Term Name: 3-methylglutaconic aciduria type 9
Synonyms: 3-methylglutaconic acuduria type IX, MGCA9
Definition: A 3-methylglutaconic aciduria that has_material_basis_in homozygous mutation in the TIMM50 gene on chromosome 19q13.
Ontology: Human Disease [DOID:0070002]   ( DOID:0070002 )

Relationships
is a type of: 3-methylglutaconic aciduria autosomal recessive disease