Overview
Progressive myoclonic epilepsy is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Unverricht-Lundborg syndrome(child)
Lafora disease(child)
PRICKLE1-related progressive myoclonic epilepsy with ataxia(child)
Jankovic-Rivera syndrome(child)
Early-onset Lafora body disease(child)
Progressive myoclonus epilepsy with dystonia(child)
AMRF - action myoclonus renal failure(child)
AFG3L2 (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome(child)
Progressive myoclonic epilepsy type 8(child)
Progressive myoclonic epilepsy due to KCTD7 deficiency(child)
Progressive myoclonic epilepsy type 6(child)
Progressive myoclonus epilepsy type 5(child)
Progressive myoclonus epilepsy type 7(child)
Progressive myoclonic epilepsy type 9(child)
Epilepsy syndrome with progressive neurological deterioration(parent)
Quick Facts
- SNOMED CT
- 267581004
- UMLS CUI
- C0751778
- Fully Specified Name
- Progressive myoclonic epilepsy (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.