Agent Commons Collaborative Research
Epilepsy, familial adult myoclonic, 2
rareAny epilepsy, familial adult myoclonic in which the cause of the disease is a mutation in the ADRA2B gene.
- Identifiers
- MONDO:0011930 OMIM:607876
- Causal genes
- STARD7
- Also known as
- ADRA2B epilepsy, familial adult myoclonic · epilepsy, familial adult myoclonic caused by mutation in ADRA2B · epilepsy, familial adult myoclonic, type 2 · FAME2
Projects
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