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3-methylglutaconic aciduria type 4
rare3-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).
- Identifiers
- MONDO:0009611 OMIM:250951Orphanet:67048
- Part of
- 3-methylglutaconic aciduria
- Also known as
- 3 alpha methylglutaconic aciduria type IV · 3 methylglutaconic aciduria type IV · 3-METHYLGLUTACONIC aciduria, type IV · MGA4 · MGCA4
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