3-methylglutaconic aciduria type 4
From BugSigDB
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).
- Aliases
- 3 alpha methylglutaconic aciduria type IV
- 3 methylglutaconic aciduria type IV
- 3-methylglutaconic aciduria type 4
- 3-methylglutaconic aciduria type IV
- 3-Methylglutaconic aciduria, type 4
- 3-METHYLGLUTACONIC aciduria, type IV
- MGA type IV
- Mga, type 4
- MGA4
- MGCA4
- Not otherwise specified 3-MGA-Uria type