Glycogen phosphorylase kinase deficiency, autosomal recessive

disorder

SNOMED 297252005CUI C0574105

Overview

Glycogen phosphorylase kinase deficiency, autosomal recessive is a disorder.

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

Related Conditions

Cardiac glycogen phosphorylase kinase deficiency(child)

Hepatic and muscle glycogen phosphorylase kinase deficiency(child)

Hepatic glycogen phosphorylase kinase deficiency(child)

Glycogen phosphorylase kinase deficiency(parent)

Quick Facts

SNOMED CT: 297252005
UMLS CUI: C0574105
Fully Specified Name: Glycogen phosphorylase kinase deficiency, autosomal recessive (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.