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epilepsy, familial adult myoclonic, 5 | RareConnect | RareConnect.io

/epilepsy, familial adult myoclonic

/epilepsy, familial adult myoclonic, 5

epilepsy, familial adult myoclonic, 5

Rare Disease

MONDO:0014167

Also Known As

CNTN2 epilepsy, familial adult myoclonicepilepsy, familial adult myoclonic caused by mutation in CNTN2epilepsy, familial adult myoclonic, 5epilepsy, familial adult myoclonic, type 5epilepsy, myoclonic, familial adult, 5FAME5cortical myoclonic tremor with epilepsy, familial, 5epilepsy, familial ADULT myoclonic, 5

Definition

Any epilepsy, familial adult myoclonic in which the cause of the disease is a mutation in the CNTN2 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:615400 ↗

GARD

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