Overview
Metabolic myopathy is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Lipid storage myopathy(child)
Familial periodic paralysis(child)
Chronic myopathy with hypocalcaemia and hypophosphataemia(child)
Nutritional myopathy(child)
Endocrine myopathy(child)
Muscle AMP deaminase deficiency(child)
Luft's hypermetabolic myopathy(child)
Glycogen storage disease, muscular form(child)
Mitochondrial myopathy(child)
Myopathy co-occurrent and due to hypercalcemia(child)
Metabolic myopathy due to lactate transporter defect(child)
PGBM1 - polyglucosan body myopathy type 1(child)
Muscle and heart glycogen synthase deficiency(child)
Polyglucosan body myopathy type 2(child)
Disease of skeletal muscle(parent)
Quick Facts
- SNOMED CT
- 26111005
- UMLS CUI
- C0270984
- Fully Specified Name
- Metabolic myopathy (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.