Term Name: 3-methylglutaconic aciduria type 5
Synonyms: 3-methylglutaconic aciduria type V, DCMA, DCMA syndrome, dilated cardiomyopathy with ataxia, MGA5, MGCA5
Definition: A 3-methylglutaconic aciduria that has_material_basis_in homozygous mutation in the DNAJC19 gene on chromosome 3q26.
Ontology: Human Disease [DOID:0110000]   ( DOID:0110000 )

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