Congenital Nystagmus

About the Disease
Congenital Nystagmus, also known as nystagmus, congenital, is related to nystagmus 7, congenital, autosomal dominant and nystagmus 6, congenital, x-linked, and has symptoms including deficiencies of smooth pursuit movements An important gene associated with Congenital Nystagmus is FRMD7 (FERM Domain Containing 7), and among its related pathways/superpathways are Visual Cycle in Retinal Rods and Visual signal transduction: Cones. Affiliated tissues include eye, brain and fetal brain, and related phenotypes are behavior/neurological and vision/eye

Common Targets
TRNR | TYR | Voltage-Gated Sodium Channel Complex | Sodium channel (nonspecified subtype) | ND1 | Acetylcholine Receptors (Nicotinic) (nAChR) (nonspecified subtype) | TULP1 | POLG | NMDA receptor | ATP6 | PAX6 | CRYBA1 | CASK | COL11A1 | SLC38A8 | TYRP1 | CACNA1F | FRMD7

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