Related Conditions
Neonatal hypermethioninemia(child)
Hepatic methionine adenosyltransferase deficiency(child)
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency(child)
Hypermethioninemia due to deficiency of glycine N-methyltransferase(child)
Hypermethioninemia encephalopathy due to deficiency of adenosine kinase(child)
Disorder of sulphur-bearing amino acid metabolism(parent)
Quick Facts
- SNOMED CT
- 43123004
- UMLS CUI
- C4048705
- Fully Specified Name
- Hypermethioninemia (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.