3-methylglutaconic aciduria type 1 (Q27677578)
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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
| Language | Label | Description | Also known as |
|---|---|---|---|
| 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 |
|
Statements
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C98683
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Identifiers
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