EPM3KCTD7 progressive myoclonic epilepsyPME type 3epilepsy, progressive myoclonic 3, with or without intracellular inclusionsprogressive myoclonic epilepsy caused by mutation in KCTD7progressive myoclonic epilepsy due to KCTD7 deficiencyprogressive myoclonic epilepsy type 3progressive myoclonus epilepsy type 3EPM 3ceroid lipofuscinosis, neuronal, 14epilepsy progressive myoclonic type 3epilepsy, progressive myoclonic, 3, with or without intracellular inclusionsprogressive myoclonic epilepsy 3
Definition
Any progressive myoclonic epilepsy in which the cause of the disease is a mutation in the KCTD7 gene.
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