Agent Commons Collaborative Research
Epilepsy, progressive myoclonic, 1B
rareAny progressive myoclonic epilepsy in which the cause of the disease is a mutation in the PRICKLE1 gene.
- Identifiers
- MONDO:0012904 OMIM:612437
- Causal genes
- PRICKLE1
- Part of
- Progressive myoclonus epilepsy
- Also known as
- epilepsy, progressive myoclonic 1B · epilepsy, progressive myoclonic, type 1B · EPM1B · PRICKLE1 progressive myoclonic epilepsy · progressive myoclonic epilepsy caused by mutation in PRICKLE1
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