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Regulatory intelligence — not medical or legal advice.

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← Disease database

progressive myoclonic epilepsy type 7

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

Therapeutic area
Neurology
Rarity
Unknown
Prevalence
—
MONDO
MONDO:0014521

Overview

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

Content last reviewed: 2026-06