3-methylglutaconic aciduria type 5
MONDO:0012435A syndrome characterized by severe early onset (before the age of three years) dilated cardiomyopathy (DCM) with conduction defects (long QT syndrome), non-progressive cerebellar ataxia, testicular dysgenesis, and 3-methylglutaconic aciduria.
Also known as: 3-methylglutaconic aciduria caused by mutation in DNAJC19, 3-methylglutaconic aciduria type 5, 3-methylglutaconic aciduria type V, DCMA, DCMA syndrome, DNAJC19 3-methylglutaconic aciduria, MGA5, MGCA5
0 clinical trials for this condition and its sub-types, 0 tagged with 3-methylglutaconic aciduria type 5 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.