial) (essential) (multifocal) (simplex) - in the ICD-10-CM Index

Browse the ICD-10-CM codes with references applicable to the clinical term "myoclonus, myoclonic, myoclonia (familial) (essential) (multifocal) (simplex)"

• Myoclonus, myoclonic, myoclonia (familial) (essential) (multifocal) (simplex) - G25.3 Myoclonus

  • drug-induced - G25.3 Myoclonus

  • epilepsy - See Also: Epilepsy, generalized, specified NEC; - G40.4 Other generalized epilepsy and epileptic syndromes

    • familial (progressive) - See: Epilepsy, myoclonus;

    • Lafora - See: Epilepsy, myoclonus, progressive, Lafora;

  • epileptica - See Also: Epilepsy, myoclonus; - G40.409 Other generalized epilepsy and epileptic syndromes, not intractable, without status epilepticus

    • with status epilepticus - G40.401 Other generalized epilepsy and epileptic syndromes, not intractable, with status epilepticus

  • facial - G51.3 Clonic hemifacial spasm

  • familial progressive - G25.3 Myoclonus

    • epilepsy - See: Epilepsy, myoclonus, progressive;

  • Friedreich's - G25.3 Myoclonus

  • jerks - G25.3 Myoclonus

  • massive - G25.3 Myoclonus

  • palatal - G25.3 Myoclonus

  • pharyngeal - G25.3 Myoclonus

Epilepsy: A disorder characterized by recurrent episodes of paroxysmal brain dysfunction due to a sudden, disorderly, and excessive neuronal discharge. Epilepsy classification systems are generally based upon: (1) clinical features of the seizure episodes (e.g., motor seizure), (2) etiology (e.g., post-traumatic), (3) anatomic site of seizure origin (e.g., frontal lobe seizure), (4) tendency to spread to other structures in the brain, and (5) temporal patterns (e.g., nocturnal epilepsy). (From Adams et al., Principles of Neurology, 6th ed, p313)