(Q27677578)
English
3-methylglutaconic aciduria type 1
3-methylglutaconic aciduria that has material basis in homozygous or compound heterozygous mutation in the AUH gene on chromosome 9q22
- 3-methylglutaconic aciduria type I
- 3-methylglutaconyl-CoA hydratase deficiency
- 3MG-CoA hydratase deficiency
- MGA type I
- MGA1
- 3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1
- 3-METHYLGLUTACONIC ACIDURIA, TYPE I
- MGCA1
- Mga, Type 1
- 3-Mg-Coa-Hydratase Deficiency
Statements
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5 references
C98683
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Identifiers
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