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Epilepsy, idiopathic generalized, susceptibility to, 11

MONDO:0011875

An inherited susceptibility or predisposition to developing epilepsy, idiopathic generalized, in which the cause of the disease is a mutation in the CLCN2 gene.

Also known as: CLCN2 generalised epilepsy, CLCN2 generalized epilepsy, EIG11, epilepsy, idiopathic generalized, susceptibility to, 11, epilepsy, idiopathic generalized, susceptibility to, type 11, generalised epilepsy caused by mutation in CLCN2, generalized epilepsy caused by mutation in CLCN2, epilepsy, juvenile absence, susceptibility to, 2

0 clinical trials for this condition and its sub-types, 0 tagged with Epilepsy, idiopathic generalized, susceptibility to, 11 itself.

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↑ Epilepsy, juvenile absence, susceptibility to (0)

Including sub-types (0) Tagged with Epilepsy, idiopathic generalized, susceptibility to, 11 (0)

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