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Disease Ontology Browser
3-methylglutaconic aciduria type 1 (DOID:0110002)
Alliance: disease page
Synonyms: 3-methylglutaconic aciduria type I; 3-methylglutaconyl-CoA hydratase deficiency; 3MG-CoA hydratase deficiency; MGA1; MGA type I
Alt IDs: OMIM:250950, MESH:C562801, ORDO:67046
Definition: A 3-methylglutaconic aciduria that has_material_basis_in homozygous or compound heterozygous mutation in the AUH gene on chromosome 9q22.


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
11/21/2023
MGI 6.22
The Jackson Laboratory