About   Help   FAQ
Disease Ontology Browser
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome (DOID:0110001)
Alliance: disease page
Synonyms: 3-methylglutaconic aciduria type 6; MEGDEL; MEGDEL syndrome; MGCA6
Alt IDs: OMIM:614739, ORDO:352328
Definition: A 3-methylglutaconic aciduria that has_material_basis_in homozygous or compound heterozygous mutation in the SERAC1 gene on chromosome 6q25.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
02/04/2020
MGI 6.14
The Jackson Laboratory