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 of mature T cells in the lymphatic system.
reduces limb blood flow from narrowed arteries, causing walking leg pain (claudication).
is a common cause of sudden dizziness from inner ear problems.
is a noncancerous growth in the lining of the abdomen.
is cancer of the peritoneum (abdominal lining), causing pain and fluid buildup.
is a rare tumor of the abdominal lining with fluid-filled cysts.
is a rare cancer of the abdominal lining, often linked to asbestos.
is a rare cancer that starts in the lining of the abdomen.
is a rare cancer of the abdominal lining, similar to ovarian cancer.
is inflammation of the abdominal lining, usually caused by infection.
is a rare tumor that can develop in many body organs.
is a rare tumor that can develop in soft tissues or organs.
is a rare growth around blood vessels, with behavior varying by type.
is a brain injury affecting white matter near the brain's ventricles.
is a brain development disorder with nerve cell nodules near ventricles.
is a rare genetic disorder affecting bone growth, joints, and movement.
is a rare inherited overgrowth disorder with kidney anomalies and tumor risk.
is a lifelong thyroid hormone deficiency present from birth.
is a rare, lifelong diabetes starting before 6 months, usually genetic.
is a rare genetic disorder causing permanent newborn diabetes and cerebellar abnormalities.
is an autoimmune condition that causes vitamin B12 deficiency and anemia.
causes weakness or numbness in the lower leg and foot.
is a rare inherited peroxisomal disorder affecting fatty acid breakdown, causing neurodegeneration.