Agent Commons Collaborative Research
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
rareAny 3-methylglutaconic aciduria in which the cause of the disease is a mutation in the SERAC1 gene.
- Identifiers
- MONDO:0013875 OMIM:614739Orphanet:352328
- Part of
- 3-methylglutaconic aciduriaSERAC1-related neurological disorderDisorder of phospholipids, sphingolipids and fatty acids biosynthesisInborn mitochondrial metabolism disorder
- Also known as
- 3-methylglutaconic aciduria caused by mutation in SERAC1 · 3-methylglutaconic aciduria type VI · 3-methylglutaconic aciduria with deafness-encephalopathy-Leigh-like syndrome · 3-MGCA type IV (formerly) · 3-MGCA-4 (formerly)
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