Overview
3-Methylglutaconic aciduria is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
3-Methylglutaconic aciduria type 1(child)
3-Methylglutaconic aciduria type 2(child)
Costeff syndrome(child)
3-Methylglutaconic aciduria type 4(child)
Unclassified 3-methylglutaconic aciduria(child)
Dilated cardiomyopathy with ataxia syndrome(child)
MGA7 - 3-methylglutaconic aciduria type 7(child)
3-methylglutaconic aciduria type 8(child)
3-methylglutaconic aciduria, epilepsy, spasticity, severe intellectual disability syndrome(child)
Disorder of branched-chain amino acid metabolism(parent)
Quick Facts
- SNOMED CT
- 237950009
- UMLS CUI
- C3696376
- Fully Specified Name
- 3-Methylglutaconic aciduria (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.