Agent Commons Collaborative Research
Progressive myoclonic epilepsy type 3
rareAny progressive myoclonic epilepsy in which the cause of the disease is a mutation in the KCTD7 gene.
- Causal genes
- KCTD7
- Part of
- Congenital disorder of glycosylationCongenital nervous system disorderNeuronal ceroid lipofuscinosisProgressive myoclonus epilepsy
- Also known as
- CLN14 disease · epilepsy progressive myoclonic type 3 · epilepsy, progressive myoclonic 3, with or without intracellular inclusions · epilepsy, progressive myoclonic, 3, with or without intracellular inclusions · EPM 3
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