early infantile epileptic encephalopathy 39 (Q60195347)
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infantile epileptic encephalopathy that has material basis in mutation in the SLC25A12 gene on chromosome 2q31
- epileptic encephalopathy with global cerebral demyelination
- AGC1 deficiency
- mitochondrial aspartate-glutamate carrier 1 deficiency
- obsolete early infantile epileptic encephalopathy 39
- DEE39
- EIEE39
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | early infantile epileptic encephalopathy 39 |
infantile epileptic encephalopathy that has material basis in mutation in the SLC25A12 gene on chromosome 2q31 |
|
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