has material basis in germline mutation in disease has major feature DNAJC19 Dilated cardiomyopathy 3-methylglutaconic aciduria type 5 https://rarediseases.info.nih.gov/diseases/10344/3-methylglutaconic-aciduria-type-v https://www.malacards.org/card/3_methylglutaconic_aciduria_type_v_2 OMIM:610198 NCIT:C173146 MEDGEN:347542 MGCA5 DNAJC19 3-methylglutaconic aciduria MESH:C565706 DCMA syndrome SCTID:711412004 DOID:0110000 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. 3-METHYLGLUTACONIC aciduria, type V UMLS:C1857776 3 methylglutaconic aciduria type V icd11.foundation:422277813 3-methylglutaconic aciduria type V MONDO:0012435 MGA V Orphanet:66634 DCMA 3-methylglutaconic aciduria caused by mutation in DNAJC19 3 alpha methylglutaconic aciduria type V 3-methylglutaconic aciduria type 5 GARD:0012964 MGA 5 MGA5 dilated cardiomyopathy with ataxia obsolete syndrome associated with dilated cardiomyopathy 3-methylglutaconic aciduria