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.