Epilepsy, familial focal, with variable foci 3

MONDO:0014925

Any epilepsy, familial focal, with variable foci in which the cause of the disease is a mutation in the NPRL3 gene.

Also known as: FFEVF3, NPRL3 epilepsy, familial focal, with variable foci, epilepsy, familial focal, with variable foci 3, epilepsy, familial focal, with variable foci 3; FFEVF3, epilepsy, familial focal, with variable foci caused by mutation in NPRL3, epilepsy, familial focal, with variable foci type 3

10 clinical trials for this condition and its sub-types, 0 tagged with Epilepsy, familial focal, with variable foci 3 itself.

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↑ Familial focal epilepsy with variable foci (0)

Including sub-types (10) Tagged with Epilepsy, familial focal, with variable foci 3 (0)

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