Term Name:	3-methylglutaconic aciduria type 1
Synonyms:	3-methylglutaconic aciduria type I, 3-methylglutaconyl-CoA hydratase deficiency, 3MG-CoA hydratase deficiency, MGA type I, MGA1
Definition:	A 3-methylglutaconic aciduria that has_material_basis_in homozygous or compound heterozygous mutation in the AUH gene on chromosome 9q22.
Ontology:	Human Disease [DOID:0110002]   ( DOID:0110002 )