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 that starts in myoepithelial cells, usually in glands.
is a rare tumor of myoepithelial cells, usually in salivary glands.
is a chronic pain disorder caused by sensitive trigger points in muscles.
is a group of inherited muscle disorders causing progressive weakness.
is an inherited muscle disorder causing weakness and abnormal protein buildup.
is a rare inherited muscle disorder causing weakness and movement problems.
is a genetic muscle disorder causing progressive muscle weakness.
is an inherited muscle disorder causing progressive weakness, sometimes heart problems.
is a genetic muscle disorder causing progressive weakness and sometimes heart involvement.
is a rare genetic muscle disorder causing progressive weakness and cardiomyopathy.
is a rare inherited muscle disease causing progressive weakness and muscle damage.
is a rare inherited muscle disease causing progressive weakness and movement problems.
is a usually noncancerous tumor of fibrous tissue, often in infancy.
is a condition where muscle breakdown releases myoglobin into the urine.
is a usually noncancerous growth of muscle tissue, often in the uterus.
is a rare inherited disorder causing muscle weakness and loose, fragile joints.
is a rare gut muscle disorder causing blockage-like symptoms without obstruction.
is a muscle disease that causes weakness and movement problems.
is a muscle disease linked with weakness and diabetes.
affects the eye muscles, causing limited movement and often drooping eyelids.
is a rare inherited muscle disease causing weakness and abnormal muscle fibers.
is a rare inherited mitochondrial disorder affecting muscles, blood, and energy production.
is a rare inherited disorder causing muscle weakness, lactic acidosis, and anemia.