Overview
Metabolic encephalopathy is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Hepatic encephalopathy(child)
Uremic encephalopathy(child)
Hypertensive encephalopathy(child)
Hypoglycemic encephalopathy(child)
Dialysis disequilibrium syndrome(child)
Dialysis dementia(child)
Glucose transporter protein type 1 deficiency syndrome(child)
Myxoedema encephalopathy(child)
Myxedema coma(child)
Encephalopathy due to vitamin deficiency(child)
Hyponatraemic encephalopathy(child)
Secondary amyloid encephalopathy(child)
Hypermethioninemia encephalopathy due to deficiency of adenosine kinase(child)
Progressive external ophthalmoplegia, myopathy, emaciation syndrome(child)
Progressive polyneuropathy with bilateral striatal necrosis(child)
SLC35A2-CDG - solute carrier family 35 member A2 congenital disorder of glycosylation(child)
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency(child)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency(child)
Transport and golgi organization 2 homolog-related metabolic encephalopathy, arrhythmia syndrome(child)
Encephalopathy due to mitochondrial and peroxisomal fission defect(child)
Quick Facts
- SNOMED CT
- 50122000
- UMLS CUI
- C0006112
- Fully Specified Name
- Metabolic encephalopathy (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.