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 thyroid cancer that usually grows slowly and is often treatable.
is a rare thyroid cancer that can sometimes spread beyond the gland.
is a rare thyroid cancer from C cells, sometimes inherited (MEN2).
is a very rare thyroid cancer with mixed mucus-producing and squamous cells.
is the most common thyroid cancer and often highly treatable.
is a rare birth condition where one thyroid lobe never develops.
is a rare genetic condition causing poor response to thyroid hormone.
is a usually benign thyroid tumor made of Hurthle cells.
is a rare thyroid tumor that is usually benign.
is a congenital condition where the thyroid gland is underdeveloped or absent.
is a rare thyroid cancer that can cause a fast-growing neck lump.
is a birth defect where the thyroid gland forms abnormally.
is a rare cancer that begins in the thyroid gland's tissues.
is inflammation of the thyroid gland that can affect hormone levels.
is an autoimmune thyroid-related eye condition causing bulging eyes and irritation.
causes sudden episodes of muscle weakness from low potassium due to hyperthyroidism.
is a condition where too much thyroid hormone speeds up the body.
is a rare, slow-growing bone cancer that usually affects the shinbone.
is a genetic condition causing absent shinbones and split hands or feet.
is inflammation of a fluid-filled sac near the inner knee.
is a rare birth difference where the shinbone is underdeveloped or missing.
is a rare genetic condition affecting leg, thumb, and toe development.
is a late-onset muscle disease causing lower-leg weakness and foot drop.
is nerve damage causing foot weakness, numbness, and trouble pointing toes.