epileptic encephalopathy with global cerebral demyelination
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epileptic encephalopathy with global cerebral demyelination
Summary
epileptic encephalopathy with global cerebral demyelination is a developmental defect during embryogenesis[1].
Key Facts
- epileptic encephalopathy with global cerebral demyelination's instance of is recorded as developmental defect during embryogenesis[2].
- epileptic encephalopathy with global cerebral demyelination's instance of is recorded as rare disease[3].
- epileptic encephalopathy with global cerebral demyelination's instance of is recorded as class of disease[4].
- epileptic encephalopathy with global cerebral demyelination is a type of neonatal epilepsy syndrome[5].
- epileptic encephalopathy with global cerebral demyelination is a type of mitochondrial substrate carrier disorder[6].
- epileptic encephalopathy with global cerebral demyelination is a type of rare genetic developmental defect during embryogenesis[7].
- epileptic encephalopathy with global cerebral demyelination's genetic association is recorded as SLC25A12[8].
- epileptic encephalopathy with global cerebral demyelination's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_353217[9].