Seizures, benign familial infantile, 5

MONDO:0014903

Any benign familial infantile epilepsy in which the cause of the disease is a mutation in the SCN8A gene.

Also known as: BFIS5, SCN8A benign familial infantile epilepsy, benign familial infantile epilepsy caused by mutation in SCN8A, seizures, benign familial infantile, 5, seizures, benign familial infantile, 5; BFIS5, seizures, benign familial infantile, type 5, convulsions, benign familial infantile, 5

7 clinical trials for this condition and its sub-types, 0 tagged with Seizures, benign familial infantile, 5 itself.

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↑ Benign familial infantile epilepsy (0)

Including sub-types (7) Tagged with Seizures, benign familial infantile, 5 (0)

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