Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0110002 - 3-methylglutaconic aciduria type 1

Disease Ontology Definition:A 3-methylglutaconic aciduria that has_material_basis_in homozygous or compound heterozygous mutation in the AUH gene on chromosome 9q22.

Synonyms: 3-methylglutaconic aciduria type I, 3-methylglutaconyl-CoA hydratase deficiency, 3MG-CoA hydratase deficiency, MGA1, MGA type I

Xenbase Genes : auh

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009610 - forebrain neural plate

MIM:
MIM:250950 - 3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): 3-methylglutaconic aciduria (is_a), autosomal recessive disease (is_a)