glutaric acidemia type 3

Summary

DOID:0112246 - glutaric acidemia type 3

Disease Ontology 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 the SUGCT gene on chromosome 7p14.1.

Synonyms: GA3, GA III, glutaric aciduria 3, glutaric aciduria III, glutaric aciduria type 3, glutaryl-CoA oxidase deficiency

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: sugct

MIM:

MIM:231690 - GLUTARIC ACIDURIA III; GA3

MIM:231690 - GLUTARIC ACIDURIA III; GA3

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), peroxisomal disease (is_a)