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Nystagmus 1, congenital, X-linked

MONDO:0010693

Any congenital nystagmus in which the cause of the disease is a mutation in the FRMD7 gene.

Also known as: FRMD7 congenital nystagmus, congenital nystagmus caused by mutation in FRMD7, nystagmus 1, congenital, X-linked, NYS1, NYSTAGMUS 1, congenital, X-linked, Nystagmus 1, congenital, X- linked, Nystagmus 1, infantile, X-linked, Nystagmus, congenital motor, 1

1 clinical trial for this condition and its sub-types, 0 tagged with Nystagmus 1, congenital, X-linked itself.

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