3-methylglutaconic aciduria type 4
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 April 2024
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3-methylglutaconic aciduria type 4?
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