Cone-Rod Dystrophy, X-Linked, 3 (CORDX3)

Cone-Rod Dystrophy, X-Linked, 3, also known as x-linked cone-rod dystrophy 3, is related to cone-rod dystrophy, x-linked, 1 and x-linked congenital stationary night blindness. An important gene associated with Cone-Rod Dystrophy, X-Linked, 3 is CACNA1F (Calcium Voltage-Gated Channel Subunit Alpha1 F), and among its related pathways/superpathways are Neuropathic Pain-Signaling in Dorsal Horn Neurons and Celecoxib Pathway, Pharmacodynamics. Affiliated tissues include eye, and related phenotypes are nystagmus and photophobia