3-methylglutaconic aciduria type 5

MONDO:0012435

A 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

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