3-methylglutaconic aciduria (3-MGA) type IV, or unclassified 3-MGA, is a clinically heterogeneous disorder characterized by increased 3-methylglutaconic acid excretion in individuals that cannot be classified as having one of the other forms of 3-MGA (3-MGA I, II or III).
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3-methylglutaconic aciduria type 1
MONDO:0009610
3-methylglutaconic aciduria type 3
MONDO:0009787
Barth syndrome
MONDO:0010543
3-methylglutaconic aciduria type 5
MONDO:0012435
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
MONDO:0013875
3-methylglutaconic aciduria, type VIIB
MONDO:0014561