Overview
Disorder of fatty acid metabolism is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Combined deficiency of long chain 3-hydroxyacyl-CoA dehydrogenase and enoyl-CoA hydratase(child)
Succinyl-CoA acetoacetate transferase deficiency(child)
Malonic aciduria(child)
Glutaric aciduria, type 2(child)
Phytanic acid storage disease(child)
Carnitine palmitoyltransferase deficiency(child)
Long-chain fatty acid transport deficiency(child)
Deficiency of carnitine acetyltransferase(child)
Deficiency of 2,4-dienoyl-CoA reductase(child)
Carnitine deficiency due to inborn error of metabolism(child)
3-hydroxy-3-methylglutaryl-coenzyme A synthase deficiency(child)
Fatty acid oxidation defect(child)
CMAMMA - combined malonic and methylmalonic aciduria(child)
Inborn error of metabolism(parent)
Disorder of organic acid metabolism(parent)
Disorder of lipoprotein AND/OR lipid metabolism(parent)
Quick Facts
- SNOMED CT
- 39929009
- UMLS CUI
- C0268634
- Fully Specified Name
- Disorder of fatty acid metabolism (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.