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Epilepsy, idiopathic generalized, susceptibility to, 10

MONDO:0013103

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

Also known as: EIG10, epilepsy, idiopathic generalized, 10, epilepsy, idiopathic generalized, susceptibility to, 10, epilepsy, idiopathic generalized, susceptibility to, type 10, epilepsy, juvenile myoclonic, susceptibility to, susceptibility to idiopathic generalised epilepsy 10, susceptibility to idiopathic generalized epilepsy 10, GEFS+, type 5, susceptibility to

0 clinical trials for this condition and its sub-types, 0 tagged with Epilepsy, idiopathic generalized, susceptibility to, 10 itself.

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