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's subclass of is recorded as neonatal epilepsy syndrome^[5].
• epileptic encephalopathy with global cerebral demyelination's subclass of is recorded as mitochondrial substrate carrier disorder^[6].
• epileptic encephalopathy with global cerebral demyelination's subclass of is recorded as rare genetic developmental defect during embryogenesis^[7].
• epileptic encephalopathy with global cerebral demyelination's MeSH descriptor ID is recorded as C567847^[8].
• epileptic encephalopathy with global cerebral demyelination's OMIM ID is recorded as 612949^[9].
• epileptic encephalopathy with global cerebral demyelination's KEGG ID is recorded as H01305^[10].
• epileptic encephalopathy with global cerebral demyelination's Orphanet ID is recorded as 353217^[11].
• epileptic encephalopathy with global cerebral demyelination's genetic association is recorded as SLC25A12^[12].
• epileptic encephalopathy with global cerebral demyelination's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_353217^[13].
• epileptic encephalopathy with global cerebral demyelination's UMLS CUI is recorded as C2751855^[14].
• epileptic encephalopathy with global cerebral demyelination's ICD-10-CM is recorded as G31.8^[15].
• epileptic encephalopathy with global cerebral demyelination's Mondo ID is recorded as MONDO_0013056^[16].