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.

Disease References using Mouse Models (1)

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, and Privacy Statement
Send questions and comments to User Support.
last database update
01/17/2023
MGI 6.22
The Jackson Laboratory