Progressive myoclonus epilepsy type 5

disorder

SNOMED 783055005CUI C5190799

Overview

Progressive myoclonus epilepsy type 5 is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Autosomal dominant hereditary disorder(parent)

Chronic brain syndrome(parent)

Progressive myoclonic epilepsy(parent)

Hereditary disorder of nervous system(parent)

Quick Facts

SNOMED CT: 783055005
UMLS CUI: C5190799
Fully Specified Name: Progressive myoclonic epilepsy type 5 (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.