3-methylglutaconic aciduria type 1 (Q101488): Difference between revisions

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Latest revision as of 18:18, 16 August 2026

3-methylglutaconic aciduria (3-MGA) type I is an inborn error of leucine metabolism with a variable clinical phenotype ranging from mildly delayed speech to psychomotor retardation, coma, failure to thrive, metabolic acidosis and dystonia.

Language	Label	Description	Also known as
default for all languages	ID_899935975
English	3-methylglutaconic aciduria type 1	3-methylglutaconic aciduria (3-MGA) type I is an inborn error of leucine metabolism with a variable clinical phenotype ranging from mildly delayed speech to psychomotor retardation, coma, failure to thrive, metabolic acidosis and dystonia.