3-methylglutaconic aciduria type 4

Definition

3-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).

Also known as MGA4, MGCA4 — per MONDO

Also identified as

• DOID 0110006 per MONDO
• MESH C565393 per MONDO
• OMIM 250951 per MONDO
• Orphanet 67048 per MONDO
• SCTID 297233004 per MONDO
• UMLS C1855126 per MONDO