3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
MONDO:0013875Any 3-methylglutaconic aciduria in which the cause of the disease is a mutation in the SERAC1 gene.
Also known as: 3-methylglutaconic aciduria caused by mutation in SERAC1, 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome, 3-methylglutaconic aciduria with deafness-encephalopathy-Leigh-like syndrome, MEGDEL, MEGDEL syndrome, MGCA6, SERAC1 3-methylglutaconic aciduria, 3-MGCA type IV (formerly)
13 clinical trials for this condition and its sub-types.
Follow this condition to get notified about new trialsBroader categories
Disease
(717)
Nervous system disorder
(243)
Metabolic disease
(241)
Inherited lipid metabolism disorder
(199)
Hereditary disease
(188)
Inborn mitochondrial metabolism disorder
(59)
Inborn errors of metabolism
(47)
Mitochondrial disease
(40)
Human disease
(15)
Developmental defect during embryogenesis
(8)