Glycogen synthase deficiency

disorder

SNOMED 237964009CUI C0342748

Overview

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

Related Conditions

Hepatic glycogen synthase deficiency(child)

Glycogen storage disease(parent)

Disease of skeletal muscle(parent)

Digestive system hereditary disorder(parent)

Hepatopathy(parent)

Hereditary disorder of musculoskeletal system(parent)

Disorder of digestive system specific to fetus OR newborn(parent)

Quick Facts

SNOMED CT: 237964009
UMLS CUI: C0342748
Fully Specified Name: Glycogen synthase deficiency (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.