rs2032582 is a genetic variant on gene ABCB1 associated with Inflammatory bowel disease 13.
rs10876864 is a genetic variant on gene IKZF4 associated with Intelligence and Allergic disease.
rs11540652 is a genetic variant on gene TP53 associated with Li-fraumeni syndrome 1 and Multiple myeloma.
rs104894226 is a genetic variant on gene HRAS associated with Costello syndrome and Large congenital melanocytic nevus.
rs7274581 is a genetic variant associated with Alzheimer's disease.
rs10808546 is a genetic variant associated with Abdominal aortic aneurysm.
is a rare condition with abnormal blood vessel connections affecting the spine.
is a rare inherited disorder affecting muscles, eye movement, and nerve function.
is a usually slow-growing tumor in the spinal canal or cord.
is a tumor inside the spinal canal but outside the spinal cord.
is cancer that begins in or spreads to the spine.
is a rare, slow-growing bone cancer that forms along the spine.
is a rare spinal cord tumor that can affect movement and sensation.
is a rare, benign cyst in or near the spinal cord.
is a spinal cord condition causing movement, sensation, or bladder problems.
causes damage to the spinal cord, affecting movement, feeling, and body functions.
is a rare tumor containing different tissues within the spinal cord.
is a fatty growth on the spinal cord, present at birth.
is a rare cancer affecting the spinal cord and nearby tissues.
is a rare cancer arising from pigment-making cells in the spinal cord.
is a rare cancer from immature nerve cells near the spine.
is a rare spinal cord tumor arising from oligodendrocyte-like cells.
is a rare spinal cord cancer made of immature nerve cells.
is a rare cancer that starts in tissues around the spinal cord.
is a rare birth defect linking skin to the spinal canal.
is a broad term for conditions affecting the spine and nerves.
is a birth defect where spinal tissues protrude through the back.
is a rare, aggressive spinal cord tumor linked to extra MYCN copies.