Epileptic encephalopathy with global cerebral demyelination

disorder

SNOMED 726702005CUI C4512050

Overview

Epileptic encephalopathy with global cerebral demyelination is a disorder.

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

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Mitochondrial cytopathy(parent)

Hereditary disorder of nervous system(parent)

Congenital anomaly of cerebrum(parent)

Developmental hereditary disorder(parent)

DEE - developmental and epileptic encephalopathy(parent)

Quick Facts

SNOMED CT: 726702005
UMLS CUI: C4512050
Fully Specified Name: Epileptic encephalopathy with global cerebral demyelination (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.