3-methylglutaconic aciduria type 4

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Synonyms: MGA4

3-methylglutaconic aciduria (3-MGA) type IV or unclassified 3-MGA is a clinically heterogeneous disorder characterised 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).

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version June 2024

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3-methylglutaconic aciduria type 4?

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Clinical Trials

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