3-methylglutaconic aciduria type 4

MONDO:0009611

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).

Also known as: MGA4, MGCA4, 3 alpha methylglutaconic aciduria type IV, 3 methylglutaconic aciduria type IV, 3-METHYLGLUTACONIC aciduria, type IV, 3-Methylglutaconic aciduria, type 4, Mga, type 4, Not otherwise specified 3-MGA-Uria type

0 clinical trials for this condition and its sub-types, 0 tagged with 3-methylglutaconic aciduria type 4 itself.

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Including sub-types (0) Tagged with 3-methylglutaconic aciduria type 4 (0)

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