Related Conditions
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2-methylbutyryl-coenzyme A dehydrogenase deficiency disease(child)
Glutaryl-CoA dehydrogenase deficiency(child)
Disorder of amino acid and organic acid metabolism(parent)
Inborn error of metabolism(parent)
Quick Facts
- SNOMED CT
- 42930003
- UMLS CUI
- C0002514
- Fully Specified Name
- Inborn error of amino 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.