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GTR Home > Conditions/Phenotypes > Epilepsy, idiopathic generalized, susceptibility to, 11

Epilepsy, idiopathic generalized, susceptibility to, 11

Synonyms
CLCN2-Related Juvenile Myoclonic Epilepsy

Summary

Both juvenile myoclonic epilepsy and juvenile absence epilepsy are subtypes of idiopathic generalized epilepsy (EIG). For a general phenotypic description and a discussion of genetic heterogeneity of these disorders, see EIG1 (600669), EJM1 (254770), and EJA1 (607631). [from OMIM]

Available tests

30 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (30 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CIC-2, CLC2, ECA2, ECA3, EGI11, EGI3, EGMA, EJM6, EJM8, FHA2, FHII, HALD2, LKPAT, clC-2, CLCN2
    Summary: chloride voltage-gated channel 2

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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