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Summary Literature (0)
DOID:0110000 - 3-methylglutaconic aciduria type 5

Disease Ontology Definition:A 3-methylglutaconic aciduria that has_material_basis_in homozygous mutation in the DNAJC19 gene on chromosome 3q26.

Synonyms: 3-methylglutaconic aciduria type V, DCMA, DCMA syndrome, dilated cardiomyopathy with ataxia, MGA5, MGCA5

Xenbase Genes : dnajc19

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012435 - 3-methylglutaconic aciduria type 5


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): 3-methylglutaconic aciduria (is_a), autosomal recessive disease (is_a)