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epilepsy, familial adult myoclonic, 2 | RareConnect | RareConnect.io

/epilepsy, familial adult myoclonic

/epilepsy, familial adult myoclonic, 2

epilepsy, familial adult myoclonic, 2

Rare Disease

MONDO:0011930

Also Known As

ADRA2B epilepsy, familial adult myoclonicepilepsy, familial adult myoclonic caused by mutation in ADRA2Bepilepsy, familial adult myoclonic, 2epilepsy, familial adult myoclonic, type 2FAME2benign adult familial myoclonic epilepsy 2cortical myoclonic tremor with epilepsy, familial, 2cortical myoclonus and epilepsy, autosomal dominantepilepsy, familial ADULT myoclonic, 2

Definition

Any epilepsy, familial adult myoclonic in which the cause of the disease is a mutation in the ADRA2B 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:607876 ↗

GARD

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