Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 17
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the GNAO1 gene.
- Identifiers
- MONDO:0014199 OMIM:615473
- Causal genes
- GNAO1
- Also known as
- DEE17 · developmental and epileptic encephalopathy 17 · early infantile epileptic encephalopathy caused by mutation in GNAO1 · early infantile epileptic encephalopathy-17 · EIEE17
Projects
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