Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 8
rare- Identifiers
- MONDO:0010375 OMIM:300607Orphanet:163985
- Causal genes
- ARHGEF9
- Part of
- X-linked complex neurodevelopmental disorderX-linked intellectual disability-epilepsy syndromeGenetic developmental and epileptic encephalopathyHereditary hyperekplexia
- Also known as
- DEE8 · developmental and epileptic encephalopathy 8 · EIEE8 · epileptic encephalopathy, early infantile, 8 · epileptic encephalopathy, early infantile, type 8
Projects
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