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

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Broader categories

Disease (717) Metabolic disease (241) Hereditary disease (188) Inborn errors of metabolism (47) Human disease (15) Inborn disorder of amino acid metabolism (6) Inborn organic aciduria (5) Amino acid metabolism disease (2) Disease of genetic or genomic mechanism (2) 3-methylglutaconic aciduria (0)

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