Glucose transporter protein type 1 deficiency syndrome

disorder

SNOMED 445252005CUI C2919264

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Metabolic encephalopathy(parent)

Hereditary disorder of nervous system(parent)

Autosomal dominant hereditary disorder(parent)

Quick Facts

SNOMED CT: 445252005
UMLS CUI: C2919264
Fully Specified Name: Glucose transporter protein type 1 deficiency syndrome (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.