Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 18
rare- Identifiers
- MONDO:0014201 OMIM:615476Orphanet:369894
- Causal genes
- SZT2
- Part of
- Congenital nervous system disorderGenetic developmental and epileptic encephalopathyMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- DEE18 · developmental and epileptic encephalopathy 18 · early infantile epileptic encephalopathy without suppression burst · EIEE18 · epileptic encephalopathy, early infantile, 18
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