3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome (Q27677577)
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3-methylglutaconic aciduria that has material basis in homozygous or compound heterozygous mutation in the SERAC1 gene on chromosome 6q25
- 3-methylglutaconic aciduria type 6
- MEGDEL
- MEGDEL syndrome
- MGCA6
- 3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL
- 3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME
- 3-Methylglutaconic Aciduria, Type 6
- 3-methylglutaconic aciduria with deafness-encephalopathy-Leigh-like syndrome
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome |
3-methylglutaconic aciduria that has material basis in homozygous or compound heterozygous mutation in the SERAC1 gene on chromosome 6q25 |
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