Related Conditions
Adenosylcobalamin and methylcobalamin synthesis defect(child)
Adenosylcobalamin synthesis defect(child)
CMAMMA - combined malonic and methylmalonic aciduria(child)
Fatal infantile lactic acidosis co-occurrent with methylmalonic aciduria(child)
Methylmalonic acidemia due to methylmalonyl-CoA racemase deficiency(child)
Methylmalonic acidaemia TCb1R type(child)
Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with methylmalonic aciduria(child)
Acidemia(parent)
Non-amino organic acidemia AND/OR aciduria(parent)
Disorder of branched-chain amino acid metabolism(parent)
Disorder of propionate AND/OR methylmalonate metabolism(parent)
Quick Facts
- SNOMED CT
- 42393006
- UMLS CUI
- C0268583
- Fully Specified Name
- Methylmalonic acidemia (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.