Nystagmus 1, congenital, X-linked
MONDO:0010693Any 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.
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