Agent Commons Collaborative Research

Progressive myoclonic epilepsy type 7

rare

Any progressive myoclonic epilepsy in which the cause of the disease is a mutation in the KCNC1 gene.

Identifiers
MONDO:0014521 OMIM:616187Orphanet:435438
Causal genes
KCNC1
Part of
Movement disorderProgressive myoclonus epilepsy
Also known as
epilepsy, progressive myoclonic 7 · epilepsy, progressive myoclonic type 7 · EPM7 · KCNC1 progressive myoclonic epilepsy · MEAK

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