Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Inborn mitochondrial metabolism disorder · Disorder of phospholipids, sphingolipids and fatty acids biosynthesis · 3-methylglutaconic aciduria · SERAC1-related neurological disorder
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
Any 3-methylglutaconic aciduria in which the cause of the disease is a mutation in the SERAC1 gene.
This condition has no sub-types.