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 cancer affecting the membranes surrounding the spinal cord.
is a rare spinal cord lining tumor that can return after treatment.
is a genetic disorder that weakens muscles and affects breathing.
is a rare genetic disorder causing muscle weakness and brain abnormalities.
is a very severe genetic muscle-weakness disorder present before birth.
is a rare inherited muscle-weakness disorder mainly affecting the legs.
is a rare inherited disorder causing progressive leg weakness and muscle wasting.
is a genetic nerve disorder causing progressive leg weakness and muscle wasting.
is a rare inherited muscle weakness disorder mainly affecting the legs.
is a rare genetic neuromuscular disorder causing infant breathing and muscle weakness.
is a rare inherited disorder causing muscle weakness and serious breathing problems.
is a very rare genetic condition affecting muscles, brain development, and eyes.
is a rare inherited disorder causing muscle weakness and recurrent seizures.
is a rare genetic disorder causing nerve tumors mainly along the spine.
is a viral infection that can affect nerves and cause paralysis.
causes narrowing in the spine that can press on nerves.
is a rare, benign blood vessel growth usually affecting hands or feet.
is a rare eye cancer that starts in pigment-producing cells.
is a rare, benign fatty tumor usually found under the skin.
is a rare cancer of fatty tissue with spindle-shaped tumor cells.
is a rare, usually noncancerous tumor of the pituitary gland.
is a rare cancer of muscle-forming tissue, usually affecting children.
is a rare connective tissue cancer arising from spindle-shaped cells.
is a rare soft tissue cancer that often starts near joints.