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Progressive myoclonic epilepsy type 8

MONDO:0014545

Any progressive myoclonic epilepsy in which the cause of the disease is a mutation in the CERS1 gene.

Also known as: CERS1 progressive myoclonic epilepsy, EPM8, PME type 8, epilepsy, progressive myoclonic, type 8, progressive myoclonic epilepsy caused by mutation in CERS1, progressive myoclonic epilepsy due to CERS1 deficiency, progressive myoclonus epilepsy type 8, epilepsy, progressive myoclonic, 8

7 clinical trials for this condition and its sub-types, 0 tagged with Progressive myoclonic epilepsy type 8 itself.

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↑ Disorder of phospholipids, sphingolipids and fatty acids biosynthesis (15) ↑ Progressive myoclonus epilepsy (12)

Including sub-types (7) Tagged with Progressive myoclonic epilepsy type 8 (0)

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