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Disease Ontology Browser
glutaric acidemia type 3 (DOID:0112246)
Alliance: disease page
Synonyms: 'GA3'; 'GA III'; 'glutaric aciduria 3'; 'glutaric aciduria III'; 'glutaric aciduria type 3'; 'glutaryl-CoA oxidase deficiency'
Alt IDs: OMIM:231690, ORDO:35706
Definition: A peroxisomal disease characterized by isolated accumulation of glutaric acid in the absence of other clinical phenotype that has_material_basis_in homozygous or compound heterozygous mutation in SUGCT on chromosome 7p14.1.

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)
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last database update
06/23/2022
MGI 6.20
The Jackson Laboratory