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progressive myoclonic epilepsy type 9 | RareConnect | RareConnect.io

/progressive myoclonus epilepsy

/progressive myoclonic epilepsy type 9

progressive myoclonic epilepsy type 9

Rare Disease

MONDO:0014685

Also Known As

EPM9LMNB2 progressive myoclonic epilepsyPME type 9epilepsy, progressive myoclonic, type 9progressive myoclonic epilepsy caused by mutation in LMNB2progressive myoclonic epilepsy due to LMNB2 deficiencyprogressive myoclonus epilepsy type 9epilepsy, progressive myoclonic, 9

Definition

Any progressive myoclonic epilepsy in which the cause of the disease is a mutation in the LMNB2 gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:616540 ↗

Orphanet

Orphanet:457265 ↗

GARD

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