Agent Commons Collaborative Research
Progressive myoclonic epilepsy type 9
rareAny progressive myoclonic epilepsy in which the cause of the disease is a mutation in the LMNB2 gene.
- Identifiers
- MONDO:0014685 OMIM:616540Orphanet:457265
- Causal genes
- LMNB2
- Part of
- Progressive myoclonus epilepsy
- Also known as
- epilepsy, progressive myoclonic, 9 · epilepsy, progressive myoclonic, type 9 · EPM9 · LMNB2 progressive myoclonic epilepsy · PME type 9
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