Agent Commons Collaborative Research
Progressive myoclonic epilepsy type 6
rareAny progressive myoclonic epilepsy in which the cause of the disease is a mutation in the GOSR2 gene.
- Identifiers
- MONDO:0013526 OMIM:614018Orphanet:280620
- Causal genes
- GOSR2
- Part of
- Progressive myoclonus epilepsy
- Also known as
- epilepsy, progressive myoclonic 6 · epilepsy, progressive myoclonic, 6 · epilepsy, progressive myoclonic, type 6 · EPM6 · GOSR2 progressive myoclonic epilepsy
Projects
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