X-linked cone-rod dystrophy 1

X-linked cone-rod dystrophy 1 is a rare inherited eye condition that affects the retina. This condition is known by several names, including COD1, CORDX1, and X-linked cone-rod dystrophy type 1. People with this condition have changes in their retina that can impact the functioning of cones and rods, the cells responsible for seeing color and light in low-light conditions, respectively. The information available from the provided sources is limited, but it is noted that the RPGR gene is associated with this condition. The fact that the condition follows an X-linked inheritance pattern means that the gene change is located on the X chromosome, which can influence who is affected in a family.

Information about symptoms is currently limited for this condition.

X-linked cone-rod dystrophy 1 is linked to changes in the RPGR gene, which plays a role in the normal function of the retina. The condition follows an X-linked pattern of inheritance, meaning that the gene change is found on the X chromosome. This genetic factor is a key cause of the condition.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about current research is currently limited for this condition.