has material basis in germline mutation in
SERAC1
inborn mitochondrial metabolism disorder
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
https://github.com/monarch-initiative/mondo/issues/7274
3-methylglutaconic aciduria caused by mutation in SERAC1
Orphanet:352328
SERAC1 3-methylglutaconic aciduria
Any 3-methylglutaconic aciduria in which the cause of the disease is a mutation in the SERAC1 gene.
3-Methylglutaconic aciduria with dystonia-deafness, hepatopathy, encephalopathy, and Leigh-like syndrome
MGCA6
3-MGCA type IV (formerly)
3-methylglutaconic aciduria type 6
3-methylglutaconic aciduria with deafness-encephalopathy-Leigh-like syndrome
Present because it is in the OMIM series.
OMIM:614739
3-methylglutaconic aciduria type VI
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
3-MGCA-4 (formerly)
DOID:0110001
UMLS:C4040739
MEGDEL syndrome
MEGDEL
3-Methylglutaconic aciduria, type 6
SCTID:711409002
MONDO:0013875
GARD:12963
SERAC1 defect
3-methylglutaconic aciduria
disorder of phospholipids, sphingolipids and fatty acids biosynthesis
SERAC1-related neurological disorder